The present disclosure provides a nitrogen-containing compound, and an electronic component and an electronic device including the same, and belongs to the technical field of organic electroluminescence. The nitrogen-containing compound provided by the present disclosure has polycyclic conjugation properties, the compound has a core structure of fused indolocarbazole. The bond energy between the atoms is high, thus the compound has a good thermal stability, and facilitates solid state accumulation between the molecules. The electroluminescence device with the compound as a luminescent layer material has a long service life. According to the nitrogen-containing compound provided by the present disclosure with an indolocarbazole structure connecting with a nitrogen-containing group (triazine, pyridine and pyrimidine) and a benzoxazole or benzothiazole group respectively has a high dipole moment, thereby improving the polarity of the material. Using the nitrogen-containing compound of the present disclosure as the luminescent layer material of the organic electroluminescence device, the electron transport performance of the device can be improved, and the luminous efficiency and service life of the device can be improved.

An organic electroluminescence device includes: an emitting region provided between a cathode and an anode; and a hole transporting zone provided between the anode and the emitting region, in which the hole transporting zone includes at least a first anode side organic layer and a second anode side organic layer, the first anode side organic layer is in direct contact with the second anode side organic layer, a total film thickness of the hole transporting zone is in a range from 20 nm to 80 nm, the first anode side organic layer contains no compound contained in the second anode side organic layer, the first anode side organic layer contains a first organic material and a second organic material, the first organic material is different from the second organic material, and a content of the first organic material in the first anode side organic layer is less than 50 mass %.

The present application relates to a compound which contains an indenocarbazole group, a particular arylamino group and an electron-deficient group bonded to the indenocarbazole group. The compound is suitable for use in electronic devices, in particular in organic electroluminescent devices.

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.

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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.

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

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.

Compounds that are organic radicals that can have a dual function. The compounds can be fluorescent emitters that emit in the near-IR. The compounds can also facilitate reverse intersystem crossing (RISC) to convert triplet excitons in an OLED to singlet excited states to maximize utilization of generated excitons in the OLED and approach 100% internal quantum efficiency.

A database system uses byte ordering for keys and a trie index to reference stored data. The keys of a database are converted into byte-comparable sequences of byte values. The trie index is generated including nodes connected by edges defining paths from a root node to leaf nodes. Each edge is associated with at least one byte value such that each path from the root node to a leaf node through one or more edges defines a unique byte prefix for a byte-comparable sequence of byte values. The leaf node of each path is associated with a database location value. A record is accessed in the database using a database location value determined from referencing the trie index using a byte-comparable sequence of byte values of the record generated from a key of the record. A trie structure and byte ordered keys may be used for partition or row indices.

A composition for manufacturing an organic electronic device includes at least three organic functional materials H1, H2, and H3, and at least one organic solvent. The organic functional materials H1 and H2 can form a type II semiconductor heterojunction structure. A LUMO value of the organic functional material H3 is greater than or equal to that of the organic functional materials H1 and H2, and a HOMO value thereof is less than or equal to that of the organic functional materials H1 and H2.