Single-compartment, self-erasing, solution-phase electrochromic devices, solutions for use therein, and uses thereof

Claim 2

A single-compartment, self-erasing, solution-phase electrochromic device which comprises, as the medium of reversibly variable transmittance to light, a solution which comprises (A) a solvent; (B) at least one cathodic electrochromic compound which, in a voltammogram done in the solvent at room temperature, displays at least two chemically reversible reduction waves, with the first of said reductions accompanied by an increase in molar extinction coefficient at at least one wavelength in the visible range; (C) at least one anodic electrochromic compound which, in a voltammogram done in the solvent at room temperature, displays at least two chemically reversible oxidation waves, with the first of said oxidations accompanied by an increase in molar extinction coefficient at at least one wavelength in the visible range; and (D) if all cathodic and anodic compounds in their zero-potential equilibrium states in the solution are not ionic, an inert current-carrying electrolyte.

Claim 3

A device according to claim 1 wherein, in the solution, (A) the solvent is a liquid at room temperature and selected from propylene carbonate, gamma-butyrolactone, gamma-valerolactone, and any homogeneous mixture that is liquid at room temperature of any two or more of said solvents or any one or more of said solvents with ethylene carbonate; (B) the cathodic compounds are selected from (i) compounds of Formula II ##STR12## wherein R 21 and R 22 are the same or different and are each selected from alkyl of 1 to 10 carbon atoms, phenyl optionally substituted at any one position with chloride, bromide, iodide, cyano, or an alkyl group of 1 to 4 carbon atoms, and benzyl, wherein the phenyl group of the benzyl group is optionally substituted at any one position with chloride, bromide, iodide, cyano or an alkyl group of 1 to 4 carbon atoms; and wherein X 23 - and X 24 - are the same or different and are each selected from chloride, bromide, iodide, BF 4 - , PF 6 - , AsF 6 - , ClO 4 - and NO 3 - ; and (ii) compounds of Formula III ##STR13## wherein R 21 and R 22 are the same or different and are defined as above for the compound of Formula II, R 31 is alkylene of 1 to 10 carbon atoms, and X 31 - , X 32 - , X 33 - and X 34 - are the same or different and are each selected from chloride, bromide, iodide, BF 4 - , PF 6 - , AsF 6 - , ClO 4 - and NO 3 - ; (C) the anodic compounds are selected from (i) compounds of Formula IV ##STR14## wherein R 41 , R 42 , R 43 and R 44 are the same or different and are each selected from hydrogen, alkyl of 1 to 10 carbon atoms, phenyl optionally substituted at any one position with chloride, bromide, iodide, cyano, or an alkyl group of 1 to 4 carbon atoms, and benzyl, wherein the phenyl moiety of the benzyl group is optionally substituted at any one position with chloride, bromide, iodide, cyano, or an alkyl group of 1 to 4 carbon atoms; (iii) compounds of Formula V ##STR15## wherein R 53 is the same as or different from R 55 and both R 53 and R 55 are selected from alkyl of 1 to 10 carbon atoms, phenyl optionally substituted at any one position with chloride, bromide, iodide, cyano, or alkyl of 1 to 4 carbon atoms, or benzyl, optionally substituted at any one position of the phenyl group of the benzyl group with chloride, bromide, iodide, cyano, or alkyl of 1 to 4 carbon atoms; (iii) compounds of Formula VI ##STR16## wherein R 61 , R 62 , R 63 and R 64 are the same or different and are each selected from alkyl of 1 to 10 carbon atoms or phenyl; and R 65 and R 66 are the same or different and are each selected from hydrogen or alkyl of 1 to 10 carbon atoms, provided that both R 65 and R 66 are hydrogen or both are alkyl, and if R 65 and R 66 are both hydrogen, not more than one of R 61 and R 62 is hydrogen and not more than one of R 63 and R 64 is hydrogen; (iv) compounds of Formula VII ##STR17## wherein R 71 is oxygen or sulfur, R 75 is hydrogen or dialylamino, wherein the alkyl groups are the same or different and are each selected from alkyl of 1 to 6 carbon atoms, and R 72 , R 73 and R 74 are the same or different and are each selected from hydrogen, alkyl of 1 to 6 carbon atoms, phenyl, optionally substituted at any one position with an alkyl group of 1 to 6 carbon atoms, and benzyl, optionally substituted at any one position of the phenyl group of the benzyl group with an alkyl group of 1 to 6 carbon atoms; and (v) compounds of Formula VIII ##STR18##

Claim 4

A device according to claim 2 wherein, in the solution, (A) the solvent is propylene carbonate; (B) the solution includes one or two different cathodic compounds, each at a concentration of 0.01 M to 0.1 M in the solution at 25° C. at zero-potential equilibrium, and (C) the solution includes one or two different anodic compounds, each at a concentration of 0.01 M to 0.1 M in the solution at 25° C. at zero-potential equilibrium.

Claim 5

A device according to claim 2 wherein, in the solution, (A) the cathodic compounds are selected from compounds of Formula X ##STR19## wherein R 101 is n-heptyl, phenyl or benzyl and X 101 - is BF 4 - or ClO 4 - ; and the compounds of Formula XI ##STR20## wherein X 112 - is BF 4 - or PF 6 - ; and (B) the anodic compounds are selected from the compounds of Formula XII ##STR21## wherein R 121 is methyl or phenyl; and the compounds of Formula XIII ##STR22## wherein R 131 is methyl or phenyl.

Claim 6

A device according to claim 4 wherein, in the solution,, the cathodic compounds are selected from 1,1'-dibenzyl-4,4'-bipyridinium difluoroborate and tetramethylene bis[4(1-benzylpyridine-4'-yl)pyridinium]tetra(hexafluorophosphate), the anodic compounds are selected from 5,10-dihydro-5,10-dimethylphenazine and N,N,N'N'-tetramethyl-1,4-phenylenediamine, the total concentration of the cathodic compounds is 0.01 M to 0.05 M at 25° C., and the total concentration of the anodic compounds is 0.01 M to 0.05 M at 25° C.

Claim 7

A device according to claim 2 wherein, in the solution, the anodic compound is 5,10-dihydro-5,10-dimethylphenazine.

Claim 8

A device according to claim 4 wherein, in the solution, the anodic compound is 5,10-dihydro-5,10-dimethylphenazine.

Claim 9

A device according to claim 5 wherein, in the solution, the anodic compound is 5,10-dihydro-5,10-dimethylphenazine.

Claim 10

A device according to claim 8 wherein, in the solution, the cathodic compound is 1,1'-dibenzyl-4,4'-bipyridinium difluoroborate.

Claim 13

A device according to claim 10 wherein the solution includes an inert, current-carrying electrolyte, at a concentration of 0.01 M to 1.0 M in the solution at 25° C., selected from an alkali metal salt of Formula M 31 + X 35 - , a tetraalkylammonium salt of Formula M 32 + X 35 - , aluminum chloride, aluminum bromide and any combination of the foregoing salts, wherein M 31 + is potassium, sodium or lithium, M 32 + is tetraalkylammonum wherein the alkyl groups are the same or different and are each selected from alkyl of 1 to 10 carbon atoms, and X 35 - is chloride, bromide, BF 4 - , PF 6 - , AsF 6 - , ClO 4 - or NO 3 - .

Claim 14

A device according to claim 11 wherein the solution includes an inert, current-carrying electrolyte of Formula M + 42 (BF - 4 ), wherein M + 42 is tetra-n-alkylammonium, wherein the n-alkyl groups are the same and are of 1 to 6 carbon atoms.

Claim 15

A device according to claim 12 wherein the solution includes an inert, current-carrying electrolyte of Formula M + 42 (BF - 4 ), wherein M + 42 is tetra-n-alkylammonium, wherein the n-alkyl groups are the same and are of 1 to 6 carbon atoms.

Claim 16

A device according to claim 13 wherein the inert current-carrying electrolyte is tetra-n-butylammonium fluoroborate at a concentration of 0.05 M to 0.5 M at 25° C.

Claim 17

A device according to claim 14 wherein the inert current-carrying electrolyte is tetra-n-butylammonium fluoroborate at a concentration of 0.05 M to 0.5 M at 25° C.