Please use this identifier to cite or link to this item: https://libjncir.jncasr.ac.in/xmlui/handle/10572/323
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKundu, Asish K-
dc.contributor.authorPralong, V-
dc.contributor.authorCaignaert, V-
dc.contributor.authorRao, C N R-
dc.contributor.authorRaveau, B-
dc.date.accessioned2012-02-07T09:36:00Z-
dc.date.available2012-02-07T09:36:00Z-
dc.date.issued2007-
dc.identifier0959-9428en_US
dc.identifier.citationJournal of Materials Chemistry 17(31), 3347-3353 (2007)en_US
dc.identifier.urihttps://libjncir.jncasr.ac.in/xmlui/10572/323-
dc.description.abstractThe substitution of cobalt and nickel for manganese in the perovskite manganate LaBiMn2O6+delta. has been realized, leading to the perovskites LaBiMn2-MxO6+delta, with M = Co, Ni and 0 <= x <= 2/3. In contrast to the literature these phases are found to be orthorhombic with Pnma symmetry. More importantly, it is shown that ferromagnetism is enhanced, TC being increased from 80 K for the parent compound (x = 0) to 97 K for the Ni phase, and to 130 K for the Co phase. Moreover, strong competition between ferromagnetism and a glassy- ferromagnetic state in the case of nickel or spin- glass behaviour in the case of cobalt is observed. These phenomena are interpreted in the frame of a phase separation scenario, where the ferromagnetic Mn4+/Ni2+ and Mn4+/Co2+ interactions reinforce the Mn3+/Mn4+ interactions. These compounds are found to be insulating with a relatively large positive value of thermoelectric power.en_US
dc.description.urihttp://dx.doi.org/10.1039/b705027een_US
dc.language.isoenen_US
dc.publisherRoyal Society Chemistryen_US
dc.rights© 2007 The Royal Society of Chemistryen_US
dc.subjectTransitionsen_US
dc.subjectLa2nimno6en_US
dc.subjectBehavioren_US
dc.subjectStatesen_US
dc.titleEnhancement of ferromagnetism by Co and Ni substitution in the perovskite LaBiMn2O6+den_US
dc.typeArticleen_US
Appears in Collections:Research Papers (Prof. C.N.R. Rao)

Files in This Item:
File Description SizeFormat 
2007 J.Mater.Chem.17,3347.pdf345.24 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.