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  Unraveling a Cavity-Induced Molecular Polarization Mechanism from Collective Vibrational Strong Coupling

Sidler, D., Schnappinger, T., Obzhirov, A., Ruggenthaler, M., Kowalewski, M., & Rubio, A. (2024). Unraveling a Cavity-Induced Molecular Polarization Mechanism from Collective Vibrational Strong Coupling. The Journal of Physical Chemistry Letters, 15(19), 5208-5214. doi:10.1021/acs.jpclett.4c00913.

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Supporting Information: Theoretical and computational details including the choices of simulation parameters; additional simulation results for an aligned Shin–Metiu setup as well as for the HF molecules under VSC (PDF); Transparent Peer Review report available (PDF)
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https://arxiv.org/abs/2306.06004 (Preprint)
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 Creators:
Sidler, D.1, 2, 3, 4, Author           
Schnappinger, T.5, Author
Obzhirov, A.2, 3, 4, Author           
Ruggenthaler, M.2, 3, 4, Author           
Kowalewski, Markus5, Author
Rubio, A.2, 3, 4, 6, 7, Author           
Affiliations:
1Laboratory for Materials Simulations, Paul Scherrer Institute, ou_persistent22              
2Theory Group, Theory Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society, ou_2266715              
3Center for Free-Electron Laser Science, ou_persistent22              
4The Hamburg Center for Ultrafast Imaging, ou_persistent22              
5Department of Physics, Stockholm University, AlbaNova University Center, ou_persistent22              
6Center for Computational Quantum Physics, Flatiron Institute, ou_persistent22              
7Nano-Bio Spectroscopy Group, University of the Basque Country (UPV/EHU), ou_persistent22              

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Free keywords: Cavities, Molecules, Polarization, Quantum mechanics, Thermodynamics
 Abstract: We demonstrate that collective vibrational strong coupling of molecules in thermal equilibrium can give rise to significant local electronic polarizations in the thermodynamic limit. We do so by first showing that the full nonrelativistic Pauli–Fierz problem of an ensemble of strongly coupled molecules in the dilute-gas limit reduces in the cavity Born–Oppenheimer approximation to a cavity–Hartree equation for the electronic structure. Consequently, each individual molecule experiences a self-consistent coupling to the dipoles of all other molecules, which amount to non-negligible values in the thermodynamic limit (large ensembles). Thus, collective vibrational strong coupling can alter individual molecules strongly for localized ”hotspots” within the ensemble. Moreover, the discovered cavity-induced polarization pattern possesses a zero net polarization, which resembles a continuous form of a spin glass (or better polarization glass). Our findings suggest that the thorough understanding of polaritonic chemistry, requires a self-consistent treatment of dressed electronic structure, which can give rise to numerous, so far overlooked, physical mechanisms.

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Language(s): eng - English
 Dates: 2024-05-012024-03-272024-05-032024-05-08
 Publication Status: Published online
 Pages: 7
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: arXiv: 2306.06004
DOI: 10.1021/acs.jpclett.4c00913
 Degree: -

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Project name : -
Grant ID : 852286
Funding program : Horizon 2020 (H2020)
Funding organization : European Commission (EC)
Project name : We thank I-Te Lu, Simone Latini, Abraham Nitzan, and Gerrit Groenhof for inspiring discussions and helpful comments. This work was made possible through the support of the RouTe Project (13N14839), financed by the Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung (BMBF)) and supported by the European Research Council (ERC-2015-AdG694097), the Cluster of Excellence “CUI: Advanced Imaging of Matter” of the Deutsche Forschungsgemeinschaft (DFG), EXC 2056, Project ID 390715994, and the Grupos Consolidados (IT1249-19). The Flatiron Institute is a division of the Simons Foundation. M.K. acknowledges funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (Grant Agreement No. 852286). Open access funded by Max Planck Society.
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Source 1

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Title: The Journal of Physical Chemistry Letters
  Abbreviation : J. Phys. Chem. Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 15 (19) Sequence Number: - Start / End Page: 5208 - 5214 Identifier: ISSN: 1948-7185
CoNE: https://pure.mpg.de/cone/journals/resource/1948-7185