With the recent discovery of High T_c ceramic superconducting materials, many potential applications which were considered impossible just a few years ago are now being realized. These new uses of superconductors will take place in electronics and energy systems where many different materials are used together. If these superconducting materials are to be used successfully, they must be characterized. Film quality was characterized by measuring the electrical properties under different conditions. Films were tested on alumina and magnesia substrates, to characterize the substrate interactions. Films were printed in different thicknesses and different widths, to determine the effect of film geometry on film quality. Finally these films were aged in a room ambient to determine the effect of atmospheric exposure. The results of these tests show that thick film Superconductors can be easily fabricated on magnesia substrates. Superconducting thick films can also be fabricated on alumina substrates, provided the film thickness is greater than 100μm and line width is greater than 50 mils. On either substrate material, critical currents of the films consistently decreased with thinner, narrower lines and environmental exposure. The maximum critical current on 2 magnesia substrates was 635 A/cm² for an unaged 77μm thick by 200 mil wide line, and the minimum was 345 A/cm² for a 25μm thick by 50 mil wide line aged for thirty days. Alumina substrates showed the same trend with a maximum of 75 A/cm² for an unaged 125μm thick by 200 mil wide line and a minimum of 47 A/cm² for a 100μm thick by 100 mil wide line aged for thirty days. / Master of Science

Strongly correlated metals are known to give rise to a variety of exotic states. In particular, if a system is tuned towards a quantum critical point, new ordered phases may arise. Sr₃Ru₂O₇ is a quasi-two dimensional metal in which field-tuned quantum criticality has been observed. In very pure single crystals of this material, a phase with unusual transport properties forms in the vicinity of its quantum critical point. Upon the application of a small in-plane field, electrical resistivity becomes anisotropic, a phenomenon which has led to the naming of this phase as an `electron nematic'. The subject of this thesis is a study of the electrical transport in high purity crystals of Sr₃Ru₂O₇. We modified an adiabatic demagnetisation refrigerator to create the conditions by which the entire temperature-field phase diagram can be explored. In particular, this allowed us to access the crossover between the low-temperature Fermi liquid and the quantum critical region. We also installed a triple axis `vector magnet' with which the applied magnetic field vector can be continuously rotated within the anisotropic phase. We conclude that the low- and high-field Fermi liquid properties have a complex dependence on magnetic field and temperature, but that a simple multiple band model can account for some of these effects, and reconcile the measured specific heat, dHvA quasiparticle masses and transport co-efficients. At high temperatures, we observe similarities between the apparent resistive scattering rate at critical tuning and those observed in other quantum critical systems and in elemental metals. Finally, the anisotropic phase measurements confirm previous reports and demonstrate behaviour consistent with an Ising-nematic, with the anisotropy aligned along either of the principal crystal axes. Our observations are consistent with the presence of a large number of domains within the anisotropic phase, and conclude that scattering from domain walls is likely to contribute strongly to the large measured anisotropy.

This thesis presents an investigation into a wide range of potential materials for organic photovoltaic (PV) devices. A variety of optical techniques are used to define physical parameters for each material such as the photoluminescence quantum yield (PLQY), absorption coefficient and exciton diffusion length. Electrical characterisation is used to determine the optimal structure for devices fabricated with these materials. A number of novel materials are presented in this thesis. These include new polymers, both soluble and precursor, and a relatively new class of material, the conjugated dendrimer. These are highly configurable branching molecular structures that enable fine tuning of material properties. Work on polymers presented in this thesis investigates how such materials can be improved by testing the effect of small changes to their molecular structure. One of these changes had significant effects upon the overall material characteristics. The introduction of a dipole across a polymer successfully created a charge separating material without the need for an extra species such as C60 to be present. The introduction of the conjugated dendrimer to PV applications allows significant scope for molecular engineering. Dendrimers enable tight control over certain aspects of the molecular properties. Small changes can be made such as colour tuning or solubility that enable optimisation to be performed on the molecular level, rather than on device structure. Such changes produced significantly higher internal quantum efficiencies (> 90%) than typical polymer devices and offer the prospect of power conversion efficiencies in excess of 10%. Time-resolved luminescence (TRL) spectroscopy was used to characterise the behaviour of photogenerated excitons within organic films. The investigation of exciton diffusion length was performed upon two polymers, each utilising two different time-resolved methods; diffusion to a quencher and exciton-exciton annihilation. It was found that diffusion in polythiophene films is anisotropic and the photoluminescence lifetime is dependent upon film thickness. This is explained by the formation of self-ordered microstructures during the spin coating process. Data modelling was performed which took into account both the thickness variation and the interaction of excitons with a quenching interface producing a much more realistic approach than previously published work.

FePt/B4C multilayer thin films are deposited on silicon substrates using magnetron sputtering with different B4C layer thickness. Experimental results suggest that the B4C layers effectively serve as spacers to separate the FePt layers, making the multilayer configuration stable even after film annealing at elevated temperatures. On the other hand, B and C are found to be incorporated into the FePt layer, which is responsible for the FePt grain growth confinement and grain separation, and eventually affects the properties of the composite film. Based on the experimental results of multilayer composite film, particle (FePt)/matrix (B4C) monolayer composite thin films on Si substrate are synthesized, in which a record coercivity of 2200 Oe is achieved compared to similar system. The size uniformity of the FePt nanoparticles, the well-defined particle-particle separation, together with the good magnetic property and high temperature thermal stability of the overall composite film, make it a very promising candidate for the ultrahigh density magnetic storage media. / Functional nanostructures serve as the basic building blocks for nanodevices and significant efforts have been devoted to their morphology control and properties optimization. In present study, four functional nanostructures, i.e., FePt/B4C multilayer composite film, particle (FePt)/matrix (B4C) monolayer composite film, Ga-doped ZnO nanowire arrays, and CdSe nanotube arrays are designed, synthesized and characterized in detail, in which the first two are expected to be prominent candidates for ultrahigh-density magnetic storage media while the later two have potential applications in solar energy conversion. / Semiconductor based one-dimensional nanostructures are investigated as promising building blocks for solar energy conversion devices. Two aspects are explored, aiming at increasing the energy conversion efficiency, i.e., facilitating electron transport and enhancing photon absorbing. In the first case, large area Ga-doped ZnO nanowire arrays are grown on transparent conducting substrate. Experimental results reveal the well-aligned array morphology and the uniform Ga concentration in these nanowires. In particular, direct I-V measurements performed on single nanowire-on-ITO substrate disclose its Ohmic contact with the conducting substrate and the significant conductivity improvement compared to undoped ZnO nanowire, In the second case, a novel synthesis strategy for nanotube arrays is developed and CdSe is used for demonstration, which material possessing more appropriate band gap as effective light harvester compared to that of materials for existing semiconductor nanotube arrays. The controllable tube wall thickness that can be increased until continuous CdSe porous network is obtained. The experimental results suggest a nanotube array formation mechanism that can be generally applied to a wide range of materials. / Zhou, Minjie = 功能纳米结构在磁性和能源方面的应用 / 周民杰. / Adviser: Li Quan. / Source: Dissertation Abstracts International, Volume: 72-11, Section: B, page: . / Thesis (Ph.D.)--Chinese University of Hong Kong, 2009. / Includes bibliographical references (leaves 91-100). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [201-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract also in Chinese. / Zhou, Minjie = Gong neng na mi jie gou zai ci xing he neng yuan fang mian de ying yong / Zhou Minjie.

Ph.D. / In the search to improve the conversion efficiency of solar cells such as α-Si and CuInSe2 cells, attention have recently been focused on the use of transparent conducting oxides (TCO's) as window layers and top electrodes in these cells. Materials such as indium tin oxide (ITO) and fluorine-doped tin oxide (FTO) thin films were used due to their excellent electro-optical properties, but it was found that they were unstable when subjected to a hydrogen plasma (during the a-Si deposition) and that the materials reduced to their metallic forms, degrading their electrical and optical properties. Zinc oxide (ZnO), however, possess electrical and optical properties equal to ITO and FTO, but is stable in the presence of a hydrogen plasma. In this study a system for the deposition of ZnO thin films by spray pyrolysis was developed and the films successfully deposited. The films were also doped with A1C1 3 in an attempt to further improve the films' conductivities. The films were then characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), electrical measurements (Hall and four-point probe measurements) and optical analyses of the films. The films were compared with films deposited by atomic layer epitaxy (ALE) and DC sputtering. It was found that the films were crystalline with a predominantly (002) preferred orientation. The addition of Al as dopant, however, resulted in the film structure deteriorating. The SEM micrographs obtained of the films indicated films with a close-packed structure, existing of small grains and the film surface having a textured appearance. It was further found that the deposition parameters of the films influenced both the structures of the films and the morphologies and the micrographs indicated that the addition of Al as dopant resulted in the film formation being inhibited and even resulting in no proper film being deposited. It was found that the as-deposited ZnO films were resistive and that the films had to be subjected to a post-deposition annealing to decrease the film resistivity. The annealing conditions were investigated and it was found that annealing the films in hydrogen at their deposition temperature for an hour resulted in the largest decrease in the films' resistivities, typically two orders of magnitude. Studies of the substrate temperature indicated that the films had to be deposited at between 350 and 420°C and that a reduction in the substrate temperature resulted in the film resistivity increasing. Contrary to literature, it was found that the addition of Al as dopant had no beneficial influence on the electrical properties of the films and that dopant concentrations exceeding 1.0 at.% resulted in the film resistivity increasing. The films were characterized optically by analysing the transmission spectra obtained of the films, using the envelope technique. It was found that the films had transmissions exceeding 95% and that the refractive indices and optical gaps centred around 1.99 and 3.3 eV respectively. Both properties were affected by the deposition parameters. The ZnO films deposited by spray pyrolysis compared excellently with the films prepared by ALE and DC sputtering in all aspects. It is hence clear that ZnO films, with characteristics suitable for solar cell application, can be deposited by the simple and inexpensive technique of spray pyrolysis.

DC resistance and AC conductance and capacitance have been measured under various conditions in an effort to electrically characterize and make electrical-mechanical correlations for 15 carbon black filled rubber samples. Resistance, conductance and capacitance have been monitored as functions of uniaxial compressive stress, time, temperature, and mechanical and thermal history. Capacitance and conductance have also been monitored as functions of frequency under various degrees of compressive loading and before and after specific heat treatments. A direct relationship has been found between sample • conductance and capacitance under any thermal and/or mechanical condition. This is in agreement with previous theories of conduction network formation and percolation. Various conduction mechanisms have been enumerated and an equivalent circuit of a network of lumped R-C "microelements'' has been qualitatively described. Stress, relaxation, frequency, and temperature dependences of the macroscopic parameters measured ( conductivity and capacitance) are discussed in terms of this model. / M.S.

Indiana University-Purdue University Indianapolis (IUPUI) / Rechargeable lithium ion batteries are widely used in portable consumer electronics such as cellphones, laptops, etc. These batteries are capable to provide high energy density with no memory effect and they have small self-discharge when they are not in use, which increases their potential for future electric vehicles. Investigators are attempting to improve the performance of these cells by focusing on the energy density, cost, safety, and durability. The energy density improves with high operation voltage and high capacity. Before any further development of high voltage materials, safe electrolytes with high ionic conductivity, wide electrochemical window, and high stability with both electrodes need to be developed. In this thesis a new strategy was investigated to develop electrolytes that can contribute to the further development of battery technology. The first study is focused on preparing a hybrid electrolyte, the combination of inorganic solid and organic liquid, for lithium based rechargeable batteries to illustrate the effect of electrode/electrolyte interfacing on electrochemical performance. This system behaves as a self-safety device at higher temperatures and provides better performance in comparison with the solid electrolyte cell, and it is also competitive with the pure liquid electrolyte cell. Then a multilayer electrolyte cell (MEC) was designed and developed as a new tool for investigating electrode/electrolyte interfacial reactions in a battery system. The MEC consists of two liquid electrolytes (L.E.) separated by a solid electrolyte (S.E.) which prevents electrolyte crossover while selectively transporting Li+ ions. The MEC successfully reproduced the performance of LiFePO4 comparable with that obtained from coin cells. In addition, the origin of capacity fading in LiNi0.5Mn1.5O4full-cell (with graphite negative electrode) was studied using the MEC. The performance of LiNi0.5Mn1.5O4 MEC full-cell was superior to that of coin full-cell by eliminating the Mn dissolution problem on graphite negative electrode as evidenced by transmission electron microscopy (TEM) analysis. The MEC can be a strong tool for identifying the electrochemical performances of future high voltage positive electrode materials and their electrode/electrolyte interfacial reactions. Finally, by employing the multilayer electrolyte concept, a new application will be introduced to recycle the lithium. This study demonstrates the feasibility of using water and the contents of waste Li-ion batteries for the electrodes in a Li-liquid battery system. Li metal was collected electrochemically from a waste Li-ion battery containing Li-ion source materials from the battery’s anode, cathode, and electrolyte, thereby recycling the Li contained in the waste battery at the room temperature.

One of the most important electrical requirements in high performance electronic systems or high speed integrated circuits, is to process larger numbers of electrical signals at much higher speeds. Signal propagation delay must be minimized in order to maximize signal velocities. Therefore, material with low dielectric constant and low dissipation factor is being sought. In this thesis research measurements of dielectric constant and dissipation factor were performed on commercially available polyimides that are used in multilayer interconnect structures. Capacitor structures with a polyimide dielectric were measured up to a 1GHz frequency and 220°C temperature. Polyimides were concluded to be compatible for use in high performance systems such as multilayer interconnect structures.

The first part of the dissertation focuses on understanding and modeling the conduction mechanism of conductive adhesives. The contact resistance is measured between silver rods with different coating materials, and the relationship between tunnel resistivity and contact pressure is obtained based on the experimental results. Three dimensional microstructure models and resistor networks are built to simulate electrical conduction in conductive adhesives. The bulk resistivity of conductive adhesives is calculated from the computer-simulated model. The effects of the geometric properties of filler particles, such as size, shape and distribution, on electrical conductivity are studied by the method of factorial design. The second part of the dissertation evaluates the reliability and investigates the failure mechanism of conductive adhesives subjected to fatigue loading, moisture conditioning and drop impacts. In fatigue tests it is found that electrical conduction failure occurs prior to mechanical failure. The experimental data show that electrical fatigue life can be described well by the power law equation. The electrical failure of conductive adhesives in fatigue is due to the impaired epoxy-silver interfacial adhesion. Moisture uptake in conductive adhesives is measured after moisture conditioning and moisture recovery. The fatigue life of conductive adhesives is significantly shortened after moisture conditioning and moisture recovery. The moisture accelerates the debonding of silver flakes from epoxy resin, which results in a reduced fatigue life. Drop tests are performed on test vehicles with conductive adhesive joints. The electrical conduction failure happens at the same time as joint breakage. The drop failure life is found to be correlated with the strain energy caused by the drop impact, and a power law life model is proposed for drop tests. The fracture is found to be interfacial between the conductive adhesive joints and components/substrates. This research provides a comprehensive understanding of the conduction mechanism of conductive adhesives. The computer-simulated modeling approach presents a useful design tool for the conductive adhesive industry. The reliability tests and proposed failure mechanisms are helpful to prevent failure of conductive adhesives in electronic packages. Moreover, the fatigue and impact life models provide tools in product design and failure prediction of conductive adhesives.

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