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

Delft University of Technology; Delft University of Technology; Delft University of Technology; Delft University of Technology; Delft University of Technology
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Publisher: ACS
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Abstract AITranslate

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.

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DOI:https://doi.org/10.1021/acsenergylett.8b00472

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Citation Information:

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.

quote

GB/T 7714-2015 [1] Ming Ma, Kai Liu, Jie Shen, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.8b00472.
MLA [1] Ming Ma, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.8b00472.
APA [1] Ming Ma, Kai Liu, Jie Shen, Recep Kas, & Wilson A. Smith. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.8b00472
IEEE [1] Ming Ma, Kai Liu, Jie Shen, Recep Kas, and Wilson A. Smith, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.8b00472.