WO2016017734A1 - 有機el発光装置 - Google Patents
有機el発光装置 Download PDFInfo
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- WO2016017734A1 WO2016017734A1 PCT/JP2015/071605 JP2015071605W WO2016017734A1 WO 2016017734 A1 WO2016017734 A1 WO 2016017734A1 JP 2015071605 W JP2015071605 W JP 2015071605W WO 2016017734 A1 WO2016017734 A1 WO 2016017734A1
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- organic
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Images
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/85—Arrangements for extracting light from the devices
- H10K50/854—Arrangements for extracting light from the devices comprising scattering means
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/02—Details
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/85—Arrangements for extracting light from the devices
- H10K50/856—Arrangements for extracting light from the devices comprising reflective means
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/85—Arrangements for extracting light from the devices
- H10K50/858—Arrangements for extracting light from the devices comprising refractive means, e.g. lenses
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2102/00—Constructional details relating to the organic devices covered by this subclass
- H10K2102/301—Details of OLEDs
- H10K2102/331—Nanoparticles used in non-emissive layers, e.g. in packaging layer
Definitions
- the present invention relates to an organic EL light emitting device.
- organic EL is an abbreviation for organic electroluminescence.
- organic EL light-emitting device in which a light-emitting layer is provided between a plurality of electrodes to obtain light emission has been studied for use as a display device in place of a liquid crystal cell.
- organic EL light-emitting devices are also being considered for use as surface light source devices such as flat-type illuminations and backlights for liquid crystal display devices, taking advantage of their high luminous efficiency, low voltage drive, light weight, and low cost. Yes.
- an organic EL light-emitting device When an organic EL light-emitting device is used as a light source of a surface light source device, it is a problem to extract useful light from the element with high efficiency.
- the light emitting layer itself of an organic EL light emitting device has high luminous efficiency, depending on conditions such as a difference in refractive index between layers constituting the device, there is a loss of light until light is transmitted through the layer and emitted. growing. Therefore, it is required to reduce such light loss as much as possible.
- Patent Document 1 proposes forming a pyramid-shaped recess on the light exit surface of an organic EL light emitting device. This is expected to improve the light extraction efficiency.
- the array of prisms can be easily manufactured with fewer steps than the pyramidal concave and convex portions. Therefore, in general, the array of prisms can be manufactured at a lower cost than the pyramidal concave and convex portions.
- the present invention has been made in view of the above-described problems, and an object thereof is to provide an organic EL light emitting device having a row-like prism and excellent in light extraction efficiency.
- the inventor of the present invention in an organic EL light emitting device including a light emitting layer, a light scattering layer, and a row of prisms in this order, the thickness of the light scattering layer and the mean free path of light scattering. And satisfying the predetermined requirements, the light extraction efficiency of the organic EL light emitting device can be increased, and the present invention has been completed. That is, the present invention is as follows.
- a light emitting layer capable of generating light;
- a first light scattering layer comprising first light scattering particles having an average particle diameter of 0.1 ⁇ m to 1 ⁇ m;
- a row of prisms in this order The organic EL light-emitting device wherein the mean free path L1 of light scattering in the first light scattering layer and the thickness D1 of the first light scattering layer are D1 / L1 ⁇ 6.
- the organic EL light emitting device according to any one of [1] to [7], further including a second light scattering layer capable of scattering the light between the prism and the light emitting layer.
- a second light scattering layer capable of scattering the light between the prism and the light emitting layer.
- the second light scattering layer is provided between the light emitting layer and the first light scattering layer.
- the organic EL light-emitting device according to any one of [1] to [9], wherein the first light scattering layer has adhesiveness.
- an organic EL light emitting device that includes a row of prisms and is excellent in light extraction efficiency.
- FIG. 1 is a perspective view schematically showing an organic EL light emitting device according to the first embodiment of the present invention.
- FIG. 2 is a cross-sectional view schematically showing a cross section of the prism layer of the organic EL light emitting device according to the first embodiment of the present invention.
- FIG. 3 is a graph showing the relationship between the mean free path of a light scattering layer according to a certain example and the particle diameter of light scattering particles contained in the light scattering layer.
- FIG. 4 is a perspective view schematically showing an organic EL light emitting device according to the second embodiment of the present invention.
- FIG. 5 is a perspective view schematically showing an organic EL light emitting device according to the third embodiment of the present invention.
- FIG. 1 is a perspective view schematically showing an organic EL light emitting device according to the first embodiment of the present invention.
- FIG. 2 is a cross-sectional view schematically showing a cross section of the prism layer of the organic EL light emitting device according to the first embodiment of the
- FIG. 6 is a plan view schematically showing a light exit surface of a prism layer according to an example.
- FIG. 7 is a graph showing the relationship between D1 / L1 and the total luminous flux obtained in the simulation according to Example 3 and Comparative Example 2 of the present invention.
- FIG. 8 is a graph showing the relationship between the apex angle of the prism and the total luminous flux obtained in the simulation according to Example 4 of the present invention.
- FIG. 9 is a graph showing the relationship between D1 / L1 and the total luminous flux obtained in the simulations according to Examples 3 and 5 and Comparative Example 2 of the present invention.
- FIG. 10 is a graph showing the relationship between the concentration of the light scattering particles obtained in Reference Example 1 and D / L.
- FIG. 1 is a perspective view schematically showing an organic EL light emitting device 100 according to the first embodiment of the present invention.
- the organic EL light emitting device 100 according to the first embodiment of the present invention is a device for emitting light generated inside the organic EL light emitting device 100 through a light emitting surface 100U.
- the organic EL light emitting device 100 includes a light emitting surface structure layer 110, a first light scattering layer 120, a substrate layer 130 as a supporting substrate, a light emitting element layer 140, and a sealing layer 150 in this order from the side closer to the light emitting surface 100U. Prepare.
- the light exit surface structure layer 110 includes a prism layer 111 having a row of prisms 160 and a base film layer 112.
- the “row-shaped prism” represents a set of a plurality of unit prisms 161 arranged side by side so as to continuously extend by a certain length.
- the light emitting element layer 140 includes a transparent electrode layer 141 as a first electrode layer, a reflective electrode layer 143 as a second electrode layer, and a light emitting layer 142 provided between the transparent electrode layer 141 and the reflective electrode layer 143. Is provided.
- the organic EL light emitting device 100 includes a sealing layer 150, a reflective electrode layer 143, a light emitting layer 142, a transparent electrode layer 141, a substrate layer 130, a first light scattering layer 120, and a base material in the thickness direction of the organic EL light emitting device 100.
- the film layer 112 and the prism layer 111 are provided in this order. Accordingly, the light generated in the light emitting layer 142 is transmitted through the transparent electrode layer 141 or after being reflected by the reflective electrode layer 143 and then transmitted through the light emitting layer 142 and the transparent electrode layer 141, The light passes through the light scattering layer 120, the base film layer 112, and the prism layer 111, and is emitted through the light exit surface 100U.
- the light exit surface structure layer 110 includes a prism layer 111 and a base film layer 112. Further, the surface of the light emitting surface structure layer 110 opposite to the light emitting element layer 140 is the surface of the prism layer 111 opposite to the base film layer 112 and is exposed on the outermost surface of the organic EL light emitting device 100. ing. Therefore, the surface of the prism layer 111 opposite to the base film layer 112 is a light emitting surface 100U as the organic EL light emitting device 100, that is, a light emitting surface 100U when light is emitted from the organic EL light emitting device 100 to the outside of the device. It is.
- the prism layer 111 has an array of prisms 160 on the light exit surface 100U. Therefore, the light exit surface 100U is not a flat surface when viewed microscopically. However, since the unit prism 161 included in the row-shaped prism 160 is small, when the light exit surface 100U is viewed macroscopically, the light exit surface 100U can be a flat surface parallel to the main surface of the organic EL light emitting device 100. Therefore, in the following description, being parallel or perpendicular to the light exit surface 100U is parallel or perpendicular to the light exit surface 100U macroscopically ignored unless otherwise noted. That means.
- the organic EL light emitting device 100 will be described in a state where the light emitting surface 100U is placed so as to be parallel and upward with respect to the horizontal direction unless otherwise specified. Further, the fact that the component is “parallel” or “vertical” may include an error within a range that does not impair the effects of the present invention, for example, ⁇ 5 °.
- the row-shaped prism 160 formed on the light exit surface 100U includes a plurality of unit prisms 161 extending in a direction parallel to the light exit surface 100U. Normally, these unit prisms 161 all extend in the same direction. Further, these unit prisms 161 may be formed in a gap as long as the effects of the present invention are not significantly impaired, but are usually formed side by side without a gap. Further, the shape of the cross section obtained by cutting the unit prism 161 on a plane perpendicular to the direction in which the unit prism 161 extends is usually a triangle, and preferably an isosceles triangle. However, when the prism 160 is manufactured by transferring it from the mold, the tip of the prism 160 may be rounded.
- the tip of the unit prism 161 is flattened or rounded. It includes what is. Note that, by flattening or rounding the tip of the outermost unit prism 161, there is an effect of enhancing the scratch resistance.
- the array of prisms 160 includes a set of unit prisms 161 as a plurality of convex portions extending in one direction.
- Each of the unit prisms 161 has an isosceles triangle shape in a cross section obtained by cutting the unit prism 161 along a plane perpendicular to the direction in which the unit prism 161 extends. Further, these unit prisms 161 are arranged in parallel with each other with no gap on the entire surface of the light exit surface 100U.
- FIG. 2 is a cross-sectional view schematically showing a cross section of the prism layer 111 of the organic EL light emitting device 100 according to the first embodiment of the present invention.
- the apex angle ⁇ 160 of the row-shaped prism 160 is preferably 10 ° or more, more preferably 20 ° or more, particularly preferably 30 ° or more, preferably 80 ° or less, more preferably. Is 70 ° or less, particularly preferably 65 ° or less.
- the prism 160 can be prevented from being damaged by setting the apex angle ⁇ 160 of the prism 160 to be equal to or higher than the lower limit value of the range, and the light extraction efficiency of the organic EL light emitting device 100 can be increased by setting the apex angle ⁇ 160 to be equal to or lower than the upper limit value.
- the tip 162 of the unit prism 161 is flattened or rounded, the apex angle ⁇ 160 of the row-shaped prism 160 is not parallel to the main surface of the organic EL light emitting device 100 of the unit prism 161. It is assumed that the angle at which the slopes 163 and 164 intersect is shown.
- the dimensions of the unit prism 161 can be arbitrarily set as long as the effects of the present invention are not significantly impaired.
- the pitch P 161 of the unit prisms 161 is usually 1 ⁇ m or more, preferably 5 ⁇ m or more, more preferably 10 ⁇ m or more, and is usually 500 ⁇ m or less, preferably 100 ⁇ m or less, more preferably 50 ⁇ m or less.
- the height (or depth) H 161 of the unit prism 161 is usually 1 ⁇ m or more, preferably 5 ⁇ m or more, more preferably 10 ⁇ m or more, and usually 500 ⁇ m or less, preferably 100 ⁇ m or less, more preferably 50 ⁇ m or less. .
- the material of the prism layer 111 a transparent material is usually used.
- the material being “transparent” means that the material has a light transmittance suitable for use in an optical member.
- the total light transmittance of the material in terms of 1 mm thickness is In general, it means 80% or more, preferably 90% or more.
- the total light transmittance can be measured in accordance with JIS K7361-1997.
- thermoplastic resins examples include thermoplastic resins; thermosetting resins; and energy ray curable resins such as ultraviolet curable resins and electron beam curable resins.
- thermoplastic resin examples include a polyester resin, a polyacrylate resin, and a cycloolefin resin.
- ultraviolet curable resin examples include epoxy resins, acrylic resins, urethane resins, ene / thiol resins, and isocyanate resins.
- these resins preferably contain a polymer having a plurality of polymerizable functional groups. Moreover, these may be used alone or in combination of two or more at any ratio.
- the material of the prism layer 111 is preferably a material having high hardness at the time of curing from the viewpoint that the prism 160 is easily formed and the scratch resistance of the prism 160 is easily obtained.
- a material having a pencil hardness of 7 Bm or less in a state without an uneven structure is preferably a material of HB or higher, more preferably a material of H or higher, and more preferably a material of 2H or higher.
- the thickness T 111 of the prism layer 111 is preferably 1 ⁇ m or more, more preferably 5 ⁇ m or more, and may be 10 ⁇ m or more.
- the thickness T 111 of the prism layer 111 is preferably 500 ⁇ m or less, more preferably 100 ⁇ m or less, and may be 50 ⁇ m or less.
- the thickness T 111 of the prism layer 111 by the upper limit or less of the range, to prevent deformation such as curl of the prism layer 111 due to the curing shrinkage can be realized a prism layer 111 of good shape.
- the base film layer 112 shown in FIG. 1 is an arbitrary layer and is usually made of a transparent material film.
- the base film layer 112 may be formed of the same material as the prism layer 111.
- the light-emitting surface structure layer 110 having various characteristics can be obtained by forming the base film layer 112 from a material different from the prism layer 111.
- the prism layer 111 is preferably formed of a material having high hardness
- the base film layer 112 is preferably formed of a flexible material.
- Examples of the material of the base film layer 112 include an alicyclic olefin polymer and polyester. Moreover, these may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- the refractive index of the base film layer 112 is preferably close to the refractive index of the binder of the first light scattering layer 120.
- the binder of the first light scattering layer 120 may be referred to as a “first binder” as appropriate.
- the specific difference between the refractive index of the base film layer 112 and the refractive index of the first binder is preferably 0.15 or less, more preferably 0.1 or less, and even more preferably 0.05 or less. Thereby, the light extraction efficiency of the organic EL light emitting device 100 can be increased.
- the refractive index can be measured by an ellipsometer (for example, “M-2000” manufactured by JA Woollam Japan Co., Ltd.).
- the thickness of the base film layer 112 is preferably 20 ⁇ m to 300 ⁇ m.
- the light exit surface structure layer 110 can be manufactured by forming the prism layer 111 on the surface 112U of the base film layer 112 by the photopolymer method (2P method) using the material of the prism layer 111 described above.
- the first light scattering layer 120 is a layer provided between the prism layer 111 and the light emitting element layer 140 and includes first light scattering particles.
- the first light scattering layer 120 includes a first binder.
- the first light scattering layer 120 satisfies the following requirement (A) and requirement (B).
- the organic EL light emitting device 100 includes the first light scattering layer 120 that satisfies the requirement (A) and the requirement (B), thereby adopting a row-shaped prism 160 as the concavo-convex structure formed on the light exit surface 100U.
- the requirement (A) and the requirement (B) thereby adopting a row-shaped prism 160 as the concavo-convex structure formed on the light exit surface 100U.
- high light extraction efficiency can be realized.
- these requirements will be described in detail.
- the average particle diameter of the first light scattering particles is usually 0.1 ⁇ m or more, preferably 0.3 ⁇ m or more, more preferably 0.4 ⁇ m or more, and usually 1 ⁇ m or less, preferably 0.9 ⁇ m or less.
- the average particle diameter refers to the volume average particle diameter unless otherwise specified.
- the volume average particle diameter is a particle diameter at which the cumulative volume calculated from the small diameter side in the particle diameter distribution measured by the laser diffraction method is 50%.
- D1 / L1 is usually less than 6, preferably less than 5, and more preferably less than 4.5.
- D1 / L1 is usually less than 6, preferably less than 5, and more preferably less than 4.5.
- D1 / L1 is usually less than 6, preferably less than 5, and more preferably less than 4.5.
- D1 / L1 represents the thickness of the first light scattering layer 120.
- L1 represents the mean free path of light scattering in the first light scattering layer 120.
- the lower limit of D1 / L1 is not particularly limited, but is usually greater than 0, preferably greater than 0.5, more preferably greater than 1. Thereby, the light extraction efficiency can be increased as in the case of the upper limit.
- the number density of light scattering particles is the number of light scattering particles per unit volume.
- the value of the volume per light scattering particle is usually used.
- the particle diameter of the light scattering particle may be used.
- the volume average particle diameter of the light scattering particles can be used as a representative value as the particle diameter used for calculating the number density of the light scattering particles.
- the shape of the light scattering particle can be calculated assuming a sphere.
- the scattering cross section can be obtained by Mie scattering theory (MIE THEORY).
- the intensity distribution I ( ⁇ , ⁇ ) depending on the angle of the scattered light is expressed by the following equation (1).
- the scattering efficiency K ( ⁇ ) is expressed by the following equation (2).
- ⁇ is an amount corresponding to the radius r of the spherical particle represented by the following formula (3) and normalized by the wavelength ⁇ of light in the medium.
- (1) i 1 and i 2 in the formula is represented by equation (4).
- a and b with the subscript ⁇ in the expressions (2) to (4) are expressed by the expression (5).
- P (cos ⁇ ) with the superscript 1 and the subscript ⁇ is composed of a Legendre polynomial.
- “A” and “b” with subscript ⁇ are composed of first and second-order Recati-Bessel functions ⁇ v and ⁇ v (where v means subscript ⁇ ) and their derivatives.
- n scatter represents the refractive index of the spherical particles.
- N matrix represents the refractive index of the medium.
- an average free path L of a light scattering layer including a binder having a refractive index of 1.56 and approximately 10.6% by weight (8% by volume) of silicone particles having a refractive index of 1.43 as light scattering particles is obtained in a vacuum.
- 3 is calculated by the above method for light having a wavelength of 550 nm.
- the mean free path L is shown when the volume concentration of the light scattering particles in the light scattering layer is constant and the particle diameter of the light scattering particles is changed to 200 nm, 600 nm, 1000 nm, 1500 nm, and 2000 nm. Yes.
- the specific gravity of the binder was 1 g / cm 3 and the specific gravity of the light scattering particles was 1.32 g / cm 3 .
- the shape of the light scattering particles was assumed to be a sphere. Assuming that the shape of the light scattering particle is a sphere in this manner is applicable when the actual shape of the light scattering particle is close to a sphere. Furthermore, even when the actual shape of the light-scattering particles is not a shape close to a sphere, the tendency of the mean free path L and the particle diameter of the light-scattering particles is a matter of size, so it is considered that the same tendency is exhibited.
- Arbitrary light-scattering particles can be used as the first light-scattering particles within a range that satisfies the requirements (A) and (B).
- Light scattering particles are particles that can scatter light.
- the first light-scattering particles can scatter light when passing through the first light-scattering layer 120, thereby increasing the light extraction efficiency of the organic EL light-emitting device 100.
- an inorganic material or an organic material may be used as the first light scattering particles.
- the inorganic material of the first light scattering particles include metals and metal compounds.
- the metal compound include metal oxides and nitrides. Specific examples thereof include metals such as silver and aluminum; metal compounds such as silicon oxide, aluminum oxide, zirconium oxide, silicon nitride, tin-added indium oxide, and titanium oxide.
- the organic material for the first light scattering particles include resins such as silicone resin, acrylic resin, and polystyrene resin. These materials for the first light scattering particles may be used alone or in combination of two or more at any ratio.
- the 1st light-scattering layer 120 is manufactured using the coating liquid suitable for manufacturing the 1st light-scattering layer 120.
- FIG. 1 the first light scattering particles tend to settle, and in particular, when the inorganic particles having a high specific gravity are included, the first light scattering particles are likely to settle. In contrast, the first light scattering particles made of an organic material are unlikely to settle. Therefore, the 1st light-scattering layer 120 which contains the 1st light-scattering particle uniformly without unevenness by using the 1st light-scattering particle which consists of organic materials is realizable. Thus, the 1st light-scattering layer 120 which contains a 1st light-scattering particle uniformly can express characteristics, such as adhesiveness, stably, and is preferable.
- first light scattering particles made of an organic material are listed as trade names.
- a particle made of a silicone resin trade name “XC-99” (Momentive Performance Materials, volume average particle) A diameter of 0.7 ⁇ m).
- grains which consist of acrylic resins a brand name "MP series” (the Soken Chemical Co., Ltd. make, volume average particle diameter of 0.8 micrometer) can be mentioned, for example.
- grains which consist of polystyrene resin a brand name "SX series” (the Soken Chemical Co., Ltd. make, volume average particle diameter of 3.5 micrometers) can be mentioned, for example.
- the 1st light-scattering particle may be used individually by 1 type, and may be used combining two or more types by arbitrary ratios.
- the refractive index of the first light-scattering particles is usually 1.2 or more, preferably 1.3 or more, more preferably 1.4 or more, and usually 1.6 or less, preferably 1.55 or less, more preferably 1 .5 or less.
- the ratio of the first light scattering particles in the first light scattering layer 120 is preferably 0.5% by weight or more, more preferably 1% by weight or more, and preferably 40% by weight or less, more preferably 20% by weight. It is as follows. By keeping the ratio of the first light scattering particles in the above range, the light extraction efficiency of the organic EL light emitting device 100 can be effectively increased. Further, usually, a desired light scattering effect can be obtained, and color unevenness corresponding to the polar angle direction on the light exit surface 100U can be suppressed.
- the first binder has a function of holding the first light scattering particles in the first light scattering layer 120. In the first light scattering layer 120, the first light scattering particles are dispersed in the first binder.
- the first binder is transparent, and light passing through the transparent first binder is reflected at the interface between the first binder and the first light scattering particles, whereby light can be scattered.
- thermoplastic resins examples include thermoplastic resins, thermosetting resins, and energy ray curable resins such as ultraviolet curable resins and electron beam curable resins. Of these, thermosetting resins and energy beam curable resins are preferred from the viewpoints of high hardness and production efficiency.
- thermoplastic resin examples include a polyester resin, a polyacrylate resin, and a cycloolefin resin.
- ultraviolet curable resin examples include epoxy resins, acrylic resins, urethane resins, ene / thiol resins, and isocyanate resins. These resins are preferably those having a plurality of polymerizable functional groups.
- the first binder an adhesive resin may be used as the first binder.
- the first light scattering layer 120 can be provided with adhesiveness. Since the first light-scattering layer 120 has adhesiveness, the light-emitting surface structure layer 110 and the substrate layer 130 can be easily bonded to each other via the first light-scattering layer 120, so that the organic EL light-emitting device 100 is manufactured. Can be easily performed.
- the “pressure-sensitive adhesive” includes not only a pressure-sensitive adhesive in a narrow sense but also a hot-melt type pressure-sensitive adhesive.
- the narrow-sense pressure-sensitive adhesive means a pressure-sensitive adhesive having a shear storage elastic modulus at 23 ° C. of less than 1 MPa and exhibiting adhesiveness at room temperature.
- the hot-melt type pressure-sensitive adhesive is a pressure-sensitive adhesive having a shear storage elastic modulus at 23 ° C. of 1 MPa to 500 MPa and exhibiting no adhesiveness at room temperature.
- the pressure-sensitive adhesive it is preferable to use a narrow-sense pressure-sensitive adhesive that exhibits adhesiveness at room temperature.
- a narrow-sense pressure-sensitive adhesive that exhibits adhesiveness at room temperature.
- Such an adhesive in a narrow sense is a pressure-sensitive adhesive that can be adhered by applying pressure, and can be easily bonded without affecting the light-emitting layer 142 due to deterioration due to heating.
- adhesives examples include rubber adhesives, acrylic adhesives, silicone adhesives, urethane adhesives, vinyl alkyl ether adhesives, polyvinyl alcohol adhesives, polyvinyl pyrrolidone adhesives, polyacrylamide adhesives. And a cellulose-based pressure-sensitive adhesive. One of these may be used alone, or two or more of these may be used in combination at any ratio. Among these, an acrylic pressure-sensitive adhesive having excellent properties such as transparency, weather resistance, and heat resistance is preferable.
- An acrylic adhesive generally contains an acrylic polymer as an adhesive material.
- An acrylic polymer is a polymer containing a structural unit having a structure formed by polymerizing an acrylic monomer. Examples of such an acrylic polymer include a polymer obtained by polymerizing an acrylic monomer; or a polymer obtained by polymerizing a mixture (monomer mixture) of an acrylic monomer and a monomer copolymerizable therewith.
- acrylic monomers include alkyl (meth) acrylates.
- (meth) acrylate includes acrylate, methacrylate, and combinations thereof.
- the average carbon number of the alkyl group of the alkyl (meth) acrylate is preferably 1 or more, more preferably 3 or more, preferably 12 or less, more preferably 8 or less.
- Specific examples of the alkyl (meth) acrylate include methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, and isooctyl (meth) acrylate.
- these may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- Preferred examples of the monomer that can be copolymerized with the acrylic monomer include a monomer having a functional group, a nitrogen atom-containing monomer, and a modified monomer.
- Examples of the monomer having a functional group include a monomer having a carboxyl group, a monomer having a hydroxyl group, and a monomer having an epoxy group.
- Examples of the monomer having a carboxyl group include acrylic acid, methacrylic acid, fumaric acid, maleic acid, and itaconic acid.
- Examples of the monomer having a hydroxyl group include 2-hydroxyethyl (meth) acrylate, hydroxybutyl (meth) acrylate, hydroxyhexyl (meth) acrylate, and N-methylol (meth) acrylamide.
- Examples of the monomer having an epoxy group include glycidyl (meth) acrylate.
- the ratio of both is 60% to 99.8% by weight of the acrylic monomer, where the total of the acrylic monomer and the monomer having a functional group is 100% by weight.
- the monomer having a functional group is preferably 40% by weight to 0.2% by weight.
- nitrogen atom-containing monomers include (meth) acrylamide, N, N-dimethyl (meth) acrylamide, N, N-diethyl (meth) acrylamide, (meth) acryloylmorpholine, (meth) acetonitrile, vinylpyrrolidone, N- Examples include cyclohexylmaleimide, itaconimide, and N, N-dimethylaminoethyl (meth) acrylamide.
- the ratio of the two is such that the total of the acrylic monomer and the nitrogen atom-containing monomer is 100% by weight, the acrylic monomer is 60% to 99.8% by weight, It is preferred that the monomer content is 40 wt% to 0.2 wt%.
- modifying monomers examples include vinyl acetate and styrene.
- the ratio of the two is such that the total of the acrylic monomer and the modified monomer is 100% by weight, the acrylic monomer is 60% to 99.8% by weight, It is preferably 40% by weight to 0.2% by weight.
- These monomers that can be copolymerized with the acrylic monomer may be used alone or in combination of two or more at any ratio.
- the amount of the polymer as the adhesive material is preferably 10% by weight or more, more preferably 20% by weight or more, preferably 80% by weight or less, more preferably 70% by weight or less, as a ratio to the total amount of the first binder. It is.
- the first binder may contain highly refractive nanoparticles.
- highly refractive nanoparticles the refractive index of the first binder can be easily adjusted.
- the refractive index of the pressure-sensitive adhesive can be increased by including highly refractive nanoparticles in the pressure-sensitive adhesive having a low refractive index.
- a high refractive nanoparticle a particle having a smaller average particle diameter and a higher refractive index than that of an adhesive not containing a high refractive nanoparticle is usually used.
- particles having a volume average particle diameter of less than 100 nm and a refractive index of 1.6 or more can be used.
- Examples of the highly refractive nanoparticles include particles made of an inorganic material and particles made of an organic material having a refractive index of 1.6 or more.
- inorganic materials include oxides such as zirconia, titania, tin oxide, and zinc oxide; titanates such as barium titanate and strontium titanate; CdS, CdSe, ZnSe, CdTe, ZnS, HgS, HgSe, PdS, Examples thereof include sulfides such as SbSe, selenides and tellurides.
- Examples of the organic material having a refractive index of 1.6 or more include polystyrene resin. One of these may be used alone, or two or more of these may be used in combination at any ratio.
- the surface of these highly refractive nanoparticles may be surface-modified with various functional groups for improving dispersibility, silane coupling agents, and the like.
- the reactive modified metal oxide particle refers to a particle containing a metal oxide and an organic substance having a reactive functional group that modifies the surface of the metal oxide. More specifically, the reactive modified metal oxide particles are coated particles containing metal oxide particles and an organic substance having a reactive functional group that modifies the surface of the particles.
- the reactive functional group in an organic substance having a reactive functional group may be in a state having an interaction such as a hydrogen bond with a metal oxide particle, or in a state where it can interact with another substance without such a state. May be.
- reactive functional groups include hydroxyl groups, phosphate groups, carboxyl groups, amino groups, alkoxy groups, isocyanate groups, acid halides, acid anhydrides, glycidyl groups, chlorosilane groups, and alkoxysilane groups. One of these may be used alone, or two or more of these may be used in combination at any ratio.
- an organic substance having an isocyanate group is particularly preferable because the stability between the metal oxide and the surrounding substance can be improved.
- the organic substance having an isocyanate group include acryloxymethyl isocyanate, methacryloxymethyl isocyanate, acryloxyethyl isocyanate, methacryloxyethyl isocyanate, acryloxypropyl isocyanate, methacryloxypropyl isocyanate, 1,1-bis (acryloxymethyl) Ethyl isocyanate is mentioned. Moreover, these may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- metal oxides contained in the reactive modified metal oxide particles include titanium oxide, zinc oxide, zirconium oxide, antimony oxide, tin-doped indium oxide (ITO), antimony-doped tin oxide (ATO), and fluorine-doped tin oxide.
- FTO phosphorus-doped tin oxide
- PTO phosphorus-doped tin oxide
- AZO zinc antimonate
- IZO indium-doped zinc oxide
- aluminum-doped zinc oxide gallium-doped zinc oxide, cerium oxide, aluminum oxide, and tin oxide.
- these may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- the ratio of the organic substance having a reactive functional group may be 1 to 40 parts by weight with respect to 100 parts by weight of the metal oxide.
- the reactive modified metal oxide particles are mixed, for example, with metal oxide particles, an organic substance having a reactive functional group, an organic solvent, and optional additives as required, and further into the resulting mixture as necessary.
- a treatment such as ultrasonic treatment, a suspension in which particles are dispersed in an organic solvent can be obtained.
- organic solvents examples include ketones such as methyl ethyl ketone, methyl isobutyl ketone, acetone and cyclohexanone, aromatic hydrocarbons such as benzene, toluene, xylene and ethylbenzene, methanol, ethanol, isopropyl alcohol, n-butanol, iso-butanol and the like Alcohols, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, and other ethers, ethyl acetate, butyl acetate, ethyl lactate, ⁇ -butyrolactone, propylene glycol monomethyl ether Esters such as acetate and propylene glycol monoethyl ether acetate, dimethylform Bromide, N, N- dimethyl acetoacetamide,
- an additive As an example of an optional additive, a metal chelating agent can be mentioned. Moreover, an additive may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- the reactive modified metal oxide particles are obtained as a suspension in which the particles are dispersed in an organic solvent
- the suspension is preferably adjusted so as to contain the reactive modified metal oxide particles at 1 wt% to 50 wt% by adjusting conditions such as the amount of the solvent.
- a mixer such as a bead mill.
- secondary particles or higher order particles can be pulverized to the primary particle level, and the surface can be treated in the state of primary particles. Thereby, uniform surface treatment can be performed.
- the ultrasonic treatment can be performed using an apparatus such as an ultrasonic cleaner, an ultrasonic homogenizer, or an ultrasonic disperser. By such treatment, a good suspension can be obtained.
- the reactive modified metal oxide particles may be used as the reactive modified metal oxide particles.
- a slurry of reactive modified metal oxide particles containing ZrO 2 as a metal oxide trade name “ZR-010” (manufactured by Solar Co., Ltd., solvent: methyl ethyl ketone, particle content 30%, reaction for modifying the surface)
- An organic substance having a polymerizable functional group an isocyanate having a polymerizable functional group, and a volume average particle diameter of 15 nm).
- a trade name “NOD-742GTF” manufactured by Nagase ChemteX Corporation, solvent: polyethylene glycol monomethyl ether, particle content 30%, Volume average particle diameter of 48 nm.
- one kind of highly refractive nanoparticles may be used alone, or two or more kinds may be used in combination at any ratio.
- the volume average particle diameter of the highly refractive nanoparticles is preferably 5 nm or more, more preferably 10 nm or more, particularly preferably 15 nm or more, and preferably less than 100 nm, more preferably 50 nm or less.
- the volume average particle diameter of the highly refractive nanoparticles By setting the volume average particle diameter of the highly refractive nanoparticles to be equal to or less than the upper limit of the above range, the color of the first light scattering layer can be reduced and the light transmittance can be improved.
- the high refractive nanoparticle of such a size can be easily dispersed.
- the range of the volume average particle size may be the range of the primary particle size.
- the ratio of the highly refractive nanoparticles is preferably 20% by weight or more, more preferably 30% by weight or more, and preferably 80% by weight or less, more preferably as the ratio with respect to the total amount of the first binder. Is 70% by weight or less.
- the refractive index of a 1st binder can be raised by making the ratio of a highly refractive nanoparticle more than the lower limit of the said range. Moreover, by making it below an upper limit, the raise of the hardness of a 1st binder can be suppressed and the fall of adhesive force can be suppressed.
- the amount of the highly refractive nanoparticles falls within the above-described range.
- the first binder may contain a plasticizer.
- a plasticizer By using a plasticizer, the viscosity of the first binder can be lowered and the adhesiveness of the first light scattering layer 120 can be increased.
- it is preferable to use a plasticizer because the viscosity of the first binder tends to increase and the adhesiveness of the first light scattering layer 120 tends to decrease.
- plasticizer examples include polybutene, vinyl ether compound, polyether compound (including polyalkylene oxide and functionalized polyalkylene oxide), ester compound, polyol compound (for example, glycerin), petroleum resin, hydrogenated petroleum resin, and styrene. Based compounds (for example, ⁇ -methylstyrene).
- ester compounds are preferable because they have good miscibility with adhesive materials and a relatively high refractive index, and ester compounds containing aromatic rings such as benzoic acid and phthalic acid are particularly preferable.
- benzoic acid ester examples include diethylene glycol dibenzoate, dipropylene glycol dibenzoate, benzyl benzoate, and 1,4-cyclohexanedimethanol dibenzoate. Particularly preferred among these are, for example, benzoic acid ester compounds such as dipropylene glycol dibenzoate and benzyl benzoate; dimethyl phthalate, diethyl phthalate, dibutyl phthalate, butyl benzyl phthalate, dicyclohexyl phthalate, and ethyl phthalyl ethyl glycolate. Phthalic acid ester compounds.
- plasticizer As an example of a commercially available plasticizer, a trade name “BENZOFLEX 9-88SG” (manufactured by Eastman) can be mentioned. Moreover, a plasticizer may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- the proportion of the plasticizer is preferably 1 part by weight or more, more preferably 5 parts by weight or more, and preferably 35 parts by weight or less, more preferably 30 parts by weight with respect to 100 parts by weight of the polymer. Or less.
- the refractive index of the first binder is usually 1.5 or more, preferably 1.52 or more, more preferably 1.55 or more, and usually 1.9 or less, preferably 1.85 or less, more preferably 1.8. It is as follows.
- the value of D1 / L1 can be easily adjusted to a suitable range with a small amount of the first light scattering particles. Therefore, it is possible to prevent the amount of the first light scattering particles from becoming excessive, so that the surface of the first light scattering layer 120 can be smoothed or the first light scattering layer 120 can be formed when the first light scattering layer is an adhesive layer. It is easy to increase the adhesiveness.
- the upper limit value or less it is easy to disperse particles when blending highly refractive nanoparticles, and when the first light scattering layer is an adhesive layer, the change in adhesive with time can be reduced, The layer can be softened.
- the first light scattering layer 120 is preferably formed only of the first light scattering particles and the first binder. Therefore, the amount of the first binder in the first light scattering layer 120 is preferably set so that the sum of the ratio of the first light scattering particles and the ratio of the first binder is 100% by weight.
- the thickness D1 of the first light scattering layer 120 is usually 1 ⁇ m or more, preferably 2 ⁇ m or more, more preferably 3 ⁇ m or more, and usually 50 ⁇ m or less, preferably 40 ⁇ m or less, more preferably 25 ⁇ m or less.
- the planar shape of the 1st scattering layer can be formed by setting it as below an upper limit.
- first light scattering layer 120 for example, a coating liquid suitable for forming the first light scattering layer 120 is applied to a desired support surface, and a curing process such as a drying process is performed as necessary. Can be produced. At this time, as the coating liquid, a liquid composition containing the first light scattering particles and the first binder can be used.
- the coating liquid may contain arbitrary components as necessary.
- the optional component include additives such as a silane coupling agent and a curing agent; and a solvent.
- silane coupling agent examples include vinyltrimethoxysilane, vinyltriethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, and 3-glycidoxypropyl.
- silane coupling agent is trade name “KBM-803” (manufactured by Shin-Etsu Chemical Co., Ltd.).
- a silane coupling agent may be used individually by 1 type, and may be used combining two or more types by arbitrary ratios.
- the amount of the silane coupling agent is preferably 0.05 parts by weight or more, more preferably 0.2 parts by weight or more, and preferably 5 parts by weight or less with respect to 100 parts by weight of the polymer in the first binder. More preferably, it is 3 parts by weight or less.
- curing agent examples include isocyanate compounds.
- Specific examples of the curing agent include isocyanate addition polymers containing isophorone diisocyanate (for example, “NY-260A” manufactured by Mitsubishi Chemical Corporation).
- curing agent may be used individually by 1 type, and may be used combining two or more types by arbitrary ratios.
- the amount of the curing agent is preferably 0.01 parts by weight or more, more preferably 0.05 parts by weight or more, and preferably 5 parts by weight or less, based on 100 parts by weight of the polymer in the first binder.
- the amount is preferably 1 part by weight or less.
- Examples of the solvent include the same examples as those given as examples of the organic solvent used for the production of the reactive modified metal oxide particles. Moreover, a solvent may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- each component contained in the coating liquid when manufacturing each component contained in the coating liquid, those components may be obtained as a solution or suspension dissolved or dispersed in a solvent. Furthermore, even when a commercially available product is purchased as each component contained in the coating liquid, these components may be obtained as a solution or a suspension. In such a case, the solvent contained in the solution or suspension may be used as part or all of the solvent of the coating solution.
- the amount of the solvent is preferably 50 parts by weight or more, more preferably 100 parts by weight or more, and preferably 300 parts by weight or less, more preferably 250 parts by weight with respect to 100 parts by weight of the total solid content of the coating liquid. Or less.
- the solid content of the coating liquid refers to a component remaining after drying of the coating liquid.
- the first light-scattering layer 120 may be produced by applying the coating liquid to the surface 112D of the base film layer 112 and performing a curing treatment as necessary.
- the first light-scattering layer 120 obtained in this way can contain the components contained in the coating liquid, but some of the components may be changed by reaction, and some of the components volatilize and disappear. You may do it.
- reactive components such as a silane coupling agent and a curing agent may react to form another substance in the drying step, or the solvent may be volatilized and disappear.
- Substrate layer 130 As the substrate layer 130, a transparent sheet is usually used. As an example of the material of the substrate layer, glass or transparent resin can be used. Examples of the transparent resin that can be used for the substrate layer 130 include a thermoplastic resin, a thermosetting resin, an ultraviolet curable resin, and an electron beam curable resin, and among them, the thermoplastic is easy in processing. Resins are preferred. Examples of thermoplastic resins include polyester resins, polyacrylate resins, and cycloolefin resin resins. Moreover, these may be used individually by 1 type and may be used combining two or more types by arbitrary ratios.
- the refractive index of the substrate layer 130 is preferably close to the refractive index of the first binder of the first light scattering layer 120.
- the specific difference between the refractive index of the substrate layer 130 and the refractive index of the first binder is preferably 0.15 or less, more preferably 0.1 or less, and even more preferably 0.05 or less. Thereby, the light extraction efficiency of the organic EL light emitting device 100 can be increased.
- the thickness of the substrate layer 130 is preferably 20 ⁇ m to 300 ⁇ m in the case of the substrate layer 130 made of resin, for example.
- the thickness is preferably 10 ⁇ m to 1100 ⁇ m.
- the substrate layer 130 may or may not have flexibility. Therefore, for example, 700 ⁇ m thick non-flexible glass may be employed as the substrate layer.
- the light-emitting element layer 140 generally includes two or more electrode layers and a light-emitting layer that is provided between the electrode layers and can generate light when a voltage is applied from the electrode layers. Such a light emitting element layer can be formed by sequentially forming layers such as an electrode layer and a light emitting layer on a substrate by a known method such as sputtering. In this embodiment, the light emitting element layer 140 including the transparent electrode layer 141, the light emitting layer 142, and the reflective electrode layer 143 in this order will be described as an example.
- the light emitting material of the light emitting layer 142 is not particularly limited and may be appropriately selected from known materials.
- the light emitting material in the light emitting layer 142 is not limited to one type, and two or more types may be used in combination at any ratio.
- the light-emitting layer 142 can be a single-layer layer including only one layer. Further, the light emitting layer 142 may be a layer having a multilayer structure including a combination of a plurality of layers in order to suit the use as a light source. As a result, the light emitting layer 142 can generate white or near-color light.
- each of the electrode layers may be a single layer structure including only one layer, or may be a multilayer structure including two or more layers.
- the light emitting element layer 140 is an arbitrary layer (for example, a hole injection layer, a hole transport layer, an electron transport layer, an electron injection layer) between the transparent electrode layer 141 and the reflective electrode layer 143 (see FIG. (Not shown). Further, the light emitting element layer 140 may further include arbitrary components such as a wiring for energizing the transparent electrode layer 141 and the reflective electrode layer 143 and a peripheral structure for sealing the light emitting layer 142.
- the material constituting the layer that can be included in the light-emitting element layer 140 is not particularly limited, but specific examples include the following.
- Examples of the material for the transparent electrode layer include ITO (indium tin oxide).
- Examples of the material for the reflective electrode layer include aluminum and silver.
- Examples of the material for the hole injection layer include starburst aromatic diamine compounds.
- Examples of the material for the hole transport layer include triphenyldiamine derivatives.
- Examples of the host material for the yellow light-emitting layer include triphenyldiamine derivatives, and examples of the dopant material for the yellow light-emitting layer include tetracene derivatives.
- Examples of the material for the green light emitting layer include pyrazoline derivatives.
- Examples of the host material for the blue light emitting layer include anthracene derivatives, and examples of the dopant material for the blue light emitting layer include perylene derivatives.
- Examples of the material for the red light emitting layer include europium complexes.
- Examples of the material for the electron transport layer include an aluminum quinoline complex (Alq).
- the light-emitting layer 142 may be a light-emitting layer that generates light having a complementary color relationship, which is referred to as a stacked type or a tandem type, by combining a plurality of layers.
- the combination of complementary colors may be, for example, yellow / blue or green / blue / red.
- the sealing layer 150 is a layer for blocking water.
- the sealing layer 150 preferably has a function of blocking not only water but also oxygen. Thereby, the organic material in the light emitting element layer 140 can be prevented from being deteriorated by water vapor and oxygen.
- the sealing layer 150 may be formed of an organic material such as a resin, or may be formed of an inorganic material such as a metal and a metal compound. Such a sealing layer 150 can be formed, for example, by attaching a sealing film or the like formed of an appropriate material to the surface of the light emitting element layer 140.
- the light emitting layer 142 generates light when voltage is applied from the transparent electrode layer 141 and the reflective electrode layer 143.
- the light thus generated is transmitted through the transparent electrode layer 141, or after being reflected by the reflective electrode layer 143 and then transmitted through the light emitting layer 142 and the transparent electrode layer 141, and then the substrate layer 130, the first light.
- the light passes through the scattering layer 120, the base film layer 112, and the concavo-convex structure layer 111, and exits through the light exit surface 100U.
- the organic EL light emitting device 100 satisfies the requirements (A) and (B) described above. Thereby, since the light generated in the light emitting layer 142 is easily emitted to the outside through the light emitting surface 100U, the organic EL light emitting device 100 according to the present embodiment can obtain high light extraction efficiency.
- the light extraction efficiency can be evaluated based on the value of the light extraction efficiency Q obtained by comparing the organic EL light emitting device 100 according to the present embodiment with the control light emitting device.
- the control light-emitting device a light-emitting device different from the organic EL light-emitting device 100 according to the present embodiment can be used only in the presence or absence of a part of layers.
- a light emitting device having a structure similar to that of the organic EL light emitting device 100 except that a layer closer to the light emitting surface 100U than the transparent electrode layer 141 (that is, a layer from the light emitting surface structural layer 110 to the substrate layer 130) is not provided.
- a layer closer to the light emitting surface 100U than the transparent electrode layer 141 that is, a layer from the light emitting surface structural layer 110 to the substrate layer 130
- it may be used as a control light-emitting device, it may be different in other configurations that do not significantly affect the light extraction efficiency.
- the color unevenness refers to a phenomenon in which the color of the observed light varies depending on the observation direction when the light exit surface 100U is observed.
- the organic EL light-emitting device of the present invention can include arbitrary layers.
- the organic EL light emitting device of the present invention includes a second light scattering layer that can scatter light generated by the light emitting layer between the array of prisms and the light emitting layer in combination with the first light scattering layer. May be.
- a second light scattering layer that can scatter light generated by the light emitting layer between the array of prisms and the light emitting layer in combination with the first light scattering layer. May be.
- an example of an organic EL light emitting device including the second light scattering layer will be described with reference to the drawings.
- FIG. 4 is a perspective view schematically showing an organic EL light emitting device 200 according to the second embodiment of the present invention.
- the organic EL light emitting device 200 shown in FIG. 4 the same parts as those of the organic EL light emitting device 100 according to the first embodiment are denoted by the same reference numerals as used in the description of the first embodiment.
- the organic EL light emitting device 200 according to the second embodiment of the present invention includes a second light scattering layer 270 between the first light scattering layer 120 and the light emitting element layer 140. More specifically, the organic EL light emitting device 200 is the same as the organic EL light emitting device 100 according to the first embodiment except that the second light scattering layer 270 is provided between the substrate layer 130 and the light emitting element layer 140. It has the structure of.
- the second light scattering layer 270 is a layer that can function as a light scattering structure that can scatter light, and includes second light scattering particles.
- the second light scattering layer 270 usually includes a second binder in order to hold the second light scattering particles in the second light scattering layer 270.
- the second light scattering particles are dispersed in the second binder.
- the second binder is transparent, and light passing through the transparent second binder is reflected at the interface between the second binder and the second light scattering particles, whereby light can be scattered.
- the second light scattering layer 270 When the second light scattering layer 270 includes the second light scattering particles, the second light scattering layer 270 preferably satisfies (D1 / L1 + D2 / L2) ⁇ 6.
- D2 represents the thickness of the second light scattering layer 270.
- L2 represents the mean free path of light scattering in the second light scattering layer 270. More specifically, the value of (D1 / L1 + D2 / L2) is preferably 0.5 or more, more preferably 0.8 or more, particularly preferably 1.4 or more, usually 6 or less, preferably 5 or less, More preferably, it is 4.5 or less. Thereby, the light extraction efficiency of the organic EL light emitting device 200 can be further increased.
- the second light scattering particle a particle selected from the range of particles described as the first light scattering particle can be arbitrarily used.
- the second light scattering particles may be used alone or in combination of two or more at any ratio.
- the refractive index of the second light scattering particles is usually 1.2 or more, preferably 1.3 or more, more preferably 1.4 or more, and usually 1.6 or less, preferably 1.55 or less, more preferably 1 .5 or less.
- the average particle diameter of the second light scattering particles is preferably 0.2 ⁇ m or more, more preferably 0.3 ⁇ m or more, particularly preferably 0.4 ⁇ m or more, preferably 1 ⁇ m or less, more preferably 0.9 ⁇ m or less, particularly Preferably it is 0.6 micrometer or less.
- the second light scattering layer 270 disposed in the vicinity of the light emitting element layer 140 also in that sense.
- the average particle diameter of the light scattering particles is preferably small as described above.
- the ratio of the second light scattering particles in the second light scattering layer 270 is preferably 0.5% by weight or more, more preferably 1% by weight or more, and preferably 40% by weight or less, more preferably 20% by weight. It is as follows. By keeping the ratio of the second light scattering particles in the above range, a desired light scattering effect can be obtained, and color unevenness corresponding to the polar angle direction on the light exit surface 100U can be suppressed.
- a material selected from the range of materials described as the first binder can be arbitrarily used.
- the refractive index of the second binder is usually 1.52 or more, preferably 1.55 or more, more preferably 1.65 or more, and usually 1.9 or less, preferably 1.85 or less, more preferably 1.8. It is as follows.
- the refractive index of the second binder By setting the refractive index of the second binder to be equal to or higher than the lower limit of the above range, the value of D2 / L2 can be easily adjusted to a suitable range even when the amount of the second light scattering particles is small. Therefore, it is possible to prevent the amount of the second light scattering particles from becoming excessive, and thus the surface of the second light scattering layer 270 can be easily smoothed.
- the refractive index difference between the light emitting element layer 140 and the second binder can be reduced to suppress reflection, and particle dispersion when blending highly refractive nanoparticles can be facilitated. .
- the second light scattering layer 270 is preferably formed only by the second light scattering particles and the second binder. Therefore, the amount of the second binder in the second light scattering layer 270 is preferably set so that the sum of the ratio of the second light scattering particles and the ratio of the second binder is 100% by weight.
- the thickness D2 of the second light scattering layer 270 is usually 1 ⁇ m or more, preferably 2 ⁇ m or more, more preferably 3 ⁇ m or more, and usually 30 ⁇ m or less, preferably 20 ⁇ m or less, more preferably 10 ⁇ m or less.
- the second light scattering layer 270 can be manufactured, for example, in the same manner as the method described as the manufacturing method of the first light scattering layer 120.
- the organic EL light emitting device 200 including the second light scattering layer 270 can be used in the same manner as the organic EL light emitting device 100 according to the first embodiment, and is the same as the organic EL light emitting device 100 according to the first embodiment. Benefits can be gained.
- the second light scattering layer including the second light scattering particles and the second binder in combination with the first light scattering layer has been described as an example.
- the structure of the arbitrary layer is not limited to the layer that can scatter light by the light-scattering particles.
- an example of an organic EL light emitting device in which a layer capable of scattering light by elements other than light scattering particles and a first light scattering layer will be described with reference to the drawings.
- FIG. 5 is a perspective view schematically showing an organic EL light emitting device 300 according to the third embodiment of the present invention.
- the same parts as those of the organic EL light emitting device 100 according to the first embodiment are denoted by the same reference numerals as used in the description of the first embodiment.
- the organic EL light emitting device 300 according to the third embodiment of the present invention is the first embodiment except that a light scattering structure layer 370 is provided between the substrate layer 130 and the light emitting element layer 140. It has the same structure as the organic EL light emitting device 100 according to the above.
- the light scattering structure layer 370 includes a first light transmissive layer 371 and a second light transmissive layer 372 having different refractive indexes.
- the first light transmissive layer 371 and the second light transmissive layer 372 are in contact with each other at the boundary surface 373. Further, the first light transmissive layer 371 and the second light transmissive layer 372 are formed with non-uniform thicknesses. Therefore, the boundary surface 373 is an uneven surface that is not flat, and includes a plurality of surface portions 373A, 373B, and 373C that are not parallel to each other.
- the boundary surface 373 When light passes through the boundary surface 373, the light is normally refracted according to an incident angle to the boundary surface 373.
- the boundary surface 373 includes a plurality of surface portions 373A to 373C that are not parallel to each other as described above. Accordingly, the light transmitted through the boundary surface 373 is refracted for each of the surface portions 373A to 373C, and thus the light transmitted through the boundary surface 373 travels in a plurality of different directions. Therefore, light can be scattered by the light scattering structure layer 370.
- the organic EL light emitting device 300 including such a light scattering structure 370 can be used in the same manner as the organic EL light emitting device 100 according to the first embodiment, and has the same advantages as the organic EL light emitting device 100 according to the first embodiment. Obtainable.
- FIG. 6 is a plan view schematically showing the light exit surface 400U of the prism layer 411 according to an example.
- a row-shaped prism 460 may be provided by a set of unit prisms 461 extending to bend in a plurality of different directions.
- the height of the unit prisms included in the array of prisms is not constant as in the above-described embodiment, and may be different.
- each unit prism 161 is continuously provided on the entire light exit surface 100U in the extending direction of the unit prism 161 .
- the unit prism 161 is not necessarily the unit prism.
- the light emitting surface 100U may not be continuously provided in the extending direction of 161.
- a gap that divides each unit prism 161 into a plurality in the extending direction of the unit prism 161 (the depth direction in FIG. 1). May be provided.
- the reflective electrode layer 143 according to the above-described embodiment may be replaced with a transparent electrode layer.
- an organic EL light emitting device capable of emitting light from both sides can be obtained.
- the position of the layer may be changed.
- the first light scattering layer 120 may be provided between the substrate layer 130 and the transparent electrode layer 141.
- the positions of the first light scattering layer 120 and the second light scattering layer 270 are switched, and the first light scattering layer 120 is changed to the light emitting element layer side, Even if the two-light-scattering layer 270 is on the prism side, the same effect as in the second embodiment can be obtained.
- the first light scattering layer 120 and the light scattering structure layer 370 may be interchanged.
- the organic EL light emitting device may not include the base film layer 112, the substrate layer 130, and the sealing layer 150. Further, the organic EL light emitting device may further include an arbitrary layer in addition to the above-described layers.
- the organic EL light-emitting device of the present invention can be used for applications such as lighting fixtures and backlight devices.
- the lighting fixture includes the organic EL light-emitting device of the present invention as a light source, and may further include arbitrary components such as a member that holds the light source and a circuit that supplies power.
- the backlight device has the organic EL light-emitting device of the present invention as a light source, and further includes a housing, a circuit for supplying power, a diffusion plate, a diffusion sheet, a prism sheet, etc. for making the emitted light more uniform. The following components may be included.
- the use of the backlight device can be used as a backlight of a display device such as a liquid crystal display device that displays an image by controlling pixels and a display device that displays a fixed image such as a signboard.
- Example 1 (1-1. Production of organic EL device) On one surface of a glass substrate having a thickness of 0.7 mm and a refractive index of 1.52, a transparent electrode layer having a thickness of 100 nm, a hole transport layer having a thickness of 10 nm, a yellow light emitting layer having a thickness of 20 nm, a blue light emitting layer having a thickness of 15 nm, and a layer having a thickness of 15 nm An electron transport layer, an electron injection layer having a thickness of 1 nm, and a reflective electrode layer having a thickness of 100 nm were formed in this order. The hole transport layer to the electron transport layer were all formed of an organic material. The yellow light-emitting layer and the blue light-emitting layer had different emission spectra.
- each layer from the transparent electrode layer to the reflective electrode layer was as follows.
- Yellow luminescent layer 1.5% by weight of rubrene added
- ⁇ -NPD Blue light emitting layer 10% by weight of iridium complex added 4,4′-dicarbazolyl-1,1′-biphenyl (CBP) -Electron transport layer; phenanthroline derivative (BCP) -Electron injection layer; lithium fluoride (LiF) -Reflective electrode layer: Al
- the transparent electrode layer was formed by a reactive sputtering method using an ITO target.
- the formation from the hole injection layer to the reflective electrode layer is performed by placing a glass substrate on which a transparent electrode layer has already been formed in a vacuum evaporation apparatus, and sequentially using the material from the hole transport layer to the reflective electrode layer by a resistance heating method. This was done by vapor deposition. Vapor deposition was performed at an internal pressure of 5 ⁇ 10 ⁇ 3 Pa and an evaporation rate of 0.1 nm / s to 0.2 nm / s.
- This container was placed on a ball mill base and ball mill dispersion was performed at a rate of 2 revolutions per second for 30 minutes. After dispersing the ball mill, the contents of the container were sieved to remove the zirconia balls, whereby a mixture 1 was obtained.
- a pressure-sensitive adhesive composition A ′ containing no silicone particles was obtained in the same manner as in the step (1-2) except that no silicone particles were added.
- This pressure-sensitive adhesive composition A ′ was applied to one side of a glass plate so that the thickness after drying was 10 ⁇ m, and dried at 80 ° C. for 5 minutes to form a test pressure-sensitive adhesive layer.
- the refractive index of this test adhesive layer was measured with an ellipsometer (“M-2000” manufactured by JA Woollam Japan Co., Ltd.), and the refractive index was 1.56.
- the pressure-sensitive adhesive composition A obtained above has a thickness of 40 ⁇ m after drying on one side of a 100 ⁇ m-thick base film layer (“Zeonor film ZF14-100” manufactured by Nippon Zeon Co., Ltd., refractive index 1.52). And then dried at 80 ° C. for 5 minutes. Thereby, the 1st light-scattering layer (scattering adhesion layer) which has adhesiveness was formed on the base film layer, and the scattering adhesive sheet provided with a base film layer and a 1st light-scattering layer was obtained.
- a 100 ⁇ m-thick base film layer (“Zeonor film ZF14-100” manufactured by Nippon Zeon Co., Ltd., refractive index 1.52).
- a UV curable resin (“P5790PS3C” manufactured by Daido Kasei Kogyo Co., Ltd.) with a thickness of 10 ⁇ m was applied to the surface of the scattering adhesive sheet opposite to the first light scattering layer.
- a mold was placed on the applied UV curable resin film.
- a concavo-convex concavo-convex structure having a shape in which unit prisms having an isosceles triangular cross section with a pitch of 10 ⁇ m and an apex angle of 60 ° were uniformly arranged was formed.
- This mold was applied to the UV curable resin film, and the UV curable resin film was irradiated with 500 mJ ultraviolet rays through the first light scattering layer. Thereby, the film
- the scattering adhesive sheet provided with the prism was attached to the surface of the light emitting device obtained in the step (1-1) on the glass substrate side.
- (prism) / (base film layer) / (first light scattering layer comprising pressure-sensitive adhesive composition A) / (glass substrate) / (transparent electrode layer) / (hole transport layer) / (yellow light emitting layer) ) / (Blue light emitting layer) / (electron transport layer) / (electron injection layer) / (reflective electrode layer) / (sealing substrate) was obtained, and an organic EL light emitting device was obtained.
- Example 2 (2-1. Preparation of adhesive composition B) A reaction vessel equipped with a cooling tube, a nitrogen introduction tube, a thermometer and a stirrer was prepared. In this reaction vessel, 233 parts of ethyl acetate as a solvent; and 30 parts of butyl acrylate, 70 parts of phenoxyethyl acrylate, 0.5 part of acrylic acid, 0.3 part of 4-hydroxybutyl acrylate, and 2,2′-azo 0.2 part of bisisobutyronitrile was added.
- the temperature inside the reaction vessel was raised to 55 ° C., and a polymerization reaction was carried out for 15 hours to obtain a solution of an acrylic copolymer having a weight average molecular weight of 810,000.
- the refractive index of this acrylic copolymer was 1.53.
- the solid content of the acrylic copolymer is 100 parts; a copolymer of ⁇ -methylstyrene and styrene (“Crystalex 3085” manufactured by Eastman Chemical Co., Ltd., softening point 82 ° C. to 88 ° C. as a tackifier.
- a pressure-sensitive adhesive composition B ′ containing no silicone particles was obtained in the same manner as in the step (2-1) except that no silicone particles were added.
- This pressure-sensitive adhesive composition B ′ was applied to one side of a glass plate so that the thickness after drying was 10 ⁇ m, and dried at 80 ° C. for 5 minutes to form a test pressure-sensitive adhesive layer.
- the refractive index of this test adhesive layer was measured with an ellipsometer (“M-2000” manufactured by JA Woollam Japan Co., Ltd.), and the refractive index was 1.56.
- Example 3 and Comparative Example 2 Range of D1 / L1
- the total luminous flux was calculated by optical simulation using a program (“Light Tools” manufactured by ORA).
- the organic EL light emitting device modeled in Example 3 is (prism) / (base film layer) / (glass substrate) / (first light scattering layer) / (transparent electrode layer) / (light emitting layer) / (reflection).
- the electrode layer was set to have a layer structure.
- the prism was set to have a concavo-convex structure in which unit prisms having an isosceles triangular cross section were uniformly arranged. This prism was set with a pitch of 20 ⁇ m, a prism apex angle of 60 °, and a refractive index of 1.52.
- the base film layer was set to have a refractive index of 1.52 and a thickness of 100 ⁇ m.
- the glass substrate was set to have a refractive index of 1.52 and a thickness of 600 ⁇ m.
- the first light scattering layer was set such that the average particle diameter of the first light scattering particles was 0.5 ⁇ m, the refractive index of the first light scattering particles was 1.43, and the refractive index of the binder was 1.75.
- the transparent electrode layer was set to have a refractive index of 1.8 and a thickness of 0.15 ⁇ m.
- the light emitting layer was set to have a refractive index of 1.8 and a thickness of 0.2 ⁇ m.
- the reflective electrode layer was set to have a reflectance of 85%.
- a virtual light emitting surface of Lambertian light distribution was set at the interface between the transparent electrode layer and the first light scattering layer.
- Comparative Example 2 an organic EL light emitting device similar to that in Example 3 was modeled except that no prism was provided.
- the value of D1 / L1 was changed by changing the thickness of the first light scattering layer and the concentration of the first light scattering particles in the first light scattering layer.
- the total luminous flux was calculated.
- the calculated total luminous flux results are shown as relative values in FIG.
- Example 3 when the value of D1 / L1 is less than 6, the total luminous flux larger than the maximum value of the total luminous flux in Comparative Example 2 is obtained, so that D1 / L1 ⁇ 6. It turns out that it is preferable.
- Example 4 Vertical angle of prism
- the total luminous flux was calculated by optical simulation using a program (“Light Tools” manufactured by ORA).
- the organic EL light emitting device modeled in Example 4 is (prism) / (base film layer) / (glass substrate) / (first light scattering layer) / (transparent electrode layer) / (light emitting layer) / (reflection).
- the electrode layer was set to have a layer structure.
- the prism was set to have a concavo-convex structure in which prisms having an isosceles triangular cross section were uniformly arranged. In this concavo-convex structure layer, a prism pitch of 20 ⁇ m and a refractive index of 1.52 were set.
- the base film layer was set to have a refractive index of 1.52 and a thickness of 100 ⁇ m.
- the glass substrate was set to have a refractive index of 1.52 and a thickness of 600 ⁇ m.
- the first light scattering layer was set such that the average particle diameter of the first light scattering particles was 0.5 ⁇ m, the refractive index of the first light scattering particles was 1.43, the refractive index of the binder was 1.75, and the thickness was 5 ⁇ m.
- the transparent electrode layer was set to have a refractive index of 1.8 and a thickness of 0.15 ⁇ m.
- the light emitting layer was set to have a refractive index of 1.8 and a thickness of 0.2 ⁇ m.
- the reflective electrode layer was set to have a reflectance of 85%.
- a virtual light emitting surface of Lambertian light distribution was set at the interface between the transparent electrode layer and the first light scattering layer.
- the total luminous flux when the apex angle of the prism was changed was calculated.
- the calculation of the total luminous flux is performed in each of the cases where the value of D1 / L1 is set to 0.4, 0.8, 1.5 and 3 by changing the concentration of the first light scattering particles in the first light scattering layer. It was.
- the result of the calculated total luminous flux is shown as a relative value in FIG.
- FIG. 8 shows that when the value of D1 / L1 is as small as about 0.4 to 1.5, the total luminous flux becomes maximum when the apex angle of the prism is around 60 ° to 70 °. It can also be seen that when the value of D1 / L1 is large, the apex angle of the prism is acute and the total luminous flux is large. Therefore, the light extraction efficiency can be particularly increased by setting the apex angle of the prism to approximately 80 ° or less.
- Example 5 Combination of first light scattering layer and second light scattering layer
- the total luminous flux was calculated by optical simulation using a program (“Light Tools” manufactured by ORA).
- the modeled organic EL light emitting device is the organic EL modeled in Example 3 except that a second light scattering layer including second light scattering particles and a binder is provided between the prism and the glass substrate. It was set as having the same layer structure as the light emitting device.
- the light extraction efficiency can be increased in a wide range of D1 / L1 by combining the second light scattering layer with the first light scattering layer. This shows that the light extraction efficiency can be stabilized even if D1 / L1 of the first light scattering layer and D2 / L2 of the second light scattering layer vary. Moreover, it turns out that the combination of a prism, a 1st light-scattering layer, and a 2nd light-scattering layer is applicable to the organic electroluminescent light-emitting device which has D1 / L1 of a wide range.
- FIG. 10 shows the ratio D / L between the thickness D of the layer containing the light scattering particles and the binder and the mean free path L of the light scattering when a binder having a refractive index of 1.48 or 1.56 is used.
- the thickness of the layer was 20 ⁇ m
- the average particle diameter of the light scattering particles was 0.7 ⁇ m
- the refractive index of the light scattering particles was 1.43.
- the specific gravity of the binder was 1, and the specific gravity of the light scattering particles was 1.32. From FIG. 10, it can be seen that a larger D / L value can be obtained by using a binder having a high refractive index with a small amount of light scattering particles. Therefore, it can be seen that when a binder having a high refractive index is used, it is easy to obtain a desired D / L, and as a result, it is easy to improve the light extraction efficiency.
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Abstract
Description
すなわち、本発明は以下の通りである。
平均粒子径0.1μm~1μmの第一光散乱粒子を含む第一光散乱層と、
条列状のプリズムと、をこの順に備え、
前記第一光散乱層における光散乱の平均自由行程L1、及び、前記第一光散乱層の厚みD1が、D1/L1<6である、有機EL発光装置。
〔2〕 前記プリズムの頂角が80°以下である、〔1〕記載の有機EL発光装置。
〔3〕 前記第一光散乱層が、第一バインダを含む、〔1〕又は〔2〕記載の有機EL発光装置。
〔4〕 前記第一バインダの屈折率が、1.5以上である、〔3〕記載の有機EL発光装置。
〔5〕 前記第一バインダが、高屈折ナノ粒子を含む、〔3〕又は〔4〕記載の有機EL発光装置。
〔6〕 前記高屈折率ナノ粒子は、前記第一バインダの全量に対する割合として、20重量%以上80重量%以下である、〔5〕記載の有機EL発光装置。
〔7〕 前記第一光散乱層における前記第1光散乱粒子の割合が0.5重量%以上40重量%以下である、〔1〕~〔6〕のいずれか1項に記載の有機EL発光装置。
〔8〕 前記プリズム及び前記発光層の間に、前記光を散乱しうる第二光散乱層を備える、〔1〕~〔7〕のいずれか1項に記載の有機EL発光装置。
〔9〕 前記第二光散乱層を、前記発光層及び前記第一光散乱層の間に備える、〔8〕記載の有機EL発光装置。
〔10〕 前記第一光散乱層が、粘着性を有する、〔1〕~〔9〕のいずれか1項に記載の有機EL発光装置。
図1は、本発明の第一実施形態に係る有機EL発光装置100を模式的に示す斜視図である。
図1に示すように、本発明の第一実施形態に係る有機EL発光装置100は、当該有機EL発光装置100の内部で生じた光を出光面100Uを通じて出光するための装置である。この有機EL発光装置100は、出光面100Uに近い方から、出光面構造層110、第一光散乱層120、支持基板としての基板層130、発光素子層140及び封止層150を、この順に備える。また、出光面構造層110は、条列状のプリズム160を有するプリズム層111、及び、基材フィルム層112を備える。ここで「条列状のプリズム」とは、ある長さだけ連続して延在するように並んで設けられた複数の単位プリズム161の集合のことを表す。さらに、発光素子層140は、第一電極層としての透明電極層141、第二電極層としての反射電極層143、並びに、透明電極層141及び反射電極層143の間に設けられた発光層142を備える。
出光面構造層110は、プリズム層111及び基材フィルム層112を備える。また、この出光面構造層110の発光素子層140とは反対側の面は、プリズム層111の基材フィルム層112とは反対側の面であり、有機EL発光装置100の最表面に露出している。よって、プリズム層111の基材フィルム層112とは反対側の面は、有機EL発光装置100としての出光面100U、即ち、有機EL発光装置100から装置外部に光が出光する際の出光面100Uである。
図2に示すように、条列状のプリズム160の頂角θ160は、好ましくは10°以上、より好ましくは20°以上、特に好ましくは30°以上であり、好ましくは80°以下、より好ましくは70°以下、特に好ましくは65°以下である。プリズム160の頂角θ160を前記範囲の下限値以上にすることによりプリズム160の破損を抑制でき、また、上限値以下にすることにより有機EL発光装置100の光取出効率を高めることができる。単位プリズム161の先端部分162が平らになっていたり丸くなっていたりする場合、条列状のプリズム160の頂角θ160は、単位プリズム161の有機EL発光装置100の主面に平行でない2つの斜面163及び164が交差した角度を示すものとする。
(1.2.1.第一光散乱層120が満たす要件)
図1に示すように、第一光散乱層120は、プリズム層111と発光素子層140との間に設けられる層であり、第一光散乱粒子を含む。また通常、第一光散乱層120は、第一バインダを含む。さらに、第一光散乱層120は、下記の要件(A)及び要件(B)を満たす。
要件(A):第一光散乱粒子の平均粒子径が、0.1μm~1μmである。
要件(B):第一光散乱層120における光散乱の平均自由行程L1、及び、第一光散乱層120の厚みD1が、D1/L1<6を満たす。
有機EL発光装置100は、前記の要件(A)及び要件(B)を満たす第一光散乱層120を備えることにより、出光面100Uに形成された凹凸構造として条列状のプリズム160を採用しながら、高い光取出効率を実現することができる。
以下、これらの要件について詳細に説明する。
第一光散乱粒子の平均粒子径は、通常0.1μm以上、好ましくは0.3μm以上、より好ましくは0.4μm以上であり、通常1μm以下、好ましくは0.9μm以下である。本明細書において、平均粒子径とは、別に断らない限り、体積平均粒子径のことを指す。体積平均粒子径は、レーザー回折法で測定された粒子径分布において小径側から計算した累積体積が50%となる粒子径である。第一光散乱粒子の平均粒子径を前記範囲の下限値以上にすることにより、散乱させるべき光の波長よりも第一光散乱粒子の粒子径を安定して大きくできるので、第一光散乱粒子によって可視光を安定して散乱させることができる。また、上限値以下にすることにより、粒子径を小さくできるので第一光散乱粒子に当たった光をより広範な範囲に反射させることができるため、第一光散乱粒子によって可視光を効率的に散乱させることができる。
第一光散乱層120は、D1/L1が、通常6未満、好ましくは5未満、より好ましくは4.5未満である。D1/L1をこのような範囲にすることによって、有機EL発光装置100の光取出効率を効果的に高めることができる。ここで、「D1」は、第一光散乱層120の厚みを表す。また、「L1」は、第一光散乱層120における光散乱の平均自由行程を表す。D1/L1の下限は、特に制限はないが、通常0より大きく、好ましくは0.5より大きく、より好ましくは1より大きい。これにより、上限の時と同様に光取出効率を高めることができる。
前記の要件(A)及び(B)を満たす範囲において、第一光散乱粒子としては任意の光散乱粒子を用いうる。光散乱粒子は、光を散乱させうる粒子である。第一光散乱粒子により、第一光散乱層120を通る際に光を散乱させて、有機EL発光装置100の光取出効率を高めることができる。
第一光散乱粒子の無機材料としては、例えば、金属及び金属化合物が挙げられる。また、金属化合物としては、例えば、金属の酸化物及び窒化物を挙げることができる。その具体例としては、銀、アルミニウム等の金属;酸化ケイ素、酸化アルミ、酸化ジルコニウム、窒化珪素、錫添加酸化インジウム、酸化チタンなどの金属化合物を挙げることができる。
また、第一光散乱粒子の有機材料としては、例えば、シリコーン樹脂、アクリル樹脂、及びポリスチレン樹脂等の樹脂が挙げられる。
これらの第一光散乱粒子の材料は、1種類を単独で用いてもよく、2種類以上を任意の比率で組み合わせて用いてもよい。
また、第一光散乱粒子は、1種類を単独で用いてもよく、2種類以上を任意の比率で組み合わせて用いてもよい。
前記の要件(A)及び(B)を満たす範囲において、第一バインダとして任意の材料を用いうる。第一バインダは、第一光散乱粒子を第一光散乱層120に保持する機能を有する。また、第一光散乱層120において、第一光散乱粒子は、第一バインダ中に分散している。通常、第一バインダは透明であり、この透明な第一バインダ中を透過する光が第一バインダと第一光散乱粒子との界面で反射されることで光の散乱が行われうる。
第一光散乱層120の厚みD1は、通常1μm以上、好ましくは2μm以上、より好ましくは3μm以上であり、通常50μm以下、好ましくは40μm以下、より好ましくは25μm以下である。第一光散乱層120の厚みを前記範囲の下限値以上にすることにより、十分に光を散乱することができる。また、上限値以下にすることにより、平らな第一散乱層の面状を形成することができる。
第一光散乱層120は、例えば、第一光散乱層120を形成するのに適した塗工液を所望の支持面に塗布し、必要に応じて乾燥処理等の硬化のための処理を行うことによって、作製できる。この際、塗工液としては、第一光散乱粒子及び第一バインダを含む液状の組成物を用いうる。
基板層130としては、通常、透明のシートを用いる。この基板層の材料の例としては、ガラス、又は透明樹脂を用いうる。基板層130に用いうる透明樹脂の例としては、熱可塑性樹脂、熱硬化性樹脂、紫外線硬化性樹脂、および電子線硬化性樹脂を挙げることができ、この中でも加工が容易である点で熱可塑性樹脂が好ましい。熱可塑性樹脂の例としては、ポリエステル樹脂、ポリアクリレート樹脂、およびシクロオレフィン樹脂の樹脂を挙げられる。また、これらは、1種類を単独で用いてもよく、2種類以上を任意の比率で組み合わせて用いてもよい。
発光素子層140は、通常、2層以上の電極層と、これらの電極層の間に設けられ、電極層から電圧を印加されることにより光を生じうる発光層とを備える。このような発光素子層は、電極層、発光層等の層を、スパッタリング等の既知の方法で基材上に順次形成することにより形成しうる。本実施形態では、透明電極層141、発光層142及び反射電極層143をこの順に備えた発光素子層140を例に挙げて説明する。
透明電極層の材料としては、ITO(酸化インジウムスズ)が挙げられる。
反射電極層の材料としては、アルミニウム、銀等が挙げられる。
正孔注入層の材料としては、スターバースト系芳香族ジアミン化合物等が挙げられる。
正孔輸送層の材料としては、トリフェニルジアミン誘導体等が挙げられる。
黄色発光層のホスト材料としては、トリフェニルジアミン誘導体等が挙げられ、黄色発光層のドーパント材料としては、テトラセン誘導体等が挙げられる。
緑色発光層の材料としては、ピラゾリン誘導体等が挙げられる。
青色発光層のホスト材料としては、アントラセン誘導体等が挙げられ、青色発光層のドーパント材料としては、ペリレン誘導体等が挙げられる。
赤色発光層の材料としては、ユーロピウム錯体等が挙げられる。
電子輸送層の材料としては、アルミニウムキノリン錯体(Alq)等が挙げられる。
封止層150は、水を遮断するための層である。また、封止層150は、水だけでなく酸素を遮断する機能も有することが好ましい。これにより、発光素子層140内の有機材料が水蒸気及び酸素により劣化することを防ぐことができる。封止層150は、例えば、樹脂等の有機材料で形成してもよく、金属及び金属化合物等の無機材料で形成してもよい。このような封止層150は、例えば、適切な材料で形成された封止フィルム等を発光素子層140の表面に貼り合わせることで形成しうる。
上述した構成を有する有機EL発光装置100では、透明電極層141及び反射電極層143から電圧を印加されることにより、発光層142が光を生じる。このようにして生じた光は、透明電極層141を透過した後、又は、反射電極層143で反射されてから発光層142及び透明電極層141を透過した後で、基板層130、第一光散乱層120、基材フィルム層112及び凹凸構造層111を透過して、出光面100Uを通って出光する。この際、前記の光は、第一光散乱層120に含まれる第一光散乱粒子の表面での反射により、第一光散乱層120を透過するときに散乱される。また、出光面100Uにプリズム171が設けられているため、前記の光は、出光面100Uに対して前記出光面100Uを透過しうる入射角で入射し易い。
そして、これらの事項に加えて、本実施形態に係る有機EL発光装置100は、上述した要件(A)及び(B)を満たしている。これにより、発光層142で生じた光は、出光面100Uを通って外部に出光し易いので、本実施形態に係る有機EL発光装置100は、高い光取出効率を得ることができる。
本発明の有機EL発光装置は、第一実施形態において説明した層以外にも、任意の層を備えうる。例えば、本発明の有機EL発光装置は、第一光散乱層に組み合わせて、条列状のプリズム及び発光層の間に、発光層が生じた光を散乱しうる第二光散乱層を備えていてもよい。以下、第二光散乱層を備えた有機EL発光装置の例を、図面を示して説明する。
図4に示すように、本発明の第二実施形態に係る有機EL発光装置200は、第一光散乱層120と発光素子層140との間に、第二光散乱層270を備える。より具体的には、有機EL発光装置200は、基板層130と発光素子層140との間に第二光散乱層270を備えること以外は、第一実施形態に係る有機EL発光装置100と同様の構造を有する。
上述した第二実施形態では、第一光散乱層に組み合わせて、第二光散乱粒子及び第二バインダを含む第二光散乱層を例示して説明した。しかし、第一光散乱層と光を散乱させうる任意の層とを組み合わせる場合、任意の層の構造は、このように光散乱粒子によって光を散乱させうる層に限定されるものでは無い。以下、光散乱粒子以外の要素によって光を散乱させうる層を第一光散乱層と組み合わせた有機EL発光装置の例を、図面を示して説明する。
図5に示すように、本発明の第三実施形態に係る有機EL発光装置300は、基板層130と発光素子層140との間に光散乱構造層370を備えること以外は、第一実施形態に係る有機EL発光装置100と同様の構造を有する。
本発明は上述した実施形態に限定されるものでは無く、更に変更して実施しうる。
例えば、凹凸構造に含まれる単位プリズムは、一方向に直線状に延在するものに限られない。図6は、ある例に係るプリズム層411の出光面400Uを模式的に示す平面図である。例えば、図6に示すように、複数の異なる方向に屈曲するように延在する単位プリズム461の集合によって、条列状のプリズム460を設けてもよい。
また、例えば、条列状のプリズムに含まれる単位プリズムの高さは、上述した実施形態のように一定でなく、異なっていてもよい。
本発明の有機EL発光装置は、例えば、照明器具及びバックライト装置等の用途に用いうる。照明器具は、本発明の有機EL発光装置を光源として有し、さらに、光源を保持する部材、電力を供給する回路等の任意の構成要素を含みうる。バックライト装置は、本発明の有機EL発光装置を光源として有し、さらに、筐体、電力を供給する回路、出光する光をさらに均一にするための拡散板、拡散シート、プリズムシート等の任意の構成要素を含みうる。バックライト装置の用途は、液晶表示装置等、画素を制御して画像を表示させる表示装置、並びに、看板等の固定された画像を表示させる表示装置のバックライトとして用いうる。
以下の実施例及び比較例において、材料の量を表す「%」及び「部」は、別に断らない限り、重量基準である。また、実施例及び比較例中の操作は、別に断らない限り常温常圧の環境下で行った。
さらに、以下の実施例及び比較例において、光散乱層における光散乱の平均自由行程の計算は、真空中での波長550nmの光に対して、ミー散乱理論を用いた前述の方法によって行った。
[実施例1]
(1-1.有機EL素子の製造)
厚み0.7mm、屈折率1.52のガラス基板の一方の面に、厚み100nmの透明電極層、厚み10nmのホール輸送層、厚み20nmの黄色発光層、厚み15nmの青色発光層、厚み15nmの電子輸送層、厚み1nmの電子注入層、および厚み100nmの反射電極層を、この順に形成した。ホール輸送層から電子輸送層までは、全て有機材料により形成した。黄色発光層および青色発光層は、それぞれ異なる発光スペクトルを有していた。
・透明電極層;錫添加酸化インジウム(ITO)
・ホール輸送層;4,4’-ビス[N-(ナフチル)-N-フェニルアミノ]ビフェニル(α-NPD)
・黄色発光層;ルブレン1.5重量%添加 α-NPD
・青色発光層;イリジウム錯体10重量%添加 4,4’-ジカルバゾリル-1,1’-ビフェニル(CBP)
・電子輸送層;フェナンスロリン誘導体(BCP)
・電子注入層;フッ化リチウム(LiF)
・反射電極層;Al
また、ホール注入層から反射電極層までの形成は、透明電極層を既に形成したガラス基板を真空蒸着装置内に設置し、上記のホール輸送層から反射電極層までの材料を抵抗加熱式により順次蒸着させることにより行なった。蒸着は、系内圧は5×10-3Pa、蒸発速度0.1nm/s~0.2nm/sで行った。
プラスチック容器に、高屈折ナノ粒子としての反応性修飾ジルコニア酸化物を含むスラリー(ソーラー社製「ZR-010」、溶媒:メチルエチルケトン、粒子含有割合30%、粒子比重約4、反応性修飾ジルコニア酸化物の粒子の体積平均粒子径15nm、屈折率約1.9)85重量部、第一光散乱粒子としてのシリコーン粒子(モメンティブ・パフォーマンス・マテリアルズ社製「XC-99」、体積平均粒子径0.7μm、比重1.32、屈折率1.43)5重量部、及び、分散用のジルコニアボール(ニッカトー社製「YTZ-0.5」)500重量部を入れた。
この容器をボールミル架台に載せ、毎秒2回転の速度で30分間、ボールミル分散を行った。ボールミル分散後、容器の内容物をふるいにかけてジルコニアボールを取り除き、混合物1を得た。
シリコーン粒子を加えなかった以外は前記工程(1-2)と同様に操作して、シリコーン粒子を含まない粘着剤組成物A’を得た。
この粘着剤組成物A’を、ガラス板の片面に、乾燥後の厚みが10μmとなるように塗布し、80℃で5分乾燥させて、試験用粘着層を形成した。この試験用粘着層の屈折率を、エリプソメーター(ジェー・エー・ウーラム・ジャパン株式会社製「M-2000」)にて測定したところ、屈折率は1.56であった。
上記で得られた粘着剤組成物Aを、厚み100μmの基材フィルム層(日本ゼオン社製「ゼオノアフィルムZF14-100」、屈折率1.52)の片面に、乾燥後の厚みが40μmとなるように塗布し、80℃で5分乾燥させた。これにより、基材フィルム層上に粘着性を有する第一光散乱層(散乱粘着層)を形成して、基材フィルム層及び第一光散乱層を備える散乱粘着シートを得た。
前記散乱粘着シートの第一光散乱層とは反対側の面に、UV硬化性樹脂(大同化成工業社製「P5790PS3C」)を厚さ10μmで塗布した。塗布されたUV硬化性樹脂の膜上に、金型を配置した。この金型の表面には、ピッチ10μm、頂角60°の二等辺三角形の断面を有する単位プリズムが一様に並んだ形状を有する条列状の凹凸構造が形成されていた。この金型をUV硬化性樹脂の膜に当て、第一光散乱層を通して500mJの紫外線をUV硬化性樹脂の膜に照射した。これによりUV硬化性樹脂の膜が固まって、基材フィルムの第一光散乱層とは反対側に条列状のプリズムが形成された。
プリズムを設けられた散乱粘着シートを、前記工程(1-1)で得られた発光素子のガラス基板側の表面に貼り付けた。これにより、(プリズム)/(基材フィルム層)/(粘着剤組成物Aからなる第一光散乱層)/(ガラス基板)/(透明電極層)/(ホール輸送層)/(黄色発光層)/(青色発光層)/(電子輸送層)/(電子注入層)/(反射電極層)/(封止基板)の層構成を有する、有機EL発光装置を得た。
(2-1.粘着剤組成物Bの調製)
冷却管、窒素導入管、温度計及び撹拌機を備えた反応容器を用意した。この反応容器に、溶媒としての酢酸エチル233部;並びに、ブチルアクリレート30部、フェノキシエチルアクリレート70部、アクリル酸0.5部、4‐ヒドロキシブチルアクリレート0.3部、及び2,2’-アゾビスイソブチロニトリル0.2部を入れた。窒素置換を行った後、反応容器内を55℃に昇温し、15時間重合反応を行なって、重量平均分子量81万のアクリル系共重合体の溶液を得た。このアクリル系共重合体の屈折率は、1.53であった。
シリコーン粒子を加えなかったこと以外は前記工程(2-1)と同様に操作して、シリコーン粒子を含まない粘着剤組成物B’を得た。
この粘着剤組成物B’を、ガラス板の片面に、乾燥後の厚みが10μmとなるように塗布し、80℃で5分乾燥させて、試験用粘着層を形成した。この試験用粘着層の屈折率を、エリプソメーター(ジェー・エー・ウーラム・ジャパン株式会社製「M-2000」)にて測定したところ、屈折率は1.56であった。
前記工程(1-4)において粘着剤組成物Aの代わりに粘着剤組成物Bを用いたこと以外は実施例1と同様にして、(プリズム)/(基材フィルム層)/(粘着剤組成物Bからなる第一光散乱層)/(ガラス基板)/(透明電極層)/(ホール輸送層)/(黄色発光層)/(青色発光層)/(電子輸送層)/(電子注入層)/(反射電極層)/(封止基板)の層構成を有する、有機EL発光装置を得た。
前記工程(1-4)において、粘着剤組成物Aの代わりに、シリコーン粒子を含まない粘着剤組成物A’を用いたこと以外は実施例1と同様にして、(プリズム)/(基材フィルム層)/(粘着剤組成物A’からなる粘着層)/(ガラス基板)/(透明電極層)/(ホール輸送層)/(黄色発光層)/(青色発光層)/(電子輸送層)/(電子注入層)/(反射電極層)/(封止基板)の層構成を有する、有機EL発光装置を得た。
〔第一光散乱層における光散乱の平均自由行程の計算〕
上述した実施例1及び2について、第一光散乱層の厚み35μm、バインダの屈折率1.56、第一光散乱粒子の平均粒子径0.7μm、第一光散乱層の固形分に対する第一光散乱粒子の濃度6.9重量%として、ミー散乱理論に基づいて第一光散乱層の平均自由行程L1を計算したところ、実施例1及び2のいずれにおいても、L1=14μmであった。よって、実施例1及び2のいずれにおいても、第一光散乱層ではD1/L1=2.9であった。
上述した実施例及び比較例で製造した有機EL発光装置の全光束を、高速配光測定システム(RADIENT社製「IMAGING SHERE」)にて測定した。測定された全光束の値を、実施例1の工程(1-1)で得た発光素子の全光束の値で割って、光取出効率を求めた。その結果を、下記の表に示す。
また、実施例2のように実施例2のように屈折率の高い重合体をバインダとして用いた第一光散乱層においては、ジルコニア酸化物等の高価な高屈折ナノ粒子が不要である。また、高屈折ナノ粒子の分散のためのボールミル処理等の煩雑な操作も不要である。そのため、バインダとしては、屈折率の高い重合体を含むものを用いることが好ましい。
[実施例3及び比較例2:D1/L1の範囲]
有機EL発光装置のモデルについて、プログラム(ORA社製「Light Tools」)を用いた光学シミュレーションにより、全光束を計算した。
プリズムでは、二等辺三角形の断面を有する単位プリズムが一様に並んだ凹凸構造を有すると設定した。このプリズムは、ピッチ20μm、プリズムの頂角60°、屈折率1.52と設定した。
基材フィルム層は、屈折率1.52、厚み100μmと設定した。
ガラス基材は、屈折率1.52、厚み600μmと設定した。
第一光散乱層は、第一光散乱粒子の平均粒子径0.5μm、第一光散乱粒子の屈折率1.43、バインダの屈折率1.75と設定した。
透明電極層は、屈折率1.8、厚み0.15μmと設定した。
発光層は、屈折率1.8、厚み0.2μmと設定した。
反射電極層は、反射率85%と設定した。
そうして透明電極層と第一光散乱層の界面に、ランバーシアン配光の仮想発光面を設定した。
有機EL発光装置のモデルについて、プログラム(ORA社製「Light Tools」)を用いた光学シミュレーションにより、全光束を計算した。
プリズムは、二等辺三角形の断面を有するプリズムが一様に並んだ凹凸構造を有すると設定した。この凹凸構造層において、プリズムのピッチ20μm、屈折率1.52と設定した。
基材フィルム層は、屈折率1.52、厚み100μmと設定した。
ガラス基材は、屈折率1.52、厚み600μmと設定した。
第一光散乱層は、第一光散乱粒子の平均粒子径0.5μm、第一光散乱粒子の屈折率1.43、バインダの屈折率1.75、厚み5μmと設定した。
透明電極層は、屈折率1.8、厚み0.15μmと設定した。
発光層は、屈折率1.8、厚み0.2μmと設定した。
反射電極層は、反射率85%と設定した。そうして透明電極層と第一光散乱層の界面に、ランバーシアン配光の仮想発光面を設定した。
有機EL発光装置のモデルについて、プログラム(ORA社製「Light Tools」)を用いた光学シミュレーションにより、全光束を計算した。
また、第二光散乱層は、第二光散乱粒子の平均粒子径0.7μm、第二光散乱粒子の屈折率1.43、第二光散乱粒子の体積濃度8%、バインダの屈折率1.56、厚み20μmとした。D2/L2=1.5であった。
光散乱粒子及びバインダを含む層の厚みDと光散乱の平均自由行程Lとの比D/Lを、屈折率が1.48又は1.56のバインダを用いた場合それぞれについて、図10に示す。この際、層の厚み20μm、光散乱粒子の平均粒子径0.7μm、光散乱粒子の屈折率1.43とした。またバインダの比重を1、光散乱粒子の比重1.32とした。
図10から、屈折率の高いバインダを使う方が、少ない量の光散乱粒子によって大きなD/Lの値を得ることができることが分かる。よって、屈折率の高いバインダを用いると、所望のD/Lを得ることが容易になり、結果として光取出効率を向上させることが容易になることが分かる。
100U 出光面
111 プリズム層
112 基材フィルム層
112D 基材フィルム層の面
120 第一光散乱層
130 基板層
140 発光素子層
141 透明電極層
142 発光層
143 反射電極層
150 封止層
160 条列状のプリズム
161 単位プリズム
200 有機EL発光装置
270 第二光散乱層
300 有機EL発光装置
370 光散乱構造層
371 第一透光層
372 第二透光層
373 境界面
373A~373C 面部
400U 出光面
411 プリズム層
460 条列状のプリズム
461 単位プリズム
Claims (10)
- 光を生じうる発光層と、
平均粒子径0.1μm~1μmの第一光散乱粒子を含む第一光散乱層と、
条列状のプリズムと、をこの順に備え、
前記第一光散乱層における光散乱の平均自由行程L1、及び、前記第一光散乱層の厚みD1が、D1/L1<6である、有機EL発光装置。 - 前記プリズムの頂角が80°以下である、請求項1記載の有機EL発光装置。
- 前記第一光散乱層が、第一バインダを含む、請求項1又は2記載の有機EL発光装置。
- 前記第一バインダの屈折率が、1.5以上である、請求項3記載の有機EL発光装置。
- 前記第一バインダが、高屈折ナノ粒子を含む、請求項3又は4記載の有機EL発光装置。
- 前記高屈折率ナノ粒子は、前記第一バインダの全量に対する割合として、20重量%以上80重量%以下である、請求項5記載の有機EL発光装置。
- 前記第一光散乱層における前記第1光散乱粒子の割合が0.5重量%以上40重量%以下である、請求項1~6のいずれか1項に記載の有機EL発光装置。
- 前記プリズム及び前記発光層の間に、前記光を散乱しうる第二光散乱層を備える、請求項1~7のいずれか1項に記載の有機EL発光装置。
- 前記第二光散乱層を、前記発光層及び前記第一光散乱層の間に備える、請求項8記載の有機EL発光装置。
- 前記第一光散乱層が、粘着性を有する、請求項1~9のいずれか1項に記載の有機EL発光装置。
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US15/327,752 US10074828B2 (en) | 2014-07-31 | 2015-07-30 | Light scattering layer having particles for an organic EL light-emitting device |
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