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Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products

In alkaline and neutral MEA CO(2) electrolyzers, CO(2) rapidly converts to (bi)carbonate, imposing a significant energy penalty arising from separating CO(2) from the anode gas outlets. Here we report a CO(2) electrolyzer uses a bipolar membrane (BPM) to convert (bi)carbonate back to CO(2), preventi...

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Autores principales: Xie, Ke, Miao, Rui Kai, Ozden, Adnan, Liu, Shijie, Chen, Zhu, Dinh, Cao-Thang, Huang, Jianan Erick, Xu, Qiucheng, Gabardo, Christine M., Lee, Geonhui, Edwards, Jonathan P., O’Brien, Colin P., Boettcher, Shannon W., Sinton, David, Sargent, Edward H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232613/
https://www.ncbi.nlm.nih.gov/pubmed/35750665
http://dx.doi.org/10.1038/s41467-022-31295-3
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author Xie, Ke
Miao, Rui Kai
Ozden, Adnan
Liu, Shijie
Chen, Zhu
Dinh, Cao-Thang
Huang, Jianan Erick
Xu, Qiucheng
Gabardo, Christine M.
Lee, Geonhui
Edwards, Jonathan P.
O’Brien, Colin P.
Boettcher, Shannon W.
Sinton, David
Sargent, Edward H.
author_facet Xie, Ke
Miao, Rui Kai
Ozden, Adnan
Liu, Shijie
Chen, Zhu
Dinh, Cao-Thang
Huang, Jianan Erick
Xu, Qiucheng
Gabardo, Christine M.
Lee, Geonhui
Edwards, Jonathan P.
O’Brien, Colin P.
Boettcher, Shannon W.
Sinton, David
Sargent, Edward H.
author_sort Xie, Ke
collection PubMed
description In alkaline and neutral MEA CO(2) electrolyzers, CO(2) rapidly converts to (bi)carbonate, imposing a significant energy penalty arising from separating CO(2) from the anode gas outlets. Here we report a CO(2) electrolyzer uses a bipolar membrane (BPM) to convert (bi)carbonate back to CO(2), preventing crossover; and that surpasses the single-pass utilization (SPU) limit (25% for multi-carbon products, C(2+)) suffered by previous neutral-media electrolyzers. We employ a stationary unbuffered catholyte layer between BPM and cathode to promote C(2+) products while ensuring that (bi)carbonate is converted back, in situ, to CO(2) near the cathode. We develop a model that enables the design of the catholyte layer, finding that limiting the diffusion path length of reverted CO(2) to ~10 μm balances the CO(2) diffusion flux with the regeneration rate. We report a single-pass CO(2) utilization of 78%, which lowers the energy associated with downstream separation of CO(2) by 10× compared with past systems.
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spelling pubmed-92326132022-06-26 Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products Xie, Ke Miao, Rui Kai Ozden, Adnan Liu, Shijie Chen, Zhu Dinh, Cao-Thang Huang, Jianan Erick Xu, Qiucheng Gabardo, Christine M. Lee, Geonhui Edwards, Jonathan P. O’Brien, Colin P. Boettcher, Shannon W. Sinton, David Sargent, Edward H. Nat Commun Article In alkaline and neutral MEA CO(2) electrolyzers, CO(2) rapidly converts to (bi)carbonate, imposing a significant energy penalty arising from separating CO(2) from the anode gas outlets. Here we report a CO(2) electrolyzer uses a bipolar membrane (BPM) to convert (bi)carbonate back to CO(2), preventing crossover; and that surpasses the single-pass utilization (SPU) limit (25% for multi-carbon products, C(2+)) suffered by previous neutral-media electrolyzers. We employ a stationary unbuffered catholyte layer between BPM and cathode to promote C(2+) products while ensuring that (bi)carbonate is converted back, in situ, to CO(2) near the cathode. We develop a model that enables the design of the catholyte layer, finding that limiting the diffusion path length of reverted CO(2) to ~10 μm balances the CO(2) diffusion flux with the regeneration rate. We report a single-pass CO(2) utilization of 78%, which lowers the energy associated with downstream separation of CO(2) by 10× compared with past systems. Nature Publishing Group UK 2022-06-24 /pmc/articles/PMC9232613/ /pubmed/35750665 http://dx.doi.org/10.1038/s41467-022-31295-3 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
Xie, Ke
Miao, Rui Kai
Ozden, Adnan
Liu, Shijie
Chen, Zhu
Dinh, Cao-Thang
Huang, Jianan Erick
Xu, Qiucheng
Gabardo, Christine M.
Lee, Geonhui
Edwards, Jonathan P.
O’Brien, Colin P.
Boettcher, Shannon W.
Sinton, David
Sargent, Edward H.
Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products
title Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products
title_full Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products
title_fullStr Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products
title_full_unstemmed Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products
title_short Bipolar membrane electrolyzers enable high single-pass CO(2) electroreduction to multicarbon products
title_sort bipolar membrane electrolyzers enable high single-pass co(2) electroreduction to multicarbon products
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232613/
https://www.ncbi.nlm.nih.gov/pubmed/35750665
http://dx.doi.org/10.1038/s41467-022-31295-3
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