IP Library › Granted Patent US 12,178,064
Granted Patent B2
US 12,178,064 · App. 18/348,291 · Granted Dec 24, 2024

Materials for forming a nucleation-inhibiting coating and devices incorporating same

Inventors: Yi-Lu Chang (Mississauga, CA); Qi Wang (Mississauga, CA); Scott Nicholas Genin (Mississauga, CA); Michael Helander (Mississauga, CA); Jacky Qiu (Mississauga, CA); Zhibin Wang (Mississauga, CA); Benoit Lessard (Mississauga, CA)
Assignee: OTI Lumionics Inc.
H10K50/824H10K85/00H10K85/622
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Quick Facts
Patent No.
US 12,178,064
App. No.
18/348,291
Granted
Dec 24, 2024
Kind
B2
Abstract

An opto-electronic device includes a substrate, a first electrode disposed over the substrate, a semiconducting layer disposed over the first electrode, a second electrode disposed over the semiconducting layer, the second electrode having a first portion and a second portion, a nucleation inhibition coating disposed over the first portion of the second electrode; and a conductive coating disposed over the second portion of the second electrode, wherein the nucleation inhibition coating is a compound of Formula (I)

Claims (23)

1. An opto-electronic device comprising:

a nucleating inhibiting coating (NIC) disposed on a first layer surface of the device in a first portion of a lateral aspect thereof; and

a conductive coating disposed on a second layer surface of the device in a second portion of the lateral aspect thereof;

wherein:

the NIC comprises a compound comprising a core moiety and at least one terminal moiety bonded thereto;

the at least one terminal moiety is independently selected from a group consisting of: I-A, I-B, I-C, I-D, I-E, I-F, a fluorene moiety, and a phenylene moiety;

in I-A, A 1 , A 2 , A 3 , A 4 , and A 5 are each independently selected from a group consisting of: hydrogen (H), deuteron (D), fluorine (F), chlorine (Cl), alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy;

in I-B, at least one of B 1 , B 2 , B 3 , B 4 , B 5 , B 6 , B 7 , and B 8 represents an attachment to the core moiety, and the remainder of B 1 , B 2 , B 3 , B 4 , B 5 , B 6 , B 7 , and B 8 are each independently selected from a group consisting of: H, D, F, Cl, alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy;

in I-C, at least one of C 1 , C 2 , C 3 , C 4 , C 5 , C 6 , C 7 , C 8 , C 9 , and C 10 represents an attachment to the core moiety, and the remainder of C 1 , C 2 , C 3 , C 4 , C 5 , C 6 , C 7 , C 8 , C 9 , and C 10 are independently selected from a group consisting of: H, D, F, Cl, alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy;

in I-D, at least one of D 1 , D 2 , D 3 , D 4 , D 5 , D 6 , D 7 , D 8 , D 9 , and D 10 represents an attachment to the core moiety, and the remainder of D 1 , D 2 , D 3 , D 4 , D 5 , D 6 , D 7 , D 8 , D 9 , and D 10 are independently selected from a group consisting of: H, D, F, Cl, alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy;

in I-E, at least one of E1, E2, E3, E4, E5, E6, E7, E8, E9, E10, E11, and E12 represents an attachment to the core moiety, and the remainder of E1, E2, E3, E4, E5, E6, E7, E8, E9, E10, E11, and E12 are each independently selected from a group consisting of: H, D, F, Cl, alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy;

in I-F, at least one of F 1 , F 2 , F 3 , F 4 , F 5 , F 6 , F 7 , F 8 , F 9 , and F 10 represents an attachment to the core moiety, and the remainder of F 1 , F 2 , F 3 , F 4 , F 5 , F 6 , F 7 , F 8 , F 9 , and F 10 are each independently selected from a group consisting of: H, D, F, Cl, alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy; and

in I-G, at least one of G 1 , G 2 , G 3 , G 4 , G 5 , G 6 , G 7 , G 8 , G 9 , G 10 , G 11 , and G 12 represents an attachment to the core moiety, and the remainder of G 1 , G 2 , G 3 , G 4 , G 5 , G 6 , G 7 , G 8 , G 9 , G 10 , G 11 , and G 12 are each independently selected from a group consisting of: H, D, F, Cl, alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy.

2. The opto-electronic device of claim 1 , wherein the fluoroaryl moiety is selected from one of: a spirobifluorene moiety, a dimethylfluorene moiety, and a difluorofluorene moiety.

3. The opto-electronic device of claim 1 , wherein the phenylene moiety is a triphenylene moiety.

4. The opto-electronic device of claim 1 , wherein the core moiety is an anthracene moiety represented by Formula I:

5. The opto-electronic device of claim 1 , wherein the at least one terminal moiety is bonded to the core moiety by one of: directly, and via a linker moiety.

6. The opto-electronic device of claim 1 , wherein the linker moiety is selected from one of: —O—, —S—, a cyclic hydrocarbon moiety, and an acyclic hydrocarbon moiety.

7. The opto-electronic device of claim 1 , wherein at least one carbon (C) in the compound is substituted by a heteroatom.

8. The opto-electronic device of claim 7 , wherein the heteroatom is selected from one of: sulfur(S) and nitrogen (N).

9. The opto-electronic device of claim 1 , wherein the compound comprises at least one F atom.

10. The opto-electronic device of claim 1 , wherein the NIC comprises a compound selected from a group consisting of compounds A 1 -A 66 :

wherein X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 , and X 10 are each independently selected from a group consisting of: H, D, F, Cl, alkyl, cycloalkyl, silyl, fluoroalkyl, arylalkyl, aryl, heteroaryl, alkoxy, and fluoroalkoxy.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2026
From: CHANG, YI-LU; WANG, QI; GENIN, SCOTT NICHOLAS; HELANDER, MICHAEL; QIU, JACKY; WANG, ZHIBIN; LESSARD, BENOIT
To: OTI LUMIONICS INC.
Reel/Frame 073603/0042 →
Continuity (5)
Continuation 16965585
Provisional Application 62770360 · Nov 21, 2018
Provisional Application 62625722 · Feb 2, 2018
Provisional Application 62625710 · Feb 2, 2018
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