Composite negative electrode material for lithium ion battery, and preparation method thereof
A lithium-ion battery and negative electrode material technology, applied in the field of lithium-ion batteries, can solve the problems of high rate continuous charge and discharge capacity and low temperature performance, low specific capacity of graphite negative electrode, etc., to achieve excellent cycle performance, improve rate, increase The effect of structural stability
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[0043] In the present application, the present invention also provides a method of preparing a composite negative electrode material for a lithium ion battery, the composite anode material comprising a composite negative electrode material for a lithium ion battery as described above, wherein the method comprnt step :
[0044] Prepare carbonaceous material precursors, silicon particles and carbon source materials;
[0045] The carbonaceous material precursor was sintered in the inert gas environment for 2 h-5 h at 300 ° C to 500 ° C, and the first burning material was obtained;
[0046] The first burning rear material is soaked using dilute hydrochloric acid, and then the first burning material is cleaned until the pH of the soaking solution is 6-8, and the first purge is obtained;
[0047] The first purified material was sintered and the second burning material was obtained in an inert gas environment.
[0048] The second burning material is pulverized and the carbonaceous materi...
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[0056] Example 1
[0057] In the present application embodiment, the method of preparing a composite negative material for a lithium ion battery according to the present application includes the following steps:
[0058] (1) Take 1 kg of coconut shell crude material (carbonaceous material precursor) in the box, into nitrogen, until the oxygen content in the box furnace is less than 100 ppm, then warmed up to 300 at 3 ° / min At ° C, calcined for 5 h, 0.34 kg of burning rear material. The burn was placed in dilute hydrochloric acid, repeatedly washed, remove impurities, and then rinsed with pure water until the pH of the solution was 6 to 8, dried. The dried material was placed in a box furnace, and nitrogen was introduced until the oxygen content in the box furnace was less than 100 ppm, and then heated at 3 ° / min to 1300 ° C, sintered 2 h. The burning rear material was pulverized, and the particle size D50 after pulverization was 3 ± 1 μm to obtain a carbonaceous material.
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Example Embodiment
[0062] Example 2
[0063] The difference from the first embodiment is that the precursor of the carbonaceous material in the step (1) is a phenol resin, a low temperature sintering temperature of 350 ° C, sintered 4h; high temperature sintering temperature is 1200 ° C, sintering 3H; burn material pulverized particle size D50 is 5 ± 1 μM to obtain a carbonaceous material.
[0064] The step (2) is used in the liquid phase composite, and the carbonaceous material and the silicon oxide are added to the ethanol solution to the ethanol solution, and the mix is mixed, and then dried to obtain a composite powder.
[0065] The carbon source gas used in step (3) is acetylene, the treatment temperature is 800 ° C, and the content of deposition carbon is 10 wt.% To obtain a composite negative electrode material.
[0066] Among the composite negative electrode materials, the proportion of carbonaceous materials is 72.0 wt.%, And the proportion of silicon particles is 18 wt.% And coated carbo...
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