Long-Range Cationic Disordering Induces two Distinct Degradation Pathways in Co-Free Ni-Rich Layered Cathodes.
Wei-Bo HuaJilu ZhangSuning WangYi ChengHang LiJochi TsengZhonghua WuChong-Heng ShenOleksandr DolotkoHao LiuSung-Fu HungWei TangMingtao LiMichael KnappHelmut EhrenbergSylvio IndrisXiao-Dong GuoPublished in: Angewandte Chemie (International ed. in English) (2023)
Ni-rich layered oxides are one of the most attractive cathode materials in high-energy-density lithium-ion batteries, their degradation mechanisms are still not completely elucidated. Herein, we report a strong dependence of degradation pathways on the long-range cationic disordering of Co-free Ni-rich Li 1-m (Ni 0.94 Al 0.06 ) 1+m O 2 (NA). Interestingly, a disordered layered phase with lattice mismatch can be easily formed in the near-surface region of NA particles with very low cation disorder (NA-LCD, m≤0.06) over electrochemical cycling, while the layered structure is basically maintained in the core of particles forming a "core-shell" structure. Such surface reconstruction triggers a rapid capacity decay during the first 100 cycles between 2.7 and 4.3 V at 1 C or 3 C. On the contrary, the local lattice distortions are gradually accumulated throughout the whole NA particles with higher degrees of cation disorder (NA-HCD, 0.06≤m≤0.15) that lead to a slow capacity decay upon cycling.