Photonic band structure of silver nanorod waveguide using embedding method N A Giannakis1, J E Inglesfield2, P A Belov1, Y Zhao1, and Y Hao1 11 Department of Electronic Engineering, Queen Mary University of London, Mile End Road, London, E1 4NS, United Kingdom,…… 2 School of Physics and Astronomy, Cardiff University, The Parade, Cardiff, CF24 3AA Abstract In this work we calculate the photonic band structure of an infinite line array of long silver nanorods, using the embedding method. The boundaries between the array of nanorods and free space is treated exactly by the embedding method. The calculation of the dispersion diagram reveals branches of longitudinal and transverse guided modes as well as flat plasmon bands. At lower frequencies a phase matching occurs between the transverse modes and the light in free space. Flat bands are observed around the single rod resonance frequency. 1. Introduction A plasmonic waveguide consists of a chain of metallic particles (like Au, Ag), and the energy of light is propagated along the array, due to the plasmon near-field interaction between the particles. The lateral confinement of the propagating wave is below the diffraction limit / 2n (where n is the refractive index and is the wavelength). This makes it a good candidate for a sub-wavelength light guide. Theoretically this light waveguide was first introduced by Quinten et al [1]. Maier and et al subsequently fabricated and did experimental measurements on such a guide [3]. A number of authors have calculated the dispersion diagram of a metallic chain of spheres using Mie theory [1], a quasistatic approximation [2], as well as point dipole approximations [4]. Here we will use the embedding method, which is a full wave solution, for an infinite onedimensional array of silver nanorods, with infinite length, for TE polarization (magnetic field parallel to the rods). 2. Conceptual description of the model The embedding method [5, 6] is a plane wave method, which calculates the region of interest by applying an embedding potential along the boundary surface. Using this method we solve the problem in region I (see figure 1), which is in between the inner boundary of unit cell and the outer surface part of cylinder, by defining the embedding potential operator along the vacuum and cylindrical boundaries. vacuum Periodic boundary I Periodic boundary y II vacuum x Figure 1, Unit cell with periodic and vacuum boundaries. In region that we solve the problem, region I, the dielectric constant is a constant value ( 1), and eventually we do not need to expand the dielectric constant, like in classic plane wave methods, and this makes the embedding method more efficient. By defining the Green function of region I [5], which is expanded in terms of electric field basis functions of region I, we can calculate the (photonic) local density of states (LDOS) ( r , ) 2 ImG I ( r , r ; i ) (1) and density of states (DOS) nI () d r ( r ,) I (2) in region I. By definition the LDOS is the number of photon states per unit volume per unit frequency and DOS is the number of photon states per unit frequency. We notice that the LDOS is proportional to the electric field intensity [8]. In our calculations, we assume that the angular frequency and wavevector are ~ implemented in reduced units, a / 2c , k y k y a / 2 respectively. The lattice ~ a / 2 ) and the radius is 25nm ( ~ a / 3 ). The dielectric constant is a 75nm ( a constant of metallic rods is expressed by the Drude dielectric constant, where 2p , ( ) 1 ( i ) is the damping constant. The plasma angular frequency for silver is p 6.18eV ( ~ p 0.37383 ) and we set 0.005 which corresponds to an almost lossless metal (for simplicity). 3. Results The DOS converges for 140 plane waves and it is plotted for different wavectors ~ ky . The frequency peak points of DOS (fig.2) construct the photonic band structure (3.1a). In the photonic band structure the lower branch is the transverse guided modes, where at lower frequencies occurs a phase matching between transverse modes and the light 200 180 160 140 DOS 120 100 80 60 40 20 0 0.00 0.05 0.10 0.15 0.20 0.25 0.30 Figure 2, DOS versus frequency for wavector ~ k y 0.33 . The first two peak values correspond to transverse and longitudinal modes respectively. The next two peaks are plasmon modes. line. At higher frequencies the group velocity changes smoothly and beyond 0.415 the group velocity becomes zero. The next upper branch is a longitudinal guided mode. In those modes the zero group velocity appears from frequency 0.458. The flat bands regime are plasmon states, which is centered at the single rod plasmon frequency, p / 2 , in which the incident light is strongly absorbed [7,9]. 0.30 0.25 0.20 0.15 0.10 0.05 0.00 0.0 0.1 0.2 0.3 0.4 0.5 ky 1) 2) Figure 3, 1) Photonic band structure. The black lines are allowed modes of region I and the blue line is the light line, 2) LDOS of region I for allowed frequencies of wavector transverse, b) longitudinal, c), d) plasmon modes. ~ k y 0.381 . 2a) The polarization of the mentioned modes can proved, by plotting the LDOS of electric ~ field at wavector k y 0.381 for different frequency states, shown in figure 3.2. Starting from the lowest point, a strong electric field intensity is on the poles along the x direction, corresponding to the transverse modes (fig. 3.2a). The second upper state is polarized along the y-axis which is a longitudinal mode (fig. 3.2b). And the next two edge states of flat bands are plasmon states and the LDOS pattern shows strong field localization on the cylinder surface and higher order plasmon poles (fig. 3.2c,d). 4. Conclusion In conclusion we have formalized the embedding method to silver nanorod chain. The advantage of this method is that excludes difficult area of dispersive cylinder by applying the embedding operator. The dispersive diagram was calculated by the DOS and the LDOS of electric field was used to confirm the polarization of transverse, longitudinal and plasmon modes. References [1] M Quinten, A Leitner, J R Krenn, and F R Aussenegg. Opt. Lett. 23, 1331 (1998). [2] S Yong, D Stroud, Phys. Rev. B 69 125418 (2004). [3] S A Maier, M L Brongersman, P G Kik and H A Atwater, Phys. Rev. B 65, 193408 (2002). [4] W H Weber and G W Ford, Phys. Rev. B 70 125429 (2004). [5] J E Inglesfield, J. Phys. C:Solid State Phys. 14, 3795 (1981). [6] R Kemp and J E Inglesfield, Phys. Rev. B 65, 115103 (2002). [7] J E Inglesfield, J M Pitarke and R Kemp, Phys. Rev. B 69, 233103 (2004). [8] G Colas des Francs, C Girard, A Dereux, J. Chem. Phys. 117, 4659 (2002). [9] G Veronis, R W Dutton, and S Fan, J. Appl. Phys. 97, 093104 (2005).