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CO tolerance of PdPt/C and PdPtRu/C anodes for PEMFC

Texto completo
Autor(es):
Garcia‚ A.C. ; Paganin‚ V.A. ; Ticianelli‚ E.A.
Número total de Autores: 3
Tipo de documento: Artigo Científico
Fonte: Electrochimica Acta; v. 53, n. 12, p. 4309-4315, 2008.
Resumo

The performance of H-2/O-2 proton exchange membrane fuel cells (PEMFCs) fed with CO-contaminated hydrogen was investigated for anodes with PdPt/C and PdPtRu/C electrocatalysts. The physicochemical properties of the catalysts were characterized by energy dispersive X-ray (EDX) analyses, X-ray diffraction (XRD) and "in situ" X-ray absorption near edge structure (XANES). Experiments were conducted in electrochemical half and single cells by cyclic voltammetry (CV) and I-V polarization measurements, while DEMS was employed to verify the formation of CO2 at the PEMFC anode outlet. A quite high performance was achieved for the PEMFC fed with H-2 + 100 ppm CO with the PdPt/C and PdPtRu/C anodes containing 0.4 mg metal cm(-2), with the cell presenting potential losses below 200 mV at 1 A cm(-2), with respect to the system fed with Pure H-2. For the PdPt/C catalysts no CO2 formation was seen at the PEMFC anode outlet, indicating that the CO tolerance is improved due to the existence of more free surface sites for H-2 electrooxidation, probably due to a lower Pd-CO interaction compared to pure Pd or Pt. For PdPtRu/C the CO tolerance may also have a contribution from the bifunctional mechanism, as shown by the presence of CO2, in the PEMFC anode outlet. (c) 2008 Elsevier Ltd. All rights reserved. (AU)

Processo FAPESP: 04/10788-5 - Estudos fundamentais e aplicados dos processos eletródicos em células a combustível de baixas temperaturas
Beneficiário:Edson Antonio Ticianelli
Modalidade de apoio: Auxílio à Pesquisa - Temático