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arXiv 2411.02443cond-mat.mtrl-scicond-mat.mes-hallcond-mat.str-elphysics.app-ph
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双层FeSe中热电子驱动的结构膨胀与磁性塌缩

Hot Electron-Driven Structural Expansion and Magnetic Collapse in Bilayer FeSe

Sam Azadi, A. Principi, M. S. Bahramy

AI总结:

本文通过第一性原理计算发现光激发热电子可诱导双层FeSe同时发生结构膨胀和反铁磁序塌缩,提出利用超快激光调控铁基薄膜量子相的新途径。

摘要:

低维系统中光与物质相互作用所引发的量子现象为未来量子技术带来了巨大潜力。本文利用包含非局域范德瓦尔斯相互作用和Hubbard修正的第一性原理计算,报道了光激发热电子诱导双层FeSe同时发生结构膨胀和磁性塌缩。计算结果表明,尽管体相FeSe如实验所观测为顺磁性,双层FeSe在低温下表现出稳健的交错反铁磁序,其每个Fe位点的净磁矩约为2.75 μB。然而,随着光激发电子密度的增加,内部电子熵系统性增强,导致反铁磁序完全塌缩,并伴随层间距的突然膨胀。研究结果表明,FeSe薄膜的结构和磁性可以通过超快激光激发进行精细调控,为通过电子温度调控铁基化合物中的量子相提供了一条途径。

英文摘要:

Quantum phenomena emerging from the interaction of light and matter in low-dimensional systems hold great potential for future quantum technologies. Here, using first-principles calculations incorporating non-local van der Waals interactions and Hubbard corrections, we report simultaneous structural expansion and magnetic collapse in bilayer FeSe induced by photoexcited hot electrons. Our calculations reveal that, while bulk FeSe is paramagnetic, as observed experimentally, double-layer FeSe exhibits robust {\it staggered} antiferromagnetic order at low temperatures with a net site magnetization of $\sim 2.75~μ_B$/Fe. However, increasing the density of photoexcited electrons systematically enhances the internal electronic entropy, leading to a complete collapse of antiferromagnetic order accompanied by an abrupt expansion of the interlayer separation. Our findings suggest the structural and magnetic properties of FeSe thin films can be finely tuned via ultrafast laser excitation, offering a pathway to control quantum phases in iron-based compounds through electronic temperature.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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