Double layer charging driven carbon dioxide adsorption limits the rate of electrochemical carbon dioxide reduction on Gold

Stefan Ringe (), Carlos G. Morales-Guio, Leanne D. Chen, Meredith Fields, Thomas F. Jaramillo, Christopher Hahn and Karen Chan ()
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Stefan Ringe: Stanford University
Carlos G. Morales-Guio: Stanford University
Leanne D. Chen: University of Guelph
Meredith Fields: Stanford University
Thomas F. Jaramillo: Stanford University
Christopher Hahn: Stanford University
Karen Chan: Technical University of Denmark

Nature Communications, 2020, vol. 11, issue 1, 1-11

Abstract: Abstract Electrochemical CO$$_{2}$$2 reduction is a potential route to the sustainable production of valuable fuels and chemicals. Here, we perform CO$$_{2}$$2 reduction experiments on Gold at neutral to acidic pH values to elucidate the long-standing controversy surrounding the rate-limiting step. We find the CO production rate to be invariant with pH on a Standard Hydrogen Electrode scale and conclude that it is limited by the CO$$_{2}$$2 adsorption step. We present a new multi-scale modeling scheme that integrates ab initio reaction kinetics with mass transport simulations, explicitly considering the charged electric double layer. The model reproduces the experimental CO polarization curve and reveals the rate-limiting step to be *COOH to *CO at low overpotentials, CO$$_{2}$$2 adsorption at intermediate ones, and CO$$_{2}$$2 mass transport at high overpotentials. Finally, we show the Tafel slope to arise from the electrostatic interaction between the dipole of *CO$$_{2}$$2 and the interfacial field. This work highlights the importance of surface charging for electrochemical kinetics and mass transport.

Date: 2020
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DOI: 10.1038/s41467-019-13777-z

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