Publication | Open Access
Understanding the Role of Commercial Separators and Their Reactivity toward LiPF<sub>6</sub> on the Failure Mechanism of High‐Voltage NCM523 || Graphite Lithium Ion Cells
61
Citations
89
References
2021
Year
EngineeringTheir ReactivityChemistryChemical EngineeringNanoengineeringHigh ReactivitySeparator ArchitectureFailure MechanismTransition MetalSodium BatteryMaterials ScienceBattery Electrode MaterialsCommercial SeparatorsAdvanced Electrode MaterialLithium-ion BatteryLithium-ion BatteriesEnergy StorageSolid-state BatteryElectrochemistryElectric BatteryLi-ion Battery MaterialsElectrochemical Energy StorageBatteriesAnode Materials
Abstract NCM523 || graphite lithium ion cells operated at 4.5 V are prone to an early “rollover” failure, due to electrode cross‐talk, that is, transition metal (TM = Mn, Ni, and Co) dissolution from NCM523 and deposition at graphite, subsequent formation of Li metal dendrites, and, in the worst case, generation of (micro‐)short‐circuits by dendrites growing to the cathode. Here, the impact of different separators on the high‐voltage performance of NCM523 || graphite cells is elucidated focusing on the separators’ structural properties (e.g., membrane vs fiber) and their reactivity toward LiPF 6 (e.g., ceramic‐coated separators). First, the separator architecture has a major impact on cycle life. Fiber‐structured separators can prevent the “rollover” failure by a more homogeneous deposition of TMs and formation of Li metal dendrites, thus, hindering penetration of dendrites to the cathode. In contrast, porous membrane‐structured separators cannot prevent the cell failure due to inhomogeneous TM deposits/Li metal dendrites. Second, it is demonstrated that different types of ceramic‐coated separators (Boehmite (γ‐AlO(OH)) vs α‐Al 2 O 3 ) exhibit different reactivities toward LiPF 6 . While α‐Al 2 O 3 shows a minor reactivity toward LiPF 6 , the γ‐AlO(OH) coating leads to in situ formation of the beneficial difluorophosphate anion in high amounts due the high reactivity toward LiPF 6 decomposition, which significantly improves cycle life.
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