阴极
钒
电化学
材料科学
电极
溶解
水溶液
电池(电)
化学工程
氧化钒
复合数
锌
氧化物
无机化学
冶金
复合材料
化学
功率(物理)
物理化学
工程类
物理
量子力学
作者
Junqi Liu,Hao Hu,Tongtong Yuan,Pengbo Zhao,Hangchen Liu,Haoyan Cheng
标识
DOI:10.1016/j.apsusc.2023.159005
摘要
The vanadium oxide cathode material is widely regarded as a promising candidate for aqueous zinc-ion batteries (AZIBs). However, its low activity, poor cycling stability, and inadequate rate performance have significantly impeded its commercial viability. In this study, we report a composite electrode material of V2O5 modified with La3+ and phytic acid (LPVO) with enhanced electrochemical performance. The La3+ are capable of intercalating into the interlayer of V2O5, effectively expanding the interlayer spacing for fast Zn2+ transport, and facilitating the exposure of more Zn2+ storage sites with improved capacity. Additionally, the encapsulated phytic acid could serve as a protective layer to prevent the detachment and dissolution of vanadium compounds during cycles, thereby improving the electrochemical stability. Under the current density of 0.1 A g−1, the capacity of LPVO electrode reaches as high as 385 mAh g−1. Even after 2000 charge–discharge cycles, the capacity retention rate remains as high as 75% (at 3 A g−1). Compared to commercial V2O5, the Zn2+ diffusion rate of the LPVO composite is improved by nearly 1000 times, reaching 5∼7 × 10−10 cm2 s−1. This approach is universally applicable to enhance electrochemical performance of diverse layered electrode materials, aiding the rapid advancement of cathode design for AZIBs.
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