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Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction
Rational design and synthesis of superior electrocatalysts for ethanol oxidation is crucial to practical applications of direct ethanol fuel cells. Here, we report that the construction of Pd-Zn dual sites with well exposure and uniformity can significantly improve the efficiency of ethanol electro-...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421426/ https://www.ncbi.nlm.nih.gov/pubmed/34489455 http://dx.doi.org/10.1038/s41467-021-25600-9 |
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author | Qiu, Yajun Zhang, Jian Jin, Jing Sun, Jiaqiang Tang, Haolin Chen, Qingqing Zhang, Zedong Sun, Wenming Meng, Ge Xu, Qi Zhu, Youqi Han, Aijuan Gu, Lin Wang, Dingsheng Li, Yadong |
author_facet | Qiu, Yajun Zhang, Jian Jin, Jing Sun, Jiaqiang Tang, Haolin Chen, Qingqing Zhang, Zedong Sun, Wenming Meng, Ge Xu, Qi Zhu, Youqi Han, Aijuan Gu, Lin Wang, Dingsheng Li, Yadong |
author_sort | Qiu, Yajun |
collection | PubMed |
description | Rational design and synthesis of superior electrocatalysts for ethanol oxidation is crucial to practical applications of direct ethanol fuel cells. Here, we report that the construction of Pd-Zn dual sites with well exposure and uniformity can significantly improve the efficiency of ethanol electro-oxidation. Through synthetic method control, Pd-Zn dual sites on intermetallic PdZn nanoparticles, Pd-Pd sites on Pd nanoparticles and individual Pd sites are respectively obtained on the same N-doped carbon coated ZnO support. Compared with Pd-Pd sites and individual Pd sites, Pd-Zn dual sites display much higher activity for ethanol electro-oxidation, exceeding that of commercial Pd/C by a factor of ~24. Further computational studies disclose that Pd-Zn dual sites promote the adsorption of ethanol and hydroxide ion to optimize the electro-oxidation pathway with dramatically reduced energy barriers, leading to the superior activity. This work provides valuable clues for developing high-performance ethanol electro-oxidation catalysts for fuel cells. |
format | Online Article Text |
id | pubmed-8421426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84214262021-09-22 Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction Qiu, Yajun Zhang, Jian Jin, Jing Sun, Jiaqiang Tang, Haolin Chen, Qingqing Zhang, Zedong Sun, Wenming Meng, Ge Xu, Qi Zhu, Youqi Han, Aijuan Gu, Lin Wang, Dingsheng Li, Yadong Nat Commun Article Rational design and synthesis of superior electrocatalysts for ethanol oxidation is crucial to practical applications of direct ethanol fuel cells. Here, we report that the construction of Pd-Zn dual sites with well exposure and uniformity can significantly improve the efficiency of ethanol electro-oxidation. Through synthetic method control, Pd-Zn dual sites on intermetallic PdZn nanoparticles, Pd-Pd sites on Pd nanoparticles and individual Pd sites are respectively obtained on the same N-doped carbon coated ZnO support. Compared with Pd-Pd sites and individual Pd sites, Pd-Zn dual sites display much higher activity for ethanol electro-oxidation, exceeding that of commercial Pd/C by a factor of ~24. Further computational studies disclose that Pd-Zn dual sites promote the adsorption of ethanol and hydroxide ion to optimize the electro-oxidation pathway with dramatically reduced energy barriers, leading to the superior activity. This work provides valuable clues for developing high-performance ethanol electro-oxidation catalysts for fuel cells. Nature Publishing Group UK 2021-09-06 /pmc/articles/PMC8421426/ /pubmed/34489455 http://dx.doi.org/10.1038/s41467-021-25600-9 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Qiu, Yajun Zhang, Jian Jin, Jing Sun, Jiaqiang Tang, Haolin Chen, Qingqing Zhang, Zedong Sun, Wenming Meng, Ge Xu, Qi Zhu, Youqi Han, Aijuan Gu, Lin Wang, Dingsheng Li, Yadong Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction |
title | Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction |
title_full | Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction |
title_fullStr | Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction |
title_full_unstemmed | Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction |
title_short | Construction of Pd-Zn dual sites to enhance the performance for ethanol electro-oxidation reaction |
title_sort | construction of pd-zn dual sites to enhance the performance for ethanol electro-oxidation reaction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421426/ https://www.ncbi.nlm.nih.gov/pubmed/34489455 http://dx.doi.org/10.1038/s41467-021-25600-9 |
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