Potassium phosphate monobasic induced decoration from the surface into the bulk lattice for Ni-rich cathode materials with enhanced cell performance

被引:11
作者
Zhang, Dianwei [1 ,2 ]
Li, Yunjiao [1 ,2 ]
Xi, Xiaoming [3 ]
Chang, Shenghong [1 ,2 ]
Wang, Shan [1 ,2 ]
Yang, Jiachao [1 ,2 ]
Zheng, Junchao [1 ,2 ]
Li, Wei [1 ,4 ]
机构
[1] Cent South Univ, Sch Met & Environm, Changsha 410083, Peoples R China
[2] Cent South Univ, Engn Res Ctr, Minist Educ Adv Battery Mat, Changsha 410083, Peoples R China
[3] Changsha Res Inst Min & Met, Changsha 410083, Peoples R China
[4] Cit Dameng Min Ind Ltd, Nanning 530028, Peoples R China
来源
SUSTAINABLE ENERGY & FUELS | 2020年 / 4卷 / 07期
关键词
LITHIUM-ION BATTERIES; ELECTROCHEMICAL PERFORMANCE; STRUCTURAL TRANSITION; STORAGE PROPERTY; COATING LAYER; OXIDE CATHODE; LI; VOLTAGE; IMPROVEMENT; LINI0.8CO0.15AL0.05O2;
D O I
10.1039/d0se00403k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interfacial instability and intrinsic structural degradation of cathodes, which cause performance loss and even a safety hazard, are a critical challenge in Ni-rich cathodes during long-term cycling. Herein, potassium phosphate monobasic modified LiNi0.8Co0.1Mn0.1O2, whereby a Li(3)PO(4)coating layer coupled with trace-levels of co-doped K(+)and PO(4)(3-)are synchronously constructed, was successfully synthesizedviaa one-step calcination process at high temperature. Impressively, the optimized 2@KP-NCM delivered superior electrochemical performance, particularly at high rate and elevated temperature. High capacity retention rates of 90.6% at a 5C-rate at room temperature after 200 cycles and 92% at a 1C-rate at 55 degrees C after 100 cycles in the voltage range of 3.0-4.4 V were reached, and these are clearly higher than those of the pristine cathode (only 73.4% and 51%, respectively). Such a great improvement on the cycling stability is mainly attributed to the pillaring effect of doped-ions on stabilizing the layered structure and suppressing the deleterious irreversible phase-transition as well as the interfacial protective layer effectively protecting the active core cathode from the chemical attack of side products.
引用
收藏
页码:3352 / 3362
页数:11
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