Preparation method of tungsten-based catalyst/nano carbon fiber composite electrode for full-vanadium flow battery
An all-vanadium redox flow battery and nano-carbon fiber technology, which is applied to battery electrodes, circuits, electrical components, etc., can solve the problems of low surface activity of electrode materials and unstable electrocatalytic performance of electrode materials, and achieve excellent electrocatalytic activity and electrocatalytic performance. Improvement of chemical activity and improvement of energy efficiency
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[0033] In a specific embodiment of the present invention, the preparation method of tungsten-based catalyst / carbon nanofiber electrode for all-vanadium redox flow battery comprises the following steps and process method:
[0034] 1) Preparation of spinning solution: adding polyacrylonitrile or polyethylene glycol into dimethylformamide or dimethylacetamide in a certain proportion, stirring evenly under water bath conditions;
[0035] Among them, the average molecular weight of polyacrylonitrile is 50,000-200,000, the average molecular weight of polyethylene glycol is 2,000-10,000, and the mass ratio of polyacrylonitrile or polyethylene glycol to dimethylformamide or dimethylacetamide is 5 : 95 to 20: 80 (preferably 10: 90 to 15: 85), the water bath temperature is 40 ~ 80 ° C, the stirring time of polyacrylonitrile or polyethylene glycol in dimethylformamide or dimethylacetamide 0.5 to 24 hours (preferably 3 to 6 hours).
[0036] 2) Add tungsten salts (one or more of tungsten-...
Embodiment 1
[0049] 1) Add polyacrylonitrile with a mass fraction of 10% into dimethylformamide under stirring conditions, and stir for 2 hours at a water bath temperature of 60° C. to obtain a spinning solution. The average molecular weight of polyacrylonitrile is 150,000.
[0050] 2) Add tungstic acid to the spinning solution, the mass ratio of the added tungstic acid to the polyacrylonitrile in the solution is 1:50, stir for 12 hours, and then ultrasonic for 6 hours to obtain a uniform composite spinning solution.
[0051] 3) adding the composite spinning solution obtained in step 2) into a 20ml syringe, and using electrospinning technology to obtain a nanofiber membrane, the thickness of the nanofiber membrane is 0.5 mm;
[0052] Among them, the electrospinning process parameters are: the needle aperture is 0.3 mm, the distance between the needle and the nanofiber film collecting plate on the roller is 12 cm, the spinning voltage between the needle and the roller is 25 kV, and the colle...
Embodiment 2
[0057] 1) Polyethylene glycol with a mass fraction of 10% was added to dimethylacetamide under stirring conditions, and the temperature of the water bath was 40° C. and stirred for 3 hours to obtain a spinning solution. The average molecular weight of polyethylene glycol was 8,000.
[0058] 2) Add tungstic acid to the spinning solution, the mass ratio of the added tungstic acid to polyethylene glycol in the solution is 1:50, stir for 12 hours, and then ultrasonic for 6 hours to obtain a uniform composite spinning solution.
[0059] 3) adding the composite spinning solution obtained in step 2) into a 20ml syringe, and using electrospinning technology to obtain a nanofiber membrane, the thickness of the nanofiber membrane is 0.5 mm;
[0060] Among them, the electrospinning process parameters are: the aperture of the needle head is 0.6 mm, the distance between the needle head and the nanofiber film collecting plate on the rotating roller is 15 cm, the spinning voltage between the ...
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