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Nature 436, 1136-1138 (25 August 2005) | doi:10.1038/nature04039; Received 2 May 2005; Accepted 11 July 2005

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Ferroelectricity from iron valence ordering in the charge-frustrated system LuFe2O4

Naoshi Ikeda1, Hiroyuki Ohsumi1, Kenji Ohwada2, Kenji Ishii2, Toshiya Inami2, Kazuhisa Kakurai3, Youichi Murakami4, Kenji Yoshii2, Shigeo Mori5, Yoichi Horibe5 & Hijiri Kitô6

  1. Japan Synchrotron Radiation Research Institute, SPring-8, Hyogo 679-5198, Japan
  2. Synchrotron Radiation Research Center, SPring-8, Japan Atomic Energy Research Institute, Hyogo 679-5148, Japan
  3. Japan Atomic Energy Research Institute, Ibaraki 319-1195, Japan
  4. Department of Physics, Tohoku University, Sendai 980-8578, Japan
  5. Department of Physical Science, Osaka Prefecture University, Sakai, Osaka 599-8531, Japan
  6. National Institute of Advanced Industrial Science and Technology, Tsukuba 305-8561, Japan

Correspondence to: Naoshi Ikeda1 Correspondence and requests for materials should be addressed to N.I. (Email: ikedan@spring8.or.jp).

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Ferroelectric materials are widely used in modern electric devices such as memory elements, filtering devices and high-performance insulators. Ferroelectric crystals have a spontaneous electric polarization arising from the coherent arrangement of electric dipoles1 (specifically, a polar displacement of anions and cations). First-principles calculations2, 3 and electron density analysis4 of ferroelectric materials have revealed that the covalent bond between the anions and cations, or the orbital hybridization of electrons on both ions, plays a key role in establishing the dipolar arrangement. However, an alternative model—electronic ferroelectricity5—has been proposed in which the electric dipole depends on electron correlations, rather than the covalency. This would offer the attractive possibility of ferroelectric materials that could be controlled by the charge, spin and orbital degrees of freedom of the electron. Here we report experimental evidence for ferroelectricity arising from electron correlations in the triangular mixed valence oxide, LuFe2O4. Using resonant X-ray scattering measurements, we determine the ordering of the Fe2+ and Fe3+ ions. They form a superstructure that supports an electric polarization consisting of distributed electrons of polar symmetry. The polar ordering arises from the repulsive property of electrons—electron correlations—acting on a frustrated geometry.

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