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Abstract Fluoride ion batteries (FIBs) have garnered significant attention due to their ultrahigh theoretical energy density, dendrite‐free safety, and resource abundance. Although some anion acceptors have been proposed to address the insolubility of inorganic fluoride salts, the difficulty in dissociating fluoride ions from acceptors results in short lifespan and extremely low specific capacity of FIBs. Here, a fluoride ion battery is demonstrated with unprecedented long life and ultrahigh specific capacity through the design of an acceptor‐multi‐F state electrolyte. The high Lewis acidity of triphenylantimony chloride (TSbCl) as a novel anion acceptor in electrolyte facilitates the complete dissociation of CsF, and the resulting TSbCl‐F complex can further interact with fluoride ions to form the acceptor‐multi‐F states. This strategy combines the high dissociation capability for fluoride salts with the minimal thermodynamic barriers for releasing fluoride ions at electrode‐electrolyte interface. This electrolyte design endows FIBs with durable reversible fluorination/defluorination reaction (3700 cycles with high coulombic efficiency of 99.5% and small voltage polarization of 30 mV) and ultrahigh reversible capacity (580 mAh g −1 after 40 cycles at 100 mA g −1 ). The high‐output voltage FIBs of CuF 2 //Li configuration (with discharge plateau of 2.9 V) and larger‐sized pouch‐type FIBs of CuF 2 //Sn+SnF 2 configuration (with reversible capacity of 530 mAh g −1 ) are demonstrated.
Li et al. (Mon,) studied this question.