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Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry
Highly porous iridium oxide structures are particularly well-suited for the preparation of porous catalyst layers needed in proton exchange membrane water electrolyzers. Herein, we report the formation of iridium oxide nanostructured cages, via a water-based process performed at room temperature, us...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580478/ https://www.ncbi.nlm.nih.gov/pubmed/36320917 http://dx.doi.org/10.1039/d2sc03640a |
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author | Elmaalouf, Marine Da Silva, Alexandre Duran, Silvia Tard, Cédric Comesaña-Hermo, Miguel Gam-Derouich, Sarra Briois, Valérie Alloyeau, Damien Giraud, Marion Piquemal, Jean-Yves Peron, Jennifer |
author_facet | Elmaalouf, Marine Da Silva, Alexandre Duran, Silvia Tard, Cédric Comesaña-Hermo, Miguel Gam-Derouich, Sarra Briois, Valérie Alloyeau, Damien Giraud, Marion Piquemal, Jean-Yves Peron, Jennifer |
author_sort | Elmaalouf, Marine |
collection | PubMed |
description | Highly porous iridium oxide structures are particularly well-suited for the preparation of porous catalyst layers needed in proton exchange membrane water electrolyzers. Herein, we report the formation of iridium oxide nanostructured cages, via a water-based process performed at room temperature, using cheap Cu(2)O cubes as the template. In this synthetic approach, based on Pearson's hard and soft acid–base theory, the replacement of the Cu(2)O core by an iridium shell is permitted by the difference in hardness/softness of cations and anions of the two reactants Cu(2)O and IrCl(3). Calcination followed by acid leaching allow the removal of residual copper oxide cores and leave IrO(2) hierarchical porous structures with outstanding activity toward the oxygen evolution reaction. Fundamental understanding of the reaction steps and identification of the intermediates are permitted by coupling a set of ex situ and in situ techniques including operando time-resolved X-ray absorption spectroscopy during the synthesis. |
format | Online Article Text |
id | pubmed-9580478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-95804782022-10-31 Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry Elmaalouf, Marine Da Silva, Alexandre Duran, Silvia Tard, Cédric Comesaña-Hermo, Miguel Gam-Derouich, Sarra Briois, Valérie Alloyeau, Damien Giraud, Marion Piquemal, Jean-Yves Peron, Jennifer Chem Sci Chemistry Highly porous iridium oxide structures are particularly well-suited for the preparation of porous catalyst layers needed in proton exchange membrane water electrolyzers. Herein, we report the formation of iridium oxide nanostructured cages, via a water-based process performed at room temperature, using cheap Cu(2)O cubes as the template. In this synthetic approach, based on Pearson's hard and soft acid–base theory, the replacement of the Cu(2)O core by an iridium shell is permitted by the difference in hardness/softness of cations and anions of the two reactants Cu(2)O and IrCl(3). Calcination followed by acid leaching allow the removal of residual copper oxide cores and leave IrO(2) hierarchical porous structures with outstanding activity toward the oxygen evolution reaction. Fundamental understanding of the reaction steps and identification of the intermediates are permitted by coupling a set of ex situ and in situ techniques including operando time-resolved X-ray absorption spectroscopy during the synthesis. The Royal Society of Chemistry 2022-09-23 /pmc/articles/PMC9580478/ /pubmed/36320917 http://dx.doi.org/10.1039/d2sc03640a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Elmaalouf, Marine Da Silva, Alexandre Duran, Silvia Tard, Cédric Comesaña-Hermo, Miguel Gam-Derouich, Sarra Briois, Valérie Alloyeau, Damien Giraud, Marion Piquemal, Jean-Yves Peron, Jennifer Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry |
title | Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry |
title_full | Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry |
title_fullStr | Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry |
title_full_unstemmed | Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry |
title_short | Green synthesis of water splitting electrocatalysts: IrO(2) nanocages via Pearson's chemistry |
title_sort | green synthesis of water splitting electrocatalysts: iro(2) nanocages via pearson's chemistry |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580478/ https://www.ncbi.nlm.nih.gov/pubmed/36320917 http://dx.doi.org/10.1039/d2sc03640a |
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