The present invention provides an organic electroluminescent element which comprises: an anode; a cathode; and an organic layer interposed between the anode and the cathodes, wherein the organic layer comprises one or more types of layer from the group consisting of a hole-injection layer, hole-transport layer, light-emitting layer, lifetime enhancement layer, electron-transport layer, and electron-injection layer.

A thermally activated, sensitized phosphorescence organic electroluminescence device includes a luminescent layer formed of a host material consisting of two materials, one being a hole transport material, and the other an electron transport material, at least one which is a thermally activated delayed fluorescence material. The host material is doped by a phosphorescent dye. The triplet state energy level of the CT excited state of the fluorescence material is higher than the triplet state energy level of the n-π excited state by 0 to 0.3 or the triplet state energy level of the CT excited state of the fluorescence material is higher than the triplet state energy level of the n-π excited state, wherein the difference is above 1.0 eV, and, a difference between the second triplet state energy level of its n-π excited state and the first singlet state energy level of its CT excited state is −0.1 to 0.1 eV.

The present disclosure relates to an organic electroluminescent compound and an organic electroluminescent device comprising the same. By comprising the organic electroluminescent compound of the present disclosure, it is possible to provide an organic electroluminescent device having low driving voltage and/or improved lifespan properties.

The present invention describes compounds having an acceptor group and a donor group, especially for use in electronic devices. The invention further relates to a process for preparing the compounds of the invention and to electronic devices comprising these.

The present disclosure relates to an OLED display panel. With the OLED display panel, a higher luminous efficiency is achieved by selecting a thermally activated delayed fluorescent material for doping into an organic light emitting layer and applying a compound having a specific energy level to match, thereby the luminous efficiency of an organic photo electronic device is improved.

A photoelectric device includes a first photoelectric conversion layer including a heterojunction that includes a first p-type semiconductor and a first n-type semiconductor, a second photoelectric conversion layer on the first photoelectric conversion layer and including a heterojunction that includes a second p-type semiconductor and a second n-type semiconductor. A peak absorption wavelength (λ.sub.max1) of the first photoelectric conversion layer and a peak absorption wavelength (λ.sub.max2) of the second photoelectric conversion layer are included in a common wavelength spectrum of light that is one wavelength spectrum of light of a red wavelength spectrum of light, a green wavelength spectrum of light, a blue wavelength spectrum of light, a near infrared wavelength spectrum of light, or an ultraviolet wavelength spectrum of light, and a light-absorption full width at half maximum (FWHM) of the second photoelectric conversion layer is narrower than an FWHM of the first photoelectric conversion layer.

An organic electroluminescent material and a device thereof are disclosed. The organic electroluminescent material uses a compound having a novel carbazole structure, and can be used as hole blocking material, host material in an electroluminescent device. These novel compounds can provide better device performance, such as obtaining device performance of very low driving-voltage, high efficiency, and long lifetime.

An organic light-emitting device includes a heterocyclic compound represented by Formula 1 ##STR00001##
In Formula 1, X is O or S, one selected from R.sub.1 to R.sub.8 is a group represented by Formula 2-1, and one selected from the remaining groups is a group represented by Formula 2-2, wherein, when X is O, one selected from R.sub.1, R.sub.2, R.sub.4, R.sub.5, R.sub.7, and R.sub.8 is a group represented by Formula 2-1.

A near-infrared absorber includes a compound represented by Chemical Formula 1. A near-infrared absorbing/blocking film, a photoelectric device, an organic sensor, and an electronic device may include the near-infrared absorber. ##STR00001## In Chemical Formula 1, X.sup.1, X.sup.2, Y.sup.1, Y.sup.2, Ar, Ar.sup.1, and Ar.sup.2 are the same as defined in the detailed description.

Organic compounds containing indolocarbazoles as electron donor connected with electron acceptors such aza-triphenylene or dibenzoquinoxaline that can improve the performance of phosphorescent organic light emitting devices are disclosed.