溶剂化
溶解
电解质
材料科学
粘度
离子液体
化学工程
电导率
离子电导率
溶剂
普鲁士蓝
化学
无机化学
离子
离子键合
强电解质
金属
分解
电阻率和电导率
电池(电)
工作(物理)
碳纤维
电极
化学稳定性
作者
Zhiming Zhou,Yun Wan,Xu Xu,Wenxi Kuang,Xiaoyan Shi,Xiaomin Chen,Jian Chen,Junxiang Liu,Xingqiao Wu,Xunzhu Zhou,Shulei Chou,L Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-01-07
卷期号:11 (2): 1642-1650
被引量:4
标识
DOI:10.1021/acsenergylett.5c02835
摘要
High-concentration electrolytes (HCE) with unique anion-rich solvation chemistry have attracted extensive attention for sodium-ion full batteries. Unfortunately, they suffer from unsatisfactory physicochemical properties, which inevitably hinder their practical application. Herein, a trade-off between the physicochemical properties and anion-rich solvation chemistry in HCE is achieved by employing methyl propionate (MP) with moderate coordination ability and low viscosity as the sole solvent. The enhanced ionic conductivity and low viscosity of the MP-based HCE significantly enhance ion transport efficiency and electrode wettability, whereas the anion-rich solvation chemistry promotes the formation of robust electrode–electrolyte interphase, which effectively suppresses transition metal dissolution and continuous electrolyte decomposition as well as accelerates the interfacial ion transport kinetics. As a result, the Prussian blue||hard carbon (PB||HC) full cell shows an enhanced rate performance and cycling stability at a wide temperature range of −20–100 °C. This work highlights the importance of solvent coordination ability in electrolyte design for sodium-ion batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI