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    Experimental Studies of GrapheneCoated Polymer Electrolyte Membranes for Direct Methanol Fuel Cells

    Source: Journal of Electrochemical Energy Conversion and Storage:;2022:;volume( 020 ):;issue: 002::page 20903
    Author:
    Metzger, Nathan;Vlassiouk, Ivan;Smirnov, Sergei;Mariscal, Gabriel;Spragg, Ryan;Li, Xianglin
    DOI: 10.1115/1.4056269
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: The two main technical limitations of direct methanol fuel cells (DMFCs) are the slow kinetic reactions of the methanol oxidation reaction (MOR) in the anode and the crossing over of unreacted methanol through the proton exchange membrane (PEM). It is a common practice to use Nafion membranes as PEMs, which have high ion exchange capacity. However, Nafionbased membranes also have high fuel permeability, decreasing fuel utilization, and reducing the potential power density. This article focuses on using graphenecoated (Grcoated) PEMs to reduce fuel crossover. Protons can permeate across graphene, and thus, it can be employed in various devices as a proton conductive membrane. Here, we report the efficiency of Grcoated Nafions. We tested performance and crossover at three different temperatures with four different fuel concentrations and compared it to a Nafion PEM that underwent the same test conditions. We found that the adhesion of Gr on to PEMs is insufficient for prolonging fuel cell operation, resulting in Gr delamination at high temperatures and higher fuel crossover values compared to lower temperature testing. The results for 7.5M methanol fuel show a reduction of up to 25% in methanol crossover, translating to a peak power density that increases from 3.9 to 9.5 mW/cm2 when using a Grcoated PEM compared to a Nafion PEM at 30 °C.
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      Experimental Studies of GrapheneCoated Polymer Electrolyte Membranes for Direct Methanol Fuel Cells

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    contributor authorMetzger, Nathan;Vlassiouk, Ivan;Smirnov, Sergei;Mariscal, Gabriel;Spragg, Ryan;Li, Xianglin
    date accessioned2023-04-06T12:53:59Z
    date available2023-04-06T12:53:59Z
    date copyright12/9/2022 12:00:00 AM
    date issued2022
    identifier issn23816872
    identifier otherjeecs_20_2_020903.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4288730
    description abstractThe two main technical limitations of direct methanol fuel cells (DMFCs) are the slow kinetic reactions of the methanol oxidation reaction (MOR) in the anode and the crossing over of unreacted methanol through the proton exchange membrane (PEM). It is a common practice to use Nafion membranes as PEMs, which have high ion exchange capacity. However, Nafionbased membranes also have high fuel permeability, decreasing fuel utilization, and reducing the potential power density. This article focuses on using graphenecoated (Grcoated) PEMs to reduce fuel crossover. Protons can permeate across graphene, and thus, it can be employed in various devices as a proton conductive membrane. Here, we report the efficiency of Grcoated Nafions. We tested performance and crossover at three different temperatures with four different fuel concentrations and compared it to a Nafion PEM that underwent the same test conditions. We found that the adhesion of Gr on to PEMs is insufficient for prolonging fuel cell operation, resulting in Gr delamination at high temperatures and higher fuel crossover values compared to lower temperature testing. The results for 7.5M methanol fuel show a reduction of up to 25% in methanol crossover, translating to a peak power density that increases from 3.9 to 9.5 mW/cm2 when using a Grcoated PEM compared to a Nafion PEM at 30 °C.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleExperimental Studies of GrapheneCoated Polymer Electrolyte Membranes for Direct Methanol Fuel Cells
    typeJournal Paper
    journal volume20
    journal issue2
    journal titleJournal of Electrochemical Energy Conversion and Storage
    identifier doi10.1115/1.4056269
    journal fristpage20903
    journal lastpage209038
    page8
    treeJournal of Electrochemical Energy Conversion and Storage:;2022:;volume( 020 ):;issue: 002
    contenttypeFulltext
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