Improvement of water management in polymer electrolyte membrane fuel cell thanks to cathode cracks

2010 ◽  
Vol 195 (16) ◽  
pp. 5228-5234 ◽  
Author(s):  
Nicolas Karst ◽  
Vincent Faucheux ◽  
Audrey Martinent ◽  
Pierre Bouillon ◽  
Jean-Pierre Simonato
2020 ◽  
Vol 45 (31) ◽  
pp. 15618-15629
Author(s):  
Qadir Esmaili ◽  
Majid Eshagh Nimvari ◽  
Nima Fallah Jouybari ◽  
Yong-Song Chen

2014 ◽  
Vol 11 (3) ◽  
Author(s):  
A. Iranzo ◽  
A. Salva ◽  
E. Tapia ◽  
F. Rosa

The thermal conductivity of the polymer electrolyte membrane (PEM) of fuel cells is an important property affecting the overall cell performance. However, very few studies or fuel cell models include the dependence of this property on temperature and humidification conditions. In addition, no detailed studies have been reported for the quantitative understanding of how this property influences important aspects of the cell such as performance, water management, and membrane durability. This work presents results of a sensibility study performed for different membrane thermal conductivities, analyzing the influence of this parameter on the main cell response variables. The work has been performed with the aid of a computational fluid dynamics (CFD) model developed for a 50 cm2 fuel cell with serpentine flow field bipolar plates, previously validated against experimental measurements. The results show to what extent the cell performance, water management, and durability issues such as MEA temperature gradients are influenced by the membrane thermal conductivity, especially at high current densities, leading up to a 50% increase in the cell electric power at 1000 mA/cm2 when the thermal conductivity of the membrane is set to 0.26 W/(m K) instead of to the base value of 0.13 W/(m K).


2021 ◽  
Vol 11 (13) ◽  
pp. 5964
Author(s):  
Wei-Wei Yuan ◽  
Kai Ou ◽  
Seunghun Jung ◽  
Young-Bae Kim

Water management is one issue that must be surpassed to ensure high membrane proton conductivity and adequate reactant transport in the membrane-electrode assembly (MEA) simultaneously. A well-designed water management system is based on a comprehensive understanding of water transport in the inner part of the polymer electrolyte membrane (PEM) fuel cell. In this work, the water transport phenomena in the MEA PEM fuel cell are analyzed by using a mathematical model. The transport of diluted species interface is used to model the transport of water in the ionomer phase in the catalytic layer and the membrane domains. The molecular flux of water is defined using Nernst–Planck equations, including migration and Fickian diffusion using parameters obtained experimentally for diffusivity and mobility based on water drag for a fully humidified membrane. The proposed model 1D model includes anode gas channel, cathode gas channel, anode gas diffusion layer (GDL), cathode GDL, anode catalyst layer, cathode catalyst layer, and proton exchange membrane. Water activity, ionomer conductivity, and output voltage are predicted by changing the humidity on the anode side of the fuel cell.


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