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contributor authorGarcأ­a
contributor authorColأ³n
contributor authorHerrington, Kevin
contributor authorFox, Elise B.
date accessioned2017-05-09T01:09:01Z
date available2017-05-09T01:09:01Z
date issued2014
identifier issn2381-6872
identifier otherfc_011_03_031001.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/155122
description abstractHigh temperature direct methanol fuel cells (DMFCs) using polybenzimidazole (PBI) membranes could improve the energy density of portable power sources. This study examines the polarization of vapor phase PBI DMFCs constructed with commercial membranes manufactured by a solgel method. The polarization of the high temperature DMFCs is compared to similar low temperature membrane electrode assemblies (MEAs) using Nafionآ® membranes. The results showed that the cathode of the PBI DMFC had higher kinetic losses that are likely due to phosphate poisoning of the Pt electrocatalyst. At the tested conditions, the membrane conductivity of the PBI MEAs was comparable to the Nafionآ® MEA even with no humidification. Higher cell temperatures significantly improved PBI DMFC performance for Pt electrocatalyst electrodes. In full cell tests, the PBI DMFC MEAs had higher performance than Nafionآ® MEAs with similar catalyst loadings. The Pt and PtRu catalysts were tested for methanol oxidation and oxygen reduction activity by a rotating disk electrode (RDE) under 0.5 M H2SO4 and 0.5 M H3PO4. The combination of the polarization and RDE results for the PBI and Nafionآ® DMFCs suggest that Pt is a more active electrocatalyst for methanol oxidation in PBI than in Nafionآ®.
publisherThe American Society of Mechanical Engineers (ASME)
titlePolarization and Electrocatalyst Selection for Polybenzimidazole Direct Methanol Fuel Cells
typeJournal Paper
journal volume11
journal issue3
journal titleJournal of Fuel Cell Science and Technology
identifier doi10.1115/1.4025523
journal fristpage31001
journal lastpage31001
identifier eissn2381-6910
treeJournal of Fuel Cell Science and Technology:;2014:;volume( 011 ):;issue: 003
contenttypeFulltext


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