Foamed nickel-based erbium-doped nickel-cobalt bimetallic phosphide nano array as well as preparation method and application thereof
A nano-array, nickel foam technology, applied in electrodes, electrolysis processes, electrolysis components, etc., can solve the problems of low catalytic activity, long-term corrosion resistance, unsatisfactory electrocatalytic performance and practical industrial application, etc., and achieve catalytic activity. High, improve the intrinsic catalytic activity, optimize the effect of Gibbs free energy
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[0031] The present invention provides a kind of preparation method of nickel-cobalt bimetallic phosphide nano-array (Er-NiCoP / NF) doped with foam nickel-based erbium, comprising the following steps:
[0032] Mixing soluble trivalent erbium salt, soluble divalent nickel salt, soluble divalent cobalt salt, urea, ammonium fluoride and water to obtain a mixed solution;
[0033] Soaking the nickel foam with the mixed solution and then performing a hydrothermal reaction to obtain a hydrothermal product;
[0034] The phosphorus source and the hydrothermal product are calcined in a protective atmosphere to obtain the nickel-cobalt double-metal phosphide nano-array doped with nickel-based erbium foam.
[0035] In the present invention, the source of each raw material is not particularly limited, and commercially available products well known to those skilled in the art can be used.
[0036] The invention mixes soluble trivalent erbium salt, soluble divalent nickel salt, soluble divale...
Embodiment 1
[0062] 1mmol Ni(NO 3 ) 2 ·6H 2 O, 1mmol Co(NO 3 ) 2 ·6H 2 O, urea (6mmol) and NH 4 F (2.5 mmol) was dissolved in 30 mL of water, and after stirring for 30 minutes, it was aged at room temperature for 1 hour. The solution was then transferred to a 50 mL stainless steel autoclave lined with Teflon, and a piece of nickel foam (area 6 cm 2 , with a thickness of 1.5mm and a surface density of 350g·cm -2 ) was immersed in the reaction solution and kept at 120° C. for 6 hours. When the temperature was cooled to room temperature, the obtained NiCo nanowire array precursor (NiCo NWAs precursor / NF) was washed once with water and ethanol, and dried overnight at 60 °C in a vacuum drying oven.
[0063] NaH 2 PO 2 ·H 2 O (500 mg) and pre-prepared NiCo NWAs precursor / NF were placed on the upstream side and center of the tube furnace, respectively. The sample was then calcined at 350 °C for 2 h in an Ar atmosphere with a heating rate of 2 °C min -1 . Finally, NiCoP / NF was obtain...
Embodiment 2
[0065] 1mmol Ni(NO 3 ) 2 ·6H 2 O, 1mmol Co(NO 3 ) 2 ·6H 2 O, 0.05mmol Er(NO 3 ) 3 ·6H 2 O (molar ratio Er:Ni=5%), urea (6mmol) and NH 4 F (2.5 mmol) was dissolved in 30 mL of water, and after stirring for 30 minutes, it was aged at room temperature for 1 hour. The solution was then transferred to a 50 mL stainless steel autoclave lined with Teflon, and a piece of nickel foam (area 6 cm 2 , with a thickness of 1.5mm and a surface density of 350g·cm -2 ) into the reaction solution and kept at 100°C for 10 hours. When the temperature was cooled to room temperature, the obtained Er-doped NiCo nanowire array precursor (Er-NiCo NWAs precursor / NF) was washed several times with water and ethanol, and dried overnight at 60 °C in a vacuum oven.
[0066] NaH 2 PO 2 ·H 2 O (500 mg) and pre-prepared Er-NiCo NWAs precursor / NF were placed on the upstream side and center of the tube furnace, respectively. The sample was then calcined at 300 °C for 3 h in an Ar atmosphere with a...
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