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Surface Protonics Promotes Catalysis

Catalytic steam reforming of methane for hydrogen production proceeds even at 473 K over 1 wt% Pd/CeO(2) catalyst in an electric field, thanks to the surface protonics. Kinetic analyses demonstrated the synergetic effect between catalytic reaction and electric field, revealing strengthened water pre...

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Autores principales: Manabe, R., Okada, S., Inagaki, R., Oshima, K., Ogo, S., Sekine, Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131306/
https://www.ncbi.nlm.nih.gov/pubmed/27905505
http://dx.doi.org/10.1038/srep38007
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author Manabe, R.
Okada, S.
Inagaki, R.
Oshima, K.
Ogo, S.
Sekine, Y.
author_facet Manabe, R.
Okada, S.
Inagaki, R.
Oshima, K.
Ogo, S.
Sekine, Y.
author_sort Manabe, R.
collection PubMed
description Catalytic steam reforming of methane for hydrogen production proceeds even at 473 K over 1 wt% Pd/CeO(2) catalyst in an electric field, thanks to the surface protonics. Kinetic analyses demonstrated the synergetic effect between catalytic reaction and electric field, revealing strengthened water pressure dependence of the reaction rate when applying an electric field, with one-third the apparent activation energy at the lower reaction temperature range. Operando–IR measurements revealed that proton conduction via adsorbed water on the catalyst surface occurred during electric field application. Methane was activated by proton collision at the Pd–CeO(2) interface, based on the inverse kinetic isotope effect. Proton conduction on the catalyst surface plays an important role in methane activation at low temperature. This report is the first describing promotion of the catalytic reaction by surface protonics.
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spelling pubmed-51313062016-12-15 Surface Protonics Promotes Catalysis Manabe, R. Okada, S. Inagaki, R. Oshima, K. Ogo, S. Sekine, Y. Sci Rep Article Catalytic steam reforming of methane for hydrogen production proceeds even at 473 K over 1 wt% Pd/CeO(2) catalyst in an electric field, thanks to the surface protonics. Kinetic analyses demonstrated the synergetic effect between catalytic reaction and electric field, revealing strengthened water pressure dependence of the reaction rate when applying an electric field, with one-third the apparent activation energy at the lower reaction temperature range. Operando–IR measurements revealed that proton conduction via adsorbed water on the catalyst surface occurred during electric field application. Methane was activated by proton collision at the Pd–CeO(2) interface, based on the inverse kinetic isotope effect. Proton conduction on the catalyst surface plays an important role in methane activation at low temperature. This report is the first describing promotion of the catalytic reaction by surface protonics. Nature Publishing Group 2016-12-01 /pmc/articles/PMC5131306/ /pubmed/27905505 http://dx.doi.org/10.1038/srep38007 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Manabe, R.
Okada, S.
Inagaki, R.
Oshima, K.
Ogo, S.
Sekine, Y.
Surface Protonics Promotes Catalysis
title Surface Protonics Promotes Catalysis
title_full Surface Protonics Promotes Catalysis
title_fullStr Surface Protonics Promotes Catalysis
title_full_unstemmed Surface Protonics Promotes Catalysis
title_short Surface Protonics Promotes Catalysis
title_sort surface protonics promotes catalysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131306/
https://www.ncbi.nlm.nih.gov/pubmed/27905505
http://dx.doi.org/10.1038/srep38007
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