水溶液
氢键
共晶体系
电解质
分子
溶剂化
材料科学
冰点
化学物理
共金键结
结晶学
化学工程
化学
物理化学
合金
热力学
有机化学
物理
电极
复合材料
工程类
作者
Changhao Zhu,Xuye He,Yun Shi,Zhenkang Wang,Baojiu Hao,Wan-Hao Chen,Hao Yang,Lifang Zhang,Haoqing Ji,Jie Liu,Chenglin Yan,Jinqiu Zhou,Tao Qian
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-11-02
卷期号:17 (21): 21614-21625
被引量:25
标识
DOI:10.1021/acsnano.3c06687
摘要
Despite the numerous advantages of aqueous Zn batteries, their practical application under cryogenic conditions is hindered by the freezing of the electrolyte because the abundance of hydrogen bonds (H-bonds) between H2O molecules drives the aqueous system to transform to an orderly frozen structure. Here, a design of H-bond interactions based on the guiding ideology of "strong replaces weak" is proposed. The strong H-bonds formed between introduced eutectic components and water molecules break down the weak H-bonds in the original water molecule network, which contributes to an ultralow freezing point and a high ionic conductivity of 1.7 mS cm-1 at -40 °C. Based on multiperspective theoretical simulations and tailor-made in situ cooling Raman characterizations, it has been demonstrated that substituting weak H-bonds with strong H-bonds facilitates the structural reshaping of Zn2+ solvation and remodeling of the H-bond network in the electrolyte. Endowed with this advantage, reversible and stable Zn plating/stripping behaviors could be realized at -40 °C, and the full cells display a high discharge capacity (200 mA h g-1) at -40 °C with ∼75% capacity retention after 1000 cycles. This study will expand the design philosophy of antifreezing aqueous electrolytes and provide a perspective to promote the adoption of Zn metal batteries for cryogenic environment large-scale energy storage.
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