阴极
阳极
水溶液
材料科学
电池(电)
储能
插层(化学)
化学工程
电解质
化学
电极
无机化学
物理化学
物理
工程类
功率(物理)
量子力学
作者
Ning Zhang,Yang Dong,Ming Jia,Xu Bian,Yuanyuan Wang,Mande Qiu,Jianzhong Xu,Yongchang Liu,Lifang Jiao,Fangyi Cheng
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-05-16
卷期号:3 (6): 1366-1372
被引量:1048
标识
DOI:10.1021/acsenergylett.8b00565
摘要
We report an aqueous Zn–V 2 O 5 battery chemistry employing commercial V 2 O 5 cathode, Zn anode, and 3 M Zn(CF 3 SO 3 ) 2 electrolyte. We elucidate the Zn-storage mechanism in the V 2 O 5 cathode to be that hydrated Zn 2+ can reversibly (de)intercalate through the layered structure. The function of the co-intercalated H 2 O is revealed to be shielding the electrostatic interactions between Zn 2+ and the host framework, accounting for the enhanced kinetics. In addition, the pristine bulk V 2 O 5 gradually evolves into porous nanosheets upon cycling, providing more active sites for Zn 2+ storage and thus rendering an initial capacity increase. As a consequence, a reversible capacity of 470 mAh g –1 at 0.2 A g –1 and a long-term cyclability with 91.1% capacity rentention over 4000 cycles at 5 A g –1 are achieved. The combination of the good battery performance, safety, scalable materials synthesis, and facile cell assembly indicates this aqueous Zn–V 2 O 5 system is promising for stationary grid storage applications.
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