Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/66025

TítuloNear-unity light absorption in a monolayer WS2 van der Waals heterostructure cavity
Autor(es)Epstein, Itai
Terrés, Bernat
Chaves, André J.
Pusapati, Varun-Varma
Rhodes, Daniel A.
Frank, Bettina
Zimmermann, Valentin
Qin, Ying
Watanabe, Kenji
Taniguchi, Takashi
Giessen, Harald
Tongay, Sefaattin
Hone, James C.
Peres, N. M. R.
Koppens, Frank
Palavras-chaveTMD Excitons
Unity absorption
2D materials
Light-matter interaction
Exciton complexes
Data2020
EditoraAmerican Chemical Society
RevistaNano Letters
Resumo(s)Excitons in monolayer transition-metal-dichalcogenides (TMDs) dominate their optical response and exhibit strong light-matter interactions with lifetime-limited emission. While various approaches have been applied to enhance light-exciton interactions in TMDs, the achieved strength have been far below unity, and a complete picture of its underlying physical mechanisms and fundamental limits has not been provided. Here, we introduce a TMD-based van der Waals heterostructure cavity that provides near-unity excitonic absorption, and emission of excitonic complexes that are observed at ultralow excitation powers. Our results are in full agreement with a quantum theoretical framework introduced to describe the light-exciton-cavity interaction. We find that the subtle interplay between the radiative, nonradiative and dephasing decay rates plays a crucial role, and unveil a universal absorption law for excitons in 2D systems. This enhanced light-exciton interaction provides a platform for studying excitonic phase-transitions and quantum nonlinearities and enables new possibilities for 2D semiconductor-based optoelectronic devices.
TipoArtigo
URIhttps://hdl.handle.net/1822/66025
DOI10.1021/acs.nanolett.0c00492
ISSN1530-6984
e-ISSN1530-6992
Versão da editorahttps://pubs.acs.org/doi/10.1021/acs.nanolett.0c00492
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:PHYSICS OF QUANTUM MATERIALS AND BIONANOSTRUCTURES (2018 - ...)

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