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Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer
Ethylene glycol is a widely utilized commodity chemical, the production of which accounts for over 46 million tons of CO(2) emission annually. Here we report a paired electrocatalytic approach for ethylene glycol production from methanol. Carbon catalysts are effective in reducing formaldehyde into...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387065/ https://www.ncbi.nlm.nih.gov/pubmed/37516779 http://dx.doi.org/10.1038/s41467-023-40296-9 |
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author | Xia, Rong Wang, Ruoyu Hasa, Bjorn Lee, Ahryeon Liu, Yuanyue Ma, Xinbin Jiao, Feng |
author_facet | Xia, Rong Wang, Ruoyu Hasa, Bjorn Lee, Ahryeon Liu, Yuanyue Ma, Xinbin Jiao, Feng |
author_sort | Xia, Rong |
collection | PubMed |
description | Ethylene glycol is a widely utilized commodity chemical, the production of which accounts for over 46 million tons of CO(2) emission annually. Here we report a paired electrocatalytic approach for ethylene glycol production from methanol. Carbon catalysts are effective in reducing formaldehyde into ethylene glycol with a 92% Faradaic efficiency, whereas Pt catalysts at the anode enable formaldehyde production through methanol partial oxidation with a 75% Faradaic efficiency. With a membrane-electrode assembly configuration, we show the feasibility of ethylene glycol electrosynthesis from methanol in a single electrolyzer. The electrolyzer operates a full cell voltage of 3.2 V at a current density of 100 mA cm(−2), with a 60% reduction in energy consumption. Further investigations, using operando flow electrolyzer mass spectroscopy, isotopic labeling, and density functional theory (DFT) calculations, indicate that the desorption of a *CH(2)OH intermediate is the crucial step in determining the selectively towards ethylene glycol over methanol. |
format | Online Article Text |
id | pubmed-10387065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103870652023-07-31 Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer Xia, Rong Wang, Ruoyu Hasa, Bjorn Lee, Ahryeon Liu, Yuanyue Ma, Xinbin Jiao, Feng Nat Commun Article Ethylene glycol is a widely utilized commodity chemical, the production of which accounts for over 46 million tons of CO(2) emission annually. Here we report a paired electrocatalytic approach for ethylene glycol production from methanol. Carbon catalysts are effective in reducing formaldehyde into ethylene glycol with a 92% Faradaic efficiency, whereas Pt catalysts at the anode enable formaldehyde production through methanol partial oxidation with a 75% Faradaic efficiency. With a membrane-electrode assembly configuration, we show the feasibility of ethylene glycol electrosynthesis from methanol in a single electrolyzer. The electrolyzer operates a full cell voltage of 3.2 V at a current density of 100 mA cm(−2), with a 60% reduction in energy consumption. Further investigations, using operando flow electrolyzer mass spectroscopy, isotopic labeling, and density functional theory (DFT) calculations, indicate that the desorption of a *CH(2)OH intermediate is the crucial step in determining the selectively towards ethylene glycol over methanol. Nature Publishing Group UK 2023-07-29 /pmc/articles/PMC10387065/ /pubmed/37516779 http://dx.doi.org/10.1038/s41467-023-40296-9 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Xia, Rong Wang, Ruoyu Hasa, Bjorn Lee, Ahryeon Liu, Yuanyue Ma, Xinbin Jiao, Feng Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer |
title | Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer |
title_full | Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer |
title_fullStr | Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer |
title_full_unstemmed | Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer |
title_short | Electrosynthesis of ethylene glycol from C(1) feedstocks in a flow electrolyzer |
title_sort | electrosynthesis of ethylene glycol from c(1) feedstocks in a flow electrolyzer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387065/ https://www.ncbi.nlm.nih.gov/pubmed/37516779 http://dx.doi.org/10.1038/s41467-023-40296-9 |
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