C09K2211/1018

Dye-loaded fluorescent polymeric nanoparticles as nano-antenna

Dye-loaded fluorescent polymeric nanoparticles working as light-harvesting nano-antenna, which efficiently transfer the excitation energy to acceptor dyes and, therefore, amplifies emission of the latter are provided.

Heterocyclic compound and organic light-emitting element using same

The present application relates to a hetero-cyclic compound represented by Chemical Formula 1, and an organic light emitting device comprising the same.

Light Emitting Device and Light Emitting Display Device Including the Same

A light emitting device and a light emitting display device that are capable of improving efficiency, driving voltage, and lifespan by varying the configuration of a layer adjacent to a blue light emitting layer in a blue fluorescent stack contacting a cathode are disclosed. The light emitting device includes stacks between an anode and a cathode, wherein an n.sup.th stack contacting the cathode is a first blue stack that includes a first hole transport layer, a first electron-blocking layer, a first blue light emitting layer containing a boron-based dopant having an emission peak of 430 nm to 480 nm, a first electron transport layer contacting the first blue light emitting layer, and an electron injection layer having two sides contacting the first electron transport layer and the cathode, respectively, wherein the first electron transport layer contains a mixture of a first material and a second material.

LIGHT EMITTING ELEMENT

A light emitting element that includes a first compound represented by a specific chemical formula in which an ortho-type or kind penta-phenyl group is bonded to a fused polycyclic compound including at least one boron atom and a heteroatom is provided. The light emitting element has a long-lifetime.

LIGHT EMITTING DEVICE AND LIGHT EMITTING DISPLAY DEVICE INCLUDING THE SAME
20230217824 · 2023-07-06 ·

Disclosed are a light emitting device that includes an additional layer adjacent to a light emitting layer and thus is capable of utilizing, in light emission, holes not used in the light emitting layer, to improve efficiency and lifespan, and a light emitting display device including the same. The light emitting device includes a first electrode and a second electrode facing each other, and an unit comprising a hole transport layer, a light emitting layer, an efficiency-improving layer, and an electron transport layer sequentially stacked between the first electrode and the second electrode, wherein the light emitting layer includes a first host comprising an anthracene derivative and a first blue light emitting dopant, and the efficiency-improving layer includes a second host having bipolarity and a second blue light emitting dopant.

PLURALITY OF HOST MATERIALS AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

The present disclosure relates to a plurality of host materials comprising at least one first host compound represented by the following formula 1 and at least one second host compound represented by the following formula 2, and an organic electroluminescent device comprising the same. By comprising the specific combination of the compound according to the present disclosure as host materials, an organic electroluminescent device having high luminous efficiency and/or long lifespan characteristics can be provided.

Thermally activated delayed fluorescent molecular material, a synthesizing method therefor, and an electroluminescent device

A thermally activated delayed fluorescent molecular material, a synthesizing method therefor, and an electroluminescent device are provided. The thermally activated delayed fluorescent molecular containing an indenobenzoselenoheteroaromatic ring donor is synthesized, so that an electron donating ability of the donor is increased, and an non-radiative transition rate is effectively inhibited, thereby increasing photo-luminescence quantum yield (PLQY) of the molecule; and increasing the twist angle between the electron donor and the electron acceptor. Meanwhile, electron cloud overlapping between highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) is reduced, thereby obtaining a smaller ΔE.sub.ST value. The organic electroluminescent device adopts the thermally activated delayed fluorescent molecular material prepared according to the synthesizing method, and thus has high luminous efficiency and long service life.

Compound for organic electronic element, organic electronic element using the same, and an electronic device thereof

The present invention provides a novel compound capable of improving the luminous efficiency, stability and lifespan of a device, an organic electronic element using the same, and an electronic device thereof, wherein the compound is represented by Formula (1): ##STR00001## wherein: A is a substituent represented by Formula (A-1)-(A-2); ##STR00002##

POLYCYCLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING POLYCYCLIC COMPOUND, AND ELECTRONIC APPARATUS INCLUDING ORGANIC LIGHT-EMITTING DEVICE

Provided are a polycyclic compound represented by Formula 1, an organic light-emitting device including the polycyclic compound, and an electronic apparatus including the organic light-emitting device:

##STR00001##

Formula 1 may be understood by referring to the description of Formula 1 provided herein.

Organic molecules for optoelectronic devices
11545632 · 2023-01-03 · ·

An organic molecule is disclosed herein having a structure of formula I: ##STR00001##
wherein
n=0 or 1 at each occurrence,
m=1-n at each occurrence; i.e. if n is 1, m is 0 and vice versa,
o=0 or 1 at each occurrence, and
p=1-o at each occurrence;
T is selected from the group consisting of a direct bond, NR.sup.3, Si(R.sup.3).sub.2, C(R.sup.3).sub.2, BR.sup.3, O, S, S(O) and S(O).sub.2.
V is selected from the group consisting of a direct bond, NR.sup.3, Si(R.sup.3).sub.2, C(R.sup.3).sub.2, BR.sup.3, O, S, S(O) and S(O).sub.2.
Z is at each occurrence independently form another selected from the group consisting of a direct bond, CR.sup.3R.sup.4, C═CR.sup.3R.sup.4, C═O, C═NR.sup.3, O, SiR.sup.3R.sup.4, S, S(O) and S(O).sub.2.