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dc.contributor.authorBlanchard, Peter E R
dc.contributor.authorHuang, Zixin
dc.contributor.authorKennedy, Brendan J
dc.contributor.authorLiu, Samuel
dc.contributor.authorMiiller, Wojciech
dc.contributor.authorReynolds, Emily
dc.contributor.authorZhou, Qingdi
dc.contributor.authorAvdeev, Maxim
dc.contributor.authorZhang, Z
dc.contributor.authorAitken, J B
dc.contributor.authorCowrie, B C C
dc.contributor.authorJang, L-Y
dc.contributor.authorLi, Sean
dc.contributor.authorLing, Chris D
dc.date.accessioned2022-08-09T04:06:32Z
dc.date.available2022-08-09T04:06:32Z
dc.date.issued2014en_AU
dc.identifier.urihttps://hdl.handle.net/2123/29380
dc.description.abstractThe key role played by bismuth in an average intermediate oxidation state in the magnetoelastic spin-gap compounds Ba3BiRu2O9 and Ba3BiIr2O9 has been confirmed by systematically replacing bismuth with La3+ and Ce4+. Through a combination of powder diffraction (neutron and synchrotron), X-ray absorption spectroscopy, and magnetic properties measurements, we show that Ru/Ir cations in Ba3BiRu2O9 and Ba3BiIr2O9 have oxidation states between +4 and +4.5, suggesting that Bi cations exist in an unusual average oxidation state intermediate between the conventional +3 and +5 states (which is confirmed by the Bi L3-edge spectrum of Ba3BiRu2O9). Precise measurements of lattice parameters from synchrotron diffraction are consistent with the presence of intermediate oxidation state bismuth cations throughout the doping ranges. We find that relatively small amounts of doping (~10 at%) on the bismuth site suppress and then completely eliminate the sharp structural and magnetic transitions observed in pure Ba3BiRu2O9 and Ba3BiIr2O9, strongly suggesting that the unstable electronic state of bismuth plays a critical role in the behaviour of these materials.en_AU
dc.language.isoenen_AU
dc.publisherAmerican Chemical Societyen_AU
dc.relation.ispartofInorganic Chemistryen_AU
dc.titleThe key role of bismuth in the magnetoelastic transitions of Ba3BiIr2O9 and Ba3BiRu2O9 as revealed by chemical dopingen_AU
dc.typeArticleen_AU
dc.subject.asrc0302 Inorganic Chemistryen_AU
dc.identifier.doi10.1021/ic4023745
dc.type.pubtypeAuthor accepted manuscripten_AU
dc.relation.arcDP110102662
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume53en_AU
usyd.citation.spage952en_AU
usyd.citation.epage960en_AU
workflow.metadata.onlyNoen_AU


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