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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
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.
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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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