Method for preparing porous graphene silicon negative electrode material
A technology of porous graphene and silicon anode, applied in the field of lithium ion batteries, can solve the problems of difficult scale application, graphene structure damage, high cost, etc., and achieve the effect of avoiding irreversible damage and high structural regularity.
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Embodiment 1
[0021] Using ferric chloride as intercalation agent and 300 mesh flake graphite as precursor, ferric chloride-graphite intercalation compound was prepared by molten salt intercalation method. Add 1g of ferric chloride-graphite intercalation compound into 1000mL of acetone solvent, ultrasonicate for 3 hours, then centrifuge at a speed of 5000r / min, pour off the supernatant, and freeze-dry the precipitate to obtain ferric chloride- Graphene Interlayer Compounds. The ferric chloride-graphene interlayer compound was placed in a muffle furnace for heat treatment, and kept at 400° C. for 2 hours to obtain an iron oxide-graphene composite material. Disperse 1g of iron oxide-graphene composite material in 500mL of water and ethanol mixed solution (ratio: 5:1), 1g of silicon material and CTAB dispersed in the same 500mL of water and ethanol mixed solution, respectively, ultrasonic treatment for 30 minutes , the silicon material dispersion liquid is slowly added dropwise into the graph...
Embodiment 2
[0023] Using ferric chloride as intercalation agent and 1000 mesh flake graphite as precursor, ferric chloride-graphite intercalation compound was prepared by molten salt intercalation method. Add 1g of ferric chloride-graphite intercalation compound into 1000mL of isopropanol solvent, use a high-pressure homogenizer to carry out 5 cycles of stripping, then perform centrifugation at a speed of 6000r / min, pour off the supernatant, and remove the precipitate Freeze-drying is carried out to obtain ferric chloride-graphene interlayer compound. The ferric chloride-graphene interlayer compound was placed in a muffle furnace for heat treatment, and kept at 550° C. for 2 hours to obtain an iron oxide-graphene composite material. Disperse 5g of iron oxide-graphene composite material in 1000mL of water and acetone mixed solution (ratio: 6:1), 5g of silicon material and PEG dispersed in the same 1000mL of water and acetone mixed solution, respectively, ultrasonic treatment for 60 minutes...
Embodiment 3
[0025] Using ferric chloride and nickel chloride as co-intercalation agents and carbon fiber as precursor, ferric chloride-nickel chloride-carbon fiber interlayer compound was prepared by molten salt intercalation method. Add 5g of ferric chloride-nickel chloride-carbon fiber interlayer compound to 1000mL N-methylpyrrolidone, use a high-pressure homogenizer to perform 10 cycles of stripping, then perform centrifugation at a speed of 4000r / min, and pour off the supernatant , and freeze-dry the precipitate to obtain the ferric chloride-nickel chloride-graphene interlayer compound. The ferric chloride-nickel chloride-graphene interlayer compound was placed in a muffle furnace for heat treatment, and kept at 600° C. for 1 hour to obtain an iron oxide-nickel oxide-graphene composite material. Disperse 10g of iron oxide-nickel oxide-graphene composite material in 1000mL water and isopropanol mixed solution (ratio: 4:1), 10g silicon material and PVP are dispersed in the same 1000mL w...
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