Time-domain observation of interlayer exciton formation and thermalization in a MoSe2/WSe2 heterostructure

被引:18
|
作者
Policht V.R. [1 ,6 ]
Mittenzwey H. [2 ]
Dogadov O. [1 ]
Katzer M. [2 ]
Villa A. [1 ]
Li Q. [3 ]
Kaiser B. [4 ]
Ross A.M. [1 ]
Scotognella F. [1 ,7 ]
Zhu X. [3 ]
Knorr A. [2 ]
Selig M. [2 ]
Cerullo G. [1 ,5 ]
Dal Conte S. [1 ]
机构
[1] Department of Physics, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano
[2] Institut für Theoretische Physik, Nichtlineare Optik und Quantenelektronik, Technische Universität Berlin, Hardenbergstraße 36, Berlin
[3] Department of Chemistry, Columbia University, 3000 Broadway, New York, 10027, NY
[4] Zuse-Institut Berlin, Takustraße 7, Berlin
[5] CNR-IFN, Piazza Leonardo da Vinci 32, Milano
[6] NRC Postdoc residing at U.S. Naval Research Laboratory, 4555 Overlook Avenue SW, Washington, 20375, DC
[7] Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino
基金
欧盟地平线“2020”; 欧洲研究理事会; 美国国家科学基金会;
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D O I
10.1038/s41467-023-42915-x
中图分类号
学科分类号
摘要
Vertical heterostructures of transition metal dichalcogenides (TMDs) host interlayer excitons with electrons and holes residing in different layers. With respect to their intralayer counterparts, interlayer excitons feature longer lifetimes and diffusion lengths, paving the way for room temperature excitonic optoelectronic devices. The interlayer exciton formation process and its underlying physical mechanisms are largely unexplored. Here we use ultrafast transient absorption spectroscopy with a broadband white-light probe to simultaneously resolve interlayer charge transfer and interlayer exciton formation dynamics in a MoSe2/WSe2 heterostructure. We observe an interlayer exciton formation timescale nearly an order of magnitude (~1 ps) longer than the interlayer charge transfer time (~100 fs). Microscopic calculations attribute this relative delay to an interplay of a phonon-assisted interlayer exciton cascade and thermalization, and excitonic wave-function overlap. Our results may explain the efficient photocurrent generation observed in optoelectronic devices based on TMD heterostructures, as the interlayer excitons are able to dissociate during thermalization. © 2023, The Author(s).
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