WO2015170882A1 - Matériau hôte à constituants multiples et dispositif électroluminescent organique comprenant ledit matériau - Google Patents

Matériau hôte à constituants multiples et dispositif électroluminescent organique comprenant ledit matériau Download PDF

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WO2015170882A1
WO2015170882A1 PCT/KR2015/004534 KR2015004534W WO2015170882A1 WO 2015170882 A1 WO2015170882 A1 WO 2015170882A1 KR 2015004534 W KR2015004534 W KR 2015004534W WO 2015170882 A1 WO2015170882 A1 WO 2015170882A1
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group
substituted
unsubstituted
host
organic electroluminescent
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PCT/KR2015/004534
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English (en)
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Hee-Choon Ahn
Young-Kwang Kim
Doo-Hyeon Moon
Su-Hyun Lee
Chi-Sik Kim
Seon-Woo Lee
Ji-Song JUN
Kyoung-Jin Park
Nam-Kyun Kim
Young-Jun Cho
Kyung-Hoon Choi
Jae-Hoon Shim
Yoo-Jin DOH
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Rohm And Haas Electronic Materials Korea Ltd.
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Priority claimed from KR1020150063037A external-priority patent/KR102395933B1/ko
Application filed by Rohm And Haas Electronic Materials Korea Ltd. filed Critical Rohm And Haas Electronic Materials Korea Ltd.
Priority to US15/308,182 priority Critical patent/US20170062730A1/en
Priority to CN201580021213.5A priority patent/CN106232770A/zh
Priority to JP2016564953A priority patent/JP6700196B2/ja
Priority to EP15789715.8A priority patent/EP3140367B1/fr
Publication of WO2015170882A1 publication Critical patent/WO2015170882A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • 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
    • H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
    • 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
    • H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K2101/00—Properties of the organic materials covered by group H10K85/00
    • H10K2101/10—Triplet emission
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K2101/00—Properties of the organic materials covered by group H10K85/00
    • H10K2101/90—Multiple hosts in the emissive layer
    • 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
    • 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
    • H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
    • 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
    • H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene

Definitions

  • the present invention relates to a multi-component host material and an organic electroluminescent device comprising the same.
  • An electroluminescent (EL) device is a self-light-emitting device with the advantages of providing a wider viewing angle, a greater contrast ratio, and a faster response time.
  • the first organic EL device was developed by Eastman Kodak, by using small aromatic diamine molecules and aluminum complexes as materials for forming a light-emitting layer (see Appl. Phys. Lett. 51, 913, 1987).
  • An organic EL device changes electric energy into light by the application of electric voltage to an organic light-emitting material, and commonly comprises an anode, a cathode, and an organic layer formed between the two electrodes.
  • the organic layer of the organic EL device may be composed of a hole injection layer (HIL), a hole transport layer (HTL), an electron blocking layer (EBL), a light-emitting layer (EML) (containing host and dopant materials), an electron buffer layer, a hole blocking layer (HBL), an electron transport layer (ETL), an electron injection layer (EIL), etc.; the materials used in the organic layer can be classified into a hole injection material, a hole transport material, an electron blocking material, a light-emitting material, an electron buffer material, a hole blocking material, an electron transport material, an electron injection material, etc., depending on functions.
  • the organic EL device In the organic EL device, holes from an anode and electrons from a cathode are injected into a light-emitting layer by electric voltage, and an exciton having high energy is produced by the recombination of holes and electrons.
  • the organic light-emitting compound moves into an excited state by the energy and emits light from energy when the organic light-emitting compound returns to the ground state from the excited state.
  • the most important factor determining luminous efficiency in an organic EL device is light-emitting materials.
  • the light-emitting materials are required to have the following features: high quantum efficiency, high movement degree of an electron and a hole, and formability of a uniform and stable layer.
  • the light-emitting materials are classified into blue light-emitting materials, green light-emitting materials, and red light-emitting materials according to the light-emitting color, and further include yellow light-emitting materials or orange light-emitting materials.
  • the light-emitting material is classified into a host material and a dopant material in a functional aspect. Recently, an urgent task is the development of an organic EL device having high efficiency and long operating lifespan.
  • a host material should have high purity and a suitable molecular weight in order to be deposited under vacuum. Furthermore, a host material is required to have high glass transition temperature and pyrolysis temperature for guaranteeing thermal stability, high electrochemical stability for long lifespan, easy formability of an amorphous thin film, good adhesion with adjacent layers, and no movement between layers.
  • a mixed system of a dopant/host material can be used as a light-emitting material to improve color purity, luminous efficiency, and stability.
  • the device having the most excellent EL properties comprises the light-emitting layer, wherein a dopant is doped onto a host. If the dopant/host material system is used, the selection of the host material is important because the host material greatly influences efficiency and performance of a light-emitting device.
  • WO 2013/112557 A1 discloses organic EL devices comprising a dopant and multi-component host.
  • the above literature uses a host having a carbazole-carbazole skeleton as a first host and a benzothiophene, benzofuran, dibenzothiophene, or dibenzofuran-based compound as a second host.
  • an organic EL device which uses a multi-component host as a host, which has a bicarbazole derivative containing pyridine and a carbazole derivative including a nitrogen-containing heteroaryl group, has high efficiency and long lifespan.
  • the object of the present invention is to provide an organic EL device having high efficiency and long lifespan.
  • an organic EL device comprising at least one light-emitting layer between an anode and a cathode, wherein the light-emitting layer comprises a host and a phosphorescent dopant; the host consists of multi-component host compounds; at least a first host compound of the multi-component host compounds is represented by the following formula 1 which is a bicarbazole derivative containing pyridine, and a second host compound is represented by the following formula 2 which is a carbazole derivative including a nitrogen-containing heteroaryl group:
  • Ar 1 represents a substituted or unsubstituted (C6-C30)aryl group
  • L 1 and L 2 each independently represent a single bond, or a substituted or unsubstituted (C6-C30)arylene group, wherein the substituent(s) of the substituted arylene group is independently selected from the group consisting of hydrogen, deuterium, a halogen, a cyano group, a substituted or unsubstituted (C1-C30)alkyl group, a substituted or unsubstituted (C2-C30)alkenyl group, a substituted or unsubstituted (C2-C30)alkynyl group, a substituted or unsubstituted (C3-C30)cycloalkyl group, a substituted or unsubstituted (C6-C60)aryl group, a substituted or unsubstituted 3- to 30-membered heteroaryl group, a substituted or unsubstituted tri(C1-C30)alkylsilyl group, a substituted or unsubsti
  • R 1 to R 16 , R 21 , and R 25 to R 32 each independently represent hydrogen, deuterium, a halogen, a cyano group, a substituted or unsubstituted (C1-C30)alkyl group, a substituted or unsubstituted (C2-C30)alkenyl group, a substituted or unsubstituted (C2-C30)alkynyl group, a substituted or unsubstituted (C3-C30)cycloalkyl group, a substituted or unsubstituted (C6-C60)aryl group, a substituted or unsubstituted 3- to 30-membered heteroaryl group, a substituted or unsubstituted tri(C1-C30)alkylsilyl group, a substituted or unsubstituted tri(C6-C30)arylsilyl group, a substituted or unsubstituted di(C1-C30)alkyl(
  • one of R 5 to R 8 is linked to one of R 9 to R 12 via a single bond
  • Ar 2 represents a substituted or unsubstituted nitrogen-containing 5- to 30-membered heteroaryl group
  • n 0, 1, 2, 3 or 4;
  • the heteroaryl group contains at least one hetero atom selected from B, N, O, S, Si, and P;
  • the heteroaryl group is a monocyclic-based heteroaryl group, such as pyrrolyl, imidazolyl, pyrazolyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, etc., or a fused ring-based heteroaryl group, such as benzoimidazolyl, isoindolyl, indolyl, indazolyl, benzothiadiazolyl, quinolyl, isoquinolyl, cinnolinyl, quinazolinyl, quinoxalinyl, carbazolyl, naphthyridinyl, phenanthridinyl, etc., which may be substituted with a (C6-C20)aryl group, a tri(C6-C12)arylsilyl group, a S- or O-containing
  • an organic EL device having high efficiency and long lifespan is provided and the production of a display device or a lighting device is possible by using the organic EL device.
  • the compound of formula 1 may be represented by the following formula 3, 4, 5, or 6:
  • Ar 1 , L 1 , R 1 to R 16 , R 21 , and m are as defined in claim 1.
  • Ar 1 may represent a substituted or unsubstituted (C6-C30)aryl group; preferably, a substituted or unsubstituted (C6-C18)aryl group.
  • L 1 and L 2 each independently may represent a single bond, or a substituted or unsubstituted (C6-C30)arylene group; and preferably, a single bond, or a substituted or unsubstituted (C6-C18)arylene group.
  • Ar 2 may represent a substituted or unsubstituted nitrogen-containing 5- to 30-membered heteroaryl group; preferably, a monocyclic-based heteroaryl group, such as pyrrolyl, imidazolyl, pyrazolyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, etc., or a fused ring-based heteroaryl group, such as benzoimidazolyl, isoindolyl, indolyl, indazolyl, benzothiadiazolyl, quinolyl, isoquinolyl, cinnolinyl, quinazolinyl, quinoxalinyl, carbazolyl, naphthyridinyl, phenanthridinyl, etc.; and more preferably, triazinyl, pyrimidiny
  • R 25 to R 32 each independently may represent hydrogen, deuterium, a halogen, a cyano group, a substituted or unsubstituted (C1-C30)alkyl group, a substituted or unsubstituted (C2-C30)alkenyl group, a substituted or unsubstituted (C2-C30)alkynyl group, a substituted or unsubstituted (C3-C30)cycloalkyl group, a substituted or unsubstituted (C6-C60)aryl group, a substituted or unsubstituted 3- to 30-membered heteroaryl group, a substituted or unsubstituted tri(C1-C30)alkylsilyl group, a substituted or unsubstituted tri(C6-C30)arylsilyl group, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl
  • (C1-C30)alkyl(ene) is meant to be a linear or branched alkyl(ene) having 1 to 30 carbon atoms, in which the number of carbon atoms is preferably 1 to 20, more preferably 1 to 10, and includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, etc.
  • (C2-C30)alkenyl is meant to be a linear or branched alkenyl having 2 to 30 carbon atoms, in which the number of carbon atoms is preferably 2 to 20, more preferably 2 to 10, and includes vinyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylbut-2-enyl, etc.
  • (C2-C30)alkynyl is a linear or branched alkynyl having 2 to 30 carbon atoms, in which the number of carbon atoms is preferably 2 to 20, more preferably 2 to 10, and includes ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methylpent-2-ynyl, etc.
  • (C3-C30)cycloalkyl is a mono- or polycyclic hydrocarbon having 3 to 30 carbon atoms, in which the number of carbon atoms is preferably 3 to 20, more preferably 3 to 7, and includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.
  • “3- to 7-membered heterocycloalkyl” is a cycloalkyl having at least one heteroatom selected from the group consisting of B, N, O, S, Si, and P, preferably O, S, and N, and 3 to 7, preferably 5 to 7 ring backbone atoms, and includes tetrahydrofuran, pyrrolidine, thiolan, tetrahydropyran, etc.
  • (C6-C30)aryl(ene) is a monocyclic or fused ring derived from an aromatic hydrocarbon having 6 to 30 carbon atoms, in which the number of carbon atoms is preferably 6 to 20, more preferably 6 to 15, and includes phenyl, biphenyl, terphenyl, naphthyl, fluorenyl, phenanthrenyl, anthracenyl, indenyl, triphenylenyl, pyrenyl, tetracenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, etc.
  • “3- to 30-membered heteroaryl(ene)” is an aryl group having at least one, preferably 1 to 4 heteroatom selected from the group consisting of B, N, O, S, Si, and P, and 3 to 30 ring backbone atoms; is a monocyclic ring, or a fused ring condensed with at least one benzene ring; has preferably 3 to 20, more preferably 3 to 15 ring backbone atoms; may be partially saturated; may be one formed by linking at least one heteroaryl or aryl group to a heteroaryl group via a single bond(s); and includes a monocyclic ring-type heteroaryl, such as furyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl, tetrazinyl,
  • “Nitrogen-containing 5- to 30-membered heteroaryl(ene) group” is an aryl group having at least one heteroatom N and 5 to 30 ring backbone atoms. 5 to 20 ring backbone atoms and 1 to 4 heteroatom are preferable, and 5 to 15 ring backbone atoms are more preferable.
  • substituted in the expression “substituted or unsubstituted” means that a hydrogen atom in a certain functional group is replaced with another atom or group, i.e., a substituent.
  • Substituents of the substituted alkyl(ene) group, the substituted alkenyl group, the substituted alkynyl group, the substituted cycloalkyl group, the substituted aryl(ene) group, the substituted heteroaryl(ene) group, the substituted trialkylsilyl group, the substituted triarylsilyl group, the substituted dialkylarylsilyl group, the substituted mono- or di-arylamino group, or the substituted mono- or polycyclic, (C3-C30) alicyclic or aromatic ring in the above formulae are each independently at least one selected from the group consisting of deuterium; a halogen; a cyano group; a carboxyl group; a nitro group;
  • the compound of formula 1 as a first host compound may be selected from the group consisting of the following compounds, but is not limited thereto:
  • the compound of formula 2 as a second host compound may be selected from the group consisting of the following compounds, but is not limited thereto:
  • the organic EL device may comprise an anode, a cathode, and at least one organic layer between the two electrodes, wherein the organic layer comprises a light-emitting layer, the light-emitting layer comprises a host and a phosphorescent dopant; the host consists of multi-component host compounds; at least a first host compound of the multi-component host compounds is represented by formula 1 which is a bicarbazole derivative containing pyridine, and a second host compound is represented by formula 2 which is a carbazole derivative including a nitrogen-containing heteroaryl group.
  • the light-emitting layer means a layer that light is emitted therefrom and may be a single layer or multi-layers consisting of two or more layers.
  • the doping concentration of dopant compounds to host compounds in the light-emitting layer is preferably less than 20 wt%.
  • the dopants included in the organic EL device of the present invention are preferably one or more phosphorescent dopants.
  • the phosphorescent dopant material applied to the organic EL device of the present invention is not specifically limited, but preferably may be selected from complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), more preferably ortho metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), and even more preferably ortho metallated iridium complex compounds.
  • the dopants included in the organic EL device of the present invention may be selected from the group consisting of the compounds represented by the following formulae 7 to 9:
  • L is selected from the following structures:
  • R 100 represents hydrogen, deuterium, a substituted or unsubstituted (C1-C30)alkyl group, or a substituted or unsubstituted (C3-C30)cycloalkyl group;
  • R 101 to R 109 and R 111 to R 123 each independently represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl group unsubstituted or substituted with a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl group, a cyano group, a substituted or unsubstituted (C1-C30)alkoxy group, or a substituted or unsubstituted (C6-C30)aryl group;
  • R 120 to R 123 may be linked to an adjacent substituent(s) to form a substituted or unsubstituted fused ring, for example, quinoline;
  • R 124 to R 127 each independently represent hydrogen, deuterium, a halogen, a substituted or unsubstituted (C1-C30)alkyl group, or a substituted or unsubstituted (C6-C30)aryl group; when R 124 to R 127 are aryl groups, they may be linked to an adjacent substituent(s) to form a substituted or unsubstituted mono- or polycyclic, (C3-C30) alicyclic, aromatic, or a heteroaromatic ring, for example, fluorene, dibenzothiophene, or dibenzofuran;
  • R 201 to R 211 each independently represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl group unsubstituted or substituted with a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl group, or a substituted or unsubstituted (C6-C30)aryl group;
  • R 208 to R 211 may be linked to an adjacent substituent(s) to form a substituted or unsubstituted mono- or polycyclic, (C3-C30) alicyclic, aromatic, or a heteroaromatic ring, for example, fluorene, dibenzothiophene, or dibenzofuran;
  • f and g each independently represent an integer of 1 to 3; where f or g is an integer of 2 or more, each of R 100 may be the same or different; and
  • n an integer of 1 to 3.
  • the dopant material includes the following:
  • the organic EL device of the present invention may further include at least one compound selected from the group consisting of arylamine-based compounds and styrylarylamine-based compounds in the organic layer.
  • the organic layer may further comprise at least one metal selected from the group consisting of metals of Group 1, metals of Group 2, transition metals of the 4 th period, transition metals of the 5 th period, lanthanides, and organic metals of d-transition elements of the Periodic Table, or at least one complex compound comprising the metal.
  • a surface layer selected from a chalcogenide layer, a metal halide layer and a metal oxide layer may be placed on an inner surface(s) of one or both electrode(s).
  • a chalcogenide (including oxides) layer of silicon or aluminum is placed on an anode surface of a light-emitting medium layer, and a metal halide layer or metal oxide layer is placed on a cathode surface of an electroluminescent medium layer.
  • the surface layer provides operating stability for the organic EL device.
  • the chalcogenide includes SiO X (1 ⁇ X ⁇ 2), AlO X (1 ⁇ X ⁇ 1.5), SiON, SiAlON, etc.;
  • the metal halide includes LiF, MgF 2 , CaF 2 , a rare earth metal fluoride, etc.; and the metal oxide includes Cs 2 O, Li 2 O, MgO, SrO, BaO, CaO, etc.
  • a hole injection layer, a hole transport layer, an electron injection layer, or their combinations can be used between an anode and a light-emitting layer.
  • the hole injection layer may be multi-layers in order to lower a hole injection barrier (or hole injection voltage) from an anode to a hole transport layer or electron blocking layer, wherein each of the multi-layers simultaneously may use two compounds.
  • the hole transport layer or the electron blocking layer may also be multi-layers.
  • An electron buffer layer, a hole blocking layer, an electron transport layer, an electron injection layer, or their combinations can be used between a light-emitting layer and a cathode.
  • the electron buffer layer may be multi-layers in order to control the injection of an electron and improve interface properties between the light-emitting layer and the electron injection layer, wherein each of the multi-layers simultaneously may use two compounds.
  • the hole blocking layer or the electron transport layer may also be multi-layers, wherein each of the multi-layers may use a multi-component of compounds.
  • a mixed region of an electron transport compound and a reductive dopant, or a mixed region of a hole transport compound and an oxidative dopant may be placed on at least one surface of a pair of electrodes.
  • the electron transport compound is reduced to an anion, and thus it becomes easier to inject and transport electrons from the mixed region to a light-emitting medium.
  • the hole transport compound is oxidized to a cation, and thus it becomes easier to inject and transport holes from the mixed region to a light-emitting medium.
  • the oxidative dopant includes various Lewis acids and acceptor compounds; and the reductive dopant includes alkali metals, alkali metal compounds, alkaline earth metals, rare-earth metals, and mixtures thereof.
  • a reductive dopant layer may be employed as a charge-generating layer to prepare an organic EL device having two or more light-emitting layers and emitting white light.
  • each layer constituting the organic EL device of the present invention dry film-forming methods, such as vacuum deposition, sputtering, plasma, ion plating methods, etc., or wet film-forming methods, such as ink jet printing, nozzle printing, slot printing, spin coating, dip coating, flow coating methods, etc., can be used.
  • dry film-forming methods such as vacuum deposition, sputtering, plasma, ion plating methods, etc.
  • wet film-forming methods such as ink jet printing, nozzle printing, slot printing, spin coating, dip coating, flow coating methods, etc.
  • co-deposition or mixed-deposition may be used.
  • a thin film is formed by dissolving or dispersing the material constituting each layer in suitable solvents, such as toluene, xylene, anisole, chlorobenzene, ethanol, chloroform, tetrahydrofuran, dioxane, etc.
  • suitable solvents such as toluene, xylene, anisole, chlorobenzene, ethanol, chloroform, tetrahydrofuran, dioxane, etc.
  • suitable solvents such as toluene, xylene, anisole, chlorobenzene, ethanol, chloroform, tetrahydrofuran, dioxane, etc.
  • a display device or a light device can be produced by using the organic EL device of the present invention.
  • the organic EL devices having high efficiency and long lifespan are provided.
  • the host materials comprising at least two kinds of the derivatives may be deposited by at least two methods including the following methods:
  • Co-deposition At least two different materials are added into separate crucibles and electric current is simultaneously applied to the two or more cells to evaporate the materials.
  • Device Examples 1-1 to 1-12 Production of an OLED device by co-deposition of the first host compound and the second host compound according to the present invention as a host
  • OLED devices comprising the luminous material of the present invention were produced as follows: A transparent electrode indium tin oxide (ITO) thin film (10 ⁇ /sq) on a glass substrate for an OLED device (Samsung Corning, Republic of Korea) was subjected to an ultrasonic washing with trichloroethylene, acetone, ethanol, and distilled water, sequentially, and was then stored in isopropanol. Next, the ITO substrate was mounted on a substrate holder of a vacuum vapor depositing apparatus. HI-1 was introduced into a cell of the vacuum vapor depositing apparatus, and the pressure in the chamber of the apparatus was then controlled to 10 -6 torr.
  • ITO indium tin oxide
  • HIL hole injection layer
  • HIL-2 was then introduced into another cell of the vacuum vapor depositing apparatus, and an electric current was applied to the cell to evaporate the introduced material, thereby forming a second hole injection layer (HIL) HI-2 having a thickness of 3 to 5 nm on the first hole injection layer (HIL) HI-1.
  • HIL-1 was introduced into another cell of the vacuum vapor depositing apparatus.
  • HTL hole transport layer
  • EML light-emitting layer
  • the two host materials were evaporated at the same rates of 1:1, and the dopant material was evaporated at a different rate and deposited in a doping amount of 15 wt%, based on the total weight of the host and dopant, to form a light-emitting layer having a thickness of 40 nm on the hole transport layer HT-1.
  • ET-1 or ET-2 and EI-1 were evaporated at the rates of 5:5 to 4:6 on another two cells to form an electron transport layer (ETL) having a thickness of 30 to 35 nm on the light-emitting layer.
  • ETL electron transport layer
  • an Al cathode was then deposited by another vacuum vapor deposition apparatus on the electron injection layer.
  • EIL electron injection layer
  • Comparative Examples 1-1 to 1-4 Production of an OLED device by using only the first host compound according to the present invention as a host
  • OLED devices were produced in the same manner as in Device Examples 1-1 to 1-12, except that only the first host compounds of Comparative Examples 1-1 to 1-4 disclosed in Table 1 below were used as a host in a light-emitting layer.
  • Comparative Examples 2-1 to 2-7 Production of an OLED device by using only the second host compound according to the present invention as a host
  • OLED devices were produced in the same manner as in Device Examples 1-1 to 1-12, except that only the second host compounds of Comparative Examples 2-1 to 2-7 disclosed in Table 1 below were used as a host in a light-emitting layer.
  • the driving voltage at a luminance of 1,000 nit, luminous efficiency, CIE color coordinate, and the lifespan taken to be reduced from 100% to 90% of a luminance of 15,000 nit at the constant current of the OLED devices produced in Device Examples 1-1 to 1-12, Comparative Examples 1-1 to 1-4, and Comparative Examples 2-1 to 2-7 are as provided in Table 2 below.
  • X * means “unmeasurable.” (It was not possible to measure the lifespan at a luminance of 15,000 nit of the device of Comparative Example 1-3 of Table 2 above since the device of Comparative Example 1-3 has very low efficiency.)

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  • Electroluminescent Light Sources (AREA)

Abstract

La présente invention concerne un dispositif électroluminescent organique comprenant au moins une couche électroluminescente entre une anode et une cathode, la couche électroluminescente comprenant un hôte et un dopant phosphorescent ; l'hôte est constitué de composés hôtes à constituants multiples ; au moins un premier composé hôte des composés hôtes à constituants multiples est un dérivé de bicarbazole contenant de la pyridine et un deuxième composé hôte est un dérivé de carbazole comprenant un groupe hétéroaryle contenant de l'azote. Selon la présente invention, un dispositif électroluminescent organique utilisant les composés hôtes à constituants multiples présente une efficacité élevée et une longue durée de vie par rapport à un dispositif classique utilisant un constituant d'un hôte.
PCT/KR2015/004534 2014-05-07 2015-05-07 Matériau hôte à constituants multiples et dispositif électroluminescent organique comprenant ledit matériau WO2015170882A1 (fr)

Priority Applications (4)

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US15/308,182 US20170062730A1 (en) 2014-05-07 2015-05-07 Multi-component host material and organic electroluminescent device comprising the same
CN201580021213.5A CN106232770A (zh) 2014-05-07 2015-05-07 多组分主体材料以及包含其的有机电致发光装置
JP2016564953A JP6700196B2 (ja) 2014-05-07 2015-05-07 多成分ホスト材料及びそれを含む有機電界発光デバイス
EP15789715.8A EP3140367B1 (fr) 2014-05-07 2015-05-07 Matériau hôte à constituants multiples et dispositif électroluminescent organique comprenant ledit matériau

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KR10-2014-0053997 2014-05-07
KR20140053997 2014-05-07
KR10-2015-0063037 2015-05-06
KR1020150063037A KR102395933B1 (ko) 2014-05-07 2015-05-06 복수종의 호스트 재료와 이를 포함하는 유기 전계 발광 소자

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CN106986835A (zh) * 2016-01-21 2017-07-28 德山新勒克斯有限公司 有机电气元件用化合物、利用其的有机电气元件及其电子装置
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CN106986835B (zh) * 2016-01-21 2021-02-02 德山新勒克斯有限公司 有机电气元件用化合物、利用其的有机电气元件及其电子装置
CN107033128A (zh) * 2016-02-03 2017-08-11 Sfc有限责任公司 有机发光化合物和包括其的有机发光装置
US11476426B2 (en) 2016-02-03 2022-10-18 Sfc Co., Ltd. Organic light emitting compounds and organic light emitting devices including the same
JP2019519096A (ja) * 2016-05-17 2019-07-04 ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド 有機電界発光化合物、有機電界発光材料、及びそれを含む有機電界発光デバイス
US10840458B2 (en) 2016-05-25 2020-11-17 Universal Display Corporation Organic electroluminescent materials and devices
DE102016115853A1 (de) * 2016-08-25 2018-03-01 Cynora Gmbh Organische Moleküle, insbesondere zur Verwendung in organischen optoelektronischen Vorrichtungen
DE102016115853B4 (de) * 2016-08-25 2020-10-15 Cynora Gmbh Organische Moleküle, insbesondere zur Verwendung in organischen optoelektronischen Vorrichtungen
TWI647225B (zh) * 2016-11-16 2019-01-11 南韓商Ｌｇ化學股份有限公司 有機發光裝置
US11800730B2 (en) 2016-11-16 2023-10-24 Lg Chem, Ltd. Organic light emitting device
US10454056B1 (en) 2017-03-30 2019-10-22 Lg Chem, Ltd. Organic light emitting device
JP2018188421A (ja) * 2017-05-01 2018-11-29 ユニバーサル ディスプレイ コーポレイション 有機エレクトロルミネセンス材料及びデバイス
JP7174533B2 (ja) 2017-05-01 2022-11-17 ユニバーサル ディスプレイ コーポレイション 有機エレクトロルミネセンス材料及びデバイス
US11702420B2 (en) 2017-05-01 2023-07-18 Universal Display Corporation Organic electroluminescent materials and devices
JP7498241B2 (ja) 2017-05-01 2024-06-11 ユニバーサル ディスプレイ コーポレイション 有機エレクトロルミネセンス材料及びデバイス
EP3438104A1 (fr) * 2017-08-01 2019-02-06 Samsung Display Co., Ltd. Composé hétérocyclique et dispositif électroluminescent organique le comprenant
US11393991B2 (en) 2017-08-01 2022-07-19 Samsung Display Co., Ltd. Heterocyclic compound and organic electroluminescence device including the same

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