In this work, argon, hydrogen and methane are used as gas sources and nitrogen is used as the doping source. Microwave plasma chemical vapor deposition and two-steps deposition processes have been applied to grow the nitrogen-doped diamond thin film on n-type (111) silicon substrate. Systematical experiments are performed to study the dependence of grown process on working pressure, temperature, microwave power, DC bias, the duration of growth time and the flow rates of gas mixture of argon, methane and nitrogen. The nitrogen-doped diamond thin films are examined by SEM, XRD, Raman and I-V. Raman spectroscopy is the most efficient tool for analyzes the quality of diamond thin films growth. The results show that a positive DC bias can enhance the doping concentration and the qualities of diamond thin films. Form the analyzing results, nitrogen is doped in the sp2 structural grain boundaries of crystallites. The longer diamond thin film grown is, the crystallites become larger and the grain boundaries become smaller, that leads to the larger resistivity of the thin films.

The objective of the research in this thesis was to develop high-efficiency n-type silicon solar cells at low-cost to reach grid parity. This was accomplished by reducing the electrical and optical losses in solar cells through understanding of fundamental physics and loss mechanisms, development of process technologies, cell design, and modeling. All these technology enhancements provided a 3.44% absolute increase in efficiency over the 17.4% efficient n-type PERT solar cell. Finally, 20.84% efficient n-type PERT (passivated emitter and rear totally diffused) solar cells were achieved on commercial grade 239cm2 n-type Cz silicon wafers with optimized front boron emitter without boron-rich layer and phosphorus back surface field, silicon dioxide/silicon nitride stack for surface passivation, optimized front grid pattern with screen printed 5 busbars and 100 gridlines, and improved rear contact with laser opening and physical vapor deposition aluminum. This thesis also suggested research directions to improve cell efficiency further and attain ≥21% efficient n-type solar cells which involves three additional technology developments including the use of floating busbars, selective emitters, and negatively charged aluminum oxide (Al2O3) film for boron emitter surface passivation.

A series of heteroleptic and homoleptic platinum(II) complexes has been synthesized and characterized towards their use in thin film devices such as organic light-emitting diodes (OLEDs) and organic thin film transistors (OTFTs). Pyridylpyrazolate- and pyridyltetrazolate-containing ligands were selected due to their structural rigidity and ease of functionalization. Single-crystal x-ray diffraction studies of two selected heteroleptic complexes show strong aggregation with preferential stacking into vertical columns with a varying degree of overlap of the neighboring square planar molecular units. It is shown that the close proximity of the molecules to one another in the stack increases semiconducting character, phosphorescence quantum yields, and shorter radiative lifetimes. The potential for these materials towards incorporation into high-efficiency doping free white OLEDs (DFW-OLEDs) for solid-state lighting and display applications has been realized and will be expanded upon by present and future embodiments of materials in this thesis.

<p> </p><p>Organic semiconductors are prime candidates for thermoelectric applications, because one can maximize the dimensionless figure of merit ZT (by maximizing the Seebeck coefficient and electrical conductivity) while simultaneously minimizing the thermal conductivity. In this work, we explore a few materials and try to find their thermoelectric characteristics. For the n-leg of the thermogenerator, we studied a modified fullerene (PCBM) which is doped with TDAE vapor. For the p-leg, we studied PEDOT and found the TDAE dedoping level at which the figure of merit is maximized.</p>

Carbon nanotubes were dispersed and functionalized with polyethylene imine (PEI) before incorporation in a polyvinyl acetate matrix. The resulting samples exhibit air-stable N-type characteristics with electrical conductivities as great as 1600 S/m and thermopowers as high as 100 microV/K. Thermopowers and electrical conductivities correlate, in a reversal of the trend found in typical materials. This phenomenon is believed to be due to the increase in the number of tubes that are evenly coated in a better dispersed sample. Increasing the amount of PEI relative to the other constituents positively affects thermopower but not conductivity. Air exposure reduces both thermopower and conductivity, but a stable value is reached within seven days following film fabrication. The atmospheric effects on the electrical conductivity prove to be reversible. Oxygen is believed to be the primary contributor to the decay.

Organic semiconductors are prime candidates for thermoelectric applications, because one can maximize the dimensionless figure of merit ZT (by maximizing the Seebeck coefficient and electrical conductivity) while simultaneously minimizing the thermal conductivity. In this work, we explore a few materials and try to find their thermoelectric characteristics. For the n-leg of the thermogenerator, we studied a modified fullerene (PCBM) which is doped with TDAE vapor. For the p-leg, we studied PEDOT and found the TDAE dedoping level at which the figure of merit is maximized.

Calcium ions (Ca2+) are admitted into presynaptic nerve terminals through voltage gated calcium channels and diffuse to bind and activate the secretory vesicle discharge mechanism. Current research favors a highly ‘modal’ organization where the release sites are activated by one or a few closely apposed channels (Stanley, 1997). To fully understand the nanophysiology of transmitter release site activation, it is necessary to determine the rate of Ca2+ flux through individual channels at normal physiological external concentrations. OBJECTIVE: To explore the relationship between CaV2.2 channel conductance and external Ca2+ across the physiological range. CONCLUSION: The conductance of the CaV2.2 channel was determined across the range of 1-100 mM [Ca2+]EXT . With 2 mM [Ca2+]EXT, the conductance was determined to be 2.76 ± 0.24 pS.

Calcium ions (Ca2+) are admitted into presynaptic nerve terminals through voltage gated calcium channels and diffuse to bind and activate the secretory vesicle discharge mechanism. Current research favors a highly ‘modal’ organization where the release sites are activated by one or a few closely apposed channels (Stanley, 1997). To fully understand the nanophysiology of transmitter release site activation, it is necessary to determine the rate of Ca2+ flux through individual channels at normal physiological external concentrations. OBJECTIVE: To explore the relationship between CaV2.2 channel conductance and external Ca2+ across the physiological range. CONCLUSION: The conductance of the CaV2.2 channel was determined across the range of 1-100 mM [Ca2+]EXT . With 2 mM [Ca2+]EXT, the conductance was determined to be 2.76 ± 0.24 pS.

Organic electronics have received significant development in the last few decades. p- Type materials are much more in availability than n-type now. There are only a few examples of air-stable n-type materials. The design and synthesis of novel air-stable ntype materials is still a focus of research. Herein is described a study to evaluate the effectiveness of a novel electron-withdrawing group, composed of three electronwithdrawing groups connected in series, to impart material properties known to be favorable for obtaining air-stable n-types. The smaller acenes, naphthalene and anthracene, carrying these electron-withdrawing groups were prepared and studied by UV-Vis absorption spectroscopy and solution electrochemical measurements to estimate changes in frontier molecular orbital energies and single crystal X-ray diffraction to determine packing motif. These measurements suggest that the new materials could be promising as n-type semiconductors in organic field effect transistor (OFET) and as acceptors for organic photovoltaic (OPV) cells. The reasons are based on: (1) the close intermolecular contacts seen in X-ray crystal structures, some of them showing 3D faceto- face stack. (2) Electrochemical measurements indicate LUMO energy levels suitable for air-stable n-type materials.

Over the past few decades, metal phthalocyanines (MPcs) have been thoroughly investigated as active materials in organic field-effect transistors (OFETs) towards the commercialization of flexible integrated circuits and displays. One of several advantages to MPcs as building blocks for OFETs is the high degree of functionality, from which the choice of metal ion, substituents along with the phthalocyanine framework and axially bound ligands can synergistically tune the physical and self-assembly properties of the material. Recent interest has been directed to the introduction of main-group elements as the central ion of MPcs as an avenue to install both hole and electron transport properties and improve device performance. To prepare materials that are suitable to be employed as the semiconducting active layer in organic field-effect transistors, a family of novel silicon phthalocyanine derivatives was prepared. The synthesis and optoelectronic properties of those new axially disubstituted silicon phthalocyanines are detailed in this work. Axial ligand variation mainly includes alkylsiloxy derivatives. The emphasis of the current thesis, however, is on tailoring the Pc backbone, which includes replacing the four benzene units with pyrazine moieties, extending the degree of conjugation with naphthalene, and introducing substituents on their peripheral positions. Several metal-containing tetra-2,3-pyrazinoporphyrazines are also described, but their applications are limited due to the difficulty of purification. Specifically, Chapter 1 serves as a comprehensive review of main-group phthalocyanines and their use as active materials in organic field-effect transistors. In Chapter 2, silicon tetra-2,3-pyrazinoporphyrazine complexes are explored. The isosteric substitution of CH groups in Pc macrocycle for nitrogen atoms leads to an obvious hypsochromic shift in their main absorption band, and their relatively low energy levels make them promising air-stable n-type organic semiconducting materials for OFETs. The synthesis and characterization of silicon tetra(tert-butyl)-2,3-naphthalocyanine complexes are described in Chapter 3. The extension of π-conjugation leads to obvious bathochromic shifts in the main absorption band. In addition, the introduction of tert-butyl groups on the periphery of the molecule reduces the tendency of the naphthalocyanine molecules to aggregate, thereby increase their solubility. Chapter 4 covers the synthesis and characterization of zinc tetra-2,3-pyrazinoporphyrazine and cobalt tetra-2,3-pyrazinoporphyrazine, whereas more future works are expected. The fifth chapter provides a conclusion to this work, and possible future directions of the research conducted herein.