Weakly Solvating Electrolytes for Safe and Fast-Charging Sodium Metal Batteries

Abstract

Electrolytes for high-performance sodium metal batteries (SMBs) are expected to have high electrode compatibility, low solvation energy, and nonflammability. However, conventional flammable carbonate ester electrolytes show high Na⁺ desolvation energy and poor compatibility with sodium metal anodes, leading to slow Faradaic reactions and significant degradation of SMBs. Herein, we report a weakly solvating electrolytes (WSEs) design developed by an ionized ether-induced solvent molecule polarization strategy. The steric hindrance and electron-withdrawing effect of the pyrrolidine cation weaken the solvation ability of the ionized ether and enable carbonate ester with low solvation energy through intermolecular polarization interactions. It enables WSEs with fast Na⁺ migration kinetics and electric-field-reinforced cationic electrode/electrolyte interface, thereby promoting the stability and reversibility of SMBs even under high-charge-rate conditions. The Na||Na₃V₂(PO₄)₃ battery with ionized ether-based WSEs exhibits a capacity retention of 83.5% with an average Coulombic efficiency (CE) of 99.69% after 500 cycles at 10C. Furthermore, the Na||Na₂Fe₂(SO₄)₃ cells maintained 92.8% capacity retention after 1000 cycles at 5C with an average CE of 99.77% at a cutoff voltage of 4.5 V. The ionized ether also eliminates the fire and safety risks associated with WSEs. This work offers valuable insights into the design of WSEs for safe and high-performance sodium metal batteries.