Investigation of Pd-based electrocatalysts for oxygen reduction in PEMFCs operating under automotive conditions (Articolo in rivista)

Type
Label
  • Investigation of Pd-based electrocatalysts for oxygen reduction in PEMFCs operating under automotive conditions (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/jjpowsour.2012.09.002 (literal)
Alternative label
  • Stassi A.; Gatto I.; Baglio V.; Passalacqua E.; Arico A.S. (2013)
    Investigation of Pd-based electrocatalysts for oxygen reduction in PEMFCs operating under automotive conditions
    in Journal of power sources (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Stassi A.; Gatto I.; Baglio V.; Passalacqua E.; Arico A.S. (literal)
Pagina inizio
  • 390 (literal)
Pagina fine
  • 399 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/inward/record.url?eid=2-s2.0-84871483791&partnerID=q2rCbXpz (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 222 (literal)
Rivista
Note
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • CNR-ITAE Istituto di Tecnologie Avanzate per l'Energia Nicola Giordano, Via Salita S. Lucia sopra Contesse 5, 98126 Messina, Italy (literal)
Titolo
  • Investigation of Pd-based electrocatalysts for oxygen reduction in PEMFCs operating under automotive conditions (literal)
Abstract
  • Composite Pd-based electrocatalysts consisting of a surface layer of Pt (5% wt.) supported on a core Pd3Co1 alloy were prepared. Two preparation approaches were investigated. One consisting of a singlestep reduction procedure; in the second method, preparation of the PdCo alloy and deposition of a Pt overlayer occurred in two distinct steps. The catalyst prepared by a one-step process showed oxidised Pt species on the surface even if characterized by a smaller crystallite size with respect to the two-step Pdbased catalyst (4 nm vs. 6 nm). Moreover, the two-step process showed an enrichment of Pt on the surface and a smaller content of Co in the outermost layers. The enhanced surface characteristics of the two-step Pd catalyst resulted in a better performance. At 80 ?C, the mass activity was lower than a Pt3Co1 alloy catalyst with the same crystallographic structure. Interestingly, the composite PtPdCo catalyst showed a significant increase of performance as the temperature was increased to 110 ?C whereas the Pt3Co1 showed a decrease due to a prevailing effect of ionomer dry-out in the catalytic layer. The composite catalyst appeared sufficiently stable after 104 electrochemical cycles between 0.6 and 0.9 V at 110 ?C and 33% R.H. (literal)
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