Joseph Wragg
;
Luca Bolzonello
;
Ludovica Donati
;
Karuppasamy Pandian Soundarapandian
;
Riccardo Bertini
;
Seth Ariel Tongay
;
Kenji Watanabe
(National Institute for Materials Science)
;
Takashi Taniguchi
(National Institute for Materials Science)
;
Frank H. L. Koppens
;
Niek F. van Hulst
Description:
(abstract)While it’s long been accepted that the role of momentum dark excitons in the photoresponse of transition metal dichalcogenides (TMD’s) is critical, their weak optical signature has made any observation confined to cryogenic conditions. Here we surpass this limit, and expose the room temperature contributions of both bright and dark excitons to the behaviour of a TMD, WSe2, from monolayer to multilayer to bulk. To do so, we present dual action spectroscopy, a photocurrent and luminescence detected Fourier-transform excitation spectroscopy scheme to microscopically map the energy landscape of WSe2. While bright excitons naturally dominate the luminescence response of the material, dark excitons dominate the current response. Notably, the dark KK' exciton is more accessible than the ground state KΛ, while the current maps reveal a disparity in the diffusivity of the two states. This work provides the basis for a new current-detected approach to study the dynamics of dark exciton states across different materials.
Rights:
Keyword: dual action spectroscopy , bright and dark excitons , WSe2
Date published: 2025-05-14
Publisher: American Chemical Society (ACS)
Journal:
Funding:
Manuscript type: Publisher's version (Version of record)
MDR DOI:
First published URL: https://doi.org/10.1021/acs.nanolett.4c06349
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Updated at: 2026-02-17 08:30:29 +0900
Published on MDR: 2026-02-16 18:00:51 +0900
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