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Ultrastrong Coupling of a Single Molecule to a Plasmonic Nanocavity: A First-Principles Study
[Image: see text] Ultrastrong coupling (USC) is a distinct regime of light-matter interaction in which the coupling strength is comparable to the resonance energy of the cavity or emitter. In the USC regime, common approximations to quantum optical Hamiltonians, such as the rotating wave approximati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931765/ https://www.ncbi.nlm.nih.gov/pubmed/35308405 http://dx.doi.org/10.1021/acsphotonics.2c00066 |
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author | Kuisma, Mikael Rousseaux, Benjamin Czajkowski, Krzysztof M. Rossi, Tuomas P. Shegai, Timur Erhart, Paul Antosiewicz, Tomasz J. |
author_facet | Kuisma, Mikael Rousseaux, Benjamin Czajkowski, Krzysztof M. Rossi, Tuomas P. Shegai, Timur Erhart, Paul Antosiewicz, Tomasz J. |
author_sort | Kuisma, Mikael |
collection | PubMed |
description | [Image: see text] Ultrastrong coupling (USC) is a distinct regime of light-matter interaction in which the coupling strength is comparable to the resonance energy of the cavity or emitter. In the USC regime, common approximations to quantum optical Hamiltonians, such as the rotating wave approximation, break down as the ground state of the coupled system gains photonic character due to admixing of vacuum states with higher excited states, leading to ground-state energy changes. USC is usually achieved by collective coherent coupling of many quantum emitters to a single mode cavity, whereas USC with a single molecule remains challenging. Here, we show by time-dependent density functional theory (TDDFT) calculations that a single organic molecule can reach USC with a plasmonic dimer, consisting of a few hundred atoms. In this context, we discuss the capacity of TDDFT to represent strong coupling and its connection to the quantum optical Hamiltonian. We find that USC leads to appreciable ground-state energy modifications accounting for a non-negligible part of the total interaction energy, comparable to k(B)T at room temperature. |
format | Online Article Text |
id | pubmed-8931765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89317652022-03-18 Ultrastrong Coupling of a Single Molecule to a Plasmonic Nanocavity: A First-Principles Study Kuisma, Mikael Rousseaux, Benjamin Czajkowski, Krzysztof M. Rossi, Tuomas P. Shegai, Timur Erhart, Paul Antosiewicz, Tomasz J. ACS Photonics [Image: see text] Ultrastrong coupling (USC) is a distinct regime of light-matter interaction in which the coupling strength is comparable to the resonance energy of the cavity or emitter. In the USC regime, common approximations to quantum optical Hamiltonians, such as the rotating wave approximation, break down as the ground state of the coupled system gains photonic character due to admixing of vacuum states with higher excited states, leading to ground-state energy changes. USC is usually achieved by collective coherent coupling of many quantum emitters to a single mode cavity, whereas USC with a single molecule remains challenging. Here, we show by time-dependent density functional theory (TDDFT) calculations that a single organic molecule can reach USC with a plasmonic dimer, consisting of a few hundred atoms. In this context, we discuss the capacity of TDDFT to represent strong coupling and its connection to the quantum optical Hamiltonian. We find that USC leads to appreciable ground-state energy modifications accounting for a non-negligible part of the total interaction energy, comparable to k(B)T at room temperature. American Chemical Society 2022-03-02 2022-03-16 /pmc/articles/PMC8931765/ /pubmed/35308405 http://dx.doi.org/10.1021/acsphotonics.2c00066 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Kuisma, Mikael Rousseaux, Benjamin Czajkowski, Krzysztof M. Rossi, Tuomas P. Shegai, Timur Erhart, Paul Antosiewicz, Tomasz J. Ultrastrong Coupling of a Single Molecule to a Plasmonic Nanocavity: A First-Principles Study |
title | Ultrastrong Coupling of a Single Molecule to a Plasmonic
Nanocavity: A First-Principles Study |
title_full | Ultrastrong Coupling of a Single Molecule to a Plasmonic
Nanocavity: A First-Principles Study |
title_fullStr | Ultrastrong Coupling of a Single Molecule to a Plasmonic
Nanocavity: A First-Principles Study |
title_full_unstemmed | Ultrastrong Coupling of a Single Molecule to a Plasmonic
Nanocavity: A First-Principles Study |
title_short | Ultrastrong Coupling of a Single Molecule to a Plasmonic
Nanocavity: A First-Principles Study |
title_sort | ultrastrong coupling of a single molecule to a plasmonic
nanocavity: a first-principles study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931765/ https://www.ncbi.nlm.nih.gov/pubmed/35308405 http://dx.doi.org/10.1021/acsphotonics.2c00066 |
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