Preparation method of molecular metal phthalocyanine (phthalocyanine)/graphene (graphene oxide) composite material
A metal phthalocyanine and composite material technology, which can be used in the manufacture of hybrid/electric double layer capacitors, hybrid capacitor electrodes, etc. Effect
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[0029]Example 1
[0030]Dissolve 0.2 g of phthalocyanine iron in 20 mL of sulfuric acid, dilute in an ice bath to adjust the pH to neutral, and dry at 60°C to obtain amorphous iron phthalocyanine.
[0031]Take 0.2 g of graphene oxide powder, add 20 mL of concentrated sulfuric acid with a concentration of 98%, and obtain a uniformly dispersed sulfuric acid dispersion of graphene oxide through ultrasound for 30 minutes.
[0032]Add 0.2 g of iron phthalocyanine powder to the graphene sulfuric acid dispersion while stirring, and stir for 12 hours after ultrasonic treatment for 30 minutes to obtain an iron phthalocyanine / graphene oxide composite dispersion, which is washed with water to neutrality to obtain a sample.
[0033]Drying in a blast drying oven at 60°C for 12 hours to obtain a black sample powder.
[0034]among themfigure 1 It is the SEM image of the purified iron phthalocyanine, which obviously changed from a crystalline structure to an amorphous structure.figure 2 There is a Mapping image o...
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[0035]Example 2
[0036]Dissolve 0.2 g nickel phthalocyanine in 20 mL sulfuric acid, dilute in an ice bath environment to adjust the pH to neutral, and dry at 60°C to obtain amorphous nickel phthalocyanine.
[0037]Take 0.2 g of graphene oxide powder, add 20 mL of concentrated sulfuric acid with a concentration of 98%, and obtain a uniformly dispersed sulfuric acid dispersion of graphene oxide through ultrasound for 30 minutes.
[0038]Add 0.2 g of nickel phthalocyanine powder to the graphene sulfuric acid dispersion while stirring, and stir for 12 hours after ultrasonic treatment for 30 minutes to obtain a nickel phthalocyanine / graphene oxide composite dispersion, which is washed with water to neutrality to obtain a sample.
[0039]Drying in a blast drying oven at 60°C for 12 hours to obtain a black sample powder.
Example Embodiment
[0040]Example 3
[0041]Dissolve 0.2 g of cobalt phthalocyanine in 20 mL of sulfuric acid, dilute in an ice bath to adjust the pH to neutral, and dry at 60°C to obtain amorphous cobalt phthalocyanine.
[0042]Take 0.2 g of graphene oxide powder, add 20 mL of concentrated sulfuric acid with a concentration of 98%, and obtain a uniformly dispersed sulfuric acid dispersion of graphene oxide through ultrasound for 30 minutes.
[0043]Add 0.2 g of cobalt phthalocyanine powder to the graphene sulfuric acid dispersion while stirring, and stir for 12 hours after ultrasonic treatment for 30 minutes to obtain a cobalt phthalocyanine / graphene oxide composite dispersion, which is washed with water to neutrality to obtain a sample.
[0044]Drying in a blast drying oven at 60°C for 12 hours to obtain a black sample powder.
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