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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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Published in: | Frontiers of chemical science and engineering 2024-03, Vol.18 (3), Article 30 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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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. |
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ISSN: | 2095-0179 2095-0187 |
DOI: | 10.1007/s11705-024-2393-5 |