Modulating the
d‑Band Center of Palladium via
Ethylene Glycol Modification: Accelerating H<sub>ad</sub> Desorption
for Enhanced Formate Electrooxidation
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 (H<sub>ad</sub>) adsorption on Pd catalysts. We developed WO<sub>3</sub>-supported
Pd nanoparticles (EG–Pd/WO<sub>3</sub>) via an organic reduction
method using ethylene glycol (EG), aiming to modulate the d-band center
of Pd and alter H<sub>ad</sub> adsorption dynamics. Cyclic voltammetry
demonstrated significantly improved H<sub>ad</sub> desorption kinetics
in EG–Pd/WO<sub>3</sub> 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 H<sub>ad</sub> 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.