Yuansheng Shi, Yifan Xu, Jiaqi Cao, Pengfeng Jiang, Fushan Geng, Chade Lv, Ju Zhao, Weixin Chen, Dilxat Muhtar, Erhai Hu, Dongshuang Wu, Jinfeng Dong, Okkyun Seo, Jialu Li, Jinghua Guo, Yang Sun, Xia Lu, Qingyu Yan
Sodium-based P2-type layered cathodes are of interest for sodium-ion batteries due to their fast Na + transport and good cycling reversibility at elevated voltages. However, their low sodium content and irreversible Na loss on the anode side limit their practical use. Here, a self-compensated P2-Na 0.8 Li 0.06 □ 0.04 Ni 0.23 Mn 0.67 O 2 (P2-NLNM-Va) is developed with approximately 4% cation vacancies in the transition metal layer to regulate lattice oxygen activity during charge and counterbalance anode-side Na loss. The vacancies activate additional charge capacity without sacrificing discharge capacity, rate capability, or air/cycling stability. As a result, the full cells of P2-NLNM-Va//hard carbon exhibit an initial discharge capacity of 100.6 mAh/g and retain 83% capacity after 300 cycles, compared with 80.2 mAh/g and 62% for the vacancy-free counterpart. This self-compensation strategy raises energy density by about 20% to 245 Wh/kg (total mass of cathode and anode), offering a route toward practical P2-type oxide-based sodium-ion batteries.