| Literature DB >> 32267670 |
Pengfei Yang1,2, Shuqing Zhang3, Shuangyuan Pan1,2, Bin Tang4, Yu Liang5, Xiaoxu Zhao6, Zhepeng Zhang1,2, Jianping Shi1,2, Yahuan Huan1,2, Yuping Shi1,2, Stephen John Pennycook6, Zefeng Ren5, Guanhua Zhang5, Qing Chen4, Xiaolong Zou3, Zhongfan Liu1, Yanfeng Zhang1,2.
Abstract
Two-dimensional (2D) semiconducting transition metal dichalcogenides (TMDs) have emerged as attractive platforms in next-generation nanoelectronics and optoelectronics for reducing device sizes down to a 10 nm scale. To achieve this, the controlled synthesis of wafer-scale single-crystal TMDs with high crystallinity has been a continuous pursuit. However, previous efforts to epitaxially grow TMD films on insulating substrates (e.g., mica and sapphire) failed to eliminate the evolution of antiparallel domains and twin boundaries, leading to the formation of polycrystalline films. Herein, we report the epitaxial growth of wafer-scale single-crystal MoS2 monolayers on vicinal Au(111) thin films, as obtained by melting and resolidifying commercial Au foils. The unidirectional alignment and seamless stitching of the MoS2 domains were comprehensively demonstrated using atomic- to centimeter-scale characterization techniques. By utilizing onsite scanning tunneling microscope characterizations combined with first-principles calculations, it was revealed that the nucleation of MoS2 monolayer is dominantly guided by the steps on Au(111), which leads to highly oriented growth of MoS2 along the ⟨110⟩ step edges. This work, thereby, makes a significant step toward the practical applications of MoS2 monolayers and the large-scale integration of 2D electronics.Entities:
Keywords: epitaxial; gold; molybdenum disulfide; orientation; single crystal
Year: 2020 PMID: 32267670 DOI: 10.1021/acsnano.0c01478
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881