We investigate the influence of a stochastically fluctuating step-barrier potential on bimolecular reaction rates by exact analytical theory and stochastic simulations. We demonstrate that the system exhibits a new "resonant reaction" behavior with rate enhancement if an appropriately defined fluctuation decay length is of the order of the system size. Importantly, we find that in the proximity of resonance, the standard reciprocal additivity law for diffusion and surface reaction rates is violated due to the dynamical coupling of multiple kinetic processes. Together, these findings may have important repercussions on the correct interpretation of various kinetic reaction problems in complex systems, as, e.g., in biomolecular association or catalysis.
Communication: Resonance reaction in diffusion-influenced bimolecular reactions.
Jakob J. Kolb,S. Angioletti-Uberti,J. Dzubiella
Published 2016 in Journal of Chemical Physics
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- Publication year
2016
- Venue
Journal of Chemical Physics
- Publication date
2016-02-24
- Fields of study
Medicine, Physics, Chemistry
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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