Volume 129, Issue 15 pp. 4307-4310
Zuschrift

Successive Charge Transitions of Unusually High-Valence Fe3.5+: Charge Disproportionation and Intermetallic Charge Transfer

Dr. Yoshiteru Hosaka

Dr. Yoshiteru Hosaka

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011 Japan

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Dr. Fabio Denis Romero

Dr. Fabio Denis Romero

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011 Japan

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Dr. Noriya Ichikawa

Dr. Noriya Ichikawa

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011 Japan

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Prof. Dr. Takashi Saito

Prof. Dr. Takashi Saito

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011 Japan

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Prof. Dr. Yuichi Shimakawa

Corresponding Author

Prof. Dr. Yuichi Shimakawa

Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011 Japan

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First published: 20 March 2017
Citations: 3

Abstract

A perovskite-structure oxide containing unusually high-valence Fe3.5+ was obtained by high-pressure synthesis. Instability of the Fe3.5+ in Ca0.5Bi0.5FeO3 is relieved first by charge disproportionation at 250 K and then by intermetallic charge transfer between A-site Bi and B-site Fe at 200 K. These previously unobserved successive charge transitions are due to competing intermetallic and disproportionation charge instabilities. Both transitions change magnetic and structural properties significantly, indicating strong coupling of charge, spin, and lattice in the present system.

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