Electrochromic thin-film systems and components thereof

• US 6,005,705 A
• Filed: 04/09/1997
• Issued: 12/21/1999
• Est. Priority Date: 04/18/1994
• Status: Expired due to Term

• Current Assignee: Institut für Neue Materialien Gemeinnützige GmbH
• Original Assignee: Institut für Neue Materialien Gemeinnützige GmbH
• Inventors: Krug, Herbert, Berni, Anette, Merl, Norbert, Moses, Anke, Judeinstein, Patrick, Schmidt, Helmut
• Primary Examiner(s): Sugarman, Scott J.
• Assistant Examiner(s): BURKE, MARGARET A
• Application Number:
  US08/722,151
• Time in Patent Office: 986 Days
• Field of Search: 252/519.31, 252/519.33, 528/14, 528/31, 427/226, 427/108, 427/77, 427/58, 427/126.3, 359/265, 359/270, 359/272, 359/273, 359/274, 423/606, 429/188, 429/194
• US Class Current: 359/265
• CPC Class Codes: C08G 77/46 containing polyether sequences
• CPC Class Codes: C08G 77/50 by carbon linkages C08G77/485 takes precedence
• CPC Class Codes: C09K 9/00 Tenebrescent materials, i.e. materials for which the range of wavelengths for energy absorption is changed as a result of excitation by some form of energy
• CPC Class Codes: C23C 18/1216 Metal oxides C23C18/1212 takes precedence
• CPC Class Codes: C23C 26/00 Coating not provided for in groups C23C2/00 - C23C24/00
• CPC Class Codes: G02F 1/1524 Transition metal compounds
• CPC Class Codes: G02F 1/1525 characterised by a particular ion transporting layer, e.g. electrolyte

Abstract

A description is given of electrochromic thin-film systems and their components, especially an improved electrochromic thin-film based on tungsten oxide and/or molybdenum oxide into which alkali metal ions are incorporated, an electrolyte which is improved in particular with respect to its conductivity and is based on pre-hydrolysed, organically modified alkoxysilane and on organic diol (triol), and an improved process for producing a noncolouring ion insertion layer based on cerium oxides and titanium oxides.

Claims

1. A method of preparing an electrochromic oxide layer, which comprises applying to a substrate a coating solution for the electrochromic layer which is prepared by reacting hydrogen peroxide with tungsten or molybdenum or both, wherein, in said coating solution or a precursor thereof or both, an alkali metal hydroxide is dissolved in an overall quantity of from about 0.001 to 1.0 mol of alkali metal per mole of tungsten or molybdenum or both and thermally after-treating the applied layer to form an electrochromic oxide.

2. The method of claim 1, wherein the alkali metal is Li, Na, K or a combination thereof.

3. The method of claim 1, wherein the alkali metal hydroxide is lithium hydroxide.

4. The method of claim 1, wherein the alkali metal hydroxide is employed in an overall quantity of from about 0.01 to 0.5 mol of alkali metal per mole of tungsten or molybdenum or both.

5. The method of claim 1, wherein said coating solution has an alcohol solvent which is liquid at room temperature.

6. The method of claim 1, wherein a concentration of tungsten or molybdenum or both in the coating solution is from about 1 to 50 percent by weight, based on MO₃, wherein M is tungsten or molybdenum or both.

7. The method of claim 1, wherein the coating solution is applied at a temperature of from about 15 to 25°

C. and at a relative atmospheric humidity of from about 5 to 50%.

8. The method of claim 1, wherein the thermal after-treatment is effected at a temperature from about 80 to 400°

C. for from 10 minutes to 2 days.

9. The method of claim 2, wherein the alkali metal is Li, Na or a combination thereof.

10. The method of claim 5, wherein the alcohol has 14 carbon atoms.

11. The method of claim 7, wherein the coating solution is applied by dipping, spraying or spin coating.

12. An electrolyte obtained by

(a) partial hydrolysis and condensation of at least one silane of the general formula

View Dependent Claims (13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29)

13. The electrolyte according to claim 12, wherein in stage (a) from 10 to 90% of all hydrolyzable groups present are eliminated by hydrolysis.

14. The electrolyte according to claim 12, wherein groups X in formulae (I) and (II) are of the formula OR" in which R" is alkyl having 1 to 8 carbon atoms.

15. The electrolyte according to claim 12, wherein at least one of the groups R in formula (I) has an ethylenically unsaturated bond and/or an epoxide ring.

16. The electrolyte according to claim 12, wherein n in formula (I) is 1.

17. The electrolyte according to claim 12, wherein the diol and/or triol which is liquid at room temperature is an alkylene oxide adduct of a diol and/or triol.

18. The electrolyte according to claim 12, wherein the diol which is liquid at room temperature is a poly-C_2-6 -alkylene glycol.

19. The electrolyte according to claim 12, wherein the initiator is selected from the group consisting of organic amines, amino-containing silanes, organoaluminium compounds and aluminum salts which are derived from organic and inorganic acids.

20. The electrolyte according to claim 12, wherein m in the formula (II) is 0 or R'"'"'0 is C_1-4 -alkyl.

21. The electrolyte according to claim 12, wherein the alkali metal salt is a salt of Li, Na or K.

22. The electrolyte according to claim 12, wherein:

(i) from 0.01 to 3.0 mol of diol and/or triol;

(ii) from 0.01 to 2.0 mol of alkali metal salt;

(iii) from 0.01 to 1.0 mol of initiator;

(iv) from 0.01 to 0.3 mol of silane of the formula (II) are employed per mole of silane of the general formula (I).

23. The electrolyte according to claim 12, wherein the acid in stage (c) is employed in a quantity of from 0.01 to 1.5 mol per mole of silane of the formula (I).

24. The electrolyte according to claim 12, wherein the thermal treatment is carried out at from 50 to 150°

C. for from 10 minutes to 48 hours.

25. The electrolyte of claim 14, wherein R" is alkyl having 1-4 carbon atoms.

26. The electrolyte of claim 18, wherein the poly-C_2-6 -alkylene glycol is a polyethylene glycol, a polypropylene glycol or a mixture thereof.

27. The electrolyte of claim 21, wherein the alkali metal salt is a perchlorate.

28. An electrolyte precursor obtained by the process of claim 12 without step (e) and with or without step (c).

29. An electrochromic thin-film system, comprising:

(a) an electrochromic oxide layer,

(b) a noncoloring ion insertion layer, and

(c) an electrolyte located between these layers, wherein component (c) is the electrolyte according to claim 12.