In Situ Fabrication and Reactivation of Highly Selective and Stable Ag Catalysts for Electrochemical CO2 Conversion

Journal Article (2018)
Author(s)

M Ma (TU Delft - ChemE/Materials for Energy Conversion and Storage)

K. Liu (TU Delft - ChemE/Materials for Energy Conversion and Storage)

J. Shen (TU Delft - QRD/Kouwenhoven Lab, TU Delft - QuTech Advanced Research Centre)

R. Kas (TU Delft - ChemE/Materials for Energy Conversion and Storage)

WA Smith (TU Delft - ChemE/Materials for Energy Conversion and Storage)

Research Group
ChemE/Materials for Energy Conversion and Storage
Copyright
© 2018 M. Ma, K. Liu, J. Shen, R. Kas, W.A. Smith
DOI related publication
https://doi.org/10.1021/acsenergylett.8b00472
More Info
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Publication Year
2018
Language
English
Copyright
© 2018 M. Ma, K. Liu, J. Shen, R. Kas, W.A. Smith
Research Group
ChemE/Materials for Energy Conversion and Storage
Issue number
6
Volume number
3
Pages (from-to)
1301-1306
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Abstract

In this work, the highly selective and stable electrocatalytic reduction of CO2 to CO on nanostructured Ag electrocatalysts is presented. The Ag electrocatalysts are synthesized by the electroreduction of Ag2CO3 formed by in situ anodic-etching of Ag foil in a KHCO3 electrolyte. After 3 min of this etching treatment, the Ag2CO3-derived nanostructured Ag electrocatalysts are capable of producing CO with up to 92% Faradaic efficiency at an overpotential as low as 290 mV, which surpasses all of the reported Ag catalysts at identical conditions to date. In addition, the anodic-etched Ag retained ∼90% catalytic selectivity in the electroreduction of CO2 to CO for more than 100 h. The Ag2CO3-derived Ag is able to facilitate the activation of CO2 via reduction of the activation energy barrier of the initial electron transfer and provide an increased number of active sites, resulting in the dramatically improved catalytic activity for the reduction of CO2 to CO.