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衬底对称性对二硫化钼单层取向的影响。

Effect of substrate symmetry on the orientations of MoS monolayers.

作者信息

Pan Shuangyuan, Yang Pengfei, Zhu Lijie, Hong Min, Xie Chunyu, Zhou Fan, Shi Yuping, Huan Yahuan, Cui Fangfang, Zhang Yanfeng

机构信息

Department of Materials Science and Engineering, College of Engineering, Peking University, Beijing 100871, People's Republic of China.

Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, People's Republic of China.

出版信息

Nanotechnology. 2021 Feb 26;32(9):095601. doi: 10.1088/1361-6528/abc566.

Abstract

Two-dimensional (2D) semiconducting transition metal dichalcogenides (TMDs) are promising platforms for developing next-generation electronic and optoelectronic devices due to their unique properties. To achieve this, the growth of large single-crystal TMDs is a critical issue. Unraveling the factors affecting the nucleation and domain orientation should hold fundamental significance. Herein, we design the chemical vapor deposition growth of monolayer MoS triangles on Au(111) and Au(100) facets, for exploring the substrate facet effects on the domain orientations. According to multi-scale characterizations, we find that, the obtained triangular MoS domains present two preferential orientations on the six-fold symmetric Au(111) facet, whereas four predominant orientations on the four-fold symmetric Au(100) facet. Using on-site scanning tunneling microscopy, we further reveal the preferred alignments of monolayer MoS triangles along the close-packed directions of both Au(111) and Au(100) facets. Moreover, bunched substrate steps are also found to form along the close-packed directions of the crystal facets, which guides the preferential nucleation of monolayer MoS along the step edges. This work should hereby deepen the understanding of the substrate facet/step effect on the nucleation and orientation of monolayer MoS domains, thus providing fundamental insights into the controllable syntheses of large single-crystal TMD monolayers.

摘要

二维(2D)半导体过渡金属二硫属化物(TMDs)因其独特的性质,是开发下一代电子和光电器件的有前途的平台。要实现这一目标,生长大尺寸单晶TMDs是一个关键问题。揭示影响成核和畴取向的因素具有重要的基础意义。在此,我们设计在Au(111)和Au(100)晶面上化学气相沉积生长单层MoS三角形,以探索衬底晶面对畴取向的影响。根据多尺度表征,我们发现,在六重对称的Au(111)晶面上获得的三角形MoS畴呈现两种优先取向,而在四重对称的Au(100)晶面上呈现四种主要取向。使用原位扫描隧道显微镜,我们进一步揭示了单层MoS三角形沿Au(111)和Au(100)晶面的密排方向的优先排列。此外,还发现沿晶面的密排方向形成了成束的衬底台阶,这引导了单层MoS沿台阶边缘优先成核。这项工作将加深对衬底晶面/台阶对单层MoS畴成核和取向影响的理解,从而为大尺寸单晶TMD单层的可控合成提供基础见解。

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