Electrochemical properties of Sn-doped Li3V2(PO4)3 cathode material synthesized via a citric acid assisted sol-gel method

被引:13
作者
Xia, Yang [1 ]
Shi, Si [1 ]
Li, Chongge [1 ,2 ]
Liang, Chu [1 ]
Gan, Yongping [1 ]
Huang, Hui [1 ,3 ]
Tao, Xinyong [1 ]
Zhang, Wenkui [1 ]
机构
[1] Zhejiang Univ Technol, Coll Mat Sci & Engn, Hangzhou 310014, Zhejiang, Peoples R China
[2] Hangzhou Haina Semicond Co Ltd, Ctr Tech, Hangzhou 310053, Zhejiang, Peoples R China
[3] Zhejiang Univ, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium vanadium phosphate; Tin; Sol-gel method; Cathode material; Lithium ion battery; LITHIUM VANADIUM PHOSPHATE; HIGH-RATE CAPABILITY; PERFORMANCE; COMPOSITE; MN; NANOCOMPOSITE; NANOPARTICLES; PHASE; TI;
D O I
10.1016/j.jallcom.2015.08.234
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
A series of Sn-doped Li3V2-xSnx(PO4)(3)/C (x = 0, 0.1, 0.15, 0.2) samples were synthesized via a citric acid assisted sol-gel method. XRD patterns indicated that all the Li3V2-xSnx(PO4)(3)/C samples were pure single phase with a monoclinic structure (space group P2(1)/n) and well crystallized. The structural refinement results and HRTEM analysis both indicated that Sn-doping did not alter the lattice structure of Li3V2(PO4)(3), but increased the unit cell volume. SEM images revealed that Sn-doping has no obvious effects on the morphology and particle size of Li3V2(PO4)(3). HRTEM, XRF and Raman results demonstrated that a thin carbon layer was coated on the surface of Li3V2-xSnx(PO4)(3)/C samples with a similar carbon content and good quality. The electrochemical performance was evaluated using coin-type half cells. Among the samples synthesized in this work, Li3V1.85Sn0.15(PO4)(3)/C exhibited the electrochemical performance in terms of specific capacity, rate capability, cycling performance. CV and EIS results implied that optimizing Sn-doping contents with x = 0.15 could greatly enhance the structural stability of Li3V2(PO4)(3) during the charge-discharge processes, as well as increase electrical conductivity with a lower charge transfer resistance and a higher Li+ diffusion coefficient. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:298 / 306
页数:9
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