Graphite composite negative electrode material for lithium ion battery, preparation method and lithium ion battery
A lithium-ion battery and negative electrode material technology, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of difficulty in controlling the uniformity and thickness of the coating layer, affecting the conductivity of raw materials, and reducing the wettability of electrolyte, etc., to achieve Improve liquid retention performance, increase specific surface area, and improve electrical conductivity
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Embodiment 1
[0050] Fully dissolve ferric nitrate in water to make a solution with an iron ion concentration of 0.001mol / L, then add flake graphite with a purity of 99.90% and stir well, soak for 24 hours, filter out the solution, and then dry at 99°C to obtain graphite Composite material precursor: Put the above-mentioned graphite composite material precursor into a rotary furnace, in a helium atmosphere with a flow rate of 0.1L / min and at 400°C, pass acetylene at a flow rate of 10L / min for chemical vapor deposition, and the reaction lasts for 0.1 h, to generate carbon nanotubes and / or carbon nanofibers; the product obtained by the above chemical vapor deposition was calcined in vacuum at 2000° C. for 10 h; ℃ for 5 h at a constant temperature, and then naturally cooled to room temperature to obtain a graphite composite negative electrode material.
Embodiment 2
[0052] Fully dissolve nickel chloride in water to form a solution with a nickel ion concentration of 0.01mol / L, then add microcrystalline graphite with a purity of 95.00% and stir thoroughly, soak for 15 hours, filter out the solution, and then dry at 90°C. Obtain the precursor of graphite composite material; put the above precursor of graphite composite material into the tube furnace, in the neon gas atmosphere with the flow rate of 0.5L / min and at 600°C, feed methane with the flow rate of 5L / min for chemical vapor deposition, The reaction lasts for 1 hour to generate carbon nanotubes and / or carbon nanofibers; the product obtained by the above chemical vapor deposition is soaked in a mixed strong acid of nitric acid, hydrochloric acid and sulfuric acid for 0.5 hours, then washed with water, dehydrated, and dried; the above acid The purified product was placed in a tubular sintering furnace, calcined at a constant temperature of 400° C. for 1 h in an air atmosphere, and then na...
Embodiment 3
[0054] Fully dissolve cobalt sulfate in water to form a solution with a cobalt ion concentration of 0.1mol / L, then add a needle coke graphitization product with a purity of 99.00% and stir thoroughly, soak for 10 hours, filter out the solution, and then bake at 80°C dry to obtain the precursor of graphite composite material; put the above precursor of graphite composite material into a box furnace, in an argon atmosphere with a flow rate of 1L / min and at 800°C, feed ethylene at a flow rate of 1L / min for chemical vapor deposition , the reaction continued for 2h to generate carbon nanotubes and / or carbon nanofibers; the product obtained by the above chemical vapor deposition was calcined for 5h under nitrogen and 2500°C; the product obtained by the above calcining was placed in a high-temperature microwave ashing furnace, Oxygen atmosphere and constant temperature calcination at 500° C. for 0.5 h, and then naturally cooled to room temperature to obtain a graphite composite negati...
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