A flame-retardant polymer electrolyte for high performance lithium metal batteries with an expanded operation temperature

Polymer electrolytes with high ionic conductivity, good interfacial stability and safety are in urgent demand for practical rechargeable lithium metal batteries (LMBs). Herein we propose a novel flame-retardant polymerized 1,3-dioxolane electrolyte (PDE), which is in situ formed via a multifunctional tris(pentafluorophenyl)borane (TB) additive. The in situ formed PDE not only affords an integrated battery structure with stabilized electrode-electrolyte interface, but also achieves good flame retardancy, significantly expanded operating temperature limit and improved oxidative stability. Moreover, TB also contributes to a highly stable LiF-rich solid electrolyte interphase (SEI). In addition, the PDE has good compatibility with electrodes and polypropylene (PP) separator, hardly increasing the thickness of the battery, and the amount of additive TB is small, so there is no loss of gravimetric or volumetric energy density due to the polymerization. Based on the in situ formed PDE, Li-S batteries without the addition of LiNO3 demonstrate excellent cycle stability (>500 cycles) and a wide operating temperature (-20 to 50 degrees C); the high voltage Li-LiNi0.6Co0.2Mn0.2O2 and Li-LiFePO4 batteries both exhibit excellent electrochemical performance (>1200 cycles). In addition, the ultrasonic imaging technique developed by our group also demonstrates no gas generation inside pouch cells using PDE. This work provides a facile and practical approach to design a highly stable polymer electrolyte for high performance LMBs.

Automated summary

A novel flame-retardant polymerized 1,3-dioxolane electrolyte (PDE) is proposed in this study, which is formed in situ via a multifunctional tris(pentafluorophenyl)borane (TB) additive. The PDE not only stabilizes the electrode-electrolyte interface, but also achieves good flame retardancy, expanded operating temperature limit, and improved oxidative stability.