Organic electroluminescent device containing exciton confinement layer
An organic electroluminescent device is disclosed. The organic electroluminescent device achieves low driving voltage and high luminous efficiency as well as long lifespan by including an exciton confinement layer (ECL), in which a predetermined physical property is adjusted, in an area of an electron transporting area, including at least two layers, that is adjacent to an emissive layer.
1. An organic electroluminescent device, comprising:
an anode; a hole transporting area; an emissive layer; an electron transporting area, and a cathode, which are stacked in this order,
wherein the emissive layer includes a host,
wherein the electron transporting area includes a first layer and a second layer, and
wherein the first layer of the electron transporting area, which is in contact with the emissive layer, is an exciton confinement layer, and a density of states for LUMO (DOS LUMO ECL ) of the exciton confinement layer satisfies at least one or more of the following conditions (i) and (ii):
(i) the density of states for LUMO (DOS LUMO ECL ) of the exciton confinement layer having a DOS that overlaps more than 0% of a density of states for LUMO (DOS LUMO HOST ) of the host; and
(ii) the density of states for LUMO (DOS LUMO ECL ) of the exciton confinement layer having a DOS that overlaps more than 0% of a density of states for LUMO (DOS LUMO ET ) of the second layer of the electron transporting area except the exciton confinement layer,
wherein the exciton confinement layer comprises at least one EWG moiety of a 6-membered moiety represented by the following Formula 1; a 5-membered moiety represented by the following Formula 2; or a polycyclic moiety in which the 6-membered moiety and the 5-membered moiety are condensed,
in Formula 1 or 2, X 1 to X 6 and Y 1 to Y 5 may be the same as or different from each other, each independently being N or C(R), while at least one of X 1 to X 6 and Y 1 to Y 5 is N,
when C(R) is plural in number, the plurality of R may be the same as or different from each other, each independently being selected from the group consisting of: hydrogen, deuterium, a halogen group, a cyano group, a nitro group, an amino group, a C 1 to C 40 alkyl group, a C 2 to C 40 alkenyl group, a C 2 to C 40 alkynyl group, a C 3 to C 40 cycloalkyl group, a heterocycloalkyl group having 3 to 40 nuclear atoms, a C 6 to C 60 aryl group, a heteroaryl group having 5 to 60 nuclear atoms, a C 1 to C 40 alkyloxy group, a C 6 to C 60 aryloxy group, a C 1 to C 40 alkylsilyl group, a C 6 to C 60 arylsilyl group, a C 1 to C 40 alkylboron group, a C 6 to C 60 arylboron group, a C 6 to C 60 arylphosphine group, a C 6 to C 60 arylphosphine oxide group and a C 6 to C 60 arylamine group, or may be bonded with an adjacent group to form a condensed ring,
the alkyl group, the alkenyl group, the alkynyl group, the aryl group, the heteroaryl group, the aryloxy group, the alkyloxy group, the cycloalkyl group, the heterocycloalkyl group, the arylamine group, the alkylsilyl group, the alkylboron group, the arylboron group, the arylphosphine group, the arylphosphine oxide group, and the arylamine group of R may each independently be substituted or unsubstituted with one or more kinds of sub stituents selected from the group consisting of hydrogen, deuterium (D), halogen, a cyano group, a nitro group, a C 1 to C 40 alkyl group, a C 2 to C 40 alkenyl group, a C 2 to C 40 alkynyl group, a C 3 to C 40 cycloalkyl group, a heterocycloalkyl group having 3 to 40 nuclear atoms, a C 6 to C 60 aryl group, a heteroaryl group having 5 to 60 nuclear atoms, a C 1 to C 40 alkyloxy group, a C 6 to C 60 aryloxy group, a C 1 to C 40 alkylsilyl group, a C 6 to C 60 arylsilyl group, a C 1 to C 40 alkylboron group, a C 6 to C 60 arylboron group, a C 6 to C 60 arylphosphine group, a C 6 to C 60 arylphosphine oxide group and a C 6 to C 60 arylamine group, and when the substituents are plural in number, the substituents may be the same as or different from each other.
2. The organic electroluminescent device of claim 1 , wherein the second layer of the electron transporting area includes an electron transporting layer, an electron injection layer, or a combination thereof.
3. The organic electroluminescent device of claim 2 , wherein the electron transporting area comprises:
(a) the exciton confinement layer and the electron injection layer; or
(b) the exciton confinement layer, the electron transporting layer, and the electron injection layer.
4. The organic electroluminescent device of claim 1 , wherein a triplet energy (T 1 ECL ) of the exciton confinement layer is 1.5 eV or more.
5. The organic electroluminescent device of claim 1 , wherein a singlet energy (S 1 ECL ) of the exciton confinement layer is 2.0 eV or more.
6. The organic electroluminescent device of claim 1 , wherein an absolute value of HOMO of the exciton confinement layer is 5.0 eV or more.
7. The organic electroluminescent device of claim 1 , wherein a band gap energy of the exciton confinement layer is 2.0 eV or more.
8. The organic electroluminescent device of claim 1 , wherein the exciton confinement layer has a lowest energy level of bond-dissociation energy in a ground state of 1.50 eV or more.
9. The organic electroluminescent device of claim 1 , wherein an absolute value difference (ΔLUMO) between a LUMO energy level of the exciton confinement layer and a LUMO energy level of the host is 2.0 eV or less.
10. The organic electroluminescent device of claim 1 , wherein an absolute value difference (ΔLUMO) between a LUMO energy level of the exciton confinement layer and a LUMO energy level of the second layer of the electron transporting area that is adjacent to the exciton confinement layer is 2.0 eV or less.
11. The organic electroluminescent device of claim 1 , wherein an absolute value difference (ΔHOMO) between a HOMO energy level of the exciton confinement layer and a HOMO energy level of the host is 2.0 eV or less.
12. The organic electroluminescent device of claim 1 , wherein an absolute value difference (ΔHOMO) between a HOMO energy level of the exciton confinement layer and a HOMO energy level of the second layer of the electron transporting area that is adjacent to the exciton confinement layer is 2.0 eV or less.
13. The organic electroluminescent device of claim 1 , wherein an electronic affinity (EA) of the exciton confinement layer is 0.5 eV or more.
14. The organic electroluminescent device of claim 1 , wherein the exciton confinement layer has a refractive index (n) of 0.7 or more in a blue wavelength region ranging from 400 to 470 nm.
15. The organic electroluminescent device of claim 1 , wherein a dipole moment of the exciton confinement layer is greater than zero.
16. The organic electroluminescent device of claim 1 , wherein the exciton confinement layer has an electron mobility (μ) of at least 1×10 −8 cm 2 /Vs or more.
17. The organic electroluminescent device of claim 1 , wherein the emissive layer includes a host and a dopant, and a mixing ratio of the host and dopant is 70-99.5:0.5-30 in a weight ratio.
18. The organic electroluminescent device of claim 1 , comprising a plurality of emissive layer stacks including at least one emissive layer.
19. The organic electroluminescent device of claim 1 , wherein the exciton confinement layer comprises a compound selected from the group consisting of compounds 1-16:
or a combination thereof.