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hal.structure.identifierDepartemento de Quimica e Bioquimica
dc.contributor.authorCARVALHO, M. D.
hal.structure.identifierDepartemento de Quimica e Bioquimica
dc.contributor.authorRAMOS, T.
hal.structure.identifierCFMC
hal.structure.identifierDepartm. Física
dc.contributor.authorFERREIRA, L. P.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorWATTIAUX, Alain
dc.date.issued2010
dc.identifier.issn1293-2558
dc.description.abstractEnThe La<sub>1</sub><sub>−</sub><i><sub>x</sub></i>Sr<i><sub>x</sub></i>Fe<sub>0.8</sub>Cr<sub>0.2</sub>O<sub>3</sub><sub>−</sub><i><sub>y</sub></i> (<i>x</i> = 0.2, 0.4, 0.6 and 0.8) phases were studied by X-ray photoelectron spectroscopy at room temperature and <sup>57</sup>Fe Mössbauer spectroscopy at different temperatures. Mixed valence states were observed both for chromium and iron ions, justifying the complex magnetic behaviour exhibited by these compounds. The Mössbauer results indicate the simultaneous presence of Fe<sup>3+</sup>, Fe<sup>4+</sup> and Fe<sup>5+</sup> at 4.2 K and the co-existence of Fe<sup>3+</sup> and Fe<sup>(3</sup><sup>+</sup><i><sup>n</sup></i><sup>)+</sup> at <i>T</i> = 293 K, with the latter fraction increasing with increasing strontium content. The presence of Cr<sup>3+/4+</sup> is interpreted as being mainly responsible for the incomplete charge disproportionation reaction of iron at low temperature, as deduced from the Mössbauer results.
dc.language.isoen
dc.publisherElsevier
dc.subject.enMössbauer spectroscopy
dc.subject.enX-ray photoelectron spectroscopy
dc.subject.enDisproportionation reaction
dc.subject.enPerovskite oxides
dc.typeArticle de revue
dc.identifier.doi10.1016/j.solidstatesciences.2009.12.011
dc.subject.halChimie/Matériaux
bordeaux.journalSolid State Sciences
bordeaux.page476-481
bordeaux.volume12
bordeaux.issue4
bordeaux.peerReviewedoui
hal.identifierhal-00470661
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00470661v1
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