A ternary PdNiMo alloy as a bifunctional nanocatalyst for the oxygen reduction reaction and hydrogen evolution reaction. Issue 24 (9th November 2022)

• Record Type: Journal Article
• Authors: Wu, Xiao; Liu, Xiangnan; He, Yi; Lei, Lecheng; Hao, Shaoyun; Zhang, Xingwang
• Is Part Of: Inorganic chemistry frontiers. Volume 9:Issue 24(2022)
• Page Start: 6574
• Page End: 6583
• Publication Date: 2022-11-09
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d2qi01317g
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : Mo0.2 Pd3 Ni/NC shows superior electrochemical performances for both ORR and HER due to the charge redistribution among Ni, Pd, and Mo, tuning the electronic structure of Pd. Abstract : Proton exchange membrane (PEM) electrolyzers are one of the most significant technologies for producing green hydrogen energy, in which nanostructured catalysts occupy an important role. At commercial densities, the nanocatalysts on the cathode side in PEM electrolyzers often suffer from undesirable oxidation with the slight oxygen passing through the membrane. In this study, we designed a ternary Mo x Pd y Ni nanocatalyst supported on N-doped carbon (NC) from the pyrolysis of ZIF-8 toward the hydrogen evolution reaction (HER), while at the same time avoiding a loss of the activity toward the oxygen reduction reaction (ORR). Taking advantage of the charge redistribution among these elements, the representative Mo0.2 Pd3 Ni/NC exhibited a low overpotential ( η 10 = 53 mV) toward HER with a low Tafel slope of 35.8 mV dec −1 in H2 SO4 . In addition, Mo0.2 Pd3 Ni/NC also exhibited a half-wave potential of 0.90 V toward ORR with a mass activity of 0.78 A mgPd −1, which was twice that of Pt/C (0.38 A mgPt −1 ). Micro-structured analyses and density functional theory calculations revealed that the d-band center of Pd was downshifted by the synergistic effect between Ni and Mo, which weakened the binding energy of the intermediates with Pd, thus lowering the energy barrier toward HER and ORR. This strategy could significantly enhance the HER stability, which could be extended to the design of other bifunctional nanocatalysts for other reactions.