材料科学
电解质
位阻效应
化学工程
小袋
降级(电信)
钠
分子
乙醚
工作(物理)
纳米技术
复合材料
两亲性
电流密度
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
摘要
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.
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