阴极
氧化物
结构稳定性
材料科学
结构变化
降级(电信)
相变
化学工程
复合氧化物
兴奋剂
相(物质)
氧气
过渡金属
纳米技术
格子(音乐)
工作(物理)
电极
化学物理
对偶(语法数字)
机制(生物学)
化学
双重角色
电化学
作者
Yaru Qin,Yu Miao,Yonglin Tang,Qizheng Zheng,Yuan Tian,Lianpeng Li,Yizhen Huang,Chenglong Shi,Maolin Yang,Yu Qiao,Shi‐Gang Sun
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-09-04
卷期号:26 (37): 12481-12490
标识
DOI:10.1021/acs.nanolett.6c03314
摘要
The high-voltage stability of P2-type layered oxide cathodes for sodium-ion batteries is closely related to their intrinsic structural characteristics. However, complex phase transitions and structural degradation at high voltage lead to rapid capacity decay. Here, a synergistic Li/Nb co-doped P2-type layered cathode is developed. Li doping disrupts Na+/vacancy ordering and redirects the high-voltage phase-transition pathway from a deleterious P2→O2 transition toward a milder Z-like O/P intergrowth evolution. Nb incorporation preserves this pathway while further reinforcing the transition-metal coordination environment. This dual modification suppresses local structural distortion, alleviates lattice strain, and mitigates irreversible oxygen release. Consequently, Na0.67Ni0.21Li0.11Mn0.63Nb0.05O2 exhibits 93.1% capacity retention after 100 cycles at 2C within 2.0-4.3 V. This work elucidates how elemental co-doping regulates local coordination and structural evolution during charge and discharge, offering a strategy for stabilizing P2-type layered oxide cathodes under high-voltage operation.
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