A kind of preparation method of nanoscale silicon negative electrode of lithium ion battery

A lithium-ion battery, nano-scale technology, applied in the direction of battery electrodes, secondary batteries, circuits, etc., can solve the problems of no discovery, low carbon residue rate, etc., and achieve the effects of improving cycle efficiency, simple polymerization method, and wide application range

Inactive Publication Date: 2020-06-26
XIAMEN UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] To sum up, it can be seen that in order to obtain a buffer space sufficient for the volume expansion of silicon during the lithiation process, the skeleton structure can be designed, the reduction of silicon dioxide, or the etching of silicon dioxide, etc., but in the process of consulting the literature, there is no Articles that use polymer pyrolysis to obtain this buffer space are found. Because most linear polymers have extremely low carbon residue rate or even 100% decomposition during the pyrolysis process, the polymer introduces silicon cores and The middle of the shell carbon precursor layer is used as a medium layer. When the carbon layer is prepared by pyrolysis, the carbon layer precursor is pyrolyzed and converted into a carbon shell layer, and at the same time, the polymer medium layer filled between the silicon core and the carbon precursor is decomposed to obtain Expansion space of silicon spheres

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of preparation method of nanoscale silicon negative electrode of lithium ion battery

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0027] 1) At room temperature, put 1 g of nano-silicon spheres into 100 ml of a mixed solution of concentrated sulfuric acid and hydrogen peroxide with a volume ratio of 7:3 and stir for 2 hours, then centrifuge and wash and separate 3 times to obtain the hydrophilic-treated nano-silicon spheres with hydroxyl groups on the surface. Silicon ball;

[0028] 2) Ultrasonically disperse 1 g of silicon spheres obtained in step 1) into 7 ml of 28% ammonia water and 100 ml of ethanol mixture, and dissolve 1 g of (2-bromo-2-methyl)hexyl trimethoxypropionate in a water bath at 40°C A mixed solution of silane and 10ml of ethanol was added dropwise to the suspension of silicon spheres, and the reaction was continued for 24 hours after the addition was completed, and the product was centrifuged three times with ethanol to obtain silicon spheres with groups on the surface that could initiate atom transfer radical polymerization;

[0029] 3) Mix 1 g of silicon spheres obtained in step 2) acco...

Embodiment 2

[0033] 1) At room temperature, place 1g of nano-silicon spheres under 100w ultraviolet light for 1 hour to obtain nano-silicon spheres with hydroxyl groups on the surface;

[0034] 2) Ultrasonically disperse 1 g of silicon spheres obtained in step 1) into 14 ml of 28% ammonia water and 180 ml of ethanol mixture, and dissolve 2 g of (2-bromo-2-methyl)hexyl trimethoxypropionate in a water bath at 60°C A mixed solution of silane and 20ml of ethanol was added dropwise to the suspension of silicon spheres, and the reaction was continued for 12 hours after the addition was completed, and the product was centrifuged three times with ethanol to obtain silicon spheres with groups on the surface that could initiate atom transfer radical polymerization;

[0035] 3) Mix 1 g of silicon spheres obtained in step 2) according to the ratio of initiator: methyl methacrylate: cuprous bromide: bipyridine in the ratio of 1:300:1:3, and initiate at 70°C under the condition of isolated air The monom...

Embodiment 3

[0039] 1) At room temperature, put 1 g of nano-silicon spheres into 100 ml of a mixed solution of concentrated sulfuric acid and hydrogen peroxide with a volume ratio of 7:3 and stir for 2 hours, then centrifuge and wash and separate 3 times to obtain the hydrophilic-treated nano-silicon spheres with hydroxyl groups on the surface. Silicon ball;

[0040] 2) Put the silicon ball obtained in step 1) into 1g, 10mL SOCl 2 ,10mL CHCl 3 , Stirred and refluxed for 36 hours, distilled off the unreacted solution, and obtained chlorinated silicon balls after vacuum drying. 1 g of chlorinated silica spheres, 15 mL of 1,4-dioxane, 3 mL of tert-butyl hydroperoxide (TBHP), 0.05 g of NaHCO 3 Mix, react under nitrogen protection at room temperature for 12 hours, centrifuge, wash with methanol, and dry in vacuum to obtain silicon spheres whose surface contains groups that can initiate oxygen and nitrogen free radicals to regulate polymerization;

[0041] 3) Add 1 g of silicon spheres obtain...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
current efficiencyaaaaaaaaaa
current efficiencyaaaaaaaaaa
Login to view more

Abstract

The invention discloses a preparation method of a nanometer silicon negative electrode for lithium ion batteries, and relates to the lithium ion batteries. The nanometer silicon negative electrode for the lithium ion batteries is a silicon @ hole @ carbon structure silicon negative electrode, and an initiator is grafted on the surface of a silicon ball through surface modification to obtain an initiator grafted silicon ball; the obtained initiator grafted silicon ball grafts a polymer which can be completely thermally decomposed as a medium layer through active free radical polymerization; a carbon clad layer is clad on the surface layer of an obtained sample as a carbon layer precursor; the obtained sample is oxidatively cross-linked in an air atmosphere and is thermally decomposed in an inert atmosphere, the medium layer is completely decomposed to obtain a silicon expanded hole space, and the carbon layer precursor is thermally decomposed and carbonized to obtain shell carbon, so that the nanometer silicon negative electrode for the lithium ion batteries is obtained. The preparation method is effectively combined with an active free radical polymerization process with relatively high controllability. Different carbon sources can be regulated, controlled and used. The operation controllability is high, and the expansion space of the silicon ball and the thickness of the carbon layer can be effectively adjusted. The operation process is easy to perform, little in dangerousness and easy for amplification.

Description

technical field [0001] The invention relates to a lithium ion battery, in particular to a preparation method of a nanoscale silicon negative electrode of a lithium ion battery. Background technique [0002] With the development of science and technology and economy, high-performance electronic devices and electric vehicles emerge in an endless stream. However, the lithium-ion battery with graphite negative electrode (theoretical capacity 370mA h / g) commonly used in the market cannot meet the requirements of high capacity and low cycle loss. Therefore, it is necessary to design electrode active materials with better performance, such as: Si, Ge, SnO 2 , SiOC and so on. In continuous research, it is found that the theoretical capacity of Si is very high, about 10 times that of graphite (when forming an alloy with Li, Li 15 Si 4 The capacity is 3579mA·h / g), and it has a low lithiation / delithiation potential, so it has attracted widespread attention in the industry. However,...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/36H01M4/583H01M4/62H01M4/38H01M10/0525H01M4/60
CPCH01M4/366H01M4/386H01M4/583H01M4/602H01M4/625H01M10/0525Y02E60/10
Inventor 刘安华吴鹏飞苏智明胡志明刘星煜郭长青
Owner XIAMEN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products