范德瓦尔斯力
堆积
半导体
材料科学
单层
超晶格
外延
凝聚态物理
原子单位
光电子学
化学物理
过渡金属
图层(电子)
纳米技术
分子
化学
物理
催化作用
量子力学
生物化学
有机化学
作者
Gangtae Jin,Chang‐Soo Lee,Odongo Francis Ngome Okello,Sukho Lee,Min Yeong Park,Soonyoung Cha,Seung‐Young Seo,Gunho Moon,Seok Young Min,Dong‐Hwan Yang,Cheolhee Han,Hyungju Ahn,Jekwan Lee,Hyunyong Choi,Jonghwan Kim,Si‐Young Choi,Moon‐Ho Jo
标识
DOI:10.1038/s41565-021-00942-z
摘要
A broad range of transition metal dichalcogenide (TMDC) semiconductors are available as monolayer (ML) crystals, so the precise integration of each kind into van der Waals (vdW) superlattices (SLs) could enable the realization of novel structures with previously unexplored functionalities. Here we report the atomic layer-by-layer epitaxial growth of vdW SLs with programmable stacking periodicities, composed of more than two kinds of dissimilar TMDC MLs, such as MoS2, WS2 and WSe2. Using kinetics-controlled vdW epitaxy in the near-equilibrium limit by metal-organic chemical vapour depositions, we achieved precise ML-by-ML stacking, free of interlayer atomic mixing, which resulted in tunable two-dimensional vdW electronic systems. As an example, by exploiting the series of type II band alignments at coherent two-dimensional vdW heterointerfaces, we demonstrated valley-polarized carrier excitations-one of the most distinctive electronic features in vdW ML semiconductors-which scale with the stack numbers n in our (MoS2/WS2)n SLs on optical excitations.
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