Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of silicon carbon negative electrode precursor

A technology of precursor and negative electrode, applied in the field of preparation of silicon carbon negative electrode precursor, can solve the problems of poor controllability of composite structure and particle size, poor material capacity, and difficulty in commercial use, so as to ensure the activity of nano-silicon and improve the first effect. and cycle performance, the effect of improving stability

Active Publication Date: 2019-10-18
CHANGSHA RES INST OF MINING & METALLURGY
View PDF9 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This material has good electrical conductivity, but the composite structure and particle size controllability of the material are poor, which eventually leads to poor performance of the material capacity, only 450mAh / g, and the first effect is as low as 85%. This method is difficult to be commercialized in the future.

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

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of silicon carbon negative electrode precursor
  • Preparation method of silicon carbon negative electrode precursor
  • Preparation method of silicon carbon negative electrode precursor

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] A method for preparing a silicon-carbon negative electrode precursor of the present invention, comprising the following steps:

[0041] (1) Add nano-silica powder with a particle diameter of D50=120nm and artificial graphite powder with a particle diameter of D50=6 μm in N-methylpyrrolidone (wherein the mass ratio of nano-silicon powder and artificial graphite powder is 20:100, powder The mass ratio to the solvent is 30:100), and then placed in a sand mill for dispersion (the grinding process is sealed and nitrogen gas is introduced for protection), the sanding speed is 1200rpm, and the sanding time is 1h to obtain a uniformly dispersed slurry of nano-silicon A;

[0042] (2) Dissolve stearic acid in N-methylpyrrolidinium in a mass ratio of 40:100, and fully mix and stir it with a mechanical stirrer at a speed of 1500 rpm for 30 minutes to prepare slurry B;

[0043] (3) Graphene is dissolved in N-methylpyrrolidinium in a mass ratio of 2:100, and the mixed solution is ul...

Embodiment 2

[0061] A method for preparing a silicon-carbon negative electrode precursor of the present invention, comprising the following steps:

[0062] (1) Add the nano silicon powder of particle diameter D50=100nm and the mesophase carbon microsphere of particle diameter D50=8 μ m in dehydrated alcohol (the mass ratio of nano silicon powder and mesocarbon microsphere is 25:100, powder The mass ratio to the solvent is 30:100), and the sand mill is used for dispersing (nitrogen protection) grinding, the sand milling speed is 1500rpm, and the sand milling time is 45min, and the slurry A with uniform dispersion of nano-silicon is obtained;

[0063] (2) Dissolve palmitic acid in absolute ethanol at a mass ratio of 50:100, fully mix and stir the mixture with a mechanical stirrer at a rotating speed of 1500 rpm, and stir for 30 minutes to obtain slurry B;

[0064] (3) dissolving the carbon nanotubes in absolute ethanol at a mass ratio of 5:100, and ultrasonically dispersing the mixed solutio...

Embodiment 3

[0068] A method for preparing a silicon-carbon negative electrode precursor of the present invention, comprising the following steps:

[0069] (1) Add the nano silicon powder of particle diameter D50=100nm and the natural graphite micropowder of particle diameter D50=6 μm in acetone (the mass ratio of medium nanometer silicon powder and natural graphite micropowder is 20:100, the mass ratio of powder material and solvent 25:100), disperse with a planetary ball mill (nitrogen protection during the sand milling process), the ball milling speed is 1800rpm, the ball milling time is 45min, and the slurry A with uniform dispersion of nano-silicon is obtained;

[0070] (2) Dissolve sebacic acid in acetone at a mass ratio of 40:100, fully mix and stir with a mechanical stirrer, rotate at 1500 rpm, and take 30 minutes to prepare slurry B;

[0071] (3) Graphene is dissolved in acetone by the mass ratio of 2:100, carries out ultrasonic dispersion with ultrasonic disperser, frequency 10kh...

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 sizeaaaaaaaaaa
Particle sizeaaaaaaaaaa
Particle sizeaaaaaaaaaa
Login to View More

Abstract

The invention discloses a preparation method of a silicon carbon negative electrode precursor. The preparation method comprises the steps of adding nanometer silicon powder and carbon micro powder into an organic solvent, and performing grinding and dispersion to form paste A; adding a nanometer carbon material into the organic solvent, and performing uniform dispersion to form paste B; adding a binding agent into the organic solvent, and performing uniform dispersion to form paste C; mixing and uniformly dispersing the paste A, the paste B and the paste C to form paste D; and performing spraydrying granulation on the paste D to obtain the silicon carbon negative electrode precursor. Multi-step dispersion is employed, the dispersion performance and the stability of the mixed paste are improved, the dispersion process time is reduced, the dispersion efficiency is improved, a relevant risk such as granulation plug is reduced, and subsequent application and mass production are facilitated; meanwhile, the carbon micro powder and the nanometer carbon material are introduced, on one hand, the problem of silicon conductivity is solved, the internal resistance is reduced, and the initialcoulombic efficiency and the rate performance are improved; and on the other hand, the volume expansion during the charge-discharge process of silicon is solved, the integral expansion rate of the material is reduced, the material pulverization is prevented, and the cycle property is improved.

Description

technical field [0001] The invention belongs to the field of lithium-ion battery materials, and in particular relates to a preparation method of a structurally stable silicon-carbon negative electrode precursor. Background technique [0002] Lithium-ion batteries have the characteristics of high working voltage, high energy density, light weight, and environmental friendliness, and are widely used in various portable electronic devices and electric vehicles. At present, the commercial lithium-ion battery anode materials are mainly graphite, but the low specific capacity (theoretical specific capacity is 372mAh / g) limits its further development in the energy density of lithium-ion batteries. As a representative of new high-capacity materials, silicon materials have the advantages of high lithium storage capacity (theoretical specific capacity 4200mAh / g), low discharge platform, and abundant reserves, which has become a breakthrough to solve the goal of 300Wh / kg. [0003] How...

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
IPC IPC(8): H01M4/36H01M4/38H01M4/62H01M10/0525
CPCH01M4/364H01M4/366H01M4/386H01M4/625H01M4/628H01M10/0525H01M2004/021H01M2004/027Y02E60/10
Inventor 汤刚彭青姣杨乐之涂飞跃陈涛余林遇史诗伟罗磊王艳华殷敖庄子龙刘志宽覃事彪
Owner CHANGSHA RES INST OF MINING & METALLURGY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products