Suppr超能文献

ε-FeOOH的高压中子衍射研究:自旋重取向转变与氢键对称化

High-Pressure Neutron Diffraction Study on ε-FeOOH: The Spin-Reorientation Transition and Hydrogen-Bond Symmetrization.

作者信息

Ikeda Osamu, Yamamoto Hajime, Sano-Furukawa Asami, Sakamaki Tatsuya, Kuribayashi Takahiro, Noda Yukio, Suzuki Akio

机构信息

Department of Earth Science, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan.

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Sendai 980-8577, Japan.

出版信息

J Am Chem Soc. 2025 Feb 5;147(5):4005-4016. doi: 10.1021/jacs.4c11982. Epub 2025 Jan 23.

Abstract

The compression behavior of iron oxyhydroxide ε-FeOOH is complex, with variations in its magnetic property and bonding character. In this study, in situ powder neutron diffraction experiments were conducted on ε-FeOOH and ε-FeOOD up to pressures exceeding 20 GPa to investigate a spin-reorientation (spin-flop) transition, hydrogen-bond (H-bond) symmetrization, and their correlation. The magnetic transition was observed at 8 GPa in both ε-FeOOH and ε-FeOOD. The Fe-spins aligned in an A-type antiferromagnetic order and reoriented from the -direction to the -direction above 8 GPa. The crystal symmetry and H-bonds of ε-FeOOH transitioned from 2 with asymmetric H-bonds to with disordered H-bonds at 17.90 GPa, while ε-FeOOD remained asymmetric. The pressure evolution of the interatomic angles and distances indicates that the coordinate geometry of Fe transitioned toward H-bond symmetrization and would have affected the magnetic anisotropy. This study provides insights into the pressure effect of the magnetic transition on compounds containing hydrogen bonds.

摘要

羟基氧化铁ε-FeOOH的压缩行为很复杂,其磁性和键合特性会发生变化。在本研究中,对ε-FeOOH和ε-FeOOD进行了原位粉末中子衍射实验,压力超过20 GPa,以研究自旋重取向(自旋翻转)转变、氢键(H键)对称化及其相关性。在ε-FeOOH和ε-FeOOD中均在8 GPa处观察到磁性转变。Fe自旋以A型反铁磁顺序排列,并在8 GPa以上从-方向重新取向至-方向。ε-FeOOH的晶体对称性和H键在17.90 GPa时从具有不对称H键的2转变为具有无序H键的,而ε-FeOOD保持不对称。原子间角度和距离的压力演化表明,Fe的配位几何向H键对称化转变,这可能影响了磁各向异性。本研究为含氢键化合物中磁性转变的压力效应提供了见解。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验