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    Investigation of Gradient Platinum Loading and Porosity Distribution for Anion Exchange Membrane Fuel Cells

    Source: Journal of Electrochemical Energy Conversion and Storage:;2022:;volume( 020 ):;issue: 004::page 41001
    Author:
    Mousa, Hassan;Xing, Lei;Das, Prodip K.
    DOI: 10.1115/1.4056029
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Anion exchange membrane fuel cells (AEMFCs) are in development as a lowcost alternative to proton exchange membrane fuel cells (PEMFCs). AEMFCs produce water at the anode side and consume it at the cathode side, resulting in no cathode water flooding like in PEMFCs. However, it brings complexity to water transportation behavior and requires appropriate water balance to avoid membrane drying out. In this study, a twodimensional twophase multiphysics model has been developed to investigate the impacts of three key electrode parameters (porosity, catalyst loading, and ionomer content) that are responsible for water production and transport as well as the performance of an AEMFC. A piecewise constant function along the xdirection (reactant diffusion direction) is used to apply the gradient on the porosity and platinum loading. The present results show that a larger porosity gradient near the cathode gas diffusion layer (GDL)/flow channel interface and lower near the GDL/microporous layer (MPL) interface can enhance mass transport and water removal, which is benefited the AEMFC performance. However, anode GDL porosity gradients show a lower AEMFC performance compared to the cathode porosity gradients. Moreover, it was confirmed that for both electrodes, the performance of AEMFC was significantly dependent on each electrode parameter.
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      Investigation of Gradient Platinum Loading and Porosity Distribution for Anion Exchange Membrane Fuel Cells

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    contributor authorMousa, Hassan;Xing, Lei;Das, Prodip K.
    date accessioned2023-04-06T12:54:42Z
    date available2023-04-06T12:54:42Z
    date copyright11/11/2022 12:00:00 AM
    date issued2022
    identifier issn23816872
    identifier otherjeecs_20_4_041001.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4288744
    description abstractAnion exchange membrane fuel cells (AEMFCs) are in development as a lowcost alternative to proton exchange membrane fuel cells (PEMFCs). AEMFCs produce water at the anode side and consume it at the cathode side, resulting in no cathode water flooding like in PEMFCs. However, it brings complexity to water transportation behavior and requires appropriate water balance to avoid membrane drying out. In this study, a twodimensional twophase multiphysics model has been developed to investigate the impacts of three key electrode parameters (porosity, catalyst loading, and ionomer content) that are responsible for water production and transport as well as the performance of an AEMFC. A piecewise constant function along the xdirection (reactant diffusion direction) is used to apply the gradient on the porosity and platinum loading. The present results show that a larger porosity gradient near the cathode gas diffusion layer (GDL)/flow channel interface and lower near the GDL/microporous layer (MPL) interface can enhance mass transport and water removal, which is benefited the AEMFC performance. However, anode GDL porosity gradients show a lower AEMFC performance compared to the cathode porosity gradients. Moreover, it was confirmed that for both electrodes, the performance of AEMFC was significantly dependent on each electrode parameter.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleInvestigation of Gradient Platinum Loading and Porosity Distribution for Anion Exchange Membrane Fuel Cells
    typeJournal Paper
    journal volume20
    journal issue4
    journal titleJournal of Electrochemical Energy Conversion and Storage
    identifier doi10.1115/1.4056029
    journal fristpage41001
    journal lastpage4100112
    page12
    treeJournal of Electrochemical Energy Conversion and Storage:;2022:;volume( 020 ):;issue: 004
    contenttypeFulltext
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