Electroluminescent device, and display device comprising thereof
US-10749130-B2 · Aug 18, 2020 · US
US12161005B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12161005-B2 |
| Application number | US-202117522316-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 9, 2021 |
| Priority date | Nov 10, 2020 |
| Publication date | Dec 3, 2024 |
| Grant date | Dec 3, 2024 |
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A light emitting device including a first electrode and a second electrode each having a surface opposite the other, a light emitting layer disposed between the first electrode and the second electrode, and an electronic auxiliary layer disposed between the light emitting layer and the second electrode, wherein the electron auxiliary layer includes metal oxide nanoparticles and an orthosilicate compound.
Opening claim text (preview).
What is claimed is: 1. A light emitting device, comprising a first electrode and a second electrode each having a surface opposite the other, a light emitting layer disposed between the first electrode and the second electrode, and an electronic auxiliary layer disposed between the light emitting layer and the second electrode, wherein the electron auxiliary layer comprises metal oxide nanoparticles and an orthosilicate compound. 2. The light emitting device of claim 1 , wherein at least a portion of the orthosilicate compound is bound to a surface of the metal oxide nanoparticles. 3. The light emitting device of claim 1 , wherein the metal oxide nanoparticles comprise a coating layer on a surface of the metal oxide nanoparticles, the coating layer including at least a portion of the orthosilicate compound. 4. The light emitting device of claim 1 , wherein the orthosilicate compound is represented by Chemical Formula 1: wherein, in Chemical Formula 1, R 11 to R 14 are independently a hydroxy group, a halogen, a substituted or unsubstituted C1 to C8 linear or branched alkoxy group, or a substituted or unsubstituted C6 to C12 aryloxy group. 5. The light emitting device of claim 1 , wherein the orthosilicate compound comprises tetramethylorthosilicate, tetraethylorthosilicate, tetrapropylorthosilicate, tetrabutylorthosilicate, or a combination thereof. 6. The light emitting device of claim 1 , wherein the orthosilicate compound is present in an amount of about 5 parts by weight to about 500 parts by weight, based on 100 parts by weight of the metal oxide nanoparticles. 7. The light emitting device of claim 1 , wherein the electron auxiliary layer further comprises a first silane compound represented by Chemical Formula 2: (R 21 ) p —Si—(R 22 ) 4-p Chemical Formula 2 wherein, in Chemical Formula 2, R 21 is a substituted or unsubstituted C6 to C20 aryl group, a substituted or unsubstituted C1 to C20 linear or branched alkyl group, a substituted or unsubstituted C1 to C20 aminoalkyl group, a substituted or unsubstituted C6 to C12 aryloxy group, a substituted or unsubstituted C2 to C20 alkynyl group, C2 to C20 alkenyl group, a substituted or unsubstituted C1 to C20 amine group, —C(═O)OR′, wherein R′ is a 01 to C20 linear or branched alkyl group, or —C(═O)ONR′R″, wherein R′ and R″ are independently a C1 to C20 linear or branched alkyl group, R 22 is a hydroxy group, a halogen, a substituted or unsubstituted C1 to C8 linear or branched alkoxy group, a substituted or unsubstituted C6 to C12 aryloxy group, a substituted or unsubstituted C2 to C10 carbonylalkyl group, or a substituted or unsubstituted C2 to C10 carbonylalkoxy group, and p is an integer of 1 to 3. 8. The light emitting device of claim 7 , wherein the first silane compound comprises trimethoxysilane, methyltrimethoxysilane, ethyltrimethoxysilane, propyltrimethoxysilane, butyltrimethoxysilane, pentyltrimethoxysilane, hexyltrimethoxysilane, octyltrimethoxysilane, triethoxysilane, methyltriethoxysilane, ethyltriethoxysilane, propyltriethoxysilane, butyltriethoxysilane, pentyltriethoxysilane, hexyltriethoxysilane, octyltriethoxysilane, dimethoxysilane, dimethyldimethoxysilane, diethyldimethoxysilane, dipropyldimethoxysilane, dibutyldimethoxysilane, dipentyldimethoxysilane, dihexyldimethoxysilane, dioctyldimethoxysilane, diethoxysilane, dimethyldiethoxysilane, diethyldiethoxysilane, dipropyldiethoxysilane, dibutyldiethoxysilane, dipentyldiethoxysilane, dihexyldiethoxysilane, dioctyldiethoxysilane, phenyltrimethoxysilane, diphenyldimethoxysilane, phenyltriethoxysilane, diphenyldiethoxysilane, aminomethyltrimethoxysilane, aminoethyltrimethoxysilane, aminopropyltrimethoxysilane, am inobutyltrimethoxysilane, aminopentyltrimethoxysilane, aminohexyltrimethoxysilane, aminooctyltrimethoxysilane, aminomethyltriethoxysilane, aminoethyltriethoxysilane, aminopropyltriethoxysilane, aminobutyltriethoxysilane, aminopentyltriethoxysilane, aminohexyltriethoxysilane, aminooctyltriethoxysilane, trichlorosilane, methyltrichlorosilane, ethyltrichlorosilane, propyltrichlorosilane, butyltrichlorosilane, pentyltrichlorosilane, hexyltrichlorosilane, octyltrichlorosilane, or a combination thereof. 9. The light emitting device of claim 1 , wherein the electron auxiliary layer further comprises a second silane compound represented by Chemical Formula 3: (R 31 ) q —Si—(R 32 ) 4-q Chemical Formula 3 wherein, in Chemical Formula 3, R 31 is a reactive functional group capable of photo-crosslinking or thermal-crosslinking including: a vinyl group; a vinyloxy group; a (meth)acryl group; a (meth)acryloxy group; an epoxy group; a substituted or unsubstituted C2 to C30 alkenyl group; a substituted or unsubstituted C2 to C30 alkynyl group; spiro-orthoester group; a substituted or unsubstituted C3 to C30 alicyclic organic group having a double bond or a triple bond in the ring; a substituted or unsubstituted C3 to C30 heterocycloalkyl group having a double bond or a triple bond in the ring; a C3 to C30 alicyclic organic group substituted with a C2 to C30 alkenyl group or a C2 to C30 alkynyl group; or a C3 to C30 heterocycloalkyl group substituted with a C2 to C30 alkenyl group or a C2 to C30 alkynyl group, R 32 is a hydroxy group, a halogen, a substituted or unsubstituted C1 to C8 linear or branched alkoxy group, a substituted or unsubstituted C6 to C12 aryloxy group, a substituted or unsubstituted C2 to C10 carbonylalkyl group, or a substituted or unsubstituted C2 to C10 carbonylalkoxy group, and q is an integer of 1 to 3. 10. The light emitting device of claim 9 , wherein the second silane compound comprises vinyl trimethoxysilane, vinyl triethoxysilane, vinyl tris(2-methoxyethoxysilane), or a combination thereof. 11. The light emitting device of claim 9 , wherein the first silane compound, and the second silane compound, are present at a concentration independent of the other though in a total amount of about 1 part by weight to about 100 parts by weight, based on 100 parts by weight of the orthosilicate compound. 12. The light emitting device of claim 1 , wherein the metal oxide nanoparticles of the electron auxiliary layer are surface-treated with a base including a hydroxy group (OH). 13. The light emitting device of claim 1 , wherein the metal oxide comprises Zn, Mg, Ca, Zr, W, Li, Ti, Y, Al, Rb, or a combination thereof. 14. The light emitting device of claim 1 , wherein the metal oxide is represented by Chemical Formula 4: Zn 1-x M x O Chemical Formula 4 wherein, in Chemical Formula 4, M is Mg, Ca, Zr, W, Li, Ti, Y, Al, Rb, or a combination thereof, and 0≤x≤0.5. 15. The light emitting device of claim 1 , wherein the metal oxide nanoparticles have an average particle size of about 1 nanometer to about 100 nanometer. 16. The light emitting device of claim 1 , wherein the light emitting layer comprises quantum dots. 17. The light emitting device of claim 1 , wherein the light emitting device further comprises a hole auxiliary layer including a hole injecting layer, a hole transporting layer, an electron blocking layer, or a combination thereof, between the first electrode and the light emitting layer. 18. A method of manufacturing a light emitting device, comprising mixing metal oxide nanoparticles and an orthosilicate compound to prepare a mixed solution; and applying the mixed solution to form an electron auxiliary layer. 19. The method of claim 18 , wherein the a
Highest occupied molecular orbital [HOMO], lowest unoccupied molecular orbital [LUMO] or Fermi energy values · CPC title
Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers · CPC title
Organosilicon compounds, e.g. TIPS pentacene · CPC title
using liquid deposition, e.g. spin coating · CPC title
characterised by the electroluminescent [EL] layers · CPC title
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