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    Lattice Boltzmann Simulations of Non-Homogeneous Li–O2 Battery Cathode: The Effect of Spatial and Temporal Porosity Variations

    Source: Journal of Electrochemical Energy Conversion and Storage:;2024:;volume( 021 ):;issue: 004::page 41005-1
    Author:
    Mohan, T. Ajeesh
    ,
    Jithin, M.
    ,
    Das, Malay K.
    DOI: 10.1115/1.4063489
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: The porosity of the cathode in a lithium–oxygen battery is a crucial parameter that influences oxygen transport and active surface area availability. This study explores various cathode models with different initial porosity distributions and analyzes the porosity evolution during discharge. The objective is to maximize the active surface area utilization of the cathode and increase the battery’s discharge capacity. The simulations employ a recently developed lattice Boltzmann method (LBM) model proposed by Chen et al. (2017, “Simulation of Double Diffusive Convection in Fluid-Saturated Porous Media by Lattice Boltzmann Method,” Int. J. Heat Mass Transfer, 108, pp. 1501–1510), which is capable of handling spatial and temporal variations in diffusion coefficient values. The results demonstrate that a hierarchical porous cathode provides a better specific capacity than a uniform porous cathode with the same average initial porosity. The specific capacity increases as the magnitude of initial porosity variation in the domain increases. Furthermore, incorporating oxygen channels improves oxygen transport in the cathode and offers a better specific capacity than the hierarchical porous cathode. A combination of hierarchical porous media and oxygen channels delivers the best specific capacity among all the other cathode models, as it efficiently balances oxygen transport and active surface area.
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      Lattice Boltzmann Simulations of Non-Homogeneous Li–O2 Battery Cathode: The Effect of Spatial and Temporal Porosity Variations

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    contributor authorMohan, T. Ajeesh
    contributor authorJithin, M.
    contributor authorDas, Malay K.
    date accessioned2024-12-24T19:04:24Z
    date available2024-12-24T19:04:24Z
    date copyright1/8/2024 12:00:00 AM
    date issued2024
    identifier issn2381-6872
    identifier otherjeecs_21_4_041005.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4303237
    description abstractThe porosity of the cathode in a lithium–oxygen battery is a crucial parameter that influences oxygen transport and active surface area availability. This study explores various cathode models with different initial porosity distributions and analyzes the porosity evolution during discharge. The objective is to maximize the active surface area utilization of the cathode and increase the battery’s discharge capacity. The simulations employ a recently developed lattice Boltzmann method (LBM) model proposed by Chen et al. (2017, “Simulation of Double Diffusive Convection in Fluid-Saturated Porous Media by Lattice Boltzmann Method,” Int. J. Heat Mass Transfer, 108, pp. 1501–1510), which is capable of handling spatial and temporal variations in diffusion coefficient values. The results demonstrate that a hierarchical porous cathode provides a better specific capacity than a uniform porous cathode with the same average initial porosity. The specific capacity increases as the magnitude of initial porosity variation in the domain increases. Furthermore, incorporating oxygen channels improves oxygen transport in the cathode and offers a better specific capacity than the hierarchical porous cathode. A combination of hierarchical porous media and oxygen channels delivers the best specific capacity among all the other cathode models, as it efficiently balances oxygen transport and active surface area.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleLattice Boltzmann Simulations of Non-Homogeneous Li–O2 Battery Cathode: The Effect of Spatial and Temporal Porosity Variations
    typeJournal Paper
    journal volume21
    journal issue4
    journal titleJournal of Electrochemical Energy Conversion and Storage
    identifier doi10.1115/1.4063489
    journal fristpage41005-1
    journal lastpage41005-16
    page16
    treeJournal of Electrochemical Energy Conversion and Storage:;2024:;volume( 021 ):;issue: 004
    contenttypeFulltext
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