IP Library Granted Patent US 8,673,503
Granted Patent B2
US 8,673,503 · App. 12/794,261 · Granted Mar 18, 2014

Polyurethane gel electrolytes with improved conductance and/or solvent retention

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Quick Facts
Patent No.
US 8,673,503
App. No.
12/794,261
Granted
Mar 18, 2014
Kind
B2
Abstract

Disclosed are gel electrolytes comprising a polymer, which is a cross-linked polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound; a lithium salt; and a solvent, which is a carbonate solvent, a lactone solvent, or mixtures thereof.

Claims (31)

1. A gel electrolyte comprising:

a polymer in about 20 to about 70 wt %;

a lithium salt in about 1 to about 8 wt. %; and

a solvent comprising a carbonate solvent, a lactone solvent, or a mixture thereof;

wherein the polymer is a polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound, the polymer is sufficiently cross-linked to form a gel in the presence of the solvent, the poly(alkyleneoxide) triol is selected from:

where m, n, and p are selected to form a polymer having molecular weight of about 1,000 to 100,000 g/mol.

2. The gel electrolyte according to claim 1 , wherein the poly(alkyleneoxide) triol comprises glycerin-type poly(alkyleneoxide).

3. The gel electrolyte according to claim 1 , wherein the poly(alkyleneoxide) triol is

where m is selected to form a polymer having molecular weight of about 1,000 to 100,000 g/mol.

4. The gel electrolyte according to claim 1 , wherein the diisocyanate compound is selected from: methylenediphenyl diisocyante (MDI), p-phenylene diisocyante (PPDI), toluene diisocyanate (TDI), o-tolidine diisocyanate (TODD, hexamethylene diisocyanate (HDI), and isophorone diisocyanate (IPDI).

5. The gel electrolyte according to claim 4 , wherein the diisocyanate compound comprises 4,4′-methylenediphenyl diisocyante (MDI).

6. The gel electrolyte according to claim 1 , wherein the polymer is present in about 25-50 wt %.

7. The gel electrolyte according to claim 1 , wherein the polymer is present in about 35 wt %.

8. The gel electrolyte according to claim 1 , wherein the lithium salt comprises lithium perchlorate.

9. The gel electrolyte according to claim 1 , wherein the lithium salt is present in about 3-6 wt %.

10. The gel electrolyte according to claim 1 , wherein the solvent comprises carbonate solvent.

11. The gel electrolyte according to claim 10 , wherein the carbonate solvent comprises dimethyl carbonate, diethyl carbonate, propylene carbonate, ethylene carbonate, vinylene carbonate, or a mixture thereof.

12. The gel electrolyte according to claim 10 , wherein the carbonate solvent comprises propylene carbonate, ethylene carbonate, or a mixture thereof.

13. The gel electrolyte according to claim 1 , wherein the solvent comprises lactone solvent.

14. The gel electrolyte according to claim 13 , wherein the lactone solvent comprises β-propiolactone, γ-butyrolactone, α-methyl-γ-butyrolactone, γ-crotonolactone, δ-valerolactone, γ-valerolactone, γ-caprolactone, ε-caprolactone, or mixtures thereof.

15. The gel electrolyte according to claim 13 , wherein the lactone solvent comprises γ-butyrolactone.

16. The gel electrolyte according to claim 1 , wherein the solvent comprises a mixture of the carbonate solvent and the lactone solvent.

17. The gel electrolyte according to claim 16 , wherein the carbonate solvent comprises propylene carbonate or ethylene carbonate, and the lactone solvent is γ-butyrolactone.

18. A battery comprising:

an anode;

a cathode;

a gel electrolyte between the anode and the cathode where the gel electrolyte includes

a polymer in about 20 to about 70 wt %;

a lithium salt in about 1 to about 8 wt. %; and

a solvent comprising a carbonate solvent, a lactone solvent, or a mixture thereof; wherein the polymer is a polyurethane prepared from a poly(alkyleneoxide) triol and a diisocyanate compound, the polymer is sufficiently cross-linked to form a gel in the presence of the solvent, the poly(alkyleneoxide) triol is selected from:

where m, n, and p are selected to form a polymer having molecular weight of about 1,000 to 100,000 g/mol.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Jul 31, 2019
From: CRESTLINE DIRECT FINANCE, L.P.
To: EMPIRE TECHNOLOGY DEVELOPMENT LLC
Reel/Frame 049924/0794 →
SECURITY INTEREST Recorded Jan 29, 2019
From: EMPIRE TECHNOLOGY DEVELOPMENT LLC
To: CRESTLINE DIRECT FINANCE, L.P.
Reel/Frame 048373/0217 →