IP Library › Granted Patent US 8,097,387
Granted Patent B2
US 8,097,387 · App. 12/243,400 · Granted Jan 17, 2012

Photoreceptors comprising aligned nano-sized domains of charge transport components that have significant intermolecular pi-pi orbital overlap

Assignee: Xerox Corporation
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Quick Facts
Patent No.
US 8,097,387
App. No.
12/243,400
Granted
Jan 17, 2012
Kind
B2
Abstract

Described herein are photoreceptor devices that include aligned domains of charge transport materials that have a pi-pi orbital overlap.

Claims (26)

1. A photoreceptor device, comprising:

at least a substrate; a charge generating layer; and a charge transport layer having charge transport materials,

wherein the charge transport materials are discotic liquid crystals selected from the group consisting of fused ring aromatic hydrocarbon components, p-type fused ring hetero-aromatic components, n-type fused ring hetero-aromatic components, and mixtures thereof wherein the charge transport materials include:

where X is —S. —Se, —O, or —NR, where R is an alkyl or aryl having from 1 to about 20 carbon atoms.

2. The photoreceptor device according to claim 1 , wherein the charge transport materials are arranged such that intermolecular spacings form pi-pi stacking.

3. The photoreceptor device according to claim 1 , wherein the pi-pi stacking forms domains where the charge transport materials are highly ordered such that the domains are aligned together in a manner where a vector sum of individual domain directors is within about 45 degrees from a normal line to the substrate.

4. The photoreceptor device according to claim 3 , wherein the vector sum of the individual domain directors is within about 30 degrees from a normal line to the substrate.

5. The photoreceptor device according to claim 3 , wherein the vector sum of the individual domain directors is perpendicular to the substrate.

6. The photoreceptor device according to claim 1 , wherein the intermolecular spacings are from more than about 0 to about 5 nm.

7. The photoreceptor device according to claim 6 , wherein the intermolecular spacings are less than about 5 Å.

8. The photoreceptor device according to claim 1 , wherein the charge transport materials are selected from the group consisting of polycyclic aromatic ring, a nitrogen-containing hetero ring, triazines, indolocarbazoles, carbazole, N-ethyl carbazole, N-isopropyl carbazole, N-phenyl carbazole, tetraphenylpyrene, 1-methyl pyrene, perylene, chrysene, anthracene, tetraphene, 2-phenyl naphthalene, azopyrene, 1-ethyl pyrene, acetyl pyrene, 2,3-benzoclirysene, 2,4-benzopyrene, 1,4-bromopyrene, poly(N-vinylcarbazole), poly(vinylpyrene), poly(vinyltetraphene), poly(vinyltetracene), poly(vinylperylene), 2,4,7-trinitro-9-fluorenone, 2,4,5,7-tetranitro-fluorenone, dinitroanthracene, dinitroacridene, tetracyanopyrene, dinitroanthraquinone, butylcarbonylfluorenemalononitrile, arylamines, and mixtures thereof.

9. The photoreceptor device according to claim 1 , wherein the charge transport layer further includes a binder.

10. The photoreceptor device according to claim 9 , wherein the binder is capable of forming a self-assembled patterned layer.

11. A photoreceptor device, comprising:

at least a substrate; and a single layer including charge transport materials and charge generating materials,

wherein the charge transport materials are discotic liquid crystals selected from the group consisting of fused ring aromatic hydrocarbon components, p-type fused ring hetero-aromatic components, n-type fused ring hetero-aromatic components, and mixtures thereof wherein the charge transport materials include:

where X is —S. —Se, —O, or —NR, where R is an alkyl or aryl having from 1 to about 20 carbon atoms.

12. The photoreceptor device according to claim 11 , wherein the charge transport materials are arranged such that intermolecular spacings form pi-pi stacking.

13. The photoreceptor device according to claim 11 , wherein the pi-pi stacking forms domains where the charge transport materials are highly ordered such that the domains are aligned together in a manner where a vector sum of individual domain directors is within about 45 degrees from a normal line to the substrate.

14. The photoreceptor device according to claim 13 , wherein the vector sum of the individual domain directors is within about 30 degrees from a normal line to the substrate.

15. The photoreceptor device according to claim 13 , wherein the vector sum of the individual domain directors is perpendicular to the substrate.

16. The photoreceptor device according to claim 11 , wherein the intermolecular spacings are from more than about 0 to about 5 nm.

17. The photoreceptor device according to claim 16 , wherein the intermolecular spacings are less than about 5 Å.

18. The photoreceptor device according to claim 11 , wherein the charge transport materials are selected from the group consisting of polycyclic aromatic ring, a nitrogen-containing hetero ring, triazines, indolocarbazoles, carbazole, N-ethyl carbazole, N-isopropyl carbazole, N-phenyl carbazole, tetraphenylpyrene, 1-methyl pyrene, perylene, clrysene, anthracene, tetraphene, 2-phenyl naphthalene, azopyrene, 1-ethyl pyrene, acetyl pyrene, 2,3-benzoclirysene, 2,4-benzopyrene, 1,4-bromopyrene, poly(N-vinylcarbazole), poly(vinylpyrene), poly(vinyltetraphene), poly(vinyltetracene), poly(vinylperylene), 2,4,7-trinitro-9-fluorenone, 2,4,5,7-tetranitro-fluorenone, dinitroantliracene, dinitroacridene, tetracyanopyrene, dinitroanthraquinone, butylcarbonylfluorenemalononitrile, arylamines, and mixtures thereof.

19. The photoreceptor device according to claim 11 , wherein the charge transport layer further includes a binder.

20. The photoreceptor device according to claim 19 , wherein the binder is capable of forming a self-assembled patterned layer.

Assignments (7)
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT RF 064760/0389 Recorded Feb 13, 2024
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: XEROX CORPORATION
Reel/Frame 068261/0001 →
SECURITY INTEREST Recorded Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
SECURITY INTEREST Recorded Nov 20, 2023
From: XEROX CORPORATION
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 065628/0019 →
SECURITY INTEREST Recorded Jun 22, 2023
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 064760/0389 →
RELEASE OF SECURITY INTEREST IN PATENTS AT R/F 062740/0214 Recorded May 18, 2023
From: CITIBANK, N.A., AS AGENT
To: XEROX CORPORATION
Reel/Frame 063694/0122 →
SECURITY INTEREST Recorded Nov 10, 2022
From: XEROX CORPORATION
To: CITIBANK, N.A., AS AGENT
Reel/Frame 062740/0214 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2008
From: AZIZ, HANY; DE JONG, KATHY L.
To: XEROX CORPORATION
Reel/Frame 021621/0667 →
Continuity (2)
Provisional Application 61034716 · Mar 7, 2008
Related Publication 20090226829A1 · Sep 10, 2009