A silicon carbon composite negative electrode material and negative electrode sheet, its preparation method and lithium ion battery
A silicon-carbon composite material and negative electrode material technology, which is applied in the direction of battery, negative electrode, electrode manufacturing, etc., can solve the problems of volume expansion, electrochemical performance and cycle life to be improved, and poor cycle performance of lithium-ion batteries
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[0034] The present invention also provides a method for preparing a negative electrode sheet. The method includes uniformly mixing a negative electrode material with a conductive agent, a binder and a solvent to obtain electrode slurry, coating the electrode slurry on the surface of the current collector, and drying it. Dry, wherein, the negative electrode material is the above-mentioned silicon carbon composite negative electrode material.
[0035] The main improvement of the preparation method of the negative electrode sheet provided by the present invention is that a new negative electrode material is adopted, and the specific types of the conductive agent, the binder and the solvent, as well as the amount of them and the negative electrode material, etc. can be compared with the existing ones. The technology is the same. For example, specific examples of the conductive agent include, but are not limited to, at least one of super carbon black, graphene, carbon fiber, and gr...
Embodiment 1
[0042] S1. Mix 100mL of ethanol and 20mL of water and heat to 60°C, add 2.5mL of ammonia water (concentration is 5wt%, the same below) and 0.5mL of ethylenediamine and mix well, then add 1g of 3-aminophenol, 2mL of formaldehyde and 4mL of silicic acid Ethyl ester was vigorously stirred at 30 rpm for 6 hours to form a precipitated product. The precipitated product was centrifuged, and the obtained solid product was dried at 60 °C for 3 h to obtain a silica / phenolic composite with a fractal structure.
[0043] S2. Take 2g of the above-mentioned silica / phenolic compound and 2g of magnesium powder, grind and mix them evenly and put them into a tube furnace. The tube furnace is protected by argon gas containing 1% hydrogen, and the tube furnace is heated to 350° C. The heat preservation reaction was performed for 10 hours, and the composite material powder of silicon and amorphous carbon with fractal structure was obtained by the reaction. The composite powder is taken out, treated...
Embodiment 2
[0046] S1. Mix 90 mL of ethanol and 10 mL of water and heat to 80°C, add 2 mL of ammonia water and 0.3 mL of ethylenediamine and mix well, then add 1.5 g of 3-aminophenol, 3.2 mL of formaldehyde and 6 mL of ethyl silicate, and stir vigorously at 150 rpm After 4 hours, a precipitated product was formed by the reaction, and the precipitated product was centrifuged, and the obtained solid product was dried at 90° C. for 1 h to obtain a silica / phenolic complex with a fractal structure.
[0047] S2: Take 2g of the above-mentioned silica / phenolic compound and put it into a tube furnace, pass argon gas containing 1% hydrogen into the tube furnace for protection, and heat the tube furnace to 1000° C. for calcination for 0.5h. The calcined product was cooled to room temperature, crushed, ground and mixed with 3 g of aluminum powder, and then put into the tube furnace again. hours, the reaction obtains a composite powder of silicon and amorphous carbon with a fractal structure. The com...
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