par Papageorgiou, Alexia
;Rongy, Laurence
;Doneux, Thomas 
Référence Journal of the Electrochemical Society, 173, 14, 145501
Publication Publié, 2026-07-16
;Rongy, Laurence
;Doneux, Thomas 
Référence Journal of the Electrochemical Society, 173, 14, 145501
Publication Publié, 2026-07-16
Article révisé par les pairs
| Résumé : | In investigations of stepwise proton coupled electron transfer (PCET) reactions, it is often assumed, explicitly or implicitly, that the proton transfer (PT) step is at equilibrium, meaning that the buffering conditions are examined from a strictly thermodynamic perspective. In the present work, the implications of the Brönsted acid-base catalysis on the voltammetric responses of reversible (fast electron transfer) electroactive species are examined in the context of a 1 e−, 1 H+ square scheme, by numerical simulations accounting explicitly for the PT kinetics. Depending on the pKa’s of the electroactive species and those of the buffer components, PT kinetics can be slowed down to such an extent that voltammetric features akin to non-buffered conditions can appear even at high buffering capacities. This kinetic buffering is intrinsically asymmetric, the PT rate being affected only in one direction as a natural consequence of the Brönsted catalysis mechanism. |



