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dc.contributor.authorGabriel L, Murphy
dc.contributor.authorBrendan J, Kennedy
dc.contributor.authorZhaoming, Zhang
dc.contributor.authorAvdeev, Maxim
dc.contributor.authorHelen, Brand
dc.contributor.authorPhilip, Kegler
dc.contributor.authorEvgeny V, Alekseev
dc.date.accessioned2019-02-21
dc.date.available2019-02-21
dc.date.issued2017-01-01
dc.identifier.citationGabriel L. Murphy, Brendan J. Kennedy, Zhaoming Zhang, Maxim Avdeev, Helen E.A. Brand, Philip Kegler, Evgeny V. Alekseev, Structure and phase transition in BaThO3: A combined neutron and synchrotron X-ray diffraction study, Journal of Alloys and Compounds,Volume 727,2017,Pages 1044-1049,ISSN 0925-8388, https://doi.org/10.1016/j.jallcom.2017.08.200.en
dc.identifier.urihttp://hdl.handle.net/2123/20037
dc.description.abstractThe structure of BaThO3, obtained by solid state synthesis, was refined for the first time by the Rietveld method using a combination of synchrotron X-ray and neutron powder diffraction data. BaThO3 has an orthorhombic structure at room temperature, in space group Pbnm with a = 6.3491(5), b = 6.3796(4) and c = 8.9907(7) Å. Heating BaThO3 to above 700 °C results in a continuous transition to a second orthorhombic structure, in space group Ibmm, demonstrated by both in situ neutron and synchrotron X-ray powder diffraction measurements. The coefficient of volumetric thermal expansion for BaThO3 is determined to be 1.04 x 10-5 oC-1 from 50 to 625 oC (Pbnm phase), and 9.43 x 10-6 oC-1 from 800 to 1000 oC (Ibmm phase). BaThO3 was found to decompose upon exposure to atmospheric moisture resulting in the formation of ThO2. The thermal expansion of ThO2, which invariably co-exists with BaThO3, is also described.en
dc.description.sponsorshipAustralian Synchrotron Australian Research Councilen
dc.publisherElsevieren
dc.relationARCen
dc.rightsOtheren
dc.subjectPerovskiteen
dc.titleStructure and phase transition in BaThO3: A combined neutron and synchrotron X-ray diffraction studyen
dc.typeArticleen
dc.subject.asrcFoR::030206 - Solid State Chemistryen
dc.identifier.doi10.1016/j.jallcom.2017.08.200
dc.type.pubtypePreprinten
dc.description.embargo2019-12-15
usyd.facultyFaculty of Science, School of Chemistry


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