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Si/C nano composite anode material as well as preparation method and application thereof

A nano-composite, anode material technology, applied in the direction of nanotechnology, nanotechnology, nanotechnology for materials and surface science, etc., can solve the problems of reduced performance, unfavorable mass production, decreased capacitance density, etc., to improve electrochemical performance. performance, facilitating electron transport, reducing the effect of capacity drop

Pending Publication Date: 2018-10-19
BLUE OCEAN & BLACK STONE TECH CO LTD BEIJING
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But these methods can lead to agglomeration of the treated graphene and reduce its performance
[0003] Due to the complex synthesis method and high synthesis cost of the silicon electrode material synthesized by the existing method, it is not conducive to large-scale production, and the volume change will occur during the charging and discharging process, which will reduce the capacitance density.

Method used

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  • Si/C nano composite anode material as well as preparation method and application thereof
  • Si/C nano composite anode material as well as preparation method and application thereof
  • Si/C nano composite anode material as well as preparation method and application thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0030] 1mol of phenol (94g), 0.85mol of formaldehyde 37% (0.69g) and 0.1mol of oxalic acid (1.45g) were dissolved in 10ml of deionized water to obtain a mixed solution, and the mixed solution was added to 250ml with a magnetic stirring bar, refluxed and condensed In a three-necked flask with a thermometer and a thermometer, heat and reflux for 1 hour under constant stirring, then add 30ml for precipitation, then pour off the upper layer, take the lower layer and distill under reduced pressure for 1 hour at 120°C; dissolve the polymer in ethanol , and then precipitated with distilled water, the purified polymer was obtained by this method, and the phenolic resin was obtained.

[0031] Mix 3 g of phenolic resin in 100 ml of acetone, then keep stirring until it becomes milky white, then add 1 g of silicon nanoparticles to the solution, ultrasonicate the light yellow solution at 40 °C for 3 hours, then continue stirring for 24 h, and The solution was evaporated to dryness, and the...

Embodiment 2

[0035] 1mol of phenol (94g), 0.85mol of formaldehyde 37% (0.69g) and 0.1mol of oxalic acid (1.45g) were dissolved in 10ml of deionized water to obtain a mixed solution, and the mixed solution was added to 250ml with a magnetic stirring bar, refluxed and condensed In a three-necked flask with a thermometer and a thermometer, heat and reflux for 1 hour under constant stirring, then add 30ml for precipitation, then pour off the upper layer, take the lower layer and distill under reduced pressure for 1 hour at 120°C; dissolve the polymer in ethanol , and then precipitated with distilled water, the purified polymer was obtained by this method, and the phenolic resin was obtained.

[0036] Mix 3 g of the above-mentioned phenolic resin in 100 ml of acetone, then keep stirring until it becomes milky white, then add 1 g of silicon nanoparticles to the solution, ultrasonicate the light yellow solution at 40° C. for 3 hours, then continue stirring for 24 h, The solution was evaporated to...

Embodiment 3

[0039] 1mol of phenol (94g), 0.85mol of formaldehyde 37% (0.69g) and 0.1mol of oxalic acid (1.45g) were dissolved in 10ml of deionized water to obtain a mixed solution, and the mixed solution was added to 250ml with a magnetic stirring bar, refluxed and condensed In a three-necked flask with a thermometer and a thermometer, heat and reflux for 1 hour under constant stirring, then add 30ml for precipitation, then pour off the upper layer, take the lower layer and distill under reduced pressure for 1 hour at 120°C; dissolve the polymer in ethanol , and then precipitated with distilled water, the purified polymer was obtained by this method, and the phenolic resin was obtained.

[0040] Mix 3 g of the above-mentioned phenolic resin in 100 ml of acetone, then keep stirring until it becomes milky white, then add 1 g of silicon nanoparticles to the solution, ultrasonicate the light yellow solution at 40° C. for 3 hours, then continue stirring for 24 h, The solution was evaporated to d...

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Abstract

The invention discloses a preparation method of a Si / C nano composite anode material. The method comprises the following steps of adding phenolic resin, which serves as a carbon source, into acetone,stirring continuously until turning milk white, then adding silicon nano particles into mixed emulsion, enabling an obtained mixed solution to be subjected to ultrasound, afterwards stirring for 24h continuously, drying the solution by distillation, extracting and drying in vacuum at 60 DEG C to obtain a Si / C nano composite precursor; performing pyrolysis on the Si / C nano composite precursor in aninert atmosphere, wherein the pyrolysis temperature is 800-1,000 DEG C and the pyrolysis time is 4-5h, cooling to room temperature, then grinding pyrolysis products to a micro order to obtain the Si / C nano composite anode material. The phenolic resin is adopted as the carbon source to combine with an ultrasonic method to prepare nano silicon-containing porous carbon, the pores of carbon and abundant spaces between carbon layers provide more interfaces for reaction between the carbon and lithium ions, so that the electrochemical property of silicon is greatly improved, the declination of capacity is reduced, by tests, the specific capacity is up to 880mAhg-1, the electric current density is 100mAg-1, and the Si / C nano composite anode material still has capacity retention ratio after circulating 500 times.

Description

technical field [0001] The invention belongs to the technical field of lithium ion batteries, and in particular relates to a Si / C nanocomposite anode material and a preparation method and application thereof. Background technique [0002] The development of lithium-ion batteries has been receiving much attention, but the existing graphene materials on the market as battery electrodes have very limited capacity (the capacity is about 370mAh / g at a current density of 100mA / g). Many precursors with modified structures have been investigated to improve the performance of anode materials, and silicon-based polymer ceramic (PDC) materials are a good candidate (theoretical capacitance is around 4000mAh / g). However, the silicon-based electrode will expand in volume during the charge and discharge process, causing its surface to break and its volume to decrease rapidly. This limits the wide application of silicon-based cathode materials. Using double-doped graphene (NSGs) can effec...

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
CPCB82Y30/00H01M4/362H01M4/386H01M4/583H01M10/0525H01M2004/021Y02E60/10
Inventor 罗贺斌孔杰王旭东唐玉生
Owner BLUE OCEAN & BLACK STONE TECH CO LTD BEIJING
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