Li, Xiyi;
Wang, Chao;
Tang, Junwang;
(2022)
Methane transformation by photocatalysis.
Nature Reviews Materials
, 7
pp. 617-632.
10.1038/s41578-022-00422-3.
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Abstract
Methane hydrate and shale gas are predicted to have substantial reserves, far beyond the sum of other fossil fuels. Using methane instead of crude oil as a building block is, thus, a very attractive strategy for synthesizing valuable chemicals. Because methane is so inert, its direct conversion needs a high activation energy and typically requires harsh reaction conditions or strong oxidants. Photocatalysis, which employs photons operated under very mild conditions, is a promising technology to reduce the thermodynamic barrier in direct methane conversion and to avoid the common issues of overoxidation and catalyst deactivation. In this Review, we cover the development of photocatalysts and co-catalysts, including the use of inorganic materials and polymeric semiconductors, and explain how the use of batch or flow reaction systems affects the reaction kinetics and product selectivity. We also discuss efforts to understand the underlying reaction mechanisms from both a photophysical and a chemical perspective. Finally, we present our view of the challenges facing this field and suggest potential solutions.
Type: | Article |
---|---|
Title: | Methane transformation by photocatalysis |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1038/s41578-022-00422-3 |
Publisher version: | https://doi.org/10.1038/s41578-022-00422-3 |
Language: | English |
Additional information: | This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions. |
Keywords: | Materials Science, Photocatalysis |
UCL classification: | UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science > Dept of Chemical Engineering UCL > Provost and Vice Provost Offices > UCL BEAMS UCL |
URI: | https://discovery.ucl.ac.uk/id/eprint/10148526 |




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