si/siox/c composite negative electrode material, its preparation method and lithium ion battery
A negative electrode material and conductive carbon technology, applied in battery electrodes, secondary batteries, circuits, etc., can solve the problems of complex preparation process, easy damage to particle structure, and degradation of cycle performance, so as to reduce volume expansion effect and improve cycle stability The effect of maintaining stability and cycle stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0059] The present invention also provides a preparation method of Si / SiOx / C composite negative electrode material, comprising the following steps:
[0060] A) silicon alloy is acid-etched, and after drying, a porous silicon precursor is obtained;
[0061] B) Mix the porous silicon precursor, SiOx powder, carbon-containing compound, conductive carbon material, dispersant and solvent, spray dry, and sinter to obtain Si / SiOx / C composite negative electrode material.
[0062] In the invention, the silicon alloy is acid-etched and dried to obtain a porous silicon precursor.
[0063] In the present invention, the alloying elements in the silicon alloy preferably include one or more of Al, Sn, Cu, Fe, Mn, Mg and Ga; more preferably one of Al, Sn, Cu and Mg or several. In some embodiments of the present invention, the silicon alloy is silicon-magnesium alloy, silicon-aluminum alloy, silicon-iron alloy or silicon-aluminum-copper alloy. The particle size of the silicon alloy is prefe...
Embodiment 1
[0100] At 50°C, silicon-magnesium alloy powder with a particle size of 15 μm was first corroded with hydrochloric acid with a mass concentration of 20% for 16 hours, and then corroded with hydrofluoric acid with a mass concentration of 10% for 8 hours, and the product obtained by acid corrosion was deionized Centrifuge and wash with water until the pH of the product is neutral, then place in a vacuum oven and dry at 100° C. for 8 hours to obtain a porous silicon precursor.
[0101] SiO 1.5 Particles are first pulverized with a crusher for 0.5h, the speed of the crusher is 1600r / min, and then crushed for 1h under the air pressure of 0.8MPa with the jet mill, and the speed of the classifier is 1800r / min when the jet pulverizer is pulverized , to obtain SiO with a particle size of 300nm to 3μm 1.5 Powder.
[0102] With 100g described porous silicon precursor, 800g SiO 1.5 Powder, 20g of glucose, 1g of graphene with a particle size of 5 μm, 1g of polyvinyl alcohol and 5000mL of...
Embodiment 2
[0114] At 50°C, the silicon-aluminum alloy powder with a particle size of 10 μm was corroded with sulfuric acid with a mass concentration of 30% for 14 hours, and then with hydrofluoric acid with a mass concentration of 10% for 10 hours, and the product obtained by acid corrosion was deionized Centrifuge and wash with water until the pH of the product is neutral, then place in a vacuum oven and dry at 100° C. for 8 hours to obtain a porous silicon precursor.
[0115] The SiO particles are first pulverized with a crusher for 0.5h, the speed of the crusher is 1800r / min, and then the jet pulverizer is used for pulverization at an air pressure of 0.8MPa for 0.5h, and the speed of the classifier during the pulverization of the jet pulverizer is 1800r / min, to obtain SiO powder with a particle size of 300nm-2μm.
[0116] 200g of the porous silicon precursor, 800g of SiO powder, 30g of sucrose, 1g of graphene with a particle size of 5 μm, 1g of conductive carbon black with a particle ...
PUM
| Property | Measurement | Unit |
|---|---|---|
| specific surface area | aaaaa | aaaaa |
| pore size | aaaaa | aaaaa |
| particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


