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Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst

Electrochemical alcohols oxidation offers a promising approach to produce valuable chemicals and facilitate coupled H(2) production. However, the corresponding current density is very low at moderate cell potential that substantially limits the overall productivity. Here we report the electrooxidati...

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Autores principales: Li, Zhenhua, Yan, Yifan, Xu, Si-Min, Zhou, Hua, Xu, Ming, Ma, Lina, Shao, Mingfei, Kong, Xianggui, Wang, Bin, Zheng, Lirong, Duan, Haohong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748678/
https://www.ncbi.nlm.nih.gov/pubmed/35013339
http://dx.doi.org/10.1038/s41467-021-27806-3
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author Li, Zhenhua
Yan, Yifan
Xu, Si-Min
Zhou, Hua
Xu, Ming
Ma, Lina
Shao, Mingfei
Kong, Xianggui
Wang, Bin
Zheng, Lirong
Duan, Haohong
author_facet Li, Zhenhua
Yan, Yifan
Xu, Si-Min
Zhou, Hua
Xu, Ming
Ma, Lina
Shao, Mingfei
Kong, Xianggui
Wang, Bin
Zheng, Lirong
Duan, Haohong
author_sort Li, Zhenhua
collection PubMed
description Electrochemical alcohols oxidation offers a promising approach to produce valuable chemicals and facilitate coupled H(2) production. However, the corresponding current density is very low at moderate cell potential that substantially limits the overall productivity. Here we report the electrooxidation of benzyl alcohol coupled with H(2) production at high current density (540 mA cm(−2) at 1.5 V vs. RHE) over a cooperative catalyst of Au nanoparticles supported on cobalt oxyhydroxide nanosheets (Au/CoOOH). The absolute current can further reach 4.8 A at 2.0 V in a more realistic two-electrode membrane-free flow electrolyzer. Experimental combined with theoretical results indicate that the benzyl alcohol can be enriched at Au/CoOOH interface and oxidized by the electrophilic oxygen species (OH*) generated on CoOOH, leading to higher activity than pure Au. Based on the finding that the catalyst can be reversibly oxidized/reduced at anodic potential/open circuit, we design an intermittent potential (IP) strategy for long-term alcohol electrooxidation that achieves high current density (>250 mA cm(−2)) over 24 h with promoted productivity and decreased energy consumption.
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spelling pubmed-87486782022-01-20 Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst Li, Zhenhua Yan, Yifan Xu, Si-Min Zhou, Hua Xu, Ming Ma, Lina Shao, Mingfei Kong, Xianggui Wang, Bin Zheng, Lirong Duan, Haohong Nat Commun Article Electrochemical alcohols oxidation offers a promising approach to produce valuable chemicals and facilitate coupled H(2) production. However, the corresponding current density is very low at moderate cell potential that substantially limits the overall productivity. Here we report the electrooxidation of benzyl alcohol coupled with H(2) production at high current density (540 mA cm(−2) at 1.5 V vs. RHE) over a cooperative catalyst of Au nanoparticles supported on cobalt oxyhydroxide nanosheets (Au/CoOOH). The absolute current can further reach 4.8 A at 2.0 V in a more realistic two-electrode membrane-free flow electrolyzer. Experimental combined with theoretical results indicate that the benzyl alcohol can be enriched at Au/CoOOH interface and oxidized by the electrophilic oxygen species (OH*) generated on CoOOH, leading to higher activity than pure Au. Based on the finding that the catalyst can be reversibly oxidized/reduced at anodic potential/open circuit, we design an intermittent potential (IP) strategy for long-term alcohol electrooxidation that achieves high current density (>250 mA cm(−2)) over 24 h with promoted productivity and decreased energy consumption. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748678/ /pubmed/35013339 http://dx.doi.org/10.1038/s41467-021-27806-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Zhenhua
Yan, Yifan
Xu, Si-Min
Zhou, Hua
Xu, Ming
Ma, Lina
Shao, Mingfei
Kong, Xianggui
Wang, Bin
Zheng, Lirong
Duan, Haohong
Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst
title Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst
title_full Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst
title_fullStr Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst
title_full_unstemmed Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst
title_short Alcohols electrooxidation coupled with H(2) production at high current densities promoted by a cooperative catalyst
title_sort alcohols electrooxidation coupled with h(2) production at high current densities promoted by a cooperative catalyst
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748678/
https://www.ncbi.nlm.nih.gov/pubmed/35013339
http://dx.doi.org/10.1038/s41467-021-27806-3
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