NiFe3N/NF electrochemical catalyst and preparation method and application thereof
A catalyst and electrochemical technology, applied in physical/chemical process catalysts, chemical instruments and methods, chemical/physical processes, etc., can solve the problem of poor electron conductivity of Ni-based catalysts, inability to large-scale production, and scarcity of crustal content, etc. problem, to achieve the effect of low cost of raw materials, easy operation, and improved oxygen evolution performance
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Embodiment 1
[0045] (1) Acid pretreatment: Prepare a hydrochloric acid solution with a concentration of 3 M, pour it into a single-necked round bottom flask, and put it in an oil bath; cut the foam nickel into a size of 1×2 cm, clean it with deionized water, and put it in a container. In a flask containing hydrochloric acid, heat to 90°C for 30 minutes, then cool to room temperature and wash with water;
[0046] (2) Surface oxidation treatment: The nickel foam after hydrochloric acid pretreatment is oxidized in the air for 2 days to keep it in a wet state at a temperature of 30°C and an air humidity of 85%.
[0047] The morphology of nickel oxide formed on the foamed nickel after surface oxidation treatment is as follows: figure 1 shown by figure 1 It can be seen that a thin layer of nickel oxide layer that grows uniformly is formed on the surface of the foamed nickel sheet.
Embodiment 2
[0049] (1) Prepare a hydrochloric acid solution with a concentration of 3 M, pour it into a single-necked round-bottomed flask, put it into an oil bath, cut the nickel foam into a size of 1×2 cm, clean it with deionized water, and put it into a flask filled with hydrochloric acid. In the flask, heat to 90°C for 30 minutes, then cool to room temperature and clean with water; the nickel foam is oxidized in the air for 2 days to keep it in a wet state, the temperature is 30°C, and the air humidity is 85%;
[0050] (2) Prepare 20 mL of K with a concentration of 0.02 mol / L 4 Fe(CN) 6 Solution, immerse a piece of 1×2cm surface oxidized nickel foam in K 4 Fe(CN) 6 In the solution, add 0.015mol / L trisodium citrate, and use the nickel oxide on the surface of the nickel foam as the nickel source to make the ligand K 4 Fe(CN) 6 The Fe source in the mixture was combined with the nickel source, and the MOF material (NiFe-PBA / NF) was obtained by standing at room temperature for 6h, 12h,...
Embodiment 3
[0053] (1) Prepare a hydrochloric acid solution with a concentration of 3 M, pour it into a single-necked round-bottomed flask, put it into an oil bath, cut the nickel foam into a size of 1×2 cm, clean it with deionized water, and put it into a flask filled with hydrochloric acid. In the flask, heat to 90°C for 30 minutes, then cool to room temperature and clean with water; the nickel foam is oxidized in the air for 2 days to keep it in a wet state, the temperature is 30°C, and the air humidity is 85%;
[0054] (2) Prepare 20mL of K with concentrations of 0.01mol / L, 0.015mol / L, and 0.02mol / L 4 Fe(CN) 6 Solution, immerse a piece of 1×2cm surface oxidized nickel foam in K 4 Fe(CN) 6 In the solution, add the trisodium citrate of 0.015mol / L, take the nickel oxide on the surface of the nickel foam as the nickel source to make the ligand K 4 Fe(CN) 6 The Fe source and the nickel source in the mixture were combined, and the MOF material (NiFe-PBA / NF) was obtained by standing at r...
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