Electrochemical Doping as a Way to Enhance Water Photooxidation on Nanostructured Nickel Titanate and Anatase Electrodes

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Títol: Electrochemical Doping as a Way to Enhance Water Photooxidation on Nanostructured Nickel Titanate and Anatase Electrodes
Autors: Díez García, María Isabel | Monllor-Satoca, Damián | Vinoth, Victor | Anandan, Sambandam | Lana-Villarreal, Teresa
Grups d'investigació o GITE: Grupo de Fotoquímica y Electroquímica de Semiconductores (GFES)
Centre, Departament o Servei: Universidad de Alicante. Departamento de Química Física | Universidad de Alicante. Instituto Universitario de Electroquímica
Paraules clau: Nickel titanate | Anatase | Electrochemical doping | Photoelectrochemistry | Water splitting
Àrees de coneixement: Química Física
Data de publicació: de juny-2017
Editor: Wiley-VCH Verlag GmbH & Co. KGaA
Citació bibliogràfica: ChemElectroChem. 2017, 4(6): 1429-1435. doi:10.1002/celc.201700039
Resum: A number of metal oxides have been proposed as useful materials for the photoelectrochemical (PEC) production of hydrogen from water. However, up to now, an ideal standalone material has not been found. We have investigated the possible use of nickel titanate (NiTiO3) nanorods as a photoanode. Although these electrodes absorb visible light, they show a modest PEC behavior. Interestingly, the photocurrent for water oxidation undergoes a 30-fold enhancement after an optimized reductive electrochemical pretreatment. Here, the induced doping is studied and compared with the corresponding for anatase nanoporous electrodes. The results reveal the key role of the electrolyte pH as well as the size of the electrode building blocks. The photocurrent promotion upon the electrochemical pretreatment can be ascribed to an enhanced charge transport linked to the ability of proton insertion in the crystal structure.
Patrocinadors: We are grateful to the Spanish Ministry of Economy and Competitiveness (MINECO) for financial support through projects PRI-PIBIN-2011-0816, MAT2012-37676 and MAT2015-71727-R (co-financed with FEDER funds by the European Union). S.A. also thanks DST, New Delhi, for the sanction of an India–Spain collaborative research grant (DST/INT/Spain/P-37/11 dt.16th Dec 2011). D.M.-S. acknowledges MINECO for financial support through project MAT2014-59961-C2-2-R, and the Spanish Ministry of Education and Science for the award of an FPI Fellowship (BES-2004-5194).
URI: http://hdl.handle.net/10045/67482
ISSN: 2196-0216
DOI: 10.1002/celc.201700039
Idioma: eng
Tipus: info:eu-repo/semantics/article
Drets: © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Revisió científica: si
Versió de l'editor: http://dx.doi.org/10.1002/celc.201700039
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