ORGANIC LIGHT-EMITTING DIODE STRUCTURE AND DISPLAY DEVICE
20230141206 · 2023-05-11
Inventors
Cpc classification
H10K2101/30
ELECTRICITY
H10K85/6574
ELECTRICITY
H10K2101/40
ELECTRICITY
H10K85/626
ELECTRICITY
H10K85/6572
ELECTRICITY
H10K85/636
ELECTRICITY
H10K85/615
ELECTRICITY
H10K85/6576
ELECTRICITY
Y02E10/549
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
International classification
Abstract
The present disclosure provides an organic light-emitting diode structure and a display device. The electron blocking layer, the luminescent layer and the hole blocking layer in the organic light-emitting diode structure satisfy: HOMO.sub.host−HOMO.sub.EBL≤0.3 eV, LUMO.sub.host>LUMO.sub.HBL, and HOMO.sub.HBL−HOMO.sub.host≥0.1 eV, wherein HOMO is the highest occupied molecular orbital, LUMO is the lowest unoccupied molecular orbital, host refers to the host material, EBL refers to the electron blocking layer, and HBL refers to the hole blocking layer.
Claims
1. An organic light-emitting diode structure, wherein the organic light-emitting diode structure comprises an anode, an electron blocking layer, a luminescent layer, a hole blocking layer and a cathode that are arranged in layer configuration, a material forming the luminescent layer comprises a host material and a guest material, and the electron blocking layer, the luminescent layer and the hole blocking layer satisfy the following conditions: HOMO.sub.host−HOMO.sub.EBL≤0.3 eV, LUMO.sub.host>LUMO.sub.HBL, and HOMO.sub.HBL−HOMO.sub.host≥0.1 eV, wherein HOMO.sub.host is a highest occupied molecular orbital of the host material, LUMO.sub.host is a lowest unoccupied molecular orbital of the host material, HOMO.sub.EBL is a highest occupied molecular orbital of the electron blocking layer, HOMO.sub.HBL is a highest occupied molecular orbital of the hole blocking layer, and LUMO.sub.HBL is a lowest unoccupied molecular orbital of the hole blocking layer.
2. The organic light-emitting diode structure according to claim 1, wherein the luminescent layer further satisfies the following conditions: HOMO.sub.dopant≤HOMO.sub.host, and LUMO.sub.dopant<LUMO.sub.host, wherein HOMO.sub.dopant is a highest occupied molecular orbital of the guest material, and LUMO.sub.dopant is a lowest unoccupied molecular orbital of the guest material.
3. The organic light-emitting diode structure according to claim 2, wherein the host material has a structure I, and the guest material has a structure III, ##STR00013##
4. The organic light-emitting diode structure according to claim 3, wherein a hole mobility/electron mobility of the host material is ≥0.001.
5. The organic light-emitting diode structure according to claim 3, wherein substituents Ar1, Ar2 and Ar3 in the structure I are independently selected from optionally substituted aryl of a ring-carbon-atom quantity of 6-30 or heteroaryl of a ring-atom quantity of 5-20.
6. The organic light-emitting diode structure according to claim 5, wherein the substituent Ar2 or Ar3 is an optionally substituted structure II, and a substituent X in the structure II is an oxygen atom, ##STR00014##
7. The organic light-emitting diode structure according to claim 5, wherein the substituents Ar1, Ar2 and Ar3 in the structure I are independently selected from phenyl, naphthyl, anthryl, phenanthryl, dibenzofuran, dibenzothiophene, benzonaphthofuran and benzonaphthothiophene.
8. The organic light-emitting diode structure according to claim 7, wherein the host material is selected from: ##STR00015## ##STR00016##
9. The organic light-emitting diode structure according to claim 3, wherein an emission wavelength of the guest material is 400-500 nm.
10. The organic light-emitting diode structure according to claim 3, wherein substituents R1, R2, R3, R4 and R5 in the structure III are independently selected from hydrogen, or optionally substituted heteroatom, amino, C1-20 alkyl, and aryl or heteroaryl of a ring-carbon-atom quantity of 6-20, wherein a substituent in the aryl or heteroaryl comprises silyl, cyano, halogen or diplogen.
11. The organic light-emitting diode structure according to claim 10, wherein R1, R2, R3, R4 and R5 are independently selected from methyl, tert-butyl, benzo, diphenylamino, 3-methyldiphenylamino and trimethylsilyl.
12. The organic light-emitting diode structure according to claim 11, wherein the guest material is selected from: ##STR00017## ##STR00018##
13. The organic light-emitting diode structure according to claim 3, wherein a doping amount of the guest material is 1-10 wt %.
14. A display device, wherein the display device comprises the organic light-emitting diode structure according to claim 1.
15. The display device according to claim 14, wherein the luminescent layer further satisfies the following conditions: HOMO.sub.dopant≤HOMO.sub.host, and LUMO.sub.dopant<LUMO.sub.host, wherein HOMO.sub.dopant is a highest occupied molecular orbital of the guest material, and LUMO.sub.dopant is a lowest unoccupied molecular orbital of the guest material.
16. The display device according to claim 15, wherein the host material has a structure I, and the guest material has a structure III, ##STR00019##
17. The display device according to claim 16, wherein a hole mobility/electron mobility of the host material is ≥0.001.
18. The display device according to claim 16, wherein substituents Ar1, Ar2 and Ar3 in the structure I are independently selected from optionally substituted aryl of a ring-carbon-atom quantity of 6-30 or heteroaryl of a ring-atom quantity of 5-20.
19. The display device according to claim 18, wherein the substituent Ar2 or Ar3 is an optionally substituted structure II, and a substituent X in the structure II is an oxygen atom, ##STR00020##
20. The display device according to claim 18, wherein the substituents Ar1, Ar2 and Ar3 in the structure I are independently selected from phenyl, naphthyl, anthryl, phenanthryl, dibenzofuran, dibenzothiophene, benzonaphthofuran and benzonaphthothiophene.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0035] The above-described aspects of the present disclosure will be interpreted with reference to the following description on the embodiments with reference to the drawings, wherein in the drawings:
[0036]
[0037]
[0038]
REFERENCE NUMERALS
[0039] 100 anode
[0040] 200 hole injection layer
[0041] 300 hole transporting layer
[0042] 400 electron blocking layer
[0043] 500 luminescent layer
[0044] 600 hole blocking layer
[0045] 700 electron transporting layer
[0046] 800 electron injection layer
[0047] 900 cathode
DETAILED DESCRIPTION
[0048] The embodiments of the present disclosure will be described in detail below. A person skilled in the art can understand that the following embodiments are intended to interpret the present disclosure, and should not be deemed as a limitation on the present disclosure. Unless indicated particularly, where the particular techniques or conditions of an embodiment in the following are not clearly described, a person skilled in the art may implement the embodiment by using commonly used techniques or conditions in the art or according to the specification of the product.
[0049] In an aspect of the present disclosure, the present disclosure provides an organic light-emitting diode structure.
[0050] According to an embodiment of the present disclosure, the organic light-emitting diode structure includes an anode, an electron blocking layer, a luminescent layer, a hole blocking layer and a cathode that are arranged in layer configuration. In some embodiments of the present disclosure, referring to
[0051] The inventor of the present disclosure has found out in the studying process that, referring to the schematic diagram of the energy-level relation of the host and the guest of the luminescent material and the adjacent layers shown in
[0052] In some embodiments of the present disclosure, (4) HOMO.sub.dopant≤HOMO.sub.host, which facilitates the guest material to capture some holes; and (5) LUMO.sub.dopant<LUMO.sub.host, which may scatter some electrons. Accordingly, the inventor regulates the combination of the energy levels of the host material and the guest material, which may further facilitate the transport of the charge carriers into the luminescent layer, thereby further reducing the accumulation of the charge carriers at the EBL/EML interface.
[0053] According to an embodiment of the present disclosure, a material forming the luminescent layer includes a host material and a guest material, wherein the host material has a structure I, and the guest material has a structure III. All of the 5 hydrogen atoms in the benzene ring at one end of the host material are replaced by diplogen atoms, which may increase the bond energy between the benzene ring and the substituent Ar1, thereby enabling the host material to have a better stability. Moreover, the structure III is selected by the intermediate structure of the guest material, this fused structure may reduce the wagging vibration and the stretching vibration of the atoms, reduce non-radiative transition, and purify the spectral colors, thereby increasing the front-face luminous efficiency of the luminescent material.
##STR00003##
[0054] By using the AC3 test, the HOMO.sub.host of the host material having the structure I is 5.8-5.9 eV, the LUMO.sub.host is 2.9-3.0 eV; the HOMO.sub.dopant of the guest material having the structure III is 5.1-5.4 eV, and the LUMO.sub.dopant is 2.5-2.7 eV; the HOMO.sub.EBL of the material forming the electron blocking layer (for example, mCBP) is 5.6-5.7 eV; and the HOMO.sub.HBL of the material forming the hole blocking layer (for example, TPBI) is 6.1-6.3 eV, and the LUMO.sub.HBL is 2.3-2.5 eV. Accordingly, the host material forming the luminescent layer has the structure I and the guest material has the structure III, which may satisfy the following formulas: (1) HOMO.sub.host−HOMO.sub.EBL≤0.3 eV; (2) HOMO.sub.HBL−HOMO.sub.host≥0.1 eV; (3) LUMO.sub.host>LUMO.sub.HBL; (4) HOMO.sub.dopant≤HOMO.sub.host; and (5) LUMO.sub.dopant<LUMO.sub.host.
[0055] According to an embodiment of the present disclosure, in the structure I of the host material, the substituents Ar1, Ar2 and Ar3 may be independently selected from optionally substituted aryl of a ring-carbon-atom quantity of 6-30 or heteroaryl of a ring-atom quantity of 5-20. Accordingly, by selecting rigid aryl or heteroaryl as the substituents of the host material, the host material may have a better stability. In some embodiments of the present disclosure, the aryl of a ring-carbon-atom quantity of 6-30 may be at least one of phenyl, naphthyl, anthryl and phenanthryl. In some other embodiments of the present disclosure, the heteroaryl of a ring-atom quantity of 5-20 may be at least one of dibenzofuran, dibenzothiophene, benzonaphthofuran and benzonaphthothiophene. Accordingly, by selecting the above substituents of a strong conjugacy, the host material may have a better luminous performance.
[0056] In some particular embodiments of the present disclosure, the substituent Ar2 or Ar3 may be an optionally substituted structure II, and the substituent X in the structure II may be an oxygen atom (O). Accordingly, by selecting dibenzofuran as the substituent Ar2 or Ar3, that may further facilitate the transport of the holes.
##STR00004##
[0057] In some particular embodiments, the host material may be selected from one of the following 11 compounds. Accordingly, by selecting any one of 1-1 to 1-11, the hole mobility/electron mobility in the mobility of the host material (measured by using the SCLC method) may be ≥0.001, thereby further facilitating the transport of the holes. In some particular embodiments, the host material in the luminescent layer may be 1-2 or 1-7, which may increase the service life of the organic light emitting diode by above 20%.
##STR00005## ##STR00006##
[0058] According to an embodiment of the present disclosure, in the structure III of the guest material, the substituents R1, R2, R3, R4 and R5 may be independently selected from hydrogen, or optionally substituted heteroatom, amino, C1-20 alkyl, and aryl or heteroaryl of a ring-carbon-atom quantity of 6-20, wherein a substituent in the aryl or heteroaryl includes silyl, cyano, halogen or diplogen. Accordingly, by selecting the above chemical groups as the five substituents in the structure III, the luminescent material may have a higher front-face luminous efficiency. Furthermore, the adjacent substituents R1-R5 may form a ring, or be integrated with the benzene ring to form fused aromatic hydrocarbons.
[0059] In some embodiments of the present disclosure, R1, R2, R3, R4 and R5 may be independently selected from methyl, tert-butyl, benzo, diphenylamino, 3-methyldiphenylamino and trimethylsilyl. Accordingly, by selecting the above types of substituents, the rigidity of the guest material may be further increased, whereby the luminescent material may have a higher front-face luminous efficiency.
[0060] In some particular embodiments, the guest material may be selected from one of the following 6 compounds. Accordingly, by selecting any one of 2-1 to 2-6, the emission wavelength of the guest material may be between 400 nm and 500 nm, which cannot only increase the rigidity of the guest material, but may also enable the light emitted by the luminescent material to have a higher color purity. In some particular embodiments, the guest material may be 2-3 or 2-5, which may increase the luminous efficiency of the organic light emitting diode by above 10%.
##STR00007## ##STR00008##
[0061] According to an embodiment of the present disclosure, based on the total weight of the luminescent-material composition, the doping amount of the guest material may be 1-10 wt %. Accordingly, by merely adding the guest material 1/99-1/9 of the weight of the host material, the service life of the organic light emitting diode containing the luminescent layer may be increased by above 20% and at the same time the luminous efficiency may be increased by above 10%.
[0062] According to an embodiment of the present disclosure, the material forming the hole injection layer (HIL) 200 may be an inorganic oxide, which particularly includes, for example, molybdenum oxide, titanium oxide, vanadium oxide, rhenium oxide, ruthenium oxide, chromium oxide, zirconium oxide, hafnium oxide, tantalum oxide, silver oxide, tungsten oxide and manganese oxide. It may also be a P-type dopant of a strong electrophilic system and a dopant of a hole transport material, which particularly includes, for example, hexacyanohexazatriphenylene, 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoparaquinonedimethane (F4TCNQ), and 1,2,3-tri[(cyano)(4-cyano-2,3,5,6-tetrafluorophenyl) methylene] cyclopropane.
[0063] According to an embodiment of the present disclosure, the materials forming the hole transporting layer (HTL) 300 and the electron blocking layer (EBL) 400 may independently be an arylamine-type or carbazole-type material having the characteristic of hole transport, which particularly includes, for example, 4,4′-bis[N-(1-naphthyl)-N-phenylamino] biphenyl (NPB), N,N′-bis(3-methylphenyl)-N,N′-diphenyl-[1,1′-biphenyl]-4,4′-diamine (TPD), 4-phenyl-4′-(9-phenylfluoren-9-yl)triphenylamine (BAFLP), 4,4′-bis[N-(9,9-dimethylfluoren-2-yl)-N-phenylamino] biphenyl (DFLDPBi), 4,4′-di(9-carbazolyl) biphenyl (CBP), and 9-phenyl-3-[4-(10-phenyl-9-anthryl) phenyl]-9H-carbazole (PCzPA).
[0064] According to an embodiment of the present disclosure, the materials forming the hole blocking layer (HBL) 600 and the electron transporting layer (ETL) 700 may independently be an aromatic heterocyclic compound, which includes, for example, a benzimidazole derivative, an imidazopyridine derivative, an imidazole derivative such as a benziimidazophenanthridine derivative, a pyrimidine derivative, an azine derivative such as a triazine derivative, and a compound containing a nitrogen-containing six-membered ring such as a phenanthroline derivative, a quinoline derivative, an iso-quinoline derivative. It also includes a compound in which a heterocyclic ring has a phosphine-oxide-series substituent, which particularly includes, for example, 2-(4-biphenyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole (PBD), 1,3-bis[5-(p-tert-butylphenyl)-1,3,4-oxadiazol-2-yl] benzene (OXD-7), 3-(4-tert-butylphenyl)-4-phenyl-5-(4-biphenyl)-1,2,4-triazole (TAZ), 3-(4-tert-butylphenyl)-4-(4-ethylphenyl)-5-(4-biphenyl)-1,2,4-triazole (p-EtTAZ), bathophenanthroline (BPhen), bathocuproine (BCP), and 4,4′-bis(5-methylbenzoxazol-2-yl) stilbene (BzOs).
[0065] According to an embodiment of the present disclosure, the material forming the electron injection layer (EIL) 800 may be an alkali metal or a metal, which particularly includes, for example, LiF, Yb, Mg, Ca and compounds thereof.
[0066] In conclusion, according to the embodiments of the present disclosure, the present disclosure provides an organic light-emitting diode structure, wherein the combination between the energy-level relation of the host material and the guest material of the luminescent layer and the adjacent electron blocking layer and hole blocking layer may enable the organic light-emitting diode structure to have a higher stability and a higher luminous efficiency, which may enable the organic light-emitting diode structure to have a longer service life and a lower power consumption.
[0067] In another aspect of the present disclosure, the present disclosure provides a display device. According to an embodiment of the present disclosure, the display device includes the organic light-emitting diode structure stated above.
[0068] According to an embodiment of the present disclosure, the particular type of the display device is not particularly limited, and particularly includes, for example, a display screen, a television set, a mobile phone, a tablet personal computer and a smart watch, which may be selected by a person skilled in the art correspondingly according to the practical usage requirements of the display device, and are not discussed herein further. It should be noted that, besides the organic light-emitting diode structure, the display device further includes other necessary components and elements, and, taking an OLED display screen as an example, particularly includes, for example, a displaying back plate, a thin-film transistor and a touch component, which may be added by a person skilled in the art correspondingly according to the functions of the display device, and are not discussed herein further.
[0069] In conclusion, according to the embodiments of the present disclosure, the present disclosure provides a display device, wherein its organic light-emitting diode structure has a higher stability and a higher luminous efficiency, which may enable the display device to have a longer service life and a lower power consumption. A person skilled in the art can understand that the features and the advantages described above with respect to the organic light-emitting diode structure apply to the display device, and are not discussed herein further.
[0070] The present disclosure will be described below with reference to the particular embodiments. It should be noted that those embodiments are merely illustrative, and do not limit the present disclosure in any way.
COMPARATIVE EXAMPLE 1
[0071] In this comparative example, an organic light-emitting diode is fabricated. The material of the luminescent layer is a comparative host material and a comparative guest material, the material of HIL is F4TCNQ, the material of HTL is m-MTDATA, the material of EBL is mCBP, the material of HBL is TPBI, and the material of ETL is BCP.
##STR00009##
[0072] comparative host material (comparative host)
##STR00010##
[0073] comparative guest material (comparative dopant)
##STR00011## ##STR00012##
COMPARATIVE EXAMPLE 2
[0074] In this comparative example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the host material of the luminescent layer is 1-2.
COMPARATIVE EXAMPLE 3
[0075] In this comparative example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the host material of the luminescent layer is 1-7.
COMPARATIVE EXAMPLE 4
[0076] In this comparative example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the guest material of the luminescent layer is 2-3.
COMPARATIVE EXAMPLE 5
[0077] In this comparative example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the guest material of the luminescent layer is 2-5.
EXAMPLE 1
[0078] In this Example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the host material of the luminescent layer is 1-7 and the guest material is 2-3.
EXAMPLE 2
[0079] In this Example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the host material of the luminescent layer is 1-7 and the guest material is 2-5.
EXAMPLE 3
[0080] In this Example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the host material of the luminescent layer is 1-2 and the guest material is 2-3.
EXAMPLE 4
[0081] In this Example, an organic light-emitting diode is fabricated. It differs from Comparative Example 1 in that the host material of the luminescent layer is 1-2 and the guest material is 2-5.
SUMMARY
[0082] Tests on the voltages, the luminous efficiencies and the lives are performed on the organic light-emitting diodes of Comparative Example 1-5 and Examples 1-4, wherein the life tests follow LT95@1000nit. The test results of the organic light emitting diodes are shown in Table 1.
TABLE-US-00001 TABLE 1 The test results of the OLEDs of the comparative examples and examples luminous material combination voltage efficiency life comparative host comparative dopant 100% 100% 100% host 1-2 comparative dopant 100% 102% 120% host 1-7 comparative dopant 98% 105% 129% comparative host dopant 2-3 98% 113% 103% comparative host dopant 2-5 96% 119% 104% host 1-7 dopant 2-3 96% 118% 131% host 1-7 dopant 2-5 94% 123% 137% host 1-2 dopant 2-3 99% 115% 126% host 1-2 dopant 2-5 97% 120% 130%
[0083] In the description of the present disclosure, the description referring to the terms “an embodiment”, “some embodiments”, “example”, “particular example” or “some examples” and so on means that particular features, structures, materials or characteristics described with reference to the embodiment or example are comprised in at least one of the embodiments or examples of the present disclosure. In the description, the illustrative expressions of the above terms do not necessarily relate to the same embodiment or example. Furthermore, the described particular features, structures, materials or characteristics may be combined in one or more embodiments or examples in a suitable form. Moreover, subject to avoiding contradiction, a person skilled in the art may combine different embodiments or examples described in the description and the features of the different embodiments or examples.
[0084] Although the embodiments of the present disclosure have already been illustrated and described above, it can be understood that the above embodiments are illustrative, and should not be construed as a limitation on the present disclosure, and a person skilled in the art may make variations, modifications, substitutions and improvements to the above embodiments within the scope of the present disclosure.