Finding materials based on non-rare earth metals is vital for the global transition to a more sustainable economy. Discovering useful properties in common metal oxides is a promising avenue for new materials. In this work we have investigated the properties of Ru(x)CoMo(1-x) to evaluate the feasibility of its use as an electrocatalyst for the oxygen evolution reaction (OER). Herein, the plasma spray deposition on FTO and glass is reported as a method for production of low Ru content-CoMo oxide. The material showed a good performance in an alkaline electrolyte for OER, with no loss on stability and overpotentials to achieve a current density of 10 mA cm-2 of 528, 483, 455, 439 mV for 0, 10, 20, and 30 At% of Ru, respectively. The final material is shown to be composed entirely of Co and Mo oxides, as well as Ru which is present in the crystal structure of these metal oxides as observed using optical characterization techniques, XRD, Raman and SEM. With the aim of maximising performance and decreasing the amount of Ru used, we find a Ru content of 20 At% is most optimal for OER in alkaline. We find therefore Ru(0.2)(CoMo)(0.8) to be an effective electrocatalyst for OER in alkaline, while examples from literature outperforms it in other applications, it is still a good basis for further work and development.

No description available.

Conjugated semiconducting polymers have garnered substantial interest in recent years due to the potential for use in various applications, particularly in the field of electronic devices such as photovoltaic cells and light emitting diodes. Conjugated polymers offer numerous advantages in these applications, including low cost and high flexibility, but electronic devices based on these materials are currently limited by poor performance. Because of these limitations, increased focus has been placed on improving conjugated polymers for use in commercially viable products. Here, a novel core shell hybrid nanocomposite based on anisotropic zinc oxide nanowires and a side-chain functionalized polythiophene is reported. This nanocomposite exhibits confirmed covalent side-on linkage between the polymer and the nanowires, and the crystalline, thermal and photophysical properties of the nanocomposite are investigated, revealing elongated conjugation length in the polymer backbone, increased crystallinity and thermal stability and rapid charge transfer. Additionally, the conformational transitions of side-chain functionalized polythiophenes are investigated in dilute solution through the use of ultraviolet-visible absorption spectrophotometry. A coil-to-rod conformational transition is identified, and is found to be induceable through temperature and solvent changes. Study into the kinetics of the transition reveals a first-order rate law, and the effects of polymer structure on the conformational transition are substantiated.

Two dimensional (2D) materials have received growing interest because of their unique properties compared to their bulk counterparts. Graphene is the archetype 2D solid, but other materials beyond graphene, such as MoS2 and BN have become potential candidates for several applications. Recently, a new family of 2D materials of early transition metal carbides and carbonitrides (Ti2CTx, Ti3C2Tx, Ti3CNTx, Ta4C3Tx, and more), labelled MXenes, has been discovered, where T stands for the surface-terminating groups. Before the present work, MXenes had only been synthesized in the form of exfoliated and delaminated powders, which is not suitable for electronic applications. In this thesis, I demonstrate the synthesis of MXenes as epitaxial thin films, a more suitable form for electronic and photonic applications. Results show that 2D epitaxial Ti3C2Tx films - produced by HF and NH4HF2 etching of magnetron sputter-grown Ti3AlC2 - exhibit metallic conductive behaviour down to 100 K and are 90% transparent to light in the visible-infrared range. The results from this work may open the door for MXenes as potential candidates for transparent conductive electrodes as well as in electronic, photonic and sensing applications. MXenes have been shown to intercalate cations and molecules between their layers that in turn can alter the surface termination groups. There is therefore a need to study the surface chemistries of synthetized MXenes to be able to study the effect of intercalation as well as altering the surface termination groups on the electronic structure and chemical states of the elements present in MXene layers. X-ray Photoelectron Spectroscopy (XPS) in-depth characterization was used to investigate surface chemistries of Ti3C2Tx and Ti2CTx. This thesis includes the discussion of the effect of Ar+ sputtering and the number of layers on the surface chemistry of MXenes. This study serves as a baseline for chemical modification and tailoring of the surface chemistry groups to potential uses and applications. New MXene phases, Nb2CTx and V2CTx, are shown in this thesis to be produced from HF chemical etching of Nb2AlC and V2AlC powders. Characterization of the produced MXenes was carried out using Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD), Transmission Electron Microscope (TEM) and XPS. Nb2CTx and V2CTx showed promising performance as electrodes for Li-ion batteries. In this thesis, electrochemical etching was used in an attempt to produce 2D metal carbides (MXene) from their ternary metal carbides, Ti3SiC2, Ti3AlC2 and Ti2AlC MAX phases. MAX phases in the form of highly dense bulk produced by Hot Isostatic Press. Several etching solutions were used such as HF, NaCl and HCl. Unlike the HF chemical etching of MAX phases, which results in MXenes, the electrochemical etching resulted in Carbide Derived Carbon (CDC). Here, I show the characterization of the produced CDC using several techniques such as XRD, TEM, Raman spectroscopy, and XPS. Electrochemical characterization was performed in the form of cyclic voltammetry, which sheds light on the etching mechanism. / <p>The series name <em>Linköping Studies in Science and Technology Licentiate Thesis</em> in this publication is incorrect. Correct name is <em>Linköping Studies in Science and Technology. Thesis</em>.</p>

In the agricultural industry, cultivator tines are used for stubble cultivation and seedbed preparation. They are exposed to rapidly developing abrasive wear, which becomes a major economic problem. The occurring wear in the tines is heavily dependent on the characteristics of the soil which it passes through. In this master thesis the goal is to produce a method which, in a laboratory environment, can reproduce the circumstances which real cultivator tines are exposed to in the field. The method will enable analysis and evaluation of the initial wear mechanisms causing the wear. In order to simulate the tillage, a pendulum setup was constructed. With this, a series of repeated impact tests were performed into a soil sample. Throughout the tests, the “cultivator tine” samples were made of aluminium. This material choice would enable an accelerated wear rate, following its low hardness. All tests were performed in the same soil, with moisture content being the only varying parameter;~0% and 18% respectively. The samples which had passed through soil with higher moisture showed reduced wear compared to those which had passed through dry soil. The pendulum setup contributed to the tests being executed in a controlled and reliable manner. Hence, it is determined to be suitable for further use in any future project work related to the subject.

In this project, different molecules have been investigated with the purpose of creating anohmic contact between metals and carbon nano materials. In particular, we considered simplemolecules connecting a graphene layer and a copper-slab. In order to determine the capability of such systems, the electronic structure was computedusing Density Functional Theory (DFT). Structural relaxation was performed in order to findcandidates where the metal and the graphene binds chemically with the hypothesis that thehybridization of the states will induce more states at the Fermi level. Six different molecularchains were tested and three of them were found to chemisorb to the graphene sheet and thecopper surface simultaneously. The electronic properties for these systems were then furtherinvestigated using the density of states (DOS). An overlap density of states (ODOS) wasdefined in order to evaluate the respective contribution of the graphene, metal and molecule. From the DOS analysis, we report that these systems did not form ohmic contacts as the resultshows too few states close to the Fermi level. The most interesting case was using a hexanolchain which had some partially overlapping states seen from the ODOS of the graphenemoleculeand graphene-Cu at the Fermi level. However, these were only small contributions.Further research is crucial in order to find a more suitable molecular chain between thegraphene and the copper for an ohmic contact.

<p>Series of rare-earth intermetallic compounds were synthesized and studied.</p> <p>The Gd₄Ge_3-<em>x</em><em>Pn_x</em> (<em>Pn</em> = P, Sb, Bi; <em>x</em> = 0.5 - 3) series of compounds were synthesized to explore the stability of the non-existent Gd₄Ge₃ binary through partial <em>Pn</em> substitutions to increase valence electron concentrations. Electronic band structure calculations were performed to elucidate the relationships between the hypothetical "Gd₄Ge₃" and Gd₅Ge₄ binaries. All Gd₄Ge_3-<em>x</em><em>Pn_x</em> phases order ferromagnetically with relatively high Curie temperatures of 234 to 356 K.</p> <p>The Gd₅Ge_4-<em>x</em>P<em>_x</em> phases were synthesized to explore the effects of both atomic size and valence electron concentration differences between Ge and P atoms. Partial substitution of P for Ge atoms occur on the interslab site, which causes the interslab distances to increase. In Gd₅Ge_4-<em>x</em>P<em>_x</em>, only a small amount of P substitution (<em>x</em> = 0.25) is required to induce ferromagnetic ordering. The appearance of a Griffiths phase is also discussed.</p> <p>The temperature dependence of the different <em>RE</em>₂Fe₁₇ (<em>RE</em> = Gd - Ho) phases was tracked by reciprocal space images generated from single crystal X-ray diffraction.</p> <p>GdCo₄B was synthesized by arcmelting and tri-arc techniques to confirm the presence of magnetostriction. Single crystal and powder X-ray diffraction, dilatometer and magnetic measurements were done.</p> / Master of Science (MSc)

Combustion engines today are primarily powered by fossil fuels, resulting in emissions of pollutants that pose significant environmental challenges. Therefore, transitioning to alternative fuels that reduce these emissions is crucial. One promising alternative fuel is ammonia, which, in addition to being carbon-free, benefits from an already developed infrastructure. However, switching to new fuels creates a different chemical environment inside the engine, and the impact on engine materials has not been well studied. Thus, in this master’s thesis, nine different engine materials (copper, brass, aluminum, cast iron, ball bearing steel, stainless steel, titanium, titanium nitride, and diamond-like carbon (DLC)) were studied before and after ammonia exposure, as well as after a tribological test, to increase the knowledge in this field. The materials were analyzed using SEM and EDS before and after exposure, and additional techniques, LOM and XPS, were also used after the exposure. All materials showed some degree of reaction in the ammonia solution. Copper, brass, and aluminum were altered to a depth of many micrometers, and the surface layer broke under tribological contact. Cast iron also reacted, but to a lesser extent, as parts of its surface remained unchanged. Ball bearing steel, stainless steel and titanium reacted mildly, primarily superficial oxidation of the surfaces. Titanium nitride and DLC were almost unaffected by ammonia. This suggests that titanium nitride, DLC, ball bearing steel, stainless steel, and titanium are more suitable for use in an ammonia driven combustion engine than copper, brass, aluminum, and cast iron.

京都大学 / 新制・課程博士 / 博士(工学) / 甲第25505号 / 工博第5272号 / 新制||工||2003(附属図書館) / 京都大学大学院工学研究科分子工学専攻 / (主査)教授 今堀 博, 教授 寺村 謙太郎, 教授 SIVANIAH Easan / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

Carbon quantum dots (CQDs) are the latest generation of carbon nanomaterials in applications where fullerenes, carbon nanotubes, and graphene are abundantly used. With several attractive properties such as tunable optical property, edge-functionalization, and defect-rich chemical structure, CQDs have the potential to revolutionize optoelectronics, electro- and photocatalysis, and biomedical applications. Chemical modifications through the addition of heteroatoms, chemical reduction, and surface passivation are found to alter the band gap, spectral position, and emission pathways of CQDs. Despite extensive studies, fundamental understanding of structure-property relationship remains unclear due to the inhomogeneity in chemical structure and a complex emission mechanism for CQDs. This dissertation outlines a series of works that investigate the structure-property relationship of CQDs and its impact in a variety of applications. First, this relationship was explored by modifying specific chemical functionalities of CQDs and relating them to differences observed in optical, catalytic, and pharmacological performance. While a number of scientific articles reported that top-down or bottom-up synthesized CQDs yielded similar properties, the results herein present dissimilar chemical structures as well as photoluminescent and metal sensing properties. Second, the role of nitrogen heteroatoms in top-down synthesized CQD was studied. The effect of nitrogen atoms on spectral position and fluorescence quantum yield was considerably studied in past reports; however, thorough investigation to differentiate various nitrogen related chemical states was rarely reported. By finely tuning both the quantity of nitrogen doping and the distribution of nitrogen-related chemical states, we found that primary amine and pyridine induce a red-shift in emission while pyrrolic and graphitic nitrogen produced a blue-shift in emission. The investigation of nitrogen chemical states was extended to bottom-up synthesized CQDs with similar results. Finally, top-down, bottom-up, nitrogen-doped and chemically reduced CQDs were separately tested for their ability to act as photodynamic anti-cancer agents. This series of experiments uncovered the distribution of reactive oxygen species produced during light exposure which elucidated the photodynamic mechanisms of cancer cytotoxicity. The results presented in this dissertation provide key insight into engineering finely-tailored CQDs as the ideal nanomaterial for a broad range of applications.