IP Library Granted Patent US 12,633,540
Granted Patent B2
US 12,633,540 · App. 18/138,742 · Granted May 19, 2026

Negative electrode active material and preparation method thereof

Inventors: Baida Deng (Ningde, CN); Meng Kang (Ningde, CN); Chen Zeng (Ningde, CN); Libing He (Ningde, CN)
Assignee: CONTEMPORARY AMPEREX TECHNOLOGY (HONG KONG) LIMITED
H01M4/583C01B32/20C01B32/21C01B32/23H01M4/364H01M4/587H01M2004/027
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Quick Facts
Patent No.
US 12,633,540
App. No.
18/138,742
Granted
May 19, 2026
Kind
B2
Abstract

This application provides a negative electrode active material and a preparation method thereof. The negative electrode active material may be self-embedded graphite composed of graphite A and graphite B, where the surface of the graphite A may have a tenon structure, the surface of the graphite B may have a mortise structure, the tenon structure of the graphite A and the mortise structure of the graphite B may be mutually embedded, and a hydrogen bond may be formed between the tenon structure of the graphite A and the mortise structure of the graphite B.

Claims (52)

1 . A negative electrode active material, wherein

the negative electrode active material is self-embedded graphite composed of graphite A and graphite B;

a surface of the graphite A has a tenon structure, and a surface of the graphite B has a mortise structure; and

the tenon structure of the graphite A and the mortise structure of the graphite B are mutually embedded, and a hydrogen bond is formed between the tenon structure of the graphite A and the mortise structure of the graphite B.

2 . The negative electrode active material according to claim 1 , wherein

the tenon structure of the graphite A is formed by an oxygen-containing metal salt, and a contact angle between the graphite A and a blank electrolyte is less than or equal to 20°; and

the blank electrolyte is formed by dissolving lithium hexafluorophosphate at a concentration of 1 mol/L in a solvent that is formed by mixing ethylene carbonate and dimethyl carbonate at a mass ratio of 1:1.

3 . The negative electrode active material according to claim 2 , wherein

the surface of the mortise structure of the graphite B has a hydroxyl group, and a contact angle between the graphite B and the blank electrolyte is less than or equal to 15°.

4 . The negative electrode active material according to claim 2 , wherein

the oxygen-containing metal salt is an oxygen-containing lithium metal salt or an oxygen-containing sodium metal salt, and is selected from at least one of lithium metaaluminate, lithium metazincate, sodium metaaluminate, or sodium metazincate.

5 . The negative electrode active material according to claim 1 , wherein

a contact angle between the self-embedded graphite and a blank electrolyte is less than or equal to 15°; and

the blank electrolyte is formed by dissolving lithium hexafluorophosphate at the concentration of 1 mol/L in the solvent that is formed by mixing ethylene carbonate and dimethyl carbonate at the mass ratio of 1:1.

6 . A preparation method of negative electrode active material, comprising the following steps:

(1) adding a first graphite matrix into a polar solvent, then adding a raw material for preparing an oxygen-containing metal salt to make an amount of the oxygen-containing metal salt coating a surface of the first graphite matrix be 1-5 wt % of a weight of the first graphite matrix, followed by stirring, evaporation, and drying, and then calcining the resulting mixture in a nitrogen atmosphere at a temperature of 500-1200° C. for 8-24 hours to obtain graphite A having a tenon structure;

(2) adding a second graphite matrix into an alkaline solution having a pH greater than or equal to 13, stirring at a constant temperature of 60-100° C. for 8-36 hours, and after filtering, cleaning, and drying the resulting product to obtain graphite B having a mortise structure; and

(3) mixing the graphite A and the graphite B to obtain a negative electrode active material.

7 . The preparation method according to claim 6 , wherein

the first graphite matrix and the second graphite matrix are different from each other.

8 . The preparation method according to claim 6 , wherein

the first graphite matrix and the second graphite matrix are the same or different artificial graphite.

9 . The preparation method according to claim 6 , wherein

the raw material for preparing the oxygen-containing metal salt comprises:

(1) any one of lithium nitrate, sodium nitrate, and potassium nitrate; and

(2) at least one of aluminum nitrate, zinc nitrate, or ferric nitrate.

10 . The preparation method according to claim 6 , wherein

D v 50 of the first graphite matrix and the second graphite matrix each satisfy the following condition:

3.0 μm≤ D v 50≤15.0 μm.

11 . The preparation method according to claim 6 , wherein

D v 50, D v 90, and D v 10 of the first graphite matrix and the second graphite matrix each satisfy the following condition:

1.0≤( D+ 90− D v 50)/ D v 50≤2.0.

12 . The preparation method according to claim 6 , wherein

length-diameter ratios D L /D W of the first graphite matrix and the second graphite matrix each satisfy the following condition:

1.0≤ D L /D w ≤2.5.

13 . The preparation method according to claim 6 , wherein

the oxygen-containing metal salt is an oxygen-containing lithium metal salt or an oxygen-containing sodium metal salt, and is selected from at least one of lithium metaaluminate, lithium metazincate, sodium metaaluminate, or sodium metazincate.

14 . The preparation method according to claim 6 , wherein

in step (1), the contact angle between the obtained graphite A and a blank electrolyte is less than or equal to 20°;

in step (2), the contact angle between the obtained graphite B and the blank electrolyte is less than or equal to 15°; and

the blank electrolyte is formed by dissolving lithium hexafluorophosphate at a concentration of 1 mol/L in a solvent that is formed by mixing ethylene carbonate and dimethyl carbonate at a mass ratio of 1:1.

15 . The preparation method according to claim 6 , wherein

the obtained negative electrode active material is self-embedded graphite composed of the graphite A and the graphite B, the tenon structure of the graphite A and the mortise structure of the graphite B are mutually embedded, and a hydrogen bond is formed between the tenon structure of the graphite A and the mortise structure of the graphite B.

16 . The preparation method according to claim 15 , wherein

a contact angle between the self-embedded graphite and a blank electrolyte is less than or equal to 15°; and

the blank electrolyte is formed by dissolving lithium hexafluorophosphate at the concentration of 1 mol/L in the solvent that is formed by mixing ethylene carbonate and dimethyl carbonate at the mass ratio of 1:1.

17 . A negative electrode plate, wherein

the negative electrode plate comprises a negative electrode active material layer, and the negative electrode active material layer comprises the negative electrode active material according to claim 1 .

18 . The negative electrode plate according to claim 17 , wherein

the negative electrode active material layer further comprises a binder, and relative to a weight of the negative electrode active material layer, a proportion of the binder is more than 1.3 wt % and less than 2.0 wt %.

19 . A secondary battery, wherein the secondary battery comprises the negative electrode plate according to claim 17 .

20 . An electric apparatus, wherein the electric apparatus comprises the secondary battery according to claim 19 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 6, 2024
From: CONTEMPORARY AMPEREX TECHNOLOGY CO., LIMITED
To: CONTEMPORARY AMPEREX TECHNOLOGY (HONG KONG) LIMITED
Reel/Frame 068338/0402 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2023
From: DENG, BAIDA; KANG, MENG; ZENG, CHEN; HE, LIBING
To: CONTEMPORARY AMPEREX TECHNOLOGY CO., LIMITED
Reel/Frame 063425/0948 →
Continuity (2)
Continuation PCTCN2022070617 · Jan 7, 2022
Related Publication 20230268505A1 · Aug 24, 2023
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