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Temperature-induced magnetization reversal in BiFe0.5Mn0.5O3 synthesized at high pressure

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dc.contributor.author Mandal, P
dc.contributor.author Sundaresan, A
dc.contributor.author Rao, C N R
dc.contributor.author Iyo, A
dc.contributor.author Shirage, P M
dc.contributor.author Tanaka, Y
dc.contributor.author Simon, Ch
dc.contributor.author Pralong, V
dc.contributor.author Lebedev, O I
dc.contributor.author Caignaert, V
dc.contributor.author Raveau, B
dc.date.accessioned 2011-03-04T07:13:49Z
dc.date.available 2011-03-04T07:13:49Z
dc.date.issued 2010-09-28
dc.identifier 1098-0121 en_US
dc.identifier.citation Physical Review B 82(10), 100416-1-4 (2010) en_US
dc.identifier.uri https://libjncir.jncasr.ac.in/xmlui/10572/62
dc.description.abstract BiFe0.5Mn0.5O3 could be stabilized in the perovskite structure by preparing it under high pressure and temperature. It has an orthorhombic structure with a possible ordered arrangement of Fe and Mn double rows and shows a magnetic ordering at high temperature (270 K). Low-temperature isothermal-magnetization measurements indicate the ground state to be antiferromagnetic with a spin canting. Surprisingly, it exhibits magnetization reversal at low applied fields below a compensation temperature, T*. Below T*, the sign of the magnetization can be switched between negative and positive value reversibly by increasing and decreasing the field. Magnetization reversal in this oxide seems to result from a competition between single-ion magnetocrystalline anisotropy and antisymmetric Dzyaloshinsky-Moriya interactions. en_US
dc.description.sponsorship Department of Science and Technology (DST), India, Japan Science and Technology (JST), Japan en_US
dc.description.uri http://dx.doi.org/10.1103/PhysRevB.82.100416 en_US
dc.language.iso en en_US
dc.publisher The American Physical Society en_US
dc.rights © 2010 The American Physical Society en_US
dc.subject N-Type Ferrimagnetism en_US
dc.subject Weak Ferromagnetism en_US
dc.subject Perovskite en_US
dc.title Temperature-induced magnetization reversal in BiFe0.5Mn0.5O3 synthesized at high pressure en_US
dc.type Article en_US


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