阴极
材料科学
反铁磁性
原子轨道
化学物理
结构稳定性
三元运算
凝聚态物理
共价键
氧化物
格子(音乐)
价(化学)
分子物理学
各向异性
结晶学
石墨烯
密度泛函理论
联轴节(管道)
电子结构
纳米技术
镍
化学
作者
Chenzhaosha Li,Yujia He,Weiping Li,Kai Jia,Pengfei Li,Kunzhi Hou,Guorui Yang,Ming Xu,Shujiang Ding,Kai Xi
标识
DOI:10.1002/anie.202522851
摘要
ABSTRACT Direct regeneration of spent layered ternary oxide cathodes offers a sustainable pathway for resource recovery and circular battery manufacturing. However, their long‐term stability is fundamentally constrained by intrinsic electronic interactions. In particular, the inherent π‐type hybridization between Ni 3 d orbitals and O 2 p orbitals facilitates detrimental Ni migration and rock‐salt phase formation, ultimately leading to rapid capacity degradation. Here, we leverage the preexisting Li vacancies in spent LiNi 0.5 Co 0.2 Mn 0.3 O 2 (NCM) as orientation sites to induce localized lattice stress fields during regeneration. The resulting lattice perturbation modulates the spin configuration of bridging O anions, thereby triggering antiferromagnetic coupling between adjacent Ni cations and O anions. Consequently, the Ni─O orbital hybridization transitions from weak π‐dominated to robust σ‐dominated interactions, as evidenced by enhanced covalent character of the Ni─O bonds. This reinforced bonding framework effectively suppresses Ni migration and defect propagation during repeated lithiation/delithiation cycles. As a result, the regenerated NCM cathode exhibits significantly improved durability, retaining ∼60% of its initial capacity after 750 cycles. These findings reveal a direct correlation between the local valence bond evolution and cycling reversibility of cathode materials, offering new design principles and mechanistic insights for stabilizing regenerated cathode materials.
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