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Nano Research 2020, 13(5): 1399-1405 https://doi.org/10.1007/s12274-020-2652-9
Research Article | Issue | Published: 10 February 2020

Dynamics of exciton energy renormalization in monolayer transition metal disulfides

Show Author's Information Jiaxin Zhao1,§,  Weijie Zhao1,§,  Wei Du1,  Rui Su1,  Qihua Xiong1,2( )
Division of Physics and Applied Physics, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore
State Key Laboratory of Low-Dimensional Quantum Physics and Department of Physics, Tsinghua University, Beijing 100084, China

§Jiaxin Zhao and Weijie Zhao contributed equally to this work.

Keywords:
transient absorption spectroscopy, exciton dynamics, transitional metal disulfide, renormalization, carrier screening effect, exciton-exciton interactions
Topics:
Absorption spectroscopyDynamics MonolayersOptical latticesSulfur compoundsTemperatureTransition metalsTungsten compounds
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Zhao J, Zhao W, Du W, et al. Dynamics of exciton energy renormalization in monolayer transition metal disulfides. Nano Research, 2020, 13(5): 1399-1405. https://doi.org/10.1007/s12274-020-2652-9
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Abstract Full text Electronic supplementary material About this article

Fundamental understandings on the dynamics of charge carriers and excitonic quasiparticles in semiconductors are of central importance for both many-body physics and promising optoelectronic and photonic applications. Here, we investigated the carrier dynamics and many-body interactions in two-dimensional (2D) transition metal dichalcogenides (TMDs), using monolayer WS2 as an example, by employing femtosecond broadband pump-probe spectroscopy. Three time regimes for the exciton energy renormalization are unambiguously revealed with a distinct red-blue-red shift upon above-bandgap optical excitations. We attribute the dominant physical process in the three typical regimes to free carrier screening effect, Coulombic exciton-exciton interactions and Auger photocarrier generation, respectively, which show distinct dependence on the optical excitation wavelength, pump fluences and/or lattice temperature. An intrinsic exciton radiative lifetime of about 1.2 picoseconds (ps) in monolayer WS2 is unraveled at low temperature, and surprisingly the efficient Auger nonradiative decay of both bright and dark excitons puts the system in a nonequilibrium state at the nanosecond timescale. In addition, the dynamics of trions at low temperature is observed to be significantly different from that of excitons, e.g., a long radiative lifetime of ~ 108.7 ps at low excitation densities and the evolution of trion energy as a function of delay times. Our findings elucidate the dynamics of excitonic quasiparticles and the intricate many-body physics in 2D semiconductors, underpinning the future development of photonics, valleytronics and optoelectronics based on 2D semiconductors.


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About this article

Dynamics of exciton energy renormalization in monolayer transition metal disulfides

Show Author's information Jiaxin Zhao1,§, Weijie Zhao1,§, Wei Du1, Rui Su1, Qihua Xiong1,2( )
Division of Physics and Applied Physics, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore
State Key Laboratory of Low-Dimensional Quantum Physics and Department of Physics, Tsinghua University, Beijing 100084, China

§Jiaxin Zhao and Weijie Zhao contributed equally to this work.

Abstract

Fundamental understandings on the dynamics of charge carriers and excitonic quasiparticles in semiconductors are of central importance for both many-body physics and promising optoelectronic and photonic applications. Here, we investigated the carrier dynamics and many-body interactions in two-dimensional (2D) transition metal dichalcogenides (TMDs), using monolayer WS2 as an example, by employing femtosecond broadband pump-probe spectroscopy. Three time regimes for the exciton energy renormalization are unambiguously revealed with a distinct red-blue-red shift upon above-bandgap optical excitations. We attribute the dominant physical process in the three typical regimes to free carrier screening effect, Coulombic exciton-exciton interactions and Auger photocarrier generation, respectively, which show distinct dependence on the optical excitation wavelength, pump fluences and/or lattice temperature. An intrinsic exciton radiative lifetime of about 1.2 picoseconds (ps) in monolayer WS2 is unraveled at low temperature, and surprisingly the efficient Auger nonradiative decay of both bright and dark excitons puts the system in a nonequilibrium state at the nanosecond timescale. In addition, the dynamics of trions at low temperature is observed to be significantly different from that of excitons, e.g., a long radiative lifetime of ~ 108.7 ps at low excitation densities and the evolution of trion energy as a function of delay times. Our findings elucidate the dynamics of excitonic quasiparticles and the intricate many-body physics in 2D semiconductors, underpinning the future development of photonics, valleytronics and optoelectronics based on 2D semiconductors.

Keywords: transient absorption spectroscopy, exciton dynamics, transitional metal disulfide, renormalization, carrier screening effect, exciton-exciton interactions

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Acknowledgements

Publication history

Received: 30 September 2019
Revised: 30 December 2019
Accepted: 10 January 2020
Published: 10 February 2020
Issue date: May 2020

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2020

Acknowledgements

Q. H. X. gratefully acknowledges the support from Singapore Ministry of Education via AcRF Tier 3 Programme (No. MOE2018-T3-1-002) and Tier 2 project (No. MOE2017-T2-1-040), and Singapore National Research Foundation via NRF-ANR project (No. NRF2017-NRF-ANR005 2D-Chiral).

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