Solvent-mediated outer-sphere CO2 electro-reduction mechanism over the Ag111 surface

The electrocatalytic CO2 reduction reaction (CO2RR) is one of the key technologies of the clean energy economy. Molecular-level understanding of the CO2RR process is instrumental for the better design of electrodes operable at low overpotentials with high current density. The catalytic mechanism und...

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Vydáno v:Chemical science (Cambridge) Ročník 13; číslo 13; s. 3803 - 3808
Hlavní autoři: Sinha, Vivek, Khramenkova, Elena, Pidko, Evgeny A
Médium: Journal Article
Jazyk:angličtina
Vydáno: Cambridge Royal Society of Chemistry 30.03.2022
The Royal Society of Chemistry
Témata:
Carbon dioxide
Chemical reduction
Chemistry
Clean energy
Conversion
Dehydration
Electrocatalysts
Electrolytes
Electron transfer
Molecular dynamics
Selectivity
ISSN:2041-6520, 2041-6539
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Shrnutí:The electrocatalytic CO2 reduction reaction (CO2RR) is one of the key technologies of the clean energy economy. Molecular-level understanding of the CO2RR process is instrumental for the better design of electrodes operable at low overpotentials with high current density. The catalytic mechanism underlying the turnover and selectivity of the CO2RR is modulated by the nature of the electrocatalyst, as well as the electrolyte liquid, and its ionic components that form the electrical double layer (EDL). Herein we demonstrate the critical non-innocent role of the EDL for the activation and conversion of CO2 at a high cathodic bias for electrocatalytic conversion over a silver surface as a representative low-cost model cathode. By using a multiscale modeling approach we demonstrate that under such conditions a dense EDL is formed, which hinders the diffusion of CO2 towards the Ag111 electrocatalyst surface. By combining DFT calculations and ab initio molecular dynamics simulations we identify favorable pathways for CO2 reduction directly over the EDL without the need for adsorption to the catalyst surface. The dense EDL promotes homogeneous phase reduction of CO2via electron transfer from the surface to the electrolyte. Such an outer-sphere mechanism favors the formation of formate as the CO2RR product. The formate can undergo dehydration to CO via a transition state stabilized by solvated alkali cations in the EDL.
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ISSN:2041-6520
2041-6539
DOI:10.1039/d1sc07119j