Physical properties of Co-substituted iron perovskite systems

被引:19
作者
Kawasaki, S [1 ]
Takano, M
Takeda, Y
机构
[1] Kyoto Univ, Inst Chem Res, Uji 611, Japan
[2] Mie Univ, Fac Engn, Dept Chem, Tsu, Mie 514, Japan
关键词
perovskite oxide; charge disproportionation; ferromagnetic metal; Mossbauer spectroscopy;
D O I
10.1016/S0167-2738(98)00042-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
ABO(3) type perovskite systems, CaFe1-xCoxO3 (0 less than or equal to x less than or equal to 0.5) and Sr2/3La1/3Fe1-xCoxO3 (0 less than or equal to x less than or equal to 1) were prepared by using a high pressure technique in the presence of an oxidizer KClO4. The parent Fe4+-oxides, CaFeO3 and Sr2/3La1/3FeO3, are both characterized by a charge disproportionation leading to an antiferromagnetic and insulating state, which is 2Fe(4+) --> Fe3+ + Fe5+ for the former and 3Fe(11/3+) --> 2Fe(3+) + Fe5+ for the latter. The Co-substitution leads to a switching to a ferromagnetic and metallic phase. In comparison with the cubic Sr-analogue, the ferromagnetic Curie temperature is lower and the saturation magnetization is smaller, while the coercive force is larger and the resistivity is higher. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:221 / 226
页数:6
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