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A set of lithium-ion cells containing a -based positive electrode and a graphite negative electrode were cycled nonintrusively at high power (5C rate) and elevated temperature . The aged cells were characterized at prescribed cycle numbers (up to 5250 cycles) by a three-electrode cell, capacity measurement, and electrochemical impedance spectroscopy (EIS). Excellent cyclability of these cells under typical hybrid-electric vehicle conditions is demonstrated by 18% capacity fade after 5250 cycles, and the discharge capacity shows a mainly parabolic behavior with the cycle number (dependent on ) in the initial stage and a linear behavior (dependent on ) for subsequent cycles. Using a lithium reference electrode further reveals that the capacity fade during cycling is primarily caused by the positive electrode, where discharge capacity may be limited by a decrease in active lithium intercalation sites in the oxide particles. The increase in full-cell impedance with cycling is evident from the increase in midfrequency arc width , composed of charge-transfer kinetic resistance and transport resistance through the solid electrolyte interphase (SEI), . More specifically, the cell-impedance rise comes mainly from the rising and of the positive electrode. Based on individual electrode EIS spectra and equivalent-circuit analysis, it is found that the rise in the positive electrode is far more influential than the change in . Therefore, property modification and thickening of the SEI layer of the positive electrode during cycling appear to be dominant factors in cell-impedance rise and power fade.
Zhang et al. (2009) studied this question.
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