Compatibility between lithium difluoro (oxalate) borate-based electrolytes and Li1.2Mn0.54Ni0.13Co0.13O2 cathode for lithium-ion batteries

被引:33
|
作者
Li, Shiyou [1 ,2 ,3 ]
Liang, Youwei [1 ]
Xie, Jing [1 ]
Ai, Ling [1 ]
Xie, Yingchun [1 ]
Li, Chunlei [1 ,3 ]
Wang, Chao [1 ]
Cui, Xiaoling [1 ,2 ,3 ]
机构
[1] Lanzhou Univ Technol, Coll Petrochem Technol, Lanzhou 730050, Gansu, Peoples R China
[2] Qinghai Green Grass New Energy Technol Co Ltd, Qinghai Res Ctr Low Temp Lithium Ion Battery Tech, Xining 810000, Qinghai, Peoples R China
[3] Gansu Engn Lab Electrolyte Mat Lithium Ion Batter, Lanzhou 730050, Gansu, Peoples R China
关键词
Lithium-ion batteries; Li1.2Mn0.54Ni0.13Co0.13O2; Lithium difluoro (oxalate) borate; Compatibility; ELECTROCHEMICAL PERFORMANCE; HIGH-CAPACITY; SURFACE; DIFLUORO(OXALATO)BORATE; PARTICIPATION; REACTIVITY; ELECTRODES; INTERFACE; STABILITY; MECHANISM;
D O I
10.1016/j.jelechem.2018.07.019
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Lithium-rich layered oxide is a promising cathode material for high-energy density lithium ion batteries. Generally, it is essential to develop high-voltage electrolyte because electrolyte is one of the key factors that determines the capacity of cathode materials. In this work, lithium difluoro(oxalato) borate (LiODFB) is introduced as a novel lithium-salt for lithium-rich cathodes. The investigation reveals that the LiODFB modifies the surface film and forms a uniform and electrochemical stable cathode electrolyte interface (CEI) on the lithium-rich cathode. The LiODFB-derived CEI layer effectively suppresses severe electrolyte decomposition at high voltages and hinders undesirable phase transformation from layered to spinel-like phases during cycling. Furthermore, the Li1.2Mn0.54Ni0.13Co0.13O2/Li cell with the LiODFB-based electrolyte exhibits high capacity retention of 91.73% after 50 cycles and better rate capability of 195 mAh g(-1) at 2 C. The unique function of the LiODFB on the surface chemistry of lithium-rich cathodes is confirmed through X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy analyses.
引用
收藏
页码:688 / 696
页数:9
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