Rubbing alignment has been used popularly in display industry. However, the alignment mechanisms of rubbed polymer are still not well understood. The purpose of this study is to investigate the relationship between anisotropy of rubbed polyimide thin film and liquid crystal alignment. In this study, we discuss the effects of surface energy and RAS on the surface roughness and pretilt angle of liquid crystal molecules. RAS is a non-contact optical probing technique developed originally for real-time, in situ monitoring of semiconductor growth . In this technique the normalized difference in reflectivity along two orthogonal directions is measured. Recently, the prospect of using RAS for process control in the fabrication of liquid crystal devices is investigated. On the other hand, we have known that the magnitude of surface energy is related to the strength of molecular bond. We can obtain the variation of surface properties by measuring the difference of surface energy. We found that the RA signal, pretilt angle and surface roughness are increasing with an increase in rubbing strength, but surface energy was decreased..

Thesis (M.S.)--University of Michigan, 1970.

Thesis (M.S.)--University of Michigan, 1970.

No description available.

Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2007. / Committee Chair: Mizaikoff, Boris; Committee Member: Bottomley, Lawrence; Committee Member: Hunt, William; Committee Member: Janata, Jiri; Committee Member: Josowicz, Miroslawa.

The use of Attenuated Total Reflectance as an analytical technique in infrared spectroscopy has become increasingly important in the past few years. ATR (Attenuated Total Reflectance) is a relatively new analytical method. Producing spectra of compounds by this method requires no solvent for dissolving the sample and no salts for making pellets. The only requirements for spectra production, similar in quality to those produced by conventional methods, are that there is enough sample to cover both sides of the reflector be similar. The index of the sample is fixed; therefore, the index of the reflector is controlled by selecting a reflector with one similar to the sample. Reflectors with indices from 1.2 to 4.12 are commercially produced. Since no solvents or salts are used in ATR, this method allows complete recovery of the sample without using separation or abstraction processes. The elimination of solvents and salts should also lower the cost of spectra production. The ATR method eliminates the weighing and measuring of samples and salts and the time consuming process of pellet making; therefore, it should be a quicker method than any of the conventional methods. The principles of ATR have been applied to several fields of infrared analysis. Harris and Svoboda used ATR as a means of determination of Alkyl and Monomer Modified Resins; Katlaksky and Keller used ATR to study aqueous solutions. Ahliyah and MOoney used ATR in preparing spectra of Polyatomic Anions, and Deley and Liotti used ATR as a means of identifying coating on paper. Materials for which ATR has been useful in analysis include fabrics, polymers which cannot be easily prepared for other types of analysis, and surfaces of semiconductors. In this project, spectra of several pure barbiturates, drug compositions containing barbiturates, and several related compounds were prepared using ATR; these were compared to spectra produced by the conventional pellet method.

Structural changes of electroactive species during electrochemical reactions cannot be determined from the electroanalytical technique alone. By incorporating spectroscopic techniques with electrochemistry, additional information about analyte structure and composition of the double layer can be obtained during electrochemical processes. Several spectroscopic methodologies have been tailored for this purpose including electronic and vibrational spectroscopies. Mid-infrared ATR spectroscopy is especially interesting as it provides in-situ information about adsorbates at the electrode surface. Mass transport limitations present in mid-infrared (mid-IR) external reflection and transmission spectroelectrochemistry are circumvented with attenuated total reflectance (ATR) spectroelectrochemistry. However, limitations of appropriate electrode materials for internal reflection configurations have hindered widespread adoption of the technique. The work described in this thesis focuses on the development and coupling of electrically conducting DLC films with mid-IR transparent multi-reflection waveguides for ATR spectroelectrochemistry. Conducting diamondlike carbon (DLC) thin films were developed utilizing pulsed laser deposition systems in collaboration with Joanneum Research (Leoben, Austria) and at the University of North Carolina (Chapel Hill). Nitrogen doping and incorporation of noble metal nanoclusters were investigated as approaches aimed at improving the electrical conductivity of DLC. Detailed compositional studies of nitrogen-doped DLC layers showed that sp2-hybridized carbon is responsible for the observed electrochemical activity. Optical transparency of thin (~ 40 nm) DLC layers in the mid-IR regime was confirmed by transmission-absorption measurements upon deposition on zinc selenide ATR waveguides. Additionally, the first spectroelectrochemical application of conducting DLC films was demonstrated via the electropolymerization of polyaniline onto coated ATR elements. Metal-DLC nanocomposite layers were investigated with various analytical techniques obtaining detailed compositional information. Improved electrochemical activity of metal-DLC demonstrated their suitability as electrode materials. Sufficient mid-IR transmissivity of metal-DLC coated germanium waveguides was displayed to enable spectroelectrochemical application. Finally, electropolymerization of poly(4-vinylpyridine) in acetonitrile was pursued to produce highly cross-linked ion-exchange membranes for spectroelectrochemical sensing. The composition of the pre-polymerization mixture and deposition conditions were tailored to obtain uniform semipermeable membranes. Diffusion of cations to electrodes is restricted by performing the electropolymerization as established herein. By employing the described electropolymerization procedure at DLC-coated waveguides, spectroelectrochemical sensing strategies can now be extended into the mid-IR regime.

The optical touch pointer (OTP), a fluorescence spectroscopy based system, assists brain surgeons during guided brain tumor resection in patients with glioblastoma multiforme (GBM). After recording and analyzing the autofluorescence spectrum of the tissue, it is possible to distinguish malignant from healthy brain tissue. A challenge during the intraoperative measurements is the interference of blood. If it gets in contact with the laser pointer, the blood blocks the light transmission to and from the tissue. The purposes of the project were to study and categorize patterns of blood interference and to present possible solutions to avoid signal blocking by blood. To measure fluorescence and reflection two devices were used respectively, the OTP which has a spectrometer and a blue laser, and the diffused reflection spectroscopy system (DRS) which has a spectrometer and a white light source. Both operate independently from each other and are connected to a fiber optical probe. A similar scenario to the one in the operation theater was simulated in the lab. Fluorescence and diffuse reflection measurements with and without blood were realized on skin and on two different plastic fluorescent standards. The results were analyzed with the aid of MatLAB, and compared with data collected in the hospital during brain tumor resection. The highest autofluorescence of brain tissue and skin is reached at approximately 506 nm. Although skin and both plastic standards have different optical properties regarding color or rather fluorescence, all of them presented very similar curves when blood on them blocked partially or completely the light transmission. A blood layer of more than 0.1 mm thickness blocks the blue laser light. Blood absorption happens at 541 and 577 nm due to oxy-hemoglobin (HbO2) in both liquid and dried blood. When the fluorescence spectrum is available but weak, the reflection spectrum contains two dips (traces of HbO2 at 541 and 577 nm). In brain there were cases in which light absorption occurred additionally at other wavelengths than the absorption peaks of deoxyhemoglobin (Hb) and HbO2. Blood interference during the OP can be prevented if the probe rests in a saline solution after every measurement. In this way the fresh blood sticking on the probe dissolves in the solution. For dried or coagulated blood, additional manual cleansing is needed.

The objective of this dissertation is to shed light on the physical properties of InN epilayers grown by High-Pressure Chemical Vapor Deposition (HPCVD) for optical device applications. Physical properties of HPCVD grown InN layers were investigated by X-ray diffraction, Raman scattering, infrared reflection spectroscopies, and atomic force microscopy. The dependencies of physical properties as well as surface morphologies of InN layers grown either directly on sapphire substrates or on GaN/sapphire templates on varied growth conditions were studied. The effect of crucial growth parameters such as growth pressure, V/III molar ratio, precursor pulse separation, substrate material, and mass transport along the flow direction on the optical and structural properties, as well as on the surface morphologies were investigated separately. At present, growth of high-quality InN material by conventional growth techniques is limited due to low dissociation temperature of InN (~600 ºC) and large difference in the partial pressures of TMI and NH3 precursors. In this research, HPCVD technique, in which ambient nitrogen is injected into reaction zone at super-atmospheric growth pressures, was utilized to suppress surface dissociation of InN at high temperatures. At high pressures, long-range and short-range orderings indicate that c-lattice constant is shorter and E2(high) mode frequency is higher than those obtained from low-pressure growth techniques, revealing that InN structure compressed either due to a hydrostatic pressure during the growth or thermal contraction during the annealing. Although the influence of varied growth parameters usually exhibit consistent correlation between long-range and short-range crystalline orderings, inconsistent correlation of these indicate inclination of InN anisotropy. InN layers, grown directly on α-sapphire substrates, exhibit InN (1 0 1) Bragg reflex. This might be due to a high c/a ratio of sapphire-grown InN epilayers compared to that of GaN/sapphire-grown InN epilayers. Optical analysis indicates that free carrier concentration, ne, in the range of 1–50 × 1018 cm–3 exhibits consistent tendency with longitudinal-optic phonon. However, for high ne values, electrostatic forces dominate over inter-atomic forces, and consistent tendency between ne and LO phonon disappears. Structural results reveal that growth temperature increases ~6.6 ºC/bar and V/III ratio affects indium migration and/or evaporation. The growth temperature and V/III ratio of InN thin films are optimized at ~850 ºC and 2400 molar ratio, respectively. Although high in-plane strain and c/a ratio values are obtained for sapphire-grown epilayers, FWHM values of long-range and short-range orderings and free carrier concentration value are still lower than those of GaN/sapphire-grown epilayers. Finally, vibrational and optical properties of chalcopyrite ZGP crystal on the (001), (110), and (10) crystalline planes were investigated by Raman scattering and infrared (IR) reflection spectroscopies. Raman scattering exhibits a nonlinear polarizability on the c-plane, and a linear polarizability on the a- and b-planes of ZGP crystal. Also, birefringence of ZGP crystal was calculated from the hydrostatic pressure difference between (110) and (10) crystalline planes for mid-frequency B2(LO) mode.

As the miniaturization of functional devices in integrated circuit (IC) continues to scale down to sub-nanometer size, the process complexity increases and makes materials characterization difficult. One of our research effort demonstrates the development and application of novel Multiple Internal Reflection Infrared Spectroscopy (MIR-IR) as a sensitive (sub-5 nm) metrology tool to provide precise chemical bonding information that can effectively guide through the development of more efficient process control. In this work, we investigated the chemical bonding structure of thin fluorocarbon polymer films deposited on low-k dielectric nanostructures, using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). Complemented by functional group specific chemical derivatization reactions, fluorocarbon film was established to contain fluorinated alkenes and carbonyl moieties embedded in a highly cross-linked, branched fluorocarbon structure and a model bonding structure was proposed for the first time. In addition, plasma induced damage to high aspect ratio trench low-k structures especially on the trench sidewalls was evaluated both qualitatively and quantitatively. Damage from different plasma processing was correlated with Si-OH formation and breakage of Si-CH3 bonds with increase in C=O functionality. In another endeavor, TiN hard mask defect formation after fluorocarbon plasma etch was characterized and investigated. Finding suggest the presence of water soluble amines that could possibly trigger the formation of TiN surface defect. An effective post etch treatment (PET) methods were applied for etch residue defect removal/suppression.