Hydrogen-Mediated Thin Pt Layer Formation on Ni3N Nanoparticles for the Oxygen Reduction Reaction

A simple wet-chemical route for the preparation of core–shell-structured catalysts was developed to achieve high oxygen reduction reaction (ORR) activity with a low Pt loading amount. Nickel nitride (Ni3N) nanoparticles were used as earth-abundant metal-based cores to support thin Pt layers. To realize the site-selective formation of Pt layers on the Ni3N core, hydrogen molecules (H2) were used as a mild reducing agent. As H2oxidation is catalyzed by the surface of Ni3N, the redox reaction between H2and Pt(IV) in solution was facilitated on the Ni3N surface, which resulted in the selective deposition of Pt on Ni3N. The controlled Pt formation led to a subnanometer (0.5–1 nm)-thick Pt shell on the Ni3N core. By adopting the core–shell structure, higher ORR activity than the commercial Pt/C was achieved. Electrochemical measurements showed that the thin Pt layer on Ni3N nanoparticle exhibits 5 times higher mass activity and specific activity than that of commercial Pt/C. Furthermore, it is expected that the proposed simple wet-chemical method can be utilized to prepare various transition-metal-based core–shell nanocatalysts for a wide range of energy conversion reactions.