Imaging member having a dual charge transport layer

• US 7,125,633 B2
• Filed: 12/12/2003
• Issued: 10/24/2006
• Est. Priority Date: 12/16/2002
• Status: Expired due to Fees

• Current Assignee: Xerox Corporation (Xerox Holdings Corp.)
• Original Assignee: Xerox Corporation (Xerox Holdings Corp.)
• Inventors: Foley, Geoff, Tong, Yuh, Yanus, Jack, Silvestri, Markus R., Yu, Robert C., Mishra, Satchidanand, Dinh, Kenny-tuan, Horgan, Anthony M., Renfer, Dale, Fuller, Timothy, Yuh, Houy Jen
• Primary Examiner(s): Dote, Janis L.
• Application Number:
  US10/734,380
• Publication Number:
  US 20040151999A1
• Time in Patent Office: 1,047 Days
• Field of Search: 430/58.05, 430/58.65, 430/58.75, 430/58.85, 430/58.3, 430/73.66, 430/58.8, 430/58.4
• US Class Current: 430/58.3
• 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 5/0535 Polyolefins; Polystyrenes; Waxes
• CPC Class Codes: G03G 5/0539 Halogenated polymers
• CPC Class Codes: G03G 5/0542 Polyvinylalcohol, polyallylalcohol; Derivatives thereof, e.g. polyvinylesters, polyvinylethers, polyvinylamines
• CPC Class Codes: G03G 5/0546 Polymers comprising at least one carboxyl radical, e.g. polyacrylic acid, polycrotonic acid, polymaleic acid; Derivatives thereof, e.g. their esters, salts, anhydrides, nitriles, amides
• CPC Class Codes: G03G 5/055 Polymers containing hetero rings in the side chain
• CPC Class Codes: G03G 5/0567 Other polycondensates comprising oxygen atoms in the main chain; Phenol resins
• CPC Class Codes: G03G 5/0575 Other polycondensates comprising nitrogen atoms with or without oxygen atoms in the main chain
• CPC Class Codes: G03G 5/0601 Acyclic or carbocyclic compounds
• CPC Class Codes: G03G 5/061443 benzidine
• CPC Class Codes: G03G 5/061473 plural alkenyl groups linked directly to the same aryl group
• CPC Class Codes: G03G 5/0616 Hydrazines; Hydrazones
• CPC Class Codes: G03G 5/0672 containing two or more methine or polymethine groups

Abstract

An imaging member having a charge transport layer with multiple regions or layers is provided. The charge transport layer includes at least two charge transport layers coated from solutions of different components and concentrations, wherein the second (top) transport layer comprises a lower concentration of different charge transport compound than the first (bottom) charge transport layer. The charge transport compound included in the second (top) charge transport layer is a high mobility hole transport compound. The charge transport compound in each layer is dissolved or molecularly dispersed in an electrically inactive film forming polymer to form a solid solution. In such a construction, the resulting dual charge transport layer exhibits enhanced cracking suppression, improves wear resistance, provides excellent imaging member electrical performance, and delivers improved print quality.

Claims

1. An imaging member comprising

an electrically conductive supporting substrate or a supporting substrate comprising an electrically conductive layer;

an optional hole blocking layer;

a charge generating layer; and

a charge transport layer having at least a first (bottom) charge transport layer and a second (top) charge transport layer each of which comprises a hole mobility organic transport compound molecularly dispersed in a film forming polymer binder;

wherein the first (bottom) charge transport layer comprises a hole mobility organic transport compound selected from the group consisting of triphenylmethane;

bis(4-diethylamine-2-methylphenyl)phenylmethane;

4,4′

-bis(diethylamino)-2,2′

-dimethyltriphenyl-methane;

N,N′

-diphenyl-N,N′

-bis(3-methylphenyl)-[1,1′

-biphenyl]-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(4-methylphenyl)-[1,1′

-biphenyl]-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(alkylphenyl)-1,1′

-biphenyl-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(chlorophenyl)-1,1′

-biphenyl-4,4′

-diamine;

tritolylamine;

N,N′

-bis-(3,4-dimethylphenyl)-4-biphenyl amine;

N,N′

-bis-(4-methylphenyl)-N,N′

-bis(4-ethylphenyl)-1,1′

-(3,3′

-dimethylbiphenyl)-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(halophenyl)-1,1′

-biphenyl-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(hydroxyphenyl)-1,1′

-biphenyl-4,4′

-diamine;

phenanthrene diamine;

arylamine;

enamine;

stilbene; and

hydrazone molecules; and

wherein the first (bottom) charge transport layer comprises between about 50 and about 90 weight percent hole mobility organic transport compound based on the total weight of the first (bottom) charge transport layer;

wherein the second (top) charge transport layer comprises a film forming polymer binder and a high hole mobility organic transport compound selected from the group consisting of a diamine represented by the formula;

2. An imaging member according to claim 1, wherein the second (top) charge transport layer comprises between about 20 to about 45 weight percent of the high hole mobility diamine organic charge transport compound of Formula (II) based upon the total weight of the second charge transport layer.

3. An imaging member according to claim 1, wherein the second (top) charge transport layer comprises between about 30 to about 40 weight percent of the high hole mobility diamine organic charge transport compound of Formula (II) based upon the total weight of the second charge transport layer.

4. An imaging member according to claim 1, wherein the first (bottom) charge transport layer comprises between about 50 to about 70 weight percent of the hole mobility organic charge transport compound based upon the total weight of the first charge transport layer.

5. An imaging member according to claim 1, wherein the hole transport compound in the first (bottom) charge transport layer is comprised of an aryl amine, N,N′

-diphenyl-N,N′

-bis(alkylphenyl)-1,1′

-biphenyl-4,4′

-diamine, represented by;

6. An imaging member of claim 5, wherein the aryl diamine in the first (bottom) charge transport layer is N,N′

-diphenyl-N,N′

-bis(3-methylphenyl)-[1,1′

-biphenyl]-4,4′

-diamine.

7. An imaging member of claim 5, wherein the aryl diamine in the first (bottom) charge transport layer is N,N′

-diphenyl-N,N′

-bis(4-methylphenyl)-[1,1′

-biphenyl]-4,4′

-diamine.

8. An imaging member of claim 1, wherein the film forming binder used in the transport layers is a polycarbonate selected from the group consisting of poly(4,4′

-isopropylidene diphenyl) carbonate and poly(4,4′

-diphenyl)-1,1′

-cyclohexane carbonate.

9. An imaging member of claim 1, wherein the film forming binder used in both transport layers is the same.

10. An imaging member comprising

an electrically conductive supporting substrate or a supporting substrate comprising an electrically conductive layer;

an optional hole blocking layer;

a charge generating layer; and

a dual charge transport layer having a first (bottom) and a second (top) charge transport layer each of which is a solid solution comprising a hole mobility organic transport compound molecularly dispersed or dissolved in a film forming polymer binder;

wherein the first (bottom) charge transport layer comprises a hole mobility organic transport compound selected from the group consisting of triphenylmethane;

bis(4-diethylamine-2-methylphenyl)phenylmethane;

4,4′

-bis(diethylamino)-2,2′

-dimethyltriphenylmethane;

N,N′

-diphenyl-N,N′

-bis(3-methylphenyl)-[1,1′

-biphenyl]-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(4-methylphenyl)-[1,1′

-biphenyl]-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(alkylphenyl)-1,1′

-biphenyl-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(chlorophenyl)-1,1′

-biphenyl-4,4′

-diamine;

tritolylamine;

N,N′

-bis-(3,4-dimethylphenyl)-4-biphenyl amine;

N,N′

-bis-(4-methylphenyl)-N,N′

-bis(4-ethylphenyl)-1,1′

-(3,3′

-dimethylbiphenyl)-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(halophenyl)-1,1′

-biphenyl-4,4′

-diamine;

N,N′

-diphenyl-N,N′

-bis(hydroxyphenyl)-1,1′

-biphenyl-4,4′

-diamine;

phenanthrene diamine;

arylamine;

enamine;

stilbene; and

hydrazone molecules; and

wherein the first (bottom) charge transport layer comprises between about 50 and about 90 weight percent hole mobility organic transport compound based on the total weight of the first (bottom) charge transport layer;

wherein the second (top) charge transport layer comprises a film forming polymer binder and a high hole mobility organic transport compound selected from the group consisting of a diamine represented by the formula;