摘要
Green hydrogen production by alkaline water electrolysis is an important technology in the decarbonization of the current industry. However, its large-scale application is limited by mediocre performance of conventional Raney Ni electrocatalysts. Herein, high-performance NiMoZn alloy catalysts of the Raney Ni type are developed by pulse electrodeposition for the hydrogen evolution reaction (HER). The optimized catalyst, NMZ-CA, exhibits an overpotential of 37 mV at 10 mA⋅cm −2 and a Tafel slope of 27 mV⋅dec −1 in 1 mol·L –1 KOH. Tafel slope measurements, X-ray photoelectron spectroscopy, and H 2 temperature-programmed desorption experiments show that the incorporation of Mo and Zn in Ni weakens the binding of HER intermediate (H ads ) on strongly adsorbing sites, leading to improved electrochemical kinetics. Electron microscopy and X-ray diffraction study reveals that a phase-pure Mo-doped Ni 2 Zn 11 intermetallic precatalyst formed via pulse electrodeposition and subsequent heat treatment is key to the structure integrity and performance of the catalyst after activation by alkaline leaching. Modification of NMZ-CA with PTFE enhances its HER performance by facilitating gas removal and improving structure integrity. A practical alkaline water electrolyzer built on the modified NMZ/PTFE-CA electrode delivers 2.0 A⋅cm −2 at 1.92 V cell voltage and operates for 250 h without decay. This work provides insights into the synergy between Ni, Mo, and Zn in Raney Ni-type catalysts, and demonstrates the hydrophobic modification as an effective strategy for electrode development in high-performance alkaline water electrolysis.
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