CN112086494A

CN112086494A - Organic light-emitting display panel

Info

Publication number: CN112086494A
Application number: CN202010959900.4A
Authority: CN
Inventors: 刘勇; 王芬; 周钰明; 卜小海
Original assignee: Nanjing Bready Electronics Co Ltd
Current assignee: Nanjing Bready Electronics Co Ltd
Priority date: 2020-09-14
Filing date: 2020-09-14
Publication date: 2020-12-15
Anticipated expiration: 2040-09-14
Also published as: CN112086494B

Abstract

An embodiment of the present application provides an organic light emitting display panel, which includes: a blue backlight source emitting blue light; the composite optical film comprises a red quantum dot optical film corresponding to the red sub-pixel R, a green quantum dot optical film corresponding to the green sub-pixel G and a blue optical film corresponding to the blue sub-pixel B; the composite optical film comprises a light coupling layer and a light extraction layer, the light coupling layer is arranged between the light extraction layer and the blue backlight source, and the refractive index of the light coupling layer is greater than that of the light extraction layer; the light extraction layer comprises a long-range ordered porous reticular patterning structure which is arranged in an array mode, and the red quantum dots, the green quantum dots and the blue quantum dots are distributed on the edges of meshes of the reticular patterning structure. The embodiment of the application solves the defects of high manufacturing cost, low luminous efficiency and low color purity in the prior art.

Description

Organic light-emitting display panel

Technical Field

The present invention relates to an organic light emitting display panel, and more particularly, to an organic light emitting display panel having a composite optical film.

Background

In recent years, Organic Light-Emitting Diode (OLED) display devices have become very popular flat panel display device products at home and abroad because OLED display devices have the characteristics of self-luminescence, wide viewing angle, short reaction time, high luminous efficiency, wide color gamut, thin thickness, large size and flexibility, simple manufacturing process, and the like, and have the potential of low cost.

The organic light emitting display device can be classified into three modes of RGB-OLED, W-OLED + Color Filter (Color Filter), B-OLED + Color conversion layer according to the colorization mode. The RGB-OLED mode uses three light-emitting materials of red, green and blue to respectively manufacture organic light-emitting layers to form RGB pixels, has the characteristic of good light-emitting efficiency, and does not need a color filter or a thin film of a color change layer. However, the RGB-OLED three-color process adopts a shielding (shadow mask) evaporation method, so that the high-precision pixels have high requirements on the process precision, and the manufacturing cost is greatly increased; and most organic luminescent materials emit with wide spectrum, so that the color purity of the compounded organic luminescent materials is not high. The W-OLED is an organic light-emitting layer made of a white light-emitting material, a layer of color filter is added in the middle, and the light-emitting efficiency is far lower than that of an RGB-OLED mode because other light rays except the sub-pixels with the corresponding colors are filtered in the filtering process. The organic light emitting layer is made of blue light emitting materials in a B-OLED + color conversion layer mode, a layer of film of the color conversion layer is arranged at an interval during light emitting, the film of the color conversion layer absorbs blue light emitted by the blue light emitting materials and then emits red light and green light respectively, and due to energy loss in down conversion, the light emitting efficiency of the device is not the same as that of an RGB-OLED mode.

The foregoing description is provided for general background information and is not admitted to be prior art.

Disclosure of Invention

Embodiments of the present application provide an organic light emitting display panel having a composite optical film with color conversion performance.

The present invention provides an organic light emitting display panel, which includes:

a blue backlight source emitting blue light;

the composite optical film comprises a red quantum dot optical film corresponding to the red sub-pixel R, a green quantum dot optical film corresponding to the green sub-pixel G and a blue optical film corresponding to the blue sub-pixel B;

the red quantum dots in the red quantum dot optical film convert the blue light into red light, the green quantum dots in the green quantum dot optical film convert the blue light into green light, and the blue optical film directly emits the blue light or converts the blue light into another blue light with different emission wavelengths;

the composite optical film comprises a light coupling layer and a light extraction layer, the light coupling layer is arranged between the light extraction layer and the blue backlight source, and the refractive index of the light coupling layer is greater than that of the light extraction layer;

the light extraction layer comprises a long-range ordered porous reticular patterning structure which is arranged in an array mode, and the red quantum dots, the green quantum dots and the blue quantum dots are distributed on the edges of meshes of the reticular patterning structure.

Preferably, the method for preparing the composite optical film comprises the following steps:

step S1, providing a substrate;

step S2, preparing a light extraction layer precursor solution, wherein the light extraction layer precursor solution comprises an amphiphilic block copolymer, metal ions and a first solvent, and the first solvent is a nonpolar solvent;

step S3, forming a light extraction layer precursor solution thin film layer on the substrate;

step S4, forming a second solvent aerosol in the closed space, wherein the second solvent aerosol comprises a second solvent and non-metal ions, and the second solvent is a polar solvent; transferring the substrate into the closed space, heating the closed space to volatilize the first solvent and the second solvent, and self-assembling and curing to form a light extraction layer, wherein the light extraction layer has a long-range ordered porous reticular patterning structure which is arranged in an array; in the process of forming the light extraction layer by self-assembly curing, the non-metal ions in the second solvent and the metal ions in the precursor solution of the light extraction layer grow in situ to form the quantum dots.

Preferably, in step S4, the substrate is masked by patterning using a mask corresponding to the sub-pixel pattern, and in the self-assembly curing process, the in-situ growth time of the quantum dots is different by controlling the curing time, so that the particle diameters of the quantum dots at the composite optical film corresponding to different sub-pixels are different, and further, the composite optical film emits color light of different colors.

Preferably, in step S4, the non-metal ions are contained or not contained in the second solvent during the self-assembly curing process of the blue optical film, so that the blue optical film obtained by curing contains blue quantum dots or does not contain quantum dots.

Preferably, the composite optical film further includes a release layer disposed on a side of the light coupling layer away from the light extraction layer.

Preferably, the release layer is peeled off and then directly applied to the light-emitting side of the blue backlight.

Preferably, the red quantum dot optical film, the green quantum dot optical film and the blue optical film are isolated from each other by a black matrix.

Preferably, the red quantum dot optical film, the green quantum dot optical film and the blue optical film have a half-peak width of 5 nm to 50 nm.

Preferably, the blue backlight source includes an anode, a cathode, and an organic layer located between the anode and the cathode, and a microcavity structure is formed between the anode and the cathode.

Preferably, in step S4, small droplets of uniform particle size in the second solvent mist are adsorbed on the surface of the thin film of the light extraction layer precursor solution thin film layer; in the process of forming the light extraction layer by self-assembly curing, the amphiphilic block copolymer takes liquid drops as a template to form the long-range ordered porous reticular patterning structure arranged in an array.

Has the advantages that: the composite optical film is used as a color conversion layer of an organic light-emitting display panel, the defects of high manufacturing cost, low luminous efficiency and low color purity of three colorization modes in the prior art are overcome, a light extraction layer with a quantum dot long-range ordered porous reticular patterning structure is generated in situ, blue light of a blue backlight source can be converted into RGB (red, green and blue) colored light, and the reticular structure is favorable for coupling light; the light extraction layer is matched with the light coupling layer, and the total reflection of blue light of the blue backlight source is also obviously reduced.

Drawings

The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments consistent with the present application and together with the description, serve to explain the principles of the application.

FIG. 1 is a flow chart of a method of making a composite optical film according to a first embodiment of the present disclosure;

fig. 2 is a schematic cross-sectional view of an organic light emitting display panel according to a second embodiment of the present application.

With the above figures, there are shown specific embodiments of the present application, which will be described in more detail below. These drawings and written description are not intended to limit the scope of the inventive concepts in any manner, but rather to illustrate the inventive concepts to those skilled in the art by reference to specific embodiments.

Detailed Description

Reference will now be made in detail to the exemplary embodiments, examples of which are illustrated in the accompanying drawings. When the following description refers to the accompanying drawings, like numbers in different drawings represent the same or similar elements unless otherwise indicated. The embodiments described in the following exemplary embodiments do not represent all embodiments consistent with the present application. Rather, they are merely examples of apparatus and methods consistent with certain aspects of the present application, as detailed in the appended claims.

It should be noted that, in this document, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, the recitation of an element by the phrase "comprising an … …" does not exclude the presence of additional like elements in the process, method, article, or apparatus that comprises the element, and further, where similarly-named elements, features, or elements in different embodiments of the disclosure may have the same meaning, or may have different meanings, that particular meaning should be determined by their interpretation in the embodiment or further by context with the embodiment.

It should be understood that although the terms first, second, third, etc. may be used herein to describe various information, such information should not be limited to these terms. These terms are only used to distinguish one type of information from another. For example, first information may also be referred to as second information, and similarly, second information may also be referred to as first information, without departing from the scope herein. The word "if" as used herein may be interpreted as "at … …" or "when … …" or "in response to a determination", depending on the context. Also, as used herein, the singular forms "a", "an" and "the" are intended to include the plural forms as well, unless the context indicates otherwise. It will be further understood that the terms "comprises," "comprising," "includes" and/or "including," when used in this specification, specify the presence of stated features, steps, operations, elements, components, items, species, and/or groups, but do not preclude the presence, or addition of one or more other features, steps, operations, elements, components, species, and/or groups thereof. The terms "or" and/or "as used herein are to be construed as inclusive or meaning any one or any combination. Thus, "A, B or C" or "A, B and/or C" means "any of the following: a; b; c; a and B; a and C; b and C; A. b and C ".

It should be understood that, although the steps in the flowcharts in the embodiments of the present application are shown in order as indicated by the arrows, the steps are not necessarily performed in order as indicated by the arrows. The steps are not performed in the exact order shown and may be performed in other orders unless explicitly stated herein. Moreover, at least some of the steps in the figures may include multiple sub-steps or multiple stages that are not necessarily performed at the same time, but may be performed at different times, in different orders, and may be performed alternately or at least partially with respect to other steps or sub-steps of other steps.

It should be noted that step numbers such as S1 and S2 are used herein for the purpose of more clearly and briefly describing the corresponding content, and do not constitute a substantial limitation on the sequence, and those skilled in the art may perform S2 first and then S1 in specific implementation, which should be within the scope of the present application.

The following describes in detail the technical solutions of the embodiments of the present application and how to solve the above technical problems with specific embodiments. The following several specific embodiments may be combined with each other, and details of the same or similar concepts or processes may not be repeated in some embodiments. Embodiments of the present application will be described below with reference to the accompanying drawings.

The embodiment of the application provides a preparation method of optical film, optical film is composite optical film, including optical coupling layer and light extraction layer, the light extraction layer has the long-range orderly porous netted patterned structure that is the array and arranges, contain the quantum dot in the light extraction layer and be used as the light conversion material, the quantum dot distribute in the netted patterned structure's of light extraction layer mesh edge, the hole is that through hole or arc are sunken. As shown in fig. 1, the preparation method comprises:

s1, providing a substrate;

illustratively, the substrate may be used as a light coupling layer for a composite optical film. However, the substrate may be used only as a film formation substrate of the composite optical film, and a light coupling layer may be additionally provided on a side of the film formation substrate adjacent to the light extraction layer.

The visible light transmittance of the light coupling layer is 30% -100%, the refractive index is 1.5-2.0, and the thickness of the light coupling layer is 100 nanometers-10 micrometers.

The optical coupling layer is a transparent layer body, and the preparation material of the optical coupling layer can be at least one of polymethyl methacrylate, polyimide, polydimethylsiloxane, polyethylene terephthalate, epoxy resin, polycarbonate, nylon, acrylonitrile-styrene copolymer, transparent polypropylene, transparent ABS (acrylonitrile-butadiene-styrene copolymer), butadiene-styrene copolymer polyvinyl chloride, ethylene, polyethylene naphthalate, polyether sulfone resin or polyethylene imine.

The preparation process of the optical coupling layer is common knowledge in the field, and is not described herein again, a film can be formed on the sacrificial layer by a pre-dissolved transparent polymer through a solution processing mode, then the film is cured through heating or ultraviolet irradiation to form a film, and then the optical coupling layer is obtained after the sacrificial layer is stripped. In addition, the sacrificial layer may not be stripped, and the sacrificial layer directly serves as the substrate in the step S1.

S2, preparing a light extraction layer precursor solution;

illustratively, the light extraction layer precursor solution includes an amphiphilic block copolymer, a metal ion, and a first solvent.

Preferably, the amphiphilic block copolymer is soluble in the first solvent. Specifically, the amphiphilic block copolymer is a block copolymer containing a block of polyacrylic acid, polyethylene oxide, polyvinyl pyridine, polyvinyl pyrrolidone, or N-vinyl imidazole, and is preferably one or more of polystyrene-b-polyacrylic acid, polystyrene-b-polyethylene oxide, and polyvinyl pyridine-b-polyethylene oxide.

Preferably, the metal ion is used as a first precursor for generating the quantum dot, and specifically, the metal ion may be an ion formed by a group II element or a group IV element, wherein the group II element is a group IIb element Zn, Cd, Hg, and the group IV element is a group IVa element Pb, Sn.

Preferably, the first solvent may be a non-polar solvent, and the first solvent is volatile. Specifically, the first solvent is one or more of toluene, benzene, chloroform and dichloromethane. Preferably, the first solvent is immiscible with the material of the light coupling layer.

As a preferred example, the amphiphilic block copolymer has a group that coordinates to the metal ion, such as quinoline, acridine, phenanthridine, oxazole, thiazole, oxadiazole, thiadiazole, pyridine, benzimidazole, benzothiazole, bipyridine, phenanthroline, and the like. When the quantum dots are formed by metal ions, the amphiphilic block copolymer is coordinated with the metal ions, so that the quantum dots can be stabilized better, and the service life of the quantum dots can be prolonged. However, applicants have found that quantum dots can still be formed at later stages of the reaction when the amphiphilic block copolymer does not have a coordinating group. Therefore, the above-mentioned coordination conditions are not essential.

Preferably, in the precursor solution, the concentration of the amphiphilic block copolymer is 10 to 40 mass%, and the concentration of the metal ion is 0.5 to 10 mass%.

S3, forming a light extraction layer precursor solution film layer on the substrate;

for example, the light extraction layer precursor solution thin film layer may be formed by any solution film forming method known in the art. Specifically, the solution film forming method includes one or more of spin coating, drop casting, inkjet printing, cast film forming, and nozzle printing.

S4, self-assembling and curing to form a light extraction layer;

illustratively, the self-assembly curing process is performed in an enclosed space, and after the substrate is transferred into the enclosed space, a second solvent aerosol is formed in the enclosed space, wherein the second solvent aerosol comprises a second solvent and non-metal ions.

Preferably, the second solvent can be a polar solvent, and is suitable for forming aerosol in the closed space in a spraying mode and the like, wherein the aerosol contains liquid drops with uniform particle size, and the particle size of the liquid drops is 100 nanometers-5 micrometers. Specifically, the second solvent may be one or more of water, acetone, ethanol, chloroform, diethyl ether, acetic acid, acetone, acetonitrile, isopropanol, and methanol. The second solvent is immiscible with the first solvent, but the amphiphilic front-stage copolymer is soluble in the second solvent.

Preferably, the non-metal ions are used as a second precursor for generating quantum dots, and the non-metal ions are dissolved in the second solvent, that is, the second solvent aerosol formed in the enclosed space while having the non-metal ions. Specifically, the non-metallic ions include ions composed of group VI elements, which are group VIa S, Se, Te.

Preferably, the self-assembly process is as follows: and after the substrate is transferred into the closed space, forming second solvent aerosol containing the non-metal ions in the closed space, wherein small drops with uniform particle sizes in the aerosol are adsorbed on the surface of the film of the precursor solution film layer of the light extraction layer to form a uniform drop layer, and meanwhile, because the first solvent and the second solvent are not mutually soluble, the drop layer is still distributed on the surface of the film in a plurality of independent drop shapes, and a continuous second solvent film cannot be formed. That is, the final second solvent droplets form a large area of long-range ordered patterned arrangement in the form of an array. Meanwhile, the polar block in the amphiphilic block copolymer in the first solvent enters the interior of the liquid drop, and the non-polar block wraps the periphery of the liquid drop, so that an effective stabilizing effect is provided, and the phenomenon that the regularity of the array template is damaged due to the convergence among the liquid drops is prevented.

And heating the closed space, wherein the heating temperature is preferably 20-80 ℃, and the heating temperature is preferably lower than the boiling points of the first solvent and the second solvent, so that the first solvent and the second solvent can volatilize at a slow speed, and the applicant finds that when the heating temperature is too high, the solvent can volatilize rapidly, and therefore, the self-assembly effect cannot be realized or the porous morphology of the self-assembled film is not uniform. With the volatilization of the solvent, the viscosity of the precursor solution gradually rises, and the amphiphilic block copolymer is primarily fixed by taking the liquid drop as a template to form a porous structure surface; finally, after the first solvent and the second solvent are volatilized in sequence, the appearance of the liquid drops is remained on the surface of the film formed by solidification, and a long-range ordered porous reticular patterning structure arranged in an array is formed.

Meanwhile, along with the self-assembly process, the non-metal ions in the second solvent react with the metal ions in the precursor solution to form quantum dots, and the quantum dots are only formed at the edges of the porous network structure. In addition, when the amphiphilic block copolymer in the first solvent has a group coordinated to a metal ion, it has a stabilizing effect on the quantum dot generated by the reaction, and thus it is possible to generate a fluorescent quantum dot having a higher quantum efficiency. Specifically, the quantum dots may be one or more of CdS, ZnS, PbS, CdSe, ZnSe, PbSe, CdTe, ZnTe, PbTe, CdTeS, ZnTeS.

Preferably, the visible light transmittance of the light extraction layer is 20% -80%, the refractive index is 1.3-1.8, the refractive index of the light extraction layer is smaller than that of the light coupling layer, the thickness of the light extraction layer is 100 nanometers-10 micrometers, and the aperture of the light extraction layer is preferably 200 nanometers-5 micrometers.

Therefore, as the preparation method of the optical film according to the first embodiment of the present application, by using the mutual solubility relationship among the amphiphilic block copolymer, the first solvent, and the second solvent, the droplet of the second solvent is creatively used as a template, and the amphiphilic block copolymer is self-assembled to form a large-area long-range ordered porous network patterning structure in the process of curing the thin film, and the network patterning structure is beneficial to coupling light out. And in the curing process, the in-situ generation of the fluorescent quantum dots is also accompanied, the porous light extraction layer with the fluorescent quantum dots is prepared by a one-step method, and the quantum dots have photoluminescence performance and can convert incident light into light with different colors.

Therefore, the light extraction layer and the light coupling layer form the composite optical film in the invention, which is suitable for being used as a color conversion layer of an optical device, and color light emitted by the optical device is converted into color light absorbed by quantum dots in the composite optical film and emits color light corresponding to the quantum dots; meanwhile, the light extraction layer has a porous structure, so that the light extraction efficiency of the composite optical film can be remarkably improved; furthermore, the light extraction layer has a large number of porous net structures, so that the light transmittance and the refractive index of the light extraction layer are lower than those of the optical functional film in the optical device, and therefore, the invention also creatively arranges the optical coupling layer between the light extraction layer and the optical device, and the light transmittance and the refractive index of the optical coupling layer are between those of the optical functional film and the light extraction layer in the optical device, so that the total reflection of light between the optical functional film and the light extraction layer interface in the optical device can be obviously reduced, and the light extraction efficiency of the optical device is further enhanced.

In particular, the composite optical film and the method for preparing the same are also applicable to optical devices, exemplarily, organic light emitting display panels, and particularly, the composite optical film can be used as a color conversion layer of the organic light emitting display panels. This will be explained below by means of a second embodiment of the invention according to fig. 2.

Fig. 2 is a schematic cross-sectional view of an organic light emitting display panel according to a second embodiment of the present disclosure, wherein the organic light emitting display panel includes a composite optical film 100 and a blue backlight 200, and the blue backlight 200 may be formed of a blue light emitting organic light emitting layer. Further, the composite optical film 100 may be prepared by the preparation method according to the first embodiment of the present disclosure, and the light coupling layer of the composite optical film 100 is disposed between the light extraction layer and the blue backlight 200.

The composite optical film 100 includes a red quantum dot optical film corresponding to the red sub-pixel R, a green quantum dot optical film corresponding to the green sub-pixel G, and a blue optical film corresponding to the blue sub-pixel B. The three-color optical films have the same porous structure, and are different only in that quantum dots contained in the optical films are different, the red quantum dot optical film contains quantum dots capable of emitting red light, the green quantum dot optical film contains quantum dots capable of emitting green light, and the blue optical film does not contain quantum dots or contains quantum dots capable of emitting blue light. Specifically, in step S4, the substrate is masked by patterning using a mask corresponding to the sub-pixel pattern, and in the self-assembly curing process, the in-situ growth time of the quantum dots is varied by controlling the curing time, so that the particle diameters of the quantum dots at the composite optical film corresponding to different pixels are varied, and the quantum dots emit different colors of light. Illustratively, the self-assembly curing time of the red quantum dot optical film corresponding to the red sub-pixel R is 20 minutes to 120 minutes, the self-assembly curing time of the green quantum dot optical film corresponding to the green sub-pixel G is 10 minutes to 100 minutes, and the self-assembly curing time of the blue optical film corresponding to the blue sub-pixel B is 5 minutes to 90 minutes.

Preferably, the composite optical film 100 of the present application further has a release layer disposed on one side of the light coupling layer away from the light extraction layer, which can protect the composite optical film. When the composite optical film 100 is used, the release layer may be peeled off and directly attached to the light-emitting side of the blue backlight 200. Therefore, the preparation process of the composite optical film and the preparation process of the blue backlight source 200 are independent from each other, so that the influence of a solvent in the preparation process of the composite optical film on the blue backlight source 200 is avoided, and meanwhile, the composite optical film can be directly pasted after the release layer is peeled off, so that the use is convenient, and the preparation process cost is favorably reduced.

For example, as shown in fig. 2, an anode 201 and a cathode 202 are disposed on two sides of the blue light emitting layer, when the organic light emitting display panel is used for displaying, the anode 201 and the cathode 202 receive a voltage signal, and under the action of a voltage difference between the anode 201 and the cathode 202, the organic light emitting layer emits blue light, and after the blue light is emitted to the composite optical film 100, the blue light is emitted through a red quantum dot optical film included in the red sub-pixel R, and the red quantum dot optical film converts the blue light into red light, so that the red sub-pixel R emits red light. The blue light is converted into green light by the green quantum dot optical film, so that the green sub-pixel G emits the green light. As an embodiment, the blue optical film corresponding to the blue sub-pixel B may be an optical film with a porous structure that does not include quantum dots, and blue light emitted by the blue backlight source may be emitted as blue light at a position of the blue sub-pixel, so that the blue sub-pixel B emits blue light; as another embodiment, a blue quantum dot optical film including blue quantum dots may be disposed at an optical film corresponding to the blue sub-pixel B, the blue light is emitted through the blue quantum dot optical film included in the blue sub-pixel B, and the blue quantum dot optical film converts the blue light into another blue light with a different emission wavelength, so that the blue sub-pixel B emits the blue light to realize color display of the organic light emitting display panel.

Illustratively, to improve the sub-pixel resolution, the red quantum dot optical film, the green quantum dot optical film, and the blue optical film in this embodiment may be isolated from each other by a black matrix. In addition, the red, green and blue optical films in this embodiment are further provided with glass substrates on the sides thereof away from the blue backlight 200. The quantum dots in the red quantum dot optical film, the green quantum dot optical film and the blue optical film can be made of the same material due to the quantum size effect, and the difference is only that the particle size of the quantum dots in each color is different, specifically, the red quantum dots have the particle size of 8-20 nanometers, the green quantum dots have the particle size of 5-15 nanometers, the blue quantum dots have the particle size of 2-10 nanometers, the particle size of the red quantum dots is larger than that of the green quantum dots, and the particle size of the green quantum dots is larger than that of the blue quantum dots. In the process of preparing the optical film, the growth particle size of the quantum dots can be controlled by controlling the time length of a self-assembly curing process, specifically, the time length of the self-assembly curing process of the red quantum dot optical film is 0.5-2 hours, the time length of the self-assembly curing process of the green quantum dot optical film is 0.2-1.5 hours, the time length of the self-assembly curing process of the blue quantum dot optical film is 5-40 minutes, the time length of the self-assembly curing process of the red quantum dot optical film is longer than that of the self-assembly curing process of the green quantum dot optical film, and the time length of the self-assembly curing process of the green quantum dot optical film is longer than that of the self-assembly curing process of the blue quantum dot optical film.

Illustratively, in order to improve the color purity of the organic light emitting display panel, the red quantum dot optical film, the green quantum dot optical film and the blue optical film in this embodiment preferably have a full width at half maximum (FWHM) of 5 nm to 50 nm, so that the color purity of the color light compounded by the organic light emitting material is significantly higher than that of the color light compounded by the organic light emitting material, which is more beneficial to improving the display quality of the display panel.

Illustratively, as shown in fig. 2, the organic light emitting display panel further includes a pixel circuit 400, and the pixel circuit 400 includes a thin film transistor T and a storage capacitor Cst. The anode 201 is connected to the drain of the corresponding thin film transistor T through a via hole. Note that fig. 2 only illustrates the storage capacitor Cst in the pixel circuit and one thin film transistor T directly connected to the anode 201, and the layer structure of the other thin film transistors in the pixel circuit may be the same as that of the thin film transistor.

Illustratively, as shown in fig. 2, the organic light emitting display panel further includes a support pillar 500 positioned between the composite optical film 100 and the blue backlight 200.

Illustratively, the anode 201 and the cathode 202 have an organic layer therebetween, and the specific configuration of the organic layer is not limited and may be various known configurations, except for including the aforementioned organic light emitting layer emitting blue light. For example, the organic layer may have: a layered structure of a hole transport layer, an organic light emitting layer, and an electron transport layer; a layered structure of a hole transport layer and a light emitting layer also serving as an electron transport layer; a layered structure of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, and an electron injection layer, and the like. Further, in the case where these layered structures and the like are "series units", the organic layer may have a two-stage series structure in which a first series unit, a connection layer, and a second series unit are stacked. Alternatively, the organic layer may have a series structure of three or more stages in which three or more stages of series units are stacked.

For example, the organic layer is formed by vacuum evaporation of an organic material. However, the present embodiment is not limited to such an example, and the organic layer may be formed by various known methods. Examples of a method that can be used as a method of forming an organic layer include: a physical vapor deposition method (PVD method) such as a vacuum evaporation method; a printing method such as a screen printing method and an inkjet printing method; a laser transfer method of transferring an organic layer by separating the organic layer formed on a laser-light absorbing layer on a transfer substrate by emitting laser light to a layered structure of the laser-light absorbing layer and the organic layer; various coating methods, etc.

Since the organic light emitting display panel is a top emission type, the anode 201 includes a material capable of reflecting light from the organic layer. For example, the anode 201 includes an alloy of aluminum and neodymium (Al — Nd alloy). The film thickness of the anode 201 is, for example, about 0.1 to 1 μm. However, the present embodiment is not limited to such an example, and the anode 201 may include various known materials used as a material of a light reflection side electrode used as an anode in a general-purpose organic EL display device. Further, the film thickness of the anode 201 is not limited to the above-described example, and the anode 201 may be formed as appropriate within the range of the film thickness generally employed in an organic EL display device.

For example, the anode 201 may include a metal having a high work function, such as platinum (Pt), gold (Au), silver (Ag), chromium (Cr), tungsten (W), nickel (Ni), copper (Cu), iron (Fe), cobalt (Co), or tantalum (Ta), or an alloy (e.g., an Ag — Pd — Cu alloy containing silver as a main component, palladium (Pd) in an amount of 0.3 to 1 mass%, and copper in an amount of 0.3 to 1 mass%, or an Al — Nd alloy). Alternatively, as the anode 201, a conductive material having a low work function value and a high light reflectance, such as aluminum or an alloy containing aluminum, may be used. In this case, it is preferable to improve the hole injection performance by providing an appropriate hole injection layer or the like on the anode 201. Alternatively, the anode 201 may have a structure in which a transparent conductive material having excellent hole injection characteristics, such as Indium Tin Oxide (ITO) or Indium Zinc Oxide (IZO), is laminated on a dielectric multilayer film, or a reflective film having high light reflectance, such as aluminum.

The cathode 202 includes a material capable of transmitting light from the organic layer. For example, the cathode 202 includes an alloy of magnesium and silver (Mg — Ag alloy). Further, the film thickness of the cathode 202 is, for example, about 10 nm. However, the present embodiment is not limited to such an example, and the cathode 202 may include various known materials used as a material of a light-transmitting side electrode used as a cathode in a general-purpose organic EL display device. Further, the thickness of the cathode 202 is not limited to the above-described example, and the cathode 202 may be formed as appropriate within the range of the film thickness generally employed in the organic EL display device.

For example, the cathode 202 may include aluminum, silver, magnesium, calcium (Ca), sodium (Na), strontium (Sr), an alloy of an alkali metal and silver, an alloy of an alkaline earth metal and silver (e.g., an alloy of magnesium and silver (Mg-Ag alloy)), an alloy of magnesium and calcium (Mg-Ca alloy), an alloy of aluminum and lithium (Al-Li alloy), and the like. In the case where these materials are used as a single layer, the film thickness of the cathode 202 is, for example, about 4 nm to 50 nm. Alternatively, the cathode 202 may have a structure in which the above-described material layer and the transparent electrode (for example, a thickness from about 30 nm to 1 μm) include, for example, ITO or IZO layered from the organic layer 111 side. In the case of such a layered structure, the thickness of the above-mentioned material layer can also be reduced to, for example, about 1 to 4 nm. Alternatively, the cathode 202 may include only a transparent electrode. Alternatively, for the cathode 202, a bus electrode (auxiliary electrode) including a low-resistance material such as aluminum, an aluminum alloy, silver, a silver alloy, copper, a copper alloy, gold, a gold alloy, or the like may be provided to achieve low resistance of the cathode 202 as a whole.

Illustratively, the anode 201 is preferably a reflective electrode and the cathode 202 is preferably a semi-reflective and semi-transmissive electrode, and thus a micro-cavity structure is formed between the anode 201 and the cathode 202 to facilitate the light extraction efficiency of the organic layer.

For example, the anode 201 and the cathode 202 are formed by depositing a material having a predetermined thickness by a vacuum evaporation method, and then patterning the film by an etching method. However, the present embodiment is not limited to such an example, and the anode 201 and the cathode 202 may be formed by various known methods. Examples of a method of forming the anode 201 and the cathode 202 include: evaporation methods, including electron beam evaporation methods, hot filament evaporation methods, and vacuum evaporation methods; sputtering; chemical Vapor Deposition (CVD); metal Organic Chemical Vapor Deposition (MOCVD); a combination of an ion plating method and an etching method; various printing methods (e.g., screen printing method, ink-jet printing method, metal mask printing method, etc.); an electroplating method (an electroplating method, a chemical plating method, etc.); a peeling method; a laser ablation method; sol-gel methods, and the like.

Therefore, as a second embodiment of the present application, the composite optical film in the present application is used as a color conversion layer of an organic light emitting display panel, so that the defects of high manufacturing cost, low light emitting efficiency and low color purity of three colorization modes in the prior art are overcome, a light extraction layer with a quantum dot long-range ordered porous mesh patterned structure is generated in situ, and not only can blue light of a blue backlight source be converted into RGB colored light, but also the mesh structure is beneficial to light coupling; the light extraction layer is matched with the light coupling layer, and the total reflection of blue light of the blue backlight source is also obviously reduced.

The embodiment of the invention also provides a display device which comprises the display panel, wherein the display panel comprises the optical film and the blue backlight source. As a specific example, the display device may be any electronic device with a display function, such as a mobile phone, a tablet computer, a notebook computer, an electronic book, or a television.

Other embodiments of the present application will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. The embodiments of the present application are intended to cover any variations, uses, or adaptations of the application following, in general, the principles of the application and including such departures from the present disclosure as come within known or customary practice within the art to which the application pertains. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the application being indicated by the following claims.

It will be understood that the present application is not limited to the precise arrangements described above and shown in the drawings and that various modifications and changes may be made without departing from the scope thereof. The scope of the application is limited only by the appended claims.

Claims

1. An organic light emitting display panel, comprising:

a blue backlight source emitting blue light;

2. The organic light-emitting display panel according to claim 1, wherein the method for preparing the composite optical film comprises:

step S1, providing a substrate;

3. The organic light-emitting display panel according to claim 2, wherein in step S4, the substrate is patterned and masked by a mask corresponding to the sub-pixel pattern, and in the self-assembly curing process, the in-situ growth time of the quantum dots is varied by controlling the curing time, so that the particle size of the quantum dots at the composite optical film corresponding to different sub-pixels is varied, and the quantum dots emit different colors of light.

4. The organic light-emitting display panel according to claim 2, wherein in step S4, the blue optical film obtained by curing contains blue quantum dots or does not contain quantum dots by controlling the content or the absence of non-metal ions in the second solvent during the self-assembly curing process of the blue optical film.

5. The organic light-emitting display panel according to claim 1, wherein the composite optical film further comprises a release layer disposed on a side of the light coupling layer away from the light extraction layer.

6. The organic light-emitting display panel according to claim 5, wherein the release layer is peeled off and directly attached to the light-emitting side of the blue backlight.

7. The organic light-emitting display panel according to claim 1, wherein the red quantum dot optical film, the green quantum dot optical film, and the blue optical film are isolated from each other by a black matrix.

8. The organic light-emitting display panel according to claim 1, wherein the red quantum dot optical film, the green quantum dot optical film, and the blue optical film have a half-peak width of 5 nm to 50 nm.

9. The organic light-emitting display panel according to claim 1, wherein the blue backlight comprises an anode, a cathode, and an organic layer between the anode and the cathode, and a microcavity structure is formed between the anode and the cathode.

10. The organic light-emitting display panel according to claim 2, wherein in step S4, the small droplets with uniform particle size in the second solvent aerosol are adsorbed on the surface of the thin film of the light extraction layer precursor solution thin film layer; in the process of forming the light extraction layer by self-assembly curing, the amphiphilic block copolymer takes liquid drops as a template to form the long-range ordered porous reticular patterning structure arranged in an array.