Proton-coupled electron transfer in the electrocatalysis of CO2 reduction: prediction of sequential vs. concerted pathways using DFT† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6sc02984a Click here for additional data file

• Published in: Chemical science (Cambridge) Vol. 8; no. 1; pp. 458 - 465
• Main Authors: Göttle, Adrien J., Koper, Marc T. M.
• Format: Journal Article
• Language: English
• Published: Royal Society of Chemistry 22.08.2016
• Subjects: Chemistry
• ISSN: 2041-6520; 2041-6539
• DOI: 10.1039/c6sc02984a

We provide a complete and computationally detailed picture of the mechanism of the initial stages of the electrocatalytic reduction of CO 2 in water catalysed by cobalt porphyrin complexes. Herein we investigate computationally in detail the mechanism of the formation of the carboxylate adduct during the electroreduction of CO 2 in water catalysed by cobalt porphyrin complexes. Specifically, we address qualitatively the competition between the concerted and sequential pathways for the proton-coupled electron transfer. We use a simple methodology for accurate computation of the p K a of the neutral and anionic carboxylate intermediates, [CoP–COOH] and [CoP–COOH] – (where CoP is a cobalt porphine complex), based on the isodesmic proton-exchange reaction scheme. The predicted values are used as in input for a theoretical model that describes the transition between the sequential and concerted pathways. The activation of the sequential pathway (ET–PT) that leads to the formation of the neutral [CoP–COOH] intermediate at pH ≈ 3.5 (p K a [CoP–COOH] = 3.5 ± 0.4), as predicted by the calculations, is in good agreement with the drastic increase in the faradaic efficiency of the CO 2 reduction reaction towards CO at pH = 3 compared to pH = 1, as experimentally observed. This confirms the existence of the CO 2 anionic adduct [CoP–CO 2 ] – as a viable intermediate at pH = 3 and its crucial role for the pH dependence of the faradaic efficiency for the CO 2 reduction. The analysis also shows that when the pH is significantly higher than the p K a of the neutral carboxylate adduct, the CO 2 reduction has to go through an alternative pathway with the formation of the anionic carboxylate intermediate [CoP–COOH] – . It is formed through a concerted proton–electron transfer step from the anionic CO 2 adduct [CoP–CO 2 ] – when the pH is below ∼8.6 (p K a [CoP–COOH] – = 8.6 ± 0.4). At pH ≈ 8.6 and above, another decoupled ET–PT is predicted to take place, leading to the formation of a dianionic CO 2 adduct [CoP–CO 2 ] 2– .