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.
| Original language | English |
|---|---|
| Article number | e73421 |
| Journal | Advanced Materials |
| Volume | 38 |
| Issue number | 35 |
| DOIs | |
| State | Published - 23 Jun 2026 |
Keywords
- anode-free
- electrolyte chemistry
- high-temperature
- molecular design
- sodium batteries
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