Pressure-induced intermetallic valence transition in BiNiO3

被引:109
作者
Azuma, Masaki [1 ]
Carlsson, Sandra
Rodgers, Jennifer
Tucker, Matthew G.
Tsujimoto, Masahiko
Ishiwata, Shintaro
Isoda, Seiji
Shimakawa, Yuichi
Takano, Mikio
Attfield, J. Paul
机构
[1] Kyoto Univ, Inst Chem Res, Kyoto 6110011, Japan
[2] Univ Edinburgh, Ctr Sci Extreme Condit, Edinburgh EH9 3JZ, Midlothian, Scotland
[3] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JZ, Midlothian, Scotland
[4] Rutherford Appleton Lab, ISIS Facil, Didcot OX11 0QX, Oxon, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1021/ja074880u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The valence state change of BiNiO3 perovskite under pressure has been investigated by a powder neutron diffraction study and electron ic-state calculations. At ambient pressure, BiNiO3 has the unusual charge distribution Bi0.53+Bi0.55+Ni2+O3 with ordering of Bi3+ and Bi5+ charges on the A sites of a highly distorted perovskite structure. High-pressure neutron diffraction measurements and bond valence sum calculations show that the pressure-induced melting of the charge disproportionated state leads to a simultaneous charge transfer from Ni to Bi, so that the high-pressure phase is metallic Bi3+Ni3+O3. This unprecedented charge transfer between A and B site cations coupled to electronic instabilities at both sites leads to a variety of ground states, and it is predicted that a Ni-charge disproportionated state should also be observable.
引用
收藏
页码:14433 / 14436
页数:4
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