材料科学
钇
锌
电解质
金属
水溶液
离子键合
无机化学
化学工程
吸附
剥离(纤维)
冶金
离子
有机化学
物理化学
化学
电极
工程类
氧化物
复合材料
作者
Liansheng Li,Chun Chen,Pengyu Meng,Yijie Zhang,Qinghua Liang
标识
DOI:10.1002/adfm.202406965
摘要
Abstract Aqueous batteries employing Zinc metal anodes (ZMAs) are considered to be promising next‐generation energy storage systems. However, the severe interfacial side reactions and dendrite growth restrict the practical application of ZMAs in aqueous electrolytes. Herein, a water‐insoluble dual‐ionic electrolyte additive of yttrium 2,4,5‐trifluorophenylacetate (YTFPAA) is developed to stabilize the aqueous ZMAs. Notably, the ethanol‐solvated TFPAA − can capture H + and thus buffer the decreased electrolyte pH caused by the hydrolysis of Y 3+ . Furthermore, the ethanol‐solvated TFPAA − can dynamically adsorb onto the surface of ZMAs through a reversible oxidation‐reduction reaction, effectively suppressing the interfacial side reactions by forming a water‐poor interface, and enhancing the reversibility of Zn 2+ deposition/stripping by redistributing the Zn 2+ flux. These favorable effects of TFPAA − combined with the dynamic electrostatic shielding effect of Y 3+ ultimately enable uniform and dense Zn 2+ deposition. As a result, the Zn/Zn cells assembled with 0.25YTFPAA electrolyte exhibit an impressive cycle life of 2100 h at 0.5 mA cm −2 –0.25 mAh cm −2 . More importantly, the assembled V 2 O 5 /Zn full cell shows an ultra‐long cycle life of up to 18000 cycles at 5.0 A g −1 . This work highlights the rational design of multifunctional ionic additives for stabilizing aqueous ZMAs.
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