This U.S. non-provisional patent application claims priority under 35 U.S.C. §119 of Korean Patent Application No. 10-2013-0076994, filed on Jul. 2, 2013, 10-2013-0149227, filed on Dec. 3, 2013, the entire contents of which are hereby incorporated by reference.
The present invention disclosed herein relates to a method of manufacturing an organic light emitting diode, and more particularly, to a method of manufacturing an organic light emitting diode including a light scattering layer.
Recently, there is an increase in demand for lightweight, miniaturization, and low price in electronic products such as mobile phones, or notebooks and lighting devices. In order to meet these demands, organic light emitting devices attract attention as display devices and light emitting devices mounted in the electronic products and lighting devices. In particular, organic light emitting devices have advantages in low voltage driving performance, lightweight, and low cost, and thus have utilization in the electronic products and lighting devices.
Nowadays, increasing light emitting efficiency of an organic light emitting device is being researched. In particular, various researches are performed on increasing light emitting efficiency of an organic light emitting device even in a low voltage by extracting a light lost inside the organic light emitting device externally.
The present invention provides a method of manufacturing an organic light emitting device having improved light extraction efficiency.
The present invention also provides a method of manufacturing an organic light emitting device that is able to be easily manufactured at a low cost.
Embodiments of the present invention provide methods of manufacturing an organic light emitting diode, including: forming a light scattering layer on a substrate; forming a metal mask layer on the light scattering layer; forming a metal mask pattern by performing a heat treatment process on the metal mask layer; forming a nano structure by pattering the light scattering layer by using the metal mask pattern as an etching mask; and forming a planarizing layer to cover the nano structure on the substrate, wherein the heat treatment process is performed at temperature of 80° C. to about 200° C.
In some embodiments, the heat treatment process may be performed in a vacuum state.
In other embodiments, the heat treatment process may be performed in an inert gas atmosphere.
In still other embodiments, the heat treatment process may be performed in an inert gas atmosphere.
In even other embodiments, the light scattering layer has a smaller refractive index than the substrate.
In even other embodiments, the refractive index of the light scattering layer may be about 1.1 to about 1.5.
In yet other embodiments, the light scattering layer may include fluorine resin, silicone oxide, magnesium oxide, or a combination thereof.
In further embodiments, the nano structure may include a plurality of nano patterns protruding in a vertical direction to a top surface of the substrate; and recess regions defined by side walls of the plurality of nano patterns, wherein a height of the plurality of nano patterns is defined as a distance between a top surface of the nano patterns and a bottom surface of the recess regions, and the height of the nano patterns is about 150 nm to 600 nm.
In still further embodiments, the metal mask pattern may include openings exposing the light scattering layer, and the forming of the nano structure comprises forming the recess regions by etching the light scattering layer exposed by the openings.
In even further embodiments, the method may further include removing the metal mask pattern after the forming of the nano structure, wherein the metal mask pattern is removed by using an acid solution.
In yet further embodiments, the acid solution may include nitric acid, sulfuric acid, aqua regia, or phosphoric acid.
In much further embodiments, the method may further include: forming a first electrode on the planarizing layer; forming an organic light emitting layer on the first electrode; and forming a second electrode on the organic light emitting layer, wherein the planarizing layer has substantially the same refractive index as the first electrode.
In still much further embodiments, the method may further include: forming a first electrode on the planarizing layer; forming a second electrode on an organic light emitting layer on the first electrode; and forming a second electrode on the organic light emitting layer, wherein the planarizing layer has a greater refractive index than the first electrode.
In even much further embodiments, the refractive index of the planarizing layer may be about 1.8 to about 2.5.
In yet much further embodiment, the method may further include forming a polymer film between the substrate and the light scattering layer, wherein the polymer film comprises at least one of polyacrylic, polyimide, polycarbonate, perylene, polyethylene, and polystyrene.
The accompanying drawings are included to provide a further understanding of the present invention, and are incorporated in and constitute a part of this specification. The drawings illustrate exemplary embodiments of the present invention and, together with the description, serve to explain principles of the present invention. In the drawings:
Preferred embodiments of the present invention will be described below in more detail with reference to the accompanying drawings. The present invention may, however, be embodied in different forms and should not be constructed as limited to the embodiments set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the present invention to those skilled in the art. In the drawings, the dimensions of layers and regions are exaggerated for clarity of illustration. Like reference numerals refer to like elements throughout.
The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. Unless otherwise defined, all terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains, and should not be interpreted as having an excessively comprehensive meaning nor as having an excessively contracted meaning. Hereinafter, it will be described about an exemplary embodiment of the present invention in conjunction with the accompanying drawings.
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The heat treatment process A may be performed in a vacuum state or an inert gas atmosphere (for example, a nitride atmosphere). Accordingly, compared to a case where the heat treatment process A is performed in the air, the heat treatment process A may be performed at relatively low temperature. The heat treatment process A may be performed at temperature of about 80° C. to about 200° C. When the heat treatment process A is performed at temperature lower than about 80° C., the dewetting phenomenon of the metal mask layer 30 does not sufficiently occur, and it may be accordingly difficult to form the metal mask pattern 35. When the treatment process A is performed at temperature higher than about 200° C., yellowing and cracks may occur in the substrate 10 and the light scattering layer 20 disposed under the metal mask layer 30 during the heat treatment process A.
First, a light scattering layer was formed which includes silicon oxide on a soda-lime glass substrate. A comparative sample was manufactured by forming a metal mask layer including a silver alloy on the light scattering layer, and then heat-treating the metal mask layer for 30 minutes at temperature of about 250° C. in the air.
First, a light scattering layer was formed which includes silicon oxide on a soda-lime glass substrate and then a metal mask layer including a silver alloy was formed on the light scattering layer. Thereafter, experimental samples are heat-treated according to conditions described below.
1) Experimental sample 1 was heat-treated for 2 hours at temperature of about 200° C. in a vacuum oven.
2) Experimental sample 2 was heat-treated for 10 minutes at temperature of about 180° C. on a heating plate in a nitride atmosphere.
3) Experimental sample 3 was heat-treated for 1 hour at temperature of about 160° C. in a vacuum oven.
4) Experimental sample 4 was heat-treated for 1 hour at temperature of about 120° C. in a vacuum oven.
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According to an embodiment, the forming of the recess regions R may include dry-etching the light scattering layer 20. The dry etching process may be, for example, a reactive ion etching or inductively coupled plasma etching process. The recess regions R may be formed to expose a part of top surface of the substrate 10.
The nano structure 40 may have a plurality of nano patterns P protruding in a vertical direction on the top surface of the substrate 10, and the recess regions R may be defined by side walls of the nano patterns P. A height h of the nano patterns P, which is defined to be a distance between the top surface of the nano patterns P and the bottom surface of the recess regions R, may be about 150 nm to about 600 nm.
According to a concept of the present invention, the metal mask pattern 35 may be easily formed at relatively low temperature. The nano structure 40 may be easily formed which includes the nano patterns P having relatively high height by using the metal mask pattern 35. Accordingly, an organic light emitting diode having improved light extraction efficiency may be easily manufactured at a low cost.
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Furthermore, a planarizing layer 50 may be formed (S50) to cover the nano structure 40 on the substrate 10. The planarizing layer 50 may fill the recess regions R of the nano structure 40 and cover the top surface of the nano patterns P. Surface roughness Ra of the planarizing layer 50 may be 10 nm or smaller.
The planarizing layer 50 may include a transparent material. That is, the visible light transmittance of the planarizing layer 50 may be about 90% or higher. The refractive index of the planarizing layer 50 may be about 1.8 to about 2.5. The planarizing layer 50 may be formed from an inorganic material, such as TiO2, ZrO2, TiO2—SiO2, SnO2, or In2O3, an organic-inorganic hybrid material including the inorganic material, polyimide, or a composite material of the inorganic material and a polymer.
In detail, the planarizing layer 50 may be formed by a spin coating, dip coating, slit coating, bar coating, or spray coating method. The planarizing layer 50 is coated by the above-described coating method, and then the planarizing layer 50 may hardened by using heat treatment or a UV irradiation process.
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The first electrode 60 may be formed of a transparent electrode or a reflective electrode. When the first electrode 60 is a transparent electrode, the first electrode 60 is formed from, for example, indium tin oxide (ITO), indium zinc oxide, or tin oxide. When the first electrode 60 is a reflective electrode, the first electrode 60 is formed from, for example, silver (Ag), aluminum (Al), Nickel (Ni), platinum (Pt), or palladium (Pd). The refractive index of the first electrode 60 may be substantially the same as or smaller than that of the planarizing layer 50.
The organic light emitting layer 70 may include an organic light emitting material containing at least any one of a polyfluorene derivative, a (poly)paraphenylenevinylene derivative, a polyphenylene derivative, a polyvinylcarbazole derivative, a polythiopliene derivative, an anthracene derivative, a butadiene derivative, a tetracene derivative, a distyrylarylene derivative, a benzazole derivative, or a carbazole derivative. In addition, the organic light emitting layer 70 may include an organic light emitting material containing a dopant. For example, the dopant may include at least any one of xanthene, perylene, cumarine, rhodamine, rubrene, dicyanomethylenepyran, thiopyran, (thia)pyrilium, periflanthene derivative, indenoperylene derivative, carbostyryl, Nile red, or quinacridone.
The organic light emitting layer 70 may include at least any one of a hole injecting layer, a hole transfer layer, an electron transfer layer, or an electron injecting layer. The organic light emitting layer 70 may generate a light by using recombination of a hole and an electron provided from the first electrode 60 or the second electrode 80.
The second electrode 80 may include a translucent or reflective conductive metal. The second electrode 80 may include, for example, at least one of gold, silver, iridium, molybdenum, palladium, or platinum.
The protection layer 90 may perform a function of protecting the second electrode 80. The protecting layer 90 may include a transparent material, and be formed by using a polymeric material.
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Processes thereafter are the same as the method of manufacturing an organic light emitting diode according to an embodiment of the present invention described in relation to
First, as described in relation to
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The forming of the recess regions R may include a wet-etching the light scattering layer 20. The wet etching process may be an etching process using hydrofluoric acid, buffered oxide etchant (BOE), or an organic solvent. After the wet etching process, a part of the light scattering layer 20 under the recess regions R may be not etched and remain.
The nano structure 40 may have a plurality of nano patterns P protruding in a vertical direction to a top surface of the substrate 10 and the recess regions R may be defined by side walls of the nano patterns P. The height of the nano patterns P, which is defined as a distance between the top surface of the nano patterns P and the bottom surface of the recess regions R, may be about 150 nm to about 600 nm.
Processes thereafter are the same as the method of manufacturing an organic light emitting diode according to an embodiment of the present invention described in relation to
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Processes thereafter are the same as the method of manufacturing an organic light emitting diode according to an embodiment of the present invention described in relation to
According to a concept of the present invention, a metal mask pattern can be easily formed at relatively low temperature. By using the metal mask pattern, a nano structure can be easily formed which includes nano patterns having a relatively high height. Accordingly, an organic light emitting diode having improved light extraction efficiency can be easily manufactured at a low cost.
The above-disclosed subject matter is to be considered illustrative, and not restrictive, and the appended claims are intended to cover all such modifications, enhancements, and other embodiments, which fall within the true spirit and scope of the present invention. Thus, to the maximum extent allowed by law, the scope of the present invention is to be determined by the broadest permissible interpretation of the following claims and their equivalents, and shall not be restricted or limited by the foregoing detailed description.
Number | Date | Country | Kind |
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10-2013-0076994 | Jul 2013 | KR | national |
10-2013-0149227 | Dec 2013 | KR | national |