Color tuning of electrochromic devices using an organic dye

• US 10,323,178 B2
• Filed: 05/14/2015
• Issued: 06/18/2019
• Est. Priority Date: 05/16/2014
• Status: Active Grant

• Current Assignee: University of Connecticut (State of Connecticut)
• Original Assignee: University of Connecticut (State of Connecticut)
• Inventors: Sotzing, Gregory Allen, Invernale, Michael A.
• Primary Examiner(s): Deherrera, Kristina M
• Application Number:
  US14/712,389
• Publication Number:
  US 20150331293A1
• Time in Patent Office: 1,496 Days
• Field of Search: 359273, 359265, 351 44, 35115939, 257 40, 252500
• CPC Class Codes: C09K 2211/1458 containing sulfur as the only heteroatom
• CPC Class Codes: C09K 2211/1466 containing nitrogen as the only heteroatom
• CPC Class Codes: C09K 2211/1491 containing other combinations of heteroatoms
• CPC Class Codes: C09K 9/02 Organic tenebrescent materials
• CPC Class Codes: C25B 3/00 Electrolytic production of organic compounds
• CPC Class Codes: G02F 1/0018 Electro-optical materials
• CPC Class Codes: G02F 1/15 based on an electrochromic effect
• CPC Class Codes: G02F 1/15165 Polymers
• CPC Class Codes: G02F 2001/164 the electrolyte is made of polymers

Abstract

Disclosed is a method to color tune an electrochromic device by the use of a standard dye. By following the “subtractive color mixing” theory and selecting the appropriate standard dye to compliment or accentuate the electrochromic material, tuning of the optical and colorimetric properties of the resulting electrochromic device can be achieved. The method can also be used to prepare electrochromic devices that will switch between two neutral colors.

Claims

1. An electrochromic device, comprising:

an electrochromic material and a standard dye disposed between at least two electrodes, or an electrochromic material disposed between at least two electrodes and a standard dye external to the at least two electrodes,

wherein the electrochromic material is a conjugated polymer, an inorganic electrochromic material, or an oligomeric electrochromic material, and

wherein the standard dye

is a solvent dye,

does not undergo redox (reduction or oxidation) processes within the potential window for operation of the electrochromic device, and

does not react with the electrochromic material.

2. The device of claim 1, wherein the electrochromic material is an electrodeposited conjugated polymer, a solvent cast conjugated polymer, or an in situ formed conjugated polymer.

3. The device of claim 1, wherein the device is a solid state electrochromic device or a liquid state electrochromic device.

4. The device of claim 1, wherein the standard dye is Solvent Yellow 1, Solvent yellow 114, Solvent Yellow 14, Solvent Yellow 16, Solvent yellow 163, Solvent yellow 176, Solvent Yellow 18, Solvent Yellow 2, Solvent Yellow 21, Solvent Yellow 3, Solvent Yellow 33, Solvent Yellow 34, Solvent Yellow 56, Solvent Yellow 62, Solvent Yellow 7, Solvent Yellow 72, Solvent Yellow 82, Solvent Yellow 93, Solvent yellow 98, Solvent Black 27, Solvent Black 29, Solvent Black 45, Solvent blue 104, Solvent blue 122, Solvent blue 35, Solvent blue 36, Solvent Blue 4, Solvent blue 59, Solvent blue 78, Solvent blue 97, Solvent Brown 1, Solvent Brown 2, Solvent Brown 3, Solvent Brown 4, Solvent Brown 5, Solvent green 28, Solvent Green 3, Solvent green 5, Solvent Green 7, Solvent orange 107, Solvent Orange 3, Solvent orange 60, Solvent Orange 62, Solvent orange 63, Solvent Orange 7, Solvent Orange 99, Solvent Red 1, Solvent Red 111, Solvent Red 122, Solvent Red 132, Solvent red 135, Solvent red 149, Solvent Red 168, Solvent red 179, Solvent red 196, Solvent red 197, Solvent red 207, Solvent Red 23, Solvent Red 24, Solvent red 242, Solvent red 27, Solvent Red 4, Solvent Red 49, Solvent Red 52, Solvent Red 8, Solvent Red 91, Solvent violet 13, Solvent Violet 14, Solvent violet 31, Solvent violet 36, Solvent Violet 58, Solvent violet 59, Solvent Violet 8, Solvent Violet 9, or a combination thereof.

5. A method of forming the electrochromic device of claim 1, comprising

placing a standard dye and an electrochromic material or electrochromic material precursor between at least two electrodes to form the electrochromic device.

6. A method of color tuning the electrochromic device of claim 1, comprising

selecting an electrochromic material;

selecting a standard dye that appropriately compliments or accentuates the electrochromic material in the bleached state, the colored state, or both; and

forming an electrochromic device comprising a combination of the electrochromic material and the standard dye disposed between at least two electrodes.

7. The electrochromic device of claim 1, wherein the standard dye appropriately compliments or accentuates the electrochromic material in the bleached state, the colored state, or both.

8. A method of forming a solid-state electrochromic device, comprising:

applying voltage to a device comprising at least two electrodes,

a combination of a crosslinked gel electrolyte composition, an electroactive monomer, and a standard dye, the combination disposed between the at least two electrodes, and

a potential source in electrical connection with the at least two electrodes;

wherein the applying voltage polymerizes the electroactive monomer to form a composite comprising conjugated polymer, standard dye, and crosslinked gel electrolyte composition;

and

wherein the standard dye is a solvent dye,

is soluble in a gel electrolyte precursor solvent used to prepare the crosslinked gel electrolyte composition,

does not undergo redox (reduction or oxidation) processes within the potential window for operation of the electrochromic device,

does not react with the conjugated polymer when oxidized, reduced, or neutral, and optionally appropriately compliments or accentuates the conjugated polymer in the bleached state, the colored state, or both.

9. The method of claim 8, further comprising tuning the electrochromic device to a neutral color transition by

determining molar absorptivity of the standard dye in the gel electrolyte precursor solvent;

determining molar absorptivity of the conjugated polymer; and

selecting a concentration of the standard dye in the gel electrolyte precursor solvent that balances the standard dye'"'"'s absorbance intensity with the conjugated polymer'"'"'s absorbance intensity.

10. The method of claim 8, wherein the standard dye is Solvent Yellow 1, Solvent yellow 114, Solvent Yellow 14, Solvent Yellow 16, Solvent yellow 163, Solvent yellow 176, Solvent Yellow 18, Solvent Yellow 2, Solvent Yellow 21, Solvent Yellow 3, Solvent Yellow 33, Solvent Yellow 34, Solvent Yellow 56, Solvent Yellow 62, Solvent Yellow 7, Solvent Yellow 72, Solvent Yellow 82, Solvent Yellow 93, Solvent yellow 98, Solvent Black 27, Solvent Black 29, Solvent Black 45, Solvent blue 104, Solvent blue 122, Solvent blue 35, Solvent blue 36, Solvent Blue 4, Solvent blue 59, Solvent blue 78, Solvent blue 97, Solvent Brown 1, Solvent Brown 2, Solvent Brown 3, Solvent Brown 4, Solvent Brown 5, Solvent green 28, Solvent Green 3, Solvent green 5, Solvent Green 7, Solvent orange 107, Solvent Orange 3, Solvent orange 60, Solvent Orange 62, Solvent orange 63, Solvent Orange 7, Solvent Orange 99, Solvent Red 1, Solvent Red 111, Solvent Red 122, Solvent Red 132, Solvent red 135, Solvent red 149, Solvent Red 168, Solvent red 179, Solvent red 196, Solvent red 197, Solvent red 207, Solvent Red 23, Solvent Red 24, Solvent red 242, Solvent red 27, Solvent Red 4, Solvent Red 49, Solvent Red 52, Solvent Red 8, Solvent Red 91, Solvent violet 13, Solvent Violet 14, Solvent violet 31, Solvent violet 36, Solvent Violet 58, Solvent violet 59, Solvent Violet 8, Solvent Violet 9, or a combination thereof.

11. The method of claim 8, wherein the device exhibits a neutral color transition.

12. The method of claim 8, wherein the electroactive monomer is thiophene, substituted thiophene, carbazole, 3,4-ethylenedioxythiophene, thieno[3,4-b]thiophene, substituted thieno[3,4-b]thiophene, dithieno[3,4-b:

3′

,4′

-d]thiophene, thieno[3,4-b]furan, substituted thieno[3,4-b]furan, bithiophene, substituted bithiophene, pyrrole, substituted pyrrole, acetylene, phenylene, substituted phenylene, naphthalene, substituted naphthalene, biphenyl and terphenyl and their substituted versions, phenylene vinylene (e.g., p-phenylene vinylene), substituted phenylene vinylene, aniline, substituted aniline, indole, substituted indole, or a combination thereof.

13. The method of claim 8, wherein the electroactive monomer is

14. The method of claim 8, wherein the crosslinked gel electrolyte composition comprises a lithium, sodium, or potassium salt, or an ionic liquid.

15. The method of claim 8, wherein the crosslinked gel electrolyte is formed by crosslinking a gel electrolyte precursor in the presence of the electroactive monomer and the standard dye to form a layer of crosslinked gel electrolyte comprising the electroactive monomer and the standard dye.

16. The method of claim 8, wherein the crosslinked gel electrolyte is prepared from a gel electrolyte precursor mixture comprising a gel electrolyte precursor, a solvent, and a salt or ionic liquid.

17. A solid-state electrochromic device prepared according to the method of claim 8.

18. A solid-state electrochromic device, comprising:

at least two electrodes; and

a composite disposed between the at least two electrodes, the composite comprising a conjugated polymer, a standard dye, and a crosslinked gel electrolyte composition;

wherein the composite is formed by in situ polymerization of an electroactive monomer in a combination comprising the crosslinked gel electrolyte composition, the standard dye, and the electroactive monomer, wherein the conjugated polymer is not formed as a discrete film; and

wherein the standard dye is a solvent dye,

is soluble in a gel electrolyte precursor solvent used to prepare the crosslinked gel electrolyte composition,

does not undergo redox (reduction or oxidation) processes within the potential window for operation of the electrochromic device,

does not react with the conjugated polymer when oxidized, reduced, or neutral, and

optionally appropriately compliments or accentuates the conjugated polymer in the bleached state, the colored state, or both.

19. The device of claim 18, wherein the device exhibits a neutral color transition.

20. The device of claim 18, wherein the standard dye is a quinoline dye.

21. The device of claim 18, wherein the standard dye is CI Yellow 114.

22. The device of claim 18, wherein the electroactive monomer is thiophene, substituted thiophene, carbazole, 3,4-ethylenedioxythiophene, thieno[3,4-b]thiophene, substituted thieno[3,4-b]thiophene, dithieno[3,4-b:

3′

,4′

-d]thiophene, thieno[3,4-b]furan, substituted thieno[3,4-b]furan, bithiophene, substituted bithiophene, pyrrole, substituted pyrrole, acetylene, phenylene, substituted phenylene, naphthalene, substituted naphthalene, biphenyl and terphenyl and their substituted versions, phenylene vinylene (e.g., p-phenylene vinylene), substituted phenylene vinylene, aniline, substituted aniline, indole, substituted indole, or a combination thereof.

23. The device of claim 18, wherein the electroactive monomer is

24. The device of claim 18, wherein the crosslinked gel electrolyte composition comprises a lithium, sodium, or potassium salt, or an ionic liquid.

25. The device of claim 18, wherein the crosslinked gel electrolyte is formed by crosslinking a gel electrolyte precursor in the presence of the electroactive monomer and the standard dye to form a layer of crosslinked gel electrolyte comprising the electroactive monomer and the standard dye.

26. The device of claim 18, wherein the crosslinked gel electrolyte is prepared from a gel electrolyte precursor mixture comprising a gel electrolyte precursor, a solvent, and a salt or ionic liquid.