Electrochromic devices
View Patent ↗Conventional electrochromic devices frequently suffer from poor reliability and poor performance. Improvements are made using entirely solid and inorganic materials. Electrochromic devices are fabricated by forming an ion conducting electronically-insulating interfacial region that serves as an IC layer. In some methods, the interfacial region is formed after formation of an electrochromic and a counter electrode layer. The interfacial region contains an ion conducting electronically-insulating material along with components of the electrochromic and/or the counter electrode layer. Materials and microstructure of the electrochromic devices provide improvements in performance and reliability over conventional devices. In various embodiments, a counter electrode is fabricated to include a base anodically coloring material and one or more additives.
1. A method of fabricating an electrochromic device, the method comprising:
(a) forming a cathodically coloring layer comprising a cathodically coloring electrochromic material;
(b) forming an anodically coloring layer comprising an anodically coloring electrochromic material and one or more additives, wherein the cathodically coloring layer and the anodically coloring layer are in contact with one another to form a stack, and wherein (a) and/or (b) includes forming a superstoichiometric oxygenated form of at least one of the cathodically coloring electrochromic material and the anodically coloring electrochromic material at an interface between the cathodically coloring layer and the anodically coloring layer;
(c) exposing the stack to lithium; and
(d) heating the stack to form an ionically conducting and electrically insulating material at the interface between the cathodically coloring layer and the anodically coloring layer.
2. The method of claim 1 , wherein the anodically coloring electrochromic material comprises one or more materials selected from the group consisting of: cobalt oxide, chromium oxide, iron oxide, iridium oxide, manganese oxide, nickel oxide, rhodium oxide, ruthenium oxide, vanadium oxide, and combinations thereof.
3. The method of claim 1 , wherein the additive is selected from the group consisting of: silver (Ag), aluminum (Al), arsenic (As), gold (Au), boron (B), barium (Ba), beryllium (Be), bismuth (Bi), calcium (Ca), cadmium (Cd), cerium (Ce), cesium (Cs), copper (Cu), europium (Eu), gallium, (Ga), gadolinium (Gd), germanium (Ge), hafnium (Hf), mercury (Hg), indium (In), potassium (K), lithium (Li), lanthanum (La), magnesium (Mg), molybdenum (Mo), sodium (Na), niobium (Nb), neodymium (Nd), osmium (Os), protactinium (Pa), lead (Pb), palladium (Pd), promethium (Pm), polonium (Po), praseodymium (Pr), platinum (Pt), radium (Ra), rubidium (Rb), rhenium (Re), antimony (Sb), scandium (Sc), selenium (Se), silicon (Si), samarium (Sm), tin (Sn), strontium (Sr), tantalum (Ta), terbium (Tb), technetium (Tc), tellurium (Te), thorium (Th), titanium (Ti), thallium (Tl), uranium (U), tungsten (W), yttrium (Y), zinc (Zn), and zirconium (Zr), and combinations thereof.
4. The method of claim 3 , wherein the additive in the anodically coloring layer is selected from the group consisting of: Al, As, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Cs, Cu, Eu, Ga, Gd, Ge, Hf, Hg, In, K, Li, La, Mg, Mo, Na, Nb, Nd, Os, Pa, Pb, Pd, Po, Pm, Pr, Pt, Rb, Ra, Re, Sb, Sc, Se, Si, Sm, Sn, Sr, Ta, Tb, Tc, Te, Th, Ti, U, W, Y, Zn, Zr, and combinations thereof.
5. The method of claim 3 , wherein the additive is selected from the group consisting of: Ag, As, Au, B, Cd, Cs, Cu, Eu, Ga, Gd, Ge, Hg, Os, Pb, Pd, Pm, Po, Pt, Ra, Rb, Tb, Tc, Th, Tl, and combinations thereof.
6. The method of claim 1 , wherein the anodically coloring electrochromic material is nickel oxide.
7. The method of claim 6 , wherein the additive comprises at least one of Ga, Gd, and Ge.
8. The method of claim 1 , wherein at least one of the cathodically coloring layer and the anodically coloring layer is formed through sputter deposition with a sputter gas having an oxygen concentration of between about 70-100% O 2 during deposition of the superstoichiometric oxygenated form of the at least one of the cathodically coloring electrochromic material and the anodically coloring electrochromic material.
9. The method of claim 1 , wherein the anodically coloring electrochromic material is substantially amorphous.
10. The method of claim 1 , wherein the cathodically coloring electrochromic material is substantially crystalline.
11. The method of claim 1 , wherein the heating is between about 150° C. and about 450° C.
12. An electrochromic device, the device comprising:
(a) a layer of cathodically coloring material; and
(b) a layer of anodically coloring material comprising an anodically coloring electrochromic material and one or more additives,
wherein an interfacial region between the layer of cathodically coloring material and the layer of anodically coloring material comprises an ionically conductive and electrically insulating material formed in situ by reaction of a superstoichiometrically oxygenated form of at least one of the anodically coloring electrochromic material and the cathodically coloring electrochromic material, with lithium in the presence of heat.
13. The electrochromic device of claim 12 , wherein the anodically coloring electrochromic material comprises one or more materials selected from the group consisting of: cobalt oxide, chromium oxide, iron oxide, iridium oxide, manganese oxide, nickel oxide, rhodium oxide, ruthenium oxide, vanadium oxide, and mixtures thereof.
14. The electrochromic device of claim 12 , wherein the additive is selected from the group consisting of: silver (Ag), aluminum (Al), arsenic (As), gold (Au), boron (B), barium (Ba), beryllium (Be), bismuth (Bi), calcium (Ca), cadmium (Cd), cerium (Ce), cesium (Cs), copper (Cu), europium (Eu), gallium, (Ga), gadolinium (Gd), germanium (Ge), hafnium (Hf), mercury (Hg), indium (In), potassium (K), lithium (Li), lanthanum (La), magnesium (Mg), molybdenum (Mo), sodium (Na), niobium (Nb), neodymium (Nd), osmium (Os), protactinium (Pa), lead (Pb), palladium (Pd), polonium (Po), promethium (Pm), praseodymium (Pr), platinum (Pt), radium (Ra), rubidium (Rb), rhenium (Re), antimony (Sb), scandium (Sc), selenium (Se), silicon (Si), samarium (Sm), tin (Sn), strontium (Sr), tantalum (Ta), terbium (Tb), technetium (Tc), tellurium (Te), thorium (Th), titanium (Ti), thallium (Tl), uranium (U), tungsten (W), yttrium (Y), zinc (Zn), zirconium (Zr), and combinations thereof.
15. The electrochromic device of claim 12 , wherein the additive is selected from the group consisting of: Al, As, Au, B, Ba, Be, Bi, Ca, Cd, Ce, Cs, Cu, Eu, Ga, Gd, Ge, Hf, Hg, In, K, Li, La, Mg, Mo, Na, Nb, Nd, Os, Pa, Pb, Pd, Po, Pm, Pr, Pt, Rb, Ra, Re, Sb, Sc, Se, Si, Sm, Sn, Sr, Ta, Tb, Tc, Te, Th, Ti, U, W, Y, Zn, Zr, and combinations thereof.
16. The electrochromic device of claim 15 , wherein the additive is selected from the group consisting of: Al, Au, Ga, Gd, Ge, Mg, Nb, Si, Ta, Zr, and combinations thereof.
17. The electrochromic device of claim 16 , wherein the additive is selected from the group consisting of: Al, Mg, Nb, Si, Ta, Zr, and combinations thereof.
18. The electrochromic device of claim 17 , wherein the additive is selected from the group consisting of: Al, Mg, Ta, and combinations thereof.
19. The electrochromic device of any of claim 12 , wherein the anodically coloring electrochromic material comprises a metal selected from the group consisting of: Ir, Ru, Rh, and combinations thereof.
20. The electrochromic device of claim 12 , wherein the anodically coloring electrochromic material is nickel oxide.
21. The electrochromic device of claim 20 , wherein the additive comprises at least one of Ga, Gd, and Ge.