Design, Fabrication and Metrology of Precision Molded Freeform Plastic Optics DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Likai Li Graduate Program in Industrial and Systems Engineering The Ohio State University 2014 Dissertation Committee: Dr. Allen Y. Yi, Advisor Dr. Jose M. Castro Dr. Thomas W. Raasch Copyright by Likai Li 2014 Abstract The main focus of this dissertation is to seek scientific knowledge and fundamental understanding of molding process for freeform optical lens fabrication by integrating freeform optical design, precision freeform molding making, numerical modeling of polymer lens forming process, and evaluation of the molded freeform optics. Compared with conventional optics, freeform optics provides more flexibilities and better performance. However, due to the complex nature of freeform optics manufacturing processes, the productivity and quality is difficult to improve, which subsequently results in higher manufacturing cost. Therefore, in order to create affordable freeform lenses with high quality, the method combining ultraprecision diamond machining and optical molding is proposed. Ultraprecision diamond machining is a process that allows us to generate precision freeform optical features on mold surfaces without post polishing, while microinjection/compression molding is proven high volume manufacturing process used to reduce production cost. The diamond machining for both regular metal materials and brittle materials are discussed to obtain high quality molds with optical finish. In addition, two novel process designs are presented to fabricate hybrid glass-polymer achromatic lenses using compression molding and injection molding, respectively. Once the low cost molded freeform optical components are achieved, their optical performance needs to be characterized to ensure quality in mass production. The ii refractive index variation and geometric deformation are two important factors that influence the final optical performance considerably. So, finite element method is utilized to simulate the manufacturing processes to obtain inhomogeneous refractive index distribution and thickness variation. The obtained FEM information is used to derive and predict the optical performance based on wavefront optics theory. In order to verify the simulated results, conventional measurement setups are modified based on characteristics of specific freeform optics to evaluate its optical properties. The numerical simulation and experimental results are in good agreement with each other. Therefore in order to solve the major challenges in manufacturing affordable high quality freeform optics, this dissertation will include several key steps: 1) Establish point-topoint mapping freeform optics design strategy using freeform microlens array for uniform beam shaping as an example; 2) Evaluate ultraprecision mold machining on both regular metal materials and brittle materials to achieve high quality molds with optical finish; 3) Develop novel manufacturing process designs to fabricate compression molded hybrid achromatic glass-polymer microlens array and injection molded hybrid glasspolymer achromatic lens; 4) Establish a methodology combining finite element method and wavefront optics theory to model the optical performances of molded freeform lenses; 5) Design proper measurement systems including Shack-Hartmann sensor and wet cell based optical interferometer to evaluate the molded freeform lenses and verify the previously modeled results. Overall, this dissertation describes a comprehensive understanding of affordable freeform optics manufacturing. iii Dedication This dissertation is dedicated to my parents, Mr. Zhengping Li and Mrs. Xihong Han. iv Acknowledgments I owe my gratitude to all those people who have made this dissertation possible and because of whom my PhD experience has been one that I will cherish forever. I would like to express my most sincere gratitude to my advisor, Prof. Allen Yi. I thank him for guiding me into the world of precision optics. It is my great pleasure to work with him, a patient and understanding advisor. Prof. Yi offers me enough free space to expand my knowledge independently. We share the wonders and frustrations of the engineering research during my entire PhD life. He is always ready to provide me guidance, encouragement and support. As an old Chinese saying goes, he is a good mentor but also a nice friend. I enjoyed working with Prof. Thomas Raasch for building up the Shack-Hartmann sensor and conducting the wavefront optics metrology. I like to thank assistance and comments from other faculty members at Ohio State who I have worked with: Prof. Jose Castro and Prof. James Lee. My thanks also go to my colleagues in Germany for providing me support on fabrication of molded glass and plastic optics: Fritz Klocke, Fei Wang, Kyriakos Georgiadis and Olaf Dambon at Fraunhofer Institute for Production Technology (IPT) in Aachen; Ingo Sieber and Ulrich Gengenbach at Karlsruhe Institute of Technology (KIT) in Eggenstein-Leopoldshafen; Erik Beckert, Ralf Steinkopf at Fraunhofer Institute for Angewandte Optik und Feinmechanik (IOF) in Jena. In addition, v I thank the continuous professional technical support from the engineers of Moldex3D North America in Michigan. Sincere thanks are extended to all my colleagues and fellow students, for our inspiring discussion and incredible cooperative work: Dr. Lei Li, Dr. Yang Chen, Dr. Lijuan Su, Dr. Can Yang, Dr. Hao Zhang, Dr. Bo Tao, Dr. Jingbo Zhou, Peng He, Hui Li, David McCray, Neil Naples, Joshua Hassenzahl and Amin Moghaddas. Perhaps my lunch conference with nine-year classmates Peng and Hui would be the most unforgettable meeting during my life. I would like to appreciate the Graduate Research Fellowship from NSF Center for Affordable Nanoengineering of Polymeric Biomedical Devices (CANPBD) and the Presidential Fellowship from the Graduate School of The Ohio State University. I am indebted to my parents, Mr. Zhengping Li and Mrs. Xihong Han. They plant the tree. It has always been watered and growing. Last but not least, my special thanks are due to my wife Ziwei Zhao. During my PhD life, she is the only person who always accompanies me and knows my happiness and pains. Without her, this dissertation could have been finished one year earlier though. vi Vita September 1987 ..............................Born, Jintan, Jiangsu, China July 2009 .........................................B.S. Precision Engineering University of Science and Technology of China Hefei, Anhui, China December 2011 ...............................M.S. Industrial and Systems Engineering The Ohio State University, Columbus, OH September 2009 ~ April 2014 .........Graduate Research Fellow Department of Integrated Systems Engineering The Ohio State University, Columbus, OH May 2014 ~ present ........................Presidential Graduate Fellow Graduate School The Ohio State University, Columbus, OH Publications 1. Li, L., Raasch, T. W., Sieber, I., Beckert, E., Steinkopf, R., Gengenbach, U., &Yi, A.Y. (2014). Fabrication of microinjection-molded miniature freeform alvarez lenses. Applied Optics, 53 (19), 4248-4255. vii 2. He, P., Li, L., Li, H., Yu, J., Lee, L. J., & Yi, A. Y. (2014). Compression molding of glass freeform optics using diamond machined silicon mold. Manufacturing Letters, 2 (2), 17-20. 3. Li, L., Raasch, T. W., & Yi, A. Y. (2013). Simulation and measurement of optical aberrations of injection molded progressive addition lenses. Applied Optics, 52 (24), 6022-6029. 4. Li, L., & Yi, A. Y. (2013). An affordable injection-molded precision hybrid glass–polymer achromatic lens. The International Journal of Advanced Manufacturing Technology, 69 (7), 1461-1467. 5. He, P., Wang, F., Li, L., Georgiadis, K., Dambon, O., Klocke, F., & Yi, A. Y. (2011). Development of a low cost high precision fabrication process for glass hybrid aspherical diffractive lenses. Journal of Optics, 13 (8), 085703. 6. Li, L., & Yi, A. Y. (2011). Design and fabrication of a freeform microlens array for uniform beam shaping. Microsystem Technologies, 17 (12), 1713-1720. 7. Li, L., He, P., Wang, F., Georgiadis, K., Dambon, O., Klocke, F., & Yi, A. Y. (2011). A hybrid polymer–glass achromatic microlens array fabricated by compression molding. Journal of Optics, 13 (5), 055407. 8. Sieber, I., Martin, T., Yi, A., Li, L., & Ruebenach, O. (2014). Optical design and tolerancing of an ophthalmological system. In SPIE Optical Engineering+ Applications (Vol. 9195, pp. 919504). 9. Li, L., Raasch, T. W., Yi, A.Y., Sieber, I., Gengenbach, U., Beckert, E., & Steinkopf, R. (2014). Fabrication of microinjection-molded miniature freeform viii alvarez lenses. In ASPE/ASPEN Summer Topical Meeting, Kohala Coast, Hawaii, USA. 10. Sieber, I., Yi, A., Li, L., Beckert, E., Steinkopf, R., & Gengenbach, U. (2014). Design of freeform optics for an ophthalmological application. In Proc. of SPIE (Vol. 9131, pp. 913108-1). 11. Li, L., Yi, A. (2013). Design and manufacturing of an affordable injection molded precision hybrid glass-polymer achromatic lens. In Proc. of ANTEC Annual Conference, Cincinnati, OH, USA. 12. He, P., Wang, F., Li, L., Georgiadis, K., Klocke, F., & Yi, A. Y. (2010). Compression molding of refractive and diffractive hybrid glass lenses. In ASPE Annual Conference, Atlanta, GA, USA. Fields of Study Major Field: Industrial and Systems Engineering ix Table of Contents Abstract ............................................................................................................................... ii Dedication .......................................................................................................................... iv Acknowledgments............................................................................................................... v Vita.................................................................................................................................... vii Table of Contents ................................................................................................................ x List of Tables ................................................................................................................... xiv List of Figures ................................................................................................................... xv Chapter 1. Introduction ................................................................................................... 1 1.1 Optical design ....................................................................................................... 1 1.2 Ultraprecision machining ..................................................................................... 3 1.3 Molding processes ................................................................................................ 5 1.4 Molded freeform optics modeling and metrology................................................ 7 Chapter 2. Research Objectives .................................................................................... 10 Chapter 3. Freeform Optics Design .............................................................................. 11 3.1 Design of the freeform microlens array ............................................................. 11 3.2 Manufacturing process for the freeform microlens array................................... 16 x 3.2.1 Geometric design of tool path ..................................................................... 16 3.2.2 Fabrication of freeform microlenses ........................................................... 17 3.3 Geometric and optical evaluations ..................................................................... 19 3.3.1 Surface geometry measurement .................................................................. 19 3.3.2 Ray tracing simulations............................................................................... 21 3.3.3 Optical performance measurement ............................................................. 22 Chapter 4. 4.1 Precision Machining for Optical Molding .................................................. 26 Diamond machining on regular metals .............................................................. 26 4.1.1 Slow tool servo machining.......................................................................... 26 4.1.2 Diamond turning ......................................................................................... 29 4.1.3 Surface coating for nickel glass mold ......................................................... 30 4.2 Diamond machining on silicon wafer ................................................................ 32 4.2.1 Modeling of 3D damage distribution .......................................................... 34 4.2.2 Machining experiments ............................................................................... 37 4.2.3 Glass molding experiments ......................................................................... 39 4.2.4 Results and discussions ............................................................................... 41 4.3 Tool path optimization ....................................................................................... 48 Chapter 5. 5.1 Molding Processes for Achromatic Lenses................................................. 51 Achromatic lens design ...................................................................................... 52 xi 5.2 Compression molded hybrid achromatic microlens array.................................. 53 5.2.1 Optical design of hybrid microlens array.................................................... 54 5.2.2 Compression molding processes ................................................................. 55 5.2.3 Simulation of compression molding ........................................................... 62 5.2.4 Geometry and optical evaluation ................................................................ 68 5.3 Injection molded hybrid glass-plastic achromatic lens ...................................... 72 5.3.1 Design of fabrication processes .................................................................. 72 5.3.2 Microinjection molding simulations ........................................................... 76 5.3.3 Lens fabrications ......................................................................................... 80 5.3.4 Optical measurements ................................................................................. 82 Chapter 6. Modeling of Optical Performance of Molded Freeform Optics ................. 84 6.1 FEM modeling for precision molding ................................................................ 85 6.2 Prediction of optical performance influenced by molding process .................... 88 Chapter 7. 7.1 Optical Metrology of Molded Freeform Optics .......................................... 91 Shack-Hartmann wavefront sensing measurement ............................................ 92 7.1.1 PAL design.................................................................................................. 93 7.1.2 PALs fabrication ......................................................................................... 94 7.1.3 Simulated wavefront pattern of PALs......................................................... 96 7.1.4 Wavefront measurement of PALs ............................................................... 97 xii 7.1.5 7.2 Results and discussions ............................................................................... 99 Interferometer measurements ........................................................................... 105 7.2.1 Optical design ........................................................................................... 106 7.2.2 Manufacturing of Alvarez lenses .............................................................. 107 7.2.3 Wavefront prediction and simulation........................................................ 109 7.2.4 Results and discussions ............................................................................. 113 Chapter 8. Conclusions ............................................................................................... 121 References ....................................................................................................................... 123 Appendix A: Replicated Microoptical Arrays for Multiple 3D Optical Trapping ......... 137 A.1 Introduction .......................................................................................................... 137 A.2 Competitive analysis ............................................................................................ 137 A.3 Experiment setup and results ................................................................................ 138 A.4 Summary and future work .................................................................................... 141 xiii List of Tables Table 4.1. Rough and fine machining parameters ............................................................ 38 Table 5.1. Mechanical and thermal properties of P-SK57 glass. ..................................... 62 Table 5.2. Structural relaxation rarameters of P-SK57 used in numerical simulation. .... 63 Table 5.3. Boundary Conditions for Glass and Polymer Molding. .................................. 63 Table 5.4. Mechanical and thermal properties of polycarbonate. .................................... 66 Table 5.5. Viscoelastic parameters of polycarbonate used in numerical simulation. ...... 67 Table 5.6. Design parameters for the aspherical surface.................................................. 76 Table 5.7. Simulation process conditions used for two different thicknesses.................. 78 Table 6.1. Material parameters of PMMA. ...................................................................... 86 Table 6.2. Injectin molding condition. ............................................................................. 87 Table 7.1. Injection molding conditions for design of experiment ................................ 104 Table 7.2. Microinjection molding conditions ............................................................... 109 xiv List of Figures Figure 3.1. Geometry of ray tracking using Snell's law. .................................................. 13 Figure 3.2. (a) Geometrical layout of light redistribution from the microcell region L to the target region M. In the example illustrated in this figure, P = 4 and Q = 3; (b) shaded model of the light redistribution by the freeform microlens. ............................................ 14 Figure 3.3. (a) A single freeform microlens surface. (b) Layout of ray tracing of a single freeform microlenslet projecting onto the target surface. (c) Close-up view of ray tracing of a single freeform microlenslet. ..................................................................................... 16 Figure 3.4. Schematic of tool compensation. ................................................................... 17 Figure 3.5. (a) Pictures of the finished mold insert and the injection molded freeform microlens arrays. (b) Two buffer areas indicated in the pictures are designed to protect the tool cutting edge from making oversize cut into the work piece. ............................... 19 Figure 3.6. The solid lines are measured 2D surface profiles along the line y=0 mm from the center to the edge (corresponding to Figure 3.3(a)) of the mold insert and the molded lens. The dashed lines are geometry errors of surface profiles along the line y=0 mm of molding insert and molded piece. ..................................................................................... 20 Figure 3.7. (a) Surface roughness measurement of the mold insert. (b) Surface roughness measurement of the molded microlens. ............................................................................ 21 Figure 3.8. Simulated light distribution on the target surface. ......................................... 22 Figure 3.9. Measured light distribution on the target surface. ......................................... 23 xv Figure 3.10. (a) Comparison of the simulated and experimental corresponding line distributions along the x axis across the center of the illumination. (b) Comparison of the simulated and experimental line distribution along the y axis across the center of the illumination. ...................................................................................................................... 24 Figure 3.11. Schematic of overcut due to the radius of the diamond tool. ...................... 25 Figure 4.1. Broaching tool path for: (a) glass microlens array, (b) polycarbonate microlens array. The spacing between neighboring steps is reduced and the return tool paths are removed for clarity. ........................................................................................... 27 Figure 4.2. Pictures of the finished (a) copper nickel mold for glass and (b) aluminum mold for polymer. ............................................................................................................. 28 Figure 4.3. Picture of the finished ultraprecision diamond turned mold inserts for the hybrid lens microinjection molding. ................................................................................. 29 Figure 4.4. SEM (scanning electron microscope) photo of the Pt-Ir coating with nickel adhesion layer. .................................................................................................................. 31 Figure 4.5. Brittle to ductile transition based on STS machining process configuration. 35 Figure 4.6. Flowchart of the 3D damage distribution calculation program ..................... 36 Figure 4.7. Design of a square microlens array. Unit is m. ........................................... 37 Figure 4.8. Microscopic pictures of the microlens arrays machined under conditions of (a) condition 1 and (b) condition 2 in Table 4.1............................................................... 39 Figure 4.9. Silicon mold and molded glass microlens array. ........................................... 40 Figure 4.10. (a) Measured profiles of the silicon mold and (b) the molded glass microlens array. (c) Geometry deviation between the mold and molded glass optics. Unit is mm. . 41 xvi Figure 4.11. Calculated 3D damage distributions of a microlens machined under (a) condition 1 and (b) condition 2. (c) and (d) are the top views of (a) and (b) respectively. Microscopic pictures of a microlens machined under (e) condition 1 and (f) condition 2. Unit is mm......................................................................................................................... 43 Figure 4.12. Calculated subsurface damage distributions of a microlens if the constant damage depth model is used. Unit is mm. ........................................................................ 44 Figure 4.13. 3D damage distribution simulations of the microlens on silicon at the middles of the (a) 5th, (b) 8th, (c) 11th and (d) 18th machining pass of the machining experiments conducted under condition 2. Unit is mm. ................................................... 46 Figure 4.14. Cutting path planning strategies: (a) constant cutting depth; (b) constant cutting ratio. Unit is mm. .................................................................................................. 47 Figure 4.15. Cross sections of concave, spherical lenslets on convex, spherical substrates. (a) Traditional, unblended, discontinuous lenslet. The thick blue line is machined, discontinuity and all. (b) Traditional lenslet blended with a torus. The thick blue line is machined, blend and all. (c) Lenslet with blending in the air. Only the thick blue line is machined, which is exactly the whole, original lenslet. Original lenslet aperture is marked by 2 magenta asterisks. ..................................................................................................... 49 Figure 4.16. Lenslet close-ups. (a) Traditional STS method with unblended lenslets. Sliced apertures are clearly visible, rendering the component useless. (b) Close up of unblended lenslet. (c) Blended lenslets machined with the original blend torus method. The tool path and physical array are both clearly continuous. (d) Close of up blended lenslet. A reduction in aperture radius can be seen as compared to a discontinuous lenslet of the same size. (e) Totally discontinuous lenslets machined with the BTA method. The xvii tool path in this case was totally continuous. (f) Close up of lenslet machined with BTA method. The aperture is discontinuous and visibly seems to be of superb quality. This method does not compromise an optical design in any way. ............................................ 50 Figure 5.1. Geometric layout of the achromat doublet design. ........................................ 54 Figure 5.2. Chromatic focal shift of one hybrid polymer-glass microlens doublets. ....... 55 Figure 5.3. Molding processes for the hybrid polymer-glass microlens array: (a)~(c) glass molding process, (d)~(f) polymer molding process. ................................................ 57 Figure 5.4. (a) Molding force and lower mold position as function of time. (b) Molding force and temperature control as function of time. ........................................................... 58 Figure 5.5. (a) Molded glass microlens array. (b) The finished hybrid polymer-glass microlens array.................................................................................................................. 61 Figure 5.6. Material properties of the P-SK57 glass used in the simulation. (a) Thermal conductivity [W/m°C] as a function of temperature [°C]. (b) Specific heat [J/kg °C] variation as a function of temperature [°C]. (c) Coefficient of thermal expansion [/°C] as a function of temperature [°C]. (d) Stress relaxation properties curve: shear constant [Pa] versus time [s] (in logarithm scale). .................................................................................. 64 Figure 5.7. (a) Meshed FEM model of glass molding for microlens. (b) Final shape of the glass microlens after cooling. ........................................................................................... 65 Figure 5.8. Comparison of simulated and experiment surface profiles of one microlens for (a) P-SK57 glass and (b) polycarbonate. ..................................................................... 68 Figure 5.9. 2D surface profiles and geometry errors along the diameter of the mold and the molded sample of one single microlens. (a) Surface profiles of the mold and molded glass lens. (b) Surface profiles of the mold and molded polymer lens. ............................ 69 xviii Figure 5.10. Schematic of the setup for measuring the chromatic focal shift: (1) laser source, (2) linear polarizers, (3) pinhole, (4) field lens, (5) hybrid lens mounted on a precision translation stage and (6) CCD camera............................................................... 70 Figure 5.11. Comparison of calculated and experiment results of chromatic focal shift of the hybrid polymer-glass doublet...................................................................................... 71 Figure 5.12. Manufacturing processes of the hybrid glass-polymer lens by microinjection molding. The right mold insert is used to house the glass lens while the left side has the aspherical surface for the polymer lens. The blue area is the glass lens and the red is the injection molded polycarbonate polymer.......................................................................... 73 Figure 5.13. Achromatic doublet design (unit: mm). ....................................................... 74 Figure 5.14. (a) Meshed Model I for the injection molded part and the part insert and (b) meshed microinjection molding system model including the cooling channels and mold base. .................................................................................................................................. 77 Figure 5.15. Comparison of simulation (a and c) and experimental results (b and d) of the melt front flow pattern for Model I during filling............................................................. 78 Figure 5.16. Melt front (shown in time) of the injection molded polymer part of Model II during filling. .................................................................................................................... 79 Figure 5.17. Simulated part deformation under different packing pressure. ................... 80 Figure 5.18. Picture of a complete hybrid glass-polymer lens manufactured by microinjection molding (shown with gate, runner and spruce). ....................................... 81 Figure 5.19. Comparison of the calculated and measured results of the chromatic focal shift of the hybrid lens. ..................................................................................................... 82 xix Figure 6.1. Meshed FEM model of a Progressive Addition Lens (PAL). Node(i,1) is numbered along number i line at the bottom surface of PAL, and Node(i,N) is the node along number i line at its top surface. ............................................................................... 85 Figure 7.1. Freeform surface of the backside of the PAL. The first polynomial term was removed to show the freeform geometry. ......................................................................... 94 Figure 7.2. Finished ultraprecision diamond turned mold inserts for PAL injection molding. ............................................................................................................................ 95 Figure 7.3. PALs manufactured by microinjection molding. .......................................... 95 Figure 7.4. Schematic of the wavefront measuring system. 1: Distant source; 2: PAL under test; 3 and 4: 150 mm fl lenses; 5: Shack-Hartmann sensor. .................................. 98 Figure 7.5. Simulated refractive index variation of an injection molded PAL. ............... 99 Figure 7.6. Simulated thickness change in xy plane of the molded PAL. ...................... 101 Figure 7.7. Spherical power M of the molded PAL (a) design (b) simulation (c) measurement ................................................................................................................... 102 Figure 7.8. Cylindrical component J0 of the injection molded PAL (a) design (b) simulation (c) measurement ............................................................................................ 103 Figure 7.9. Comparison of (a) design, (b) simulated and (c) measured cylindrical component J45 of the injection molded PAL................................................................... 103 Figure 7.10. Top freeform surface of Alvarez lens. ....................................................... 107 Figure 7.11. (a) Finished ultraprecision diamond machined mold for injection molding. (b) 3D model of the molded Alvarez lens with small straight pins and flats designed for assembly. ......................................................................................................................... 108 Figure 7.12. An injection molded Alvarez lens. ............................................................ 109 xx Figure 7.13. FEM mesh model of the Alvarez lens. Node (i, 1) is numbered along the vertical line at coordinates (xi, yi) at the bottom surface, and Node (i, N) is the node along the vertical line at coordinates (xi, yi) at its top surface. ................................................. 110 Figure 7.14. Interferometry setup for measuring wavefront pattern of microinjection molded Alvarez lens immersed in a wet cell. 1: He-Ne laser light source; 2: optical pin hole; 3: collimation lens; 4: beam splitter A; 5: flat mirror A; 6: flat mirror B; 7: Alvarez lens immersed in a wet cell; 8: beam splitter B; 9: CCD camera; 10: PZT stage. .......... 112 Figure 7.15. (a) Simulated and (b) measured bottom surface deformations of the microinjection molded Alvarez lens. .............................................................................. 114 Figure 7.16. Simulation plot of the deformed microinjection molded Alvarez lens with a magnification scale of 50X. ............................................................................................ 115 Figure 7.17. (a) Simulated and (b) measured wavefront pattern describing refractive index distribution of the microinjection molded Alvarez lenses. ................................... 116 Figure 7.18. (a) Nominal and (b) measured wavefront pattern describing surface power distribution of the microinjection molded Alvarez lenses. (c) Difference between the simulated and the measured results................................................................................. 117 Figure 7.19. Optical path change on the freeform surface. ............................................ 119 Figure A.1. Optical setup of the integrated multiple trapping system. .......................... 139 Figure A.2. Compression molded glass microlens array used in hybrid glass-polymer microlens assmely. .......................................................................................................... 140 Figure A.3. (a) Multiple laser focal spots generated by the optical setup discussed before (b) trapped polystyrene beads ......................................................................................... 141 xxi Chapter 1. Introduction A freeform optical component in this research is loosely defined as an optical element that is not symmetric around its optical axis. It provides some attractive features to optical designers to create innovative products: a) more design flexibilities of surface geometry; b) ability to correct multiple aberrations with fewer or one optical surfaces; c) reduced number of optical elements, package size and weight; d) easy system integration (Fang, et al., 2013). Because of the benefits brought by freeform optics, manufacturing of freeform optics is a promising technology today in various fields, such as biomedical engineering, mobile electronic device, energy, automobile, aerospace and so on. The entire freeform optics manufacturing consists of design, machining, forming, metrology and characterization. All these fields and their standardization are still developing. This dissertation focuses on the fabrication processes of affordable freeform plastic optics and its related optical design and metrology. 1.1 Optical design Usually the freeform optics design can be realized by multi parameter optimization and direct mapping. In the approach of multi-parameter optimization, the freeform surface can be described a certain polynomial equation with multiple parameterized coefficients. According to design requirements, a merit function is defined that how far the current design is away from the target, while the coefficients defining the freeform surface are 1 varied to find local or global minimum of the merit function. However, due to intrinsic complicated nature of freeform optics, the results usually are not satisfied. Therefore, some advanced direct mapping methods are proposed to solve the challenges in the freeform optics design. Partial differential equation (PDE) is used to establish the relationship between the target surface, freeform optical surface and space vector of incident light (Ries & Rabl, 1994). This method is based on the energy conservation and tailoring theory which redistribute the radiation of light source onto a given desired distribution (Winston, et al., 2005; Ries & Muschaweck, 2002). Ries & Muschaweck obtained the tailored freeform surface for an arbitry irradiance distribution by solving a set of partial deiffential equation with the curvature and slope. However, when the target patten becomes more complicated, the solutions of partial differential equation method are more challenging. Oliker presented an alternate freeform reflector design with riorous mathematical theory but for a generic application (Oliker, 2005; Oliker, 2006). He established an iteration process of combining a series of elliptical reflector into one freeform surface to redistribute the irradiance of a point light source to an arbitrary pattern. Similar to Oliker’s idea, Michaelis et al. developed a method that assembles sets of Cartesian ovals into a freeform refraction surface in order to redistribute light into arbitrary pattern (Michaelis, et al., 2011). These two approaches avoids the complicated process of solving partial differential equation set. Another method for constructing the equation between the source surface and target surface is called point-to-point mapping (Fang, et al., 2013). In order to achieve certain irradiance distribution, Parkyn & Pelka proposed to divide the source and the target surface into grids using the same topology (Parkyn & Pelka, 2006). The edge relations of 2 corresponding pairs of source grid and target grid are utilized to derive the normal vectors of the lens to generate smooth surface. The topology of target grid is based on the intensity distribution of the source grid. This point-to-point mapping method has frequently been applied to LED package illumination (Wang, et al., 2010; Belousov, et al., 2008; Luo, et al., 2010). The freeform microlens array discussed in this dissertation was designed by the point-topoint mapping method (Li & Yi, 2011). It is capable of redistributing a collimated light into a pre-determined, in this case, a uniform pattern. This freeform microlens array design requires fewer optical elements compared with classic uniform illumination system, and also reduces alignment difficulty. The fabricated optical element in this research could achieve light re-distribution at the target with approximately 80% uniformity. 1.2 Ultraprecision machining In recent years, different methods have been investigated for fabrication of optical freeform surfaces in order to obtain high quality components. These techniques include diamond micromilling (Brinksmeier & Autschbach, 2004; Stoebenau & Sinzinger, 2009), ultraprecision diamond turning (Yi & Li, 2005; Yi, et al., 2006), diamond flycutting (Stoebenau & Sinzinger, 2009) and ultraprecision grinding (Van Ligten & Venkatesh, 1985). Diamond micromilling is an alternative to machining aspheric or complex lenses with small positive and negative curvatures. Diamond flycutting can be employed to generate optical elements with small radius of curvature and high aspect ratio. Ultraprecision grinding is capable of providing very fine surfaces but it is difficult to set 3 up and has relatively long machining cycles. On the other hand, diamond turning process is one of the widely used machining processes in optical industry, for example, well established fast tool servo (FTS) is applied in the area of contact lens and freeform lens manufacturing (Michaelis, et al., 2008). In a fast tool servo process, the diamond tool is mounted on a piezoelectric actuator which is capable of oscillating at extremely high frequency, and the oscillation position is determined according to both the radial and the angular position of the workpiece. However fast tool servo method also has limitations, such as the typical travel range is less than 1 mm (Tohme & Lowe, 2003). The approach used in this dissertation is slow tool servo (STS) diamond machining which is a similar but uniquely different process to fast tool servo. In slow tool servo machining, z axis slide provides the control in the direction of cutting depth. This arrangement allows large deviation on machined surfaces but has limits on the dynamic movement of the cutting tool due to inertia of the heavy mechanical slide used. The slow tool servo diamond machining can be easily applied to fabricate regular metal mold materials with optical quality, such as aluminum and copper nickel alloy. However, the machining on brittle materials, for example crystalline silicon, leads to micro fractures during material removal. Hence, ultraprecision machining of (crystalline) silicon has been studied frequently in the last two decades. The focus of the investigations has been largely on the basic understanding of the brittle to ductile transition (Blake & Scattergood, 1990). One of the key findings of these studies shows that a large negative rake angle is a critical process condition in reducing fractures and enhancing tool life (Blackley & Scattergood, 1991). In practice, diamond tool tip is simply titled against the silicon substrate, therefore the clearance angle is usually much 4 larger than the nominal value. Fang et al. introduced a concept of extrusion as opposed to shearing to explain the nanometer scale diamond turning mechanism (Fang, et al., 2005). A large negative rake angle increases the pressure on the substrate and resulting in threedimensional volumetric deformation (Patten & Gao, 2001). In a more classic view using shearing (plane) concept, energy is more concentrated on the shearing plane, generally a 2D scenario (Yan, et al., 2009). Therefore it is of great interest to understand and predict the damage distribution threedimensionally and further optimize the machining process when freeform optics is in consideration. In this dissertation, the subsurface damage model was modified to study 3D damage distribution in slow tool servo diamond machined silicon. The prediction of the 3D damage distributions on freeform surfaces were compared with experimental results and their close match demonstrated the feasibility of using this modeling technique to effectively assist freeform diamond machining on silicon or other similar brittle materials. In addition, the development of the damage distribution and two different machining strategies were analyzed in order to understand brittle material machining process and improve surface quality. 1.3 Molding processes The third step, replication process, has to be a low cost manufacturing process. For optical manufacturing, microinjection molding (Lee, et al., 2004) and hot compression molding (Yi & Jain, 2005) are two most common techniques that can be utilized. In injection molding, material is heated up above its transition temperature, then mixed, and finally forced into a mold cavity where it cools and hardens to the configuration of the 5 mold cavity. As a subset of injection molding, microinjection molding process is considered as one of the significant technologies of manufacturing high precision micro features with mass-production capability. Microinjection molding offers molded parts more accuracy and less variability by means of its special design features, i.e., a) plasticizing screw and injection plunger are separated, and both are manufactured with high precision to provide stable and uniform polymer melt, b) direct clamping pressure by central ram construction provides even distribution of clamping pressure on the platen. For hot compression molding process, the general setup is a piece of glass or polymer sandwiched between two mold halves. The blank is heated up in the vacuum furnace above its transition temperature and then squeezed between the two mold halves. Afterwards the positions of the mold halves are held for a certain period of time, and annealing is started when compression is completed. The good availability of these two replication processes ensures that the study of these two methods can be done easily both in industry and education research institute. Moreover, a wide range of transparent materials including polymer and glass both, such as polymethylmethacrylate (PMMA), polycarbonate (PC), P-SK57 glass, and BK7 glass, can be selected to work with these two methods. This dissertation presents an innovative compression process for hybrid polymer-glass microlens array (Li, et al., 2011). Both of the glass and polymer optical elements were fabricated by thermal compression molding. First a P-SK57 glass blank was pressed in a compression molding operation into the shape of a finished microlens array together with the fiducial features for subsequent alignment in thermal forming of polymer lenses. Annealing was performed after the compression molding process to minimize thermal 6 shrinkage. Compression molding is inherently designed for freeform (including microlenses) optical element fabrication (Yi, et al., 2006). One of the major advantages of a hybrid polymer-glass microlens lies in its improved performance from the thermal stability of glass and the benefit of lower manufacturing cost using commercial grade optical polymers. Besides compression molding, microinjection molding was utilized to apply the aspheric polycarbonate layer directly onto the N-BK7 glass lens surface in this unique study for its capabilities of precision micro feature replication and mass production (Li & Yi, 2013). So the combination of polycarbonate (flint glass) and N-BK7 (crown glass) can also be used to correct chromatic aberration. To ensure high precision in the fabricated hybrid lens, mechanical alignment features were created on the mold inserts to position the finished polymer lens along with the insert that housed the glass lens. It was demonstrated in this study that with properly designed manufacturing processes, an integrated hybrid glass-polymer lens could be fabricated without further mechanical alignment. 1.4 Molded freeform optics modeling and metrology The high quality requirement for freeform optical devices often leads to high manufacturing cost. Microinjection molding encounters several quality issues for optical applications. These include thermally induced shrinkage, non-uniform refractive index and birefringence. To ameliorate these quality related issues, a finite element method (FEM) has been used to model the process (Kim & Turng, 2006) and analyze its influences on optical performance of injection molded freeform optics. For example, Park 7 and Joo simulated the ray tracing inside an injection molded lens according to the FEM results (Park & Joo, 2008). Suhara constructed the refractive index distribution of an injection molded lens by using computed tomography technique (Suhara, 2002). Yang et al. studied the impact of packing pressure on refractive index variation of an injection molded flat lens and compared the simulated results with experiments (Yang, et al., 2011). Li et al. previously analyzed the optical aberrations of injection molded progressive addition lenses (Li, et al., 2013), and investigated how to apply injection molding to hybrid glass-polymer lens fabrication (Li & Yi, 2013). This study focuses on how injection molding process influences freeform optics in terms of the part’s surface deformation and refractive index variation. In this dissertation, an innovative metrology setup was proposed to evaluate the optical wavefront patterns in the molded lenses by using a Shack-Hartmann sensor or an interferometer based wavefront measurement system (Li, et al., 2013; Li, et al., 2014). The measurement system based on a Shack-Hartmann wavefront sensor was used to measure the wavefront of the lens which is pivoted around horizontal and vertical axes. The intersection of the two axes mimics the center of rotation of an eye behind the lens. For the other setup, the interferometer based measurement system utilized an optical matching liquid to reduce or eliminate the lenses’ surface power such that the wavefront pattern with large deviation from the freeform lenses can be measured by a regular wavefront setup.The previously obtained FEM simulation results were used to explain the differences between the nominal and experimentally measured wavefront patterns of the microinjection molded lenses. In summary, the proposed method combining simulation 8 and wavefront measurements is shown to be an effective approach for studying injection molding of freeform optics. 9 Chapter 2. Research Objectives The main focus of this dissertation is to seek scientific knowledge and fundamental understanding of molding process for freeform optical lens fabrication by integrating freeform optical design, precision freeform molding making, numerical modeling of polymer lens forming process, and evaluation of the molded freeform optics. Overall, this dissertation describes a comprehensive understanding of affordable freeform optics manufacturing. In order to solve the major challenges in manufacturing affordable high quality freeform optics, this dissertation will include several key steps: 1) Establish point-to-point mapping freeform optics design strategy using freeform microlens array for uniform beam shaping as an example; 2) Evaluate ultraprecision mold machining onto both regular metal materials and brittle materials to achieve high quality molds with optical finish; 3) Develop novel manufacturing process designs to fabricate compression molded hybrid achromatic glass-polymer microlens array and injection molded hybrid glass-polymer achromatic lens; 4) Combine finite element method and wavefront optics theory to model the optical performances of molded freeform plastic lenses; 5) Design proper measurement systems including Shack-Hartmann sensor and wet cell based optical interferometer to evaluate the molded freeform lenses and verify the previously modeled optical performances. 10 Chapter 3. Freeform Optics Design Optical systems using freeform lenses are becoming a viable solution to both imaging and non-imaging optics for its ability of reducing the number of elements in an optical system and accurately controlling light irradiation. A freeform lens in this research is loosely defined as an optical element that is not symmetric around its optical axis. The first reported freeform lens applied to large scale commercial use was a folding single lens reflex (SLR) pack film camera developed by Polaroid SX-70 in 1972 (Plummer, 1982). The freeform lenses in that design were injection molded. Ultraprecision grinding and polishing were adopted to fabricate the molds, which was laborious and difficult to control. However, there are many applications that can benefit from freeform optics, such as LED illumination (Ding, et al., 2008; Wang, et al., 2010), projection displays (Yi, et al., 2006), phase aberration correction (Yi & Raasch, 2005), computational imaging (Kubala, et al., 2003), and compact prism display system (Cheng, et al., 2009), to name a few. 3.1 Design of the freeform microlens array Michaelis et al. generalized a method to design a freeform element in given optical system (Michaelis, et al., 2011), while the basic concept of the simple optical design here is to use a panel with freeform microlens array to redistribute the incoming light into a pre determined pattern on the target (Sun, et al., 2009). The aim of this research design is 11 focused on the development of the fabrication process. The proposed method is demonstrated in a generic freeform microlens array design therefore permits its immediate implementation in optical industry. For the optical design, first of all, it is assumed that the incoming light is collimated. Second, once the light energy area is meshed into tiny cells, each cell can be statistically treated as having uniform radiation even if the entire radiation of incoming light is not uniform. Third, the relative location of the neighboring microlens cells is ignored, since the microlens cell size is considered to be much smaller than the distance between the freeform microlens panel and the target plane. As a result, the uniform redistributed patterns on the target plane produced by these microlens cells overlap at the same location on the target plane. Therefore the shape of only one microlens cell needs to be calculated for redistributing the light on to the target plane. Based on the hypothesis discussed above, the desired redistributed radiation pattern can be determined. In a classic uniform illumination system called fly’s-eye condenser, one or two pieces of microlens array are typically used along with a condenser lens to achieve uniform irradiance at the target plane. Schreiber et al. manufactured a double sided array and analyzed the aberration and diffraction caused by the microlens array in their fly’s-eye condenser system (Schreiber, et al., 2005). Buttner et al. investigated influence of microlens diameter, on-axis microlens aberration and array illumination to the fly’s-eye system consisting of either one or two microlens arrays (Buttner & Zeitner, 2002). However, compared to the design in this research, this conventional uniform illumination system requires more optical elements which involves in more alignment. Both of the conventional and freeform microlens arrays have great usage potentials in optical 12 industry, particularly in LED illumination. However, the intrinsic light divergence from the emitting surface of the LED sources will lead to decreased homogenization effect. A discussion bridging microlens array and LED uniform illumination can be found in (Buttner & Zeitner, 2002). To build the ray tracing model, vector form of the Snell's law’s is used. The incident ray is travelling in a direction defined by vector r, and the reflected and refracted ray direction can be defined as vector rL and rR respectively, which are shown is Figure 3.1. N is the normal vector at incident point O on the incident surface (the front surface of the microlenses). After the ray passes through the incident surface, the refracted ray reaches point E on the target surface. The refractive indices of the surrounding medium of the incident and refractive light space are n1 and n2, respectively. Since | r | = n1 and | rR | = n2, the normal vector of N can be obtained using Equation (1) from reference (Chaves, 2008): N r rR r rR Figure 3.1. Geometry of ray tracking using Snell's law. 13 (1) According to the “edge-ray principle”, if the light coming from the edge of the light source is refracted by the freeform microlens onto the edge of the target region, the light within the source region will be redistributed within the target region (Chaves, 2008). Figure 3.2. (a) Geometrical layout of light redistribution from the microcell region L to the target region M. In the example illustrated in this figure, P = 4 and Q = 3; (b) shaded model of the light redistribution by the freeform microlens. As mentioned above, only one microlens cell needs to be calculated. Thus, if both the microlens cell and the redistributed region are meshed into P × Q grids (the grid sizes are the same) and each grid node of the microcell region is mapped to the corresponding grid node of the redistributed region on the target, the directions of the refracted ray can be determined, as shown in Figure 3.2. In addition, the direction of the incident rays is assumed to be perpendicular to the target surface from the assumption. Since r and rR are already obtained, the normal vectors at the grid nodes of the microcell region can be easily calculated using: 14 Ni, j 1 j 1 i 1 ( A( ) i , B( ) j ,(C nm ) k ) Q 1 2 P 1 2 j 1 2 i 1 2 2 2 (2) A( ) B ( ) (C nm ) Q 1 2 P 1 2 2 i 0,1, 2,..., P 1 j 0,1, 2,..., Q 1 A A1 A2 B B B 1 2 A2 ( j 1 )2 B 2 ( i 1 ) 2 C 2 Q 1 2 P 1 2 where A1 and B1 are the length and width of the rectangular target respectively, A2 and B2 are the length and width of the source rectangle respectively, C is the distance between the target and the source, and nm is the refractive index of the material of the freeform microlens. If the microcell mesh is dense enough, an accurate freeform microlens can be generated and represented by B-spline function (Piegl & Tiller, 1997). The proposed design was aimed to redistribute the collimated light from a 1 mm×2 mm size rectangle into a 20 mm×40 mm size rectangle. The illumination distance was set as 200 mm. Each microlens was divided into 99×199 meshes. Polymethylmethacrylate (PMMA) was chosen as the microlens material whose refractive index was 1.492 at the wavelength of 632.8 nm. The generated freeform microlens is shown in Figure 3.3. The maximum profile deviation of the design value of the freeform lens with respect to a spherical lens is 3.4 µm. 15 Figure 3.3. (a) A single freeform microlens surface. (b) Layout of ray tracing of a single freeform microlenslet projecting onto the target surface. (c) Close-up view of ray tracing of a single freeform microlenslet. 3.2 3.2.1 Manufacturing process for the freeform microlens array Geometric design of tool path Since the grid points of the lens surface and their normal vectors were known, the tool path could be generated. The model of the tool path generation with tool geometry is schematically shown in Figure 3.4 with a fixed tool nose radius. Suppose the radius of the tool nose is R. OT is the center of the tool nose, PO is the cutting point, and N is the freeform surface normal vector at PO. nT is the normal vector of the cutting plane, so it 16 can be assumed as (0, 1, 0). Vector nC is the projection of the freeform surface normal vector N in the cutting plane. nC0 is the unit vector of nC. The position of the tool center OT can be obtained by Equation (4): nC N ( N nT ) nT n nC C0 n C (3) OT PO R nC 0 (4) Figure 3.4. Schematic of tool compensation. 3.2.2 Fabrication of freeform microlenses In this research, ultraprecision machining was performed on the Freeform Generator 350 (Moore Nanotechnology, Inc., Keene, New Hampshire). A diamond tool with radius 0.378 mm was utilized in the current study. Since the radius of the tool and the normal vectors of the mesh nodes were known, the tool radius compensation was included in the tool trajectory generation. The material of the mold insert was 6061 aluminum alloy. 17 Prior to machining the freeform surface, the top surface of the mold insert was diamond turned flat. The rotational speed of the C axis was set at 2,000 rpm. The cutting depth and the feedrate of the finishing cutting were 2 m and 5 mm/min, respectively. In most cases, two types of tool path generation methods are available for slow tool servo process, i.e., spiral path and linear broaching path. The broaching path generation was selected to fabricate the freeform microlens array because of the rectangular shape of the microlens (Li, et al., 2006). In this process, the workpiece was moving along the y axis, while the positions of x axis and z axis were determined by the cutting path with proper tool radius compensation. Once an individual pass was finished, the tool was retracted and moved to the next starting point for next vertical pass. This process eliminated the need for alignment for the symmetry axis of the tool with the C axis, compared with the fast tool servo diamond turning. The size of one freeform microlens in this study was 1 mm×2 mm, and the number of the matrix of the microlens array was 8×4. The entire machining process was divided into 10 cycles while for each cycle the depth of cut was 10 m. For rough cutting, the diamond tool cross-feed step size was 30 m, and the feedrate was 40 mm/min. For finish cutting, the cross-feed step size was 10 m, and the feedrate was 20 mm/min. Microinjection molding process was applied to replicate the low cost freeform microlens array. The processing parameters used in this research are: the injection temperature was 250˚C, the injection speed was 200 mm/s, the injection pressure was 180 MPa, the packing pressure was 80 MPa, and the packing time was 3 sec. The optical grade PMMA 18 (Plexiglas® V825, GE polymerland) was used to perform this experiment. The mold insert and the molded samples are shown in Figure 3.5. Figure 3.5. (a) Pictures of the finished mold insert and the injection molded freeform microlens arrays. (b) Two buffer areas indicated in the pictures are designed to protect the tool cutting edge from making oversize cut into the work piece. 3.3 3.3.1 Geometric and optical evaluations Surface geometry measurement The surface profile measurement was performed on a Wyko NT9100 noncontact optical profilometer. The solid lines of Figure 3.6 show the designed and measured surface profiles along the line y=0 mm of microinjection molding insert and molded part. As shown by the dashed lines in Figure 3.6, both of the measured mold insert and the molded microlens profiles match the designed freeform profile well. For the mold insert, the maximum error between the achieved and the designed profile is 0.3 m. For the 19 microlens, the maximum error of the profile in height is around 0.5 m, and the maximum peak-peak deviation of the geometry error is roughly 600 nm. Figure 3.6. The solid lines are measured 2D surface profiles along the line y=0 mm from the center to the edge (corresponding to Figure 3.3(a)) of the mold insert and the molded lens. The dashed lines are geometry errors of surface profiles along the line y=0 mm of molding insert and molded piece. Figure 3.7 are the measurements for surface roughness of the mold insert and molded microlens. The Ra values of the surfaces of the mold insert and the molded microlens are 29 nm and 25 nm, respectively. No post polishing was performed after the diamond machining. 20 Figure 3.7. (a) Surface roughness measurement of the mold insert. (b) Surface roughness measurement of the molded microlens. 3.3.2 Ray tracing simulations The overall size of the freeform microlens array is 8 mm×8 mm, and the distance between the microlens array panel and the target surface is 200 mm. To evaluate the performance of the freeform microlens array, the optical setup was simulated in Zemax (3001 112th Avenue NE, Suite 202, Bellevue, WA 98004-8017). Non-sequential ray tracing mode was applied to trace the propagation of the rays after refracted by the freeform microlens array. Rays were randomly generated by a rectangular light source, and after refraction, the rays reached the rectangular detector. To build the model of the freeform microlens array, polygen object was utilized in this simulation. Polygen object is one of the user-defined objects in Zemax, which consists of a collection of quadrangles. The neighboring fours vertexes of the entire series of quadrangles were selected from the fitted freeform surface nodes. 21 Figure 3.8. Simulated light distribution on the target surface. For a single freeform microlens, total 20,100 quadrangles were defined based on the model of polygon object. Zemax used the built-in object type “Array” to arrange 32 microlenses in an 8×4 array. Light source and detector were placed on the designed positions. The number of rays used in analysis was 1,000,000. The size of the rectangular source was 8 mm×8 mm, and at the end of this optical setup the intensity was detected by a 50 mm×40 mm size rectangular detector that had a resolution of 200 ×100 pixels. The uniform distribution was the core in this study rather than the absolute intensity of the light, thus the simulated results of the absolute luminance of light source was ignored. Figure 3.8 is the detector image of the irradiation refracted by the microlens array. 3.3.3 Optical performance measurement A He-Ne laser was used as the illumination source. A translucent plastic plate worked as the target plane surface. Figure 3.9 shows the grey value of the red pixel of the illumination picture taken behind the translucent plastic plate. The value of the red pixel ranges from 0 to 255, which quantitatively represents the intensity of light. 22 Figure 3.9. Measured light distribution on the target surface. In order to compare the simulated and the experimental results, the simulated and measured intensity of the light was normalized. The uniformity is defined as Equation (5): u 1 I max I min I avg (5) Where Imax is the maximum intensity value, Imin is the minimum intensity value and Iavg is the averaged intensity value of all the pixels. As a result, for simulated result, 82.1% uniformity of designed area is achieved in the illuminated area; for experimental result, 82.0% uniformity of target area is obtained. 23 Figure 3.10. (a) Comparison of the simulated and experimental corresponding line distributions along the x axis across the center of the illumination. (b) Comparison of the simulated and experimental line distribution along the y axis across the center of the illumination. Figure 3.10 illustrates the comparison of the line distributions along x axis and y axis across the center of the illuminated area of the experimental and simulated results. Majority of the line distributions along x axis and y axis from simulated and experimental results are consistent with each other, as shown in Figure 3.10. Thus, the uniformity of the redistributed illumination was achieved. However, there are factors that may lead to the uniformity error. For instance, the illumination image was taken behind the translucent plastic plate, which might cause the surrounding scattering shown in Figure 3.9. Also, in the optical measurement the light source was laser while interference between the radiations refracted by the different cells was not considered, so the optical design needs to be improved when coherent effects are included. The usage of LED source can be employed to avoid the interference problem 24 caused by the laser, but the lights need to be corrected. Moreover, the exact value of the refractive index of PMMA before and after molding was not known at certain wavelength used in the experiment which also possibly leaded to more errors. In addition, the size limitation of the diamond tool might cause the manufacturing quality as well. As discussed above, tool compensation calculation was included in the tool path generation. In the compensated tool path, the edge of the tool bit was considered as an arc with a fixed radius and the position of the cutting point on the edge of the tool bit depended on the normal vector of the surface that was being machined. Thus, it was almost impossible to avoid the overcut by a fixed radius cutter toward a convex surface during the diamond machining process, as illustrated in Figure 3.11. Smaller diamond tool will reduce the overcut area, which can achieve higher uniformity of the beam shaping. However, studies also indicated that a too small cutting tool could result in deterioration of the machined surface quality (Li, et al., 2010). Figure 3.9 indicates that the uneven radiation distributions on both the left and the right side were created by the overcut problem. Figure 3.11. Schematic of overcut due to the radius of the diamond tool. 25 Chapter 4. Precision Machining for Optical Molding Various micromachining techniques were developed in recent years, such as photolithography, thermal reflow, laser micromachining, micro milling, micro electrical discharge machining and ultraprecision diamond machining. One of the approaches used in this thesis research is slow tool servo diamond machining, a noncleanroom method requiring minimal setup with a considerable manufacturing flexibility. In slow tool servo machining (Yi & Li, 2005), a mechanical slide (z axis in the setup in system used in this study) provides the control in the direction of the depth of cutting. This arrangement allows large deviations on optical surfaces to be machined but limits the dynamic response of the cutting tool due to the inertia of the heavy mechanical slides. In this section, both the glass and polymer molds were fabricated by the slow tool servo machining technique. Ultraprecision machining was performed on the Freeform Generator 350 (Moore Nanotechnology, Inc., Keene, New Hampshire). The basic information of this machining process can be found in (Yi & Li, 2005). The diamond machining for both regular metal materials and brittle materials are discussed. 4.1 4.1.1 Diamond machining on regular metals Slow tool servo machining A diamond tool with a radius of 0.378 mm was utilized in the current study. The tool nose radius of the diamond cutter was compensated off line in the calculation for tool 26 path trajectory. Linear broaching method was adopted to generate the tool paths. In this process, the workpiece was moving along the y axis, while the positions of x axis and z axis were determined by the cutting path with tool radius compensation. Once an individual pass was finished, the tool was retracted and moved to the starting point for the next vertical pass. The number the microlens array is 4×4 and the spacing between horizontal or vertical centers of a pair of the neighboring lenslets or pitch in both direction is 2.2 mm (Li, et al., 2011). Figure 4.1 depicts the broaching CNC (Computer Numerical Control) tool paths for both the glass and polymer microlens arrays. (a) (b) Figure 4.1. Broaching tool path for: (a) glass microlens array, (b) polycarbonate microlens array. The spacing between neighboring steps is reduced and the return tool paths are removed for clarity. The material used for glass mold was 715 copper nickel alloy (www.farmerscopper.com, Galveston, TX). For polymer molding, 6061 aluminum alloy was employed. Prior to machining the microlens array pattern, the top surface of the mold was diamond turned flat. The rotational speed of the C axis (main spindle) was set to at 2,000 rpm. The cutting 27 depth and the feedrate of the finishing cutting were 1 m and 1 mm/min, respectively. For the microlens array pattern, the entire machining process was divided into 18 cycles (infeed) on the nickel mold, 9 cycles (infeed) on the aluminum mold. For each cycle the depth of cutting was 10 µm. For rough cutting, the diamond tool cross-feed step was 30 µm, and the feedrate was 40 mm/min. For finish cutting, the cross-feed step was 10 µm, and the feedrate was 20 mm/min. In addition, the rectangular pocket on the top surface of the aluminum mold was micromilled by an ultraprecision high speed air bearing spindle made by Professional Instrument (ISO 6000, maximum speed 60,000 rpm). The two chisel shaped cavities used for positioning were machined by broaching simultaneously with the microlenses to ensure high position tolerance. Figure 4.2 shows the finished copper nickel mold for glass compression molding and aluminum alloy mold for polymer compression molding. (a) (b) Figure 4.2. Pictures of the finished (a) copper nickel mold for glass and (b) aluminum mold for polymer. 28 4.1.2 Diamond turning In the fabrication process of axisymmetric mold, the diamond turning of the mold inserts used in this study was also performed on the Freeform Generator 350 (Moore Nanotechnology, Inc., Keene, New Hampshire). This diamond machining technique provides a lot of flexibility in generating complex freeform surface while still maintaining high precision. The mold material was 6061 aluminum alloy. A diamond tool with controlled radius 2.6055 mm was used in the study. The tool nose radius of the diamond cutter was compensated off line for tool path trajectory. In the finishing machining path for the aspherical optical surface, the cutting depth was 1.5 m and the feedrate was 1 mm/min. Figure 4.3 shows the finished aluminum mold for the hybrid lens injection molding. The surface roughness of the optical surface is approximately 8 nm as measured by Wyko NT9100 optical profilometer. Figure 4.3. Picture of the finished ultraprecision diamond turned mold inserts for the hybrid lens microinjection molding. 29 4.1.3 Surface coating for nickel glass mold Molds for precision glass molding must withstand high mechanical stresses and oxidation under high temperatures. In order to improve the lifetime of the molds under these difficult conditions, protective coatings are applied on the optical surfaces of the molds (Ma, et al., 2008). The goal of these thin film coatings is to reduce the interactions between the glass and the mold, thus reducing the opportunity of glass adhering to the mold surface during and after molding. Ceramic coatings (TiAlN, SiC, and CrBN), noble metal coatings such as Pt-Ir and DLC coatings (Aoki, et al., 1987; Hagerty, et al., 1988; Hirabayashi, et al., 1991) have all been used for this application. Comparisons of ceramic and noble metal coatings indicated that noble metal coatings showed better characteristics in contact with glass samples (Klocke, et al., 2010). Based on that experience, a Pt-It coating was deposited on the nickel alloy mold. Since the substrate was 715 copper nickel instead of the usually used tungsten carbide, the deposition parameters had to be adjusted. Firstly, the temperature of the substrate during coating was reduced from 450°C to 150°C in order to reduce the possibility of structural changes or recrystallization in the substrate material. Secondly, the duration of the physical etching of the substrate prior to coating was reduced from 20 min to 5 min, since copper and nickel alloy is more easily sputtered than tungsten carbide. During physical etching, a few nanometers of the substrate surface material were sputtered by argon ion plasma before coating. This cleans and activates the surface thus improving the adhesion of the subsequently deposited coating. However, if the cleaning and activation process is used excessively, it can lead to increased surface roughness. Using the adjusted etching parameters, no change in surface roughness was observed before and after 30 coating. Thirdly, a 50 nm nickel adhesion layer was deposited between the substrate and the Pt-Ir coating. Since nickel was also present in the substrate, strong adhesion was ensured. This prevents delamination of the coating during molding, especially around the sharp edges where mechanical stresses are the highest. Finally, a 250 nm Pt-Ir coating was deposited using unbalanced magnetron sputtering with a segmented target, the composition of the coating consists of 40 % Pt and 60% Ir. Figure 4.4 shows the Pt-Ir coating with nickel adhesion layer. The low coating thickness ensures that neither the form accuracy nor the surface roughness of the mold is affected by the thin Pt-Ir coating layer. Figure 4.4. SEM (scanning electron microscope) photo of the Pt-Ir coating with nickel adhesion layer. 31 4.2 Diamond machining on silicon wafer Silicon is a versatile engineering material for a wide range of applications such as electronics, biology (Silicon, 2013) and mold applications (He, et al., 2013; He, et al., 2014) because its attractive material properties and precision manufacturing processes that have been developed over the last few decades. Among the processes available, photolithography is a conventional industrial processing technology for high volume silicon production. However, this technology requires cleanroom environment and complex processing procedures. More importantly, it cannot be used to create true freeform features on silicon substrate. As such, ultraprecision diamond machining of single crystalline silicon has been investigated as an alternative in non-axisymmetric or freeform optics fabrication. Compared with photolithography technique, diamond machining can be readily used to create high precision freeform surfaces and structures, but the biggest challenge for this process is the brittle nature of the silicon material. Because silicon is brittle, it is difficult to avoid the micro fractures on and below the wafer surface caused by diamond machining. Studies of silicon machining have been conducted to address this issue. For example, Blake and Scattergood proposed the diamond machining theory for brittle materials that in ductile-regime, the micro fracture damage could be eliminated if the effective cutting depth was below the critical cutting depth (Blake & Scattergood, 1990). Blackley and Scattergood further analyzed the influences to the fracture damage from various machining parameters, such as rake angle, tool radius, and machining environment (Blackley & Scattergood, 1991). Shibata et al. and Leung et al. extended the investigations to diamond turning process (Shibata, et al., 1996; Leung, et al., 1998). Yan 32 et al. examined the thickness and structure of the subsurface damage of diamond machined silicon (Yan, et al., 2009). Yu et al. determined the subsurface damage depth using a novel method (Yu, Wong, & Hong, A novel method for determination of the subsurface damage depth in diamond turning of brittle materials, 2011). To study freeform optics, Yu et al. and Jasinevicius et al. investigated the application of diamond machining on brittle materials to unconventional optical components (Yu, Wong, & Hong, Ultraprecision machining of micro-structured functional surfaces on brittle materials, 2011; Jasinevicius, et al., 2013). However, the previous studies assumed that subsurface damage depth remained constant during the entire machining process whereas our experimental studies showed that different damages were created when different depth of cut was used. Moreover, in a few studies designed for slow tool servo (STS) diamond machining, only 2D damage prediction was reported (Yu, Wong, & Hong, Ultraprecision machining of microstructured functional surfaces on brittle materials, 2011). To accurately predict the damages in machining, 3D damage distribution prediction is of great interest especially when non-axisymmetric or freeform optics are employed. The 3D damage distribution modeling in our study can accurately predict the pitting damages caused by diamond machining and can be further utilized to optimize the machining process without conducting the actual experiments. This modeling approach has great industrial potentials in freeform optics field, such as, machining of infrared glass lens, and compression molding of glass optics (He, et al., 2013). The main objectives of this silicon machining research are organized as follows: firstly, develop a novel subsurface damage model for the STS diamond machining of silicon and 33 apply this model to simulate the damage distribution three-dimensionally. Secondly, verify the damage predictions by comparing them with the machining experiments. Finally, fabricate a molded glass microlens array by using the machined silicon as mold. In addition, the applications and optimization of the 3D simulation of damage distribution will be discussed. 4.2.1 Modeling of 3D damage distribution In the past, researchers proposed the hypothesis that brittle materials undergo brittle to ductile transition at a critical cutting depth tc (Blake & Scattergood, 1990). When effective cutting depth is below this threshold, machining is carried out in plastic deformation mode, which is called ductile regime machining. Hence, the machining for brittle materials should be maintained within ductile regime to achieve optical quality surface finish. They also assumed that subsurface damage is generated at a constant depth even when the cutting depth is beyond that threshold (Blake & Scattergood, 1990; Yu, Wong, & Hong, A novel method for determination of the subsurface damage depth in diamond turning of brittle materials, 2011). Nevertheless, unlike previous assumption, our studies of STS machining discovered that more micro fracture damages can be observed with the increase of cutting depth. Therefore, the subsurface damage model is revised as shown in Figure 4.5. 34 Figure 4.5. Brittle to ductile transition based on STS machining process configuration. In this subsurface damage model illustrated in Figure 4.5, similar with previous researches, no micro fracture damage occurs if the cutting depth is less than tc, and it is assumed that the micro fracture with a depth of yc is initialized beneath the cutting surface when the local cutting depth is equal to the critical cutting depth tc. In addition, our experiments show that when the cutting depth is more than a certain value (about 2 µm in our studies), the machining produces the fish-scale-shaped cracks which are much more severe than the micro factures or pitting damages under brittle-ductile transition mode. This cutting depth value for crack initialization is marked as tcr in Figure 4.5. Therefore, with a cutting depth larger than tcr the surface damage is increased tremendously; on the other hand, with a cutting depth between tc and tcr, it is assumed that the micro fracture damage depth has an approximately linear relationship with the cutting depth beyond the critical cutting depth. This linear relationship assumption is based our experimental experience, and needs to be investigated further in the future. In this way, the revised subsurface damage model can be used to simulate the 3D distribution of 35 subsurface micro fracture damages of the diamond machined silicon. The influence of crystalline direction of silicon to the micro fracture generation during the STS machining was not taken into account in this study. Figure 4.6. Flowchart of the 3D damage distribution calculation program Based on the subsurface damage model discussed above, a MATLAB computer code was programmed to simulate how material is removed while calculating the consequent local damage depth. Figure 4.6 shows the flowchart of this computer program. If the current effective cutting depth at the cutting point is small than tc, no new damage is generated, 36 and the local damage depth is reduced by the effective cutting depth until it reaches zero. On the contrary, if the current effective cutting depth at the cutting point is larger than tc, the damage depth is updated as a linearly function of the effective cutting depth. Thus, with the information of tool path and subsurface damage model, the damage distribution of STS diamond machined silicon can be visualized three-dimensionally. 4.2.2 Machining experiments The STS machining on silicon wafer was performed on the Freeform Generator 350 FG (Moore Nanotechnology System, Inc., Keene, New Hampshire). The machining tool path can be either spiral or broaching method. In this study, the broaching tool path was adopted (Li, et al., 2011; Li & Yi, 2011). The diamond tool crossfeed rate was 20 mm/min. The tool nose radius of the diamond cutter was 3.05 mm, the rake angle was 24.95° rake angle and the clearance angle was 10°. The odorless mineral oil was used as coolant during the entire machining process. The distance between each broaching path before the compensation for tool radius was 5 µm. Figure 4.7. Design of a square microlens array. Unit is m. 37 An array of square microlenses with 7.1119 mm radius and 0.36 x 0.36 mm apertures was machined on a single crystalline silicon wafer. The sag of each microlens was 4.5 µm. Figure 4.7 shows the layout of the square microlens array. The fabrication process consisted of rough and fine machining. Two sets of rough and fine cutting combinations were experimented in order to balance surface quality and cycle time because even though more fine cutting passes could reduce micro factures it would considerably increase machining time. The detailed parameters of rough and fine cutting are summarized in Table 4.1. Table 4.1. Rough and fine machining parameters Condition 1 2 Depth of rough cut (nm) 333 350 # of passes 12 10 Depth of finish cut (nm) 100 100 # of passes 5 10 According to the machining results, the machining condition 2 was later adopted to fabricate the silicon mold for glass molding experiments for its damage free surface finish. Figure 4.8 shows the microscopic pictures of the microlens arrays machined under the conditions listed in Table 4.1. It shows that the left edge of the microlenses machined under condition 1 has micro fractures in contrast to the microlenses with optical quality machined under condition 2. The damages on the edge of the microlenses in the left column (produced by the overcut of the round diamond tool) are negligible because those spots are not used as effective optical area. Furthermore, these damages can be eliminated by increasing the number of the fine cutting while the machining cycle time needs to be increased considerably. 38 (a) (b) Figure 4.8. Microscopic pictures of the microlens arrays machined under conditions of (a) condition 1 and (b) condition 2 in Table 4.1. 4.2.3 Glass molding experiments A coating process is necessary to protect silicon mold from damage due to adhesion between silicon and glass at high temperature (Yi & Jain, 2005). It has been demonstrated that a thin film coating of graphene-like structure on silicon mold can be an effective way to prevent adhesion (He, et al., 2013). In the coating process, the silicon mold was placed in a nitrogen gas purged furnace. Benzene in the form of bubbles was introduced into furnace as carbon source with Ar gas at an elevated temperature. After coating, a thin layer of graphene-like structures is deposited on the silicon wafer, which has silver like metal appearance. Precision glass molding is a hot forming process to replicate optical features from molds to glass blanks. It has been used as a high volume, low cost process to fabricate various optical components (He, et al., 2011; Li, et al., 2011; Yi & Jain, 2005). In a molding process, glass preform is heated to an elevated temperature then compression molded between two optical polished molds. Controlled cooling is applied after glass was pressed 39 to prevent thermal crack and reduce residual stresses in the molded glass optics (Tao, et al., 2014). The molding experiment was carried out on a DTI glass molding press. A 5 x 10 x 0.6 mm glass sheet was used to replicate the micro features from the silicon mold. The molding temperature was 560 °C for the selected glass type P-SK57 (Schott Glass). The heating ramp rate was limited at 2 °C/s and the soaking time was 10 min. Those heating parameters were chosen to balance uniform temperature distribution and production efficiency. A molding force of 200 N was applied to glass when the molding system reached the desired temperature. After 1 min of holding time, the system was cooled with an initial cooling rate of 0.6 °C/s from 560 °C to 480 °C then cooled with nitrogen forced cooling. The molded glass was removed from the mold at about 200 °C. Figure 4.9. Silicon mold and molded glass microlens array. Figure 4.9 shows the silicon mold and the achieved molded glass microlens array. The machined surface was measured by Wyko NT 9100 optical profiler. The surface 40 roughness Ra value of the damage free area is about 15 nm. Figure 4.10 shows the measured profiles of the machined mold, molded glass optics and the geometry deviation between the mold and the molded part. The optical profilometer collected multiple measurement data and then stitched them into a single surface covering the entire measured area. The stitched measurements indicate about 500 nm maximum geometry deviation for the entire molded part. The peak-valley deviation within the aperture of each microlens is mainly due to the local tilt. So if the local tilts are subtracted, the geometry deviation turns to be less than 100 nm. The large local tilt possibly results from the accuracy of the stitching algorithm and the x-y stage translation of the Wyko profilometer. Figure 4.10. (a) Measured profiles of the silicon mold and (b) the molded glass microlens array. (c) Geometry deviation between the mold and molded glass optics. Unit is mm. 4.2.4 Results and discussions In order to apply the subsurface damage model to the 3D machining simulation, similar experiments such as the ones Yan et al. conducted were carried out to determine the value of the critical cutting depth tc (Yan, et al., 2009). This value was determined to be 130 nm 41 in our experiments. The initial subsurface damage depth yc was set as 700 nm based on previous studies (Blake & Scattergood, 1990; Blackley & Scattergood, 1991; Yu, Wong, & Hong, A novel method for determination of the subsurface damage depth in diamond turning of brittle materials, 2011). The empirical coefficient of the linear relation was set as 2.5. Therefore, the 3D distribution prediction of the subsurface micro fracture damages can be generated based on how the machining path is calculated, as illustrated in Figure 4.11 (a) and (b). Since the machining path of each microlens is the same, only the 3D damage distribution of the microlens in the most left column are shown as an example for the above two machining conditions. The round left edge of the microlens is due to the overcut of the round tool nose and therefore only the microlenses in the most left and right column have this pattern. The experiments of the STS diamond machining on silicon wafers were performed under the same machining conditions used in the calculation of subsurface damages. The calculation shows that the surface micro fracture damages of these two experiment conditions have different degrees of damages and distribution patterns, as shown in Figure 4.11 (e) and (f). Figure 4.11 demonstrate that the calculated and experimental results are in good agreement with each other. The revised subsurface damage model discussed in Section 4.2.1 was applied to calculate the 3D damage distribution of the STS diamond machined silicon, providing more details of the damaged surface. 42 (a) (b) (c) (d) (e) (f) Figure 4.11. Calculated 3D damage distributions of a microlens machined under (a) condition 1 and (b) condition 2. (c) and (d) are the top views of (a) and (b) respectively. Microscopic pictures of a microlens machined under (e) condition 1 and (f) condition 2. Unit is mm. 43 For example, Figure 4.11(c) shows the damage pattern (red dots) along the right edge of the lens. In addition, the density of the red dots representing the damaged area in Figure 4.11 (d) is less than Figure 4.11 (c). These details can be confirmed in the corresponding experimental micro fracture damage distributions shown in Figure 4.11(e) and Figure 4.11(f). The minor differences between the calculated and experimental results may be due to the fluctuation of the temperature control of the machine during the machining process, the accuracy of the subsurface damage model, and the material uniformity. Figure 4.12 shows the calculated damage distribution of a microlens when the constant damage depth is applied. From Figure 4.12 it can be concluded that if the constant damage depth model is used in the calculation for 3D damage distribution, neither the detailed damage distribution of Figure 4.11(c) nor the variation of damage degree in Figure 4.11(d) can be obtained. It should be noted that the tc was increased to 1,000 nm for Figure 4.11(a) to compare these two subsurface damage depth models, because even no damage was predicted with the same tc value 700 nm used in the other calculations. (a) (b) Figure 4.12. Calculated subsurface damage distributions of a microlens if the constant damage depth model is used. Unit is mm. 44 Additionally, the calculation of the 3D damage distribution can provide the micro fracture layouts at any stage during the machining process without “interrupting” it, which helps us understand the ductile mode machining for brittle materials. Figure 4.13 show the development of the damage distribution during the entire machining process using machining condition 2 as an example. The damage is not initialized (Figure 4.13(a)) for the first couple of passes because of the small effective cutting depth, and starts to grow when the geometric slope between the neighboring paths increases (Figure 4.13(b)). During this stage, it shows that large rough cutting depth does not necessarily result in large effective cutting depth. The damaged area then continues increasing (Figure 4.13(c)) until the condition 2 was switched to the finer cutting depth which is even smaller than the critical cutting depth (Figure 4.13(d)), such that ductile regime machining mode is maintained. This way, the damaged area is reduced significantly in effective area that requires optical quality after the fine cutting passes (Figure 4.13(b)). This study confirms the previous researches that the brittle-ductile regime machining damage is associated with many factors, such as geometry, tool radius and cross feedrate. This study is a visual approach to present the development of damage distribution in brittle-ductile machining mode. Therefore, this technique will be very helpful for monitoring the 3D damage distribution of diamond machined brittle materials especially when complex freeform geometries or multiple machining passes are involved. 45 (a) (b) (c) (d) Figure 4.13. 3D damage distribution simulations of the microlens on silicon at the middles of the (a) 5th, (b) 8th, (c) 11th and (d) 18th machining pass of the machining experiments conducted under condition 2. Unit is mm. 46 (a) (b) Figure 4.14. Cutting path planning strategies: (a) constant cutting depth; (b) constant cutting ratio. Unit is mm. Since single point diamond machining is conducted at nanometer scale, the micron scale freeform optics features have to be divided into several steps to avoid fracture damages of brittle materials. Hence, two different dividing strategies were compared to minimize damages as shown in Figure 4.14. Figure 4.14(a) uses a constant cutting depth for each pass, while Figure 4.14(b) employs a constant ratio of the final sag for the cutting depth for each pass. In order to compare these two machining dividing methods, the machining condition 2 listed in Table 4.1 was selected as an example for the constant cutting depth method. For the constant cutting ratio method, the cutting depth of condition 2 in Table 1 was set as the maximum cutting depth for each pass. For example, the maximum cutting depth is 350 nm and the final sag height is 4.5 µm, the ratio for this pass is 0.35/4.5=0.0778. According to the calculate damage distribution results, the constant cutting depth method has 3.54% damaged area, whereas the constant cutting ratio method 47 results in 7.95% damaged area. The difference is due to the fact that the damages were initialized at the very beginning of the machining under the latter condition. Therefore the accumulated damages incurred during initial cutting could not be removed by the following passes using the latter method. The calculated results suggest that even the same maximum cutting depth can still lead to different degrees of damage when different machining strategies are utilized. With the increasing use of freeform optics in the past few years, diamond machining on silicon or other brittle materials has been explored frequently. The STS diamond machining is capable of providing true 3D feature generation on silicon, compared with limited and complicated cleanroom technologies. However, the brittleness of silicon impedes its diamond machinability. Thus, it is important to understand the damage distribution of STS diamond machined silicon in 3D when freeform optics is involved. In this research, we have demonstrated a unique process utilizing single point STS diamond machining process to create microlens arrays on single crystalline silicon substrate with zero or minimum damages. 4.3 Tool path optimization In machining of the microlens array on either flat substrate or curved substrate, it was found that the sharp discontinuities occur at peripheral regions of microlenses due to the discontinuous surface normal vectors at the edge of the microlenses (Scheiding, et al., 2011). Therefore, two alternative modifications have been proposed to improve the surface quality and reduce cycle time as shown in Figure 4.15 (Naples, 2014). 48 Figure 4.15. Cross sections of concave, spherical lenslets on convex, spherical substrates. (a) Traditional, unblended, discontinuous lenslet. The thick blue line is machined, discontinuity and all. (b) Traditional lenslet blended with a torus. The thick blue line is machined, blend and all. (c) Lenslet with blending in the air. Only the thick blue line is machined, which is exactly the whole, original lenslet. Original lenslet aperture is marked by 2 magenta asterisks. Figure 4.15(a) shows the traditional, unblended, discontinuous lenslet. Figure 4.15(b) illustrates the first alternative by removing the lenslet/substrate intersection discontinuity with a “blend” torus that a tangent to the lenslet and substrate. In this way, relatively small acceleration gradients can be achieved among all the mechanical slides, so one is able to greatly reduce machining time and improve the overall quality of the array. There is, however, a variation on the blend torus method that allows one to machine perfectly 49 discontinuous lens arrays on flat and non-flat substrates without physically machining a blend torus on the part. In the further optimized strategy shown in Figure 4.15(c), the physically machined part is the originally designed lenslet, while the machining path on the Blend Torus is in the Air (BTA). Figure 4.16 shows close lenslet close-up pictures for allthree methods (spherical lenslets machined on spherical substrates). Figure 4.16. Lenslet close-ups. (a) Traditional STS method with unblended lenslets. Sliced apertures are clearly visible, rendering the component useless. (b) Close up of unblended lenslet. (c) Blended lenslets machined with the original blend torus method. The tool path and physical array are both clearly continuous. (d) Close of up blended lenslet. A reduction in aperture radius can be seen as compared to a discontinuous lenslet of the same size. (e) Totally discontinuous lenslets machined with the BTA method. The tool path in this case was totally continuous. (f) Close up of lenslet machined with BTA method. The aperture is discontinuous and visibly seems to be of superb quality. This method does not compromise an optical design in any way. 50 Chapter 5. Molding Processes for Achromatic Lenses In recent years various techniques of creating achromatic lenses have been investigated for polychromatic applications in order to correct chromatic aberration. These efforts include, for example, chromatic aberration characterizing and measuring method (Juskaitis & Wilson, 1999; Seong & Greivenkamp, 2008; Dorrer, 2004; Fernández, et al., 2005), post-processing algorithm (Wach, et al., 1998; Kozubek & Matula, 2000; Wang, et al., 2006), liquid achromatic lens (Sigler, 1990; Reichelt & Zappe, 2007), diffractive achromatic lens (Stone & George, 1998; Dobson, et al., 1997), electron optical achromats (Rempfer, et al., 1997) and superachromatic lenses (Herzberger & McClure, 1963). In addition, other researches related to lowering chromatic aberration were conducted in the field of telescopes, surface defect analysis (Tiziani, et al., 2000), focusing of ultrashort light pulses (Kempe & Rudolph, 1993) and scaling laws for aberration in optics (Lohmann, 1989). Achromatic lenses are usually designed in the form of achromatic doublets, in which materials with different optical dispersion characteristics are assembled together to form a hybrid lens or a diffractive optical achromat, where the complementary dispersion characteristics of the diffractive structure and the optical material are utilized. The most common approach to creating hybrid lenses is to use two materials with different dispersion properties in the form of achromatic doublets. One of the advantages of using doublets is that it allows wide range selection of the glass materials compared 51 with standard micromachining techniques such as RIE etching where only limited number of materials available. Historically, Abbe number is used to quantify material dispersion in relation to refractive index. For flint glass, the Abbe number is less than 50 while for crown glass it is more than 50. Therefore, both selecting the proper materials and the assembly of these two materials to the required tolerance are key process steps to manufacturing hybrid lenses. Oliva et al. proposed the best normal flint glass suitable for the design of lens systems working in the infrared up to 2.5 µm (Oliva & Gennari, 1998). Zwiers et al. fabricated a hybrid polymer-glass aspherical lens using UV-polymerizable coatings (Zwiers & Dortant, 1985). Lim et al. compensated the shrinkage error during the UV imprinting process for fabricating hybrid lenses (Lim, et al., 2008). Verstegen et al. analyzed the shape accuracy of optical components influenced by the reaction mechanism (Verstegen, et al., 2003). 5.1 Achromatic lens design The refractive index of an optical material varies as a function of wavelength. Therefore the focal length of a glass lens varies as a function of light color. As aforementioned, Abbe number is the measure of variation of refractive index with wavelength, and is defined as (Laikin, 2010): V nD 1 nF nc (6) where nD, nF and nC are the refractive indices of the material at the wavelengths of the Fraunhofer D, F and C spectral lines (589.2 nm, 486.1 nm and 656.3 nm respectively). The lower the Abbe number V an optical material has, the higher its dispersion is. On the 52 other hand, the power of the lens can be expressed in the form of the lens surface curvatures and its refractive index if the lens is used in air: (n 1)(c1 c2 ) (7) where n is the refractive index of the lens material, c1 and c2 are the curvatures of the two surfaces of the lens. The common technique for achromatic doublets to correct chromatic aberration is to cement flint glass and crown glass together using UV (ultraviolet) curing adhesive. The total optical power of such a cemented doublet is equal to the sum of the powers of two single lenses. The requirements to correct chromatic aberration are described in Equation (8) (Laikin, 2010): 1 2 1 2 V V 0 1 2 (8) where is the total power of the doublet, 1 and 2 are the power of flint glass lens and crown glass lens, respectively, V1 and V2 are the Abbe numbers of two single lenses, respectively. From here the power of two lenses can be obtained from Equation (9): V1 1 V V 1 2 V 2 2 V V2 1 5.2 (9) Compression molded hybrid achromatic microlens array Microlens arrays play an important role in optical industry. For instance, components used in telecommunication devices, digital projectors, machine vision systems and 53 compact imaging applications. The application of microlens array in low cost multiple optical trapping can be found in Appendix A. Therefore, there is a growing demand to develop large volume, high precision production techniques for manufacturing microlens arrays. 5.2.1 Optical design of hybrid microlens array In our study, Polycarbonate (PC) was used for being widely available in industry with an Abbe number V1 of 29.91. P-SK57 glass was selected as crown glass with an Abbe number V2 59.60 for its low glass transition temperature to alleviate the requirement for high temperature molding conditions. The nominal refractive index of polycarbonate used in this research is 1.5855, and the refractive index of P-SK57 is 1.5870. The material parameters are obtained from the optical design software Zemax. The design effective focal length is then 10 mm, and the diameter of each microlenslet is chosen as 2 mm. Figure 5.1. Geometric layout of the achromat doublet design. 54 After obtaining the calculated lens parameters, these data were entered into Zemax for further optimization. Figure 5.1 shows the geometric layout of the achromat doublet design. The radius R1 of the convex surface of the crown glass microlens is 2.92167 mm, and the radius R2 of the convex surface of the flint glass microlens is 5.88252 mm. The edge thicknesses of the glass and polymer microlens in Figure 5.1 are 1.82354 mm and 1.63221 mm. Figure 5.2. Chromatic focal shift of one hybrid polymer-glass microlens doublets. Figure 5.2 illustrates the chromatic focal shift of this doublet for wavelength from 486.1 nm to 656.3 nm calculated using Zemax. The maximum focal shift range is 7.16 µm. The capability of chromatic aberration correction by the hybrid polymer-glass doublet is clearly demonstrated in Figure 5.2. 5.2.2 Compression molding processes The fabrication process is schematically illustrated in Figure 5.3. Figure 5.3(a)~(c) describe the compression molding process for the glass microlens array. The general setup was that a piece of P-SK57 glass was sandwiched between two mold halves. The 55 glass piece was heated up in the vacuum furnace above its transition temperature and then squeezed between the two mold halves. The positions of the mold halves were held for a certain period of time, and cooling was started after compression was completed. Two chisel shaped shaped cavities were designed on the glass mold and would be machined simultaneously when the microlens array was created so the polymer lens layer could be precisely aligned in a self-assembly fashion. The thickness of the glass piece was controlled by the vertical gap between the two mold halves as in Figure 5.3(b). The molded glass piece was then used as the top mold half for the subsequent polymer compression molding procedure shown in Figure 5.3(d). The forming of the polymer microlens array was shown in Figure 5.3(d)~(f). Two chisel shaped shaped cavities with identical shapes on the nickel alloy mold, that would be used as fiducial features, were also machined on the top surface (Figure 5.3(d)) of the aluminum mold using identical design parameters and the same relative position to the microlens array pattern uninterruptedly. The horizontal relative position of the chisel shaped shape cavities next to the microlens array pattern was the same as that in the glass mold. The chisel shaped cavities were used to precisely align the glass and polymer parts during forming of the polymer half. As to the polycarbonate compression molding, the glass piece was first placed on the top surface of the polymer sheet. After the entire system was heated to 10 ˚C above the transition temperature of the polymer, pressure was applied to the bottom half of the mold to form the polymer microlens array. As with the compression process for glass, cooling came after the molds have been held for a while. In both the glass and polymer molding processes, internal stresses were introduced by the pressing action. Furthermore, during and after annealing, stress relaxation as a function of 56 time occurred because of the viscoelastic nature of these two materials, and thus a permanent lens-shaped curvature was developed (Firestone & Yi, et al., 2005). Figure 5.3. Molding processes for the hybrid polymer-glass microlens array: (a)~(c) glass molding process, (d)~(f) polymer molding process. The glass molding experiments were conducted on a Toshiba GMP-211 V machine at Fraunhofer Institute for Production Technology (IPT) in Germany, and the details of the machine and glass molding process can be found in (Yi & Jain, 2005, Yi, et al., 2006, Chen, et al., 2008). The molding conditions were selected based on the previous experience. These conditions were found to be effective but not optimized as the focus of this dissertation is the implementation of compression molding to the hybrid lens array. The hybrid lenses were molded under the following steps: (Firestone, et al., 2005) (1) Vacuum was applied to remove the oxygen before the nitrogen purge. Nitrogen was used during the entire process as a protective atmosphere and the forced nitrogen flow was applied during cooling for adjusting the cooling rate. 57 (2) The lower mold was pushed upward to the heating position, which left about 2 mm gap between glass blank and the upper mold to allow materials to expand during heating. The molds and glass blank were heated up from the initial temperature to the molding temperature of 570 °C at a rate of 2.4 °C/s. (a) (b) Figure 5.4. (a) Molding force and lower mold position as function of time. (b) Molding force and temperature control as function of time. (3) After the molds reached the molding temperature, a soaking phase of about 4 minutes was carried out to ensure that the entire mold and lens system had a homogenous temperature distribution. At the beginning of the molding phase, vacuum was applied again to ensure no nitrogen bubbles existed between the glass blank and the mold. The lower mold was moved upward again at a velocity of 0.44 mm/s to initialize the compression. When the glass blank touched the upper mold, the lower mold was continuously pressing the glass blank at a constant load of 1.5 kN by a servo feedback system. During the entire process, position of the lower mold and the molding force were precisely monitored and 58 recorded with a sampling frequency of 1 Hz. The monitoring file of lower mold position control during molding process is shown in Figure 5.4(a). Cooling began after the lower mold arrived at the desired position. (4) With the start of cooling, the molding force was reduced to a constant holding force of 186 N during the gradual cooling phase with a cooling rate of 0.84 °C/s lasting for 87 seconds. The cooling rate was controlled by the forced nitrogen flow. Once the system reached 500 °C, a faster cooling rate of 1 °C/s was employed until the mold temperature reached 215 °C. The contact between molded glass lenses and the upper mold was released to allow the lens to cool freely. The displayed molding force of 255 N at the fast cooling stage is actually a result of air pressure by the forced nitrogen flow. The temperature control for molding and cooling is shown in Figure 5.4(b). At last, the lenses were removed from the molding machine and cooled down to room temperature. Figure 5.5(a) shows the sample of a molded glass microlens array. The polycarbonate molding experiments were conducted on an experimental apparatus at The Ohio State University designed for compression molding of both glass and polymer optics. The details of the machine and its operation can be found in (Firestone, et al., 2005). The polycarbonate microlens array and the final microlens array assembly were completed as follows: (1) The polycarbonate blanks were placed in a vacuum oven to remove moisture to prevent bubbles from occurring inside the polycarbonate blank during molding. The temperature of the vacuum oven was set at 70 ˚C, and the entire drying time 59 was 48 hours. The polycarbonate blanks used in this study are LEXAN® clear polycarbonate sheet with 2.26 mm measured thickness. (2) A vacuum environment is also critical to compression molding of polycarbonate microlens array to avoid oxidation and remove air from the gap between the polycarbonate blank and the mold. Heating began when the air pressure dropped to 27 Pa. The temperature of the mold halves was increased to 205 ˚C from room temperature in 20 minutes. To enhance the heat transfer and reduce heating time, the lower mold was moved upward until the contact was made with the upper mold. The load between the polycarbonate blank sandwiched by the mold halves was held at 60±8 N and controlled by adjusting the lower mold position using an encoder based feedback element. The heating was provided by four 700 W watlow electrical heating elements. The details of the heating unit can be found elsewhere (Fischbach, et al., 2010). (3) It took 20 minutes for temperature of the molds to reach the steady state, and then the molding process was initialized. The air pressure inside the heating chamber was 4 Pa, and molding force was around 140 N. The molding speed was set as 8 m/s. The lower mold stopped moving upward when the upper glass mold touched the top plate fixed in the heating chamber and the load increased to around 380 N. (4) Cooling was started before the vacuum was turned off, because the polycarbonate blank was molded at just 10 ˚C above its transition temperature and required time to allow the residual stresses to dissipate. The cooling started at a slow rate of 60 0.0139 ˚C/s for 1 hour. At about 110 ˚C, vacuum was turned off and it took another 3 hours for the entire system to cool down to room temperature. (a) (b) Figure 5.5. (a) Molded glass microlens array. (b) The finished hybrid polymer-glass microlens array. The polycarbonate blank was bonded to the glass top mold half, but did not stick to the bottom aluminum alloy mold, therefore the hybrid polymer-glass mircrolens array could be removed easily from the mold after molding. Finally, the hybrid polymer-glass mircrolens array was obtained, as shown in Figure 5.5(b). To secure the plastic lens half to the glass lens substrate, a drop of hot glue can be applied. The annealing process is crucial to residual stresses that lead to birefringence. The annealing in both the thermal compression moldings of P-SK57 and polymer was very carefully controlled to reduce the residual internal stresses. The internal residual stresses were measured using a polarimeter (PS-100-SF, Strainoptics, Inc., 108 W. Montgomery 61 Ave, North Wales, PA 19454 USA), and both the residual internal stresses of glass and hybrid lenses were below 1 MPa that can be safely neglected in this experiment. 5.2.3 Simulation of compression molding Table 5.1. Mechanical and thermal properties of P-SK57 glass. Material Properties Value Elastic modulus, E [Mpa] 93,000 Poisson’s ratio, v 0.25 Density, ρ [kg/m3] 3,200 Friction coefficient, µ 0.5 Thermal conductivity, kc [W/m°C] Figure 5.6(a) Specific heat, Cp [J/kg °C] Figure 5.6(b) Transition temperature, Tg [°C] 493 Coefficient of thermal expansion, α [/°C] Figure 5.6(c) Finite element method (FEM) has been extensively utilized to study the lens shape change, internal stresses and refractive index change in optical elements in recent years (Yi & Jain, et al., 2005; Chen, et al., 2008; Yi, et al., 2006; Su, et al., 2008). Thermal forming processes affect the final optical performance of a microlens array. For glass molding, the Narayanaswamy model can be used to describe the structural relaxation characteristics during the forming of glass microlens arrays (Narayanaswamy, 1971). One single microlens in axisymmetric form was created in MSC/MARC. Both the top and bottom mold halves were simplified as rigid bodies because the Young's modulus of the mold material is much higher than the glass when the temperature is above its transition temperature. The entire simulation can be divided into two major steps: (1) the glass blank was molded after the entire system was heated up above its transition temperature, 62 (2) uniform cooling was applied to all meshed glass blank during the cooling phase. The mechanical and thermal properties of P-SK57 are listed in Table 5.1, its structural relaxation parameters are listed in Table 5.2, and Table 5.3 describes the details of the boundary conditions for all the two-step simulation. Table 5.2. Structural relaxation rarameters of P-SK57 used in numerical simulation. Material Properties Value 493 Reference temperature, T [°C] 73,300 Activation energy/gas constant, ΔH/R [°C] 1 Fraction parameter, x Figure 5.6(d) Stress relaxation curve Table 5.3. Boundary Conditions for Glass and Polymer Molding. Mechanical boundary condition Thermal boundary condition 63 Molding Cooling No slip Isolated Simple shear friction Uniform cooling (a) (b) (c) (d) Figure 5.6. Material properties of the P-SK57 glass used in the simulation. (a) Thermal conductivity [W/m°C] as a function of temperature [°C]. (b) Specific heat [J/kg °C] variation as a function of temperature [°C]. (c) Coefficient of thermal expansion [/°C] as a function of temperature [°C]. (d) Stress relaxation properties curve: shear constant [Pa] versus time [s] (in logarithm scale). The molding temperature for the glass microlens array was 570 ˚C, and the mold traveled 805 m at a velocity of 5.5 µm/s to complete the molding process. The cooling rate applied in this simulation from 0 to 87 s was about 0.84 ˚C/s and 1.01 ˚C/s from 88 to 366 s. The lenses were then cooled down to 25 ˚C in 1,000 s. The FEM simulation was 64 based on the transient mechanical-thermal coupled analysis. The glass blank was meshed into 7,260 four-node isoparametric quadrilateral elements as shown in Figure 5.7(a), and Figure 5.7(b) illustrates the molded deformable model after cooling. (a) (b) Figure 5.7. (a) Meshed FEM model of glass molding for microlens. (b) Final shape of the glass microlens after cooling. The principles of compression molding process for P-SK57 and polycarbonate are similar. The Williams-Landel-Ferry (WLF) equation was used to describe the temperature dependence of rheological properties (Juang, et al., 2002). An axisymmetric model of one single microlens was built for reducing the number of elements and calculating time. The top glass mold half and bottom aluminum alloy mold half were simplified as rigid bodies during relevant simulation. Two simulation steps, i.e., compression molding and uniform cooling, consist of the entire process. The mechanical and thermal properties of polycarbonate are listed in Table 5.4 (Autodesk Moldflow 65 Insight, 2011; Mirkhalaf, et al., 2010), its viscoelastic parameters are listed in Table 5.5 (Juang, et al., 2002), and the boundary conditions for the polymer molding are the same as for the glass molding shown in Table 5.3. Table 5.4. Mechanical and thermal properties of polycarbonate. Material Properties Value Elastic modulus, E [Mpa] 2,280 0.37 Poisson’s ratio, v Density, ρ [kg/m3] 1,191.5 0.3 Friction coefficient, µ Thermal conductivity, kc [W/m°C] 0.31 Specific heat, Cp [J/kg °C] 2,052 Transition temperature, Tg [°C] 150 Solid coefficient of thermal expansion, αg [/°C] 7×10-5 Liquid coefficient of thermal expansion, αl [/°C] 5.72×10-4 Molding temperature for the polymer microlens array was 160 ˚C, 10 ˚C above its transition temperature [39, 40]. The top mold half moved downward at a speed of 7.28 m/s for 100 s to press the polymer blank. It took one hour for the polycarbonate sheet to cool down to 110 ˚C, and another 3.16 hours to 25 ˚C. The FEM simulation was also based on transient mechanical-thermal coupled analysis. The polycarbonate blank was meshed into 3,738 four-node isoparametric quadrilateral elements (see Figure 5.7(a)), and the FEM model of the molded polycarbonate microlens is shown in Figure 5.7(b) after cooling. 66 Table 5.5. Viscoelastic parameters of polycarbonate used in numerical simulation. Material Properties Reference temperature, T [°C] Empirical constant, C1 Empirical constant, C2 Value 160 7.68 24.35 Time [s] Shear modulus [Pa] 0.158 1.995×105 0.316 9.9×105 1 1×106 10 1.585×106 Shear modulus vs. time (a) (b) Figure 5.7. (a) Meshed FEM model of the polymer microlens. (b) Final shape of the polymer microlens after cooling. In order to verify whether this FEM simulation could be used to accurately predict the compression molding process and the final shape of the microlens, surface geometry measurements for the microlens were performed on a Wyko NT9100 noncontact optical profilometer (Bruker AXS Inc., 5465 East Cheryl Parkway Madison, WI). Figure 5.8 67 shows the surface profile comparisons of simulated and experimental results. Simulation results were found to be in good agreement with experimental results. Therefore, future work would include reducing the error of the lens curvature to obtain a complete spherical surface by optimizing the process. (a) (b) Figure 5.8. Comparison of simulated and experiment surface profiles of one microlens for (a) P-SK57 glass and (b) polycarbonate. 5.2.4 Geometry and optical evaluation The surface measurement was also performed on the Wyko NT9100 optical profilometer. The solid lines shown in Figure 5.9 are the designed and the measured surface profiles along the diameter of the mold and a single microlens in the molded microlens array. Figure 5.9(a) shows the P-SK57 glass convex surface and Figure 5.9(b) shows the polycarbonate convex surface. Shown as the dashed lines in Figure 5.9, both the measured profiles of the mold and the molded microlens match the designed profile well. For P-SK57 glass compression molding, the maximum error of the mold in height is 68 about 1.8 m and the maximum error of the molded microlens is around 2.7 m. For polycarbonate compression molding, the maximum error of the mold in height is approximate 1.0 m and the maximum error of the molded microlens is about 1.8 m. The surface roughness of the mold and molded part was measured as well. For glass microlens array, the surface roughness Ra value of the copper nickel mold and the molded glass microlens are 28.05 nm and 48.59 nm, respectively. For polymer microlens array, its Ra value for aluminum alloy mold and the molded microlens are 28.27 nm and 26.47 nm, respectively. As mentioned before, no post machining polishing was performed to either the nickel or the aluminum mold. The surface roughness of the molded glass microlens is higher than the mold surface, but the Ra value of the molded polycarbonate microlens is only slightly better than the aluminum mold. (a) (b) Figure 5.9. 2D surface profiles and geometry errors along the diameter of the mold and the molded sample of one single microlens. (a) Surface profiles of the mold and molded glass lens. (b) Surface profiles of the mold and molded polymer lens. 69 The schematic of the setup for measuring chromatic aberration and the focal length is shown in Figure 5.10. Collimated lasers with three different wavelengths (λ = 405 nm, 532 nm and 632.8 nm) were used as the light source. To visualize the image of the focal spot, a zoom lens imaging system (VZMTM 450i, Edmund Optics, Inc., 101 East Gloucester Pike, Barrington, NJ 08007-1380) and a CCD camera (PL-B957F, pixeLINK, 1465 N. Fiesta Blvd., Gilbert, AZ 85233-1002) were used in the optical setup. The criterion for locating the focal spot is finding the smallest spot by varying the position of the hybrid lens, while the image of the focal spot is viewed through the zoom lens system. Figure 5.10. Schematic of the setup for measuring the chromatic focal shift: (1) laser source, (2) linear polarizers, (3) pinhole, (4) field lens, (5) hybrid lens mounted on a precision translation stage and (6) CCD camera. To measure the chromatic focal shift of the microlens, λ = 405 nm laser was the first to be used in this measurement. The precision stage on which the microlens was mounted was adjusted until the focal spot could be observed from the CCD camera, and the position of the stage d1 was recorded. Second, a laser with wavelength of λ = 532 nm was used and the stage was adjusted to find the new focal position. The focal position at this 70 wavelength was recorded as d2. Third, λ = 632.8 nm laser was employed and the focal position was recorded as d3. The chromatic focal shift from 405 nm to 532 nm is d1-d2 and the shift from 532 nm to 632.8 nm is d3-d2. For d1-d2, the measured average is 60.1 µm with a standard deviation less than 5.1 µm as comparing to the calculated value is 65.5 µm. For d3-d2, the measured average is 5.4 µm with a standard deviation less than 2.1 µm, while the calculated value is 4.06 µm. As shown in Figure 5.11, the chromatic shift for 532 nm laser is assumed to be zero and the blue solid curve represents the calculated results of chromatic focal shift with respect to wavelength in Zemax. The measured chromatic shifts are plotted as red asterisks in this figure for comparison. The theoretical values and experimental results are consistent to each other. Figure 5.11. Comparison of calculated and experiment results of chromatic focal shift of the hybrid polymer-glass doublet. The focal lengths of the hybrid microlens array were also evaluated in this study. A HeNe laser of wavelength 632.8 nm was used in this measurement. First, a molded lenslet was moved manually along the optical axis such that the flat surface of the microlens was 71 focused on the CCD camera. Then the microlens was moved away from the camera until the sharp focus of the collimated beam was displayed in the monitor. The distance between these two positions was the focal length. In order to evaluate the uniformity of the microlens array, the focal length of each microlens was measured in the same fashion. The measured focal length is 9.864 mm with a standard deviation less than 0.054 mm. Therefore, a hybrid polymer-glass achromatic microlens array was fabricated by compression molding. Polycarbonate and P-SK57 were selected for the doublets array since they have opposite dispersion properties. The geometry error is about 2.7 m for the molded glass microlens, and is approximately 1.8 m for the molded polymer microlenses. As for the surface roughness, the Ra value of the glass microlens is 48.59 nm, and is 26.47 nm for the polymer microlens. The focal length measurement verifies that this hybrid polymer-glass achromatic microlens is capable of correcting chromatic aberration as designed. Future work would include designing new precision assembly technique, optimizing the thermal compression molding process to compensate the geometry, analyzing refractive index change caused by the molding process, and improving ultraprecision machining method to increase the optical quality of the mold surface. If the requirement for optical performance increases, the knowledge of the exact values of the material properties becomes crucial since it significantly influences the initial calculation of the optical design and the simulation of the compression molding. 5.3 5.3.1 Injection molded hybrid glass-plastic achromatic lens Design of fabrication processes 72 Unlike conventional UV curing method for polymer coatings, in this research microinjection molding was utilized to apply a layer of polymer to the glass lens surface. The competitive advantages of injection molding over conventional UV curing method come from the fact that injection molding is ideal for mass production thus can significantly lower manufacturing cost. As a subset of injection molding, microinjection is considered as one of the crucial technologies for its uniqueness of replicating high precision micro scale features. (a) (b) (c) (d) Figure 5.12. Manufacturing processes of the hybrid glass-polymer lens by microinjection molding. The right mold insert is used to house the glass lens while the left side has the aspherical surface for the polymer lens. The blue area is the glass lens and the red is the injection molded polycarbonate polymer. Figure 5.12 shows the manufacturing processes for the hybrid lens by microinjection molding. Firstly, two mold inserts are diamond machined to the print. In the layout used in this study, the left mold has the aspherical curvature, and the right mold is used to 73 house the glass lens. Once the glass lens with spherical surface is placed in the circular pocket of the right insert, two mold halves are closed and the polymer melt is injected into the cavity between the glass lens and the aspherical surface. Figure 5.13. Achromatic doublet design (unit: mm). The diameter of the polymer lens is slightly larger than the glass lens as shown in Figure 5.13. In this design the edge of the polymer lens will apply compression stress to the glass lens after the melt polymer cools down. Therefore, the glass lens and the polymer lens are integrated into one hybrid glass-polymer aspherical lens that can be removed from the mold without further alignment in a single uninterrupted process. The fitting tolerance for the glass lens outside diameter and the circular pocket inside diameter is of slide fit so as to leave some room during polymer filling stage to avoid cracking while still allows the glass lens to be positioned within the accuracy of a couple of microns. Additionally, the axial alignment accuracy of these two mold inserts is secured by the mold base assembly. 74 The manufacturing process design is then followed by the optical design. Polycarbonate (PC) is chosen as the higher dispersion flint glass with Abbe number of 29.9 while NBK7 is chosen as the lower dispersion crown glass with Abbe number of 64.1. These two materials are selected for their availability and low cost. Figure 5.13 shows the geometric layout of the achromatic doublet design. The radius of the spherical glass lens is 51.5 mm and its thickness from the top to the flat bottom is 3.59 mm. In this design, the thickness t of the center of the polymer layer is relatively thin which can be difficult to manufacture. In addition the change of the polymer thickness ranging from 0.1 mm to 2 mm does not significantly affect its optical performances, such as RMS spot size or chromatic focal shift. The actual value will be discussed according to the process simulation in the next section. The aspherical curvature of the polycarbonate lens is described by the equation below: z cr 2 1 1 1 k c r 2 2 r2 (10) where z is the sag of the aspherical surface which is a function of the radial coordinate, c is the curvature or the reciprocal of the radius, r is the radial coordinate, k is the conic constant and is a constant coefficient. Table 5.6 shows the design values of these parameters for the hybrid lens in this study. With the geometry design of the hybrid glasspolymer lens, the chromatic focal shift from wavelength 486.1 nm to 656.3 nm in ZEMAX clearly demonstrates its capability for chromatic aberration correction. The nominal focal length of the hybrid lens is 200 mm, and the maximum focal shift range from wavelength 486.1 nm to 656.3 nm is 480.5 m. 75 Table 5.6. Design parameters for the aspherical surface. c k α 5.3.2 -1/88.51123 -1.16867 2.3731×10-4 Microinjection molding simulations Since considerable thermal and fluidic phenomena are involved in the microinjection molding, the visualization of molding process can help understand and improve the manufacturing process. For example, flow pattern (Kim & Turng, 2006), welding lines, refractive index variation (Yang, et al., 2011), geometrical curve deviation and internal stresses (Lu & Khim, 2001), can be predicted by finite element method (FEM) simulation, and the predicted information accompanied by the experimental results will feedback to the parameter control of the mold machining and microinjection molding to optimize the fabrication of the hybrid lens in the further study. A commercial FEM software package Moldex3D was used in this injection molding research. In this simulation, the mold base and cooling pipes were also included in the meshed model to improve accuracy. The glass lens was modeled as a part insert, and Moldex3D assumed the part insert and the injected part were completely bonded together after filling, sharing the same interface temperature and deformation. This way, the insert injection molding modeling can evaluate the deformation of the polymer lens in the integrated part. Moreover, for the challenges of injecting the polymer melt into the thin cavity and controlling the shrinkage of the polymer lens, the simulation was focused on melt front flow pattern during filling and warpage after cooling. 76 As mentioned in the before, the thin center of the polymer lens might lead to an unfilled hole or weld line defects. Thus two different center thickness designs of the polymer part were modeled in FEM simulation, one being 0.1257 mm for Model I and the other one being 0.7257 mm for Model II. Figure 5.14(a) shows the meshed Model I for the injected polycarbonate part and the glass lens part insert. The three dimensional mesh is based on layer-by-layer strategy to increase the accuracy of the numerical analysis (Park & Joo, 2008). Figure 5.14(b) shows the entire meshed model for the injection molding simulation including the cooling channels and mold base. After the meshed models were imported into the Moldex3D software package, the molding process was simulated to find a better thickness design. The Sabic Lexan OQ1020 was selected as the material for simulation and its material database was provided by the software. Table 5.7 summarizes the process conditions used for the two different thickness designs of the injection molded hybrid glass-polymer lens. (a) (b) Figure 5.14. (a) Meshed Model I for the injection molded part and the part insert and (b) meshed microinjection molding system model including the cooling channels and mold base. 77 Table 5.7. Simulation process conditions used for two different thicknesses. Injection temperature 330 °C Injection time 0.1 s Packing pressure 80 MPa Packing time 5s Cooling temperature 82 °C (a) (b) (c) (d) Cooling time 35 s Figure 5.15. Comparison of simulation (a and c) and experimental results (b and d) of the melt front flow pattern for Model I during filling. The melt front patterns during the filling stage were obtained by the post processing analysis in Moldex3D, as shown in the left column in Figure 5.15. There were two highly possible issues in injection molding, one being an unfilled hole and the second one being welding lines in the center. Both issues were later confirmed in the experiment as shown in the right column in Figure 5.15. The minor difference between the simulation 78 and experiment may result from the material properties provided in the commercial software, the interface assumption between the glass and the polymer melt in simulation, and the actual operation status of the machine used in the experiment. However, the simulation for Model II shows that the melt front passes the center and pushes the potential welding line to the edge of the polymer lens as illustrated in Figure 5.16, thus the larger thickness of 0.7257 mm was adopted in further study for the hybrid lens. Figure 5.16. Melt front (shown in time) of the injection molded polymer part of Model II during filling. Besides the melt front flow patterns, the effect of the packing pressure to the deformation of the polymer lens edge was also studied in simulation because too much shrinkage may result in large deformations and high internal stresses. 40 MPa and 80 MPa were used as the two levels of the packing pressure in the process simulation, while other process parameters were kept the same as listed in Table 5.7. Figure 5.17 shows the results of the deformations of the molded part under the two packing pressures. The results show that the edge deformation on the condition with packing pressure 80 MPa is smaller than 79 with the packing pressure 40 MPa, thus a higher packing pressure is adopted in all later experiments. Figure 5.17. Simulated part deformation under different packing pressure. 5.3.3 Lens fabrications The diamond turned mold inserts were installed in the microinjection molding machine (LD30EH2, Sodick Plustech) for molding test. The microinjection molding machine employed in this study can apply up to 30 ton maximum clamping force and 250 mm/s maximum injection velocity. The uniqueness of this machine is that its injection system is consisted of a screw plasticizing unit and a plunger injection unit for precisely managing the micro feature replication by their independent controls. The diameter of the plasticizing screw is 18 mm, and a 16 mm diameter injection plunger can produce an injection stroke up to 70 mm. The optical grade polycarbonate (SABIC Lexan OQ1022 Resin) was used in this experiment. 80 Figure 5.18. Picture of a complete hybrid glass-polymer lens manufactured by microinjection molding (shown with gate, runner and spruce). In this experimental test, firstly, the polycarbonate pellets were placed in an electrical dryer for 24 hours at 100 °C in a ventilation environment to remove the moisture. Secondly, the processing parameters were entered the machine as follows: the injection temperature was 330 °C, the injection speed was 200 mm/s, the maximum injection pressure was 150 MPa, the packing pressure was 80 MPa with a 5 seconds packing time and the temperature of the cycled cooling water was 82 °C with a 35 seconds cooling time. Next, a glass lens was placed in the circular pocket of the right mold insert illustrated in Figure 5.12(b). When the temperature of the glass lens reached a steady state from room temperature to the temperature of the mold insert, the mold halves were closed. Lastly, the polymer melt was injected into the cavity to form a polymer layer over the glass lens surface. The cooling time was set to be relative long to reduce stresses 81 formed during the filling stage. A complete hybrid glass-polymer lens manufactured by microinjection molding is shown in Figure 5.18. The surface roughness of the polycarbonate lens is about 8 nm which is close to the measurement result of the mold insert mentioned in the first paragraph of this section. 5.3.4 Optical measurements The schematic of the setup for measuring the chromatic aberration is the same as shown in Figure 5.10. Three different wavelengths ( = 405 nm, 532 nm and 632.8 nm) lasers were employed as the light source. Similar procedures were repeated for the other three wavelengths laser. Hence, the chromatic focal shift from 532 nm to 632.8 nm is d2-d1 and the shift from 405 nm to 532 nm is d3-d2. For d2-d1, the measured average is 248 m with a standard deviation 12.1 m as comparing to the calculated value of 157 µm. For d3-d2, the measured average is 2,563 m with a standard deviation 50.4 m, while the calculated value is 2,115 m. Figure 5.19. Comparison of the calculated and measured results of the chromatic focal shift of the hybrid lens. 82 Figure 5.19 shows the calculated focal shift of the hybrid lens with respect to wavelength by ZEMAX. The focal shift from 486.1 nm to 656.3 nm is very small as discussed in the optical design. The measured chromatic shifts are plotted as red asterisks in this figure for comparison. The experimental results show a good agreement with the theoretical values. Some factors, such as the optical alignment, the optical properties of the material, the stability of the laser source and manufacturing quality control, may result in the difference between the measured and theoretical data. In addition, the hybrid lens was examined by the polarimeter (PS-100-SF, Strainoptics, Inc., North Wales, PA), and the residual stresses in the center part of the polymer lens were below 10 MPa although the edge shows relatively high internal stresses but it is outside of the clear aperture. Hence, microinjection molding is also demonstrated to be an effective tool to precisely replicate micro features in optical mass production to correct color aberrations. Besides its improved optical performance and easy mechanical alignment, the hybrid lenses are also chemical corrosion resistant. These lenses also have reduced weight, compact size and robust thermal stability (Doushkina, 2010). 83 Chapter 6. Modeling of Optical Performance of Molded Freeform Optics Injection molding processes are ideal for high-volume production, and can work with a wide range of materials including optical grade polymer materials. However injection molded freeform optical components have several major issues. These issues include, for example, large geometric shrinkage, refractive index variation and birefringence. Hence, it is of great interest to utilize numerical modeling to investigate and predict the manufacturing process. Kim and Turng used a finite element method (FEM) to model the filling phase of the injection molding process for an optical lens and verified the filling pattern experimentally (Kim & Turng, 2006). Park and Joo applied FEM analysis results of an injection molded lens to a ray tracing simulation (Park & Joo, 2008) and concluded that inhomogeneous distribution of refractive index could occur if molding conditions were not carefully controlled. Besides the simulations for refractive index distribution, Huang (Huang C. , 2008) and Yang et al. (Yang, et al., 2011) discussed the refractive index variation of injection molded precision optical lenses using two different experimental setups. Suhara constructed the refractive index distribution of an injection molded lens by using computed tomography technique (Suhara, 2002). Furthermore, Su et al. compensated the refractive index change and geometric deviation during glass molding process to improve lens forming quality (Su, et al., 2014). 84 Based on the aforementioned research, geometric deformation induced by cooling shrinkage can be minimized in the production of precision freeform optics. In addition, uniform refractive index distribution also plays a crucial role in high quality optical elements. Therefore, in this chapter we focus on modeling of the injection molding process, including how geometric deformation and refractive index variation are related to wavefront of molded freeform optics. 6.1 FEM modeling for precision molding Figure 6.1. Meshed FEM model of a Progressive Addition Lens (PAL). Node(i,1) is numbered along number i line at the bottom surface of PAL, and Node(i,N) is the node along number i line at its top surface. After the geometric model was constructed, a 3D model example was generated using HyperMesh (www.altair.com) as shown in Figure 6.1. The meshed model was then imported to a commercial software package Moldex3D (http://www.moldex3d.com/en/) to complete the FEM simulation. The entire lens model was divided into 12 surface 85 layers of prism elements, and each element layer could be considered as a lens surface. In addition to the lens itself, the mold base and cooling pipes were also included in the model to ensure accuracy but were omitted from Figure 6.1 for clarity. Table 6.1. Material parameters of PMMA. PVT Tait Model Parameters Values b1L (cc/g) 0.85982 b1S (cc/g) 0.860702 b2L (cc/g·k) 0.0005697 b2S (cc/g·k) 0.0001995 2 b3L (dyne/cm ) 2.09×109 2 b3S (dyne/cm ) 2.73×109 b4L (1/K) 0.0049083 b4s (1/K) 0.003394 b5 (K) 383 b6 (cm2·K/dyne) 2×10-8 0.0894 C Viscosity Cross WLF Model Parameters Values 0.21 n 6 * 2 1.48×10 (dyne/cm ) B (g/cm·s) 1×10-16 Tb (K) 24294 In this simulation, three stages of the injection molding process were analyzed: filling, packing and cooling. An optical grade polymethylmethacrylate (PMMA, trade name Plexiglas V825) was selected for molding the freeform lens. The PVT properties of the PMMA are expressed by the modified Tait Model as follows, V V0 1 Cln 1 P / B (11) b b2 ST , if T Tt V0 1S b1L b2 LT , if T Tt (12) b3S exp b4 ST , if T Tt B b3Lexp b4 LT , if T Tt (13) T T b5 (14) 86 Tt b5 b6 P (15) where V is specific volume in cm2, P is pressure in dyne/cm2, T is temperature in kelvin, and the remaining parameters are constants listed in the left half part of Table 6.1. The modified Cross WLF model describes the viscosity behavior of the PMMA material used in this study in the following equations, 0 (16) 1 n 1 0* Tb T 0 Bexp (17) where is viscosity in g/cm·s, is shear rate in dyne/cm2, and the remaining parameters are shown in the right half of Table 6.1. These material properties were directly taken from the Moldex3D database. Additionally, Table 6.2 also summarizes the values of the molding condition used in this work. Table 6.2. Injectin molding condition. Molding parameters Melt temperature (ºC) Mold temperature (ºC) Injection velocity (mm/s) Maximum injection pressure (MPa) Velocity/pressure switch (vol %) Packing pressure (MPa) Packing time (s) Cooling time (s) Coolant temperature (ºC) Values 250 75 200 100 90 80 6 25 65 As mentioned previously, the computed geometric deformation and refractive index distribution were exported from the FEM calculation for later discussion. The geometric 87 deformation primarily has an impact on optical refraction, so the nodes’ positions on the top and bottom surface meshes were extracted for numerical analysis of its optical aberrations in next section. Furthermore, uneven cooling as well as the polymer’s rheological properties could result in an unevenly distributed density that consequently causes variation in refractive index (Yang, et al., 2011). Therefore refractive index information at each node was also collected for optical aberration analysis. It should be noted here that birefringence is defined as a variation in refractive index with polarization angle at any point inside the lens. Previously, Isayev investigated the refractive index through birefringence approach with consideration of flow-induced stress and relaxation effect (Isayev, 1983). Different from Isayev’s work, refractive index in this study is considered to be a scalar, which can vary with lens location. 6.2 Prediction of optical performance influenced by molding process After the FEM computation is completed, the geometric deformation and refractive index variation were exported for later analysis. The geometric deformation primarily affects refraction at the surface, while refractive index variation affects internal propagation. As for the surface warpage, in this study it was defined as the geometric deformation in lens thickness. The coordinate positions of the nodes on both top and bottom surfaces were recorded. For example, the original thickness at the coordinates (xi, yi) line is defined as, ti z i, N z i,1 88 (18) where z(i, 1) and z(i, N) are z coordinate positions of the Node (i, 1) on the nominal bottom and top surfaces, respectively. The deformed thickness between top and bottom surface at the coordinates (xi, yi) line was calculated using the following equation, ti' z i, N z i,1 (19) where z’(i, 1) and z’(i, N) are z coordinate positions of Node (i, j) on the fitted deformed bottom surface and Node (i,N) on the fitted deformed top surfaces, respectively. Due to non-uniform cooling rate at different locations of the microinjection molded Alvarez lens, uneven density distribution is formed inside the lens. This density deviation leads to refractive index variation. It should be noted that in this study refractive index is considered to be a scalar, varying with location inside the lens. In order to simplify the problem of refractive index variation, one index value over the xy plane corresponds to the refractive index information on one vertical line at certain xy coordinates. More specifically, the index value along the vertical lines at coordinates (xi, yi) is the average of the refractive index values of all the nodes along this line in the thickness direction of the Alvarez lens, or, N ni n i, j / N j 1 (20) where ni is the average refractive index value along the line at coordinates (xi, yi) in the thickness direction, n (i, j) is the refractive index of the Node (i, j) or the jth node on the line, N is the number of the nodes on the Number i line. Figure 6.1 illustrates the numbering scheme. Hence, the refractive index variation at coordinates (xi, yi) can be obtained by 89 NV ni ni n j / NV (21) j 1 where NV is the number of the vertical lines along the z direction in the mesh model. Therefore, the optical path when both inhomogeneous refractive index and geometric deformation were considered can be calculated depending on the specific cases. 90 Chapter 7. Optical Metrology of Molded Freeform Optics Traditionally, the freeform optics measurement is challenging because of its nonaxisymmetric nature as compared with conventional optics. Savio et al. reviewed general freeform surfaces measurement for various applications (Savio, et al., 2007). The measurement methods are divided into two types, i.e., contact and non-contact techniques. Coordinate measuring machines (CMM) are the most widely used contact measurement tool for large measurement range, although its uncertainty is at the micron level (Schellekens, et al., 1998). For non-contact methods, optical imaging and interferometry techniques can provide fast measurement with low uncertainty, but they are sensitive to ambient influences such as surface roughness, defects, light transmission, dust, oil or water coats (Fang, et al., 2013). Fringe Reflection Technique (FRT) is another non-contact robust system for measuring freeform surfaces by converting fringe spacing variations to local surface gradients (Bothe, et al., 2004). An interferometry based setup is an ideal way to evaluate flat, spherical surfaces with nanometer resolution. If interferometers are used to measure an aspheric or freeform surface with large deviation, a null lens or some type of wavefront modulator must be added to the optical setup. The techniques mentioned above require either expensive equipment or complex procedures, so we present two simple approaches to quantifying freeform wavefront patterns. One is realized by customized Shack-Hartmann sensor (Lane & Tallon, 1992), while the other one is achieved by a wet cell based interferometer. 91 7.1 Shack-Hartmann wavefront sensing measurement Progressive addition lenses (PALs) have been widely accepted for the compensation of presbyopia (i.e. the decline in ocular accommodation with age) over the past 60 years. Compared with conventional bifocal lenses, PALs provide users a continuous change in spherical optical power through different regions of the lenses. PALs are typically manufactured using a casting process. In this process, a monomer is injected into the mold cavity, and then either an initiator is injected, or ultraviolet (UV) exposure is turned on to cure the monomer. However, manufacturing cost for the traditional methods is high due to limited production rate. Therefore, in recently years, new more affordable molding techniques have been proposed to produce PALs, such as glass molding (Lochegnies, et al., 2013) and plastic injection molding (Hsu, et al., 2010; Cheung, et al., 2012). Comprehensive methods for evaluating and measuring their optical properties have been developed. Castellini et al. modified the Hartmann test to accurately measure the prismatic deviation and spherical power of PALs (Castellini, et al., 1994). Villegas and Artal set up a Shack-Hartmann wavefront sensor system to perform spatially revolved aberration measurement of PALs either isolated or in combination with the eye (Villegas & Artal, 2003). Huang compared the wavefront sensing method with a moiré interferometer-based method and a coordinate measuring machine (CMM) method, and discovered that those three methods were comparable for measuring optical powers of PALs (Huang, et al., 2012). This research utilized a custom optical measurement system based on a Shack-Hartmann wavefront sensor to evaluate second order wavefront aberrations of injection molded PALs, to verify FEM simulated results (Li, et al., 2013). 92 7.1.1 PAL design The front convex surface of the PAL in this research is a spherical shape, and its geometry can be described by the radially symmetric second order Zernike term . z 0.462 3 2 x 2 2 y 2 1 (22) where z is surface height in mm, x and y are normalized coordinate positions ranging from -1 to +1, and the nominal radius is 20 mm. The front surface has a peak-valley difference of approximately 1.6 mm and a radius of curvature of 125 mm. Assuming a refractive index of 1.49, this surface has a dioptric power of approximately 3.9 D. The back concave surface height, in mm, is a freeform surface described by Zernike polynomials: z 0.462 3 2 x 2 2 y 2 1 0.015 2 2 3x 2 y y 3 0.046 2 2 3x 2 y 3 y 3 2 y 0.007 2 2 3x 3 3xy 2 2 x (23) 0.007 2 2 x 3 3xy 2 0.0064 2 3 10 x 4 y 20 x 2 y 3 12 x 2 y 10 y 5 12 y 3 3 y Figure 7.1 shows the freeform surface of the backside of the PAL where the first polynomial term representing the spherical shape is removed for clarity to show the freeform pattern. The center thickness of the PAL is 2.285 mm. In terms of Zernike polynomials, this freeform surface is the sum of third order coma and trefoil, and fifth order secondary vertical coma. 93 Figure 7.1. Freeform surface of the backside of the PAL. The first polynomial term was removed to show the freeform geometry. 7.1.2 PALs fabrication For the mold fabrication process, the mold insert with the convex freeform surface was also machined on the Freeform Generator 350 (Moore Nanotechnology, Inc., Keene, New Hampshire) using ultraprecision diamond slow tool servo to optical quality. In this study, a diamond tool with a controlled radius of 2.6055 mm was utilized. The tool path trajectory was compensated offline by the tool radius. On the finishing machining path for the convex freeform optical surface, the cutting depth was 5 m and the feedrate was 20 mm/min. 6061 aluminum alloy was used as the material of the mold inserts. Figure 7.2 shows the finished aluminum mold inserts for the PAL. The surface roughness of the convex surface was approximately 10 nm measured using the Wyko NT9100 optical profilometer. The concave spherical mold surface was machined by conventional 94 ultraprecision diamond turning and its surface roughness was measured to be about 8 nm. No post-polishing was performed on the inserts. Figure 7.2. Finished ultraprecision diamond turned mold inserts for PAL injection molding. Figure 7.3. PALs manufactured by microinjection molding. The diamond turned mold inserts were then installed in the microinjection molding machine (LD30EH2, Sodick Plustech) for molding test. The microinjection molding machine employed in this study can generate up to 250 mm/s maximum injection 95 velocity with a 30 ton maximum clamping force. The special injection system of this machine has separated screw plasticizing unit and plunger injection unit to precisely manage the micro feature replication by their independent controls. Same as the material modeled in the simulation, the optical grade PMMA, Plexiglas V825, was used in the experiment. The experimental molding conditions were the same as in the simulations listed in Table 6.2. The injection molded PALs are shown in Figure 7.3. 7.1.3 Simulated wavefront pattern of PALs With the exported FEM results obtained in Chapter 6, the optical path difference (OPD) when both inhomogeneous refractive index and geometric deformation were considered can be calculated by: OPD ni n0 1 (di' t0 ) (24) where n0 is the nominal refractive index of the PMMA material, which is 1.49, t0 is the center thickness of the PAL, which is 2.285 mm in this study. The calculated OPD was fitted to a Zernike polynomial up to the 8th order, or 45 terms using a least square method. The Zernike coefficients of the 45 terms were annotated as a column vector cc. Moreover, if a subaperture was translated within the original aperture of the lens, the Zernike coefficient vector for the newly translated subaperture could be calculated by the following equation cc' TZ ZT x, y cc .*rs j (25) where, cc' is transformed Zernike coefficient vector, TZ and ZT(x,y) are matrices for Taylor-to-Zernike and Zernike-to-Taylor transform respectively, rsj is a column vector of 96 size rescaling terms, and ‘.*’ represents element-by-element multiplication. The detailed explanation of this method for calculating transformed Zernike coefficients can be found in (Raasch, 2011). In this fashion, the spherocylindrical power with this subaperture can be obtained according to the second order Zernike polynomial coefficients: c20 4 3 M r2 (26) J0 c22 2 6 r2 (27) J 45 c22 2 6 r2 (28) where M, J0, J45, in units of diopters, are spherical defocus, orthogonal astigmatism and oblique astigmatism, respectively (Thibos, et al., 2004). In Equations (26)~(28), these second order Zernike coefficients C2m have meridional frequency m, and have units of µm. The radius of the subaperture, r, has a unit of mm. Finally, the calculated spherocylindrical powers of all the arrayed subapertures or pupils are assembled in their corresponding positions to plot the figures of the optical powers for the entire PAL. 7.1.4 Wavefront measurement of PALs Figure 7.4 shows a schematic of the wavefront sensor measuring system. A small, distant white light source produces a nearly flat wavefront in the plane of the tested PAL. The refracted wavefront traverses two relay lenses, and arrives at the Shack-Hartmann sensor. The two relay lenses (elements 3 and 4 in Figure 7.4) are positioned such that the PAL and the microlens array are in optically conjugate planes. To position any given location of the PAL along the measurement axis, the lens is pivoted around horizontal and vertical 97 axes, the intersection of which represents the center of rotation of an eye 27 mm behind the lens. Lens positioning is performed with stepper-motors that pivot the lens mount around the horizontal and vertical rotation axes (not shown in the figure). 150 mm 1 2 300 mm 3 150 mm 4 5 Figure 7.4. Schematic of the wavefront measuring system. 1: Distant source; 2: PAL under test; 3 and 4: 150 mm fl lenses; 5: Shack-Hartmann sensor. The Shack-Hartmann sensor consists of a microlens array and a CCD camera. A 3.5 mm virtual stop is placed at the microlens array, and since it is conjugate with the lens plane at unit magnification, it represents a 3.5 mm eye pupil centered at that lens position. Each microlens is 0.36 mm on a side, and with a 3.5 mm diameter pupil, approximately 70 lenslet spot images are contained in the camera image. When a wavefront enters the sensor, it is partitioned by the microlens array. The local tilt of the wavefront within each subaperture causes a displacement of the focal spot from the reference central position. Thus, these deviations can be assembled to reconstruct the wavefront variation (Shack & Platt, 1971). Wavefront aberration arises from the freeform nature of the PAL, the nonuniform refractive index distribution, and geometric deformation of the lens surfaces. 98 7.1.5 Results and discussions Figure 7.5. Simulated refractive index variation of an injection molded PAL. As discussed in Chapter 6, the rheological phenomenon and uneven cooling lead to the refractive index variation of the injection molded PAL. The FEM results show that the refractive index on one surface layer varies in the scale of 10-4, whereas the variation scale among the multiple surface layers along the thickness direction is 10-3. Figure 7.5 illustrates the refractive index variation of the molded PAL calculated by Equation (21). The location of the injection gate is at the bottom of this picture. Although the upper limit of the injection pressure was set as 100 MPa, the actual maximum injection pressure was about 80 MPa indicated by the FEM simulation which was almost equal to the packing pressure. This is an effective packing with high packing pressure and long packing time. Thus, compared with previous studies (Park & Joo, 2008; Yang, et al., 2011), the 99 distribution variation is relatively small with a maximum deviation of 6×10-4. In addition to the small deviation, because higher packing pressure occurs closer to the injection gate, the general trend of the distribution decreases along the flow direction. Despite of the dominant effects by the sufficient packing, the uneven cooling may outweigh the packing effects. For example, the material at the region farther away from the center in the radial direction cools and shrinks faster than the central region. This causes denser material formation resulting in a higher refractive index. More specifically, as an example, some region at the top may have higher refractive index than the lower part although the top region is farther away from the injection gate. Additionally, since a thinner area cools faster than a thicker area, this analysis can also apply to the thinner top region when compared with the thicker bottom. In Figure 7.5, the index variation is similar to the freeform geometry pattern illustrated in Figure 7.1, which suggests that regional thickness discrepancies may be more important than radial position differences for refractive index variation in terms of thermal transportation. So, with all of these effects combined, the highest refractive index happens at the bottom half of the PAL surrounded by an ox-horn-shaped transition region from the bottom to the top. Geometric deformation is another important factor that influences the PAL’s optical performance. As defined before, the geometric deformation is the thickness deviation between the design and the molded parts. The simulated thickness for the molded lens between the top and bottom surfaces can be calculated by Equation (19). If similar derivations are applied to the original design, the thickness deviation is the discrepancy between the design and simulation. Figure 7.6 shows the simulated thickness deviation between the design and the molded PAL. As seen in this figure, the thicker bottom part of 100 the PAL has more shrinkage in thickness, although it is closer to the injection gate or the highest packing pressure location. Consistent with the analysis above, the larger shrinkage in the thicker region may also result in higher refractive index. In this situation, the regional thickness difference largely contributes to the thickness change of the molded PAL. Figure 7.6. Simulated thickness change in xy plane of the molded PAL. Considering both the refractive index variation and geometric deformation, each component of the optical aberrations of the injection molded PAL can be determined by the derivations developed in Section 7.1.3. Figure 7.7 ~ Figure 7.9 show the PAL’s spherical power M, and the two cylindrical components J0 and J45 respectively, in terms of the design, simulation and measurement results. It can be seen that the variation scales of the simulated optical powers and aberrations are slightly larger than the design. 101 Figure 7.7(b) shows that the magnitude of the simulation is smaller than the design. In addition the optical aberration patterns were also slightly changed when the injection molding process was taken into consideration. For instance, as the simulated spherical power in Figure 7.7(b), a round corner appears at the left side of the bottom red area in contrast to the flat slope at the transition area between red and yellow region in Figure 7.7(a). There is a falling tip pattern on the right side of the blue area though smooth progression in design. Additionally, as can be observed in Figure 7.8(b), the top area in the red zone is larger than the blue area at the bottom while the overall pattern is rotational symmetric in the original design as shown in Figure 7.8(a). Moreover, the simulated cylindrical aberration component J45 in Figure 7.9(b) displays the sagging blue area and red area, but these two areas are symmetric about the horizontal direction in the design as illustrated in Figure 7.9 (a). Finally, the Shack-Hartmann sensor measurements (Figure 7.7(c), Figure 7.8(c), Figure 7.9c), appear to be in relatively good agreement with the simulations. (a) (b) (c) Figure 7.7. Spherical power M of the molded PAL (a) design (b) simulation (c) measurement 102 (a) (b) (c) Figure 7.8. Cylindrical component J0 of the injection molded PAL (a) design (b) simulation (c) measurement (a) (b) (c) Figure 7.9. Comparison of (a) design, (b) simulated and (c) measured cylindrical component J45 of the injection molded PAL. There are many other possible reasons that can potentially affect the accuracy of the evaluation process. For example, in ophthalmic applications, the distance between the lens and the entrance pupil of the eye is typically about 15 mm. The wavefront will, in 103 general, change shape as it travels that distance. However, in this instance, curvatures are not high enough for this difference to be clinically meaningful. In addition, meshing strategies, materials models and boundary conditions also have an influence on the final simulated results. Furthermore, in the optical measurement apparatus, the PAL was rotated around an ocular center of rotation 27 mm behind the lens to select each measurement area. This was done to imitate a rotating eye as it views through different locations on the lens. Nevertheless, large oblique incidence will affect wavefront shape, which is not yet accounted for in this modeling. Finally, precision of centering and positioning the PAL could be improved. Table 7.1. Injection molding conditions for design of experiment Process number Packing pressure (Kg/cm2) Packing time (s) Injection time (s) 800 3 0.125 1 1,200 3 0.125 2 1,200 6 0.125 3 800 6 0.125 4 800 3 0.1 5 800 6 0.1 6 1,200 3 0.1 7 1,200 6 0.1 8 In this research, the goal was to search for a preferred injection molding condition for the PALs. Specifically, packing pressure, packing time, and injection time, were investigated. Two levels of each parameter were investigated, as listed in Table 7.1. Our conclusions can be summarized as: (a) neither the packing time nor the injection time has a significant impact on the optical properties of the PALs, (b) higher packing pressure results in smaller refractive index variation and smaller thickness change (refractive index variation 104 -1.5×10-4 ~ 3.5×10-4, thickness change -15.5 ~ -11 µm), (c) the patterns and the scales of the second order optical powers and aberrations do not change dramatically when the injection molding process conditions are varied. The first conclusion can be explained by the fact that packing times were adequate to offset shrinkage. Further, the higher packing pressure reduced the absolute amount of thickness deformation. However, deformation patterns plotted in the same way as Figure 7.6 were still quite similar between the two packing pressure levels. From the test conditions, the No. 2 process condition was adopted for future production of PALs because of its shorter cycle time, less power requirement, more uniform refractive index distribution and less geometric deformation. This research presents a new approach to fabricate PALs using the combination of ultraprecision diamond turning and precision injection molding. This approach has wide industrialization potential due to its affordability. Also, it is demonstrated that the modeling of the injection molded PALs can be used to successfully predict their optical aberrations. The numerical modeling can also be utilized to optimize manufacturing processes. 7.2 Interferometer measurements A simple approach to quantifying freeform wavefront patterns with large deviation is accomplished by reducing the lens’s surface powers. The power reduction is realized by immersing the freeform lens in a wet cell containing an optical liquid with controlled refractive index (Li, et al., 2014). By comparing the collected wavefront patterns with the nominal values, the differences can be obtained and evaluated by comparing to the FEM 105 simulation. This also improves the understanding of the quality control of microinjection molded freeform optics. 7.2.1 Optical design Alvarez lens is used as an example in the wet cell based interferometer study. The purpose of Alvarez lens is to realize variable refraction powers by a simple and compact approach. Previous studies showed that the optical refraction power of Alvarez lens pair could be varied by shifting the two freeform surfaces perpendicular to the optical axis (Simonov, et al., 2006; Barbero, 2009). In this study, the bottom surface of the Alvarez lens is flat while its top surface height, in mm, can be described by the polynomial below: z a1 x 2 y a2 y 3 (29) where x and y are coordinate positions ranging within a 6 mm diameter circular aperture, and a1 and a2 are 0.019583063 and 0.0062879497 respectively. The deviation from the actual value of a2/a1 to the standard ratio of 1/3 is due to a compensation of spherical aberrations by means of the freeform surface (Sieber, 2014). More details of the optical design can be found in (Sieber, 2014). Figure 7.10 shows the color map of the top freeform surface. The surface pattern is axisymmetric about y axis and negatively rotationally symmetric with respect to x axis. The maximum (peak-valley) deviation is 493.4 µm. 106 Figure 7.10. Top freeform surface of Alvarez lens. 7.2.2 Manufacturing of Alvarez lenses Ultraprecision diamond machining can be utilized to directly fabricate Alvarez lens pair for either infrared light (Smilie, et al., 2011) or visible light (Barbero & Rubinstein, 2013). Furthermore, in order to achieve high volume production, molding techniques have to be employed. For the mold fabrication process, the mold insert with the freeform surface was machined using ultraprecision diamond fast tool servo (FTS) machining for its capability of delivering optical quality surfaces with high precision. Nickel alloy was used as the material of the mold inserts. Figure 7.11(a) shows the finished mold for the Alvarez lens. The arithmetic average surface roughness Ra of the optical surface was approximately 6 nm as measured by a Wyko NT9100 optical profilometer. No postpolishing was performed on the inserts. Some mechanical features were machined into the stainless steel mold housing the mold insert. These features were used to assemble the lens into an automatic driven system. The 3D model of the lens with mechanical features 107 is shown in Figure 7.11(b). The performance of this molded lens will be discussed in a different publication (Sieber, 2014). (a) (b) Figure 7.11. (a) Finished ultraprecision diamond machined mold for injection molding. (b) 3D model of the molded Alvarez lens with small straight pins and flats designed for assembly. The diamond machined mold inserts were then mounted in the microinjection molding machine (LD30EH2, Sodick Plustech) for freeform lens fabrication. The same optical grade polymethylmethacrylate (PMMA), Plexiglas V825, was used in the experiment. The experimental molding conditions are listed in Table 7.2. The inlet of plastic melt is located at the lower right side of the lens shown in Figure 7.11(b). The thickness of the Alvarez lens ranges from 100 µm to 594 µm. A microinjection molded miniature Alvarez lens is shown in Figure 7.12. Not only was the optical surface quality successfully achieved, the small mechanical features were also precisely replicated. 108 Table 7.2. Microinjection molding conditions Molding parameters Values Melt temperature C) 250 Mold temperature C) 35 Injection velocity (mm/s) 220 Maximum injection pressure (MPa) 150 Velocity/pressure switch (vol %) 89 Packing pressure (MPa) 120 Packing time (s) 3 Cooling time (s) 50 Coolant temperature C) 25 Figure 7.12. An injection molded Alvarez lens. 7.2.3 Wavefront prediction and simulation A 3D FEM model for the freeform Alvarez lens was established using HyperMesh (http://www.altair.com) as shown in Figure 7.13. The meshed model was then imported into a commercial FEM software package Moldex3D (http://www.moldex3d.com/en/) to perform the FEM simulation. The entire lens model was meshed, based on a layer-bylayer structure (Li, et al., 2013). There are 10 total surface layers of prism elements, with each layer considered to be a lens surface. Besides the lens itself, the runner, mold base and cooling pipes were also included in the model to ensure accuracy but were omitted 109 from Figure 7.13 for clarity. The material properties of the selected PMMA Plexiglas V825, such as PVT properties and viscosity behaviors, can be found in the Chapter 6. The conditions for the molding simulation were the same as in the experiments listed in Table 7.2. Figure 7.13. FEM mesh model of the Alvarez lens. Node (i, 1) is numbered along the vertical line at coordinates (xi, yi) at the bottom surface, and Node (i, N) is the node along the vertical line at coordinates (xi, yi) at its top surface. One approach to evaluating the optical performance of an Alvarez lens is to measure a wavefront passing through the lens. The Shack-Hartmann sensor system can be used for measuring wavefront deviations in ophthalmic applications (Liang, et al., 1994). However, if large wavefront deviations are involved, the large displacement of the focal spots will result in overlap on the sensor. On the other hand, if interferometers are used, as mentioned previously, a freeform null lens or light modulator has to be added, which significantly increases complexity of this freeform lens measurement system. Therefore, 110 in order to reduce the optical power, such that the entire wavefront variation can be measured using the interferometer, we immersed the lens in one optical liquid with controlled refractive index close to the lens’ nominal refractive index (Joo & Jung, 2012; Barbero, et al., 2003; Tayag & Bachim, 2010). The phase delay was reduced by a conversion factor (Jeong, et al., 2005): CF nlens nliquid nlens nair (30) where nlens is the nominal surface refractive index of the lens, nliquid is the refractive index of the optical liquid, and nair is the refractive index of air. Reliable and repeatable measurement of wavefront aberrations using a wet cell technique was demonstrated in previous studies, for example (Jeong, et al., 2005). In this study, the wet cell technique was introduced to measure the wavefront pattern of the microinjection molded freeform optics compared with conventional axisymmetric optics, and Shack-Hartmann sensor based metrology system was replaced by an interferometer in order to increase accuracy and resolution. Figure 7.14 shows the interferometry setup for the wavefront map measurement of the microinjection molded Alvarez lens. The proposed setup is similar to a previously used scheme studied in (Yun, et al., 1998) except in the current layout the previous double pass setup was modified to a single pass arrangement to accommodate the large deviation in freeform lens geometry. If double pass setup is adopted, the freeform characteristics of the lens, such as freeform surface power and uneven refractive index distribution will be coupled with the measured wavefront. 111 If the controlled refractive index of the optical liquid matches the lens’ refractive index at the lens surface, the measured wavefront deviation reflects the information of refractive index variation (Suhara, 2002; Yang, et al., 2011). This is because with a matching index immersion fluid the surface power of the lens is eliminated. Figure 7.14. Interferometry setup for measuring wavefront pattern of microinjection molded Alvarez lens immersed in a wet cell. 1: He-Ne laser light source; 2: optical pin hole; 3: collimation lens; 4: beam splitter A; 5: flat mirror A; 6: flat mirror B; 7: Alvarez lens immersed in a wet cell; 8: beam splitter B; 9: CCD camera; 10: PZT stage. Next, the measured wavefront pattern due to refractive index variation can be compared with the simulated results. Back to the FEM simulated results, the optical path located at the (xi, yi) line passing through the microinjection molded lens can be computed by OPi ni ti' nliquid Tchamber ti' (31) where Tchamber is the thickness of the wet cell housing the molded lens. Consequently, the simulated optical path deviation can be simply obtained using: 112 NV OPi OPi OPj / NV (32) j 1 In addition, if the controlled refractive index of the optical liquid is not equal but close to the nominal refractive index of the lens, the number of interference fringes can be decreased to a number recognizable to the computer. In this scenario, the surface power of the freeform lens in the air can be reconstructed by multiplying the measured wavefront by the conversion factor: Wair xi , yi CF Wliquid xi , yi (33) where Wair(xi, yi) is the wavefront aberration at coordinates (xi, yi) if lens is placed in the air, Wair(xi, yi) is the wavefront aberration at coordinates (xi, yi) if the lens is immersed in the optical matching liquid. The microinjection molded Alvarez lenses are immersed into two optical liquids from Cargille Labs (http://www.cargille.com/): one with refractive index 1.4917 for PMMA’s nominal refractive index and the other one with 1.5167 for BK7 glass. Once the measured wavefront patterns were obtained, a mask for locating the effective area was manually placed within the aperture region. The positioning of the effective measured wavefront was also manually iterated to achieve minimum deviation from the simulated results by a MATLAB program. 7.2.4 Results and discussions Surface deformation has its primary impact on refraction at the lens surface/air interface. The deformation in injection molding is due to the polymer’s rheological properties and thermal history of the molding process. According to the FEM simulation mentioned in 113 Chapter 6, the surface displacements of the top freeform surface and bottom flat surface are very similar. Therefore, in order to assess the surface deformation of the Alvarez lens, only the bottom surface displacement was selected as evaluation parameter to study the geometry deformation of the microinjection molded Alvarez lenses. Figure 7.15 shows the (a) simulated and (b) measured bottom surface deformations. The injection direction is from the top of the plot to the bottom. The surface measurement was conducted by the stitching program of the Wyko NT9100 optical profilometer. (a) (b) Figure 7.15. (a) Simulated and (b) measured bottom surface deformations of the microinjection molded Alvarez lens. The simulated and measured surfaces have very closely matched variation tendency and range. As can be seen in Figure 7.15, the positive (red) areas are on the left and right corners of the bottom half, where the thinnest areas and two assembly pins are located. But the top areas with higher thickness have an opposite deformation trend compared 114 with the bottom corners. Moreover, the transition region exists between the top half and bottom corners. So the deformation is affected by the freeform surface variation and the surrounding mechanical assemble features. Generally speaking, the deformation is mainly influenced by the geometric structure of the Alvarez lens. Figure 7.16 shows the deformed Alvarez lens with a magnification scale of 50X. Figure 7.16. Simulation plot of the deformed microinjection molded Alvarez lens with a magnification scale of 50X. The residual stresses of the molded Alvarez lenses were measured using a polariscope (PS-100-SF, Strainoptics, Inc), and its value was below 3 MPa, small enough to be safely neglected in this experiment. The maximum residual stress occurred in the thinnest region of the molded lens. Injection molding process has three stages including filling, packing and cooling. The refractive index inside the microinjection molded Alvarez lenses vary with the location of 115 the point of interest. The refractive index variation is a result of the uneven cooling rate at different locations, Figure 7.17 show the refractive index variation maps of simulation and measurement results. Again, the gate of the lens mold is at the top of the plot. For both results, most of the areas have less than 1 λ wavefront deviation. The small deviation is contributed by the effective packing indicated by the simulation. The general trend of the simulation and measured deviations is in good agreement with each other. The peak to valley value of the simulated wavefront deviation is about 1 λ while the value is about 0.5 λ for the measurement. The RMS value of the measured wavefront is 0.082 λ. (a) (b) Figure 7.17. (a) Simulated and (b) measured wavefront pattern describing refractive index distribution of the microinjection molded Alvarez lenses. The highest values occur at the bottom left and right corners, because these are the thinnest parts of the freeform lens leading to the fastest cooling rate. Faster cooling causes denser material formation and then produces higher refractive index. In contrast, 116 the top left and right corners are thicker, which slows the cooling process, so these two areas have lower refractive index. This refractive index effect is relatively small, so the regional thickness distortion tends to have the larger effect on the refractive properties of the lens. Although from Figure 7.10 the center portion of the Alvarez lens has a relatively uniform thickness, for both the simulation and measurement plots, the wavefront deviation decreases from the top center to the bottom center. This is because the top center area is closer to the gate where higher packing pressure is expected, and higher packing pressure yields denser material structure. This pattern may help explain the astigmatism observed in injection molded optics. So the combined effects mentioned above are responsible for the refractive index deviation within the aperture of the microinjection molded Alvarez lens as illustrated in Figure 7.17. (a) (b) (c) Figure 7.18. (a) Nominal and (b) measured wavefront pattern describing surface power distribution of the microinjection molded Alvarez lenses. (c) Difference between the simulated and the measured results. 117 However, there are still some differences between the simulations and measurements for the above two factors. These differences may be due to reasons that can affect the evaluation accuracy. For example, in the FEM calculation, the simulation parameters and boundary conditions may not be accurate enough, such as the materials properties, boundary conditions, and mesh strategies. Moreover, in the wavefront measurement, the position of the lens, the mirror flatness, and the refractive index accuracy of the optical liquids at the current wavelength may also need to be enhanced in the future. When the optical liquid is switched to higher refractive index of 1.5167, the wavefront pattern from the surface power can be measured. Figure 7.18 show the nominal wavefront pattern of an undeformed Alvarez lens with uniform refractive index, the measured wavefront pattern of the microinjection molded Alvarez lens and their difference map, respectively. The nominal wavefront deviation is 15.89 λ while the measured wavefront deviation is 15.8 λ, so the deviation values are close, and were normalized for comparison in Figure 7.18. The maximum local difference of these two wavefront patterns is less than 5%. In addition, as can be seen in Figure 7.18 (c), the major differences come from the center and corner areas. The deviation trend of the wavefront differences between the nominal and the measurement is a combined result of surface deformation and refractive index variation. It can be observed in Figure 7.16 that the overall shape of the top half of the lens in the positive y axis is concave, and the shape of the bottom half is convex. Nevertheless, when taking the geometric deformation into account, the absolute values of the radii of both the concave and convex curvature are increased. In another words, the top concave surface becomes slightly more concave while the bottom convex surface becomes more convex. 118 This leads to the larger optical path for the light traveling through the top region since the ambient optical liquid has higher refractive index, as illustrated in Figure 7.19. In addition to the surface deformation, the refractive index variation factor shown in Figure 7.17(b) further increases the optical path difference between the central top half and the central bottom half. Figure 7.19. Optical path change on the freeform surface. In addition, the positive optical path difference in the top center results in the phase delay at the top left and top right corners, and the opposite trend occurs at the two bottom corners. The described patterns can be confirmed by the surface deformation and refractive index variation at the local corners. Thus, the combined effects of the surface deformation and refractive index variation largely result in the differences between the nominal and the measured wavefront patterns in Figure 7.18. Injection molding has its own intrinsic advantages over conventional glass materials for its capability of providing affordable freeform optics in high volume. This research 119 combined the techniques of ultraprecision diamond machining and microinjection molding to fabricate miniature Alvarez lenses. However, the geometric deformation and uneven density distribution caused by the microinjection molding process complicates its application to precision freeform optics. Therefore, we present an FEM simulation approach to visualize how both the surface deformation and refractive index variation affect the wavefront change. Moreover, a simple and fast wavefront measurement technique by using an optical matching wet cell for injection molded freeform optics is proposed to validate the simulation. 120 Chapter 8. Conclusions This dissertation discusses the fundamental understanding of the freeform optical lens fabrication and its related freeform optical design, ultraprecision mold machining, numerical modeling, and optical metrology. At the first part of this dissertation, a freeform microlens array, which was made of PMMA and had 32 freeform microlenses, was fabricated using the combination of ultraprecision diamond machining and microinjection molding. This method was demonstrated in manufacturing high volume and low cost beam shaping freeform microlens arrays. The design, fabrication, simulation and measurement of a specific freeform microlens were discussed. Ultraprecision slow tool servo diamond machining provides the mold with optical quality without the need for post-polishing. The diamond machining on both of regular materials and brittle materials were evaluated to achieve optical finish. A computer code was programmed to visualize the development of micro fractures distribution on diamond machined silicon surface in 3D. In addition, the novel compression molding and microinjection molding processes were developed to fabricate axisymmetric and asymmetric affordable achromatic optics with high precision. The molding method was selected according to the specific design requirements. By performing the measurement of chromatic focal shifts, these two novel molding processes have been demonstrated as 121 effective approaches for manufacturing affordable and highly flexible optical components. If injection molding is employed, refractive index variation and geometric deformation of injection molded optics influence its optical performance. Finite element modeling were used to calculate the above two factors. 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Applied Optics, 24(24), 44834488. 136 Appendix A: Replicated Microoptical Arrays for Multiple 3D Optical Trapping A.1 Introduction Conventional laser optical tweezers require a high magnification microscope objective lens with high numerical aperture (N.A.) to achieve adequate 3D manipulation. In addition to high cost, limited depth of field, and limited field of view associated with such lenses, the conventional design only allows a single laser trapping spot for manipulating individual micro object. Since the ultimate goal is to process large number of cancer cells simultaneously and these cells have to be manipulated in a specific fashion, a low cost, microlens array based trapping system has been developed. Here we describe our program involving in replicated microoptical lenses fabricated using a combination of diamond machining and microinjection molding. A.2 Competitive analysis Simultaneous multiple trapping of micro objects is of great interest to the state-of-the-art biomedical research since it provides maximum flexibility and capacity for cell manipulation and is also non-invasive to living cells. There are three major solutions available today, namely, time-sharing laser beam, holographic optical elements and microoptics array. The first two methods are expensive and complicated because the delicate optical components used in the system. The third method using microoptics can 137 be made more economic with the combination of ultraprecision machining and molding processes. Ultraprecision diamond machining provides a means to produce arbitrary array patterns for the microlens array in addition to lower optical aberrations. High volume productivity by molding processes makes the devices very affordable. After individual parts are fabricated, the optical devices can be inserted into the conventional optical trapping setup utilizing the proper mechanical alignment features to obtain the precise focal spots for multiple trapping, providing a unique solution to biomedical and medical research. Our work is one of the first attempts to use replicated optical devices made by combining ultraprecision diamond machining and proper replication processes to create multiple trapping, and it will also represent the first affordable integrated device with future commercialization potential thus establishing the foundation for lost cost multiple trapping using microlens arrays. A.3 Experiment setup and results Figure A.1 shows the optical layout of the integrated multiple trapping system constructed for this research. In this design, the collimated infrared laser beam passes through the microlens array (MLA) forming an array of “beamlets”. Assuming proper optical alignment is established, these beamlets are then transferred by the field lens again to form a set of laser traps at the focal plane of the microscope objective (MO). The resulting optical traps can be utilized to manipulate multiple micro objects (in this case living cells) as shown in the figure. Additionally, the fabricated device can be integrated with NEP chip in the future. As illustrated at the bottom of Figure A.1, multiple 138 nanochannels allow multiple cells to be placed in required areas for high efficiency multiple trapping. Figure A.1. Optical setup of the integrated multiple trapping system. Ultraprecision diamond machining has many advantages over more conventional cleanroom based technologies since it can eliminate complicated process steps, avoid high lab maintenance expense and provide more flexibility in 3D pattern manipulation. In addition, ultraprecision machining of freeform optics provides a unique solution to eliminate many optical aberrations that are associated with the optics made with conventional lithography, such as spherical aberration. Once the optical mold is finished, replication processes are utilized for high volume manufacturing while maintaining high precision and quality. One of the replication process options here is microinjection molding which provides an economic way to produce high volume and low cost devices. 139 A couple of designs for the polymer microlens array have been manufactured to evaluate their optical performance. However, because of the high energy laser required in this study, glass microlens array may be desired to avoid the "burn out" issue involved in the experiment. To this end, glass microlens arrays were fabricated to demonstrate their manufacturing feasibility as shown in Figure A.2. Figure A.2. Compression molded glass microlens array used in hybrid glass-polymer microlens assmely. Figure A.3(a) shows the multiple trapping spots obtained by using the combination of a glass microlens array and a microscope objective. The intensity of the laser spots was not completely uniform, and typically brighter spots lead to higher trapping force. Moreover, as shown in Figure A.3(b) the multiple polystyrene beads with approximate 3 m diameter were successfully trapped by this design. The formation pattern of trapped micro objects are determined by the arrangement of the microlens array, therefore the trapping pattern layout can be adjusted according to the need of the specific applications. In addition to multiple trapping, these micro objects can 140 be positioned, such as moved or rotated, to the desired locations by steering the incoming laser beam. (a) (b) Figure A.3. (a) Multiple laser focal spots generated by the optical setup discussed before (b) trapped polystyrene beads A.4 Summary and future work Precision replicated microoptics with high quality provide a low cost alternative for multiple optical trapping, because they can be manufactured by using the combination of ultraprecision diamond machining and molding replication processes. In addition to cost, they offer the advantages of more flexibility of trapping formation pattern and reducing common optical aberrations. The future focus will include the evaluating the performance of optical design, optimizing the optical setup, fabricating suitable microlens arrays with low cost and integrating the device with the NEP chip system. Our ultimate goal is to realize disposable assembled multiple optical trapping devices by replacing the microscope objective with affordable molded precision optical components. 141