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dc.contributor.authorBrown, Alex J.
dc.contributor.authorAvdeev, Maxim
dc.contributor.authorManjón-Sanz, Alicia
dc.contributor.authorBrand, Helen E. A.
dc.contributor.authorLing, Chris D.
dc.date.accessioned2024-11-11T03:11:31Z
dc.date.available2024-11-11T03:11:31Z
dc.date.issued2023en_AU
dc.identifier.urihttps://hdl.handle.net/2123/33252
dc.description.abstractOxygen-deficient perovskite compounds with the general formula Ba3RFe2O7.5 present a good opportunity to study competing magnetic interactions between Fe3+ 3d cations with and without the involvement of unpaired 4f electrons on R3+ cations. From analysis of neutron powder diffraction data, complemented by ab initio density functional theory calculations, we determined the magnetic ground states when R3+ = Y3+ (non-magnetic) and Dy3+ (4f9). They both adopt complex long-range ordered antiferromagnetic structures below TN = 6.6 and 14.5 K, respectively, with the same magnetic space group Ca2/c (BNS #15.91). However, the dominant influence of f-electron magnetism is clear in temperature dependence and differences between the size of the ordered moments on the two crystallographically independent Fe sites, one of which is enhanced by R–O–Fe superexchange in the Dy compound, while the other is frustrated by it. The Dy compound also shows evidence for temperature- and field-dependent transitions with hysteresis, indicating a field-induced ferromagnetic component below TN.en_AU
dc.language.isoenen_AU
dc.publisherAmerican Chemical Societyen_AU
dc.relation.ispartofInorganic Chemistryen_AU
dc.rightsOtheren_AU
dc.titleCompeting Magnetic Interactions and the Role of Unpaired 4f Electrons in Oxygen-Deficient Perovskites Ba3RFe2O7.5 (R = Y, Dy)en_AU
dc.typeArticleen_AU
dc.identifier.doi10.1021/acs.inorgchem.3c00524
dc.type.pubtypeAuthor accepted manuscripten_AU
dc.relation.arcDP200100959
dc.rights.otherThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © 2023 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see doi:10.1021/acs.inorgchem.3c00524.en_AU
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume62en_AU
usyd.citation.issue17en_AU
usyd.citation.spage6786en_AU
usyd.citation.epage6793en_AU
workflow.metadata.onlyNoen_AU


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