Oxygen vacancy ordering and magnetism in the rare earth stabilised perovskite form of "SrCoO3-δ"

被引:35
作者
James, M
Cassidy, D
Wilson, KF
Horvat, J
Withers, RL
机构
[1] Australian Nucl Sci & Technol Org, Bragg Inst, Menai, NSW 2234, Australia
[2] Univ New S Wales, Sch Phys, Sydney, NSW 2052, Australia
[3] Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2522, Australia
[4] Australian Natl Univ, Res Sch Chem, Canberra, ACT 0200, Australia
基金
澳大利亚研究理事会;
关键词
strontium doped cobaltate; solid solution limits; perovskite superstructure; spin glass magnetism;
D O I
10.1016/j.solidstatesciences.2003.03.001
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We have demonstrated that SrCoO3-delta can be stabilised into phase pure perovskite forms by the introduction of small amounts similar to5% of certain rare earth ions (Sm3+-Yb3+). At the same doping levels, La3+ and Pr3+ crystallise with the same isostructural trigonal structure as Sr6Co5O15; while the Nd3+ composition shows a mixture of both structure types. Powder X-ray diffraction showed only a simple cubic perovskite structure, however, a combination of electron and neutron diffraction has revealed a tetragonal (P4/mmm) a(p) x a(p) x 2a(p) superstructure. Strontium and the rare earth ions are disordered over a single site, while the oxygen vacancies are localised on the apical 02 sites. Magnetisation measurements show that these materials undergo transitions to a spin-glass state at temperatures below 150 K, and that significant coupling occurs between the rare earth ions and the mixed Co3+/(4+) ions. Magnetisation measurements as a function of applied field reveals that below the transition temperature ferromagnetic ordering takes place at relatively large fields. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:655 / 662
页数:8
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