IP Library Granted Patent US 11,618,800
Granted Patent B2
US 11,618,800 · App. 17/553,369 · Granted Apr 4, 2023

Composition and method for lamination of silicon dominant electrodes

Inventors: Ambica Nair (Irvine, CA); Giulia Canton (Irvine, CA); Ian Browne (Irvine, CA); Michael Buet (Irvine, CA)
Assignee: Enevate Corporation
C08F277/00H01M4/043H01M4/0404H01M4/0471H01M4/1395H01M4/364H01M4/386H01M4/587H01M4/661H01M4/667H01M4/668H01M2004/027
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Quick Facts
Patent No.
US 11,618,800
App. No.
17/553,369
Granted
Apr 4, 2023
Kind
B2
Abstract

Disclosed are maleic anhydride-grafted cyclic olefin copolymers, methods for preparing maleic anhydride-grafted cyclic olefin copolymers, low temperature methods for laminating anodes comprising the maleic anhydride-grafted cyclic olefin copolymers, and anodes and alkali ion batteries that comprise the maleic anhydride-grafted cyclic olefin copolymers.

Claims (20)

1. A solid film comprising an electrochemically active material and a polymer layer comprising a maleic anhydride-grafted cyclic olefin copolymer.

2. The solid film of claim 1 wherein the electrochemically active material is a silicon dominant material.

3. The solid film according to claim 1 , wherein the polymer layer has a final thickness of about 2 microns to about 5 microns.

4. The solid film according to claim 3 , wherein the polymer layer has a final thickness of about 3 microns.

5. The solid film according to claim 1 , wherein the cyclic olefin copolymer has a structure according to Formula I:

wherein A is a C 5 -C 12 carbocyclic ring, optionally substituted with one or more C1-6 alkyl, C2-6 alkenyl, or aryl groups; and

x and y are integers, wherein the ratio of x:y falls within a range of about 6:1 to about 1.5:1.

6. The solid film according to claim 5 , wherein A is selected from the group consisting of cyclopentyl, tetracyclododecenes, tetracyclododecenes, norbornanes (bicyclo[2.2.1]heptanes), and norbornenes (bicyclo[2.2.1]hept-2-enes).

7. The solid film according to claim 1 , wherein said maleic anhydride-grafted cyclic olefin copolymer is prepared by mixing a solution comprising a cyclic olefin copolymer with a solution of maleic anhydride to form a reaction mixture;

adding a radical initiator to the reaction mixture; and

maintaining the reaction mixture under conditions that allow for the formation of the maleic anhydride-grafted olefin copolymer.

8. The solid film according to claim 7 , wherein the radical initiator is selected from the group consisting of azo compounds and peroxides.

9. The solid film according to claim 8 , wherein the radical initiator is azobisisobutyronitrile (AIBN).

10. The solid film according to claim 7 , wherein the reaction mixture comprises a cyclohexane/toluene solvent system.

11. The solid film according to claim 7 , wherein the conditions that allow for the formation of the maleic anhydride-grafted olefin copolymer comprise heating the reaction mixture to a temperature range of 40° C. to 100° C.

12. The solid film according to claim 11 , wherein the conditions that allow for the formation of the maleic anhydride-grafted olefin copolymer comprise heating the reaction mixture to a temperature range of 50° C. to 60° C.

13. The solid film according to claim 12 , wherein the conditions that allow for the formation of the maleic anhydride-grafted olefin copolymer comprise heating the reaction mixture to a temperature range of about 55° C.

14. The solid film according to claim 7 , wherein the conditions that allow for the formation of the maleic anhydride-grafted olefin copolymer are maintained for about 8 hours to about 20 hours.

15. The solid film according to claim 14 , wherein the conditions that allow for the formation of the maleic anhydride-grafted olefin copolymer are maintained for about 16 hours.

16. The solid film according to claim 7 , wherein the conditions that allow for the formation of the maleic anhydride-grafted olefin copolymer comprise heating the reaction mixture to a temperature range of 50° C. to 60° C. for about 16 hours.

Assignments (1)
SECURITY INTEREST Recorded Mar 10, 2026
From: ENEVATE CORPORATION
To: MCANDREWS, HELD & MALLOY LTD.
Reel/Frame 075093/0935 →
Continuity (2)
Continuation 16548476 · Aug 22, 2019
Related Publication 20220106425A1 · Apr 7, 2022