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Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water
Solar-driven CO(2) reduction by abundant water to alcohols can supply sustainable liquid fuels and alleviate global warming. However, the sluggish water oxidation reaction has been hardly reported to be efficient and selective in CO(2) conversion due to fast charge recombination. Here, using transie...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242399/ https://www.ncbi.nlm.nih.gov/pubmed/32439875 http://dx.doi.org/10.1038/s41467-020-16227-3 |
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author | Wang, Yiou Liu, Xu Han, Xiaoyu Godin, Robert Chen, Jialu Zhou, Wuzong Jiang, Chaoran Thompson, Jamie F. Mustafa, K. Bayazit Shevlin, Stephen A. Durrant, James R. Guo, Zhengxiao Tang, Junwang |
author_facet | Wang, Yiou Liu, Xu Han, Xiaoyu Godin, Robert Chen, Jialu Zhou, Wuzong Jiang, Chaoran Thompson, Jamie F. Mustafa, K. Bayazit Shevlin, Stephen A. Durrant, James R. Guo, Zhengxiao Tang, Junwang |
author_sort | Wang, Yiou |
collection | PubMed |
description | Solar-driven CO(2) reduction by abundant water to alcohols can supply sustainable liquid fuels and alleviate global warming. However, the sluggish water oxidation reaction has been hardly reported to be efficient and selective in CO(2) conversion due to fast charge recombination. Here, using transient absorption spectroscopy, we demonstrate that microwave-synthesised carbon-dots ((m)CD) possess unique hole-accepting nature, prolonging the electron lifetime (t(50%)) of carbon nitride (CN) by six folds, favouring a six-electron product. (m)CD-decorated CN stably produces stoichiometric oxygen and methanol from water and CO(2) with nearly 100% selectivity to methanol and internal quantum efficiency of 2.1% in the visible region, further confirmed by isotopic labelling. Such (m)CD rapidly extracts holes from CN and prevents the surface adsorption of methanol, favourably oxidising water over methanol and enhancing the selective CO(2) reduction to alcohols. This work provides a unique strategy for efficient and highly selective CO(2) reduction by water to high-value chemicals. |
format | Online Article Text |
id | pubmed-7242399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72423992020-05-29 Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water Wang, Yiou Liu, Xu Han, Xiaoyu Godin, Robert Chen, Jialu Zhou, Wuzong Jiang, Chaoran Thompson, Jamie F. Mustafa, K. Bayazit Shevlin, Stephen A. Durrant, James R. Guo, Zhengxiao Tang, Junwang Nat Commun Article Solar-driven CO(2) reduction by abundant water to alcohols can supply sustainable liquid fuels and alleviate global warming. However, the sluggish water oxidation reaction has been hardly reported to be efficient and selective in CO(2) conversion due to fast charge recombination. Here, using transient absorption spectroscopy, we demonstrate that microwave-synthesised carbon-dots ((m)CD) possess unique hole-accepting nature, prolonging the electron lifetime (t(50%)) of carbon nitride (CN) by six folds, favouring a six-electron product. (m)CD-decorated CN stably produces stoichiometric oxygen and methanol from water and CO(2) with nearly 100% selectivity to methanol and internal quantum efficiency of 2.1% in the visible region, further confirmed by isotopic labelling. Such (m)CD rapidly extracts holes from CN and prevents the surface adsorption of methanol, favourably oxidising water over methanol and enhancing the selective CO(2) reduction to alcohols. This work provides a unique strategy for efficient and highly selective CO(2) reduction by water to high-value chemicals. Nature Publishing Group UK 2020-05-21 /pmc/articles/PMC7242399/ /pubmed/32439875 http://dx.doi.org/10.1038/s41467-020-16227-3 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Wang, Yiou Liu, Xu Han, Xiaoyu Godin, Robert Chen, Jialu Zhou, Wuzong Jiang, Chaoran Thompson, Jamie F. Mustafa, K. Bayazit Shevlin, Stephen A. Durrant, James R. Guo, Zhengxiao Tang, Junwang Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water |
title | Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water |
title_full | Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water |
title_fullStr | Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water |
title_full_unstemmed | Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water |
title_short | Unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water |
title_sort | unique hole-accepting carbon-dots promoting selective carbon dioxide reduction nearly 100% to methanol by pure water |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242399/ https://www.ncbi.nlm.nih.gov/pubmed/32439875 http://dx.doi.org/10.1038/s41467-020-16227-3 |
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