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Preparation method for NiCoP nanowire electro-catalytic electrode

A technology of catalytic electrode and rice wire electricity, applied in the direction of electrode, nanotechnology, nanotechnology, etc., can solve the problems of small specific surface area of ​​coating, high product toxicity, easy pollution of the environment, etc., meet the requirements of conventional equipment, improve catalytic activity, and rich raw materials Effect

Inactive Publication Date: 2016-09-21
HUBEI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But its disadvantage is that the specific surface area of ​​the prepared coating is too small, which leads to poor durability, and it will cause a decline in performance after a period of time.
[0005] The patent application No. 201410133843.9 discloses a method for preparing a high-performance nickel-based ruthenium-containing composite oxide hydrogen evolution electrode, which mainly uses a solvothermal synthesis method to grow nickel-ruthenium oxide nanorods in situ on a foamed nickel substrate to obtain The specific surface area of ​​the electrode is large, and it is firmly combined with the substrate. The resulting product has a large specific surface area, many active sites and strong catalytic activity. It has excellent hydrogen evolution performance and high stability, but its disadvantage is that the prepared product High toxicity and easy to pollute the environment

Method used

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  • Preparation method for NiCoP nanowire electro-catalytic electrode
  • Preparation method for NiCoP nanowire electro-catalytic electrode
  • Preparation method for NiCoP nanowire electro-catalytic electrode

Examples

Experimental program
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Effect test

Embodiment 1

[0029] (1) remove the nickel foam surface oxide layer, first prepare 120ml deionized water and 3ml 36.8-38wt% concentrated hydrochloric acid solution, then soak the foam nickel sheet of 4cm * 7cm size in the above solution, after 20 minutes, take out the foam nickel The sheet was washed with ethanol and deionized water three times in sequence, and finally dried in an oven at 60°C for 4 hours to obtain a foamed nickel sheet without an oxide layer on the surface;

[0030] (2) Hydrothermal growth of nickel-cobalt salt compound precursor, first dissolve 2mmol nickel chloride and 4mmol cobalt chloride powder in 60mL deionized water, add 12mmol urea until completely dissolved, and then fix the treated foam nickel sheet vertically In the polytetrafluoroethylene liner (100mL) containing the above solution, after sealing with an autoclave, place it in an oven at 120°C for 8 hours, and finally wash and dry the reaction product to obtain the nickel-cobalt salt compound precursor;

[0031...

Embodiment 2

[0033](1) Remove the nickel foam surface oxide layer, first prepare 150ml deionized water and 5ml 36.8-38wt% concentrated hydrochloric acid solution, then soak the foam nickel sheet of 4cm * 7cm size in the above solution, after 18 minutes, take out the foam nickel The sheet was washed with ethanol and deionized water four times in sequence, and finally dried in an oven at 70°C for 4 hours to obtain a nickel foam sheet without an oxide layer on the surface.

[0034] (2) Hydrothermal growth of nickel-cobalt salt compound precursor, first dissolve 3mol nickel chloride and 6mol cobalt chloride powder in 60mL deionized water, add 18mmol urea until completely dissolved, and then fix the treated foam nickel sheet vertically In a polytetrafluoroethylene liner (100mL) filled with the above solution, seal it with an autoclave, place it in an oven at 120°C for 8 hours, and finally wash and dry the reaction product to obtain the nickel-cobalt salt compound precursor.

[0035] (3) Phospha...

Embodiment 3

[0037] (1) Remove the surface oxide layer of foamed nickel, first prepare 200ml deionized water and 5ml 36.8-38wt% concentrated hydrochloric acid solution, then soak the foamed nickel sheet of 4cm * 7cm size in the above solution, after 22 minutes, take out the foamed nickel The sheet was washed with ethanol and deionized water five times in sequence, and finally dried in an oven at 80°C for 3 hours to obtain a nickel foam sheet without an oxide layer on the surface.

[0038] (2) Hydrothermal growth of nickel-cobalt salt compound precursor, first dissolve 3mol nickel chloride and 6mol cobalt chloride powder in 60mL deionized water, add 18mmol urea until completely dissolved, and then fix the treated foam nickel sheet vertically In a polytetrafluoroethylene liner (100mL) filled with the above solution, seal it with an autoclave, place it in an oven at 120°C for 8 hours, and finally wash and dry the reaction product to obtain the nickel-cobalt salt compound precursor.

[0039] (...

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PUM

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Abstract

The invention discloses a preparation method for a NiCoP nanowire electro-catalytic electrode. A NiCo salt nanowire is adopted as a phosphorization precursor, hypophosphite is used as a phosphorus source, and the phosphorization process of the NiCo salt nanowire is achieved by controlling the annealing technique in a stored program control tube type annealing furnace. The diameter of the NiCoP nanowire obtained through the method is 140 nanometers, the length of the obtained NiCoP nanowire is about 3.2 micrometers, and the surface of the nanowire is roughly and evenly grown on a 3D netty foamed nickel substrate, so that the specific surface area and the electric conductivity of an electro-catalytic material are effectively improved, and the electro-catalytic hydrogen evolution performance and stability of an electrode material are improved. The electro-catalytic hydrogen production performance of the electrode is tested in 1M of a KOH electrolyte, the overpotential under the electric current density of 10 mA / cm<2> is 109 mV, and the Tafel slope is 88.5 mV / dec, so that the material has the superior electro-catalytic hydrogen production performance compared with common electro-catalytic hydrogen evolution materials. Meanwhile, the preparation technique is simple, the equipment requirement is conventional, reactive materials are abundant, price is low, and the electrode is environmentally friendly.

Description

technical field [0001] The invention relates to a catalytic hydrogen production material for electrolysis of water, in particular to a preparation method of a NiCoP electrocatalytic hydrogen production material for electrolysis of water. Background technique [0002] Due to the serious energy demand and environmental pollution, it is imminent to find an efficient, clean and sustainable energy source. Hydrogen, as an abundant, renewable and clean energy source, is considered to be one of the most promising energy materials in the future [[1] Bard , A.J.; Fox, M.A. Acc. Chem. Res. 1995, 28, 141]. At present, there are many ways to produce hydrogen, among which hydrogen production by electrolysis of water has attracted much attention due to its simple equipment, no pollution, and high product purity. The hydrogen production reaction of electrolyzed water occurs on the electrode surface, including two basic half-reactions, the cathodic hydrogen evolution reaction and the anode ...

Claims

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Application Information

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IPC IPC(8): C25B11/06C25B11/03C25B1/04B82Y40/00B82Y30/00
CPCB82Y30/00B82Y40/00C25B1/04C25B11/031C25B11/073Y02E60/36
Inventor 童锐王喜娜王浩周小龙肖凌峰郑铮
Owner HUBEI UNIV
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