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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Synthesis and Magnetism of Low-dimensional Compounds by Mixed Anion Strategy / 複合アニオン戦略による合成と磁性

Matsumoto, Yuki 23 March 2023 (has links)
京都大学 / 新制・課程博士 / 博士(工学) / 甲第24629号 / 工博第5135号 / 新制||工||1981(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 陰山 洋, 教授 安部 武志, 教授 藤田 晃司 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM
2

The structures and properties of layered pnictides and oxychalcogenides

Pitcher, Michael J. January 2011 (has links)
This work focuses principally on two compounds, CeCu<sub>1-x</sub>OS and LiFeAs, which have related layered structures but exhibit radically different physical properties. The nature of the air sensitivity of the ZrCuSiAs-type oxysulfide CeCu<sub>1-x</sub>OS has been investigated by neutron diffraction and magnetometry. It was found that this compound can be made fully stoichiometric, with structural and magnetic properties that are consistent with other LnCuOS compounds, indicating that this is a bona-fide Ce<sup>3+</sup> compound. Upon air exposure, Cu ions are extruded from the sulfide layer to leave a Cu-deficient phase with contracted unit cell parameters and a diminished paramagnetic moment consistent with mixed-valence Ce<sup>3+/4+</sup>.The extruded Cu forms CuO and can be re-inserted into the sulfide layer by heating under a reducing atmosphere. This explains the anomalous behaviour of CeCuOS reported throughout the literature and has implications for the behaviour of other layered Cu-sulfides with oxidisable cations. At low temperatures Cu-deficient CeCu<sub>0.8</sub>OS was found to exhibit structural ordering of Cu<sup>+</sup> ions and vacancies, resulting in a √5a x √5a basal expansion of the high-temperature unit cell. The layered iron arsenide LiFeAs was synthesised and found to be superconducting below 17 K. Joint XRD/NPD measurements showed unambiguously that the compound adopts the anti-PbFCl structure with Li ions in a square-pyramidal LiAs5 environment. No evidence was found for an orthorhombic structural distortion at low temperatures. Further diffraction experiments showed that the compound can be made with non-stoichiometric compositions Li<sub>1-y</sub>Fe<sub>1-y</sub> for small values of y (&lt;0.05), as Fe can be accommodated on the Li site. This type of non-stoichiometry was found to strongly inhibit superconductivity (which was quenched entirely when y&gt;0.02). Three series of compounds of type LiFe<sub>1-x</sub>M<sub>x</sub>As (M = Mn, Co, Ni) were synthesised and characterised struturally bu high-resolution XRD and/or NPD. Substitution by Co and Ni was found to cause a monotonic decrease in T<sub>c</sub>, and Ni was found to be twice as effective at suppressing T<sub>c</sub> as Co. MuSR measurements showed the penetration depth increasing with Co and Ni substitution, consisitent with the superconducting state becoming less robust. Substitution by Mn was found to strongly inhibit superconductivity, and this behaviour is reminiscent of the non-stoichiometric Li<sub>1-y</sub>Fe<sub>1-y</sub>As materials. The structures and superconducting properties of LiFeAs and NaFeAs were studied under high pressures. Equations of state were obtained for each compound. Hydrostatic pressure was found to distort of the FeAs<sub>4</sub> away from ideal tetrahedral geometry in both compounds. These changes caused a monotonic decrease in T<sub>c</sub> in LiFeAs, but has a smaller and more complex effect on the T<sub>c</sub> of NaFeAs. Furthermore, NaFeAs was found to undergo a structural transition above P = 22 GPa, but the high-pressure structure could not be solved and this will become a target for future work.

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