High-compaction silicon-carbon composite negative electrode material as well as preparation and application thereof
A technology of silicon-carbon composite materials and silicon-carbon composites, which is applied in the preparation/purification of carbon, silicon compounds, silicon oxide, etc., can solve the problems of difficult control of oxygen content, low compaction density of silicon-carbon composite materials, and weak interface bonding, etc. problems, to achieve the effect of improving the tap density, improving the electrochemical performance, and improving the interface binding effect
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Embodiment 1
[0095] Using SiO coarse powder with an average particle size of 0.5 mm as raw material, after crushing and crushing, SiO fine powder with an average particle size of 1 μm is obtained; chemical vapor deposition method is used, acetylene is used as raw material gas, argon is used as carrier gas, and the deposition temperature is at 650°C, holding time 1h, gas flow rate of acetylene 120ml / min, argon 40ml / min, coating a thin carbon layer on the surface of SiO fine powder to obtain silicon monoxide particles (SiO@C) wrapped in a thin layer of carbon; SiO @C particles, metallic Mg, non-metallic B powder, mixed salt (LiCl:NaCl molar ratio 7:3, eutectic point 570°C) were mixed and granulated by extrusion granulation according to the mass ratio of 1:0.2:0.05:1 pellets to obtain a composite precursor; put the composite precursor into a sintering boat and place it in a muffle furnace for sintering reaction under an argon atmosphere, and heat up to 700°C at a speed of 5°C / min, react for 6 ...
Embodiment 2
[0100] Mix the low-oxygen porous silicon prepared in Example 1, artificial graphite powder with a particle size of 6 μm, pitch with a particle size of 3 μm, and toluene in a mass ratio of 1:0.5:0.08:4 and mix them uniformly in a high-speed disperser, then Spray granulation was performed to obtain a silicon-carbon precursor; the silicon-carbon precursor was placed in a cauldron and subjected to carbonization heat treatment at 950° C. for 2 hours under an argon atmosphere. After cooling, disperse with a jet mill to obtain a silicon-carbon intermediate with an average particle size of 13 μm; carry out particle size grading with artificial graphite with a particle size of 20 μm in a mass ratio of 1:1 to obtain the high-compact silicon-carbon composite negative electrode material .
[0101] The silicon carbon negative plate was assembled into a CR2032 lithium-ion button battery, and the electrochemical performance was tested in the voltage range of 0.01-2V at room temperature, and ...
Embodiment 3
[0103] Mix the low-oxygen porous silicon prepared in Example 1, artificial graphite powder with a particle size of 2 μm, phenolic resin with a particle size of 1 μm, and acetone at a mass ratio of 1:2:0.2:8 and mix them uniformly in a high-speed disperser. Then spray granulation was carried out to obtain the silicon-carbon precursor; the silicon-carbon precursor was placed in a cauldron and subjected to carbonization heat treatment at 800° C. for 4 hours under an argon atmosphere. After cooling, disperse with a jet mill to obtain a silicon-carbon intermediate with an average particle size of 8 μm; carry out particle size grading with artificial graphite with a particle size of 15 μm in a mass ratio of 1:1 to obtain the high-pressure compacted silicon-carbon composite negative electrode material .
[0104] The silicon carbon negative plate was assembled into a CR2032 lithium-ion button battery, and the electrochemical performance was tested in the voltage range of 0.01-2V at ro...
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