Breakdown of the static dielectric screening approximation of Coulomb interactions in atomically thin semiconductors

Fuente: arXiv
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Auteurs principaux: Mhenni, Amine Ben, Van Tuan, Dinh, Geilen, Leonard, Petrić, Marko M., Erdi, Melike, Watanabe, Kenji, Taniguchi, Takashi, Tongay, Sefaattin, Müller, Kai, Wilson, Nathan P., Finley, Jonathan J., Dery, Hanan, Barbone, Matteo
Format: Preprint
Publié: 2024
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author Mhenni, Amine Ben
Van Tuan, Dinh
Geilen, Leonard
Petrić, Marko M.
Erdi, Melike
Watanabe, Kenji
Taniguchi, Takashi
Tongay, Sefaattin
Müller, Kai
Wilson, Nathan P.
Finley, Jonathan J.
Dery, Hanan
Barbone, Matteo
author_facet Mhenni, Amine Ben
Van Tuan, Dinh
Geilen, Leonard
Petrić, Marko M.
Erdi, Melike
Watanabe, Kenji
Taniguchi, Takashi
Tongay, Sefaattin
Müller, Kai
Wilson, Nathan P.
Finley, Jonathan J.
Dery, Hanan
Barbone, Matteo
contents Coulomb interactions in atomically thin materials are uniquely sensitive to variations in the dielectric screening of the environment, which can be used to control quasiparticles and exotic quantum many-body phases. A static approximation of the dielectric response, where increased dielectric screening is predicted to cause an energy redshift of the exciton resonance, has been until now sufficient. Here, we use charge-tunable exciton resonances to study screening effects in transition metal dichalcogenide monolayers embedded in materials with dielectric constants ranging from 4 to more than 1000. In contrast to expectations, we observe a blueshift of the exciton resonance exceeding 30 meV for larger dielectric constant environments. By employing a dynamical screening model, we find that while the exciton binding energy remains mostly controlled by the static dielectric response, the exciton self-energy is dominated by the high-frequency response. Dielectrics with markedly different static and high-frequency screening enable the selective addressing of distinct many-body effects in layered materials and their heterostructures, expanding the tunability range and offering new routes to detect and control correlated quantum many-body states and to design optoelectronic and quantum devices.
format Preprint
id arxiv_https___arxiv_org_abs_2402_18639
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Breakdown of the static dielectric screening approximation of Coulomb interactions in atomically thin semiconductors
Mhenni, Amine Ben
Van Tuan, Dinh
Geilen, Leonard
Petrić, Marko M.
Erdi, Melike
Watanabe, Kenji
Taniguchi, Takashi
Tongay, Sefaattin
Müller, Kai
Wilson, Nathan P.
Finley, Jonathan J.
Dery, Hanan
Barbone, Matteo
Mesoscale and Nanoscale Physics
Materials Science
Coulomb interactions in atomically thin materials are uniquely sensitive to variations in the dielectric screening of the environment, which can be used to control quasiparticles and exotic quantum many-body phases. A static approximation of the dielectric response, where increased dielectric screening is predicted to cause an energy redshift of the exciton resonance, has been until now sufficient. Here, we use charge-tunable exciton resonances to study screening effects in transition metal dichalcogenide monolayers embedded in materials with dielectric constants ranging from 4 to more than 1000. In contrast to expectations, we observe a blueshift of the exciton resonance exceeding 30 meV for larger dielectric constant environments. By employing a dynamical screening model, we find that while the exciton binding energy remains mostly controlled by the static dielectric response, the exciton self-energy is dominated by the high-frequency response. Dielectrics with markedly different static and high-frequency screening enable the selective addressing of distinct many-body effects in layered materials and their heterostructures, expanding the tunability range and offering new routes to detect and control correlated quantum many-body states and to design optoelectronic and quantum devices.
title Breakdown of the static dielectric screening approximation of Coulomb interactions in atomically thin semiconductors
topic Mesoscale and Nanoscale Physics
Materials Science
url https://arxiv.org/abs/2402.18639