Method of preparing negative electrode active material for lithium secondary battery and lithium secondary battery using the same

Patent metadata

Field	Value
Publication number	US-2018269519-A1
Application number	US-201615751916-A
Country	US
Kind code	A1
Filing date	Dec 9, 2016
Priority date	Dec 10, 2015
Publication date	Sep 20, 2018
Grant date	—

Abstract

The present invention relates to a method of preparing a negative electrode active material for a secondary battery which may prevent oxidation during the preparation of nano-sized silicon particles, a negative electrode active material for a secondary battery prepared thereby, and a negative electrode for a secondary battery and a lithium secondary battery including the same.

First claim

1 . A method of preparing a negative electrode active material for a lithium secondary battery, the method comprising steps of:
depositing an amorphous silicon layer on a surface of a glass substrate by applying silane gas at a rate of 10 sccm/60 min to 50 sccm/60 min in a temperature range of 500° C. to 700° C. and in a pressure range of 10 −8 Torr to 760 Torr (S1) through chemical vapor deposition (CVD) using silane (SiH 4 ) gas as a source (S1); immersing the glass substrate having the amorphous silicon layer deposited thereon in an acetone solution and then performing ultrasonic milling of the amorphous silicon layer at a power of 50 W to 200 W for 10 minutes to 20 minutes at room temperature using an ultrasonic milling machine to prepare amorphous silicon particles (S2); dispersing the amorphous silicon particles in a carbon-based precursor solution to prepare a dispersion solution (S3); spray drying the dispersion solution to prepare a silicon-based composite precursor (S4); and heat treating the silicon-based composite precursor to form a silicon composite which includes an amorphous carbon coating layer containing at least one amorphous silicon particle in inside thereof (S5).

2 . (canceled)

3 . The method of claim 1 , wherein a thickness of the deposited amorphous silicon layer is in a range of 20 nm to 500 nm.

4 . (canceled)

5 . The method of claim 1 , wherein the method further comprises collecting the milled amorphous silicon particles by volatilizing an acetone solvent, after the amorphous silicon particle preparing step S2 and before the dispersion solution preparing step S3.

6 . The method of claim 1 , wherein the milled amorphous silicon particles have an average particle diameter (D50) of 5 nm to 500 nm.

7 . The method of claim 1 , wherein the dispersion solution preparing step S3 is performed by mixing a carbon-based material capable of being carbonized at a temperature of 1,000° C. or less with distilled water to prepare the carbon-based precursor solution, and dispersing the amorphous silicon particles.

8 . The method of claim 7 , wherein the carbon-based material comprises a single material selected from the group consisting of sucrose, glucose, fructose, galactose, maltose, and lactose, or a mixture of two or more thereof.

9 . The method of claim 1 , wherein the carbon-based precursor solution is used in an amount of 25 parts by weight to 4,000 parts by weight based on 100 parts by weight of the amorphous silicon particles.

10 . The method of claim 1 , wherein at least one conductive carbon-based material selected from the group consisting of crystalline carbon and amorphous carbon is additionally dispersed during the dispersing of the amorphous silicon particles.

11 . (canceled)

12 . The method of claim 1 , wherein the dispersion solution spray-drying step S4 is performed by providing the precursor solution to a sprayer to form droplets by spraying, followed by drying the droplets at a same time.

13 . The method of claim 1 , wherein the spray drying is performed at a rate of 10 mL/min to 50 mL/min in a temperature range of 50° C. to 300° C.

14 . The method of claim 1 , wherein the silicon-based composite precursor heat treating step S5 is performed in a temperature range of 400° C. to 1,000° C. for about 10 minutes to about 1 hour.

15 . A negative electrode active material for a lithium secondary battery prepared by the method of claim 1 , the negative electrode active material comprising a silicon composite including:
an amorphous carbon coating layer; and at least one amorphous silicon particle included in the amorphous carbon coating layer; wherein the amorphous silicon particles are included in an amount of 1 wt % to 95 wt % based on a total weight of the negative electrode active material; wherein a weight ratio of the amorphous silicon particles: the amorphous carbon coating layer is in a range of 1:99 to 95:5.

16 . The negative electrode active material for a lithium secondary battery of claim 15 , wherein the amorphous silicon particle comprises a single particle or a secondary amorphous silicon particle which is formed by agglomeration of primary amorphous silicon particles composed of the single particle.

17 . (canceled)

18 . (canceled)

19 . (canceled)

20 . (canceled)

21 . The negative electrode active material for a lithium secondary battery of claim 15 , wherein the negative electrode active material further comprises at least one conductive carbon-based material selected from the group consisting of crystalline carbon and amorphous carbon in the amorphous carbon coating layer.

22 . The negative electrode active material for a lithium secondary battery of claim 21 , wherein the negative electrode active material comprises a silicon composite which includes an amorphous carbon coating layer; and at least one amorphous silicon particle and amorphous carbon included in the amorphous carbon coating layer.

23 . The negative electrode active material for a lithium secondary battery of claim 22 , wherein the amorphous carbon is included in an amount of 0.1 wt % to 50 wt % based on a total weight of the negative electrode active material.

24 . The negative electrode active material for a lithium secondary battery of claim 21 , wherein the negative electrode active material comprises an amorphous carbon coating layer; and at least one amorphous silicon particle and crystalline carbon included in the amorphous carbon coating layer,
wherein the at least one amorphous silicon particle is distributed on a surface of the crystalline carbon; wherein the crystalline carbon has an average particle diameter (D50) of 300 nm to 30 μm and is included in an amount of 10 wt % to 90 wt % based on a total weight of the negative electrode active material.

25 . (canceled)

26 . (canceled)

27 . (canceled)

28 . (canceled)

29 . A negative electrode comprising:
a current collector; and the negative electrode active material of claim 15 which is formed on at least one surface of the current collector.

30 . (canceled)

Assignees

• Lg Chemical Ltd

Inventors

• Jo Rae Hwan
• Lee Yong Ju
• Kim Eun Kyung

Classifications

• H01M10/052 Primary

  Li-accumulators · CPC title

• H01M2004/027

  Negative electrodes · CPC title

• H01M4/386

  Silicon or alloys based on silicon · CPC title

• H01M4/583

  Carbonaceous material, e.g. graphite-intercalation compounds or CFx · CPC title

• H01M4/587

  for inserting or intercalating light metals · CPC title