dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorCtr Tecnol Informação Renato Archer CTI
dc.contributorUniv Jaume 1
dc.date.accessioned2014-05-20T14:18:38Z
dc.date.accessioned2022-10-05T15:16:45Z
dc.date.available2014-05-20T14:18:38Z
dc.date.available2022-10-05T15:16:45Z
dc.date.created2014-05-20T14:18:38Z
dc.date.issued2011-10-25
dc.identifierCatalysis Communications. Amsterdam: Elsevier B.V., v. 14, n. 1, p. 58-61, 2011.
dc.identifier1566-7367
dc.identifierhttp://hdl.handle.net/11449/25625
dc.identifier10.1016/j.catcom.2011.07.008
dc.identifierWOS:000296213700012
dc.identifier0477045906733254
dc.identifier0000-0003-2827-0208
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3898708
dc.description.abstractIn this work we propose the use of platinum-coated nanostructured oxides for improving the redox rate of active electrodes for applications in catalysts for water splitting, fuel cells, organic depollution, etc. In order to test this concept, CaCu(3)Ti(4)O(12) nanorods were grown by magnetron sputtering over Si/SiO(2)/Ti/Pt substrates and coated with a platinum layer using the same technique. The performance of this active electrode was studied by cyclic voltammetry and electrochemical impedance spectroscopy. Other Pt films (both dense and porous) deposited on oxidized silicon, and platinum-coated FTO-glass, when tested under the same conditions, were less efficient. The charge transfer resistance and the capacitance of one dimensional platinum-coated nanostructured electrodes were at least one order of magnitude better than those measured for platinum-coated FTO-glass. (C) 2011 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationCatalysis Communications
dc.relation3.463
dc.relation0,929
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectActive electrode
dc.subjectNanostructures
dc.subjectCatalysis
dc.subjectPlatinum
dc.titlePlatinum-coated nanostructured oxides for active catalytic electrodes
dc.typeArtigo


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