IP Library Granted Patent US 7,450,293
Granted Patent B2
US 7,450,293 · App. 10/997,483 · Granted Nov 11, 2008

Electrochromic salts, solutions, and devices

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Quick Facts
Patent No.
US 7,450,293
App. No.
10/997,483
Granted
Nov 11, 2008
Kind
B2
Abstract

Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

Claims (42)

1. An electrolyte solution for an electrochromic device, comprising:

(a) a molten salt solvent comprising at least one anion selected from the group consisting of bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide;

(b) at least one reductant soluble in said molten salt solvent, wherein said reductant comprises at least one phenazine; and

(c) at least one oxidant soluble in said molten salt solvent, said oxidant having the chemical formula [A][B] 2

wherein B is selected from the group consisting of bis(perfluoroethylsulfonyl)imide and tris(trifluoromethylsulfonyl)methide and wherein A is a dication having the structural formula

wherein R 1 and R 1 ′ are independently selected from alkyl having 1-20 carbons, aryl, alkyl-substituted aryl having 7-20 carbons, methoxy-substituted aryl having 7-20 carbons, nitro-substituted aryl having 6-20 carbons, cyano-substituted aryl having 7-20 carbons, trifluoromethyl-substituted aryl having 7-20 carbons;

wherein R 2 , R 2′ , R 3 and R 3′ are independently selected from hydrogen, alkyl having 1-20 carbons, aryl, alkyl-substituted aryl having 7-20 carbons, methoxy-substituted aryl having 7-20 carbons, nitro-substituted aryl having 6-20 carbons, cyano-substituted aryl having 7-20 carbons, trifluoromethyl-substituted aryl having 7-20 carbons;

or wherein A is a dication having the structural formula

wherein R 4 and R 4 ′ are independently selected from alkyl having 1-20 carbons; wherein R 5 , R 5′ , R 6 , R 6′ , R 7 , R 7′ , R 8 , and R 8′ are independently selected from hydrogen, alkyl having 1-20 carbons, aryl, alkyl-substituted aryl having 7-20 carbons, methoxy-substituted aryl having 7-20 carbons, nitro-substituted aryl having 6-20 carbons, cyano-substituted aryl having 7-20 carbons, trifluoromethyl-substituted aryl having 7-20 carbons.

2. The electrolyte solution of claim 1 , wherein A is a dication having the structural formula

wherein R 1 ′ is alkyl having 1 to 9 carbons or trimethylphenyl or methoxyphenyl and R 1 is alkyl having 1 to 9 carbons and R 2 ═R 2′ ═R 3 ═R 3 ′=hydrogen; wherein R 1 ═R 1 ′=m-xylyl and R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen; wherein R 1 is phenyl and R 1 ′ is alkyl substituted aryl having 18 carbons and R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen; wherein R 1 R 1 ′=methyl and R 2 is alkyl substituted aryl having 8 or 9 carbons or alkyl having 6 carbons and R 2 ′, R 3 , and R 3 ′ independently selected from the group consisting of hydrogen, alkyl having from 1 to 9 carbons, and alkyl substituted aryl having from 7-20 carbons.

3. The electrolyte solution of claim 1 , wherein R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen and wherein R 1 and R 1′ are independently selected from alkyl having 1-9 carbons, aryl, and alkyl-substituted aryl having 7-20 carbons.

4. The electrolyte solution of claim 1 , wherein R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen and wherein R 1 ═R 1 ′ and are selected from the group consisting of alkyl having 1-9 carbons, aryl, and alkyl-substituted aryl having 7-20.

5. The electrolyte solution of claim 1 , wherein R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen and wherein R 1 ═R 1′ and are selected from methyl and benzyl.

6. The electrolyte solution of claim 1 , wherein said phenazine is selected from the group consisting of 2,5,10-trimethyl-3-phenyl-5,10-dihydrophenazine, 5-ethyl-10-methyl-5,10-dihydrophenazine, 5,10-dimethyl-5,10-dihydrobenzo(A)phenazine, 2,7-diphenoxy-5,10-dimethyl-5,10-dihydrophenazine, 2-phenoxy-5,10-dimethyl-5,10-dihydrophenazine, 2,7-bis(o-tolyl)-5,10-dimethyl-5,10-dihydrophenazine,2,3-dimethyl-7-trifluoromethyl-5,10-diethyl-5,10-dihydrophenazine, 5,10-dimethyl-5,10-dihydrophenazine, 2,3-diphenyl-5,10-dimethyl-5,10-dihydrophenazine, 2,7-diphenyl-5,10-dimethyl-5,10-dihydrophenazine, 2-vinyl-5,10-dimethyl-5,10-dihydrophenazine, 2-phenyl-5,10-dimethyl-5,10-dihydrophenazine, 5,10-diisopropyl-5,10-dihydrophenazine, 5,10-dimethyl-5,10-dihydrodibenzo(A,C)phenazine, 1,5,10-trimethyl-2-phenyl-5,10-dihydrophenazin, 2,3,5,10-tetramethyl-7-trifluoromethyl-5,10-dihydrophenazine, 2,3,5,10-tetramethyl-5,10-dihydrobenzo(B)phenazine, ferrocene, 1,1′-dimethylferrocene, and decamethylferrocene.

7. The electrolyte solution of claim 1 , wherein said electrolyte solution does not include chloride, bromide, iodide, perchlorate, tetrafluoroborate, tetraphenylborate, carboxylate, carbonate, hexafluorophosphate, or hexafluoroantimonate anions.

8. The electrolyte solution of claim 1 , wherein said molten salt comprises cations selected from the group consisting of quarternary ammonium cations.

9. The electrolyte solution of claim 8 , wherein said quarternary ammonium cations comprise pyridinium, pyridazinium, pyrimidinium, pyrazinium, imidazolium, pyrazolium, thiazolium, oxazolium, triazolium, tetraalkylammonium cations, and N-methyl morpholinium cations.

10. The electrolyte solution of claim 9 , wherein said quarternary ammonium cations have the formula (CH 3 CH 2 ) 3 N(R 24 ), wherein R 24 is alkyl having 2-10 carbons; or having the formula (CH 3 ) 2 (CH 3 CHCH 3 )N(R 25 ), wherein R 25 is alkyl having 2-10 carbons; or having the structural formula

wherein R 26 is alkyl having 2-10 carbons;

or having the structural formula

wherein R 27 is alkyl having 2-10 carbons.

11. An electrolyte solution prepared by dissolving at least one reductant and at least one electrochromic ionic compound into a molten salt, wherein reductamt comprises at least one phenazine, said molten salt comprising an anion selected from the group consisting of bis(perfluoroethylsulfonyl)imide and tris(trifluoromethylsulfonyl)methide, said electrochromic compound having the chemical formula

[A][B] 2

wherein B is selected from the group consisting of bis(perfluoroethylsulfonyl)imide and tris(trifluoromethylsulfonyl)methide and wherein A is a dication having the structural formula

wherein R 1 and R 1 ′ are independently selected from alkyl having 1-20 carbons, aryl, alkyl-substituted aryl having 7-20 carbons, methoxy-substituted aryl having 7-20 carbons, nitro-substituted aryl having 6-20 carbons, cyano-substituted aryl having 7-20 carbons, trifluoromethyl-substituted aryl having 7-20 carbons;

wherein R 2 , R 2′ , R 3 and R 3′ are independently selected from hydrogen, alkyl having 1-20 carbons, aryl, alkyl-substituted aryl having 7-20 carbons, methoxy-substituted aryl having 7-20 carbons, nitro-substituted aryl having 6-20 carbons, cyano-substituted aryl having 7-20 carbons, trifluoromethyl-substituted aryl having 7-20 carbons;

or wherein A is a dication having the structural formula

wherein R 4 and R 4 ′ are independently selected from alkyl having 1-20 carbons; wherein R 5 , R 5′ , R 6 , R 6′ , R 7 , R 7′ , R 8 , and R 8′ are independently selected from hydrogen, alkyl having 1-20 carbons, aryl, alkyl-substituted aryl having 7-20 carbons, methoxy-substituted aryl having 7-20 carbons, nitro-substituted aryl having 6-20 carbons, cyano-substituted aryl having 7-20 carbons, trifluoromethyl-substituted aryl having 7-20 carbons.

12. The electrolyte solution of claim 11 , wherein A is a dication having the structural formula

wherein R 1 ′ is alkyl having 1 to 9 carbons or trimethylphenyl or methoxyphenyl and R 1 is alkyl having 1 to 9 carbons and R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen; wherein R 1 ═R 1 ′=m-xylyl and R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen; wherein R 1 is phenyl and R 1 ′ is alkyl substituted aryl having 18 carbons and R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen; wherein R 1 ═R 1 ′=methyl and R 2 is alkyl substituted aryl having 8 or 9 carbons or alkyl having 6 carbons and R 2 ′, R 3 , and R 3 ′ independently selected from the group consisting of hydrogen, alkyl having from 1 to 9 carbons, and alkyl substituted aryl having from 7 to 20 carbons.

13. The electrolyte solution of claim 11 , wherein R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen and wherein R 1 and R 1′ are independently selected from alkyl having 1-9 carbons, aryl, and alkyl-substituted aryl having 7-20 carbons.

14. The electrolyte solution of claim 11 , wherein R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen and wherein R 1 ═R 1′ and are selected from the group consisting of alkyl having 1-9 carbons, aryl, and alkyl-substituted aryl having 7-20 carbons.

15. The electrolyte solution of claim 11 , wherein R 2 ═R 2 ′═R 3 ═R 3 ′=hydrogen and wherein R 1 ═R 1′ and are selected from methyl and benzyl.

16. The electrolyte solution of claim 11 , wherein said molten salt comprises at least one quarternary ammonium cation.

17. The electrolyte solution of claim 16 , wherein said quarternary ammonium cation comprises pyridinium, pyridazinium, pyrimidinium, pyrazinium, imidazolium, pyrazolium, thiazolium, oxazolium, triazolium, tetraalkylammonium cations, and N-methyl morpholinium.

18. The electrolyte solution of claim 17 , wherein said quarternary ammonium cations having the formula (CH 3 CH 2 ) 3 N(R 24 ), wherein R 24 is alkyl having 2-10 carbons; or having the formula (CH 3 ) 2 (CH 3 CHCH 3 )N(R 25 ), wherein R 25 is alkyl having 2-10 carbons; or having the structural formula

wherein R 26 is alkyl having 2-10 carbons;

or having the structural formula

wherein R 27 is alkyl having 2-10 carbons.

19. The electrolyte solution of claim 11 wherein said electrolyte solution does not include chloride anion, bromide anion, iodide anion, perchlorate anion, tetrafluoroborate anion, tetraphenylborate anion, carboxylate anion, carbonate anion, hexafluorophosphate anion, or hexafluoroantimonate anion.

20. The electrolyte solution of claim 11 , wherein said phenazine is selected from the group consisting of N,N,N′,N′-tetramethyl-p-phenylenediamine, 2,5,10-trimethyl-3-phenyl-5,10-dihydrophenazine, 5-ethyl-10-methyl-5,10-dihydrophenazine, 5,10-dimethyl-5,10-dihydrobenzo(A)phenazine, 2,7-diphenoxy-5,10-dimethyl-5,10-dihydrophenazine, 2-phenoxy-5,10-dimethyl-5,10-dihydrophenazine, 2,7-bis(o-tolyl)-5,10-dimethyl-5,10-dihydrophenazine,2,3-dimethyl-7-trifluoromethyl-5,10-diethyl-5,10-dihydrophenazine, 5,10-dimethyl-5,10-dihydrophenazine, 2,3-diphenyl-5,10-dimethyl-5,10-dihydrophenazine, 2,7-diphenyl-5,10-dimethyl-5,10-dihydrophenazine, 2-vinyl-5,10-dimethyl-5,10-dihydrophenazine, 2-phenyl-5,10-dimethyl-5,10-dihydrophenazine, 5,10-diisopropyl-5,10-dihydrophenazine, 5,10-dimethyl-5,10-dihydrodibenzo(A,C)phenazine, 1,5,10-trimethyl-2-phenyl-5,10-dihydrophenazin, 2,3,5,10-tetramethyl-7-trifluoromethyl-5,10-dihydrophenazine, and 2,3,5,10-tetramethyl-5,10-dihydrobenzo(B)phenazine.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2018
From: LOS ALAMOS NATIONAL SECURITY, LLC
To: TRIAD NATIONAL SECURITY, LLC
Reel/Frame 047446/0849 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2006
From: REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE
To: LOS ALAMOS NATIONAL SECURITY, LLC
Reel/Frame 017917/0647 →