Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Angew Chem Int Ed Engl. 2017 Apr 3;56(15):4243-4246. doi: 10.1002/anie.201700881. Epub 2017 Mar 20.
A perovskite-structure oxide containing unusually high-valence Fe was obtained by high-pressure synthesis. Instability of the Fe in Ca Bi FeO 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.
通过高压合成得到了一种含有异常高价态 Fe 的钙钛矿结构氧化物。在 250 K 时,通过电荷歧化首先缓解了 Ca Bi FeO 中 Fe 的不稳定性,然后在 200 K 时通过 A 位 Bi 和 B 位 Fe 之间的金属间电荷转移进一步缓解。这些以前未观察到的连续电荷跃迁归因于竞争的金属间和歧化电荷不稳定性。这两种转变都显著改变了磁和结构性质,表明在当前体系中电荷、自旋和晶格的强耦合。