| Literature DB >> 33347267 |
Ce Xu1, Hui Wen Yong1, Jinlu He2, Run Long2, Alisson R Cadore3, Ioannis Paradisanos3, Anna K Ott3, Giancarlo Soavi3,4, Sefaattin Tongay5, Giulio Cerullo6,7, Andrea C Ferrari3, Oleg V Prezhdo8, Zhi-Heng Loh1,9.
Abstract
Electron transport across the transition-metal dichalcogenide (TMD)/metal interface plays an important role in determining the performance of TMD-based optoelectronic devices. However, the robustness of this process against structural heterogeneities remains unexplored, to the best of our knowledge. Here, we employ a combination of time-resolved photoemission electron microscopy (TR-PEEM) and atomic force microscopy to investigate the spatially resolved hot-electron-transfer dynamics at the monolayer (1L) MoS2/Au interface. A spatially heterogeneous distribution of 1L-MoS2/Au gap distances, along with the sub-80 nm spatial- and sub-60 fs temporal resolution of TR-PEEM, permits the simultaneous measurement of electron-transfer rates across a range of 1L-MoS2/Au distances. These decay exponentially as a function of distance, with an attenuation coefficient β ∼ 0.06 ± 0.01 Å-1, comparable to molecular wires. Ab initio simulations suggest that surface plasmon-like states mediate hot-electron-transfer, hence accounting for its weak distance dependence. The weak distance dependence of the interfacial hot-electron-transfer rate indicates that this process is insensitive to distance fluctuations at the TMD/metal interface, thus motivating further exploration of optoelectronic devices based on hot carriers.Entities:
Keywords: TMD/metal interface; hot carriers; time-resolved photoemission electron microscopy; transition-metal dichalcogenides; ultrafast spectroscopy
Year: 2020 PMID: 33347267 DOI: 10.1021/acsnano.0c07350
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881