Unravelling the Influence of Synthetic Paths on the Cation Arrangement in Lithium-rich Layered Oxide Cathode Materials

Lithium-rich layered oxides (LLOs) have garnered substantial attention due to their superior reversible capacity. However, oxygen release and transition metal migration are likely to occur during the charging and discharging process because of the inherently unstable structure of LLOs, which hampers their commercialization process. Present studies suggest that the local structure and atomic arrangement have a considerable impact on the stability of LLOs. Hence, researchers have been trying to determine how to implement the control of atomic ordering. Herein, we propose a new strategy to modify the cation arrangement of LLOs by adjusting the mixing order of cations through the sol-gel method. As a result, the optimized S-LLO sample presents a more ordered cation arrangement than that of the pristine M-LLO sample. The S-LLO cathode, meanwhile, provides a high discharging capacity of 249.5 mAh center dot g 1 accompanied by a coulombic efficiency of 73.7% at 0.1 C and can still maintain a capacity of 91.8 mAh center dot g 1 at 10 C. More importantly, a high-capacity retention of 71.7% can be obtained after 150 cycles at 1 C for the optimized LLO cathode, whereas the pristine M-LLO sample retains a retention of only 45.5%.