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Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction
Transitional metal-nitrogen-carbon system is a promising candidate to replace the Pt-based electrocatalyst due to its superior activity, durability and cost effectiveness. In this study, we have designed a simple strategy to fabricate carbon nanotubes-supported binary-nitrogen-carbon catalyst via we...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667450/ https://www.ncbi.nlm.nih.gov/pubmed/31363157 http://dx.doi.org/10.1038/s41598-019-47575-w |
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author | Begum, Halima Ahmed, Mohammad Shamsuddin Lee, Dong-Weon Kim, Young-Bae |
author_facet | Begum, Halima Ahmed, Mohammad Shamsuddin Lee, Dong-Weon Kim, Young-Bae |
author_sort | Begum, Halima |
collection | PubMed |
description | Transitional metal-nitrogen-carbon system is a promising candidate to replace the Pt-based electrocatalyst due to its superior activity, durability and cost effectiveness. In this study, we have designed a simple strategy to fabricate carbon nanotubes-supported binary-nitrogen-carbon catalyst via wet-chemical method. Palladium and transitional metals (M, i.e. manganese cobalt and copper) nanoparticles are anchored through four-nitrogen system onto carbon nanotubes (denoted as PdM-N(4)/CNTs). This material has been used as bifunctional electrocatalyst for electrochemical ethanol oxidation reaction and hydrogen evolution reaction for the first time. The N(4)-linked nanoparticles onto carbon nanotubes plays a crucial role in intrinsic catalytic activity for both reactions in 1 M KOH electrolyte. Among three PdM-N(4)/CNTs catalysts, the PdMn-N(4)/CNTs catalyst exhibits higher catalytic activity in terms of current density, mass activity and stability compared to the benchmark Pt/C. The robust electrocatalysis are inherited from the better attachment of PdMn through N(4)-system onto carbon nanotubes, comparatively smaller particles formation with better dispersion and higher electrical conductivity. |
format | Online Article Text |
id | pubmed-6667450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66674502019-08-06 Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction Begum, Halima Ahmed, Mohammad Shamsuddin Lee, Dong-Weon Kim, Young-Bae Sci Rep Article Transitional metal-nitrogen-carbon system is a promising candidate to replace the Pt-based electrocatalyst due to its superior activity, durability and cost effectiveness. In this study, we have designed a simple strategy to fabricate carbon nanotubes-supported binary-nitrogen-carbon catalyst via wet-chemical method. Palladium and transitional metals (M, i.e. manganese cobalt and copper) nanoparticles are anchored through four-nitrogen system onto carbon nanotubes (denoted as PdM-N(4)/CNTs). This material has been used as bifunctional electrocatalyst for electrochemical ethanol oxidation reaction and hydrogen evolution reaction for the first time. The N(4)-linked nanoparticles onto carbon nanotubes plays a crucial role in intrinsic catalytic activity for both reactions in 1 M KOH electrolyte. Among three PdM-N(4)/CNTs catalysts, the PdMn-N(4)/CNTs catalyst exhibits higher catalytic activity in terms of current density, mass activity and stability compared to the benchmark Pt/C. The robust electrocatalysis are inherited from the better attachment of PdMn through N(4)-system onto carbon nanotubes, comparatively smaller particles formation with better dispersion and higher electrical conductivity. Nature Publishing Group UK 2019-07-30 /pmc/articles/PMC6667450/ /pubmed/31363157 http://dx.doi.org/10.1038/s41598-019-47575-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Begum, Halima Ahmed, Mohammad Shamsuddin Lee, Dong-Weon Kim, Young-Bae Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction |
title | Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction |
title_full | Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction |
title_fullStr | Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction |
title_full_unstemmed | Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction |
title_short | Carbon nanotubes-based PdM bimetallic catalysts through N(4)-system for efficient ethanol oxidation and hydrogen evolution reaction |
title_sort | carbon nanotubes-based pdm bimetallic catalysts through n(4)-system for efficient ethanol oxidation and hydrogen evolution reaction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667450/ https://www.ncbi.nlm.nih.gov/pubmed/31363157 http://dx.doi.org/10.1038/s41598-019-47575-w |
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