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

Pending Publication Date: 2022-04-08
HUIZHOU LIWINON NEW ENERGY TECH CO LTD
View PDF5 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] However, silicon still has the following problems as a negative electrode material: 1) It will produce huge volume expansion during the alloying process with lithium, which will lead to the fragmentation of active materials, the shedding of active materials and current collectors, and then the continuous rupture and regeneration of the SEI film. Shows extremely poor cycle stability; 2) Silicon is used as a semiconductor with an intrinsic conductivity of 2.52×10 -4 S / m, showing poor rate performance; 3) Silicon anode materials are also easily corroded by HF decomposed by the electrolyte
For the field of silicon-carbon composites, the selection of carbon sources and the combination of silicon and carbon are the research directions of most researchers, but the current silicon-carbon composite methods still have shortcomings such as slow reaction speed and poor uniformity.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

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.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
particle diameteraaaaaaaaaa
electrical conductivityaaaaaaaaaa
Login to view more

Abstract

The invention provides a preparation method of a silicon negative electrode material, which comprises the following steps of: preparing a silicon dioxide layer containing more hydroxyl groups on the surface of a silicon material, and recording the silicon dioxide layer as Si-coated SiO2; the preparation method comprises the following steps: by taking Si-coated SiO2 as a raw material, enabling the Si-coated SiO2 to be subjected to a coupling reaction with a silane coupling agent through hydroxyl, enabling a tail amino group on the silane coupling agent to face outwards so as to obtain amino-modified Si-coated SiO2, taking aniline as a carbon source, enabling the amino group to have an electrostatic force effect on the aniline, and generating nucleation sites for oriented growth of the aniline, so that the surface of the Si-coated SiO2 is uniformly coated with polyaniline, and the surface of the Si-coated SiO2 is uniformly coated with the polyaniline. The polyaniline serving as a conductive polymer has high conductivity, and the conjugated structure of the polyaniline also has relatively high rigidity, so that the polyaniline has a very good inhibition effect on the expansion problem of the silicon material. Therefore, according to the obtained silicon negative electrode material, the reaction speed of silicon-carbon compounding is increased, the requirement for silicon particles is low, a high-quality, high-conductivity and uniformly-coated polyaniline layer can be formed, and the expansion problem of the silicon material can be effectively inhibited.

Description

technical field [0001] The invention relates to the field of secondary batteries, in particular to a preparation method, product and application of a silicon negative electrode material. Background technique [0002] The development of digital 3C, new energy vehicles and energy storage equipment puts forward higher requirements on the energy density, cycle life and safety performance of lithium-ion batteries. At present, the energy and power density of commercialized graphite anodes (specific capacity = 372mAh / g) are approaching the limit, and the development of high-capacity anode material systems is an important prerequisite for the development of high-capacity lithium-ion batteries. Silicon has the highest theoretical specific capacity (4200mAh / g) among the current negative electrode materials with lithium intercalation activity, and has a higher lithium-to-lithium potential than graphite, which can effectively avoid the safety hazard caused by high-magnification lithium ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/38H01M4/48H01M4/62
CPCY02E60/10
Inventor 杨承成吴秋丽张凯马斌陈杰杨山
Owner HUIZHOU LIWINON NEW ENERGY TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products