Physical Chemistry

Grand canonical rate theory for electrochemical and electrocatalytic systems I: General formulation and proton-coupled electron transfer reactions

Marko Melander Department of Chemistry, University of Jyväskylä

Abstract

A generally valid rate theory at fixed potentials is developed to treat electrochemical and electrocatalytic potential-dependent electron, proton, and proton-coupled electron reactions. Both classical and quantum reactions in adiabatic and non-adiabatic limits are treated. The applicability and new information obtained from the theory is demonstrated for the gold catalyzed acidic Volmer reaction.

Version notes

This is the 5th and revised version with new results

Content

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Supplementary material

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supporting info
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appendix