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dc.contributor.authorWang, Chun-Hai
dc.contributor.authorAvdeev, Maxim
dc.contributor.authorKennedy, Brendan J
dc.contributor.authorKuepers, M
dc.contributor.authorLing, Chris D
dc.date.accessioned2022-07-22T03:57:15Z
dc.date.available2022-07-22T03:57:15Z
dc.date.issued2016en_AU
dc.identifier.urihttps://hdl.handle.net/2123/29316
dc.description.abstractWe report a new gaudefroyite-type compound YCa3(CrO)3(BO3)4, in which Cr3+ ions (3d3, S = 3/2) form an undistorted kagomé lattice. Using a flux agent, the synthesis was significantly accelerated with the typical calcining time reduced from more than two weeks to two days. The structure of YCa3(CrO)3(BO3)4 was determined by combined Rietveld refinements against X-ray and neutron diffraction data. Symmetry distortion refinement starting from a disordered YCa3(MnO)3(BO3)4 model was applied to avoid over-parameterization. There are two ordering models, K2-1 and K2-2 with the space groups P63 (#173) and (#147) respectively that differ in the [BO3] ordering between different channels (in-phase or out-of-phase). Both models give similarly good fits to the diffraction data. YCa3(CrO)3(BO3)4 is an insulator with the major band gap at Eg = 1.65eV and a second transition at 1.78 eV. Magnetically, YCa3(CrO)3(BO3)4 is dominated by antiferromagnetic exchange along edge-sharing CrO6 octahedral chains perpendicular to the kagomé planes, with Θ ≈ –120 K and μeff ≈ 3.92 μB. The compound shows no spin ordering or freezing observed down to at least 2 K.en_AU
dc.language.isoenen_AU
dc.publisherAmerican Chemical Societyen_AU
dc.relation.ispartofInorganic Chemistryen_AU
dc.rightsOtheren_AU
dc.subjectElectrical conductivityen_AU
dc.subjectLatticesen_AU
dc.subjectMagnetic propertiesen_AU
dc.subjectPhysical and chemical processesen_AU
dc.subjectQuantum mechanicsen_AU
dc.titleYCa3(CrO)3(BO3)4: a Cr3+ kagomé lattice compound showing no magnetic order down to 2 Ken_AU
dc.typeArticleen_AU
dc.subject.asrc0302 Inorganic Chemistryen_AU
dc.identifier.doi10.1021/acs.inorgchem.6b00923
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.6b00923en_AU
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume55en_AU
usyd.citation.issue15en_AU
usyd.citation.spage7535en_AU
usyd.citation.epage7541en_AU
workflow.metadata.onlyNoen_AU


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