Thesis (Ph. D.)--UCLA, 2009. / Vita. Description based on print version record. Includes bibliographical references (leaves 347-368).

Colloidal nanocrystal assemblies offer an attractive opportunity for designer metamaterials. The ability to permute chemical composition, size, shape, and arrangement of nanocrystals leads to an astounding number of unique materials properties that find use in an extensive array of applications---ranging from solar cells to medicine. However, to take full advantage of these materials in useful applications, the nature of their assembly and their behavior under external stimuli must be well understood. Additionally, the assembly of colloidal nanocrystals into thin films provides a promising pathway to the solution-processing of inorganic materials that are prohibitively too expensive and/or difficult to deposit by conventional methods. Nanocrystal superlattices (NCSLs) of sterically stabilized nanocrystals were assembled by slow evaporation of colloidal dispersions on various substrates. Detailed analysis of the NCSL structures was carried out using transmission and scanning electron microscopy (TEM and SEM) and small-angle x-ray scattering (SAXS). Body-centered cubic (bcc) NCSLs, in particular, were studied in detail and ligand packing frustration was proposed as a significant driving force for their assembly. The behavior of NCSLs was also studied by SAXS under mild heating and solvent vapor exposure revealing several remarkable order-order, order-disorder, and amorphous-crystalline structural transitions. Colloidal Cu(In [subscript 1-x] Ga [subscript x])Se₂ (CIGS) nanocrystals were synthesized by arrested precipitation and formulated into inks. These inks were spray deposited into thin films under ambient conditions to serve as the active light absorbing material in printed low-cost photovoltaic (PV) devices. These devices, which were fabricated without the need for high temperature processes, have achieved power conversion efficiencies above 3 % under AM1.5 illumination. While the efficiencies of these devices are still too low for commercial viability, this work does provide a proof of concept that reasonable efficient solar cells can be created with a low-cost printable process using nanocrystal inks. Since high temperatures are not used to form the light-absorbing layer, nanocrystal-based solar cells were built on flexible light weight plastic substrates. The main obstacle to achieving high power conversation efficiencies was found to be the ability to extract the photo induced charge carriers. Nanocrystal films suffer from poor transport that leads to high recombination rates in thicker films. To date, the best efficiencies have been achieved with thin light absorber layers that only absorb a fraction of the incident light. / text

This thesis presents the design and synthesis of nanowires (NW) with targeted and tunable optical properties. Moreover, we show how single and assembled NW devices can enable new photovoltaic (PV) and photonic platforms. Beginning with an investigation of axially modulated p-i-n junction NWs, we established several fundamental parameters dictating solar cell performance at the nanoscale and demonstratred the first series integration of multiple solar cells on a single NW. Thereafter, implementation of the first silicon NW photovoltaic device with radially modulated p-n junctions showed that power conversion efficiencies of 3-4% are attainable from a nanoscale architecture, exceeding efficiencies for many organic and hybrid organic-inorganic solar cells. Despite these achievements, the poor electrical characteristics and insufficient control over absorption properties characterizing the aforementioned devices would limit the promise of silicon NWs for next generation solar cells. We overcome these limitations with a class of polymorphic core/multi-shell silicon NWs with highly-crystalline hexagonally-faceted shells and embedded coaxial p/i/n junctions. NW PV devices 200-300 nm in diameter exhibit open-circuit voltages of 0.5 V and fill-factors of 73% under one-sun solar illumination. Single-NW wavelength-dependent photocurrent measurements agree quantitatively with FDTD simulations. Synthetic manipulation of NW size and morphology drives tuning of optical resonances such that optimized structures can yield current densities double those for films of comparable thickness. Further optimized NW devices achieve current densities of 17 mA/cm2 and power conversion efficiencies of 6%. We also present steps toward rational assembly of larger-scale NW PV arrays. Parallel integration of NWs preserves PV metrics while assembly of vertically-stacked NWs yields current densities of \(25 mA/cm^2\) and projected efficiencies of ~15% for \(1 \mu m\) thick assemblies. Finally, we present the first ever NW material possessing 3 degrees of structural freedom, thus expanding the NW "structome." Such NWs were achieved through the first demonstration of facet selective growth of silicon and germanium in the gas phase. Photonic devices based on this new material present intriguing optical properties, including selective attenuation, enhancement, and wavelength tunability of resonant cavity modes. / Chemistry and Chemical Biology

This thesis presents the theoretical studies of electronic transport in molecular electronic devices. Such devices have been proposed and investigated as a promising new approach that complements conventional silicon-based electronics. To design and fabricate future nanoelectronic devices, it is essential to understand the conduction mechanism at a molecular or atomic level. Our approach is based on the non-equilibrium Green's function method (NEGF) combined with density functional theory (DFT). We apply the method to study the electronic transport properties of two-probe systems consisting of molecules or atomic wires sandwiched between leads. A few molecular electronic devices are characterized; namely, conducting molecular wires, molecular switches and molecular recognition sensors. The considered applications are interconnection of different nanoelectronic units with cumulene molecular wires; adding switching functionality to the molecular connectors by applying stress to the CNT-cumulene-CNT junction or by introducing phthalocyanine unit; sensing of individual nucleotides, e.g., for DNA sequencing applications. The obtained results provide useful insights into the electron transport properties of molecules. Several interesting and significant features are analyzed and explained in particular such as, level pinning, negative differential resistance, interfering of conducting channels etc.

Thesis (M.S.) in Electrical Engineering--University of Maine, 2008. / Includes vita. Includes bibliographical references (leaves 47-48).

No description available.

abstract: Raman scattering from Ge-Si core-shell nanowires is investigated theoretically and experimentally. A theoretical model that makes it possible to extract quantitative strain information from the measured Raman spectra is presented for the first time. Geometrical and elastic simplifications are introduced to keep the model analytical, which facilitates comparison with experimental results. In particular, the nanowires are assumed to be cylindrical, and their elastic constants isotropic. The simple analytical model is subsequently validated by performing numerical calculations using realistic nanowire geometries and cubic, anisotropic elastic constants. The comparison confirms that the analytic model is an excellent approximation that greatly facilitates quantitative Raman work, with expected errors in the strain determination that do not exceed 10%. Experimental Raman spectra of a variety of core-shell nanowires are presented, and the strain in the nanowires is assessed using the models described above. It is found that all structures present a significant degree of strain relaxation relative to ideal, fully strained Ge-Si core-shell structures. The analytical models are modified to quantify this strain relaxation. / Dissertation/Thesis / Ph.D. Physics 2011

abstract: ABSTRACT The unique structural features of deoxyribonucleic acid (DNA) that are of considerable biological interest also make it a valuable engineering material. Perhaps the most useful property of DNA for molecular engineering is its ability to self-assemble into predictable, double helical secondary structures. These interactions are exploited to design a variety of DNA nanostructures, which can be organized into both discrete and periodic structures. This dissertation focuses on studying the dynamic behavior of DNA nanostructure recognition processes. The thermodynamics and kinetics of nanostructure binding are evaluated, with the intention of improving our ability to understand and control their assembly. Presented here are a series of studies toward this goal. First, multi-helical DNA nanostructures were used to investigate how the valency and arrangement of the connections between DNA nanostructures affect super-structure formation. The study revealed that both the number and the relative position of connections play a significant role in the stability of the final assembly. Next, several DNA nanostructures were designed to gain insight into how small changes to the nanostructure scaffolds, intended to vary their conformational flexibility, would affect their association equilibrium. This approach yielded quantitative information about the roles of enthalpy and entropy in the affinity of polyvalent DNA nanostructure interactions, which exhibit an intriguing compensating effect. Finally, a multi-helical DNA nanostructure was used as a model `chip' for the detection of a single stranded DNA target. The results revealed that the rate constant of hybridization is strongly dominated by a rate-limiting nucleation step. / Dissertation/Thesis / Ph.D. Chemistry 2011

The aim of this project is to develop novel approaches for the detection and characterisation of engineered and other potentially harmful nanoparticles in the air. In particular we wish to distinguish specific nanomaterials from the background atmospheric aerosol to provide a means of measuring human exposure to nanomaterials that may present a risk to health. Ideally, solutions should be practically deployable in the field. The metrics considered for measurement across this project are: size, number, chemical nature and surface area. Two main approaches are chosen to address these requirements: online size selective surface area controlled nucleation, and quantitative assessment of size resolved Raman spectroscopic maps. The first approach is based on the discovery of a different regime type of heterogeneous nucleation. In this case nucleation probability is determined by the surface area of the aerosol rather than the number of nuclei present. A portable DMA has also been developed allowing for the pre-separation of particles according to size in a compact package. Combining this DMA with the novel nucleation technology provides a means of measuring surface area distributions of particles. Finally, a novel Raman spectroscopic methodology is presented for the chemically specific quantification of aerodynamically size selected samples. Particles are first aerodynamically size segregated from the air in a wide size range sampler. These size fractionated samples are analysed by Raman spectroscopy. Imaging analysis is then applied to Raman spatial maps to provide chemically specific quantification against the substrate as a proxy for background aerosol. Analysing this data in combination with the known deposition efficiency of aerosols in the respiratory tract (provided by the sampling method), can then provide a complete exposure measurement approach.

abstract: In today's world there is a great need for sensing methods as tools to provide critical information to solve today's problems in security applications. Real time detection of trace chemicals, such as explosives, in a complex environment containing various interferents using a portable device that can be reliably deployed in a field has been a difficult challenge. A hybrid nanosensor based on the electrochemical reduction of trinitrotoluene (TNT) and the interaction of the reduction products with conducting polymer nanojunctions in an ionic liquid was fabricated. The sensor simultaneously measures the electrochemical current from the reduction of TNT and the conductance change of the polymer nanojunction caused from the reduction product. The hybrid detection mechanism, together with the unique selective preconcentration capability of the ionic liquid, provides a selective, fast, and sensitive detection of TNT. The sensor, in its current form, is capable of detecting parts per trillion level TNT in the presence of various interferents within a few minutes. A novel hybrid electrochemical-colorimetric (EC-C) sensing platform was also designed and fabricated to meet these challenges. The hybrid sensor is based on electrochemical reactions of trace explosives, colorimetric detection of the reaction products, and unique properties of the explosives in an ionic liquid (IL). This approach affords not only increased sensitivity but also selectivity as evident from the demonstrated null rate of false positives and low detection limits. Using an inexpensive webcam a detection limit of part per billion in volume (ppbV) has been achieved and demonstrated selective detection of explosives in the presence of common interferences (perfumes, mouth wash, cleaners, petroleum products, etc.). The works presented in this dissertation, were published in the Journal of the American Chemical Society (JACS, 2009) and Nano Letters (2010), won first place in the National Defense Research contest in (2009) and has been granted a patent (WO 2010/030874 A1). In addition, other work related to conductive polymer junctions and their sensing capabilities has been published in Applied Physics Letters (2005) and IEEE sensors journal (2008). / Dissertation/Thesis / Ph.D. Electrical Engineering 2012