Abstract:
The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device including the organic compound. Applying the organic compound into an emissive layer makes the OLED and the organic light emitting device lower their driving voltage, improves their luminous efficiency and color purity.
Abstract:
An organic light emitting diode (OLED) device includes a first electrode; a second electrode facing the first electrode; an emitting material layer disposed between the first and second electrodes and a horizontally oriented liquid crystal type emitting material.
Abstract:
The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device including the organic compound. The organic compound can be a bipolar compound having a p-type moiety and an n-type moiety and has high energy level and proper energy bandgap for an emissive layer of the OLED. As the organic compound is applied into the emissive layer, the OLED can maximize its luminous properties as holes and electrons are recombined uniformly over the whole area in an emitting material layer (EML).
Abstract:
The present disclosure relates to an emitting compound and organic light emitting device including the same, more specifically, relates to an emitting compound of following and an organic light emitting diode and an organic light emitting device each including the emitting compound.
Abstract:
Discussed is an organic compound of Formula 1 and an organic light emitting diode and an OLED device including the organic compound. In the organic compound, Ar1 is a heteroaryl group comprising a nitrogen atom, and Ar2 is a C6 to C30 aryl group, and R is a C1 to C10 alkyl group. The organic compound may be included in an emitting material layer of the organic light emitting diode as a host such that an emitting efficiency and a lifespan of the organic light emitting diode and the OLED device are improved.
Abstract:
Discussed is a space-through charge transfer compound including a naphthalene core; an electron donor moiety selected from carbazole and phenylcarbazole; and an electron acceptor moiety selected from pyridine, diazine, triazole, and phenyl benzodiazole, wherein the electron donor moiety and the electron acceptor moiety are combined to first and eighth positions of the naphthalene core with a benzene linker, respectively.
Abstract:
The present invention provides an organic compound of following formula and an organic light emitting diode and an OLED device including the organic 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 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:
The present disclosure relates to an organic light emitting diode including an emitting material layer that has a host and two different delayed fluorescent materials whose energy levels are controlled and an organic light emitting device including the diode. Exciton energy is transferred from a first delayed fluorescent dopant to a second delayed fluorescent dopant, which has singlet and triplet energy levels lower than singlet and triplet energy levels of the first delayed fluorescent dopant and a narrow FWHM (full-width at half maximum) compared to the first delayed fluorescent dopant so that efficient light emission can be realized.