Multiple proton-coupled electron transfer for electrochemical generation of fuels
Marc Koper a
a Leiden University, Leiden Institute of Chemistry, Leiden, 2300, Netherlands
Materials for Sustainable Development Conference (MATSUS)
Proceedings of September Meeting 2016 (NFM16)
Berlin, Germany, 2016 September 5th - 13th
Organizers: Marin Alexe, Enrique Cánovas, Celso de Mello Donega, Ivan Infante, Thomas Kirchartz, Maksym Kovalenko, Federico Rosei, Lukas Schmidt-Mende, Laurens Siebbeles, Peter Strasser, Teodor K Todorov, Roel van de Krol and Ulrike Woggon
Invited Speaker, Marc Koper, presentation 004
Publication date: 14th June 2016

This talk will outline a simple but general theoretical analysis for multiple proton-electron transfer reactions, based on the microscopic theory of proton-coupled electron transfer reactions, recent developments in the thermodynamic theory of multi-step electron transfer reactions, and the experimental realization that many multiple proton-coupled electron transfer reactions feature decoupled proton-electron steps in their mechanism. It is shown that decoupling of proton and electron transfer leads to a strong pH dependence of the overall catalytic reaction, implying an optimal pH for high catalytic turnover, and an associated optimal catalyst at the optimal pH. When more than one catalytic intermediate is involved, scaling relationships between intermediates may dictate the optimal catalyst and limit the extent of reversibility that may be achievable for a multiple proton-electron-transfer reaction. These scaling relationships follow from a valence-bond-type binding of intermediates to the catalyst surface. The theory is discussed in relation to the experimental results for a number of redox reactions that are of importance for sustainable energy conversion, including the electrocatalytic reduction of CO2, focusing on their pH dependence and structure sensitivity.



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