Preparation method of lead graphene battery negative plate
A battery negative electrode and graphene technology, applied in the direction of lead-acid battery electrodes, etc., can solve the problems of difficulty in uniform distribution, poor dispersion of graphene materials, and failure to achieve the desired effect
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Embodiment 1
[0024] The preparation method of the lead graphene battery negative plate of this embodiment includes steps S1-S5. details as follows.
[0025] S1. Weigh 10 mg of graphene oxide and add it to 50 ml of dimethylformamide (DMF), heat the solution to 50° C., keep stirring for 3 hours, and then centrifuge and dry to obtain graphene oxide with a negatively charged surface modified by functional groups.
[0026] S2, the graphene oxide that step S1 obtains is all dispersed into 0.5mol / L Pb(NO of 100ml 3 ) 2 In the solution, ultrasonication was performed for 1 hour, followed by continuous stirring for 2 hours to obtain graphene oxide with lead ions adsorbed on the surface.
[0027] S3. Transfer the solution of the above step S2 into a hydrothermal kettle, and conduct a hydrothermal reaction at 160° C. for 6 hours. Obtain reduced graphene lead oxide composite material.
[0028] S4, the graphene lead oxide composite material that step S3 obtains is all dispersed in the 2ml sulfuric a...
Embodiment 2
[0031] The preparation method of the lead graphene battery negative plate of this embodiment includes steps S1-S5. details as follows.
[0032] S1. Weigh 7 mg of graphene oxide and add it to 50 ml of dimethylformamide (DMF), heat the solution to 50° C., keep stirring for 3 hours, and then centrifuge and dry to obtain functional group-modified graphene oxide with a negatively charged surface.
[0033] S2, all the graphene oxide obtained in step S1 is dispersed into 0.5mol / L RbNO 3 In the solution, ultrasonication was performed for 1 hour, followed by continuous stirring for 2 hours to obtain graphene oxide with rubidium ions adsorbed on the surface.
[0034] S3. Transfer the solution of the above step S2 into a hydrothermal kettle, and conduct a hydrothermal reaction at 160° C. for 6 hours. A reduced graphene rubidium oxide composite material is obtained.
[0035] S4, the graphene rubidium oxide composite material that step S3 obtains is all dispersed in the 2ml sulfuric aci...
Embodiment 3
[0038] S1. Weigh 1 mg of graphene oxide and add it to 50 ml of nitrogen-methylpyrrolidone, heat the solution to 55° C., keep stirring for 5 hours, and then centrifuge and dry to obtain graphene oxide with a negatively charged surface modified by functional groups.
[0039] S2, disperse 1mg of graphene oxide obtained in step S1 into 50ml of 0.2mol / L MnCl 2 The solution was ultrasonicated for 1 hour, and then continuously stirred for 2 hours to obtain graphene oxide with manganese ions adsorbed on the surface.
[0040] S3. Transfer the solution of the above step S2 into a hydrothermal kettle, and conduct a hydrothermal reaction at 170° C. for 3 hours. A reduced graphene manganese oxide composite material is obtained.
[0041] S4. Disperse 10 mg of the graphene manganese oxide composite material obtained in step S3 into 3 ml of sulfuric acid solution with 0.02 g of polyaspartic acid added, and add 6 ml of deionized water, and ultrasonically disperse for 1 hour to obtain graphene...
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