Anthracite-Derived Dual-Phase Carbon-Coated Li3V2(PO4)3 as High-Performance Cathode Material for Lithium Ion Batteries

被引:54
作者
Ding, Xiao-Kai [1 ]
Zhang, Lu-Lu [1 ]
Yang, Xue-Lin [1 ]
Fang, Hui [2 ]
Zhou, Ying-Xian [1 ]
Wang, Ji-Qing [1 ]
Ma, Di [1 ]
机构
[1] China Three Gorges Univ, Coll Mat & Chem Engn, Hubei Prov Collaborat Innovat Ctr New Energy Micr, 8 Dame Rd, Yichang 443002, Hubei, Peoples R China
[2] Sam Houston State Univ, Dept Phys, Huntsville, TX 77341 USA
基金
中国国家自然科学基金;
关键词
lithium ion battery; cathode material; lithium vanadium phosphate; anthracite; dual-phase carbon; SOL-GEL METHOD; ELECTROCHEMICAL PERFORMANCE; VANADIUM PHOSPHATE; COMPOSITE; MICROSPHERES; DENSITY; COAL;
D O I
10.1021/acsami.7b14117
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this study, low cost anthracite-derived dual-phase carbon-coated Li3V2(PO4)(3) composites have been successfully prepared via a traditional solid-phase method. XRD results show that the as-prepared samples have high crystallinity and anthracite introduction has no influence on the LVP crystal structure. The LVP/C particles are uniformly covered with a dual-phase carbon layer composed of amorphous carbon and graphitic carbon. The effect of the amount of anthracite on the battery performance of LVP as a cathode material has also been studied. The LVP/C composite obtained with 10 wt % anthracite (LVP/C-10) delivers the highest initial charge/discharge capacities of 186.1/168.2 mAh g(-1) at 1 C and still retains the highest discharge capacity of 134.0 mAh g(-1) even after 100 cycles. LVP/C-10 also displays an outstanding average capacity of 140.8 mAh g(-1) at 5 C. The superior rate capability and cycling stability of LVP/C-10 is ascribed to the reduced particle size, decreased charge-transfer resistance, and improved lithium ion diffusion coefficient. Our results demonstrate that using anthracite as a carbon source opens up a new strategy for larger-scale synthesis of LVP and other electrode materials with poor electronic conductivity for lithium ion batteries.
引用
收藏
页码:42788 / 42796
页数:9
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