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Ultrahigh PEMFC Performance of a Thin-Film, Dual-electrode Assembly with Tailored Electrode Morphology

Title
Ultrahigh PEMFC Performance of a Thin-Film, Dual-electrode Assembly with Tailored Electrode Morphology
Author
이성철
Issue Date
2014-01
Publisher
WILEY-V C H VERLAG GMBH, BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY
Citation
CHEMSUSCHEM,2014,7(2), p 466-473(8)
Abstract
A dual-electrode membrane electrode assembly (MEA) for proton exchange membrane fuel cells with enhanced polarization under zero relative humidity (RH) is fabricated by introducing a phase-separated morphology in an agglomerated catalyst layer of Pt/C (platinum on carbon black) and Nafion. In the catalyst layer, a sufficient level of phase separation is achieved by dispersing the Pt catalyst and the Nafion dispersion in a mixed-solvent system (propane-1,2,3-triol/1-methyl-2-pyrrolidinone). The high polymer chain mobility results in improved water uptake and regular pore-size distribution with small pore diameters. The electrochemical performance of the dual-film electrode assembly with different levels of phase separation is compared to conventional electrode assemblies. As a result, good performance at 0% RH is obtained because self-humidification is dramatically improved by attaching this dense and phase-separated catalytic overlayer onto the conventional catalyst layer. A MEA prepared using the thin-film, dual-layered electrode exhibits 39-fold increased RH stability and 28-fold improved start-up recovery time during the on-off operation relative to the conventional device. We demonstrate the successful operation of the dual-layered electrode comprised of discriminatively phase-separated agglomerates with an ultrahigh zero RH fuel-cell performance reaching over 95% performance of a fully humidified MEA.
URI
http://onlinelibrary.wiley.com/doi/abs/10.1002/cssc.201301043http://hdl.handle.net/20.500.11754/54832
ISSN
1864-5631
DOI
10.1002/cssc.201301043
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > CHEMICAL ENGINEERING(화학공학과) > Articles
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