Spatially Strengthened Ion‐Dipole Electrolyte Enables High‐Temperature Anode‐Free Sodium Batteries

作者：Hao Lan, S Wang, Jiangchun Chen, Liqiang Wu, Jingwen Jiang, Dandan Yu, Shuai Dong, Xinyu Sun, Qiaonan Zhu, Daojun Yang, Wei Wei, Guang Yang, Bin Dong, H Wang · 发表于：Advanced Materials · 年份：2026 · DOI：10.1002/adma.73421 · 被引用次数：3 · 研究领域：Advanced Battery Materials and Technologies、Advancements in Battery Materials、Thermal Expansion and Ionic Conductivity

ABSTRACT Practical anode‐free sodium batteries (AFSBs) require high‐temperature adaptability, e.g., stable operation at 45°C. However, current AFSBs are usually confined to room/low temperatures, and pouch cell‐level AFSBs capable of stable cycling >25°C have rarely been reported. Here we report high‐temperature AFSBs via spatially strengthened ion‐dipole electrolyte chemistry. Specifically, a novel solvent, namely, ethyl tetrahydrofurfuryl ether (ETFE) is designed. The reversely anchored rigid cyclic head endows ETFE molecule with weakened steric hindrance effect and stronger cyclic ethereal O─Na + interaction accordingly, hence spatially strengthening overall ion‐dipole interaction. Consequently, less vulnerable free solvents, ameliorated electrolyte decomposition, and formation of stable electrode/electrolyte interphases enable highly reversible Na plating/stripping behaviors at elevated temperatures. Further, an ampere hour (Ah)‐level pouch cell capable of 200 cycles at 45°C with a capacity retention of 89.1% is realized even after initial 300‐cycle ageing at 25°C, featuring the first long‐term HT evaluation toward pouch cell‐level AFSBs. This work should expedite the practicability of AFSBs.