KR102118629B1 - Organic light emitting device - Google Patents

Abstract

The present invention provides an organic light emitting device.

Description

Organic light emitting device {ORGANIC LIGHT EMITTING DEVICE}

The present invention relates to an organic light emitting device.

In general, 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. In order to increase the efficiency and stability of the organic light emitting device, the organic material layer is often formed of a multi-layered structure composed of different materials, and may be formed of, for example, a hole injection layer, a hole transport layer, a light emitting layer, an electron transport layer, or an electron injection layer. When a voltage is applied between two electrodes in the structure of the organic light emitting device, holes are injected at the anode and electrons are injected at the cathode, and excitons are formed when the injected holes meet the electrons. When it falls to the ground again, it glows.

The development of new materials for organic materials used in the organic light emitting device as described above is continuously required.

Korean Patent Publication No. 10-2000-0051826

The present invention provides an organic light emitting device.

The present invention is an anode; A cathode provided opposite the anode; And one or more organic material layers provided between the anode and the cathode, wherein the organic material layer includes a light emitting layer, and the light emitting layer includes a compound represented by Formula 1 below, and between the anode and the light emitting layer. It provides an organic light-emitting device comprising a compound represented by the formula (2).

[Formula 1]

In Chemical Formula 1,

L ¹ is a single bond, or a substituted or unsubstituted C _6-60 arylene,

L ² is a single bond, substituted or unsubstituted C _6-60 arylene, or substituted or unsubstituted C _2-60 heteroarylene comprising one or more of O, N, Si and S,

Y ¹ to Y ³ are each independently N or CR ¹ , at least one of which is N, R ¹ is hydrogen or substituted or unsubstituted C _1-40 alkyl,

Ar ¹ and Ar ² are each independently substituted or unsubstituted C _6-60 aryl, or substituted or unsubstituted C _2-60 heteroaryl including one or more of O, N, Si and S,

Ar ³ is substituted or unsubstituted C _6-60 aryl,

m is an integer from 1 to 2,

[Formula 2]

In Chemical Formula 2,

Ar ⁴ and Ar ⁵ are each independently substituted or unsubstituted C _6-60 aryl,

R ¹ and R ² are each independently substituted or unsubstituted C _6-20 aryl,

n1 and n2 are each independently 0 or 1.

The present invention uses the compound represented by the formula (1) as the host material of the light emitting layer, and the compound represented by the formula (2) as the material of the organic layer between the anode and the light emitting layer, low voltage driving is possible, high efficiency and It is possible to provide an organic light emitting device exhibiting long life characteristics.

1 is composed of a substrate 1, an anode 2, a hole injection layer 3, a hole transport layer 5, an electron blocking layer 6, a light emitting layer 7, an electron transport layer 8 and a cathode 4 An example of an organic light emitting device is shown.

Hereinafter, it will be described in more detail in order to help the understanding of the present invention.

The present invention provides an organic light emitting device in which the light emitting layer includes the compound represented by Chemical Formula 1 and the compound represented by the Chemical Formula 2 between the anode and the light emitting layer.

는 다른 화합물에 연결되는 결합을 의미하고, 단일 결합은 L¹ 또는 L²로 표시되는 부분에 별도의 원자가 존재하지 않은 경우를 의미한다. 예컨대, 화학식 1의 L¹이 단일 결합이고, Y¹ 내지 Y³가 N이면, Ar¹ 및 Ar²로 치환된 트리아진 치환기가 디벤조퓨란에 직접 연결될 수 있다. In this specification,

Means a bond connected to another compound, and a single bond means a case where a separate atom does not exist in a portion represented by L ¹ or L ² . For example, L ¹ is a single bond in the formula (I), when Y ¹ to Y ³ is N, may be a triazine substituted with a substituent Ar ¹ and Ar ² be directly connected to the dibenzofuran.

In this specification the term "substituted or unsubstituted" may be substituted or means a unsubstituted by R ^a, R ^a is heavy hydrogen, a halogen, a cyano group, a nitro group, an amino group, an alkyl group having 1 to 40 carbon atoms, 1 to 40 haloalkyl groups, substituted or unsubstituted O, N, Si and one or more of C 1 to 40 carbon atoms containing one or more of substituted, unsubstituted O, N, Si and S It may be a C 1 to C 40 hetero haloalkyl group, or a C 2 to C 40 alkenyl group.

Halogen herein may be fluorine, chlorine, bromine or iodine.

In the present specification, the alkyl group having 1 to 40 carbon atoms may be a straight chain, branched chain, or cyclic alkyl group. Specifically, the alkyl group having 1 to 40 carbon atoms is a straight chain alkyl group having 1 to 40 carbon atoms; A straight chain alkyl group having 1 to 20 carbon atoms; A straight-chain alkyl group having 1 to 10 carbon atoms; A branched or cyclic alkyl group having 3 to 40 carbon atoms; A branched or cyclic alkyl group having 3 to 20 carbon atoms; Or it may be a branched or cyclic alkyl group having 3 to 10 carbon atoms. More specifically, the alkyl group having 1 to 40 carbon atoms is a methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, iso-butyl group, t-butyl group, n-pentyl group, iso-pentyl group, neo-pentyl group or cyclohexyl group. However, it is not limited thereto.

In the present specification, a heteroalkyl group having 1 to 40 carbon atoms may be one or more carbons, each independently substituted with O, N, Si or S. For example, as an example of a straight-chain alkyl group, a heteroalkyl group in which 1 carbon of n-butyl group is substituted with O is an n-propoxy group, a heteroalkyl group substituted with N is an n-propylamino group, and a heteroalkyl group substituted with Si is n -It is a propyl silyl group, and the heteroalkyl group substituted by S is an n-propyl thio group. And, as an example of a branched chain alkyl group, the heteroalkyl group in which the 1st carbon of the neo-pentyl group is substituted with O is a t-butoxy group, the heteroalkyl group substituted with N is a t-butylamino group, and the heteroalkyl group substituted with Si is t -Butylsilyl group, and the heteroalkyl group substituted with S is a t-butylthio group. In addition, as an example of the cyclic alkyl group, the heteroalkyl group in which the second carbon of the cyclohexyl group is substituted with O is a 2-tetrahydropyranyl group, and the heteroalkyl group substituted with N is a 2-piperidinyl group, The heteroalkyl group substituted with Si is a 1-sila-cyclohexyl group, and the heteroalkyl group substituted with S is a 2-tetrahydrothiopyranyl group. Specifically, a heteroalkyl group having 1 to 40 carbon atoms is a straight chain, branched chain or cyclic hydroxyalkyl group having 1 to 40 carbon atoms; A straight chain, branched chain or cyclic alkoxy group having 1 to 40 carbon atoms; A straight chain, branched chain or cyclic alkoxyalkyl group having 2 to 40 carbon atoms; A straight chain, branched chain or cyclic aminoalkyl group having 1 to 40 carbon atoms; A straight chain, branched chain or cyclic alkylamino group having 1 to 40 carbon atoms; A linear, branched or cyclic alkylaminoalkyl group having 1 to 40 carbon atoms; A linear, branched or cyclic silylalkyl (oxy) group having 1 to 40 carbon atoms; A straight chain, branched chain or cyclic alkyl (oxy) silyl group having 1 to 40 carbon atoms; A linear, branched or cyclic alkyl (oxy) silylalkyl (oxy) group having 1 to 40 carbon atoms; A straight chain, branched chain or cyclic mercaptoalkyl group having 1 to 40 carbon atoms; A straight chain, branched chain or cyclic alkylthio group having 1 to 40 carbon atoms; Or it may be a straight chain, branched chain, or cyclic alkylthioalkyl group having 2 to 40 carbon atoms. More specifically, the heteroalkyl group having 1 to 40 carbon atoms is hydroxymethyl group, methoxy group, ethoxy group, n-propoxy group, iso-propoxy group, t-butoxy group, cyclohexoxy group, methoxymethyl group, iso-pro Foxymethyl group, cyclohexoxymethyl group, 2-tetrahydropyranyl group, aminomethyl group, methylamino group, n-propylamino group, t-butylamino group, methylaminopropyl group, 2-piperidinyl group, n- Propylsilyl group, trimethylsilyl group, dimethylmethoxysilyl group, t-butylsilyl group, 1-sila-cyclohexyl group, n-propylthio group, t-butylthio group or 2-tetra And hydrothiopyranyl (2-tetrahydrothiopyranyl) groups. However, it is not limited thereto.

In the present specification, an alkenyl group having 2 to 40 carbon atoms may be a straight chain, branched chain, or cyclic alkenyl group. Specifically, an alkenyl group having 2 to 40 carbon atoms is a straight chain alkenyl group having 2 to 40 carbon atoms; A straight-chain alkenyl group having 2 to 20 carbon atoms; A straight-chain alkenyl group having 2 to 10 carbon atoms; A branched alkenyl group having 3 to 40 carbon atoms; A branched alkenyl group having 3 to 20 carbon atoms; A branched alkenyl group having 3 to 10 carbon atoms; A cyclic alkenyl group having 5 to 40 carbon atoms; A cyclic alkenyl group having 5 to 20 carbon atoms; Or it may be a cyclic alkenyl group having 5 to 10 carbon atoms. More specifically, an alkenyl group having 2 to 40 carbon atoms may be an ethenyl group, a propenyl group, a butenyl group, a pentenyl group, or a cyclohexenyl group. However, it is not limited thereto.

In the present specification, the aryl group having 6 to 60 carbon atoms may be a monocyclic aryl group or a polycyclic aryl group. Specifically, an aryl group having 6 to 60 carbon atoms has a monocyclic or polycyclic aryl group having 6 to 30 carbon atoms; Or it may be a monocyclic or polycyclic aryl group having 6 to 20 carbon atoms. More specifically, an aryl group having 6 to 60 carbon atoms may be a phenyl group, a biphenyl group, or a terphenyl group as a monocyclic aryl group, and may be a naphthyl group, anthracenyl group, tetrasenyl group, phenanthryl group, triphenyle as a polycyclic aryl group It may be a nil group, a fluoranthenyl group, a pyrenyl group, a perylenyl group, a chrysenyl group or a fluorenyl group.

In addition, aryl groups having 6 to 60 carbon atoms may have a structure in which two or more selected from the group consisting of monocyclic aryl groups and polycyclic aryl groups are connected to each other. Specifically, an aryl group having 6 to 60 carbon atoms may have a structure in which a polycyclic aryl group and/or a monocyclic aryl group are connected to a polycyclic aryl group. More specifically, an aryl group having 6 to 60 carbon atoms is a naphthylphenyl group, anthracenylphenyl group, phenanthrylphenyl group, triphenylenylphenyl group, pyrenylphenyl group, perylenylphenyl group, chrysenylphenyl group, fluorenylphenyl group, phenylnaphthyl group, It may be a phenyl anthracenyl group, a phenyl terphenyl group, or a phenyl naphthylphenyl group. However, it is not limited thereto.

등이 될 수 있다. 다만, 이에 한정되는 것은 아니다.In the present specification, the fluorenyl group may be substituted, and two substituents may combine with each other to form a spiro structure. When the fluorenyl group is substituted,

It can be back. However, it is not limited thereto.

In the present specification, a heteroaryl group having 2 to 60 carbon atoms may be one or more carbons of the aryl group, each independently substituted with O, N, Si or S. For example, the heteroaryl group in which carbon 9 of the fluorenyl group is substituted with O is a dibenzofuranyl group, the heteroaryl group substituted with N is a carbazoli group, and the heteroaryl group substituted with Si is a 9-sila-floorenyl group , S-substituted heteroaryl group is a dibenzothiophenyl group. Specifically, a heteroaryl group having 2 to 60 carbon atoms is a heteroaryl group having 2 to 30 carbon atoms; Or it may be a heteroaryl group having 2 to 20 carbon atoms. More specifically, a heteroaryl group having 2 to 60 carbon atoms is a thiophene group, a furan group, a pyrrol group, an imidazole group, a thiazole group, an oxazole group, an oxadiazole group, a triazole group, a pyridyl group, a bipyridyl group, a pyrimidyl group, Triazine group, triazole group, acridil group, pyridazine group, pyrazinyl group, quinolinyl group, quinazolinyl group, quinoxalinyl group, phthalazinyl group, pyrido pyrimidinyl group, pyrido pyrazinyl group, pyrazino pyra Genyl group, isoquinoline group, indole group, carbazole group, benzoxazole group, benzoimidazole group, benzothiazole group, benzocarbazole group, benzothiophene group, dibenzothiophene group, benzofuranyl group, phenanthroline group (phenanthroline ), a thiazolyl group, an isooxazolyl group, an oxadiazolyl group, a thiadiazolyl group, a benzothiazolyl group, a phenothiazinyl group, and a dibenzofuranyl group, but is not limited thereto.

In the present specification, the arylene group means a divalent organic group from which any one hydrogen radical of the above-described aryl group is removed, and the heteroarylene group means a divalent organic group from which any one hydrogen radical of the above-described heteroaryl group is removed. .

In Chemical Formula 1, L ¹ may be a single bond or phenylene, and more specifically, a single bond.

In Chemical Formula 1, Y ¹ to Y ³ are each independently N or CH, but at least one may be N.

In Formula 1, Ar ¹ and Ar ² are each independently benzene, biphenyl, terphenyl, naphthalene, phenanthrene, triphenylene, 9,9-dimethylfluorene, 9,9-diphenylfluorene, spiro[ Group consisting of fluorene-9,9'-fluorene], dibenzofuran, dibenzothiophene, N-phenylcarbazole, phenyl-9,9-dimethylfluorene, phenyldibenzofuran and phenyldibenzothiophene It may be a monovalent residue derived from the arene or heteroarene selected from.

Specifically, Ar ¹ and Ar ² may each independently be a monovalent residue derived from arenes selected from the group consisting of benzene, biphenyl, and terphenyl.

More specifically, Ar ¹ and Ar ² may each independently be phenyl or biphenyl.

In Chemical Formula 1, L ² is a single bond or benzene, naphthalene, 9,9-dimethylfluorene, 9,9-diphenylfluorene, spiro[fluorene-9,9'-fluorene], dibenzofuran , Dibenzothiophene, benzothieno[2,3-d]pyrimidine and benzothieno[3,2-d]pyrimidine (benzothieno[3,2-d ]pyrimidene) may be a divalent residue derived from arene or heteroarene selected from the group consisting of.

In Formula 1, Ar ³ is benzene, biphenyl, terphenyl, naphthalene, anthracene, tetracene, chrysene, phenanthrene, triphenylene, fluoranthene, pyrene, and perylene It may be a monovalent residue derived from arenes selected from the group consisting of (perylene).

In Chemical Formula 1, L ² -Ar ³ may be a substituent selected from the group consisting of the following substituents.

The compound represented by Formula 1 may be a compound selected from the group consisting of compounds represented by Formulas 1-1 and 1-2 below.

[Formula 1-1]

In Chemical Formula 1-1,

L ¹ , Y ¹ to Y ³ , Ar ¹ and Ar ² are the same as in Chemical Formula 1,

L ^2a is a single bond, substituted or unsubstituted C _6-60 arylene, or C _2-60 heteroarylene comprising one or more of substituted or unsubstituted O, N, Si and S,

Ar ^3a is substituted or unsubstituted C _6-60 aryl,

[Formula 1-2]

In Chemical Formula 1-2,

L ¹ , Y ¹ to Y ³ , Ar ¹ and Ar ² are the same as in Chemical Formula 1,

L ^2b and L ^2c are each independently a single bond, a substituted or unsubstituted C _6-60 arylene, or a substituted or unsubstituted C _2-60 heteroaryl including one or more of O, N, Si and S. It's Rengi,

Ar ^3b and Ar ^3c are each independently substituted or unsubstituted C _6-60 aryl.

L ^1, Y ¹ to Y ^3, Ar ¹ and Ar ² of Formula 1-1 and 1-2 are the same as L ^1, Y ¹ to Y ^3, Ar ¹ and Ar ² in Formula 1, L ^2a to L ^2c corresponds to L ² of Formula 1, Ar ^3a to Ar ^3c corresponds to Formula 1 and Ar ³ , and specific examples of L ¹ and L ² , Y ¹ to Y ³ , Ar ¹ to Ar ³ are described in detail above. Since it has been described, a detailed description is omitted here.

The compound represented by Formula 1 may be selected from the group consisting of the following compounds.

In the above Chemical Formula 2, Ar ⁴ and Ar ⁵ are each independently benzene, biphenyl, terphenyl, naphthalene, phenanthrene, triphenylene, phenylterphenyl, phenylnaphthalene, phenylphenanthrene, 9,9-dimethylfluorene , 9,9-diphenylfluorene and spiro[fluorene-9,9'-fluorene] may be monovalent residues derived from arenes selected from the group consisting of.

Specifically, Ar ⁴ and Ar ⁵ may each independently be a monovalent residue derived from arenes selected from the group consisting of benzene, biphenyl, terphenyl, triphenylene, phenylterphenyl, phenylnaphthalene and phenylphenanthrene.

In Chemical Formula 2, R ¹ and R ² are phenyl, and n1 and n2 may each independently be 0 or 1. When n1 or n2 is 0, it means that the carbazole of Formula 2 is not substituted with R ¹ or R ² .

The compound represented by Formula 2 may be selected from the group consisting of the following compounds.

The organic light emitting device of the present invention includes an anode; A cathode provided opposite the anode; And at least one organic layer provided between the anode and the cathode. The organic material layer has a multilayer structure in which two or more organic material layers are stacked. Specifically, the organic material layer may include a hole injection layer adjacent to the anode, a hole transport layer provided on the hole injection layer, an electron blocking layer provided on the hole transport layer, and a light emitting layer provided on the electron blocking layer. have. In addition, the organic light emitting device may include an electron transport layer and an electron injection layer between the light emitting layer and the cathode. However, the structure of the organic light emitting device is not limited to this, and may include a smaller number of organic material layers.

The organic light emitting device according to the present invention may be an organic light emitting device having a structure in which an anode, one or more organic material layers and a cathode are sequentially stacked on a substrate (normal type). Further, the organic light emitting device according to the present invention may be an organic light emitting device of an inverted type in which a cathode, one or more organic material layers, and an anode are sequentially stacked on a substrate. For example, the structure of the organic light emitting device according to an embodiment of the present invention is illustrated in FIG. 1.

1 is composed of a substrate 1, an anode 2, a hole injection layer 3, a hole transport layer 5, an electron blocking layer 6, a light emitting layer 7, an electron transport layer 8 and a cathode 4 An example of an organic light emitting device is shown. In this structure, the compound represented by the formula (1) is included in the light emitting layer (7), the compound represented by the formula (2) of the hole injection layer (3), hole transport layer (5) and electron blocking layer (6) It can be included in one or more organic material layers to lower the driving voltage of the organic light emitting device and improve efficiency and life.

The organic light emitting device according to the present invention includes a compound represented by Formula 1 in the light emitting layer, and a compound represented by Formula 2 in at least one organic layer of the hole injection layer, the hole transport layer, and the electron blocking layer Except for that, it can be made of materials and methods known in the art. Further, the plurality of organic material layers may be formed of the same material or different materials.

For example, the organic light emitting device according to the present invention may be manufactured by sequentially stacking one electrode of an anode and a cathode, an organic material layer, and another electrode of the anode and the cathode on a substrate. At this time, a positive electrode is formed by depositing a metal or conductive metal oxide or alloys thereof on a substrate using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation. Then, 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. In addition to this method, an organic light emitting device may be manufactured by sequentially depositing a cathode material, an organic material layer, and a cathode material on a substrate (WO 2003/012890). However, the manufacturing method is not limited thereto.

In addition, the compound represented by the formula (1) and the compound represented by the formula (2) may be formed into an organic material layer by a solution coating method as well as a vacuum deposition method when manufacturing an organic light emitting device. Here, 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.

The positive electrode material is preferably a material having a large work function so that hole injection into the organic material layer is smooth. Specific examples of 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); Metal and oxide combinations 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 an organic material layer. Specific examples of 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 hole injection layer is a layer for injecting holes from an electrode, and has the ability to transport holes as a hole injection material, and thus has a hole injection effect at an anode, an excellent hole injection effect for a light emitting layer or a light emitting material, and is generated in the light emitting layer. A compound that prevents migration to the electron injection layer or electron injection material of the exciton and is excellent in the ability to form a thin film is preferable. As the hole injection material, a compound represented by Chemical Formula 2 or a compound known as a conventional hole injection material may be used. 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. Specific examples of the hole injection material include metal porphyrin, oligothiophene, arylamine-based organic matter, hexanitrile hexaazatriphenylene-based organic matter, quinacridone-based organic matter, and perylene-based Organic materials, anthraquinones, polyaniline and polythiophene-based conductive polymers, and the like, but are not limited thereto.

The hole transport layer is a layer that receives holes from the hole injection layer and transports holes to the light emitting layer, and a compound represented by Chemical Formula 2 may be used as a material for forming the hole transport layer. Since the compound represented by Chemical Formula 2 has been described in detail above, a detailed description is omitted here.

The compound represented by Chemical Formula 2 is suitable for transporting holes from the anode or the hole injection layer and transferring them to the light emitting layer because the mobility of the holes is large.

On the other hand, if the hole injection layer or the electron blocking layer is formed of a compound represented by Chemical Formula 2, the hole transport layer may be formed of a hole transport material known in the art. Specific examples of the hole transport material include, but are not limited to, arylamine-based organic materials, conductive polymers, and block copolymers having conjugated and non-conjugated portions.

An electron blocking layer may be formed between the hole transport layer and the emission layer to prevent electrons transferred to the emission layer from moving toward the anode. As the material forming the electron blocking layer, a compound represented by Chemical Formula 2 may be used. In particular, when the electron blocking layer is formed of the compound represented by Chemical Formula 2, the efficiency of the organic light emitting device can be remarkably improved.

The light-emitting layer is a layer capable of emitting light in the visible region by transporting and combining holes and electrons from the hole transport layer and the electron transport layer, respectively. The light emitting layer may include a host material and a dopant material.

As the host material, a compound represented by Chemical Formula 1 may be used. Since the compound represented by Chemical Formula 1 has been described in detail above, a detailed description is omitted here.

In addition, a compound represented by Chemical Formula 1 and a compound represented by Chemical Formula 3 may be used as the host material.

[Formula 3]

In Chemical Formula 3,

Ar ⁷ and Ar ⁸ are each independently substituted or unsubstituted C _6-60 aryl.

In Chemical Formula 3, Ar ⁷ and Ar ⁸ are each independently benzene, biphenyl, terphenyl, naphthalene, phenanthrene, triphenylene, 9,9-dimethylfluorene, 9,9-diphenylfluorene, spiro[ Fluorene-9,9'-fluorene], phenylterphenyl, phenylnaphthalene, and phenylphenanthrene.

The compound represented by Chemical Formula 3 may be selected from the group consisting of the following compounds.

The light emitting layer may further include a host material known in the art to which the present invention pertains, in addition to the compounds represented by Chemical Formulas 1 and 3. Specific examples of such host materials include condensed aromatic ring derivatives or heterocyclic compounds. Specifically, condensed aromatic ring derivatives include anthracene derivatives, pyrene derivatives, naphthalene derivatives, pentacene derivatives, phenanthrene compounds, fluoranthene compounds, etc., and heterocyclic compounds include carbazole derivatives, dibenzofuran derivatives, and ladder types Furan compounds, pyrimidine derivatives, and the like, but are not limited thereto.

Examples of the dopant material include aromatic amine derivatives, strylamine compounds, boron complexes, fluoranthene compounds, and metal complexes. Specifically, the aromatic amine derivative is a condensed aromatic ring derivative having a substituted or unsubstituted arylamino group, and includes pyrene, anthracene, chrysene, periplanene, etc. having an arylamino group, and substituted or unsubstituted as a 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. Specifically, styrylamine, styryldiamine, styryltriamine, styryltetraamine, and the like, but are not limited thereto. Further, examples of the metal complex include an iridium complex, a platinum complex, and the like, but are not limited thereto.

The electron transport layer is a layer that receives electrons from the electron injection layer and transports electrons to the light emitting layer. As the electron transport material, a material capable of receiving electrons from the cathode and transferring them to the light emitting layer, a material having high mobility for electrons 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 thereto. The electron transport layer can be used with any desired cathode material, as used according to the prior art. In particular, examples of 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, followed by an aluminum layer or a silver layer in each case.

The electron injection layer is a layer that injects electrons from an electrode, has the ability to transport electrons, has an electron injection effect from a cathode, an excellent electron injection effect on a light emitting layer or a light emitting material, and injects holes of excitons generated in the light emitting layer A compound that prevents migration to the layer and has excellent thin film forming ability is preferred. Specifically, 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, and 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-naphtolato) aluminum, bis (2-methyl-8-quinolinato) (2-naphtholato) gallium, It is not limited to this.

The organic light emitting device according to the present invention may be a front emission type, a back emission type, or a double-sided emission type, depending on the material used.

Manufacturing of the above-described organic light emitting device will be described in detail in the following Examples. However, the following examples are intended to illustrate the invention, and the scope of the invention is not limited by them.

Example  1: Preparation of organic light emitting device

A glass substrate coated with ITO (indium tin oxide) at a thickness of 1300 에 was placed in distilled water in which detergent was dissolved and washed with ultrasonic waves. At this time, Fischer Co. product was used as the detergent, and distilled water filtered secondarily using a filter of Millipore Co. was used as the distilled water. After the ITO substrate was washed for 30 minutes, ultrasonic cleaning was repeated twice with distilled water for 10 minutes. After washing with distilled water, the ITO substrate was ultrasonically cleaned with a solvent of isopropyl alcohol, acetone and methanol, dried, and then transferred to a plasma cleaner. Then, the ITO substrate was cleaned for 5 minutes using oxygen plasma and then transferred to a vacuum evaporator.

The following compound HI-1 was thermally vacuum-deposited on the prepared ITO electrode to a thickness of 50 Å to form a hole injection layer. The following compound HT-1 was thermally vacuum deposited on the hole injection layer to a thickness of 1200 Å to form a hole transport layer, and the following compound 2-1 was vacuum deposited on the hole transport layer to a thickness of 400 전자 to form an electron blocking layer. . Subsequently, the following compound 1-1 and 6% by weight of phosphorescent dopant YGD-1 with respect to the weight of the compound 1-1 were co-deposited on the electron blocking layer to form a light emitting layer with a thickness of 350 MPa. The following compound ET-1 was vacuum-deposited to a thickness of 200 위에 on the light emitting layer to form an electron transport layer, and co-deposited 2% by weight of Li with respect to the weight of the following compound ET-2 and the compound ET-2 was 100 Å. An electron injection layer was formed to a thickness. Aluminum was deposited on the electron injection layer to a thickness of 1000 Å to form a cathode.

In the above process, the deposition rate of the organic material was maintained at 0.4 to 0.7 Å/sec, and the aluminum was maintained at the deposition rate of 2 Å/sec, and the vacuum degree during deposition was maintained at 1×10 ^-7 to 5×10 ^-8 torr. Thus, an organic light emitting device was manufactured.

Example  2 to 16: Preparation of organic light emitting device

An organic light emitting device was manufactured in the same manner as in Example 1, except that the compound for forming the electron blocking layer and/or the light emitting layer was changed as shown in Table 1 below. In Table 1, 1-2, 1-3, 1-4, 2-2, 2-3, and 2-4 compounds are as follows.

Comparative example 1 to 15: Preparation of organic light emitting device

An organic light emitting device was manufactured in the same manner as in Example 1, except that the compound for forming the electron blocking layer and/or the light emitting layer was changed as shown in Table 1 below. In Table 1, HT-2, HT-3, YGH-1, and YGH-2 compounds are as follows.

Experimental Example : Performance evaluation of organic light emitting device

At a current density of 10 mA/cm ² , voltages, efficiencies and lifetimes of the organic light emitting devices manufactured according to Examples 1 to 16 and Comparative Examples 1 to 15 were measured and the results are shown in Table 1. The life (LT95) is defined as the time required to decrease to 95% of the initial luminance (6000 nit), and was measured at a current density of 20 mA/cm ² .

Electronic blocking layer Emitting layer Voltage (V) Current efficiency (cd/A) LT95(hr) Example 1 2-1 1-1 3.83 6.32 290 Example 2 2-1 1-2 3.86 6.37 290 Example 3 2-1 1-3 3.85 6.35 315 Example 4 2-1 1-4 3.84 6.36 280 Example 5 2-2 1-1 3.61 6.56 290 Example 6 2-2 1-2 3.62 6.52 290 Example 7 2-2 1-3 3.63 6.53 320 Example 8 2-2 1-4 3.65 6.51 270 Example 9 2-3 1-1 3.71 6.35 295 Example 10 2-3 1-2 3.72 6.36 285 Example 11 2-3 1-3 3.73 6.37 330 Example 12 2-3 1-4 3.74 6.39 270 Example 13 2-4 1-1 3.85 6.33 305 Example 14 2-4 1-2 3.86 6.32 315 Example 15 2-4 1-3 3.85 6.37 335 Example 16 2-4 1-4 3.84 6.30 310 Comparative Example 1 HT-2 YGH-1 4.11 5.95 225 Comparative Example 2 HT-3 YGH-1 4.15 6.12 240 Comparative Example 3 HT-2 YGH-2 4.44 5.83 205 Comparative Example 4 2-1 YGH-1 4.09 6.46 250 Comparative Example 5 2-2 YGH-1 3.98 6.44 265 Comparative Example 6 2-3 YGH-1 4.09 6.46 255 Comparative Example 7 2-4 YGH-1 4.07 6.33 250 Comparative Example 8 HT-2 1-1 4.08 6.16 270 Comparative Example 9 HT-2 1-2 4.04 6.18 275 Comparative Example 10 HT-2 1-3 4.05 6.03 295 Comparative Example 11 HT-2 1-4 3.94 6.12 280 Comparative Example 12 2-1 YGH-3 4.07 6.43 220 Comparative Example 13 2-2 YGH-3 3.99 6.47 215 Comparative Example 14 2-3 YGH-3 4.06 6.49 225 Comparative Example 15 2-4 YGH-3 4.04 6.36 230

In Table 1, an organic light-emitting device using a conventional compound (Comparative Examples 1 to 3), an organic light-emitting device using a compound represented by Formula 2 as an electron blocking layer, but using a conventional compound as a light-emitting layer material (Comparative Examples 4 to 7) and the compound represented by Chemical Formula 1 are used as the light emitting layer material, but basic characteristics of the organic light emitting device (Comparative Examples 8 to 11) using the existing compound as the electron blocking layer material are shown.

When comparing the examples and the comparative examples, when using the compounds represented by the formulas 1 and 2 as the material of the light-emitting layer and the electron blocking layer, it exhibits a lower driving voltage, higher efficiency, and longer life compared to the conventional organic light emitting device. Is confirmed. In particular, when the compound 2-2 was used as the electron blocking layer material, the driving voltage was the lowest and the efficiency was the highest, and when 1-3 was used as the light emitting layer material, the lifetime was the longest.

On the other hand, when comparing Comparative Examples 1 to 15, in Examples 4 to 7, Comparative Examples 12 to 15, in which the electron blocking layer material was changed to the compound represented by Chemical Formula 2, efficiency is improved, and the light emitting layer material is expressed as Chemical Formula 1. In Comparative Examples 8 to 11 changed to the compound to be displayed, the lifespan was improved. However, it did not show the efficiency and lifetime of the example level.

Thus, the organic light emitting device of the present invention exhibits improved efficiency by including a compound having an arylamine-substituted structure containing a benzidine type linker at the 9th position of carbazole as shown in Formula 2 between the anode and the light emitting layer, A compound having a structure in which the 4-position of dibenzofuran having electron stability as shown in 1 is substituted with triazine having excellent electron injection ability and thermal stability is included in the light-emitting layer, exhibiting a low driving voltage and improved efficiency while exhibiting long life. Is confirmed.

1: substrate 2: anode
3: hole injection layer 4: cathode
5: hole transport layer 6: electron blocking layer
7: light emitting layer 8: electron transport layer

Claims (15)

anode; A cathode provided opposite the anode; And one or more organic material layers provided between the anode and the cathode,
The organic layer includes a light emitting layer,
The light emitting layer includes a compound represented by Formula 1 below,
Comprising a compound represented by the following formula (2) between the anode and the light emitting layer,
Organic light emitting device:
[Formula 1]

In Chemical Formula 1,
L ¹ is a single bond, or a substituted or unsubstituted C _6-60 arylene,
L ² is a single bond or benzene, naphthalene, 9,9-dimethylfluorene, 9,9-diphenylfluorene, spiro[fluorene-9,9'-fluorene], dibenzofuran, dibenzothi With offen, benzothieno[2,3-d]pyrimidine and benzothieno[3,2-d]pyrimidine A divalent residue derived from arene or heteroarene selected from the group consisting of,
Y ¹ to Y ³ are each independently N or CR ¹ , at least one of which is N, R ¹ is hydrogen, or substituted or unsubstituted C _1-40 alkyl,
Ar ¹ and Ar ² are each independently substituted or unsubstituted C _6-60 aryl, or substituted or unsubstituted C _2-60 heteroaryl including one or more of O, N, Si and S,
Ar ³ is substituted or unsubstituted C _6-60 aryl,
m is 1 or 2,
[Formula 2]

In Chemical Formula 2,
Ar ⁴ and Ar ⁵ are each independently substituted or unsubstituted C _6-60 aryl,
R ¹ and R ² are each independently substituted or unsubstituted C _6-20 aryl,
n1 and n2 are each independently 0 or 1.
According to claim 1,
L ¹ is a single bond, or phenylene,
Organic light emitting device.
According to claim 1,
Y ¹ to Y ³ are each independently N or CH, at least one of which is N,
Organic light emitting device.
According to claim 1,
Ar ¹ and Ar ² are each independently benzene, biphenyl, terphenyl, naphthalene, phenanthrene, triphenylene, 9,9-dimethylfluorene, 9,9-diphenylfluorene, spiro[fluorene-9, 9'-fluorene], dibenzofuran, dibenzothiophene, N-phenylcarbazole, phenyl-9,9-dimethylfluorene, phenyldibenzofuran and arene or hetero selected from the group consisting of phenyldibenzothiophene A monovalent residue derived from arene,
Organic light emitting device.
delete According to claim 1,
Ar ³ is composed of benzene, biphenyl, terphenyl, naphthalene, anthracene, tetracene, chrysene, phenanthrene, triphenylene, fluoranthene, pyrene and perylene A monovalent residue derived from arenes selected from the group,
Organic light emitting device.
According to claim 1,
L ² -Ar ³ is a substituent selected from the group consisting of the following substituents,
Organic light emitting device:

.
According to claim 1,
The compound represented by Formula 1 is selected from the group consisting of compounds represented by the following Formulas 1-1 and 1-2,
Organic light emitting device:
[Formula 1-1]

In Chemical Formula 1-1,
L ¹ , Y ¹ to Y ³ , Ar ¹ and Ar ² are the same as in Chemical Formula 1,
L ^2a is a single bond, substituted or unsubstituted C _6-60 arylene, or C _2-60 heteroarylene comprising one or more of substituted or unsubstituted O, N, Si and S,
Ar ^3a is substituted or unsubstituted C _6-60 aryl,
[Formula 1-2]

In Chemical Formula 1-2,
L ¹ , Y ¹ to Y ³ , Ar ¹ and Ar ² are the same as in Chemical Formula 1,
L ^2b and L ^2c are each independently a single bond, a substituted or unsubstituted C _6-60 arylene, or a C _2-60 heteroaryl containing one or more of substituted or unsubstituted O, N, Si and S. It's Rengi,
Ar ^3b and Ar ^3c are each independently substituted or unsubstituted C _6-60 aryl.
According to claim 1,
The compound represented by Formula 1 is selected from the group consisting of the following compounds,
Organic light emitting device:

According to claim 1,
Ar ⁴ and Ar ⁵ are each independently benzene, biphenyl, terphenyl, naphthalene, phenanthrene, triphenylene, phenylterphenyl, phenylnaphthalene, phenylphenanthrene, 9,9-dimethylfluorene, 9,9- A monovalent residue derived from arene selected from the group consisting of diphenylfluorene and spiro[fluorene-9,9'-fluorene],
Organic light emitting device.
According to claim 1,
R ¹ and R ² are phenyl,
n1 and n2 are each independently 0 or 1,
Organic light emitting device.
According to claim 1,
The compound represented by Formula 2 is selected from the group consisting of the following compounds, an organic light emitting device:

According to claim 1,
The light emitting layer further comprises a compound represented by the formula (3),
Organic light emitting device:
[Formula 3]

In Chemical Formula 3,
Ar ⁷ and Ar ⁸ are each independently substituted or unsubstituted C _6-60 aryl.
The method of claim 13,
Ar ⁷ and Ar ⁸ are each independently benzene, biphenyl, terphenyl, naphthalene, phenanthrene, triphenylene, 9,9-dimethylfluorene, 9,9-diphenylfluorene, spiro[fluorene-9, 9'-fluorene], a monovalent residue derived from arenes selected from the group consisting of phenylterphenyl, phenylnaphthalene and phenylphenanthrene,
Organic light emitting device.
The method of claim 13,
The compound represented by Formula 3 is selected from the group consisting of the following compounds,
Organic light emitting device:

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