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Rechargeable secondary batteries operating through fluoride-ion shuttling between the positive and negative electrodes, referred to as fluoride shuttle batteries (FSBs), offer a potentially promising solution to overcoming the energy-density limitations of current lithium-ion battery systems. However, there are many technical issues that need to be resolved to achieve high-quality fluoride-carrying electrolytes and ensure reversible transformations between a metal and its fluoride counterpart at both electrodes. Here, we introduce novel lactone-based liquid electrolytes consisting either of CsF or KF, which are prepared by a solvent substitution method. Although the maximum fluoride-ion concentration achieved by the method is approximately 0.05 M, these systems behave as strong electrolytes where CsF(KF) is almost fully dissociated into Cs+(K+) and F− ions to give a maximum ionic conductivity of 0.8 mS.cm−1. Hence, the solvent supports electrochemically active fluoride ions that can drive reversible metal/metal-fluoride transformations at room temperature for a wide range of metal electrodes. However, irreversible reductive reactions of the solvent, also promoted by the fluoride ions, limit currently the negative potential window to approximately −1.5 V vs the standard hydrogen electrode.

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Tracer diffusion coefficients D* of lithium ions in Li x Mn2O4 (0.2 < x < 1) thin films were measured as a function of the composition x by using secondary ion mass spectrometry. For this purpose, a new “step-isotope-exchange method” was developed to observe the time dependence of the 6Li isotope concentration ratio in the Li x Mn2O4 film which is in contact with a 6Li-enriched electrolyte to exchange Li+ ions. A steep decrease in D* depending on the Li composition was observed for Li x Mn2O4, with D* = 8 × 10–13 cm2 s–1 for x = 0.2 and decreasing to 1.5 × 10–17 cm2 s–1 for x = 1.0 (bulk diffusion coefficient, D b *). This behavior is well explained by a vacancy diffusion model for the α phase on Li x Mn2O4 (0.77 < x < 1.0). Chemical diffusion coefficients D̃ were also measured in the range of 0.2 < x < 1.0 by an electrochemical method, which was compared with the D* to evaluate the effect of thermodynamic factors. The thermodynamic factors and interactions between Li+ ions were found to strongly influence the chemical diffusion coefficient. The tracer diffusion measurements are important to understand the charge–discharge mechanism in the electrodes of lithium-ion batteries.

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