Direct Detection of Electron Transfer Reactions Underpinning the Tin-Catalyzed Electrochemical Reduction of CO2 using Fourier-Transformed ac Voltammetry

Ying Zhang, Lu Chen, Fengwang Li, Christopher D. Easton, Jiezhen Li, Alan M. Bond, Jie Zhang

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Two underlying electron transfer processes that directly underpin the catalytic reduction of carbon dioxide (CO2) to HCOO- and CO at Sn electrodes have been detected using the higher order harmonic components available in Fourier-transformed large-amplitude ac voltammetry. Both closely spaced electron transfer processes are undetectable by dc voltammetry and are associated with the direct reduction of CO2 species and have reversible potentials of approximately -1.27 and -1.40 V vs Ag/AgCl (1 M KCl). A mechanism involving a reversible inner-sphere one-electron reduction of CO2 followed by a rate-determining CO2 •- protonation step is proposed. Molecular CO2 has been identified as the dominant electroactive species that undergoes a series of coupling electron transfer and chemical reactions to form the final products. The substantial difference in the catalytic responses of Sn(SnOx)-modified glassy carbon and Sn foil electrodes are attributed to their strongly preferred Sn (200) orientation and polycrystalline states, respectively. The Fourier-transformed ac technique should be generally applicable for predicting the performance of Sn catalysts.

Original languageEnglish
Pages (from-to)4846-4853
Number of pages8
JournalACS Catalysis
Volume7
Issue number7
DOIs
Publication statusPublished - 7 Jul 2017

Keywords

  • CO reduction
  • electrocatalysis
  • Fourier-transformed ac voltammetry
  • mechanism
  • tin

Cite this

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title = "Direct Detection of Electron Transfer Reactions Underpinning the Tin-Catalyzed Electrochemical Reduction of CO2 using Fourier-Transformed ac Voltammetry",
abstract = "Two underlying electron transfer processes that directly underpin the catalytic reduction of carbon dioxide (CO2) to HCOO- and CO at Sn electrodes have been detected using the higher order harmonic components available in Fourier-transformed large-amplitude ac voltammetry. Both closely spaced electron transfer processes are undetectable by dc voltammetry and are associated with the direct reduction of CO2 species and have reversible potentials of approximately -1.27 and -1.40 V vs Ag/AgCl (1 M KCl). A mechanism involving a reversible inner-sphere one-electron reduction of CO2 followed by a rate-determining CO2 •- protonation step is proposed. Molecular CO2 has been identified as the dominant electroactive species that undergoes a series of coupling electron transfer and chemical reactions to form the final products. The substantial difference in the catalytic responses of Sn(SnOx)-modified glassy carbon and Sn foil electrodes are attributed to their strongly preferred Sn (200) orientation and polycrystalline states, respectively. The Fourier-transformed ac technique should be generally applicable for predicting the performance of Sn catalysts.",
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author = "Ying Zhang and Lu Chen and Fengwang Li and Easton, {Christopher D.} and Jiezhen Li and Bond, {Alan M.} and Jie Zhang",
year = "2017",
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doi = "10.1021/acscatal.7b01305",
language = "English",
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Direct Detection of Electron Transfer Reactions Underpinning the Tin-Catalyzed Electrochemical Reduction of CO2 using Fourier-Transformed ac Voltammetry. / Zhang, Ying; Chen, Lu; Li, Fengwang; Easton, Christopher D.; Li, Jiezhen; Bond, Alan M.; Zhang, Jie.

In: ACS Catalysis, Vol. 7, No. 7, 07.07.2017, p. 4846-4853.

Research output: Contribution to journalArticleResearchpeer-review

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AU - Zhang, Jie

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AB - Two underlying electron transfer processes that directly underpin the catalytic reduction of carbon dioxide (CO2) to HCOO- and CO at Sn electrodes have been detected using the higher order harmonic components available in Fourier-transformed large-amplitude ac voltammetry. Both closely spaced electron transfer processes are undetectable by dc voltammetry and are associated with the direct reduction of CO2 species and have reversible potentials of approximately -1.27 and -1.40 V vs Ag/AgCl (1 M KCl). A mechanism involving a reversible inner-sphere one-electron reduction of CO2 followed by a rate-determining CO2 •- protonation step is proposed. Molecular CO2 has been identified as the dominant electroactive species that undergoes a series of coupling electron transfer and chemical reactions to form the final products. The substantial difference in the catalytic responses of Sn(SnOx)-modified glassy carbon and Sn foil electrodes are attributed to their strongly preferred Sn (200) orientation and polycrystalline states, respectively. The Fourier-transformed ac technique should be generally applicable for predicting the performance of Sn catalysts.

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