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  Chirality-Dependent Dynamic Evolution for Trions in Monolayer WS2

Xiang, B., Wang, R., Chen, Y., Wang, Y., Qin, T., Zhang, M., et al. (2024). Chirality-Dependent Dynamic Evolution for Trions in Monolayer WS2. Nano Letters, 24(22), 6592-6600. doi:10.1021/acs.nanolett.4c01082.

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xiang-et-al-2024-chirality-dependent-dynamic-evolution-for-trions-in-monolayer-ws2.pdf (Publisher version), 2MB
 
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Supporting Information: Sample preparation, helicity-resolved setup, linear-response regime analysis, time traces of A-exciton induced by different energy excitation at room temperature, population recombination dynamics of monolayer WS2, Raman and PL spectra of monolayer WS2 at different temperatures, transient differential transmission spectra of monolayer WS2, normalized time traces of trions/excitons at different temperatures in the SCP and OCP configurations, and theoretical calculation
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 Creators:
Xiang, B.1, 2, Author
Wang, R.1, Author
Chen, Y.2, Author
Wang, Y.1, 2, Author
Qin, T.2, Author
Zhang, M.2, Author
Watanabe, K.3, Author
Taniguchi, T.4, Author
Duan, W.5, 6, Author
Tang, P.7, 8, 9, Author           
Liu, H.10, Author
Xiong, Qihua1, 6, 10, 11, Author
Affiliations:
1State Key Laboratory of Low-Dimensional Quantum Physics and Department of Physics, Tsinghua University, ou_persistent22              
2Beijing Academy of Quantum Information Sciences, ou_persistent22              
3Research Center for Electronic and Optical Materials, National Institute for Materials Science, Tsukuba, ou_persistent22              
4Research Center for Materials Nanoarchitectonics, National Institute for Materials Science, Tsukuba, ou_persistent22              
5State Key Laboratory of Low-Dimensional Quantum Physics and Department of Physics and Institute for Advanced Study, Tsinghua University, ou_persistent22              
6Frontier Science Center for Quantum Information, ou_persistent22              
7School of Materials Science and Engineering, Beihang University, ou_persistent22              
8Theory Group, Theory Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society, ou_2266715              
9Center for Free-Electron Laser Science, ou_persistent22              
10Beijing Academy of Quantum Information Science, ou_persistent22              
11Collaborative Innovation Center of Quantum Matter, Beijing, ou_persistent22              

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Free keywords: chirality, transient transmission spectroscopy, trion dynamics, transition metal dichalcogenides, many-body interaction
 Abstract: Monolayer transition metal dichalcogenides exhibit valley-dependent excitonic characters with a large binding energy, acting as the building block for future optoelectronic functionalities. Herein, combined with pump–probe ultrafast transient transmission spectroscopy and theoretical simulations, we reveal the chirality-dependent trion dynamics in h-BN encapsulated monolayer tungsten disulfide. By resonantly pumping trions in a single valley and monitoring their temporal evolution, we identify the temperature-dependent competition between two relaxation channels driven by chirality-dependent scattering processes. At room temperature, the phonon-assisted upconversion process predominates, converting excited trions to excitons within the same valley on a sub-picosecond (ps) time scale. As temperature decreases, this process becomes less efficient, while alternative channels, notably valley depolarization process for trions, assume importance, leading to an increase of trion density in the unpumped valley within a ps time scale. Our time-resolved valley-contrast results provide a comprehensive insight into trion dynamics in 2D materials, thereby advancing the development of novel valleytronic devices.

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Language(s): eng - English
 Dates: 2024-05-172024-03-072024-05-172024-05-242024-06-05
 Publication Status: Issued
 Pages: 9
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/acs.nanolett.4c01082
 Degree: -

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Project name : Q.X. gratefully acknowledges strong funding support by the National Key Research and Development Program of China (grant no. 2022YFA1204700), National Natural Science Foundation of China (grant nos. 12020101003 and 12250710126), funding support from the State Key Laboratory of Low-Dimensional Quantum Physics of Tsinghua University, and the Tsinghua University Initiative Scientific Research Program. P.T. was supported by the National Natural Science Foundation of China (grant nos. 12234011 and 12374053). H.L. acknowledges support from the National Natural Science Foundation of China (grant no. 92056204). W.D. acknowledges the support of the Basic Science Center Project of NSFC (grant no. 52388201), Innovation Program for Quantum Science and Technology (grant no. 2023ZD0300500), and the Beijing Advanced Innovation Center for Future Chip (ICFC). K.W. and T.T. acknowledge support from the JSPS KAKENHI (Grant Numbers 20H00354 and 23H02052) and World Premier International Research Center Initiative (WPI), MEXT, Japan.
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Source 1

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Title: Nano Letters
  Abbreviation : Nano Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 24 (22) Sequence Number: - Start / End Page: 6592 - 6600 Identifier: ISSN: 1530-6984
CoNE: https://pure.mpg.de/cone/journals/resource/110978984570403