Journal of The Electrochemical Society · 2010 · 344 citations · 47 references
Performance LossCrystal StructureEngineeringChemical EngineeringSodium BatteryBattery DegradationMaterials ScienceElectrical EngineeringBattery Electrode MaterialsElectrochemical Power SourceLithium-ion BatteryLithium-ion BatteriesStructural AnalysesEnergy StorageSolid-state BatteryElectrochemistryElectric BatteryLi-ion Battery MaterialsCathode MaterialsGrapheneElectrochemical Energy StorageBatteriesAnode Materials
The study examines how carbon negative degradation and loss of active lithium jointly limit LiFePO₄ battery capacity within a unified degradation mechanism. Performance loss was investigated by galvanostatic charge–discharge, AC impedance, hybrid pulse power measurements, and by destructive physical and ex‑situ electrochemical analyses on selected cells. Loss of lithium and cracking/delamination of the carbon negative, along with graphite crystal‑structure changes, were found to limit cell capacity, with active‑lithium depletion directly correlating with degradation.
The performance loss of lithium-ion batteries with lithium iron phosphate positive chemistry was analyzed using electrochemical characterization techniques such as galvanostatic charge–discharge at different rates, ac impedance, and hybrid pulse power characterization measurements. Differentiation analysis of the discharge profiles as well as in situ reference electrode measurement revealed loss of lithium as well as degradation of the carbon negative; the cell capacity, however, was limited by the amount of active lithium. Destructive physical analyses and ex situ electrochemical analyses were performed at test completion on selected cells. While no change in positive morphology and performance was detected, significant cracking and delamination of the carbon negative was observed. In addition, X-ray diffraction analysis confirmed the changes in the crystal structure of the graphite during cycling. The degradation of the carbon negative is consistent with the observations from the electrochemical analysis. Ex situ electrochemical analysis confirmed that active lithium controlled cell capacity and its loss with cycling directly correlated with cell degradation. The relationship between carbon negative degradation and loss of active lithium is discussed in the context of a consistent overall mechanism.
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