H10K85/636

ORGANIC ELECTROLUMINESCENT DEVICE

In the organic electroluminescent device having at least an anode, a hole injection layer, a first hole injection layer, a second hole injection layer, a light emitting layer, an electron transport layer and a cathode in this order, the hole injection layer includes an arylamine compound of the following general formula (1) and an electron acceptor.

##STR00001##

In the formula, Ar.sub.1 to Ar.sub.4 may be the same or different, and represent a substituted or unsubstituted aromatic hydrocarbon group, a substituted or unsubstituted aromatic heterocyclic group, or a substituted or unsubstituted condensed polycyclic aromatic group.

SPIRO-TYPE COMPOUND AND ORGANIC LIGHT EMITTING ELEMENT COMPRISING SAME
20180006233 · 2018-01-04 · ·

The present specification provides a compound having a spiro structure, and an organic light emitting device including the same.

ORGANIC PHOTOELECTRONIC DEVICE AND IMAGE SENSOR

An organic photoelectronic device includes a first electrode and a second electrode facing each other and a light-absorption layer between the first electrode and the second electrode and including a photoelectric conversion region including a p-type light-absorbing material and an n-type light-absorbing material and a doped region including an exciton quencher and at least one of the p-type light-absorbing material and the n-type light-absorbing material, wherein at least one of the p-type light-absorbing material and the n-type light-absorbing material selectively absorbs a part of visible light, and an image sensor includes the same.

Carbazole Derivative, and Light-Emitting Element, Light-Emitting Device, and Electronic Device Using the Carbazole Derivative

To provide a light-emitting element having high luminous efficiency and to provide a light-emitting device and an electronic device which consumes low power and is driven at low voltage, a carbazole derivative represented by the general formula (1) is provided. In the formula, α.sup.1, α.sup.2, α.sup.3, and α.sup.4 each represent an arylene group having less than or equal to 13 carbon atoms; Ar.sup.1 and Ar.sup.2 each represent an aryl group having less than or equal to 13 carbon atoms; R.sup.1 represents any of a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted biphenyl group; and R.sup.2 represents any of an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted phenyl group, and a substituted or unsubstituted biphenyl group. In addition, l, m, and n are each independently 0 or 1.

MATERIAS FOR ELECTRONIC DEVICES

The present invention relates to a compound of the formula (I), (II) or (III), to the use of the compound in an electronic device, and to an electronic device comprising a compound of the formula (I), (II) or (III). The present invention furthermore relates to a process for the preparation of a compound of the formula (I), (II) or (III) and to a formulation comprising one or more compounds of the formula (I), (II) or (III).

ORGANIC ELECTROLUMINESCENT ELEMENT

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.

THERMALLY-ACTIVATED SENSITIZED PHOSPHORESCENT ORGANIC ELECTROLUMINESCENT DEVICE

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.

ORGANIC LIGHT-EMITTING DIODE HAVING LOW DRIVING VOLTAGE AND LONG LIFESPAN

The present disclosure relates to an organic light-emitting diode having a low driving voltage and long lifespan and more particularly, to an organic light-emitting diode, comprising a first electrode, a second electrode facing the first electrode, and a light-emitting layer interposed therebetween, wherein the light-emitting layer contains at least one of the amine compounds represented by the following Chemical Formula A or Chemical Formula B, plus the compound represented by Chemical Formula D. The structures of Chemical Formulas A, B, and D are the same as in the specification.

Metal amides for use as HIL for an organic light-emitting diode (OLED)
11711934 · 2023-07-25 · ·

The present invention relates to metal amides of general Formula Ia and for their use as hole injection layer (HIL) for an Organic light-emitting diode (OLED), and a method of manufacturing Organic light-emitting diode (OLED) comprising an hole injection layer containing a metal amide of general Formula Ia: ##STR00001##

Compounds with an acceptor and a donor group

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.