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Combined effects of sea urchin-like structure and mixed Cu+/Cu0 states on promoting C2 formation in electrocatalytic CO2 reduction

Surface engineering and Cu valence regulation are essential factors in improving the C 2 selectivity during the electrochemical reduction of CO 2 . Herein, we present a sea urchin-like CuO/Cu 2 O catalyst derived from rhombic dodecahedra Cu 2 O through one-step oxidation/etching method where the mix...

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Bibliographic Details
Published in:Frontiers of chemical science and engineering 2024-03, Vol.18 (3), Article 30
Main Authors: Shan, Mengqing, Lu, Dongsheng, Dong, Jiatong, Yan, Shen, Han, Jinyu, Wang, Hua
Format: Article
Language:English
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Summary:Surface engineering and Cu valence regulation are essential factors in improving the C 2 selectivity during the electrochemical reduction of CO 2 . Herein, we present a sea urchin-like CuO/Cu 2 O catalyst derived from rhombic dodecahedra Cu 2 O through one-step oxidation/etching method where the mixed Cu + /Cu 0 states are formed via in situ reduction during electrocatalysis. The combined effects of the morphology and the mixed Cu + /Cu 0 states on C–C coupling are evaluated by the Faradaic efficiency of C 2 and the C 2 /C 1 ratio obtained in an H-cell. R-CuO/Cu 2 O exhibited 49.5% Faradaic efficiency of C 2 with a C 2 /C 1 ratio of 3.1 at −1.4 V vs. reversible hydrogen electrode, which are 1.5 and 3.2 times higher than those of R-Cu 2 O, respectively. Using a flow-cell, 68.0% Faradaic efficiency of C 2 is achieved at a current density of 500 mA·cm −2 . The formation of the mixed Cu + /Cu 0 states was confirmed by in situ Raman spectra. Additionally, the sea urchin-like structure provides more active sites and enables faster electron transfer. As a result, the excellent C 2 production on R-CuO/Cu 2 O is primarily attributed to the synergistic effects of the sea urchin-like structure and the stable mixed Cu + /Cu 0 states. Therefore, this work presents an integrated strategy for developing Cu-based electrocatalysts for C 2 production through electrochemical CO 2 reduction.
ISSN:2095-0179
2095-0187
DOI:10.1007/s11705-024-2393-5