Journal of The Electrochemical Society · 2018 · 70 citations · 43 references
Natural SciencesMaterials EngineeringMaterials ScienceElectrochemical EngineeringElectrochemistryEnergy MaterialsBattery MaterialsBattery TechnologyElectrochemical CellsElectrochemical Energy StorageElectrochemical KineticsElectrode MaterialsBattery ModelingElectrochemical CharacterizationElectrochemical ModelingElectrode DesignElectrode PolarizationGraphite AnodesLithium-ion BatteriesOverpotential
The influence of the negative electrode design on its electrochemical performance with regard to Li insertion/de-insertion is analyzed in this work. A combined experimental/modeling approach is undertaken relying on Newman continuum model. Various designs of industry-grade graphite electrodes (2-6 mAh cm -2 ) were previously characterized by measuring geometric and physical parameters that are used as input parameters in the present model analysis. The half-cell model is successfully validated against rate-capability experiments without any further parameter fitting. The various polarization contributions are then identified based on the model analysis of rate-capability tests on the various electrodes. It emerges that low-loading electrodes suffer from larger particle-scale limitations (mainly solid-diffusion limitation) than high-loading electrodes because of a lower active surface area per geometric area. However, high-loading electrodes undergo large liquid-phase limitations at medium to high current densities: a large overpotential develops because of the formation of a large salt concentration gradient across the cell. Finally, the graphite electrode model is used into a full-cell model vs. LiNi 0.33 Mn 0.33 Co 0.33 O 2 (NMC) as the positive electrode. Simulations allow for a forecast of the occurrence of Li plating for various cell designs with the constraint of a constant ratio of negative to positive electrode loading.
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Porous‐electrode theory with battery applications
John Newman, William Tiedemann · AIChE Journal · 1975 · 1.2K citations · Full text