Demonstrates reduced voltage hysteresis in sulfide all-solid-state batteries, implying improved energy efficiency.
Conversion‐type metal fluorides are promising cathode candidates for high‐energy‐density post‐lithium batteries. Unfortunately, their practical implementation has been severely impeded by pronounced voltage hysteresis (VH). Herein, we report a gas‐phase treatment strategy to realize oxygen doping and nano‐disordering of FeF 2 , which reduces the VH of FeF 2 to a record low level of 153 mV at 80°C when integrated into sulfide all‐solid‐state batteries. Specifically, crystalline FeF 2 is doped with oxygen and refined to nanocrystals dispersed in a disordered FeOF matrix, which narrows the band gap of FeF 2 from 1.84 to 1.36 eV, decreases the ionic migration energy barrier from 2.2 to 1.2 eV, enhances its electronic conductivity from 4.1 × 10 −6 mS/cm to 0.48 mS/cm, ionic conductivity from 1.1 × 10 −6 mS/cm to 4.8 × 10 −5 mS/cm. The dramatically increased electronic and ionic conductivity boosts the charge transport kinetics and reduces the charge transfer barrier, thus suppressing the VH. Notably, the oxygen doping strategy is not restricted to FeF 2 , but is valid for a broad class of metal fluorides. These results provide a versatile solution to the long‐standing VH bottleneck in metal fluorides and are expected to accelerate the industrial adoption of metal fluoride cathodes to enable high‐energy‐density lithium batteries.
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Chen et al. (2026) studied this question.
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