WO2018056645A1 - Dispositif électroluminescent organique comprenant une couche tampon d'électrons et une couche de transport d'électrons - Google Patents

Dispositif électroluminescent organique comprenant une couche tampon d'électrons et une couche de transport d'électrons Download PDF

Info

Publication number
WO2018056645A1
WO2018056645A1 PCT/KR2017/010110 KR2017010110W WO2018056645A1 WO 2018056645 A1 WO2018056645 A1 WO 2018056645A1 KR 2017010110 W KR2017010110 W KR 2017010110W WO 2018056645 A1 WO2018056645 A1 WO 2018056645A1
Authority
WO
WIPO (PCT)
Prior art keywords
substituted
unsubstituted
organic electroluminescent
electron
electroluminescent device
Prior art date
Application number
PCT/KR2017/010110
Other languages
English (en)
Inventor
Sang-Hee Cho
Doo-Hyeon Moon
Original Assignee
Rohm And Haas Electronic Materials Korea Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from KR1020170114048A external-priority patent/KR102455656B1/ko
Application filed by Rohm And Haas Electronic Materials Korea Ltd. filed Critical Rohm And Haas Electronic Materials Korea Ltd.
Priority to CN201780055061.XA priority Critical patent/CN109716549B/zh
Priority to US16/327,955 priority patent/US11107997B2/en
Publication of WO2018056645A1 publication Critical patent/WO2018056645A1/fr

Links

Images

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/14—Carrier transporting layers
    • H10K50/16—Electron transporting layers
    • H10K50/166—Electron transporting layers comprising a multilayered structure
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/17—Carrier injection layers

Definitions

  • the present disclosure relates to an organic electroluminescent device comprising an electron buffer layer and an electron transport layer.
  • An electroluminescent (EL) device is a self-light-emitting device with the advantages of providing a wider viewing angle, a greater contrast ratio, and a faster response time.
  • the first organic EL device was developed by Eastman Kodak, by using small aromatic diamine molecules and aluminum complexes as materials for forming a light-emitting layer ( see Appl. Phys. Lett. 51, 913, 1987).
  • An organic EL device changes electric energy into light by the injection of a charge into an organic light-emitting material, and commonly comprises an anode, a cathode, and an organic layer formed between the two electrodes.
  • the organic layer of the organic EL device may be composed of a hole injection layer, a hole transport layer, an electron blocking layer, a light-emitting layer (containing host and dopant materials), an electron buffer layer, a hole blocking layer, an electron transport layer, an electron injection layer, etc.; the materials used in the organic layer can be classified into a hole injection material, a hole transport material, an electron blocking material, a light-emitting material, an electron buffer material, a hole blocking material, an electron transport material, an electron injection material, etc., depending on functions.
  • the organic EL device In the organic EL device, holes from an anode and electrons from a cathode are injected into a light-emitting layer by electric voltage, and an exciton having high energy is produced by the recombination of the holes and electrons.
  • the organic light-emitting compound moves into an excited state by the energy and emits light from energy when the organic light-emitting compound returns to the ground state from the excited state.
  • an electron transport material actively transports electrons from a cathode to a light-emitting layer and inhibits transport of holes which are not recombined in the light-emitting layer to increase recombination opportunity of holes and electrons in the light-emitting layer.
  • electron-affinitive materials are used as an electron transport material.
  • Organic metal complexes having light-emitting function such as Alq 3 are excellent in transporting electrons, and thus have been conventionally used as an electron transport material.
  • Alq 3 has problems in that it moves to other layers and shows reduction of color purity when used in blue light-emitting devices. Therefore, new electron transport materials have been required, which do not have the above problems, are highly electron-affinitive, and quickly transport electrons in organic EL devices to provide organic EL devices having high luminous efficiency.
  • the electron buffer layer is a layer for solving the problem of a change in luminance caused by the change of a current characteristic of the device when exposed to a high temperature during a process of producing a panel.
  • the characteristic of the compound comprised in the electron buffer layer is important.
  • a fluorescent material provides lower efficiencies than a phosphorescent material. Accordingly, there have been attempts to improve efficiencies by developing a specific fluorescent material such as a combination of an anthracene-based host and a pyrene-based dopant. However, the proposed combination makes holes become greatly trapped, which can cause light-emitting sites in a light-emitting layer to shift to the side close to a hole transport layer, thereby light being emitted at an interface. The light-emission at the interface decreases lifespan of a device, and efficiencies are not satisfactory. Accordingly, there have been attempts to solve both efficiency and lifespan problems by inserting an electron buffer layer between the light-emitting layer and the electron transport layer as a method to solve the problems of fluorescent materials.
  • Korean Patent Appln. Laying-Open No. 2015-0080213 A discloses an organic electroluminescent device comprising a bilayer-structured electron transport layer comprising an anthracene-based compound and a heteroaryl-based compound.
  • Korean Patent Appln. Laying-Open No. 2016-0034804 A discloses an organic electroluminescent device comprising a compound in which a nitrogen-containing heteroaryl is bonded to a benzocarbazole, etc., via a linker comprising two or more aryl groups as an electron transport material.
  • Korean Patent Appln. Laying-Open No. 2015-0108330 A discloses an organic electroluminescent device comprising a compound in which a nitrogen-containing heteroaryl is bonded to a carbazole, etc., as an electron buffer material.
  • an organic electroluminescent device comprising a compound comprising a nitrogen-containing heteroaryl as an electron buffer material and a compound in which a nitrogen-containing heteroaryl is bonded to a benzocarbazole, etc., via a linker of a naphthylene as an electron transport material.
  • a hetero compound in which a nitrogen-containing heteroaryl is bonded to a benzocarbazole, etc. via a linker comprising two or more aryl groups as an electron transport material, the LUMO energy level gets lower. Thus, it is not appropriate as an electron transport material.
  • the objective of the present disclosure is to provide an organic electroluminescent device having high efficiency and/or long lifespan by comprising a specific combination of an electron buffer material and an electron transport material.
  • an organic electroluminescent device comprising a first electrode, a second electrode facing the first electrode, a light-emitting layer between the first electrode and the second electrode, and an electron transport layer and an electron buffer layer between the light-emitting layer and the second electrode, wherein the electron buffer layer comprises a compound represented by the following formula 1, and the electron transport layer comprises a compound represented by the following formula 2:
  • X 1 to X 5 each independently represent CR 1 or N;
  • R 1 represents hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted mono- or di- (C1-C30)alkylamino, or a substituted or
  • L represents a single bond, a substituted or unsubstituted (C6-C50)arylene, or a substituted or unsubstituted (5- to 50-membered)heteroarylene;
  • Ar represents a substituted or unsubstituted (C6-C50)aryl, or a substituted or unsubstituted (5- to 50-membered)heteroaryl;
  • Ar 1 and Ar 2 each independently represent a substituted or unsubstituted (C6-C30)aryl
  • L 1 represents a naphthylene
  • ring A and ring B each independently represent a benzene, a phenylbenzene, or a naphthalene, with a proviso that at least one of ring A and ring B represent naphthalene;
  • n an integer of 1 to 3;
  • the heteroaryl(ene) contains at least one heteroatom selected from B, N, O, S, Si, and P.
  • the present disclosure provides an organic electroluminescent device having high efficiency and/or long lifespan, and a display system or a lighting system can be produced by using the device.
  • Figure 1 illustrates a schematic sectional view of an organic electroluminescent device according to one embodiment of the present disclosure.
  • Figure 2 illustrates an energy gap relationship among the layers of the organic electroluminescent device according to one embodiment of the present disclosure.
  • Figure 3 is a graph illustrating a current efficiency versus a luminance of organic electroluminescent devices of Comparative Example 1 and Device Example 2.
  • organic electroluminescent compound in the present disclosure means a compound that may be used in an organic electroluminescent device, and may be comprised in any layer constituting an organic electroluminescent device, as necessary.
  • organic electroluminescent material in the present disclosure means a material that may be used in an organic electroluminescent device, and may comprise at least one compound.
  • the organic electroluminescent material may be comprised in any layer constituting an organic electroluminescent device, as necessary.
  • the organic electroluminescent material may be a hole injection material, a hole transport material, a hole auxiliary material, a light-emitting auxiliary material, an electron blocking material, a light-emitting material, an electron buffer material, a hole blocking material, an electron transport material, or an electron injection material.
  • an electron buffer layer can be inserted between the light-emitting layer and the second electrode to focus on obtaining high efficiency and/or long lifespan due to electron injection controlled by the LUMO energy level of the electron buffer layer.
  • LUMO energy level (A) and HOMO energy level are expressed in absolute values in the present disclosure.
  • the values of the LUMO energy level are compared based on absolute values. Values measured by density functional theory (DFT) are used for LUMO energy levels and HOMO energy levels in the present disclosure.
  • DFT density functional theory
  • the LUMO energy levels can be easily measured by known various methods. Generally, LUMO energy levels are measured by cyclic voltammetry or ultraviolet photoelectron spectroscopy (UPS). Therefore, a person skilled in the art can easily comprehend the electron buffer layer, light-emitting layer, and electron transport layer that satisfy the equational relationship of the LUMO energy levels of the present disclosure, and practice the present disclosure. HOMO energy levels can be easily measured by the same method of measuring LUMO energy levels.
  • the present disclosure is directed to an organic electroluminescent device comprising a first electrode, a second electrode facing the first electrode, a light-emitting layer between the first electrode and the second electrode, and an electron transport layer and an electron buffer layer between the light-emitting layer and the second electrode, wherein the electron buffer layer comprises a compound represented by formula 1, and the electron transport layer comprises a compound represented by formula 2.
  • the electron buffer layer and the electron transport zone are inserted between the light-emitting layer and the second electrode.
  • the electron buffer layer may be located between the light-emitting layer and the electron transport zone, or between the electron transport zone and the second electrode.
  • the electron buffer material comprised in the electron buffer layer indicates a material controlling an electron flow. Therefore, the electron buffer material may be, for example, a material which traps electrons, blocks electrons, or lowers an energy barrier between an electron transport zone and a light-emitting layer.
  • the electron buffer material may be used for preparing an electron buffer layer, or may be incorporated into another area such as an electron transport zone or a light-emitting layer.
  • the electron buffer layer may be formed between a light-emitting layer and an electron transport zone, or between an electron transport zone and a second electrode of an organic electroluminescent device.
  • the electron buffer material may further comprise materials which are conventionally used for preparing an organic electroluminescent device besides the compound of formula 1.
  • the electron transport material comprised in the electron transport layer actively transports electrons from a cathode to a light-emitting layer and inhibits transport of holes which are not recombined in the light-emitting layer to increase recombination opportunity of holes and electrons in the light-emitting layer.
  • electron-affinitive materials are used as an electron transport material.
  • the electron transport layer may be formed in an electron transport zone between a second electrode and a light-emitting layer of an organic electroluminescent device.
  • the electron transport material may further comprise materials which are conventionally used for preparing an organic electroluminescent device besides the compound of formula 2.
  • (C1-C30)alkyl is meant to be a linear or branched alkyl having 1 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 1 to 10, more preferably 1 to 6, and includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, etc.
  • (C2-C30)alkenyl is meant to be a linear or branched alkenyl having 2 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 2 to 20, more preferably 2 to 10, and includes vinyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylbut-2-enyl, etc.
  • (C2-C30)alkynyl is a linear or branched alkynyl having 2 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 2 to 20, more preferably 2 to 10, and includes ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methylpent-2-ynyl, etc.
  • (C3-C30)cycloalkyl is a mono- or polycyclic hydrocarbon having 3 to 30 ring backbone carbon atoms, in which the number of carbon atoms is preferably 3 to 20, more preferably 3 to 7, and includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.
  • (3- to 7-membered)heterocycloalkyl is a cycloalkyl having at least one heteroatom selected from the group consisting of B, N, O, S, Si, and P, preferably O, S, and N, and 3 to 7 ring backbone atoms, and includes tetrahydrofuran, pyrrolidine, thiolan, tetrahydropyran, etc.
  • (C6-C30)aryl(ene) is a monocyclic or fused ring derived from an aromatic hydrocarbon having 6 to 30 ring backbone carbon atoms and may be partially saturated, in which the number of ring backbone carbon atoms is preferably 6 to 20, more preferably 6 to 15, and includes phenyl, biphenyl, terphenyl, naphthyl, binaphthyl, phenylnaphthyl, naphthylphenyl, fluorenyl, phenylfluorenyl, benzofluorenyl, dibenzofluorenyl, phenanthrenyl, phenylphenanthrenyl, anthracenyl, indenyl, triphenylenyl, pyrenyl, tetracenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, etc.
  • (3- to 30-membered)heteroaryl(ene) is an aryl group having at least one, preferably 1 to 4 heteroatoms selected from the group consisting of B, N, O, S, Si, and P, and 3 to 30 ring backbone atoms, in which the number of ring backbone atoms is preferably 3 to 20, more preferably 5 to 15; is a monocyclic ring, or a fused ring condensed with at least one benzene ring; may be partially saturated; may be one formed by linking at least one heteroaryl or aryl group to a heteroaryl group via a single bond(s); and includes a monocyclic ring-type heteroaryl including furyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl,
  • substituted in the expression “substituted or unsubstituted” means that a hydrogen atom in a certain functional group is replaced with another atom or functional group, i.e., a substituent.
  • the compound of formula 1 comprised in the electron buffer layer may be represented by the following formula 3 or 4:
  • Ar 3 and Ar 4 are identical to the definition of R 1 ;
  • the compound of formula 2 comprised in the electron transport layer may be represented by the following formula 5 or 6:
  • X 1 , L 1 , Ar 1 , and Ar 2 are as defined in formula 1;
  • n 0 or 1.
  • X 2 to X 5 each independently represent CR 1 or N.
  • R 1 represents hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted mono- or di- (C1-C30)alkylamino, or a substituted or
  • R 1 preferably represents hydrogen, a substituted or unsubstituted (C6-C20)aryl, or a substituted or unsubstituted (5- to 15-membered)heteroaryl; or may be linked to an adjacent substituent to form a substituted or unsubstituted, mono- or polycyclic, (C6-C15) alicyclic, aromatic, or a combination of alicyclic and aromatic ring; and more preferably represents hydrogen, a (C6-C20)aryl unsubstituted or substituted with a (C1-C6)alkyl or a (5- to 15-membered)heteroaryl, or an unsubstituted (5- to 15-membered)heteroaryl; or may be linked to an adjacent substituent to form an unsubstituted, mono- or polycyclic, (C6-C15) alicyclic, aromatic, or a combination of alicyclic and aromatic ring.
  • L represents a single bond, a substituted or unsubstituted (C6-C50)arylene, or a substituted or unsubstituted (5- to 50-membered)heteroarylene.
  • L preferably represents a single bond, a substituted or unsubstituted (C6-C20)arylene, or a substituted or unsubstituted (5- to 40-membered)heteroarylene, and more preferably represents a single bond, a (C6-C20)arylene unsubstituted or substituted with a (C1-C6)alkyl or a (C6-C12)aryl, or a (5- to 40-membered)heteroarylene unsubstituted or substituted with a (C1-C6)alkyl or a (C6-C12)aryl.
  • Ar represents a substituted or unsubstituted (C6-C50)aryl, or a substituted or unsubstituted (5- to 50-membered)heteroaryl.
  • Ar preferably represents a substituted or unsubstituted (C6-C20)aryl, or a substituted or unsubstituted (5- to 40-membered)heteroaryl, and more preferably represents a (C6-C20)aryl unsubstituted or substituted with a (C1-C6)alkyl or a (C6-C12)aryl, or a (5- to 40-membered)heteroaryl unsubstituted or substituted with a (C1-C6)alkyl or a (C6-C12)aryl.
  • Ar 1 and Ar 2 each independently represent a substituted or unsubstituted (C6-C30)aryl.
  • Ar 1 and Ar 2 preferably, each independently represent a substituted or unsubstituted (C6-C20)aryl, and more preferably, each independently represent an unsubstituted (C6-C20)aryl.
  • L 1 represents a naphthylene. Specifically, L 1 may be represented by any one of the following formulae 8 to 10:
  • ring A and ring B each independently represent a benzene, a phenylbenzene, or a naphthalene, with a proviso that at least one of ring A and ring B represent naphthalene.
  • Formula 1 may be represented by formula 11 or 12:
  • Ar 3 , Ar 4 , L, and n are as defined in formulae 3 and 4;
  • Ar 5 and Ar 6 each independently represent hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C3-C30)cycloalkenyl, a substituted or unsubstituted (3- to 7-membered)heterocycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6
  • heteroaryl(ene) and the heterocycloalkyl each independently contain at least one heteroatom selected from B, N, O, S, Si, and P;
  • s and t each independently represent an integer of 1 to 4, and where s or t is an integer of 2 or more, each of Ar 5 or each of Ar 6 may be the same or different.
  • the compound represented by formula 1 may be selected from the group consisting of the following compounds, but is not limited thereto:
  • the compound represented by formula 2 may be selected from the group consisting of the following compounds, but is not limited thereto:
  • the compound of formulae 1 and 2 according to the present disclosure can be prepared by known methods to a person skilled in the art, and can be prepared, for example, by Bromination, Suzuki reaction, Buchwald-Hartwig reaction, Ullmann reaction, etc.
  • the host compound to be used in the present disclosure may be a phosphorescent host compound or a fluorescent host compound.
  • the kinds of host compound to be used are not particularly limited, and may be compounds having the aforementioned LUMO energy level and selected from compounds known in the art.
  • the host compound may be a fluorescent host compound.
  • the fluorescent host compound may be an anthracene-based compound represented by the following formula 30:
  • Ar 31 and Ar 32 each independently, represent a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (5- to 30-membered) heteroaryl;
  • Ar 33 and Ar 34 each independently, represent hydrogen, deuterium, a halogen, a cyano, a nitro, a hydroxy, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered) heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted (C1-C30)alkylsilyl, a substituted or unsubstituted (C6-C30)aryls
  • the compound of formula 30 includes the following compounds, but is not limited thereto:
  • the dopant compound to be used in the present disclosure may be a phosphorescent dopant compound or a fluorescent dopant compound.
  • the dopant compound may be a fluorescent dopant compound.
  • the fluorescent dopant compound may be a condensed polycyclic amine derivative represented by the following formula 40:
  • Ar 41 represents a substituted or unsubstituted (C6-C50)aryl or styryl;
  • L a represents a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene;
  • Ar 42 and Ar 43 each independently, represent hydrogen, deuterium, a halogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl, or may be linked to an adjacent substituent(s) to form a mono- or polycyclic, (C3-C30) alicyclic, aromatic, or a combination of alicyclic and aromatic ring whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, and
  • a preferable aryl for Ar 41 includes a substituted or unsubstituted phenyl, a substituted or unsubstituted fluorenyl, a substituted or unsubstituted anthryl, a substituted or unsubstituted pyrenyl, a substituted or unsubstituted chrysenyl, a substituted or unsubstituted benzofluorenyl, and spiro[fluoren-benzofluorene], etc.
  • the compound of formula 40 includes the following compounds, but is not limited thereto:
  • the organic electroluminescent device of the present disclosure may further comprise a hole injection layer or a hole transport layer between the first electrode and the light-emitting layer.
  • Figure 1 illustrates a schematic sectional view of an organic electroluminescent device according to one embodiment of the present disclosure.
  • Figure 1 shows an organic electroluminescent device 100 comprising a substrate 101, a first electrode 110 formed on the substrate 101, an organic layer 120 formed on the first electrode 110, and a second electrode 130 formed on the organic layer 120 and facing the first electrode 110.
  • the organic layer 120 comprises a hole injection layer 122, a hole transport layer 123 formed on the hole injection layer 122, a light-emitting layer 125 formed on the hole transport layer 123, an electron buffer layer 126 formed on the light-emitting layer 125, and an electron transport zone 129 formed on the electron buffer layer 126; and the electron transport zone 129 comprises an electron transport layer 127 formed on the electron buffer layer 126, and an electron injection layer 128 formed on the electron transport layer 127.
  • the light-emitting layer 125 may be prepared with a host compound and a dopant compound.
  • the kinds of host compound and dopant compound to be used are not particularly limited, and may be selected from compounds known in the art. The examples of the host compound and the dopant compound are as described above.
  • the dopant can be doped in an amount of less than about 25 wt%, and preferably less than 17 wt%, based on the total amount of the dopant and host of the light-emitting layer.
  • the light emitting layer 125 is composed of two or more layers, each of the layers may be prepared to emit color different from one another.
  • the device may emit white light by preparing three light-emitting layers 125 which emit blue, red, and green colors, respectively.
  • the device may include light-emitting layers which emit yellow or orange color, if necessary.
  • the electron buffer layer 126 may employ the compound of formula 1 of the present disclosure or other compounds for the electron buffer.
  • the thickness of the electron buffer layer 126 is 1 nm or more, but is not particularly limited thereto. Specifically, the thickness of the electron buffer layer 126 may be in the range of from 2 nm to 200 nm.
  • the electron buffer layer 126 may be formed on the light-emitting layer 125 by using known various methods such as vacuum deposition, wet film-forming methods, laser induced thermal imaging, etc.
  • the electron buffer layer indicates a layer controlling an electron flow. Therefore, the electron buffer layer may be, for example, a layer which traps electrons, blocks electrons, or lowers an energy barrier between an electron transport zone and a light-emitting layer.
  • the electron transport zone 129 means a zone in which electrons are transported from the second electrode to the light-emitting layer.
  • the electron transport zone 129 can comprise an electron transport compound, a reductive dopant, or a combination thereof.
  • the electron transport compound can be at least one selected from a group comprising triazine-based compounds, oxazole-based compounds, isoxazole-based compounds, triazole-based compounds, isothiazole-based compounds, oxadiazole-based compounds, thiadiazole-based compounds, perylene-based compounds, anthracene-based compounds, aluminum complexes, and gallium complexes.
  • the reductve dopant may be selected from alkali metals, alkali metal compounds, alkaline earth metals, rare-earth metals, and halides, oxides, and complexes thereof.
  • the reductive dopant includes lithium quinolate, sodium quinolate, cesium quinolate, potassium quinolate, LiF, NaCl, CsF, Li 2 O, BaO, and BaF 2 , but are not limited thereto.
  • the electron transport zone 129 can comprise an electron transport layer 127, an electron injection layer 128, or both of them.
  • the electron transport layer 127 and the electron injection layer 128 can each be composed of two or more layers.
  • the electron transport layer 127 can comprise an electron transport material including the compound represented by formula 2.
  • the electron transport layer 127 can further comprise the reductive dopant above.
  • the electron injection layer 128 may be prepared with any electron injection material known in the art, which includes lithium quinolate, sodium quinolate, cesium quinolate, potassium quinolate, LiF, NaCl, CsF, Li 2 O, BaO, and BaF 2 , but is not limited thereto.
  • the aforementioned description regarding the organic electroluminescent device shown in Figure 1 is intended to explain one embodiment of the invention, and is not meant in any way to restrict the scope of the invention.
  • the organic electroluminescent device can be constructed in another way.
  • any one optional component such as a hole injection layer may not be comprised in the organic electroluminescent device of Figure 1, except for a light-emitting layer and an electron buffer layer.
  • an optional component may be further comprised therein, which includes one or more of an impurity layer such as n-doping layer and p-doping layer.
  • the organic electroluminescent device may be a both side emission type in which a light-emitting layer is placed on each of both sides of the impurity layer.
  • the two light-emitting layers on the impurity layer may emit different colors.
  • the organic electroluminescent device may be a bottom emission type in which a first electrode is a transparent electrode and a second electrode is a reflective electrode.
  • the organic electroluminescent device may be a top emission type in which a first electrode is a reflective electrode and a second electrode is a transparent electrode.
  • the organic electroluminescent device may have an inverted type structure in which a cathode, an electron transport layer, a light-emitting layer, a hole transport layer, a hole injection layer, and an anode are sequentially stacked on a substrate.
  • Figure 2 illustrates an energy gap relationship among the layers of the organic electroluminescent device according to one embodiment of the present disclosure.
  • a hole transport layer 123, a light-emitting layer 125, an electron buffer layer 126, and an electron transport zone 129 are sequentially stacked. Electrons (e - ) injected from a cathode are transported to a light-emitting layer 125 through an electron transport zone 129 and an electron buffering layer 126.
  • the LUMO energy level of the electron buffer layer 126 has a medium value of the LUMO energy level of the host compound and the dopant compound of the light-emitting layer 125 and the LUMO energy level of the electron transport layer 127.
  • the LUMO energy levels of the layers have a relationship of the electron transport layer > electron buffer layer > light-emitting layer.
  • a LUMO energy gap of 0.5 eV or greater occurs between the light-emitting layer and the electron transport layer.
  • an electron buffer layer there is an advantage in that electrons can be actively transported.
  • the LUMO energy level of the light-emitting layer (Ah) is higher than the LUMO energy level of the dopant compound (Ad).
  • the LUMO energy level of the electron transport layer (Ae) is higher than the LUMO energy level of the electron buffer layer (Ab).
  • the LUMO energy level of the electron transport layer (Ae) and the LUMO energy level of the light-emitting layer (Ah) satisfy the following equation.
  • the LUMO energy level of the electron transport layer (Ae) and the LUMO energy level of the electron buffer layer (Ab) satisfy the following equation.
  • results according to the relationship of the LUMO energy levels of the electron transport layer (Ae), electron buffer layer (Ab), and the light-emitting layer (Ah) are for explaining the rough tendency of the device in accordance with the overall LUMO energy groups, and so results other than the above can appear according to the inherent property of the specific derivatives, and the stability of the materials.
  • the electron buffer layer can be comprised in organic electroluminescent devices emitting every color including blue, red, and green. Preferably, it can be comprised in an organic electroluminescent device emitting blue light (i.e. the main peak wavelength is from 430 to 470 nm, preferably, in the 450's nm).
  • a display system for example, for smartphones, tablets, notebooks, PCs, TVs, or vehicles, or a lighting system, for example, an indoor or outdoor lighting system, can be produced.
  • An OLED device not according to the present disclosure was produced as follows: A transparent electrode indium tin oxide (ITO) thin film (10 ⁇ /sq) on a glass substrate for an OLED (GEOMATEC CO., LTD., Japan) was subjected to an ultrasonic washing with acetone and isopropyl alcohol, sequentially, and then was stored in isopropanol. Next, the ITO substrate was mounted on a substrate holder of a vacuum vapor deposition apparatus.
  • ITO indium tin oxide
  • Compound H-82 as a host was introduced into one cell of the vacuum vapor deposition apparatus and compound D-38 as a dopant was introduced into another cell of the apparatus.
  • the two materials were evaporated at a different rate and the dopant was deposited in a doping amount of 2 wt%, based on the total weight of the host and dopant, to form a light-emitting layer having a thickness of 20 nm on the second hole transport layer.
  • BCP compound ETL-1
  • an electron transport material was introduced into one cell of the vacuum vapor deposition apparatus and evaporated to form an electron transport layer having a thickness of 35 nm on the light-emitting layer.
  • an Al cathode having a thickness of 80 nm was deposited by another vacuum vapor deposition apparatus on the electron injection layer.
  • All the materials used for producing the OLED device were purified by vacuum sublimation at 10 -6 torr.
  • the driving voltage, luminous efficiency, CIE color coordinates, and the time period for the luminance to decrease from 100% to 90% at a luminance of 1,000 nits of the produced OLED device are provided in Table 1 below.
  • a current efficiency versus a luminance of the organic electroluminescent device of Comparative Example 1 is illustrated in Figure 3 as a graph.
  • An OLED device was produced in the same manner as in Comparative Example 1, except that Alq 3 (compound ETL-2 ) was used as an electron transport material, and evaluated.
  • the evaluation results of the OLED device of Comparative Example 2 are provided in Table 1 below.
  • OLED devices were produced in the same manner as in Comparative Example 1, except that BCP (compound ETL-1 ) was evaporated as an electron buffer layer of 5 nm and Alq 3 (compound ETL-2 ) was evaporated as an electron transport layer of 30 nm (Comparative Example 3), and compound B-21 was evaporated as an electron buffer layer of 5 nm and compound ETL-3 and Liq in a weight ratio of 50:50 were evaporated as an electron transport layer of 30 nm (Comparative Example 4) instead of forming an electron transport layer of 35 nm, and evaluated.
  • the evaluation results of the OLED device of Comparative Examples 3 and 4 are provided in Table 1 below.
  • OLED devices were produced in the same manner as in Comparative Example 1, except that an electron buffer layer is not formed and the compounds of Table 1 and Liq in a weight ratio of 50:50 were evaporated as an electron transport layer of 30 nm, and evaluated.
  • the evaluation results of the OLED device of Comparative Examples 5 to 8 are provided in Table 1 below.
  • OLED devices were produced in the same manner as in Comparative Example 1, except that compound B-21 was evaporated as an electron buffer layer of 5 nm and the compounds of Table 1 and Liq in a weight ratio of 50:50 were evaporated as an electron transport layer of 30 nm, and evaluated.
  • the evaluation results of the OLED device of Device Examples 1 to 4 are provided in Table 1 below.
  • a current efficiency versus a luminance of the organic electroluminescent device of Device Example 2 is illustrated in Figure 3 as a graph.
  • OLED devices were produced in the same manner as in Comparative Example 1, except for using compound H-15 as the host compound and using the electron transport material as in Table 2, and evaluated.
  • the evaluation results of the OLED device of Comparative Examples 9 and 10 are provided in Table 2 below.
  • An OLED device was produced in the same manner as in Comparative Examples 9 and 10, except that BCP (compound ETL-1 ) was evaporated as an electron buffer layer of 5 nm and Alq 3 (compound ETL-2 ) was evaporated as an electron transport layer of 30 nm instead of forming an electron transport layer of 35 nm, and evaluated.
  • BCP compound ETL-1
  • Alq 3 compound ETL-2
  • OLED devices were produced in the same manner as in Comparative Examples 9 and 10, except that an electron buffer layer is not formed and the compounds of Table 2 and Liq in a weight ratio of 50:50 were evaporated as an electron transport layer of 30 nm, and evaluated.
  • the evaluation results of the OLED device of Comparative Examples 12 to 14 are provided in Table 2 below.
  • OLED devices were produced in the same manner as in Comparative Examples 9 and 10, except that compound B-28 was evaporated as an electron buffer layer of 5 nm and the compounds of Table 2 and Liq in a weight ratio of 50:50 were evaporated as an electron transport layer of 30 nm, and evaluated.
  • the evaluation results of the OLED device of Device Examples 5 to 7 are provided in Table 2 below.
  • the OLED devices of Device Examples 1 to 4 and Device Examples 5 and 7 provide lower driving voltage, higher efficiency, and longer lifespan compared to Comparative Examples 1 to 4 and Comparative Examples 9 to 11, respectively, by appropriately combining the electron buffer layer and the electron transport layer of the present disclosure.
  • Comparative Examples 5 to 8 and Comparative Examples 12 to 14 with Device Examples 1 to 4 and Device Examples 5 and 7, respectively, it can be seen that the driving voltage, efficiency, and lifespan characteristics are all improved according to the insertion of the electron buffer layer between the light-emitting layer and the electron transport layer. This means that the electron injection characteristic can be improved according to the combination of the electron buffer layer and the electron transport layer, which may be due to an active cascade of the LUMO energy level.
  • the LUMO energy level of the light-emitting layer may be 1.6 eV, and when a 1,4-naphthyl group is comprised as a linker between a carbazole derivative and a triazine, the LUMO energy level may be 2.1 eV.
  • the energy barrier between the light-emitting layer and the electron transport layer is as high as about 0.5 eV so that a high driving voltage and low efficiency characteristics can be shown as in Comparative Examples 5 to 8.
  • an electron buffer layer of the compound of the present disclosure is inserted between the light-emitting layer and the electron transport layer, the electron injection barrier is improved as in Figure 2 so that the driving voltage, efficiency, and lifespan characteristics are all improved.
  • the combination of the electron buffer layer and the electron transport layer is considered to be easily applied to flexible displays, lightings, and vehicle displays which require long lifespan.

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Electroluminescent Light Sources (AREA)

Abstract

La présente invention concerne un dispositif électroluminescent organique. Le dispositif électroluminescent organique de la présente invention comprend une combinaison spécifique d'un matériau tampon d'électrons et d'un matériau de transport d'électrons qui peut offrir une efficacité élevée et/ou une longue durée de vie.
PCT/KR2017/010110 2016-09-22 2017-09-15 Dispositif électroluminescent organique comprenant une couche tampon d'électrons et une couche de transport d'électrons WO2018056645A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201780055061.XA CN109716549B (zh) 2016-09-22 2017-09-15 包含电子缓冲层和电子传输层的有机电致发光装置
US16/327,955 US11107997B2 (en) 2016-09-22 2017-09-15 Organic electroluminescent device comprising an electron buffer layer and an electron transport layer

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
KR20160121692 2016-09-22
KR10-2016-0121692 2016-09-22
KR1020170114048A KR102455656B1 (ko) 2016-09-22 2017-09-06 전자 버퍼층 및 전자 전달층을 포함하는 유기 전계 발광 소자
KR10-2017-0114048 2017-09-06

Publications (1)

Publication Number Publication Date
WO2018056645A1 true WO2018056645A1 (fr) 2018-03-29

Family

ID=61689968

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2017/010110 WO2018056645A1 (fr) 2016-09-22 2017-09-15 Dispositif électroluminescent organique comprenant une couche tampon d'électrons et une couche de transport d'électrons

Country Status (1)

Country Link
WO (1) WO2018056645A1 (fr)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109346500A (zh) * 2018-06-29 2019-02-15 云谷（固安）科技有限公司 一种有机电致发光装置
WO2019206290A1 (fr) * 2018-04-28 2019-10-31 江苏三月光电科技有限公司 Dispositif électroluminescent organique
WO2020045976A1 (fr) * 2018-08-29 2020-03-05 Rohm And Haas Electronic Materials Korea Ltd. Pluralité de matériaux hôtes et dispositif électroluminescent organique les comprenant
EP3551623A4 (fr) * 2016-12-09 2020-04-29 Rohm And Haas Electronic Materials Korea Ltd. Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
WO2020130392A1 (fr) * 2018-12-17 2020-06-25 덕산네오룩스 주식회사 Composé pour élément électrique organique, élément électrique organique l'utilisant et dispositif électronique comprenant ledit élément électrique organique
US20210028369A1 (en) * 2018-03-27 2021-01-28 Rohm And Haas Electronic Materials Korea Ltd. Composition material for organic electroluminescent device, plurality of host materials, and organic electroluminescent device comprising the same
WO2021157635A1 (fr) 2020-02-05 2021-08-12 出光興産株式会社 Composé, matériau pour éléments électroluminescents organiques, élément électroluminescent organique et dispositif électronique
WO2021157636A1 (fr) 2020-02-05 2021-08-12 出光興産株式会社 Élément électroluminescent organique et dispositif électronique
WO2024029581A1 (fr) * 2022-08-03 2024-02-08 出光興産株式会社 Composé, matériau d'élément électroluminescent organique, élément électroluminescent organique et dispositif électronique

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014104720A1 (fr) * 2012-12-24 2014-07-03 Rohm And Haas Electronic Materials Korea Ltd. Composés électroluminescents organiques et dispositif électroluminescent organique les comprenant
WO2015142040A1 (fr) * 2014-03-17 2015-09-24 Rohm And Haas Electronic Materials Korea Ltd. Matériau tampon d'électrons et dispositif électroluminescent organique
WO2015142036A1 (fr) * 2014-03-17 2015-09-24 Rohm And Haas Electronic Materials Korea Ltd. Matériau tampon de confinement d'électrons et dispositif électroluminescent organique comportant de matériau
WO2016018076A1 (fr) * 2014-07-29 2016-02-04 Rohm And Haas Electronic Materials Korea Ltd. Matériau tampon d'électrons et dispositif électroluminescent organique
WO2016129819A1 (fr) * 2015-02-12 2016-08-18 Rohm And Haas Electronic Materials Korea Ltd. Composés électroluminescents organiques et dispositifs électroluminescents organiques les comprenant

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014104720A1 (fr) * 2012-12-24 2014-07-03 Rohm And Haas Electronic Materials Korea Ltd. Composés électroluminescents organiques et dispositif électroluminescent organique les comprenant
WO2015142040A1 (fr) * 2014-03-17 2015-09-24 Rohm And Haas Electronic Materials Korea Ltd. Matériau tampon d'électrons et dispositif électroluminescent organique
WO2015142036A1 (fr) * 2014-03-17 2015-09-24 Rohm And Haas Electronic Materials Korea Ltd. Matériau tampon de confinement d'électrons et dispositif électroluminescent organique comportant de matériau
WO2016018076A1 (fr) * 2014-07-29 2016-02-04 Rohm And Haas Electronic Materials Korea Ltd. Matériau tampon d'électrons et dispositif électroluminescent organique
WO2016129819A1 (fr) * 2015-02-12 2016-08-18 Rohm And Haas Electronic Materials Korea Ltd. Composés électroluminescents organiques et dispositifs électroluminescents organiques les comprenant

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3551623A4 (fr) * 2016-12-09 2020-04-29 Rohm And Haas Electronic Materials Korea Ltd. Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
US11495750B2 (en) 2016-12-09 2022-11-08 Rohm And Haas Electronic Materials Korea Ltd. Organic electroluminescent compound and organic electroluminescent device comprising the same
US20210028369A1 (en) * 2018-03-27 2021-01-28 Rohm And Haas Electronic Materials Korea Ltd. Composition material for organic electroluminescent device, plurality of host materials, and organic electroluminescent device comprising the same
WO2019206290A1 (fr) * 2018-04-28 2019-10-31 江苏三月光电科技有限公司 Dispositif électroluminescent organique
CN110416419A (zh) * 2018-04-28 2019-11-05 江苏三月光电科技有限公司 有机电致发光器件
CN109346500A (zh) * 2018-06-29 2019-02-15 云谷（固安）科技有限公司 一种有机电致发光装置
CN109346500B (zh) * 2018-06-29 2020-12-01 云谷（固安）科技有限公司 一种有机电致发光装置
WO2020045976A1 (fr) * 2018-08-29 2020-03-05 Rohm And Haas Electronic Materials Korea Ltd. Pluralité de matériaux hôtes et dispositif électroluminescent organique les comprenant
WO2020130392A1 (fr) * 2018-12-17 2020-06-25 덕산네오룩스 주식회사 Composé pour élément électrique organique, élément électrique organique l'utilisant et dispositif électronique comprenant ledit élément électrique organique
WO2021157635A1 (fr) 2020-02-05 2021-08-12 出光興産株式会社 Composé, matériau pour éléments électroluminescents organiques, élément électroluminescent organique et dispositif électronique
WO2021157636A1 (fr) 2020-02-05 2021-08-12 出光興産株式会社 Élément électroluminescent organique et dispositif électronique
KR20220138380A (ko) 2020-02-05 2022-10-12 이데미쓰 고산 가부시키가이샤 화합물, 유기 전기발광 소자용 재료, 유기 전기발광 소자 및 전자 기기
KR20220137648A (ko) 2020-02-05 2022-10-12 이데미쓰 고산 가부시키가이샤 유기 전기발광 소자 및 전자 기기
WO2024029581A1 (fr) * 2022-08-03 2024-02-08 出光興産株式会社 Composé, matériau d'élément électroluminescent organique, élément électroluminescent organique et dispositif électronique

Similar Documents

Publication Publication Date Title
WO2018056645A1 (fr) Dispositif électroluminescent organique comprenant une couche tampon d'électrons et une couche de transport d'électrons
WO2018062778A1 (fr) Dispositif électroluminescent organique comprenant une couche de transport d'électrons et une couche tampon d'électrons
EP3119751A1 (fr) Matériau tampon d'électrons et dispositif électroluminescent organique
WO2015142040A1 (fr) Matériau tampon d'électrons et dispositif électroluminescent organique
EP3344606A1 (fr) Composés électroluminescents organiques et dispositif électroluminescent organique les comprenant
WO2015084021A1 (fr) Nouveaux composés organiques électroluminescents et dispositif organique électroluminescent les comprenant
WO2015099485A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique comprenant ce composé
WO2015037965A1 (fr) Nouveaux composés électroluminescents organiques et dispositif électroluminescent organique les comprenant
WO2015099486A1 (fr) Nouveaux composés organiques électroluminescents et dispositif organique électroluminescent les comprenant
WO2013165192A1 (fr) Nouveaux composés électroluminescents organiques et dispositif électroluminescent organique les contenant
WO2013109045A1 (fr) Nouveaux composés électroluminescents organiques et dispositif électroluminescent organique les utilisant
WO2013165189A1 (fr) Nouveaux composés électroluminescents organiques et dispositif électroluminescent organique les contenant
WO2014196805A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
WO2013151297A1 (fr) Nouveaux composés électroluminescents organiques et dispositif électroluminescent organique les comprenant
WO2013122402A1 (fr) Nouveaux composés organiques électroluminescents et dispositif organique électroluminescent les utilisant
WO2018151520A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
EP2831197A1 (fr) Nouveaux composés à électroluminescence organique et dispositif à électroluminescence organique les contenant
EP3563437A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
WO2018124697A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
WO2014104720A1 (fr) Composés électroluminescents organiques et dispositif électroluminescent organique les comprenant
EP3256453A1 (fr) Composés électroluminescents organiques et dispositifs électroluminescents organiques les comprenant
WO2015194839A1 (fr) Matériau de mise en tampon d'électrons et dispositif électroluminescent organique
EP3189035A1 (fr) Matériau de transport de trous et dispositif électroluminescent organique comprenant celui-ci
WO2017030283A1 (fr) Composés électroluminescents organiques et dispositif électroluminescent organique les comprenant
WO2014104704A1 (fr) Nouveaux composés électroluminescents organiques et dispositif électroluminescent organique les comprenant

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17853359

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17853359

Country of ref document: EP

Kind code of ref document: A1