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Published December 2022 | Published
Journal Article Open

First-principles ultrafast exciton dynamics and time-domain spectroscopies: Dark-exciton mediated valley depolarization in monolayer WSe₂

Abstract

Calculations combining first-principles electron-phonon (e-ph) interactions with the Boltzmann equation enable studies of ultrafast carrier and phonon dynamics. However, in materials with weak Coulomb screening, electrons and holes form bound excitons so their scattering processes become correlated, posing additional challenges for modeling nonequilibrium physics. Here we show calculations of ultrafast exciton dynamics and related time-domain spectroscopies using ab initio exciton-phonon (ex-ph) interactions together with an excitonic Boltzmann equation. Starting from the nonequilibrium exciton populations, we develop simulations of time-domain absorption and photoemission spectra that take into account electron-hole correlations. We use this method to study monolayer WSe₂, where our calculations predict subpicosecond timescales for exciton relaxation and valley depolarization and reveal the key role of intermediate dark excitons. The approach introduced in this paper enables a quantitative description of nonequilibrium dynamics and ultrafast spectroscopies in materials with strongly bound excitons.

Additional Information

Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI. The authors thank Ivan Maliyov and Jinsoo Park for fruitful discussions. This material is based upon work supported by the U.S. Department of Energy, Office of Science, Office of Advanced Scientific Computing Research and Office of Basic Energy Sciences, Scientific Discovery through Advanced Computing (SciDAC) program under Award No. DESC0022088, which supported method development. M.B. was partially supported by the Liquid Sunlight Alliance, which is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Award No. DE-SC0021266. Code development was partially funded by the National Science Foundation under Grant No. OAC-2209262. H.-Y. Chen was partially supported by the J. Yang Fellowship. D.S. acknowledges funding from Italian MIUR, PRIN BIOX Grant No. 20173B72NB, and from the EU MaX project Materials design at the eXascale H2020-INFRAEDI-2018-2020, Grant Agreement No. 824143. This research used resources of the National Energy Research Scientific Computing Center (NERSC), a U.S. Department of Energy Office of Science User Facility located at Lawrence Berkeley National Laboratory, operated under Contract No. DE-AC02-05CH11231.

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Additional details

Created:
August 22, 2023
Modified:
October 23, 2023