Is Cu instability during the CO2 reduction reaction governed by the applied potential or the local CO concentration?

Cu-based catalysts have shown structural instability during the electrochemical CO2 reduction reaction (CO2RR). However, studies on monometallic Cu catalysts do not allow a nuanced differentiation between the contribution of the applied potential and the local concentration of CO as the reaction int...

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Bibliographic Details
Published in:Chemical science (Cambridge) 2021-01, Vol.12 (11), p.4028-4033
Main Authors: Wilde, Patrick, O'Mara, Peter B, Junqueira, João R C, Tarnev, Tsvetan, Benedetti, Tania M, Andronescu, Corina, Yen-Ting, Chen, Tilley, Richard D, Schuhmann, Wolfgang, Gooding, J Justin
Format: Article
Language:English
Subjects:
Bimetals
Carbon dioxide
Catalysts
Chemical reduction
Chemistry
Copper
Crystal lattices
Crystal structure
Electron beams
Image resolution
Nanoparticles
Palladium
Reaction intermediates
Selectivity
Silver
Stability analysis
Structural stability
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Summary:Cu-based catalysts have shown structural instability during the electrochemical CO2 reduction reaction (CO2RR). However, studies on monometallic Cu catalysts do not allow a nuanced differentiation between the contribution of the applied potential and the local concentration of CO as the reaction intermediate since both are inevitably linked. We first use bimetallic Ag-core/porous Cu-shell nanoparticles, which utilise nanoconfinement to generate high local CO concentrations at the Ag core at potentials at which the Cu shell is still inactive for the CO2RR. Using operando liquid cell TEM in combination with ex situ TEM, we can unequivocally confirm that the local CO concentration is the main source for the Cu instability. The local CO concentration is then modulated by replacing the Ag-core with a Pd-core which further confirms the role of high local CO concentrations. Product quantification during CO2RR reveals an inherent trade-off between stability, selectivity and activity in both systems.
ISSN:2041-6520
2041-6539
DOI:10.1039/d0sc05990k