并五苯
异质结
材料科学
扫描隧道显微镜
密度泛函理论
范德瓦尔斯力
纳米技术
纳米电子学
分子束外延
基质(水族馆)
光电子学
化学物理
分子
外延
化学
计算化学
薄膜晶体管
图层(电子)
地质学
有机化学
海洋学
作者
Francesco Tumino,Andi Rabia,Andrea Li Bassi,Sergio Tosoni,Carlo S. Casari
标识
DOI:10.1021/acs.jpcc.1c06661
摘要
Mixed-dimensional van der Waals heterostructures formed by molecular assemblies and 2D materials provide a novel platform for fundamental nanoscience and future nanoelectronics applications. Here we investigate a prototypical hybrid heterostructure between pentacene molecules and 2D MoS2 nanocrystals, deposited on Au(111) by combining pulsed laser deposition and organic molecular beam epitaxy. The obtained structures were investigated in situ by scanning tunneling microscopy and spectroscopy and analyzed theoretically by density functional theory calculations. Our results show the formation of atomically thin pentacene/MoS2 lateral heterostructures on the Au substrate. The most stable pentacene adsorption site corresponds to MoS2 terminations, where the molecules self-assemble parallel to the direction of MoS2 edges. The density of states changes sharply across the pentacene/MoS2 interface, indicating a weak interfacial coupling, which leaves the electronic signature of MoS2 edge states unaltered. This work unveils the self-organization of abrupt mixed-dimensional lateral heterostructures, opening to hybrid devices based on organic/inorganic one-dimensional junctions.
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