Room-Temperature Magnetism Realized by Doping Fe into Ferroelectric LiTaO3
We synthesize LiTal-x FexO3-σ (LTFO) remain single phase up to x = 0.09 ceramics by the conventional solid-state reaction method. The samples The magnetic measurements show that the doping of Fe successfully realizes ferromagnetism of LTFO at room temperature. The dielectric measurements indicate th...
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Published in | 中国物理快报:英文版 no. 1; pp. 161 - 164 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
2014
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Subjects | |
Online Access | Get full text |
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Summary: | We synthesize LiTal-x FexO3-σ (LTFO) remain single phase up to x = 0.09 ceramics by the conventional solid-state reaction method. The samples The magnetic measurements show that the doping of Fe successfully realizes ferromagnetism of LTFO at room temperature. The dielectric measurements indicate that LTFO is ferroelectric, similarly to LiTaO3 (LTO), but its ferroelectric Curie temperature seems to decrease with the increasing Fe content. By means of doping Fe ions into LTO, the coexistence of spontaneous electric polarization and spontaneous magnetic moment is realized at room temperature. |
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Bibliography: | 11-1959/O4 We synthesize LiTal-x FexO3-σ (LTFO) remain single phase up to x = 0.09 ceramics by the conventional solid-state reaction method. The samples The magnetic measurements show that the doping of Fe successfully realizes ferromagnetism of LTFO at room temperature. The dielectric measurements indicate that LTFO is ferroelectric, similarly to LiTaO3 (LTO), but its ferroelectric Curie temperature seems to decrease with the increasing Fe content. By means of doping Fe ions into LTO, the coexistence of spontaneous electric polarization and spontaneous magnetic moment is realized at room temperature. SONG Ying-Jie, ZHANG Qing-Hua, SHEN Xi, NI Xiao-Dong, YAO Yuan, YU Ri-Cheng( 1 Department of Physics, University of Science and Technology Beijing, Beijing 100083 2 Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190) |
ISSN: | 0256-307X 1741-3540 |
DOI: | 10.1088/0256-307X/31/1/017501 |