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On ZnAlCe-THs Nanocomposites Electrocatalysts for Electrocatalytic Carbon Dioxide Reduction to Carbon Monoxide.

Authors :
Tan, Fang
Liu, Tianxia
Liu, Errui
Zhang, Yaping
Source :
Catalysis Letters; Jan2024, Vol. 154 Issue 1, p11-22, 12p
Publication Year :
2024

Abstract

Reducing the use of fossil fuels is critical to human society. In recent years, electrocatalytic carbon dioxide (CO<subscript>2</subscript>) reduction has attracted widespread attention. A suitable CO<subscript>2</subscript> reduction catalyst is essential to convert CO<subscript>2</subscript> into more valuable chemical products with high selectivity and efficiency. In this paper, a highly selective ZnAlCe-Ternary metal hydroxides (ZnAlCe-THs) nanocomposite electrocatalyst material was designed and prepared, and its performance as an electrocatalyst for catalytic reduction of CO<subscript>2</subscript> to carbon monoxide (CO) was explored. The layered structure of ZnAlCe-THs nanocomposites facilitates electron transfer as well as CO<subscript>2</subscript> and proton transfer, providing a high specific surface area for the electroactive sites of the electrocatalytic reduction reaction. At the same time, the ZnAlCe-THs catalyst generates CO at an overpotential of − 0.5 V. At − 1.2 V versus the reversible hydrogen electrode (vs. RHE), the bias current density is about 10.46 mA cm<superscript>−2</superscript> with high selectivity of 89.3% Faraday efficiency. Its excellent electrochemical properties make it a good catalyst for the selective reduction of CO<subscript>2</subscript> to CO. In this paper, ZnAlCe-Ternary mental hydroxides (ZnAlCe-THs) with a layered hydrotalclike structure were prepared by hydrothermal and co-precipitation methods. It showed excellent catalytic performance in the electrocatalytic reduction of carbon dioxide to carbon monoxide with a Faraday efficiency of 89.3% at − 1.2 V vs. RHE and a current density of 10.46 mA cm<superscript>−2</superscript> for higher selectivity for CO. In addition, the ZnAlCe-THs catalyst is stable and it can operate for 5 h without particularly significant deactivation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1011372X
Volume :
154
Issue :
1
Database :
Complementary Index
Journal :
Catalysis Letters
Publication Type :
Academic Journal
Accession number :
174578973
Full Text :
https://doi.org/10.1007/s10562-023-04302-5