Coupling Between Magnetic Exchange and Charge Activation in Cu-Doped LaFeO3

Material research on perovskite‐type oxides (ABO3) has been driven by the recognition of their unique properties primarily attributed to the presence of oxygen octahedron (BO6). Since 2003, the discovery of strong coupling in TbMnO3 and BiFeO3 has stimulated new interests in understanding the relati...

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Published inJournal of the American Ceramic Society Vol. 99; no. 6; pp. 2035 - 2039
Main Authors Dogdibegovic, Emir, Cai, Qingsheng, James, William J., Yelon, William B., Anderson, Harlan U., Yang, Jin-Bo, Zhou, Xiao-Dong
Format Journal Article
LanguageEnglish
Published Columbus Blackwell Publishing Ltd 01.06.2016
Wiley Subscription Services, Inc
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Summary:Material research on perovskite‐type oxides (ABO3) has been driven by the recognition of their unique properties primarily attributed to the presence of oxygen octahedron (BO6). Since 2003, the discovery of strong coupling in TbMnO3 and BiFeO3 has stimulated new interests in understanding the relationship between magnetic and electric properties in perovskites. In this article, we report our recent work on the magnetic superexchange interaction and charge formation in copper‐doped LaFeO3 using high‐temperature neutron diffraction and thermoelectric measurements. In situ neutron diffraction measurements show a loss of antiferromagnetic ordering above 450°C. With an increase in Cu content, the (Fe, Cu)‐O bond length decreases and the (Fe, Cu)–O–(Fe, Cu) bond angle increases, which leads to an enhancement of the Fe–O–Fe superexchange interaction. Thermoelectric and electrical measurements show that the formation of electron holes in Cu‐doped LaFeO3 is a thermally activated process with two distinct regions with a transition temperature near 450°C, in congruence with the magnetic measurements. Our work show that Cu is in 3+ state in La(Fe,Cu)O3 at room temperature, resulting in the maximum superexchange interaction between Fe3+ ions.
Bibliography:ark:/67375/WNG-KQXLRDG8-8
ArticleID:JACE14061
National Science Foundation - No. DMR-1006113
Department of Energy - No. FE0023475
istex:A5EFEBDE9E9D3E5A34921A72D84652CFD53D8B37
National Natural Science Foundation of China - No. 51171001; No. 51371009
ISSN:0002-7820
1551-2916
DOI:10.1111/jace.14061