Abstract: An organic compound having a fused heteroaromatic moiety as an electron donor and a tri-pyrimidine moiety sharing an arylene group as an electron acceptor bonded to the fused heteroaromatic moiety, an organic light-emitting diode and an organic light-emitting device including the organic compound are disclosed, where the organic compound leads to enhanced luminous efficiency and lower driving voltages.

Abstract: An organic light emitting diode includes an emitting material layer including first and second layers; a first electrode on a side of the emitting material layer; and a second electrode on the other side of the light emitting material layer and facing the first electrode, wherein the first layer includes a first compound, and the second layer includes a second compound, wherein the first compound has a difference, between a singlet energy and a triplet energy, less than 0.3 eV, and wherein the singlet energy of the first compound is greater than a singlet energy of the second compound.

Abstract: An organic compound having a naphtho fluoranthene core and a hetero aromatic group bonded to a specific position of the naphtho fluoranthene core, an organic light-emitting diode and an organic light-emitting device including the compound are disclosed. Since the organic compound has a narrow Stokes Shift between an absorption wavelength and an emission wavelength, the organic compound has a broad overlapped area between its absorption peak and an emission peak of a delayed fluorescent material, and therefore it can emit blue light with high color purity. It is possible to manufacture an organic light-emitting diode (OLED) and an organic light-emitting device that enhance luminous efficiency and color purity using the organic compound.

Abstract: The present disclosure provides an organic emitting compound of the following Formula, and an organic light emitting diode, which includes a first electrode; a second electrode facing the first electrode; and a first emitting material layer positioned between the first electrode and the second electrode and including a first host and the organic emitting compound, and an organic light emitting display device including the organic light emitting diode.

Abstract: Embodiments relate to a delayed fluorescence compound of The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: Discussed is a space-through charge transfer compound including a paracyclophane core, an electron donor moiety selected from the group consisting of carbazole and diphenyl amine, and an electron acceptor moiety selected from the group consisting of pyrimidine, diphenyltriazine, and triazole. The electron donor moiety and the electron acceptor moiety are indirectly or directly combined to the paracyclophane core with or without a linker, respectively.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.

Abstract: An organic light emitting diode includes an emitting material layer including first and second layers; a first electrode on a side of the emitting material layer; and a second electrode on the other side of the light emitting material layer and facing the first electrode, wherein the first layer includes a first compound, and the second layer includes a second compound, wherein the first compound has a difference, between a singlet energy and a triplet energy, less than 0.3 eV, and wherein the singlet energy of the first compound is greater than a singlet energy of the second compound.

Abstract: Discussed is a delayed fluorescence compound including a first electron donor moiety of indolo-[3,2,1-j,k]carbazole; a second electron donor moiety selected from indolo-[3,2,1-j,k]carbazole, carbazole, or triphenylamine; and an electron acceptor moiety selected from dibenzothiophene sulfone or diphenyl sulfone, wherein the first and second electron donor moieties are combined to the electron acceptor moiety, and the electron acceptor moiety is combined to a third position or a sixth position of the first electron donor moiety.

Abstract: Discussed is a delayed fluorescence compound of Formula 1: wherein n is 1 or 0, and A is selected from Formula 2: wherein D is selected from Formula 3: and each of “L1” and “L2” is independently selected from Formula 4: wherein R1 in the Formula 2 is selected from hydrogen or phenyl, and each of X, Y, and Z is independently selected from carbon and nitrogen, and wherein at least two selected from X, Y, and Z are nitrogen, and R2 in the Formula 4 is selected from one of hydrogen and C1 alkyl through C10 alkyl.

Abstract: Discussed is an organic electroluminescent device including a first charge carrying layer being disposed adjacent to a first electrode; and a second charge carrying layer disposed adjacent to a second electrode, wherein the first charge carrying layer includes an emitting part, a hole injection part and a hole transporting part between the hole injection part and the emitting part, wherein at least one of the hole injection part, the hole transporting part and the emitting part includes a host material having an organic compound of Formula: wherein R is substituted or non-substituted C1 to C12 alkyl, and A and B are symmetrically or asymmetrically positioned in 2-position or 7-position of the fluorene core, and wherein each of A and B is independently selected from substituted or non-substituted aromatic group or substituted or non-substituted heterocyclic group.

Abstract: Discussed is an organic electroluminescent device including a first charge carrying layer being disposed adjacent to a first electrode; and a second charge carrying layer disposed adjacent to a second electrode, wherein the first charge carrying layer includes an emitting part, a hole injection part and a hole transporting part between the hole injection part and the emitting part, wherein at least one of the hole injection part, the hole transporting part and the emitting part includes a host material having an organic compound of Formula: wherein R is substituted or non-substituted C1 to C12 alkyl, and A and B are symmetrically or asymmetrically positioned in 2-position or 7-position of the fluorene core, and wherein each of A and B is independently selected from substituted or non-substituted aromatic group or substituted or non-substituted heterocyclic group.

Abstract: Discussed is a space-through charge transfer compound including a paracyclophane core, an electron donor moiety selected from the group consisting of carbazole and diphenyl amine, and an electron acceptor moiety selected from the group consisting of pyrimidine, diphenyltriazine, and triazole. The electron donor moiety and the electron acceptor moiety are indirectly or directly combined to the paracyclophane core with or without a linker, respectively.

Abstract: Discussed is an organic electroluminescent device including a first charge carrying layer being disposed adjacent to a first electrode; and a second charge carrying layer disposed adjacent to a second electrode, wherein the first charge carrying layer includes an emitting part, a hole injection part and a hole transporting part between the hole injection part and the emitting part, wherein at least one of the hole injection part, the hole transporting part and the emitting part includes a host material having an organic compound of Formula: wherein R is substituted or non-substituted C1 to C12 alkyl, and A and B are symmetrically or asymmetrically positioned in 2-position or 7-position of the fluorene core, and wherein each of A and B is independently selected from substituted or non-substituted aromatic group or substituted or non-substituted heterocyclic group.

Abstract: Discussed is an organic electroluminescent device including a first charge carrying layer being disposed adjacent to a first electrode; and a second charge carrying layer disposed adjacent to a second electrode, wherein the first charge carrying layer includes an emitting part, a hole injection part and a hole transporting part between the hole injection part and the emitting part, wherein at least one of the hole injection part, the hole transporting part and the emitting part includes a host material having an organic compound of Formula: wherein R is substituted or non-substituted C1 to C12 alkyl, and A and B are symmetrically or asymmetrically positioned in 2-position or 7-position of the fluorene core, and wherein each of A and B is independently selected from substituted or non-substituted aromatic group or substituted or non-substituted heterocyclic group.

Abstract: Embodiments relate to a delayed fluorescence compound of Formula 1: or Formula 2: The excitons in the triplet state are engaged in emission such that the emitting efficiency of the delayed fluorescent compound is increased. Embodiments also relate to a display device with an organic light emitting diode (OLED) that includes the delayed fluorescence compound.