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Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution
Electrochemical deposition is a facile strategy to prepare functional materials but suffers from limitation in thin films and uncontrollable interface engineering. Here we report a universal electrosynthesis of metal hydroxides/oxides on varied substrates via reduction of oxyacid anions. On graphiti...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006371/ https://www.ncbi.nlm.nih.gov/pubmed/29915288 http://dx.doi.org/10.1038/s41467-018-04788-3 |
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author | Yan, Zhenhua Sun, Hongming Chen, Xiang Liu, Huanhuan Zhao, Yaran Li, Haixia Xie, Wei Cheng, Fangyi Chen, Jun |
author_facet | Yan, Zhenhua Sun, Hongming Chen, Xiang Liu, Huanhuan Zhao, Yaran Li, Haixia Xie, Wei Cheng, Fangyi Chen, Jun |
author_sort | Yan, Zhenhua |
collection | PubMed |
description | Electrochemical deposition is a facile strategy to prepare functional materials but suffers from limitation in thin films and uncontrollable interface engineering. Here we report a universal electrosynthesis of metal hydroxides/oxides on varied substrates via reduction of oxyacid anions. On graphitic substrates, we find that the insertion of nitrate ion in graphene layers significantly enhances the electrodeposit–support interface, resulting in high mass loading and super hydrophilic/aerophobic properties. For the electrocatalytic oxygen evolution reaction, the nanocrystalline cerium dioxide and amorphous nickel hydroxide co-electrodeposited on graphite exhibits low overpotential (177 mV@10 mA cm(−2)) and sustains long-term durability (over 300 h) at a large current density of 1000 mA cm(−2). In situ Raman and operando X-ray diffraction unravel that the integration of cerium promotes the formation of electrocatalytically active gamma-phase nickel oxyhydroxide with exposed (003) facets. Therefore, combining anion intercalation with cathodic electrodeposition allows building robust electrodes with high electrochemical performance. |
format | Online Article Text |
id | pubmed-6006371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60063712018-06-20 Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution Yan, Zhenhua Sun, Hongming Chen, Xiang Liu, Huanhuan Zhao, Yaran Li, Haixia Xie, Wei Cheng, Fangyi Chen, Jun Nat Commun Article Electrochemical deposition is a facile strategy to prepare functional materials but suffers from limitation in thin films and uncontrollable interface engineering. Here we report a universal electrosynthesis of metal hydroxides/oxides on varied substrates via reduction of oxyacid anions. On graphitic substrates, we find that the insertion of nitrate ion in graphene layers significantly enhances the electrodeposit–support interface, resulting in high mass loading and super hydrophilic/aerophobic properties. For the electrocatalytic oxygen evolution reaction, the nanocrystalline cerium dioxide and amorphous nickel hydroxide co-electrodeposited on graphite exhibits low overpotential (177 mV@10 mA cm(−2)) and sustains long-term durability (over 300 h) at a large current density of 1000 mA cm(−2). In situ Raman and operando X-ray diffraction unravel that the integration of cerium promotes the formation of electrocatalytically active gamma-phase nickel oxyhydroxide with exposed (003) facets. Therefore, combining anion intercalation with cathodic electrodeposition allows building robust electrodes with high electrochemical performance. Nature Publishing Group UK 2018-06-18 /pmc/articles/PMC6006371/ /pubmed/29915288 http://dx.doi.org/10.1038/s41467-018-04788-3 Text en © The Author(s) 2018 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 Yan, Zhenhua Sun, Hongming Chen, Xiang Liu, Huanhuan Zhao, Yaran Li, Haixia Xie, Wei Cheng, Fangyi Chen, Jun Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution |
title | Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution |
title_full | Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution |
title_fullStr | Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution |
title_full_unstemmed | Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution |
title_short | Anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution |
title_sort | anion insertion enhanced electrodeposition of robust metal hydroxide/oxide electrodes for oxygen evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006371/ https://www.ncbi.nlm.nih.gov/pubmed/29915288 http://dx.doi.org/10.1038/s41467-018-04788-3 |
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