Graphene-coated silicon composite negative electrode material and its preparation method and application
A technology of graphene coating and negative electrode materials, which is applied in the direction of battery electrodes, structural parts, electrical components, etc., can solve the problems of high cost, distance from the theoretical capacity of silicon, complex operation, etc., to achieve improved conductivity, low cost, and material The effect of structural stability
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[0033] The preparation method of graphite oxide among the present invention is as follows:
[0034] In a water bath at 0-20°C, add 3-5g of graphite powder into 100-150mL of concentrated sulfuric acid, add 10-20g of potassium permanganate while stirring, stir for 3-4 hours, and when the temperature rises to 30-35°C, add 300-500mL Deionized water, stirred for 1-3 hours, added 15-25mL of 30% hydrogen peroxide solution, stirred for 5-20 minutes, centrifuged, washed repeatedly with 5% hydrochloric acid solution and deionized water, and dried Finally, graphite oxide is obtained.
[0035] The assembly and testing methods of lithium-ion batteries are as follows:
[0036]The pea-shaped graphene-coated silicon composite negative electrode material of the present invention and 20wt.% binder (solid content is 2wt.% styrene-butadiene rubber-sodium carboxymethyl cellulose emulsion or concentration is 0.02g / mL poly N-methylpyrrolidone solution of vinylidene fluoride) mixed with 20wt.% cond...
Embodiment 1
[0039] This embodiment relates to a preparation method of a pea-shaped graphene-coated silicon composite negative electrode material, the method comprising the following steps:
[0040] Disperse 80mg of nano-silica powder with a particle size of about 20nm and 40mg of graphite oxide powder in 20ml of deionized water. After ultrasonic dispersion, freeze-dry at -50°C and a pressure of 5Pa for 36 hours, and then disperse the dried sample in 40ml In anhydrous ethanol, put it in a polytetrafluoroethylene-lined reactor for solvothermal reaction, the reaction temperature is 170 ° C, react for 12 hours, the product after the reaction is washed with deionized water, at -50 ° C, the pressure is 5Pa Freeze-dried for 24 hours to obtain a pea-shaped graphene-coated silicon composite negative electrode material. In the composite material, the mass proportion of silicon nanoparticles is about 83%.
[0041] The SEM image of the pea-shaped graphene-coated silicon composite negative electrode ...
Embodiment 2
[0047] This embodiment relates to a preparation method of a pea-shaped graphene-coated silicon composite negative electrode material, the method comprising the following steps:
[0048] Disperse 80mg of nano-silica powder with a particle size of about 1nm and 10mg of graphite oxide powder in 50ml of deionized water. After ultrasonic dispersion, freeze-dry at 10°C and a pressure of 101000Pa for 72 hours, and then disperse the dried sample in 10ml of N , in N-dimethylformamide, placed in a polytetrafluoroethylene-lined reactor for solvothermal reaction, the reaction temperature is 240 ° C, reacted for 2 hours, the product after the reaction was washed with deionized water, at 10 ° C , freeze-dried for 72 hours at a pressure of 101,000 Pa to obtain a pea-shaped graphene-coated silicon composite. In the composite material, the mass ratio of silicon nanoparticles is about 95%.
[0049] The pea-shaped graphene-coated silicon composite negative electrode material prepared in this ex...
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