Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuisma, Mikael, Rousseaux, Benjamin, Czajkowski, Krzysztof M., Rossi, Tuomas P., Shegai, Timur, Erhart, Paul, Antosiewicz, Tomasz J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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
_version_ 1784671330397847552
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
work_keys_str_mv AT kuismamikael ultrastrongcouplingofasinglemoleculetoaplasmonicnanocavityafirstprinciplesstudy
AT rousseauxbenjamin ultrastrongcouplingofasinglemoleculetoaplasmonicnanocavityafirstprinciplesstudy
AT czajkowskikrzysztofm ultrastrongcouplingofasinglemoleculetoaplasmonicnanocavityafirstprinciplesstudy
AT rossituomasp ultrastrongcouplingofasinglemoleculetoaplasmonicnanocavityafirstprinciplesstudy
AT shegaitimur ultrastrongcouplingofasinglemoleculetoaplasmonicnanocavityafirstprinciplesstudy
AT erhartpaul ultrastrongcouplingofasinglemoleculetoaplasmonicnanocavityafirstprinciplesstudy
AT antosiewicztomaszj ultrastrongcouplingofasinglemoleculetoaplasmonicnanocavityafirstprinciplesstudy