H10K85/623

Organic electroluminescent compound and organic electroluminescent device comprising the same

The present disclosure relates to an organic electroluminescent compound and an organic electroluminescent device comprising the same. By using the organic electroluminescent compound of the present disclosure, an organic electroluminescent device having high luminous efficiency and/or long lifespan properties can be provided compared to conventional organic electroluminescent devices.

COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE COMPRISING SAME

Provided is a compound of Chemical Formula 1:

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wherein n is 0 or 1, when n is 0, at least one of R1 to R10 is a group of Chemical Formula A, and when n is 1, at least one of R1 to R12 is a group of Chemical Formula A:

##STR00002##

wherein L1 is a direct bond, or a substituted or unsubstituted arylene or heteroarylene group; l1 is an integer of 1 to 5; m is an integer of 1 to 3; when l1 is 2 or greater, the two or more L1s are the same as or different from each other, and an organic light emitting device including the same.

Organic electroluminescence device and electronic apparatus

An organic electroluminescence device including: an anode, a cathode, and at least one emitting layer between the cathode and the anode, wherein the emitting layer contains a first host material, a second host material, and a dopant material, the first host material is a compound having at least one deuterium atom, and the emitting layer contains the first host material in the proportion of 1% by mass or more.

NITROGEN-CONTAINING COMPOUND, ORGANIC ELECTROLUMINESCENT DEVICE, AND ELECTRONIC APPARATUS
20230124929 · 2023-04-20 ·

Provided are a nitrogen-containing compound, an organic electroluminescent device and an electronic apparatus. The nitrogen-containing compound has a structure as shown in chemical formula 1; Ar.sub.1 and Ar.sub.2 are the same or different, and each is independently selected from a substituted or unsubstituted C6-C30 aryl, or a substituted or unsubstituted C3-C30 heteroaryl; and R.sub.0 is selected from hydrogen, a C1-C6 alkyl, a substituted or unsubstituted C6-C30 aryl, or a substituted or unsubstituted C3-C30 heteroaryl. The nitrogen-containing compound acts as a hole transporting material or a host material of a luminescent layer and can effectively improve the performance of organic electroluminescent devices.

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ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC DEVICE
20230123637 · 2023-04-20 · ·

An organic EL device includes: an anode; a cathode; an anode side emitting unit; a cathode side emitting unit; a charge generating unit; a first organic layer having a thickness of 40 nm or less; and a second organic layer, in which the anode side emitting unit includes a first emitting layer which is provided close to the anode, a difference between an ionization potential Ip(H1) of a first host material in the first emitting layer and an ionization potential Ip(EBL) of a first organic material in the first organic layer satisfies a relationship of a numerical formula (Numerical Formula A1) below,


Ip(H1)−Ip(EBL)≤0.4 eV  (Numerical Formula A1).

LIGHT-RECEIVING DEVICE AND LIGHT-EMITTING AND LIGHT-RECEIVING APPARATUS

A light-receiving device in which an increase in driving voltage is inhibited is provided. Any of the following light-receiving devices is provided: a light-receiving device that includes a light-receiving layer between a pair of electrodes and in which the light-receiving layer includes an active layer, a buffer layer, and an electron-transport layer, the buffer layer is between the active layer and the electron-transport layer and is in contact with the active layer, and the buffer layer includes an organic compound having an electron-withdrawing group; a light-receiving device that includes a light-receiving layer between a pair of electrodes and in which the light-receiving layer includes an active layer, a buffer layer, and an electron-transport layer, the buffer layer is between the active layer and the electron-transport layer and is in contact with the active layer, and the buffer layer includes a heteroaromatic compound having an electron-withdrawing group.

LIGHT EMITTING ELEMENT AND POLYCYCLIC COMPOUND FOR LIGHT EMITTING ELEMENT

Provided is a polycyclic compound and a light emitting element including the polycyclic compound. The light emitting element includes a first electrode, a second electrode facing the first electrode, light emitting structures disposed between the first electrode and the second electrode, and a charge generation layer disposed between adjacent ones of the light emitting structures and including a polycyclic compound represented by Formula 1, thereby exhibiting high luminous efficiency.

##STR00001##

COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE COMPRISING SAME

A compound of Chemical Formula 1, and an organic light emitting device including the same are provided. The compound is used as a material of an organic material layer of an organic light emitting device, and provides enhanced efficiency, low driving voltage and/or increased lifetime properties of the organic light emitting device.

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LIGHT-EMITTING DEVICE AND ELECTRONIC APPARATUS INCLUDING THE SAME

A light-emitting device includes a first electrode, a second electrode facing the first electrode, and an interlayer disposed between the first electrode and the second electrode. The emission layer includes a first emission layer and a second emission layer. The first emission layer includes a first compound, and the second emission layer includes a second compound. The first compound includes at least one deuterium (D), and the second compound does not include deuterium. An electronic apparatus including the light-emitting device is also provided.

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC DEVICE

A compound has, in a molecule, a cyclic structure represented by a formula (1) below; and at least one cyclic structure selected from the group consisting of a cyclic structure represented by a formula (10) below and a cyclic structure represented by a formula (11) below. In the formula (1): R.sub.1 to R.sub.16 are each independently a hydrogen atom, an alkyl group or the like; and R.sub.X and R.sub.Y are each independently an alkyl group.

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