Preparation method, product and application of silicon negative electrode material
A technology of silicon negative electrode and negative electrode sheet, which is applied to battery electrodes, electrical components, circuits, etc., can solve the problems of corrosion of negative electrode materials, broken active materials, poor cycle stability, etc., to improve the reaction speed, suppress expansion problems, and expand problems. inhibiting effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0022] The first aspect of the present invention aims to provide a method for preparing a silicon negative electrode material, comprising the following steps:
[0023] S1. Clean the impurities on the surface of nano-silicon, then mix and stir with ammonia water, and get SiO on the surface after centrifugal washing. 2 The Si material of the layer is denoted as Si@SiO 2 ;
[0024] S2, the Si@SiO obtained in step S1 2 Place it in the amino group-containing silane coupling agent solution, react and reflux at 100-120°C for 0.8-2 hours under the protection of a protective atmosphere, suction filter and clean the obtained product, and then remove the unreacted amino group-containing silane coupling agent, dried to obtain amino-modified Si@SiO 2 , recorded as Si@SiO 2 -NH 2 ;
[0025] S3, the Si@SiO obtained in step S2 2 -NH 2 Mix and disperse with hydrochloric acid in the reaction bottle, add aniline monomer, place the reaction bottle in the cooling liquid at -4~0°C, and add ...
Embodiment 1
[0051] A method for preparing a silicon negative electrode material, comprising the steps of:
[0052] S1. Accurately weigh 5.00g of Si with D50=100nm, add nano-silicon into 0.1M hydrochloric acid solution according to the solid-to-liquid ratio of 5:100, put it in a water bath at 30°C and stir it at a speed of 150rpm / min for 12h. After the reaction is completed, transfer the product to a centrifuge tube and put it in a centrifuge for centrifugation at a centrifugal speed of 8000rpm / min. The washing liquid is deionized water until the pH value of the supernatant is neutral, and then transfer it to a vacuum drying oven at 60°C. Drying in medium for 12h to obtain Si particles after cleaning;
[0053] S2. Accurately weigh 2.8g of Si particles obtained in step S1 and 50mL of ethanol solution for 15 minutes of ultrasonic dispersion to obtain solution A; prepare 50mL of concentrated ammonia water-ethanol solution consisting of 2mL of concentrated ammonia water (14.5M), 8mL of deioniz...
Embodiment 2
[0057] The difference from Embodiment 1 is step S4.
[0058] S4, the Si@SiO obtained in step S3 2 -NH 2 Put it into a three-necked bottle, add 50mL of 1M hydrochloric acid to ultrasonically disperse for 30 minutes, then stir and disperse for 30 minutes; then weigh 0.3g of aniline monomer into the three-necked bottle, place the three-necked bottle in a cooling liquid at 25°C and stir at a speed of 150rpm / min; then weigh 0.3g of ammonium persulfate (APS) and dissolve it in 10mL of 1M hydrochloric acid, and use a constant flow pump to add the prepared ammonium persulfate solution dropwise into the three-neck flask, and control the addition within 15min , reacted for 5h; then the solution was washed and filtered with 1M hydrochloric acid, acetone, and distilled water, and dried in a vacuum oven at 60°C for 12h to obtain a silicon negative electrode material, denoted as Si@SiO 2 @PANI.
[0059] The rest are the same as in Embodiment 1, and will not be repeated here.
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
electrical conductivity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap