Study of Oxygen Diffusion in the Cathode Catalyst Layer and Gas Diffusion Layer for Polymer Electrolyte Fuel Cells with EIS

Author(s):  
Samuel Cruz-Manzo ◽  
Paul Greenwood
2021 ◽  
Vol MA2021-02 (37) ◽  
pp. 1087-1087
Author(s):  
Makoto Uchida ◽  
Kayoko Tamoto ◽  
Takumi Nagasaka ◽  
Chihiro Taguchi ◽  
Shimao Yoneyama

Author(s):  
Deepashree Thumbarathy ◽  
Gaurav Gupta ◽  
Mohamed Mamlouk ◽  
Prodip K. Das

Abstract Gas diffusion layer (GDL) and its interfaces with the flow-channel and microporous layer or catalyst layer in polymer electrolyte fuel cells (PEFCs) play a significant role in water management and heat removal from the cells. Both surface morphology and surface wettability of GDL influence and control the water transport in PEFCs. Thus, the surface morphology and selectivity of its surface wettability are critical for PEFCs to provide optimum outputs. In this study, we have reported the fabrications of GDLs with a selective wetting pattern. Sigracet® GDLs were used as a substrate and two different monomers, polydimethylsiloxane (PDMS) added with fumed silica (Si) and fluorinated ethylene propylene (FEP), were used to print a selective pattern on the GDL surfaces. The evaluations of printed GDL surfaces, by means of static contact angle, sliding angles, and scanning electron microscopy image show that superhydrophobicity was achieved with both FEP and PDMS-Si coatings. Fourier transform infrared spectroscopy analysis confirmed the successful introduction of the functional groups in both the coatings. Finally, pore size distributions, sliding angle measurements, and adhesion forces were used to investigate the interactions between the water droplets and GDL surfaces. The results of this study demonstrate that the present approach provides a novel but simple way to tune GDL surfaces with selective wetting properties and obtain superhydrophobic interfaces. The electrochemical results showed that an improvement can be achieved for the performance of PEFCs with patterned GDL/flow-channel interfaces.


2008 ◽  
Vol 86 (7) ◽  
pp. 657-667 ◽  
Author(s):  
Zetao Xia ◽  
Qianpu Wang ◽  
Michael Eikerling ◽  
Zhongsheng Liu

In this work, we analyze effectiveness factors of Pt utilization in perfluorosulfonate ionomer (PFSI) bonded thin film cathode catalyst layers of polymer electrolyte fuel cells. We define the effectiveness factor of Pt utilization as the apparent rate of current conversion exhibited by a specific catalyst layer design divided by the ideal rate obtained if all Pt atoms were used equally in electrochemical reactions at the specified electrode overpotential and externally provided reactant concentrations. This definition includes statistical factors at all relevant scales as well as non-uniformities of reaction rate distributions under operation. Our model is based on the random composite agglomerated morphology of the catalyst layer. It accounts for the interplay of transport phenomena and electrochemical kinetics. At the mesoscopic scale, limited effectiveness of Pt utilization in agglomerates is mainly an electrostatic effect. We determined spatial distributions of effectiveness factors of agglomerates in the through-plane direction, and thereafter calculated overall effectiveness factors of the cathode catalyst layer. Our results show that small agglomerate radius, low operating current density, high operating temperature, and high oxygen partial pressure result in high effectiveness factors of Pt utilization. Finally, we compared PFSI-bonded thin film cathode catalyst layers with ultrathin two-phase cathode catalyst layers in terms of effectiveness factors. Including the surface to volume atom ratio of Pt nanoparticles, the two different types of structures exhibit similar effectiveness factors of Pt utilization, which are found to be distinctly below 10%.Key words: polymer electrolyte fuel cells, fuel cell modeling, cathode catalyst layer, Pt utilization, effectiveness factor.


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