WO2015091783A1

WO2015091783A1 - Method for producing a nanowire top electrode for optoelectronic components and use thereof

Info

Publication number: WO2015091783A1
Application number: PCT/EP2014/078443
Authority: WO
Inventors: Lars MÜLLER-MESKAMP; Franz SELZER; Jan Ludwig BORMANN; Nelli WEISS; Christoph SACHSE; Nikolai Gaponik; Alexander EYCHMÜLLER; David KNEPPE
Original assignee: Technische Universität Dresden
Priority date: 2013-12-20
Filing date: 2014-12-18
Publication date: 2015-06-25
Also published as: DE102013226998A1; DE102013226998B4

Abstract

The invention relates to a method for producing a nanowire top electrode for optoelectronic components and to the use thereof. The problem of the invention is that the precipitation of nanowires from a solvent on solvent-sensitive layers of the optoelectronic component cannot be achieved or can only be achieved to a limited extent. The invention therefore provides a method for producing a transparent, electrically conductive layer, an inert nanowire dispersion in fluorine phase for precipitating a percolative nanowire network in such a method as well as a nanowire top electrode for optoelectronic components, in particular for components made of solvent-sensitive small molecules and polymers, and an optoelectronic component having a nanowire top electrode precipitated out of fluorine phase.

Description

Method for producing a nanowire cover electrode for optoelectronic components and their use

The invention relates to a method for producing a transparent, electrically conductive layer, an inert nanowire dispersion in fluorous phase for depositing a percolatable nanowire network in such a method, a nanowire cover electrode for optoelectronic devices, in particular for devices made of solvent-sensitive small molecules and polymers, and a An optoelectronic component comprising a nanofire cover electrode deposited from a fluorous phase.

State of the art

Mechanically flexible optoelectronic components, such as organic light emitting diodes (OLEDs) and organic solar cells (OSCs), are based on organic semiconductors from organic polymers (PLED - polymer light emitting diode) or small molecules or oligomers (SMOLED - small molecule organic light emitting diode) can be realized. In particular, molecules which can be deposited in vacuo by thermal evaporation or molecules of similar molecular weight for solvent processing are referred to as small molecules. Usually, so-called small molecules have a molecular weight of less than 1000 g / mol, e.g. Fullerenes or pthalocyanines.

While semiconductor layers of organic polymers can be produced in simple screen-printing and wet-deposition methods, semiconductor layers of small molecules generally require deposition from the gas phase. The semiconducting organic layers are produced solvent-free and are very sensitive to molecules deposited from solution due to lack of protective groups. A solvent-resistant configuration of the small molecules and polymers would reduce the effectiveness of the semiconductor layers produced.

In order to produce flexible electronics that can be used, it is necessary to contact the semiconducting organic layers from the outside. Thin-film electrodes used for this purpose must ensure high flexibility and electrical conductivity. In addition, a transparency of the electrodes is desirable. Depending on the arrangement of an electrode, a distinction is made between ground contacts and cover contacts. The substrate-near electrode is referred to as a ground contact. Conventional thin-film electrodes have hitherto been made, for example, by vapor deposition of thin metal layers (Schubert et al., Advanced Energy Materials 2013, 3 (4), 438-443) or sputtering of metal or metal oxide layers, for example of indium tin oxide (ITO) or aluminum-doped zinc oxide (AZO) or in stamp transfer processes from thin layers of free-standing carbon nanotubes (Kim et al., Solar Energy Materials and Solar Cells 2012, 96, 244-250).

The deposition or sputtering of the metallic layers takes place under high temperatures, vacuum and at low speeds, and is thus time-consuming and energy-intensive. Thereafter, thermal annealing ("armealing") of the layer is usually necessary, which means that the processes are only suitable to a limited extent for roll-to-roll mass production and coating on sensitive organic semiconductor layers, and thin metal oxide layers are limited in their ability to bend robust and networks of carbon nanotubes comparatively poorly conductive (Lee et al., Nano Lett. 2008, 8 (2), 689-692).

Another possibility for realizing flexible, transparent thin-film electrodes with high electrical conductivity are percolative networks of metallic nanowires. Such networks can also be applied in stamp transfer processes or by depositing the nanowires from solution onto optoelectronic components.

In transfer processes, nanowires deposited on a glass substrate are laminated on the layer sequence of an organic solar cell in a solution-based manner (Lee et al., Nano Lett. 2010, 10 (4), 1276-1279; Hardin et al., Organic Electronics 201 1, 12, 875-879). In this case, mechanical stresses occur which cause damage to the vacuum-processed organic layers. Scaling to industrial scales is also problematic. Furthermore, contacting problems may occur at the interface between the nanowire top contact and the corresponding component.

The solvent-based deposition of nanowire networks under semiconducting organic layers presents a multitude of problems. Due to the high roughness of the ground contact deposited networks, conductive or semiconductive organic layers deposited thereon may be shorted. This problem is more pronounced in optoelectronic devices produced by vacuum evaporation of small molecules (Lee et al., Nano Lett. 2008, 8 (2), 689-692). In the deposition of nanowires as a cover contact there is a risk of damage to the underlying solvent-sensitive organic layers by the solvent used.

For polymer solar cells, Krantz et al. and Reinhard et al. Recently, a method for producing a silver nanowire top contact by spray coating (Krantz et al., Advanced Functional Materials 2013, 23 (13), 171 1 -1717) or drip coating (Reinhard et al., Organic Electronics 2013, 14 (3), 273 -277). To protect the polymer layers, a functional layer, in this case PEDOT: PSS (Krantz et al.) Or V ₂ 0 ₅ (Reinhard et al.), Can be applied. Depending on the stack construction, however, such protective layers can have a disadvantageous effect on the electrical properties of the component, or shield the disadvantageous effect of nanowire processing only incompletely.

Energetic barrier-free transitions at the interfaces of SMOLEDs by molecular doping problem (Walzer et al., Chemical Reviews 2007 ^', 107 (49) 1233- 1271). However, the use of common solvents in SMOLEDs is always associated with damage to the layers of vacuum-processed small molecules. This results in losses in the efficiency or complete destruction of the optoelectronic components. The same problems also apply to organic solar cells with active layers of small molecules (SM OPV) or solvent-sensitive layers of polymers.

In known processes for depositing nanowire base contacts on substrates, nanowires suspended in aqueous, polar or organic solvents have hitherto been used (Hu et al., ACS nano 2010, 4 (5), 2955-2963, WO 20061 13207 A2 "Nano - Wire dispersion compositions and uses thereof, "US 2008 / 0283799A1" Nanowire-based transparent conductors "). The nanowire network, after drying the solvent i.d.R. a low conductivity, which is improved by subsequent annealing at high temperatures (Sachse et al., Organic Electronics 2013, 14 (1), 143-148.) In the case of a cover contact of nanowires, the sensitive ones can be used Organic layers of the underlying component are damaged by the heating and the efficiency of the device can be reduced.

The aim of the invention is the realization of a metallic nanowire top contact for optoelectronic devices made of solvent-sensitive small molecules or polymers. For this purpose, a method for producing a transparent, electrically conductive layer by deposition from a nanowire suspension is proposed, in which a Damage to sensitive organic layers is avoided. In addition, a liquid-based nanowire electrode with high transparency and electrical conductivity as well as an optoelectronic component with such a nanowire electrode should be proposed.

The object according to the invention is achieved by a method for producing an electrically conductive layer, comprising the following method steps:

a) wetting of an organic layer of an optoelectronic component with a homogeneous nanowire suspension in fluorous phase, containing

i) an orthogonal, fluorinated solvent and

ii) surface-modified nanowires with an organic stabilizer, wherein the nanowires consist of electrically conductive or semiconducting material, b) percolation of the nanowires on the organic layer by evaporation of the solvent.

In the process according to the invention, a homogeneous nanowire suspension made from a fluorinated orthogonal solvent and surface-modified nanowires with a fluorinated organic stabilizer is used as starting material. The nanowires have an elongated shape and consist of electrically conductive or semiconducting materials, such as, for example, metal, metal alloys, semiconductors or carbon.

An organic layer is understood as meaning a layer comprising at least one organic semiconductive material. The organic layer may be formed, for example, as a mixed layer of organic materials, wherein the organic materials form, for example, a donor-acceptor system. In addition, the organic layer may also be formed as a charge carrier transport layer. The organic layer may also be doped, partially doped or undoped. As organic semiconductive materials, for example, organic polymers or small molecules can be used.

"Orthogonal" refers to the property of the fluorinated solvent not to mix with polar protic, polar aprotic or apolar organic or hydroxylic compounds, but only with highly fluorinated or perfluorinated organic compounds or act as a solvent for these.

For the purposes of the present invention, a nanowire is understood to mean a wire with a diameter of 20-200 nm, and an aspect ratio = length / diameter of at least 100. Hochfluoriert is an organic compound (ie, substances which primarily consist of carbon and hydrogen) in the context of this application when at least 40%, preferably at least 60%, more preferably at least 80% of the hydrogen atoms contained in the organic compound substituted by fluorine atoms and / or at least 40%, preferably at least 60%, more preferably at least 80% of the halogen atoms contained are fluorine. For organic compounds containing fluoride atoms and other hydrogen atoms, both conditions must be met. The fluorine content can be determined in a conventional manner by elemental analysis, preferably by atomic spectroscopy, particularly preferably by atomic absorption spectrometry, atomic emission spectrometry, atomic fluorescence spectroscopy, mass spectrometry or nuclear magnetic resonance spectroscopy.

Suspension of the nanowires in fluorinated solvents requires their surface modification with a fluorinated stabilizer. In one embodiment, the fluorinated stabilizer has at least one functional group bonding to the surface of the nanowires and a fluorinated alkyl or aryl group. The bonding functional group effects the spontaneous, preferably coordinative, binding of the stabilizer to the nanowires and the fluorination of the alkyl or aryl group the solubility of the surface-modified nanowires in the fluorinated solvent.

For the purposes of the present invention, the surface of the nanowire is understood to be the topmost layer of the nanowire which interacts with the stabilizer and is modified. Depending on the configuration of the nanowire, the surface may be formed, for example, metallically or by a polymer layer, such as PVP or another stabilizer layer. In the case of polymer layers, modification of the surface according to the invention, in particular in the case of monomeric stabilizers, involves ligand exchange, the polymer molecules being replaced by the stabilizer, which with its functional group adheres to the metal surface of the nanowire. The modification of wires with stabilizer surfaces does not necessarily require a ligand exchange, the coordinate binding of the polymeric stabilizers advantageously also takes place on the stabilizer layer (eg PVP) by non-covalent interactions (eg, Keesom interaction) or spatial entanglement (eg London dispersion interaction ) or other Van der Waals interactions. In one embodiment of the invention, the stabilizer has at least one functional group which binds to the surface of the nanowires and is at least partially or perfluorinated.

In an alternative embodiment, the stabilizer is formed as a fluorinated aliphatic or aromatic polymer. The polymer preferably has coordinating functional groups which bind to the nanowire surface.

Polymeric stabilizers bind to the wires or their stabilizer layer via coordinative bonds, such as hydrogen bonds, van der Waals forces, and spatial entanglement. In addition to electrostatic stabilization by shielding the (polar) nanowire surface, polymer stabilizers cause steric stabilization of the nanowires by preventing their agglomeration by steric repulsion.

In an alternative embodiment, the surface of the nanowires is not directly modified, but the organic shell of the nanowires is modified as previously discussed. The organic shell consists of the usual stabilizer molecules, which allow a stable dispersion of the nanowires in conventional polar protic, polar aprotic or apolar organic or hydroxylic solvents. This shell is altered by incorporation of the fluorinated stabilizer, which mixes with or binds to the shell, thereby enabling solubility of the surface-modified nanowires in the fluorinated solvent.

The nanowires are preferably made of metal, in particular of gold, silver, nickel, copper, palladium, iridium, cobalt, chromium, aluminum, iron, titanium, ruthenium, platinum, tin, zinc, tungsten, molybdenum or metal alloys, conductive polymers, carbon and / or combinations thereof. More preferably, silver nanowires are used.

The nanowires are produced, for example, by template-based synthesis, for example in channels of nanotubes or nano- to microporous materials, by attachment to DNA chains or on the surfaces of solid substrates, or by reduction of metallic salts in solution.

Nanowires are preferably synthesized by reduction of silver nitrate in the presence of polyvinylpyrrolidone (PVP) in ethylene glycol, the latter simultaneously acting as solvent and reducing agent in the polyol process (Lee et al., Nano Lett. 2008, 8 (2), 689-692). The PVP macromolecules adsorb to the surface of the resulting silver nanoparticles. As a stabilizer of the nanowires, they are responsible for their directed growth in an elongated form, via Ostwald ripening and adsorption and desorption to various interfaces (Sun et al, Nano Lett. 2002, 2 (2), 165-168).

Immediately after the synthesis, nanowires synthesized in the polyol process have a PVP layer a few nanometers thick (about 1 -2 nm) on their surface. For the modification of the surface according to the invention, in particular in the case of monomeric stabilizers, a ligand exchange takes place, the PVP molecules being replaced by the functional group of the stabilizer. The modification of the wires with polymeric stabilizers does not necessarily require a ligand exchange, the coordinate binding of the polymeric stabilizers is advantageously also on the PVP layer by non-covalent interactions (eg, Keesom interaction) or spatial entanglement (eg London dispersion interaction).

To modify the nanowires, the stabilizer is preferably added to a standard solution of unmodified nanowires and mixed intensively with this. Shakers, magnetic stirrers or ultrasonic mixers are preferably used for this purpose. Subsequently, the separation of the nanowires, eg. By centrifugation, and optionally a washing step with fluorinated solvent. The successful modification of the nanowires is verifiable via fluorogen detection, for example by XPS (X-ray photoelectron spectroscopy, FIB-SIMS (Focused Ion Beam Secondary Ion Mass Spectrometry), SNMS (Secondary Neutral Particle Mass Spectrometry), RBS or LEIS (low energy ion scattering spectroscopy, low energy ion scattering spectroscopy).

Surface-modified nanowires are then suspended in fluorinated solvent to produce a nanowire suspension in a fluorous phase. Shakers, magnetic stirrers or ultrasonic mixers are preferably used for their homogenization. This treatment is preferably repeated just prior to use of the nanowire suspension to avoid sedimentation of the nanowires. Due to the orthogonality of the fluorinated solvent used, the organic layers, in particular the organic layers of vacuum-processed small molecules and polymers, are inert to the nanowire suspension (Zhadikov et al., Organic Electronics 2012, 13 (3), 356-360).

As the next step for producing a transparent and electrically conductive layer, the wetting of the organic layer of the optoelectronic component with the suspension takes place in a thin-film deposition method. Depending on the nature of the method, a correspondingly diluted suspension is applied once or several times to the substrate surface applied, wherein between the individual wetting the fluorinated solvent is evaporated.

As the solvent evaporates, the nanowires are stochastically placed on the surface of the organic layer. Due to the elongated shape of the wires, even at low surface coverage, their percolation and the formation of a nanowire network as a preferably transparent and electrically conductive layer occur. The electrical conductivity of the nanowire network depends on the conductivity of the individual nanowires, the number of nanowires deposited overall, as well as the number of nanowire intersections and the resistance at the points of contact.

The surface coverage of the organic layer, from which at least one continuous conduction path is formed, is also referred to as the "percolation threshold." With increasing continuous paths of crosslinked nanowires, the electrical resistance of the layer decreases Transmission, so that the optical and electrical characteristics of the nanowire network can be adjusted by the type and number of wetting steps.

The organic layer is preferably a solvent-sensitive layer, more preferably a layer of vacuum-processed small molecules or a multilayer structure of organic layers. These are not attacked by the fluorinated solvent of the nanowire suspension, so the deposition of the nanowire network is not associated with damage to the underlying layer or adverse surface effects.

Further advantageously, the layers deposited in the method according to the invention have instantaneously sufficient conductivity. Thermal annealing of the nano-wire networks is unnecessary, which protects underlying layers.

The fluorine chemistry used for the first time for the preparation of nanowire suspensions leads to advantageous properties of the layers produced in the process according to the invention. Due to the entanglement of the alkyl or aryl groups of the stabilizers used or the crosslinking of the polymeric stabilizers used, the deposited layers advantageously have an increased abrasion resistance and an increased resistance to delamination. For comparable effects, a subsequent coating of the nanowire electrodes with a 20 nm thick Teflon film was hitherto necessary (Hu et al., ACS nano 2010, 4 (5), 2955-2963). Furthermore, the surface modification with fluorinated group causes Advantageously, a reduction of the surface energy of the electrically conductive layer, whereby this hydrocarbon oils, silicones and aqueous solutions rejects (Barriet et al., Current Opinion in Colloid and Interface Science 2003, 8, 236-242) and thus an anticorrosive equipment on the constituting constituent nanowires.

The remaining on the nanowires fluorinated stabilizers can be advantageously detected by a fluorine analysis, for example. By FIB-SIMS, SNMS, RBS or LEIS.

In one embodiment, in the process chlorofluorocarbons (CFCs): C _x Cl _y F ₂ , chlorofluorocarbons (HCFCs): C _x C _y F _z H _w , hydrofluorocarbons (HFCs): C _x FyH _z , perfluorinated fluorocarbons (FCs): C _x F _y , hydrofluoroethers (HFEs): C _x H _y OC _z F _w , perfluoroethers: C _x F _y OC ₂ F _w , perfluoroamines: (C _x F _y ) ₃ N, trifluoromethyl (CF ₃ ) -substituted aromatic solvents, etc. used as orthogonal fluorinated solvent. The indices assume only positive integer and stoichiometrically permissible values.

At least 40%, preferably 60% and particularly preferably 80% of the hydrogen atoms contained in the compound are substituted by fluorine atoms and / or at least 40% are preferred in all of these fluoroorganic solvents, which are originally composed primarily of carbon, hydrogen and optionally oxygen at least 60%, more preferably at least 80% of the halogen atoms contained fluorine.

In a further embodiment of the invention, linear or branched fluorinated alkyl ethers of the general formula (CF ₃ ) ₀ (CF ₂ ) n (CF) _m -OR, R = - (CH ₂ ) i CH ₃ , where i, m, n and o independently assume an integer value between 1 and 4, and / or their mixtures used as a fluorinated solvent. These hydrofluoroethers (HFE) are particularly environmentally friendly, non-flammable and near-non-toxic solvents that are commercially available in various forms. In addition, the compatibility of hydrofluoroethers with organic thin films by Zakidov et al. by operating therein an unencapsulated organic light-emitting diode without changing its performance parameters (Zakhidov et al., Organic Electronics 2012, 13 (3), 356-360). In one embodiment of the embodiment, the ratio of indices n: i is at least 2: 3, more preferably 3: 2 or 4: 1.

Particularly preferred fluorinated alkyl ethers (HFEs) are methyl nonafluorobutyl ethers, methyl nonafluoroisobutyl ethers, isomeric mixtures of methyl nonafluorobutyl ether and methyl nonafluoroisobutyl ether, ethyl nonafluorobutyl ether, ethyl nonafluoroisobutyl ether, isomeric See mixtures of ethyl nonafluorobutyl ether and ethyl nonafluoroisobutyl ether, 3-ethoxy-l, 1, 1, 2,3,4,4,5, 5, 6,6,6-dodecafluoro-2-trifluoromethyl-hexane, 1, 1, 1, 2 , 2,3,4,5,5,5-decafluoro-3-methoxy-4-trifluoromethyl-pentane, 1,1,1,3,3,3-hexafluoro-4- (1,1,2,3, 3,3, hexafluoropropoxy) pentanes and mixtures thereof. Further examples can be found in WO2009 / 143357A2.

In a further embodiment of the invention, the functional groups of the non-polymeric stabilizer are preferably thiol groups (-SH), amino groups (-NH ₂ , = NH), hydroxyl groups (-OH) or carboxy groups (-COOH). The functional group advantageously binds to the metal surface of the nanowire, wherein the functional group of partially or perhalogenated fluorohydrocarbon acts as an agent for the fluorinated solvent. The functional groups have a strong binding affinity for nanoparticles with polar metal surfaces, in particular for Au, Ag and Cu surfaces. The non-polymeric stabilizer thus has a general form R-SH, R-NH ₂ ,

R-COOH with Ri, R ₂ = Rf as a highly fluorinated or perfluorinated alkyl or aryl radical. In one embodiment of the embodiment, the highly fluorinated or perfluorinated alkyl or aryl radical has 8 to 10 carbon atoms. As a partially halogenated or perhalogenated fluorohydrocarbon, preference is given to 1H, 1H, 2H, 2H-perfluorodecanethiol, 2-trifluoromethylbenzyl mercaptan, 1H, 1H, 2H, 2H-perfluorooxethane ethiol, 3,3,4,4,4-pentafluoro-1 Butanediol, 2,2,3,3,3-pentafluoropropionic acid, perfluorobutanesulfonic acid, perfluorooctanoic acid, perfluorooctane sulfonate or mixtures thereof.

In a further embodiment of the invention, the non-polymeric stabilizer additionally has a spacer group located between the top and end groups. The stabilizer is highly fluorinated or perfluorinated. Thus, in the stabilizer at least 40%, preferably 60% and more preferably 80% of the hydrogen atoms contained in the compound substituted by fluorine atoms and / or at least 40%, preferably at least 60%, more preferably at least 80% of the halogen atoms contained fluorine.

Stabilizers form highly organized dense layers on the wire surface. These advantageously enable a particularly agglomeration-free suspension of the nanowires and protect them from disintegration effects occurring in solvents (Lee et al., Small 2013, 1-8). Adverse effects of the stabilizer layer on the conductivity of the nano-wire network can be reduced by annealing. The fluorinated solvent preferably has a low vapor pressure and a boiling point in the range of 60 to 160 ° C. From the suitable combination of stabilizer and solvent, advantageously lower heating temperatures can be achieved compared to previously used methods. ger 160 ° C, preferably less 60 ° C, more preferably less than 30 ° C can be achieved. The non-polymeric stabilizer has up to 25 C atoms, preferably up to 20 C atoms in the carbon skeleton and a molar mass between 20 -4000 g / mol.

In a further embodiment of the invention, the polymeric stabilizer is a partially or perfluorinated organic polymer selected from the group comprising polymethacrylate, polymethyl methacrylate, polyvinylpyrrolidone, polyvinyl alcohol, polyethylene glycol, polystyrene sulfonate or their heteropolymers, and amorphous fluoropolymers based on tetrafluoroethylene (US Pat. TFE) which are soluble in orthogonal solvents such as CYTOP (http://www.agcce.com/Cytop.asp), Hyflon (http://www.solvayplastics.com/sites/solvayplastics/EN/specialty_polymers/FullyFluorinatedP olymers / Pages / Hyflon_AD.aspx), Dyneon ™ Perfluoroelastomer, DuPont Kalrez ™ or DuPont Teflon ™ AF. Further examples can be found in US7323514 and US6734227. The polymeric stabilizer has a molar mass between 5000 and 100,000 g / mol.

In one embodiment of the invention, polymethacrylates and polymethyl methacrylates are used as stabilizers prepared from the following fluorinated monomers: 1H, 1H, 7H-dodecafluoroheptyl methacrylate, 1,1,1,3,3,3-hexafluoroisopropyl- acrylate, 1,1,1,3,3,3-hexafluoroisopropyl methacrylate, 2,2,2-trifluoroethyl acrylate, 2,2,2-trifluoroethyl methacrylate, 1H, 1H, 2H, 2H-heptadecafluorodecyl- acrylate, 1 Η, Ι H, 2H, 2H-heptadecafluorodecyl acrylate, 1H, 1H, 2H, 2H-heptadecafluorodecyl methacrylate, 1H, 1H-heptafluorobutyl acrylate, 1H, 1H, 3H-hexafluorobutyl- acrylate, bis (1,1,3,3,3,3-hexafluoroisopropyl) itaconate, bis (2,2,2-trifluoroethyl) itaconate, hexafluoroisopropyl methacrylate, 1H, 1H, 5H- Octafluoropentyl acrylate, 1H, 1H, 5H-octafluoropentyl methacrylate, pentafluorophenyl acrylate, pentafluorophenyl methacrylate, 1H, 1H, 3H-tetrafluoropropyl methacrylate, 2,2,2-trifluoroethyl acrylate, 2,2, 2-trifluoroethyl methacrylates

The fluorinated polymethacrylates bind predominantly coordinatively, so that the stabilization takes place by spatial entanglement of the wires. This interaction binds the electrons involved weaker compared to the covalent bond, for example. For fluorinated thiols and therefore causes lower electrical resistance at wire crossings. By using fluorinated polymers, in particular of EGC2702, highly conductive transparent electrodes can thus be realized immediately after deposition. Even though the polymeric stabilizers additionally have head groups which covalently bind to the wire surface, the number of binding sites is small in comparison with the polymer size or the occupied wire surface. In a further embodiment of the invention, the wetting of the substrate with the nanowire suspension takes place by a thin-layer application method selected from spray coating (Lee et al., Small 2013, 1-8), dip coating, spin coating, Mayer rod coating (Hu et al. , ACS nano 2010, 4 (5), 2955-2963) or Slot Die Coating or via a printing process such as inkjet, offset, gravure printing.

The wetting is preferably carried out by spray coating a nanowire suspension onto a substrate which has preferably been cleaned in an oxygen plasma. The wetting is repeated until the desired transmission is achieved. Advantageously, the availability of commercial spray robots makes this application process easily scalable to industry roll-to-roll standards. Spray wetting also has the advantage that the nanowires are thrown onto the substrate with high kinetic energy. As a result, the wires are bent at intersections and partially fused together, thus reducing crossover resistances (Lee et al., Small 2013, 1-8).

In a further embodiment of the invention nanowire suspensions are used with a nanowire concentration of 0.01 to 3 m%, and preferably from 0.15 to 0.3 m%. The strong dilution improves the sprayability of the suspension. For wetting with spray coating, the nanowires have, for example, a diameter between 30 and 100 nm and a length between 10 and 30 μm.

In one embodiment of the embodiment, the suspension contains additional metallic nanoparticles as optical scattering centers.

In a further embodiment of the invention, the wetting of the organic layer takes place at temperatures below 160 ° C., preferably below 60 ° C., more preferably below 30 ° C. at ambient pressure and under air or inert gas atmosphere. By dispensing with vacuum technology, the method is advantageously scalable on an industrial scale. Due to the comparatively low temperatures, sensitive substrates, in particular organic layers, are spared. Particularly preferably, the wetting takes place under an inert gas atmosphere, for example under a nitrogen atmosphere, in order to protect the organic layers which are sensitive to oxygen and water exposure.

In a further embodiment of the invention, after the wetting and percolation of the nanowires, the formed network is repeatedly washed with a fluorinated solvent. By removing the surface coating from fluorinated organic Stabilizer, the sheet resistance of the nanowire network is advantageously reduced (Lee et al., Small 2013, 1-8), wherein damage to the underlying organic layers due to the orthogonality of the fluorinated solvent is avoided. The washing thus represents an alternative to thermal annealing in known processes. Disadvantageously, the washing effects a reduction in the advantageous properties of the nanoproducts coated with fluorine, in particular their abrasion and delamination strength and the hydrophobicity of the network.

In an alternative embodiment of the embodiment, the washing of the nanowires takes place after the separation and before the deposition on the organic layer.

An optimization of the conductivity of the nanowire network takes place alternatively or additionally by mechanical pressing of the nanowires onto the organic layer. For this purpose, for example, a glass plate with a defined pressure, preferably of up to 100 GPa, is pressed onto the percolative nanowire network. In addition to a reduction of the sheet resistance by a factor of ten, an improvement of the surface morphology, in particular a reduction of the roughness, is thereby achieved (Hu et al., ACS nano 2010, 4 (5), 2955-2963). It is also conceivable to ensure mechanical pressing by means of rollers. This is particularly advantageous in the context of a roll-to-roll processing.

In one embodiment of the invention, the organic layer is formed as one or more thin layers of vacuum-processed small molecules or organic polymers. A variety of vacuum-processed small molecule and polymer based optoeletronic devices are known in the art (Walzer et al., Chemical Review 2007, 107 (4), 1233-1271, Peumans et al., J. Appl. Phys , 93 (7), 3693-3722).

In a further embodiment of the invention, before the nanowires are deposited, a cover contact mask is introduced over the organic layer, which covers a part of the surface. By masking these areas on the organic layer, the nano-wire electrode can be deposited in a structured manner. In this case, the electrode is deposited only in the desired areas, namely the unmasked areas. This is particularly advantageous if a structured nanowire electrode is to be deposited.

In a further embodiment of the invention, structuring of the nanowire cover electrode deposited on the organic layer takes place by means of laser structuring. In a further embodiment of the invention, the structuring of the nanowire cover electrode is effected by photolithography. In a further embodiment of the invention, structuring takes place by deposition of a structured passivation layer between the organic layer and the nanowire cover electrode. The passivation layer is characterized in that it is not electrically conductive. The electrode can then be deposited over the entire area or in a structured manner, but only contacts the component in the areas which have been cleared by the passivation layer.

In a further embodiment of the invention, a directed deposition of the nanowires on the organic layer takes place. The directional deposition causes an orientation of the nanowires on the surface. As a result, for example, the nanowires can be aligned in parallel. However, it is also possible to generate gradients. In one embodiment of the embodiment, the directional deposition of the (magnetic) nanowires takes place by the action of an external magnetic field. The magnetic field aligns the nanowires with their polarization.

In a further embodiment of the embodiment, the directional deposition of the nanowires takes place by immersing in and pulling out the component from the nanowire suspension.

In a further embodiment of the embodiment, the directed deposition takes place by a microfluidic system. Microfluidic systems have small channel widths which allow a laminar flow. With the appropriate design of the microfluidic system, targeted areas of the organic layer to be coated can be controlled and coated.

Likewise provided by the invention is a nanowire suspension in fluorous phase for depositing a percolative nanowire network on an organic layer of an optoelectronic component, comprising:

a) a fluorinated solvent and

b) with a stabilizer surface-modified nanowires, wherein

the nanowires consist of electrically conductive or semiconducting material.

The nanowire suspension according to the invention advantageously makes it possible to prevent the deposition of a percolative nanowire network on organic layers of an optoelectronic component without damaging it. Thus, nanowire networks can be deposited on organic layers without adversely affecting their functionality, for example, in light absorption or emission. In addition, the fluorinated organic stabilizer improves the properties of the deposited nanowire network, in particular by increasing its abrasion and delamination resistance and hydrophobicity.

In one embodiment of the invention, the orthogonally fluorinated solvent is chlorofluorocarbons (CFCs): CxClyF ₂ , chlorofluorocarbons (HCFCs): C _x ClyF _z H _w , hydrofluorocarbons (HFCs): C _x F _y H _z , perfluorinated fluorohydrocarbons ( FCs): C _x F _y , hydrofluoroethers (HFEs): CxH _y OC _z F _w , perfluoroethers: C _x F _y OC ₂ F _w , perfluoroamines: (C _x F _y ) ₃ N, trifluoromethyl (CF ₃ ) -substituted aromatic Solvents and / or mixtures thereof. The indices assume only positive integer and stoichiometrically permissible values.

In one embodiment of the invention, wherein the fluorinated solvent is linear or branched fluorinated alkyl ether of the general formula (CF ₃₎ ₀ (CF ₂₎ _n (CF) _m -OR, R = - (CH ₂₎ I _3, where i , m, n and o independently assume an integer value between 1 and 4, and / or mixtures thereof. In one embodiment of the embodiment, the ratio of indices n: i is at least 2: 3, more preferably 3: 2 or 4: 1. The fluorinated alkyl ethers (HFEs) are preferably methylnonafluorobutyl ether, methyl nonafluoroisobutyl ether, isomeric mixtures of methyl nonafluorobutyl ether and methyl nonafluoroisobutyl ether, ethyl nonafluorobutyl ether, ethyl nonafluoroisobutyl ether, isomeric mixtures of ethyl nonafluorobutyl ether and ethyl nonafluoroisobutyl ether, 3-ethoxy-1, 1, 2,3,4,4,5,5,6,6,6-dodecafluoro-2-trifluoromethyl-hexane, 1,1,1,2,3,4,5,5,5-decafluoro- 3-methoxy-4-trifluoromethyl-pentanes, 1,1,1,3,3,3-hexafluoro-4- (1,1,3,3,3,3-hexafluoropropoxy) -pentanes and / or mixtures thereof. Further examples can be found in WO2009 / 143357A2.

In one embodiment of the invention, at least 40%, preferably 60% and particularly preferably 80% of the hydrogen atoms contained in the compound are substituted by fluorine atoms in all these fluoroorganic solvents and / or at least 40%, preferably at least 60%, particularly preferably at least 80 % of the halogen atoms contained fluorine.

In a further embodiment of the invention, the stabilizer has at least one group bound to the surface of the nanowires and a fluorinated alkyl or aryl group. The bonding functional group effects the spontaneous, preferably coordinative, binding of the stabilizer to the nanowires and the fluorination of the alkyl or aryl group the solubility of the surface-modified nanowires in the fluorinated solvent. In another embodiment, the stabilizer is formed as a fluorinated aliphatic or aromatic polymer. The polymer preferably has coordinating functional groups which bind to the nano wire surface. Polymeric stabilizers bind to the wires via coordinative bonds, such as hydrogen bonds, van der Waals forces, and spatial entanglement. In addition to electrostatic stabilization by shielding the (polar) nanowire surface, polymer stabilizers cause steric stabilization of the nanowires by preventing their agglomeration by steric repulsion.

The functional groups of the stabilizer are preferably thiol groups (-SH), amino groups (-NH ₂ , = NH), hydroxyl groups (-OH) or carboxy groups (-COOH). These functional head groups have a strong binding affinity for nanoparticles with polar metal surfaces, especially for Au, Ag, and Cu surfaces. The monomeric stabilizer thus has a general form R-SH, R-NH ₂ ,

R-COOH with R1, R ₂ = Rf as a highly fluorinated or perfluorinated alkyl or aryl radical. Particularly preferably, the highly fluorinated or perfluorinated alkyl or aryl radical has from 8 to 10 carbon atoms. The partially halogenated fluorohydrocarbons are preferably 1H, 1H, 2H, 2H-perfluorodecanethiol, 2-trifluoromethylbenzyl mercaptan, 1H, 1H, 2H, 2H-

Perfluorooxethanethiol, 3,3,4,4,4-pentafluoro-1-butanethiol, 2,2,3,3,3-pentafluoropropionic acid, perfluorobutanesulfonic acid, perfluorooctanoic acid, perfluorooctane sulfonate or mixtures thereof.

In a further embodiment of the invention, the non-polymeric stabilizer additionally has a spacer group located between the top and end groups. Advantageously, the stabilizer is highly fluorinated or perfluorinated. Thus, in the stabilizer at least 40%, preferably 60% and more preferably 80% of the hydrogen atoms contained in the compound substituted by fluorine atoms and / or at least 40%, preferably at least 60%, more preferably at least 80% of the halogen atoms contained fluorine. In perfluorinated carbonaceous stabilizers, the ratio of carbon atoms to fluorine atoms is between 1: 4 and 4: 1, preferably 1: 2, 1: 3 or 1: 4.

The polymeric stabilizer is preferably formed as fluorinated polymethacrylate and / or as its heteropolymers.

The nanowire suspension preferably contains nanowires with a concentration of 0.01 to 3 m%, preferably of 1 to 1, 5 m%. At these concentrations, a spontaneous No aggregation of the suspended nanowires is avoided, as a result of which the suspension is long-term stable and storable. For use of the suspension in the process according to the invention is preferably carried out a dilution of the suspension with an orthogonal solvent depending on the coating method in a ratio of storable nanowire suspension to solvent between 1: 2 and 1:20, and a re-suspension sedimented nanowires using shakers, magnetic stirrers or ultrasonic mixers. Particularly preferably, the nanowires have a diameter of between 30 and 120 nm and a length of more than 30 μm. Furthermore, the suspension according to the invention preferably contains additional metallic nanoparticles as optical scattering centers.

The nanowire suspension according to the invention preferably enables the production of a conductive layer in the process according to the invention. The invention likewise relates to the use of this nanowire suspension in the method according to the invention for depositing a nanowire electrode on an organic layer of an optoelectronic component.

Likewise provided by the invention is a nanowire electrode having an electrically conductive layer for an optoelectronic component, produced by a method according to the invention. The nanowire electrode is preferably arranged as a nanowire cover electrode on sensitive organic layers.

An optoelectronic component is understood here to mean an organic light-emitting diode (OLED), an organic solar cell (OSC), an organic field-effect transistor (OFET) or an organic thin-film transistor (OTFT). Organic means that the component comprises at least one layer with at least one organic material.

Advantageously, the nanowire electrode has a high electrical conductivity with high optical transmission. Particularly advantageously, the nanowire electrode is constituted by surface-modified nanowires and thus has a high abrasion and delamination resistance. The surface modification of the nanowires by fluorinated organic stabilizers also advantageously brings about a reduction in the surface energy of the nanowire electrode, thereby rejecting hydrocarbon oils, silicones and aqueous solutions. The nanowire electrode according to the invention thus advantageously has an intrinsic anti-corrosive finish.

Likewise provided by the invention is an optoelectronic component, comprising a) an electrode and a counterelectrode, wherein the electrode is arranged close to the substrate and wherein b) at least one organic layer is arranged between the electrode and the counterelectrode, the organic layer comprising at least one organic material,

c) wherein the counter electrode is formed as the uppermost layer of nanowires with a fluorine-containing surface functionalization.

The optoelectronic component according to the invention is preferably a generic solar cell or light-emitting diode. Such a device usually has a layer structure, wherein the respective lowermost and uppermost layer are formed as an electrode and counter electrode for electrical contacting. The optoelectronic component is arranged on a substrate, such as glass, plastic (PET, etc.) or a metal strip. At least one organic layer comprising at least one organic material is arranged between the substrate-near electrode and the counterelectrode. As organic material hereby small organic molecules or polymers can be used. In one embodiment, the organic layer is a photoactive layer, wherein the photoactive layer is formed, for example, as a mixed layer of a donor and an acceptor material. Adjacent to the at least one photoactive layer can be arranged charge carrier transport layers. Depending on their design, these can preferably transport electrons or holes from or to the respective electrodes. In one embodiment, the optoelectronic component is designed as a tandem or multiple component. In this case, at least two optoelectronic components are deposited as a layer system one above the other. On the formed as a contact base and cover layers may be followed by additional layers for coating or encapsulation of the device or other components.

The optoelectronic component has a bottom layer formed as a base contact and a nanowire cover electrode, the latter being constituted by surface-modified nanowires. As a result, the optoelectronic component has a high abrasion and delamination resistance on the part of the cover electrode. The surface modification of the nanowires by fluorinated organic stabilizers also advantageously brings about a reduction in the surface energy of the nanowire electrode, thereby rejecting hydrocarbon oils, silicones and aqueous solutions. The nanowire electrode according to the invention thus advantageously has an intrinsic anti-corrosive finish. This advantageously allows a long service life of the optoelectronic component. The remaining on the nanowires of the top electrode of the device fluorinated stabilizers can be advantageously detected by a fluorine analysis, for example. By FIB-SIMS, SNMS, RBS or LEIS.

The optoelectronic component according to the invention is preferably organic light-emitting diodes (OLEDs) and organic solar cells (OSCs) with a photoactive layer of vacuum-processed, solvent-sensitive small molecules or polymers. On this vacuum-processed thin-film component, a solvent-based, preferably transparent electrode is applied as a cover contact layer. For the production of the component can advantageously be dispensed with high temperature steps above 160 ° C, preferably the deposition is carried out at below 60 ° C, more preferably below 30 ° C. Optionally, the conductivity of the cover contact layer can be improved by post-processing of the component, for example by repeated washing or by pressing the nanowire layer.

The nanowire network applied as a cover contact layer consists of nanowires which have a diameter of preferably 30 to 120 nm, and thus has a high roughness, i.d.R. of a few hundred nanometers. Deposited thin films of small molecules or polymers often only have a thickness between 30 and 60 nm. When using nanowire electrodes as a ground contact thus the risk of short circuits is large. The formation of a cover contact layer as a nanowire electrode also makes it possible to exploit the excellent properties of nanowire electrodes for devices having layers of vacuum-processed small molecules or polymers.

In one embodiment of the invention, the deposition of the cover contact layer is carried out by a method according to the invention. In this case, a homogeneous nanowire suspension in a fluorous phase containing a fluorinated solvent and with an organic stabilizer surface-modified nanowires is deposited on the organic layer. The nanowires consist of an electrically conductive or semiconducting material. The stabilizer has at least one functional group bonding to the surface of the nanowires and is at least partially or perfluorinated, wherein the bonding functional group has a fluorinated alkyl or aryl group or is formed as a fluorinated or partially fluorinated aliphatic or aromatic polymer. Subsequently, a percolation of the nanowires on the organic layer by evaporation of the solvent.

In one embodiment of the invention, the base contact of the optoelectronic component is formed as a thin metal band. The deposition of the organic layers and the cover contact layer on the thin metal strip advantageously allow a very cost-effective ten efficient production of the optoelectronic component. In addition, the metal strip has a high reflection, whereby the transparency of the entire component minimized and its luminous efficacy is increased.

In a further embodiment of the invention, the photoactive layer is formed as an organic light-emitting layer and the component as an OLED, particularly preferably as a SMOLED. The light-emitting diode is preferably top-emitting and has as a base contact on a metal strip. The emitted light thus passes through the transparent nanowire cover electrode and is thereby scattered. As a result, the light extraction and color stability of the LEDs is advantageously optimized at large viewing angles compared to conventional OLEDs.

In a further embodiment of the invention, additional nanoparticles are contained in the nano-wire electrode, which reinforce an advantageous scattering of the light. The nanoparticles themselves may have a surface modification according to the method of the invention. For example, metal or metal oxide particles, such as TiO ₂ or Ag nanoparticles, can be used as nanoparticles. The nanoparticles have a dimensioning in the range between 1 to 100 nm. In addition, the nanoparticles improve the contacting of the nanowires by deposition in the intermediate regions of the nanowires, thereby improving the conduction paths.

In a further embodiment of the invention, at least one photoactive layer is formed as an organic light-absorbing layer and the component as an OSC. The light incidence in the solar cell is preferably done by the cover contact layer and has as a base contact on a metal strip. The incident light thus passes through the transparent nanowire cover electrode and is thereby scattered. Thus, even at small angles obliquely incident on the solar cell light is scattered in the photoactive layer, whereby the efficiency of the solar cell compared to conventional organic solar cells is advantageously increased.

In a further embodiment of the embodiment, additional nanoparticles are contained in the nanowire electrode, which reinforce an advantageous scattering of the light. The nanoparticles themselves may have a coating according to the method of the invention

To implement the invention, it is also expedient to combine the above-described embodiments and features of the claims. In the following the invention will be explained in more detail with reference to an embodiment and figures, without being limited thereto. Showing:

FIG. 1: j-U characteristic curve of an organic solar cell with a nanowire cover electrode deposited in the fluorous phase method according to the invention.

A) Preparation of a nanowire suspension according to the invention

To 4 ml of ethanol solution of silver nanowires (about 1 .25 mg / ml) was added 30 μΙ to 3 ml of 2% solution of EGC-2702 in HFE-7200 (3M ™ Novec ™) and stirred vigorously using a magnetic stirrer for 1 to 120 minutes. The nanowires functionalized with the fluorinated polymer were separated from the ethanol solution by centrifugation and then dispersed in 50 ml of HFE-7100.

Alternatively, the functionalized nanowires may be washed with 3 ml of HFE-7100 (3M) prior to dispersion in HFE-7100.

Alternatively, to 3 ml of ethanol solution of silver nanowires (about 0.5 mg / ml)

1 H, 1 H, 2H, 2H-perfluorodecanethiol in the ratio Ag: thiol = 1: 1 to 1: 20 was added and stirred vigorously by means of magnetic stirrer for 10 to 360 min. The nanowires functionalized with the fluorinated thiol were then separated from the ethanol solution by centrifugation, washed with 3 ml HFE-7100 (3M), and then dispersed in 25 ml HFE-7100.

B) Production of a Nanowire Electrode According to the Invention

The solution according to the invention was then suspended in the ultrasonic bath (Sonorex Digital 10P, Bandelin) for 15 minutes and then introduced into a spray robot (F7300N series 3-Axis Robot, Fisnar / Vieweg).

Subsequently, a pre-cleaned glass substrate treated for 10 minutes by means of oxygen plasma (Plasma Cleaner: Sterilizer Model PDC-002, Harrick Scientific Corp.) was heated to 30 ° C. and wetted with the nanowire suspension according to the invention. Subsequently, the spraying of the substrate was repeated until the desired transmission was achieved. C) Preparation and Characterization of a Device According to the Invention

The nano-wire electrode was used as a cover contact to organic solar cells (ITO / C ₆ o: W2 (hpp) ₄ / C6o / ZnPc: C6o / ZnPc / BF-DFP: NDP9 / NDP9) is deposited as described above.

Thereafter, the samples were tempered for 30 or 60 min at 100 ° C. Table 1 compares the characteristic values of the individual samples determined below. Heating the Ag nanowire solar cell at 100 ° C for 30 minutes significantly improves the parameters.

Table 1

FIG. 1 also shows the jU characteristic of nanowires deposited on glass. The silver nanowires had a diameter of 90 nm and were deposited in the solvent HFE7100 with the stabilizer EGC2702. Graphs with unfilled symbols represent the dark curves. Here, too, heating the Ag nanowire solar cell at 100 ° C for 30 minutes improves the parameters. Further heating essentially reduces the current of the solar cell in the forward direction, so that one must assume with the second heating step to damage the solar cell. In other words, the optimum of the heating time should be between 30 and 60 minutes.

The patent specification cites the following non-patent literature:

[Kim2009] Kim, Y.-K., Kang, P.S., Kim, D.-i, Shin, G., Kim, G.T., & Ha, J.S. (2009). Fabrication of nanowire channels with unidirectional alignment and controlled length by a simple, gas-blowing-assisted, selective-transfer-printing technique. Small (Weinheim an der Bergstrasse, Germany), 5 (6), 727-34. doi: 10.1002 / smll.200801362

[Lee2010] Lee, J.-Y., Connor, S.T., Cui, Y., & Peumans, P. (2010). Semitransparent organic photovoltaic cells with laminated top electrode. Nano letters, 10 (4), 1276-9. doi: 10.1021 / nl903892x

[Lee2013] Lee J, Lee I, Kim TS, Lee JY (2013), Efficient welding of silver nanowire networks without post-processing. Small 9 (17), 2887-94.

[Hardin2011] Hardin, B.E., Gaynor, W., Ding, I.-K, Rim, S.-B., Peumans, P., & McGehee, M.

D. (2011). Laminating solution-processed silver nanowire mesh electrodes onto solid-state dye-sensitized solar cells. Organic Electronics, 12 (6), 875-879. doi: 10.1016 / j.orgel.2011.03.006

[Azulai2012] Azulai, D., Givan, U., Shpaisman, N., Belenkova, T.L., Gilon, H., Patolsky, F., & Markovich, G. (2012). On-Surface Formation of Metal Nanowire Transparent Top Electrodes on CdSe Nanowire Array-Based Photoconductive Devices. ACS Appl. Mater. Interfaces. doi: 10.1021 / am3004895

[Reinhard2013] Reinhard, M., Eckstein, R., Slobodskyy, A., Lemmer, U., & Colsmann, A. (2013). Solution-processed polymer-silver nanowire top electrodes for inverted semitransparent solar cells. Organic Electronics, 14 (1), 273-277. doi: 10.1016 / j.orgel.2012.10.039

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E., et al. (2013). Spray Coated Silver Nanowires as Top Electrode Layer in Semitransparent P3HT: PCBM-Based Organic Solar Cell Devices. Advanced Functional Materials, 23 (13), 1711-1717. doi: 10.1002 / adfm.201202523 patents

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Claims

claims

1 . Process for producing an electrically conductive layer, comprising the following process steps:

i) an orthogonal, fluorinated solvent and

ii) surface-modified nanowires with a stabilizer, wherein the nanowires consist of electrically conductive or semiconducting material, b) percolation of the nanowires on the organic layer by evaporation of the solvent.

2. The method according to claim 1, characterized in that as orthogonal, fluorinated solvent chlorofluorocarbons (CFCs), chlorofluorocarbons (HCFCs), partially halogenated fluorohydrocarbons (HFCs), perfluorinated fluorocarbons (FCs), hydrofluoroethers (HFEs), perfluoroethers, perfluoroamines or other teilflourierte organic Connections are used.

3. The method according to any one of claims 1 and 2, characterized in that used as orthogonally fluorinated solvent fluorinated alkyl ethers of the general formula CF ₃ (CF ₂ ) _n - OR, R = - (CH ₂ ) _m CH ₃ and / or mixtures thereof become.

4. The method according to any one of the preceding claims, characterized in that the stabilizer comprises at least one bonding to the surface of the nanowires functional group and a fluorinated alkyl or aryl group.

5. The method according to any one of claims 1 to 3, characterized in that the stabilizer is formed as a fluorinated or partially fluorinated aliphatic or aromatic polymer.

6. Process according to one of the preceding claims, characterized in that the functional groups are thiol, amino, hydroxyl or carboxy groups.

7. The method according to any one of the preceding claims, characterized in that the non-polymeric stabilizer has the general form R-SH, R-NH ₂ , R ₁ R ₂ -NH, R-COOH with R ^ R2 = CF ₃ (CF ₂ ) n has.

8. The method according to any one of the preceding claims, characterized in that as polymeric stabilizers partially or fully fluorinated polymethacrylates, their hetero polymers or other teilflourierte polymers are used.

9. The method according to any one of the preceding claims, characterized in that the deposition in a thin film application method by means of spray coating, dip coating, spin coating, Mayer rod coating, slot Die Coating or via a printing process such as inkjet, offset, gravure printing or a related Printing technique is done.

10. The method according to any one of the preceding claims, characterized in that the deposition of the nanowires is directed.

1 1. Method according to one of the preceding claims, characterized in that a nanowire suspension is used with a nanowire concentration of 0.01 to 3 m%.

12. The method according to any one of the preceding claims, characterized in that the wetting takes place at temperatures below 160 ° C, preferably below 60 ° C, more preferably below 30 ° C at ambient pressure and / or inert gas atmosphere.

13. The method according to any one of the preceding claims, characterized in that the percolated nanowires on the organic layer repeatedly washed with an orthogonal, fluorinated solvent and / or pressed with a defined pressure.

14. The method according to any one of the preceding claims, characterized in that a structuring of the nanowires takes place on the organic layer.

15. The method according to claim 14, characterized in that the structuring is effected by means of laser or photolithography or passivation layer.

16. A nanowire suspension in a fluorous phase for depositing a percolative nanowire network on an organic layer of an optoelectronic device, comprising: a) an orthogonal, fluorinated solvent and

b) with a stabilizer surface-modified nanowires, wherein

i) the nanowires consist of electrically conductive or semiconducting material.

17. nanowire suspension according to claim 16, characterized in that the nano- wire suspension contains nanowires with a concentration of 0.01 to 3m%.

18. nanowire suspension according to one of claims 16 or 17, characterized in that the stabilizer has at least one binding to the surface of the nanowires functional group and a fluorinated alkyl or aryl group.

19. nanowire suspension according to any one of claims 16 or 17, characterized in that the stabilizer is formed as a fluorinated aliphatic or aromatic polymer.

20. nanowire electrode for an optoelectronic component with a transparent, electrically conductive layer, produced in a method according to one of claims 1 to 15.

21. Optoelectronic component comprising

a) an electrode and a counter electrode, wherein the electrode is arranged close to the substrate and wherein

b) at least one organic layer is arranged between the electrode and the counterelectrode, the organic layer comprising at least one organic material,

wherein the counter electrode is formed as the uppermost layer of nanowires with a fluorine-containing surface functionalization.

22. Optoelectronic component according to claim 21, characterized in that the organic layer is formed as a photoactive layer.

23. Optoelectronic component according to claim 21 or 22, characterized in that the organic layer is formed from vacuum-processed, solvent-sensitive small molecules, oligomers or polymers.

24. Optoelectronic component according to one of claims 21 to 23, characterized in that the photoactive layer as the organic light-emitting layer and the Component is designed as an organic light-emitting diode (OLED) or the photoactive layer is formed as an organic light-absorbing layer and the device as an organic photovoltaic cell.