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Silicon/mesoporous carbon composites with three-dimensional conductive network structure

A composite material and network structure technology, applied in the field of silicon/mesoporous carbon composite materials, can solve the problems of low capacity and short life of lithium ion batteries, and achieve the effect of improving electrochemical contact, good elasticity and high conductivity

Inactive Publication Date: 2019-01-08
JIANGSU RONGSHENG ELECTRONICS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The purpose of the present invention is to solve the problems of low capacity and short service life of lithium-ion batteries at present, and provide a method that can effectively prolong the cycle life of silicon-carbon negative electrode materials and improve reversible capacity on the problems of existing silicon-based carbon coating materials. Retention, lithium-ion battery anode materials that improve the cycle performance of silicon-carbon anode materials, the composite material has an ordered mesoporous structure; the silicon / carbon mass ratio in the composite material is (0.1-0.9): 1; nano-silicon powder is Si or SiO x One or more of (02 g -1 , the pore volume is 0.2-3.0cm 3 g -1

Method used

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  • Silicon/mesoporous carbon composites with three-dimensional conductive network structure

Examples

Experimental program
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Effect test

Embodiment example 1

[0032] 1.61g phenol, add 10ml 1.5 mol L -1 KOH solution, stirred for 20min, added 5.0ml of 37% formaldehyde solution, stirred for 1h, added 3.0g of F-127 into 20g of methanol, stirred until transparent, added into phenolic resin, stirred at 65°C for 1h. Cool to room temperature, use 1.0 mol L -1 HNO 3 The pH of the solution was adjusted to 7. The obtained solution was rotary evaporated at 55°C, and the obtained resin was dispersed in methanol, stirred, and centrifuged at 5000r min -1 , 20min, filtered to obtain a methanol solution of phenolic resin. The obtained solution was transferred to a Petri dish, volatilized at room temperature for 10 h, and solidified at 120° C. for more than 24 h to obtain a transparent material. The obtained material was put into a tube furnace with nitrogen protection at 10°C min -1 The temperature was raised to 400°C at a high speed, kept for 4 hours, then raised to 600°C, kept for 3 hours, and then naturally cooled to room temperature to obta...

Embodiment example 2

[0036] 1.61g phenol, add 10ml 1.5 mol L -1 KOH solution, stirred for 20min, added 5.0ml of 37% formaldehyde solution, stirred for 1h, added 3.0g of F-127 into 20g of methanol, stirred until transparent, added into phenolic resin, stirred at 65°C for 1h. Cool to room temperature, use 1.0 mol L -1 HNO 3 The pH of the solution was adjusted to 7. The obtained solution was rotary evaporated at 55°C, and the obtained resin was dispersed in methanol, stirred, and centrifuged at 5000r min -1 , 20min, filtered to obtain a methanol solution of phenolic resin. The carbon nanotubes were acidified, ultrasonicated for 3 hours in 40ml of concentrated sulfuric acid and concentrated nitric acid (3:1, V / V), washed with deionized water and filtered until neutral, and dried in vacuum for later use.

[0037] Take carbon nanotubes accounting for 10% of the total mass and 20% silicon powder (50-100nm) according to a predetermined ratio, add appropriate amount of methanol respectively, ultrasoni...

Embodiment example 3

[0041] 1.61g phenol, add 10ml 1.5 mol L -1 KOH solution, stirred for 20min, added 5.0ml of 37% formaldehyde solution, stirred for 1h, added 3.0g of F-127 into 20g of methanol, stirred until transparent, added into phenolic resin, stirred at 65°C for 1h. Cool to room temperature, use 1.0 mol L -1 HNO 3 The pH of the solution was adjusted to 7. The obtained solution was rotary evaporated at 55°C, and the obtained resin was dispersed in methanol, stirred, and centrifuged at 5000r min -1 , 20min, filtered to obtain a methanol solution of phenolic resin. The carbon nanotubes were acidified, ultrasonicated for 3 hours in 40ml of concentrated sulfuric acid and concentrated nitric acid (3:1, V / V), washed with deionized water and filtered until neutral, and dried in vacuum for later use.

[0042] Take carbon nanotubes accounting for 10% of the total mass and silicon powder (50-100nm) with a mass of 40% according to a predetermined ratio, add appropriate amount of methanol respect...

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Abstract

The invention discloses a silicon / mesoporous carbon composite material with a three-dimensional conductive network structure, As that composite material has good electrical conductivity, so that it iselastic, mesoporous carbon has a high specific surface area, Stabilizing mechanical properties and uniform ordered pore structure, carbon nanotubes and mesoporous carbon constitute a new network structure, which can effectively buffer the stress caused by the volume change of silicon during charging and discharging. The three-dimensional network provides a channel for the rapid transport of lithium ions and electrons. As the cathode material of lithium batteries, it shows excellent electrochemical performance.

Description

technical field [0001] The invention relates to a silicon / mesoporous carbon composite material with a three-dimensional conductive network structure. The material is obtained through thermal polymerization and high-temperature annealing through a method of solvent volatilization induction combination, and belongs to the field of new energy. Background technique [0002] Lithium-ion batteries have the advantages of high energy storage density, high open circuit voltage, and low self-discharge rate, and are widely used in portable electronic equipment, aerospace equipment, and electric vehicles. The rapid development of electronic devices and electric vehicles has placed increasing demands on the capacity and energy density of lithium-ion batteries. [0003] At present, in commercial lithium-ion battery systems, graphite-based anode materials are limited by their theoretical capacity (372mAh g -1 ), researchers began to look for new anode materials to replace graphite anodes....

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/36H01M4/38H01M4/587H01M4/62H01M10/0525B82Y30/00
CPCB82Y30/00H01M4/366H01M4/386H01M4/587H01M4/625H01M10/0525Y02E60/10
Inventor 陈仕谋陈建军
Owner JIANGSU RONGSHENG ELECTRONICS