Catalyst for efficiently electrocatalytically synthesizing ammonia and preparation method thereof
A technology for electrocatalysis and ammonia synthesis, which is applied to electrodes, electrolysis components, electrolysis processes, etc., can solve problems such as low Faradaic efficiency of catalysts, and achieve the effects of improving the activity and selectivity of NH3 synthesis, simple operation and low cost.
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Embodiment 1
[0036] This embodiment provides a NiCoP / CoMoP / Co(Mo 3 Se 4 ) 4 The @C / NF catalyst was prepared as follows:
[0037] (1) The NiCoMo-OH-urea precursor deposited on the nickel foam substrate was prepared by hydrothermal reaction:
[0038] 3mmol cobalt nitrate, 2mmol sodium molybdate, 2mmol urea and 2mmol ammonium fluoride were mixed in 50mL deionized water, stirred for 4 hours to be completely dissolved; then mixed solution and the foam nickel of 1cm × 5cm size were put into the reactor together. The reaction was carried out at 120 °C for 5 hours, and the reactants were naturally cooled to room temperature; the reacted nickel foam was washed and washed alternately with ethanol and deionized water for three times, and then vacuum-dried. The vacuum drying box was set to 35 °C and dried for 12 hours. NiCoMo-OH-urea precursor.
[0039] (2) Preparation of NiCoP / CoMoP / Co(Mo 3 Se 4 ) 4 @C / NF Catalyst:
[0040] Place 2mmol selenium powder, NiCoMo-OH-urea precursor obtained in ste...
Embodiment 2
[0044] This embodiment provides a NiCoP / CoMoP / Co(Mo 3 Se 4 ) 4 The @C / NF catalyst was prepared as follows:
[0045] (1) The NiCoMo-OH-urea precursor deposited on the nickel foam substrate was prepared by hydrothermal reaction:
[0046] 3mmol cobalt nitrate, 1mmol sodium molybdate, 2mmol urea and 2mmol ammonium fluoride were mixed in 50mL deionized water, stirred for 4 hours to be completely dissolved; then mixed solution and the foam nickel of 1cm × 3cm size were put into the reactor together. The reaction was carried out at 120 °C for 5 hours, and the reactants were naturally cooled to room temperature; the reacted nickel foam was washed and washed alternately with ethanol and deionized water for three times, and then vacuum-dried. The vacuum drying box was set to 35 °C and dried for 12 hours. NiCoMo-OH-urea precursor.
[0047] (2) Preparation of NiCoP / CoMoP / Co(Mo 3 Se 4 ) 4 @C / NF Catalyst:
[0048] Place 2mmol selenium powder, NiCoMo-OH-urea precursor obtained in ste...
Embodiment 3
[0051] This embodiment provides a NiCoP / CoMoP / Co(Mo 3 Se 4 ) 4 The @C / NF catalyst was prepared as follows:
[0052] (1) The NiCoMo-OH-urea precursor deposited on the nickel foam substrate was prepared by hydrothermal reaction:
[0053] 3mmol cobalt nitrate, 2mmol sodium molybdate, 2mmol urea and 2mmol ammonium fluoride were mixed in 50mL deionized water, stirred for 4 hours to be completely dissolved; The mixed solution and the foam nickel of 1cm×4cm size were put into the reactor together. The reaction was carried out at 110 °C for 5 hours, and the reactant was naturally cooled to room temperature; the reacted nickel foam was washed and washed alternately with ethanol and deionized water three times, and then vacuum-dried. The vacuum drying box was set to 40 °C and dried for 10 hours to obtain NiCoMo-OH-urea precursor.
[0054] (2) Preparation of NiCoP / CoMoP / Co(Mo 3 Se 4 ) 4 @C / NF Catalyst:
[0055] Place 2mmol selenium powder, NiCoMo-OH-urea precursor obtained in step ...
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