普鲁士蓝
钒
阴极
电解质
材料科学
阳极
化学工程
水溶液
溶解
无机化学
共晶体系
锌
电化学
化学
电极
冶金
合金
物理化学
工程类
作者
Huan Pang,Yuxin Shi,Biao Yang,Gongjing Song,Zhidong Chen,Mohsen Shakouri,Wenfeng Zhou,Xiaoxing Zhang,Guoqiang Yuan
标识
DOI:10.1002/anie.202411579
摘要
Prussian blue analogues (PBAs) have been widely studied in aqueous zinc‐ion batteries (AZIBs) due to the characteristics of large specific surface area, open aperture, and straightforward synthesis. In this work, vanadium‐based PBA nanocubes were firstly prepared using a mild in‐situ conversion strategy at room temperature without the protection of noble gas. Benefiting from the multiple‐redox active sites of V3+/V4+, V4+/V5+ and Fe2+/Fe3+, the cathode exhibited an excellent discharge specific capacity of 200 mA h g‐1 in AZIBs, which is much higher than those of other metal‐based PBAs nanocubes. To further improve the long‐term cycling stability of the V‐PBA cathode, a high concentration water‐in‐salt electrolyte (4.5 M ZnSO4 + 3 M Zn(OTf)2), and a water‐based eutectic electrolyte (5.55 M glucose + 3 M Zn(OTf)2) were designed to successfully inhibit the dissolution of vanadium and improve the deposition of Zn2+ onto the zinc anode. More importantly, the assembled AZIBs maintained 55% of their highest discharge specific capacity even after 10000 cycles at 10 A g‐1 with superior rate capability. This study provides a new strategy for the preparation of pure PBA nanostructures and a new direction for enhancing the long‐term cycling stability of PBA‐based AZIBs at high current densities for industrialization prospects.
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