Abstract:
A borole compound is represented by Formula 1: X11—(R11)b11. X11, R11, and b11 are as defined herein. An organic light-emitting device includes the borole compound. The organic light-emitting device includes a first electrode, a second electrode, and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer. The organic layer includes the borole compound.
Abstract:
A borole compound is represented by Formula 1: X11—(R11)b11. X11, R11, and b11 are as defined herein. An organic light-emitting device includes the borole compound. The organic light-emitting device includes a first electrode, a second electrode, and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer. The organic layer includes the borole compound.
Abstract:
A dibenzoborole-based compound and an organic light-emitting device including the same. The dibenzoborole-based compound is represented by the formula A1-(A2)n1, wherein A1 may be selected from specific aromatic and non-aromatic carbocycles and heterocycles, n1 may be an integer selected from 1 to 10, and each A2 moiety may independently be selected from a group represented by Formula 2: The dibenzoborole-based compound may be included in the hole transport region or hole transport layer. When the dibenzoborole-based compound has strong electron acceptor characteristics, the hole injection barrier between the anode and the organic layer may be reduced, and thus, an organic light-emitting device including the dibenzoborole-based compound may have high efficiency and a long lifespan.
Abstract:
A dibenzoborole-based compound and an organic light-emitting device including the same. The dibenzoborole-based compound is represented by the formula A1-(A2)n1, wherein A1 may be selected from specific aromatic and non-aromatic carbocycles and heterocycles, n1 may be an integer selected from 1 to 10, and each A2 moiety may independently be selected from a group represented by Formula 2: The dibenzoborole-based compound may be included in the hole transport region or hole transport layer. When the dibenzoborole-based compound has strong electron acceptor characteristics, the hole injection barrier between the anode and the organic layer may be reduced, and thus, an organic light-emitting device including the dibenzoborole-based compound may have high efficiency and a long lifespan.
Abstract:
A light-emitting device includes a first electrode, a second electrode facing the first electrode, an interlayer arranged between the first electrode and the second electrode and including an emission layer, and a capping layer, wherein the emission layer includes a first emitter, the first emitter is configured to emit first light having a first emission spectrum, the capping layer is arranged in a path on which the first light is configured to travel, an emission peak wavelength of the first light is in a range of about 610 nm to about 720 nm, the first emitter includes iridium, the capping layer includes an amine-containing compound, a value of ratio of reflective index to full width at half maximum of the first light configured to be extracted to the outside through the capping layer is 2.0 or more, and the RRF value is calculated by Equation 1.
Abstract:
An organometallic compound includes a hexadentate ligand bonded to a metal atom (M1). An energy level (E3MC) of a 3MC state (triplet metal centered state) of the organometallic compound is higher than an energy level (E3MLCT) of a 3MLCT state (triplet metal-to-ligand charge transfer state) of the organometallic compound.
Abstract:
An organometallic compound and an organic light-emitting device including the same are provided. The organometallic compound may be represented by Formula 1, wherein L1 is a ligand represented by Formula 2A and L2 is a ligand represented by Formula 2B. Further details about the compounds are presented in the disclosure. M(L1)n1(L2)n2, wherein M is iridium.