Constructing a Size-Controllable Spherical P2-Type Layered Oxides Cathode That Achieves Practicable Sodium-Ion Batteries

被引:5
|
作者
Yin, Shuo [1 ]
Tao, Zongzhi [2 ]
Zhang, Yuying [1 ]
Zhang, Xinpeng [1 ]
Yu, Lai [2 ]
Ji, Fangli [1 ]
Ma, Xinyi [2 ]
Yuan, Guohe [1 ]
Zhang, Genqiang [2 ]
机构
[1] CNGR Adv Mat Co Ltd, Changsha 410600, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
sodium-ion battery; layered metal oxides; controllingprecursors; morphological design; cylindrical cell; NI; CHALLENGES; PHASE; CO; LI;
D O I
10.1021/acsami.4c04855
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
P2-type layered metal oxides are regarded as promising cathode materials for sodium-ion batteries due to their high voltage platform and rapid Na+ diffusion kinetics. However, limited capacity and unfavorable cycling stability resulting from inevitable phase transformation and detrimental structure collapse hinder their future application. Herein, based on P2-type Na0.67Ni0.18Mn0.67Cu0.1Zn0.05O2, we synthesized a series of secondary spherical morphology cathodes with different radii derived from controlling precursors prepared by a coprecipitation method, which can be promoted to large-scale production. Consequently, the synthesized materials possessed a high tap density of 1.52 g cm(-3) and a compacted density of 3.2 g cm(-3). The half cells exhibited a specific capacity of 111.8 mAh g(-1) at a current density of 0.1 C as well as an 82.64% capacity retention with a high initial capacity of 85.80 mAh g(-1) after 1000 cycles under a rate of 5 C. Notably, in situ X-ray diffraction revealed a reversible P2-OP4 phase transition and displayed a tiny volume change of 6.96% during the charge/discharge process, indicating an outstanding cycling stability of the modified cathode. Commendably, the cylindrical cell achieved a capacity of 4.7 Ah with almost no change during 1000 cycles at 2 C, suggesting excellent potential for future applications.
引用
收藏
页码:26340 / 26347
页数:8
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