Thesis (Ph.D.)--University of Delaware, 2006. / Principal faculty advisor: Dionisios G. Vlachos, Dept. of Chemical Engineering. Includes bibliographical references.

Thesis (Ph. D.)--Oregon State University, 2007. / Printout. Includes bibliographical references. Also available on the World Wide Web.

Thesis (Ph. D.)--University of Washington, 2006. / Vita. Includes bibliographical references (leaves 112-120).

A mathematical model is developed to describe the micro/nano-scale fluid flow and heat/mass transfer phenomena in an evaporating extended meniscus, focusing on the transition film region under nonisothermal interfacial conditions. The model incorporates thermocapillary stresses at the liquid-vapor interface, a slip boundary condition on the solid wall, polarity contributions to the working fluid field, and binary mixture evaporation. The analytical results show that the adsorbed film thickness and the thin film length decrease with increasing superheat by the thermocapillary stresses, which influences detrimentally the evaporation process by degrading the wettability of the evaporating liquid film. In contrast, the slip effect and the binary mixture enhance the stability of thin film evaporation. The slip effect at the wall makes the liquid in the transition region flow with smaller flow resistance and thus the length of the transition region increases. In addition, the total evaporative heat flow rate increases due to the slip boundary condition. The mixture of pentane and decane increases the length of the thin film by counteracting the thermocapillary stress, which enhances the stability of the thin film evaporation. The polarity effect of water significantly elongates the thin film length due to the strong adhesion force of intermolecular interaction. The strong interaction force restrains the liquid from evaporation for a polar liquid compared to a non-polar liquid. In the experimental part, laser induced fluorescence (LIF) thermometry has been used to measure the microscale temperature field of a heated capillary tube with a 1 mm by 1 mm square cross section. For the temperature measurement, the calibration curve between the temperature and the fluorescent intensity ratio of Rhodamine-B and Rhodamine-110 has been successfully obtained. The fluorescent intensity ratio provides microscale spatial resolution and good temperature dependency without any possible bias error caused by illuminating light and background noise usually encountered in conventional LIF techniques. For the validation of the calibration curve obtained, thermally stratified fields established inside a glass cuvette of 10 mm width were measured. The measurement result showed a good agreement with the linear prediction. The temperature measurement in a 1 mm capillary tube could provide the feasible method of temperature measurement for the thin film region in the future.

Copper has become the metal of choice for metallization, owing to its high electrical and thermal conductivity, relatively higher melting temperature and correspondingly lower rate of diffusivity. Most of the current studies can get high strength copper thin films but on an expense of conductivity. This study proposes a technique to deposit high strength and high conductivity copper thin films on different silicon substrates at room temperature. Single crystal Cu (100) and Cu (111) have been grown on Si (100) and Si (110) substrates, respectively. Single crystal Cu (111) films have a high density of growth twins, oriented parallel to the substrate surface due to low twin boundary energy and a high deposition rate. The yield strengths of these twinned Cu films are much higher than that of bulk copper, with an electrical resistivity value close to that of bulk copper. X-ray diffraction, transmission electron microscopy and nanoindentation techniques were used to show that high density twins are sole reason for the increase in hardness of these thin films. The formation of growth twins and their roles in enhancing the mechanical strength of Cu films while maintaining low resistivity are discussed.

High tunability and low loss tangent of ferroelectric thinfilms offer unique opportunity for the development of variousmicrowave devices. Silver tantalate niobate, which showsexcellent microwave properties, was selected for this study.Ag(Ta,Nb)O3(ATN) showed week dielectric dispersion in a widefrequency range from 1 kHz up to 100 GHz, negligible losses upto 30 GHz, and ease to tailor paraelectric state in a widetemperature range by Ta:Nb ratio. This thesis is mainly based on the synthesis andcharacterization of niobate ferroelectric ATN thin films. Thinfilms for various measurements were prepared by pulsed laserdeposition and rf-magnetron sputtering techniques. X-ray diffraction (XRD) pattern show that ATN/Pt80Ir20films have been found to be (001) preferentiallyoriented, while the epitaxial quality of ATN/LaAlO3heterostructures have been ascertained. Dielectricproperties were analyzed by measuring the relationship betweendielectric permittivity and frequency as well as dielectricpermittivity and temperature. Reliable tracing of theferroelectric hysteresis polarization versus electric loopsindicate the ferroelectric state in ATN films at temperaturebelow 125 K and yields the remanant polarization of 0.4µC/cm2@ 77 K. The fundamental current-voltage behavior in Ag(Ta,Nb)O3ferroelectric films was measured usingMe/Ag(Ta,Nb)O3/Pt80Ir20, Me = Pd, Au, Cr, and Al, vertical capacitivecell structures with different top electrodes. Various kinds ofconduction mechanisms such as Schottky emission, Poole-Frenkel,Fowler-Nordheim, and ionic conduction were classified. Finally, by fabricating interdigital capacitors on the oxidesubstrates, the characteristics and performances of Ag(Ta,Nb)O3varactors were examined. Au/Cr/ATN/LaAlO3interdigital capacitors exhibited loss tangent aslow as 0.0033 @ 1 MHz, weak frequency dispersion of 5.8 % in 1kHz to 1 MHz range, tunability as high as 16.4 %,K-factor (tunability/tanδ) higher than 48.

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The effect of pH and ionic strength on the equilibrium adsorptive behavior of β-lactoglobulin onto hydrophobic and hydrophilic silicon surfaces was studied using ellipsometry. Plots of amount adsorbed (μg protein/cm²) as a function of protein concentration (mg/ml) exhibited attainment of plateau values beyond a protein concentration of 0.250 mg/ml. At a given pH and ionic strength, plateau values associated with hydrophobic surfaces were observed to be greater than those associated with hydrophilic surfaces. The Langmuir adsorption isotherm was chosen as the most appropriate model to represent the data and was used to compare results obtained under different experimental conditions. Effects of pH and ionic strength on protein adsorption at hydrophilic surfaces indicate that electrostatics played a major role, while pH and ionic strength effects on adsorption to hydrophobic surfaces reflect a greater importance of nonelectrostatic interactions. / Graduation date: 1991

The dichroism in amorphous As2Se3 induced by a polarized beam of near band-gap light (λ = 632.8 nm) was measured in films that ranged in thickness from 0.25 µm to 1.93 µm. Most noncrystalline materials are initially isotropic and homogeneous. When amorphous As2Se3 (a chalcogenide glass) absorbs an intense pump-beam of polarized light, the absorption coefficient for light polarized in the same direction as the pump-beam is less than for the perpendicular polarization, i.e. the sample becomes anisotropic (dichroic). The induced dichroism is reversible by rotating the polarization of the pump light by 90°. Induced dichroism is potentially useful in various photonic devices including optical switches, optical memory, and photowritable polarizers.<p>Several aspects of photoinduced anisotropy in a-As2Se3 have been analyzed:<p>(i) rate of photoinduced anisotropy buildup as a function of inducing beam intensity and sample thickness, <p>(ii) the kinetics of the photoinduced anisotropy buildup in terms of a stretched exponential curve, <p>(iii) the stretched exponent, β, as a function of inducing beam intensity and sample thickness, <p>(iv) reversibility of the photoinduced anisotropy, (v) saturation level of photoinduced anisotropy as a function of inducing beam intensity and sample thickness.<p>The anisotropy buildup kinetics has been found to follow a stretched exponential behavior and that there exists an inverse relationship between the pump intensity and the time constant, τ. The τ(I) vs intensity (I) relationship more closely follows a logistic dose response curve than a simple straight line or power law relationship. There exists a direct relationship between the time contact  and the sample thickness, where a longer anisotropy buildup time is required as the sample thickness increases. The stretched exponent, β, was found to be approximately 0.6 and has a slight dependence on the inducing light intensity. The correlation of the stretching exponent, β, to sample thickness, L, was found to have a weak inverse relationship, that is β tends to decrease as the sample thickness increases.<p>The findings in this work demonstrate that the anisotropy orientation could be changed indefinitely since it was found that even after 100 orientation changes the anisotropy saturation had no measurable fatiguing. The anisotropy saturation level was found to be independent of the inducing beam intensity and linearly proportional to the sample thickness.