Electrically controllable spontaneous magnetism in nanoscale mixed phase multiferroics

Magnetoelectrics and multiferroics present exciting opportunities for electric-field control of magnetism. However, there are few room-temperature ferromagnetic-ferroelectrics. Among the various types of multiferroics the bismuth ferrite system has received much attention primarily because both the...

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Published inNature communications Vol. 2; no. 1; p. 225
Main Authors He, Q, Chu, Y. -H, Heron, J. T, Yang, S. Y, Liang, W. I, Kuo, C.Y, Lin, H. J, Yu, P, Liang, C. W, Zeches, R. J, Kuo, W. C, Juang, J. Y, Chen, C. T, Arenholz, E, Scholl, A, Ramesh, R
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.03.2011
Nature Publishing Group
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Summary:Magnetoelectrics and multiferroics present exciting opportunities for electric-field control of magnetism. However, there are few room-temperature ferromagnetic-ferroelectrics. Among the various types of multiferroics the bismuth ferrite system has received much attention primarily because both the ferroelectric and the antiferromagnetic orders are quite robust at room temperature. Here we demonstrate the emergence of an enhanced spontaneous magnetization in a strain-driven rhombohedral and super-tetragonal mixed phase of BiFeO 3 . Using X-ray magnetic circular dichroism-based photoemission electron microscopy coupled with macroscopic magnetic measurements, we find that the spontaneous magnetization of the rhombohedral phase is significantly enhanced above the canted antiferromagnetic moment in the bulk phase, as a consequence of a piezomagnetic coupling to the adjacent tetragonal-like phase and the epitaxial constraint. Reversible electric-field control and manipulation of this magnetic moment at room temperature is also shown. Complex oxide interfaces are important for electronic and spintronic applications. In this study, the authors show the emergence of spontaneous magnetism at one such interface between two phases of BiFeO 3 due to strain effects and piezoelectric coupling.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms1221