Ammonium Cation-Promoted CO<sub>2</sub> Electroreduction on Au in Acidic Media

The electrochemical reduction of CO<sub>2</sub> in acidic media has received considerable attention, as it can mitigate the carbonate formation issue. However, the available protons in acidic media can boost the hydrogen evolution reaction (HER), so alkali metal cations are generally employed to promote the CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) while suppressing the HER. Here we report that NH<sub>4</sub><sup>+</sup> cations are more effective promoters of CO<sub>2</sub> electrolysis on Au in acidic media than Na<sup>+</sup> and K<sup>+</sup>, achieving a 3-fold improvement in the CO<sub>2</sub>RR activity. The promotional effect of NH<sub>4</sub><sup>+</sup> cations is mainly attributed to their enhanced electrostatic stabilization of the CO<sub>2</sub> adsorption, which is the rate-limiting step for the CO<sub>2</sub>RR on Au. An estimation of the local pH under relevant conditions indicates that NH<sub>4</sub><sup>+</sup> can mitigate the interfacial pH swing during the CO<sub>2</sub>RR compared to Na<sup>+</sup> and K<sup>+</sup>. Further studies on Au nanocatalysts of varying sizes indicate that the cation effect is independent of the catalytic sites. Our work advances the understanding of the cation effect on CO<sub>2</sub>RR using nonmetal cations and demonstrates a viable cation strategy to enhance CO<sub>2</sub> electrolysis.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-06-18
DOI
https://doi.org/10.1021/jacs.5c08017
Citations
18
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
Field-Weighted Citation Impact
6.54

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article

Ammonium Cation-Promoted CO2 Electroreduction on Au in Acidic Media

William E. Kaden, Xiaofeng Feng, Talat S. Rahman, Daniel W. Israel et al.
18 citations
Journal of the American Chemical Society
CO2 Reduction Techniques and Catalysts
6.54
article

Ammonium Cation-Promoted CO2 Electroreduction on Au in Acidic Media

William E. Kaden, Xiaofeng Feng, Talat S. Rahman, Daniel W. Israel, Duy Le, Zhuanghe Ren, Zhen Meng, Kaige Shi, John Janisch
article en
18 citations

Abstract

The electrochemical reduction of CO<sub>2</sub> in acidic media has received considerable attention, as it can mitigate the carbonate formation issue. However, the available protons in acidic media can boost the hydrogen evolution reaction (HER), so alkali metal cations are generally employed to promote the CO<sub>2</sub> reduction reaction (CO<sub>2</sub>RR) while suppressing the HER. Here we report that NH<sub>4</sub><sup>+</sup> cations are more effective promoters of CO<sub>2</sub> electrolysis on Au in acidic media than Na<sup>+</sup> and K<sup>+</sup>, achieving a 3-fold improvement in the CO<sub>2</sub>RR activity. The promotional effect of NH<sub>4</sub><sup>+</sup> cations is mainly attributed to their enhanced electrostatic stabilization of the CO<sub>2</sub> adsorption, which is the rate-limiting step for the CO<sub>2</sub>RR on Au. An estimation of the local pH under relevant conditions indicates that NH<sub>4</sub><sup>+</sup> can mitigate the interfacial pH swing during the CO<sub>2</sub>RR compared to Na<sup>+</sup> and K<sup>+</sup>. Further studies on Au nanocatalysts of varying sizes indicate that the cation effect is independent of the catalytic sites. Our work advances the understanding of the cation effect on CO<sub>2</sub>RR using nonmetal cations and demonstrates a viable cation strategy to enhance CO<sub>2</sub> electrolysis.

Journal of the American Chemical SocietyVol. 147(26)
University of Central Florida (US)
University of Central Florida, National Energy Research Scientific Computing Center, Basic Energy Sciences
Openalex Percentile: Top 3%
CO2 Reduction Techniques and Catalysts
6.54
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