电解质
化学
溶剂化
法拉第效率
水溶液
电池(电)
离子
电化学
电极
化学工程
储能
锌
热传导
无机化学
分子动力学
熵(时间箭头)
离子运输机
电化学储能
低能
化学物理
可持续能源
作者
Lei Ye,Jiaqi Wei,Song Yuan,Jifeng Wang,Ying Wang,Can Cao,Fu Lun Tan,Hanchen Shen,Rongrong Qin,Yanzhen Li,Xiaodong Chen
摘要
Aqueous batteries hold great promise for safe, sustainable energy storage, but their operation at low temperatures is limited by electrolyte freezing that impedes bulk ion transport and by sluggish cation desolvation at the electrode interface. Herein, we report a high-entropy hydrogel electrolyte (HEE) that leverages polymeric complexity to enhance ion conduction and interfacial desolvation at low temperatures, enabling aqueous battery operation down to -80 °C. The increased mixing entropy from various polymer-water interactions disrupts the ordered water network, suppressing ice formation with preserved ion-conducting pathways at low temperatures. Concurrently, the enhanced solvation entropy generates varying ion coordination environments with loosely bound solvation shells, promoting desolvation and stabilizing the solid-electrolyte interphase. As a proof of concept, the HEE achieves highly reversible zinc (Zn) plating/stripping with an average Coulombic efficiency of 99.7%, exhibits stable cycling for over 4000 h, and supports aqueous Zn-based battery operation even at -80 °C. This entropy-engineering strategy offers an effective route for realizing energy storage under extreme conditions.
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