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Ni and Co-based bifunctional electrocatalysts supported on TiO2@C for oxygen evolution and reduction reactions

dc.contributor.authorFernandes, Diana M.
dc.contributor.authorAbdelkader-Fernandez, Victor K.
dc.contributor.authorFayad, Ali
dc.contributor.authorAnia, Conchi O.
dc.contributor.authorPraxedes, Fabiano R. [UNESP]
dc.contributor.authorLanfredi, Silvania [UNESP]
dc.contributor.authorRodríguez-Castellón, Enrique
dc.contributor.authorRodríguez-Aguado, Elena
dc.contributor.authorHernández-Garrido, Juan C.
dc.contributor.authorQuintana-González, Juan J.
dc.contributor.authorPoon, Po S.
dc.contributor.authorMatos, Juan
dc.contributor.institutionUniversidade do Porto
dc.contributor.institutionUniversity of Granada
dc.contributor.institutionUniversité d'Orléans
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversity of Malaga
dc.contributor.institutionUniversity of Cadiz
dc.contributor.institutionUniversidad de Concepción
dc.contributor.institutionUniversidad Autónoma de Chile
dc.date.accessioned2025-04-29T19:34:28Z
dc.date.issued2024-12-01
dc.description.abstractIn the search for affordable, ecofriendly, and sustainable catalysts for energy-related processes, series of Ni and Co-based bifunctional hybrid electrocatalysts supported on TiO2@C were prepared and studied in the oxygen evolution (OER) and oxygen reduction reactions (ORR). The hybrid TiO2@C supports were prepared using three biomass precursors: furfural, chitosan and saccharose. The nature and dispersion of the metallic phases on those supports was evaluated as a function of the biomass-derived precursors. The prepared materials showed electrocatalytic activity towards ORR and OER reaction, being more active for the latter. Despite a lower performance than Pt/C benchmark, these materials are clearly at much lower costs. The long-term stability and performance of the catalysts were also performed. The number of electrons involved in both processes was determined and a mechanism is proposed for the understanding of the mechanism of reactions using the present materials. It can be concluded that the Ni and mainly Co-based electrocatalysts show a remarkable potential for use as alternative catalysts in fuel cells-related reactions.en
dc.description.affiliationLAQV-REQUIMTE Departamento de Química e Bioquímica Faculdade de Ciências Universidade do Porto, Rua do Campo Alegre s/n
dc.description.affiliationInorganic Chemistry Department Sciences Faculty University of Granada, Av. Fuentenueva s/n, Granada
dc.description.affiliationCEMHTI CNRS (UPR 3079) Université d'Orléans
dc.description.affiliationDept. Chemistry and Biochemistry São Paulo State University (Unesp) School of Technology and Sciences, SP
dc.description.affiliationInorganic Chemistry Department Faculty of Science Instituto Interuniversitario de Investigación en Biorrefinerías I3B University of Malaga
dc.description.affiliationDept. Materials Science and Metallurgy Engineering and Inorganic Chemistry Faculty of Sciences University of Cadiz
dc.description.affiliationUnidad de Desarrollo Tecnológico (UDT) Universidad de Concepción, Barrio Universitario s/n
dc.description.affiliationUnidad de Cambio Climático y Medio Ambiente (UCCMA) Instituto Iberoamericano de Desarrollo Sostenible (IIDS) Facultad de Arquitectura Construcción y Medio Ambiente Universidad Autónoma de Chile
dc.description.affiliationUnespDept. Chemistry and Biochemistry São Paulo State University (Unesp) School of Technology and Sciences, SP
dc.identifierhttp://dx.doi.org/10.1016/j.electacta.2024.145030
dc.identifier.citationElectrochimica Acta, v. 506.
dc.identifier.doi10.1016/j.electacta.2024.145030
dc.identifier.issn0013-4686
dc.identifier.scopus2-s2.0-85203405112
dc.identifier.urihttps://hdl.handle.net/11449/304286
dc.language.isoeng
dc.relation.ispartofElectrochimica Acta
dc.sourceScopus
dc.subjectFuel-cells
dc.subjectNiCo-based electrocatalysts
dc.subjectOER
dc.subjectORR
dc.subjectTiO2@C supports
dc.titleNi and Co-based bifunctional electrocatalysts supported on TiO2@C for oxygen evolution and reduction reactionsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbbcf06b3-c5f9-4a27-ac03-b690202a3b4e
relation.isOrgUnitOfPublication.latestForDiscoverybbcf06b3-c5f9-4a27-ac03-b690202a3b4e
unesp.author.orcid0000-0001-5263-2737[1]
unesp.author.orcid0000-0002-6419-1278 0000-0002-6419-1278[2]
unesp.author.orcid0009-0007-4768-949X[3]
unesp.author.orcid0000-0001-7355-4387[5]
unesp.author.orcid0000-0003-4751-1767[7]
unesp.author.orcid0000-0002-9888-5964[8]
unesp.author.orcid0000-0001-8499-0395[9]
unesp.author.orcid0000-0001-9917-6126[12]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências e Tecnologia, Presidente Prudentept

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