IP Library Granted Patent US 9,000,294
Granted Patent B2
US 9,000,294 · App. 13/869,426 · Granted Apr 7, 2015

Tunable photoactive compounds

Inventors: Michael D. Irwin (El Paso, TX); Vivek V. Dhas (El Paso, TX); Robert D. Maher, III (Plano, TX); Jerred A. Chute (Dallas, TX)
Assignee: Hunt Energy Enterprises, LLC
H01L51/0058
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Quick Facts
Patent No.
US 9,000,294
App. No.
13/869,426
Granted
Apr 7, 2015
Kind
B2
Abstract

Photoactive compositions of matter, methods for their design and synthesis, and various applications of such compositions of matter are disclosed. Such photoactive compositions may, for example, include any one or more of the following: a core moiety; a primary electron donor moiety; an electron-withdrawing moiety; and an alkyl tail. Some photoactive compositions may further include multiple additional electron donor moieties, electron-withdrawing moieties, and alkyl tails. Applications of such photoactive compositions of matter may include use in photovoltaic cells (e.g., as a p- or n-type material of the active layer of some photovoltaic cells, or as a dye to be employed in other photovoltaic cells); batteries, field-effect transistors; and light-emitting diodes.

Claims (49)

1. A photovoltaic device comprising:

a first electrode;

an active layer comprising a photoactive organic compound; and

a second electrode;

wherein the active layer is between the first and second electrodes;

wherein the photoactive organic compound comprises:

a primary electron donor moiety comprising at least one substituent selected from the group consisting of: aryl amine; aryl phosphine; aryl arsine; aryl stibine; aryl sulfide; aryl selenide; phenyl; phenol; alkoxy phenyl; dialkoxy phenyl; alkyl phenyl, and any combination thereof;

a core moiety comprising at least one aryl substituent selected from the group consisting of: benzothiophene, dibenzothiophene, naphthothiophene, dinaphthothiophene, benzonaphthothiophene, naphthyl, benzothiazole, benzo[b]naphtha[2,3-d]thiophene, 4H-cyclopenta[1,2-b:5,4-b′]bisthiophene, dinaphtho[2,3-d]thiophene, thieno[3,2-b]thiophene, naphthalene, anthracene, and any combination thereof;

a second electron donor moiety comprising at least one pi-electron donor substituent selected from the group consisting of: thiophene, benzene, benzothiophene, thienothiophene; and any combination thereof; and

an electron-withdrawing moiety comprising at least one substituent selected from the group consisting of: a carboxylic acid; a monocyanocomplex; a dicyanocomplex; a thiocyanocomplex; an isothiocyanocomplex, and any combination thereof.

2. The photovoltaic device of claim 1 wherein the active layer comprises one or both of a p-type material and an n-type material; and

wherein at least one of the p-type and the n-type material comprises the photoactive organic compound.

3. The photovoltaic device of claim 1 wherein the active layer comprises an electrolyte and a dye;

wherein the dye comprises the photoactive organic compound.

4. The photovoltaic device of claim 1 wherein the active layer comprises a hole-transport material and a dye;

wherein the dye comprises the photoactive organic compound.

5. The photovoltaic device of claim 2 wherein the primary electron donor moiety comprises a multi-aryl amine.

6. The photovoltaic device of claim 2 wherein the core moiety comprises at least one aryl substituent sourced from asphaltene.

7. The photovoltaic device of claim 3 wherein the primary electron donor moiety comprises a multi-aryl amine.

8. The photovoltaic device of claim 3 wherein the core moiety comprises at least one aryl substituent sourced from asphaltene.

9. The photovoltaic device of claim 4 wherein the primary electron donor moiety comprises a multi-aryl amine.

10. The photovoltaic device of claim 4 wherein the core moiety comprises at least one aryl substituent sourced from asphaltene.

11. The photovoltaic device of claim 2 wherein the primary electron donor moiety comprises a dialkoxyphenylamine.

12. The photovoltaic device of claim 2 wherein the core moiety comprises a dibenzothiophene.

13. The photovoltaic device of claim 11 wherein the core moiety comprises a dibenzothiophene.

14. The photovoltaic device of claim 13 wherein the photoactive organic compound has the structural formula:

wherein R comprises the second electron donor moiety and the electron-withdrawing moiety.

15. The photovoltaic device of claim 3 wherein the primary electron donor moiety comprises a dialkoxyphenylamine.

16. The photovoltaic device of claim 3 wherein the core moiety comprises a dibenzothiophene.

17. The photovoltaic device of claim 16 wherein the core moiety comprises a dibenzothiophene.

18. The photovoltaic device of claim 17 wherein the photoactive organic compound has the structural formula:

wherein R comprises the second electron donor moiety and the electron-withdrawing moiety.

19. The photovoltaic device of claim 4 wherein the primary electron donor moiety comprises a dialkoxyphenylamine.

20. The photovoltaic device of claim 4 wherein the core moiety comprises a dibenzothiophene.

21. The photovoltaic device of claim 20 wherein the core moiety comprises a dibenzothiophene.

22. The photovoltaic device of claim 17 wherein the photoactive organic compound has the structural formula:

wherein R comprises the second electron donor moiety and the electron-withdrawing moiety.

23. A photovoltaic device comprising:

a first electrode;

an active layer comprising a photoactive organic compound; and

a second electrode;

wherein the active layer is between the first and second electrodes; and

wherein the photoactive organic compound has the structural formula:

24. The photovoltaic device of claim 23 wherein the active layer comprises one or both of a p-type material and an n-type material; and

wherein at least one of the p-type and the n-type material comprises the photoactive organic compound.

25. The photovoltaic device of claim 23 wherein the active layer comprises an electrolyte and a dye;

wherein the dye comprises the photoactive organic compound.

26. The photovoltaic device of claim 23 wherein the active layer comprises a hole-transport material and a dye;

wherein the dye comprises the photoactive organic compound.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2021
From: CUBIC PEROVSKITE LLC
To: CUBICPV INC.
Reel/Frame 058517/0919 →
CHANGE OF NAME Recorded Aug 1, 2021
From: HUNT PEROVSKITE TECHNOLOGIES, L.L.C.
To: CUBIC PEROVSKITE LLC
Reel/Frame 057047/0232 →
CHANGE OF NAME Recorded Apr 13, 2020
From: HEE SOLAR, L.L.C.
To: HUNT PEROVSKITE TECHNOLOGIES, L.L.C.
Reel/Frame 052385/0490 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2017
From: HUNT ENERGY ENTERPRISES, L.L.C.
To: HEE SOLAR, L.L.C.
Reel/Frame 043174/0690 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2014
From: IRWIN, MICHAEL D.; DHAS, VIVEK V.; MAHER, ROBERT D., III; CHUTE, JERRED A.
To: HUNT ENERGY ENTERPRISES, L.L.C.
Reel/Frame 032411/0411 →
Continuity (2)
Continuation 13839349 · Mar 15, 2013
Related Publication 20140261692A1 · Sep 18, 2014