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EP3028319A1 - Dispositif électroluminescent - Google Patents

Dispositif électroluminescent

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Publication number
EP3028319A1
EP3028319A1 EP14735855.0A EP14735855A EP3028319A1 EP 3028319 A1 EP3028319 A1 EP 3028319A1 EP 14735855 A EP14735855 A EP 14735855A EP 3028319 A1 EP3028319 A1 EP 3028319A1
Authority
EP
European Patent Office
Prior art keywords
conducting
polymer
hole
group
predominantly
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
EP14735855.0A
Other languages
German (de)
English (en)
Inventor
Junyou Pan
Frank Egon Meyer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Patent GmbH
Original Assignee
Merck Patent GmbH
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
Application filed by Merck Patent GmbH filed Critical Merck Patent GmbH
Priority to EP14735855.0A priority Critical patent/EP3028319A1/fr
Publication of EP3028319A1 publication Critical patent/EP3028319A1/fr
Ceased legal-status Critical Current

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Classifications

    • 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
    • H10K85/10—Organic polymers or oligomers
    • H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
    • H10K85/115—Polyfluorene; Derivatives thereof
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    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • H—ELECTRICITY
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    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/10—Organic polymers or oligomers
    • H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
    • H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
    • H10K85/1135—Polyethylene dioxythiophene [PEDOT]; Derivatives thereof
    • H—ELECTRICITY
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    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/10—Organic polymers or oligomers
    • H10K85/151—Copolymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/12—Copolymers
    • C—CHEMISTRY; METALLURGY
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/12—Copolymers
    • C08G2261/124—Copolymers alternating
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/14—Side-groups
    • C08G2261/148—Side-chains having aromatic units
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/10—Definition of the polymer structure
    • C08G2261/18—Definition of the polymer structure conjugated
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
    • C08G2261/312—Non-condensed aromatic systems, e.g. benzene
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
    • C08G2261/314—Condensed aromatic systems, e.g. perylene, anthracene or pyrene
    • C08G2261/3142—Condensed aromatic systems, e.g. perylene, anthracene or pyrene fluorene-based, e.g. fluorene, indenofluorene, or spirobifluorene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
    • C08G2261/316—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain bridged by heteroatoms, e.g. N, P, Si or B
    • C08G2261/3162—Arylamines
    • C—CHEMISTRY; METALLURGY
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/50—Physical properties
    • C08G2261/51—Charge transport
    • C08G2261/512—Hole transport
    • C—CHEMISTRY; METALLURGY
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/50—Physical properties
    • C08G2261/52—Luminescence
    • C08G2261/522—Luminescence fluorescent
    • C—CHEMISTRY; METALLURGY
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    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/50—Physical properties
    • C08G2261/52—Luminescence
    • C08G2261/524—Luminescence phosphorescent
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/90—Applications
    • C08G2261/95—Use in organic luminescent diodes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
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    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1408—Carbocyclic compounds
    • C09K2211/1416—Condensed systems
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    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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    • C09K2211/1425—Non-condensed systems
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    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1408—Carbocyclic compounds
    • C09K2211/1433—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K2101/00—Properties of the organic materials covered by group H10K85/00
    • H10K2101/10—Triplet emission
    • 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]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H—ELECTRICITY
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    • 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
    • H10K50/15—Hole transporting layers
    • H—ELECTRICITY
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    • 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
    • Y—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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/549—Organic PV cells
    • Y—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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the present invention relates to an electroluminescent device containing a polymer with hole-conducting or predominantly hole-conducting properties in the emitter layer.
  • light-sensitive organic materials e.g., phthalocyanines
  • organic charge transport materials e.g., triarylamine-based hole transporters
  • OLED organic light-emitting diodes
  • OLEDs consisting of all three basic colors
  • OLEDs are not good enough for many applications.
  • the combination of good color coordinates with high efficiency is still in need of improvement.
  • the above reasons require improvements in the production of OLEDs.
  • an organic electroluminescent device consists of several layers, which by means of vacuum methods or different printing methods, in particular solution-based printing methods, such as inkjet printing, or solvent-free printing methods, such as
  • a support plate or substrate preferably of glass or of
  • a transparent anode preferably of indium tin oxide ("ITO”); at least one hole injection layer ("Hole Injection Layer” or
  • HIL e.g. based on conductive polymers with hole conductor properties, e.g. Polyaniline (PANI) or polythiophene derivatives (such as PEDOT);
  • PANI Polyaniline
  • PEDOT polythiophene derivatives
  • interlayer optionally an intermediate layer
  • hole transporting layer e.g. based on triarylamine units containing polymers (WO 2004/084260 A);
  • an EML preferably has fluorescent dyes, e.g. ⁇ , ⁇ '-diphenylquinacridone (QA), or
  • Phosphorescent dyes eg tris- (phenyl-pyridyl) -iridium (Ir (PPy) 3 ) or tris- (2-benzothiephenyl-pyridyl) -iridium (Ir (BTP) 3 ), as well as doped matrix materials, eg 4,4'-bis (carbazol-9-yl) -biphenyl (CBP).
  • an EML can also consist of polymers, mixtures of polymers, mixtures of polymers with low molecular weight compounds or mixtures of various low molecular weight compounds;
  • HBL hole-blocking layer
  • an HBL preferably contains materials which have a deep HOMO and block the transport of holes, e.g. BCP (2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline or bathocuproine) or bis (2-methyl-8-quinolinolato) -4- (phenyl-phenolato) -aluminum (III) (BAIq );
  • ETL electron transport Layer
  • AlQ 3 aluminum tris-8-hydroxyquinoxalate
  • an electron injection layer (Electron Injection
  • EIL layer which may partially coincide with the aforementioned EML, HBL or ETL layers or a small part of the cathode is specially treated or specially deposited, whereby this EIL layer may be a thin layer, which consists of a material with a high dielectric constant, eg a layer of LiF, Li 2 O, BaF 2 , MgO or NaF;
  • a cathode preferably employing metals, metal combinations or low work function metal alloys, e.g. Ca, Ba, Cs, Mg, Al, In or Mg / Ag.
  • individual layers such as HBL, ETL and / or EIL layers
  • hybrid devices can also be produced by vapor deposition in vacuo, instead of by application from solution, whereby so-called hybrid devices are produced.
  • the entire device is structured accordingly (depending on the application), contacted and finally usually hermetically sealed, since the life of such devices can drastically shorten in the presence of water and / or air. The same applies to so-called.
  • the anode is constructed, for example, of Al / Ni / NiOx or of Al / Pt / PtO x or of other metal / metal oxide combinations which have a workfunction greater than 5 eV.
  • the cathode is constructed of the same materials described above, although the metal or the metal alloy is applied very thinly and thus is transparent.
  • the layer thickness is preferably below 50 nm, more preferably below 30 nm, and most preferably below 10 nm, whereby a portion of the emitted light is always absorbed thereby.
  • Another transparent material can be applied to this transparent cathode, for example ITO or IZO ("indium-zinc-oxide").
  • Anode / hole injection layer / emitter layer / cathode In structures of this type, the recombination of the electrons with the holes and thus the generation of radiation takes place in the emitter layer. Holes migrate into the emitter layer, which usually contains at least one predominantly electron-conducting material in addition to the emitter molecules, and recombine there with the excitation of the emitter molecules
  • Electrons Most of the polymers used today in OLED have higher mobility for electrons than for holes (see Friend et al., Nature, Vol. 434, pp. 194). Predominantly hole-conducting, conjugated electroluminescent polymer materials have hitherto not been described and have hitherto not been used in emitter layers. The use of these materials in Emitter layers would, in addition to the simple method of production of the layer, decisively improve the choices and enable the construction of new OLEDs.
  • WO 2008/034758 A discloses an OLED with a longer service life, which comprises a light-emitting layer with a phosphorescent emitter and with a hole-conducting material.
  • an electron-conducting layer is arranged between the light-emitting layer and the cathode.
  • This document describes mainly hole-conducting materials that consist of small organic molecules.
  • hole-conducting polymers have also been described; however, only polyvinylcarbazole, PEDOT or PANI are disclosed.
  • PEDOT and PANI are materials that need to be doped with protic acids to achieve adequate hole conductivity. Such materials are unsuitable for emitter layers, since the presence of protons the
  • Polyvinylcarbazole is a saturated hydrocarbon main chain polymer in which the conductivity-promoting carbazole groups are located in the side chains. Such electrically conductive polymers have only limited stability.
  • WO 2006/076092 A discloses phosphorescent OLEDs which have an exciton-blocking layer.
  • the emitter layer used therein contains, in addition to the light-emitting material, a hole-conducting material and an electron-conducting material. Only emitter layers composed of small organic molecules are disclosed. Also, no emitter layers with predominantly hole-conducting properties are disclosed, but only emitter layers with predominantly electron-conducting properties.
  • WO 2005/112 47 A discloses an organic light emitting diode with improved lifetime. This is due to the presence of a layer achieved from an aryl borane copolymer between the cathode and emitter layer and / or between the anode and emitter layer. Details of the structure of the light emitting diode or on the design of the emitter layer or other layers are not disclosed.
  • Emitter layer recombine and stimulate the emitter molecules located there to glow.
  • the present invention is therefore based on the object, a
  • Another object of the present invention is the
  • Yet another object of the present invention is to provide an electroluminescent device with a simple structure, which is characterized by a long life and a high luminous efficacy.
  • the device according to the invention should be easy to manufacture, be capable of broadband emission and have high radiation efficiency.
  • the present invention thus provides an electroluminescent device containing
  • At least one emitter layer which contains at least one emitter and which is arranged between the anode and the cathode
  • at least one electron transport layer which comprises at least one material with electron-conducting or predominantly electron-conducting
  • the at least one emitter layer contains at least one polymer, preferably a polymer, with hole-conducting or predominantly hole-conducting properties. Under a polymer with hole-conducting or predominantly hole-conducting
  • the mobility of the holes in this polymer must be at least one, preferably at least two, more preferably at least three orders of magnitude higher than the mobility of the electrons.
  • the hole mobility of the polymers employed in this invention having predominantly hole-conducting properties at 25 ° C preferably at least 10 "4 cm 2 A * sec, measured by the" time-of-flight "method in an electric field strength of 5 ⁇ 10 7 V / m.
  • This electric field strength corresponds to an OLED with 80 nm layer thickness and 4 V.
  • the electron mobility at 25 ° C is preferably at most 10 "5 cm 2 / V * sec, measured by the time-of-flight method at an electric field strength of 5 * 10 7 V / m.
  • the operation of the electroluminescent device according to the invention can of course also be carried out at other electric field strengths, for example at field strengths in the range of 10 7 to 10 10 V / m.
  • the mobility of free charge carriers in polymers can be determined by various methods known to the person skilled in the art.
  • the "time-of-flight” method is used (see: “Organic Photoreceptors for Xerography”, Paul M. Borsenberger, 1998, Marcel Dekker).
  • a material with electron-conducting or predominantly electron-conducting properties is to be understood as meaning a material which can conduct only electrons or which can conduct both holes and electrons.
  • the mobility of the electrons in this material must be at least one, preferably at least two, more preferably at least three orders of magnitude higher than the mobility of the holes.
  • These materials may be low molecular weight organic compounds, polymers or a mixture of polymers with low molecular weight organic
  • the emitter is incorporated as a repeating unit in a polymer, more preferably in the polymer with hole-conducting or predominantly hole-conducting properties.
  • the emitter is mixed into a matrix material, which may be a small molecule, a polymer, an oligomer, a dendrimer or a mixture thereof.
  • emitter unit or emitter refers to a device or compound in which, upon receipt of an exciton or formation of an exciton, radiation decay occurs with light emission.
  • fluorescent emitter refers to materials or compounds that undergo a radiation transition from an excited singlet state to its ground state.
  • phosphorescent emitter refers to luminescent materials or compounds containing transition metals. These typically include materials in which the light emission is caused by spin-forbidden transitions, e.g. Transitions of excited triplet and / or
  • an emitter selected from the group of:
  • fluorescent emitter is selected. Many examples of fluorescent emitters have already been published, e.g. Styrylamine derivatives such as e.g. in JP 2913116 B and in the
  • the fluorescent emitters are preferably polyaromatic compounds, such as 9,10-di (2-naphthylanthracene) and other anthracene derivatives, derivatives of tetracene, xanthene, perylene, such as 2,5,8,11-tetra-t- butylperylene, phenylene, eg 4,4 '- (bis (9-ethyl-3-carbazovinylene) -1, 1'-biphenyl, fluorene, arylpyrene (US 2006/0222886), arylenevinylenes (US 5121029, US 5130603 ), Derivatives of rubrene, coumarin, rhodamine, quinacridone, such as ⁇ , ⁇ '-dimethylquinacridone (DMQA),
  • Other preferred fluorescent emitters are selected from the class of monostyrylamines, distyrylamines, tristyrylamines, tetrastyrylamines, styrylphosphines, styryl ethers and arylamines.
  • a monostyrylamine is meant a compound containing a substituted or unsubstituted styryl group and at least one, preferably aromatic, amine.
  • a distyrylamine is meant a compound which is two substituted or unsubstituted
  • Styryl groups and at least one, preferably aromatic, amine are to be understood as meaning a compound which contains three substituted or unsubstituted styryl groups and at least one, preferably aromatic, amine.
  • a tetrastyrylamine is meant a compound containing four substituted or unsubstituted styryl groups and at least one, preferably aromatic, amine.
  • the styryl groups are particularly preferably stilbenes, which may also be further substituted.
  • the corresponding phosphines and ethers are defined analogously to the amines.
  • aromatic amine to understand a compound containing three substituted or unsubstituted aromatic or heteroaromatic ring systems which are directly bonded to the nitrogen. At least one of these aromatic or heteroaromatic ring systems is preferably a fused ring system, preferably having at least 14 aromatic ring atoms. Preferred examples of these are aromatic anthracene amines, aromatic anthracenediamines, aromatic pyrenamines, aromatic pyrenediamines, aromatic Chrysenamine and aromatic chrysene diamines. Under a
  • aromatic anthracenamine is a compound in which a diarylamino group is bonded directly to an anthracene group, preferably in the 9-position.
  • aromatic anthracenediamine is meant a compound in which two diarylamino groups are bonded directly to an anthracene group, preferably in the 9,10-position.
  • Aromatic pyrenamines, pyrenediamines, chrysenamines and chrysenediamines are defined analogously thereto, the diarylamino groups on the pyrene preferably being bonded in the 1-position or in the 1, 6-position.
  • fluorescent emitters are indenofluorenamines and indenofluorodiamines, e.g. according to WO 2006/122630, benzoin-indenofluoreneamines and benzoindenofluorodiamines, e.g. according to WO 2008/006449, and dibenzoindenofluorenamines and dibenzoindeno-fluoro-diamines, e.g. according to WO 2007/140847.
  • Examples of emitters from the class of styrylamines are substituted or unsubstituted tristilbenamines or the dopants described in WO 2006/000388, WO 2006/058737, WO 2006/000389, WO 2007/065549 and WO 2007/115610. Distyrylbenzene and distyryl biphenyl derivatives are described in US 5121029. Further,
  • Styrylamines can be found in US 2007/0122656 A1.
  • styrylamine emitters and triarylamine emitters are the compounds of the formulas (1) to (6) as described in US Pat. No. 7,250,532 B2, DE 102005058557 A1, CN 1583691 A, JP 08053397 A, US Pat
  • fluorescent emitters are from the derivatives of naphthalene, anthracene, tetracene, fluorene, periflanthene, indenoperylene, phenanthrene, perylene (US 2007/0252517 A1), pyrene, chrysene, decacycles, coronene, tetraphenylcyclopentadiene, pentaphenylcyclopentadiene, fluorene, spirofluorene, Rubrene, coumarin (US 4769292, US 6020078, US 2007/0252517 A1), pyran, oxazone, benzoxazole, benzothiazole, benzimidazole, pyrazine, cinnamic esters, diketopyrrolopyrrole, acridone and quinacridone (US 2007/0252517 A1).
  • 9,10-substituted anthracenes e.g. 9,10-diphenylanthracene and 9,10-bis (phenylethynyl) anthracene, more preferably. 1,4-bis (9'-ethynylanthracenyl) benzene is also a preferred dopant.
  • an emitter in the emitter layer which is selected from the group consisting of the blue-fluorescent, the green-fluorescent or the yellow-fluorescent emitter.
  • an emitter in the emitter layer which is selected from the group of red fluorescent emitters.
  • a particularly preferred red-fluorescent emitter is selected from the group of perylene derivatives, for example of the formula (7), as disclosed, for example, in US 2007/0104977 A1.
  • an emitter in the emitter layer which is selected from the group of phosphorescent emitters.
  • Examples of phosphorescent emitters are disclosed in WO 00/070655, WO 01/041512, WO 02/002714, WO 02/015645, EP 1191613, EP 1191612, EP 1191614 and WO 2005/033244.
  • the phosphorescent emitter may be a metal complex, preferably of the formula M (L) Z in which M is a metal atom, L on each occurrence independently represents an organic ligand attached to M via one, two or more positions or is coordinated therewith, and z is an integer greater than 1, preferably 1, 2, 3, 4, 5 or 6, and in which, where appropriate, these groups are accompanied by a polymer via one or more, preferably one, two or three positions, preferably via the ligands L, are linked.
  • M is preferably a metal atom which consists of transition metals, preferably of transition metals of the VIII group, Lanthanides or actinides, more preferably from Rh, Os, Ir, Pt, Pd, Au, Sm, Eu, Gd, Tb, Dy, Re, Cu, Zn, W, Mo, Pd, Ag or Ru and most preferably from Os , Ir, Ru, Rh, Re, Pd or Pt. M can also mean Zn.
  • Preferred ligands are 2-phenylpyridine derivatives, 7,8-benzoquinoline derivatives, 2- (2-thienyl) pyridine derivatives, 2- (1-naphthyl) pyridine derivatives or 2-phenylquinoline derivatives. These compounds may each be substituted, e.g. by fluorine or trifluoromethyl substituents for blue.
  • Secondary ligands are preferably acetylacetonate or picric acid.
  • tetradentate ligands of formula (8) as disclosed, for example, in US 2007/0087219 A1, in which R 1 to R 14 and Z 1 to Z 5 are as defined in US 2007/0087219 A1, Pt-porphyrin complexes having an enlarged Ring system (US 2009/0061681 A1) and Ir complexes, for example 2,3,7,8,12,13,17,18-octa-ethyl-21H, 23H-porphyrin-Pt (II), tetraphenyl-Pt ( II) -tetrabenzoporphyrin (US 2009/0061681 A1), cis-bis (2-phenylpyridinato-N, C2 ') Pt (II), cis-bis (2- (2'-thienyl) pyridinato-N, C3') Pt (II), cis-bis (2- (2'-thienyl) quinolinato-N, C
  • phosphorescent emitters are compounds of the following formulas (9) and (10) as well as further compounds as disclosed, for example, in US 2001/0053462 A1 and WO 2007/095118 A1.
  • an emitter in the emitter layer which is selected from the group of metaliorganischen complexes.
  • suitable metal complexes according to the present invention are selected from transition metals, rare earth elements, lanthanides and actinides.
  • the metal is selected from Ir, Ru, Os, Eu, Au, Pt, Cu, Zn, Mo, W, Rh, Pd and Ag.
  • the proportion of emitter structural units in the polymer having hole-conducting or predominantly hole-conducting properties which is used in the emitter layer is preferably in the range from 0.01 to 20 mol%, particularly preferably in the range from 0.5 to 10 mol%, very particularly preferably in the range of 1 to 8 mol%, and in particular in the range of 1 to 5 mol%.
  • the hole-conducting properties of the copolymer used in the emitter layer are also determined by the selection of suitable structural units. scored.
  • the polymer having the hole-conducting or predominantly hole-conducting properties contains at least one repeating unit selected from the group of hole transport materials (HTM), preferably with at least one repeating unit forming the polymer backbone.
  • HTM hole transport materials
  • any HTM known to the person skilled in the art can be used as a repeating unit in the polymer having the hole-conducting or predominantly hole-conducting properties.
  • HTM is preferably selected from amines, triarylamines, thiophenes,
  • the HTM is more preferably selected from amines, triarylamines, thiophenes, carbazoles, phthalocyanines and porphyrins.
  • Suitable HTM repeating units are phenylenediamine derivatives (US 3615404), arylamine derivatives (US 3567450), amino-substituted
  • Copolymers e.g., porphyrin compounds (JP-A-63-2956965), aromatic dimethylidene-type compounds, carbazole compounds, e.g. CDBP, CBP and mCP, aromatic tertiary amine and styrylamine compounds (US 4127412) and monomeric triarylamines (US 3,180,730).
  • triarylamine groups are present in the polymer.
  • aromatic tertiary amines containing at least two tertiary amine units such as 4,4'-bis [N- (1-naphthyl) -N-phenylamino] biphenyl (NPD) (US 5061569) or MTDATA (JP A 4-308688), N, N, N ', N'-tetra (4-biphenyl) diaminobiphenylene (TBDB), 1, 1-bis (4-di-p-tolylaminophenyl) cyclohexane (TAPC), 1 , 1-bis (4-di-p-tolylaminophenyl) -3-phenylpropane (TAPPP), 1, 4-bis [2- [4- [N, N-di (p-tolyl) -amino] phenyl] vinyl] benzene (BDTAPVB), N, N, N ', N'-tetra-p-to-tol
  • tertiary amines containing carbazole units such as 4- (9H-carbazol-9-yl) -N, N-bis [4- (9H -carbazol-9-yl) -phenyl] -benzolamine (TCTA). Also preferred are hexaazatriphenylene compounds according to US 2007/0092755 A1.
  • HTM units are, for example, triarylamine, benzidine, tetraaryl-para-phenylenediamine, carbazole, azulene, thiophene, pyrrole and furan derivatives, and also O, S or N-containing heterocycles.
  • Ar 1 which may be the same or different, independently, when in different repeat units, represents a single bond or an optionally substituted mononuclear or polynuclear aryl group,
  • Ar 2 which may be the same or different, independently, when in different repeating units, represent an optionally substituted mononuclear or polynuclear aryl group
  • Ar 3 which may be the same or different, independently, when in different repeating units, represent an optionally substituted mononuclear or polynuclear aryl group
  • m is 1, 2 or 3.
  • Preferred repeat units of the formula (17) are selected from the following formulas (18) to (20):
  • R which may be the same or different at each instance, is selected from H, substituted or unsubstituted aromatic or heteroaromatic group, alkyl, cycloalkyl, alkoxy, aralkyl, aryloxy, arylthio, alkoxycarbonyl, silyl, carboxy group, halogen, cyano, nitro or hydroxy group is
  • r 0, 1, 2, 3 or 4 and
  • the polymer having hole-conducting or predominantly hole-conducting properties contains at least one of the following repeat units of the formula (21):
  • T 1 and T 2 are independently selected from thiophene, selenophene, thieno [2,3b] thiophene, thieno [3,2b] thiophene, dithienothiophene, pyrrole, aniline, all of which are optionally substituted with R 5 ,
  • the groups T 1 and T 2 are preferably selected from Thiophene-2,5-diyl, o [3,2b] thiophene-2,5-o [2,3b] thiophene-2,5-nonhiophene-2,6-diyl-2,5-diyl,
  • R ° and R 5 can assume the same meaning as R in the formulas (18) to (20).
  • Preferred units of formula (21) are selected from the group consisting of the following formulas:
  • R ° can assume the same meaning as R in the formulas (18) to (20).
  • the proportion of the HTM structural units in the hole-conducting or predominantly hole-conducting polymer which is used in the emitter layer is preferably in the range from 10 to 99 mol%, particularly preferably in the range from 20 to 80 mol%, and very particularly preferably in the range from 30 to 60 mol%.
  • the polymer used in the emitter layer preferably also has further structural units which form the backbone of the polymer.
  • the structural units that form the polymer backbone contain aromatic or heteroaromatic structures having 6 to 40 carbon atoms.
  • aromatic or heteroaromatic structures having 6 to 40 carbon atoms.
  • these are, for example, 4,5-dihydropyrene derivatives, 4,5,9,10-tetrahydropyrene derivatives, fluorene derivatives as disclosed, for example, in US Pat. No. 5,962,631, WO 2006/052457 A2 and WO 2006 / 118345A1, 9, 9'-spirobifluorene derivatives, as disclosed, for example, in WO 2003/020790 A1, 9,10-phenanthrene derivatives, for example in WO 2005/104264 A1 discloses 9,10-dihydrophenanthrene derivatives, such as in the
  • WO 2005/014689 A2 discloses 5,7-dihydrodibenzooxepine derivatives and cis and trans indenofluorene derivatives, e.g. in WO 2004/041901 A1 and WO 2004/113412 A2, and binaphthylene derivatives, such as e.g. in WO 2006/063852 A1, and also units such as e.g. in WO 2005 / 056633A1, EP 1344788A1, WO 2007 / 043495A1, WO 2005/033174 A1, WO 2003/099901 A1 and DE 102006003710.
  • Particularly preferred structural units which form the polymer backbone are selected from fluorene, e.g. in US 5,962,631, WO
  • 2006/052457 A2 and WO 2006/118345 A1 discloses spirobifluorene, such as e.g. in WO 2003/020790 A1 discloses benzofluorene,
  • Very particularly preferred structural units which form the polymer backbone are units of the following formula (22):
  • X means halogen
  • R ° and R 00 are each independently H or an optionally substituted carbyl or hydrocarbyl group optionally containing one or more heteroatoms; g is each independently 0 or 1 and the corresponding h in the same subunit for the other of 0 or 1, m is an integer> 1,
  • Ar 1 and Ar 2 are independently mono- or polynuclear aryl or heteroaryl optionally substituted and optionally fused to the 7,8-positions or 8,9-positions of the indenofluorene group, and a and b are independently 0 or 1 stand.
  • R 1 and R 2 form a spiro group with the fluorene group to which they are attached, these are preferably spirobifluorene.
  • the structural units of the formula (22) are preferably selected from the following formulas (23) to (27): -29 -
  • Particularly preferred structural units of the formula (22) are selected from the following formulas (28) to (31):
  • L is H, halogen or optionally fluorinated, linear or branched alkyl or alkoxy having 1 to 12 C atoms and preferably H, F, methyl, i-propyl, t-butyl, n-pentoxy or trifluoromethyl, and
  • the polymer in the emitter layer is a conjugated polymer having at least one emitting moiety, at least one hole-carrying moiety, and at least one moiety forming the polymer backbone.
  • Heteroatom-containing units have, for example, arylamines, aryiphosphines or heterocycles in which the conjugation partially on N, O, P or S atoms take place, or organometallic complexes in which the conjugation takes place partially via metal atoms.
  • Conjugated polymers are therefore to be understood in the broadest sense. These may be, for example, random polymers, block polymers or graft polymers.
  • Very particularly preferred structural units which form the polymer backbone are selected from fluorene, spirobifluorene, indenofluorene, phenanthrene, dihydrophenanthrene, dibenzothiophene, dibenzofuran and derivatives thereof.
  • conjugated polymers containing hole transporting units are disclosed in WO 2007/131582 A1 and WO 2008 / 009343A1.
  • the polymer of the emitter layer is not one
  • the non-conjugated or partially contains
  • the unconjugated polymer backbone moiety is included
  • X and Y are independently selected from the group consisting of H, F, a Ci -4 o-alkyl group, a C2 -4 o-alkenyl group, an alkynyl group C2-40-, an optionally substituted C6-4o-aryl, and optionally substituted 5- to 25-membered heteroaryl group.
  • non-conjugated polymer backbone structural units are selected from fluorene, phenanthrene, dihydrophenanthrene and indenofluorene derivatives of the following formulas (34a) to (37d), as described, for example, in U.S. Pat. in WO 2010/1361 1 1 A1 are disclosed:
  • R1 to R4 can have the same meanings as X and Y in formulas (32) and (33).
  • the proportion of the structural units forming the polymer backbone in the hole-conducting or predominantly hole-conducting polymer which is used in the emitter layer is preferably in the range from 10 to 99 mol%, more preferably in the range of 20 to 80 mol%, and most preferably in the range of 30 to 60 mol%.
  • the electronic device of the present invention comprises an electron transporting layer (ETL) which has electron-conducting or predominantly electron-conducting properties.
  • ETL electron transporting layer
  • any electron transport material known to those skilled in the art can be used either as a low molecular weight compound or, preferably, as a repeating unit in a polymer of the electron transporting layer.
  • ETMs are preferably selected from imidazoles, pyridines, pyrimidines,
  • Anthracenes benzanthracenes, pyrenes, perylenes, benzimidazoles, triazines, ketones, phosphine oxides, phenazines, phenanthrolines, triarylboranes and their isomers and derivatives.
  • Suitable ETM moieties are metal chelates of 8-hydroxyquinoline (for example, Liq, Alq 3, Gaq 3, MgQ 2, ZnQ 2, lnq 3, Zrq 4), Balq, 4-Azaphenanthren-5- ol / Be complexes (US 5,529,853 A eg formula 7), butadiene derivatives
  • Benzazoles e.g. 1, 3,5-tris (2-N-phenylbenzimidazolyl) benzene (TPBI) (US Pat. No. 5,763,779, Formula 8), 1,3,5-triazine derivatives (US Pat. No. 6,229,012 B1, US Pat. No. 6,225,467 B1, DE 10312675 A1, WO 98 / 04007A1 and US 6352791 B1), pyrenes, anthracenes, tetracenes, fluorenes, spirobifluorenes, dendrimers, tetracenes, eg Rubrene derivatives, 1, 10-phenanthroline derivatives
  • JP 2003/115387, JP 2004/311184, JP 2001/267080, WO 2002/043449 silacylcyclopentadiene derivatives
  • EP 1480280, EP 1478032, EP 1469533 silacylcyclopentadiene derivatives
  • pyridine derivatives JP 2004/200162 Kodak
  • phenanthrolines for example BCP and Bphen, as well as a number of bonded via biphenyl or other aromatic groups phenanthrolines (US 2007/0252517 A1) or anthracene-bound phenanthrolines (US 2007/0122656 A1, eg
  • Formulas 9 and 10 1, 3,4-oxadiazoles, e.g. Formula 11, triazoles, e.g. Formula 12, triarylboranes, benzimidazole derivatives and other N-heterocyclic compounds (see US 2007/0273272 A1), Silacyclopentadienderivate, borane derivatives, Ga-oxinoid complexes.
  • R and R 1 "8 each independently represent a hydrogen atom, a substituted or unsubstituted aromatic cyclic hydrocarbon group having 6 to 50 carbon atoms in the nucleus, a substituted or unsubstituted aromatic heterocyclic group having 5 to 50 nucleus atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 50 carbon atoms in the nucleus, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted aralkyl group having 6 to 50 carbon atoms in the nucleus, a substituted or unsubstituted aryloxy group having 5 to 50 carbon atoms in the nucleus, a substituted or unsubstituted arylthio group having 5 to 50 carbon atoms in the nucleus, a substituted or unsubsti
  • ETM structural units are from the group consisting of:
  • R is a hydrogen atom, a C 6-60 aryl group which may have a substituent, a pyridyl group which may have a substituent, a quinolyl group which may have a substituent, a C 1-20 alkyl group which may have a substituent, or a C 1-6 alkyl group which may have a substituent C1-20 alkoxy group which may have a substituent;
  • m is an integer from 0 to 4;
  • R 1 is a C 6-60 aryl group which may have a substituent, a pyridyl group which may have a substituent, a quinolyl group which may have a substituent, a C 1-20 alkyl group which may have a substituent, or a C 1-6 alkyl group which may have a substituent 20-alkoxy group which may have a substituent;
  • R 2 is a hydrogen atom, a C 6-60 aryl group which may have a substituent, a pyridyl group which may have a substituent, a quinolyl group which may have a substituent, a C 1-20 alkyl group which may have a substituent, or a C 1-20 alkoxy group which may have a substituent; and
  • L is a C6-60 arylene group which may have a substituent, a pyridinylene group which may have a substituent, a quinoline and a fluorenylene group which may have a substituent, and
  • Ar 1 represents a C 6-60 aryl group which may have a substituent, a pyridinyl group which may have a substituent, or a quinolinyl group which may have a substituent.
  • 2,9,10-substituted anthracenes with 1- or 2-naphthyl and 4- or 3-biphenyl
  • molecules containing two anthracene moieties such as e.g. disclosed in US 2008/0193796 A1.
  • the ETM materials are selected from heteroaromatic ring systems of the following formulas (40) to (45):
  • anthracene benzimidazole derivatives of formulas (46) through (48), e.g. in US 6878469 B2, US 2006/147747 A and EP 1551206 A1 are disclosed:
  • Copolymers contain structural units with electron-conducting
  • R to R 4 can assume the same meanings as R in formula
  • the proportion of materials having electron-conducting properties or the proportion of structural units having electron-conducting properties in the polymer in the electron-transporting layer which have electron-conducting or predominantly electron-conducting properties is preferably in the range from 10 to 99 mol%, particularly preferably in the range from 20 to 80 mol%, and most preferably in the range of 30 to 60 mol%.
  • the electron-conducting material is incorporated as a structural unit in a polymer, and thus an electron-conducting polymer.
  • the electron-conducting polymer has at least one further structural unit selected from polymer backbone structural units as described above with respect to the polymers of the emitter layer.
  • the proportion of the at least one polymer backbone structural unit in the electron-conducting polymer is preferably in the range from 10 to 99 mol%, particularly preferably in the range from 20 to 80 mol%, and very particularly preferably in the range from 30 to 60 mol%.
  • Very particularly preferred structural units which form the polymer backbone in the electron-conducting polymer are selected from fluorene,
  • the electron-conducting polymer is a conjugated polymer.
  • Particularly preferred polymer backbone structural units of the conjugated polymer are selected from the above-mentioned structural units of the formulas (23) to (31).
  • the electron-conducting polymer is a non-conjugated or partially conjugated polymer.
  • Particularly preferred polymer backbone structural units of the unconjugated or partially conjugated polymer are selected from those mentioned above
  • the electron-conducting layer contains exclusively low-molecular-weight electron transport materials, as described above.
  • the electron-conducting layer contains a mixture of at least one low-molecular-weight electron-transport material and a polymer.
  • Particularly preferred polymer backbone structural units of this polymer are selected from fluorene, spirobifluorene, indenofluorene, phenanthrene and dihydrophenanthrene and their derivatives.
  • this too Polymer additionally having electron-conducting repeating units as described above.
  • Another object of the present application are to provide a third object of the present application.
  • Formulations containing the hole-conducting or predominantly hole-conducting polymer and at least one solvent are included in Formulations containing the hole-conducting or predominantly hole-conducting polymer and at least one solvent.
  • the electronic device according to the present invention may further include other layers which may be selected from, among others, hole injection layer, emitter layer, electron blocking layer, hole blocking layer, exciton generating layer and electron injection layer.
  • the at least one emitter layer of the device according to the invention is applied from solution.
  • Electron transport layer of the electroluminescent device according to the invention applied from solution.
  • a preferred embodiment of the electroluminescent device according to the invention has the structure described below, which is advantageous in particular for top emission displays:
  • a cathode typically metals, metal combinations or low work function metal alloys are used, such as Ca, Ba, Cs, Mg, Al, In or Mg / Ag,
  • EIL electron injection layer
  • ETL electron transport layer
  • EML emitter layer of the material described above
  • HIL hole injection layer
  • ITO indium tin oxide
  • an air-stable cathode is used in the electroluminescent device according to the invention.
  • Such air-stable cathodes may be TiO 2 as described by Haque et al., Adv. Mater. 2007, 19, 683-687 or from ZrO 2 as described by Bradley et al. in Adv. Mater. DOI: 10. 002 / adma.200802594, or from ZnO, as reported by Bolink et al. in Adv. Mater. 2009, 21, 79-82 is reported.
  • Another object of the present application are electroluminescent polymers, the hole-conducting or predominantly hole-conducting
  • the polymer with hole-conducting or predominantly hole-conducting properties has at least one hole-transporting property
  • Emitter layer of the electroluminescent device according to the invention described structural units can be selected.
  • the material according to the invention has
  • hole-conducting or predominantly hole-conducting properties additionally at least one polymer backbone structural unit, which can be selected from the above-described polymer backbone structural units.
  • polymer backbone structural units which comprise the
  • Forming polymer backbone selected from fluorene, spirobifluorene,
  • the hole-transporting structural units are selected from amines, triarylamines, thiophenes, carbazoles and the abovementioned structural units of the formulas (18) to (21).
  • the polymer according to the invention is a nonconjugated or partially conjugated polymer.
  • a particularly preferred, non-conjugated or partially conjugated polymer of the invention contains a non-conjugated one
  • Polymer backbone moiety The unconjugated polymer backbone moiety is included
  • non-conjugated polymer backbone structural units are selected from the above-described fluorene, phenanthrene, dihydrophenanthrene and indenofluorene derivatives of formulas (34a) to (37d).
  • Has properties is preferably in the range of 10 to 99 mol%, more preferably in the range of 20 to 80 mol%, and most preferably in the range of 30 to 60 mol%.
  • the proportion of hole-transporting structural units in the polymer according to the invention which has hole-conducting or predominantly hole-conducting properties is preferably in the range from 10 to 99 mol%, particularly preferably in the range from 20 to 80 mol%, and very particularly preferably in the range from 30 to 60 mol %.
  • Has properties is preferably in the range of 0.01 to 20 mol%, more preferably in the range of 0.5 to 10 mol%, and most preferably in the range of 1 to 5 mol%.
  • the present application also relates to a mixture comprising at least one polymer according to the invention having hole-conducting or predominantly hole-conducting properties, as described above.
  • the present application further provides a formulation containing at least one polymer according to the invention with hole-conducting or predominantly hole-conducting properties, as described above, and at least one solvent.
  • the formulation forms a homogeneous solution, that is, only one homogeneous phase exists.
  • the formulation forms an emulsion, that is, both a continuous phase and a
  • the at least one solvent is selected from the group of organic solvents.
  • the organic solvent is selected from dichloromethane, trichloromethane, monochlorobenzene, o-dichlorobenzene, tetrahydrofuran, anisole, morpholine, toluene, o-xylene, m-xylene, p-xylene, 1, 4-dioxane, acetone, methyl ethyl ketone, 1, 2-dichloroethane, 1, 1-trichloroethane, 1, 1, 2,2-tetrachloroethane, ethyl acetate, n-butyl acetate, dimethylformamide, dimethylacetamide, dimethyl sulfoxide, tetralin, decalin, indane and mixtures thereof.
  • the concentration of the polymer according to the invention in the formulation is preferably in the range from 0.001 to 50% by weight, more preferably in the range from 0.01 to 20% by weight, very particularly preferably in the range from 0.1 to 10% by weight, and in particular in the range of 0.1 to 5 wt.%.
  • the formulation may additionally contain at least one binder in order to adjust the Theological properties can, such. As described in WO 2005/055248 A1.
  • the present application also relates to the use of the polymer according to the invention having hole-conducting or predominantly hole-conducting properties, or a mixture containing the same polymer according to the invention with hole-conducting or predominantly
  • the subject matter of the present application is likewise an electronic device containing the polymer according to the invention with hole-conducting or predominantly hole-conducting properties.
  • the electronic device preferably has 2, 3, 4, 5 or 6
  • the electronic device has two electrodes, an anode and a cathode.
  • the electronic device according to the invention can be used to emit light, to collect light or to detect light.
  • the electronic device is selected from
  • organic light-emitting diodes OLED
  • PLED polymeric light-emitting diodes
  • electrochemical cells organic field effect transistors (OFET), thin film transistors (TFT), organic solar cells (O-SC), organic laser diodes (O-lasers), organic integrated circuits (O-IC), RFID (radio frequency identification) Labels, photodetectors, sensors, logic circuits, memory elements, capacitors,
  • Charge injection layers Schottky diodes, planarization layers, antistatic films, conductive substrates or patterns, photoconductors, electrophotographic elements, organic light emitting transistors (OLET), spintronic organic devices, and
  • An electrophotographic element comprises a substrate, an electrode, and a charge transport layer over the electrode and optionally a charge generation layer between the electrode and the
  • Such a device preferably contains a nano-diamontide or a polymer according to the invention with hole-conducting or predominantly hole-conducting properties, particularly preferably in the charge transport layer.
  • a preferred organic Spintronic device is a so-called “spin valve” device as described by Z.H. Xiong et al., Described in Nature 2004 Vol. 427, 821, which contains two ferromagnetic electrodes and at least one organic layer between the two ferromagnetic electrodes, wherein at least one of the organic layers
  • OLEDs organic light-emitting electrochemical cells
  • OLEDs contain two electrodes, as well as a mixture or blend of an electrolyte and a fluorescent species, as first described by Pei & Heeger in Science 1995, 269, 1086-1088.
  • nano-diamontoides or polymers according to the invention with hole-conducting or predominantly hole-conducting properties in such
  • Dye solar cells also called “dye-sensitized solar cells (DSSCs)"
  • DSSCs contain a working electrode, a thin nanoporous layer of titanium dioxide (TiO 2 ), a thin layer of a photosensitive dye, the
  • the liquid electrolyte can be replaced by a solid hole transport layer, e.g. in Nature 1998, 395, 583-585.
  • the electronic device according to the invention is particularly preferably an organic light-emitting diode (OLED).
  • OLEDs have the following typical layer structure:
  • HIL hole injection layer
  • HTL hole transport layer
  • Electron blocking layer (EBL)
  • ETL electron transport layer
  • HBL hole blocking layer
  • EIL electron injection layer
  • excitons are generated in the active layer by electrical excitation, in which a voltage is applied between the anode and the cathode, which emit light by radiation decay. This is a light-emitting device.
  • excitons are generated in the active layer by light absorption, and free charge transport is produced by dissociation of the excitons. It is a photovoltaic cell or a solar cell.
  • Example 1 Polymer 1 is a copolymer which has substantially hole transport properties and has the following composition:
  • Polymer 2 is a copolymer which has essentially electron transport properties and has the following composition:
  • OLED 1 is a single-layer device in which polymer 1 is used as an emitter in the emitter layer. OLED 1 is manufactured as follows:
  • OLED 2 is a two-layer device in which polymer 1 is used as emitter in the emitter layer and polymer 2 as electron transport material in the electron transport layer. OLED 2 is made as follows:
  • OLED 3 is a monolayer device in which polymer 2 is used as an emitter in the emitter layer.
  • the manufacturing steps for producing OLED 3 are the same as for the production of OLED 1, except that in step 2, polymer 2 is used instead of polymer 1.
  • the produced OLED devices OLED 1 and OLED 3 have the construction shown in FIG. 2, and the OLED device OLED 2 according to the invention has the structure shown in FIG.
  • FIG. 3 shows the EL spectra of the three OLEDs 1 to 3. As FIG. 3 shows, the spectra of OLED 1 and OLED 2 are virtually identical, which proves that the emission in both OLEDs originates from predominantly hole-conducting polymer P1.
  • the properties of the three prepared OLEDs are summarized in Table 1. As Table 1 shows, the use of predominantly Hole conductive polymer 1 in the emitter layer and the predominantly electron-conducting polymer 2 in the electron transport layer to a significant improvement of all measured properties, compared with the monolayer devices of the OLEDs 1 and 3. The essential properties of the three OLEDs are also shown in Figures 4-7.
  • the "hole current" in the OLED 1 is very high, that is, the holes reach the cathode without first recombining with the electrons, therefore, the efficiency of this OLED is very low, and hence a determination of Lifespan not possible.

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  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Electroluminescent Light Sources (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
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Abstract

La présente invention concerne un dispositif électroluminescent contenant : a) une anode, b) une cathode, c) au moins une couche émettrice qui contient au moins une matière électroluminescente et qui est disposée entre l'anode et la cathode, et d) au moins une couche de transport d'électrons qui contient au moins une matière présentant des propriétés de conduction d'électrons ou essentiellement de conduction électrons et qui est disposée entre l'au moins une couche émettrice et la cathode. L'invention est caractérisée en ce que l'au moins une couche émettrice contient un polymère présentant des propriétés de conduction de trous ou essentiellement de conduction de trous. Le dispositif électroluminescent de l'invention est caractérisé par une longue durée de vie et un rendement de rayonnement élevé.
EP14735855.0A 2013-07-29 2014-07-01 Dispositif électroluminescent Ceased EP3028319A1 (fr)

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CN105409021A (zh) 2016-03-16
JP2016534551A (ja) 2016-11-04
KR20160038015A (ko) 2016-04-06
US20160181537A1 (en) 2016-06-23
JP6567519B2 (ja) 2019-08-28
WO2015014429A1 (fr) 2015-02-05
KR102206694B1 (ko) 2021-01-22
CN105409021B (zh) 2018-07-13

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