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Photoelectrochemical characterization of ITO/TiO2 electrodes obtained by cathodic electrodeposition from aqueous solution

dc.contributor.authorMarchesi, L. F.
dc.contributor.authorFreitas, R. G.
dc.contributor.authorSpada, E. R.
dc.contributor.authorPaula, F. R. [UNESP]
dc.contributor.authorGoes, M. S.
dc.contributor.authorGarcia, J. R.
dc.contributor.institutionUniv Tecnol Fed Parana
dc.contributor.institutionUniversidade Federal de Mato Grosso do Sul (UFMS)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv Integracao Latinoamer
dc.contributor.institutionUniversidade Estadual de Ponta Grossa (UEPG)
dc.date.accessioned2018-11-26T17:55:37Z
dc.date.available2018-11-26T17:55:37Z
dc.date.issued2015-08-01
dc.description.abstractIn the present work, the photoelectrochemical characterization of ITO/TiO2 electrodes electrosynthesized at two distinct TiO2 film charges (0.35 and 1.00 C) was performed. Scanning electron microscopy presented a globular-like nanostructure and a typical morphology that are dependent on the growing charge, where the photoelectrode synthesized at 0.35 C presented a more homogeneous morphology. Such dependence was also observed at the photoelectrochemical response, once the photoactivity for the photoelectrode synthesized at 0.35 C was better than the photoelectrode synthesized at 1.00 C, which was explained by the surface recombination process and the electron lifetime. In order to explore the charge-transfer process and the displacement of the quasi-Fermi level upon illumination, electrochemical impedance spectroscopy (EIS) was performed at distinct applied potentials. EIS results corroborate the previous results, presenting a higher charge-transfer resistance and a lower chemical capacitance for the 1.00 C electrode film, the last one in accordance with the open-circuit voltage decay.en
dc.description.affiliationUniv Tecnol Fed Parana, BR-84016210 Ponta Grossa, PR, Brazil
dc.description.affiliationUniv Fed Mato Grosso, GENMAT Grp Eletroquim & Novos Mat, BR-78060900 Cuiaba, MT, Brazil
dc.description.affiliationUniv Sao Paulo, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
dc.description.affiliationUniv Estadual Paulista, BR-15385000 Ilha Solteira, SP, Brazil
dc.description.affiliationUniv Integracao Latinoamer, BR-85866000 Foz Do Iguacu, PR, Brazil
dc.description.affiliationUniv Estadual Ponta Grossa, BR-84030900 Ponta Grossa, PR, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, BR-15385000 Ilha Solteira, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipNational Institute for Science and Technology on Organic Electronics (INEO)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipFundacao Araucaria do Estado do Parana
dc.description.sponsorshipIdCNPq: 446320/2014-5
dc.description.sponsorshipIdCNPq: 158984/2014-5
dc.format.extent2205-2211
dc.identifierhttp://dx.doi.org/10.1007/s10008-015-2848-1
dc.identifier.citationJournal Of Solid State Electrochemistry. New York: Springer, v. 19, n. 8, p. 2205-2211, 2015.
dc.identifier.doi10.1007/s10008-015-2848-1
dc.identifier.fileWOS000358546700002.pdf
dc.identifier.issn1432-8488
dc.identifier.urihttp://hdl.handle.net/11449/164690
dc.identifier.wosWOS:000358546700002
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofJournal Of Solid State Electrochemistry
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectPhotoanodes
dc.subjectITO/TiO2 electrodes
dc.subjectCathodic electrodeposition
dc.subjectElectrochemical impedance spectroscopy
dc.titlePhotoelectrochemical characterization of ITO/TiO2 electrodes obtained by cathodic electrodeposition from aqueous solutionen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Física Teórica (IFT), São Paulopt

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