材料科学
氧化还原
阴极
氧化物
化学工程
无机化学
电化学
氧还原反应
纳米技术
电极
锂离子电池的纳米结构
催化作用
氧还原
作者
Ting Liu,Hongjie Tan,Jianyuan Wang,Chengyu Li,Z L Liu,Zhenting Wu,Yong‐Sheng Hu,Shanglong Peng
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-05-05
卷期号:20 (19): 14145-14154
被引量:7
标识
DOI:10.1021/acsnano.6c00915
摘要
The exploitation of high-capacity, long-cycle cathode materials with reversible anionic redox activity and robust structural stability remains an essential challenge for sodium-ion batteries. Herein, we address these limitations through Na–O–A configuration modulation in P2–Na 0.67 [Ni x Li y Mn 1– x–y ]O 2, which fundamentally enables reversible anionic redox reactions and ensures structural stability. The obtained P2–Na 0.67 Ni 0.23 Mn 0.67 Li 0.08 Nb 0.02 O 2 cathodes deliver a remarkable reversible capacity of 158.4 mAh g –1 at 0.1C while maintaining extraordinary cycling stability with 98.2% capacity retention after 500 cycles at 5C (a minimal capacity fade of only 0.0036% per cycle). The introduction of the Na–O–Li/Nb configuration enables dual cationic and anionic redox reactions (ARR) to enhance capacity. Meanwhile, the high-valence Nb 5+ species not only suppresses oxygen release through robust Nb–O bonds, thereby improving the reversibility of ARR, but also reinforces the structural rigidity of the transition metal-layer framework. Ultimately, this modulation strategy provides a universal pathway for designing highly stable, high-energy cathodes for next-generation sodium-ion batteries.
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