http://www.cnr.it/ontology/cnr/individuo/prodotto/ID289140
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
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Stassi A.; Gatto I.; Baglio V.; Passalacqua E.; Arico A.S. (literal)
- Pagina inizio
- Pagina fine
- 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
- Rivista
- Note
- 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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