Initiating a Room-Temperature Rechargeable Aqueous Fluoride-Ion Battery with Long Lifespan through a Rational Buffering Phase Design

Previously reported fluoride-ion batteries (FIBs) can only work at high temperatures (>150 degrees C) with solid electrolytes or organic electrolytes. Aqueous FIB has barely been reported due to the unstable F- electrochemistry in aqueous electrolytes. In addition, the electrode materials commonly suffer from serious and adverse volume expansion during the conversion reaction. Herein, a stable aqueous F- electrochemistry is realized by a rational buffering phase design in which stagger distribution of BiF3 and Bi7F11O5 phases is achieved. The enhanced F- electrochemistry is systematically studied and suggests that the Bi7F11O5 phase plays a vital role in the stability and reversibility of the electrode due to its lower volume change and higher electronic conductivity. Pulverization and dissolution of active species issues are also suppressed. As a result, the assembled battery delivers excellent cycling stability, high reversibility, and superior rate capability, which is far better than conventional solid fluoride shuttle batteries. Mechanism studies demonstrate that the capacity comes from reversible conversion between Bi3+ and Bi-0 with an intermediate phase of Bi7F11O5. This work initiates room-temperature FIBs with aqueous electrolytes and provides a good cycling lifespan, which pave the way to a more practical fluoride ion storage system.

Automated summary

This study successfully demonstrates a stable aqueous fluoride-ion battery with superior cycling stability and high rate capability through rational design, paving the way for a more practical fluoride-ion storage system.