钨
钒
插层(化学)
电化学
阴极
材料科学
结构稳定性
钨酸盐
钒酸盐
动力学
氧气
离子
化学
化学工程
无机化学
电极
物理化学
物理
量子力学
有机化学
工程类
冶金
结构工程
作者
Fengxian Gao,Hongge Gao,Kang Zhao,Xiaoyu Cao,Junwei Ding,Shiwen Wang
标识
DOI:10.1016/j.jcis.2022.09.010
摘要
The tunnel structure of the bronze phase vanadium dioxide (VO2(B)) can be used as the zinc ion storage active sites. However, the intense charge repulsion of divalent Zn2+ causes a sluggish reaction kinetics in the tunnel VO2(B). Here, a tungsten-oxygen bond pre-introduced (TOBI) approach is proposed to modulate the tunnel structure of VO2(B). The VO2(B) cathodes with TOBI of 0.5 at% to 3.0 at% have been controllably synthesized by a simple hydrothermal method. The results from structural analysis uncover that the pre-introduced W6+ replaces the V4+ in VO2(B) to form WO6 octahedra. Benefiting from the rapid diffusion kinetics, enhanced structural stability and improved conductivity enabled by the TOBI, the optimal VO2(B) nanoribbons with 1.5 at% shows a high reversible capacity of 265 mAh g-1, a high rate-performance of up-to 10 A g-1 and a long cycling stability of 2000 cycles. Moreover, a pseudo-capacitive dominated Zn2+ intercalation/de-intercalation behavior is solidly determined by the electrochemical kinetics testing and structural characterizations. This TOBI method is referential for developing other multivalent ion battery cathodes with outstanding performances.
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