Selective Enhancement of Methane Formation in Electrochemical CO₂ Reduction Enabled by a Raman-Inactive Oxygen-Containing Species on Cu
Abstract
The role of oxygen-containing species on Cu catalysts in the electrochemical CO₂ reduction reaction (CO₂RR) remains unclear due to the difficulty in its stabilization under reaction conditions. Co-electrolysis of CO₂ with an oxidant is an effective strategy to introduce oxygen-containing species on Cu during the CO₂RR. In this work, we present concrete evidence demonstrating that an oxygen-containing species is able to not only enhance the rate of the CO₂RR but also tune selectivities for certain products. Co-electrolysis of CO₂ with H₂O₂ on Cu selectively accelerates the CH4 production rate by up to a factor of 200, but with only a slight enhancement of C₂₊ products. Combined investigations using in situ Raman spectroscopy with density functional theory calculations reveal that a Raman-inactive Cu oxide species is responsible for the improved CH₄ production. Results reported in this work highlight the possibility of enhancing Cu-based CO₂RR catalysts by introducing stable oxygen-containing catalytic structures.
Additional Information
© 2022 American Chemical Society. Received 6 January 2022. Revised 23 March 2022. Published online 6 May 2022. Published in issue 20 May 2022. This work is supported by the National Key Research and Development Program of China (grant number 2017YFA0208200) and the National Natural Science Foundation of China (grant number 21872079). X.C. and B.X. acknowledge the support of Beijing National Laboratory for Molecular Sciences, as well as the National Science Foundation CAREER Program (Award No. CBET-1651625). W.A.G. thanks the Department of Energy (DE-SC0021266) for support. All NMR experiments were performed at the BioNMR facility, Tsinghua University Branch of China National Center for Protein Sciences (Beijing). The authors thank Dr. Ning Xu for assistance in NMR data collection. The authors thank Zenan Wang for assistance in AFM measurement. The authors declare no competing financial interest.Attached Files
Supplemental Material - cs2c00087_si_001.pdf
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Additional details
- Eprint ID
- 114837
- Resolver ID
- CaltechAUTHORS:20220520-388227000
- National Key Research and Development Program of China
- 2017YFA0208200
- National Natural Science Foundation of China
- 21872079
- NSF
- CBET-1651625
- Department of Energy (DOE)
- DE-SC0021266
- Created
-
2022-05-20Created from EPrint's datestamp field
- Updated
-
2022-08-14Created from EPrint's last_modified field
- Other Numbering System Name
- WAG
- Other Numbering System Identifier
- 1520