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Theoretical Advances in Polariton Chemistry and Molecular Cavity Quantum Electrodynamics
[Image: see text] When molecules are coupled to an optical cavity, new light–matter hybrid states, so-called polaritons, are formed due to quantum light–matter interactions. With the experimental demonstrations of modifying chemical reactivities by forming polaritons under strong light–matter intera...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450711/ https://www.ncbi.nlm.nih.gov/pubmed/37552606 http://dx.doi.org/10.1021/acs.chemrev.2c00855 |
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author | Mandal, Arkajit Taylor, Michael A.D. Weight, Braden M. Koessler, Eric R. Li, Xinyang Huo, Pengfei |
author_facet | Mandal, Arkajit Taylor, Michael A.D. Weight, Braden M. Koessler, Eric R. Li, Xinyang Huo, Pengfei |
author_sort | Mandal, Arkajit |
collection | PubMed |
description | [Image: see text] When molecules are coupled to an optical cavity, new light–matter hybrid states, so-called polaritons, are formed due to quantum light–matter interactions. With the experimental demonstrations of modifying chemical reactivities by forming polaritons under strong light–matter interactions, theorists have been encouraged to develop new methods to simulate these systems and discover new strategies to tune and control reactions. This review summarizes some of these exciting theoretical advances in polariton chemistry, in methods ranging from the fundamental framework to computational techniques and applications spanning from photochemistry to vibrational strong coupling. Even though the theory of quantum light–matter interactions goes back to the midtwentieth century, the gaps in the knowledge of molecular quantum electrodynamics (QED) have only recently been filled. We review recent advances made in resolving gauge ambiguities, the correct form of different QED Hamiltonians under different gauges, and their connections to various quantum optics models. Then, we review recently developed ab initio QED approaches which can accurately describe polariton states in a realistic molecule–cavity hybrid system. We then discuss applications using these method advancements. We review advancements in polariton photochemistry where the cavity is made resonant to electronic transitions to control molecular nonadiabatic excited state dynamics and enable new photochemical reactivities. When the cavity resonance is tuned to the molecular vibrations instead, ground-state chemical reaction modifications have been demonstrated experimentally, though its mechanistic principle remains unclear. We present some recent theoretical progress in resolving this mystery. Finally, we review the recent advances in understanding the collective coupling regime between light and matter, where many molecules can collectively couple to a single cavity mode or many cavity modes. We also lay out the current challenges in theory to explain the observed experimental results. We hope that this review will serve as a useful document for anyone who wants to become familiar with the context of polariton chemistry and molecular cavity QED and thus significantly benefit the entire community. |
format | Online Article Text |
id | pubmed-10450711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104507112023-08-26 Theoretical Advances in Polariton Chemistry and Molecular Cavity Quantum Electrodynamics Mandal, Arkajit Taylor, Michael A.D. Weight, Braden M. Koessler, Eric R. Li, Xinyang Huo, Pengfei Chem Rev [Image: see text] When molecules are coupled to an optical cavity, new light–matter hybrid states, so-called polaritons, are formed due to quantum light–matter interactions. With the experimental demonstrations of modifying chemical reactivities by forming polaritons under strong light–matter interactions, theorists have been encouraged to develop new methods to simulate these systems and discover new strategies to tune and control reactions. This review summarizes some of these exciting theoretical advances in polariton chemistry, in methods ranging from the fundamental framework to computational techniques and applications spanning from photochemistry to vibrational strong coupling. Even though the theory of quantum light–matter interactions goes back to the midtwentieth century, the gaps in the knowledge of molecular quantum electrodynamics (QED) have only recently been filled. We review recent advances made in resolving gauge ambiguities, the correct form of different QED Hamiltonians under different gauges, and their connections to various quantum optics models. Then, we review recently developed ab initio QED approaches which can accurately describe polariton states in a realistic molecule–cavity hybrid system. We then discuss applications using these method advancements. We review advancements in polariton photochemistry where the cavity is made resonant to electronic transitions to control molecular nonadiabatic excited state dynamics and enable new photochemical reactivities. When the cavity resonance is tuned to the molecular vibrations instead, ground-state chemical reaction modifications have been demonstrated experimentally, though its mechanistic principle remains unclear. We present some recent theoretical progress in resolving this mystery. Finally, we review the recent advances in understanding the collective coupling regime between light and matter, where many molecules can collectively couple to a single cavity mode or many cavity modes. We also lay out the current challenges in theory to explain the observed experimental results. We hope that this review will serve as a useful document for anyone who wants to become familiar with the context of polariton chemistry and molecular cavity QED and thus significantly benefit the entire community. American Chemical Society 2023-08-08 /pmc/articles/PMC10450711/ /pubmed/37552606 http://dx.doi.org/10.1021/acs.chemrev.2c00855 Text en © 2023 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 | Mandal, Arkajit Taylor, Michael A.D. Weight, Braden M. Koessler, Eric R. Li, Xinyang Huo, Pengfei Theoretical Advances in Polariton Chemistry and Molecular Cavity Quantum Electrodynamics |
title | Theoretical
Advances in Polariton Chemistry and Molecular
Cavity Quantum Electrodynamics |
title_full | Theoretical
Advances in Polariton Chemistry and Molecular
Cavity Quantum Electrodynamics |
title_fullStr | Theoretical
Advances in Polariton Chemistry and Molecular
Cavity Quantum Electrodynamics |
title_full_unstemmed | Theoretical
Advances in Polariton Chemistry and Molecular
Cavity Quantum Electrodynamics |
title_short | Theoretical
Advances in Polariton Chemistry and Molecular
Cavity Quantum Electrodynamics |
title_sort | theoretical
advances in polariton chemistry and molecular
cavity quantum electrodynamics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450711/ https://www.ncbi.nlm.nih.gov/pubmed/37552606 http://dx.doi.org/10.1021/acs.chemrev.2c00855 |
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