Order-disorder competition in the Sc2VO5+δ system. Review and experimental pursuit of A3+2VO5 and Sc2VO5+δ-inspired solid phases

dc.contributor.authorVrublevskiy, Dmitry
dc.contributor.examiningcommitteeSchreckenbach, H. Georg (Chemistry)en_US
dc.contributor.examiningcommitteeWiebe, Christopher (Chemistry)en_US
dc.contributor.examiningcommitteeHu, Can-Ming (Physics and Astronomy)en_US
dc.contributor.examiningcommitteeMozharivskyj, Yurij (McMaster University)en_US
dc.contributor.supervisorBieringer, Mario
dc.date.accessioned2023-01-23T17:27:55Z
dc.date.available2023-01-23T17:27:55Z
dc.date.copyright2023-01-18
dc.date.issued2023-01-18
dc.date.submitted2023-01-18T15:59:14Zen_US
dc.degree.disciplineChemistryen_US
dc.degree.levelDoctor of Philosophy (Ph.D.)en_US
dc.description.abstractThis work was motivated by the proclivity of oxygen-deficient metal oxides to enable oxide transport at high temperatures. This property depends on the composition and metal-oxygen connectivities within the structure and requires vacant crystallographic sites. The project initially focused on non-conducting derivatives of oxygen defect fluorites AO2-δ, namely split-cation A2BO5-type superstructures, but eventually turned into a broader experimental and theoretical investigation of formation regimes and metal-oxygen connectivities of these phases and, to a degree, their structural competitors – A2B2O7 and A4B3O12. At the core of this work is the defect fluorite superstructure Sc2VO5+δ with tunable δ. It belongs to the structurally diverse yet scarce A2VO5 family of compounds. The high-temperature tetragonal polymorph t-Sc2VO5+δ is predominantly ordered – cation-ordered and oxygen-vacancy-ordered, and its vanadium sublattice is charge-ordered. Doping of the vanadium sublattice with commensurate cations Ge, Ti, Sn, and Cr replaced either V3+…4+ or V5+ in it in proportion to the octahedral ionic size of the dopant, also affecting δ and the average cation ordering. Increasing the content of the dopant led to formation of competing phases – Sc2B2O7 and Sc4B3O12, which are also discussed. The low-temperature cubic polymorph c-Sc2VO5+δ is fully disordered on average but partially ordered on the local scale, insofar as its vanadium sublattice accumulates smaller V5+ species. This cubic phase can be oxidatively obtained from either its tetragonal polymorph or a cation-disordered bixbyite Sc2VO4.5, in both cases inheriting the average ordering scheme of its precursor. Key phases were investigated with a tandem of ex-situ and in-situ average and local structure probes, such as X-ray and neutron powder diffraction, X-ray absorption near-edge structure spectroscopy, and X-ray and neutron total scattering. Results led to a discussion on the evolution of coordination and connectivities in the cation sublattices, oxygen driven phase transitions, limit of oxygen concentration, oxide vacancy structure, the crucial role of the cation radius in phase formation, and the order-disorder interplay. Discussed vanadates with 2:1 and 1:1 stoichiometric ratio of A3+ and aliovalent vanadium were compared across their joint phase diagram and discussed with the help of stability maps.en_US
dc.description.noteMay 2023en_US
dc.description.sponsorshipMario Bieringer's NSERC granten_US
dc.identifier.urihttp://hdl.handle.net/1993/37160
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectOrder-disorderen_US
dc.subjectFluorite-type structuresen_US
dc.subjectOxide defectsen_US
dc.subjectTopotactic and reconstructive synthesisen_US
dc.subjectTransition metalsen_US
dc.subjectVanadatesen_US
dc.subjectFluorite superstructuresen_US
dc.subjectX-ray powder diffractionen_US
dc.subjectNeutron powder diffractionen_US
dc.subjectX-ray absorption near edge structure spectroscopyen_US
dc.subjectPair distribution functionen_US
dc.titleOrder-disorder competition in the Sc2VO5+δ system. Review and experimental pursuit of A3+2VO5 and Sc2VO5+δ-inspired solid phasesen_US
dc.typedoctoral thesisen_US
local.subject.manitobanoen_US
oaire.awardTitleUniversity of Manitoba Graduate Fellowshipen_US
oaire.awardURIhttps://umanitoba.ca/graduate-studies/funding-awards-and-financial-aid/university-manitoba-graduate-fellowship-umgfen_US
project.funder.nameUniversity of Manitobaen_US
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