Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/12453
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dc.contributor.authorChang, FF-
dc.contributor.authorReehuis, M-
dc.contributor.authorHester, JR-
dc.contributor.authorAvdeev, M-
dc.contributor.authorXiang, F-
dc.contributor.authorWang, X-
dc.contributor.authorSeidel, J-
dc.contributor.authorUlrich, C-
dc.date.accessioned2021-12-13T04:06:27Z-
dc.date.available2021-12-13T04:06:27Z-
dc.date.issued2016-02-04-
dc.identifier.citationChang, F., Reehuis, M., Hester, J., Avdeev, M., Xiang, F., Wang, X., Seidel, J. & Ulrich, C. (2016). Crystallographic and magnetic structure study in SrCoO3-x by high resolution x-ray and neutron powder diffraction. Paper presented to the 40th Annual Condensed Matter and Materials Meeting, Charles Sturt University, Wagga Wagga, NSW, 2nd February – 5th February, 2016, (pp. 46-47). Retrieved from: https://physics.org.au/wp-content/uploads/cmm/2016/Wagga_2016_Conference_Handbook.pdfen_US
dc.identifier.isbn978-0-646-96433-1-
dc.identifier.otherTN2-
dc.identifier.urihttps://physics.org.au/wp-content/uploads/cmm/2016/Wagga_2016_Conference_Handbook.pdfen_US
dc.identifier.urihttps://apo.ansto.gov.au/dspace/handle/10238/12453-
dc.description.abstractTransition metal oxides (TMOs) represent a wide set of materials with a broad range of functionalities, including superconductivity, magnetism, and ferroelectricity, which can be tuned by careful choice of parameters such as strain, oxygen content, and applied electric and magnetic fields. This tunability makes TMO’s ideal candidate materials for use in developing novel information and energy technologies and SrCoO3 provides a particularly interesting system for investigation due to its propensity to form oxygen-vacancy-ordered structures as the oxygen content is decreased. The ties between structural and functional properties of this material are obvious as it undergoes simultaneously structural and magnetic phase transitions between two topotactic phases: from a ferromagnetic perovskite phase at SrCoO3.0 to the antiferromagnetic brownmillerite SrCoO2.5. In this study we have determined their crystallographic and magnetic structures of SrCoO2.50, SrCoO2.875, and cubic SrCoO3.00 using high resolution X-ray and neutron powder diffraction from 4 K to 600 K. The correct structure of oxygen-deficient end-member SrCoO2.5 was determined in space group of Imma, instead of Pnma or Ima2 proposed previously, with G-type antiferromagnetic order up to TN = 570 K. In SrCoO2.875, clear peak splitting was observed from (200) in cubic phase to (004) and (440) in tetragonal phase, indicating that the precise structure is I4/mmm with a = b = 10.829(9) Å and c = 7.684(2) Å at 95 K, and the corresponding magnetic structure is ferromagnetic with 1.86(4) μB per formula, in accordance to a spin configuration of cobalt ions with an intermediate spin state of both on Co3+ and on Co4+. The end member SrCoO3.00 possesses a simple cubic crystal structure with a = 3.817(2) Å at 95 K, and ferromagnetic order up to 280 K. The magnetic moment of 1.96(8) μB /Co4+ corresponds to an intermediate spin state of Co4+.en_US
dc.language.isoenen_US
dc.publisherAustralian Institute of Physicsen_US
dc.subjectCharged particlesen_US
dc.subjectIonsen_US
dc.subjectMagnetismen_US
dc.subjectMetalsen_US
dc.subjectMineralsen_US
dc.subjectOxide mineralsen_US
dc.subjectParticle propertiesen_US
dc.subjectPerovskitesen_US
dc.subjectPhysical propertiesen_US
dc.subjectScatteringen_US
dc.titleCrystallographic and magnetic structure study in SrCoO3-x by high resolution x-ray and neutron powder diffractionen_US
dc.typeConference Abstracten_US
dc.date.statistics2021-09-22-
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