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Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions
Direct partial oxidation of methane to liquid oxygenates has been regarded as a potential route to valorize methane. However, CH(4) activation usually requires a high temperature and pressure, which lowers the feasibility of the reaction. Here, we propose an electro-assisted approach for the partial...
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/PMC10404228/ https://www.ncbi.nlm.nih.gov/pubmed/37543676 http://dx.doi.org/10.1038/s41467-023-40415-6 |
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author | Kim, Jiwon Kim, Jae Hyung Oh, Cheoulwoo Yun, Hyewon Lee, Eunchong Oh, Hyung-Suk Park, Jong Hyeok Hwang, Yun Jeong |
author_facet | Kim, Jiwon Kim, Jae Hyung Oh, Cheoulwoo Yun, Hyewon Lee, Eunchong Oh, Hyung-Suk Park, Jong Hyeok Hwang, Yun Jeong |
author_sort | Kim, Jiwon |
collection | PubMed |
description | Direct partial oxidation of methane to liquid oxygenates has been regarded as a potential route to valorize methane. However, CH(4) activation usually requires a high temperature and pressure, which lowers the feasibility of the reaction. Here, we propose an electro-assisted approach for the partial oxidation of methane, using in-situ cathodically generated reactive oxygen species, at ambient temperature and pressure. Upon using acid-treated carbon as the electrocatalyst, the electro-assisted system enables the partial oxidation of methane in an acidic electrolyte to produce oxygenated liquid products. We also demonstrate a high production rate of oxygenates (18.9 μmol h(−1)) with selective HCOOH production. Mechanistic analysis reveals that reactive oxygen species such as ∙OH and ∙OOH radicals are produced and activate CH(4) and CH(3)OH. In addition, unstable CH(3)OOH generated from methane partial oxidation can be additionally reduced to CH(3)OH on the cathode, and so-produced CH(3)OH is further oxidized to HCOOH, allowing selective methane partial oxidation. |
format | Online Article Text |
id | pubmed-10404228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104042282023-08-07 Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions Kim, Jiwon Kim, Jae Hyung Oh, Cheoulwoo Yun, Hyewon Lee, Eunchong Oh, Hyung-Suk Park, Jong Hyeok Hwang, Yun Jeong Nat Commun Article Direct partial oxidation of methane to liquid oxygenates has been regarded as a potential route to valorize methane. However, CH(4) activation usually requires a high temperature and pressure, which lowers the feasibility of the reaction. Here, we propose an electro-assisted approach for the partial oxidation of methane, using in-situ cathodically generated reactive oxygen species, at ambient temperature and pressure. Upon using acid-treated carbon as the electrocatalyst, the electro-assisted system enables the partial oxidation of methane in an acidic electrolyte to produce oxygenated liquid products. We also demonstrate a high production rate of oxygenates (18.9 μmol h(−1)) with selective HCOOH production. Mechanistic analysis reveals that reactive oxygen species such as ∙OH and ∙OOH radicals are produced and activate CH(4) and CH(3)OH. In addition, unstable CH(3)OOH generated from methane partial oxidation can be additionally reduced to CH(3)OH on the cathode, and so-produced CH(3)OH is further oxidized to HCOOH, allowing selective methane partial oxidation. Nature Publishing Group UK 2023-08-05 /pmc/articles/PMC10404228/ /pubmed/37543676 http://dx.doi.org/10.1038/s41467-023-40415-6 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 Kim, Jiwon Kim, Jae Hyung Oh, Cheoulwoo Yun, Hyewon Lee, Eunchong Oh, Hyung-Suk Park, Jong Hyeok Hwang, Yun Jeong Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions |
title | Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions |
title_full | Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions |
title_fullStr | Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions |
title_full_unstemmed | Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions |
title_short | Electro-assisted methane oxidation to formic acid via in-situ cathodically generated H(2)O(2) under ambient conditions |
title_sort | electro-assisted methane oxidation to formic acid via in-situ cathodically generated h(2)o(2) under ambient conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404228/ https://www.ncbi.nlm.nih.gov/pubmed/37543676 http://dx.doi.org/10.1038/s41467-023-40415-6 |
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