范德华铁磁体VI3的居里温度因压力而大幅升高

J. Valenta, M. Kratochvílová, M. Míšek, Karel Carva, J. Kaštil, P. Doležal, P. Opletal, Petr Čermák, P. Proschek, K. Uhlířová, J. Prchal, M. Coak, S. Son, J-G. Park, V. Sechovský
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引用次数: 17

摘要

本文报道了范德华化合物VI3单晶在7.3 GPa外压下的磁性演化。在常压下,分别观察到T1 = 54.5 K、T2 = 53 K、TC = 49.5 K和TFM = 26 K的磁相变。前两种是由于在特定的晶体表面层中发生了铁磁性。体铁磁性表现为居里温度下的磁性有序转变和两种不同铁磁性相之间的转变,并伴随着冷却时从单斜向三斜对称的结构转变。采用三种独立的技术研究了压力对磁参数的影响。当压力达到0.6 GPa时,TC几乎不受影响,而TFM则随着压力的增加而迅速增加,并在约0.85 GPa时达到TC的三相点。在较高的压力下,随着压力的增加,只观察到一个磁相变向更高的温度移动,在7.3 GPa下达到99 K。相比之下,施加压力可以显著降低低温体磁化强度(在2.5 GPa时降低50%以上),这表明可能是压力引起的钒磁矩降低。我们结合最近的理论研究对这些结果进行了讨论,以分析交换相互作用并提供如何提高VI3的居里温度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pressure-induced large increase of Curie temperature of the van der Waals ferromagnet VI3
Evolution of magnetism in single crystals of the van der Waals compound VI3 in external pressure up to 7.3 GPa studied by measuring magnetization and ac magnetic susceptibility is reported. Four magnetic phase transitions, at T1 = 54.5 K, T2 = 53 K, TC = 49.5 K, and TFM = 26 K, respectively have been observed at ambient pressure. The first two have been attributed to the onset of ferromagnetism in specific crystal-surface layers. The bulk ferromagnetism is characterized by the magnetic ordering transition at Curie temperature TC and the transition between two different ferromagnetic phases TFM, accompanied by a structure transition from monoclinic to triclinic symmetry upon cooling. The pressure effects on magnetic parameters were studied with three independent techniques. TC was found to be almost unaffected by pressures up to 0.6 GPa whereas TFM increases rapidly with increasing pressure and reaches TC at a triple point at ~ 0.85 GPa. At higher pressures, only one magnetic phase transition is observed moving to higher temperatures with increasing pressure to reach 99 K at 7.3 GPa. In contrast, the low-temperature bulk magnetization is dramatically reduced by applying pressure (by more than 50% at 2.5 GPa) suggesting a possible pressure-induced reduction of vanadium magnetic moment. We discussed these results in light of recent theoretical studies to analyze exchange interactions and provide how to increase the Curie temperature of VI3.
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