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A kind of carbon cage type silicon-graphite composite material and preparation method thereof

A composite material and graphite technology, applied in the preparation/purification of graphite and carbon, structural parts, etc., can solve the problems of lithium ion consumption, cycle performance deterioration, volume expansion effect, etc., to increase conductivity and stability, and suppress volume Expansion effect, the effect of optimizing the skeleton structure

Active Publication Date: 2021-08-10
CHANGSHA UNIVERSITY OF SCIENCE AND TECHNOLOGY
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But silicon-based materials have always had a serious problem: the volume expansion effect
During the charging and discharging process of the battery, with the intercalation and extraction of lithium ions, the volume expansion effect of silicon reaches 297%, and the volume expansion causes the destruction of the material structure and mechanical pulverization, resulting in the separation between the electrode materials and the electrode materials and the current collector. Loss of electrical contact, resulting in rapid capacity decay and deterioration of cycle performance
Due to the severe volume effect, the SEI film on the silicon surface collapses and forms reciprocally, continuously consuming lithium ions, increasing the irreversible capacity of the electrode, and further affecting the cycle performance
[0004] Most researchers use different processes to solve the volume expansion problem of silicon by carbon coating, and synthesize carbon-coated silicon materials with different structures through a series of processes. Although the volume expansion problem of silicon has been effectively solved, However, the process steps are too complex for commercial application, and enter the bottleneck due to insufficient electrode loading and limited energy density.
[0005] The main problem of silicon-graphite composites is that the interface between graphite and silicon is not firmly bonded, and it is difficult to give full play to the synergistic lithium storage effect.
The limited surface area of ​​graphite also leads to limited loading of silicon on graphite, and the prepared electrode material cannot achieve the ideal specific capacity.
Moreover, graphite is easily deformed during cycling under the condition of low load and high energy density, which affects the cycle performance of electrode materials.

Method used

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  • A kind of carbon cage type silicon-graphite composite material and preparation method thereof
  • A kind of carbon cage type silicon-graphite composite material and preparation method thereof

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preparation example Construction

[0034] A kind of preparation method of carbon cage type silicon-graphite material, comprises the steps:

[0035] Step 1: Add 2.5-3.5 parts of graphite into 80-100 parts of concentrated sulfuric acid solution in parts by mass, and stir at room temperature to obtain suspension 1. The graphite may be natural graphite and / or artificial graphite. Concentrated sulfuric acid plays the role of intercalation and activation to oxidize the edge of graphite and SO 4 2﹣ intercalation. Preferably, the mass percent concentration of the concentrated sulfuric acid solution used is 95%-98%, and the stirring time is 3-4 hours. A mixture of concentrated sulfuric acid and phosphoric acid can also be used.

[0036] Step 2: Pour suspension 1 into 7-9 parts of potassium permanganate solution, and stir at room temperature to obtain suspension 2; pour suspension 2 into 50-65 parts of hydrogen peroxide solution, and stir at room temperature to obtain suspension 3. The main function of potassium perm...

Embodiment 1

[0044] Step 1: Add 3 g of natural graphite into 50 mL of 95%-98% concentrated sulfuric acid solution, and stir at room temperature for 3 hours to obtain suspension 1;

[0045] Step 2: Pour suspension 1 into 7-9 g of 50% potassium permanganate solution by mass, stir at room temperature for 3 hours to obtain suspension 2, and pour suspension 2 into 50 mL of 30% hydrogen peroxide by mass solution, stirred at room temperature for 2 h to obtain suspension 3;

[0046] Step 3, the suspension 3 was washed with distilled water until pH = 6.76, 1 g of nano-scale silicon powder was added, and then 1 g of polyvinylpyrrolidone was added to stir and ultrasonically disperse for 20 minutes each to obtain a suspension 4.

[0047] Step 4: Add 2 g of sucrose to the suspension 4, add 1 g of citric acid, stir for 20 minutes, and sonicate for 30 minutes to obtain a suspension 5, and put the suspension 5 into an oven to dry at 110° C. for 3 hours;

[0048] Step 5: Put the dried sample into a tube f...

Embodiment 2

[0051] Step 1: Add 3 g of artificial graphite into 50 mL of 95%-98% concentrated sulfuric acid solution, stir at room temperature for 3 hours to obtain suspension 1;

[0052] Step 2: Pour suspension 1 into 7-9 g of 50% potassium permanganate solution by mass, and stir at room temperature for 3 hours to obtain suspension 2; pour suspension 2 into 50 mL of 30% hydrogen peroxide by mass solution, stirred at room temperature for 2 h to obtain suspension 3;

[0053] Step 3, the suspension 3 was washed with distilled water until pH = 6.84, 1 g of nano-scale silicon powder was added, and then 1 g of polyvinylpyrrolidone was added to stir and ultrasonically disperse for 20 minutes each to obtain suspension 4.

[0054] Step 4: Add 2 g of sucrose to the suspension 4, add 1 g of citric acid, stir for 20 minutes, and sonicate for 30 minutes to obtain a suspension 5, and put the suspension 5 into an oven to dry at 110° C. for 3 hours;

[0055] Step 5: Put the dried sample into a tube furn...

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Abstract

The invention discloses a carbon cage type silicon-graphite composite material and a preparation method thereof. The graphite is intercalated and oxidized; the treated graphite and nano-scale silicon powder are stirred and dispersed in the presence of a dispersant to obtain a silicon-graphite composite material. Suspension of graphite composite material; adding sucrose and acid to the suspension to hydrolyze the sucrose under acid catalysis, and then drying; calcining and carbonizing the dried product under an inert atmosphere, and coating the silicon-graphite composite material without Shape the carbon layer to obtain a carbon-cage silicon-graphite composite material. The carbon cage silicon-graphite composite material prepared by this method has high specific capacity and good cycle stability. Using surface treatment technology, the combination of graphite and silicon is realized, and the volume of silicon is adjusted by a simple carbon coating method. The expansion problem is effectively controlled, and the disadvantage of low specific capacity of traditional commercial graphite electrode materials is improved.

Description

technical field [0001] The invention belongs to the field of composite materials, and in particular relates to a carbon cage silicon-graphite composite material and a preparation method thereof. Background technique [0002] my country is the country with the most abundant graphite reserves in the world, and it is also the largest producer and exporter, occupying an important position in the world graphite industry. Graphite material has good electrical conductivity, high thermal and chemical stability. But the specific capacity of graphite is only 372mA h g -1 . Moreover, the potential of the graphite negative electrode material is low, which is easy to cause lithium precipitation; poor compatibility with the electrolyte; the ion migration rate is slow, so the charge and discharge rate is low; layered graphite will generate about 10% in the process of lithium ion insertion and deintercalation. The deformation will affect the cycle life of the battery. The voltage platfo...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01B32/22C01B32/21C01B32/05H01M4/38H01M4/587H01M4/62
CPCC01B32/05C01B32/21C01B32/22H01M4/386H01M4/587H01M4/625Y02E60/10
Inventor 刘鹏杨尚泽祝欣怡李晓露梁江段克勤
Owner CHANGSHA UNIVERSITY OF SCIENCE AND TECHNOLOGY
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