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US-2024381702-A1 · Nov 14, 2024 · US
US2025056966A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2025056966-A1 |
| Application number | US-202418675348-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 28, 2024 |
| Priority date | Aug 2, 2023 |
| Publication date | Feb 13, 2025 |
| Grant date | — |
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Embodiments provide a light emitting element that includes a first electrode, a first light emitting unit disposed on the first electrode, a charge generation unit disposed on the first light emitting unit, a second light emitting unit disposed on the charge generation unit, and a second electrode disposed on the second light emitting unit. The first light emitting unit includes a first hole transport region disposed on the first electrode, a first emission layer disposed on the first hole transport region, and a first electron transport region disposed on the first emission layer. The charge generation unit includes an n-type charge generation layer disposed on the first light emitting unit, and a p-type charge generation layer disposed on the n-type charge generation layer. At least one of the p-type charge generation layer and the first hole transport region each independently includes a tertiary amine compound including a cycloalkyl moiety.
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1 . A light emitting element comprising: a first electrode; a first light emitting unit disposed on the first electrode; a charge generation unit disposed on the first light emitting unit; a second light emitting unit disposed on the charge generation unit; and a second electrode disposed on the second light emitting unit, wherein the first light emitting unit comprises: a first hole transport region disposed on the first electrode; a first emission layer disposed on the first hole transport region; and a first electron transport region disposed on the first emission layer, the charge generation unit comprises: an n-type charge generation layer disposed on the first light emitting unit; and a p-type charge generation layer disposed on the n-type charge generation layer, at least one of the p-type charge generation layer and the first hole transport region each independently comprises a tertiary amine compound comprising a cycloalkyl moiety, and a first refractive index of the p-type charge generation layer with respect to a visible light is greater than a second refractive index of the first hole transport region with respect to the visible light. 2 . The light emitting element of claim 1 , wherein the first refractive index is in a range of about 1.78 to about 2.0, and the second refractive index is in a range of about 1.50 to about 1.78. 3 . The light emitting element of claim 1 , wherein a relation between the first refractive index and the second refractive index is represented by Mathematical Equation 1: 0.001 ≤ n 1 - n 2 ≤ 0.2 [ Mathematical Equation 1 ] wherein in Mathematical Equation 1, n1 is the first refractive index, and n2 is the second refractive index. 4 . The light emitting element of claim 1 , wherein a first extinction coefficient of the p-type charge generation layer is greater than a second extinction coefficient of the first hole transport region. 5 . The light emitting element of claim 4 , wherein the relation between the first extinction coefficient and the second extinction coefficient is represented by the following Mathematical Equation 2: 0.0001 ≤ k 1 - k 2 ≤ 0.1 [ Mathematical Equation 2 ] wherein in Mathematical Equation 2, k1 is the first extinction coefficient, and k2 is the second extinction coefficient. 6 . The light emitting element of claim 1 , wherein the tertiary amine compound is represented by Formula 1: wherein in Formula 1, L 1 , L 2 , and L 3 are each independently a direct linkage, a substituted or unsubstituted arylene group of 6 to 30 ring-forming carbon atoms, a substituted or unsubstituted heteroarylene group of 2 to 30 ring-forming carbon atoms, or a substituted or unsubstituted cycloalkylene group of 5 to 30 ring-forming carbon atoms, R 1 is a substituted or unsubstituted cycloalkyl group of 5 to 30 carbon atoms, R 2 is a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a hydroxyl group, a silyl group, a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted cycloalkyl group of 5 to 30 ring-forming carbon atoms, a substituted or unsubstituted aryl group of 6 to 30 ring-forming carbon atoms, or a substituted or unsubstituted heteroaryl group of 2 to 30 ring-forming carbon atoms, and R 3 is a group represented by Formula 2: wherein in Formula 2, X is C(R y1 )(R y2 ), N(R y3 ), O, or S, R x1 to R x8 and R y1 to R y3 are each independently a hydrogen atom, a deuterium atom, a halogen atom, a cyano group, a hydroxyl group, a substituted or unsubstituted alkyl group of 1 to 20 carbon atoms, a substituted or unsubstituted cycloalkyl group of 5 to 30 ring-forming carbon atoms, a substituted or unsubstituted aryl group of 6 to 30 ring-forming carbon atoms, or a substituted or unsubstituted heteroaryl group of 2 to 30 ring-forming carbon atoms, or combined with an adjacent group to form a ring, except that one of R x1 to R x8 is a position connected with Formula 1. 7 . The light emitting element of claim 6 , wherein R 1 is a group represented by one of Formula 3-1 to Formula 3-5: wherein in Formula 3-1 to Formula 3-5, is a position connected to L 1 in Formula 1, and at least one hydrogen atom is optionally substituted with a deuterium atom. 8 . The light emitting element of claim 6 , wherein the first hole transport region comprises the compound represented by Formula 1. 9 . The light emitting element of claim 1 , wherein the first hole transport region comprises at least one compound selected from Compound Group 1: 10 . The light emitting element of cla
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