METHODS OF FORMING A PHOTORECEPTOR DEVICE HAVING A SELF-ASSEMBLED PATTERNED BINDER LAYER

• US 20080233297A1
• Filed: 03/23/2007
• Published: 09/25/2008
• Est. Priority Date: 03/23/2007
• Status: Abandoned Application

• Current Assignee: Xerox Corporation (Xerox Holdings Corp.)
• Original Assignee: Xerox Corporation (Xerox Holdings Corp.)
• Inventors: DE JONG, Kathy L., AZIZ, Hany
• Application Number:
  US11/690,548
• Publication Number:
  US 20080233297A1
• Time in Patent Office: Days
• US Class Current: 427/385.5
• CPC Class Codes: G03G 5/047 characterised by the charge-generation layers or charge transport layers G03G5/0433 and G03G5/0436 take precedence
• CPC Class Codes: G03G 5/0503 Inert supplements
• CPC Class Codes: G03G 5/0514 not comprising cyclic groups
• CPC Class Codes: G03G 5/0525 Coating methods
• CPC Class Codes: G03G 5/0535 Polyolefins; Polystyrenes; Waxes
• CPC Class Codes: G03G 5/0571 Polyamides; Polyimides
• CPC Class Codes: G03G 5/0592 Macromolecular compounds characterised by their structure or by their chemical properties, e.g. block polymers, reticulated polymers, molecular weight, acidity
• CPC Class Codes: G03G 5/0596 Macromolecular compounds characterised by their physical properties

Abstract

Methods of forming a self-assembled patterned binder layer, which may include at least one functional material, that is particularly suitable for use in photoreceptor devices.

Claims

1. A method of forming a patterned binder layer having a binder material by a self-assembly process on a substrate, comprising:

spreading a solution comprising a polymer and a solvent onto a flat support;

evaporating the solvent;

during evaporation, optionally providing a flow of gas such that non-solvent vapor condenses at an interface between air and the solution;

precipitating the polymer at the interface of the non-solvent vapor condensation to form the binder layer;

partially or fully encapsulating non-solvent droplets of the non-solvent vapor condensation within the precipitated polymer; and

evaporating the non-solvent droplets to form hollow spaces in the patterned binder layer.

2. The method according to claim 1, wherein the non-solvent is water, phenol, ether, methanol, ethanol, propanol or butane.

3. The method according to claim 1, wherein the solution further comprises at least one functional material that is a charge generation material or a charge transport material.

4. The method according to claim 3, wherein the charge generation material comprises at least one material selected from the group consisting of quinacridones, dibromo anthanthrone pigments, perylene diamines, perinone diamines, polynuclear aromatic quinones, azo pigments, oxyvanadium phthalocyanine, chloroaluminum phthalocyanine, copper phthalocyanine, oxytitanium phthalocyanine, chlorogallium phthalocyanine, hydroxygallium phthalocyanine, magnesium phthalocyanine, metal-free phthalocyanine, and combinations thereof.

5. The method according to claim 3, wherein the charge transport material comprises a tertiary aromatic amine selected from the group consisting of N,N′

-diphenyl-N,N′

-bis(3-hydroxyphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N′

-diphenyl-N,N′

-bis(3-methylphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N,N′

N′

-tetra(4-methylphenyl)-(1,1′

-biphenyl)-4,4′

-diamine, 4,4′

-(3,4-dimethylphenylazanediyl)bis(4,1-phenylene)dimethanol, N,N′

-bis(3-methylphenyl)-N,N′

-bis(4-n-butylphenyl)-1,1′

-terphenyl-4,4-diamine, and combinations thereof.

6. The method according to claim 1, wherein the gas is a saturated inert gas.

7. The method according to claim 1, wherein the flat support is located in an enclosed humid environment.

8. The method according to claim 1, wherein the gas is selected from the group consisting of air, xenon, argon, nitrogen, oxygen, and mixtures thereof.

9. The method according to claim 1, wherein the solution further comprises at least one functional material, and the hollow spaces are substantially filled with a filler or at least one other functional material.

10. The method according to claim 9, wherein the at least one other functional material in the hollow spaces is a charge generation material or a charge transport material.

11. The method according to claim 10, wherein the charge generation material comprises at least one material selected from the group consisting of quinacridones, dibromo anthanthrone pigments, perylene diamines, perinone diamines, polynuclear aromatic quinones, azo pigments, oxyvanadium phthalocyanine, chloroaluminum phthalocyanine, copper phthalocyanine, oxytitanium phthalocyanine, chlorogallium phthalocyanine, hydroxygallium phthalocyanine, magnesium phthalocyanine, metal-free phthalocyanine, and mixtures thereof.

12. The method according to claim 10, wherein the charge transport material comprises a tertiary aromatic amine selected from the group consisting of N,N′

-diphenyl-N,N′

-bis(3-hydroxyphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N′

-diphenyl-N,N′

-bis(3-methylphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N,N′

N′

-tetra(4-methylphenyl)-(1,1′

-biphenyl)-4,4′

-diamine, 4,4′

-(3,4-dimethylphenylazanediyl)bis(4,1-phenylene)dimethanol, N,N′

-bis(3-methylphenyl)-N,N′

-bis(4-n-butylphenyl)-1,1′

-terphenyl-4,4-diamine, and mixtures thereof.

13. The method according to claim 1, wherein the polymer comprises a block copolymer, a linear polymer or a branched polymer.

14. The method according to claim 13, wherein the block copolymer comprises at least one material selected from the group consisting of polystyrenes, poly(paraphenylenes) and polyimides.

15. The method according to claim 1, wherein the polymer comprises a material capable of forming micelles.

16. The method according to claim 1, wherein the solvent is at least one selected from the group consisting of carbon disulfide, tetrahydrofuran, chloroform, toluene, dichloroethane, dichloromethane, benzene, hexanes, xylene, ethylbenzene, methylene chloride, carbon tetrachloride, and mixtures thereof.

17. A method of forming a patterned binder layer having a binder material by a self-assembly process on a substrate, comprising:

depositing a block copolymer such that the block copolymer self assembles to form a binder layer, and

applying a solvent to dissolve a portion of the block copolymer to form a self-assembled patterned binder layer having hollow spaces.

18. The method according to claim 17, wherein the block copolymer includes at least one block selected from the group consisting of a polystyrene, a poly(paraphenylene), a polyimide, poly2-vinylpyridine, poly(n-alkylmethacrylate), poly(n-butylmethacrylate), poly(methyl methacrylate), poly(2-vinylpyridine), polyisoprene, poly(ferrocenyldimethylsilane), poly(cyclohaylethylene), polylactide, poly(ferrocenyldimethylsilane), poly(dimethysiloxane), poly(ethylene-propylene), polyethylene, polybutadiene, poly(ethyleneoxide), polystyrenepolybutadiene, poly(α

-methylstyrene), poly(4-hydroxystyrene), poly(methyltetraclododecene), poly(substituted-2-norbornene), poly(propyleneoxide), poly(butadienevinylpyridinium), poly(tert-butylacrylate), poly(cinnamoyl-ethylmethacrylate), pentadecyl phenol modified polystyrene, poly(4-vinylpyridine) and poly(tert-butylmethacrylate).

19. The method according to claim 17, wherein the solvent is selected from the group consisting of carbon disulfide, tetrahydrofuran, chloroform, toluene, benzene, hexanes, xylene, ethylbenzene, methylene chloride, carbon tetrachloride, dichloroethane, and mixtures thereof.

20. The method according to claim 17, further comprising filling the hollow spaces with a filler or at least one functional material selected from the group consisting of a charge generation material or a charge transport material.

21. The method according to claim 20, wherein the charge generation material comprises at least one material selected from the group consisting of quinacridones, dibromo anthanthrone pigments, perylene diamines, perinone diamines, polynuclear aromatic quinones, azo pigments, oxyvanadium phthalocyanine, chloroaluminum phthalocyanine, copper phthalocyanine, oxytitanium phthalocyanine, chlorogallium phthalocyanine, hydroxygallium phthalocyanine, magnesium phthalocyanine and metal-free phthalocyanine.

22. The method according to claim 20, wherein the charge transport material comprises a tertiary aromatic amine selected from the group consisting of N,N′

-diphenyl-N,N′

-bis(3-hydroxyphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N′

-diphenyl-N,N′

-bis(3-methylphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N,N′

N′

-tetra(4-methylphenyl)-(1,1′

-biphenyl)-4,4′

-diamine, 4,4′

-(3,4-dimethylphenylazanediyl)bis(4,1-phenylene)dimethanol, N,N′

-bis(3-methylphenyl)-N,N′

-bis(4-n-butylphenyl)-1,1′

-terphenyl-4,4-diamine, and mixtures thereof.

23. A method of forming a patterned binder layer having a binder material by a self-assembly process on a substrate, comprising:

submersing a substrate into a solution having a polymer and a solvent,

pulling the substrate out of the solution at a rate of from about 20 cm/min. to about 60 cm/min., thereby forming a film on the substrate, and

drying the film at a temperature of from about 15°

C. to about 600°

C. to form the patterned binder layer having hollow spaces.

24. The method according to claim 23, wherein the solution includes at least one functional material, and the hollow spaces are substantially filled with a filler or at least one other functional material.

25. The method according to claim 24, wherein the at least one functional material and the at least one other functional material are selected from the group consisting of a charge generation material and a charge transport material.

26. The method according to claim 25, wherein the charge generation material comprises at least one material selected from the group consisting of quinacridones, dibromo anthanthrone pigments, perylene diamines, perinone diamines, polynuclear aromatic quinones, azo pigments, oxyvanadium phthalocyanine, chloroaluminum phthalocyanine, copper phthalocyanine, oxytitanium phthalocyanine, chlorogallium phthalocyanine, hydroxygallium phthalocyanine, magnesium phthalocyanine, metal-free phthalocyanine, and mixtures thereof.

27. The method according to claim 25, wherein the charge transport material comprises a tertiary aromatic amine selected from the group consisting of N,N′

-diphenyl-N,N′

-bis(3-hydroxyphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N′

-diphenyl-N,N′

-bis(3-methylphenyl)-1,1′

-biphenyl-4,4′

-diamine, N,N,N′

N′

-tetra(4-methylphenyl)-(1,1′

-biphenyl)-4,4′

-diamine, 4,4′

-(3,4-dimethylphenylazanediyl)bis(4,1-phenylene)dimethanol, N,N′

-bis(3-methylphenyl)-N,N′

-bis(4-n-butylphenyl)-1,1′

-terphenyl-4,4-diamine, and mixtures thereof.

28. The method according to claim 23, wherein the polymer comprises a block copolymer, a linear polymer or a branched polymer.

29. The method according to claim 28, wherein the block copolymer comprises at least one material selected from the group consisting of polystyrenes, poly(paraphenylenes) and polyimides.

30. The method according to claim 23, wherein the solvent is at least one selected from the group consisting of carbon disulfide, tetrahydrofuran, chloroform, toluene, dichloroethane, dichloromethane, benzene, hexanes, xylene, ethylbenzene, methylene chloride, carbon tetrachloride, and mixtures thereof.