光激发
含时密度泛函理论
电荷密度波
共价键
振荡(细胞信号)
材料科学
相变
分子物理学
电荷密度
凝聚态物理
密度泛函理论
原子物理学
物理
化学
计算化学
量子力学
生物化学
超导电性
激发态
作者
Yu-Xiang Gu§,Wen-Hao Liu§,Zhi Wang,Shu‐Shen Li,Lin‐Wang Wang,Jun‐Wei Luo
出处
期刊:Cornell University - arXiv
日期:2022-01-01
标识
DOI:10.48550/arxiv.2209.12135
摘要
In stark contrast to the conventional charge density wave (CDW) materials, the one-dimensional CDW on the In/Si(111) surface exhibits immediate damping of the CDW oscillation during the photoinduced phase transition. Here, by successfully reproducing the experimentally observed photoinduced CDW transition on the In/Si(111) surface by performing real-time time-dependent density functional theory (rt-TDDFT) simulations, we demonstrate that photoexcitation promotes valence electrons from Si substrate to empty surface bands composed primarily of the covalent p-p bonding states of the long In-In bonds, generating interatomic forces to shorten the long bonds and in turn drives coherently the structural transition. We illustrate that after the structural transition, the component of these surface bands occurs a switch among different covalent In bonds, causing a rotation of the interatomic forces by about π/6 and thus quickly damping the oscillations in feature CDW modes. These findings provide a deeper understanding of photoinduced phase transitions.
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