Raman scattering excitation in monolayers of semiconducting transition metal dichalcogenides

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Hauptverfasser: Zinkiewicz, M., Grzeszczyk, M., Kazimierczuk, T., Bartos, M., Nogajewski, K., Pacuski, W., Watanabe, K., Taniguchi, T., Wysmołek, A., Kossacki, P., Potemski, M., Babiński, A., Molas, M. R.
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Veröffentlicht: 2023
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author Zinkiewicz, M.
Grzeszczyk, M.
Kazimierczuk, T.
Bartos, M.
Nogajewski, K.
Pacuski, W.
Watanabe, K.
Taniguchi, T.
Wysmołek, A.
Kossacki, P.
Potemski, M.
Babiński, A.
Molas, M. R.
author_facet Zinkiewicz, M.
Grzeszczyk, M.
Kazimierczuk, T.
Bartos, M.
Nogajewski, K.
Pacuski, W.
Watanabe, K.
Taniguchi, T.
Wysmołek, A.
Kossacki, P.
Potemski, M.
Babiński, A.
Molas, M. R.
contents Raman scattering excitation (RSE) is an experimental technique in which the spectrum is made up by sweeping the excitation energy when the detection energy is fixed. We study the low-temperature ($T$=5~K) RSE spectra measured on four high quality monolayers (ML) of semiconducting transition metal dichalcogenides (S-TMDs), $i.e.$ MoS$_2$, MoSe$_2$, WS$_2$, and WSe$_2$, encapsulated in hexagonal BN. The outgoing resonant conditions of Raman scattering reveal an extraordinary intensity enhancement of the phonon modes, which results in extremely rich RSE spectra. The obtained spectra are composed not only of Raman-active peaks, $i.e.$ in-plane E$'$ and out-of-plane A$'_1$, but the appearance of 1$^{st}$, 2$^{nd}$, and higher-order phonon modes is recognised. The intensity profiles of the A$'_1$ modes in the investigated MLs resemble the emissions due to neutral excitons measured in the corresponding PL spectra for the outgoing type of resonant Raman scattering conditions. Furthermore, for the WSe$_2$ ML, the A$'_1$ mode was observed when the incoming light was in resonance with the neutral exciton line. The strength of the exciton-phonon coupling (EPC) in S-TMD MLs strongly depends on the type of their ground excitonic state, $i.e.$ bright or dark, resulting in different shapes of the RSE spectra. Our results demonstrate that RSE spectroscopy is a powerful technique for studying EPC in S-TMD MLs.
format Preprint
id arxiv_https___arxiv_org_abs_2308_08320
institution arXiv
publishDate 2023
record_format arxiv
spellingShingle Raman scattering excitation in monolayers of semiconducting transition metal dichalcogenides
Zinkiewicz, M.
Grzeszczyk, M.
Kazimierczuk, T.
Bartos, M.
Nogajewski, K.
Pacuski, W.
Watanabe, K.
Taniguchi, T.
Wysmołek, A.
Kossacki, P.
Potemski, M.
Babiński, A.
Molas, M. R.
Mesoscale and Nanoscale Physics
Materials Science
Raman scattering excitation (RSE) is an experimental technique in which the spectrum is made up by sweeping the excitation energy when the detection energy is fixed. We study the low-temperature ($T$=5~K) RSE spectra measured on four high quality monolayers (ML) of semiconducting transition metal dichalcogenides (S-TMDs), $i.e.$ MoS$_2$, MoSe$_2$, WS$_2$, and WSe$_2$, encapsulated in hexagonal BN. The outgoing resonant conditions of Raman scattering reveal an extraordinary intensity enhancement of the phonon modes, which results in extremely rich RSE spectra. The obtained spectra are composed not only of Raman-active peaks, $i.e.$ in-plane E$'$ and out-of-plane A$'_1$, but the appearance of 1$^{st}$, 2$^{nd}$, and higher-order phonon modes is recognised. The intensity profiles of the A$'_1$ modes in the investigated MLs resemble the emissions due to neutral excitons measured in the corresponding PL spectra for the outgoing type of resonant Raman scattering conditions. Furthermore, for the WSe$_2$ ML, the A$'_1$ mode was observed when the incoming light was in resonance with the neutral exciton line. The strength of the exciton-phonon coupling (EPC) in S-TMD MLs strongly depends on the type of their ground excitonic state, $i.e.$ bright or dark, resulting in different shapes of the RSE spectra. Our results demonstrate that RSE spectroscopy is a powerful technique for studying EPC in S-TMD MLs.
title Raman scattering excitation in monolayers of semiconducting transition metal dichalcogenides
topic Mesoscale and Nanoscale Physics
Materials Science
url https://arxiv.org/abs/2308.08320