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学術論文

Cavity-Modulated Proton Transfer Reactions

MPS-Authors
/persons/resource/persons22028

Rubio,  A.
Center for Computational Quantum Physics, Flatiron Institute;
Theory Group, Theory Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;
Center for Free-Electron Laser Science;
Nano-Bio Spectroscopy Group and European Theoretical Spectroscopy Facility (ETSF), Universidad del Paìs Vasco (UPV/EHU);

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フルテキスト (公開)

2112.02138.pdf
(プレプリント), 2MB

付随資料 (公開)

suppl.zip
(付録資料), 465KB

引用

Pavošević, F., Hammes-Schiffer, S., Rubio, A., & Flick, J. (2022). Cavity-Modulated Proton Transfer Reactions. Journal of the American Chemical Society, 144(11), 4995-5002. doi:10.1021/jacs.1c13201.


引用: https://hdl.handle.net/21.11116/0000-0009-9651-2
要旨
Proton transfer is ubiquitous in many fundamental chemical and biological processes, and the ability to modulate and control the proton transfer rate would have a major impact on numerous quantum technological advances. One possibility to modulate the reaction rate of proton transfer processes is given by exploiting the strong light-matter coupling of chemical systems inside optical or nanoplasmonic cavities. In this work, we investigate the proton transfer reactions in the prototype malonaldehyde and Z-3-amino-propenal (aminopropenal) molecules using different quantum electrodynamics methods, in particular, quantum electrodynamics coupled cluster theory and quantum electrodynamical density functional theory. Depending on the cavity mode polarization direction, we show that the optical cavity can increase the reaction energy barrier by 10–20% or decrease the reaction barrier by ∼5%. By using first-principles methods, this work establishes strong light-matter coupling as a viable and practical route to alter and catalyze proton transfer reactions.