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    Superhydrophobic Cobalt–Graphene Composite for the Corrosion Protection of Copper Bipolar Plates in Proton Exchange Membrane Fuel Cells

    Source: Journal of Electrochemical Energy Conversion and Storage:;2022:;volume( 019 ):;issue: 003::page 31007-1
    Author:
    Mohamed, Mohamed E.
    ,
    Abd-El-Nabey, Beshier A.
    DOI: 10.1115/1.4053782
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Superhydrophobic cobalt and cobalt–graphene films were fabricated on copper bipolar plates (BPPs) using potentiostatic electrodeposition to improve their corrosion resistance and surface conductivity. A scanning electron microscope (SEM) was used to study the surface morphology of the prepared superhydrophobic films. The results show that the cobalt film modified by stearic acid (Co-SA) and cobalt–graphene composite modified by stearic acid (Co–G-SA) exhibit micro–nano structures. The results of the Fourier transforming infrared (FTIR) spectrophotometer confirm that the copper substrate was coated by Co-SA and Co–G-SA films. The wettability results of the prepared superhydrophobic films demonstrate that the films display superhydrophobicity, where the fabricated Co-SA and Co–G-SA films have contact angles (CAs) of 159 deg and 165 deg, respectively. Chemical stability, mechanical abrasion resistance, surface conductivity, and corrosion resistance in a simulated proton exchange membrane fuel cells (PEMFCs) environment are significantly higher for copper coated by Co–G-SA film. Because the copper coated with Co–G-SA has a low interfacial contact resistance (ICR) value and a high corrosion resistance, it is thought to be a good choice for PEMFC bipolar plates.
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      Superhydrophobic Cobalt–Graphene Composite for the Corrosion Protection of Copper Bipolar Plates in Proton Exchange Membrane Fuel Cells

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4285284
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    • Journal of Electrochemical Energy Conversion and Storage

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    contributor authorMohamed, Mohamed E.
    contributor authorAbd-El-Nabey, Beshier A.
    date accessioned2022-05-08T09:33:39Z
    date available2022-05-08T09:33:39Z
    date copyright3/7/2022 12:00:00 AM
    date issued2022
    identifier issn2381-6872
    identifier otherjeecs_19_3_031007.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4285284
    description abstractSuperhydrophobic cobalt and cobalt–graphene films were fabricated on copper bipolar plates (BPPs) using potentiostatic electrodeposition to improve their corrosion resistance and surface conductivity. A scanning electron microscope (SEM) was used to study the surface morphology of the prepared superhydrophobic films. The results show that the cobalt film modified by stearic acid (Co-SA) and cobalt–graphene composite modified by stearic acid (Co–G-SA) exhibit micro–nano structures. The results of the Fourier transforming infrared (FTIR) spectrophotometer confirm that the copper substrate was coated by Co-SA and Co–G-SA films. The wettability results of the prepared superhydrophobic films demonstrate that the films display superhydrophobicity, where the fabricated Co-SA and Co–G-SA films have contact angles (CAs) of 159 deg and 165 deg, respectively. Chemical stability, mechanical abrasion resistance, surface conductivity, and corrosion resistance in a simulated proton exchange membrane fuel cells (PEMFCs) environment are significantly higher for copper coated by Co–G-SA film. Because the copper coated with Co–G-SA has a low interfacial contact resistance (ICR) value and a high corrosion resistance, it is thought to be a good choice for PEMFC bipolar plates.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleSuperhydrophobic Cobalt–Graphene Composite for the Corrosion Protection of Copper Bipolar Plates in Proton Exchange Membrane Fuel Cells
    typeJournal Paper
    journal volume19
    journal issue3
    journal titleJournal of Electrochemical Energy Conversion and Storage
    identifier doi10.1115/1.4053782
    journal fristpage31007-1
    journal lastpage31007-9
    page9
    treeJournal of Electrochemical Energy Conversion and Storage:;2022:;volume( 019 ):;issue: 003
    contenttypeFulltext
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