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dc.contributor.authorBouet, L-
dc.contributor.authorTailhades, P-
dc.contributor.authorRousset, A-
dc.contributor.authorKannan, K R-
dc.contributor.authorVerelst, M-
dc.contributor.authorKulkarni, G U-
dc.contributor.authorRao, C N R-
dc.date.accessioned2012-10-31T11:23:53Z-
dc.date.available2012-10-31T11:23:53Z-
dc.date.issued1993-02-
dc.identifier0022-4596en_US
dc.identifier.citationJournal of Solid State Chemistry 102(2), 414-422 (1993)en_US
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/10572/897-
dc.descriptionRestricted Accessen_US
dc.description.abstractFerrites of the formula MoxFe3-xO4, prepared by a soft-chemistry route, show mixed valence states of both iron and molybdenum cations. Mössbauer studies show that Fe2+ and Fe3+ ions are present on both the A and B sites, giving Fe an average oxidation state between 2+ and 3+. Molybdenum is present in the 3+ and the 4+ states on the B sites. The presence of Mo in the 3+ state has been established by determining the Mo3+-O distance (2.2 Å), for the first time, by Mo K-EXAFS. The mixed valence of Fe on both the A and B sites and of Mo on the B sites is responsible for the fast electron transfer between the cations. All the Mössbauer parameters including the line width show a marked change at a composition (x ≈ 0.3) above which the concentration of Fe2+A increases rapidly.en_US
dc.description.urihttp://dx.doi.org/10.1006/jssc.1993.1053en_US
dc.language.isoenen_US
dc.publisherAcademic Press Incen_US
dc.rights© 1993 Academic Press Incen_US
dc.subjectX-Rayen_US
dc.subjectExchangeen_US
dc.titleFe-57 Mössbauer and Mo K-EXAFS Investigations of MoxFe3-xO4, an Interesting Mixed-Valent Oxide Systemen_US
dc.typeArticleen_US
Appears in Collections:Research Papers (Prof. C.N.R. Rao)

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