金属中的阿秒电子定位与筛选动力学

M. Volkov, Shunsuke A. Sato, F. Schlaepfer, L. Kasmi, N. Hartmann, M. Lucchini, L. Gallmann, Á. Rubio, U. Keller
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引用次数: 0

摘要

过渡金属及其化合物的d轨道上高度的电子局域化为有效地控制它们的光性质提供了一个杠杆。例如,VO2中的光吸收可能导致从介电态到金属态的超快电子相变[1]。电子相变的基本时间尺度与筛选动力学有关,通常属于阿秒域。其次是飞秒电子-电子热化,这可能模糊筛选引起的电荷再分配的初始印记。在这里,我们证明了过渡金属的性质原则上可以比电子热化时间尺度更快地被操纵,甚至比光学周期更快。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Attosecond Electron Localization and Screening Dynamics in Metals
A high degree of electron localization on the d-orbitals of transition metals and their compounds provides a lever to efficiently control their properties with light. For example, light absorption in VO2 may result in an ultrafast electronic phase transition from a dielectric into a metallic state [1]. The essential timescale of electronic phase transitions is connected to the screening dynamics, which typically belongs to the attosecond domain. It is followed by femtosecond electron-electron thermalization, which may blur the initial imprints of screening-induced charge re-distribution. Here we show that the properties of transition metals could in principle be manipulated much faster than the electron thermalization timescale and even faster than the optical cycle.
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