Hydrogen dissociative chemisorption and desorption on saturated subnano palladium clusters (Pdn, n = 2–9)

Abstract

H₂ sequential dissociative chemisorption on small palladium clusters was studied using density functional theory. The chosen clusters Pd_n (n = 2–9) are of the lowest energy structures for each n. H₂ dissociative chemisorption and subsequent H atom migration on the bare Pd clusters were found to be nearly barrierless. The dissociative chemisorption energy of H₂ and the desorption energy of H atom in general decrease with the coverage of H atoms and thus the catalytic efficiency decreases as the H loading increases. These energies at full cluster saturation were identified and found to vary in small energy ranges regardless of cluster size. As H loading increases, the clusters gradually change their bonding from metallic character to covalent character. For the selected Pd clusters, the capacity to adsorb H atoms increases almost proportionally with cluster size; however, it was found that the capacity of Pd clusters to adsorb H atoms is, on average, substantially smaller than that of small Pt clusters, suggesting that the catalytic efficiency of Pt nanoparticles is superior to Pd nanoparticles in catalyzing dissociative chemisorption of H₂ molecules.