The foremost aim for performing this study was to focus on the electrodeposition of mixed hydrogen molybdenum tungsten bronze films, which have the potential for e– transfer interactions carrying out the reduction of carbon dioxide. A yellow peroxymolybdic tungstate solution was prepared and used for the electrodeposition of hydrogen molybdenum tungsten bronze films on conductive carbon paper. Electrodeposition was carried out at -2.0 V from 20 - 120 minutes to determine the effect of deposition time on film thickness and CO2 reduction. These films were characterized by X-ray photoelectron spectroscopy. The deposited films served as a working electrode for CO2 electrochemical reduction utilizing 0.8 M NaHCO3 as the electrolyte. Carbon dioxide gas was bubbled into the cathode solution for an hour while bulk electrolysis was carried out at different applied potentials. Products were identified and evaluated using ion chromatography.

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第22068号 / 工博第4649号 / 新制||工||1725(附属図書館) / 京都大学大学院工学研究科材料工学専攻 / (主査)教授 邑瀬 邦明, 教授 宇田 哲也, 教授 杉村 博之 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第22459号 / 工博第4720号 / 新制||工||1737(附属図書館) / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 作花 哲夫, 教授 安部 武志, 教授 阿部 竜 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM

京都大学 / 0048 / 新制・課程博士 / 博士(エネルギー科学) / 甲第22673号 / エネ博第405号 / 新制||エネ||77(附属図書館) / 京都大学大学院エネルギー科学研究科エネルギー応用科学専攻 / (主査)教授 平藤 哲司, 教授 馬渕 守, 教授 土井 俊哉 / 学位規則第4条第1項該当 / Doctor of Energy Science / Kyoto University / DFAM

京都大学 / 0048 / 新制・課程博士 / 博士(エネルギー科学) / 甲第22798号 / エネ博第412号 / 新制||エネ||79(附属図書館) / 京都大学大学院エネルギー科学研究科エネルギー応用科学専攻 / (主査)教授 平藤 哲司, 教授 土井 俊哉, 教授 馬渕 守 / 学位規則第4条第1項該当 / Doctor of Energy Science / Kyoto University / DFAM

Strengthening, resistant and shielding properties, to name a few, can be achieved by implementing a surface material coating onto an engineering component. Various elements of these compounded parts can augment the functionality of the part, such as, increased life time and more interactive surfaces. Tungsten has proven to be a challenge to plate with other metals, but if done correctly, the results can allow for the cold spray of tungsten. Cold spraying tungsten particles alone provides a challenge because the powder is too hard and instead of adhering, it erodes the surface it is attempting to plate. Coating tungsten in a softer metal, like copper, will allow for the particles to adhere to the surface and create a strengthened and radiation shielded component. It also yields a better surface to electroplate onto in the future, as tungsten itself is hard to plate onto, so the copper layer provides the ability to easily plate other metals. The purpose of this thesis project is to encapsulate tungsten powder within copper, then scale up the process to produce bulk amounts of the material in a batch process. The particles will be encased using an electroplating method, that has been vi turned into a semi-autonomous process for the ease of producing bulk powder. While electroless deposition has previously shown positive results for attaining a uniform coating, making it a semi-batch process for bulk material would have an extreme cost in comparison to electrolytic deposition. The tungsten particles have been successfully enclosed in copper by electrolytic deposition in this set of experimentation using an HF electro-etch pretreatment and ultrasonic agitation during electroplating. Further experimentation will include improved methods of stirring and transferring powder, as the transfer takes too long between the etch and the onset of plating and the stirring method is bulky and reduces the area that can be efficiently plated on.

京都大学 / 新制・課程博士 / 博士(エネルギー科学) / 甲第23396号 / エネ博第423号 / 新制||エネ||80(附属図書館) / 京都大学大学院エネルギー科学研究科エネルギー応用科学専攻 / (主査)教授 平藤 哲司, 教授 土井 俊哉, 准教授 三宅 正男 / 学位規則第4条第1項該当 / Doctor of Energy Science / Kyoto University / DGAM

In this dissertation, nano-manufacturing of amorphous alloys for electro-catalytic applications is reported and the role of chemistry and active surface area on catalytic behavior is discussed. The catalytic activity of recently developed platinum and palladium-based metallic glasses was studied using cyclic voltammetry and localized electrochemical techniques. The synergistic effect between platinum and palladium was shown for amorphous alloys containing both these elements. The mechanism for superior catalytic behavior was investigated through electronic structure and surface chemical state of the alloys. A correlation between the work function and catalytic performance of the amorphous alloys with widely varying chemistries was established. To address the high cost associated with the noble-metal containing catalysts, the performance of non-noble Ni-P amorphous catalyst was evaluated for electro-catalysis. A facile pulsed electrodeposition approach was used for the nano-manufacturing of these amorphous catalysts. This nano-manufacturing route allowed the synthesis of fully amorphous nano-wires at room temperature for alloys with little or no noble-metal content. A wide range of nano-wires with varying aspect ratios from 25 to 120 was synthesized using commercially obtained anodic aluminum oxide (AAO) nano-molds. Cyclic voltammetry and chrono-amperometry demonstrated superior performance in terms of electrocatalytic activity and stability of the metallic glass nano-wires towards electro-oxidation of methanol. The mechanism for amorphization during pulsed electrodeposition is discussed and compared with the conventional approach of rapid quenching of the liquid melt.

Diploma thesis is involved in basic properties of nickel materials for alkaline accumulators. Practical part deals with measuring of nickel hydroxides by cyclic voltametry. Next practical part is above measuring and optimalization various proportion of nickel and cobalt in layer made by electrodeposition on nickel electrodes.

The diploma thesis deals with researching electrodeposition of silicon in anhydrous solutions. As electrolyte was used EC:DMC (1:1) with (C2H5)4NBF4, LiPF6 and LiClO4. Research was measured by cyclic voltammetry and XRD.