Biphasic high-entropy layered oxide as a stable and high-rate cathode for sodium-ion batteries

被引:39
|
作者
Mu, Jinxiao [1 ,2 ]
Cai, Tianxun [1 ,2 ]
Dong, Wujie [1 ]
Zhou, Ce [3 ,4 ]
Han, Zhen [1 ]
Huang, Fuqiang [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine M, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Peking Univ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
[4] Peking Univ, Coll Chem & Mol Engn, State Key Lab Rare Earth Mat Chem & Applicat, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
Sodium ion batteries; Layered oxide cathode; O3/P2 hybrid phase; High-entropy; Structure evolution; High-rate;
D O I
10.1016/j.cej.2023.144403
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
O3-phase layered oxides are promising cathode materials for sodium-ion batteries. However due to the strong Na+ -O2- electrostatic attraction and the large size of Na ion, the O3 type cathodes suffer inferior rate capability and undesired phase transitions induced fast capacity fading. Herein, we propose a synergetic strategy of secondary phase (P2) and high-entropy to alleviate the aforementioned problems. Such a novel biphasic highentropy (B-HE) layered cathode Na0.85Li0.05Ni0.25Cu0.025Mg0.025Fe0.05Al0.05Mn0.5Ti0.05O2 exhibits a specific capacity of 122 mAh g(-1) at 0.2C, outstanding rate capacity of 81.8 mAh g(-1) at 10C, and long-term cycling stability of similar to 90% capacity retention after 1000 cycles at 10C. In situ XRD and electrochemical characterization demonstrate reversible phase transition of O3/P2 -> P3/P2 -> OP2/OP4, and the long-term existed P phase with fast Na ion migration paths. This biphasic high-entropy design strategy provides a promising road for advanced cathodes of Sodium-ion batteries.
引用
收藏
页数:7
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