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Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy

[Image: see text] By implementing four-wave mixing (FWM) microspectroscopy, we measure coherence and population dynamics of the exciton transitions in monolayers of MoSe(2). We reveal their dephasing times T(2) and radiative lifetime T(1) in a subpicosecond (ps) range, approaching T(2) = 2T(1) and t...

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Autores principales: Jakubczyk, Tomasz, Delmonte, Valentin, Koperski, Maciej, Nogajewski, Karol, Faugeras, Clément, Langbein, Wolfgang, Potemski, Marek, Kasprzak, Jacek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518748/
https://www.ncbi.nlm.nih.gov/pubmed/27517124
http://dx.doi.org/10.1021/acs.nanolett.6b01060
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author Jakubczyk, Tomasz
Delmonte, Valentin
Koperski, Maciej
Nogajewski, Karol
Faugeras, Clément
Langbein, Wolfgang
Potemski, Marek
Kasprzak, Jacek
author_facet Jakubczyk, Tomasz
Delmonte, Valentin
Koperski, Maciej
Nogajewski, Karol
Faugeras, Clément
Langbein, Wolfgang
Potemski, Marek
Kasprzak, Jacek
author_sort Jakubczyk, Tomasz
collection PubMed
description [Image: see text] By implementing four-wave mixing (FWM) microspectroscopy, we measure coherence and population dynamics of the exciton transitions in monolayers of MoSe(2). We reveal their dephasing times T(2) and radiative lifetime T(1) in a subpicosecond (ps) range, approaching T(2) = 2T(1) and thus indicating radiatively limited dephasing at a temperature of 6 K. We elucidate the dephasing mechanisms by varying the temperature and by probing various locations on the flake exhibiting a different local disorder. At the nanosecond range, we observe the residual FWM produced by the incoherent excitons, which initially disperse toward the dark states but then relax back to the optically active states within the light cone. By introducing polarization-resolved excitation, we infer intervalley exciton dynamics, revealing an initial polarization degree of around 30%, constant during the initial subpicosecond decay, followed by the depolarization on a picosecond time scale. The FWM hyperspectral imaging reveals the doped and undoped areas of the sample, allowing us to investigate the neutral exciton, the charged one, or both transitions at the same time. In the latter, we observe the exciton–trion beating in the coherence evolution indicating their coherent coupling.
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spelling pubmed-55187482017-08-12 Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy Jakubczyk, Tomasz Delmonte, Valentin Koperski, Maciej Nogajewski, Karol Faugeras, Clément Langbein, Wolfgang Potemski, Marek Kasprzak, Jacek Nano Lett [Image: see text] By implementing four-wave mixing (FWM) microspectroscopy, we measure coherence and population dynamics of the exciton transitions in monolayers of MoSe(2). We reveal their dephasing times T(2) and radiative lifetime T(1) in a subpicosecond (ps) range, approaching T(2) = 2T(1) and thus indicating radiatively limited dephasing at a temperature of 6 K. We elucidate the dephasing mechanisms by varying the temperature and by probing various locations on the flake exhibiting a different local disorder. At the nanosecond range, we observe the residual FWM produced by the incoherent excitons, which initially disperse toward the dark states but then relax back to the optically active states within the light cone. By introducing polarization-resolved excitation, we infer intervalley exciton dynamics, revealing an initial polarization degree of around 30%, constant during the initial subpicosecond decay, followed by the depolarization on a picosecond time scale. The FWM hyperspectral imaging reveals the doped and undoped areas of the sample, allowing us to investigate the neutral exciton, the charged one, or both transitions at the same time. In the latter, we observe the exciton–trion beating in the coherence evolution indicating their coherent coupling. American Chemical Society 2016-08-12 2016-09-14 /pmc/articles/PMC5518748/ /pubmed/27517124 http://dx.doi.org/10.1021/acs.nanolett.6b01060 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Jakubczyk, Tomasz
Delmonte, Valentin
Koperski, Maciej
Nogajewski, Karol
Faugeras, Clément
Langbein, Wolfgang
Potemski, Marek
Kasprzak, Jacek
Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy
title Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy
title_full Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy
title_fullStr Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy
title_full_unstemmed Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy
title_short Radiatively Limited Dephasing and Exciton Dynamics in MoSe(2) Monolayers Revealed with Four-Wave Mixing Microscopy
title_sort radiatively limited dephasing and exciton dynamics in mose(2) monolayers revealed with four-wave mixing microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5518748/
https://www.ncbi.nlm.nih.gov/pubmed/27517124
http://dx.doi.org/10.1021/acs.nanolett.6b01060
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