Three-Dimensional Honeycomb-Structural LiAlO2-Modified LiMnPO4 Composite with Superior High Rate Capability as Li-Ion Battery Cathodes

被引:53
作者
Li, Junzhe [1 ,4 ,5 ]
Luo, Shaohua [2 ,3 ,4 ]
Ding, Xueyong [1 ]
Wang, Qing [2 ,3 ,4 ]
He, Ping [5 ]
机构
[1] Northeastern Univ, Sch Met, Shenyang 110819, Liaoning, Peoples R China
[2] Northeastern Univ, Sch Mat Sci & Engn, Shenyang 110819, Liaoning, Peoples R China
[3] Northeastern Univ Qinhuangdao, Sch Resources & Mat, Qinhuangdao 066004, Peoples R China
[4] Hebei Key Lab Dielect & Electrolyte Funct Mat, Qinhuangdao 066004, Peoples R China
[5] Cent Iron & Steel Res Inst, Met Technol Res Dept, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium-ion batteries; three-dimensional configuration; core-shell architectures; LiAlO2; templates; LiMnPO4; ELECTROCHEMICAL PERFORMANCE; CRYSTAL ORIENTATION; LOW-TEMPERATURE; POROUS ALUMINA; LIALO2; MICROBATTERIES; STORAGE; NANOPARTICLES; ELECTRODES;
D O I
10.1021/acsami.7b17597
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In the efforts toward the rapidly increasing demands for high-power application, cathode materials with three-dimensional (3D) architectures have been proposed. Here, we report the construction of the 3D LiAlO2-LiMnPO4/C cathode materials for lithium-ion batteries in an innovation way. The as-prepared 3D active materials LiMnPO4/C and the honeycomb-like Li-ion conductor LiAlO2 framework are used as working electrode directly without additional usage of polymeric binder. The electrochemical performance has been improved significantly due to the special designed core-shell architectures of LiMnPO4/C@LiAlO2. The 3D binder-free electrode exhibits high rate capability as well as superior cycling stability with a capability of similar to 105 mAh g(-1) and 98.4% capacity retention after 100 cycles at a high discharge rate of 10 C. Such synthesis method adopted in our work can be further extended to other promising candidates and would also inspire new avenues of development of 3D materials for lithium-ion batteries.
引用
收藏
页码:10786 / 10795
页数:10
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