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

被引:115
作者
Garcia, Amanda C. [1 ]
Paganin, Valdecir A. [1 ]
Ticianelli, Edson A. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
PdPt/C catalyst; PdPtRu/C catalyst; PEMFC; CO oxidation; DEMS;
D O I
10.1016/j.electacta.2008.01.006
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
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.
引用
收藏
页码:4309 / 4315
页数:7
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