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Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst

Herein, a novel approach used to enhance the conversion of electrochemical CO(2) reduction (CO(2)R), as well as the capacity to produce C(2) products, is reported. A copper oxide catalyst supported by graphite phase carbon nitride (CuO/g-C(3)N(4)) was prepared using a one-step hydrothermal method an...

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Detalles Bibliográficos
Autores principales: Yan, Zijun, Wu, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696822/
https://www.ncbi.nlm.nih.gov/pubmed/36430857
http://dx.doi.org/10.3390/ijms232214381
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author Yan, Zijun
Wu, Tao
author_facet Yan, Zijun
Wu, Tao
author_sort Yan, Zijun
collection PubMed
description Herein, a novel approach used to enhance the conversion of electrochemical CO(2) reduction (CO(2)R), as well as the capacity to produce C(2) products, is reported. A copper oxide catalyst supported by graphite phase carbon nitride (CuO/g-C(3)N(4)) was prepared using a one-step hydrothermal method and exhibited a better performance than pure copper oxide nanosheets (CuO NSs) and spherical copper oxide particles (CuO SPs). The Faradaic efficiency reached 64.7% for all the C(2) products, specifically 37.0% for C(2)H(4), with a good durability at −1.0 V vs. RHE. The results suggest that the interaction between CuO and the two-dimensional g-C(3)N(4) planes promoted CO(2) adsorption, its activation and C-C coupling. This work offers a practical method that can be used to enhance the activity of electrochemical CO(2)R and the selectivity of C(2) products through synergistic effects.
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spelling pubmed-96968222022-11-26 Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst Yan, Zijun Wu, Tao Int J Mol Sci Article Herein, a novel approach used to enhance the conversion of electrochemical CO(2) reduction (CO(2)R), as well as the capacity to produce C(2) products, is reported. A copper oxide catalyst supported by graphite phase carbon nitride (CuO/g-C(3)N(4)) was prepared using a one-step hydrothermal method and exhibited a better performance than pure copper oxide nanosheets (CuO NSs) and spherical copper oxide particles (CuO SPs). The Faradaic efficiency reached 64.7% for all the C(2) products, specifically 37.0% for C(2)H(4), with a good durability at −1.0 V vs. RHE. The results suggest that the interaction between CuO and the two-dimensional g-C(3)N(4) planes promoted CO(2) adsorption, its activation and C-C coupling. This work offers a practical method that can be used to enhance the activity of electrochemical CO(2)R and the selectivity of C(2) products through synergistic effects. MDPI 2022-11-19 /pmc/articles/PMC9696822/ /pubmed/36430857 http://dx.doi.org/10.3390/ijms232214381 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yan, Zijun
Wu, Tao
Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst
title Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst
title_full Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst
title_fullStr Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst
title_full_unstemmed Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst
title_short Highly Selective Electrochemical CO(2) Reduction to C(2) Products on a g-C(3)N(4)-Supported Copper-Based Catalyst
title_sort highly selective electrochemical co(2) reduction to c(2) products on a g-c(3)n(4)-supported copper-based catalyst
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696822/
https://www.ncbi.nlm.nih.gov/pubmed/36430857
http://dx.doi.org/10.3390/ijms232214381
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