材料科学
共晶体系
电化学
水溶液
电解质
溶剂化
无机化学
化学工程
储能
工作(物理)
分子
冰点降低
电化学电位
快离子导体
金属
电化学电池
冰点
协调数
深共晶溶剂
沉积(地质)
电化学储能
化学物理
作者
Xuemei Zhang,Qiang Tang,Hang Luo,Weihang Xie,Boya Wang,Shuyang Zhou,Shuangxiu Cao,Liming Wang,Qianyang He,Jianan Peng,Xinxiu Yan,Tao Chen,Wenlong Cai
标识
DOI:10.1002/aenm.202504638
摘要
Abstract Owing to high energy density and low cost, zinc‐ion batteries are gaining much popularity. However, frozen aqueous electrolytes and unstable interface hinder their practical application at extremely low temperature conditions. Herein, a multivariate competitive coordination structure in hydrated eutectic electrolytes is proposed to decrease the freezing point and concurrently construct a stable interface for long‐life low‐temperature applications. The introduction of second metal cations and organic additives not only breaks the hydrogen‐bond network of original water molecules but also competes to reshape Zn 2+ solvation shell. To be a result, free water content is decreased, and a stable solid electrolyte interface layer is simultaneously formed. Concomitantly, dendrite‐free Zn deposition and excellent Zn plating/stripping at −40 °C are achieved. Impressively, the Zn || Zn symmetrical cells with a competitive hydrated eutectic electrolyte demonstrate a stable cycle life of up to 4250 h at a current density of 0.5 mA cm −2 , and even work for ≈1000 h at a discharge depth of 62%. This work provides a unique view of designing anti‐freezing electrolytes for zinc‐ion batteries, and its universality and applicability will arouse the interest of a series of researchers in the field of electrochemical energy storage.
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