The
explorations of earth-abundant, noble metal-free, highly efficient
electrocatalysts for water-splitting reactions have been considered
as highly significant for imperishable energy production. Though the
metal organic framework (MOF)-based materials are highly promising
candidates in the area of material chemistry, the combined properties
associated with MOFs and the one-dimensional (1D) fibrous matrix,
which can lead to better electrocatalytic performance, have been less
explored. Herein, we ascertain a fabrication method for ZIF-67 (zeolite
imidazolate framework) nanofibers (NFs), Fe-ZIF NFs, and Fe-ZIF-67
NFs via the wet chemical combined electrospinning (ES) approach. The
as-synthesized catalysts were utilized for the electrochemical reaction,
which showed a high efficiency toward the oxygen evolution reaction
(OER). Compared to other catalysts, the Fe-ZIF-67 NF catalyst showed
a very less overpotential of 278 mV at a fixed current density of
10 mA cm–2. The obtained Tafel slope and R
ct values are 77 mV dec–1 and
1.2 Ω, respectively. The post-X-ray photoelectron spectroscopy
(XPS) analysis revealed the transformation of FeOOH during the OER
study along with Co3+ states in mixed Fe-ZIF-67 NFs. In
an alkaline electrolyzer, Fe-ZIF-67 NFs were utilized as the anode
and a Pt wire as the cathode in 1 M KOH solution, which required a
cell voltage of 1.68 V at 10 mA cm–2 current density
with astonishing stability. Hence, this work should open a new path
for the exploration of efficient non-noble metal catalysts for energy-related
applications.