Tungsten selenide/graphene/carbon nanofiber composite material and preparing method thereof
A carbon nanofiber and composite material technology, applied in the direction of carbon fiber, fiber treatment, artificial filament of inorganic raw materials, etc., can solve the problems of low electrochemical activity, low density specific surface area, and restricted performance of electrospun carbon nanofibers, and achieve Excellent electrical conductivity and electrochemical activity, good self-support and flexibility, and ingenious design ideas
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Embodiment 1
[0042] This embodiment includes the following steps:
[0043] Weigh 0.8 g of polyacrylonitrile powder and add 10 mL of N,N-dimethylformamide, and stir at high speed for 4 hours under heating in an oil bath at 80°C to obtain a transparent polyacrylonitrile solution with a yellowish color. Electrospinning is carried out on the above polyacrylonitrile solution, and the spinning process conditions are set as follows: flow rate 0.25mm / min, voltage 18kV, receiving distance 12cm. The prepared polyacrylonitrile nanofibers are finally deposited on the drum receiver in the form of nanofiber membranes, and the fiber membranes are removed and dried in a vacuum oven for 24-28 hours to remove residual solvents. The prepared polyacrylonitrile fiber membrane was fixed on a plate and placed in a programmed temperature-controlled oven for pre-oxidation treatment. The temperature was raised from room temperature to 250 °C at a rate of 1 °C / min and kept for 1 h, and then naturally cooled to room ...
Embodiment 2
[0049] This embodiment includes the following steps:
[0050] The graphene oxide prepared by the Hummers method was sonicated for 2 h to obtain a graphene oxide dispersion with a concentration of 1 mg / mL. Take 80 mg of the above-mentioned oxidized polyacrylonitrile fiber membrane and add it to 100 mL of graphene oxide dispersion and let it stand at room temperature for 48 hours, then take out the fiber membrane and rinse off the graphene oxide dispersion on the surface with absolute ethanol, and dry it in a constant temperature oven at 70°C for 48 hours . The above-mentioned graphene oxide / oxidized polyacrylonitrile nanofiber membrane was placed in a temperature-programmed tube furnace for high-temperature carbonization treatment. The carbonization conditions were as follows: the temperature was raised from room temperature to 1000°C at a heating rate of 10°C / min and kept for 1h. Cool down naturally. Finally, a graphene / carbon nanofiber composite material is obtained.
Embodiment 3
[0052] This embodiment includes the following steps:
[0053] A certain amount of selenium powder was weighed and added to the hydrazine hydrate solution, heated and stirred in an oil bath at 85° C. for 1 h to obtain a brown transparent selenium solution with a molar concentration of 2 mM, and cooled at room temperature for use. Weigh a certain amount of sodium tungstate crystals and add it into N,N-dimethylformamide to prepare a sodium tungstate solution with a molar concentration of 1mM. Weigh 10mg of graphene / carbon nanofiber composite material and add it to the above mixed solution of 10mL selenium solution and 10mL sodium tungstate, transfer it to a polytetrafluoroethylene-lined reaction kettle, and place it in a constant temperature oven at 220°C for 12 hours Then take it out, wash and dry to obtain the tungsten selenide / graphene / carbon nanofiber composite material.
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