Preparation method and application of silicon-based composite negative electrode material for lithium ion battery
A technology for lithium ion batteries and negative electrode materials, which is applied in the fields of electrochemical materials and new energy, can solve problems such as poor electrical conductivity, and achieve the effects of suppressing volume expansion, improving electronic conductivity, and improving Coulomb efficiency.
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Embodiment 1
[0024] Disperse 1 mol of nano-silicon with a particle size of 80 nm and 0.2 mol of polyaniline in absolute ethanol, set the ultrasonic power to 120 W, and the ultrasonic dispersion time to 30 min. The homogeneous mixed solution obtained after dispersion was dried into powder by using a spray dryer. The inlet air temperature of the spray dryer was 200° C., the outlet air temperature was 120° C., and the constant flow pump speed was 80 rpm. The spray-dried powder was transferred to the reaction chamber, and nitrogen gas with a flow rate of 150 sccm was introduced, and the temperature was raised to 500° C. at a rate of 5° C. / min, and maintained for 120 minutes. Then turn off the heating switch of the reaction chamber, cool down to room temperature naturally, and collect the silicon / amorphous carbon composite material. Then 0.05mol of heteropolyacid [PSi 12 o 40 ] n- Disperse together with silicon / amorphous carbon in absolute ethanol, the power of the ultrasonic wave used is 12...
Embodiment 2
[0026] Disperse 1 mol of nano-silicon with a particle size of 80 nm and 0.2 mol of polypyrrole in absolute ethanol, set the ultrasonic power to 120 W, and the dispersion time to 15 minutes. The homogeneous mixed solution obtained after dispersion was dried into powder by using a spray dryer. The inlet air temperature of the spray dryer was 200° C., the outlet air temperature was 120° C., and the constant flow pump speed was 80 rpm. The spray-dried powder was transferred to the reaction chamber, and nitrogen gas with a flow rate of 150 sccm was introduced, and the temperature was raised to 500° C. at a rate of 5° C. / min, and maintained for 120 minutes. Then turn off the heating switch of the reaction chamber, cool down to room temperature naturally, and collect the silicon / amorphous carbon composite material. Then 0.05mol of heteropolyacid [MoSi 12 o 40 ] n- Disperse together with silicon / amorphous carbon in absolute ethanol, the power of the ultrasonic wave used is 120W, an...
Embodiment 3
[0028] Disperse 1 mol of nano-silicon with a particle size of 80nm and 0.2 mol of polypyrrole in methanol, set the ultrasonic power to 100W, and the dispersion time to 25min. The homogeneous mixed solution obtained after dispersion was dried into powder by using a spray dryer. The inlet air temperature of the spray dryer was 200° C., the outlet air temperature was 120° C., and the constant flow pump speed was 80 rpm. The spray-dried powder was transferred to the reaction chamber, and nitrogen gas with a flow rate of 150 sccm was introduced, and the temperature was raised to 500° C. at a rate of 5° C. / min, and maintained for 120 minutes. Then turn off the heating switch of the reaction chamber, cool down to room temperature naturally, and collect the silicon / amorphous carbon composite material. Then 0.08mol of heteropolyacid [MoSi 12 o 40 ] n- Disperse together with silicon / amorphous carbon in propanol, the ultrasonic power used is 120W, and the dispersion time is 30min. By...
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