The DOI matches its Crossref record; 79 of the 79 references it cites were found in a registry or an index.
Linking the Dynamic Chemical State of Catalysts with the Product Profile of Electrocatalytic CO2 Reduction
Abstract
The promoted activity and enhanced selectivity of electrocatalysts is commonly ascribed to specific structural features such as surface facets, morphology, and atomic defects. However, unraveling the factors that really govern the direct electrochemical reduction of CO 2 (CO 2 RR) is still very challenging since the surface state of electrocatalysts is dynamic and difficult to predict under working conditions. Moreover, theoretical predictions from the viewpoint of thermodynamics alone often fail to specify the actual configuration of a catalyst for the dynamic CO 2 RR process. Herein, we re‐survey recent studies with the emphasis on revealing the dynamic chemical state of Cu sites under CO 2 RR conditions extracted by in situ/operando characterizations, and further validate a critical link between the chemical state of Cu and the product profile of CO 2 RR. This point of view provides a generalizable concept of dynamic chemical‐state‐driven CO 2 RR selectivity that offers an inspiration in both fundamental understanding and efficient electrocatalysts design.
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Cites
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Cited by
Stabilizing Cu2+ Ions by Solid Solutions to Promote CO2 Electroreduction to Methane
Zhou, X., Shan, J., Chen, L., Xia, B. Y., Ling, T., Duan, J., Jiao, Y., Zheng, Y., & Qiao, S.-Z. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.1c12212 · Cited by 518
Metadata
- Authors
- Wang, J., Tan, H., Zhu, Y., Chu, H., & Chen, H. M.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2021-04-13
- Volume
- 60
- Issue
- 32
- Pages
- 17254-17267
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W4243652164
- Cited by
- 322
- References
- 79
- FWCI
- 10.99
- Type
- journal article
- Language
- en
- Open access
- closed
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