Na3V2(PO4)3 with specially designed carbon framework as high performance cathode for sodium-ion batteries

被引:23
作者
Zheng, Li-Li [1 ]
Xue, Yuan [1 ]
Deng, Liang [1 ]
Wu, Guo-Rui [1 ]
Hao, Su-E. [1 ]
Wang, Zhen-bo [1 ,2 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, 92 West Da Zhi St, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Boerter Energy Technol Co LTD, 14955 Zhongyuan Rd, Harbin 150001, Heilongjiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Na3V2(PO4)(3); Electron channels; Aggregate structure; Sodium-ion batteries; ELECTROCHEMICAL PERFORMANCE; RATE CAPABILITY; GRAPHENE; HYDRODECHLORINATION; MECHANISM; ELECTRODE;
D O I
10.1016/j.ceramint.2018.11.153
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The structures of materials have great influence on their properties. For materials with low electron conductivity, fast electron transport pathway can be constructed through carbon structure design. Here we report a simple but effective method to improve the electrochemical performances of Na3V2(PO4)(3). Polyvinyl Pyrrolidone (PVP) can improve the viscosity of the precursor solution, thus forming aggregate structured material. In Na3V2(PO4)(3), primary particles with a diameter of approximately 300 nm are aggregated through a special carbon network to form micro-sized secondary particles. This kind of structure will provide easy access for electron transportation, thereby improving electrochemical performance of the material. As a cathode material for sodium-ion batteries, Na3V2(PO4)(3) delivers excellent rate (86.6 mAh g(-1) at 30 C) and cycling performance (capacity retention of 88.4% after 2000 cycles at 10 C). The material also exhibits a specific capacity of 100.2 mAh g(-1) at 5 C under 55 degrees C. The above-mentioned performance is far better than the control sample without PVP. The special carbon network provides electron transport channels which improves the electrochemical performance of the material. This method may provide new ideas for the preparation of phosphate materials.
引用
收藏
页码:4637 / 4644
页数:8
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