Engineering Sn‐based Catalytic Materials for Efficient Electrochemical CO 2 Reduction to Formate

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Engineering Sn‐based Catalytic Materials for Efficient Electrochemical CO 2 Reduction to Formate
Title:
Engineering Sn‐based Catalytic Materials for Efficient Electrochemical CO 2 Reduction to Formate
Journal Title:
ChemNanoMat
Keywords:
Publication Date:
02 March 2021
Citation:
Tay, Y. F., Tan, Z. H., Lum, Y. (2021). Engineering Sn‐based Catalytic Materials for Efficient Electrochemical CO 2 Reduction to Formate. ChemNanoMat, 7(4), 380–391. doi:10.1002/cnma.202100031
Abstract:
The electroreduction of CO2 provides a promising avenue to use renewable electricity for the sustainable production of chemicals and fuels. In particular, formate is attractive as a liquid hydrogen carrier or used directly in a fuel cell to generate electricity on demand. Sn-based catalysts have emerged as promising catalysts, however key issues such as how to reduce overpotential, enhance selectivity and maximize long-term stability are still yet to be resolved. In this minireview, we will highlight recent key advances in developing Sn-based catalysts, covering experimental and computational efforts on this front. Intriguingly, among the various strategies employed, we find that modifying the Sn oxidation state towards electron deficiency has been most effective. Finally, we also provide a perspective and outlook on future research and development of these Sn-based catalysts.
License type:
Publisher Copyright
Funding Info:
This research / project is supported by the A*STAR - Career Development Award
Grant Reference no. : 202D800037
Description:
This is the peer reviewed version of the following article: Tay, Y. F., Tan, Z. H., Lum, Y. (2021). Engineering Sn‐based Catalytic Materials for Efficient Electrochemical CO2 Reduction to Formate. ChemNanoMat, 7(4), 380–391. doi:10.1002/cnma.202100031, which has been published in final form at http://dx.doi.org/10.1002/cnma.202100031. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
ISSN:
2199-692X
2199-692X
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