IP Library Granted Patent US 10,141,376
Granted Patent B2
US 10,141,376 · App. 15/593,631 · Granted Nov 27, 2018

Organic photoelectronic device and image sensor

Inventors: Kyung Bae Park (Hwaseong-si, KR); Satoh Ryuichi (Numazu-si, JP); Gae Hwang Lee (Seongnam-si, KR); Kwang Hee Lee (Hwaseong-si, KR); Dong-Seok Leem (Hwaseong-si, KR); Yong Wan Jin (Seoul, KR); Tadao Yagi (Hwaseong-si, KR); Chul Joon Heo (Busan, KR)
Assignee: Samsung Electronics Co., Ltd.
H01L27/307H01L27/30H01L27/302H01L51/008H01L51/0094H01L51/424H01L51/4246H01L51/4253H01L51/442H01L51/447H01L25/167H01L33/06H01L51/0046H01L51/0068H01L51/44Y02E10/549
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Quick Facts
Patent No.
US 10,141,376
App. No.
15/593,631
Granted
Nov 27, 2018
Kind
B2
Abstract

Example embodiments relate to an organic photoelectronic device that includes a first electrode, a light-absorption layer on the first electrode and including a first p-type light-absorption material and a first n-type light-absorption material, a light-absorption auxiliary layer on the light-absorption layer and including a second p-type light-absorption material or a second n-type light-absorption material that have a smaller full width at half maximum (FWHM) than the FWHM of the light absorption layer, a charge auxiliary layer on the light-absorption auxiliary layer, and a second electrode on the charge auxiliary layer, and an image sensor including the same.

Claims (42)

1. An organic photoelectronic device, comprising:

a first electrode and a second electrode facing each other;

a light-absorption layer between the first electrode and the second electrode, the light-absorption layer including a first p-type light-absorption material and a first n-type light-absorption material, the first p-type light-absorption material and the first n-type light-absorption material forming a heterojunction, and

a light-absorption auxiliary layer on one side of the light-absorption layer, the light-absorption auxiliary layer including a second p-type light-absorption material or a second n-type light-absorption material, the light-absorption auxiliary layer having a smaller full width at half maximum (FWHM) than the light-absorption layer.

2. The organic photoelectronic device of claim 1 , wherein the second p-type light-absorption material or the second n-type light-absorption material has a smaller FWHM than a FWHM of the light-absorption layer by about 5 nm or more.

3. The organic photoelectronic device of claim 1 , wherein the second p-type light-absorption material is the same as or different from the first p-type light-absorption material, and

the second n-type light-absorption material is the same as or different from the first n-type light-absorption material.

4. The organic photoelectronic device of claim 1 , wherein the light-absorption auxiliary layer has an extinction coefficient that is greater than or equal to about 100,000 cm −1 at a maximum absorption wavelength (λ max ).

5. The organic photoelectronic device of claim 1 , wherein an external quantum efficiency (EQE) of the second p-type light-absorption material or the second n-type light-absorption material at a maximum absorption wavelength (λ max ) is equal to or greater than an external quantum efficiency (EQE) of the light-absorption layer at the maximum absorption wavelength (λ max ).

6. The organic photoelectronic device of claim 1 , wherein the second p-type light-absorption material or the second n-type light-absorption material is represented by the following Chemical Formula 1, and

the first p-type light-absorption material or the first n-type light-absorption material is represented by the following Chemical Formula 2:

wherein

R a to R 1 are independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen atom, a halogen-containing group, or a combination thereof,

X is a halogen atom, a halogen-containing group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 aryloxy group, a substituted or unsubstituted C1 to C30 heteroaryloxy group, a substituted or unsubstituted silyloxy group, a substituted or unsubstituted amine group, a substituted or unsubstituted arylamine group, or a combination thereof,

wherein

R m to R x are independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen atom, a halogen-containing group, or a combination thereof, and

Y is a halogen atom.

7. An organic photoelectronic device, comprising:

a light-receiving electrode and an opposing electrode,

a light-absorption layer between the light-receiving electrode and the opposing electrode, and

a light-absorption auxiliary layer between the light-receiving electrode and the opposing electrode,

wherein the light-absorption auxiliary layer includes a light-absorption material configured to absorb light in a visible wavelength region.

8. The organic photoelectronic device of claim 7 , wherein the light-absorption layer and the light-absorption auxiliary layer are configured to absorb light in a green wavelength region.

9. The organic photoelectronic device of claim 8 , wherein a FWHM of the light-absorption auxiliary layer is narrower than a FWHM of the light-absorption layer.

10. The organic photoelectronic device of claim 7 , wherein the light-absorption material of the light-absorption auxiliary layer is represented by the following Chemical Formula 1:

wherein

R a to R 1 are independently hydrogen, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C3 to C30 heteroaryl group, a halogen atom, a halogen-containing group, or a combination thereof, and

X is a halogen atom, a halogen-containing group, a substituted or unsubstituted C1 to C30 alkyl group, a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted C1 to C30 alkoxy group, a substituted or unsubstituted C1 to C30 aryloxy group, a substituted or unsubstituted C1 to C30 heteroaryloxy group, a substituted or unsubstituted silyloxy group, a substituted or unsubstituted amine group, a substituted or unsubstituted arylamine group, or a combination thereof.

11. The organic photoelectronic device of claim 7 , further comprising a charge auxiliary layer between the light receiving electrode and the opposing electrode.

12. An organic photoelectronic device, comprising:

a first electrode and a second electrode facing each other;

a light-absorption layer between the first electrode and the second electrode, the light-absorption layer including a first p-type light-absorption material and a first n-type light-absorption material, the first p-type light-absorption material and the first n-type light-absorption material forming a heterojunction, and

a light-absorption auxiliary layer on one side of the light-absorption layer,

wherein a FWHM of the light-absorption auxiliary layer is narrower than a FWHM of the light-absorption layer.

13. The organic photoelectronic device of claim 12 , wherein the light-absorption auxiliary layer has a FWHM that is less than or equal to about 90 nm.

14. The organic photoelectronic device of claim 12 , further comprising a charge auxiliary layer on one side of the light-absorption auxiliary layer.

15. An image sensor comprising the organic photoelectronic device of claim 1 .

16. An electronic device including the image sensor of claim 15 .

17. An image sensor comprising the organic photoelectronic device of claim 7 .

18. An electronic device including the image sensor of claim 17 .

19. An image sensor comprising the organic photoelectronic device of claim 12 .

20. An electronic device including the image sensor of claim 19 .

Priority Claims (1)
KR 10-2014-0089914 · Jul 16, 2014 · national
Continuity (2)
Continuation 14604185 · Jan 23, 2015
Related Publication 20170250227A1 · Aug 31, 2017
Cited By (1)
US 12,317,727