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dc.contributor.authorMohan, T. Ajeesh
dc.contributor.authorJithin, M.
dc.contributor.authorDas, Malay K.
dc.date.accessioned2024-12-24T19:04:24Z
dc.date.available2024-12-24T19:04:24Z
dc.date.copyright1/8/2024 12:00:00 AM
dc.date.issued2024
dc.identifier.issn2381-6872
dc.identifier.otherjeecs_21_4_041005.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4303237
dc.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.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleLattice Boltzmann Simulations of Non-Homogeneous Li–O2 Battery Cathode: The Effect of Spatial and Temporal Porosity Variations
dc.typeJournal Paper
dc.journal.volume21
dc.journal.issue4
dc.journal.titleJournal of Electrochemical Energy Conversion and Storage
dc.identifier.doi10.1115/1.4063489
dc.journal.fristpage41005-1
dc.journal.lastpage41005-16
dc.page16
dc.treeJournal of Electrochemical Energy Conversion and Storage:;2024:;volume( 021 ):;issue: 004
dc.contenttypeFulltext


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