Improving rate capacity and cycling performance of lithium-rich high-Mn Li1.8[Mn0.7Co0.15Ni0.15]O2.675 cathode materials by Li2SiO3 coating

被引:32
作者
Gao, Kai [1 ,2 ]
Zhao, Shi-Xi [1 ]
Guo, Shuang-Tao [1 ,2 ]
Nan, Ce-Wen [2 ]
机构
[1] Tsinghua Univ, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Sch Mat Sci & Engn, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium ion batteries; Lithium-excess high manganese layered oxides; Cathode materials; Carbonate co-precipitation method; Li2SiO3; Coating; X-RAY-ABSORPTION; ELECTROCHEMICAL PERFORMANCE; ION BATTERY; RATE CAPABILITY; IMPROVEMENT; BEHAVIOR;
D O I
10.1016/j.electacta.2016.04.085
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Spherical lithium-excess high manganese layered oxides, Li-1.8[Mn0.7Co0.15Ni0.15]O-2.675, were successfully synthesized by carbonate co-precipitation method. To further improve the electrochemical performance of this cathode materials, spherical Li-1.8[Mn0.7Co0.15Ni0.15]O-2.675 particles were functionally modified with fast Li+-ion conductor Li2SiO3 via a sol-gel method. The structural change features were systematically characterized by powder X-ray diffraction, high-resolution transmission electron microscopy, scanning electron microscopy, cyclic voltammograms and electrochemical impedance spectroscopy. The results show that Li2SiO3 coating layer can greatly improves the diffusion rate of Lithium ions at the interface between cathode materials and electrolyte, Li-1.8[Mn0.7Co0.15Ni0.15]O-2.675@ Li2SiO3 composite cathode materials exhibits outstanding rate capability(*), cycle stability and low polarization. This excellent performance is attributes to Li2SiO3 coating layer can prevent electrode from the corrosion of electrolyte and improve the diffusion rate of lithium ion. 1.5 wt% Li2SiO3 coating sample shows the highest rate capacity (approximately 250 mAh g(-1) at 0.1C and 160 mAh g(-1) at 1C) and stable cyclic performance when cycled between 2.5-4.8 V at 25 degrees C. (C) 2016 Elsevier Ltd. All rights reserved.
引用
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页码:1 / 9
页数:9
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