Dynamics of charge-transfer excitons in a transition metal dichalcogenide heterostructure

被引:16
|
作者
Bian, Ang [1 ]
He, Dawei [1 ]
Hao, Shengcai [1 ]
Fu, Yang [1 ]
Zhang, Lu [1 ]
He, Jiaqi [2 ]
Wang, Yongsheng [1 ]
Zhao, Hui [3 ]
机构
[1] Beijing Jiaotong Univ, Inst Optoelect Technol, Key Lab Luminescence & Opt Informat, Minist Educ, Beijing 100044, Peoples R China
[2] Beijing Univ Chem Technol, Coll Math & Phys, Beijing 100029, Peoples R China
[3] Univ Kansas, Dept Phys & Astron, Lawrence, KS 66045 USA
基金
中国国家自然科学基金; 美国国家科学基金会; 北京市自然科学基金; 国家重点研发计划;
关键词
INDIRECT INTERLAYER EXCITONS; FEW-LAYER; PHOTOCARRIER DYNAMICS; ENERGY-TRANSFER; MONO LAYER; MONOLAYER; PHOTOLUMINESCENCE; OPTOELECTRONICS;
D O I
10.1039/d0nr01924k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge-transfer excitons are formed by photoexcited electrons and holes following charge transfer across a heterojunction. They are important quasiparticles for optoelectronic applications of semiconducting heterostructures. The newly developed two-dimensional heterostructures provide a new platform to study these excitons. We report spatially and temporally resolved transient absorption measurements on the dynamics of charge-transfer excitons in a MoS2/WS2/MoSe2 trilayer heterostructure. We observed a non-classical lateral diffusion process of charge-transfer excitons with a decreasing diffusion coefficient. This feature suggests that hot charge-transfer excitons with large kinetic energies are formed and their cooling process persists for about 100 ps. The long energy relaxation time of excitons in the trilayer compared to its monolayer components is attributed to the reduced carrier and phonon scattering due to the dielectric screening effect in the trilayer. Our results help develop an in-depth understanding of the dynamics of charge-transfer excitons in two-dimensional heterostructures.
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页码:8485 / 8492
页数:8
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