Silicon-carbon composite for secondary battery anode material, and method for manufacturing the same.

JP2026518595APending Publication Date: 2026-06-09OCI CO LTD(KR)

Patent Information

Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
OCI CO LTD(KR)
Filing Date
2024-04-30
Publication Date
2026-06-09

AI Technical Summary

Benefits of technology

【0034】 本発明は、二次電池の充放電の際にも、シリコンの割れを防止し、体積膨張を最小化することができる条件の粒度を有するように調節されたシリコン粒子を含む、シリコン-炭素複合体、及びこれを含む二次電池用負極材を提供することができる。

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Abstract

The present invention relates to a silicon-carbon composite for secondary battery anode material and a method for manufacturing the same, and more specifically, to a silicon-carbon composite for secondary battery anode material that minimizes the volume change of silicon particles during the charging and discharging process of a secondary battery, thereby improving the characteristics of the secondary battery when applied as an anode material, and to a method for efficiently manufacturing the same.
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Claims

1. A silicon-carbon composite comprising silicon particles and a carbon material, The silicon particles are amorphous, having an average crystallite size of 10 nm or less. The sphericity of the silicon-carbon composite is 0.7 or higher. Silicon-carbon composite.

2. The sphericity of the silicon-carbon composite is 0.9 or higher. The silicon-carbon composite according to claim 1.

3. The silicon-carbon composite has a carbon-based amorphous coating layer formed from a carbon-based coating material on its surface. The silicon-carbon composite according to claim 1.

4. The carbon-based coating material comprises one or more selected from the group consisting of petroleum pitch, ethylene, acetylene, methane, ethane, epoxy resin, polyphenol, polyaniline, polyvinyl alcohol, polyvinyl chloride, and other cross-linked polymers. The silicon-carbon composite according to claim 1.

5. Based on the total weight of the silicon-carbon composite, the silicon particles constitute 55 to 70% by weight, and the carbon material constitutes 30 to 45% by weight. The silicon-carbon composite according to claim 1.

6. A silicon-carbon composite comprising the silicon-carbon composite according to any one of claims 1 to 5, Negative electrode material for secondary batteries.

7. (S1) A step of heating a rotary firing furnace to a temperature of 400°C to 650°C while purging it with an inert gas; and, (S2) A step in which silicon source gas and carbon source gas are simultaneously introduced into the rotary firing furnace, and a homogeneous reaction is carried out under atmospheric pressure conditions to obtain a silicon-carbon composite by co-deposition of silicon and carbon; Includes, The obtained silicon-carbon composite comprises silicon particles and carbon material. The average crystallite size of the silicon particles is 10 nm or less. The silicon-carbon composite D 50 The values ​​are between 1 μm and 10 μm, and the sphericity is 0.7 or higher. A method for manufacturing silicon-carbon composites.

8. The inert gas includes one or more of nitrogen gas and argon gas. A method for producing a silicon-carbon composite according to claim 7.

9. The rotary firing furnace is a chemical vapor deposition (CVD) reactor equipped with a rotary baffle. A method for producing a silicon-carbon composite according to claim 7.

10. The silicon source gas includes at least one selected from the group consisting of monosilane (SiH 4 ), disilane (Si 2 H 6 ), monochlorosilane (SiHCl 3 ), dichlorosilane (SiHCl 2 Cl 2 ), trichlorosilane (SiHCl 3 ), tetrachlorosilane (SiCl 4 ), and trimethylsilane (SiH(CH 3 )) 3 gas. A method for producing a silicon-carbon composite according to claim 7.

11. The carbon source gas includes one or more gases selected from the group consisting of methane, ethane, propane, butane, ethylene, and acetylene. A method for producing a silicon-carbon composite according to claim 7.

12. The sphericity of the silicon-carbon composite is 0.9 or higher. A method for producing a silicon-carbon composite according to claim 7.

13. The silicon-carbon composite in step (S2) above is cooled to room temperature of 15°C to 25°C to obtain a solid powder. A method for producing a silicon-carbon composite according to claim 7.

14. After the reaction (S2) described above has terminated, (S3) The step of introducing a carbon-based source gas and an inert gas for the coating material to form a carbon-based amorphous coating layer on the result obtained in (S2) to obtain the final silicon-carbon composite is further included. A method for producing a silicon-carbon composite according to claim 7.

15. The above (S3) step is performed by chemical vapor deposition. A method for producing a silicon-carbon composite according to claim 14.

16. The carbon-based source gas is one selected from the group consisting of methane gas, ethane gas, propane gas, butane gas, acetylene gas, ethylene gas, and propylene gas. A method for producing a silicon-carbon composite according to claim 14.