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dc.contributor.authorTang, Yongfu
dc.contributor.authorMu, Shichun
dc.contributor.authorYu, Shengxue
dc.contributor.authorZhao, Yufeng
dc.contributor.authorWang, Hongchao
dc.contributor.authorGao, Faming
dc.date.accessioned2017-05-09T01:09:05Z
dc.date.available2017-05-09T01:09:05Z
dc.date.issued2014
dc.identifier.issn2381-6872
dc.identifier.otherfc_011_05_051004.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl/handle/yetl/155150
dc.description.abstractTo investigate the degradation mechanism of the asprepared Pd/C catalyst, in situ and ex situ accelerated stress tests were carried out via potential cycling. Durability tests of the single cells with Pd/C catalysts were performed through an interval constant current density mode. Electrochemical impedance spectroscopy (EIS) was applied to measure the impedance of the single cell during degradation tests. Results indicate that the degradation of Pd/C catalyst may be attributed to the phase transition of absorbed خ±phase PdH to خ²phase PdH, the dissolution of Pd metal, and the size increase of Pd nanoparticles. Moreover, the degradation of single cell may be predominantly ascribed to the degradation of catalyst, the deterioration of contact between electronic/ionic conductors, as well as the flooding of gas diffusion channels.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleIn Situ and Ex Situ Studies on the Degradation of Pd/C Catalyst for Proton Exchange Membrane Fuel Cells
dc.typeJournal Paper
dc.journal.volume11
dc.journal.issue5
dc.journal.titleJournal of Fuel Cell Science and Technology
dc.identifier.doi10.1115/1.4027708
dc.journal.fristpage51004
dc.journal.lastpage51004
dc.identifier.eissn2381-6910
dc.treeJournal of Fuel Cell Science and Technology:;2014:;volume( 011 ):;issue: 005
dc.contenttypeFulltext


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