IP Library Granted Patent US 8,642,375
Granted Patent B2
US 8,642,375 · App. 12/989,298 · Granted Feb 4, 2014

Preparation method of organic photovoltaic cell's photoactive layer using aerosol jet printing

Inventors: Sung Cheol Yoon (Gyeonggi-do, KR); Hak Sung Lee (Chungcheongnam-do, KR); Chang Jin Lee (Taejeon-si, KR); Jongsun Lim (Taejeon-si, KR); Yong Gu Kang (Taejeon-si, KR)
Assignee: kOREA Research Institute of Chemical Technology
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Quick Facts
Patent No.
US 8,642,375
App. No.
12/989,298
Granted
Feb 4, 2014
Kind
B2
Abstract

Disclosed is a method of manufacturing the photoactive layer of organic photovoltaic cells using aerosol jet printing. The photoactive layer of the organic photovoltaic cell has high crystallinity and is easily formed into a multilayer structure, thus simplifying the process of manufacturing the organic photovoltaic cells. The solar power conversion efficiency of the organic photovoltaic cells including the photoactive layer is increased, thus facilitating the production of environmentally friendly energy.

Claims (31)

1. A method of manufacturing a photoactive layer of an organic photovoltaic cell using aerosol jet printing, comprising:

preparing a photoactive solution for an organic photovoltaic cell (step 1);

atomizing the photoactive solution prepared in step 1 and transferring it to an aerosol jet nozzle (step 2); and

jetting the photoactive solution in a mist form, atomized and transferred to the aerosol jet nozzle in step 2, onto a transparent electrode, thus causing spontaneous crystallization, thereby forming a photoactive layer (step 3).

2. The method according to claim 1 , wherein the photoactive solution is obtained by dissolving an electron donor and an electron acceptor in an organic solvent.

3. The method according to claim 2 , wherein the electron donor is a p-type organic semiconductor material having a band gap of 2.5˜1.4 eV.

4. The method according to claim 3 , wherein the p-type organic semiconductor material is selected from a group consisting of poly[2-methoxy-5-(2′-ethylhexyloxy)-p-phenylene vinylene] (MEH-PPV), poly[2-methoxy-5-(3,7-dimethyloctyloxy)-1,4-phenylenevinylene] (MDMO-PPV), poly(3-hexylthiophene) (P3HT), and mixtures thereof.

5. The method according to claim 2 , wherein the electron acceptor is an n-type organic semiconductor material, including fullerene and derivatives thereof.

6. The method according to claim 5 , wherein the n-type organic semiconductor material is selected from a group consisting of phenyl-C61-butyric acid methyl ester (PCBM), derivatives thereof, and mixtures thereof.

7. The method according to claim 2 , wherein the organic solvent is selected from a group consisting of benzene, toluene, trimethylbenzene, xylene, dichloromethane, chloroform, dichloroethane, trichloroethane, tetrachloroethane, dichloroethylene, trichloroethylene, tetrachloroethylene, chlorobenzene, ortho-dichlorobenzene, and mixtures thereof.

8. The method according to claim 2 , wherein, in the photoactive solution, the electron donor and the electron acceptor are used in an amount of 0.1˜2.5 wt %.

9. The method according to claim 2 , wherein a blend ratio by weight of the electron donor and the electron acceptor, which are added to the organic solvent, is set to 1:0.3˜1:5.

10. The method according to claim 1 , wherein the atomizing in step 2 is conducted by applying ultrasonic waves ranging from 20 kHz to 200 MHz to the photoactive solution prepared in step 1.

11. The method according to claim 1 , wherein the atomizing in step 2 is conducted by subjecting the photoactive solution prepared in step 1 to a pneumatic process using compressed air of 0.01˜5 psi.

12. The method according to claim 1 , wherein the photoactive solution atomized in step 2 is transferred to the aerosol jet nozzle using an inert gas as a carrier gas.

13. The method according to claim 1 , wherein the jetting in step 3 is facilitated with additional use of a sheath gas to increase a flow rate of the carrier gas.

14. The method according to claim 1 , further comprising sintering the photoactive layer deposited in step 3 (step 4).

15. The method according to claim 1 , wherein the photovoltaic layer is a single organic active layer comprising a blend of an electron donor and an electron acceptor, or multilayer structures selected from the group consisting of (a)˜(e) below:

(a) donor layer/acceptor layer

(b) donor layer/donor-acceptor blend layer/acceptor layer

(c) donor-acceptor blend layer/electron-hole recombination layer/donor-acceptor blend layer

(d) donor layer/acceptor layer/electron-hole recombination layer/donor layer/acceptor layer

(e) donor layer/donor-acceptor blend layer/acceptor layer/electron-hole recombination layer/donor layer/donor-acceptor blend layer/acceptor layer.

16. A method of fabricating organic photovoltaic cell comprising a transparent electrode layer, a hole injection layer, a photoactive layer, and an electrode layer, which are sequentially formed on a substrate, and the method comprises:

a step of preparing a substrate on which a transparent electrode layer and a hole injection layer are sequentially formed;

a step of forming a photovoltaic layer on the hole injection layer; and

a step of forming an electrode layer on the photovoltaic layer,

wherein the step of forming a photovoltaic layer comprises:

preparing a photoactive solution for an organic photovoltaic cell (step 1);

atomizing the photoactive solution prepared in step 1 and transferring it to an aerosol jet nozzle (step 2); and

jetting the photoactive solution in a mist form, atomized and transferred to the aerosol jet nozzle in step 2, onto a transparent electrode, thus causing spontaneous crystallization, thereby forming a photoactive layer (step 3).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2010
From: YOON, SUNG CHEOL; LEE, HAK SUNG; LEE, CHANG JIN; LIM, JONGSUN; KANG, YONG GU
To: KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
Reel/Frame 025183/0085 →
Priority Claims (1)
KR 10-2008-0039370 · Apr 28, 2008 · national
Continuity (1)
Related Publication 20110036403A1 · Feb 17, 2011