空位缺陷
电化学
材料科学
氮化钒
离子
钒
密度泛函理论
氮化物
阴极
化学工程
无机化学
电极
纳米技术
冶金
物理化学
化学
结晶学
计算化学
工程类
有机化学
图层(电子)
作者
Youcun Bai,Liang Luo,Wenliang Song,Shuaishuai Man,Heng Zhang,Chang Ming Li
标识
DOI:10.1002/advs.202308668
摘要
Abstract Vanadium nitride (VN) is a potential cathode material with high capacity and high energy density for aqueous zinc batteries (AZIBs). However, the slow kinetics resulting from the strong electrostatic interaction of the electrode materials with zinc ions is a major challenge for fast storage. Here, VN clusters with nitrogen‐vacancy embedded in carbon (C) (N v ‐VN/C‐SS‐2) are prepared for the first time to improve the slow reaction kinetics. The nitrogen vacancies can effectively accelerate the reaction kinetics, reduce the electrochemical polarization, and improve the performance. The density functional theory (DFT) calculations also prove that the rapid adsorption and desorption of zinc ions on N v ‐VN/C‐SS‐2 can release more electrons to the delocalized electron cloud of the material, thus adding more active sites. The N v ‐VN/C‐SS‐2 exhibits a specific capacity and outstanding cycle life. Meanwhile, the quasi‐solid‐state battery exhibits a high capacity of 186.5 mAh g −1 , ultra‐high energy density of 278.9 Wh kg −1 , and a high power density of 2375.1 W kg −1 at 2.5 A g −1 , showing excellent electrochemical performance. This work provides a meaningful reference value for improving the comprehensive electrochemical performance of VN through interface engineering.
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