Completely solid electrochromic device, electrochromic bilayer for said device, and method for producing said device

Patent metadata

Field	Value
Publication number	US-9703165-B2
Application number	US-201514867883-A
Country	US
Kind code	B2
Filing date	Sep 28, 2015
Priority date	Dec 15, 2010
Publication date	Jul 11, 2017
Grant date	Jul 11, 2017

Abstract

An all-solid electrochromic device with controlled infrared reflection or emission is provided, in particular of electro-controllable type, comprising a stack successively comprising from a back face ( 3 ) as far as a front face ( 1 ) exposed to infrared radiation ( 2 ): a substrate ( 4 ) made of an electron-conducting material, or a substrate made of a non-electron-conducting material coated with a layer made of an electron-conducting material, forming a first electrode; a layer made of a first proton storage electrochromic material ( 5 ); a layer of a proton-conducting and electron-insulating electrolyte ( 6 ); a bilayer comprising a layer of a non-electrochromic, sub-stoichiometric tungsten oxide WO 3-y forming a second electrode; said tungsten oxide WO 3-y layer being arranged underneath a layer with variable infrared reflection of a second electrochromic material with variable proton intercalation rate, chosen from among crystallized tungsten oxide H x WO 3 -c and hydrated crystallized tungsten oxide H x WO 3 .nH 2 0-c; a protective layer ( 10 ) transparent to infrared radiation.

First claim

The invention claim is:

1. A method of thermally protecting an object, comprising
protectively associating with the object to be protected an all-solid electrochromic device with controlled infrared reflection or emission,
said device comprising a stack, said stack successively comprising from a back face towards a front face exposed to infrared radiation:
a) a substrate made of an electron-conducting material, or a substrate made of a non-electron-conducting material coated with a layer made of an electron-conducting material, said substrate made of an electron-conducting material or said layer made of an electron-conducting material forming a first electrode;
b) a layer made of a first proton storage electrochromic material;
c) a layer of a proton-conducting and electron-insulating electrolyte;
d) a bilayer comprising a layer of a non-electrochromic, sub-stoichiometric tungsten oxide, WO 3-y , where y is comprised between 0.2 and 1, optically absorbent in the infrared, electron-conducting, porous, forming a second electrode; said layer of tungsten oxide WO 3-y being arranged underneath a layer with variable infrared reflection, of a second electrochromic material with variable proton intercalation rate, chosen from among crystallized tungsten oxide H x WO 3 -c where x is comprised between 0 and 1, and hydrated crystallized tungsten oxide H x WO 3 .nH 2 O-c where x is comprised between 0 and 1 and n is an integer of 1 to 2; and
e) a protective layer transparent to infrared radiation, made of an inorganic material.

2. The method according to claim 1 , wherein the object is a satellite.

3. The method according to claim 1 , wherein said substrate is made of an electron-conducting material chosen from among materials having mechanical and chemical resistance to stresses of the external medium and chemically compatible with proton-operation.

4. The method according to claim 3 , wherein said electron-conducting material is chosen from among materials chemically compatible with the first proton storage electrochromic material.

5. The method according to claim 3 , wherein said electron-conducting material is chosen from among metals.

6. The method according to claim 5 , wherein said electron conducting material is chosen from among aluminum, platinum, chromium and the alloys thereof.

7. The method according to claim 1 , wherein said substrate is made of a non-electron-conducting material chosen from among materials having mechanical and chemical resistance to stresses of the external medium and chemically compatible with proton-operation.

8. The method according to claim 7 , wherein said non-electron-conducting material is chosen from among materials chemically compatible with the first proton storage electrochromic material.

9. The method according to claim 7 , wherein said non-electron-conducting material is chosen from among glasses and organic polymers having mechanical and chemical resistance.

10. The method according to claim 9 , wherein the non-electron-conducting material is polyethylene terephthalate (PET).

11. The method according to claim 1 , wherein the layer made of an electron-conducting material is made of an electron-conducting material chosen from among materials having mechanical and chemical resistance against stresses of the external medium, and chemically compatible with proton operation.

12. The method according to claim 11 , wherein said electron-conducting material is chosen from among materials chemically compatible with the first proton storage electrochromic material.

13. The method according to claim 11 , wherein said electron-conducting material is chosen from among metals and electron-conducting metal oxides.

14. The method according to claim 13 , wherein said metals are aluminum, platinum, chromium, and alloys of aluminium, platinum and chromium, and said electron-conducting metal oxides are indium tin oxide and fluorine-doped tin oxide.

15. The method according to claim 1 , wherein the first proton storage electrochromic material is chosen from among proton storage electrochromic materials chemically compatible with proton-operation.

16. The method according to claim 15 , where said first proton storage electrochromic material is chosen from among materials chemically compatible with the proton-conducting and electron-insulating electrolyte.

17. The method according to claim 15 , wherein the first proton storage electrochromic material is chosen from among hydrated metal oxides, and mixtures of two or more of said oxides.

18. The method according to claim 17 , wherein said hydrated metal oxides are amorphous.

19. The method according to claim 17 , wherein the first proton storage electrochromic material is hydrated tungsten oxide H x WO 3 .nH 2 O where x is comprised between 0 and 1 and n is an integer of 1 to 2.

20. The method according to claim 1 , wherein the proton-conducting and electron-insulating electrolyte is chosen from among proton-conducting and electron-insulating electrolytes chemically compatible with proton-operation.

21. The method according to claim 20 , wherein the proton-conducting and electron-insulating electrolyte is chosen from among proton-conducting and electron-insulating electrolytes chemically compatible with/against crystallized tungsten oxide H x WO 3 -c (protonated tungsten oxide) or hydrated crystallized tungsten oxide H x WO 3 .nH 2 O-c.

22. The method according to claim 20 , wherein the proton-conducting and electron-insulating electrolyte is chosen from hydrated metal oxides.

23. The method according to claim 22 , wherein said hydrated metal oxides are amorphous.

24. The method according to claim 23 , wherein said metal oxides are amorphous hydrated tantalum oxide Ta 2 O 5 , amorphous hydrated zirconium oxide and mixtures of two or more of said oxides.

25. The method according to claim 1 , wherein the protective layer transparent to infrared radiation is made of a material chosen from among materials chemically compatible with crystallized tungsten oxide H x WO 3 -c or hydrated crystallized tungsten oxide H x WO 3 .nH 2 O-c.

26. The method according to claim 25 , wherein the protective layer transparent to infrared radiation is made of a material chosen from cerium oxide CeO 2 , yttrium oxide Y 2 O 3 , silica SiO 2 and mixtures of two or more of said metal or metalloid oxides.

27. The method according to claim 1 , wherein the substrate has a thickness of 0.175 mm to 1 mm.

28. The method according to claim 1 , wherein the layer made of an electron-conducting material coating the substrate made of a non-electron-conducting material has a thickness of 50 to 150 nm.

29. The method according to claim 1 , wherein the layer of a first proton storage electrochromic material has a thickness of 0.2 to 1 μm.

30. The method according to claim 1 , wherein the layer made of a proton-conducting and electron-insulating electrolyte has a thickness of 0.2 to 1 μm.

31. The method according to claim 1 , wherein the layer made of tungsten oxide WO 3-y has a thickness of 0.2 to 0.5 μm.

32. The method according to claim 1 , wherein the layer of a second electrochromic material has a thickness of 0.2 to 1 μm.

33. The method according to claim 1 , wherein the protective layer transparent to infrared radiation has a thickne

Assignees

• Commissariat Energie Atomique

Inventors

• Marcel Corinne
• Sabary Frederic
• Marteau Daniel
• Demeaux Julien

Classifications

• B64G1/58

  Thermal protection, e.g. heat shields · CPC title

• G02F1/1525 Primary

  characterised by a particular ion transporting layer, e.g. electrolyte · CPC title

• G02F1/155

  Electrodes · CPC title

• G02F1/15

  based on an electrochromic effect · CPC title

• G02F2001/1552

  Inner electrode, e.g. the electrochromic layer being sandwiched between the inner electrode and the support substrate · CPC title