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dc.contributor.authorLiang, F.
dc.contributor.authorZhou, W.
dc.contributor.authorChi, B.
dc.contributor.authorPu, J.
dc.contributor.authorJiang, San Ping
dc.contributor.authorJian, L.
dc.date.accessioned2017-01-30T13:35:22Z
dc.date.available2017-01-30T13:35:22Z
dc.date.created2014-10-08T06:00:43Z
dc.date.issued2011
dc.identifier.citationLiang, F. and Zhou, W. and Chi, B. and Pu, J. and Jiang, S.P. and Jian, L. 2011. Pd-YSZ composite cathodes for oxygen reduction reaction of intermediate-temperature solid oxide fuel cells. International Journal of Hydrogen Energy. 36: pp. 7670-7676.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/33145
dc.description.abstract

mechanicalmixing and infiltration methods. In the case of infiltration, thermal decomposition and chemical reduction processes are used to form Pd particles on the YSZ scaffold. The phase structure, morphology and electrochemical performance of the Pd-YSZ composite cathodes are characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM) and electrochemical impedance spectroscopy (EIS). The performance of mechanically mixed Pd-YSZ composite cathodes is inadequate due to significant growth and sporadical distribution of Pd particles. The 5 wt.% Pd-loaded cathode prepared by infiltration-thermal decomposition process shows the lowest polarization resistance, i.e. between 0.042 U cm2 and 1.5 U cm2 in the temperature range of 850e600 C, benefited from the formation of nano-sized Pd particles and the presence of well connected Pd network. The effect of Pd loading on the performance of the infiltratedthermal decomposed Pd-YSZ composite cathodes is also evaluated, 5 wt.% Pd loading results in the lowest polarization resistances.

dc.publisherPergamon-Elsevier Science Ltd
dc.subjectSolid oxide fuel cell
dc.subjectInfiltration
dc.subjectCathode
dc.subjectYSZ
dc.subjectPalladium
dc.titlePd-YSZ composite cathodes for oxygen reduction reaction of intermediate-temperature solid oxide fuel cells
dc.typeJournal Article
dcterms.source.volume36
dcterms.source.startPage7670
dcterms.source.endPage7676
dcterms.source.issn03603199
dcterms.source.titleInternational Journal of Hydrogen Energy
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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