Different Electronic Materials Semiconductors: Elemental (Si, Ge) & Compound (GaAs, GaN, ZnS, CdS, …) Insulators: SiO2, Al2O3, Si3N4, SiOxNy, ... Conductors: Al, Au, Cu, W, silicide, ... Organic and polymer: liquid crystal, insulator, semiconductor, conductor, superconductor Composite materials: multi-layer structures, nano-materials, photonic crystals, ... More: magnetic, bio, … Insulators, Conductors, Semiconductors Inorganic Materials E E conduction band empty Band gap Forbidden region Eg > 5eV valence band filled Insulator SiO2: Eg = 9 eV E conduction band Band gap Eg < valence band electron hole 5eV partially-filled band + Semiconductor Si: Eg = 1.1 eV Ge: Eg = 0.75 eV GaAs: Eg = 1.42 eV Conductor Electronic properties & device function of molecules Electrons in molecule occupy discrete energy levels--molecular orbitals Highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) are most important to electronic applications Bandgap of molecule: Eg = E(LUMO) - E(HOMO) Organic molecules with carbon-based covalent bonds, with occupied bond states ( band) as HOMO and empty antibonding states (* band) as LUMO Lower energy by delocalization: Benzene Conducting Polymers Polyacetylene: Eg ~ 1.7 eV ~ 104 S cm-1 Polysulphur nitride (SN)n ~ 103-106 S cm-1 Poly(phenylene-vinylene) (PPV) High luminescence efficiency Biphenyl Diodes and nonlinear devices Molecule with D--A structure C16H33Q-3CNQ D Highly conductive zwitterionic D+--Astate at 1-2V forward bias Reverse conduction state D---A+ requires bias of 9V I-V curve of Al/4-ML C16H33Q-3CNQ LB film/Al structure A Negative differential resistance (NDR): electronic structural change under applied bias, showing peak conductance 2’-amino-4-ethynylphenyl-4’ethynylphenyl-5’-nitro-1-benzennthiol Self-assembled layer between Au electrodes NDR peak-to-valley ratio ~ 1000 Molecular FET and logic gates Molecular single-electron transistor: Could achieve frequency > 1 THz switching Assembly of molecule-based electronic devices “Alligator clips” of molecules: Attaching functional atoms S for effective contact to Au High conductance through leads but surface of body is insulating Self-assembled Molecular (SAM) Layers Carene on Si(100) Simulated STM images for (c) for (a) 0.1 ML 1-nitronaphthalene adsorbed on Au(111) at 65 K Ordered 2-D clusters Self-assembled patterns of trans-BCTBPP on Au(111) at 63 K Interlocking with CN groups Conventional Organic Electronic Devices Organic Thin Film Transistors (OTFT) Organic Light Emitting Diode (OLED) For large-area flat-panel displays, circuit on plastic sheet Printing: Soft-lithographic process in fabrication of organic electronic circuits Unique electronic & opto-electronic properties of nanostructures DOS of reduced dimensionality (spectra lines are normally much narrower) Spatial localization Adjustable emission wavelength Surface/interface states Effective bandgap blue-shifted, and adjustable by size-control Optical properties of quantum dot systems Excitons in bulk semiconductors An e-h pair bound by Coulomb potential H-atom like states of exciton in effective-mass approximation: 2K 2 E Eg 13.6 (eV) 2M n 2 m r2 0 Bohr radius of the exciton: rm 0a a B 0 (a0 = 0.529 Å) M = me*+ mh*, ħK: CM momentum = me*mh*/(me*+ mh*) reduced mass Bohr radius of electron or hole: a e,h rm 0a 0 * m e,h aB = ae + ah In GaAs (me*= 0.067m0, mhh*= 0.62m0, r = 13.2) Binding energy (n = 1): 4.7 meV, aB = 115 Å Generally, binding energy in meV range, Bohr radius 50-400 Å Excitons in QDs Bohr radius is comparable or even much larger than QD size R Weak-confinement regime: R >> aB, the picture of H atom-like exciton is still largely valid: 2 2 E Eg 13.6 (eV) 2 2 2 2MR n m r 0 Strong confinement regime (R << ae and ah): model of H atom-like exciton is not valid, confinement potential of QD is more important. Lowest energy e-h pair state {1s, 1s}: 2 2 2 1 1 1 . 8 e E ( R) E g * 4 R 2 * 2R me m 0 r h Production of uniform size spherical QDs Controlled nucleation & growth in supersaturated solution All clusters nucleate at basically same moment, QD size distribution < 15% QDs of certain average size are obtained by removing them out of solution after a specific growth period Further size-selective processing to narrow the distribution to 5% Similar nucleation and growth processes of QDs also occur in glass (mixture of SiO2 and other oxides) and polymer matrices Ion implantation into glass + annealing Mono-dispersed nanocrystals of many semiconductors, such as CdS, CdSe, CdTe, ZnO, CuCl, and Si, are fabricated this way Optimal performance of QDs for semiconductor laser active layers requires 3D ordered arrays of QDs with uniform size In wet chemical QDs fabrication: proper control of solvent composition and speed of separation In SK growth of QDs: strain-mediated intra- and inter-layer interactions between the QDs Aligned array of GaN QDs in AlN Passive optic devices with nanostructures: Photonic Crystal An optical medium with periodic dielectric parameter r that generates a bandgap in transmission spectrum Luminescence from Si-based nanostructures Luminescence efficiency of porous Si (PSi) and Si QDs embedded in SiO2 ~ 104 times higher than crystalline Si Fabrication of PSi: electrochemical etching in HF solution, positive voltage is applied to Si wafer (anodization) Sizes of porous holes: from nm to m, depending on the doping type and level Nano-finger model of PSi: from Si quantum wires to pure SiO2 finger with increasing oxidation Emission spectrum of PSi: from infrared to the whole visible range Remarkable increase in luminescence efficiency also observed in porous GaP, SiC Precise control of PSi properties not easy Si-based light emitting materials and devices Digital Display Atomic structures of carbon nanotubes Stable bulk crystal of carbon Graphite Layer structure: strong intra-layer atomic bonding, weak inter-layer bonding 3.4 Å 1.42 Å Enclosed structures: such as fullerene balls (e.g., C60, C70) or nanotubes are more stable than a small graphite sheet Trade-off: curving of the bonds raises strain energy, e.g., binding energy per C atom in C60 is ~ 0.7 eV less than in graphite MWNT, layer spacing ~ 3.4 Å SWNT Index of Single-wall Carbon Nanotubes (SWNT) Armchair (n, n) Zigzag (n, 0) General (m, n) Synthesis of CNTs by Laser vaporization: Pulsed laser ablation of compound target (1.2% at. Co-Ni + 98.8% C) High yield (~70%) of SWNT ropes Carbon arc discharge: ~500 Torr He, 20-25 V across 1-mm gap between 2 carbon rods Plasma T > 3000C, CNT bundles deposited on negative electrode With catalyst (Co, Ni, Fe, Y, Gd, Fe/Ni, Co/Ni, Co/Pt) SWNTs Without catalyst MWNTs Vapor-phase synthesis: similar to CVD Substrate at ~ 700-1500C decorated with catalyst (Co, Ni or Fe) particles, exposed to hydrocarbon (e.g. CH4, C6H6) and H2 Aligned CNTs grow continuously atop of catalyst particles Regular CNT arrays on catalyst pattern Useful for flat panel display Growth mechanisms of C nanotubes 1) C2 dimer addition model: C2 dimer inserted near pentagons at cap 2) Carbon addition at open ends: attach C2 at armchair sites and C3 at zigzag sites Functions of catalyst clusters: stabilizing terminators, cracking of hydrocarbons Fit the controlled CVD process, the open-end is terminated by a catalyst cluster Structural identification of nanotubes: with TEM, electron diffraction, STM HRTEM: number of shells, diameter STM: diameter, helicity of nanotube out-shell, electronic structure Electronic properties of SWNTs SWNTs: 1D crystal If m - n = 3q metallic Otherwise semiconductor Zigzag, dt = 1.6nm =18, dt = 1.7nm =21, dt = 1.5nm =11, dt = 1.8nm Armchair, dt = 1.4nm Bandgap of semiconducting SWNTs: ta E g C C dt a t 5.4 eV, CC = 1.42 Å, overlap integral STM I-V spectroscopy Junctions between SWNTs: homojunctions, heterojunctions, Schottky junctions, but how to connect and dope? SWNT connections: insert pentagons and heptagons Natural SWNT Junctions Doping of semiconductor SWNTs N, K atoms n-type; B atoms, oxygen p-type SWNT CMOS inverter & its characteristics Other nanotubes and nanowires GaN nanowires BN nanotubes Si nanowires p-Si/n-GaN nanowire junction