Layered nickel-rich transition metal oxide has been receiving much attention as high-energy-density cathode materials for rechargeable lithium-ion batteries. However, the severe capacity fading caused by bulk structural degradation of Ni-rich cathodes during lithiation/delithiation obstructs their commercialization. Herein, we modify the LiNi 0.92 Co 0.06 Al 0.02 O 2 (NCA92) cathode materials by W 6 + cation and BO 3 3À polyanion codoping to improve the structural stability and upgrade the electrochemical reversibility. The co-doped NCA92 materials show remarkably improved cycling stability at 1 C with a capacity retention of 93.4 % after 100 cycles, whereas the pristine cathodes exhibit poor capacity retention of 53.0 % and suffer severe structural deterioration. Further studies reveal that the particle fragmentation resulted from the inherent internal strain and the structural degradation upon cycling can be effectively mitigated by W 6 + cation and BO 3 3À polyanion codoping. Besides, W 6 + and BO 3 3À co-doping could enlarge the interlayer spacing of NCA92, thus increasing lithium-ion diffusion coefficient, which is conducive to enhancing the rate capability. The present work demonstrates that cationic-anionic co-doping is an effective strategy to maintain the structural stability of Ni-rich cathode materials, and it promotes the development of stable cathode materials for high energy density lithium-ion batteries.