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Charge disproportionation and magnetoresistivity in a double perovskite with alternate Fe4+(d4) and Mn4+(d3) layers

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dc.contributor.author Subodh, G
dc.contributor.author Tassel, C
dc.contributor.author Hayashi, N
dc.contributor.author Goto, Y
dc.contributor.author Bouilly, G
dc.contributor.author Yajima, T
dc.contributor.author Kobayashi, Y
dc.contributor.author Kageyama, H
dc.date.accessioned 2014-06-26T11:21:07Z
dc.date.available 2014-06-26T11:21:07Z
dc.date.issued 2014
dc.identifier.citation European Journal of Inorganic Chemistry (15):2576-2581; May 2014 en_US
dc.identifier.issn 1099-0682
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/1565
dc.description.abstract An 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.iso en en_US
dc.publisher Wiley en_US
dc.subject Layered compounds en_US
dc.subject Perovskite phases en_US
dc.subject Topochemistry en_US
dc.subject Magnetic properties en_US
dc.subject Iron en_US
dc.subject Manganese en_US
dc.title Charge disproportionation and magnetoresistivity in a double perovskite with alternate Fe4+(d4) and Mn4+(d3) layers en_US
dc.type Article en_US


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