Thesis (M. Phil.)--Hong Kong University of Science and Technology, 2003. / Includes bibliographical references. Also available in electronic version. Access restricted to campus users.

Thesis (M.S.)--Virginia Polytechnic Institute and State University, 1994. / Vita. Abstract. Includes bibliographical references (leaves 68-70). Also available via the Internet.

Thesis (M.S.)--Oregon State University, 2009. / Printout. Includes bibliographical references (leaves 48-50). Also available on the World Wide Web.

A dissertation submitted to the Faculty of Science, University of the Witwatersrand, Johannesburg, in fulfillment of the academic requirements for the degree of Master of Science. Johannesburg, March 2016. / Zinc oxide (ZnO) continues to receive widespread attention due to its excellent optical and electronic properties; it demonstrates the combined characteristics of high transmittance and electrical conductivity. Despite the tremendous drive for its application in optoelectronic devices, the full nature of the point defects and defect complexes have not been characterised comprehensively. In this work, luminescence characteristics of the intrinsic defects in ZnO thin films and the rare-earth ions Eu3+ and Tb3+ in ZnO powders are investigated under blue-laser excitation. The thin films used in this study were deposited using the radio-frequency magnetron sputtering method over a 2 hour duration under varied power and substrate bias conditions. The powders were synthesized by the chemical bath deposition method with dopant concentrations of 1.0 mol%. Grazing incidence X-ray diffraction (XRD) was used to determine the lattice properties of the samples. Photoluminescence studies were primarily conducted at room temperature (300 K) with the 457.9 nm, 476.5 nm and 488.0 nm laser lines as excitation sources. For the ZnO thin films, XRD patterns of a hexagonal wurtzite structure with a c/a ratio of about 1.60 and a u-parameter of 0.38 were obtained. Photoluminescence measurements show a broad emission band in the 500.0-900.0 nm range, centred at 656.0 nm. Annealed films yielded relatively more intense photoluminescence spectra than the as-prepared films. The intrinsic point defects and defect level transitions responsible for the broad emission are discussed. For the ZnO powders, the XRD patterns of the annealed samples of pristine ZnO, ZnO:Eu3+ and ZnO:Tb3+ are similarly consistent with a hexagonal wurtzite ZnO phase. Energy dispersive spectroscopy (EDS) confirmed the presence of the Eu3+ and Tb3+ dopants in the respective ZnO host while scanning electron microscopy (SEM) measurements showed the morphology of the sample powders. Photoluminescence spectra of pelletized samples, obtained in the 460.0-900.0 nm range, exhibit relatively intense Eu3+ and Tb3+ emission bands superimposed on a broad emission background. The RE3+ emission bands are attributed to the 5D0 → 7FJ (J = 0, 1, 2, 3, 4) and the 5D4 → 7FJ (J = 0, 1, 2, 3, 4, 5, 6) electronic transitions of Eu3+ and Tb3+, respectively, while the background emission is attributed to intrinsic defects. Crystal-field energy levels for the Eu3+ ion and the Tb3+ ion occupying a C3v symmetry site were deduced from fitting Gaussian curves to the RE3+ emission bands. Possible channels for transfer of energy from the intrinsic defects to Eu3+ and Tb3+ are discussed. / LG2017

The observation of ferromagnetism of (Ga,Mn)As by Ohno in 1998 has inspired great interest in diluted magnetic semiconductors (DMS). DMS’s features combining ferromagnetism and semiconducting make them of great potential for conceptual spintronic devices, which is a promising field of research for the emerging electronics. The practical application of DMS requires a Curie temperature well above room temperature and an intrinsic ferromagnetism. There are several types of DMS materials. The typical ones are transition-metal (TM) doped GaAs, GaN and ZnO. The TM-doped ZnO has drawn particular attention due to the observation of room temperature ferromagnetism in this system including cobalt-doped ZnO.But the origin of ferromagnetic TM-doped ZnO is still unknown after a decade’s theoretical and experimental effort on this material. In this thesis, we do the magnetic circular dichroism(MCD) and Hall measurement of high quality Cobalt-doped ZnO thin films grown by molecular beam epitaxy (MBE). Room temperature ferromagnetism is observed in these samples. Combining the data from MCD and Hall measurement, we attribute the room temperature ferromagnetism in this system to the impurity band of the doped Cobalt cations. / published_or_final_version / Physics / Master / Master of Philosophy

Thesis (Ph. D.)--Washington State University, December 2007. / Includes bibliographical references.

ZnO is an n-type semiconducting material with high optical transparency in the visible range (400 - 750 nm) of the electromagnetic spectrum. When doped with group 13 or 14 metal oxides, ZnO exhibits almost metallic electrical conductivity. ZnO thin films have been recognised as promising alternative material for the currently widely-used but expensive indium oxide in the form of indium tin oxide (ITO), in terms of their low cost and the high abundance of zinc. At the moment, even the best solution-processed ZnO films still can not compete for ITO replacement especially in solar energy utilization and OLED lighting applications, and the performance of ZnO films needs to be further improved. The objective of this work was to enhance the electrical and optical properties of spray pyrolysed ZnO thin films by simultaneous cation and anion doping. This was achieved by growing several series of undoped, single-doped, and co-doped ZnO thin films over a wide range of conditions, in order to understand the growth behaviour of undoped and doped ZnO, and to establish the optimum growth procedure. Spray pyrolysis process has advantages over vacuum-based techniques in terms of its low-cost, high deposition rate, simple procedure and can be applied for the production of large area thin films. Various techniques were employed to characterize the properties of the prepared thin films, and thus determine the optimum growth conditions (i.e. X-ray difiraction (XRD), Xray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), scanning electron microscopy (SEM), UV-Vis-NIR spectroscopy and Hall effect measurement). The growth of doped ZnO on glass substrates using Si and F as dopants, yielded highly conducting and transparent thin films. The co-doped thin films exhibited distinct widening of band gap upon increasing deposition temperature and doping concentration as a result of increasing electron concentration up to 4.8 x 10²⁰ cm^-3 upon doping with Si and F at the same time. The resistivity of the films deposited from Zn(acac)₂ · xH₂O solutions and at the optimum temperature of 450 °C, was found to decrease from 4.6 x 10^-2 Ωcm for the best undoped ZnO film to 3.7 x 10^-3 Ωcm, upon doping with 3% Si. The films co-doped with Si and F in the ratios of [Si] / [Zn]= 3 - 4 mol% and [F] / [Zn]=30 - 40 mol% were the most conducting (p ∼ 2.0 x 10^-3 Ωcm). The associated optical transmittance of co-doped ZnO was above 85% in the whole visible range. Results compare favourably with In-doped ZnO deposited under similar conditions. Si+F co-doped ZnO films offer a suitable replacement for ITO in many applications such as LCD and touch screen displays.

No description available.

Xia, Daxue. / Thesis (Ph.D.)--Chinese University of Hong Kong, 2011. / Includes bibliographical references. / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract also in Chinese.

Vertically aligned nanocomposite (VAN) thin films have recently stimulated significant research interest to achieve better material functionality or multifunctionalities. In VAN thin films, both phases grow epitaxially in parallel on given substrates and form a unique nano-checkerboard structure. Multiple strains, including the vertical strain which along the vertical interface and the substrate induced strain which along the film and substrate interface, exist in VAN thin films. The competition of these strains gives a promise to tune the material lattice structure and future more the nanocomposite film physical properties. Those two phases in the VAN thin films are selected based on their growth kinetics, thermodynamic stability and epitaxial growth ability on given substrates. In the present work, we investigated unique epitaxial two-phase VAN (BiFeO3)x:(Sm2O3)1-x and (La0.7Sr0.3MnO3)x:(Mn3O4)1-x thin film systems by pulsed laser deposition. These VAN thin films exhibit a highly ordered vertical columnar structure with good epitaxial quality. The strain of the two phases can be tuned by deposition parameters, e.g. deposition frequency and film composition. Their strain tunability is found to be related directly to the systematic variation of the column widths and domain structures. Their physical properties, such as dielectric loss and ferromagnetisms can be tuned systematically by this variation. The growth morphology, microstructure and material functionalities of VAN thin films can be varied by modifying the phase ratio, substrate orientation or deposition conditions. Systematic study has been done on growing (SrTiO3)0.5:(MgO)0.5 VAN thin films on SrTiO3 and MgO substrates, respectively. The variation of column width demonstrates the substrate induced strain plays another important role in the VAN thin film growth. The VAN thin films also hold promise in achieving porous thin films with ordered nanopores by thermal treatment. We selected (BiFeO3)0.5:(Sm2O3)0.5 VAN thin films as a template and get uniformly distributed bi-layered nanopores. Controllable porosity can be achieved by adjusting the microstructure of VAN (BiFeO3):(Sm2O3) thin films and the annealing parameters. In situ heating experiments within a transmission electron microscope column provide direct observations into the phases transformation, evaporation and structure reconstruction during the annealing. Systematic study in this dissertation demonstrate that the vertically aligned nanocomposite microstructure is a brand new architecture in thin films and an exciting approach that promises tunable material functionalities as well as novel nanostructures.