4.8 Article

In-situ surface enhanced Raman spectroscopy investigations on surface transformations of oxide derived copper electrodes during CO2RR

Journal

JOURNAL OF CATALYSIS
Volume 423, Issue -, Pages 118-128

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2023.04.021

Keywords

CO2 reduction; Copper oxide; SERS; Malachite; C-2 products

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We investigated the catalytic activity and C2 selectivity in electrochemical CO2 reduction reaction (CO2RR) on two electrodeposited Cu oxides with distinct morphologies and structures. The compact electrode exhibited higher faradaic efficiencies of C2 products (40%). A metastable phase (malachite) formed on electrode surfaces by consuming HCO3- was found to cause a shift in local pH, as observed through electrochemical surface-enhanced Raman spectroscopy (SERS). The presence of the malachite phase was strongly correlated with strongly-adsorbed CO on electrode surfaces, inhibiting dimerization and further reduction.
We investigated the catalytic activity and C2 selectivity in electrochemical carbon dioxide reduction reac-tion (CO2RR) on two distinguished electrodeposited Cu oxides with distinct morphologies and structures. The electrode with a compact structure exhibited two times higher faradaic efficiencies of C2 products (40%). Through utilizing electrochemical surface-enhanced Raman spectroscopy (SERS), it was realized that the formation of a metastable phase (malachite) on electrode surfaces by consumption of HCO3- could cause a shift in local pH. The analysis of SERS indicated a strong correlation between the presence of the malachite phase and strongly-adsorbed CO on electrode surfaces, preventing dimerization and fur-ther reduction. This malachite phase terminating the surface can hinder the charge exchange and inter-fere with further reductions in C2 products. (c) 2023 Elsevier Inc. All rights reserved.

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