Abstract
A PEM fuel cell with a hydrophobically treated cathode catalyst layer (CL) demonstrates ∼220% peak power increase with humidified air at 70 °C. To understand the reasons of the increase, a mathematical model was developed focusing on the oxygen-water two-phase transport phenomena in the CL. It suggests the treatment affects the CL in two ways. First, the interface of the ionomer layer exposed to the gas pores becomes more hydrophobic, facilitating less liquid water coverage and faster water drainage from the CL and resulting in better performance at high current densities. Second, it also affects the hydration level in the ionomer phase resulting in higher oxygen concentration in the ionomer phase on and in the catalyst agglomerates, leading to higher performance over the whole polarization curve. The properties having significant influence on the model fitting the experimental data are the capillary pressure property of the CL, the hydrophobic ionomer ratio in the catalyst agglomerate, and the oxygen solubility/diffusivity in the Nafion® phases. With this experimentally verified model, additional case studies combining the hydrophobic gas diffusion material with the hydrophobic CL demonstrate that the membrane’s self-humidification (zero-net-water flux) and peak power enhancement (∼15%) can be reached simultaneously, providing direction for the future materials development.
Funder
Division of Chemical, Bioengineering, Environmental, and Transport Systems
Publisher
The Electrochemical Society
Subject
Materials Chemistry,Electrochemistry,Surfaces, Coatings and Films,Condensed Matter Physics,Renewable Energy, Sustainability and the Environment,Electronic, Optical and Magnetic Materials
Cited by
1 articles.
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