Accelerated Degradation of Polymer Electrolyte Membrane Fuel Cell Gas Diffusion Layers: Mass Transport Resistance and Liquid Water Accumulation at Limiting Current Density with in operando Synchrotron X-ray Radiography

被引:7
|
作者
George, Michael G. [1 ]
Liu, Hang [1 ]
Banerjee, Rupak [1 ]
Ge, Nan [1 ]
Shrestha, Pranay [1 ]
Muirhead, Dan [1 ]
Lee, Jongmin [1 ]
Chevalier, Stephane [1 ]
Hinebaugh, James [1 ]
Messerschmidt, Matthias [3 ]
Zeis, Roswitha [2 ]
Scholta, Joachim [3 ]
Bazylak, Aimy [1 ]
机构
[1] Univ Toronto, Dept Mech & Ind Engn, Thermofluids Energy & Adv Mat Lab, Toronto, ON M5S 3G8, Canada
[2] Helmholtz Inst Ulm, Karlsruhe Inst Technol, Ulm, Germany
[3] Zentrum Sonnenenergie & Wasserstoff Forsch Baden, Ulm, Germany
来源
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
D O I
10.1149/07514.0089ecst
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
An SGL 29BC gas diffusion layer (GDL) was degraded (aged) in hydrogen peroxide. The impact of ageing was measured through deviations from pristine GDLs in terms of limiting current densities, oxygen mass transport resistances, and liquid water spatial distributions in the GDL. For dry and saturated cathode conditions (oxygen concentrations of 1% and 21%, respectively) the fuel cell containing the aged GDL reached limiting current densities that were up to 10.3% lower and experienced increases in oxygen mass transport resistance of up to 11.7% versus the pristine GDL. This performance reduction was attributed to a higher liquid water content (13% more at an oxygen concentration of 21%) in the aged GDL under the channel compared to the pristine GDL. In fuel cells built with aged and pristine GDLs, up to 200% more water was present in the GDL under the land compared to under the channel at limiting current operation.
引用
收藏
页码:89 / 100
页数:12
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