An economical catalyst with excellent selectivity and high activity is eagerly desirable for H₂ generation from the decomposition of N₂H₄·H₂O. Here, a bifunctional two-dimensional NiFe/CeO₂ nanocatalyst with NiFe nanoparticles (∼5 nm) uniformly anchored on CeO₂ nanosheets supports has been successfully synthesized through a dynamic controlling coprecipitation process followed by in-situ topotactic reduction. Even without NaOH as catalyst promoter, as-designed Ni0.6Fe0.4/CeO₂ nanocatalyst can show high activity for selectively catalyzing H₂ generation (reaction rate (molN2H4 mol⁻¹NiFe h⁻¹): 5.73 h⁻¹). As ceria is easily reducible from CeO₂ to CeO2-x, the surface of CeO₂ could supply an extremely large amount of Ce³⁺, and the high-density electrons of Ce³⁺ can work as Lewis base to facilitate the absorption of N₂H₄, which can weaken the N-H bond and promote NiFe active centers to break the N-H bond preferentially, resulting in the high catalytic selectivity (over 99%) and activity for the H₂ generation from N₂H₄·H₂O.
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Wu et al. (2017) studied this question.
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