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Verfasst von:Sun, Jing [VerfasserIn]   i
 Vendrell, Oriol [VerfasserIn]   i
Titel:Modification of thermal chemical rates in a cavity via resonant effects in the collective regime
Verf.angabe:Jing Sun and Oriol Vendrell
E-Jahr:2023
Jahr:September 14, 2023
Umfang:8 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 18.01.2024
Titel Quelle:Enthalten in: The journal of physical chemistry letters
Ort Quelle:Washington, DC : ACS, 2010
Jahr Quelle:2023
Band/Heft Quelle:14(2023), 38, Seite 8397-8404
ISSN Quelle:1948-7185
Abstract:The modification of thermal chemical rates in Fabry-Perot cavities, as observed in experiments, still poses theoretical challenges. While we have a better grasp of how the reactivity of isolated molecules and model systems changes under strong coupling, we lack a comprehensive understanding of the combined effects and the specific roles played by activated and spectator molecules during reactive events. In this study, we investigate an ensemble of randomly oriented gas-phase HONO molecules undergoing a cis-trans isomerization reaction on an ab initio potential energy surface. One thermally activated molecule can overcome the reaction barrier, while the other molecules are nonactivated but coupled to the cavity as well. Using the classical reactive flux method, we analyze the transmission coefficient and determine the conditions that lead to accelerated rates within the collective regime. We identify two main mechanistic aspects: First, nonactivated molecules enhance the cavity’s ability to dissipate excess energy from the activated molecule postreactive event. Second, the activated molecule couples with the polaritonic resonance created by the nonactivated molecules and the cavity at a shifted resonance frequency with respect to the bare cavity.
DOI:doi:10.1021/acs.jpclett.3c02199
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1021/acs.jpclett.3c02199
 kostenfrei: Volltext: https://pubs.acs.org/doi/10.1021/acs.jpclett.3c02199
 DOI: https://doi.org/10.1021/acs.jpclett.3c02199
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1878417061
Verknüpfungen:→ Zeitschrift

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