Extending the cycle life of Na3V2(PO4)3 cathodes in sodium-ion batteries through interdigitated carbon scaffolding

被引:67
作者
Jiang, Xi [1 ]
Yang, Liuqing [1 ]
Ding, Bo [1 ]
Qu, Baihua [1 ,2 ,3 ]
Ji, Ge [1 ]
Lee, Jim Yang [1 ]
机构
[1] Natl Univ Singapore, Dept Chem & Biomol Engn, 10 Kent Ridge Crescent, Singapore 119260, Singapore
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, Block N4-1,Nanyang Ave, Singapore 639798, Singapore
[3] Xiamen Univ, Pen Tung Sah Inst Micronano Sci & Technol, 422 Siming South Rd, Xiamen 361005, Peoples R China
关键词
COATED NA3V2(PO4)(3); PERFORMANCE;
D O I
10.1039/c6ta05030a
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
The increasing interest in Na-ion batteries is based on their lower projected cost relative to Li-ion batteries and hence are more economically viable for the large-scale storage of electrical energy. Similar to Li-ion batteries, the capacity of Na-ion batteries is cathode-limited. Na3V2(PO4)(3) (NVP), a prevalent cathode candidate and one of the most stable Na-ion host materials, still exhibits capacity losses in prolonged cycling. We report herein a method which can improve the durability of NVP in extended use. This is done by using a carbon scaffold to constrain the movement of NVP during charge and discharge reactions. The procedure consists of the sol-gel synthesis of densely aligned dense NVP nanofibers under hydrothermal conditions, followed by sucrose infiltration into the interstices of these fibers to form an interdigitated carbon scaffold after calcination. The NVP-carbon nanocomposite fabricated as such shows ultra-stable cycling performance at very high C-rates, 99.9% capacity retention at 20C for more than 10 000 cycles, thereby demonstrating the effectiveness of the materials design principles behind this modification strategy.
引用
收藏
页码:14669 / 14674
页数:6
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