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hal.structure.identifierKey Laboratory of Superlight Materials and Surface Technology
dc.contributor.authorWANG, Jingping
hal.structure.identifierKey Laboratory of Functional Inorganic Material Chemistry [KLFIMC]
dc.contributor.authorMENG, Fuchang
hal.structure.identifierKey Laboratory of Functional Inorganic Material Chemistry [KLFIMC]
dc.contributor.authorXIA, Tian
hal.structure.identifierKey Laboratory of Functional Inorganic Material Chemistry [KLFIMC]
dc.contributor.authorSHI, Zhan
hal.structure.identifierKey Laboratory of Functional Inorganic Material Chemistry [KLFIMC]
dc.contributor.authorLIAN, Jie
hal.structure.identifierKey Laboratory of Superlight Materials and Surface Technology
dc.contributor.authorXU, Chunbo
hal.structure.identifierKey Laboratory of Functional Inorganic Material Chemistry [KLFIMC]
dc.contributor.authorZHAO, Hui
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorBASSAT, Jean-Marc.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorGRENIER, Jean-Claude
dc.date.issued2014
dc.identifier.issn0360-3199
dc.description.abstractEnThe layered perovskite PrBaxCo2O5+δ (PBxCO, x = 0.90–1.0) oxides have been synthesized by a solid-state reaction technique, and evaluated as the potential cathode materials for intermediate-temperature solid oxide fuel cells (IT-SOFCs). Room temperature X-ray diffraction patterns show the orthorhombic structures which double the lattice parameters from the perovskite cell parameter as a ≈ ap, b ≈ ap and c ≈ 2ap (ap is the cell parameter of the primitive perovskite) in the Pmmm space group. There is a good chemical compatibility between the PBxCO cathode and the Ce0.9Gd0.1O1.95 (CGO) electrolyte at 1000 °C. The electrical conductivity and thermal expansion coefficient of PBxCO are improved due to the increased amount of electronic holes originated from the Ba-deficiency. The results demonstrate the high electrochemical performance of PBxCO cathodes, as evidenced by the super low polarization resistances (Rp) over the intermediate temperature range. The lowest Rp value, 0.042 Ω cm2, and the cathodic overpotential, −15 mV at a current density of −25 mA cm−2, are obtained in the PrBa0.94Co2O5+δ cathode at 600 °C in air, which thus allow to be used as a highly promising cathode for IT-SOFCs. A CGO electrolyte fuel cell with the PrBa0.94Co2O5+δ cathode presents the attractive peak power density of ∼1.0 W cm−2 at 700 °C. Furthermore, the oxygen reduction kinetics of the PrBa0.94Co2O5+δ cathode is also studied, and the rate-limiting steps for oxygen reduction reaction are determined at different temperatures.
dc.language.isoen
dc.publisherElsevier
dc.subject.enIntermediate-temperature solid oxide fuel cell
dc.subject.enCathode material
dc.subject.enLayered perovskite
dc.subject.enElectrochemical performance
dc.subject.enOxygen reduction kinetics
dc.title.enSuperior electrochemical performance and oxygen reduction kinetics of layered perovskite PrBaxCo2O5+δ (x = 0.90–1.0) oxides as cathode materials for intermediate-temperature solid oxide fuel cells
dc.typeArticle de revue
dc.identifier.doi10.1149/2.0121414jes
dc.subject.halChimie/Matériaux
bordeaux.journalInternational Journal of Hydrogen Energy
bordeaux.page18392-18404
bordeaux.volume39
bordeaux.issue32
bordeaux.peerReviewedoui
hal.identifierhal-01080087
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01080087v1
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