单层
材料科学
范德瓦尔斯力
静电力显微镜
量子隧道
纳米结构
纳米技术
纳米尺度
库仑
六边形晶格
凝聚态物理
导电原子力显微镜
剥脱关节
Crystal(编程语言)
化学物理
光电子学
原子力显微镜
分子物理学
分子
石墨烯
化学
物理
量子力学
程序设计语言
反铁磁性
电子
有机化学
计算机科学
作者
Sheng Liu,Chee Fai Fong,Xue Liu,Beng Hau Tan,Qingyun Zeng,Yoshinori Okada,Nam‐Trung Nguyen,Hongjie An
标识
DOI:10.1002/admi.202300580
摘要
Abstract Atoms, molecules, and nanoparticles can be spatially manipulated by an atomic force microscopy (AFM) tip, through van der Waals (vdW) and/or Coulomb forces. These point‐to‐point manipulations are highly accurate at nanoscale, facilitating the construction and modification of nanostructures. Nevertheless, it is difficult to manipulate 2D layers in vdW crystals by an AFM tip, because the tip‐induced attractive force is usually insufficient to outcompete the interlaminar vdW forces. Herein, manipulation of the surface layers on a MoS 2 single crystal by a conductive AFM tip is successfully reported. By applying a bias between the tip and MoS 2 , the Coulomb attractive force allows the topmost MoS 2 layers to be picked up. These exfoliated layers are deformed into micron‐sized bubbles with sixfold symmetry, which are composed of high‐quality monolayers and visually reflecting the hexagonal lattice orientation. The underlying mechanisms of the sixfold symmetric exfoliation and the formation of monolayers are discussed by in situ monitoring of the tunneling volt‐ampere characteristics and simulation of the force distribution. The findings open a new route to obtain high‐quality transition metal dichalcogenide (TMD) monolayers and their derived nanostructures on the surface of TMD single crystals for optoelectronic and photonic device applications.
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