位阻效应
电解质
锌
水溶液
材料科学
阳极
化学工程
无机化学
钝化
纳米技术
化学
冶金
有机化学
物理化学
电极
工程类
图层(电子)
作者
Cheng Lu,Zhilong Wang,Jinjin Li,Liangming Wei
出处
期刊:Small
[Wiley]
日期:2025-07-04
卷期号:21 (35): e2506968-e2506968
被引量:1
标识
DOI:10.1002/smll.202506968
摘要
Aluminum-based electrolytes and zinc anodes respectively provide aqueous Al-Zn hybrid-ion batteries with high theoretical capacity and reversible plating/stripping behavior. However, parasitic reactions at the zinc anode/aluminum-based electrolyte interface - including dendrite growth, hydrogen evolution, and corrosion passivation - significantly limit cycle life and accelerate capacity degradation. Herein, a comparative investigation of the synergistic effects between glucose (a linear monosaccharide) and sucrose (a branched disaccharide) electrolyte additives with the ZnCr₂O₄ interface of PVDF@ZnCr₂O₄@Zn anodes is conducted, specifically examining spontaneous adsorption, steric hindrance, and conductivity enhancement effects on battery performance. The study reveals that glucose, due to its intrinsic properties and lower steric hindrance, exhibits stronger synergistic effects with the ZnCr₂O₄ interface than sucrose, leading to more effective suppression of parasitic reactions and capacity fade. The glucose/sucrose-modified electrolyte enables the battery to achieve exceptional cycling stability (19,000 and 8,000 cycles) while maintaining high specific discharge capacities (267 and 215 mAh g⁻¹). The synergistic effects between these electrolyte additives and the engineered anode interface present promising strategies and theoretical foundations for developing next-generation high-performance batteries.
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