Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1565
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dc.contributor.authorSubodh, G-
dc.contributor.authorTassel, C-
dc.contributor.authorHayashi, N-
dc.contributor.authorGoto, Y-
dc.contributor.authorBouilly, G-
dc.contributor.authorYajima, T-
dc.contributor.authorKobayashi, Y-
dc.contributor.authorKageyama, H-
dc.date.accessioned2014-06-26T11:21:07Z-
dc.date.available2014-06-26T11:21:07Z-
dc.date.issued2014-
dc.identifier.citationEuropean Journal of Inorganic Chemistry (15):2576-2581; May 2014en_US
dc.identifier.issn1099-0682-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1565-
dc.description.abstractAn oxygen-stoichiometric, B-site-ordered perovskite Ca2Fe1.1Mn0.9O6 (CFMO) with alternate stacking of Fe and Mn layers was obtained through topochemical oxidation of the corresponding brownmillerite phase under high pressure in the presence of KClO4. The structure crystallizes in the P21/m space group with a doubling of the cell along all three crystallographic axes. Mössbauer spectroscopy, susceptibility, and resistivity measurements suggest ferromagnetic interactions between Fe4+(d4) and Mn4+(d3) along [001] through a double-exchange mechanism, a situation similar to half-doped manganese perovskite oxides. Upon cooling, CFMO exhibits a ferrimagnetic transition below Tc = 90K, likely accompanied by a charge disproportionation of the iron site, 2Fe4+ Fe3+ + Fe5+. A reasonably good magnetoresistivity of 27% was observed below Tc.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectLayered compoundsen_US
dc.subjectPerovskite phasesen_US
dc.subjectTopochemistryen_US
dc.subjectMagnetic propertiesen_US
dc.subjectIronen_US
dc.subjectManganeseen_US
dc.titleCharge disproportionation and magnetoresistivity in a double perovskite with alternate Fe4+(d4) and Mn4+(d3) layersen_US
dc.typeArticleen_US
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