First-principles study of electrochemical HO production on Pd-B single-atom catalyst.

Hydrogen peroxide (HO), a versatile green compound, is increasingly in demand. The electrochemical two-electron oxygen reduction reaction (2e ORR) is a simple and environmentally friendly substitute method to the traditional anthraquinone oxidation method for HO production. This study systematically investigates the 2e ORR process on single transition metal atom-loaded boron fullerene (M - B) using density functional theory calculations. In evaluating the stability of the catalysts, we found that Au, Pd, Pt, Rh, and Ir atoms adsorbed on hexagonal or heptagonal sites of B exhibit good stability. Among these, Pd-modified B heptagonal cavity (Pd-B-heptagonal) demonstrates an ideal Gibbs free energy change for OOH* (4.49 eV) and efficiently catalyzes HO production at a low overpotential (0.27 V). Electronic structure analysis reveals that electron transfer between Pd-B-heptagonal and adsorbed O facilitates O activation. Additionally, the high 2e ORR activity of Pd-B-heptagonal is attributed to electron transfer from the Pd-d orbitals to the π* anti-bonding of p orbitals of OOH*, moderately activating the O-O bond. This study offers valuable understanding designing high-performance electrocatalysts for 2e ORR.