光激发
激子
材料科学
二硒化钨
自由电子模型
光电子学
光电导性
太赫兹光谱与技术
Crystal(编程语言)
比克西顿
太赫兹辐射
光谱学
载流子
多激子产生
分子物理学
凝聚态物理
光学
光致发光
原子物理学
激光器
太阳能电池
物理
化学
过渡金属
催化作用
激发态
程序设计语言
量子力学
生物化学
计算机科学
作者
Chuan He,Lipeng Zhu,Qiyi Zhao,Yuanyuan Huang,Zehan Yao,Wanyi Du,Yuhang He,Sujuan Zhang,Xinlong Xu
标识
DOI:10.1002/adom.201800290
摘要
Abstract The dynamics of photoexcited species is quite important for the development of next‐generation ultrafast optoelectronic devices based on transition metal dichalcogenides (TMDs). Herein, time‐resolved optical pump terahertz (THz) probe spectroscopy, which is sensitive to both bounded excitons and free electrons/holes, is employed to study the dynamics of photo‐induced carriers in the typical layered TMDs crystal tungsten diselenide (WSe 2 ). Initial photoexcitation could generate both free carriers and excitons. The free carriers decay followed by phonon‐assistance (≈30 ps) and defect‐assistance (≈200–280 ps). The excitons decay followed by the phonon‐assisted recombination (≈100 ps) and the defect‐induced exciton separation (≈40–200 ps). With the increasing of pump fluence, more free electrons and holes will bind to form excitons by many‐body effect, while with the decay of time, more excitons will dissociate into free carriers by defects. The frequency‐dependent transient complex THz photoconductivity of layered WSe 2 crystal can be well described by Drude–Smith–Lorentz model, which suggests preferential free carriers backscattering due to the defects. The ratio of free carriers to excitons suggests that free carriers dominate after the photoexcitation, which is important for the optoelectronic devices such as solar cells and photodetectors.
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