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Method for preparing porous graphene silicon negative electrode material

A technology of porous graphene and silicon anode, applied in the field of lithium ion batteries, can solve the problems of difficult scale application, graphene structure damage, high cost, etc., and achieve the effect of avoiding irreversible damage and high structural regularity.

Active Publication Date: 2019-08-09
AVIC BEIJING INST OF AERONAUTICAL MATERIALS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The main method is to load metal oxide on the surface of redox graphene, and then reduce and etch it. This method causes irreparable damage to the structure of graphene, and uses a large amount of highly toxic substances such as acid and alkali in the preparation process. , low yield, difficult to scale production
In addition, plasma sputtering, microwave method, ultrasonic treatment, gas etching and other methods are also used, but most of these technologies are expensive, poorly controllable and difficult to apply on a large scale

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] Using ferric chloride as intercalation agent and 300 mesh flake graphite as precursor, ferric chloride-graphite intercalation compound was prepared by molten salt intercalation method. Add 1g of ferric chloride-graphite intercalation compound into 1000mL of acetone solvent, ultrasonicate for 3 hours, then centrifuge at a speed of 5000r / min, pour off the supernatant, and freeze-dry the precipitate to obtain ferric chloride- Graphene Interlayer Compounds. The ferric chloride-graphene interlayer compound was placed in a muffle furnace for heat treatment, and kept at 400° C. for 2 hours to obtain an iron oxide-graphene composite material. Disperse 1g of iron oxide-graphene composite material in 500mL of water and ethanol mixed solution (ratio: 5:1), 1g of silicon material and CTAB dispersed in the same 500mL of water and ethanol mixed solution, respectively, ultrasonic treatment for 30 minutes , the silicon material dispersion liquid is slowly added dropwise into the graph...

Embodiment 2

[0023] Using ferric chloride as intercalation agent and 1000 mesh flake graphite as precursor, ferric chloride-graphite intercalation compound was prepared by molten salt intercalation method. Add 1g of ferric chloride-graphite intercalation compound into 1000mL of isopropanol solvent, use a high-pressure homogenizer to carry out 5 cycles of stripping, then perform centrifugation at a speed of 6000r / min, pour off the supernatant, and remove the precipitate Freeze-drying is carried out to obtain ferric chloride-graphene interlayer compound. The ferric chloride-graphene interlayer compound was placed in a muffle furnace for heat treatment, and kept at 550° C. for 2 hours to obtain an iron oxide-graphene composite material. Disperse 5g of iron oxide-graphene composite material in 1000mL of water and acetone mixed solution (ratio: 6:1), 5g of silicon material and PEG dispersed in the same 1000mL of water and acetone mixed solution, respectively, ultrasonic treatment for 60 minutes...

Embodiment 3

[0025] Using ferric chloride and nickel chloride as co-intercalation agents and carbon fiber as precursor, ferric chloride-nickel chloride-carbon fiber interlayer compound was prepared by molten salt intercalation method. Add 5g of ferric chloride-nickel chloride-carbon fiber interlayer compound to 1000mL N-methylpyrrolidone, use a high-pressure homogenizer to perform 10 cycles of stripping, then perform centrifugation at a speed of 4000r / min, and pour off the supernatant , and freeze-dry the precipitate to obtain the ferric chloride-nickel chloride-graphene interlayer compound. The ferric chloride-nickel chloride-graphene interlayer compound was placed in a muffle furnace for heat treatment, and kept at 600° C. for 1 hour to obtain an iron oxide-nickel oxide-graphene composite material. Disperse 10g of iron oxide-nickel oxide-graphene composite material in 1000mL water and isopropanol mixed solution (ratio: 4:1), 10g silicon material and PVP are dispersed in the same 1000mL w...

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Abstract

The invention relates to a method for preparing a porous graphene silicon negative electrode material. For the problem that the volume expansion of a current silicon negative electrode material seriously causes structural collapse to cause rapid collapse to cause the quick attenuation of energy, a metal oxide-graphene composite material is prepared by using a graphite intercalation method, a liquid phase stripping method and an in-situ growth method, the surface of a silicon material is coated with the metal oxide-graphene composite material, then the metal oxide is etched away with an acid solution, and the porous graphene silicon negative electrode material is obtained by the principle of carbothermal reaction. The excellent conductivity and porous structure of high-quality graphene facilitate the rapid transmission of electrons and lithium ions, a variety of pore graphene structures can be obtained by controlling heat treatment time and temperature, the flexible adjustment can be carried out according to conditions needed by an actual negative electrode material, the etched metal oxide leaves a buffer space, and a series of negative effects caused by the volume expansion of thesilicon material are alleviated.

Description

technical field [0001] The invention belongs to the field of lithium ion battery negative electrode materials, and in particular relates to a preparation method of a porous graphene silicon negative electrode material and a lithium ion battery using the negative electrode material. Background technique [0002] As a negative electrode material for lithium batteries, silicon materials have extremely high theoretical specific capacity (>3000mA h g-1), and are expected to become a new generation of negative electrode materials that can replace graphite materials with low lithium storage capacity. However, the volume expansion of silicon during charge and discharge is serious (about 4 times), which causes the particles to squeeze each other and cause the structure to collapse, and the silicon material is easy to fall off from the current collector, thus causing rapid energy decay of the battery. Application of negative electrode materials. [0003] Graphene, a two-dimensiona...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/36H01M4/38H01M4/485H01M4/58H01M4/587H01M4/62H01M10/0525
CPCH01M4/366H01M4/386H01M4/485H01M4/58H01M4/587H01M4/625H01M4/628H01M10/0525Y02E60/10
Inventor 齐新燕绍九南文争李秀辉洪起虎
Owner AVIC BEIJING INST OF AERONAUTICAL MATERIALS
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