Nonlinear 4 × 4 MDS diffusion layers

2021 ◽  
pp. 1-14
Author(s):  
M. R. Mirzaee Shamsabad ◽  
S. M. Dehnavi
Keyword(s):  
Diffusion Layers

scholarly journals Effect of Gas Diffusion Layer Thickness on the Performance of Anion Exchange Membrane Fuel Cells

Processes ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 718
Author(s):  
Van Men Truong ◽  
Ngoc Bich Duong ◽  
Hsiharng Yang
Keyword(s):  
Water Management ◽  
Anion Exchange ◽  
Critical Role ◽  
Gas Diffusion ◽  
Anion Exchange Membrane ◽  
Cell Performance ◽  
Water Flooding ◽  
Diffusion Layer Thickness ◽  
Diffusion Layers ◽  
Exchange Membrane

Gas diffusion layers (GDLs) play a critical role in anion exchange membrane fuel cell (AEMFC) water management. In this work, the effect of GDL thickness on the cell performance of the AEMFC was experimentally investigated. Three GDLs with different thicknesses of 120, 260, and 310 µm (denoted as GDL-120, GDL-260, and GDL-310, respectively) were prepared and tested in a single H2/O2 AEMFC. The experimental results showed that the GDL-260 employed in both anode and cathode electrodes exhibited the best cell performance. There was a small difference in cell performance for GDL-260 and GDL-310, while water flooding was observed in the case of using GDL-120 operated at current densities greater than 1100 mA cm−2. In addition, it was found that the GDL thickness had more sensitivity to the AEMFC performance as used in the anode electrode rather than in the cathode electrode, indicating that water removal at the anode was more challenging than water supply at the cathode. The strategy of water management in the anode should be different from that in the cathode. These findings can provide a further understanding of the role of GDLs in the water management of AEMFCs.

Imaging of desaturation of the frozen gas diffusion layers by synchrotron X-ray radiography

2021 ◽  
Author(s):  
Yuzhou Zhang ◽  
Viral Hirpara ◽  
Virat Patel ◽  
Chen Li ◽  
Ryan Anderson ◽  
...  
Keyword(s):  
Gas Diffusion ◽  
Gas Diffusion Layers ◽  
X Ray ◽  
Diffusion Layers

scholarly journals Water Electrolysis Using a Porous IrO2/Ti/IrO2 Catalyst Electrode and Nafion Membranes at Elevated Temperatures

Membranes ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 330
Author(s):  
Je-Deok Kim ◽  
Akihiro Ohira
Keyword(s):  
Elevated Temperatures ◽  
High Current Density ◽  
Water Electrolysis ◽  
Gas Diffusion ◽  
Membrane Electrode ◽  
Porous Ti ◽  
Diffusion Layers ◽  
Iro2 Catalyst ◽  
Ti Powder ◽  
Catalyst Electrode

Porous IrO2/Ti/IrO2 catalyst electrodes were obtained by coating IrO2 on both sides of three types of porous Ti powder sheets (sample 1, sample 2, and sample 3) using different surface treatment methods, and a hydrogen evolution catalyst electrode was obtained by coating Pt/C on carbon gas diffusion layers. A Nafion115 membrane was used as an electrolyte for the membrane electrode assemblies (MEA). Water electrolysis was investigated at cell temperatures up to 150 °C, and the electrical characteristics of the three types of porous IrO2/Ti/IrO2 catalyst electrodes were investigated. The sheet resistance of sample 1 was higher than those of samples 2 and 3, although during water electrolysis, a high current density was observed due to the nanostructure of the IrO2 catalyst. In addition, the structural stabilities of Nafion and Aquivion membranes up to 150 °C were investigated by using small angle X-ray scattering (SAXS). The polymer structures of Nafion and Aquivion membranes were stable up to 80 °C, whereas the crystalline domains grew significantly above 120 °C. In other words, the initial polymer structure did not recover after the sample was heated above the glass transition temperature.

scholarly journals Mass Transport Limitations of Water Evaporation in Polymer Electrolyte Fuel Cell Gas Diffusion Layers

Energies ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2967
Author(s):  
Adrian Mularczyk ◽  
Andreas Michalski ◽  
Michael Striednig ◽  
Robert Herrendörfer ◽  
Thomas J. Schmidt ◽  
...  
Keyword(s):  
Fuel Cell ◽  
Liquid Water ◽  
Evaporative Cooling ◽  
Gas Diffusion ◽  
Polymer Electrolyte Fuel Cell ◽  
Ex Situ ◽  
Water Evaporation ◽  
Evaporative Water ◽  
Gas Diffusion Layers ◽  
Diffusion Layers

Facilitating the proper handling of water is one of the main challenges to overcome when trying to improve fuel cell performance. Specifically, enhanced removal of liquid water from the porous gas diffusion layers (GDLs) holds a lot of potential, but has proven to be non-trivial. A main contributor to this removal process is the gaseous transport of water following evaporation inside the GDL or catalyst layer domain. Vapor transport is desired over liquid removal, as the liquid water takes up pore space otherwise available for reactant gas supply to the catalytically active sites and opens up the possibility to remove the waste heat of the cell by evaporative cooling concepts. To better understand evaporative water removal from fuel cells and facilitate the evaporative cooling concept developed at the Paul Scherrer Institute, the effect of gas speed (0.5–10 m/s), temperature (30–60 °C), and evaporation domain (0.8–10 mm) on the evaporation rate of water from a GDL (TGP-H-120, 10 wt% PTFE) has been investigated using an ex situ approach, combined with X-ray tomographic microscopy. An along-the-channel model showed good agreement with the measured values and was used to extrapolate the differential approach to larger domains and to investigate parameter variations that were not covered experimentally.

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