电化学
材料科学
复合数
电极
钒
水溶液
阴极
储能
化学工程
离子
价(化学)
纳米技术
化学
复合材料
冶金
物理化学
功率(物理)
有机化学
工程类
物理
量子力学
作者
Yanyi Wang,Ming Yang,Dingtao Ma,Minfeng Chen,Jizhang Chen,Tingshu He,Peixin Zhang
标识
DOI:10.1016/j.cej.2022.138809
摘要
Although V2O5 is considered as promising cathode for aqueous Zn-ion batteries (AZIBs), the poor intrinsic conductivity and unstable structure can significantly hamper its electrochemical energy storage capability. In this work, an in-situ formation strategy of V2O5/C composite nanosheets-derived from V4AlC3 MAX is reported, as an efficient Zn2+ storage host via electrochemically etching-induced phase transition strategy. And the mechanism behind the V4AlC3 MAX electrode conversion were systematically studied. The results revealed that the V-Al bond and Al 1s peak of V4AlC3 were gradually disappearing at prolonged cycling, meanwhile the high valence state vanadium was formed simultaneously as the V2O5/C composite. Benefiting from the efficient reaction kinetics endowed by the V2O5/C nanosheets, such V4AlC3 MAX derived electrode can deliver a high specific capacity of 102 mA h g−1 (20 A/g) at the cut-off voltage of 2.0 V, Furthermore, discharge capacity of 158 mA h g−1 after 3000 cycles at 10 A/g can be retained, confirming it a superior rate capability and cycling stability. The work demonstrates an effective strategy for green and advanced cathode material design and high-performance AZIBs.
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