In operando X-ray absorption spectroscopy study of charge rate effects on the atomic environment in graphene-coated Li-rich mixed oxide cathode

Abstract

Li2O extraction from the electrode material is known to be a dominant mechanism of irreversible battery capacity loss in the first cycle. The extraction mechanism of the Li+ ions shows dependence on the charge rate. Here for the first time we report the difference in the electrochemical behavior at two different charge rates (0.125C vs 0.5C) observed using novel design transmission coin cells in the graphene-coated Li(Li0.2Mn0.54Ni0.13Co0.13)O2 cathode by in operando X-ray absorption spectroscopy (XAS). The results obtained from Mn, Co, and Ni atom XANES/EXAFS demonstrate that, whilst during fast charge Li2O extraction is localized to the lithium slab in the crystal structure, the delithiation is deeper at the slower charge rate, when Li+ ions are removed from both the transition metal and lithium layers. In the slow charge cell, NiO bond splitting resulting from the Jahn-Teller distortion were clearly identified at approximately 4.224V when a sudden rise in the bond length was observed in the EXAFS analysis of MnO and CoO bonds. The results demonstrate the power of using the novel cell design for transmission in operando XAS.