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dc.contributor.authorChen, D.
dc.contributor.authorYang, G.
dc.contributor.authorShao, Zongping
dc.contributor.authorCiucci, F.
dc.date.accessioned2017-01-30T11:22:34Z
dc.date.available2017-01-30T11:22:34Z
dc.date.created2014-10-08T01:14:47Z
dc.date.issued2013
dc.identifier.citationChen, D. and Yang, G. and Shao, Z. and Ciucci, F. 2013. Nanoscaled Sm-doped CeO2 buffer layers for intermediate-temperature solid oxide fuel cells. Electrochemistry Communications. 35: pp. 131-134.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/11043
dc.description.abstract

A dense and crack-free nanoscaled Sm-doped CeO2 (SDC) thin film as a buffer layer for intermediate-temperature solid oxide fuel cells has been successfully deposited onto the polycrystalline yttria-stabilized zirconia (YSZ) electrolyte by pulsed laser deposition (PLD). SEM and XRD results reveal that the dense and crack-free buffer layer effectively prevents the formation of the insulating layer between the Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF) cathode and the YSZ electrolyte. The fuel cell with the as-deposited buffer layer exhibits high peak power density (e.g.,2016 mW cm-2 at 700 degrees Celcius) and low resistance. In contrast, at 700 degrees Celcius the fuel cell with an optimized SDC layer prepared by spray deposition or the fuel cell without interlayer have lower peak power densities, 1132 mW cm-2 and 60 mW cm-2 respectively, and higher resistances. The significant enhancement in peak power densities with the adoption of the SDC buffer layer by PLD is likely due to the combination of three factors: the lack of solid-state reaction between BSCF and YSZ, the thinner thickness in comparison to the SDC layer by spray deposition, as well as the improvement of the charge-transfer process.

dc.publisherElsevier Inc.
dc.subjectBuffer layer
dc.subjectPhase reaction
dc.subjectThin film
dc.subjectPulsed laser deposition
dc.subjectSolid oxide fuel cells
dc.titleNanoscaled Sm-doped CeO2 buffer layers for intermediate-temperature solid oxide fuel cells
dc.typeJournal Article
dcterms.source.volume35
dcterms.source.startPage131
dcterms.source.endPage134
dcterms.source.issn1388-2481
dcterms.source.titleElectrochemistry Communications
curtin.accessStatusFulltext not available


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