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Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports

The use of ammonia as a hydrogen vector has the potential to unlock the hydrogen economy. In this context, this paper presents novel insights into improving the ammonia decomposition activity of ruthenium nanoparticles supported on carbon nanotubes (CNT) by nitrogen doping. Our results can be applie...

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Autores principales: Bell, Tamsin E., Zhan, Guowu, Wu, Kejun, Zeng, Hua Chun, Torrente-Murciano, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961473/
https://www.ncbi.nlm.nih.gov/pubmed/32009773
http://dx.doi.org/10.1007/s11244-017-0806-0
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author Bell, Tamsin E.
Zhan, Guowu
Wu, Kejun
Zeng, Hua Chun
Torrente-Murciano, Laura
author_facet Bell, Tamsin E.
Zhan, Guowu
Wu, Kejun
Zeng, Hua Chun
Torrente-Murciano, Laura
author_sort Bell, Tamsin E.
collection PubMed
description The use of ammonia as a hydrogen vector has the potential to unlock the hydrogen economy. In this context, this paper presents novel insights into improving the ammonia decomposition activity of ruthenium nanoparticles supported on carbon nanotubes (CNT) by nitrogen doping. Our results can be applied to develop more active systems capable of delivering hydrogen on demand, with a view to move towards the low temperature target of less than 150 °C. Herein we demonstrate that nitrogen doping of the CNT support enhances the activity of ruthenium nanoparticles for the low temperature ammonia decomposition with turnover frequency numbers at 400 °C of 6200 LH(2) mol(Ru) (−1) h(−1), higher than the corresponding value of unmodified CNT supports under the same conditions (4400 LH(2) mol(Ru) (−1) h(− 1)), despite presenting similar ruthenium particle sizes. However, when the nitrogen doping process is carried out with cetyltrimethylammonium bromide (CTAB) to enhance the dispersion of CNTs, the catalyst becomes virtually inactive despite the small ruthenium particle size, likely due to interference of CTAB, weakening the metal–support interaction. Our results demonstrate that the low temperature ammonia decomposition activity of ruthenium can be enhanced by nitrogen doping of the CNT support due to simultaneously increasing the support’s conductivity and basicity, electronically modifying the ruthenium active sites and promoting a strong metal–support interaction.
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spelling pubmed-69614732020-01-29 Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports Bell, Tamsin E. Zhan, Guowu Wu, Kejun Zeng, Hua Chun Torrente-Murciano, Laura Top Catal Original Paper The use of ammonia as a hydrogen vector has the potential to unlock the hydrogen economy. In this context, this paper presents novel insights into improving the ammonia decomposition activity of ruthenium nanoparticles supported on carbon nanotubes (CNT) by nitrogen doping. Our results can be applied to develop more active systems capable of delivering hydrogen on demand, with a view to move towards the low temperature target of less than 150 °C. Herein we demonstrate that nitrogen doping of the CNT support enhances the activity of ruthenium nanoparticles for the low temperature ammonia decomposition with turnover frequency numbers at 400 °C of 6200 LH(2) mol(Ru) (−1) h(−1), higher than the corresponding value of unmodified CNT supports under the same conditions (4400 LH(2) mol(Ru) (−1) h(− 1)), despite presenting similar ruthenium particle sizes. However, when the nitrogen doping process is carried out with cetyltrimethylammonium bromide (CTAB) to enhance the dispersion of CNTs, the catalyst becomes virtually inactive despite the small ruthenium particle size, likely due to interference of CTAB, weakening the metal–support interaction. Our results demonstrate that the low temperature ammonia decomposition activity of ruthenium can be enhanced by nitrogen doping of the CNT support due to simultaneously increasing the support’s conductivity and basicity, electronically modifying the ruthenium active sites and promoting a strong metal–support interaction. Springer US 2017-06-29 2017 /pmc/articles/PMC6961473/ /pubmed/32009773 http://dx.doi.org/10.1007/s11244-017-0806-0 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Paper
Bell, Tamsin E.
Zhan, Guowu
Wu, Kejun
Zeng, Hua Chun
Torrente-Murciano, Laura
Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports
title Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports
title_full Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports
title_fullStr Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports
title_full_unstemmed Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports
title_short Modification of Ammonia Decomposition Activity of Ruthenium Nanoparticles by N-Doping of CNT Supports
title_sort modification of ammonia decomposition activity of ruthenium nanoparticles by n-doping of cnt supports
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961473/
https://www.ncbi.nlm.nih.gov/pubmed/32009773
http://dx.doi.org/10.1007/s11244-017-0806-0
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