声子
单层
材料科学
凝聚态物理
异质结
二硫化钼
基质(水族馆)
化学物理
电子
分子物理学
纳米技术
光电子学
化学
物理
量子力学
海洋学
地质学
冶金
作者
Tristan L. Britt,Qiuyang Li,Laurent P. René de Cotret,Nicholas Olsen,Martin Otto,Syed Ali Hassan,Marios Zacharias,Fabio Caruso,Xiaoyang Zhu,Bradley J. Siwick
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-06-07
卷期号:22 (12): 4718-4724
被引量:36
标识
DOI:10.1021/acs.nanolett.2c00850
摘要
Transition-metal dichalcogenide monolayers and heterostructures are highly tunable material systems that provide excellent models for physical phenomena at the two-dimensional (2D) limit. While most studies to date have focused on electrons and electron-hole pairs, phonons also play essential roles. Here, we apply ultrafast electron diffraction and diffuse scattering to directly quantify, with time and momentum resolution, electron-phonon coupling (EPC) in monolayer molybdenum disulfide and phonon transport from the monolayer to a silicon nitride substrate. Optically generated hot carriers result in a profoundly anisotropic distribution of phonons in the monolayer within ∼5 ps. A quantitative comparison with ab initio ultrafast dynamics simulations reveals the essential role of dielectric screening in weakening EPC. Thermal transport from the monolayer to the substrate occurs with the phonon system far from equilibrium. While screening in 2D is known to strongly affect equilibrium properties, our findings extend this understanding to the dynamic regime.
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