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dc.contributor.authorMartínez Arias, Arturoes_ES
dc.contributor.authorHungría, Ana B.es_ES
dc.contributor.authorIglesias Juez, Anaes_ES
dc.contributor.authorConesa Cegarra, José Carloses_ES
dc.contributor.authorMather, Glenn C.es_ES
dc.contributor.authorMunuera, Guillermoes_ES
dc.contributor.authorFernández, M.-
dc.date.accessioned2018-12-11T11:06:56Z-
dc.date.available2018-12-11T11:06:56Z-
dc.date.issued2005-10-10-
dc.identifier.citationJournal of Power Sources 151: 43-51 (2005)es_ES
dc.identifier.issn0378-7753-
dc.identifier.urihttp://hdl.handle.net/10261/173090-
dc.description.abstractHighly homogeneous (Ce,Tb) oxides are prepared by a microemulsion technique, and their structural and electronic state after high temperature calcination is examined with X-ray diffraction, high resolution transmission electron microscopy, X-ray photoelectron and absorption (XANES) spectroscopies and impedance spectroscopy measurements. Addition of Tb stabilizes significantly (in comparison to pure ceria) specific surface area and small particles sizes during high temperature calcination (up to 1100 °C); phase decomposition at these high temperatures, similar to that occurring when stabilization of ceria is carried out with Zr, does not occur, and the mixed oxide remains homogeneous throughout. Tb addition to ceria may thus be beneficial when used as a component of SOFC anodes. TEM data indicate reshaping of oxide particles and provide evidence of crystal superstructures after high temperature treatments, while XPS and XANES reveal an increase in the Tb4+/Tb3+ ratio (for a given pretreatment) with the Tb/Ce ratio; Ce seems to be less reducible to Ce3+ in the presence of Tb. Total electrical conductivity of CT samples under H2 is mediated by electron transport (involving probably only Ce) and is lower than in gadolinia-doped ceria (GCO); in air conductivity is higher than for GCO, particularly at low temperatures, and it is probable that a p-type transport mechanism predominates in this case.es_ES
dc.description.sponsorshipThanks are given to CICYT (Project MAT2003-03925) for financial support of this research, to the Universities of Madrid (Complutense) and Cádiz for the facilities given for the obtention of TEM data, to ICP-Unidad de Apoyo staff for chemical analysis results and XRD recording, to technical staff at Daresbury Laboratory Station 9.3 (Drs. I. Harvey and A.R. Lennie) for the help given during recording of the XAFS spectra, and to Mr. A. Macías for assistance in recording the XPS data.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccesses_ES
dc.subjectCerium oxidees_ES
dc.subjectTerbium oxidees_ES
dc.subjectSolid oxide fuel celles_ES
dc.subjectAnodees_ES
dc.subjectStructurees_ES
dc.subjectSurface areaes_ES
dc.titleCerium–terbium mixed oxides as potential materials for anodes in solid oxide fuel cellses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1016/j.jpowsour.2005.02.079-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.jpowsour.2005.02.079es_ES
dc.contributor.funderComisión Interministerial de Ciencia y Tecnología, CICYT (España)es_ES
dc.contributor.funderUniversidad Complutense de Madrides_ES
dc.contributor.funderUniversidad de Cádizes_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100007273es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002911es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100008723es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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