A series of ZIF-67-C-IL catalysts were prepared using ZIF-67 and 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl] imide ([ BMIM]NTf2) ionic liquid as precursors. The structure of the catalysts was characterized by XRD, TEM, SEM and XPS. The catalytic performance of the catalysts for the oxygen reduction reaction (ORR) was evaluated in a three-electrode system. The results confirmed that the high-temperature treatment of the precursors resulted in the formation of N, S codoped carbon-encapsulated Co9S8 nanoparticles. To create N, S co-doped carbon coated Co9S8 nanoparticle catalysts, ionic liquids are used as sulfur and nitrogen sources. The catalytic activity of ORR can be improved using N, S co-doped carbon to prevent the aggregation of Co9S8 nanoparticles. Graphitized and N, S co-doped carbon shells are optimal for achieving high activity stability. Optimal 600-ZIF-67-C(1:1.5)-30IL catalytic activity was observed for ORR. The half-wave potential of ORR was 0.88 V vs. RHE in 0.1 mol L− 1 KOH, with a limit current density of 4.70 mA cm− 2. Similar ORR electrocatalytic activity was observed between this catalyst and commercial Pt/C (20 wt%).

Alkaline direct liquid fuel cells (ADLFCs) employing anion-exchange membranes as a fuel barrier have attracted significant attention as promising alternative energy sources. ADLFCs are allowed to use more abundant anode catalysts which are cheaper than the catalyst used in that using hydrogen fuel. In this work, novel pore-filled anion-exchange membranes (PFAEMs) were successfully fabricated by combining a highly porous poly(tetrafluoroethylene) film and cationic polyelectrolytes with structurally stable anion-exchange sites. The results of the membrane characterizations revealed that the optimization in the crosslinking degree and hydrophilicity of membranes should be considered for the successful application of the PFAEMs to ADLFCs. (KETEP)(20153030031720) and (MOTIE) (No. 10047796).