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dc.contributor.authorBlanchard, Peter E R
dc.contributor.authorChapman, Karena W
dc.contributor.authorHeald, Steve M
dc.contributor.authorZbiri, Mohamed
dc.contributor.authorJohnson, Mark R
dc.contributor.authorKennedy, Brendan J
dc.contributor.authorLing, Chris D
dc.date.accessioned2022-07-22T04:48:14Z
dc.date.available2022-07-22T04:48:14Z
dc.date.issued2016en_AU
dc.identifier.urihttps://hdl.handle.net/2123/29317
dc.description.abstractThe hexagonal perovskites Ba3BiIr2O9, Ba3BiRu2O9 and Ba4BiIr3O12 all undergo pressure-induced 1% volume collapses above 5 GPa. These first-order transitions have been ascribed to internal transfer of valence electrons between bismuth and iridium/ruthenium, which is driven by external applied pressure because the reduction in volume achieved by emptying the 6s shell of bismuth upon oxidation to Bi5+ is greater in magnitude than the increase in volume by reducing iridium or ruthenium. Here, we report direct observation of these valence transfers for the first time, using high-pressure X-ray absorption near-edge spectroscopy (XANES) measurements. Our data also support the highly unusual “4+” nominal oxidation state of bismuth in these compounds, although the possibility of local disproportionation into Bi3+/Bi5+ cannot be definitively ruled out. Ab initio calculations reproduce the transition, support its interpretation as a valence electron transfer from Bi to Ir/Ru, and suggest that the high-pressure phase may show metallic behavior (in contrast to the insulating ambient-pressure phase).en_AU
dc.language.isoenen_AU
dc.publisherAmerican Chemical Societyen_AU
dc.relation.ispartofInorganic Chemistryen_AU
dc.rightsOtheren_AU
dc.subjectCharge transferen_AU
dc.subjectOxidation stateen_AU
dc.subjectPhase transitionsen_AU
dc.subjectTransition metalsen_AU
dc.subjectX-ray absorption near edge spectroscopyen_AU
dc.titleDirect observation of pressure-driven valence electron transfer in Ba3BiRu2O9, Ba3BiIr2O9 and Ba4BiIr3O12en_AU
dc.typeArticleen_AU
dc.subject.asrc0302 Inorganic Chemistryen_AU
dc.identifier.doi10.1021/acs.inorgchem.6b00718
dc.type.pubtypeAuthor accepted manuscripten_AU
dc.relation.arcDP150102863
dc.rights.otherThis document is the unedited Author’s version of a Submitted Work that was subsequently accepted for publication in Inorganic Chemistry, copyright © American Chemical Society after peer review. To access the final edited and published work see https://doi.org/10.1021/acs.inorgchem.6b00718en_AU
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume55en_AU
usyd.citation.issue11en_AU
usyd.citation.spage5649en_AU
usyd.citation.epage5654en_AU
workflow.metadata.onlyNoen_AU


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