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    Ultrasonic Bonding of Membrane Electrode Assemblies for Low Temperature Proton Exchange Membrane Fuel Cells

    Source: Journal of Fuel Cell Science and Technology:;2012:;volume( 009 ):;issue: 005::page 51005
    Author:
    Joseph Beck
    ,
    Daniel Walczyk
    ,
    Casey Hoffman
    ,
    Steve Buelte
    DOI: 10.1115/1.4007136
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Low temperature proton exchange membrane (PEM) fuel cells currently dominate the fuel cell market, yet there are materials-, cost-, reliability-, and manufacturing-related challenges that hinder widespread commercial success of this promising technology. With regards to manufacturing, one of the main process bottlenecks is thermal bonding of electrode and membrane components into a unitized membrane electrode assembly (MEA). Recent work has shown that ultrasonic bonding can serve as a direct replacement for thermal bonding for high-temperature PEM fuel cells with dramatic reductions in cycle time and energy consumption but no significant degradation in performance. This paper investigates the possible use of ultrasonic bonding for low-temperature PEM MEAs operated at 65 °C. Polarization curves and 1000 Hz impedance were measured for MEAs with a five-layer architecture comprised of Nafion 115 membrane and carbon paper-based gas diffusion electrodes (GDE) that were thermally bonded and ultrasonically bonded using commercial equipment. The effect of membrane condition (conditioned and dry), electrode type (commercially available, custom-made with lower platinum loadings), and process conditions are investigated. Experimental results demonstrate clear trends. Both custom-made GDEs with lower platinum loading performed best suggesting that electrode architecture and composition can be optimized for ultrasonic bonding. There was little difference in performance between dry and conditioned membrane, which helps explain current industrial practice. Statistical analysis of an experimental design where ultrasonic bonding energy and pressure were varied suggests that neither parameter significantly affects MEA performance and that the process is robust. Similar analysis of thermal bonding with temperature and pressure varied suggests that temperature has a significant effect on MEA performance. However, the most important results of all experimentation are that process cycle time and energy consumption are reduced by nearly two orders-of-magnitude using ultrasonic bonding.
    keyword(s): Pressure , Bonding , Electrodes , Membranes , Temperature , Low temperature , Sealing (Process) , Manufacturing AND Energy consumption ,
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      Ultrasonic Bonding of Membrane Electrode Assemblies for Low Temperature Proton Exchange Membrane Fuel Cells

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    https://yetl.yabesh.ir/yetl1/handle/yetl/149208
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    contributor authorJoseph Beck
    contributor authorDaniel Walczyk
    contributor authorCasey Hoffman
    contributor authorSteve Buelte
    date accessioned2017-05-09T00:51:35Z
    date available2017-05-09T00:51:35Z
    date copyrightOctober, 2012
    date issued2012
    identifier issn2381-6872
    identifier otherJFCSAU-926051#051005_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/149208
    description abstractLow temperature proton exchange membrane (PEM) fuel cells currently dominate the fuel cell market, yet there are materials-, cost-, reliability-, and manufacturing-related challenges that hinder widespread commercial success of this promising technology. With regards to manufacturing, one of the main process bottlenecks is thermal bonding of electrode and membrane components into a unitized membrane electrode assembly (MEA). Recent work has shown that ultrasonic bonding can serve as a direct replacement for thermal bonding for high-temperature PEM fuel cells with dramatic reductions in cycle time and energy consumption but no significant degradation in performance. This paper investigates the possible use of ultrasonic bonding for low-temperature PEM MEAs operated at 65 °C. Polarization curves and 1000 Hz impedance were measured for MEAs with a five-layer architecture comprised of Nafion 115 membrane and carbon paper-based gas diffusion electrodes (GDE) that were thermally bonded and ultrasonically bonded using commercial equipment. The effect of membrane condition (conditioned and dry), electrode type (commercially available, custom-made with lower platinum loadings), and process conditions are investigated. Experimental results demonstrate clear trends. Both custom-made GDEs with lower platinum loading performed best suggesting that electrode architecture and composition can be optimized for ultrasonic bonding. There was little difference in performance between dry and conditioned membrane, which helps explain current industrial practice. Statistical analysis of an experimental design where ultrasonic bonding energy and pressure were varied suggests that neither parameter significantly affects MEA performance and that the process is robust. Similar analysis of thermal bonding with temperature and pressure varied suggests that temperature has a significant effect on MEA performance. However, the most important results of all experimentation are that process cycle time and energy consumption are reduced by nearly two orders-of-magnitude using ultrasonic bonding.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleUltrasonic Bonding of Membrane Electrode Assemblies for Low Temperature Proton Exchange Membrane Fuel Cells
    typeJournal Paper
    journal volume9
    journal issue5
    journal titleJournal of Fuel Cell Science and Technology
    identifier doi10.1115/1.4007136
    journal fristpage51005
    identifier eissn2381-6910
    keywordsPressure
    keywordsBonding
    keywordsElectrodes
    keywordsMembranes
    keywordsTemperature
    keywordsLow temperature
    keywordsSealing (Process)
    keywordsManufacturing AND Energy consumption
    treeJournal of Fuel Cell Science and Technology:;2012:;volume( 009 ):;issue: 005
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
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