Compared
with traditional two-dimensional layered materials, MXene
with metal-like conductivity has excellent chemical reaction activity
and hydrophilicity, which can be used as ideal substrate materials.
Nanocomposites with the non-noble metal based on MXene have important
application prospects in the field of electrocatalytic decomposition
of water. In this study, Co4MnFe3/Ti3C2 has been successfully synthesized only by the one-step
method and prepared using ultrathin two-dimensional layered Ti3C2 as substrate materials, which is much more convenient
than most electrocatalyst hybridization. The hybrid exhibits excellent
electrochemical performance in alkaline media with an overpotential
of 263 mV and Tafel slope of 26.3 mV·dec–1,
which is much lower than that of its pure Co4MnFe3 counterparts and RuO2 catalyst in alkaline medium. When
the current density reaches 10 mA/cm2, excellent long-range
stability is displayed. Meanwhile, a fast reaction kinetics can also
be obtained. Furthermore, density functional theory calculations reveal
that, due to electron interactions and d-band center of metals, the
enhanced density of states in the vicinity of the Fermi level has
great influence on the oxygen evolution reaction property of the electrocatalyst
via adjusting the adsorption strength of intermediates, which can
improve the electrocatalytic performance of the hybrid. More importantly,
this work provides a new approach for the electrolytic water oxygen
evolution reaction of MXene-based catalysts in alkaline media and
shed light on the exploration of advanced electrocatalysts for renewable
energy conversion and storage systems.