Publication | Open Access
High‐Energy Nickel‐Cobalt‐Aluminium Oxide (NCA) Cells on Idle: Anode‐ versus Cathode‐Driven Side Reactions
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Citations
48
References
2021
Year
EngineeringEnergy ConversionChemical EngineeringTemperature DependenciesBattery DegradationMaterials ScienceElectrical EngineeringBattery Electrode MaterialsCommercial High‐energy 21700Advanced Electrode MaterialLithium-ion BatteryLithium-ion BatteriesEnergy StorageCatalysisEnergySolid-state BatteryElectrochemical ProcessElectrochemistryElectric BatteryLi-ion Battery MaterialsHigh‐energy Nickel‐cobalt‐aluminium OxideMetal AnodeCalendar AgeingElectrochemical Energy StorageBatteriesAnode Materials
Abstract We report on the first year of calendar ageing of commercial high‐energy 21700 lithium‐ion cells, varying over eight state of charge (SoC) and three temperature values. Lithium‐nickel‐cobalt‐aluminium oxide (NCA) and graphite with silicon suboxide (Gr‐SiO x ) form cathodes and anodes of those cells, respectively. Degradation is fastest for cells at 70–80 % SoC according to monthly electrochemical check‐up tests. Cells kept at 100 % SoC do not show the fastest capacity fade but develop internal short circuits for temperatures T ≥40 °C. Degradation is slowest for cells stored close to 0 % SoC at all temperatures. Rates of capacity fade and their temperature dependencies are distinctly different for SoC values below and above 60 %, respectively. Differential voltage analyses, apparent activation energy analysis, and endpoint slippage tracking provide useful insights into the degradation mechanisms and the respective roles of anode and cathode potential. We discuss how reversible losses of lithium might play a role in alleviating the rate of irreversible losses on commercial cells.
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