Enhanced low temperature electrochemical performances of LiFePO4/C by surface modification with Ti3SiC2

被引:50
作者
Cai, Guanglan [1 ]
Guo, Ruisong [1 ]
Liu, Li [1 ]
Yang, Yuexia [1 ]
Zhang, Chao [1 ]
Wu, Chen [1 ]
Guo, Weina [1 ]
Jiang, Hong [2 ]
机构
[1] Tianjin Univ, Key Lab Adv Ceram & Machining Technol, Minist Educ, Tianjin 300072, Peoples R China
[2] Guizhou Radio & Televis Univ, Guiyang 550004, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion battery; Ti3SiC2; Modification; LiFePO4; Electrochemical performance; Low temperature; LITHIUM-ION BATTERIES; CATHODE MATERIALS; COMPOSITE CATHODES; MAX PHASES; CARBON; ELECTROLYTE; ADDITIVES; GRAPHENE;
D O I
10.1016/j.jpowsour.2015.04.129
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
Ti3SiC2-modified LiFePO4/C cathode materials are prepared via a suspension mixing method followed by heat-treatment at 400 degrees C. The galvanostatic electrochemical measurements indicate that 4 wt% Ti3SiC2-modified LiFePO4/C exhibits the best electrochemical performances in the voltage range of 2.0-4.2 V. The sample shows the highest initial discharge capacity of 116.0 mAh g(-1) at the rate of 0.1 C at 20 degrees C. And it keeps a capacity retention of 97.0% at 1 C at - 10 degrees C after 100 cycles, higher than 81.2% for LiFePO4/C at the same conditions. Furthermore, Ti3SiC2-modified LiFePO4/C samples deliver lower charge-transfer resistance and higher diffusion coefficient of Li+ compared with the pristine LiFePO4/C, especially the 4 wt% Ti3SiC2-modified LiFePO4/C sample exhibits the lowest charge-transfer resistance and highest diffusion coefficient of Li+ among all the four samples. The improved electrochemical performances can be attributed to the lower charge transfer resistance and higher diffusion coefficient of lithium ions resulted from the modification of appropriate amount of Ti3SiC2. Besides, a series of electrochemical results show that the performances of the electrodes with 10 wt% super-P are superior to those of the electrodes with 5 wt% super-P. (c) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 144
页数:9
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