激子
异质结
光致发光
单层
材料科学
范德瓦尔斯力
电子
半导体
三极管
光电子学
化学物理
凝聚态物理
纳米技术
化学
物理
量子力学
分子
有机化学
作者
Yuze Meng,Tianmeng Wang,Chenhao Jin,Zhipeng Li,Shengnan Miao,Zhen Lian,Takashi Taniguchi,Kenji Watanabe,Fengqi Song,Su‐Fei Shi
标识
DOI:10.1038/s41467-020-16419-x
摘要
Abstract The heterostructure of monolayer transition metal dichalcogenides (TMDCs) provides a unique platform to manipulate exciton dynamics. The ultrafast carrier transfer across the van der Waals interface of the TMDC hetero-bilayer can efficiently separate electrons and holes in the intralayer excitons with a type II alignment, but it will funnel excitons into one layer with a type I alignment. In this work, we demonstrate the reversible switch from exciton dissociation to exciton funneling in a MoSe 2 /WS 2 heterostructure, which manifests itself as the photoluminescence (PL) quenching to PL enhancement transition. This transition was realized through effectively controlling the quantum capacitance of both MoSe 2 and WS 2 layers with gating. PL excitation spectroscopy study unveils that PL enhancement arises from the blockage of the optically excited electron transfer from MoSe 2 to WS 2 . Our work demonstrates electrical control of photoexcited carrier transfer across the van der Waals interface, the understanding of which promises applications in quantum optoelectronics.
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