...
首页> 外文期刊>International Journal of Quantum Chemistry >Synthesis, structure, and magnetic properties of SrMn1-xGaxO3-delta (x=0-0.5) perovskites
【24h】

Synthesis, structure, and magnetic properties of SrMn1-xGaxO3-delta (x=0-0.5) perovskites

机译:SrMn1-xGaxO3-δ(x = 0-0.5)钙钛矿的合成,结构和磁性

获取原文
获取原文并翻译 | 示例
           

摘要

We report the synthesis of SrMn1-xGaxO3-delta perovskite compounds and describe the dependence of their phase stability and structural and physical properties over extended cation and oxygen composition ranges. Using special synthesis techniques derived from thermogravimetric measurements, we have extended the solubility limit of random substitution of Ga3+ for Mn in the cubic perovskite phase to x = 0.5. In the cubic perovskite phase the maximum oxygen content is close to 3-x/2, which corresponds to 100% Mn4+. Maximally oxygenated solid solution compounds are found to order antiferromagnetically for x = 0-0.4, with the transition temperature linearly decreasing as Ga content increases. Increasing the Ga content introduces frustration into the magnetic system and a spin-glass state is observed for SrMn0.5Ga0.5O2.67(3) below 12 K. These properties are markedly different from the long-range antiferromagnetic order below 180 K observed for the layer-ordered compound Sr2MnGaO5.50 with nominally identical chemical composition. (c) 2005 Elsevier Inc. All rights reserved.
机译:我们报告了SrMn1-xGaxO3-δ钙钛矿化合物的合成,并描述了它们的相稳定性以及结构和物理性质对扩展的阳离子和氧组成范围的依赖性。使用从热重法测量得出的特殊合成技术,我们将Ga3 +随机替代的立方钙钛矿相中的Mn的溶解度极限扩展到x = 0.5。在立方钙钛矿相中,最大氧含量接近3-x / 2,相当于100%Mn4 +。发现最大的含氧固溶体化合物在x = 0-0.4时反铁磁性排列,并且随着Ga含量的增加,转变温度线性降低。 Ga含量的增加会给磁系统带来挫败感,并且在12 K以下观察到SrMn0.5Ga0.5O2.67(3)的自旋玻璃态。这些性质与在180 K以下观察到的远距离反铁磁有明显不同。具有名义上相同的化学组成的层序化合物Sr2MnGaO5.50。 (c)2005 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号