In sodium-ion batteries, layered oxide cathode materials offer the advantage of high electrochemical specific capacity. Especially, their crystal structure can accommodate Na+ ions with a relatively large radius and provide good diffusion pathways, thereby enabling excellent high-rate performance. Among various oxide cathode materials, P2-type layered transition-metal oxides have emerged as highly promising candidates for sodium-ion batteries due to their high capacity, good rate capability, and stable cycling performance. In this work, P2-type Na0.7CoO2 was successfully prepared using Na2CO3 and Co3O4 as raw materials through a simple high-temperature solid-state preparation method. Furthermore, the partial substitution of Na with Li is used here to prepare Na0.6Li0.1CoO2. It is confirmed from XRD analysis that both oxides, before and after Li substitution, have the P2-type layered structure with a hexagonal lattice (space group P63/mmc). A trace amount of the LiCoO2 impurity phase is detected in the Li-substituted sample. It is revealed from electrochemical measurements that the Na0.6Li0.1CoO2 cathode delivers the large discharge capacity of 129.7 mAh g−1 at 1C rate, representing a 12.6% increase over the pristine Na0.7CoO2. Meanwhile, Na0.6Li0.1CoO2 also exhibits excellent high-rate discharge capability, retaining the discharge capacity of 93.1 mAh g−1 at 20 C rate. In addition, Na0.6Li0.1CoO2 cathode shows good cycling stability, with the good capacity retention of 81.8% after 300 cycles.



