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dc.contributor.authorWollstadt, Stephan-
dc.contributor.authorIkeda, Yuji-
dc.contributor.authorSarkar, Abhishek-
dc.contributor.authorVasala, Sami-
dc.contributor.authorFasel, Claudia-
dc.contributor.authorAlff, Lambert-
dc.contributor.authorKruk, Robert-
dc.contributor.authorGrabowski, Blazej-
dc.contributor.authorClemens, Oliver-
dc.date.accessioned2022-08-30T10:38:38Z-
dc.date.available2022-08-30T10:38:38Z-
dc.date.issued2021de
dc.identifier.issn1520-510X-
dc.identifier.issn0020-1669-
dc.identifier.other181552264X-
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-123751de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/12375-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-12356-
dc.description.abstractA new vacancy-ordered perovskite-type compound Ba3Fe3O8 (BaFeO2.667) was prepared by oxidizing BaFeO2.5 (P21/c) with the latter compound obtained by a spray-pyrolysis technique. The structure of Ba3Fe3O8 was found to be isotypic to Ba3Fe3O7F (P21/m) and can be written as Ba3Fe3+2Fe4+1O8. Mössbauer spectroscopy and ab initio calculations were used to confirm mixed iron oxidation states, showing allocation of the tetravalent iron species on the tetrahedral site and octahedral as well as square pyramidal coordination for the trivalent species within a G-type antiferromagnetic ordering. The uptake and release of oxygen was investigated over a broad temperature range from RT to 1100 °C under pure oxygen and ambient atmosphere via a combination of DTA/TG and variable temperature diffraction measurements. The compound exhibits a strong lattice enthalpy driven reduction to monoclinic and cubic BaFeO2.5 at elevated temperatures.en
dc.language.isoende
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/865855de
dc.relation.uridoi:10.1021/acs.inorgchem.1c00434de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.ddc530de
dc.titleStructural and magnetic properties of newly found BaFeO2.667 synthesized by oxidizing BaFeO2.5 obtained via nebulized spray pyrolysisen
dc.typearticlede
ubs.bemerkung.externThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © 2021 The Authors, Published by American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.inorgchem.1c00434de
ubs.fakultaetChemiede
ubs.fakultaetFakultätsübergreifend / Sonstige Einrichtungde
ubs.institutInstitut für Materialwissenschaftde
ubs.institutFakultätsübergreifend / Sonstige Einrichtungde
ubs.publikation.seiten27de
ubs.publikation.sourceInorganic chemistry 60 (2021), S. 10923-10933de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:03 Fakultät Chemie

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