The synthesis of efficient hydrogen
evolution reaction (HER) electrocatalysts
is challenging for industrial-scale hydrogen generation by water splitting.
Since their discovery in 2011, MXenes have been extensively investigated
for their use in various energy applications as they possess sheet-like
morphology that provides more active surface area and facilitates
fast ion transfer. This work
utilizes a facile hydrothermal treatment to fabricate palladium-modified
MXene nanoflowers (nPdNFs). Chemical and morphological analysis of
these synthesized nPdNFs shows that nPds have been successfully incorporated
in MXene nanoflowers and act as an excellent support material for
nPds. The effect of temperature and the thermal decomposition properties
of the synthesized material were investigated by calcining it at different
temperatures like 200, 300, and 400 °C in a flow of N2 gas. It is observed that nPdNFs-3 (calcined at 300 °C) exhibits
maximum active catalytic sites for HER because its porous morphology
supports rapid ion transportation. The electrochemical active surface
area (ECSA) for all three materials was evaluated, among which nPdNFs-3
demonstrated the highest ECSA value, corroborating its HER activity
and depicting a current density of 10 mA cm−2 at
a low overpotential of 149 mV, with a Tafel slope of 96 mV dec–1 in 0.5 M H2SO4. The fabricated
nanostructured material highlights ceaseless efforts and paves the
way for developing MXenes and related materials, which can be employed
in the energy conversion and storage sector.