Carbonaceous lithium ion battery negative electrode material with nuclear shell structure and producing method thereof
A technology for lithium-ion batteries and negative electrode materials, applied in electrode manufacturing, battery electrodes, structural parts, etc., can solve the problems of poor cycle performance, high initial irreversible amount, and reduce the first irreversible amount, and achieve long cycle life and low initial irreversible Capacity, the effect of high capacity
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Embodiment 1
[0032] a) Ordinary H prepared by chemical method 2 SO 4 -H 2 o 2 The system expandable graphite is pulverized to a particle size of 5-50 μm.
[0033] b) Heating the obtained graphite intercalation compound at 250° C. for 48 hours to slowly deintercalate.
[0034] c) Prepare a phenolic resin ethanol solution with a mass fraction of 3 wt%, immerse the deintercalated graphite in the solution, stir for 6 hours, let stand for 4 hours, filter, and dry the filtered graphite powder at 300°C.
[0035] d) heating the graphite powder obtained in the previous step to 1000° C. at a rate of 300° C. / h under nitrogen protection, keeping the temperature for 4 hours, and cooling with the furnace to obtain graphite powder coated with amorphous carbon on the surface.
[0036] The first cycle efficiency of the graphite powder coated with amorphous carbon on the surface obtained by this method is greater than 90%, and the test results of 38 cycles of discharge capacity change are as follows:
Embodiment 2
[0038] a) FeCl prepared by electrochemical method 3 The intercalated expandable graphite is pulverized to a particle size of 5-50 μm.
[0039] b) Heating the obtained graphite intercalation compound at 350° C. for 72 h to slowly deintercalate.
[0040] c) Prepare a 20 wt% sucrose aqueous solution, immerse the deintercalated graphite into the solution, stir for 0.5 hours, let stand for 6 hours, filter, and dry the filtered graphite powder at 100°C.
[0041] d) Under the protection of nitrogen, the graphite powder obtained in the previous step is heated to 700°C at a rate of 500°C / h, kept at a temperature of 0.5 hours, and cooled with the furnace to obtain graphite powder coated with amorphous carbon on the surface.
Embodiment 3
[0043] a) flake graphite powder with a particle size of 5-50 μm is prepared by chemical method 2 SO 4 Intercalated graphite intercalation compound.
[0044] b) Heat the obtained graphite intercalation compound at 205° C. for 12 hours, and slowly deintercalate it.
[0045] c) Prepare a 5% mass fraction phenolic resin ethanol solution, immerse the deintercalated graphite in the solution, stir for 2 hours, let stand for 6 hours, filter, and dry the filtered graphite powder at 200°C.
[0046] d) heating the graphite powder obtained in the previous step to 1000° C. at a rate of 250° C. / h under nitrogen protection, keeping the temperature for 3 hours, and cooling with the furnace to obtain graphite powder coated with amorphous carbon on the surface.
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