Developing
a low-cost effective, readily available, highly efficient
electrocatalyst is essential to produce clean and sustainable energy.
We report the synthesis of microporous iron-anchored cobalt phosphonate
materials, i.e., FeCoPIm-6, FeCoPIm-12, FeCoPIm-24,
and FeCoPIm-48, using iminodi(methylphosphonic acid) as a ligand,
by varying the reaction time under hydrothermal condition and post-grafting
synthetic pathway. The FeCoPIm-12 catalyst exhibits excellent electrocatalytic
activity for the hydrogen evolution reaction (HER) and the oxygen
evolution reaction (OER), acquiring low overpotentials of 117 and
249 mV vs. reversible hydrogen electrode (RHE), respectively,
at the current density of 10 mA cm–2 with outstanding
long-term durability up to 100 h in a 1.0 M KOH electrolyte solution.
Also, the bifunctionalized electrocatalyst FeCoPIm-12 requires a cell
voltage of 1.53 V at 10 mA cm–2 for overall water
splitting in an alkaline medium and displays long-term stability.
The superior electrochemical performance of the FeCoPIm-12 catalyst
over the as-synthesized catalyst is due to its higher surface area
with microporous channel throughout the catalyst and the synergistic
effect of the highly active metal oxyhydroxide (FeOOH and CoOOH) components
on the pore wall.