邻接
单层
外延
材料科学
扫描隧道显微镜
凝聚态物理
结晶学
化学气相沉积
光电子学
化学物理
纳米技术
化学
图层(电子)
物理
有机化学
作者
Jingyi Hu,Wenzhi Quan,Pengfei Yang,Fangfang Cui,Fachen Liu,Lijie Zhu,Shuangyuan Pan,Yahuan Huan,Fan Zhou,Jiatian Fu,Guanhua Zhang,Peng Gao,Yanfeng Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-12-27
卷期号:17 (1): 312-321
被引量:25
标识
DOI:10.1021/acsnano.2c07978
摘要
Epitaxial growth of wafer-scale monolayer semiconducting transition metal dichalcogenide single crystals is essential for advancing their applications in next-generation transistors and highly integrated circuits. Several efforts have been made for the growth of monolayer MoS2 single crystals on high-symmetry Au(111) and sapphire substrates, while more prototype growth systems still need to be discovered for clarifying the internal mechanisms. Herein, we report the epitaxial growth of unidirectionally aligned monolayer MoS2 domains and single-crystal films on low-symmetry Au(101) vicinal facets via a facile chemical vapor deposition method. On-site scanning tunneling microscopy observations reveal the formation of a specific rectangular Moiré pattern along the [101̅] step edge of Au(101) and along its perpendicular direction. The perfect lattice constant matching of MoS2/Au(101) along the substrate high-symmetry directions (i.e., Au[101̅], Au [010]) as well as the step-edge-guiding effect are proposed to facilitate the robust epitaxy. Multiscale characterizations further confirm the domain-boundary-free feature of the monolayer MoS2 films merged by unidirectionally aligned monolayer domains. This work hereby puts forward a symmetry mismatched epitaxial system for the direct synthesis of monolayer MoS2 single crystals, which should deepen our understanding about the epitaxy of 2D layered materials and propel their applications in various fields.
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