Abstract
The slow hydrogen oxidation reaction (HOR) rate at the anode of the anion exchange membrane fuel cell currently holds back its further development. In this study, N-doped porous hollow carbon spheres (NHCSs) as a support are created, and highly dispersed small-sized IrMo nanoclusters (3.05 nm NCs) as the active species within NHCSs. The Ir1Mo5/NHCS composite exhibits excellent HOR catalytic activity in 0.1 M KOH solution with a mass activity of 2687.20 mA mg-1 and an exchange current density of 11.0 mA cm-2, which are 6.7 and 7.9 times higher than those of commercial Pt/C, respectively. Experiments and theoretical calculations suggest that Ir and Mo act as dual active sites for the H* and OH* adsorption. The high HOR catalytic activity of Ir1Mo5/NHCSs is attributed to the synergistic effect of Ir and Mo, which modulates the d-band center of the catalyst and thus optimizes the binding energy of H* and OH*. Furthermore, the spatial confinement effect of the highly porous support structure, combined with the anchoring effect of N doping, not only increases the dispersion and exposure of active IrMo NCs, but also enhances their structural stability and resistance to CO poisoning.