Journal of The Electrochemical Society · 2024 · 42 citations · 82 references
ElectrolytesEngineeringLayered Transition MetalChemistryChemical EngineeringElectrical EngineeringCell PerformanceElectrochemical Power SourceLithium-ion BatteryBattery AdditivesLithium-ion BatteriesLipf 6Lithium-ion Battery CellsEnergy StorageSolid-state BatteryElectrochemistryElectric BatteryElectrochemical Energy StorageBatteries
The trend for increased nickel content in layered transition metal oxide cathode active materials and increasing charging cut-off voltages aggravates aging of lithium-ion battery cells at high state of charge (SOC). We investigate the calendaric aging behavior of large-format automotive prototype cells and laboratory single-layer pouch cells at high but realistic cell voltages/SOCs and demonstrate that electrolyte oxidation in combination with follow-up reactions can cause a significant loss of the LiPF 6 salt in the electrolyte. For this, we analyze the LiPF 6 concentration in aged cells, the generation of H 2 upon storage, and the cell resistance for different aging conditions. We show that the LiPF 6 loss is a critical aging phenomenon, as it cannot readily be detected by capacity fading measurements at low/medium C-rates or by cell resistance measurements, while it severely reduces rate and fast-charging capability. Under certain circumstances, LiPF 6 loss can even lead to a temporary capacity increase due to conversion of the conducting salt in the electrolyte to cyclable lithium in the active material. Finally, we suggest a possible reaction mechanism and a simple accounting model to keep track of how different side reactions involved in LiPF 6 loss change the cyclable lithium inventory of a lithium-ion cell.
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Roland Jung, Michael Metzger, Filippo Maglia et al. · Journal of The Electrochemical Society · 2017 · 1.2K citations · Full text
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