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Evaluation of the stability and durability of Pt and Pt-Co/C catalysts for polymer electrolyte membrane fuel cells

Tipo de material: TextoTextoSeries ; Journal of Power Sources, 182(1), p.83-90, 2008Trabajos contenidos:
  • Zignani, S.C
  • Antolini, E
  • Gonzalez, E.R
Tema(s): Recursos en línea: Resumen: Carbon supported Pt and Pt-Co nanoparticles were prepared by reduction of the metal precursors with NaBH4. The activity for the oxygen reduction reaction (ORR)of the as-prepared Co-containing catalystwas higher than that of pure Pt. 30 h of constant potential operation at 0.8 V, repetitive potential cycling in the range 0.5-1.0V and thermal treatments were carried out to evaluate their electrochemical stability. Loss of non-alloyed and, to a less extent, alloyed cobaltwas observed after the durability tests with the Pt-Co/C catalyst. The loss in ORR activity following durability tests was higher in Pt-Co/C than in Pt/C, i.e. pure Pt showed higher electrochemical stability than the binary catalyst. The lower stability of the Pt-Co catalyst during repetitive potential cycling was not ascribed to Co loss, but to the dissolution-re-deposition of Pt, forming a surface layer of non-alloyed pure Pt. The lower activity of the Pt-Co catalyst than Pt following the thermal treatment, instead, was due to the presence of non-alloyed Co and its oxides on the catalyst surface, hindering the molecular oxygen to reach the Pt sites.
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Carbon supported Pt and Pt-Co nanoparticles were prepared by reduction of the metal precursors with NaBH4. The activity for the oxygen reduction reaction (ORR)of the as-prepared Co-containing catalystwas higher than that of pure Pt. 30 h of constant potential operation at 0.8 V, repetitive potential cycling in the range 0.5-1.0V and thermal treatments were carried out to evaluate their electrochemical stability. Loss of non-alloyed and, to a less extent, alloyed cobaltwas observed after the durability tests with the Pt-Co/C catalyst. The loss in ORR activity following durability tests was higher in Pt-Co/C than in Pt/C, i.e. pure Pt showed higher electrochemical stability than the binary catalyst. The lower stability of the Pt-Co catalyst during repetitive potential cycling was not ascribed to Co loss, but to the dissolution-re-deposition of Pt, forming a surface layer of non-alloyed pure Pt. The lower activity of the Pt-Co catalyst than Pt following the thermal treatment, instead, was due to the presence of non-alloyed Co and its oxides on the catalyst surface, hindering the molecular oxygen to reach the Pt sites.

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