Interfacial Electron Engineering of Palladium and Molybdenum Carbide for Highly Efficient Oxygen Reduction

Interfacial electron engineering between noble metal and transition metal carbide is identified as a powerful strategy to improve the intrinsic activity of electrocatalytic oxygen reduction reaction (ORR). However, this short-range effect and the huge structural differences make it a significant challenge to obtain the desired electrocatalyst with atomically thin noble metal layers. Here, we demonstrated the combinatorial strategies to fabricate the heterostructure electrocatalyst of Mo2C-coupled Pd atomic layers (AL-Pd/Mo2C) by precise control of metal-organic framework confinement and covalent interaction. Both atomic characterizations and density functional theory calculations uncovered that the strong electron effect imposed on Pd atomic layers has intensively regulated the electronic structures and d-band center and then optimized the reaction kinetics. Remarkably, AL-Pd/Mo2C showed the highest ORR electrochemical activity and stability, which delivered a mass activity of 2.055 A mg(pd)(-1) at 0.9 V, which is 22.1, 36.1, and 80.3 times higher than Pt/C, Pd/C, and Pd nanoparticles, respectively. The present work has developed a novel approach for atomically noble metal catalysts and provides new insights into interfacial electron regulation.

Automated summary

The study demonstrates the fabrication of Mo2C-coupled Pd atomic layers heterostructure electrocatalyst through precise control of metal-organic framework confinement and covalent interaction. The resulting AL-Pd/Mo2C showed the highest ORR electrochemical activity and stability, significantly outperforming traditional Pt/C, Pd/C, and Pd nanoparticles catalysts.