A Molecule Crowding Strategy to Stabilize Aqueous Sodium‐Ion Batteries

Author:

Ding Jibo1ORCID,Li Qin1,Yang Jinyu1,Wang Runting1,Ruan Jiafeng1,Fang Fang12,Sun Dalin12,Wang Fei12ORCID

Affiliation:

1. Department of Materials Science Fudan University Shanghai 200433 China

2. School of Materials Science and Engineering Anhui University Hefei 230601 China

Abstract

AbstractAqueous sodium‐ion batteries (ASIBs) have recently emerged as a compelling choice for large‐scale energy storage when considering their safe operational characteristics and cost‐effectiveness. Nonetheless, the inadequate electrochemical stability window (ESW) of water (1.23 V) and severe dissolution of electrodes in aqueous electrolytes have proven bottlenecks to enabling high energy density and long lifespan of ASIBs. Here, a molecular crowding electrolyte is introduced, featuring nonflammable polyethylene glycol dimethyl ether (PED) as a crowding agent and a hydrogen bond receptor to further diminish the water activity. The 4.5 m (mol kg−1) NaClO4‐4 wt% H2O‐96 wt% PED electrolyte displayed an impressive ESW of 3.4 V, all while maintaining a moderate salt concentration of 4.5 m. Meanwhile, this electrolyte demonstrated substantial mitigation of vanadium dissolution in Na3V2(PO4)3. Consequently, in a comprehensive evaluation, the aqueous NaTi2(PO4)3||Na3V2(PO4)3 full cell exhibited an energy density of 47 Wh kg−1 at 1 C with a 74% retention after 100 cycles, and displayed negligible capacity decay (≈0.014% per cycle) at 5 C in 1000 cycles with high average coulombic efficiency of 99.8%. This work offers a universal strategy for the design of aqueous electrolytes with wide ESW and the ability to effectively suppress vanadium dissolution.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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