Preparation method of high-specific energy porous silicon-carbon composite negative electrode material
A technology of carbon composite materials and negative electrode materials, applied in the field of preparation of high specific energy porous silicon carbon composite negative electrode materials, can solve the problems of material structure damage, high cost, low power density, etc.
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Embodiment 1
[0021] Disperse 0.1 gram of silicon powder in 0.1 liter of 0.05 mol / liter sodium carbonate aqueous solution, and slowly add the obtained suspension into 0.1 liter of 0.05 mol / liter calcium chloride aqueous solution under rapid stirring. Stirring was continued for 0.5 hours. The solid obtained in the above steps was washed with distilled water and ethanol successively, and dispersed into the asphalt ethanol solution (the mass ratio of silicon powder and asphalt was 1:1), and the stirring was continued for 1 hour. The solid obtained in the above steps was dried, pre-reacted in air at 280°C for 2 hours, and then reacted at 800°C for 2 hours under an inert atmosphere. Washed with dilute hydrochloric acid and water in turn, and dried to obtain a porous silicon-carbon composite negative electrode material, the product morphology is as follows: figure 1 shown.
Embodiment 2
[0023] Ultrasonically disperse 0.05 g of silicon powder in 0.1 liter of 0.1 mol / L sodium carbonate aqueous solution, and slowly add the obtained suspension into 0.1 liter of 0.1 mol / L calcium chloride aqueous solution under rapid stirring. Stirring was continued for 0.5 hours. The solid obtained in the above steps was washed with distilled water and ethanol successively, and dispersed into the asphalt ethanol solution (the mass ratio of silicon powder and asphalt was 1:2), and the stirring was continued for 0.5 hours. The solid obtained in the above steps was dried and reacted at 700° C. for 2 hours under an inert atmosphere. Washed with dilute hydrochloric acid and water in turn, and dried to obtain a porous silicon-carbon composite negative electrode material, the product morphology is as follows: figure 2 shown.
Embodiment 3
[0025] Ultrasonically disperse 0.1 g of silicon powder in 0.1 liter of 0.1 mol / L sodium carbonate aqueous solution, and slowly add the obtained suspension into 0.1 liter of 0.1 mol / L calcium chloride aqueous solution under rapid stirring. Stirring was continued for 1 hour and filtered. The solid obtained in the above steps was washed with distilled water and ethanol successively, and dispersed into a tetrahydrofuran solution of asphalt (the mass ratio of silicon powder and asphalt was 1:1), and the stirring was continued for 1 hour. The solid obtained in the above steps was dried and reacted at 800° C. for 2 hours under an inert atmosphere. Washed with dilute hydrochloric acid and water in turn, and dried to obtain a porous silicon-carbon composite negative electrode material, the product morphology is as follows: image 3 Shown, the X-ray powder diffraction pattern is shown in 4.
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