Electrochromic gels and devices containing them

Patent metadata

Field	Value
Publication number	US-2025043135-A1
Application number	US-202218706796-A
Country	US
Kind code	A1
Filing date	Nov 2, 2022
Priority date	Nov 5, 2021
Publication date	Feb 6, 2025
Grant date	—

Abstract

Electrochromic gels that include 20 to 99 wt. % of a polar solvent, 0.5 to 25 wt. % of a rheology modifying agent, and 0.5 to 20 wt. % of an electrochromic material. The rheology modifying agent is soluble in the polar solvent and forms a gel at ambient conditions when dissolved.

First claim

1 . An electrochromic gel comprising:
20 to 99 wt. % of a polar solvent, 0.5 to 25 wt. % of a rheology modifying agent, and 0.5 to 20 wt. % of an electrochromic material; wherein the rheology modifying agent dissolved in the polar solvent forms a thermoreversible gel; and wherein the thermoreversible gel is a gel at 25° C. and is a fluid at 120° C.

2 . The electrochromic gel according to claim 1 , wherein the polar solvent comprises C 1 to C 6 alkyl carbonates, C 1 to C 6 alkyl phosphates, acetone, methyl isobutyl ketone, methyl ethyl ketone, dimethyl formamide, C 1 to C 6 alcohols, water, formamide, and/or dimethyl sulfoxide.

3 . (canceled)

4 . The electrochromic gel according to claim 1 , wherein the rheology modifying agent comprises poly(vinylidene fluoride), poly(vinylidene fluoride-co-hexafluoropropylene), poly(vinyl chloride), poly(vinyl alcohol), poly(methyl (meth)acrylate), poly(ethylene oxide), poly(vinyl pyrrolidone) and/or poly(propylene carbonate).

5 . The electrochromic gel according to claim 1 , wherein the electrochromic material comprises a cathodic electrochromic agent and an anodic electrochromic agent.

6 . The electrochromic gel according to claim 1 , wherein the cathodic electrochromic agent comprises viologen and its derivatives, and the anodic electrochromic agent comprises phenazine, phenazine derivatives, and/or N,N,N′,N′-tetramethyl-p-phenylenediamine.

7 . A method of making the electrochromic gel according to claim 1 comprising
combining the electrochromic material and a portion of the polar solvent by mixing under ambient conditions to form an electrochromic material solution,
combining the rheology modifying agent and a portion of the polar solvent by mixing at a temperature of from 30° C. to 120° C. to form a rheology modifying agent solution,
combining the electrochromic material solution and the rheology modifying agent solution and allowing the combined solution to cool to ambient conditions to form the electrochromic gel; or
applying a first conductor over at least a portion of a first optical substrate,
applying a second conductor over at least a portion of the first optical substrate such that the second conductor is not in direct contact with the first conductor, and
applying a coating layer comprising an electrochromic gel according to claim 1 over at least a portion of the first optical substrate and optionally over at least a portion of a second optical substrate, wherein the coating layer is in contact with the first conductor and the second conductor; or
applying a first conductor over at least a portion of a first optical substrate,
applying a coating layer comprising an electrochromic gel according to claim 1 over at least a portion of the first optical substrate and in contact with the first conductor,
optionally applying a coating layer comprising an electrochromic gel according to claim 1 over at least a portion of a second optical substrate,
applying a second conductor over at least a portion of the second optical substrate, and
applying the second optical substrate over the first optical substrate, first conductor, and electrochromic gel, such that the second conductor is not in direct contact with the first conductor.

8 . (canceled)

9 . The method of making an electrochromic cell according to claim 1 comprising applying a second optical substrate over the first conductor, the second conductor and electrochromic gel.

10 . (canceled)

11 . The method according to claim 7 , wherein the first and second optical substrates are optically clear substrates and the first optically clear substrate and the second optically clear substrate each independently comprise glass, flexible polymeric materials and rigid polymeric materials selected from poly (methyl methacrylate), polycarbonate, polyethylene terephthalate, poly (allyl diglycol carbonate), polyurea, polyurethane, polythiourea, and/or polythiourethane; and/or
wherein one or both of the first conductor and second conductor are independently transparent conductors; and/or wherein the first conductor and second conductor independently comprise indium tin oxide, fluorine-doped tin oxide, partially octadecyltrichlorsilane covered indium tin oxide, metal mesh, silver nanowires, aluminium doped zinc oxide (AZO), carbon nanotubes, graphene and/or conductive polymers; and/or wherein the coating layer comprising an electrochromic gel is applied using a method comprising draw down, screen printing, spin coating, spray application, cut and stick, extrusion, casting, ink jet, gravure, and/or roll to roll.

12 . (canceled)

13 . (canceled)

14 . (canceled)

15 . The method according to claim 1 , wherein the coating layer has a thickness of from 0.1 to 12 mil; and
wherein the thickness of the coating layer that includes the electrochromic gel controls the space between the first substrate and second substrates.

16 . (canceled)

17 . The method according to claim 7 , wherein the visible light transmittance through the electrochromic cell in the clear state is from 50% to 99% measured using a Hunter UltraScan PRO at visible spectrum wavelengths between 380 nm and 780 nm.

18 . The method according to claim 7 , wherein the visible light transmittance through the electrochromic cell in the dark state is from 0.00001 to 50%, measured according to ASTM E972 at visible spectrum wavelengths between 380 nm and 780 nm; and/or
wherein the haze in the electrochromic cell in the clear state is from 0.05% to 10% measured using a spectrophotometer or Hunter UltraScan PRO at visible spectrum wavelengths between 380 nm and 780 nm at 25° C.

19 . (canceled)

20 . The method according to claim 7 , wherein the electrochromic cell transitions to a fully darkened state, upon application of a voltage, in from 0.1 seconds to 30 minutes measured using a spectrophotometer or Hunter UltraScan PRO at visible spectrum wavelengths between 380 nm and 780 nm at 25° C.

21 . An electrochromic device comprising the cell made according to a method according to claim 7 , wherein the electrochromic cell transitions to a fully clear state, upon reduction and/or removal and/or reversal of a voltage, in from 0.1 seconds to 60 minutes, measured using a spectrophotometer or a Hunter UltraScan PRO at visible spectrum wavelengths between 380 nm and 780 nm at 25° C.

22 . (canceled)

23 . The electrochromic device according to claim 21 comprising
a first optical substrate comprising,
a first conductor,
a second conductor not in direct contact with the first conductor, and
a coating layer comprising an electrochromic gel according to any of claims 1 through 7 disposed over and in contact with the first conductor and the second conductor; and

a power source;
and optionally a second optical substrate
wherein the first and/or second optical substrates are optically clear substrates.

24 . (canceled)

25 . (canceled)

26 . The electrochromic device according to claim 23 , wherein the first optical substrate and the second optical substrate comprise glass, flexible polymeric materials and rigid polymeric materials, poly (methyl methacrylate), polycarbonate, polyethylene terephthalate, poly (allyl diglycol carbonate), polyurea, polyurethane, poly-thiourea, and/or poly-thiouethane;
wherein one or both of the first conductor and second conductor are transparent conductors.

27 .

Assignees

• Ppg Ind Ohio Inc

Inventors

• Valdisera Kevin Mark
• Duarte Nicolas Benjamin
• Gonzalez Arellano David Leonardo
• Thakare Dhawal Rajendra

Classifications

• G02F1/155

  Electrodes · CPC title

• G02F1/1341

  Filling or closing of cells · CPC title

• C09K2211/1018

  Heterocyclic compounds · CPC title

• C09K9/02 Primary

  Organic tenebrescent materials · CPC title

• C09D127/16

  Homopolymers or copolymers of vinylidene fluoride · CPC title