材料科学
结构稳定性
超晶格
阴极
动力学
兴奋剂
氧化物
扩散
化学工程
理论(学习稳定性)
化学物理
结晶学
光电子学
电极
作者
Xiaoxu Yang,Zihan Li,Yue Wang,Jiaxuan Li,Jiaxuan Li,Zhifeng Guo,Lei Yue,Juan Zhang,Xindong Wang,Jianling Li,Jianling Li
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2026-06-26
卷期号:40 (27): 14839-14849
标识
DOI:10.1021/acs.energyfuels.6c01045
摘要
Sodium-ion batteries (SIBs) are highly promising for large-scale energy storage due to the abundance and low cost of sodium resources. Among various cathode materials, layered transition metal oxides are considered one of the most commercially viable systems, thanks to their high theoretical capacity, mature synthesis processes, and favorable two-dimensional ion diffusion pathways that enable fast ion transport. However, their practical application is still hindered by challenges such as structural instability and interfacial side reactions. Conventional single-element doping strategies often struggle to address these multiple issues simultaneously. This study focuses on the superlattice-structured P2–Na 0.80 Li 0.13 Ni 0.20 Mn 0.67 O 2 cathode material. A TbF 3 synergistic doping strategy is employed to achieve concurrent optimization of the crystal structure and interfacial chemistry. The doping effectively promoted reversible anionic redox reactions while suppressing electrolyte decomposition and interfacial side reactions. Electrochemical tests reveal that the optimized sample exhibits a capacity retention of 84.01% after 200 cycles at 0.5 C within the voltage range of 2–4.5 V and delivers a capacity of 94.08 mAh g –1 at a high rate of 5 C, significantly outperforming the undoped sample. This work provides a novel rare-earth and anion synergistic doping strategy for designing high-performance SIBs.
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