Multifunctional Indium Tin Oxide Electrode Generated by Unusual Surface Modification

Sarra Bouden 1 Antoine Dahi 1 Fanny Hauquier 2 Hyacinthe Randriamahazaka 1 Jalal Ghilane 1, *
* Auteur correspondant
2 LICSEN - Laboratoire Innovation en Chimie des Surfaces et NanoSciences
NIMBE UMR 3685 - Nanosciences et Innovation pour les Matériaux, la Biomédecine et l'Energie (ex SIS2M)
Abstract : The indium tin oxide (ITO) material has been widely used in various scientific fields and has been successfully implemented in several devices. Herein, the electrochemical reduction of ITO electrode in an organic electrolytic solution containing alkali metal, NaI, or redox molecule, N-(ferrocenylmethyl) imidazolium iodide, was investigated. The reduced ITO surfaces were investigated by X-ray photoelectron spectroscopy and grazing incident XRD demonstrating the presence of the electrolyte cation inside the material. Reversibility of this process after re-oxidation was evidenced by XPS. Using a redox molecule based ionic liquid as supporting electrolyte leads to fellow electrochemically the intercalation process. As a result, modified ITO containing ferrocenyl imidazolium was easily generated. This reduction process occurs at mild reducing potential around −1.8 V and causes for higher reducing potential a drastic morphological change accompanied with a decrease of the electrode conductivity at the macroscopic scale. Finally, the self-reducing power of the reduced ITO phase was used to initiate the spontaneous reduction of silver ions leading to the growth of Ag nanoparticles. As a result, transparent and multifunctional active ITO surfaces were generated bearing redox active molecules inside the material and Ag nanoparticles onto the surface.
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Scientific Reports, Nature Publishing Group, 2016, 6, pp.36708. 〈http://dx.doi.org/10.1038/srep36708〉. 〈10.1038/srep36708〉
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Sarra Bouden, Antoine Dahi, Fanny Hauquier, Hyacinthe Randriamahazaka, Jalal Ghilane. Multifunctional Indium Tin Oxide Electrode Generated by Unusual Surface Modification. Scientific Reports, Nature Publishing Group, 2016, 6, pp.36708. 〈http://dx.doi.org/10.1038/srep36708〉. 〈10.1038/srep36708〉. 〈cea-01634543〉

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