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Core-shell-structured silicon carbon negative electrode material and preparation method therefor

A technology of anode material and core-shell structure, which is applied in the field of silicon-carbon anode materials with core-shell structure and its preparation, can solve the problems of reduced delithiation capacity, damage to the conductive network, and low Coulombic efficiency, and achieve stable cycle performance and inhibition Effect of volume change and improvement of cycle performance

Active Publication Date: 2018-03-30
HEFEI GUOXUAN HIGH TECH POWER ENERGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] However, SiO also has the following problems: (1) There is a 200% volume expansion during the lithium intercalation process, which generates a large stress, which will lead to electrode pulverization, destroy the conductive network, and rapidly decay the capacity; (2) In the first lithium intercalation process The inert lithium oxide and lithium silicate phases generated in the process make the coulombic efficiency of the first cycle low; (3) in the subsequent charge and discharge process, due to the continuous formation of the solid electrolyte phase interface (SEI) film, the consumption of Li + , the Coulombic efficiency is lower than 100%, which leads to a significant reduction in the delithiation capacity of the negative electrode compared to the positive electrode in the actual battery; (4) SiO is a semiconductor, and its conductivity is much lower than that of graphite, so there will be a larger charge and discharge when the current is large. severe ohmic polarization

Method used

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  • Core-shell-structured silicon carbon negative electrode material and preparation method therefor
  • Core-shell-structured silicon carbon negative electrode material and preparation method therefor
  • Core-shell-structured silicon carbon negative electrode material and preparation method therefor

Examples

Experimental program
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Embodiment 1

[0030] (1) Mix SiO particles with a D50 of about 5 μm and NaOH at a mass ratio of 20:1, and heat at 50°C for 20 minutes in an argon protective gas to react to obtain SiO, Si, SiO 2 and nuclear materials composed of silicates;

[0031] (2) Add 0.5ml, 10wt% 3-aminopropyltriethoxysilane (APS) to the aqueous suspension of the nuclear material, heat to 40°C and continue to stir for 5h, then add a small amount of hydrochloric acid to make the solution pH 5, obtain a positively charged SiO-APS suspension.

[0032] (3) prepare the graphene quantum dot (GQDs) aqueous solution of 1.5mg / ml graphene quantum dot (GQDs) with acidification oxidation method, wherein the particle size distribution of graphene quantum dot (GQDs) is 2-10nm, and thickness is 1.6-3.2 nm;

[0033] (4) Slowly add the positively charged SiO-APS suspension in step 2) into the negatively charged graphene quantum dot (GQDs) aqueous solution, and stir for 40 min after ultrasonication. Obtain coated SiO by electrostati...

Embodiment 2

[0041] (1) Mix SiO particles with a D50 of about 5 μm and NaOH at a mass ratio of 17:1, heat at 950°C for 20 minutes in an argon protective gas, and obtain SiO, Si, and SiO by the reaction of SiO and NaOH 2 and nuclear materials composed of silicates;

[0042] (2) Add 1ml of 10wt% 3-aminopropyltriethoxysilane (APS) to the nuclear material aqueous suspension, heat to 30°C and continue to stir for 6h, then add a small amount of alkene hydrochloric acid to make the solution pH 6, An electropositive SiO-APS suspension was obtained.

[0043]Step 3) preparing an aqueous solution of carbon dots with a concentration of 3mg / ml by electrochemical method, wherein the particle size distribution of CDs is 2-10nm, and the thickness is 1.6-3.2nm;

[0044] Step 4) Slowly add the positively charged SiO-APS suspension in step 2) into the negatively charged CDs aqueous solution, and stir for 30 minutes after ultrasonication. Obtain CDs-coated SiO by electrostatic adsorption, followed by drying...

Embodiment 3

[0048] (1) Mix SiO particles with a D50 of about 5 μm and NaOH at a mass ratio of 23:1, heat at 950°C for 20 minutes in an argon protective gas, and obtain SiO, Si, and SiO by the reaction of SiO and NaOH 2 and nuclear materials composed of silicates;

[0049] (2) Add 1.5ml of 8wt% 3-aminopropyltriethoxysilane (APS) to the nuclear material aqueous suspension, heat to 50°C and continue stirring for 4h, then add a small amount of dihydrochloric acid to make the solution pH 5, An electropositive SiO-APS suspension was obtained.

[0050] Step 3) Using graphite as a raw material, prepare an aqueous solution of CDs carbon dots with a concentration of 1.5-4.5 mg / ml by an acidification oxidation method, wherein the particle size distribution of CDs is 2-10 nm, and the thickness is 1.6-3.2 nm;

[0051] Step 4) Slowly add the positively charged SiO-APS suspension in step 2) into the negatively charged CDs aqueous solution, and stir for 60 min after ultrasonication. Obtain CDs-coated S...

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Abstract

The invention discloses a core-shell-structured silicon carbon negative electrode material and a preparation method therefor. The silicon carbon negative electrode material comprise a core, a buffer layer and a shell from inside to outside in sequence; the core material consists of SiO, Si, SiO<2> and silicate; the buffer layer material comprises carbon dots or graphene quantum dots; and the shellmaterial is a hard carbon material. The core material disclosed in the invention comprises a modified SiO material; through a high-temperature reaction between SiO and NaOH, nanometer silicon and sodium silicate are generated, so that the shortcoming of low initial coulombic efficiency caused by a reaction between SiO and Li in the initial charging process can be solved; meanwhile, by taking thegenerated sodium silicate as a buffer medium, volume change of the material in the lithium de-intercalation process can be suppressed effectively, and cycle performance of the electrode can be improved; and by taking conductive carbon as a coating layer and by introducing the carbon dots or graphene quantum dots, the material conductivity is improved and a buffer effect can be played, thereby realizing stable cycle performance and high reversible capacity of the battery.

Description

technical field [0001] The invention relates to the field of negative electrode materials for lithium ion batteries, in particular to a silicon-carbon negative electrode material with a core-shell structure and a preparation method thereof. Background technique [0002] Due to the advantages of high specific capacity, high charge-discharge efficiency, good cycle performance and low cost, lithium-ion batteries have gradually become a research hotspot. The rapid development of electronic products and new energy vehicle technology has put forward higher requirements for lithium-ion batteries. As an important part of lithium-ion batteries, anode materials affect the specific energy and cycle life requirements of batteries, and have always been the focus of lithium-ion battery research. [0003] Silicon-based anode materials have high lithium storage capacity and low voltage platform, and are one of the hotspots in the research of anode materials for lithium-ion batteries. Howe...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/36H01M4/48H01M4/62H01M10/0525
CPCH01M4/366H01M4/483H01M4/625H01M4/628H01M10/0525Y02E60/10
Inventor 刘会王辉郭桂略
Owner HEFEI GUOXUAN HIGH TECH POWER ENERGY
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