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Preparation method for modified graphite anode material

A graphite negative electrode and modification technology, which is applied in the direction of battery electrodes, electrochemical generators, electrical components, etc., can solve the problems that the first irreversible capacity cannot be eliminated, the charge-discharge efficiency reduces the capacity, and the charge-discharge cycle cannot be achieved. Good cycle stability performance, improved cycle stability, and improved co-embedded performance

Inactive Publication Date: 2015-08-26
田东
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, similar to other high-capacity metals, silicon has very poor cycle performance and cannot perform normal charge-discharge cycles.
When silicon is used as a negative electrode material, the reversible formation and decomposition of Li2Si alloy is accompanied by a huge volume change during the charge-discharge cycle, which will cause mechanical splitting of the alloy (creating cracks and pulverization), resulting in the collapse of the material structure and the electrode material. The peeling of the electrode material will cause the electrode material to lose electrical contact, resulting in a sharp drop in the cycle performance of the electrode, and finally lead to electrode failure, so it is difficult to be practically applied in lithium-ion batteries
Studies have shown that small particle size silicon or its alloys have greatly improved both in terms of capacity and cycle performance. When the particles of alloy materials reach the nanometer level, the volume expansion during charge and discharge will be greatly reduced, and the performance will also be improved. It will be improved, but nanomaterials have a large surface energy and are prone to agglomeration, which will reduce the charge and discharge efficiency and accelerate the decay of capacity, thereby offsetting the advantages of nanoparticles; silicon films prepared by various deposition methods can To a certain extent, the cycle life of the material can be extended, but its high initial irreversible capacity cannot be eliminated, which restricts the practical application of this material.

Method used

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  • Preparation method for modified graphite anode material

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Experimental program
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Effect test

Embodiment 1

[0024] According to the ratio of graphite:resin:nickel powder:silicon powder=100:10:3:3, weigh 1000g artificial graphite, 100g phenolic resin, 30g nickel powder, 30g silicon powder, according to the ratio of solid content of 30%, weigh In 2706g of ethanol solvent, use zirconia grinding balls, and ball mill for 12 hours to obtain a uniform slurry; then dry the slurry at -0.1Mpa and 30°C for 10 hours to obtain a powder; then put the powder in an inert gas Under protection, the temperature was raised to 1000°C at a rate of 10°C / min, then kept at a temperature of 3 hours, the temperature was naturally lowered, and the graphite negative electrode material of the present invention was obtained by sieving after cooling.

Embodiment 2

[0026] According to the ratio of graphite:resin:nickel powder:silicon powder=100:5:5:1, weigh 1000g of natural graphite, 50g of epoxy resin, 50g of nickel powder, and 10g of silicon powder. Take 1665g of ethanol solvent, use zirconia grinding balls, and ball mill for 12 hours to obtain a uniform slurry; then dry the slurry at -0.1Mpa and 40°C for 80 hours to obtain a powder; then put the powder in an inert gas Under the protection of 20°C / min, the temperature was raised to 800°C, and then kept for 10 hours, the temperature was naturally lowered, and the graphite negative electrode material of the present invention was obtained by sieving after cooling.

Embodiment 3

[0028] According to the ratio of graphite:resin:nickel powder:silicon powder=100:8:4:3, weigh 1000g artificial graphite, 80g phenolic resin, 40g nickel powder, 30g silicon powder, according to the proportion of solid content of 30%, weigh In 2683g of ethanol solvent, ceramic grinding balls were used to mill for 12 hours to obtain a uniform slurry; then the slurry was dried at -0.1Mpa and 35°C for 9 hours to obtain a powder; then the powder was placed under the protection of an inert gas The temperature was raised to 850°C at a rate of 10°C / min, and then kept at a temperature of 14 hours, the temperature was naturally lowered, and the graphite negative electrode material of the present invention was obtained by sieving after cooling.

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Abstract

The invention discloses a preparation method for a modified graphite anode material. The preparation method comprises the following steps: (1) preparing a slurry precursor; (2) drying the precursor; (3) performing heat treatment. The prepared graphite anode material has higher specific capacity; the material is modified, so that the electrical conductivity of the material is effectively improved, and the cyclic stability of the material is improved; therefore, when the anode material is used for a lithium ion battery, higher energy density and good cyclic stability are achieved.

Description

technical field [0001] The invention relates to a preparation method of a modified graphite negative electrode material, in particular to a preparation method of a graphite negative electrode material doped with metallic nickel and metallic silicon and treated by coating. Background technique [0002] Lithium-ion batteries have the advantages of small size, high storage capacity and high discharge capacity under long-term use, so they are widely used in communication, electronic and other equipment. Based on its safety and cost considerations, "graphite" has become the mainstream raw material for lithium-ion battery anode materials; and various lithium-ion battery anode materials using graphite as raw materials, as well as related preparation methods, have gradually been developed. [0003] At present, the anode materials of commercial lithium-ion batteries use graphite-like carbon materials, which have the advantages of low lithium intercalation / deintercalation potential, s...

Claims

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Application Information

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IPC IPC(8): H01M10/0525H01M4/583H01M4/36
CPCH01M4/366H01M4/583H01M10/0525H01M4/133H01M4/134H01M4/1393H01M4/1395Y02E60/10
Inventor 田东
Owner 田东
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