WO2020091468A1 - Dispositif électroluminescent organique - Google Patents

Dispositif électroluminescent organique Download PDF

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WO2020091468A1
WO2020091468A1 PCT/KR2019/014621 KR2019014621W WO2020091468A1 WO 2020091468 A1 WO2020091468 A1 WO 2020091468A1 KR 2019014621 W KR2019014621 W KR 2019014621W WO 2020091468 A1 WO2020091468 A1 WO 2020091468A1
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group
compound
light emitting
substituted
unsubstituted
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Korean (ko)
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김성소
천민승
하재승
서상덕
홍성길
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주식회사 엘지화학
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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
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
    • 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
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons

Definitions

  • the present invention relates to an organic light emitting device having a low driving voltage, high luminous efficiency, and long life characteristics.
  • the organic light emitting phenomenon refers to a phenomenon that converts electrical energy into light energy using an organic material.
  • the organic light emitting device using the organic light emitting phenomenon has a wide viewing angle, excellent contrast, and fast response time, and has excellent luminance, driving voltage, and response speed characteristics, and thus many studies have been conducted.
  • the organic light emitting device generally has a structure including an anode and a cathode and an organic material layer between the anode and the cathode.
  • the organic material layer is often formed of a multi-layered structure composed of different materials, for example, may be formed of a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, an electron injection layer, and the like.
  • Patent Document 1 Korean Patent Publication No. 10-2000-0051826
  • the present invention is to provide an organic light emitting device having a low driving voltage, high luminous efficiency, and long life characteristics.
  • the present invention provides the following organic light emitting device:
  • the light emitting layer includes a host and a dopant
  • the dipole moment value of the host is 0.4 to 1.3
  • the electron control layer comprises a compound having a dipole moment (dipole moment) value of 0.7 to 1.3,
  • the organic light emitting device can have a low driving voltage, high luminous efficiency, and long life characteristics by using a host and an electron regulating layer material satisfying a specific dipole moment value.
  • FIG. 1 shows an example of an organic light emitting device comprising a substrate 1, an anode 2, a light emitting layer 3, an electron regulating layer 4, and a cathode 5.
  • substituted or unsubstituted refers to deuterium; Halogen group; Nitrile group; Nitro group; Hydroxy group; Carbonyl group; Ester groups; Imide group; Amino group; Phosphine oxide group; Alkoxy groups; Aryloxy group; Alkyl thioxy group; Arylthioxy group; Alkyl sulfoxy group; Aryl sulfoxyl group; Silyl group; Boron group; Alkyl groups; Cycloalkyl group; Alkenyl group; Aryl group; Aralkyl group; An alkenyl group; Alkyl aryl groups; Alkylamine groups; Aralkylamine group; Heteroarylamine group; Arylamine group; Arylphosphine group; Or substituted or unsubstituted with one or more substituents selected from the group consisting of heterocyclic groups containing one or more of N, O and S atoms, or substituted or unsubstituted with two or more
  • the number of carbon atoms of the carbonyl group is not particularly limited, but is preferably 1 to 40 carbon atoms. Specifically, it may be a compound having the following structure, but is not limited thereto.
  • the oxygen of the ester group may be substituted with a straight chain, branched or cyclic alkyl group having 1 to 25 carbon atoms or an aryl group having 6 to 25 carbon atoms. Specifically, it may be a compound of the following structural formula, but is not limited thereto.
  • the number of carbon atoms of the imide group is not particularly limited, but is preferably 1 to 25 carbon atoms. Specifically, it may be a compound having the following structure, but is not limited thereto.
  • the silyl group is specifically trimethylsilyl group, triethylsilyl group, t-butyldimethylsilyl group, vinyldimethylsilyl group, propyldimethylsilyl group, triphenylsilyl group, diphenylsilyl group, phenylsilyl group, etc. However, it is not limited thereto.
  • the boron group is specifically a trimethyl boron group, a triethyl boron group, a t-butyldimethyl boron group, a triphenyl boron group, a phenyl boron group, and the like, but is not limited thereto.
  • examples of the halogen group include fluorine, chlorine, bromine or iodine.
  • the alkyl group may be straight chain or branched chain, and carbon number is not particularly limited, but is preferably 1 to 40. According to an exemplary embodiment, the alkyl group has 1 to 20 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 10 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 6 carbon atoms.
  • alkyl group examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n -Pentyl, isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl , n-heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-octyl, 1-methylheptyl, 2-ethylhexyl
  • the alkenyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. According to one embodiment, the carbon number of the alkenyl group is 2 to 20. According to another exemplary embodiment, the alkenyl group has 2 to 10 carbon atoms. According to another exemplary embodiment, the alkenyl group has 2 to 6 carbon atoms.
  • Specific examples include vinyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 3-methyl-1- Butenyl, 1,3-butadienyl, allyl, 1-phenylvinyl-1-yl, 2-phenylvinyl-1-yl, 2,2-diphenylvinyl-1-yl, 2-phenyl-2- ( Naphthyl-1-yl) vinyl-1-yl, 2,2-bis (diphenyl-1-yl) vinyl-1-yl, steelbenyl group, styrenyl group, and the like, but are not limited thereto.
  • the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and according to an exemplary embodiment, the cycloalkyl group has 3 to 30 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 20 carbon atoms. According to another exemplary embodiment, the cycloalkyl group has 3 to 6 carbon atoms.
  • the aryl group is not particularly limited, but is preferably 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to one embodiment, the carbon number of the aryl group is 6 to 30. According to one embodiment, the carbon number of the aryl group is 6 to 20.
  • the aryl group may be a phenyl group, a biphenyl group, a terphenyl group, etc., as a monocyclic aryl group, but is not limited thereto.
  • the polycyclic aryl group may be a naphthyl group, anthracenyl group, phenanthryl group, pyrenyl group, perylenyl group, chrysenyl group, fluorenyl group, and the like, but is not limited thereto.
  • the fluorenyl group may be substituted, and two substituents may combine with each other to form a spiro structure.
  • the fluorenyl group When the fluorenyl group is substituted, It can be back. However, it is not limited thereto.
  • the heterocyclic group is a heterocyclic group containing one or more of O, N, Si, and S as heterogeneous elements, and the number of carbon atoms is not particularly limited, but is preferably 2 to 60 carbon atoms.
  • the heterocyclic group include thiophene group, furan group, pyrrol group, imidazole group, thiazole group, oxazole group, oxadiazole group, triazole group, pyridyl group, bipyridyl group, pyrimidyl group, triazine group, acridil group , Pyridazine group, pyrazinyl group, quinolinyl group, quinazolinyl group, quinoxalinyl group, phthalazinyl group, pyridopyrimidinyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group, isoquinoline group, indole group ,
  • an aryl group in an aralkyl group, an alkenyl group, an alkylaryl group, and an arylamine group is the same as the exemplified aryl group.
  • the alkyl group among the aralkyl group, alkylaryl group, and alkylamine group is the same as the above-described alkyl group.
  • the description of the heteroaryl group among heteroarylamines may be applied.
  • the alkenyl group in the alkenyl group is the same as the exemplified alkenyl group.
  • the description of the aryl group described above may be applied, except that the arylene is a divalent group.
  • the description of the heterocyclic group described above may be applied, except that the heteroarylene is a divalent group.
  • the hydrocarbon ring is not a monovalent group, and a description of the aryl group or cycloalkyl group described above may be applied, except that two substituents are formed by bonding.
  • the heterocycle is not a monovalent group, and the description of the aforementioned heterocyclic group may be applied, except that two substituents are formed by bonding.
  • the present invention the anode; A light emitting layer; Electronic control layer; Electron transport layer; And a cathode, wherein the light emitting layer includes a host and a dopant, and the compound included in the host and the electron regulating layer has a specific dipole moment value.
  • dipole moment used in the present specification means a physical quantity indicating the degree of polarity, and may be calculated as in Equation 1 below.
  • the molecular density can be calculated by calculating the dipole moment value.
  • the molecular density can be obtained by calculating the charge and dipole for each atom using the Hirshfeld Charge Analysis method, and calculating according to the following equation. Dipole Moment).
  • the dipole moment of the host compound of the light emitting layer In order to optimize the light emission characteristics of the organic light emitting device, the dipole moment of the host compound of the light emitting layer must be considered.
  • the compound included in the host and the electron control layer has a specific dipole moment value, low driving voltage and high It was confirmed that it can have luminous efficiency and long life characteristics.
  • the dipole moment value of the host is 0.4 to 1.3
  • the electron regulating layer includes a compound having a dipole moment value of 0.7 to 1.3.
  • the difference between the dipole moment value of the host and the dipole moment value of the compound included in the electron regulating layer is 0.01 to 0.8.
  • the maximum emission peak wavelength of the light emitting layer is 400 nm to 470 nm.
  • the triplet energy of the compound contained in the electron regulating layer is greater than the triplet energy of the host.
  • a compound represented by Formula 1 below may be used as the host used:
  • X 1 is O, or S
  • L 1 is a single bond, or a substituted or unsubstituted C 6-60 arylene,
  • Ar 1 is substituted or unsubstituted C 6-60 aryl
  • R 1 and R 2 are each independently hydrogen, deuterium, halogen, cyano, nitro, amino, substituted or unsubstituted C 1-60 alkyl, substituted or unsubstituted C 3-60 cycloalkyl, substituted or unsubstituted C 2-60 alkenyl, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted N, O, and C 2-60 heteroaryl containing one or more heteroatoms selected from the group consisting of S aryl , Or two adjacent ones combine with each other to form a benzene ring,
  • n1 is an integer from 0 to 3
  • n2 is an integer from 0 to 4.
  • L 1 is a single bond, or phenylene.
  • Ar 1 is phenyl, biphenylyl, terphenylyl, naphthyl, or naphthylphenyl.
  • R 1 is hydrogen, deuterium, or phenyl.
  • R 2 is hydrogen, deuterium, phenyl, biphenyl, or naphthyl.
  • the compound represented by Chemical Formula 1 may be prepared by the following Reaction Scheme 1.
  • Reaction Scheme 1 as a Suzuki coupling reaction, is preferably performed in the presence of a palladium catalyst and a base, and the reactor for the Suzuki coupling reaction can be modified as known in the art.
  • the manufacturing method may be more specific in the manufacturing examples to be described later.
  • the dopant material used in the light emitting layer is not particularly limited as long as it is used in an organic light emitting device.
  • the dopant material includes an aromatic amine derivative, a strylamine compound, a boron complex, a fluoranthene compound, and a metal complex.
  • the aromatic amine derivative is a condensed aromatic ring derivative having a substituted or unsubstituted arylamino group, and includes arylamino groups such as pyrene, anthracene, chrysene, periplanten, and the substituted or unsubstituted styrylamine compound.
  • a compound in which at least one arylvinyl group is substituted with the arylamine, a substituent selected from 1 or 2 or more from the group consisting of an aryl group, a silyl group, an alkyl group, a cycloalkyl group, and an arylamino group is substituted or unsubstituted.
  • a substituent selected from 1 or 2 or more from the group consisting of an aryl group, a silyl group, an alkyl group, a cycloalkyl group, and an arylamino group is substituted or unsubstituted.
  • styrylamine, styryldiamine, styryltriamine, styryltetraamine, and the like but are not limited thereto.
  • examples of the metal complex include an iridium complex and a platinum complex, but are not limited thereto.
  • the electron-regulating layer includes a compound represented by Formula 2 or 3 below:
  • Y is O, or S
  • X 2 are each independently N, or CH, provided that two or more of X 2 are N,
  • L 2 is a single bond, or a substituted or unsubstituted C 6-60 arylene,
  • Ar 2 and Ar 3 are each independently substituted or unsubstituted C 6-60 aryl; Or C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of substituted or unsubstituted N, O and S,
  • R 3 and R 4 are each independently hydrogen, deuterium, halogen, cyano, nitro, amino, substituted or unsubstituted C 1-60 alkyl, substituted or unsubstituted C 3-60 cycloalkyl, substituted or unsubstituted C 2-60 alkenyl, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted N, O, and C 2-60 heteroaryl containing one or more heteroatoms selected from the group consisting of S aryl ego,
  • n3 is an integer from 0 to 4,
  • n4 is an integer from 0 to 4.
  • L 2 is a single bond, phenylene, or biphenyldiyl.
  • Ar 2 and Ar 3 are each independently phenyl, biphenylyl, or terphenylyl.
  • R 3 and R 4 are hydrogen.
  • the compound represented by Chemical Formula 2 may be prepared by the same method as in Scheme 2, and may also be applied to the compound represented by Chemical Formula 3.
  • Reaction Scheme 2 as a Suzuki coupling reaction, is preferably performed in the presence of a palladium catalyst and a base, and the reactor for the Suzuki coupling reaction can be modified as known in the art.
  • the manufacturing method may be more specific in the manufacturing examples to be described later.
  • the organic light emitting devices other than the above-described light emitting layer and the electron control layer are not particularly limited as long as they can be used in the organic light emitting device, and will be described below for each configuration.
  • the positive electrode material is preferably a material having a large work function so that hole injection into the organic material layer is smooth.
  • the positive electrode material include metals such as vanadium, chromium, copper, zinc and gold or alloys thereof; Metal oxides such as zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO); A combination of metal and oxide such as ZnO: Al or SnO 2 : Sb; Conductive polymers such as poly (3-methylthiophene), poly [3,4- (ethylene-1,2-dioxy) thiophene] (PEDOT), polypyrrole, and polyaniline, but are not limited thereto.
  • the cathode material is preferably a material having a small work function to facilitate electron injection into the organic material layer.
  • the negative electrode material include metals such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead, or alloys thereof;
  • There is a multilayer structure material such as LiF / Al or LiO 2 / Al, but is not limited thereto.
  • the organic light emitting device may include a hole injection layer for injecting holes from an electrode.
  • the hole injection material it has the ability to transport holes and has a hole injection effect at the anode, an excellent hole injection effect for the light emitting layer or the light emitting material, and prevents the movement of the exciton generated in the light emitting layer to the electron injection layer or the electron injection material
  • a compound having excellent thin film formation ability is preferred. It is preferable that the highest occupied molecular orbital (HOMO) of the hole injection material is between the work function of the positive electrode material and the HOMO of the surrounding organic material layer.
  • the hole injection material examples include metal porphyrin, oligothiophene, arylamine-based organic substances, hexanitrile hexaazatriphenylene-based organic substances, quinacridone-based organic substances, and perylene-based substances.
  • the organic light emitting device may include a hole transport layer that transports holes from the anode or the hole injection layer to the hole to receive holes.
  • a material for transporting holes from the anode or the hole injection layer as a hole transport material and transferring them to the light emitting layer a material having high mobility for holes is suitable.
  • Specific examples include arylamine-based organic materials, conductive polymers, and block copolymers having a conjugated portion and a non-conjugated portion, but are not limited thereto.
  • the organic light emitting device may include an electron blocking layer that suppresses electrons injected from the cathode from being transferred toward the anode without recombination in the light emitting layer.
  • the organic light emitting device may include an electron transport layer that transports electrons from the cathode or the electron injection layer to the electron control layer by receiving electrons.
  • the electron transport material a material capable of receiving electrons well from the cathode and transferring them to the light emitting layer, a material having high mobility for electrons is suitable.
  • Specific examples include the Al complex of 8-hydroxyquinoline; Complexes including Alq 3 ; Organic radical compounds; Hydroxyflavone-metal complexes, and the like, but are not limited to these.
  • the electron transport layer can be used with any desired cathode material as used according to the prior art.
  • suitable cathode materials are those that have a low work function and are followed by an aluminum or silver layer. Specifically, cesium, barium, calcium, ytterbium and samarium, each case followed by an aluminum layer or a silver layer.
  • the organic light emitting device may include an electron injection layer that injects electrons from an electrode.
  • an electron injection material it has the ability to transport electrons, has an electron injection effect from the cathode, an excellent electron injection effect for the light emitting layer or the light emitting material, prevents movement of excitons generated in the light emitting layer to the hole injection layer, and also , A compound having excellent thin film forming ability is preferred.
  • fluorenone anthraquinodimethane, diphenoquinone, thiopyran dioxide, oxazole, oxadiazole, triazole, imidazole, perylenetetracarboxylic acid, preorenylidene methane, anthrone and the like and their derivatives, metal Complex compounds, nitrogen-containing 5-membered ring derivatives, and the like, but are not limited thereto.
  • Examples of the metal complex compound include 8-hydroxyquinolinato lithium, bis (8-hydroxyquinolinato) zinc, bis (8-hydroxyquinolinato) copper, bis (8-hydroxyquinolinato) manganese, Tris (8-hydroxyquinolinato) aluminum, tris (2-methyl-8-hydroxyquinolinato) aluminum, tris (8-hydroxyquinolinato) gallium, bis (10-hydroxybenzo [h] Quinolinato) beryllium, bis (10-hydroxybenzo [h] quinolinato) zinc, bis (2-methyl-8-quinolinato) chlorogallium, bis (2-methyl-8-quinolinato) ( There are o-cresolato) gallium, bis (2-methyl-8-quinolinato) (1-naphtholato) aluminum, bis (2-methyl-8-quinolinato) (2-naphtholato) gallium, It is not limited to this.
  • FIGS. 1 and 2 The structure of the organic light emitting device according to the present invention is illustrated in FIGS. 1 and 2.
  • FIG. 1 shows an example of an organic light emitting device comprising a substrate 1, an anode 2, a light emitting layer 3, an electron regulating layer 4, and a cathode 5.
  • An example of an organic light emitting device including an electron injection layer 10 and a cathode 5 is shown.
  • the organic light emitting device can be manufactured by sequentially stacking the above-described components.
  • a positive electrode is formed by depositing a metal or conductive metal oxide or an alloy thereof on a substrate using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation.
  • PVD physical vapor deposition
  • an organic material layer including a hole injection layer, a hole transport layer, a light emitting layer, and an electron transport layer is formed thereon, and a material that can be used as a cathode is deposited thereon.
  • an organic light emitting device may be formed by sequentially depositing a cathode material, an organic material layer, and a cathode material on a substrate.
  • the light emitting layer may be formed by a host and a dopant by a vacuum deposition method as well as a solution application method.
  • the solution application method means spin coating, dip coating, doctor blading, inkjet printing, screen printing, spraying, roll coating, and the like, but is not limited to these.
  • an organic light emitting device may be manufactured by sequentially depositing an organic material layer and a cathode material from a cathode material on a substrate (WO 2003/012890).
  • the manufacturing method is not limited thereto.
  • the organic light emitting device may be a front emission type, a back emission type or a double-sided emission type depending on the material used.
  • step 3 of Preparation Example 1-1 2- (dibenzo [b, d] furan-4-yl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolan is compound 1
  • step 3 of Preparation Example 1-1 2- (dibenzo [b, d] furan-4-yl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolan is compound 1
  • Step 2 of Preparation Example 1-1 the compound 1-7- was prepared in the same manner as in the preparation method of Compound 1-1-b, except that Compound 1-1-a was changed to Compound 1-7-a.
  • Compound 2-3 was prepared in the same manner as in Production Example 2-2, except that Compound E was used instead of Compound D in Preparation Example 2-2.
  • Compound 2-5 was manufactured by the same method as Production Example 2-2, except that compound H was used instead of compound D in Preparation Example 2-2.
  • Compound 2-6 was manufactured by the same method as the preparation example 2-1, except that compound I was used instead of compound B in Preparation Example 2-1.
  • Compound 2-7 was manufactured by the same method as Production Example 2-2, except that compound B was used instead of compound D in Preparation Example 2-2.
  • Compound 2-8 was manufactured by the same method as Production Example 2-4, except that compound J was used instead of compound G in Preparation Example 2-4.
  • a glass substrate coated with a thin film of ITO (indium tin oxide) at a thickness of 1,000 ⁇ was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves.
  • Fischer Fischer Co.
  • distilled water filtered secondarily by a filter of Millipore Co. was used as distilled water.
  • ultrasonic cleaning was repeated twice for 10 minutes with distilled water.
  • ultrasonic cleaning was performed with a solvent of isopropyl alcohol, acetone, and methanol, followed by drying and transporting to a plasma cleaner.
  • the substrate was transferred to a vacuum evaporator.
  • the following HAT compound was thermally vacuum-deposited to a thickness of 500 Pa on the prepared ITO transparent electrode to form a hole injection layer.
  • the following NPB compound was vacuum-deposited to a thickness of 300 MPa to form a hole transport layer.
  • the following HTL1 compound was vacuum-deposited to a thickness of 100 Pa on the hole transport layer to form an electron blocking layer.
  • a compound 1-1 and the following compound BD prepared above were vacuum-deposited to a thickness of 300 Pa in a weight ratio of 20: 1 to form a light emitting layer on the electron blocking layer.
  • An electron-regulating layer was formed by vacuum-depositing Compound 2-1 prepared above on the light emitting layer to a thickness of 100 MPa.
  • the following ETL compound and the following LiQ compound were vacuum-deposited to a thickness of 300 Pa in a weight ratio of 1: 1 to form an electron injection and transport layer.
  • lithium fluoride (LiF) with a thickness of 12 ⁇ and aluminum with a thickness of 2,000 ⁇ were sequentially deposited to form a negative electrode.
  • the deposition rate of the organic material was maintained at 0.4 to 0.7 ⁇ / sec
  • the lithium fluoride of the negative electrode was maintained at a deposition rate of 0.3 ⁇ / sec
  • the aluminum was maintained at a deposition rate of 2 ⁇ / sec
  • the vacuum degree during deposition was 2 ⁇ 10.
  • An organic light emitting device was manufactured by maintaining -7 to 5 x 10 -6 torr.
  • An organic light-emitting device was manufactured in the same manner as in Example 1, but using the compounds shown in Table 1 below instead of Compound 1-1 and Compound 2-1.
  • An organic light-emitting device was manufactured in the same manner as in Example 1, but using the compounds shown in Table 1 below instead of Compound 1-1 and Compound 2-1.
  • Table 1 the compounds of BH-1 to BH-8 and HB-1 to HB-9 are as follows.
  • the driving voltage, luminous efficiency, and color coordinates of the organic light-emitting device prepared in the above Examples and Comparative Examples were measured at a current density of 10 mA / cm 2 , and the results are shown in Table 1 below, and used for the host and the electron control layer. The dipole moment value of the compound was also shown.
  • the dipole moment of the host and the dipole moment of the compound used in the electron regulating layer according to the present invention have specific values, so that the balance of electrons and holes in the light emitting layer is well matched with the driving voltage. It was confirmed that the luminous efficiency was excellent.
  • the compound represented by Chemical Formula 1 of the present invention is advantageous for injection of holes and electrons, and exhibits low-low-pressure characteristics when used as a host.
  • the compound represented by Chemical Formulas 2 or 3 of the present invention not only delivers electrons to the light emitting layer well, but also has an excellent ability to block holes coming from the light emitting layer, and thus, when applied to the electron control layer, a high efficiency device can be obtained. .
  • substrate 2 anode

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Abstract

Le but de la présente invention est de fournir un dispositif électroluminescent organique, qui a une faible tension de commande, une efficacité lumineuse élevée et des caractéristiques de longue durée de vie.
PCT/KR2019/014621 2018-11-01 2019-10-31 Dispositif électroluminescent organique WO2020091468A1 (fr)

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CN113149943A (zh) * 2021-05-10 2021-07-23 吉林奥来德光电材料股份有限公司 荧光化合物及其制备方法和包含其的有机电致发光器件

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20170134264A (ko) * 2016-05-27 2017-12-06 주식회사 엘지화학 유기발광소자
KR20180057109A (ko) * 2016-11-21 2018-05-30 주식회사 두산 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자
KR20180103021A (ko) * 2017-03-08 2018-09-18 주식회사 엘지화학 유기 발광 소자
KR20180111558A (ko) * 2017-03-30 2018-10-11 주식회사 엘지화학 유기 발광 소자
KR20180115637A (ko) * 2017-04-13 2018-10-23 주식회사 엘지화학 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100430549B1 (ko) 1999-01-27 2004-05-10 주식회사 엘지화학 신규한 착물 및 그의 제조 방법과 이를 이용한 유기 발광 소자 및 그의 제조 방법

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20170134264A (ko) * 2016-05-27 2017-12-06 주식회사 엘지화학 유기발광소자
KR20180057109A (ko) * 2016-11-21 2018-05-30 주식회사 두산 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자
KR20180103021A (ko) * 2017-03-08 2018-09-18 주식회사 엘지화학 유기 발광 소자
KR20180111558A (ko) * 2017-03-30 2018-10-11 주식회사 엘지화학 유기 발광 소자
KR20180115637A (ko) * 2017-04-13 2018-10-23 주식회사 엘지화학 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113149943A (zh) * 2021-05-10 2021-07-23 吉林奥来德光电材料股份有限公司 荧光化合物及其制备方法和包含其的有机电致发光器件
CN113149943B (zh) * 2021-05-10 2023-08-22 吉林奥来德光电材料股份有限公司 荧光化合物及其制备方法和包含其的有机电致发光器件

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