The Effect of Mechanical Fatigue on the Lifetimes of Membrane Electrode Assemblies

Author(s):  
Michael Pestrak ◽  
Yongqiang Li ◽  
Scott W. Case ◽  
David A. Dillard ◽  
Michael W. Ellis ◽  
...  

Long-term durability of the membrane electrode assembly (MEA) in proton exchange membrane (PEM) fuel cells is one of the major technological barriers to the commercialization of fuel cell vehicles. The cracks in the electrode layers of the MEA, referred to as mud-cracks, are potential contributors to the failure in the PEM. To investigate how these mud-cracks affect the mechanical durability of the MEA, pressure-loaded blister tests are performed at 90°C to determine the biaxial fatigue strength of Gore-Primea® series 57 MEA. In these volume-controlled tests, leaking rate is determined as a function of fatigue cycles. The failure is defined to occur when the leaking rate exceeds a specified threshold. Postmortem characterization using bubble point testing and field emission scanning electron microscopy (FESEM) was conducted to provide visual documentation of leaking failure sites. The analysis of the experimental leaking data indicates that the MEA has much shorter lifetimes at the same nominal stress levels than membrane samples without the electrode layers. FESEM photomicrographs of leaking locations identified via the bubble point testing show cracks in the membrane that are concentrated within the mud-cracks of the electrode layer. These two pieces of information indicate that the mud-cracks within the electrode layers contribute to the leaking failures of the MEA assembly. For the fuel cell industry, this study suggests there is an opportunity to reduce the likelihood of membrane pinhole failures by reducing the size and occurrence of the mud-cracks formed during the MEA processing or by increasing the fatigue resistance (including the notch sensitivity) of the membrane material within the MEA.

2018 ◽  
Vol 778 ◽  
pp. 275-282
Author(s):  
Noaman Khan ◽  
Saim Saher ◽  
Xuan Shi ◽  
Muhammad Noman ◽  
Mujahid Wasim Durani ◽  
...  

Highly porous ZIF-67 (Zeolitic imidazole framework) has a conductive crystalline metal organic framework (MOF) structure which was served as a precursor and template for the preparation of nitrogen-doped carbon nanotubes (NCNTs) electrocatalysts. As a first step, the chloroplatinic acid, a platinum (Pt) precursor was infiltrated in ZIF-67 with a precise amount to obtain 0.12 mg.cm-2 Pt loading. Later, the infiltrated structure was calcined at 700°C in Ar:H2 (90:10 vol%) gas mixture. Multi-walled nitrogen-doped carbon nanotubes were grown on the surface of ZIF-67 crystals following thermal activation at 700°C. The resulting PtCo-NCNTs electrocatalysts were deposited on Nafion-212 solid electrolyte membrane by spray technique to study the oxygen reduction reaction (ORR) in the presence of H2/O2 gases in a temperature range of 50-70°C. The present study elucidates the performance of nitrogen-doped carbon nanotubes ORR electrocatalysts derived from ZIF-67 and the effects of membrane electrode assembly (MEA) steaming on the performance of proton exchange membrane fuel cell (PEMFC) employing PtCo-NCNTs as ORR electrocatalysts. We observed that the peak power density at 70°C was 450 mW/cm2 for steamed membrane electrode assembly (MEA) compared to 392 mW/cm2 for an identical MEA without steaming.


Energy ◽  
2007 ◽  
Vol 32 (12) ◽  
pp. 2401-2411 ◽  
Author(s):  
Apichai Therdthianwong ◽  
Phochan Manomayidthikarn ◽  
Supaporn Therdthianwong

Author(s):  
Attila Husar ◽  
Andrew Higier ◽  
Hongtan Liu

Water management is of critical importance in a proton exchange membrane (PEM) fuel cell. Yet there are very limited studies of water transfer through the membrane and no data are available for water transfer due to individual mechanisms through the membrane electrode assembly (MEA) in an operational fuel cell. Thus it is the objective of this study to measure water transfer through the MEA due to different mechanisms through the membrane electrode assembly (MEA) of an operational PEM fuel cell. The three different mechanisms of water transfer, i.e., electro-osmotic drag, diffusion and hydraulic permeation were isolated by specially imposed boundary conditions. Therefore water transfer through the MEA due to each mechanism could be measured separately. In this study, all the data were collected in an actual assembled operational fuel cell, and some of the data were collected while the fuel cell was generating power. The measured results showed that water transfer due to hydraulic permeation, i.e. the pressure difference between the anode and cathode is at least an order of magnitude lower than those due to other two mechanisms. The data for water transfers due to electro-osmosis and diffusion through the MEA are in good agreement with some of the data and model predications in the literature for the membrane. The methodology used in this study is simple and can be easily adopted for in-situ water transfer measurement due to different mechanisms in actual PEM fuel cells without any cell modifications.


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