Temperature‐Dependent Optical and Polaritonic Properties of Excitons in hBN‐Encapsulated Monolayer TMDs

Abstract Monolayer transition metal dichalcogenides (TMDs) support robust excitons in the visible to near‐infrared spectral range. Their reduced dielectric screening results in large binding energies, and combined with a direct bandgap in monolayer form, these excitons dominate the optical response of TMDs. In this work, a comprehensive investigation of the temperature‐dependent optical and polaritonic properties of high‐quality WS 2 , MoS 2 , WSe 2 , and MoSe 2 monolayers, encapsulated by hBN, in the range of 5‐300 K, is presented. Using reflection spectroscopy measurements, the optical and polaritonic constituents of the TMD excitons in terms of oscillator strength, linewidth, and negative permittivity, are evaluated and compared. It is found that MoSe 2 exhibits the most pronounced optical and polaritonic response, stemming from its rapid linewidth narrowing at low temperatures, as compared to the other TMDs. In addition, It is found that all four TMDs exhibit a temperature‐dependent negative real part permittivity, thus supporting surface‐exciton‐polaritons. The dispersion relation, confinement factor, and losses are derived and similarly reveal that MoSe 2 exhibits enhanced polaritonic properties. These findings establish a comparative framework for understanding the optical and polaritonic properties of monolayer TMDs, with implications on their utilization in optoelectronic devices based on 2D semiconductors.

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Publication Details

Journal
Advanced Optical Materials
Published
2025-11-27
DOI
https://doi.org/10.1002/adom.202502535
Citations
1
Primary Topic
Strong Light-Matter Interactions
Type
article
Field-Weighted Citation Impact
1.25

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article

Temperature‐Dependent Optical and Polaritonic Properties of Excitons in hBN‐Encapsulated Monolayer TMDs

James H. Edgar, Sefaattin Tongay, Yonatan Gershuni, Itai Epstein et al.
1 citations
Advanced Optical Materials
Strong Light-Matter Interactions
1.25
article

Temperature‐Dependent Optical and Polaritonic Properties of Excitons in hBN‐Encapsulated Monolayer TMDs

James H. Edgar, Sefaattin Tongay, Yonatan Gershuni, Itai Epstein, Thomas Poirier, Anabel Atash Kahlon, Matan Meshulam
article en
1 citations

Abstract

Abstract Monolayer transition metal dichalcogenides (TMDs) support robust excitons in the visible to near‐infrared spectral range. Their reduced dielectric screening results in large binding energies, and combined with a direct bandgap in monolayer form, these excitons dominate the optical response of TMDs. In this work, a comprehensive investigation of the temperature‐dependent optical and polaritonic properties of high‐quality WS 2 , MoS 2 , WSe 2 , and MoSe 2 monolayers, encapsulated by hBN, in the range of 5‐300 K, is presented. Using reflection spectroscopy measurements, the optical and polaritonic constituents of the TMD excitons in terms of oscillator strength, linewidth, and negative permittivity, are evaluated and compared. It is found that MoSe 2 exhibits the most pronounced optical and polaritonic response, stemming from its rapid linewidth narrowing at low temperatures, as compared to the other TMDs. In addition, It is found that all four TMDs exhibit a temperature‐dependent negative real part permittivity, thus supporting surface‐exciton‐polaritons. The dispersion relation, confinement factor, and losses are derived and similarly reveal that MoSe 2 exhibits enhanced polaritonic properties. These findings establish a comparative framework for understanding the optical and polaritonic properties of monolayer TMDs, with implications on their utilization in optoelectronic devices based on 2D semiconductors.

Advanced Optical MaterialsVol. 14(7)
Tel Aviv University (IL), Kansas State University (US), Exact Sciences (United States) (US), Arizona State University (US)
National Science Foundation, U.S. Department of Energy, European Commission, Division of Chemical, Bioengineering, Environmental, and Transport Systems
Openalex Percentile: Top 15%
Strong Light-Matter Interactions
1.25
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