Published July 31, 2020 | Version Published + Supplemental Material
Journal Article Open

Oxygen induced promotion of electrochemical reduction of CO₂ via co-electrolysis

  • 1. ROR icon Tsinghua University
  • 2. ROR icon University of Delaware
  • 3. ROR icon Columbia University
  • 4. ROR icon California Institute of Technology
  • 5. ROR icon National Cheng Kung University

Abstract

Harnessing renewable electricity to drive the electrochemical reduction of CO₂ is being intensely studied for sustainable fuel production and as a means for energy storage. Copper is the only monometallic electrocatalyst capable of converting CO₂ to value-added products, e.g., hydrocarbons and oxygenates, but suffers from poor selectivity and mediocre activity. Multiple oxidative treatments have shown improvements in the performance of copper catalysts. However, the fundamental underpinning for such enhancement remains controversial. Here, we combine reactivity, in-situ surface-enhanced Raman spectroscopy, and computational investigations to demonstrate that the presence of surface hydroxyl species by co-electrolysis of CO₂ with low concentrations of O₂ can dramatically enhance the activity of copper catalyzed CO2 electroreduction. Our results indicate that co-electrolysis of CO₂ with an oxidant is a promising strategy to introduce catalytically active species in electrocatalysis.

Additional Information

© The Author(s) 2020. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. Received 31 March 2020; Accepted 14 July 2020; Published 31 July 2020. 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 the National Science Foundation CAREER Program (Award No. CBET-1651625). W.A.G. is supported by the US National Science Foundation (CBET-1805022). M.-j.C. acknowledges financial support from the Ministry of Science and Technology of the Republic of China under Grant No. MOST 107-2113-M-006-008-MY2. Data availability: The data that support the findings of this study are available from the corresponding author upon request. Author Contributions: These authors contributed equally: Ming He, Chunsong Li. Q.L. conceived and designed the project. M.H. and C.L. carried out the electrocatalytic tests and physical characterizations. X.C. and B.X. performed in situ SERS experiments. H.Z. and M.-j.C. performed DFT calculations. J.G.C. and W.A.G. contributed to data analysis and writing of this manuscript. These authors contributed equally: M.H. and C.L. The authors declare no competing interests.

Attached Files

Published - s41467-020-17690-8.pdf

Supplemental Material - 41467_2020_17690_MOESM1_ESM.pdf

Files

s41467-020-17690-8.pdf

Files (26.3 MB)

Name Size Download all
md5:90a3cb4aaffe92e4c009173b1511c46e
22.1 MB Preview Download
md5:332dd6d991460e314d47394d039a0fcd
4.3 MB Preview Download

Additional details

Identifiers

PMCID
PMC7395777
Eprint ID
104697
Resolver ID
CaltechAUTHORS:20200803-093757604

Funding

National Key Research and Development Program of China
2017YFA0208200
National Natural Science Foundation of China
21872079
NSF
CBET-1651625
NSF
CBET-1805022
Ministry of Science and Technology (China)
MOST 107-2113-M-006-008-MY2

Dates

Created
2020-08-03
Created from EPrint's datestamp field
Updated
2021-11-16
Created from EPrint's last_modified field

Caltech Custom Metadata

Other Numbering System Name
WAG
Other Numbering System Identifier
1389