化学乱驱动的集群旋转玻璃在伪子Co2Zn10.2Mn0.8:一个实验和理论研究
Amit Mondal1, Shubham Patel2, Rahul Pan1
1Department of Chemistry, Indian Institute of Technology, Kharagpur 721302, India.
Inorganic chemistry
|March 22, 2025
概括
这项研究详细介绍了Co2Zn11中的Mn替代,揭示了23.1K以下的集群玻璃形成.磁性特性受到Mn原子旋转的影响,通过衍射技术得到证实.
科学领域:
- 凝聚物质物理学 凝聚物质物理学
- 材料科学 材料科学 材料科学
- 固态化学 固态化学
背景情况:
- -化合物因其磁性特性而引起人们的兴趣.
- 通过元素替代调整磁性行为是材料设计中的一个关键策略.
研究的目的:
- 为了研究替代的Co2Zn11.11的晶体结构和磁性.
- 了解Mn在Co2Zn11系统的磁性排序中的作用.
主要方法:
- 在高真空下进行固态合成.
- 用于结构分析的X射线和中子粉碎衍射 (NPD).
- 测量磁性易感度以探测磁性排序.
主要成果:
- Co2Zn10.2Mn0.8 在非中心对称空间组I4̅3m.m.中结晶.
- 在自旋结温度低于23.1 K的温度下,形成集群玻璃 (CG) 的证据.
- 磁矩主要来自Mn 3d状态,这表明Mn的重要作用.
结论:
- 在Co2Zn11中Mn的替代导致了集群玻璃的磁性行为.
- 结构和磁性数据证实了原子的分布及其对磁性特性的影响.
- 该研究提供了有关Mn-化-金属间的磁性相互作用的见解.
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