Iron trifluoride (FeF3), a conversion-type
cathode for
sodium-ion batteries (SIBs), is based on cheap and abundant Fe and
provides high theoretical capacity. However, the applications of FeF3-based SIBs have been hindered by their low-capacity utilization
and poor cycling stability. Herein, we report greatly enhanced performance
of FeF3 in multiple types of ionic liquid (IL) electrolytes
at both room temperature (RT) and elevated temperatures. The Pyr1,4FSI electrolyte demonstrated the best cycling stability
with an unprecedented decay rate of only ∼0.023% per cycle
after the initial stabilization and an average coulombic efficiency
of ∼99.5% for over 1000 cycles at RT. The Pyr1,3FSI electrolyte demonstrated the best cycling stability with a capacity
decay rate of only ∼0.25% per cycle at 60 °C. Cells using
Pyr1,3FSI and EMIMFSI electrolytes also showed promising
cycling stability with capacity decay rates of ∼0.039% and
∼0.030% per cycle over 1000 cycles, respectively. A protective
and ionically conductive cathode electrolyte interphase (CEI) layer
is formed during cycling in ILs, diminishing side reactions that commonly
lead to gassing and excessive CEI growth in organic electrolytes,
especially at elevated temperatures. Furthermore, the increased ionic
conductivity and decreased viscosity of ILs at elevated temperatures
help attain higher accessible capacity. The application of ILs sheds
light on designing a protective CEI for its use in stable SIBs.