Durable electrooptic devices comprising ionic liquids
View Patent ↗Electrolyte solutions for electrochromic devices such as rear view mirrors and displays with low leakage currents are prepared using inexpensive, low conductivity conductors. Preferred electrolytes include bifunctional redox dyes and molten salt solvents with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF 3 SO 3 − ), bis(trifluoromethylsulfonyl)imide ((CF 3 SO 2 ) 2 N − ), bis(perfluoroethylsulfonyl)imide ((CF 3 CF 2 SO 2 ) 2 N − ) and tris(trifluoromethylsulfonyl)methide ((CF 3 SO 2 ) 3 C − ). Electroluminescent, electrochromic and photoelectrochromic devices with nanostructured electrodes include ionic liquids with bifunctional redox dyes. Some of the electrolyte solutions color to red when devices employing the solutions are powered, leading to red or neutral electrooptic devices.
1. An electrochromic device, comprising:
a first substrate having a transparent conductor coated surface,
a second substrate having a second conductor coated surface,
an electrolyte medium comprising ionic liquid and disposed between said first substrate and said second substrate, the ionic liquid comprising anions,
at least one conductive surface on at least one of said transparent conductor coated surface and said second conductor coated surface, said conductive surface comprising a coating of nanostructured material,
an electrochromic dye attached to said nanostructured material, wherein the anion of the attached dye is same as the anion of the ionic liquid.
2. The device of claim 1 , wherein said electrolyte medium is a solid medium.
3. The device of claim 2 , wherein said solid electrolyte medium comprises a plurality of phases or crosslinked polymer.
4. An electro-optic device, comprising:
at least one chamber, and
an electrolyte medium inside the chamber and comprising a first compound of the formula
wherein Q is R 1′ or a group of the formula
wherein n=1-10, wherein A − and B − are counterions;
wherein R 1 and R 1′ are independently selected from alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, phosphorous acid having 1-20 carbons, boric acid 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 X and Y are independently selected from 0, —C(R 9 )(R 9′ ))— and —C(R 9 )(R 9′ )C(R 10 )(R 10′ ))—;
wherein R 2 , R 3 , R 3′ , R 4 , R 4′ , R 5 , R 5′ , R 6 , R 6′ , R 7 , R 7′ , R 8 , R 9 , R 9′ , R 10 , R 10′ , are independently selected from hydrogen, alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, boric acid having 1-20 carbons, phosphorous acid 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 a compound of the formula
wherein Q is R 1′ or a group of the formula
wherein n=1-10, wherein A − and B − are counterions;
wherein R 1 and R 1′ are independently selected from alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, phosphorous acid having 1-20 carbons, boric acid 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 , R 3′ , are independently selected from hydrogen, alkyl having 1-20 carbons, alkyl carboxylic acid having 1-20 carbons, alkyl phosphorous acid 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 a compound of the formula
wherein Q is R 1′ or a group of the formula
wherein n=1-10, wherein A − and B − are counterions;
wherein R 1 , R 1′ , R 2 , R 2′ , R 3 , R 3′ , R 4 , R 4′ , are independently selected from alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, boric acid having 1-20 carbons, phosphorous acid 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.
5. The electrooptic device of claim 4 , wherein said electrolyte medium comprises a salt.
6. The electrooptic device of claim 5 , wherein said electrolyte medium further comprises at least one additive selected from the group consisting of non-ionic cosolvents, polymers, thixotropic agents, and UV stabilizers.
7. The electrooptic device of claim 5 , wherein said electrolyte medium further comprises a radical cation of said first compound.
8. The electrooptic device of claim 5 , wherein said electrolyte medium further comprises at least a second compound that, in combination with said first compound, produces a neutral color when said electrooptic device is powered.
9. The electrooptic device of claim 8 , wherein said second compound is a viologen.
10. The electrooptic device of claim 5 , wherein said device is a display device.
11. The electrooptic device of claim 4 , wherein said electrolyte medium further comprises a UV stabilizer or an electron acceptor that is covalently attached to said first compound.
12. The electrooptic device of claim 4 , wherein said electrolyte medium comprises an ionic liquid.
13. The electrooptic device of claim 12 , wherein said ionic liquid comprises at least one anion selected from the group consisting of trifluoromethylsulfonate (CF 3 SO 3 − ), bis(trifluoromethylsulfonyl)imide ((CF 3 SO 2 ) 2 N − ), bis(perfluoroethylsulfonyl)imide ((CF 3 CF 2 SO 2 ) 2 N − ) and tris(trifluoromethylsulfonyl)methide ((CF 3 SO 2 ) 3 C − ).
14. An electrochromic device, comprising:
a first electrode comprising a transparent or translucent substrate, an electrically conducting coating on said substrate, and on said electrically conducting coating a nanostructured film comprising a conducting or semiconducting metal oxide having a first redox chromophore adsorbed thereto,
a second electrode comprising a transparent or translucent substrate, an electrically conducting coating on said substrate, and on the coating a nanostructured film comprising a conducting metal oxide having a second redox chromophore adsorbed thereto
an electrolyte between said first electrode and said second electrode,
wherein at least one of said first redox chromophore and said second redox chromophore comprises a compound of the formula
wherein Q is R 1′ or a group of the formula
wherein n=1-10, wherein A − and B − are counterions;
wherein R 1 and R 1′ are independently selected from alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, phosphorous acid having 1-20 carbons, boric acid 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 X and Z are independently selected from O, —C(R 9 )(R 9′ ))— and —C(R 9 )(R 9′ )C(R 10 )(R 10′ ))—;
wherein R 2 , R 3 , R 3′ , R 4 , R 4′ , R 5 , R 5′ , R 6 , R 6′ , R 7 , R 7′ , R 8 , R 9 , R 9′ , R 10 , R 10′ , are independently selected from hydrogen, alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, boric acid having 1-20 carbons, phosphorous acid 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 a compound of the formula
wherein Q is R 1′ or a group of the formula
wherein n=1-10, wherein A − and B − are counterions;
wherein R 1 and R 1′ are independently selected from alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, phosphorous acid having 1-20 carbons, boric acid 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 , R 3′ , are independently selected from hydrogen, alkyl having 1-20 carbons, alkyl carboxylic acid having 1-20 carbons, alkyl phosphorous acid 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 a compound of the formula
wherein Q is R 1′ or a group of the formula
wherein n=1-10, wherein A − and B − are counterions;
wherein R 1 , R 1′ , R 2 , R 2′ , R 3 , R 3′ , R 4 , R 4′ , are independently selected from alkyl having 1-20 carbons, carboxylic acid having 1-20 carbons, boric acid having 1-20 carbons, phosphorous acid 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.
15. An electrooptic device as in claim 14 , wherein at least one of the redox chromophores comprises a metallocene.
16. The electrooptic device of claim 15 , wherein the metallocene comprises a ferrocene or a ferrocene derivative.