CO2 or Carbonates – What is the Active Species in Electrochemical CO2 Reduction over Fe-Porphyrin?

Funding Information: Calculations were performed at the Finnish IT centre for science (CSC). All authors acknowledge financial support from the Jane and Aatos Erkko Foundation through the “Renewable energy storage to high value chemicals” project. M. B. is additionally grateful for the support throu...

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Bibliographic Details
Published in:ChemCatChem
Main Authors: Khakpour, Reza, Lindberg, Daniel, Laasonen, Kari, Busch, Michael
Other Authors: Department of Chemistry and Materials Science, Department of Chemical and Metallurgical Engineering, Computational Chemistry, Metallurgical Thermodynamics and Modelling, Aalto-yliopisto, Aalto University
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2023
Subjects:
Bicarbonate
CO reduction
Electrocatalysis
Hydrogen evolution
Porphyrin
Carbonic acid
Online Access:https://aaltodoc.aalto.fi/handle/123456789/120355
https://doi.org/10.1002/cctc.202201671
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Summary:Funding Information: Calculations were performed at the Finnish IT centre for science (CSC). All authors acknowledge financial support from the Jane and Aatos Erkko Foundation through the “Renewable energy storage to high value chemicals” project. M. B. is additionally grateful for the support through the Dr. Barbara Mez‐Stark foundation. Open Access funding enabled and organized by Projekt DEAL. Publisher Copyright: © 2023 The Authors. ChemCatChem published by Wiley-VCH GmbH. CO2 reduction is typically performed at neutral pH. Under these conditions CO2 is in equilibrium with H2CO3, HCO3− and CO32−. However, despite their presence so far most studies solely focus on the contribution of CO2 while carbonate species as alternative reactants are generally neglected. Using density functional theory (DFT) modelling we explore the possible contribution of these carbonate species to the overall CO2 reduction activity for a Fe porphyrin model catalyst. Considering only reaction Gibbs free energies, we find the reduction of carbonic acid (H2CO3), bicarbonate (HCO3−) and CO2 to be equally likely. However, owing to a very high activation barrier for the initial adsorption of CO2 onto the catalyst, bicarbonate and carbonic acid reduction are found to be several orders of magnitude faster. These data are used to model the pH dependence of the reaction rates of the different reactants. These results confirm that carbonic acid and bicarbonate are the most likely reactants independent of the pH and reactor setup. Peer reviewed

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