The Hard Ferromagnetism in FePS3 Induced by Non-Magnetic Molecular Intercalation (Adv. Phys. Res. 2/2025)

Yunbo Ou, Xiaoyin Li, Jan Kopaczek, Austin Davis, Gigi Jackson, Mohammed Sayyad, Feng Liu, Seth Ariel Tongay
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引用次数: 0

Abstract

Anisotropic ferromagnetism within antiferromagnetic crystals

The cover feature showcases the emergence of hard anisotropic ferromagnetism following the intercalation of nonmagnetic pyridinium ions into antiferromagnetic FePS3 single crystals. In article number 202400101, Yunbo Ou, Feng Liu, Seth Ariel Tongay, and colleagues report the transition from antiferromagnetism to ferromagnetism in pyridinium-intercalated FePS3, thereby highlighting both the energetically stable B-phase and metastable P-phase. These phases exhibit remarkable properties, including giant coercive fields exceeding 7 T and high Curie temperatures (72–87 K). As revealed by X-ray photoelectron spectroscopy and supported by first-principles calculations and atomistic spin dynamics simulations, electron transfer from the pyridinium ions to FePS3 plays a key role in driving this transition. This work offers crucial insights into hard magnetism in intercalated van der Waals materials, thus paving the way for advances in 2D magnet-based technologies.

Abstract Image

非磁性分子插层诱导FePS3的硬铁磁性研究[j]。研究》2/2025)
反铁磁晶体内的各向异性铁磁性覆盖特征显示了非磁性吡啶离子嵌入反铁磁FePS3单晶后出现的硬各向异性铁磁性。在文章编号202400101中,欧云波、刘峰、Seth Ariel Tongay等人报道了吡啶插层FePS3从反铁磁性到铁磁性的转变,从而强调了能量稳定的b相和亚稳的p相。x射线光电子能谱、第一性原理计算和原子自旋动力学模拟结果表明,电子从吡啶离子向FePS3的转移在这一转变过程中起着关键作用。这项工作为嵌入范德华材料的硬磁性提供了重要的见解,从而为二维磁性技术的进步铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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