IP Library Granted Patent US 11,569,508
Granted Patent B2
US 11,569,508 · App. 15/549,066 · Granted Jan 31, 2023

Binder resin for lithium secondary battery electrode, electrode for lithium secondary battery, and lithium secondary battery

Inventors: Tetsuaki Suzuki (Yokohama, JP); Shuzo Waki (Yokohama, JP); Whan Jin Roh (Seoul, KR); Seung Joon Hong (Seoul, KR)
Assignees: PI R&D CO., LTD.; TOP MATERIAL CO., LTD.
H01M4/622H01M4/0404H01M4/0471H01M4/13H01M4/485H01M4/58H01M10/052Y02T10/70
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Quick Facts
Patent No.
US 11,569,508
App. No.
15/549,066
Granted
Jan 31, 2023
Kind
B2
Abstract

Provided are a binder resin for an electrode of a lithium secondary battery containing a solvent-soluble polyimide having a repeating unit represented by the following Formula [I], and a method of producing the binder resin for an electrode. (In the formula, Z represents an aromatic or alicyclic tetracarboxylic dianhydride residue, and Ar is an aromatic diamine residue having a carboxyl group and an aromatic diamine residue having an aromatic ether bond, or an aromatic diamine residue having a phenylindan structure).

Claims (19)

1. An electrode for a lithium secondary battery, which is formed by applying a mixture material of an active material, a binder resin for an electrode of a lithium secondary battery, said binder resin containing a solvent-soluble polyimide having a repeating unit represented by the following Formula [I]:

wherein in the formula, Z represents an aromatic or alicyclic tetracarboxylic dianhydride residue; and Ar is an aromatic diamine residue having a carboxyl group and an aromatic diamine residue having an aromatic ether bond, or an aromatic diamine residue having a phenylindan-structure, and a conductive material onto a current collector,

wherein the electrode is a negative electrode using a silicon-containing substance as the active material,

wherein in cases where Ar is the aromatic diamine residue having a carboxyl group and the aromatic diamine residue having an aromatic ether bond, the aromatic diamine component having a carboxyl group is from 27% by mole to 50% by mole of a total aromatic diamine component,

wherein the content of the binder resin based on the active material is from 10% by weight to 30% by weight in terms of the weight (solid content) of the polyimide, and

wherein the silicon-containing substance is silicon (Si) or silicon alloy.

2. The electrode according to claim 1 , wherein the content of the binder resin based on the active material is from 15% by weight to 30% by weight in terms of the weight (solid content) of the polyimide.

3. A lithium secondary battery comprising a negative electrode, a positive electrode, a separation membrane, an electrolyte, and an outer packaging material, wherein the positive electrode or the negative electrode is the electrode according to claim 1 .

4. The electrode according to claim 1 , wherein the solvent-soluble polyimide is a block copolymer having a repeating unit represented by the following Formula [II] and a repeating unit represented by the following Formula [III]:

wherein in the formula, Z 1 represents an aromatic or alicyclic tetracarboxylic dianhydride residue, and Ar 1 is an aromatic diamine residue having a carboxyl group

wherein in the formula, Z 2 represents an aromatic or alicyclic tetracarboxylic dianhydride residue and Ar 2 represents an aromatic diamine residue having an aromatic ether bond.

5. The electrode according to claim 1 , said binder resin containing a solvent-soluble polyimide having a repeating unit represented by the following-Formula [IV]:

wherein in the formula, Z 3 represents an aromatic or alicyclic tetracarboxylic dianhydride residue and Ar 3 is an aromatic diamine residue having a phenylindan structure.

6. The electrode according to claim 5 , wherein the solvent-soluble polyimide is a block copolymer comprising a repeating unit represented by the following Formula [III] and a repeating unit represented by the following Formula [IV]:

wherein in the formula, Z 2 represents an aromatic or alicyclic tetracarboxylic dianhydride residue and Ar 2 represents an aromatic diamine residue having an aromatic ether bond:

wherein in the formula, Z 3 represents an aromatic or alicyclic tetracarboxylic dianhydride residue and Ar 3 is an aromatic diamine residue having a phenylindan structure.

7. The electrode according to claim 6 , wherein the aromatic diamine component having a phenylindan structure constituting the solvent-soluble polyimide is from 25% by mole to 90% by mole of the total aromatic diamine component.

8. The electrode according to claim 1 , wherein Z is the aromatic tetracarboxylic dianhydride residue, and the aromatic tetracarboxylic dianhydride for introducing the aromatic tetracarboxylic dianhydride residue is 3,4,3′,4′-biphenyltetracarboxylic acid dianhydride and 4,4′-oxydiphthalic acid dianhydride.

9. The electrode according to claim 1 , wherein the sum of the aromatic diamine component having a carboxyl group and the aromatic diamine component having an aromatic ether bond is 100% by mole among the diamine components.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2023
From: TOP MATERIAL CO., LTD.
To: PI R&D CO., LTD.
Reel/Frame 062535/0421 →
CHANGE OF NAME Recorded Oct 14, 2022
From: TOP BATTERY CO., LTD.
To: TOP MATERIAL CO., LTD.
Reel/Frame 061684/0283 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 7, 2017
From: SUZUKI, TETSUAKI; WAKI, SHUZO; ROH, WHAN JIN; HONG, SEUNG JOON
To: PI R&D CO., LTD.; TOP BATTERY CO., LTD.
Reel/Frame 043219/0060 →
Priority Claims (1)
JP JP2015-021282 · Feb 5, 2015 · national
Continuity (1)
Related Publication 20180034057A1 · Feb 1, 2018