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 method of preparing a foam-nickel-doped nickel-doped nickel-cobalt bimetalline phosphatine nano-array (ER-NICOP / NF), including the following steps:
[0032] The soluble trivalent nibquide, soluble divalent nickel salt, soluble bvilobal cobalt salt, urea, ammonium fluid, and water, to obtain a mixed solution;
[0033] After soaking the foam nickel with the mixed solution, the hydrothermal reaction is obtained.
[0034] The phosphorus source and the water heat product are calcined in the protective atmosphere to obtain the foam-nickel-plyc-doped nickel-cobalt bimetallic phosphide nano array.
[0035] The invention is not particularly limited for the source of each raw material, and the commercially available goods well known to those skilled in the art can be used.
[0036] The present invention adds soluble trivalent ribs, soluble divalent nickel salts, soluble bvilobal cobalt salts, urea, ammonium fluid, and water to obtain a mixed solutio...
Example Embodiment
[0061] Example 1
[0062] 1 mmol ni (no 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, stirred for 30 minutes, aged for 1 hour at room temperature. The solution is then transferred to a 50 ml stainless steel autoclave with TEFLON liner, and a piece of foam is 6 cm. 2 , Thickness of 1.5 mm, surface density is 350g · cm -2 Immersion in the reaction solution, maintained at 120 ° C for 6 hours. When the temperature was cooled to room temperature, the obtained NiCO nanowire array precursor (Nico Nwas Precuesor / NF) was washed with water and ethanol and dried overnight at 60 ° C in a vacuum drying tank.
[0063] Nah 2 PO 2 · H 2 O (500 mg) and pre-prepared NICO NWAS Precuesor / NF are placed on the upstream side and center of the tubular furnace, respectively. The sample was then calcined in a Ar atmosphere for 2 hours, the heating rate was 2 ° C · min. -1 . Finally, cooling to room temperature to get NiCOP / NF.
Example Embodiment
[0064] Example 2
[0065] 1 mmol ni (no 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 = 5%), urea (6mmol) and NH 4 F (2.5 mmol) was dissolved in 30 ml of water, stirred for 30 minutes, aged for 1 hour at room temperature. The solution is then transferred to a 50 ml stainless steel autoclave with TEFLON liner, and a piece of foam is 6 cm. 2 , Thickness of 1.5 mm, surface density is 350g · cm -2 Immersion in the reaction solution, maintained at 100 ° C for 10 hours. When the temperature was cooled to room temperature, the obtained ER-NWAS Precuesor / NF was washed several times a few times with water and ethanol and dried overnight at 60 ° C in a vacuum drying tank.
[0066] Nah 2 PO 2 · H 2 O (500 mg) and pre-prepared ER-NICO NWAS Precuesor / NF are placed on the upstream and centers of the tubular furnace, respectively. The sample was then calcined in a Ar atmosphere for 3 hours, and the heating rate was 2 ° C · min. -1 . Finally, coo...
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