电解质
溶剂化
水溶液
法拉第效率
化学
溶剂化壳
离子
电化学
熵(时间箭头)
分子动力学
电池(电)
化学工程
离子键合
无机化学
材料科学
化学物理
纳米技术
电化学窗口
离子液体
强电解质
工作(物理)
阳离子聚合
作者
Hance Su,Elizabeth L. Hinks,Yuxuan Chen,Sang Cheol Kim,Yuqi Li,Xiwen Chi,P. L. Zhang,Jing Wang,Il Rok Choi,Haiyan Mao,Isabella Huang,Xueer Xu,Zhouyi Chen,Jian Qin,Yi Cui
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-03-13
卷期号:11 (4): 3265-3273
被引量:3
标识
DOI:10.1021/acsenergylett.5c04154
摘要
Our study introduces a novel electrolyte design strategy for aqueous zinc-ion batteries (AZIBs), leveraging high-entropy concepts specifically within the second solvation shell rather than the commonly targeted first shell. By combining multiple zinc salts to achieve controlled entropy enhancement, we demonstrated significantly improved zinc-ion transport kinetics, ionic conductivity, and suppression of the hydrogen evolution reactions (HER). Molecular dynamics simulations and spectroscopic analyses revealed that increased second-shell entropy weakened the hydrogen-bonding network, disrupting proton transfer pathways responsible for HER. Consequently, this high-entropy electrolyte substantially extended cycle life in symmetric cells and improved Coulombic efficiency in asymmetric configurations, outperforming conventional single-salt systems by up to 4-fold. In practical dual-electrode-free Zn–MnO2 and Zn–NVO full cell setups, our electrolytes showed enhanced cycling stability, rate capability, and capacity retention. This work presents a transformative electrolyte approach, highlighting second-shell entropy manipulation as an effective avenue for advancing performance and sustainability in aqueous zinc-ion battery technology and beyond.
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