Effect and siting of Nafion in a Pt/C proton exchange membrane fuel cell catalyst |
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Authors: | Jack Z ZhangKitiya Hongsirikarn James G Goodwin Jr |
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Affiliation: | Department of Chemical and Biomolecular Engineering, Clemson University, Clemson, SC 29634-0909, USA |
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Abstract: | This paper explores the effect and siting (location) of Nafion on Pt/C as exists in a PEM fuel cell catalyst layer. The addition of 30 wt% Nafion on Pt/C (Nfn-Pt/C) resulted in a severe loss of BET surface area by filling/blocking the smaller pore structures in the carbon support. Surprisingly, the presence of this much Nafion appeared to have only a minimal effect on the adsorption capability of either hydrogen or CO on Pt. However, the presence of Nafion doubled the amount of time required to purge most of the gas-phase and weakly-adsorbed hydrogen molecules away from the catalyst during hydrogen surface concentration measurements. This strongly chemisorbed surface hydrogen was determined by a H2/D2 switch and exchange procedure. Nafion had an even more pronounced effect on the reaction of a larger molecule like cyclopropane. Results from the modeling of cyclopropane hydrogenolysis in an idealized pores suggest that partial blockage of only the pore openings by the Nafion for the meso-macropores is sufficient to induce diffusion limitations on the reaction. The facts suggest that most of the Pt particles are in the meso-macropores of the C support, whereas Nafion is present primarily on the external surface of the C where it blocks significantly the micropores but only partially the meso-macropores. |
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Keywords: | H2-D2 exchange Pt/C Nafion-Pt/C H2 activation PEMFC Hydrogen surface concentration |
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