High-capacity silicon carbon negative electrode material, and preparation method and applications thereof
A negative electrode material and high-capacity technology, applied in the field of high-capacity silicon-carbon negative electrode materials and their preparation, can solve the problems of consuming water resources and time, difficulty in realizing industrial production, high cost, etc., to reduce absolute volume expansion and relieve volume Swelling problem, effect of easy mass production
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[0039] A method for preparing a high-capacity silicon-carbon material of the present invention comprises the following steps:
[0040] S1. Ball milling: disperse the nano-silicon and carbon materials in the required metering ratio in a solvent for wet ball milling, the ball milling speed is 300-2000rpm, the ball milling time is 0.2-8.0h, preferably, the ball milling time is 0.5-2.5h;
[0041]The carbon material is any one of graphite, nanofiber, graphene, porous carbon or a combination thereof; the solvent is any one of deionized water, ethanol, N-methylpyrrolidone, acetone, ethylene glycol or a combination thereof.
[0042] S2. Ultrasonic: Dilute the ball-milled slurry to a solid content of 10-40% and perform ultrasonic treatment at 5°C. The ultrasonic power is 500-2000W, and the ultrasonic time is 0.5-2.0h;
[0043] S3. Slurry preparation: add carbon source and surfactant to the ultrasonicated slurry, stir vigorously for 0.5-5h, and rotate at 800-2000rpm;
[0044] Carbon so...
Embodiment 1
[0050] Synthesis of high-capacity silicon-carbon anode materials
[0051] (1) Ball milling: disperse silicon with a medium particle size of 230nm and graphite of 8um in ethanol at a mass ratio of 3.25:1 for ball milling, the ball-to-material ratio is 8:1, the rotating speed is 1000rpm, and the ball milling time is 2h;
[0052] (2) Ultrasonic: Adjust the solid content of the slurry after ball milling to 20%, and ultrasonicate for 30 minutes at 5°C, and the ultrasonic power is 1300W;
[0053] (3) Add surfactant and carbon source: add 0.03mol / L ethanol of PVP8000 and PEG20000 to the slurry and stir vigorously for 2.0h at a speed of 800rpm;
[0054] (4) Spray drying: the inlet and outlet temperatures are 150 and 60°C respectively, and the liquid inlet speed is 8mL / min;
[0055] (5) Heat treatment: N 2 Atmosphere, 480°C 2h+850°C 3h.
[0056] Characterization of physicochemical properties of silicon-carbon composites:
[0057] The microscopic morphology of the silicon carbon mat...
Embodiment 2
[0062] (1) Ball milling: disperse silicon with a particle size of 80nm, graphite A of 20um, and graphite B of 8um in ethanol at a mass ratio of 45:25:5 for ball milling, the ball-to-material ratio is 8:1, the ball milling speed is 400rpm, time 2h;
[0063] (2) Ultrasonic: Adjust the solid content of the slurry after ball milling to 15%, and ultrasonically perform 30 minutes at 5°C with an ultrasonic power of 1000W;
[0064] (3) Spray drying: the inlet and outlet temperatures were 150°C and 60°C respectively, and the feed rate was 5mL / min to prepare precursor C;
[0065] (4) Add carbon source: add coal tar pitch to the slurry, adjust the solid content to 10%, stir vigorously for 1.0h, and the rotating speed is 1500rpm;
[0066] (5) Spray drying: the inlet and outlet temperatures are 150 and 60°C respectively, and the liquid inlet speed is 7.5mL / min;
[0067] (6) Heat treatment: N2 atmosphere, 2h at 200°C + 3h at 850°C.
[0068] The test results of thermogravimetric method sh...
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