| Literature DB >> 33591207 |
Zilong Wang1, Patrick Altmann1, Christoph Gadermaier1,2, Yating Yang3, Wei Li4, Lavinia Ghirardini1, Chiara Trovatello1, Marco Finazzi1, Lamberto Duò1, Michele Celebrano1, Run Long3, Deji Akinwande4, Oleg V Prezhdo5,6, Giulio Cerullo1,5, Stefano Dal Conte1.
Abstract
Monolayer transition metal dichalcogenides bear great potential for photodetection and light harvesting due to high absorption coefficients. However, these applications require dissociation of strongly bound photogenerated excitons. The dissociation can be achieved by vertically stacking different monolayers to realize band alignment that favors interlayer charge transfer. In such heterostructures, the reported recombination times vary strongly, and the charge separation and recombination mechanisms remain elusive. We use two color pump-probe microscopy to demonstrate that the charge separation in a MoSe2/WSe2 heterostructure is ultrafast (∼200 fs) and virtually temperature independent, whereas the recombination accelerates strongly with temperature. Ab initio quantum dynamics simulations rationalize the experiments, indicating that the charge separation is temperature-independent because it is barrierless, involves dense acceptor states, and is promoted by higher-frequency out-of-plane vibrations. The strong temperature dependence of the recombination, on the other hand, arises from a transient indirect-to-direct bandgap modulation by low-frequency shear and layer breathing motions.Entities:
Keywords: 2D Heterostructure; TDDFT; charge transfer; femtosecond pump−probe spectroscopy; transition metal dichalcogenides
Year: 2021 PMID: 33591207 DOI: 10.1021/acs.nanolett.0c04955
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189