This study addresses the critical challenge in alkaline
direct
formate fuel cells (DFFCs) of slow formate oxidation reaction (FOR)
kinetics as a result of strong hydrogen intermediate (Had) adsorption on Pd catalysts. We developed WO3-supported
Pd nanoparticles (EG–Pd/WO3) via an organic reduction
method using ethylene glycol (EG), aiming to modulate the d-band center
of Pd and alter Had adsorption dynamics. Cyclic voltammetry
demonstrated significantly improved Had desorption kinetics
in EG–Pd/WO3 catalysts. Density functional theory
(DFT) calculations revealed that the presence of EG reduces the d-band
center of Pd, leading to weaker Pd–H bonds and enhanced Had desorption during the FOR. This research provides a new
approach to optimize catalyst efficiency in DFFCs, highlighting the
potential for more effective and sustainable energy solutions through
advanced material engineering.