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Cited by 489

The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.

Electrochemical Reduction of CO2 to CH3OH at Copper Oxide Surfaces

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Le, M., Ren, M., Zhang, Z., Sprunger, P. T., Kurtz, R. L., Flake, J. C.·2011·Journal of The Electrochemical Society

Abstract

The direct reduction of CO 2 to CH 3 OH is known to occur at several types of electrocatalysts including oxidized Cu electrodes. In this work, we examine the yield behavior of an electrodeposited cuprous oxide thin film and explore relationships between surface chemistry and reaction behavior relative to air-oxidized and anodized Cu electrodes. CH 3 OH yields (43 μmol cm −2 h −1 ) and Faradaic efficiencies (38%) observed at cuprous oxide electrodes were remarkably higher than air-oxidized or anodized Cu electrodes suggesting Cu(I) species may play a critical role in selectivity to CH 3 OH. Experimental results also show CH 3 OH yields are dynamic and the copper oxides are reduced to metallic Cu in a simultaneous process. Yield behavior is discussed in comparison with photoelectrochemical and hydrogenation reactions where the improved stability of Cu(I) species may allow continuous CH 3 OH generation.

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Metadata

Authors
Le, M., Ren, M., Zhang, Z., Sprunger, P. T., Kurtz, R. L., & Flake, J. C.
Venue
Journal of The Electrochemical Society
Published
2011
Volume
158
Issue
5
Pages
E45
ISSN
0013-4651 (ISSN-L)
OpenAlex
W2032749248
Cited by
489
References
34
FWCI
10.25
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Electrochemical Reduction of CO2 to CH3OH at Copper Oxide Surfaces. https://app.cochat.ai/papers/10.1149/1.3561636
The paper
Le, M., Ren, M., Zhang, Z., Sprunger, P. T., Kurtz, R. L., & Flake, J. C. (2011). Electrochemical Reduction of CO2 to CH3OH at Copper Oxide Surfaces. Journal of The Electrochemical Society. https://doi.org/10.1149/1.3561636

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.