Preparation method of silicon/graphene/carbon composite negative electrode material
A technology of negative electrode material and composite material, which is applied in the field of preparation of silicon/graphene/carbon composite negative electrode material, can solve the problem of the rapid volume expansion of silicon material negative electrode lithium ion battery, and the inability to protect nano-silicon particle powder and composite material well. The ability of electrical conductivity is limited, etc., to achieve the effect of increasing the charging and discharging efficiency, improving the charging and discharging efficiency, and increasing the conductivity
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Embodiment 1
[0031] (1) Disperse 80 mg of silicon nanoparticles (40 nm~60 nm) uniformly in 100 ml of absolute ethanol under ultrasonic treatment to form a silicon nanoparticle dispersion with a concentration of 0.8 mg / mL;
[0032] (2) Add 0.8 mL of aminopropyltrimethoxysilane (APS) to the silicon nanoparticle dispersion obtained in step (1) by magnetic stirring for surface modification of silicon;
[0033] (3) The dispersion obtained in step (2) was centrifuged and dried to obtain APS-modified silicon nanoparticles, and the APS-modified silicon nanoparticles were dispersed in absolute ethanol to form a dispersion with a concentration of 0.8 mg / mL. Graphene solution (1.26mg / mL) was added dropwise under magnetic stirring, so that the mass ratio of silicon nanoparticles to graphene was 10:1, and silicon nanoparticles / graphene composite materials were obtained after centrifugal washing and freeze drying;
[0034] (4) Mix the silicon nanoparticle / graphene composite material with polyvinylidene ...
Embodiment 2
[0041] (1) Disperse 80 mg of silicon nanoparticles (40 nm~55 nm) uniformly in 100 ml of absolute ethanol under ultrasonic treatment to form a silicon nanoparticle dispersion with a concentration of 0.8 mg / mL;
[0042] (2) Add 0.8 mL of aminopropyltrimethoxysilane (APS) to the silicon nanoparticle dispersion by magnetic stirring for surface modification of silicon;
[0043] (3) The dispersion obtained in step (2) was centrifuged and dried to obtain APS-modified silicon nanoparticles, and the APS-modified silicon nanoparticles were dispersed in absolute ethanol to form a dispersion with a concentration of 0.8 mg / mL. Graphene solution (1.26mg / mL) was added dropwise under magnetic stirring, so that the mass ratio of silicon nanoparticles to graphene was 10:1, and silicon nanoparticles / graphene composite materials were obtained after centrifugal washing and freeze drying;
[0044] (4) Mix the silicon nanoparticle / graphene composite material with polyvinylidene fluoride (PVDF) at a ...
Embodiment 3
[0049] (1) Disperse 80 mg of silicon nanoparticles (45 nm~60 nm) uniformly in 100 ml of absolute ethanol under ultrasonic treatment to form a silicon nanoparticle dispersion with a concentration of 0.8 mg / mL;
[0050] (2) Add 0.8 mL of aminopropyltrimethoxysilane (APS) to the silicon nanoparticle dispersion by magnetic stirring for surface modification of silicon;
[0051] (3) The dispersion obtained in step (2) was centrifuged and dried to obtain APS-modified silicon nanoparticles, and the APS-modified silicon nanoparticles were dispersed in absolute ethanol to form a dispersion with a concentration of 0.8 mg / mL. Graphene solution (1.26 mg / mL) was added dropwise under magnetic stirring, so that the mass ratio of silicon nanoparticles to graphene was 10:1, and silicon nanoparticles / graphene composites were obtained after centrifugal washing and freeze-drying;
[0052] (4) The silicon nanoparticle / graphene composite material and polyvinylidene fluoride (PVDF) were mixed uniform...
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Abstract
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