ORGANIC LIGHT-EMITTING DEVICE

Abstract

An organic light-emitting device including a first electrode, a second electrode facing the first electrode, and an emission layer disposed between the first electrode and the second electrode, wherein the emission layer includes a first material not including an electron transport moiety, a second material including at least one electron transport moiety, a third material having reorganization energy of about 0.4 eV or more, and a light-emitting material, wherein the first material, the second material, the third material, and the light-emitting material are different from one another, and wherein a ratio of a light-emitting component emitted from the light-emitting material to a total of light-emitting components emitted from the emission layer is about 90% or more.

Description

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to Korean Patent Application No. 10-2017-0154975, filed on Nov. 20, 2017, in the Korean Intellectual Property Office, and all the benefits accruing therefrom under 35 U.S.C. § 119, the content of which is incorporated herein in its entirety by reference.

BACKGROUND

1. Field

The present disclosure relates to an organic light-emitting device.

2. Description of the Related Art

Organic light-emitting devices (OLEDs) are self-emission devices that produce full-color images, and that also have wide viewing angles, high contrast ratios, short response times, and excellent characteristics in terms of brightness, driving voltage, and response speed, compared to devices in the art.

In an example, an organic light-emitting device includes an anode, a cathode, and an organic layer disposed between the anode and the cathode, wherein the organic layer includes an emission layer. A hole transport region may be disposed between the anode and the emission layer, and an electron transport region may be disposed between the emission layer and the cathode. Holes provided from the anode may move toward the emission layer through the hole transport region, and electrons provided from the cathode may move toward the emission layer through the electron transport region. The holes and the electrons recombine in the emission layer to produce excitons. These excitons transit from an excited state to a ground state, thereby generating light.

Various types of organic light emitting devices are known. However, there still remains a need in OLEDs having low driving voltage, high efficiency, high brightness, and long lifespan.

SUMMARY

Aspects of the present disclosure provide an organic light-emitting device with a long lifespan, which includes a first material, a second material, a third material, and a light-emitting material.

Additional aspects will be set forth in part in the description which follows and, in part, will be apparent from the description, or may be learned by practice of the presented embodiments.

An aspect provides an organic light-emitting device including:

a first electrode;

a second electrode facing the first electrode; and

an emission layer between the first electrode and the second electrode,

wherein the emission layer includes a first material, a second material, a third material, and a light-emitting material,

the first material does not include an electron transport moiety,

the second material includes at least one electron transport moiety,

the third material has reorganization energy of about 0.4 eV or more,

the first material, the second material, the third material, and the light-emitting material are different from one another, and

a ratio of a light-emitting component emitted from the light-emitting material to a total of light-emitting components emitted from the emission layer is 90% or more.

BRIEF DESCRIPTION OF THE DRAWING

These and/or other aspects will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the FIGURE which is a schematic view of an organic light-emitting device according to an embodiment.

DETAILED DESCRIPTION

Reference will now be made in detail to embodiments, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to like elements throughout. In this regard, the present embodiments may have different forms and should not be construed as being limited to the descriptions set forth herein. Accordingly, the embodiments are merely described below, by referring to the figures, to explain aspects of the present description. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Expressions such as “at least one of,” when preceding a list of elements, modify the entire list of elements and do not modify the individual elements of the list.

It will be understood that when an element is referred to as being “on” another element, it can be directly in contact with the other element or intervening elements may be present therebetween. In contrast, when an element is referred to as being “directly on” another element, there are no intervening elements present.

It will be understood that, although the terms first, second, third etc. may be used herein to describe various elements, components, regions, layers, and/or sections, these elements, components, regions, layers, and/or sections should not be limited by these terms. These terms are only used to distinguish one element, component, region, layer, or section from another element, component, region, layer, or section. Thus, a first element, component, region, layer, or section discussed below could be termed a second element, component, region, layer, or section without departing from the teachings of the present embodiments.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. As used herein, the singular forms “a,” “an,” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise.

The term “or” means “and/or.” It will be further understood that the terms “comprises” and/or “comprising,” or “includes” and/or “including” when used in this specification, specify the presence of stated features, regions, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components, and/or groups thereof.

Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this general inventive concept belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and the present disclosure, and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.

Exemplary embodiments are described herein with reference to cross section illustrations that are schematic illustrations of idealized embodiments. As such, variations from the shapes of the illustrations as a result, for example, of manufacturing techniques and/or tolerances, are to be expected. Thus, embodiments described herein should not be construed as limited to the particular shapes of regions as illustrated herein but are to include deviations in shapes that result, for example, from manufacturing. For example, a region illustrated or described as flat may, typically, have rough and/or nonlinear features. Moreover, sharp angles that are illustrated may be rounded. Thus, the regions illustrated in the figures are schematic in nature and their shapes are not intended to illustrate the precise shape of a region and are not intended to limit the scope of the present claims.

“About” or “approximately” as used herein is inclusive of the stated value and means within an acceptable range of deviation for the particular value as determined by one of ordinary skill in the art, considering the measurement in question and the error associated with measurement of the particular quantity (i.e., the limitations of the measurement system). For example, “about” can mean within one or more standard deviations, or within ±30%, 20%, 10%, 5% of the stated value.

In an embodiment, an organic light-emitting device is provided. The organic light-emitting device according to an embodiment may include a first electrode, a second electrode facing the first electrode, and an emission layer between the first electrode and the second electrode, wherein the emission layer may include a first material, a second material, a third material, and a light-emitting material.

The first material does not include an electron transport moiety, and the second material may include at least one electron transport moiety.

For example, the first material may include at least one π electron-depleted nitrogen-free cyclic group and may not include an electron transport moiety, and the second material may include at least one π electron-depleted nitrogen-free cyclic group and at least one electron transport moiety. The electron transport moiety may be selected from a cyano group, a π electron-depleted nitrogen-containing cyclic group, and a group represented by one of Formulae illustrated below:

In Formulae, *, *′, and *″ each indicate a binding site to a neighboring atom.

The “π electron-depleted nitrogen-containing cyclic group” means a group including a cyclic group having at least one *—N═*′ moiety and may be, for example, an imidazole group, a pyrazole group, a thiazole group, an isothiazole group, an oxazole group, an isoxazole group, a pyridine group, a pyrazine group, a pyridazine group, a pyrimidine group, an indazole group, a purine group, a quinoline group, an isoquinoline group, a benzoquinoline group, a benzoisoquinoline group, a phthalazine group, a naphthyridine group, a quinoxaline group, a benzoquinoxaline group, a quinazoline group, a cinnoline group, a phenanthridine group, a phenanthroline group, a phenazine group, a benzimidazole group, an iso-benzothiazole group, a benzoxazole group, an isobenzoxazole group, a triazole group, a tetrazole group, an oxadiazole group, a triazine group, a thiadiazole group, an imidazopyridine group, an imidazopyrimidine group, an azaindene group, an azaindole group, an azabenzofuran group, an azabenzothiophene group, an azabenzosilole group, an azafluorene group, an azacarbazole group, an azadibenzofuran group, an azadibenzothiophene group, an azadibenzosilole group, or a condensed group condensed with at least one of these groups and a cyclic group.

The π electron-depleted nitrogen-free cyclic group may be, for example, a benzene group, a heptalene group, an indene group, a naphthalene group, an azulene group, a heptalene group, an indacene group, an acenaphthylene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentacene group, a hexacene group, a pentaphene group, a rubicene group, a coronene group, an ovalene group, a pyrrole group, an iso-indole group, an indole group, a furan group, a thiophene group, a benzofuran group, a benzothiophene group, a benzosilole group, a benzocarbazole group, a dibenzocarbazole group, a dibenzofuran group, a dibenzothiophene group, a dibenzothiophene sulfone group, a carbazole group, a dibenzosilole group, an indeno carbazole group, an indolocarbazole group, a benzofurocarbazole group, a benzothienocarbazole group, a benzosilolocarbazole group, a triindolobenzene group, an acridine group, or a dihydroacridine group, but embodiments of the present disclosure are not limited thereto.

In an embodiment, the first material may include at least one of a compound represented by Formula H-1(1), a compound represented by Formula H-1(2), and a compound represented by Formula H-1(3):

A₄₁ to A₄₄ in Formulae H-1(1) to H-1(3) may each independently be a benzene group, a naphthalene group, an indene group, an indole group, a benzofuran group, a benzothiophene group, a benzosilole group, a fluorene group, a carbazole group, a dibenzofuran group, a dibenzothiophene group, or a dibenzosilole group.

For example, A₄₁ to A₄₄ may each independently be a benzene group, a fluorene group, a carbazole group, a dibenzofuran group, a dibenzothiophene group, or a dibenzosilole group, wherein at least one of A₄₁ and A₄₂ may be a benzene group, and at least one of A₄₃ and A₄₄ may be a benzene group.

In Formulae H-1(1) to H-1(3),

X₄₁ may be N-[(L₄₁₁)_c411-Z₄₁₁], C(Z₄₁₅)(Z₄₁₆), O, or S,

X₄₂ may be a single bond, N-[(L₄₁₂)_c412-Z₄₁₂], C(Z₄₁₇)(Z₄₁₈), O, or S,

X₄₃ may be N-[(L₄₁₃)_c413-Z₄₁₃], C(Z₄₁₉)(Z₄₂₀), O, or S, and

X₄₄ may be a single bond, N-[(L₄₁₄)_c414-Z₄₁₄], C(Z₄₂₁)(Z₄₂₂), O, or S.

L₄₀₁ and L₄₁₁ to L₄₁₄ may each independently be selected from:

a single bond; and

a π electron-depleted nitrogen-free cyclic group, unsubstituted or substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, a tetraphenyl group, and —Si(Q₄₀₁)(Q₄₀₂)(Q₄₀₃) (for example, a benzene group, a heptalene group, an indene group, a naphthalene group, an azulene group, a heptalene group, an indacene group, an acenaphthylene group, a fluorene group, a spiro-bifluorene group, a benzofluorene group, a dibenzofluorene group, a phenalene group, a phenanthrene group, an anthracene group, a fluoranthene group, a triphenylene group, a pyrene group, a chrysene group, a naphthacene group, a picene group, a perylene group, a pentacene group, a hexacene group, a pentaphene group, a rubicene group, a coronene group, an ovalene group, a pyrrole group, an isoindole group, an indole group, a furan group, a thiophene group, a benzofuran group, a benzothiophene group, a benzosilole group, a benzocarbazole group, a dibenzocarbazole group, a dibenzofuran group, a dibenzothiophene group, a dibenzothiophene sulfone group, a carbazole group, a dibenzosilole group, an indeno carbazole group, an indolocarbazole group, a benzofurocarbazole group, a benzothienocarbazole group, a benzosilolocarbazole group, a triindolobenzene group, an acridine group, or a dihydroacridine group, each unsubstituted or substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, a tetraphenyl group, and —Si(Q₄₀₁)(Q₄₀₂)(Q₄₀₃)).

a401 and c411 to c414 indicate the number of groups L₄₀₁ and groups L₄₁₁ to L₄₁₄, respectively, and may each independently be an integer from 1 to 10, wherein, when a401 is two or more, two or more groups L₄₀₁ may be identical to or different from each other, when c411 is two or more, two or more groups L₄₁₁ may be identical to or different from each other, when c412 is two or more, two or more groups L₄₁₂ may be identical to or different from each other, when c413 is two or more, two or more groups L₄₁₃ may be identical to or different from each other, and when c414 is two or more, two or more groups L₄₁₄ may be identical to or different from each other.

For example, a401 and c411 to c414 may each independently be 1, 2, or 3.

Z₄₁ to Z₄₄ and Z₄₁₁ to Z₄₂₂ may each independently be selected from:

hydrogen, deuterium, a C₁-C₁₀ alkyl group, and a C₁-C₁₀ alkoxy group; and

a π electron-depleted nitrogen-free cyclic group, unsubstituted or substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, a tetraphenyl group, and —Si(Q₄₀₁)(Q₄₀₂)(Q₄₀₃) (for example, a phenyl group, a biphenyl group, a terphenyl group, a tetraphenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, an isoindolyl group, an indolyl group, a furanyl group, a thiophenyl group, a benzofuranyl group, a benzothiophenyl group, a benzosilolyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a carbazolyl group, a dibenzosilolyl group, an indeno carbazolyl group, an indolocarbazolyl group, a benzofurocarbazolyl group, a benzothienocarbazolyl group, a benzosilolocarbazolyl group, an acridinyl group, or a dihydroacridinyl group, each unsubstituted or substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, a tetraphenyl group, and —Si(Q₄₀₁)(Q₄₀₂)(Q₄₀₃)).

b41 to b44 indicate the number of groups Z₄₁ to Z₄₄, respectively, and may each independently be 1, 2, 3, or 4. When b41 is two or more, two or more groups Z₄₁ may be identical to or different from each other, when b42 is two or more, two or more groups Z₄₂ may be identical to or different from each other, when b43 is two or more, two or more groups Z₄₃ may be identical to or different from each other, and when b44 is two or more, two or more groups Z₄₄ may be identical to or different from each other.

For example, b41 to b44 may each independently be 1 or 2, but embodiments of the present disclosure are not limited thereto.

Q₄₀₁ to Q₄₀₃ may each independently be hydrogen, deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, or a tetraphenyl group.

In an embodiment, L₄₀₁ and L₄₁₁ to L₄₁₄ may each independently be selected from:

a single bond; and

a benzene group, a fluorene group, a dibenzofuran group, a dibenzothiophene group, a carbazole group, a dibenzosilole group, an indeno carbazole group, an indolocarbazole group, a benzofurocarbazole group, a benzothienocarbazole group, a benzosilolocarbazole group, an acridine group, or a dihydroacridine group, each unsubstituted or substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, and a tetraphenyl group, and

Z₄₁ to Z₄₄ and Z₄₁₁ to Z₄₂₂ may each independently be selected from:

hydrogen, deuterium, a C₁-C₁₀ alkyl group, and a C₁-C₁₀ alkoxy group; and

a phenyl group, a biphenyl group, a terphenyl group, a tetraphenyl group, a fluorenyl group, a dibenzocarbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a carbazolyl group, a dibenzosilolyl group, an indenocarbazolyl group, an indolocarbazolyl group, a benzofurocarbazolyl group, a benzothienocarbazolyl group, a benzosilolocarbazolyl group, an acridinyl group, or a dihydroacridinyl group, each unsubstituted or substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, and a tetraphenyl group,

but embodiments of the present disclosure are not limited thereto.

In an embodiment, the first material may include at least one compound selected from Compounds H1 to H32, but embodiments of the present disclosure are not limited thereto:

In one or more embodiments, the second material may include at least one cyano group.

In one or more embodiments, the second material may include at least one cyano group and at least one carbazole ring.

In one or more embodiments, the second material may include a compound represented by Formula E-1:

[Ar₃₀₁]_xb11-[(L₃₀₁)_xb1-R₃₀₁]_xb21.   Formula E-1

In Formula E-1,

Ar₃₀₁ may be selected from a substituted or unsubstituted C₅-C₆₀ carbocyclic group and a substituted or unsubstituted C₁-C₆₀ heterocyclic group,

xb1 1 may be 1, 2, or 3, and

L₃₀₁ may be selected from a single bond, a group represented by one of Formulae illustrated below, a substituted or unsubstituted C₅-C₆₀ carbocyclic group, and a substituted or unsubstituted C₁-C₆₀ heterocyclic group, and *, *′, and *″ in Formulae each indicate a binding site to a neighboring atom:

xb1 may be an integer from 1 to 5,

R₃₀₁ may be selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₃₀₁)(Q₃₀₂)(Q₃₀₃), —N(Q₃₀₁)(Q₃₀₂), —B(Q₃₀₁)(Q₃₀₂), —C(═O)(Q₃₀₁), —S(═O)₂(Q₃₀₁), —S(═O)(Q₃₀₁), —P(═O)(Q₃₀₁)(Q₃₀₂), and —P(═S)(Q₃₀₁)(Q₃₀₂),

xb21 may be an integer from 1 to 5,

Q₃₀₁ to Q₃₀₃ may each independently be selected from a C₁-C₁₀ alkyl group, a alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group, and

at least one of <Condition 1> to <Condition 3> is satisfied:

Condition 1

at least one of Ar₃₀₁, L₃₀₁, and R₃₀₁ in Formula E-1 includes a π electron-depleted nitrogen-containing cyclic group;

Condition 2

L₃₀₁ in Formula E-1 is a group represented by one of Formulae illustrated below:

and

Condition 3

R₃₀₁ in Formula E-1 is selected from a cyano group, —S(═O)₂(Q₃₀₁), —S(═O)(Q₃₀₁), —P(═O)(Q₃₀₁)(Q₃₀₂), and —P(═S)(Q₃₀₁)(Q₃₀₂).

In one or more embodiments, the second material may include at least one of a compound represented by Formula E-1(1), a compound represented by Formula E-1(2), and a compound represented by Formula E-1(3):

Z₁ to Z₆ in Formulae E-1(1) to E-1(3) may each independently be:

hydrogen, deuterium, or a cyano group (CN); or

a C₁-C₂₀ alkyl group, a phenyl group, a biphenyl group, a terphenyl group, a dibenzofuranyl group, or a dibenzothiophenyl group, each unsubstituted or substituted with at least one selected from deuterium, a cyano group, a C₁-C₂₀ alkyl group, a phenyl group, and a biphenyl group.

For example, Z₁ to Z₆ in Formulae E-1(1) to E-1(3) may each independently be:

hydrogen, deuterium, or a cyano group; or

a C₃-C₁₀ alkyl group, a phenyl group, a biphenyl group, a terphenyl group, a dibenzofuranyl group, or a dibenzothiophenyl group, each unsubstituted or substituted with at least one selected from deuterium, a cyano group, a C₃-C₁₀ alkyl group, a phenyl group, and a biphenyl group.

In an embodiment, Z₁ to Z₆ in Formulae E-1(1) to E-1(3) may each independently be:

hydrogen, deuterium, or a cyano group; or

an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, a biphenyl group, or a terphenyl group, each unsubstituted or substituted with at least one selected from deuterium, a cyano group, an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, and a biphenyl group.

b1 to b6 in Formulae E-1(1) to E-1(3) indicate the number of groups Z₁ to Z₆, respectively, and may each independently be 1, 2, or 3. When b1 to b6 are two or more, two or more groups Z₁ to Z₆ are identical to or different from each other, respectively.

In Formulae E-1(1) to E-1(3), at least one of groups Z₁ in the number of b1, groups Z₂ in the number of b2, groups Z₃ in the number of b3, groups Z₄ in the number of b4, groups Z₅ in the number of b5, and groups R₆ in the number of b6 may be a cyano group. That is, Formulae Formula E-1(1) to E-1(3) essentially includes at least one cyano group.

For example, the number of cyano groups included in the compound represented by Formula E-1(1), the number of cyano groups included in the compound represented by Formula E-1(2), and the number of cyano groups included in the compound represented by Formula E-1(3) may each independently be 1, 2, or 3, but embodiments of the present disclosure are not limited thereto.

In an embodiment, in Formulae E-1(1) to E-1(3),

at least one of groups Z₁ in the number of b1 and groups Z₂ in the number of b2 may be a cyano group,

at least one of groups Z₃ in the number of b3 and groups Z₄ in the number of b4 may be a cyano group,

at least one of groups Z₅ in the number of b5 and groups Z₆ in the number of b6 may be a cyano group,

at least one of groups Z₁ in the number of b1 and groups Z₂ in the number of b2 may be a cyano group, and at least one of groups Z₃ in the number of b3 and groups Z₄ in the number of b4 may be a cyano group,

at least one of groups Z₁ in the number of b1 and groups Z₂ in the number of b2 may be a cyano group, and at least one of groups Z₅ in the number of b5 and groups Z₆ in the number of b6 may be a cyano group,

at least one of groups Z₃ in the number of b3 and groups Z₄ in the number of b4 may be a cyano group, and at least one of groups Z₅ in the number of b5 and groups Z₆ in the number of b6 may be a cyano group, or

at least one of groups Z₁ in the number of b1 and groups Z₂ in the number of b2 may be a cyano group, at least one of groups Z₃ in the number of b3 and groups Z₄ in the number of b4 may be a cyano group, and at least one of groups Z₅ in the number of b5 and groups Z₆ in the number of b6 may be a cyano group.

X₂₁ and X₂₂ in Formulae E-1(1) to E-1(3) may each independently be O or S, and m may be 0 or 1.

In an embodiment, a group represented by

in Formulae E-1(1) to E-1(3) may be one of groups represented by Formulae PO1 to PO25, PM1 to PM25, PP1 to PP18, MO1 to MO37, MM1 to MM37, MP1 to MP25, OO1 to OO37, OM1 to OM37, OP1 to OP25, O1 to O16, M1 to M16, and P1 to P9:

Z₁₀ to Z₁₉ in Formulae PO1 to PO25, PM1 to PM25, PP1 to PP18, MO1 to MO37, MM1 to MM37, MP1 to MP25, OO1 to OO37, OM1 to OM37, OP1 to OP25, O1 to O16, M1 to M16, and P1 to P9 are the same as described in connection with Z₃ and Z₄, and * and *′ each indicate a binding site to a neighboring atom.

In an embodiment, Z₁₀ to Z₁₉ in Formulae PO1 to PO25, PM1 to PM25, PP1 to PP18, MO1 to MO37, MM1 to MM37, MP1 to MP25, OO1 to OO37, OM1 to OM37, OP1 to OP25, O1 to O16, M1 to M16, and P1 to P9 may not be a cyano group.

In one or more embodiments, Z₁₀ to Z₁₉ in Formulae PO1 to PO25, PM1 to PM25, PP1 to PP18, MO1 to MO37, MM1 to MM37, MP1 to MP25, OO1 to OO37, OM1 to OM37, OP1 to OP25, O1 to O16, M1 to M16, and P1 to P9 may each independently be:

hydrogen, deuterium, or a cyano group; or

an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, a biphenyl group, or a terphenyl group, each unsubstituted or substituted with at least one selected from deuterium, a cyano group, an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, and a biphenyl group.

In one or more embodiments, a group represented by

in Formulae E-1(1) and E-1(2) may be one of groups represented by Formulae A1-1 to A1-3,

a group represented by

in Formula E-1(1) may be one of groups represented by Formulae A2-1 to A2-3,

a group represented by

in Formulae E-1(2) and E-1(3) may be one of groups represented by Formulae A2-4 to A2-17, and

a group represented by

in Formula E-1(3) may be one of groups represented by Formulae A1-4 to A1-17:

In Formulae A1-1 to A1-17 and A2-1 to A2-17, Z₂₁ to Z₂₈ are the same as described in connection with Z₁ and Z₂, Z₃₁ to Z₃₈ are the same as described in connection with Z₅ and Z₆, and * and *′ each indicate a binding site to a neighboring atom.

In an embodiment, Z₂₁ to Z₂₈ and Z₃₁ to Z₃₈ in Formulae A1-1 to A1-17 and A2-1 to A2-17a are not a cyano group.

In one or more embodiments, Z₂₁ to Z₂₈ and Z₃₁ to Z₃₈ in Formulae A1-1 to A1-17 and A2-1 to A2-17 may each independently be:

hydrogen, deuterium, or a cyano group; or

an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, a biphenyl group, or a terphenyl group, each unsubstituted or substituted with at least one selected from deuterium, a cyano group, an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, and a biphenyl group.

In an embodiment, the second material may include at least one compound selected from Compounds E1 to E8, but embodiments of the present disclosure are not limited thereto:

The third material may be selected from materials having reorganization energy of about 0.4 electron volts (eV) or more, for example, about 0.4 eV to about 1.0 eV, about 0.4 eV to about 0.9 eV, about 0.4 eV to about 0.8 eV, about 0.4 eV to about 0.7 eV, about 0.4 eV to about 0.6 eV, or about 0.4 eV to about 0.5 eV.

The “reorganization energy” means energy necessary for relaxation of a molecular structure due to movement of electrons. The third material, which has large reorganization energy in the above-described range, serves to reduce excess electrons in the emission layer and minimize polaron-triplet quenching in the emission layer. Thus, the emission layer including the third material as described above may have long lifespan characteristics.

The reorganization energy may be calculated and estimated by a density function theory using quantum chemical software (TURBOMOLE), and a more detailed evaluation method may be understood by referring to Evaluation Example 1 provided below.

In an embodiment, the third material may include a compound represented by Formula 11:

X₁ in Formula 11 may be a single bond, N-[(L₄)_c4-R₄], C(R₅)(R₆), O, or S.

For example, X₁ may be a single bond, but embodiments of the present disclosure are not limited thereto.

A₁ and A₂ in Formula 11 may each independently be a benzene group, a naphthalene group, an indene group, an indole group, a benzofuran group, a benzothiophene group, a benzosilole group, a fluorene group, a carbazole group, a dibenzofuran group, a dibenzothiophene group, or a dibenzosilole group.

For example, A₁ and A₂ may each independently be a benzene group, a fluorene group, a carbazole group, a dibenzofuran group, a dibenzothiophene group, or a dibenzosilole group, and at least one of A₁ and A₂ may be a benzene group, but embodiments of the present disclosure are not limited thereto.

L₃ and L₄ may each independently be selected from a single bond, a substituted or unsubstituted C₃-C₁₀ cycloalkylene group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkylene group, a substituted or unsubstituted C₃-C₁₀ cycloalkenylene group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenylene group, a substituted or unsubstituted C₆-C₆₀ arylene group, a substituted or unsubstituted C₁-C₆₀ heteroarylene group, a substituted or unsubstituted divalent non-aromatic condensed polycyclic group, and a substituted or unsubstituted divalent non-aromatic condensed heteropolycyclic group.

For example, L₃ and L₄ may each independently be selected from:

a single bond, a phenylene group, a naphthylene group, a fluorenylene group, a pyridinylene group, a pyrimidinylene group, a pyrazinylene group, a pyridazinylene group, a triazinylene group, a quinolinylene group, an isoquinolinylene group, a carbazolylene group, a dibenzofuranylene group, a dibenzothiophenylene group, and an indolocarbazolylene group; and

a phenylene group, a naphthylene group, a fluorenylene group, a pyridinylene group, a pyrimidinylene group, a pyrazinylene group, a pyridazinylene group, a triazinylene group, a quinolinylene group, an isoquinolinylene group, a carbazolylene group, a dibenzofuranylene group, a dibenzothiophenylene group, and an indolocarbazolylene group, each substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, an indolocarbazolyl group, —Si(Q₃₁)(Q₃₂)(Q₃₃), and —N(Q₃₄)(Q₃₅), and

Q₃₁ to Q₃₅ may each independently be selected from a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group. However, embodiments of the present disclosure are not limited thereto.

c3 and c4 indicate the number of groups L₃ and the number of groups L₄, respectively, and may each independently be an integer from 0 to 4. When c3 is two or more, two or more groups L₃ may be identical to or different from each other, and when c4 is two or more, two or more groups L₄ may be identical to or different from each other. For example, c3 and c4 may each independently be 0, 1, or 2, but embodiments of the present disclosure are not limited thereto.

R₁ to R₆ in Formula 11 may each independently be selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —Si(Q₁)(Q₂)(Q₃), —N(Q₄)(Q₅), and —B(Q₆)(Q₇).

In an embodiment, R₃ in Formula 11 may include at least one π electron-depleted nitrogen-containing cyclic group. The π electron-depleted nitrogen-containing cyclic group is the same as described above.

For example, R₃ in Formula 11 may be selected from a phenyl group, an indenyl group, a naphthyl group, a fluorenyl group, a spiro-bifluorenyl group, a benzofluorenyl group, a dibenzofluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, an isoindolyl group, an indolyl group, a furanyl group, a thiophenyl group, a silolyl group, a benzofuranyl group, a benzothiophenyl group, a benzosilolyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a dibenzosilolyl group, an indeno carbazolyl group, an indolocarbazolyl group, a benzofuracarbazolyl group, a benzothienocarbazolyl group, a benzosilolocarbazolyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyridazinyl group, a pyrimidinyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a benzoisoquinolinyl group, a phthalazinyl group, a naphthyridinyl group, a quinoxalinyl group, a benzoquinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a phenanthridinyl group, an acridinyl group, a phenanthrolinyl group, a phenazinyl group, a benzimidazolyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a thiadiazolyl group, an imidazopyridinyl group, an imidazopyrimidinyl group, an azaindenyl group, an azaindolyl group, an azabenzofuranyl group, an azabenzothiophenyl group, an azabenzosilolyl group, an azafluorenyl group, an azacarbazolyl group, an azadibenzofuranyl group, an azadibenzothiophenyl group, and an azadibenzosilolyl group, each unsubstituted or substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a (C₁-C₁₀ alkyl)phenyl group, a di(C₁-C₁₀ alkyl)phenyl group, a biphenyl group, a terphenyl group, a di(phenyl)phenyl group, a di(biphenyl)phenyl group, a (pyridinyl)phenyl group, a di(pyridinyl)phenyl group, a (pyrimidinyl)phenyl group, a di(pyridiminyl)phenyl group, a (triazinyl)phenyl group, a di(triazinyl)phenyl group, a pyridinyl group, a (C₁-C₁₀ alkyl)pyridinyl group, a di(C₁-C₁₀ alkyl)pyridinyl group, a (phenyl)pyridinyl group, a di(phenyl)pyridinyl group, a (biphenyl)pyridinyl group, a di(biphenyl)pyridinyl group, a (terphenyl)pyridinyl group, a bi(terphenyl)pyridinyl group, a (pyridinyl)pyridinyl group, a di(pyridinyl)pyridinyl group, a (pyrimidinyl)pyridinyl group, a di(pyrimidinyl)pyridinyl group, a (triazinyl)pyridinyl group, a di(triazinyl)pyridinyl group, a pyrimidinyl group, a (C₁-C₁₀ alkyl)pyrimidinyl group, a di(C₁-C₁₀ alkyl)pyrimidinyl group, a (phenyl)pyrimidinyl group, a di(phenyl)pyrimidinyl group, a (biphenyl)pyrimidinyl group, a di(biphenyl)pyrimidinyl group, a (terphenyl)pyrimidinyl group, a bi(terphenyl)pyrimidinyl group, a (pyridinyl)pyrimidinyl group, a di(pyridinyl)pyrimidinyl group, a (pyrimidinyl)pyrimidinyl group, a di(pyrimidinyl)pyrimidinyl group, a (triazinyl)pyrimidinyl group, a di(triazinyl)pyrimidinyl group, a triazinyl group, a (C₁-C₁₀ alkyl)triazinyl group, a di(C₁-C₁₀ alkyl)triazinyl group, a (phenyl)triazinyl group, a di(phenyl)triazinyl group, a (biphenyl)triazinyl group, a di(biphenyl)triazinyl group, a (terphenyl)triazinyl group, a bi(terphenyl)triazinyl group, a (pyridinyl)triazinyl group, a di(pyridinyl)triazinyl group, a (pyrimidinyl)triazinyl group, a di(pyrimidinyl)triazinyl group, a (triazinyl)triazinyl group, a di(triazinyl)triazinyl group, a fluorenyl group, a di(C₁-C₁₀ alkyl)fluorenyl group, a di(phenyl)fluorenyl group, a di(biphenyl)fluorenyl group, a carbazolyl group, a (C₁-C₁₀ alkyl)carbazolyl group, a (phenyl)carbazolyl group, a (biphenyl)carbazolyl group, a dibenzofuranyl group, a (C₁-C₁₀ alkyl)dibenzofuranyl group, a (phenyl)dibenzofuranyl group, a (C₁-C₁₀ alkyl)dibenzothiophenyl group, a (phenyl)dibenzothiophenyl group, and a (biphenyl)dibenzothiophenyl group, but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, R₃ in Formula 11 may be selected from:

a group represented by Formula 13(1) or 13(2);

a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and an indolocarbazolyl group; and

a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and an indolocarbazolyl group, each substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, an indolocarbazolyl group, and —Si(Q₃₁)(Q₃₂)(Q₃₃), and

Q₃₁ to Q₃₃ may each independently be selected from a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group:

X₁₁ to X₁₅ in Formula 13(1) may each independently be C or N, and at least one of X₁₁ to X₁₅ may be N.

For example, two or three of X₁₁ to X₁₅ may each be N.

In Formula 13(2), A₁₁ and A₁₂ may each independently be a benzene group, a naphthalene group, a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, a quinoline group, an isoquinoline group, a quinoxaline group, or a quinazoline group, and at least one of A₁₁ and A₁₂ may be a pyridine group, a pyrazine group, a pyrimidine group, a pyridazine group, a quinoline group, an isoquinoline group, a quinoxaline group, or a quinazoline group.

For example, A₁₁ may be a pyridine group, a pyrimidine group, a quinoline group, an isoquinoline group, a quinoxaline group, or a quinazoline group, and A₁₂ may be a benzene group or a naphthalene group, but embodiments of the present disclosure are not limited thereto.

In Formula 13(2), X₁₆ may be N-[(L₁₂)_a12-R₁₂], C(R₁₄)(R₁₅), O, or S, and X₁₇ may be a single bond, N-[(L₁₃)_a13-R₁₃], C(R₁₆)(R₁₇), O, or S.

For example, X₁₆ may be O or S, and X₁₇ may be a single bond, but embodiments of the present disclosure are not limited thereto.

In Formulae 13(1) and 13(2), L₁₁ to L₁₃ are the same as described in connection with L₃, a11 to a13 are the same as described in connection with c3, and R₁₁ to R₁₇ are the same as described in connection with R₁.

d16 in Formula 13(2) may be an integer from 0 to 6, and d14 in Formula 13(1) may be an integer from 0 to 4.

* in Formulae 13(1) and 13(2) indicates a binding site to a neighboring atom.

In an embodiment, R₃ in Formula 11 may be one of groups represented by Formulae 13-1 to 13-20, but embodiments of the present disclosure are not limited thereto:

In Formulae 13-1 to 13-20,

X₁₆ may be N-[(L₁₂)_a12-R₁₂], C(R₁₄)(R₁₅), O, or S,

L₁₁ and L₁₂ are the same as described in connection with L₃ ,

a11 and a12 are the same as described in connection with c3,

R₁₁, R₁₂, R₁₄, and R₁₅ are the same as described in connection with R₁,

d16 may be an integer from 0 to 6,

d15 may be an integer from 0 to 5,

d14 may be an integer from 0 to 4,

d13 may be an integer from 0 to 3,

d12 may be an integer from 0 to 2, and

* indicates a binding site to a neighboring atom.

In an embodiment, R₁, R₂, R₅, and R₆ in Formula 11 may each independently be selected from hydrogen, deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, an indolocarbazolyl group, —Si(Q₁)(Q₂)(Q₃), and —N(Q₄)(Q₅), and

Q₁ to Q₅ may each independently be selected from a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group.

a1 and a2 in Formula 11 indicate the number of groups R₁ and the number of groups R₂, respectively, and may each independently be an integer from 0 to 10. When a1 is two or more, two or more groups R₁ may be identical to or different from each other, and when a2 is two or more, two or more groups R₂ may be identical to or different from each other.

In an embodiment, the third material may include a compound represented by one of Formulae 11-1 to 11-7, but embodiments of the present disclosure are not limited thereto:

In Formulae 11-1 to 11-7,

X₁, L₃, c3, and R₁ to R₃ are the same as described herein,

X₂ may be N-[(L₅)_c5-R₇], C(R₈)(R₉), O, or S,

L₅ and c5 are the same as described in connection with L₃ and c3,

R₇ is the same as described in connection with R₃,

R₈ and R₉ are the same as described in connection with R₅ and R₆,

a16 may be an integer from 0 to 6, and

a14 and a24 may each independently be an integer from 0 to 4.

In an embodiment, in Formulae 11-1 to 11-17, 1) R₃ when X₂ is C(R₈)(R₉), O, or S, and 2) at least one of R₃ and R₇ when X₂ is N-[(L₅)_c5-R₇], may each independently include at least one π electron-depleted nitrogen-containing cyclic group as described above.

In one or more embodiments, in Formulae 11-1 to 11-17, 1) R₃ when X₂ is C(R₈)(R₉), O, or S and 2) R₃ and R₇ when X₂ is N-[(L₅)_c5-R₇], may each independently be selected from:

a group represented by Formula 13(1) or 13(2) (for example, one of groups represented by Formulae 13-1 to 13-20);

a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and an indolocarbazolyl group; and

a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and an indolocarbazolyl group, each substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, a C₁-C₁₀ alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, an indolocarbazolyl group, and —Si(Q₃₁)(Q₃₂)(Q₃₃),

1) R₃ when X₂ is C(R₈)(R₉), O, or S and 2) at least one of R₃ and R₇ when X₂ is N-[(L₅)_c5-R₇], may each independently be a group represented by Formula 13(1) or 13(2) (for example, one of groups represented by Formulae 13-1 to 13-20).

a1 and a2 in Formula 11 indicate the number of groups R₁ to the number of groups R₂, respectively, and may each independently be an integer from 0 to 10. When a1 is two or more, two or more groups R₁ may be identical to or different from each other, and when a2 is two or more, two or more groups R₂ may be identical to or different from each other. For example, a1 and a2 may each independently be 0, 1, 2, or 3, but they are not limited thereto.

In an embodiment, the third material may include at least one compound selected from Compounds M1-1 to M1-81, M2-1 to M2-81, M3-1 to M3-81, and M201 to M204, but embodiments of the present disclosure are not limited thereto:

The light-emitting material may include a phosphorescent material. Therefore, the emission layer may emit phosphorescence.

In an embodiment, the light-emitting material may include a transition metal-containing organometallic compound.

The transition metal may be, for example, iridium (Ir), platinum (Pt), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf), europium (Eu), terbium (Tb), thulium (Tm), rhodium (Rh), ruthenium (Ru), rhenium (Re), cobalt (Co), copper (Cu), rhodium (Rh), palladium (Pd), silver (Ag), or gold (Au), but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, the light-emitting material may include a transition metal-containing organometallic compound that emits blue light.

In one or more embodiments, the light-emitting material may include an organometallic compound including a bidentate ligand and a transition metal, the bidentate ligand containing at least one cyano group or at least one fluoro group.

In one or more embodiments, the light-emitting material may include an organometallic compound including a transition metal and a cyano group-containing bidentate ligand.

In one or more embodiments, the light-emitting material may include an organometallic compound including a ligand containing at least one cyano group and at least one deuterium and a transition metal.

In one or more embodiments, the light-emitting material may include a homoleptic organometallic compound including iridium and a cyano group-containing phenylimidazole-based bidentate ligand.

In one or more embodiments, the light-emitting material may include an organometallic compound represented by Formula 1:

M in Formula 1 may be selected from a first-row transition metal, a second-row transition metal, and a third-row transition metal.

For example, M may be Ir, Os, Re, Pt, Pd, or Au, but embodiments of the present disclosure are not limited thereto.

In Formula 1, L₃₁ may be selected from a monodentate ligand and a bidentate ligand, and n31 may be 0, 1, 2, 3, or 4, wherein, when n31 is two or more, two or more groups L₃₁ may be identical to or different from each other.

n32 in Formula 1 may be 1, 2, or 3.

For example, when M is Ir or Os, the sum of n31 and n32 may be 3, and when M is Pt, the sum of n31 and n32 may be 2.

In Formula 1, X₃₉ may be N or C(R₃₉), and X₄₀ may be N or C(R₄₀).

R₃₁ to R₄₀ may each independently be selected from hydrogen, deuterium, —F, —Cl, —Br, —I, —SF₅, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉). Q₁ to Q₉ are the same as described above.

For example, R₃₁ to R₄₀ may each independently be selected from:

hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, —SF₅, a C₁-C₂₀ alkyl group, and a C₁-C₂₀ alkoxy group;

a C₁-C₂₀ alkyl group and a C₁-C₂₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a biphenyl group, a naphthyl group, a pyridinyl group, and a pyrimidinyl group;

a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, and isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, and an imidazopyrimidinyl group;

a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinoinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzoimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, and an imidazopyrimidinyl group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cycloctyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a biphenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, and an imidazopyrimidinyl group; and

—N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉), and

Q₁ to Q₉ may each independently be selected from:

—CH₃, —CD₃, —CD₂H, —CDH₂, —CH₂CH₃, —CH₂CD₃, —CH₂CD₂H, —CH₂CDH₂, —CHDCH₃, —CHDCD₂H, —CHDCDH₂, —CHDCD₃, —CD₂CD₃, —CD₂CD₂H, and —CD₂CDH₂;

an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, and a naphthyl group; and

an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, and a naphthyl group, each substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, and a phenyl group,

but embodiments of the present disclosure are not limited thereto.

Two or more neighboring groups selected from R₃₁ to R₄₀ may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₂-C₃₀ heterocyclic group.

In an embodiment, at least one of R₃₁, R₃₃, and R₃₅ in Formula 1 (for example, R₃₁ and R₃₅) may each independently be:

deuterium, a cyano group, a C₁-C₂₀ alkyl group, a phenyl group, a biphenyl group, or a terphenyl group; or

a C₁-C₂₀ alkyl group, a phenyl group, a biphenyl group, or a terphenyl group, each unsubstituted or substituted with at least one selected from deuterium, a cyano group, and a C₁-C₂₀ alkyl group.

In an embodiment, a maximum emission wavelength of the organometallic compound represented by Formula 1 may be in a range of about 440 nanometers (nm) to about 470 nm (for example, about 440 nm to about 467 nm). When the maximum emission wavelength is in a range of about 440 nm to about 470 nm, an organic light-emitting device emitting a deep blue color may be provided.

In an embodiment, the light-emitting material may include at least one compound selected from Compounds 1 to 24, D1 to D11, and F₂IrPic, but embodiments of the present disclosure are not limited thereto:

The first material, the second material, the third material, and the light-emitting material in the emission layer may be different from one another. That is, the emission layer may essentially include four types of different compounds.

A ratio of a light-emitting compound emitted from the light-emitting material to a total light-emitting component emitted from the emission layer may be 90% or more, for example, 92% or more, 94% or more, 96% or more, or 98% or more.

An amount of the third material may be greater than about 0 parts by weight and equal to and less than about 10 parts by weight, for example, about 1 part by weight to about 7 parts by weight, based on 100 parts by weight of the first material, the second material, the third material, and the light-emitting material. While not wishing to be bound by theory, it is understood that when the amount of the third material is within this range, it is possible to achieve an increase in luminescent efficiency from the light-emitting material in the emission layer and achieve an effect of reducing polaron-triplet quenching in the emission layer.

An amount of the light-emitting material may be greater than about 0 parts by weight and equal to and less than about 10 parts by weight, for example, about 0.1 parts by weight to about 5 parts by weight, based on 100 parts by weight of the first material, the second material, the third material, and the light-emitting material. While not wishing to be bound by theory, it is understood that when the amount of the light-emitting material is within this range, it is possible to achieve high luminescent efficiency without concentration quenching.

The total amount of the first material and the second material may be in a range of about 50 parts by weight to about 95 parts by weight, for example, about 60 parts by weight to about 90 parts by weight, based on 100 parts by weight of the first material, the second material, the third material, and the light-emitting material. While not wishing to be bound by theory, it is understood that when the total amount of the first material and the second material is within this range, it is possible to achieve high luminescent efficiency without concentration quenching.

A weight ratio of the first material to the second material may be selected from about 1:9 to about 9:1, about 2:8 to about 8:2, about 3:7 to about 7:3, and about 4:6 to about 6:4.

The first material and the second material may act as a host in the emission layer, the light-emitting material may act as a dopant in the emission layer, and the third material may act as an additive for improvement in lifespan in the emission layer.

Since the emission layer includes the first material, the second material, the third material, and the light-emitting material at the same time as described above, an organic light-emitting device including the emission layer may have both high luminescent efficiency and long lifespan characteristics due to minimization in polaron-triplet quenching.

The FIGURE is a schematic view of an organic light-emitting device 10 according to an embodiment. Hereinafter, the structure of an organic light-emitting device according to an embodiment and a method of manufacturing an organic light-emitting device according to an embodiment will be described in connection with the FIGURE. The organic light-emitting device 10 includes a first electrode 11, an organic layer 15, and a second electrode 19, which are sequentially stacked.

A substrate may be additionally disposed under the first electrode 11 or above the second electrode 19. For use as the substrate, any substrate that is used in general organic light-emitting devices may be used, and the substrate may be a glass substrate or a transparent plastic substrate, each having excellent mechanical strength, thermal stability, transparency, surface smoothness, ease of handling, and water resistance.

The first electrode 11 may be formed by depositing or sputtering a material for forming the first electrode 11 on the substrate. The first electrode 11 may be an anode. The material for forming the first electrode 11 may be selected from materials with a high work function to facilitate hole injection. The first electrode 11 may be a reflective electrode, a semi-transmissive electrode, or a transmissive electrode. The material for forming the first electrode may be, for example, indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO₂), and zinc oxide (ZnO). In one or more embodiments, magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), or magnesium-silver (Mg—Ag) may be used as the material for forming the first electrode.

The first electrode 11 may have a single-layered structure or a multi-layered structure including two or more layers. For example, the first electrode 11 may have a three-layered structure of ITO/Ag/ITO, but the structure of the first electrode 110 is not limited thereto.

The organic layer 15 is disposed on the first electrode 11.

The organic layer 15 may include a hole transport region, an emission layer, and an electron transport region.

The hole transport region may be disposed between the first electrode 11 and the emission layer.

The hole transport region may include at least one selected from a hole injection layer, a hole transport layer, an electron blocking layer, and a buffer layer. The hole transport layer may be a single layer or may include two or more layers.

The hole transport region may include only either a hole injection layer or a hole transport layer. In an embodiment, the hole transport region may include, a hole injection layer/hole transport layer structure, a hole injection layer/hole transport layer/electron blocking layer structure, a hole transport layer/electron blocking layer structure, a hole injection layer/first hole transport layer/second hole transport layer structure, a hole injection layer/first hole transport layer/second hole transport layer/electron blocking layer structure, or a first hole transport layer/second hole transport layer/electron blocking layer structure, which are sequentially stacked in this stated order from the first electrode 11.

A hole injection layer may be formed on the first electrode 11 by using one or more suitable methods selected from vacuum deposition, spin coating, casting, or Langmuir-Blodgett (LB) deposition.

When a hole injection layer is formed by vacuum deposition, the deposition conditions may vary according to a compound that is used to form the hole injection layer, and the structure and thermal characteristics of the hole injection layer. For example, the deposition conditions may include a deposition temperature of about 100° C. to about 500° C., a vacuum pressure of about 10⁻⁸ torr to about 10⁻³ torr, and a deposition rate of about 0.01 Angstroms per second (Å/sec) to about 100 Å/sec. However, the deposition conditions are not limited thereto.

When the hole injection layer is formed using spin coating, coating conditions may vary according to the material used to form the hole injection layer, and the structure and thermal properties of the hole injection layer. For example, a coating speed may be from about 2,000 revolutions per minute (rpm) to about 5,000 rpm, and a temperature at which a heat treatment is performed to remove a solvent after coating may be from about 80° C. to about 200° C. However, the coating conditions are not limited thereto.

Conditions for forming a hole transport layer and an electron blocking layer may be understood by referring to conditions for forming the hole injection layer.

The hole transport region may include at least one selected from m-MTDATA, TDATA, 2-TNATA, NPB, β-NPB, TPD, Spiro-TPD, Spiro-NPB, methylated-NPB, TAPC, HMTPD, 4,4′,4″-tris(N-carbazolyl)triphenylamine (TCTA), polyaniline/dodecylbenzene sulfonic acid (PANI/DBSA), poly(3,4-ethylenedioxythiophene)/poly(4-styrene sulfonate) (PEDOT/PSS), polyaniline/camphor sulfonic acid (PANI/CSA), polyaniline/poly(4-styrene sulfonate) (PANI/PSS), a compound represented by Formula 201 below, and a compound represented by Formula 202 below:

In Formula 201, Ar₁₀₁ and Ar₁₀₂ may each independently be selected from:

a phenylene group, a pentalenylene group, an indenylene group, a naphthylene group, an azulenylene group, a heptalenylene group, an acenaphthylene group, a fluorenylene group, a phenalenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylenylene group, a naphthacenylene group, a picenylene group, a perylenylene group, and a pentacenylene group; and

a phenylene group, a pentalenylene group, an indenylene group, a naphthylene group, an azulenylene group, a heptalenylene group, an acenaphthylene group, a fluorenylene group, a phenalenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylenylene group, a naphthacenylene group, a picenylene group, a perylenylene group, and a pentacenylene group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group.

In Formula 201, xa and xb may each independently be an integer of 0 to 5, or may be 0, 1, or 2. For example, xa is 1 and xb is 0, but xa and xb are not limited thereto.

In Formulae 201 and 202, R₁₀₁ to R₁₀₈, R₁₁₁ to R₁₁₉, and R₁₂₁ to R₁₂₄ may each independently be selected from:

hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group (for example, a methyl group, an ethyl group, a propyl group, a butyl group, pentyl group, a hexyl group, and the like), and a C₁-C₁₀ alkoxy group (for example, a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentoxy group, and the like);

a C₁-C₁₀ alkyl group and a C₁-C₁₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, and a phosphoric acid group or a salt thereof;

a phenyl group, a naphthyl group, an anthracenyl group, a fluorenyl group, and a pyrenyl group; and

a phenyl group, a naphthyl group, an anthracenyl group, a fluorenyl group, and a pyrenyl group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group, and a C₁-C₁₀ alkoxy group, but embodiments of the present disclosure are not limited thereto.

In Formula 201, R₁₀₉ may be selected from:

a phenyl group, a naphthyl group, an anthracenyl group, and a pyridinyl group; and

a phenyl group, a naphthyl group, an anthracenyl group, and a pyridinyl group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a alkoxy group, a phenyl group, a naphthyl group, an anthracenyl group, and a pyridinyl group.

In an embodiment, the compound represented by Formula 201 may be represented by Formula 201A, but embodiments of the present disclosure are not limited thereto:

R₁₀₁, R₁₁₁, R₁₁₂, and R₁₀₉ in Formula 201A may be understood by referring to the description provided herein.

For example, the compound represented by Formula 201, and the compound represented by Formula 202 may include compounds HT1 to HT20 illustrated below, but are not limited thereto:

A thickness of the hole transport region may be in a range of about 100 Angstroms (A) to about 10,000 Å, for example, about 100 Å to about 1,000 Å. When the hole transport region includes a hole injection layer and a hole transport layer, the thickness of the hole injection layer may be in a range of about 100 Å to about 10,000 Å, and for example, about 100 Å to about 1,000 Å, and the thickness of the hole transport layer may be in a range of about 50 Å to about 2,000 Å, and for example, about 100 Å to about 1,500 Å. While not wishing to be bound by theory, it is understood that when the thicknesses of the hole transport region, the hole injection layer, and the hole transport layer are within these ranges, satisfactory hole transporting characteristics may be obtained without a substantial increase in driving voltage.

The hole transport region may further include, in addition to these materials, a charge-generation material for the improvement of conductive properties. The charge-generation material may be homogeneously or non-homogeneously dispersed in the hole transport region.

The charge-generation material may be, for example, a p-dopant. The p-dopant may be one selected from a quinone derivative, a metal oxide, and a cyano group-containing compound, but embodiments of the present disclosure are not limited thereto. Non-limiting examples of the p-dopant are a quinone derivative, such as tetracyanoquinonedimethane (TCNQ) or 2,3,5,6-tetrafluoro-tetracyano-1,4-benzoquinonedimethane (F4-TCNQ); a metal oxide, such as a tungsten oxide or a molybdenium oxide; and a cyano group-containing compound, such as Compound HT-D1 or Compound HT-D2 below, but are not limited thereto.

The hole transport region may include a buffer layer.

Also, the buffer layer may compensate for an optical resonance distance according to a wavelength of light emitted from the emission layer, and thus, efficiency of a formed organic light-emitting device may be improved.

Then, an emission layer may be formed on the hole transport region by vacuum deposition, spin coating, casting, LB deposition, or the like. When the emission layer is formed by vacuum deposition or spin coating, the deposition or coating conditions may be similar to those applied in forming the hole injection layer although the deposition or coating conditions may vary according to a compound that is used to form the emission layer.

Meanwhile, when the hole transport region includes an electron blocking layer, a material for the electron blocking layer may be selected from materials for the hole transport region described above and materials for a host to be explained later. However, the material for the electron blocking layer is not limited thereto. For example, when the hole transport region includes an electron blocking layer, a material for the electron blocking layer may be mCP.

The emission layer may include the first material, the second material, the third material, and the light-emitting material as described above.

When the organic light-emitting device is a full-color organic light-emitting device, the emission layer may be patterned into a red emission layer, a green emission layer, and a blue emission layer. In one or more embodiments, due to a stacked structure including a red emission layer, a green emission layer, and/or a blue emission layer, the emission layer may emit white light.

A thickness of the emission layer may be in a range of about 100 Å to about 1,000 Å, for example, about 200 Å to about 600 Å. While not wishing to be bound by theory, it is understood that when the thickness of the emission layer is within this range, excellent light-emission characteristics may be obtained without a substantial increase in driving voltage.

Then, an electron transport region may be disposed on the emission layer.

The electron transport region may include at least one selected from a hole blocking layer, an electron transport layer, and an electron injection layer.

For example, the electron transport region may have a hole blocking layer/electron transport layer/electron injection layer structure or an electron transport layer/electron injection layer structure, but the structure of the electron transport region is not limited thereto. The electron transport layer may have a single-layered structure or a multi-layered structure including two or more different materials.

Conditions for forming the hole blocking layer, the electron transport layer, and the electron injection layer which constitute the electron transport region may be understood by referring to the conditions for forming the hole injection layer.

When the electron transport region includes a hole blocking layer, the hole blocking layer may include, for example, at least one of BCP, Bphen, and BAlq but embodiments of the present disclosure are not limited thereto:

A thickness of the hole blocking layer may be in a range of about 20 Å to about 1,000 Å, for example, about 30 Å to about 300 Å. While not wishing to be bound by theory, it is understood that when the thickness of the hole blocking layer is within these ranges, the hole blocking layer may have improved hole blocking ability without a substantial increase in driving voltage.

The electron transport layer may further include at least one selected from BCP, Bphen, Alq₃, BAlq, TAZ, and NTAZ:

In one or more embodiments, the electron transport layer may include at least one of ET1 and ET25, but are not limited thereto:

A thickness of the electron transport layer may be in a range of about 100 Å to about 1,000 Å, for example, about 150 Å to about 500 Å. While not wishing to be bound by theory, it is understood that when the thickness of the electron transport layer is within the range described above, the electron transport layer may have satisfactory electron transport characteristics without a substantial increase in driving voltage.

Also, the electron transport layer may further include, in addition to the materials described above, a metal-containing material.

The metal-containing material may include a Li complex. The Li complex may include, for example, Compound ET-D1 (lithium quinolate, LiQ) or ET-D2:

The electron transport region may include an electron injection layer that promotes flow of electrons from the second electrode 19 thereinto.

The electron injection layer may include at least one selected from LiF, NaCl, CsF, Li₂O, and BaO.

A thickness of the electron injection layer may be in a range of about 1 Å to about 100 Å, for example, about 3 Å to about 90 Å. While not wishing to be bound by theory, it is understood that when the thickness of the electron injection layer is within the range described above, the electron injection layer may have satisfactory electron injection characteristics without a substantial increase in driving voltage.

The second electrode 19 is disposed on the organic layer 15. The second electrode 19 may be a cathode. A material for forming the second electrode 19 may be selected from metal, an alloy, an electrically conductive compound, and a combination thereof, which have a relatively low work function. For example, lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), or magnesium-silver (Mg—Ag) may be used as a material for forming the second electrode 19. In one or more embodiments, to manufacture a top-emission type light-emitting device, a transmissive electrode formed using ITO or IZO may be used as the second electrode 19.

Hereinbefore, the organic light-emitting device has been described with reference to the FIGURE, but embodiments of the present disclosure are not limited thereto.

The term “C₁-C₆₀ alkyl group” as used herein refers to a linear or branched saturated aliphatic hydrocarbon monovalent group having 1 to 60 carbon atoms, and non-limiting examples thereof include a methyl group, an ethyl group, a propyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an iso-amyl group, and a hexyl group. The term “C₁-C₆₀ alkylene group” as used herein refers to a divalent group having the same structure as the C₁-C₆₀ alkyl group.

The term “C₁-C₆₀ alkoxy group” as used herein refers to a monovalent group represented by —OA₁₀₁ (wherein A₁₀₁ is the C₁-C₆₀ alkyl group), and non-limiting examples thereof include a methoxy group, an ethoxy group, and an iso-propyloxy group.

The term “C₂-C₆₀ alkenyl group” as used herein refers to a hydrocarbon group formed by including at least one carbon-carbon double bond in the middle or at the terminus of the C₂-C₆₀ alkyl group, and examples thereof include an ethenyl group, a propenyl group, and a butenyl group. The term “C₂-C₆₀ alkenylene group” as used herein refers to a divalent group having the same structure as the C₂-C₆₀ alkenyl group.

The term “C₂-C₆₀ alkynyl group” as used herein refers to a hydrocarbon group formed by including at least one carbon-carbon triple bond in the middle or at the terminus of the C₂-C₆₀ alkyl group, and examples thereof include an ethynyl group, and a propynyl group. The term “C₂-C₆₀ alkynylene group” as used herein refers to a divalent group having the same structure as the C₂-C₆₀ alkynyl group.

The term “C₃-C₁₀ cycloalkyl group” as used herein refers to a monovalent saturated hydrocarbon monocyclic group having 3 to 10 carbon atoms, and non-limiting examples thereof include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group. The term “C₃-C₁₀ cycloalkylene group” as used herein refers to a divalent group having the same structure as the C₃-C₁₀ cycloalkyl group.

The term “C₁-C₁₀ heterocycloalkyl group” as used herein refers to a monovalent saturated monocyclic group having at least one heteroatom selected from N, O, P, Si and S as a ring-forming atom and 1 to 10 carbon atoms, and non-limiting examples thereof include a tetrahydrofuranyl group, and a tetrahydrothiophenyl group. The term “C₁-C₁₀ heterocycloalkylene group” as used herein refers to a divalent group having the same structure as the C₁-C₁₀ heterocycloalkyl group.

The term “C₃-C₁₀ cycloalkenyl group” as used herein refers to a monovalent monocyclic group that has 3 to 10 carbon atoms and at least one carbon-carbon double bond in the ring thereof and no aromaticity, and non-limiting examples thereof include a cyclopentenyl group, a cyclohexenyl group, and a cycloheptenyl group. The term “C₃-C₁₀ cycloalkenylene group” as used herein refers to a divalent group having the same structure as the C₃-C₁₀ cycloalkenyl group.

The term “C₁-C₁₀ heterocycloalkenyl group” as used herein refers to a monovalent monocyclic group that has at least one heteroatom selected from N, O, P, Si, and S as a ring-forming atom, 1 to 10 carbon atoms, and at least one carbon-carbon double bond in its ring. Examples of the C₁-C₁₀ heterocycloalkenyl group are a 2,3-dihydrofuranyl group, and a 2,3-dihydrothiophenyl group. The term “C₁-C₁₀ heterocycloalkenylene group” as used herein refers to a divalent group having the same structure as the C₁-C₁₀ heterocycloalkenyl group.

The term “C₆-C₆₀ aryl group” used herein refers to a monovalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms, and a C₆-C₆₀ arylene group used herein refers to a divalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms. Non-limiting examples of the C₆-C₆₀ aryl group include a phenyl group, a naphthyl group, an anthracenyl group, a phenanthrenyl group, a pyrenyl group, and a chrysenyl group. When the C₆-C₆₀ aryl group and the C₆-C₆₀ arylene group each include two or more rings, the rings may be fused to each other.

The term “C₁-C₆₀ heteroaryl group” as used herein refers to a monovalent group having a heterocyclic aromatic system that has at least one heteroatom selected from N, O, P, Si, and S as a ring-forming atom, and 1 to 60 carbon atoms. The term “C₁-C₆₀ heteroarylene group,” as used herein refers to a divalent group having a heterocyclic aromatic system that has at least one heteroatom selected from N, O, P, Si, and S as a ring-forming atom, and 1 to 60 carbon atoms. Non-limiting examples of the C₁-C₆₀ heteroaryl group include a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, and an isoquinolinyl group. When the C₁-C₆₀ heteroaryl group and the C₁-C₆₀ heteroarylene group each include two or more rings, the rings may be fused to each other.

The term “C₆-C₆₀ aryloxy group” used herein indicates —OA₁₀₂ (wherein A₁₀₂ is the C₆-C₆₀ aryl group), and a C₆-C₆₀ arylthio group used herein indicates —SA₁₀₃ (wherein A₁₀₃ is the C₆-C₆₀ aryl group).

The term “monovalent non-aromatic condensed polycyclic group” as used herein refers to a monovalent group (for example, having 8 to 60 carbon atoms) having two or more rings condensed to each other, only carbon atoms as ring-forming atoms, and no aromaticity in its entire molecular structure. Examples of the monovalent non-aromatic condensed polycyclic group include a fluorenyl group. The term “divalent non-aromatic condensed polycyclic group” as used herein refers to a divalent group having the same structure as the monovalent non-aromatic condensed polycyclic group.

The term “monovalent non-aromatic condensed heteropolycyclic group” as used herein refers to a monovalent group (for example, having 2 to 60 carbon atoms) having two or more rings condensed to each other, a heteroatom selected from N, O, P, Si, and S, other than carbon atoms, as a ring-forming atom, and no aromaticity in its entire molecular structure. Non-limiting examples of the monovalent non-aromatic condensed heteropolycyclic group include a carbazolyl group. The term “divalent non-aromatic condensed heteropolycyclic group” as used herein refers to a divalent group having the same structure as the monovalent non-aromatic condensed heteropolycyclic group.

The term “C₅-C₃₀ carbocyclic group” as used herein refers to a saturated or unsaturated cyclic group having, as a ring-forming atom, 5 to 30 carbon atoms only. The term “C₅-C₃₀ carbocyclic group” as used herein refers to a monocyclic group or a polycyclic group, and, according to its chemical structure, a monovalent, divalent, trivalent, tetravalent, pentavalent, or hexavalent group.

The term “C₂-C₃₀ heterocyclic group” as used herein refers to a saturated or unsaturated cyclic group having, as a ring-forming atom, at least one heteroatom selected from N, O, Si, P, and S other than 2 to 30 carbon atoms. The term “C₂-C₃₀ heterocyclic group” as used herein refers to a monocyclic group or a polycyclic group, and, according to its chemical structure, a monovalent, divalent, trivalent, tetravalent, pentavalent, or hexavalent group.

At least one substituent of the substituted C₅-C₃₀ carbocyclic group, the substituted C₂-C₃₀ heterocyclic group, the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₁-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₁-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₁-C₆₀ heteroaryl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group may be selected from:

deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group;

a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁₁)(Q₁₂), —Si(Q₁₃)(Q₁₄)(Q₁₅), —B(Q₁₆)(Q₁₇), and —P(═O)(Q₁₈)(Q₁₉);

a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group;

a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, -CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —N(Q₂₁)(Q₂₂), —Si(Q₂₃)(Q₂₄)(Q₂₅), —B(Q₂₆)(Q₂₇) and —P(═O)(Q₂₈)(Q₂₉); and

—N(Q₃₁)(Q₃₂), —Si(Q₃₃)(Q₃₄)(Q₃₅), —B(Q₃₆)(Q₃₇), and —P(═O)(Q₃₈)(Q₃₉), and

Q₁ to Q₉, Q₁₁ to Q₁₉, Q₂₁ to Q₂₉, and Q₃₁ to Q₃₉ may each independently be selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryl group substituted with at least one selected from a C₁-C₆₀ alkyl group and a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₁-C₆₀ heteroaryl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group.

Hereinafter, a compound and an organic light-emitting device according to embodiments are described in detail with reference to Synthesis Example and Examples. However, the organic light-emitting device is not limited thereto. The wording “B was used instead of A” used in describing Synthesis Examples means that an amount of A used was identical to an amount of B used, in terms of a molar equivalent.

EXAMPLES

Synthesis Example 1

Synthesis of Compound D1

(1) Synthesis of Compound L4

Compound L6 (34.70 millimoles, mmol), Compound L5 (41.64 mmol), K₂CO₃ (173.51 mmol), CuI (1.74 mmol), 1,10-phenanthroline (3.47 mmol), and 500 milliliters (mL) of DMF were added to a 1-L reaction container and refluxed for 12 hours in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was cooled to room temperature. Then, the organic layer was separated therefrom by adding dichloromethane and distilled water thereto. The separated organic layer was washed twice by using distilled water and dried by using MgSO₄, and the solvent was removed therefrom. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate and n-hexane) to obtain 26.37 mmol of Compound L4. The obtained Compound L4 was identified by LC-MS.

LC-MS (m/z): 237.22 [M+1].

(2) Synthesis of Compound L3

Compound L4 (26.37 mmol) and tetrahydrofuran were added to a reaction container and cooled to a temperature of −78° C. in a nitrogen atmosphere. n-BuLi (2.5 M in n-hexane, 27.69 mmol) was slowly added thereto at a temperature of −78° C. and then stirred. After stirring for 1 hour, Br₂ (52.74 mmol) was slowly added thereto at a temperature of −78° C. After 30 minutes, the reaction mixture was heated by removing a cooler and stirred at room temperature for 6 hours. After the reaction was completed, the organic layer was separated therefrom by adding dichloromethane and pure water thereto. The separated organic layer was washed twice by using distilled water and dried by using MgSO₄, and the solvent was removed therefrom. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate and n-hexane) to obtain Compound L3 (18.72 mmol). The obtained Compound L3 was identified by LC-MS.

LC-MS (m/z): 314.12 [M+1].

(3) Synthesis of Compound L1

Compound L3 (18.72 mmol), Compound L2 (28.08 mmol), Pd(PPh₃)₄ (1.87 mmol), K₂CO₃ (210.63 mmol), and THF:distilled water (=2:1) were added to a reaction container and refluxed for 12 hours in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was cooled to room temperature. Then, the organic layer was separated therefrom by adding dichloromethane and distilled water thereto. The separated organic layer was washed twice by using distilled water and dried by using MgSO₄, and the solvent was removed therefrom. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate and n-hexane) to obtain Compound L1 (16.47 mmol). The obtained Compound L1 was identified by LC-MS.

LC-MS (m/z): 337.24 [M+1].

(4) Synthesis of Compound D1

Ir(acac)₃ (3.29 mmol), Compound L1 (16.47 mmol), and glycerol were added to a reaction container and refluxed for 12 hours in a nitrogen atmosphere. After the reaction was completed, the reaction mixture was cooled to room temperature. Then, the organic layer was separated therefrom by adding dichloromethane and distilled water thereto. The separated organic layer was washed twice by using distilled water and dried by using MgSO₄, and the solvent was removed therefrom. The crude product was purified by silica gel column chromatography (eluent: dichloromethane and n-hexane) to obtain Compound D1 (0.49 mmol). The obtained Compound D1 was identified by MALDI-TOF.

MALDI-TOF (m/z): 529.19 [M]⁺.

Evaluation Example 1

Evaluation of Reorganization Energy

Reorganization energy was evaluated by applying a density function theory (PBE0/def2-SVP) using quantum chemical software (TURBOMOLE). Specifically, after optimizing a lowest singlet ground state of a neutral molecule (S₀) and a lowest doublet ground state of an ionic state (D₀), hole reorganization energy (λ_h) and electron reorganization energy (λ_e) were calculated by using the following equations:

λ_h=IP(v)−HEP

λ_e=EEP−EA(v).

In the equations, IP(v) (electron volts, eV) represents vertical ionization potential, EA(v) (eV) represents electron affinity, HEP (eV) represents hole extraction potential, and EEP (eV) represents electron extraction potential.

Reorganization energies of Compounds M1-41, M204, A, B, and C were evaluated by the above-described method, and results thereof are shown in Table 1.

TABLE 1
Compound No. Reorganization energy (eV)
M1-41        0.43
M204         0.43
A            0.32
B            0.29
C            0.25

Referring to Table 1, it is confirmed that Compounds M1-41 and M204 have high reorganization energy, as compared with Compounds A, B, and C.

Example 1

A glass substrate, on which an ITO electrode (first electrode, anode) having a thickness of 1,500 Angstroms (Å) was formed, was cleaned by distilled water ultrasound. After the distilled water cleaning was completed, the glass substrate was ultrasonically cleaned by using iso-propyl alcohol, acetone, and methanol in sequence and then dried. The glass substrate was provided to a plasma cleanser so that the glass substrate was cleaned for 5 minutes by using oxygen plasma. Then, the glass substrate was provided to a vacuum deposition apparatus.

Compound HT3 was vacuum-deposited on the ITO electrode of the glass substrate to form a first hole injection layer having a thickness of 3,500 Å, Compound HT-D1 was vacuum-deposited on the first hole injection layer to form a second hole injection layer having a thickness of 300 Å, TAPC was vacuum-deposited on the second hole injection layer to form an electron blocking layer having a thickness of 100 Å, thereby forming a hole transport region.

Compound H19 (first material), Compound E4 (second material), Compound M1-41 (third material), and F₂Irpic (light-emitting material) were co-deposited on the hole transport region, such that i) an amount of the third material was 10 percent by weight (wt %) based on 100 wt % of the emission layer, ii) an amount of the light-emitting material was 1 wt % based on 100% of the emission layer, iii) a total amount of the first material, the second material, and the third material was 99 wt % based on 100 wt % of the emission layer, and iv) a weight ratio of the first material to the second material was 5:5, thereby forming an emission layer having a thickness of 300 Å.

Compound ET3 was vacuum-deposited on the emission layer to form an electron transport layer having a thickness of 250 Å, ET-D1 (LiQ) was deposited on the electron transport layer to form an electron injection layer having a thickness of 5 Å, Al was deposited on the electron injection layer to form a second electrode (cathode) having a thickness of 1,000 Å, thereby completing the manufacture of an organic light-emitting device.

Example 2 and Comparative Examples A to F

Organic light-emitting devices were manufactured in the same manner as in Example 1, except that Compounds shown in Table 2 were each used as a first material, a second material, a third material, and a light-emitting material in forming an emission layer. In Comparative Examples E and F, a weight ratio of the first material (or, the second material) and the third material was 5:5.

Evaluation Example 2

Evaluation of Characteristics of Organic Light-Emitting Device

Lifespans (T₉₅) of the organic light-emitting devices manufactured according to Examples 1 and 2 and Comparative Examples A to F were evaluated, and results thereof are shown in Table 2. The lifespan (T₉₅) indicates an amount of time that lapsed when luminance was 95% of initial luminance (100%) (the measurement of the luminance was performed by using a luminance meter (Minolta Cs-1000A)). The lifespan (T₉₅) was indicated by a relative value of data of Comparative Example D.

TABLE 2
	Emission layer	Lifespan (T95)
				Light-	(at 1000
	First	Second	Third	emitting	cd/m2)
	material	material	material	material	(%)
Example 1	H19	E4	M1-41	F2Irpic	120
Example 2	H19	E4	M204	F2Irpic	110
Comparative	H19	E4	A	F2Irpic	70
Example A
Comparative	H19	E4	B	F2Irpic	64
Example B
Comparative	H19	E4	C	F2Irpic	62
Example C
Comparative	H19	E4	—	F2Irpic	100
Example D
Comparative	H19	—	M1-41	F2Irpic	60
Example E
Comparative	—	E4	M1-41	F2Irpic	40
Example F

Referring to Table 2, it is confirmed that Examples 1 and 2 have an excellent lifespan, as compared with Comparative Examples A to F.

Examples 3 and 4

Organic light-emitting devices were manufactured in the same manner as in Example 1, except that Compounds shown in Table 3 were each used as a light-emitting material in forming an emission layer.

Evaluation Example 3

Evaluation of Characteristics of Organic Light-Emitting Device

Lifespans (T₉₅) of the organic light-emitting devices manufactured according to Examples 3 and 4 were evaluated in the same manner as in Evaluation Example 2, and results thereof are shown in Table 3. The lifespan (T₉₅) was indicated by a relative value of data of Comparative Example D.

TABLE 3
	Emission layer
				Light-	Lifespan (T95)
	First	Second	Third	emitting	(at 1000 cd/m2)
	material	material	material	material	(%)
Example 3	H19	E4	M1-41	D1	143
Example 4	H19	E4	M204	D1	122

Referring to Table 3, it is confirmed that Examples 3 and 4 have an excellent lifespan, as compared with Comparative Examples A to F.

Since the organic light-emitting device includes the first material, the second material, the third material, and the light-emitting material in a predetermined condition, the organic light-emitting device may have a long lifespan.

It should be understood that embodiments described herein should be considered in a descriptive sense only and not for purposes of limitation. Descriptions of features or aspects within each embodiment should typically be considered as available for other similar features or aspects in other embodiments.

While one or more embodiments have been described with reference to the figures, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present description as defined by the following claims.

Claims

1. An organic light-emitting device comprising: a first electrode;a second electrode facing the first electrode; andan emission layer disposed between the first electrode and the second electrode,wherein the emission layer comprises a first material, a second material, a third material, and a light-emitting material,the first material does not comprise an electron transport moiety,the second material comprises at least one electron transport moiety,the third material has reorganization energy of about 0.4 electron volts or more,the first material, the second material, the third material, and the light-emitting material are different from one another, anda ratio of a light-emitting component emitted from the light-emitting material to a total of light-emitting components emitted from the emission layer is about 90% or more.

2. The organic light-emitting device of claim 1, wherein the first material comprises at least one π electron-depleted nitrogen-free cyclic group and does not comprise an electron transport moiety,the second material comprises at least one π electron-depleted nitrogen-free cyclic group and at least one electron transport moiety, andthe electron transport moiety is selected from a cyano group, a π electron-depleted nitrogen-containing cyclic group, and a group represented by one of the following Formulae:

3. The organic light-emitting device of claim 1, wherein the first material comprises at least one of a compound represented by Formula H-1(1), a compound represented by Formula H-1(2), and a compound represented by Formula H-1(3):

4. The organic light-emitting device of claim 3, wherein L401 and L411 to L414 are each independently selected from: a single bond; anda benzene group, a fluorene group, a dibenzofuran group, a dibenzothiophene group, a carbazole group, a dibenzosilole group, an indenocarbazole group, an indolocarbazole group, a benzofurocarbazole group, a benzothienocarbazole group, a benzosilolocarbazole group, an acridine group, or a dihydroacridine group, each unsubstituted or substituted with at least one selected from deuterium, a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, and a tetraphenyl group,Z41 to Z44 and Z411 to Z422 are each independently selected from:hydrogen, deuterium, a C1-C10 alkyl group, and a C1-C10 alkoxy group; anda phenyl group, a biphenyl group, a terphenyl group, a tetraphenyl group, a fluorenyl group, a dibenzocarbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a carbazolyl group, a dibenzosilolyl group, an indenocarbazolyl group, an indolocarbazolyl group, a benzofurocarbazolyl group, a benzothienocarbazolyl group, a benzosilolocarbazolyl group, an acridinyl group, or a dihydroacridinyl group, each unsubstituted or substituted with at least one selected from deuterium, a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a naphthyl group, a fluorenyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a triphenylenyl group, a biphenyl group, a terphenyl group, and a tetraphenyl group.

5. The organic light-emitting device of claim 1, wherein the second material comprises at least one cyano group.

6. The organic light-emitting device of claim 1, wherein the second material comprises at least one of a compound represented by Formula E-1(1), a compound represented by Formula E-1(2), and a compound represented by Formula E-1(3):

7. The organic light-emitting device of claim 6, wherein, in Formulae E-1(1) to E-1(3), at least one of groups Z1 in the number of b1 and groups Z2 in the number of b2 is a cyano group,at least one of groups Z3 in the number of b3 and groups Z4 in the number of b4 is a cyano group,at least one of groups Z5 in the number of b5 and groups Z6 in the number of b6 is a cyano group,at least one of groups Z1 in the number of b1 and groups Z2 in the number of b2 is a cyano group, and at least one of groups Z3 in the number of b3 and groups Z4 in the number of b4 is a cyano group,at least one of groups Z1 in the number of b1 and groups Z2 in the number of b2 is a cyano group, and at least one of groups Z5 in the number of b5 and groups Z6 in the number of b6 is a cyano group,at least one of groups Z3 in the number of b3 and groups Z4 in the number of b4 is a cyano group, and at least one of groups Z5 in the number of b5 and groups Z6 in the number of b6 is a cyano group, orat least one of groups Z1 in the number of b1 and groups Z2 in the number of b2 is a cyano group, at least one of groups Z3 in the number of b3 and groups Z4 in the number of b4 is a cyano group, and at least one of groups Z5 in the number of b5 and groups Z6 in the number of b6 is a cyano group.

8. The organic light-emitting device of claim 6, wherein a group represented by

9. The organic light-emitting device of claim 6, wherein a group represented by

10. The organic light-emitting device of claim 1, wherein the third material has reorganization energy of about 0.4 electron volts to about 1 electron volt.

11. The organic light-emitting device of claim 1, wherein the third material comprises a compound represented by Formula 11:

12. The organic light-emitting device of claim 11, wherein R3 comprises at least one π electron-depleted nitrogen-containing cyclic group.

13. The organic light-emitting device of claim 11, wherein R3 is selected from: a group represented by Formula 13(1) or 13(2);a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and an indolocarbazolyl group; anda phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and an indolocarbazolyl group, each substituted with at least one selected from deuterium, a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, a naphthyl group, a fluorenyl group, a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, an isoquinolinyl group, a carbazolyl group, a dibenzofuranyl group, a dibenzothiophenyl group, an indolocarbazolyl group, and —Si(Q31)(Q32)(Q33), andQ31 to Q33 are each independently selected from a C1-C10 alkyl group, a C1-C10 alkoxy group, a phenyl group, a biphenyl group, a terphenyl group, and a naphthyl group:

14. The organic light-emitting device of claim 11, wherein the third material comprises a compound represented by one of Formulae 11-1 to 11-7:

15. The organic light-emitting device of claim 1, wherein the light-emitting material comprises a transition metal-containing organometallic compound that emits blue light.

16. The organic light-emitting device of claim 1, wherein the light-emitting material comprises an organometallic compound comprising a bidentate ligand and a transition metal, the bidentate ligand containing at least one cyano group or at least one fluoro group.

17. The organic light-emitting device of claim 1, wherein the light-emitting material comprises an organometallic compound represented by Formula 1:

18. The organic light-emitting device of claim 17, wherein at least one of R31, R33, and R35 in Formula 1 is independently: deuterium, a cyano group, a C1-C20 alkyl group, a phenyl group, a biphenyl group, or a terphenyl group; ora C1-C20 alkyl group, a phenyl group, a biphenyl group, or a terphenyl group, each unsubstituted or substituted with at least one selected from deuterium, a cyano group, and a C1-C20 alkyl group.

19. The organic light-emitting device of claim 1, wherein an amount of the third material is greater than about 0 parts by weight and equal to or less than about 10 parts by weight based on 100 parts by weight of the first material, the second material, the third material, and the light-emitting material.

20. The organic light-emitting device of claim 1, wherein an amount of the light-emitting material is greater than about 0 parts by weight and equal to or less than about 5 parts by weight based on 100 parts by weight of the first material, the second material, the third material, and the light-emitting material.