Abstract:
A condensed cyclic compound and a device including the same are provided. The compound has the structure wherein rings A1-A4 may independently be selected from a C5-C30 carbocyclic ring and a C2-C30 heterocyclic ring, R1 to R4 may independently be selected from Formula 2-1, Formula 2-2, hydrogen, deuterium (-D), —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazino group, a hydrazono group, 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 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, —Si(Q1)(Q2)(Q3), —B(Q1)(Q2), —C(═O)(Q1), —S(═O)2(Q1), and —P(═O)(Q1)(Q2). Details, including structures of Formula 2-1 and Formula 2-2, are provided.
Abstract:
An organic light-emitting device including: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the organic layer includes a carbazole-based compound represented by Formula 1A or 1B: When the carbazole-based compound represented by Formula 1A or 1B is included in the hole transport layer, an organic light-emitting device may have improved driving voltage, efficiency, luminance, and lifespan characteristics.
Abstract:
An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the organic layer includes a compound represented by Formula 1. The organic light-emitting device including the compound may have high efficiency, low voltage, high luminance, and a long lifespan.
Abstract:
A compound represented by Formula 1, and an organic light-emitting device including the compound represented by Formula 1: When the compound represented by Formula 1 is included in the electron transport layer of an organic light-emitting device, the device may have high efficiency, a lower driving voltage, high luminance, excellent I-V-L characteristics, and/or a long lifespan.
Abstract:
A compound represented by Formula 1, and an organic light-emitting device including the compound: In Formula 1, when L1 and/or L2 is a phenyl group, a pyridyl group, a pyrimidyl group, and/or a 1,3,5-triazinyl group having binding sites that are ortho- or meta- to each other, and the compound of Formula 1 is included the second hole transport layer (HTL2), the efficiency and luminance half-life of a device may increase due to the HTL2 having a higher T1 (e.g., triplet) energy level compared to examples in the related art using a para-substituted phenyl linker.
Abstract:
The present disclosure provides a condensed-cyclic compound represented by Formula 1, in which one selected from R1 to R8 is a monoamine represented by Formula 2: The condensed-cyclic compound represented by Formula 1 may act as a hole transport material having a suitable energy level and band-gap. Further, the condensed-cyclic compound represented by Formula 1 has a fused core, and accordingly may have a high glass transition temperature (Tg), high melting point, and improved resistance to high temperatures. Therefore an organic light-emitting device including the condensed-cyclic compound represented by Formula 1 may retain high durability during storing and/or driving.
Abstract:
An organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer, wherein the organic layer includes: a condensed cyclic compound represented by Formula 1; and at least one selected from a first compound represented by Formula 11, a second compound represented by Formula 12, and a third compound represented by Formula 13: