Complementary surface confined polmer electrochromic materials, systems, and methods of fabrication therefor

• US 5,818,636 A
• Filed: 06/07/1995
• Issued: 10/06/1998
• Est. Priority Date: 02/26/1990
• Status: Expired due to Fees

• Current Assignee: BioVeris Corporation (Roche Holding AG)
• Original Assignee: Molecular Displays, Inc.
• Inventors: Leventis, Nicholas, Chung, Young C.
• Primary Examiner(s): Sugarman, Scott J.
• Assistant Examiner(s): BEY, DAWN MARIE
• Application Number:
  US08/480,078
• Time in Patent Office: 1,217 Days
• Field of Search: 359/265, 359/273, 359/275, 359/277
• US Class Current: 359/273
• CPC Class Codes: C09K 9/02 Organic tenebrescent materials
• CPC Class Codes: G02F 1/1503 caused by oxidation-reduction reactions in organic liquid solutions, e.g. viologen solutions
• CPC Class Codes: G02F 1/15165 Polymers
• CPC Class Codes: G02F 1/1524 Transition metal compounds
• CPC Class Codes: G02F 2001/1517 Cyano complex compounds, e.g. Prussian blue
• CPC Class Codes: G02F 2001/1555 Counter electrode

Abstract

Electrochromic device having electrode surface confined complementary polymer electrochromic materials, and materials, systems and methods of fabrication therefore. The electrochromic devices employ a polypyrrole-prussian blue composite material on the oxiatively coloring electrode, and a heteroaromatic substance containing at least one quaternized nitrogen atom group on the reductively coloring electrode. A bilayer material consisting substantially of metallic oxide which is conductive in at least one of its redox states and electroplated with a polymer is also disclosed for use as an electrochromic material on either the oxidatively colored or reductively colored electrodes. A method for electrodeposition of viologen polymers at a substantially neutral pH is also disclosed. A method for self-powering and self-modulating electrochromic devices by means of photovoltaic cells is also disclosed.

Claims

1. An electrochromic device comprising at least one substrate having a layer of an electrochromic metallic oxide thereon, and a layer of strongly adhered, electrode surface confined polymeric electrochromic material having a thickness of at least 2,000 Angstroms.

2. The device defined in claim 1, wherein said polymeric electrochromic material is a heteroaromatic substance containing at least one quaternized nitrogen atom group.

3. The device of claim 2, wherein said heteroaromatic substance is taken from the group of 4,4'"'"'-bipyridine, 2,2'"'"'-bipyridine, 4,9-diazafluorene and 3,7-diazafluorene.

4. The device of claim 2, wherein said heteroaromatic substance is a fused aromatic ring polyaromatic substance.

5. The device defined in claim 4, wherein said fused aromatic ring polyaromatic substance is taken from the group of 1,10-phenanthroline, 1,7-phenanthroline, 4,7-phenanthroline, 3,8-phenanthroline, 2,7-diazapyrene, and 2,9-diazaperopyrene.

6. The device of claim 1, wherein said confined polymeric electrochromic material includes at least one cross-linker derived from a trialkoxysilyl group.

7. The device of claim 6, wherein the confined polymeric electrochromic material is derived from N, N'"'"'-bis p-(trimethoxysilyl) benzyl!-4,4'"'"'-bipyridinium dichloride, N, N'"'"'-bis 3-(trimethoxysilyl)propyl!-4,4'"'"'-bipyridinium dibromide, N, N'"'"'-bis p-(trimethoxysilyl) benzyl!-2,7-diazapyrenium dichloride or N, N'"'"'-bis 3-(trimethoxysilyl)propyl!-2,7-diazapyrenium dibromide.

8. The device of claim 7, wherein said electrochromic metallic oxide is able to change from a substantially colorless state to a colored stated upon reduction and includes as a constituent a metal taken from the group of tungsten, molybdenum, niobium, vanadium and titanium.

9. The device of claim 8, wherein said electrochromic metallic oxide is tungsten trioxide.

10. A method for surface confining electrochromic materials in multiple layers onto a conductive substrate, comprising the steps of depositing a layer of an electrochromic metallic oxide which is conductive in at least one of its redox states onto said conductive substrate, and then electrodepositing a polymeric electrochromic material onto said metallic oxide layer in an ionically conductive solution.

11. The method of claim 10, wherein said electrochromic metallic oxide is deposited by sputtering.

12. The method of claim 10, wherein said electrochromic metallic oxide is able to change from a substantially colorless state to a colored state upon reduction and includes as a constituent a metal taken from the group of tungsten, molybdenum, niobium, vanadium and titanium.

13. The method of claim 12, wherein said electrochromic metallic oxide is tungsten trioxide.

14. The method of claim 10, wherein said polymeric electrochromic material is a heteroaromatic substance containing at least one quaternized nitrogen atom group.

15. The method of claim 14, wherein said heteroaromatic substance is taken from the group of 4,4'"'"'-bipyridine, 2,2'"'"'-bipyridine, 4,9-diazafluorene and 3,7-diazafluorene.

16. The method of claim 14, wherein said heteroaromatic substance is a fused aromatic ring polyaromatic substance.

17. The method of claim 16, wherein said fused aromatic ring polyaromatic substance is taken from the group of 1,10-phenanthroline, 1,7-phenanthroline, 4,7-phenanthroline, 3,8-phenanthroline, 2,7-diazapyrene, and 2,9-diazaperopyrene.

18. The method of claim 14 wherein said at least one quaternized nitrogen atom group includes at least one cross-linker derived from a trialkoxysilyl group.

19. The method of claim 18, wherein the polymeric electrochromic material is derived from N, N'"'"'-bis p-(trimethoxysilyl) benzyl!-4,4'"'"'-bipyridinium dichloride, N, N'"'"'-bis 3-(trimethoxysilyl)propyl!-4,4'"'"'-bipyridinium dibromide, N,N'"'"'bis p-(trimethoxysilyl) benzyl!-2,7-diazapyrenium dichloride or N, N'"'"'-bis 3-(trimethoxysilyl)propyl!-2,7-diazapyrenium dibromide.

20. The method of claim 10, wherein the ionically conductive solution is aqueous and adjusted to a pH in the range of about 5-9.

21. The method of claim 10, wherein the ionically conductive solution is an aqueous solution of a salt M, adjusted to a pH in the range of about 7, where M is taken from the group K₂ SO₄, KCl, NaCl, LiCl, KH₂ PO₄ /K₂ HPO₄ buffer, NaClO₄, LiClO₄, CF₃ SO₂ Li.

22. The method of claim 20 wherein the aqueous solution has a concentration in the range of 0.05 Molal to 1.5 Molar.