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Preparing method of lithium ion battery silicon carbon negative electrode material

A technology for lithium-ion batteries and negative electrode materials, applied in battery electrodes, nanotechnology for materials and surface science, secondary batteries, etc., can solve problems that hinder the industrial production of silicon/carbon composite materials, and achieve mild conditions and electric The effect of improved chemical properties and simple steps

Inactive Publication Date: 2019-01-29
TIANJIN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the preparation methods of silicon / carbon composite materials mainly include CVD method, magnesia thermal reduction method, etching method and template method, but most of these methods require expensive equipment or templates, highly toxic reactants or solvents (such as silane, tetrahydrofuran , hydrogen fluoride), complex reaction process, harsh reaction conditions (such as high temperature, high pressure), thus hindering the industrial production of silicon / carbon composites

Method used

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  • Preparing method of lithium ion battery silicon carbon negative electrode material
  • Preparing method of lithium ion battery silicon carbon negative electrode material
  • Preparing method of lithium ion battery silicon carbon negative electrode material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] (1) Disperse 0.5g of 50-80nm silicon powder in 100mL of deionized water by ultrasonication, add 5g of polydiallyldimethylammonium chloride, after ultrasonication for 2 hours, centrifuge, wash with water 3 times, vacuum at 70°C After drying for 10 hours, polymer-modified silicon nanoparticles (Si-PDDA) were obtained.

[0026] (2) Add 2g of 10-12um mesophase carbon microspheres to 90mL of a mixture of concentrated sulfuric acid and concentrated nitric acid with a volume ratio of 3:1, stir and reflux at 70°C for 10 hours, wash with water until neutral, and then dry to obtain oxidized Mesophase carbon microspheres (O-MCMB).

[0027] (3) Add 0.1g Si-PDDA to the mixture of 45ml ethanol and 5mL water, ultrasonically disperse, add 0.7gO-MCMB, stir ultrasonically for 1 hour, add 10mL 0.05g / mL sucrose aqueous solution, stir and evaporate the solvent in a water bath at 70°C.

[0028] (4) Put the dried sample into an argon-protected tube furnace for calcination at 700° C. for 2 ho...

Embodiment 2

[0034] (1) Disperse 0.5g of 200nm silicon powder in 100mL of deionized water by ultrasound, add 3mL of aminopropyltriethoxysilane, stir for 2 hours, centrifuge, wash with water 3 times, and vacuum dry at 70°C for 10 hours to obtain a polymer material-modified silicon nanoparticles (Si-APTMS).

[0035] (2) Add 2g10-12um mesocarbon microspheres and 1.5g sodium dodecyl sulfate into 80mL water, stir for 2 hours, centrifuge, and dry to obtain mesophase carbon microspheres modified by sodium dodecyl sulfate (MCMB- SDS).

[0036] (3) Add 0.15g of Si-APTMS to the mixture of 45ml of ethanol and 5mL of water, after ultrasonic dispersion, add 0.7g of MCMB-SDS, ultrasonic for 1 hour, and add 10mL of 0.05g / mL glucose solution. Stir in a water bath at 70°C and evaporate the solvent to dryness.

[0037] (4) Put the dried sample into an argon tube furnace for calcination at 800° C. for 3 hours to obtain the final product.

[0038] Figure 5 It is the scanning electron microscope picture of ...

Embodiment 3

[0041] (1) Disperse 0.5g of 500nm silicon powder in 100mL of deionized water by ultrasound, add 2g of hexadecyltrimethylammonium bromide, ultrasonic for 2 hours, centrifuge, wash with water 3 times, and vacuum dry at 70°C for 10 hours. Polymer-modified silicon nanoparticles (Si-CTAB) were obtained.

[0042] (2) Add 10-12um mesocarbon microspheres into 0.5M alkaline potassium permanganate solution, stir for 24 hours, wash with water until neutral and dry to obtain oxidized mesocarbon microspheres (O-MCMB).

[0043] (3) Add 0.2g of Si-CTAB to a mixture of 45ml of ethanol and 5mL of water, and after ultrasonic dispersion, add 0.7g of O-MCMB, stir for 3 hours, and add 0.2g of phenolic resin. Stir in a water bath at 70°C and evaporate the solvent to dryness.

[0044] (4) Put the dried sample into an argon tube furnace for calcination at 500° C. for 8 hours to obtain the final product.

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Abstract

The invention discloses a preparing method of a lithium ion battery silicon carbon negative electrode material. A compound containing amidogens or ammonium ions is adopted for modifying nanometre silicon, so that the nanometre silicon carries positive charges, a scheme of modifying negative ions or oxidizing the negative ions is adopted, so that a carbon skeleton carries negative charges, in a solvent, the silicon and the carbon skeleton which carry the opposite charges are self-assembled to a composite material, and then the surface of the composite material is coated with pyrolytic carbon. Compared with existing methods for preparing silicon / carbon composite materials, the adopted self-assembly method is mild in condition and simple in step, complicated and expensive equipment is not needed, and large-scale popularization is facilitated; meanwhile, after the prepared silicon / carbon composite material is subjected to charge-discharge cycles 200 times, the discharge specific capacity is still larger than 500 mAh.g<-1>, and the electrochemical performance of the lithium ion battery silicon carbon negative electrode material is obviously improved compared with silicon / carbon composite materials which are prepared through simple mixing.

Description

technical field [0001] The invention relates to the field of preparation of negative electrode materials for lithium ion batteries, more specifically, especially the preparation of silicon carbon negative electrode materials for lithium ion batteries. Background technique [0002] With the increasing pressure of energy shortage and environmental protection, lithium-ion batteries are considered as the most potential energy storage system. In recent years, due to its advantages of high energy density, small self-discharge, and no memory effect, it has been widely used in portable electronic equipment, electric vehicles, large power supplies and other fields. The current commercial lithium ion negative electrode material is carbon material, but its theoretical specific capacity is only 372mAh g -1 , can no longer meet the huge market demand for high specific capacity lithium ion batteries, so it is urgent to develop new lithium ion battery negative electrode materials with hig...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/36H01M4/38H01M4/583H01M10/0525B82Y30/00
CPCB82Y30/00H01M4/366H01M4/386H01M4/583H01M10/0525Y02E60/10
Inventor 单忠强刘慧添曹宗杰田建华
Owner TIANJIN UNIV
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