IP Library Granted Patent US 10,511,025
Granted Patent B2
US 10,511,025 · App. 15/314,281 · Granted Dec 17, 2019

Electrode manufacturing method

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,511,025
App. No.
15/314,281
Granted
Dec 17, 2019
Kind
B2
Abstract

Disclosed is a method for manufacturing an electrode by forming an electrode mixture layer on a surface of a current collector using an electrode mixture composition containing an aqueous polyimide precursor solution composition and a specific crosslinking agent, the aqueous polyimide precursor solution composition being obtained by dissolving a specific polyamide acid in an aqueous solvent together with a specific imidazole, and subsequently performing heat treatment to remove the solvent and perform an imidization reaction of the polyamide acid. It is preferable that the imidazole is an imidazole selected from the group consisting of 1,2-dimethylimidazole, 2-ethyl-4-methylimidazole, 4-ethyl-2-methylimidazole, and 1-methyl-4-ethylimidazole.

Claims (15)

1. A method for manufacturing an electrode, the method comprising forming an electrode mixture layer on a surface of a current collector using an electrode mixture composition containing at least an electrode active material, an aqueous polyimide precursor solution composition, and a crosslinking agent, the aqueous polyimide precursor solution composition being obtained by dissolving a polyamide acid having a repeating unit represented by a formula (1) below in an aqueous solvent together with an imidazole in an amount of 1.6 moles or more per mole of a tetracarboxylic acid component of the polyamide acid, the imidazole having two or more alkyl groups as substituents, and the crosslinking agent having a carbodiimide group or an oxazoline group; and subsequently performing heat treatment to remove the solvent and perform an imidization reaction of the polyamide acid,

wherein in the formula (1), A comprises at least one tetravalent group selected from the group consisting of tetravalent groups represented by formulae (2), (3), and (4) below, and B comprises (i) at least one divalent group selected from the group consisting of divalent groups represented by formulae (5), (6), (7), and (8) below and divalent saturated hydrocarbon groups having 4 to 10 carbon atoms; and (ii) at least one divalent group selected from the group consisting of divalent groups represented by formulae (9) and (10) below,

wherein in the formula (8), X is any of a direct bond, an oxygen atom, a sulfur atom, a methylene group, a carbonyl group, a sulfoxyl group, a sulfone group, a 1,1′-ethylidene group, a 1,2-ethylidene group, a 2,2′-isopropylidene group, a 2,2′-hexafluoroisopropylidene group, a cyclohexylidene group, a phenylene group, a 1,3-phenylenedimethylene group, a 1,4-phenylenedimethylene group, a 1,3-phenylenediethylidene group, a 1,4-phenylenediethylidene group, a 1,3-phenylenedipropylidene group, a 1,4-phenylenedipropylidene group, a 1,3-phenylenedioxy group, a 1,4-phenylenedioxy group, a biphenylenedioxy group, a methylenediphenoxy group, an ethylidenediphenoxy group, a propylidenediphenoxy group, a hexafluoropropylidenediphenoxy group, an oxydiphenoxy group, a thiodiphenoxy group, and a sulfonediphenoxy group, and

wherein in the formula (10), Y is any of a direct bond, an oxygen atom, a sulfur atom, a methylene group, a carbonyl group, a sulfoxyl group, a sulfone group, a 1,1′-ethylidene group, a 1,2-ethylidene group, a 2,2′-isopropylidene group, a 2,2′-hexafluoroisopropylidene group, a cyclohexylidene group, a phenylene group, a 1,3-phenylenedimethylene group, a 1,4-phenylenedimethylene group, a 1,3-phenylenediethylidene group, a 1,4-phenylenediethylidene group, a 1,3-phenylenedipropylidene group, a 1,4-phenylenedipropylidene group, a 1,3-phenylenedioxy group, a 1,4-phenylenedioxy group, a biphenylenedioxy group, a methylenediphenoxy group, an ethylidenediphenoxy group, a propylidenediphenoxy group, a hexafluoropropylidenediphenoxy group, an oxydiphenoxy group, a thiodiphenoxy group, and a sulfonediphenoxy group.

2. The method for manufacturing an electrode according to claim 1 , wherein the imidazole having two or more alkyl groups as substituents is an imidazole selected from the group consisting of 1,2-dimethylimidazole, 2-ethyl-4-methylimidazole, 4-ethyl-2-methylimidazole, and 1-methyl-4-ethylimidazole.

3. The method for manufacturing an electrode according to claim 1 , wherein the electrode active material is carbon powder, silicon powder, tin powder, or alloy powder containing silicon or tin.

4. The method for manufacturing an electrode according to claim 1 , wherein the electrode active material is a lithium transition metal oxide.

5. The method for manufacturing an electrode according to claim 1 , wherein an electrode for a lithium ion secondary battery is obtained.

6. The method for manufacturing an electrode according to claim 2 , wherein the electrode active material is carbon powder, silicon powder, tin powder, or alloy powder containing silicon or tin.

7. The method for manufacturing an electrode according to claim 2 , wherein the electrode active material is a lithium transition metal oxide.

8. The method for manufacturing an electrode according to claim 2 , wherein an electrode for a lithium ion secondary battery is obtained.

9. The method for manufacturing an electrode according to claim 3 , wherein an electrode for a lithium ion secondary battery is obtained.

10. The method for manufacturing an electrode according to claim 4 , wherein an electrode for a lithium ion secondary battery is obtained.

11. The method for manufacturing an electrode according to claim 6 , wherein an electrode for a lithium ion secondary battery is obtained.

12. The method for manufacturing an electrode according to claim 7 , wherein an electrode for a lithium ion secondary battery is obtained.

Assignments (2)
CHANGE OF NAME Recorded Jul 14, 2023
From: UBE INDUSTRIES, LTD.
To: UBE CORPORATION
Reel/Frame 064275/0021 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 28, 2016
From: NAKAYAMA, TAKESHIGE; NAKAYAMA, TOMONORI; KITAYAMA, NAOKI
To: UBE INDUSTRIES, LTD.
Reel/Frame 040431/0923 →