Composition for organic optoelectronic device and organic optoelectronic device and display device

Abstract

The present invention relates to a composition for an organic optoelectronic device, and an organic optoelectronic device and a display device comprising the same, the composition comprising a first compound represented by Chemical Formula 1, a second compound represented by Chemical Formula 2 or a combination of Chemical Formula 3 and Chemical Formula 4, and a third compound, and the third compound is represented by Chemical Formula 5. Details of Chemical Formulae 1 to 5 are the same as those disclosed in the specification.

Description

Technical Field

[0001] Compositions for organic optoelectronic devices, organic optoelectronic devices, and display devices are disclosed. Background Art

[0002] An organic optoelectronic device (organic optoelectronic diode) is a device capable of converting electrical energy and light energy into each other.

[0003] According to the working principle, organic optoelectronic devices can be roughly divided into two categories. One is a photoelectric device that generates electrical energy by separating excitons formed by light energy into electrons and holes and transferring the electrons and holes to different electrodes, respectively, and the other is a light-emitting device that generates light energy from electrical energy by applying a voltage or current to an electrode.

[0004] Examples of organic optoelectronic devices include organic optoelectronic devices, organic light-emitting diodes, organic solar cells, and organic photoreceptors.

[0005] Among them, due to the increasing demand for flat panel display devices, organic light-emitting diodes (OLEDs) have attracted much attention in recent years. An organic light-emitting diode is a device that converts electrical energy into light, and the performance of an organic light-emitting diode is greatly affected by the organic material between the electrodes. Summary of the Invention

[0006] Technical Problem

[0007] One embodiment provides a composition for an organic optoelectronic device capable of achieving a low-driving, high-efficiency, and long-life organic optoelectronic device.

[0008] Another embodiment provides an organic optoelectronic device including the composition for an organic optoelectronic device.

[0009] Another embodiment provides a display device including the organic optoelectronic device.

[0010] Technical Solution

[0011] According to one embodiment, a composition for an organic optoelectronic device includes a first compound, a second compound, and a third compound, wherein the first compound is represented by Chemical Formula 1, the second compound is represented by Chemical Formula 2 or a combination of Chemical Formulas 3 and 4, and the third compound is represented by Chemical Formula 5.

[0012] [Chemical Formula 1]

[0013]

[0014] In Chemical Formula 1,

[0015] Z 1 to Z 3 are each independently N or C-La -R a ,

[0016] Z 1 to Z 3 at least two of which are N,

[0017] L a and L 1 to L 3 each independently is a single bond, a substituted or unsubstituted C6 - C20 arylene, a substituted or unsubstituted C2 - C20 heterocyclic group, or a combination thereof,

[0018] R 1 to R 3 each independently is hydrogen, deuterium, cyano, a substituted or unsubstituted C1 - C10 alkyl, a substituted or unsubstituted C6 - C30 aryl, a substituted or unsubstituted C2 - C30 heterocyclic group, or a combination thereof,

[0019] Ar 1 and Ar 2 each independently is a substituted or unsubstituted C6 - C30 aryl, a substituted or unsubstituted C2 - C30 heterocyclic group, or a combination thereof,

[0020] m1 and m2 each independently is one of the integers from 1 to 4, and

[0021] m3 is one of the integers from 1 to 3;

[0022] [Chemical formula 2]

[0023]

[0024] In Chemical formula 2,

[0025] Ar 3 and Ar 4 each independently is a substituted or unsubstituted C6 - C30 aryl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted carbazolyl, a substituted or unsubstituted dibenzofuranyl, a substituted or unsubstituted dibenzothiophenyl, or a substituted or unsubstituted dibenzosilolyl,

[0026] L 4 and L 5 each independently is a single bond or a substituted or unsubstituted C6 - C20 arylene,

[0027] R 7 to R 11 each independently is hydrogen, deuterium, cyano, halogen, a substituted or unsubstituted amino group, a substituted or unsubstituted C1 - C30 alkyl, a substituted or unsubstituted silyl group, a substituted or unsubstituted C6 - C30 aryl, or a substituted or unsubstituted C2 - C30 heterocyclic group,

[0028] m8 and m9 are each independently one of the integers from 1 to 3,

[0029] m7, m10 and m11 are each independently one of the integers from 1 to 4, and

[0030] n is one of the integers from 0 to 2;

[0031]

[0032] In Chemical Formula 3 and Chemical Formula 4,

[0033] Ar 5 and Ar 6 are each independently a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group or a substituted or unsubstituted dibenzosilolyl group,

[0034] a in Chemical Formula 3 1 * to a 4 * are each independently a connecting carbon (C) or C-L b -R b ,

[0035] a 1 * to a 4 * of two adjacent ones of them are each connected to the * of Chemical Formula 4,

[0036] In a 1 * to a 4 *, the remaining two that are not connected to the * in Chemical Formula 4 are each independently C-L b -R b ,

[0037] L b 、L 6 and L 7 are each independently a single bond or a substituted or unsubstituted C6-C20 arylene group, and

[0038] R b 、R 12 and R 13 are each independently hydrogen, deuterium, cyano, halogen, a substituted or unsubstituted amino group, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C2-C30 heterocyclic group;

[0039] [Chemical Formula 5]

[0040]

[0041] In Chemical Formula 5,

[0042] Z 4 to Z 6 are each independently N or C-L c -R c ,

[0043] Z 4 to Z 6 at least two of which are N,

[0044] L c and L 8 to L 10 are each independently a single bond, a substituted or unsubstituted C6-C20 arylene group, a substituted or unsubstituted C2-C20 heterocyclic group, or a combination thereof,

[0045] R c is hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof,

[0046] Ar 7 to Ar 9 are each independently hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof,

[0047] Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted carbazolyl group, and

[0048] the remaining Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted dibenzofuranyl group or a substituted or unsubstituted dibenzothiophenyl group.

[0049] According to another embodiment, the organic optoelectronic device includes an anode and a cathode facing each other and at least one organic layer between the anode and the cathode, wherein the organic layer contains the composition for the organic optoelectronic device described above.

[0050] According to another embodiment, a display device including the organic optoelectronic device is provided.

[0051] Advantageous Effects

[0052] An organic optoelectronic device with low driving, high efficiency, and long life can be achieved. Description of the Drawings

[0053] Figure 1It is a cross-sectional view showing an organic light-emitting diode according to an embodiment.

[0054] <Description of Reference Numerals>

[0055] 100: Organic light-emitting diode

[0056] 105: Organic layer

[0057] 110: Cathode

[0058] 120: Anode

[0059] 130: Light-emitting layer

[0060] 140: Hole transport region

[0061] 150: Electron transport region Detailed Embodiments

[0062] Hereinafter, embodiments of the present invention are described in detail. However, these embodiments are exemplary, and the present disclosure is not limited thereto.

[0063] As used herein, when no other definition is provided, "substituted" means that at least one hydrogen of a substituent or a compound is replaced by the following: deuterium, halogen, hydroxyl group, amino group, substituted or unsubstituted C1-C30 amino group, nitro group, substituted or unsubstituted C1-C40 silyl group, C1-C30 alkyl group, C1-C10 alkylsilyl group, C6-C30 arylsilyl group, C3-C30 cycloalkyl group, C3-C30 heterocycloalkyl group, C6-C30 aryl group, C2-C30 heteroaryl group, C1-C20 alkoxy group, C1-C10 trifluoroalkyl group, cyano group, or a combination thereof.

[0064] In one example of the present invention, "substituted" means that at least one hydrogen of a substituent or a compound is replaced by one of the following: deuterium, cyano, C1-C30 alkyl, C1-C10 alkylsilyl, C6-C30 arylamino, C6-C30 arylsilyl, C3-C30 cycloalkyl, C3-C30 heteroalkyl, C6-C30 aryl or C2-C30 heteroaryl. In a specific example of the present invention, "substituted" means that at least one hydrogen of a substituent or a compound is replaced by one of the following: deuterium, cyano, C1-C20 alkyl, C6-C30 arylamino, C6-C30 aryl or C2-C30 heteroaryl. In a specific example of the present invention, "substituted" means that at least one hydrogen of a substituent or a compound is replaced by one of the following: deuterium, cyano, C1-C5 alkyl, C6-C20 arylamino, C6-C18 aryl, dibenzofuranyl, dibenzothiophenyl, carbazolyl or pyridyl. In a specific example of the present invention, "substituted" means that at least one hydrogen of a substituent or a compound is replaced by one of the following: deuterium, cyano, methyl, ethyl, propyl, butyl, C6-C20 arylamino, phenyl, biphenyl, terphenyl, naphthyl, triphenyl, fluorenyl, dibenzofuranyl, dibenzothiophenyl, carbazolyl or pyridyl.

[0065] In this specification, "unsubstituted" means that a hydrogen atom is not replaced by another substituent and the hydrogen atom is retained.

[0066] In this specification, "hydrogen substitution (-H)" may include "deuterium substitution (-D)" or "tritium substitution (-T)".

[0067] In this specification, when no other definition is provided, "hetero" means including one to three heteroatoms selected from N, O, S, P and Si in a functional group and the remaining carbon.

[0068] In this specification, "aryl" means a group including at least one hydrocarbon aromatic moiety, and all elements of the hydrocarbon aromatic moiety have conjugated p orbitals, such as phenyl, naphthyl, etc. Two or more hydrocarbon aromatic moieties may be connected by a σ bond and may be, for example, biphenyl, terphenyl, quaterphenyl, etc., and two or more hydrocarbon aromatic moieties are directly or indirectly fused to provide a non-aromatic fused ring, such as fluorenyl.

[0069] Aryl may include monocyclic, polycyclic or fused polycyclic (i.e., rings sharing adjacent carbon atom pairs) functional groups.

[0070] As used herein, "heterocyclic group" is a superordinate concept of heteroaryl and may include at least one heteroatom selected from N, O, S, P, and Si in place of carbon (C) in a cyclic compound such as aryl, cycloalkyl, their fused rings, or combinations thereof. When the heterocyclic group is a fused ring, the entire ring or each ring of the heterocyclic group may include one or more heteroatoms.

[0071] For example, "heteroaryl" may refer to an aryl group including at least one heteroatom selected from N, O, S, P, and Si. Two or more heteroaryl groups are directly connected by a σ bond, or when the heteroaryl group includes two or more rings, the two or more rings may be fused. When the heteroaryl group is a fused ring, each ring may include one to three heteroatoms.

[0072] More specifically, the substituted or unsubstituted C6-C30 aryl group may be a substituted or unsubstituted phenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthryl group, a substituted or unsubstituted phenanthryl group, a substituted or unsubstituted condensed tetraphenyl group, a substituted or unsubstituted pyrenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted p-terphenyl group, a substituted or unsubstituted m-terphenyl group, a substituted or unsubstituted o-terphenyl group, a substituted or unsubstituted chrysenyl group, a substituted or unsubstituted triphenylene group, a substituted or unsubstituted perylenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted indenyl group, or a combination thereof, but is not limited thereto.

[0073] More specifically, the substituted or unsubstituted C2-C30 heterocyclic group may be a substituted or unsubstituted furyl group, a substituted or unsubstituted thienyl group, a substituted or unsubstituted pyrrolyl group, a substituted or unsubstituted pyrazolyl group, a substituted or unsubstituted imidazolyl group, a substituted or unsubstituted triazolyl group, a substituted or unsubstituted oxazolyl group, a substituted or unsubstituted thiazolyl group, a substituted or unsubstituted oxadiazolyl group, a substituted or unsubstituted thiadiazolyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted pyrimidinyl group, a substituted or unsubstituted pyrazinyl group, a substituted or unsubstituted triazinyl group, a substituted or unsubstituted benzofuryl group, a substituted or unsubstituted benzothienyl group, a substituted or unsubstituted benzimidazolyl group, a substituted or unsubstituted indolyl group, a substituted or unsubstituted quinolinyl group, a substituted or unsubstituted isoquinolinyl group, a substituted or unsubstituted quinazolinyl group, a substituted or unsubstituted quinoxalinyl group, a substituted or unsubstituted naphthyridinyl group, a substituted or unsubstituted benzoxazinyl group, a substituted or unsubstituted benzothiazinyl group, a substituted or unsubstituted acridinyl group, a substituted or unsubstituted phenazinyl group, a substituted or unsubstituted phenothiazinyl group, a substituted or unsubstituted phenoxazinyl group, a substituted or unsubstituted dibenzofuryl group, a substituted or unsubstituted dibenzothienyl group, or a combination thereof, but is not limited thereto.

[0074] As used herein, hole characteristics refer to the ability to provide electrons to form holes when an electric field is applied, and due to the conductive characteristics according to the highest occupied molecular orbital (HOMO) energy level, the holes formed in the anode can be easily injected into the light-emitting layer and transported in the light-emitting layer.

[0075] In addition, electron characteristics refer to the ability to accept electrons when an electric field is applied, and due to the conductive characteristics according to the lowest unoccupied molecular orbital (LUMO) energy level, the electrons formed in the cathode can be easily injected into the light-emitting layer and transported in the light-emitting layer.

[0076] Hereinafter, a composition for an organic optoelectronic device according to one embodiment is described.

[0077] The organic optoelectronic device composition according to one embodiment is a mixture including three compounds. Specifically, the first compound includes at least one nitrogen-containing ring, thereby forming a structure that may accept electrons when an electric field is applied, thereby increasing the electron injection amount and making the electron (electrical) characteristics have relatively strong bipolar characteristics. The second compound may have relatively strong hole characteristics by including a carbazole moiety.

[0078] When the first compound and the second compound are used together in the light-emitting layer, there are the following advantages: the light-emitting efficiency and lifetime characteristics can be improved by increasing the charge mobility and enhancing the stability.

[0079] On the other hand, due to the trapping phenomena caused by the difference in HOMO energy levels between the dopant and the host, the hole and electron transport capabilities are rapidly reduced, so there is a problem of increasing the driving voltage of the organic optoelectronic device.

[0080] Therefore, by adding a third compound having excellent hole and electron characteristics, the trapping phenomena between the dopant and the host can be reduced or minimized, and the injection of holes and electrons into the light-emitting layer can be made smoother, thereby producing an organic optoelectronic device having excellent efficiency while significantly reducing the driving voltage.

[0081] By adding a third compound having excellent hole and electron characteristics, the problem of increased driving voltage that may occur when only the first and second compounds are included can be solved, thereby effectively improving the power efficiency performance of the device. In addition, by using three types of hosts, the optimal position and width of the light-emitting region can be adjusted, thereby effectively improving the efficiency and lifetime.

[0082] The first compound having electron characteristics has a structure in which a triphenylene derivative is substituted with a nitrogen-containing 6-membered ring and is represented by Chemical Formula 1.

[0083] [Chemical Formula 1]

[0084]

[0085] In Chemical Formula 1,

[0086] Z 1 to Z 3 are each independently N or C-L a -R a ,

[0087] Z 1 to Z 3 at least two of which are N,

[0088] L a and L 1 to L 3 are each independently a single bond, a substituted or unsubstituted C6-C20 arylene group, a substituted or unsubstituted C2-C20 heterocyclic group, or a combination thereof,

[0089] R 1 to R 3 are each independently hydrogen, deuterium, cyano, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof,

[0090] Ar 1 and Ar 2 are each independently a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof,

[0091] m1 and m2 are each independently one of the integers from 1 to 4, and

[0092] m3 is one of the integers from 1 to 3.

[0093] In Chemical Formula 1, when there are two or more R substituents 1 , each R 1 can be the same as or different from each other.

[0094] In Chemical Formula 1, when there are two or more R substituents 2 , each R 2 can be the same as or different from each other.

[0095] In Chemical Formula 1, when there are two or more R substituents 3 , each R 3 can be the same as or different from each other.

[0096] In Chemical Formula 1, when there are two or more R substituents a , each R amay be the same as or different from each other.

[0097] Specifically, Z in Chemical Formula 1 1 to Z 3 may each independently be N or CH, and at least two of Z 1 to Z 3 may be N.

[0098] For example, Z 1 to Z 3 may each be N.

[0099] For example, Z 1 and Z 3 may be N, and Z 2 may be CH.

[0100] L in Chemical Formula 1 1 may be a single bond, a substituted or unsubstituted phenylene, a substituted or unsubstituted biphenylene, a substituted or unsubstituted terphenylene, a substituted or unsubstituted naphthylene, a substituted or unsubstituted carbazolylene, a substituted or unsubstituted dibenzofuranylene, or a substituted or unsubstituted dibenzothiophenylene.

[0101] L in Chemical Formula 1 2 and L 3 may each independently be a single bond, a substituted or unsubstituted phenylene, or a substituted or unsubstituted biphenylene.

[0102] R in Chemical Formula 1 1 to R 3 may each independently be hydrogen, deuterium, a substituted or unsubstituted C1-C5 alkyl group, a substituted or unsubstituted C6-C12 aryl group, a substituted or unsubstituted C2-C12 heterocyclic group, or a combination thereof.

[0103] Ar in Chemical Formula 1 1 and Ar 2 may each independently be a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, a substituted or unsubstituted carbazolyl group, or a substituted or unsubstituted dibenzosilolyl group.

[0104] In a specific example of the present invention, L in Chemical Formula 1 1 may be a single bond, a substituted or unsubstituted phenylene, or a substituted or unsubstituted biphenylene.

[0105] In a specific example of the present invention, L in Chemical Formula 1 2 and L 3 may each be a single bond.

[0106] In a specific example of the present invention, R in Formula 1 1 to R 3 can each independently be hydrogen, deuterium, cyano, a substituted or unsubstituted C6 to C12 aryl group.

[0107] In a specific example of the present invention, Ar in Formula 1 1 and Ar 2 can each independently be a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, or a substituted or unsubstituted fluorenyl group.

[0108] For example, R in Formula 1 1 to R 3 can each independently be hydrogen, deuterium, cyano, or a substituted or unsubstituted phenyl group.

[0109] The first compound can have a structure that is prone to accepting electrons when an electric field is applied by including a ring containing at least one nitrogen, and thus can reduce the driving voltage of an organic optoelectronic device to which the compound is applied.

[0110] Furthermore, the first compound forms a bipolar structure by including a terphenyl structure that is prone to accepting holes and a nitrogen-containing ring portion that is prone to accepting electrons, thereby appropriately balancing the flow of holes and electrons, and thus improving the efficiency of the organic optoelectronic device to which the compound is applied.

[0111] L 1 can be, for example, one group selected from the substituted or unsubstituted groups listed in Group I.

[0112] [Group I]

[0113]

[0114] In Group I, * is the point of attachment.

[0115] The first compound represented by Formula 1 can desirably have at least two kinked structures, for example, can have 2 to 4 kinked structures.

[0116] The first compound represented by Chemical Formula 1 has the above-mentioned kink structure, and thus can exhibit excellent bipolar characteristics by appropriately localizing the terphenyl structure that tends to accept holes and the nitrogen-containing ring portion that tends to accept electrons in the above bipolar structure compound and controlling the flow of the conjugated system. In addition, according to the said structure, the first compound represented by Chemical Formula 1 can effectively prevent the stacking of organic compounds, thereby increasing the process stability and at the same time reducing the deposition temperature. When the first compound represented by Chemical Formula 1 includes a linking group (L 1 ), this anti-stacking effect can be further enhanced.

[0117] In the first compound represented by Chemical Formula 1, the structure having a linking group (L 1 ) can be represented by any one of Chemical Formulas 1-1 to 1-12, for example.

[0118]

[0119]

[0120]

[0121]

[0122] In Chemical Formulas 1-1 to 1-12, Z 1 to Z 3 , R 1 to R 3 , L 2 , L 3 , Ar 1 , Ar 2 and m1 to m3 are the same as above, R 4 to R 6 are as defined for R 1 to R 3 , and m4 to m6 are each independently one of the integers from 1 to 4.

[0123] In Chemical Formulas 1-1 to 1-12, two or more R 4 are substituted, and each R 4 can be the same as or different from each other.

[0124] In Chemical Formulas 1-1 to 1-12, two or more R 5 are substituted, and each R 5 can be the same as or different from each other.

[0125] In Chemical Formulas 1-1 to 1-12, two or more R 6 are substituted, and each R6 They may be the same as or different from each other.

[0126] The first compound may be, for example, one selected from the compounds listed in Group 1.

[0127] [Group 1]

[0128]

[0129]

[0130]

[0131]

[0132] The second compound having hole characteristics has a structure in which a C6 to C30 aryl group or a substituted or unsubstituted C2 to C30 heterocyclic group in which a carbazole or a carbazole derivative is substituted or unsubstituted, and may be represented by, for example, Chemical Formula 2 or a combination of Chemical Formula 3 and Chemical Formula 4.

[0133] [Chemical Formula 2]

[0134]

[0135] In Chemical Formula 2,

[0136] Ar 3 and Ar 4 are each independently a substituted or unsubstituted C6 to C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, or a substituted or unsubstituted dibenzosilolyl group,

[0137] L 4 and L 5 are each independently a single bond or a substituted or unsubstituted C6 to C20 arylene group,

[0138] R 7 to R 11 are each independently hydrogen, deuterium, cyano group, halogen, substituted or unsubstituted amino group, substituted or unsubstituted C1 to C30 alkyl group, substituted or unsubstituted silyl group, substituted or unsubstituted C6 to C30 aryl group, or substituted or unsubstituted C2 to C30 heterocyclic group,

[0139] m8 and m9 are each independently one of the integers from 1 to 3,

[0140] m7, m10 and m11 are each independently one of the integers from 1 to 4, and

[0141] n is one of the integers from 0 to 2;

[0142]

[0143]

[0144] In Chemical Formulas 3 and 4,

[0145] Ar 5 and Ar 6 are each independently a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, or a substituted or unsubstituted dibenzosilolyl group,

[0146] a in Chemical Formula 3 1 * to a 4 * are each independently a linking carbon (C) or C-L b -R b ,

[0147] a 1 * to a 4 * of two adjacent ones of which are each linked to the * of Chemical Formula 4,

[0148] In a 1 * to a 4 *, the remaining two that are not linked to the * in Chemical Formula 4 are each independently C-L b -R b ,

[0149] L b 、L 6 and L 7 are each independently a single bond or a substituted or unsubstituted C6-C20 arylene group, and

[0150] R b 、R 12 and R 13 are each independently hydrogen, deuterium, cyano group, halogen, a substituted or unsubstituted amino group, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted C6-C30 aryl group, or a substituted or unsubstituted C2-C30 heterocyclic group.

[0151] In Chemical Formula 2, when two or more R 7 are substituted, each R 7 can be the same as or different from each other.

[0152] In Chemical Formula 2, when two or more R 8 are substituted, each R 8 can be the same as or different from each other.

[0153] In Chemical Formula 2, when two or more R are substituted 9 each R 9 may be the same as or different from each other.

[0154] In Chemical Formula 2, when two or more R are substituted 10 each R 10 may be the same as or different from each other.

[0155] In Chemical Formula 2, when two or more R are substituted 11 each R 11 may be the same as or different from each other.

[0156] In Chemical Formula 3, when two or more R are substituted b each R b may be the same as or different from each other.

[0157] In Chemical Formula 3, when two or more R are substituted 12 each R 12 may be the same as or different from each other.

[0158] In Chemical Formula 4, when two or more R are substituted 13 each R 13 may be the same as or different from each other.

[0159] For example, in Chemical Formula 2, Ar 3 and Ar 4 may each independently be a substituted or unsubstituted phenyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted terphenyl, a substituted or unsubstituted naphthyl, a substituted or unsubstituted anthryl, a substituted or unsubstituted phenanthryl, a substituted or unsubstituted terphenylene, a substituted or unsubstituted pyridyl, a substituted or unsubstituted carbazolyl, a substituted or unsubstituted dibenzothiophenyl, a substituted or unsubstituted dibenzofuranyl, or a substituted or unsubstituted fluorenyl.

[0160] For example, in Chemical Formula 2, L 4 and L 5 may each independently be a single bond, a substituted or unsubstituted phenylene, a substituted or unsubstituted biphenylene, a substituted or unsubstituted terphenylene, a substituted or unsubstituted quaterphenylene, a substituted or unsubstituted naphthylene, a substituted or unsubstituted anthrylene, a substituted or unsubstituted terphenylene, or a substituted or unsubstituted phenanthrylene.

[0161] For example, in Chemical Formula 2, R 7 to R 11Each may independently be hydrogen, deuterium, a substituted or unsubstituted C1-C20 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof.

[0162] As a specific example, in Chemical Formula 2, R 7 to R 11 may each independently be hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C20 aryl group, or a substituted or unsubstituted C2-C20 heterocyclic group.

[0163] For example, in Chemical Formulas 3 and 4, Ar 5 and Ar 6 may each independently be a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, or a combination thereof.

[0164] For example, in Chemical Formulas 3 and 4, R b , R 12 and R 13 may each independently be hydrogen, deuterium, a cyano group, a halogen, a substituted or unsubstituted amino group, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C20 aryl group, or a substituted or unsubstituted C2-C20 heterocyclic group.

[0165] As a specific example, in Chemical Formula 2, Ar 3 and Ar 4 may each independently be a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group,

[0166] In Chemical Formula 2, L 4 and L 5 may each independently be a single bond, a substituted or unsubstituted phenylene group, a substituted or unsubstituted biphenylene group, or a substituted or unsubstituted naphthylene group,

[0167] In Chemical Formula 2, R 7 to R 11 may each independently be hydrogen, deuterium, a substituted or unsubstituted C6-C12 aryl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group, and

[0168] n may be 0 or 1.

[0169] As an example, in Chemical Formula 2 to Chemical Formula 4, "substituted" means that at least one hydrogen is replaced by deuterium, a C1-C4 alkyl group, a C6-C18 aryl group, or a C2-C30 heteroaryl group.

[0170] In a specific embodiment of the present invention, Chemical Formula 2 can be represented by one of Chemical Formulas 2-1 to 2-15.

[0171]

[0172]

[0173] In Chemical Formulas 2-1 to 2-15, R 7 to R 11 can each independently be hydrogen, deuterium, a substituted or unsubstituted C6-C12 aryl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group, and *-L 4 -Ar 3 and *-L 5 -Ar 4 can each independently be one of the substituents listed in Group II.

[0174] [Group II]

[0175]

[0176] In Group II,

[0177] R 14 to R 17 each independently are hydrogen, deuterium, a substituted or unsubstituted C1-C4 alkyl group, a substituted or unsubstituted C6-C18 aryl group, or a substituted or unsubstituted C2-C30 heteroaryl group,

[0178] m14 is one of the integers from 1 to 5,

[0179] m15 is one of the integers from 1 to 4,

[0180] m16 is one of the integers from 1 to 3,

[0181] m17 is an integer of 1 or 2, and

[0182] * is a point of attachment.

[0183] In Group II, when there are two or more R 14 substituents, each R 14 can be the same as or different from each other.

[0184] In Group II, when there are two or more R15 When each R 15 can be the same as or different from each other.

[0185] In Group II, when substituted with two or more Rs 16 When each R 16 can be the same as or different from each other.

[0186] In Group II, when substituted with two or more Rs 17 When each R 17 can be the same as or different from each other.

[0187] For example, the second compound represented by the combination of Chemical Formula 3 and Chemical Formula 4 can be represented by any one of Chemical Formula 3A, Chemical Formula 3B, Chemical Formula 3C, Chemical Formula 3D, and Chemical Formula 3E.

[0188]

[0189] In Chemical Formulas 3A to 3E, Ar 5 , Ar 6 , L 6 , L 7 , R 12 , R 13 are the same as those above,

[0190] L b1 to L b4 are defined as L 6 and L 7 described above, and

[0191] R b1 to R b4 are defined as R 12 and R 13 described above.

[0192] For example, in Chemical Formulas 3 and 4, Ar 5 and Ar 6 can each independently be a substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl, substituted or unsubstituted terphenyl, substituted or unsubstituted naphthyl, substituted or unsubstituted anthryl, substituted or unsubstituted phenanthryl, substituted or unsubstituted terphenylene, substituted or unsubstituted pyridyl, substituted or unsubstituted carbazolyl, substituted or unsubstituted dibenzothiophenyl, substituted or unsubstituted dibenzofuranyl, or substituted or unsubstituted fluorenyl.

[0193] R b1 to R b4 , R 12 and R 13Each independently may be hydrogen, deuterium, cyano, substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl, substituted or unsubstituted carbazolyl, substituted or unsubstituted dibenzofuranyl, or substituted or unsubstituted dibenzothiophenyl.

[0194] In a specific embodiment of the present invention, in Chemical Formulas 3 and 4, *-L 6 -Ar 5 and *-L 7 -Ar 6 may each independently be selected from the substituents listed in Group II.

[0195] In one embodiment, R b1 to R b4 , R 12 and R 13 may each independently be hydrogen, deuterium, cyano, substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl, substituted or unsubstituted naphthyl, substituted or unsubstituted terphenyl, substituted or unsubstituted carbazolyl, substituted or unsubstituted dibenzofuranyl, or substituted or unsubstituted dibenzothiophenyl.

[0196] For example, R b1 to R b4 , R 12 and R 13 may each independently be hydrogen, deuterium, substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl, substituted or unsubstituted carbazolyl, substituted or unsubstituted dibenzofuranyl, or substituted or unsubstituted dibenzothiophenyl, and

[0197] In a specific embodiment, R b1 to R b4 , R 12 and R 13 may each independently be hydrogen, deuterium, substituted or unsubstituted phenyl, substituted or unsubstituted carbazolyl, substituted or unsubstituted dibenzofuranyl, or substituted or unsubstituted dibenzothiophenyl.

[0198] In a specific embodiment of the present invention, the second compound may be represented by Chemical Formula 2-6 or Chemical Formula 2-8, wherein Ar 3 and Ar 4 may each independently be substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl, substituted or unsubstituted naphthyl, substituted or unsubstituted terphenyl, substituted or unsubstituted carbazolyl, substituted or unsubstituted dibenzofuranyl, or substituted or unsubstituted dibenzothiophenyl, L 4 and L 5 may each independently be a single bond or a substituted or unsubstituted C6-C20 arylene group, and R 7 to R11 Each may independently be hydrogen, deuterium, cyano, a substituted or unsubstituted phenyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted carbazolyl, a substituted or unsubstituted dibenzofuranyl, or a substituted or unsubstituted dibenzothiophenyl.

[0199] For example, *-L 4 -Ar 3 and *-L 5 -Ar 2 may each independently be selected from the substituents listed in Group II, and in one embodiment, may be any one of C-1, C-2, C-3, C-4, C-7, C-8, and C-9.

[0200] In another specific embodiment of the present invention, the third compound may be represented by Chemical Formula 3C, wherein L b1 and L b2 may be a single bond, L 6 and L 7 may each independently be a single bond or a substituted or unsubstituted C6 to C12 arylene, R b1 , R b2 , R 12 and R 13 may each be hydrogen, deuterium, a substituted or unsubstituted phenyl, a substituted or unsubstituted terphenyl, a substituted or unsubstituted carbazolyl, a substituted or unsubstituted dibenzofuranyl, or a substituted or unsubstituted dibenzothiophenyl, and Ar 5 and Ar 6 may each independently be a substituted or unsubstituted phenyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted carbazolyl, a substituted or unsubstituted dibenzofuranyl, or a substituted or unsubstituted dibenzothiophenyl.

[0201] For example, the second compound may be one of the compounds listed in Group 2, but is not limited thereto.

[0202] [Group 2]

[0203]

[0204]

[0205]

[0206]

[0207]

[0208]

[0209]

[0210] In addition, examples in which at least one hydrogen in Compounds B-1 to B-150 listed in Group 2 is replaced by deuterium are given below, but are not limited thereto.

[0211]

[0212]

[0213] (Dn refers to the number of deuterium substitutions and represents a structure substituted by one or more deuteriums).

[0214] According to the position and substitution rate of deuterium substitution, the most specific structures of Compounds B-151 to B-195 in Group 2 are presented below as examples, and are not intended to limit the scope of rights for compounds not listed below.

[0215] The scope of the present disclosure is determined by the claims, and when substituted with deuterium, it is not limited to the compounds illustrated below, and the deuterium substitution position, deuterium substitution rate, etc. may include all variable ranges within the scope of Compounds B-1 to B-195.

[0216]

[0217]

[0218]

[0219]

[0220]

[0221]

[0222] In addition, examples in which at least one hydrogen in Compounds C-1 to C-57 listed in Group 2 is replaced by deuterium are given below, but are not limited thereto.

[0223]

[0224]

[0225] (Dn refers to the number of deuterium substitutions and represents a structure substituted by one or more deuteriums).

[0226] According to the position and substitution rate of deuterium substitution, the most specific structures of Compounds C-58 to C-72 in Group 2 are presented below as examples, and are not intended to limit the scope of rights for compounds not listed below.

[0227] The scope of the present disclosure is determined by the claims, and when deuterium is substituted, it is not limited to the compounds illustrated below, and the deuterium substitution position, deuterium substitution rate, etc. may include all variable ranges within the range of Compound C-58 to Compound C-72.

[0228]

[0229]

[0230]

[0231] The second compound is a compound having relatively strong hole characteristics and can be used together with the first compound in the light-emitting layer to improve charge mobility and stability, thereby improving light-emitting efficiency and lifetime characteristics. In addition, the charge mobility can be controlled by controlling the ratio of the third compound having hole characteristics to the first compound.

[0232] In addition, the first compound and the second compound are included in a weight ratio of, for example, about 1:9 to 9:1, and specifically, the first compound and the second compound may be included in weight ratios of 2:8 to 8:2, 3:7 to 7:3, 4:6 to 6:4, and 5:5. By including within the above range, bipolar characteristics can be achieved, thereby improving both efficiency and lifetime.

[0233] In addition to the first compound and the second compound described above, the light-emitting layer 130 may further include a third compound as a host.

[0234] The third compound may be represented by Chemical Formula 5.

[0235] [Chemical Formula 5]

[0236]

[0237] In Chemical Formula 5,

[0238] Z 4 to Z 6 are each independently N or C-L c -R c ,

[0239] Z 4 to Z 6 at least two of which are N,

[0240] L c and L 8 to L 10 are each independently a single bond, a substituted or unsubstituted C6-C20 arylene group, a substituted or unsubstituted C2-C20 heterocyclic group, or a combination thereof,

[0241] Rc is hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof,

[0242] Ar 7 to Ar 9 each independently is hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof,

[0243] Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted carbazolyl group, and

[0244] the remaining Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted dibenzofuranyl group or a substituted or unsubstituted dibenzothiophenyl group.

[0245] Depending on the substitution direction of the carbazole, the third compound can be represented by Chemical Formula 5A or Chemical Formula 5B.

[0246]

[0247]

[0248] In Chemical Formula 5A and Chemical Formula 5B,

[0249] Z 4 to Z 6 and L 8 to L 10 are the same as defined in Claim 1,

[0250] Ar 9 is a substituted or unsubstituted C6-C30 aryl group,

[0251] X 1 is O or S,

[0252] R 18 to R 23 each independently is hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof,

[0253] m18, m20, m21 and m23 are each independently one of the integers from 1 to 4, and

[0254] m19 and m22 are each independently one of the integers from 1 to 3.

[0255] In Chemical Formula 5A and Chemical Formula 5B, when two or more Rs are substituted, 18 each R 18 can be the same as or different from each other.

[0256] In Chemical Formula 5A and Chemical Formula 5B, when two or more Rs are substituted, 19 each R 19 can be the same as or different from each other.

[0257] In Chemical Formula 5A and Chemical Formula 5B, when two or more Rs are substituted, 20 each R 20 can be the same as or different from each other.

[0258] In Chemical Formula 5A and Chemical Formula 5B, when two or more Rs are substituted, 21 each R 21 can be the same as or different from each other.

[0259] In Chemical Formula 5A and Chemical Formula 5B, when two or more Rs are substituted, 22 each R 22 can be the same as or different from each other.

[0260] In Chemical Formula 5A and Chemical Formula 5B, when two or more Rs are substituted, 23 each R 23 can be the same as or different from each other.

[0261] In Chemical Formula 5A and Chemical Formula 5B, when two or more Rs are substituted, c each R c can be the same as or different from each other.

[0262] For example, in Chemical Formula 5, Ar 7 to Ar 9 can each independently be a substituted or unsubstituted phenyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted terphenyl, a substituted or unsubstituted naphthyl, a substituted or unsubstituted anthryl, a substituted or unsubstituted phenanthryl, a substituted or unsubstituted terphenylene, a substituted or unsubstituted fluorenyl, a substituted or unsubstituted carbazolyl, a substituted or unsubstituted dibenzofuranyl, or a substituted or unsubstituted dibenzothiophenyl,

[0263] Ar 7 to Ar 9 at least one of which can be a substituted or unsubstituted carbazolyl, and

[0264] the remaining Ar 7 to Ar 9At least one of them may be a substituted or unsubstituted dibenzofuranyl group or a substituted or unsubstituted dibenzothiophenyl group.

[0265] In one embodiment, the third compound is represented by Chemical Formula 5A or Chemical Formula 5B, and Ar 9 may be a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthryl group, a substituted or unsubstituted phenanthryl group, a substituted or unsubstituted terphenylene group, or a substituted or unsubstituted fluorenyl group.

[0266] The third compound may be, for example, one selected from the compounds listed in Group 3.

[0267] [Group 3]

[0268]

[0269]

[0270]

[0271]

[0272]

[0273]

[0274]

[0275]

[0276]

[0277] A composition for an organic optoelectronic device according to an embodiment of the present invention includes a first compound having relatively strong electron characteristics, a second compound having relatively strong hole characteristics, and a third compound having excellent hole and electron injection and transport capabilities, all of which are in a light-emitting layer, thereby enabling an organic optoelectronic device having excellent efficiency while significantly reducing a driving voltage to be realized.

[0278] In particular, by adding a third compound having excellent electron characteristics, the problem of an increase in driving voltage that may occur when only the first compound and the second compound are included can be solved, thereby effectively improving the power efficiency performance of the device. In addition, by using three types of hosts, the optimal position and width of the light-emitting region can be adjusted, thereby effectively improving efficiency and lifetime.

[0279] The first compound and the second compound may be included in a weight ratio of, for example, 90:10 to 10:90, and specifically, the first compound and the second compound may be included in a weight ratio of 90:10 to 10:90, 85:15 to 15:85, 80:20 to 20:80, 70:30 to 30:70, 60:40 to 40:60, 50:50. Preferably, a mixture of the first compound and the second compound and the third compound may be included in a weight ratio of 90:10, 85:15, 80:20 or 70:30.

[0280] By including within the above ranges, bipolar characteristics can be more effectively achieved, which not only improves efficiency and lifespan but also significantly reduces the driving voltage.

[0281] In addition to the first compound, the second compound, and the third compound described above, the light-emitting layer 130 may further include one or more compounds as a host.

[0282] For example, a dopant may be further included. The dopant may be, for example, a phosphorescent dopant, such as a red, green, or blue phosphorescent dopant, and may be, for example, a green phosphorescent dopant.

[0283] The dopant is a material that is mixed in a small amount with a composition containing the first compound, the second compound, and the third compound to cause luminescence, and is generally a material such as a metal complex that emits light by being excited to a triplet state or more states multiple times. The dopant may be, for example, an inorganic, organic, or organic / inorganic compound, and one or more types thereof may be used.

[0284] Examples of the dopant may be phosphorescent dopants, and examples of the phosphorescent dopants may be organometallic compounds including Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, Tm, Fe, Co, Ni, Ru, Rh, Pd, or combinations thereof. The phosphorescent dopant may be, for example, a compound represented by Chemical Formula Z, but is not limited thereto.

[0285] [Chemical Formula Z]

[0286] L 11 MX 2

[0287] In Chemical Formula Z, M is a metal, and L 11 and X 2 are the same or different and are ligands that form a complex with M.

[0288] M may be, for example, Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, Tm, Fe, Co, Ni, Ru, Rh, Pd, or combinations thereof, and L 11 and X 2It can be, for example, a bidentate ligand.

[0289] The ligand represented by L 11 and X 2 Examples of the ligand can be selected from the chemical formulas listed in Group A, but are not limited thereto.

[0290] [Group A]

[0291]

[0292] In Group A,

[0293] R 300 to R 302 are each independently hydrogen, deuterium, a C1-C30 alkyl group which may or may not be substituted with a halogen, a C6-C30 aryl group which may or may not be substituted with a C1-C30 alkyl group, or a halogen, and

[0294] R 303 to R 324 are each independently hydrogen, deuterium, a halogen, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted C1-C30 alkoxy group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C2-C30 alkenyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C1-C30 heteroaryl group, a substituted or unsubstituted C1-C30 amino group, a substituted or unsubstituted C6-C30 arylamino group, SF 5 , a trialkylsilyl group having a substituted or unsubstituted C1-C30 alkyl group, a dialkylarylsilyl group having a substituted or unsubstituted C1-C30 alkyl group and a C6-C30 aryl group, or a triarylsilyl group having a substituted or unsubstituted C6-C30 aryl group.

[0295] As an example, it can include a dopant represented by Chemical Formula IV.

[0296] [Chemical Formula IV]

[0297]

[0298] In Chemical Formula IV,

[0299] R 101 to R 116 are each independently hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C20 aryl group, or -SiR 132 R 133 R 134 ,

[0300] R 132 to R 134 are each independently a C1-C6 alkyl group,

[0301] R 101 to R 116 at least one of which is a functional group represented by Chemical Formula IV-1,

[0302] L 100 is a bidentate ligand of a monovalent anion and is a ligand coordinated with iridium through a lone pair of electrons of a carbon or heteroatom, and

[0303] n1 and n2 are each independently any one of integers from 0 to 3, and n1 + n2 is any one of integers from 1 to 3,

[0304] [Chemical Formula IV-1]

[0305]

[0306] In Chemical Formula IV-1,

[0307] R 135 to R 139 are each independently hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C20 aryl group or -SiR 132 R 133 R 134 , and

[0308] * represents a moiety attached to a carbon atom.

[0309] As an example, it may include a dopant represented by Chemical Formula Z-1.

[0310] [Chemical Formula Z-1]

[0311]

[0312] In Chemical Formula Z-1, rings A, B, C, and D independently represent a 5-membered or 6-membered carbocyclic or heterocyclic ring;

[0313] R A , R B , R C and R D independently represent mono-, di-, tri- or tetra-substituted or unsubstituted;

[0314] L B , L C and L D are each independently selected from a direct bond, BR, NR, PR, O, S, Se, C=O, S=O, SO 2 , CRR', SiRR', GeRR' and combinations thereof;

[0315] When nA is 1, L ESelected from direct bond, BR, NR, PR, O, S, Se, C═O, S═O, SO 2 , CRR', SiRR', GeRR' and combinations thereof; when nA is 0, L E does not exist; and

[0316] R A , R B , R C , R D , R and R' are each independently selected from hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxyl, ester, nitrile, isonitrile, thioalkyl, sulfinyl, sulfonyl, phosphino and combinations thereof; any adjacent R A , R B , R C , R D , R and R' are optionally joined to each other to provide a ring; X B , X C , X D and X E are each independently selected from carbon and nitrogen; and Q 1 , Q 2 , Q 3 and Q 4 each represents oxygen or a direct bond.

[0317] The dopant according to one embodiment may be a platinum complex and may be represented, for example, by Chemical Formula V.

[0318] [Chemical Formula V]

[0319]

[0320] In Chemical Formula V,

[0321] X 100 is selected from O, S and NR 131 ,

[0322] R 117 to R 131 are each independently hydrogen, deuterium, substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C6-C20 aryl or -SiR 132 R 133 R 134 ,

[0323] R 132 to R 134 are each independently C1-C6 alkyl, and

[0324] R 117 to R131 At least one of them is -SiR 132 R 133 R 134 or tert-butyl.

[0325] Hereinafter, an organic optoelectronic device using the above-described composition for an organic optoelectronic device is described.

[0326] The organic optoelectronic device can be a suitable device that converts electrical energy into light energy and vice versa. For example, an organic optoelectronic device, an organic light-emitting diode, an organic solar cell, or an organic photoreceptor drum.

[0327] Herein, with reference to the drawings, an organic light-emitting diode as an example of an organic optoelectronic device is described.

[0328] Figure 1 is a cross-sectional view showing an organic light-emitting diode according to an embodiment.

[0329] Referring to Figure 1 , an organic light-emitting diode 100 according to an embodiment includes an anode 120 and a cathode 110 facing each other and an organic layer 105 disposed between the anode 120 and the cathode 110.

[0330] The anode 120 can be made of a conductor having a large work function to assist hole injection, and can be, for example, a metal, a metal oxide, and / or a conductive polymer. The anode 120 can be, for example, a metal such as nickel, platinum, vanadium, chromium, copper, zinc, gold, etc. or an alloy thereof; a metal oxide such as zinc oxide, indium oxide, indium tin oxide (ITO), indium zinc oxide (IZO), etc.; a combination of a metal and an oxide such as ZnO and Al or SnO 2 and Sb; a conductive polymer such as poly(3-methylthiophene), poly(3,4-(ethylenedioxy)thiophene) (PEDOT), polypyrrole, and polyaniline, but not limited thereto.

[0331] The cathode 110 can be made of a conductor having a small work function to assist electron injection, and can be, for example, a metal, a metal oxide, and / or a conductive polymer. The cathode 110 can include a metal such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin, lead, cesium, barium, or an alloy thereof; a multilayer structure material such as LiF / Al, LiO 2 / Al, LiF / Ca, and BaF 2 / Ca, but not limited thereto.

[0332] The organic layer 105 can contain the above-described composition for an organic optoelectronic device.

[0333] The above organic layer 105 can be formed by a dry film-forming method such as chemical vapor deposition.

[0334] The organic layer 105 may include a light-emitting layer 130, and the light-emitting layer 130 may contain the above-described composition for an organic optoelectronic device.

[0335] The composition for an organic optoelectronic device further including a dopant may be, for example, a green light-emitting composition.

[0336] The light-emitting layer 130 may contain, for example, the above-described composition for an organic optoelectronic device as a phosphorescent host.

[0337] In addition to the light-emitting layer, the organic layer may further include a charge transport region.

[0338] The charge transport region may be, for example, a hole transport region 140.

[0339] The hole transport region 140 may further improve the hole injection and / or hole mobility between the anode 120 and the light-emitting layer 130 and block electrons.

[0340] Specifically, the hole transport region 140 may include a hole transport layer between the anode 120 and the light-emitting layer 130 and a hole transport auxiliary layer between the light-emitting layer 130 and the hole transport layer, and may include at least one of the compounds in Group B in at least one of the hole transport layer and the hole transport auxiliary layer.

[0341] [Group B]

[0342]

[0343]

[0344]

[0345]

[0346]

[0347] (Dn refers to the number of deuterium substitutions and represents a structure substituted with one or more deuteriums).

[0348] In the hole transport region, in addition to the compounds described above, known compounds disclosed in US5061569A, JP1993-009471A, WO1995-009147A1, JP1995-126615A, JP1998-095973A, etc. and compounds having similar structures may also be used.

[0349] In addition, the charge transport region may be, for example, an electron transport region 150.

[0350] The electron transport region 150 can further improve the electron injection and / or electron mobility between the cathode 110 and the light-emitting layer 130 and block holes.

[0351] Specifically, the electron transport region 150 can include an electron transport layer between the cathode 110 and the light-emitting layer 130 and an electron transport auxiliary layer between the light-emitting layer 130 and the electron transport layer, and can include at least one of the compounds in Group C in at least one of the electron transport layer and the electron transport auxiliary layer.

[0352] [Group C]

[0353]

[0354]

[0355]

[0356]

[0357] One embodiment may be an organic light-emitting diode including a light-emitting layer as an organic layer.

[0358] Another embodiment may be an organic light-emitting diode including a light-emitting layer and a hole transport region as organic layers.

[0359] Another embodiment may be an organic light-emitting diode including a light-emitting layer and an electron transport region as organic layers.

[0360] As Figure 1 shown, another embodiment of the present invention may provide an organic light-emitting diode including a hole transport region 140 and an electron transport region 150 as organic layers 105 in addition to the light-emitting layer 130.

[0361] On the other hand, in addition to the light-emitting layer, the organic light-emitting diode may further include an electron injection layer (not shown), a hole injection layer (not shown), etc. as organic layers.

[0362] The organic light-emitting diode 100 can be manufactured by: forming an anode or a cathode on a substrate, then forming an organic layer by a dry film method (such as vacuum deposition, sputtering, plasma plating, and ion plating), and forming a cathode or an anode thereon.

[0363] The organic light-emitting diode can be applied to an organic light-emitting display device.

[0364] It should be understood that the present invention is not limited to the disclosed embodiments. On the contrary, it is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.

Claims

1. A composition for an organic optoelectronic device, comprising a first compound; a second compound; and a third compound, wherein, the first compound is represented by Chemical Formula 1, the second compound is represented by Chemical Formula 2 or a combination of Chemical Formula 3 and Chemical Formula 4, and the third compound is represented by Chemical Formula 5: [Chemical Formula 1] In Chemical Formula 1, Z 1 to Z 3 each independently is N or C-L a -R a , Z 1 to Z 3 at least two of which are N, L a and L 1 to L 3 each independently represents a single bond, a substituted or unsubstituted C6-C20 arylene group, a substituted or unsubstituted C2-C20 heterocyclic group, or a combination thereof, R 1 to R 3 each independently is hydrogen, deuterium, cyano, substituted or unsubstituted C1-C10 alkyl, substituted or unsubstituted C6-C30 aryl, substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof Ar 1 and Ar 2 each independently is a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof, m1 and m2 are each independently one of the integers from 1 to 4, and m3 is one of the integers from 1 to 3; [Chemical Formula 2] In Chemical Formula 2, Ar 3 and Ar 4 each independently is a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group or a substituted or unsubstituted dibenzosilolyl group, L 4 and L 5 each independently is a single bond or a substituted or unsubstituted C6-C20 arylene group, R 7 to R 11 each independently represents hydrogen, deuterium, cyano, halogen, substituted or unsubstituted amino, substituted or unsubstituted C1-C30 alkyl, substituted or unsubstituted silyl, substituted or unsubstituted C6-C30 aryl or substituted or unsubstituted C2-C30 heterocyclic group, m8 and m9 are each independently one of the integers from 1 to 3, m7, m10 and m11 are each independently one of the integers from 1 to 4, and n is one of the integers from 0 to 2; In Chemical Formula 3 and Chemical Formula 4, Ar 5 and Ar 6 each independently is a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted pyridyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, a substituted or unsubstituted dibenzothiophenyl group, or a substituted or unsubstituted dibenzosilolyl group, a in Chemical Formula 3 1 * to a 4 * are each independently a linking carbon (C) or C-L b -R b , a 1 * to a 4 * Two adjacent ones of * are each connected to * of Chemical Formula 4 In a 1 * to a 4 * Among them, the remaining two that are not connected to the * in Chemical Formula 4 are each independently C-L b -R b , L b 、L 6 and L 7 each independently represents a single bond or a substituted or unsubstituted C6-C20 arylene group, and R b 、R 12 and R 13 each independently is hydrogen, deuterium, cyano, halogen, a substituted or unsubstituted amino group, a substituted or unsubstituted C1-C30 alkyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted C6-C30 aryl group, or a substituted or unsubstituted C2-C30 heterocyclic group; [Chemical Formula 5] In Chemical Formula 5, Z 4 from Z 6 each independently is N or C-L c -R c , Z 4 from Z 6 at least two of which are N, L c and L 8 to L 10 each independently represents a single bond, a substituted or unsubstituted C6-C20 arylene group, a substituted or unsubstituted C2-C20 heterocyclic group, or a combination thereof R c is hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof, Ar 7 to Ar 9 each independently is hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted carbazolyl group, and The remaining Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted dibenzofuranyl group or a substituted or unsubstituted dibenzothiophenyl group.

2. The composition for an organic optoelectronic device according to claim 1, wherein the first compound is represented by any one of Chemical Formulas 1-1 to 1-12: In Chemical Formulas 1-1 to 1-12, Z 1 from Z to 3 、R 1 from R to 3 、L 2 、L 3 、Ar 1 、Ar 2 and m1 to m3 are the same as those defined in claim 1, R 4 to R 6 and R 1 to R 3 is the same as the definition of, and m4 to m6 are each independently one of the integers from 1 to 4.

3. The composition for an organic optoelectronic device according to claim 2, wherein the first compound is represented by Chemical Formula 1-3.

4. The composition for an organic optoelectronic device according to claim 1, wherein the second compound is represented by any one of Chemical Formulas 2-6, 2-8 and 3C: In Chemical Formulas 2-6, 2-8, and 3C, L 4 to L 7 、Ar 3 to Ar 6 、R 7 to R 10 、R 12 、R 13 、m7 to m10, m12, and m13 are the same as those defined in claim 1, L b1 and L b2 is the same as L in claim 1, and b identical, and R b1 and R b2 is the same as R in claim 1 b identical.

5. The composition for an organic optoelectronic device according to claim 1, wherein the third compound is represented by Chemical Formula 5A or Chemical Formula 5B: In Chemical Formulas 5A and 5B, Z 4 from Z 6 and L 8 to L 10 the same as defined in claim 1 Ar 9 is a substituted or unsubstituted C6-C30 aryl group, X 1 is O or S, R 18 to R 23 each independently is hydrogen, deuterium, a substituted or unsubstituted C1-C10 alkyl group, a substituted or unsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30 heterocyclic group, or a combination thereof m18, m20, m21 and m23 are each independently one of the integers from 1 to 4, and m19 and m22 are each independently one of the integers from 1 to 3.

6. The composition for an organic optoelectronic device according to claim 1, wherein In Chemical Formula 5, Ar 7 to Ar 9 each independently represents a substituted or unsubstituted phenyl group, a substituted or unsubstituted biphenyl group, a substituted or unsubstituted terphenyl group, a substituted or unsubstituted naphthyl group, a substituted or unsubstituted anthracenyl group, a substituted or unsubstituted phenanthrenyl group, a substituted or unsubstituted terphenylene group, a substituted or unsubstituted fluorenyl group, a substituted or unsubstituted carbazolyl group, a substituted or unsubstituted dibenzofuranyl group, or a substituted or unsubstituted dibenzothiophenyl group, Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted carbazolyl group, and The remaining Ar 7 to Ar 9 at least one of which is a substituted or unsubstituted dibenzofuranyl group or a substituted or unsubstituted dibenzothiophenyl group.

7. An organic optoelectronic device, comprising an anode and a cathode facing each other, and at least one organic layer between the anode and the cathode, wherein, the organic layer contains the composition for an organic optoelectronic device according to any one of claims 1 to 6.

8. The organic optoelectronic device according to claim 7, wherein the organic layer includes a light-emitting layer, and the light-emitting layer contains the composition for an organic optoelectronic device.

9. The organic optoelectronic device according to claim 7, wherein the first compound, the second compound and the third compound are each used as the host of the light-emitting layer.

10. The organic optoelectronic device according to claim 7, wherein a mixture of the first compound and the second compound and the third compound are included in a weight ratio of 90:10 to 40:

60.

11. The organic optoelectronic device according to claim 9, wherein the composition for an organic optoelectronic device further contains a phosphorescent dopant.

12. The organic optoelectronic device according to claim 11, wherein the composition for an organic optoelectronic device is a green light-emitting composition.

13. A display device, comprising the organic optoelectronic device according to claim 7.

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