Achieving high intrinsic proton conductivity is essential
for the
development of stable proton conductors in proton exchange membrane
fuel cells. Herein, an ionic liquid (IL) with a hydrosulfate anion,
an imidazole ring, and a sulfonate group beneficial to proton transfer
was used to functionalize a metal–organic framework (MOF-808)
by replacing the formates coordinated with Zr. The obtained MOF-808-IL exhibits high intrinsic proton conductivity of
1.28 × 10–1 S cm–1 at 60
°C and 100% relative humidity (RH), which exceeds those of most
of the MOF-based proton conductors. Moreover, the proton transfer
mechanism has been elucidated by the combination of the crystal structure
and variable temperature Fourier transform infrared spectra. This
study provides a strategy for achieving ultrahigh proton conductivity
and a model for analyzing the proton conducting mechanism.