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Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion of CO(2) and H(2) to CH(4) with a High Photon-to-Methane Efficiency
[Image: see text] Methane, which has a high energy storage density and is safely stored and transported in our existing infrastructure, can be produced through conversion of the undesired energy carrier H(2) with CO(2). Methane production with standard transition-metal catalysts requires high-temper...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649275/ https://www.ncbi.nlm.nih.gov/pubmed/31459835 http://dx.doi.org/10.1021/acsomega.9b00581 |
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author | Sastre, Francesc Versluis, Caroline Meulendijks, Nicole Rodríguez-Fernández, Jessica Sweelssen, Jorgen Elen, Ken Van Bael, Marlies K. den Hartog, Tim Verheijen, Marcel A. Buskens, Pascal |
author_facet | Sastre, Francesc Versluis, Caroline Meulendijks, Nicole Rodríguez-Fernández, Jessica Sweelssen, Jorgen Elen, Ken Van Bael, Marlies K. den Hartog, Tim Verheijen, Marcel A. Buskens, Pascal |
author_sort | Sastre, Francesc |
collection | PubMed |
description | [Image: see text] Methane, which has a high energy storage density and is safely stored and transported in our existing infrastructure, can be produced through conversion of the undesired energy carrier H(2) with CO(2). Methane production with standard transition-metal catalysts requires high-temperature activation (300–500 °C). Alternatively, semiconductor metal oxide photocatalysts can be used, but they require high-intensity UV light. Here, we report a Ru metal catalyst that facilitates methanation below 250 °C using sunlight as an energy source. Although at low solar intensity (1 sun) the activity of the Ru catalyst is mainly attributed to thermal effects, we identified a large nonthermal contribution at slightly elevated intensities (5.7 and 8.5 sun) resulting in a high photon-to-methane efficiency of up to 55% over the whole solar spectrum. We attribute the excellent sunlight-harvesting ability of the catalyst and the high photon-to-methane efficiency to its UV–vis–NIR plasmonic absorption. Our highly efficient conversion of H(2) to methane is a promising technology to simultaneously accelerate the energy transition and reduce CO(2) emissions. |
format | Online Article Text |
id | pubmed-6649275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66492752019-08-27 Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion of CO(2) and H(2) to CH(4) with a High Photon-to-Methane Efficiency Sastre, Francesc Versluis, Caroline Meulendijks, Nicole Rodríguez-Fernández, Jessica Sweelssen, Jorgen Elen, Ken Van Bael, Marlies K. den Hartog, Tim Verheijen, Marcel A. Buskens, Pascal ACS Omega [Image: see text] Methane, which has a high energy storage density and is safely stored and transported in our existing infrastructure, can be produced through conversion of the undesired energy carrier H(2) with CO(2). Methane production with standard transition-metal catalysts requires high-temperature activation (300–500 °C). Alternatively, semiconductor metal oxide photocatalysts can be used, but they require high-intensity UV light. Here, we report a Ru metal catalyst that facilitates methanation below 250 °C using sunlight as an energy source. Although at low solar intensity (1 sun) the activity of the Ru catalyst is mainly attributed to thermal effects, we identified a large nonthermal contribution at slightly elevated intensities (5.7 and 8.5 sun) resulting in a high photon-to-methane efficiency of up to 55% over the whole solar spectrum. We attribute the excellent sunlight-harvesting ability of the catalyst and the high photon-to-methane efficiency to its UV–vis–NIR plasmonic absorption. Our highly efficient conversion of H(2) to methane is a promising technology to simultaneously accelerate the energy transition and reduce CO(2) emissions. American Chemical Society 2019-04-23 /pmc/articles/PMC6649275/ /pubmed/31459835 http://dx.doi.org/10.1021/acsomega.9b00581 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Sastre, Francesc Versluis, Caroline Meulendijks, Nicole Rodríguez-Fernández, Jessica Sweelssen, Jorgen Elen, Ken Van Bael, Marlies K. den Hartog, Tim Verheijen, Marcel A. Buskens, Pascal Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion of CO(2) and H(2) to CH(4) with a High Photon-to-Methane Efficiency |
title | Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion
of CO(2) and H(2) to CH(4) with a High
Photon-to-Methane Efficiency |
title_full | Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion
of CO(2) and H(2) to CH(4) with a High
Photon-to-Methane Efficiency |
title_fullStr | Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion
of CO(2) and H(2) to CH(4) with a High
Photon-to-Methane Efficiency |
title_full_unstemmed | Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion
of CO(2) and H(2) to CH(4) with a High
Photon-to-Methane Efficiency |
title_short | Sunlight-Fueled, Low-Temperature Ru-Catalyzed Conversion
of CO(2) and H(2) to CH(4) with a High
Photon-to-Methane Efficiency |
title_sort | sunlight-fueled, low-temperature ru-catalyzed conversion
of co(2) and h(2) to ch(4) with a high
photon-to-methane efficiency |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6649275/ https://www.ncbi.nlm.nih.gov/pubmed/31459835 http://dx.doi.org/10.1021/acsomega.9b00581 |
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