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Cathode catalyst layer using supported Pt catalyst on ordered mesoporous carbon for direct methanol fuel cell
The development of a cathode catalyst layer based on a supported Pt catalyst using an ordered mesoporous carbon (OMC) for direct methanol fuel cell is reported. An OMC with a mesopore structure between hexagonally arranged carbon nanorods is prepared using a template method. Platinum nanoparticles a...
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Published in: | Journal of power sources 2008-06, Vol.180 (2), p.724-732 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The development of a cathode catalyst layer based on a supported Pt catalyst using an ordered mesoporous carbon (OMC) for direct methanol fuel cell is reported. An OMC with a mesopore structure between hexagonally arranged carbon nanorods is prepared using a template method. Platinum nanoparticles are supported on the OMC (Pt/OMC) with high metal loading of 60
wt.%. Compositional and morphological variations are made by varying the ionomer content and by compressing the catalyst layer to detect a parameter that determines the power performance. Increase in power density with decrease in the volume fraction of ionomer in the agglomerate comprising the Pt/OMC and the ionomer indicates that mass transport through the ionomer phase governs the kinetics of oxygen reduction. Impedance spectroscopic analysis suggests that a significant mass-transport limitation occurs at high ionomer content and in the compressed cathode. The power density of the optimum cathode layer, which employs a Pt/OMC catalyst with a Pt loading of 2
mg
cm
−2, is greater than that of a catalyst layer with 6
mg
cm
−2 Pt-black catalyst at a voltage higher than 0.4
V. This would lead to a significant reduction in the cost of the membrane electrode assembly. |
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ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2008.02.081 |