氯化胆碱
乙二醇
电解质
共晶体系
电化学
材料科学
锌
氯化物
电池(电)
水溶液
电化学窗口
无机化学
电导率
离子电导率
化学工程
核化学
化学
冶金
有机化学
微观结构
电极
功率(物理)
物理
物理化学
量子力学
工程类
作者
P. Rangaswamy,Hyocheol Lee,Hyo‐Won Bae,Do Youb Kim,Dukjoon Kim
出处
期刊:Small
[Wiley]
日期:2024-04-23
被引量:2
标识
DOI:10.1002/smll.202400692
摘要
Abstract Aqueous rechargeable zinc‐ion batteries (ARZIBs) are considered as an emerging energy storage technology owing to their low cost, inherent safety, and reasonable energy density. However, significant challenges associated with electrodes, and aqueous electrolytes restrict their rapid development. Herein, ethylene glycol‐choline chloride (Eg‐ChCl) based hydrated deep‐eutectic electrolytes (HDEEs) are proposed for RZIBs. Also, a novel V 10 O 24 · n H 2 O@rGO composite is prepared and investigated in combination with HDEEs. The formulated HDEEs, particularly the composition of 1 ml of EG, 0.5 g of ChCl, 4 ml of H 2 O, and 2 M ZnTFS (1‐0.5‐4‐2 HDEE), not only exhibit the lowest viscosity, highest Zn 2+ conductivity (20.38 mS cm −1 ), and the highest zinc (Zn) transference number ( t + = 0.937), but also provide a wide electrochemical stability window (>3.2 V vs ZnǁZn 2+ ) and enabledendrite‐free Zn stripping/plating cycling over 1000 hours. The resulting ZnǁV 10 O 24 · n H 2 O@rGO cell with 1‐0.5‐4‐2 HDEE manifests high reversible capacity of ≈365 mAh g −1 at 0.1 A g −1 , high rate‐performance (delivered ≈365/223 mAh g −1 at 0.1/10 mA g −1 ) and enhanced cycling performance (≈63.10% capacity retention in the 4000 th cycle at 10 A g −1 ). Furthermore, 1‐0.5‐4‐2 HDEE support feasible Zn‐ion storage performance across a wide temperature range (0–80 °C) FInally, a ZnǁV 10 O 24 · n H 2 O@rGO pouch‐cell prototype fabricated with 1‐0.5‐4‐2 HDEE demonstrates good flexibility, safety, and durability.
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