Preparation method for flexible graphite fibre-based asymmetric super capacitor
A supercapacitor and graphene fiber technology, which is applied in the manufacture of hybrid/electric double layer capacitors, can solve the problems of one-dimensional graphene fiber-based flexible asymmetric supercapacitors, and achieve good flexibility and bending stability. High specific capacitance, the effect of expanding the working voltage
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[0032] The steps of the preparation method of the flexible graphene fiber-based asymmetric supercapacitor are as follows:
[0033] 1) Dissolving the graphene oxide raw material in a solvent to obtain a graphene oxide spinning slurry with a mass percentage of 0.1%-3%;
[0034] The solvent can be any one of deionized water, N-methyl-2-pyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, dimethylsulfoxide, sulfolane or a variety of mixtures in any proportion.
[0035] 2) Pass the graphene oxide spinning slurry obtained in step 1 through a spinning nozzle with a diameter of 10-5000 μm at an extrusion speed of 10-2000 μL / min, stay in a coagulation solution at 5-35°C for 1-3600s, and wash, vacuum drying to obtain graphene oxide fibers;
[0036] The coagulation liquid is a water-based coagulant or an organic coagulant; the solvent of the water-based coagulant is composed of ethanol and water in a volume ratio of 1-9:3, and the solute is calcium chloride or manganese acetate. ...
Embodiment 1
[0056] 1) Dissolve the graphene oxide raw material in deionized water to obtain a mass percentage of 0.1%
[0057] 2) Pass the graphene oxide spinning slurry obtained in step 1 through a spinning nozzle with a diameter of 10 μm at an extrusion speed of 10 μL / min, and stay in the water-based coagulation solution at 35°C for 600 seconds. It is the mixed liquid of ethanol and water of 1:3, and the mass ratio of solute calcium chloride and solvent is 1:100, then washes with detergent, and detergent is made up of ethanol, 80 o C vacuum drying, obtains graphene oxide fiber;
[0058] 3) Place the graphene oxide fiber obtained in step 2 in hydrazine vapor for 90 o C reduced for 1h to obtain graphene fibers;
[0059] 4) Soak the graphene fibers obtained in step 3 in an aqueous solution of potassium permanganate with a concentration of 0.1g / L and a temperature of 5°C, react for 24 hours, take out and wash, 80 o C is vacuum-dried to obtain the graphene fiber modified by manganese diox...
Embodiment 2
[0066] 1) Dissolving the graphene oxide raw material in deionized water to obtain a graphene oxide spinning slurry with a mass percentage of 3%;
[0067] 2) Pass the graphene oxide spinning slurry obtained in step 1 through a spinning nozzle with a diameter of 5000 μm at an extrusion speed of 2000 μL / min, and stay in an organic coagulation solution at 5 °C for 300 seconds, and the organic coagulation solution is composed of acetone as a solvent , then 60 o C vacuum drying, obtains graphene oxide fiber;
[0068] 3) Place the graphene oxide fibers obtained in step 2 in 50% sodium ascorbate aqueous solution at 85°C to obtain graphene fibers;
[0069] 4) Soak the graphene fibers obtained in step 3 in an aqueous potassium permanganate solution with a concentration of 1g / L and a temperature of 70°C, react for 10 minutes, remove and wash, and dry in vacuum at 80°C to obtain manganese dioxide-modified graphene fibers ;
[0070] 5) Dissolve graphene oxide and carboxylated multi-wall...
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