Zhe Li
;
Xin-Yuan Zhang
;
Rundong Ma
;
Tong Fu
;
Yan Zeng
;
Chong Hu
;
Yufeng Cheng
;
Cheng Wang
;
Yun Wang
;
Yuhua Feng
;
Takashi Taniguchi
(National Institute for Materials Science
)
;
Kenji Watanabe
(National Institute for Materials Science
)
;
Ti Wang
;
Xiaoze Liu
;
Hongxing Xu
Description:
(abstract)Various exciton species in transition metal dichalcogenides (TMDs), such as neutral excitons, trions (charged excitons), dark excitons, and biexcitons, have been individually discovered with distinct light-matter interactions. In terms of valley-spin locked band structures and electron-hole configurations, these exciton species demonstrate flexible control of emission light with degrees of freedoms (DOFs) such as intensity, polarization, frequency and dynamics. However, it remains elusive to fully manipulate different exciton species on demand for practical applications. Here, we investigate the contrasting light-matter interactions to control multiple DOFs of emission light in a hybrid monolayer WSe2-Ag nanowire (NW) structure by taking advantages of various exciton species. These excitons, including trions, dark excitons and biexcitons, are found to couple independently with propagating surface plasmon polaritons (SPPs) of Ag NW in quite different ways, thanks to the orientations of transition dipoles. Consistent with the simulations, the dark excitons and dark trions show extremely high coupling efficiency with SPPs, while the trions demonstrate directional chiral-coupling features. This study presents a crucial step towards the ultimate goal of exploiting the comprehensive spectrum of TMD excitons for optical information processing and quantum optics.
Rights:
Keyword: Exciton species, light-matter interactions, surface plasmon polaritons
Date published: 2023-12-07
Publisher: Springer Science and Business Media LLC
Journal:
Funding:
Manuscript type: Publisher's version (Version of record)
MDR DOI:
First published URL: https://doi.org/10.1038/s41377-023-01338-5
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Updated at: 2025-02-14 16:30:22 +0900
Published on MDR: 2025-02-14 16:30:22 +0900
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