电解质
溶剂化
材料科学
离子电导率
合理设计
电导率
离子键合
纳米技术
化学工程
离子
化学物理
设计要素和原则
动力学
快离子导体
机制(生物学)
电池(电)
微观结构
储能
材料设计
工作(物理)
电化学
电极
热力学
电阻率和电导率
导电体
过程(计算)
作者
Hao-Jie Liang,Xiao-Tong Wang,Yu Cao,Han‐Hao Liu,Jia-Xin Yan,Zhi-Ming Liu,Yuan-Zheng Tang,Qing-Liang Lv,Lei Wang,Xing-Long Wu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-12-24
卷期号:11 (1): 764-773
被引量:5
标识
DOI:10.1021/acsenergylett.5c03431
摘要
Ether-based electrolytes have attracted increasing attention for the development of low-temperature sodium-ion batteries (SIBs); however, relevant performances are significantly constrained by temperature factors for lack of appropriate modification strategies. Herein, advanced design principles are proposed by integrating an entropy-motivated mechanism to customize the sodium-based solvation configuration at meso- and microscopic scales. Specifically, the tailored ionic clusters along with an increase in disorder guarantee sufficient conductivity at LTs, and the multiple solvation microstructures with weakened ion–solvent interactions concurrently facilitate the desolvation behavior at interfaces. With the assistance of accelerated ion transport kinetics and complementary organic–inorganic interphases featuring an equilibrium of thickness and robustness, Na3V2(PO4)2O2F and Na3V2(PO4)3 exhibit workability as the temperature approached −80 °C. Moreover, the assembled full cells verify the feasibility at LTs. In short, the rational design strategy with an entropy-dependent effect is introduced to provide an emerging perspective on functional ether-based electrolytes for low-temperature and high-voltage SIBs.
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