CN104183715A - Organic light-emitting device and manufacturing method thereof - Google Patents

Organic light-emitting device and manufacturing method thereof Download PDF

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Publication number
CN104183715A
CN104183715A CN201310192390.2A CN201310192390A CN104183715A CN 104183715 A CN104183715 A CN 104183715A CN 201310192390 A CN201310192390 A CN 201310192390A CN 104183715 A CN104183715 A CN 104183715A
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layer
bis
phenyl
carbazole
biphenyl
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周明杰
钟铁涛
王平
陈吉星
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Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Engineering Co Ltd
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Oceans King Lighting Science and Technology Co Ltd
Shenzhen Oceans King Lighting Engineering Co Ltd
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Priority to CN201310192390.2A priority Critical patent/CN104183715A/en
Publication of CN104183715A publication Critical patent/CN104183715A/en
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    • 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
    • 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
    • H10K50/805—Electrodes
    • H10K50/81—Anodes
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
    • 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

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  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Electroluminescent Light Sources (AREA)

Abstract

The invention relates to an organic light-emitting device which includes an anti-reflection composite layer, a substrate, an anode, a short-circuit reduction layer, a first organic light-emitting function layer, a charge generation layer, a second organic light-emitting function layer and a cathode layer, which are sequentially arranged in a laminated manner, wherein the anti-reflection composite layer includes a white glass plate and an anti-reflection membrane located at one side of the white glass plate; and the substrate is arranged on the anti-reflection membrane and a light-exiting gap is arranged between the substrate and the anti-reflection membrane. In the organic light-emitting device, through arrangement of the anti-reflection membrane beneath a light-exiting surface and arrangement of the short-circuit reduction layer on the anode layer, the light-exiting efficiency of the hole device is improved significantly. The manufacturing method is simple and convenient and has low demands on equipment so that the method can be widely popularized and applied. Moreover, the invention also relates to the manufacturing method for the organic light-emitting device.

Description

Organic electroluminescence device and preparation method thereof
Technical field
The present invention relates to electroluminescent technology field, especially relate to a kind of organic electroluminescence device and preparation method thereof.
Background technology
Organic electroluminescence device (OLED) has advantages of that some are unique: (1) OLED belongs to diffused area source, does not need by extra light-conducting system, to obtain large-area white light source as light-emitting diode (LED); (2) due to the diversity of luminous organic material, OLED illumination is the light of design color as required, no matter be little Molecule OLEDs at present, or polymer organic LED (PLED) has all obtained and has comprised white-light spectrum at the light of interior all colours; (3) OLED can make on as glass, pottery, metal or plastic or other material at multiple substrate, thereby freer while making to design lighting source; (4) adopt the mode of making OLED demonstration to make OLED illumination panel, can in illumination, show information; (5) OLED also can be used as controlled look in illuminator, allows user to regulate light atmosphere according to individual demand.Yet traditional not high problem of OLED ubiquity light extraction efficiency.
Summary of the invention
Based on this, be necessary to provide organic electroluminescence device that a kind of light extraction efficiency is higher and preparation method thereof.
An organic electroluminescence device, comprises the antireflection composite bed, substrate, anode layer, short reduction layer, the first organic luminescence function layer, charge generation layer, the second organic luminescence function layer and the cathode layer that are cascading; Wherein, the anti-reflective film that described antireflection composite bed comprises white glass plate and is positioned at described white glass plate one side, described substrate be located on described anti-reflective film and and this anti-reflective film between be provided with bright dipping space; The material of described short reduction layer is SiGe(SiGe) and In 2o 3(indium sesquioxide), ZnS(zinc sulphide), SnO 2(tin ash) or SiO 2the composite material that (silicon dioxide) forms according to mass ratio 1:1; Described the first organic luminescence function layer is included in the first hole injection layer, the first hole transmission layer, red light luminescent layer, the first green luminescence layer, the first blue light-emitting and the first electron transfer layer being cascading on described short reduction layer; Described the second organic luminescence function layer is included in the second hole injection layer, the second hole transmission layer, the second green luminescence layer, the second blue light-emitting, the second electron transfer layer and the electron injecting layer being cascading on described charge generation layer, and described cathode layer is located on described electron injecting layer.
In an embodiment, the material of described anti-reflective film is SiGe(SiGe therein), thickness is 10～20nm.
In an embodiment, the material of described substrate is polyurethane therein, described substrate near a side of described antireflection composite bed be provided with a plurality of be uniformly distributed and with the integrated projection of described substrate.
In an embodiment, described projection is conical therein, and bottom surface diameter is 5～20 μ m, is highly 5～20 μ m, spacing 5～20 μ m between adjacent protrusion.
In an embodiment, described anode layer is the ITO(tin indium oxide of thickness 100nm therein) layer.
In an embodiment, the material of described the first hole injection layer is MoO therein 3(molybdenum trioxide), WO 3(tungstic acid), V 2o 5(vanadic oxide) or ReO 3(rhenium trioxide) is entrained in N according to 25～35% doping mass ratio, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines (NPB), 4,4', 4''-tri-(carbazole-9-yl) triphenylamine (TCTA), 4,4'-bis-(9-carbazole) biphenyl (CBP), N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine (TPD) or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] the middle composite material forming of cyclohexane (TAPC);
The material of described the first hole transmission layer is N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane;
The material of described red light luminescent layer is that two (2-methyl-diphenyl [f, h] quinoxaline) (acetylacetone,2,4-pentanediones) close iridium (Ir (MDQ) 2(acac)), two [2-phenylchinoline base)-N, C2] (acetylacetone,2,4-pentanedione) close iridium (III) (PQIr), two [N-isopropyl-2-(4-fluorophenyl) benzimidazole] (acetylacetone,2,4-pentanediones) close iridium (III) ((fbi) 2ir (acac)), two [2-(2-fluorophenyl)-1,3-benzothiazole-N, C2] (acetylacetone,2,4-pentanedione) closes iridium (III) ((F-BT) 2ir (acac)), two (2-benzothiophene-2-base-pyridine) (acetylacetone,2,4-pentanediones) close iridium (III) (Ir (btp) 2 (acac)) or three (1-phenyl-isoquinolin) close iridium) (Ir (piq) 3) according to 0.5～2% doping mass ratio, be entrained in 4,4', 4''-tri-(carbazole-9-yl) triphenylamine (TCTA), 9,9'-(1,3-phenyl) two-9H-carbazole (mCP), 4,4'-bis-(9-carbazole) biphenyl (CBP), N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine (TPD), 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] two (1-naphthyl) anthracenes of cyclohexane (TAPC) or 9,10-) composite material that forms in (ADN);
The material of described the first green luminescence layer is that three (2-phenylpyridines) close iridium (Ir (ppy) 3), acetopyruvic acid two (2-phenylpyridine) iridium (Ir (ppy) 2(acac)) or three [2-(p-methylphenyl) pyridines] close iridium (III) (Ir (mppy) 3) according to 2～10% doping mass ratio, be entrained in 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 9,9'-(1,3-phenyl) two-9H-carbazole, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine, 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in two (1-naphthyl) anthracenes of cyclohexane or 9,10-;
The material of described the first blue light-emitting comprises Blue-light emitting host material, blue light guest materials and charge generating material, described Blue-light emitting host material is 4, 4'-bis-(9-carbazole) biphenyl, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 9-(4-2-methyl-2-phenylpropane base)-3, two (triphenyl the silicon)-9H-carbazoles (CzSi) of 6-, 2, two (3-(9H-carbazole-9-yl) phenyl) pyridines (26DCzPPY) of 6-, 3, two (3-(9H-carbazole-9-yl) phenyl) pyridines (35DCzPPY) or 1 of 5-, two (triphenyl silicon) benzene (UGH2) of 4--, described blue light guest materials is two (4, 6-difluorophenyl pyridine-N, C2) pyridine formyl closes iridium (FIrpic), two (4, 6-difluorophenyl pyridine)-tetra-(1-pyrazolyl) boric acid closes iridium (FIr6), three (2-(4', the fluoro-5 '-cyano group of 6'-bis-) phenylpyridine-N, C2') close iridium (FCNIr), two (4, 6-difluorophenyl pyridine)-(3-(trifluoromethyl)-5-(pyridine-2-yl)-1, 2, 4-triazole) close iridium (FIrtaz) or two (4, 6-difluorophenyl pyridine) (5-(pyridine-2-yl)-tetrazolium) closes iridium) (FIrN4), described charge generating material is MoO 3, V 2o 5, WO 3or ReO 3, the mass ratio of described Blue-light emitting host material, described blue light guest materials and described charge generating material is 1:5～20:5～10,
The material of described the first electron transfer layer is 4,7-diphenyl-1,10-phenanthroline (Bphen), 4,7-diphenyl-1,10-Phen (BCP), 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium (BAlq), oxine aluminium (Alq 3), 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole (TAZ) or 1,3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene (TPBI).
In an embodiment, the material of described charge generation layer is MoO therein 3, V 2o 5, WO 3or ReO 3, thickness is 5～30nm.
In an embodiment, the material of described the second hole injection layer is MoO therein 3, WO 3, V 2o 5or ReO 3doping mass ratio according to 25～35% is entrained in N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in cyclohexane;
The material of described the second hole transmission layer is N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane;
The material of described the second green luminescence layer is that three (2-phenylpyridines) close iridium (Ir (ppy) 3), acetopyruvic acid two (2-phenylpyridine) iridium (Ir (ppy) 2(acac)) or three [2-(p-methylphenyl) pyridines] close iridium (III) (Ir (mppy) 3) according to 2～10% doping mass ratio, be entrained in 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 9,9'-(1,3-phenyl) two-9H-carbazole, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine, 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in two (1-naphthyl) anthracenes of cyclohexane or 9,10-;
The material of described the second blue light-emitting comprises Blue-light emitting host material, blue light guest materials and charge generating material, described Blue-light emitting host material is 4, 4'-bis-(9-carbazole) biphenyl, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 9-(4-2-methyl-2-phenylpropane base)-3, two (triphenyl the silicon)-9H-carbazoles of 6-, 2, two (3-(9H-carbazole-9-yl) phenyl) pyridines of 6-, 3, two (3-(9H-carbazole-9-yl) phenyl) pyridines or 1 of 5-, two (triphenyl silicon) benzene of 4--, described blue light guest materials is two (4, 6-difluorophenyl pyridine-N, C2) pyridine formyl closes iridium, two (4, 6-difluorophenyl pyridine)-tetra-(1-pyrazolyl) boric acid closes iridium, three (2-(4', the fluoro-5 '-cyano group of 6'-bis-) phenylpyridine-N, C2') close iridium, two (4, 6-difluorophenyl pyridine)-(3-(trifluoromethyl)-5-(pyridine-2-yl)-1, 2, 4-triazole) close iridium or two (4, 6-difluorophenyl pyridine) (5-(pyridine-2-yl)-tetrazolium) closes iridium), described charge generating material is MoO 3, V 2o 5, WO 3or ReO 3, the mass ratio of described Blue-light emitting host material, described blue light guest materials and described charge generating material is 1:5～20:5～10,
The material of described the second electron transfer layer is 4,7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1,3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene;
The material of described electron injecting layer is Cs 2cO 3(cesium carbonate), CsF(cesium fluoride), CsN 3(cesium trinitride), Li 2cO 3(lithium carbonate), LiF(lithium fluoride) or Li 2o(lithia) according to 25～35% doping mass ratio, be entrained in 4,7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1, the composite material forming in 3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene.
In an embodiment, the material of described cathode layer is Ag, Al or Au therein, and thickness is 50～200nm.
A manufacture method for organic electroluminescence device, comprises the steps:
A side magnetron sputtering at white glass plate is prepared anti-reflective film, obtain the antireflection composite bed that contains individual layer anti-reflective film, simultaneously in a side deposits conductive material of substrate, make anode layer, then by the opposite side of described substrate folded be located on described anti-reflective film and and this anti-reflective film between be provided with bright dipping space;
Adopt the mode of magnetron sputtering, on described anode layer, prepare short reduction layer, material selection SiGe and the In of magnetron sputtering 2o 3, ZnS, SnO 2or SiO 2the composite material forming according to mass ratio 1:1;
On described short reduction layer, prepare successively the first hole injection layer, the first hole transmission layer, red light luminescent layer, the first green luminescence layer, the first blue light-emitting and the first electron transfer layer;
On described the first electron transfer layer, evaporation is prepared charge generation layer, and the material of described charge generation layer is MoO 3, V 2o 5, WO 3or ReO 3;
On described charge generation layer, prepare successively the second hole injection layer, the second hole transmission layer, the second green luminescence layer, the second blue light-emitting, the second electron transfer layer and electron injecting layer;
On described electron injecting layer, evaporation is prepared cathode layer, obtains described organic electroluminescence device.
Above-mentioned organic electroluminescence device by under exiting surface, anti-reflective film being set, and arranges short reduction layer on anode layer, and the light extraction efficiency of whole device improves greatly.And above-mentioned manufacture method is easy, low for equipment requirements, can wide popularization and application.
Accompanying drawing explanation
Fig. 1 is the structural representation of the organic electroluminescence device of an execution mode.
Embodiment
Mainly in conjunction with the drawings and the specific embodiments organic electroluminescence device and preparation method thereof is described in further detail below.
As shown in Figure 1, the organic electroluminescence device 100 of an execution mode comprises antireflection composite bed 110, substrate 120, anode layer 130, short reduction layer 140, the first organic luminescence function layer 150, charge generation layer 160, the second organic luminescence function layer 170 and the cathode layer 180 being cascading.
The anti-reflective film 114 that antireflection composite bed 110 comprises white glass plate 112 and is positioned at white glass plate 112 1 sides.The material of anti-reflective film 114 is SiGe, and thickness is 10～20nm.
Substrate 120 be located on anti-reflective film 114 and and this anti-reflective film 114 between be provided with bright dipping space.The material of substrate 120 is polyurethane.Substrate 120 near a side of antireflection composite bed 114 be provided with a plurality of be uniformly distributed and with substrate 120 integrated protruding 122.In the present embodiment, projection 122 is conical, and bottom surface diameter is 5～20 μ m, is highly 5～20 μ m, spacing 5～20 μ m between adjacent protrusion 122.Be appreciated that in other embodiments, the shape of projection 122 is not limited to this, as being square or hemisphere etc.Substrate 120 is provided with folded being located on antireflection composite bed 110 of a side of projection 122, thereby between the two, forms gap, and light can penetrate from this gap, and meanwhile, due to the existence of anti-reflective film 114, light extraction efficiency significantly improves.
Anode layer 130 is for covering the ITO layer of the thickness 100nm in substrate 120.
The material of short reduction layer 140 is the composite material that bi-material is mixed to form according to mass ratio 1:1, and one of them material is SiGe, and another kind of material is In 2o 3, ZnS, SnO 2or SiO 2.The thickness of short reduction layer 140 is 4～10nm.
The first organic luminescence function layer 150 is included in the first hole injection layer 151, the first hole transmission layer 152, red light luminescent layer 153, the first green luminescence layer 154, the first blue light-emitting 155 and the first electron transfer layer 156 being cascading on short reduction layer 140.
The material of the first hole injection layer 151 is the MoO for adulterating 3, WO 3, V 2o 5or ReO 3doping mass ratio according to 25～35% is entrained in N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in the material of main part such as cyclohexane.Wherein, doping quality than data representation for the material that adulterates and the mass ratio of material of main part, below in like manner.The thickness of the first hole injection layer 151 is 10～15nm.
The material of the first hole transmission layer 152 is N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane.The thickness of the first hole transmission layer 152 is 30～50nm.
The material of red light luminescent layer 153 is two (2-methyl-diphenyl [f, h] quinoxaline) (acetylacetone,2,4-pentanedione) close iridium, two [2-phenylchinoline base)-N, C2] (acetylacetone,2,4-pentanedione) close iridium (III), two [N-isopropyl-2-(4-fluorophenyl) benzimidazole] (acetylacetone,2,4-pentanediones) close iridium (III), two [2-(2-fluorophenyl)-1, 3-benzothiazole-N, C2] (acetylacetone,2,4-pentanedione) close iridium (III), two (2-benzothiophene-2-base-pyridine) (acetylacetone,2,4-pentanediones) close iridium (III) or three (1-phenyl-isoquinolin) and close iridium) doping mass ratio according to 0.5～2% is entrained in 4, 4', 4''-tri-(carbazole-9-yl) triphenylamine, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 4, 4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4, 4'-benzidine, 1, 1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane or 9, two (1-naphthyl) anthracenes of 10-) composite material forming in.The thickness of red light luminescent layer 153 is 10～30nm.
The material of the first green luminescence layer 154 is that three (2-phenylpyridines) close iridium, acetopyruvic acid two (2-phenylpyridine) iridium or three [2-(p-methylphenyl) pyridine] and close iridium (III) and be entrained in 4 according to 2～10% doping mass ratio, 4', 4''-tri-(carbazole-9-yl) triphenylamine, 9,9'-(1,3-phenyl) two-9H-carbazole, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine, 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in two (1-naphthyl) anthracenes of cyclohexane or 9,10-.The thickness of the first green luminescence layer 154 is 10～30nm.
The material of the first blue light-emitting 155 comprises Blue-light emitting host material, blue light guest materials and charge generating material, Blue-light emitting host material is 4, 4'-bis-(9-carbazole) biphenyl, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 9-(4-2-methyl-2-phenylpropane base)-3, two (triphenyl the silicon)-9H-carbazoles of 6-, 2, two (3-(9H-carbazole-9-yl) phenyl) pyridines of 6-, 3, two (3-(9H-carbazole-9-yl) phenyl) pyridines or 1 of 5-, two (triphenyl silicon) benzene of 4--, blue light guest materials is two (4, 6-difluorophenyl pyridine-N, C2) pyridine formyl closes iridium, two (4, 6-difluorophenyl pyridine)-tetra-(1-pyrazolyl) boric acid closes iridium, three (2-(4', the fluoro-5 '-cyano group of 6'-bis-) phenylpyridine-N, C2') close iridium, two (4, 6-difluorophenyl pyridine)-(3-(trifluoromethyl)-5-(pyridine-2-yl)-1, 2, 4-triazole) close iridium or two (4, 6-difluorophenyl pyridine) (5-(pyridine-2-yl)-tetrazolium) closes iridium), charge generating material is MoO 3, V 2o 5, WO 3or ReO 3, the mass ratio of Blue-light emitting host material, blue light guest materials and charge generating material is 1:5～20:5～10.The thickness of the first blue light-emitting 155 is 5～15nm.
The material of the first electron transfer layer 156 is 4,7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1,3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene.The thickness of the first electron transfer layer 156 is 10～60nm.
The material of charge generation layer 160 is MoO 3, V 2o 5, WO 3or ReO 3, thickness is 5～30nm.
The second organic luminescence function layer 170 is included in the second hole injection layer 171, the second hole transmission layer 172, the second green luminescence layer 173, the second blue light-emitting 174, the second electron transfer layer 175 and the electron injecting layer 176 being cascading on charge generation layer 160.
The material of the second hole injection layer 171 is MoO 3, WO 3, V 2o 5or ReO 3doping mass ratio according to 25～35% is entrained in N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in cyclohexane.The thickness of the second hole transmission layer 171 is 10～15nm.
The material of the second hole transmission layer 172 is N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane.The thickness of the second hole transmission layer 172 is 30～50nm.
The material of the second green luminescence layer 173 is that three (2-phenylpyridines) close iridium, acetopyruvic acid two (2-phenylpyridine) iridium or three [2-(p-methylphenyl) pyridine] and close iridium (III) and be entrained in 4 according to 2～10% doping mass ratio, 4', 4''-tri-(carbazole-9-yl) triphenylamine, 9,9'-(1,3-phenyl) two-9H-carbazole, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine, 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in two (1-naphthyl) anthracenes of cyclohexane or 9,10-.The thickness of the second green luminescence layer 173 is 10～30nm.
The material of the second blue light-emitting 174 comprises Blue-light emitting host material, blue light guest materials and charge generating material, Blue-light emitting host material is 4, 4'-bis-(9-carbazole) biphenyl, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 9-(4-2-methyl-2-phenylpropane base)-3, two (triphenyl the silicon)-9H-carbazoles of 6-, 2, two (3-(9H-carbazole-9-yl) phenyl) pyridines of 6-, 3, two (3-(9H-carbazole-9-yl) phenyl) pyridines or 1 of 5-, two (triphenyl silicon) benzene of 4--, blue light guest materials is two (4, 6-difluorophenyl pyridine-N, C2) pyridine formyl closes iridium, two (4, 6-difluorophenyl pyridine)-tetra-(1-pyrazolyl) boric acid closes iridium, three (2-(4', the fluoro-5 '-cyano group of 6'-bis-) phenylpyridine-N, C2') close iridium, two (4, 6-difluorophenyl pyridine)-(3-(trifluoromethyl)-5-(pyridine-2-yl)-1, 2, 4-triazole) close iridium or two (4, 6-difluorophenyl pyridine) (5-(pyridine-2-yl)-tetrazolium) closes iridium), charge generating material is MoO 3, V 2o 5, WO 3or ReO 3, the mass ratio of Blue-light emitting host material, blue light guest materials and charge generating material is 1:5～20:5～10.The thickness of the second blue light-emitting 174 is 5～15nm.
The material of the second electron transfer layer 175 is 4,7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1,3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene.The thickness of the second electron transfer layer 175 is 10～60nm.
The material of electron injecting layer 176 is Cs 2cO 3, CsF, CsN 3, Li 2cO 3, LiF or Li 2o is entrained in 4 according to 25～35% doping mass ratio, 7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1, the composite material forming in 3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene.The thickness of electron injecting layer 176 is 20～40nm.
Cathode layer 180 is located on electron injecting layer 176.The material of cathode layer 180 is Ag, Al or Au, and thickness is 50～200nm.
This organic electroluminescence device 100 is by anti-reflective film 114 is set under exiting surface, and short reduction layer 140 is set on anode layer 130, and the light extraction efficiency of whole device 100 improves greatly.
In addition, present embodiment also provides a kind of manufacture method of organic electroluminescence device, comprises the steps:
Step 1: the side magnetron sputtering at white glass plate is prepared anti-reflective film, obtain the antireflection composite bed that contains individual layer anti-reflective film, simultaneously in a side deposits conductive material of substrate, make anode layer, then by the opposite side of described substrate folded be located on described anti-reflective film and and this anti-reflective film between be provided with bright dipping space.
In the present embodiment, the opposite side that is also included in substrate carries out micro-pattern textureization to be made, and substrate is dried and is processed to remove the step of water and air as far as possible at vacuum state.Wherein, micro-pattern textureization is made and is specifically adopted conical tool, at the opposite side of substrate, produces and has a plurality of equally distributed conical protrusions.The bottom surface diameter of conical protrusions is 5～20 μ m, is highly 5～20 μ m, spacing 5～20 μ m between adjacent protrusion.
Step 2: adopt the mode of magnetron sputtering, prepare short reduction layer on anode layer, material selection SiGe and the In of magnetron sputtering 2o 3, ZnS, SnO 2or SiO 2the composite material forming according to mass ratio 1:1.
Step 3: prepare successively the first hole injection layer, the first hole transmission layer, red light luminescent layer, the first green luminescence layer, the first blue light-emitting and the first electron transfer layer on short reduction layer.
The making of the first hole injection layer, the first hole transmission layer, red light luminescent layer, the first green luminescence layer, the first blue light-emitting and the first electron transfer layer mainly adopts the mode of vacuum evaporation.
Step 4: charge generation layer is prepared in vacuum evaporation on the first electron transfer layer, the material of charge generation layer is MoO 3, V 2o 5, WO 3or ReO 3.
Step 5: prepare successively the second hole injection layer, the second hole transmission layer, the second green luminescence layer, the second blue light-emitting, the second electron transfer layer and electron injecting layer on charge generation layer.
The making of the second hole injection layer, the second hole transmission layer, the second green luminescence layer, the second blue light-emitting, the second electron transfer layer and electron injecting layer mainly adopts the mode of vacuum evaporation.
Step 6: cathode layer is prepared in vacuum evaporation on electron injecting layer, obtains organic electroluminescence device.
Above-mentioned manufacture method is easy, low for equipment requirements, can wide popularization and application.
Be below specific embodiment part:
Embodiment 1:
A) choose there is high refractive index transparent polyurethane plastic as high refractive index layer.First the transparent ito anode of thickness 100nm is deposited on to the surface of polyurethane plastic, adopt conical tool to carry out micro-pattern texture making on another surface of plastic film, on another surface of plastic film, making bottom surface diameter is 5～20 μ m, height 5 μ m, spacing is a plurality of equally distributed conical protrusions of 5 μ m.
Choose a white glass plate, adopt the mode of vacuum sputtering at white glass plate one side sputter one deck anti-reflective film, the material of anti-reflective film is SiGe, and base vacuum degree is 1 * 10 -5pa, thickness 20nm.
The side that plastic film is had to conical protrusions is on the anti-reflective film of white glass plate one side, and micro-patterning texture structure has been connected on anti-reflective film, has produced space between the two.By the structure obtaining vacuumize 15min at 80 ℃, reduce remaining water and gas.
The making of short reduction layer: adopt the mode of magnetron sputtering to make short reduction layer on ito anode layer, material selection SiGe and the In of short reduction layer 2o 3the composite material being mixed to form according to mass ratio 1:1, base vacuum degree is 1 * 10 -5pa, thickness 10nm.
Adopt the mode of vacuum evaporation to be prepared as follows each layer:
B) preparation of the first hole injection layer: by MoO 3be doped in NPB as the first hole injection layer, doping content 30wt%(" wt " and represent mass concentration, below in like manner), thickness 12.5nm, vacuum degree 5 * 10 -5pa, evaporation rate .
C) preparation of the first hole transmission layer: material adopts NPB, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
D) preparation of red light luminescent layer: material of main part adopts TCTA, red guest material adopts Ir (MDQ) 2(acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of red guest material and material of main part is 1:100.
E) preparation of the first green luminescence layer: material of main part adopts TCTA, green guest material adopts Ir (ppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 6:100.
F) preparation of the first blue light-emitting: material of main part adopts CBP, blue guest material to adopt FIrpic, charge generating material to adopt MoO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12.5:7.5.
G) preparation of the first electron transfer layer: electron transport material is Bphen, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 35nm.
H) preparation of charge generation layer: adopt bipolarity charge generation layer MoO 3, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 17.5nm.
I) preparation of the second hole injection layer: by MoO 3be doped in NPB as the second hole injection layer doping content 30wt%, thickness 12.5nm, vacuum degree 5 * 10 -5pa, evaporation rate .
J) preparation of the second hole transmission layer: material adopts NPB; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
K) preparation of the second green luminescence layer: material of main part adopts TCTA, green guest material adopts Ir (ppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 6:100.
L) preparation of the second blue light-emitting: material of main part adopts CBP, blue guest material to adopt FIrpic, charge generating material to adopt MoO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12.5:7.5.
M) preparation of the second electron transfer layer: material is Bphen, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 35nm.
N) preparation of electron injecting layer: adopt that N-shaped is material doped to be entered in electron transport material to form electron injecting layer, N-shaped material is Cs 2cO 3, electron transport material adopts Bphen, the doping content 30wt% of N-shaped material in electron transport material, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
O) preparation of cathode layer: metallic cathode adopts silver (Ag), and thickness is 125nm, vacuum degree 5 * 10 -5pa, evaporation rate .
Embodiment 2:
A) choose there is high refractive index transparent polyurethane plastic as high refractive index layer.First the transparent ito anode of thickness 100nm is deposited on to the surface of polyurethane plastic, adopt conical tool to carry out micro-pattern texture making on another surface of plastic film, on another surface of plastic film, making bottom surface diameter is 5～20 μ m, be highly 10 μ m, spacing is a plurality of equally distributed conical protrusions of 10 μ m.
Choose a white glass plate, adopt the mode of vacuum sputtering at white glass plate one side sputter one deck anti-reflective film, the material of anti-reflective film is SiGe, and base vacuum degree is 1 * 10 -5pa, thickness 20nm.
The side that plastic film is had to conical protrusions is on the anti-reflective film of white glass plate one side, and micro-patterning texture structure has been connected on anti-reflective film, has produced space between the two.By the structure obtaining vacuumize 15min at 80 ℃, reduce remaining water and gas.
The making of short reduction layer: adopt the mode of magnetron sputtering to make short reduction layer on ito anode layer, the composite material that the material selection SiGe of short reduction layer and ZnS are mixed to form according to mass ratio 1:1, base vacuum degree is 1 * 10 -5pa, thickness 10nm.
Adopt the mode of vacuum evaporation to be prepared as follows each layer:
B) preparation of the first hole injection layer: by WO 3be doped in TCTA as the first hole injection layer doping content 25wt%, thickness 10nm, vacuum degree 5 * 10 -5pa, evaporation rate .
C) preparation of the first hole transmission layer: material adopts TCTA, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
D) preparation of red light luminescent layer: material of main part adopts mCP, red guest material adopts PQIr; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of red guest material and material of main part is 0.5:100.
E) preparation of the first green luminescence layer: material of main part adopts mCP, green guest material adopts Ir (ppy) 2(acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of green guest material and material of main part is 2:100.
F) preparation of the first blue light-emitting: material of main part adopts mCP, blue guest material to adopt Fir6, charge generating material to adopt V 2o 5; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 5nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:5:5.
G) preparation of the first electron transfer layer: electron transport material is BCP, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm.
H) preparation of charge generation layer: adopt bipolarity charge generation layer V 2o 5, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 5nm.
I) preparation of the second hole injection layer: by WO 3be doped in TCTA as the second hole injection layer doping content 25wt%, thickness 10nm, vacuum degree 5 * 10 -5pa, evaporation rate .
J) preparation of the second hole transmission layer: material adopts TCTA; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
K) preparation of the second green luminescence layer: material of main part adopts mCP, green guest material adopts Ir (ppy) 2(acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of green guest material and material of main part is 2:100.
L) preparation of the second blue light-emitting: material of main part adopts mCP, blue guest material to adopt Fir6, charge generating material to adopt V 2o 5; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 5nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:5:5.
M) preparation of the second electron transfer layer: material is BCP, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm.
N) preparation of electron injecting layer: adopt that N-shaped is material doped to be entered in electron transport material to form electron injecting layer, N-shaped material is CsF, and electron transport material adopts BCP, the doping content 25wt% of N-shaped material in electron transport material, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm.
O) preparation of cathode layer: metallic cathode adopts silver (Al), and thickness is 50nm, vacuum degree 5 * 10 -5pa, evaporation rate .
Embodiment 3:
A) choose there is high refractive index transparent polyurethane plastic as high refractive index layer.First the transparent ito anode of thickness 100nm is deposited on to the surface of polyurethane plastic, adopt conical tool to carry out micro-pattern texture making on another surface of plastic film, on another surface of plastic film, making bottom surface diameter is 5～20 μ m, be highly 15 μ m, spacing is a plurality of equally distributed conical protrusions of 15 μ m.
Choose a white glass plate, adopt the mode of vacuum sputtering at white glass plate one side sputter one deck anti-reflective film, the material of anti-reflective film is SiGe, and base vacuum degree is 1 * 10 -5pa, thickness 20nm.
The side that plastic film is had to conical protrusions is on the anti-reflective film of white glass plate one side, and micro-patterning texture structure has been connected on anti-reflective film, has produced space between the two.By the structure obtaining vacuumize 15min at 80 ℃, reduce remaining water and gas.
The making of short reduction layer: adopt the mode of magnetron sputtering to make short reduction layer on ito anode layer, material selection SiGe and the SnO of short reduction layer 2the composite material being mixed to form according to mass ratio 1:1, base vacuum degree is 1 * 10 -5pa, thickness 10nm.
Adopt the mode of vacuum evaporation to be prepared as follows each layer:
B) preparation of the first hole injection layer: by V 2o 5be doped in CBP as the first hole injection layer doping content 35wt%, thickness 15nm, vacuum degree 5 * 10 -5pa, evaporation rate .
C) preparation of the first hole transmission layer: material adopts CBP, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 50nm.
D) preparation of red light luminescent layer: material of main part adopts CBP, red guest material adopts (fbi) 2ir (acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm, the mass ratio of red guest material and material of main part is 2:100.
E) preparation of the first green luminescence layer: material of main part adopts CBP, green guest material adopts Ir (mppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm, the mass ratio of green guest material and material of main part is 10:100.
F) preparation of the first blue light-emitting: material of main part adopts CzSi, blue guest material to adopt FCNIr, charge generating material to adopt WO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 15nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:20:10.
G) preparation of the first electron transfer layer: electron transport material is BAlq, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 60nm.
H) preparation of charge generation layer: adopt bipolarity charge generation layer WO 3, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
I) preparation of the second hole injection layer: by V 2o 5be doped in CBP as the second hole injection layer doping content 35wt%, thickness 15nm, vacuum degree 5 * 10 -5pa, evaporation rate .
J) preparation of the second hole transmission layer: material adopts CBP; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 50nm.
K) preparation of the second green luminescence layer: material of main part adopts CBP, green guest material adopts Ir (mppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm, the mass ratio of green guest material and material of main part is 10:100.
L) preparation of the second blue light-emitting: material of main part adopts CzSi, blue guest material to adopt FCNIr, charge generating material to adopt WO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 15nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:20:10.
M) preparation of the second electron transfer layer: material is BAlq, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 60nm.
N) preparation of electron injecting layer: adopt that N-shaped is material doped to be entered in electron transport material to form electron injecting layer, N-shaped material is CsN 3, electron transport material adopts BAlq, the doping content 35wt% of N-shaped material in electron transport material, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
O) preparation of cathode layer: metallic cathode adopts silver (Au), and thickness is 200nm, vacuum degree 5 * 10 -5pa, evaporation rate .
Embodiment 4:
A) choose there is high refractive index transparent polyurethane plastic as high refractive index layer.First the transparent ito anode of thickness 100nm is deposited on to the surface of polyurethane plastic, adopt conical tool to carry out micro-pattern texture making on another surface of plastic film, on another surface of plastic film, making bottom surface diameter is 5～20 μ m, be highly 20 μ m, spacing is a plurality of equally distributed conical protrusions of 20 μ m.
Choose a white glass plate, adopt the mode of vacuum sputtering at white glass plate one side sputter one deck anti-reflective film, the material of anti-reflective film is SiGe, and base vacuum degree is 1 * 10 -4pa, thickness 15nm.
The side that plastic film is had to conical protrusions is on the anti-reflective film of white glass plate one side, and micro-patterning texture structure has been connected on anti-reflective film, has produced space between the two.By the structure obtaining vacuumize 15min at 80 ℃, reduce remaining water and gas.
The making of short reduction layer: adopt the mode of magnetron sputtering to make short reduction layer on ito anode layer, material selection SiGe and the SiO of short reduction layer 2the composite material being mixed to form according to mass ratio 1:1, base vacuum degree is 1 * 10 -4pa, thickness 6nm.
Adopt the mode of vacuum evaporation to be prepared as follows each layer:
B) preparation of the first hole injection layer: by ReO 3be doped in TPD as the first hole injection layer doping content 30wt%, thickness 13nm, vacuum degree 5 * 10 -5pa, evaporation rate .
C) preparation of the first hole transmission layer: material adopts TPD, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
D) preparation of red light luminescent layer: material of main part adopts TPD, red guest material adopts (F-BT) 2ir (acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of red guest material and material of main part is 1:100.
E) preparation of the first green luminescence layer: material of main part adopts TPD, green guest material adopts Ir (ppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 5:100.
F) preparation of the first blue light-emitting: material of main part adopts 26DCzPPY, blue guest material to adopt FIrtaz, charge generating material to adopt ReO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12:7.
G) preparation of the first electron transfer layer: electron transport material is Alq 3, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
H) preparation of charge generation layer: adopt bipolarity charge generation layer ReO 3, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm.
I) preparation of the second hole injection layer: by ReO 3be doped in TPD as the second hole injection layer doping content 30wt%, thickness 12nm, vacuum degree 5 * 10 -5pa, evaporation rate .
J) preparation of the second hole transmission layer: material adopts TPD, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
K) preparation of the second green luminescence layer: material of main part adopts TPD, green guest material adopts Ir (ppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 5:100.
L) preparation of the second blue light-emitting: material of main part adopts 26DCzPPY, blue guest material to adopt FIrtaz, charge generating material to adopt ReO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12:7.
M) preparation of the second electron transfer layer: electron transport material is Alq 3, vacuum degree 5 * 10 -5pa, evaporation rate 1 / s, evaporation thickness 30nm.
N) preparation of electron injecting layer: adopt that N-shaped is material doped to be entered in electron transport material to form electron injecting layer, N-shaped material is Li 2cO 3, electron transport material adopts Alq 3, the doping content 30wt% of N-shaped material in electron transport material, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
O) preparation of cathode layer: metallic cathode adopts silver (Ag), and thickness is 100nm, vacuum degree 5 * 10 -5pa, evaporation rate .
Embodiment 5:
A) choose there is high refractive index transparent polyurethane plastic as high refractive index layer.First the transparent ito anode of thickness 100nm is deposited on to the surface of polyurethane plastic, adopt conical tool to carry out micro-pattern texture making on another surface of plastic film, on another surface of plastic film, making bottom surface diameter is 5～20 μ m, be highly 11 μ m, spacing is a plurality of equally distributed conical protrusions of 11 μ m.
Choose a white glass plate, adopt the mode of vacuum sputtering at white glass plate one side sputter one deck anti-reflective film, the material of anti-reflective film is SiGe, and base vacuum degree is 1 * 10 -5pa, thickness 15nm.
The side that plastic film is had to conical protrusions is on the anti-reflective film of white glass plate one side, and micro-patterning texture structure has been connected on anti-reflective film, has produced space between the two.By the structure obtaining vacuumize 15min at 80 ℃, reduce remaining water and gas.
The making of short reduction layer: adopt the mode of magnetron sputtering to make short reduction layer on ito anode layer, material selection SiGe and the In of short reduction layer 2o 3the composite material being mixed to form according to mass ratio 1:1, base vacuum degree is 1 * 10 -4pa, thickness 6nm.
Adopt the mode of vacuum evaporation to be prepared as follows each layer:
B) preparation of the first hole injection layer: by MoO 3be doped in TAPC as the first hole injection layer doping content 25wt%, thickness 10nm, vacuum degree 5 * 10 -5pa, evaporation rate .
C) preparation of the first hole transmission layer: material adopts TAPC, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
D) preparation of red light luminescent layer: material of main part adopts TAPC, red guest material adopts Ir (btp) 2(acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of red guest material and material of main part is 1:100.
E) preparation of the first green luminescence layer: material of main part adopts TAPC, green guest material adopts Ir (ppy) 2(acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 7:100.
F) preparation of the first blue light-emitting: material of main part adopts 35DCzPPY, blue guest material to adopt FIrN4, charge generating material to adopt MoO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12:7.
G) preparation of the first electron transfer layer: electron transport material is TAZ, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
H) preparation of charge generation layer: adopt bipolarity charge generation layer MoO 3, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm.
I) preparation of the second hole injection layer: by MoO 3be doped in TAPC as the second hole injection layer doping content 28wt%, thickness 13nm, vacuum degree 5 * 10 -5pa, evaporation rate .
J) preparation of the second hole transmission layer: material adopts TAPC, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
K) preparation of the second green luminescence layer: material of main part adopts TAPC, green guest material adopts Ir (ppy) 2(acac); Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 7:100.
L) preparation of the second blue light-emitting: material of main part adopts 35DCzPPY, blue guest material to adopt FIrN4, charge generating material to adopt MoO 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12:7.
M) preparation of the second electron transfer layer: electron transport material is TAZ, vacuum degree 5 * 10 -5pa, evaporation rate 1 / s, evaporation thickness 50nm.
N) preparation of electron injecting layer: adopt that N-shaped is material doped to be entered in electron transport material to form electron injecting layer, N-shaped material is LiF, and electron transport material adopts TAZ, the doping content 30wt% of N-shaped material in electron transport material, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
O) preparation of cathode layer: metallic cathode adopts silver (Al), and thickness is 100nm, vacuum degree 5 * 10 -5pa, evaporation rate .
Embodiment 6:
A) choose there is high refractive index transparent polyurethane plastic as high refractive index layer.First the transparent ito anode of thickness 100nm is deposited on to the surface of polyurethane plastic, adopt conical tool to carry out micro-pattern texture making on another surface of plastic film, on another surface of plastic film, making bottom surface diameter is 5～20 μ m, be highly 18 μ m, spacing is a plurality of equally distributed conical protrusions of 18 μ m.
Choose a white glass plate, adopt the mode of vacuum sputtering at white glass plate one side sputter one deck anti-reflective film, the material of anti-reflective film is SiGe, and base vacuum degree is 1 * 10 -3pa, thickness 10nm.
The side that plastic film is had to conical protrusions is on the anti-reflective film of white glass plate one side, and micro-patterning texture structure has been connected on anti-reflective film, has produced space between the two.By the structure obtaining vacuumize 15min at 80 ℃, reduce remaining water and gas.
The making of short reduction layer: adopt the mode of magnetron sputtering to make short reduction layer on ito anode layer, the composite material that the material selection SiGe of short reduction layer and ZnS are mixed to form according to mass ratio 1:1, base vacuum degree is 1 * 10 -3pa, thickness 4nm.
Adopt the mode of vacuum evaporation to be prepared as follows each layer:
B) preparation of the first hole injection layer: by WO 3be doped in NPB as the first hole injection layer doping content 30wt%, thickness 12nm, vacuum degree 5 * 10 -5pa, evaporation rate .
C) preparation of the first hole transmission layer: material adopts NPB, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
D) preparation of red light luminescent layer: material of main part adopts ADN, red guest material adopts Ir (piq) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of red guest material and material of main part is 1:100.
E) preparation of the first green luminescence layer: material of main part adopts ADN, green guest material adopts Ir (mppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 6:100.
F) preparation of the first blue light-emitting: material of main part adopts UGH2, blue guest material to adopt FIrpic, charge generating material to adopt V 2o 5; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12:7.
G) preparation of the first electron transfer layer: electron transport material is TPBI, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
H) preparation of charge generation layer: adopt bipolarity charge generation layer V 2o 5, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm.
I) preparation of the second hole injection layer: by WO 3be doped in NPB as the second hole injection layer doping content 30wt%, thickness 12nm, vacuum degree 5 * 10 -5pa, evaporation rate .
J) preparation of the second hole transmission layer: material adopts NPB, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 40nm.
K) preparation of the second green luminescence layer: material of main part adopts ADN, green guest material adopts Ir (mppy) 3; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 20nm, the mass ratio of green guest material and material of main part is 6:100.
L) preparation of the second blue light-emitting: material of main part adopts UGH2, blue guest material to adopt FIrpic, charge generating material to adopt V 2o 5; Vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 10nm, the mass ratio of material of main part, blue guest material and charge generating material is 100:12:7.
M) preparation of the second electron transfer layer: electron transport material is TPBI, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
N) preparation of electron injecting layer: adopt that N-shaped is material doped to be entered in electron transport material to form electron injecting layer, N-shaped material is Li 2o, electron transport material adopts TPBI, the doping content 30wt% of N-shaped material in electron transport material, vacuum degree 5 * 10 -5pa, evaporation rate , evaporation thickness 30nm.
O) preparation of cathode layer: metallic cathode adopts silver (Al), and thickness is 100nm, vacuum degree 5 * 10 -5pa, evaporation rate .
Table 2 is the luminous efficiency test result of the organic electroluminescence device of embodiment 1-6 making, specific as follows:
Table 2
As can be seen from Table 2, the organic electroluminescence device that embodiment 1-6 makes is owing to adopting anti-reflective film and short reduction layer, and the luminous efficiency of whole device significantly improves.
The above embodiment has only expressed several execution mode of the present invention, and it describes comparatively concrete and detailed, but can not therefore be interpreted as the restriction to the scope of the claims of the present invention.It should be pointed out that for the person of ordinary skill of the art, without departing from the inventive concept of the premise, can also make some distortion and improvement, these all belong to protection scope of the present invention.Therefore, the protection range of patent of the present invention should be as the criterion with claims.

Claims (10)

1. an organic electroluminescence device, is characterized in that, comprises the antireflection composite bed, substrate, anode layer, short reduction layer, the first organic luminescence function layer, charge generation layer, the second organic luminescence function layer and the cathode layer that are cascading; Wherein, the anti-reflective film that described antireflection composite bed comprises white glass plate and is positioned at described white glass plate one side, described substrate be located on described anti-reflective film and and this anti-reflective film between be provided with bright dipping space; The material of described short reduction layer is SiGe and In 2o 3, ZnS, SnO 2or SiO 2the composite material forming according to mass ratio 1:1; Described the first organic luminescence function layer is included in the first hole injection layer, the first hole transmission layer, red light luminescent layer, the first green luminescence layer, the first blue light-emitting and the first electron transfer layer being cascading on described short reduction layer; Described the second organic luminescence function layer is included in the second hole injection layer, the second hole transmission layer, the second green luminescence layer, the second blue light-emitting, the second electron transfer layer and the electron injecting layer being cascading on described charge generation layer, and described cathode layer is located on described electron injecting layer.
2. organic electroluminescence device as claimed in claim 1, is characterized in that, the material of described anti-reflective film is SiGe, and thickness is 10～20nm.
3. organic electroluminescence device as claimed in claim 1, is characterized in that, the material of described substrate is polyurethane, described substrate near a side of described antireflection composite bed be provided with a plurality of be uniformly distributed and with the integrated projection of described substrate.
4. organic electroluminescence device as claimed in claim 3, is characterized in that, described projection is conical, and bottom surface diameter is 5～20 μ m, is highly 5～20 μ m, spacing 5～20 μ m between adjacent protrusion.
5. organic electroluminescence device as claimed in claim 1, is characterized in that, described anode layer is the ITO layer of thickness 100nm.
6. organic electroluminescence device as claimed in claim 1, is characterized in that, the material of described the first hole injection layer is MoO 3, WO 3, V 2o 5or ReO 3doping mass ratio according to 25～35% is entrained in N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in cyclohexane;
The material of described the first hole transmission layer is N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane;
The material of described red light luminescent layer is two (2-methyl-diphenyl [f, h] quinoxaline) (acetylacetone,2,4-pentanedione) close iridium, two [2-phenylchinoline base)-N, C2] (acetylacetone,2,4-pentanedione) close iridium (III), two [N-isopropyl-2-(4-fluorophenyl) benzimidazole] (acetylacetone,2,4-pentanediones) close iridium (III), two [2-(2-fluorophenyl)-1, 3-benzothiazole-N, C2] (acetylacetone,2,4-pentanedione) close iridium (III), two (2-benzothiophene-2-base-pyridine) (acetylacetone,2,4-pentanediones) close iridium (III) or three (1-phenyl-isoquinolin) and close iridium) doping mass ratio according to 0.5～2% is entrained in 4, 4', 4''-tri-(carbazole-9-yl) triphenylamine, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 4, 4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4, 4'-benzidine, 1, 1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane or 9, two (1-naphthyl) anthracenes of 10-) composite material forming in,
The material of described the first green luminescence layer is that three (2-phenylpyridines) close iridium, acetopyruvic acid two (2-phenylpyridine) iridium or three [2-(p-methylphenyl) pyridine] and close iridium (III) and be entrained in 4 according to 2～10% doping mass ratio, 4', 4''-tri-(carbazole-9-yl) triphenylamine, 9,9'-(1,3-phenyl) two-9H-carbazole, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine, 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in two (1-naphthyl) anthracenes of cyclohexane or 9,10-;
The material of described the first blue light-emitting comprises Blue-light emitting host material, blue light guest materials and charge generating material, described Blue-light emitting host material is 4, 4'-bis-(9-carbazole) biphenyl, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 9-(4-2-methyl-2-phenylpropane base)-3, two (triphenyl the silicon)-9H-carbazoles of 6-, 2, two (3-(9H-carbazole-9-yl) phenyl) pyridines of 6-, 3, two (3-(9H-carbazole-9-yl) phenyl) pyridines or 1 of 5-, two (triphenyl silicon) benzene of 4--, described blue light guest materials is two (4, 6-difluorophenyl pyridine-N, C2) pyridine formyl closes iridium, two (4, 6-difluorophenyl pyridine)-tetra-(1-pyrazolyl) boric acid closes iridium, three (2-(4', the fluoro-5 '-cyano group of 6'-bis-) phenylpyridine-N, C2') close iridium, two (4, 6-difluorophenyl pyridine)-(3-(trifluoromethyl)-5-(pyridine-2-yl)-1, 2, 4-triazole) close iridium or two (4, 6-difluorophenyl pyridine) (5-(pyridine-2-yl)-tetrazolium) closes iridium), described charge generating material is MoO 3, V 2o 5, WO 3or ReO 3, the mass ratio of described Blue-light emitting host material, described blue light guest materials and described charge generating material is 1:5～20:5～10,
The material of described the first electron transfer layer is 4,7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1,3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene.
7. organic electroluminescence device as claimed in claim 1, is characterized in that, the material of described charge generation layer is MoO 3, V 2o 5, WO 3or ReO 3, thickness is 5～30nm.
8. organic electroluminescence device as claimed in claim 1, is characterized in that, the material of described the second hole injection layer is MoO 3, WO 3, V 2o 5or ReO 3doping mass ratio according to 25～35% is entrained in N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in cyclohexane;
The material of described the second hole transmission layer is N, N'-diphenyl-N, N'-bis-(1-naphthyl)-1,1'-biphenyl-4,4'-diamines, 4,4', 4''-tri-(carbazole-9-yl) triphenylamine, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine or 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] cyclohexane;
The material of described the second green luminescence layer is that three (2-phenylpyridines) close iridium, acetopyruvic acid two (2-phenylpyridine) iridium or three [2-(p-methylphenyl) pyridine] and close iridium (III) and be entrained in 4 according to 2～10% doping mass ratio, 4', 4''-tri-(carbazole-9-yl) triphenylamine, 9,9'-(1,3-phenyl) two-9H-carbazole, 4,4'-bis-(9-carbazole) biphenyl, N, N'-bis-(3-aminomethyl phenyl)-N, N'-diphenyl-4,4'-benzidine, 1,1-bis-[4-[N, N '-bis-(p-tolyl) amino] phenyl] composite material that forms in two (1-naphthyl) anthracenes of cyclohexane or 9,10-;
The material of described the second blue light-emitting comprises Blue-light emitting host material, blue light guest materials and charge generating material, described Blue-light emitting host material is 4, 4'-bis-(9-carbazole) biphenyl, 9, 9'-(1, 3-phenyl) two-9H-carbazole, 9-(4-2-methyl-2-phenylpropane base)-3, two (triphenyl the silicon)-9H-carbazoles of 6-, 2, two (3-(9H-carbazole-9-yl) phenyl) pyridines of 6-, 3, two (3-(9H-carbazole-9-yl) phenyl) pyridines or 1 of 5-, two (triphenyl silicon) benzene of 4--, described blue light guest materials is two (4, 6-difluorophenyl pyridine-N, C2) pyridine formyl closes iridium, two (4, 6-difluorophenyl pyridine)-tetra-(1-pyrazolyl) boric acid closes iridium, three (2-(4', the fluoro-5 '-cyano group of 6'-bis-) phenylpyridine-N, C2') close iridium, two (4, 6-difluorophenyl pyridine)-(3-(trifluoromethyl)-5-(pyridine-2-yl)-1, 2, 4-triazole) close iridium or two (4, 6-difluorophenyl pyridine) (5-(pyridine-2-yl)-tetrazolium) closes iridium), described charge generating material is MoO 3, V 2o 5, WO 3or ReO 3, the mass ratio of described Blue-light emitting host material, described blue light guest materials and described charge generating material is 1:5～20:5～10,
The material of described the second electron transfer layer is 4,7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1,3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene;
The material of described electron injecting layer is Cs 2cO 3, CsF, CsN 3, Li 2cO 3, LiF or Li 2o is entrained in 4 according to 25～35% doping mass ratio, 7-diphenyl-1,10-phenanthroline, 4,7-diphenyl-1,10-Phen, 4-biphenyl phenolic group-bis-(2-methyl-oxine) close aluminium, oxine aluminium, 3-(biphenyl-4-yl)-5-(4-tert-butyl-phenyl)-4-phenyl-4H-1,2,4-triazole or 1, the composite material forming in 3,5-tri-(1-phenyl-1H-benzimidazolyl-2 radicals-yl) benzene.
9. organic electroluminescence device as claimed in claim 1, is characterized in that, the material of described cathode layer is Ag, Al or Au, and thickness is 50～200nm.
10. a manufacture method for organic electroluminescence device, is characterized in that, comprises the steps:
A side magnetron sputtering at white glass plate is prepared anti-reflective film, obtain the antireflection composite bed that contains individual layer anti-reflective film, simultaneously in a side deposits conductive material of substrate, make anode layer, then by the opposite side of described substrate folded be located on described anti-reflective film and and this anti-reflective film between be provided with bright dipping space;
Adopt the mode of magnetron sputtering, on described anode layer, prepare short reduction layer, material selection SiGe and the In of magnetron sputtering 2o 3, ZnS, SnO 2or SiO 2the composite material forming according to mass ratio 1:1;
On described short reduction layer, prepare successively the first hole injection layer, the first hole transmission layer, red light luminescent layer, the first green luminescence layer, the first blue light-emitting and the first electron transfer layer;
On described the first electron transfer layer, evaporation is prepared charge generation layer, and the material of described charge generation layer is MoO 3, V 2o 5, WO 3or ReO 3;
On described charge generation layer, prepare successively the second hole injection layer, the second hole transmission layer, the second green luminescence layer, the second blue light-emitting, the second electron transfer layer and electron injecting layer;
On described electron injecting layer, evaporation is prepared cathode layer, obtains described organic electroluminescence device.
CN201310192390.2A 2013-05-22 2013-05-22 Organic light-emitting device and manufacturing method thereof Pending CN104183715A (en)

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Application publication date: 20141203