Patent Application
20140242350
The invention relates to a process for the production of a layered body, a layered body, a use of a layered body for the production of an electronic component, in particular a touch panel, a touch screen or an antistatic coating, and an electronic component, in particular a touch panel or a touch screen, comprising a layered body.
Conductive polymers are increasingly gaining economic importance, since polymers have advantages over metals with respect to processability, weight and targeted adjustment of properties by chemical modification. Examples of known n-conjugated, conductive polymers are polypyrroles, polythiophenes, polyanilines, polyacetylenes, polyphenylenes and poly(p-phenylene-vinylenes). Layers of conductive polymers are employed in diverse industrial uses, e.g. as polymeric counter-electrodes in capacitors or for throughplating of electronic circuit boards. The preparation of conductive polymers is carried out chemically or electrochemically by oxidation from monomeric precursors, such as e.g. optionally substituted thiophenes, pyrroles and anilines and the particular optionally oligomeric derivatives thereof. In particular, chemically oxidative polymerization is widely used, since it is easy to realize industrially in a liquid medium or on diverse substrates.
A particularly important polythiophene which is used industrially is poly(ethylene-3,4-dioxythiophene) (PEDOT or PEDT), which is described, for example, in EP 0 339 340 A2 and is prepared by chemical polymerization of ethylene-3,4-dioxythiophene (EDOT or EDT), and which has very high conductivities in its oxidized form. An overview of numerous poly(alkylene-3,4-dioxythiophene) derivatives, in particular poly(ethylene-3,4-dioxythiophene) derivatives, and their monomer units, syntheses and uses is given by L. Groenendaal, F. Jonas, D. Freitag, H. Pielartzik & J. R. Reynolds, Adv. Mater. 12, (2000) p. 481-494.
The dispersions, disclosed for example in EP 0 440 957 A2, of PEDOT with polyanions, such as e.g. polystyrenesulphonic acid (PSS), have acquired particular industrial importance. Transparent, conductive films which have found a large number of uses, e.g. as an antistatic coating or as a hole injection layer in organic light-emitting diodes (OLEDS), as shown in EP 1 227 529 A2, can be produced from these dispersions.
In this context, the polymerization of EDOT is carried out in an aqueous solution of the polyanion, and a polyelectrolyte complex is formed. Cationic polythiophenes which contain polymeric anions as counter-ions for charge compensation are also often called polythiophene/polyanion complexes in the technical field. Due to the polyelectrolyte properties of PEDOT as a polycation and PSS as a polyanion, this complex in this context is not a true solution, but rather a dispersion. The extent to which polymers or parts of the polymers are dissolved or dispersed in this context depends on the weight ratio of the polycation and the polyanion, on the charge density of the polymers, on the salt concentration of the environment and on the nature of the surrounding medium (V. Kabanov, Russian Chemical Reviews 74, 2005, 3-20). The transitions in this context can be fluid. No distinction is therefore made in the following between the terms “dispersed” and “dissolved”. Similarly little distinction is made between “dispersing” and “solution” or between “dispersing agent” and “solvent”. Rather, these terms are used as being equivalent in the following.
There is a great need for being able to structure electrically conductive layers based on conductive polymers, in particular based on complexes of polythiophenes and polyanions, similarly to ITO layers (=indium tin oxide layer), where here and in the following “structuring” is to be understood as meaning any measure which leads to an at least partial reduction, but preferably to a complete elimination of the conductivity, in a part region or in several part regions of the layer of electrically conductive polymers.
One possibility for the production of structured layers based on conductive polymers is to apply these polymers to surfaces in a structured manner via certain printing processes, as is described, for example, in EP-A-1 054 414. However, the disadvantage of this set-up for achieving the object is that the electrically conductive polymers must be converted into a paste, which sometimes causes problems in view of the tendency of conductive polymers to aggregate. Furthermore, during application of electrically conductive polymers via printing pastes there is the disadvantage that the outer region of the drops of liquid is thicker than the inner region and that accordingly on drying of the pastes the coating is thicker in the outer region than in the inner region. The resulting irregularity in the layer thickness often has an adverse effect on the electrical properties of the electrically conductive layer. A further disadvantage of structuring via printing pastes is that this is applied only in those regions in which an electrical conductivity of a substrate surface is desired. The consequence of this is that considerable differences in colour occur on the substrate surface between the regions with and without application of the printing paste, which as a rule, however, are undesirable.
In addition to the use of printing pastes, a further possibility for the production of structured coatings from conductive polymers consists of first producing a uniform, non-structured coating from electrically conductive polymers and only then structuring this, for example by photo-bleaching processes or by the use of etching solutions. Thus, for example, WO-A-2009/122923 and WO-A-2008/041461 describe processes in which layers of electrically conductive polymers are structured by means of cerium ammonium nitrate solutions having an etching action. JP-A-2010-161013 describes a process in which structuring of a layer of a conductive polymer is carried out by using a photoresist and/or a dry film resist in combination with an etching agent solution containing cerium ammonium nitrate, cerium ammonium sulphate or hypochlorite. However, the disadvantage of this set-up is, inter alia, that such etching solutions remove the coating of the electrically conductive polymer to a considerable extent, and because of these changes in the nature of the surface the external appearance of the coating is therefore adversely influenced. In particular, the colour of the coating is impaired decisively by a structuring with etching solutions containing cerium.
The present invention was based on the object of overcoming the disadvantages resulting from the prior art in connection with the structuring of layers of electrically conductive polymers, in particular of layers comprising polythiophenes.
In particular, the present invention was based on the object of providing a process for the structuring of a layer of electrically conductive polymers, in particular a layer comprising polythiophenes, with which the conductivity can be reduced, preferably eliminated completely, in certain regions of this layer without the colour of the layer being noticeably influenced by this structuring.
The present invention was also based on the object of providing a process for the structuring of a layer of electrically conductive polymers, in particular a layer comprising polythiophenes, with which the conductivity can be reduced, preferably eliminated completely, in certain regions of this layer without the thickness of the coating and therefore the external appearance of the layer being noticeably influenced by this structuring.
The present invention was furthermore based on the object of providing a process for the structuring of a layer of electrically conductive polymers, in particular a layer comprising polythiophenes, with which the conductivity can be reduced, preferably eliminated completely, in certain regions of this layer, it being possible for clearly defined sharp transitions to be achieved between the conductive regions and the regions of reduced conductivity compared with the conductive regions.
A contribution towards achieving the abovementioned objects is made by a process for the production, preferably for the modification, particularly preferably for the structuring of a layered body S2 (1) comprising the process steps:
A further contribution towards achieving the abovementioned objects is made by a process for the production, preferably for the modification, particularly preferably for the structuring of a layered body S2 (1) comprising the process steps:
In one embodiment of the invention, a) and b) are realized together.
In process step i) of the process according to the invention, a layered body S2 comprising a substrate and an electrically conductive layer which follows the substrate and comprises an electrically conductive polymer P1 is first provided. In this context, the wording “an electrically conductive layer which follows the substrate” includes both layered bodies in which the electrically conductive layer is applied directly to the substrate and layered bodies in which one or more intermediate layers are provided between the substrate and the electrically conductive layer.
In this connection, films of plastic are preferred as the substrate, very particularly preferably transparent films of plastic, which conventionally have a thickness in a range of from 5 to 5,000 μm, particularly preferably in a range of from 10 to 2,500 μm and most preferably in a range of from 25 to 1,000 μm. Such films of plastic can be based, for example, on polymers, such as polycarbonates, polyesters, such as e.g. PET and PEN (polyethylene terephthalate or polyethylene-naphthalene dicarboxylate), copolycarbonates, polysulphones, polyether sulphones (PES), polyimides, polyamides, polyethylene, polypropylene or cyclic polyolefins or cyclic olefin copolymers (COC), polyvinyl chloride, polystyrene, hydrogenated styrene polymers or hydrogenated styrene copolymers. In addition to plastics materials, possible substrates are, in particular, also substrates based on metals or metal oxides, such as, for example, ITO layers (indium tin oxide layers) or the like. Glass is furthermore preferred as the substrate.
This substrate is followed by a layer comprising an electrically conductive polymer P1, all the electrically conductive polymers known to the person skilled in the art being possible as the electrically conductive polymer P1. Examples of suitable electrically conductive polymers which may be mentioned at this point are, in particular, polythiophenes, polypyrrole or polyanilines.
Electrically conductive polymers which are particularly preferred according to the invention are polythiophenes, polythiophenes which can be employed being in principle all polymers with recurring units of the general formula (I)
in which
In a particularly preferred embodiment of the process according to the invention, polythiophenes comprising recurring units of the general formula (I-a) and/or of the general formula (I-b) are preferred:
In the context of the invention, the prefix “poly-” is to be understood as meaning that the polythiophene contains more than one identical or different recurring unit. The polythiophenes contain n recurring units of the general formula (I) in total, where n can be an integer from 2 to 2,000, preferably 2 to 100. The recurring units of the general formula (I) can in each case be identical or different within one polythiophene. Polythiophenes containing in each case identical recurring units of the general formula (I) are preferred.
The polythiophenes preferably in each case carry H on the end groups.
In particularly preferred embodiments, the polythiophene is poly(3,4-ethylenedioxythiophene), poly(3,4-ethylenoxythiathiophene) or poly(thieno[3,4-b]thiophene, poly(3,4-ethylenedioxythiophene) being most preferred.
The optionally substituted polythiophenes are cationic, “cationic” relating only to the charges on the polythiophene main chain. The polythiophenes can carry positive and negative charges in the structural unit, depending on the substituent on the radicals R7 and R8, the positive charges being on the polythiophene main chain and the negative charges optionally being on the radicals R substituted by sulphonate or carboxylate groups.
In this context, the positive charges of the polythiophene main chain can be partly or completely satisfied by the anionic groups optionally present on the radicals R. Overall, in these cases the polythiophenes can be cationic, neutral or even anionic. Nevertheless, in the context of the invention they are all regarded as cationic polythiophenes, since the positive charges on the polythiophene main chain are the deciding factor. The positive charges are not shown in the formulae, since they are mesomerically delocalized. However, the number of positive charges is at least 1 and at most n, where n is the total number of all recurring units (identical or different) within the polythiophene.
However, according to the invention it is particularly preferable for the positive charges on the polythiophene main chain to be compensated by polyanions, a polyanion preferably being understood as meaning a polymeric anion which includes at least 2, particularly preferably at least 3, still more preferably at least 4 and most preferably at least 10 identical anionic monomer recurring units, which, however, do not necessarily have to be linked directly to one another. In this case, the electrically conductive composition and therefore also the electrically conductive layer accordingly comprises a polyanion in addition to the electrically conductive polymer, in particular in addition to the polythiophene.
Polyanions here can be, for example, anions of polymeric carboxylic acids, such as polyacrylic acids, polymethacrylic acid or polymaleic acids, or of polymeric sulphonic acids, such as polystyrenesulphonic acids and polyvinylsulphonic acids. These polycarboxylic and -sulphonic acids can also be copolymers of vinylcarboxylic and vinylsulphonic acids with other polymerizable monomers, such as acrylic acid esters and styrene. Preferably, the electrically conductive layer contains an anion of a polymeric carboxylic or sulphonic acid as the polyanion.
The anion of polystyrenesulphonic acid (PSS) is particularly preferred as the polyanion. The molecular weight (Mw) of the polyacids supplying the polyanions is preferably 1,000 to 2,000,000, particularly preferably 2,000 to 500,000. The molecular weight is determined via gel permeation chromatography with the aid of polystyrenesulphonic acids of defined molecular weights as the calibration standard. The polyacids or their alkali metal salts are commercially obtainable, e.g. polystyrenesulphonic acids and polyacrylic acids, or can be prepared by known processes (see e.g. Houben Weyl, Methoden der organischen Chemie, vol. E 20 Makromolekulare Stoffe, part 2, (1987), p. 1141 et seq.).
In this connection, it is particularly preferable for the electrically conductive layer to comprise a complex of the electrically conductive polymer, in particular of the polythiophene described above, and one of the polyanions described above, particularly preferably a complex of poly(3,4-ethylenedioxythiophene) and polystyrenesulphonic acid (so-called “PEDOT/PSS complexes”). The weight ratio of polythiophene to polyanion in these complexes is preferably in a range of from 1:0.3 to 1:100, preferably in a range of from 1:1 to 1:40, particularly preferably in a range of from 1:2 to 1:20 and extremely preferably in a range of from 1:2 to 1:15.
In this connection, it is furthermore preferable for the electrically conductive layer to comprise 1 wt. % to 100 wt. %, particularly preferably at least 5 wt. % and most preferably at least 10 wt. %, in each case based on the total weight of the electrically conductive layer, of the complexes described above of an electrically conductive polymer and a polyanion, particularly preferably the complexes of poly(3,4-ethylenedioxythiophene) and polystyrenesulphonic acid.
The complexes described above of electrically conductive polymer and polyanion are preferably obtainable by oxidative polymerization, in the presence of the polyanion, of the monomers from which the electrically conductive polymer is formed. In the case of complexes of poly(3,4-ethylenedioxythiophene) and polystyrenesulphonic acid, the complexes are accordingly obtainable by the oxidative polymerization of 3,4-ethylenedioxythiophene in the presence of polystyrenesulphonic acid.
Processes for the preparation of the monomeric precursors for the preparation of the polythiophenes containing recurring units of the general formula (I) and derivatives thereof are known to the person skilled in the art and are described, for example, in L. Groenendaal, F. Jonas, D. Freitag, H. Pielartzik & J. R. Reynolds, Adv. Mater. 12 (2000) 481-494 and the literature cited therein. Mixtures of various precursors can also be used.
In the context of the invention, derivatives of the abovementioned thiophenes are understood as meaning, for example, dimers or trimers of these thiophenes. Higher molecular weight derivatives, i.e. tetramers, pentamers etc., of the monomeric precursors are also possible as derivatives. The derivatives can be built up from both identical and different monomer units and can be employed in the pure form and in a mixture with one another and/or with the abovementioned thiophenes. In the context of the invention, oxidized or reduced forms of these thiophenes and thiophene derivatives are also included in the term “thiophenes” and “thiophene derivatives” as long as the same conductive polymers are formed in their polymerization as in the case of the abovementioned thiophenes and thiophene derivatives.
Very particularly preferred thiophene monomers are optionally substituted 3,4-ethylenedioxythiophenes, the use of unsubstituted 3,4-ethylenedioxythiophene as the thiophene monomer being very particularly preferred.
In the process according to the invention, the thiophene monomers are polymerized oxidatively in the presence of the polyanions, preferably in the presence of polystyrenesulphonic acid. Oxidizing agents which can be used are the oxidizing agents which are suitable for the oxidative polymerization of pyrrole; these are described, for example, in J. Am. Chem. Soc. 85, 454 (1963). Inexpensive oxidizing agents which are easy to handle, e.g. iron-III salts, such as FeCl3, Fe(ClO4)3 and the iron-III salts of organic acids and of inorganic acids containing organic radicals, and furthermore H2O2, K2Cr2O7, alkali metal and ammonium persulphates, alkali metal perborates, potassium permanganate and copper salts, such as copper tetrafluoroborate, are preferred for practical reasons. The use of persulphates and of iron-III salts of organic acids and of inorganic acids containing organic radicals has the great advantage in use that they do not have a corrosive action. Iron-III salts of inorganic acids containing organic radicals which may be mentioned are, for example, the iron-III salts of the sulphuric acid half-esters of C1-C20-alkanols, e.g. the Fe-III salt of lauryl sulphate. Iron-III salts of organic acids which may be mentioned are, for example: the Fe-III salts of C1-C20-alkylsulphonic acids, such as methane and dodecanesulphonic acid; aliphatic C1-C20-carboxylic acids, such as 2-ethylhexylcarboxylic acid; aliphatic perfluorocarboxylic acids, such as trifluoroacetic acid and perfluorooctanoic acid; aliphatic dicarboxylic acids, such as oxalic acid, and above all of aromatic sulphonic acids optionally substituted by C1-C20-alkyl groups, such as benzenesulphonic acid, p-toluenesulphonic acid and dodecylbenzenesulphonic acid.
For the oxidative polymerization of the thiophene monomers of the formula (I), theoretically 2.25 equivalents of oxidizing agent are required per mol of thiophene (see e.g. J. Polym. Sc. Part A Polymer Chemistry vol. 26, p. 1287 (1988)). In practice, however, the oxidizing agent is used in a certain excess, e.g. an excess of from 0.1 to 2 equivalents per mol of thiophene.
The oxidative polymerization of the thiophene monomers in the presence of the polyanions can be carried out in water or in water-miscible organic solvents, such as, for example, methanol, ethanol, 1-propanol or 2-propanol, the use of water as the solvent being particularly preferred. In the case of 3,4-ethylenedioxythiophene as the thiophene monomer and polystyrenesulphonic acid as the polyanion, aqueous dispersions which are known as PEDOT/PSS dispersions and are obtainable, for example, under the trade name Clevios™ P from Heraeus Clevios GmbH are obtained in this manner. The concentration of the thiophene monomers and of the polyanions in the particular solvent is preferably chosen such that after the oxidative polymerization of the thiophene monomers in the presence of the polyanions a dispersion is obtained which contains the complexes of the polythiophene and the polyanion in a concentration in a range of from 0.05 to 50 wt. %, preferably in a range of from 0.1 to 10 wt % and still more preferably in a range of from 1 to 5 wt. %.
The dispersions obtained after the polymerization are conventionally further treated with anion and/or cation exchangers, for example in order to at least partially remove from the dispersions metal cations still present in the dispersions.
According to a preferred embodiment of the process according to the invention, the layered body S2 provided in process step i) is obtainable by a process comprising the process steps:
In process step ia), a substrate is first provided, those substrates which have already been mentioned above as preferred substrates being preferred as substrates. The surface of the substrates can be pretreated before the application of the electrically conductive layer, for example by treatment with a primer, by corona treatment, flame treatment, fluorination or plasma treatment, in order to improve the polarity of the surface and therefore the wettability and chemical affinity.
The dispersion described above which is obtained after the oxidative polymerization of the thiophene monomers in the presence of the polyanions and has preferably been treated beforehand with ion exchangers can be employed, for example, as the composition Z2 comprising the electrically conductive polymer P1 and optionally a polyanion and a solvent, which is applied to at least a part of the surface of the substrate in process step ib). Preferably, the composition Z2 applied in process step ib) contains an anion of a polymeric carboxylic or sulphonic acid as the polyanion. The composition Z2 is preferably a solution or dispersion comprising complexes of poly(3,4-ethylenedioxythiophene) and polystyrenesulphonic acid, the use of a PEDOT/PSS dispersion being particularly preferred.
Before such a dispersion is applied to the substrate surface in process step ib) as composition Z2 for the purpose of formation of an electrically conductive layer, still further additives which, for example, increase the conductivity, such as e.g. compounds containing ether groups, such as e.g. tetrahydrofuran, compounds containing lactone groups, such as butyrolactone, valerolactone, compounds containing amide or lactam groups, such as caprolactam, N-methylcaprolactam, N,N-dimethylacetamide, N-methylacetamide, N,N-dimethylformamide (DMF), N-methylformamide, N-methylformanilide, N-methylpyrrolidone (NMP), N-octylpyrrolidone, pyrrolidone, sulphones and sulphoxides, such as e.g. sulpholane (tetramethylene sulphone), dimethylsulphoxide (DMSO), sugars or sugar derivatives, such as e.g. sucrose, glucose, fructose, lactose, sugar alcohols, such as e.g. sorbitol, mannitol, furan derivatives, such as e.g. 2-furancarboxylic acid, 3-furancarboxylic acid, and/or di- or polyalcohols, such as e.g. ethylene glycol, glycerol or di- and triethylene glycol, can be added to the dispersion. Tetrahydrofuran, N-methylformamide, N-methylpyrrolidone, ethylene glycol, dimethylsulphoxide or sorbitol are particularly preferably employed as conductivity-increasing additives.
One or more binders, such as polyvinyl acetate, polycarbonate, polyvinylbutyral, polyacrylic acid esters, polyacrylamides, polymethacrylic acid esters, polymethacrylamides, polystyrene, polyacrylonitrile, polyvinyl chloride, polyvinylpyrrolidones, polybutadiene, polyisoprene, polyethers, polyesters, polyurethanes, polyamides, polyimides, polysulphones, silicones, epoxy resins, styrene/acrylic acid ester, vinyl acetate/acrylic acid ester and ethylene/vinyl acetate copolymers, polyvinyl alcohols or celluloses, can also additionally be added to the dispersion. The content of the polymeric binder, if this is employed, is conventionally in a range of from 0.1 to 90 wt. %, preferably 0.5 to 30 wt. % and very particularly preferably 0.5 to 10 wt. %, based on the total weight of the composition Z2.
Bases or acids, for example, can be added to the compositions Z2 to adjust the pH. Those additions which do not impair the film formation of the dispersions, such as e.g. the bases 2-(dimethylamino)-ethanol, 2,2′-iminodiethanol or 2,2′,2″-nitrilotriethanol, are preferred.
According to a particularly preferred embodiment of the process according to the invention, the composition Z2 can also contain crosslinking agents which render possible crosslinking of the composition Z2 after application to the substrate surface. The solubility of the coating in organic solvents can thereby be lowered. Examples of suitable crosslinking agents which may be mentioned are, for example, melamine compounds, masked isocyanates, functional silanes—e.g. tetraethoxysilane, alkoxysilane hydrolysates, e.g. based on tetraethoxysilane, or epoxysilanes, such as 3-glycidoxypropyltrialkoxysilane. These crosslinking agents can be added to the composition in an amount in a range of from 0.01 to 10 wt. %, particularly preferably in an amount in a range of from 0.05 to 5 wt. % and most preferably in an amount in a range of from 0.1 to 1 wt. %, in each case based on the total weight of the composition Z2.
This composition Z2 can be applied in process step ib) by known processes, e.g. by spin coating, dipping, impregnation, pouring, dripping on, spraying, misting, knife coating, brushing or printing, for example ink-jet, screen, gravure, offset or tampon printing, to the substrate in a wet film thickness of from 0.5 μm to 250 μm, preferably in a wet film thickness of from 2 μm to 50 μm.
In process step ic), the solvent is then at least partially removed to obtain an electrically conductive layer which comprises the complexes according to the invention or the complexes obtainable by the process according to the invention, this removal preferably being carried out by simple evaporation.
Preferably, the thickness of the electrically conductive layer is 1 nm to 50 μm, particularly preferably in a range of from 1 nm to 5 μm and most preferably in a range of from 10 nm to 500 nm.
In process step ii) of the process according to the invention, at least a part of the electrically conductive layer is now brought into contact with a composition Z1, preferably comprising an organic compound which is capable of releasing chlorine, bromine or iodine. It is preferable here for a part of the conductive layer to be wetted with this composition Z1 and for a further part of the electrically conductive layer adjacent to this part not to be wetted with the composition Z1. Alternatively, this can be effected via a release area or by heating the electrically conductive layer to a temperature in a range of from more than 40 to 200° C., preferably in a range of from more than 40 to 100° C., preferably in a range of from 50 to 90° C., particularly preferably in a range of from 55 to 85° C. Preferably, the bringing into contact is carried out under heat treatment of the electrically conductive layer. Preferably, during heating of the electrically conductive layer the remainder of the layered body S2 is also brought to the temperature of the electrically conductive layer. Alternatively, parts of the layered body S2, such as, for example, the substrate, can also have a temperature which deviates from the electrically conductive layer.
The heat treatment of at least the electrically conductive layer can be carried out in various ways. The heat transfer is preferably carried out via a gas or the surface of a solid body. For example, the layered body S2 is brought into contact with the substrate on a heated surface. Alternatively, the layer can also be brought into contact with heated gas. Alternatively, the electrically conductive layer is brought into contact directly with a liquid which serves to transfer heat.
The heated area is preferably the surface of a heating bath or of a metal plate which is in contact with a heating bath. The heating bath is preferably heated by a heatable liquid, preferably water, or a heating coil. Preferably, the surface with which the layered structure comes into contact for heat treatment is heated by means of a heatable gas. The area via which the heat is released to the electrically conductive layer can have various shapes. The heated area is preferably trapezoidal, rectangular, square, circular or polygonal. Particularly preferably, the area is trapezoidal or rectangular. The heated area preferably has an area in a range of from 0.001 cm2 to 1,000 m2, particularly preferably in a range of from 0.005 cm2 to 100 m2, very particularly preferably in a range of from 0.01 cm2 to 10 m2.
In a preferred embodiment of the process, the composition Z1 is released by means of a release area. The release area preferably comes into contact with the electrically conductive layer only on a part of the layer. The release area can be produced from all materials which are suitable for transferring the composition Z1 to a layered body.
Preferably, the release area has a pattern. In this manner, on the electrically conductive layer the layered structure can be an image of any sequence of at least one first region Du and at least one region Dd which is not brought into contact with the composition Z1. The pattern preferably has sequences of the two different regions Du and Dd with varying sizes of the two regions. Thus, depending on the use, sometimes the amount or area of Du and sometimes the amount or area of Dd can be greater. With such patterns electrical leads can be limited in a targeted manner to only tiny regions on an area.
The release area furthermore preferably comprises an absorbent material. According to the invention, absorbent material is to be understood as meaning that the release area can bind at least a part of the composition Z1. The binding is preferably a physical binding, since at least a part of the composition Z1 is to be released again to the layered structure without the composition having changed chemically.
In a preferred embodiment of the process, the release area is constructed from a material chosen from the group consisting of a porous body, a gel and a fibre material or a combination of at least two of these.
A porous body is preferably a body which has a surface which contains pores. The porous body can take up, for example, liquids or powders through the pores. Preferably, the body reacts with none of the constituents of the liquid or powder, so that on release to the electrically conductive layer the liquid is unchanged in its composition.
The gel likewise has a surface which is suitable for binding powers or liquids physically, so that at least a part of them is released in contact with the electrically conductive layer. In this context, a gel has the property of being of a configuration which is at least in part deformable or elastic under pressure, so that it can adapt to the contours of the layered structure, in particular of the electrically conductive layer.
A fibre material is preferably a material of several fibres. The fibres are preferably laid, woven, knitted or stitched. In this context, the terms woven and knitted designate arrangements of the fibres in a regular pattern, while laid and stitched also describe random arrangements of the fibres. The fibres can be natural fibres, such as silk, wool, cotton, soya or viscose as well as mixtures thereof. Alternatively or additionally, the fibres can also be synthetic fibres. Synthetic fibres are to be understood as meaning fibres of polymers. The polymers can in turn be of natural origin or synthetic origin. The synthetic fibres are preferably fibres chosen from the group consisting of polyester, polyamide, polyimide, polyamide-imide, polyphenylene sulphide, polyacrylonitrile, polytetrafluoroethylene, polyethylene, polypropylene, polyvinyl chloride and polyurethane or a mixture of at least two of these. It is preferable for the fibres to comprise mixtures of natural and synthetic fibres.
Preferably, the porous body is at least in part chosen from the group consisting of a paper, a nonwoven, a sponge and a porous ceramic or is formed from a combination of at least two of these. A porous ceramic preferably designates products from clay minerals. The ceramic can be chosen from the group consisting of silicate raw materials, oxidic raw materials or non-oxidic raw materials.
Preferably, the release area is a recess or bulge or both. This form of the release area is preferred if the composition Z1 is transferred by means of a printing process, for example by means of a printing roller. Preferably, the printing process is chosen from the group consisting of gravure printing with recesses, relief printing with bulges and screen printing or a combination of at least two of these.
Preferably, the release area is configured in the form of an often flat or rounded area adapted to the topology of the conductive layer, preferably in the form of a roll or roller. The release area furthermore preferably contains an absorbent material.
In a preferred embodiment, the heat treatment in step ii) is carried out by means of a heating bath or a heatable roll. If the heat treatment is not carried out via a heating bath, as described above, it can alternatively be carried out via a heatable roll. The roll is preferably configured in the form of a roller over which the layered body is passed. The roll preferably has a contact area in a range of from 0.001 cm2 to 1,000 m2, preferably in a range of from 0.005 cm2 to 100 m2, particularly preferably in a range of from 0.01 cm2 to 10 m2.
In a further preferred embodiment, the roll is heated, and moreover has a release area for release of the composition Z1 to the electrically conductive layer.
The electrically conductive layer is preferably brought into contact to obtain at least one first region Du, also called the contacted region, and at least one non-contacted region Dd of the electrically conductive layer. The regions Dd and Du can each be continuous or discontinuous. If, for example, the non-contacted region Dd is a continuous region, the at least one first contacted region Du can be a continuous or a discontinuous, preferably a discontinuous region Du. If the first region Du is a continuous region, the non-contacted region Dd can be a continuous or a discontinuous, preferably a discontinuous region Dd.
In connection with the process according to the invention, it is preferable for the regions Dd and Du to have a geometric shape, preferably a planar geometric shape chosen from the group consisting of a circle, a rectangle, rhombus, a triangle, tetragon, pentagon, hexagon, heptagon or octagon or a combination of at least two of these. In this connection, it is particularly preferable for the regions Dd and Du together to form a circuit design. In this connection, it is furthermore preferable for the regions Dd and Du each to have an area of at least 0.00001 mm2, preferably at least 0.0001 mm2, still more preferably at least 0.001 mm2, still more preferably at least 0.01 mm2, still more preferably at least 0.1 mm2, still more preferably at least 1 mm2 and most preferably at least 10 mm2.
Particularly preferably, in process step ii) the composition Z1 is applied as a pattern, the covered and the non-covered regions Dd and Du resulting from the pattern. The generation of these patterns is often also called structuring. The pattern can be, for example, a pattern for an electronic component, a circuit board, a touch panel, a touch screen or an antistatic coating. The transition between the regions Du and Dd is preferably very sharp. This often linear transition between the at least first region Du and the at least one non-contacted region Dd preferably has a sharpness of less than 500 μm, preferably in a range of from 1 nm to 450 μm, preferably in a range of from 10 nm to 400 μm, more preferably in a range of from 100 nm to 350 μm, still more preferably in a range of from 1 μm to 300 μm, still more preferably in a range of from 10 μm to 200 μm, still more preferably in a range of from 10 μm to 150 μm.
In process step ii) of the process according to the invention, the electrical conductivity of the electrically conductive layer is reduced in at least a part of the at least one first region Du compared with the electrical conductivity of the electrically conductive layer in the at least one non-contacted region Dd.
In a preferred embodiment of the process according to the invention, in process step ii) the electrical conductivity of the electrically conductive layer is reduced in at least a part of the at least one first region Du by a factor of at least 10, preferably by a factor of at least 100, more preferably by a factor of at least 1,000, still more preferably by a factor of at least 10,000, compared with the electrical conductivity of the electrically conductive layer in the at least one non-contacted region Dd.
Preferably, process step ii) includes at least one process step
According to the present invention, the wording “which is capable of releasing chlorine, bromine or iodine” is preferably understood as meaning an organic compound which, after addition of a solvent, preferably after addition of water, releases chlorine in the form of Cl2, HOCl, OCl− or a mixture of at least two of these chlorine compounds, or bromine in the form of Br2, HOBr, OBr− or a mixture of at least two of these bromine compounds, or iodine in the form of I2, HIO, IO− or a mixture of at least two of these iodine compounds.
An organic compound which is capable of releasing chlorine, bromine or iodine and is particularly preferred according to the invention is an organic compound which comprises at least one structural element (II)
wherein
According to a first particular embodiment of the process according to the invention, the organic compound comprises at least two structural elements (II) in which Hal represents a chlorine atom or a bromine atom and Y represents nitrogen, wherein these at least two structural elements (I) can optionally also be different. In this connection, according to a first process variant it is very particularly preferable for the organic compound to comprise the structural element (III)
in which a chlorine atom or a bromine atom is bonded to at least two of the nitrogen atoms. Among these organic compounds, sodium dichlorodiisocyanurate, sodium dibromodiisocyanurate, tribromoisocyanuric acid and trichloroisocyanuric acid are particularly preferred.
According to a second process variant of this first particular embodiment of the process according to the invention, it is preferable for the organic compound to comprise the structural element (IV)
in which a chlorine atom or a bromine atom is bonded to the two nitrogen atoms and in which R1 and R2 can be identical or different and represent a hydrogen atom or a C1-C4-alkyl group, in particular a methyl group or an ethyl group.
Particularly preferred organic compounds in this connection are chosen from the group consisting of bromo-3-chloro-5,5-dimethylhydantoin, 1-chloro-3-bromo-5,5-dimethylhydantoin, 1,3-dichloro-5,5-dimethylhydantoin and 1,3-dibromo-5,5-dimethylhydantoin.
According to a second particular embodiment of the process according to the invention, the organic compound comprises exactly one structural element (II). In this case also, Y preferably represents N.
According to a first process variant of this second particular embodiment of the process according to the invention, the organic compound is N-chlorosuccinimide or N-bromosuccinimide.
According to a second process variant of this second particular embodiment of the process according to the invention, the organic compound comprises the structural element (V)
in which a chlorine atom or a bromine atom is bonded to the nitrogen atom and in which R3, R4, R5 and R6 can be identical or different and represent a hydrogen atom or a C1-C4-alkyl group, which can optionally be substituted by bromine or chlorine. In this connection, examples of suitable organic compounds which may be mentioned are 3-bromo-5-chloromethyl-2-oxazolidinone, 3-chloro-5-chloromethyl-2-oxazolidinone, 3-bromo-5-bromomethyl-2-oxazolidinone and 3-chloro-5-bromomethyl-2-oxazolidinone.
The organic compound according to the second particular embodiment of the process according to the invention can furthermore be, for example, halazone, an N,N-dichlorosulphonamide, an N-chloro-N-alkylsulphonamide or an N-bromo-N-alkylsulphonamide, in which the alkyl group is a C1-C4-alkyl group, particularly preferably a methyl group or an ethyl group.
According to a third particular embodiment of the process according to the invention, organic compounds chosen from the group consisting of 5-chloro-2-methyl-4-isothiazolin-3-one, 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one, bromo-2-nitro-1,3-propanediol (BNPD), 2,2-dibromo-3-nitrilopropionamide, dibromonitroethyl propionate, dibromonitroethyl formate, sodium N-chloro-(4-methylbenzene)-sulphonamide or tetraglycine hydroperiodide are furthermore possible as the organic compound.
The composition employed in process step ii) is preferably an aqueous solution or dispersion in which the organic compound is dissolved or dispersed. In this connection, it is particularly preferable for the aqueous solution or dispersion to have a pH, determined at 25° C., of at least 4, particularly preferably in a range of from 4 to 12, particularly preferably in a range of from 5 to 10 and most preferably in a range of from 6 to 8.
Preferably, the composition Z1, particularly preferably the aqueous solution or dispersion, comprises the organic compound described above in a concentration in a range of from 0.1 to 50 wt. %, particularly preferably in a range of from 0.5 to 35 wt. % and most preferably in a range of from 1 to 20 wt. %, in each case based on the total weight of the composition Z1.
According to a further particular embodiment of the process according to the invention for the production of a layered body, the composition Z1 employed preferably comprises cyanuric acid as a stabilizer as a further component in addition to the organic compound described above. It has been found, surprisingly, that the rate of release of chlorine, bromine or iodine can be regulated via the addition of cyanuric acid. In the case of the use of a solution or dispersion of the organic compound in process step ii) or iia), the amount of cyanuric acid in the solution or dispersion is preferably in a range of from 1 to 500 mg/l, particularly preferably in a range of from 10 to 100 mg/l.
The bringing of the electrically conductive layer into contact with the composition Z1 in process step iia) is preferably carried out by immersion, which can partly also be carried out, however, by complete submersion, of the electrically conductive layer in the composition Z1 or by printing the electrically conductive layer with the composition Z1, in principle all the processes which have already been described above as preferred application processes in connection with the application of the composition Z2 to the substrate surface, however, also being suitable. In order to ensure an adequate structuring, the electrically conductive layer remains in contact with the composition Z1, preferably the aqueous solution or dispersion, for about 1 second to 30 minutes, particularly preferably for about 30 seconds to 15 minutes and most preferably for about 1 to 5 minutes, before it is taken out again or before the composition Z1 is removed again. The temperature of the composition Z1 during the bringing into contact with the electrically conductive layer is preferably in a range of from 10 to 40° C., particularly preferably in a range of from 20 to 30° C., the use of a composition Z1 with room temperature (approx. 22-25° C.) being most preferred.
The process according to the invention can comprise as a further process step:
wherein the washing is preferably carried out by immersion of the layered body in a solvent, for example in water, and can be followed by a drying step.
According to a particular embodiment of the process according to the invention, the bringing of the electrically conductive layer into contact with the composition Z1 is carried out under conditions such that the colour separation ΔEbefore, after is at most 4.5, particularly preferably at most 3.0 and most preferably at most 1.5, wherein the colour separation ΔEbefore, after is calculated as follows:
ΔEbefore,after=√{square root over ((L*before−L*after)2+(a*before−a*after)2+(b*before−b*after)2)}{square root over ((L*before−L*after)2+(a*before−a*after)2+(b*before−b*after)2)}{square root over ((L*before−L*after)2+(a*before−a*after)2+(b*before−b*after)2)}
In this context, L*before, a*before and b*before are the L, a and, respectively, b values of the L*a*b* colour space of the electrically conductive layer before the bringing into contact with the composition Z1 and L*after, a*after and b*after are the L, a and, respectively, b values of the L*a*b* colour space of the (formerly) electrically conductive layer after the bringing into contact with the composition Z1. In this context, for the purpose of the above requirement the layer after the bringing into contact with the composition Z1 is also still to be called the “electrically conductive layer” if the electrical conductivity is infinitesimally low as a consequence of the bringing into contact with the composition Z1.
In the process according to the invention, it is advantageous if the colour and the difference in colour between the region not brought into contact and brought into contact with the composition Z1, i.e. between the at least one first region Dd and the at least one non-contacted region Du, does not change or changes only very little during storage, during transportation or during use of the layered body. It is particularly preferable according to the invention for the L, a and b values of the L*a*b* colour space of the electrically conductive layer in the at least one covered region Dd and the at least one non-covered region Du not to change or to change only very little during storage, transportation or during use of the layered body. The changes can be measured e.g. before and after a climate test. The climate test is storage of the layered body for 1,000 hours at approx. 85° C. and approx. 85% relative atmospheric humidity. In this context, the colour separation ΔEDd, before climate test; Dd after climate test should be at most 4.5, particularly preferably at most 3.0, more preferably at most 2.2 and most preferably at most 1.5. In this context, furthermore, the colour separation ΔEDu, before climate test; Du, after climate test should be at most 4.5, particularly preferably at most 3.0 and most preferably at most 1.6. The colour separation ΔEDd, before climate test; Dd. after climate test and ΔEDu, before climate test; Du, after climate test is calculated like the colour separation ΔEbefore, after, the values L*before, a*before, b*before, L*after, a*after and b*after being replaced in the equation by the respective values L*Dd, before climate test, a*Dd, before climate test, b*Dd, before climate test, L*Dd, after climate test, a*Dd, after climate test, and b*Dd, after climate test. The colour separation ΔEDu, before climate test, Du, after climate test is calculated like the colour separation ΔEbefore, after, the values L*before, a*before, b*before, L*after, a*after and b*after being replaced in the equation by the respective values L*Du, before climate test, a*Du, before climate test, b*Du, before climate test, L*Du, after climate test, a*Du, after climate test and b*Du, after climate test. In this context, L*before climate test, a*before climate test and b*before climate test are the L, a and, respectively, b values of the L*a*b* colour space of the electrically conductive layer in the particular regions before the climate test and L*after climate test, a*after climate test and b*after climate test are the L, a and, respectively, b values of the L*a*b* colour space of the electrically conductive layer in the particular regions after the climate test. According to a particularly preferred embodiment of the layered body according to the invention, the difference in the colour separations ΔEDd, before climate test, Dd, after climate test and ΔEDu, before climate test, Du, after climate test (|ΔEDd, before climate test, Dd, after climate test−ΔEDu, before climate test, Du after climate test|) is at most 3.0, preferably 2.0, particularly preferably at most 1.0 and most preferably at most 0.7.
It is furthermore preferable in the process according to the invention for the bringing of the electrically conductive layer into contact with the composition Z1 to be carried out under conditions such that the thickness of the electrically conductive layer in those regions which are brought into contact with the composition Z1 is reduced by at most 50%, particularly preferably by at most 25% and most preferably by at most 10%.
The process according to the invention can furthermore comprise a process step
The acidic solution is preferably an aqueous solution of an organic or an inorganic acid, preferably of an inorganic acid. Preferred inorganic acids are sulphonic acid, sulphuric acid, phosphoric acid, hydrochloric acid or nitric acid, sulphuric acid being preferred. This process step serves to improve the surface resistance in the electrically conductive regions of the electrically conductive layer. The treatment is preferably carried out by immersion of the electrically conductive layer in the acidic solution or by printing the electrically conductive layer with the acidic solution, in principle all the processes which have already been described above as preferred application processes in connection with the application of the composition Z2 to the substrate surface, however, also being suitable. In order to ensure an adequate improvement of the surface resistance, the electrically conductive layer remains in contact with the acidic solution for about 1 second to 30 minutes, particularly preferably for about 30 seconds to 15 minutes and most preferably for about 1 to 5 minutes, before it is taken out again or before the acidic solution is removed again. The temperature of the acidic solution during the treatment is preferably in a range of from 10 to 40° C., particularly preferably in a range of from 20 to 30° C., the use of an acidic solution with room temperature (25° C.) being most preferred.
Preferably, according to the invention, after at least one of the process steps i) to iii) at least one washing or at least one drying or at least one washing and at least one drying are carried out, the washing preferably being carried out with water and the drying being carried out at a temperature in a range of from 10 to 200° C., preferably in a range of from 20 to 150° C., more preferably in a range of from 30 to 120° C., still more preferably in a range of from 40 to 100° C.
After process steps i) to ii), preferably after process steps i) to iii), a layered body S2 is obtained which has at least one electrically conductive region and at least one region with an electrical conductivity reduced compared with the electrically conductive region by a factor of at least 10, preferably by a factor of at least 100, more preferably by a factor of at least 1,000, still more preferably by a factor of at least 10,000. Most preferably, the electrical conductivity in the at least one region with a reduced electrical conductivity compared with the electrically conductive region is destroyed completely.
A contribution towards achieving the abovementioned objects is also made by a layered body S2 which is obtainable by the process according to the invention described above, wherein at least three, preferably at least four, preferably at least five and particularly preferably at least ten areas, preferably different from one another, follow one another, it being preferable for at least one area to be surrounded by at least one further area to the extent of at least 70%, preferably at least 80% and particularly preferably at least 90% of the outline of the at least one area. According to the invention, follow one another is understood as meaning directly in the sense of directly adjacent or indirectly in the sense of spaced by something.
The layered body S2 produced by the process according to the invention preferably has
wherein the colour separation ΔEarea A, area B is at most 4.5, particularly preferably at most 3.0 and most preferably at most 1.5.
The term “follow” here relates both to following directly in the sense of being directly adjacent and following indirectly via a separation, following directly being preferred. It is preferable for two and more areas to lie in one plane and particularly preferably in one layer. The area A preferably corresponds to the region or the regions Dd and the area B preferably corresponds to the region or the regions Du of the process according to the invention. The colour separation ΔEarea A, area B is calculated as described below.
A contribution towards achieving the abovementioned objects is also made by a layered body comprising a substrate and a layer which follows the substrate and comprises an electrically conductive polymer P, wherein the layered body comprises
wherein the colour separation ΔEarea A, area B is at most 4.5, particularly preferably at most 3.0 and most preferably at most 1.5.
The colour separation ΔEarea A, area B is calculated as follows:
ΔEarea A,area B=√{square root over ((L*area A−L*area B)2+(a*area A−a*area B)2+(b*area A−b*area B)2)}{square root over ((L*area A−L*area B)2+(a*area A−a*area B)2+(b*area A−b*area B)2)}{square root over ((L*area A−L*area B)2+(a*area A−a*area B)2+(b*area A−b*area B)2)}
In this context, L*area A, a*area A and b*area A are the L, a and, respectively, b values of the L*a*b* colour space of the areas A and L*area B, a*area B and b*area B are the L, a and, respectively, b values of the L*a*b* colour space of the areas B.
The area A preferably corresponds to the region or the regions Dd and the area B preferably corresponds to the region or the regions Du of the process according to the invention.
In the process according to the invention, it is advantageous if the colour of the area A and the colour of the area B and the difference in colour between the area A and the area B do not change or change only very little during storage, during transportation or during use of the layered body. It is particularly preferable according to the invention for the L, a and b values of the L*a*b* colour space of the electrically conductive layer in the area A and the area B not to change or to change only very little during storage, transportation or during use of the layered body. The changes can be measured e.g. before and after a climate test. A suitable climate test is storage of the layered body for 1,000 hours at approx. 85° C. and approx. 85% relative atmospheric humidity. In this context, the colour separation ΔEarea A, before climate test; area A, after climate test should be at most 4.5, particularly preferably at most 3.0, more preferably 2.2 and most preferably at most 1.5. In this context, furthermore, the colour separation ΔEarea B, before climate test; area B, after climate test should be at most 4.5, particularly preferably at most 3.0 and most preferably at most 1.6. The colour separation ΔEarea A, before climate test; area A, after climate test and ΔEarea B, before climate test; area B, after climate test is calculated like the colour separation ΔEarea A, area B, the values L*area A, a*area A, b*area A, L*area B, a*area B and b*area B being replaced in the equation by the respective values L*area A, before climate test, a*area A, before climate test, b*area A, before climate test, L*area A, after climate test, a*area A, after climate test and b*area A, after climate test. The colour separation ΔEarea B, before climate test, area B after climate test is calculated like the colour separation ΔEbefore, after, the values L*before, a*before, b*before, L*after, a*after and b*after being replaced in the equation by the respective values L*area B, before climate test, a*area B, before climate test, b*area B, before climate test, L*area B, after climate test, a*area B, after climate test and b*area B, after climate test.
In this context, the respective value L*before climate test, a*before climate test and b*before climate test for area A and for area B are the L, a and, respectively, b values of the L*a*b* colour space of the electrically conductive layer in the particular areas A and B before the climate test and L*after climate test, a*after climate test and b*after climate test for area A and for area B are the L, a and, respectively, b values of the L*a*b* colour space of the electrically conductive layer in the particular areas A and B after the climate test.
According to a particularly preferred embodiment of the layered body according to the invention, the difference in the colour separations ΔEarea A, before climate test, area A, after climate test and ΔEarea B, before climate test, area B, after climate test (|ΔEarea A, before climate test, area A, after climate test−ΔEarea B, before climate test, area B, after climate test|) is at most 3.0, preferably at most 2.0, particularly preferably at most 1.0 and most preferably at most 0.7.
Preferably, the sharpness of the transition between the area A and the area B is less than 500 μm, preferably in a range of from 1 nm to 450 μm, preferably in a range of from 10 nm to 400 μm, more preferably in a range of from 100 nm to 350 μm, still more preferably in a range of from 1 μm to 300 μm, still more preferably in a range of from 10 μm to 200 μm, still more preferably in a range of from 10 μm to 150 μm. The “transition sharpness” describes the sharpness of the transition between the area A and the area B.
Preferred substrates and electrically conductive polymers are those substrates and electrically conductive polymers which have already been mentioned above as preferred substrates and electrically conductive polymers in connection with the process according to the invention. In connection with the layered body S2 according to the invention, it is furthermore also preferable for the layer to comprise complexes of a polythiophene and a polyanion, those complexes which have already been mentioned above as preferred complexes in connection with the process according to the invention also being preferred here. In this connection, complexes of poly(3,4-ethylenedioxythiophene) and polystyrenesulphonic acid are very particularly preferred. The thickness of the layer also preferably corresponds to the thickness of the electrically conductive layer, as has been described above as the preferred layer thickness in connection with the process according to the invention.
In the case in particular of a layer which comprises complexes of poly(3,4-ethylenedioxythiophene) and polystyrenesulphonic acid, it is preferable for the surface resistance R to have a value in a range of from 1 to 109 Ω/square, particularly preferably in a range of from 10 to 106 Ω/square and most preferably in a range of from 10 to 103 Ω/square.
In connection with the layered body according to the invention, it is furthermore preferable for the following to apply to the thickness of the electrically conductive layer in the areas A (SA) and B (SB):
In this context, for the purpose of the above requirement the layer in the areas B is also to be interpreted as an “electrically conductive layer” if the electrical conductivity of this layer is infinitesimally low.
According to a particular embodiment of the layered body according to the invention, the difference in the transmission of the areas (A) and (B) (|TA−TB|) is at most 5%, particularly preferably at most 3% and most preferably at most 1% of the value of the transmission of the areas A (TA).
In connection with the layered body according to the invention, it is furthermore preferable for the areas A and B to have a geometric shape, preferably a planar geometric shape chosen from the group consisting of a circle, a rectangle, rhombus, a triangle, tetragon, pentagon, hexagon, heptagon or octagon or a combination of at least two of these. In this connection, it is particularly preferable for the areas A and B together to form a circuit design. In this connection, it is furthermore preferable for the areas A and B each to have an area of at least 0.00001 mm2, preferably at least 0.0001 mm2, still more preferably at least 0.001 mm2, still more preferably at least 0.01 mm2, still more preferably at least 0.1 mm2, still more preferably at least 1 mm2 and most preferably at least 10 mm2.
A contribution towards achieving the abovementioned objects is also made by the use of a layered body obtainable by the process according to the invention or a layered body according to the invention for the production of electronic components, in particular organic light-emitting diodes, organic solar cells or non-visible electrical leads, which are preferably provided on transparent substrates, for the production of touch panels or touch screens or for the production of an antistatic coating.
A contribution towards achieving the abovementioned objects is also made by an electronic component, a touch panel or a touch screen comprising a layered body obtainable by the process according to the invention or a layered body according to the invention. Preferred electronic components are, in particular, organic light-emitting diodes, organic solar cell.
The invention is now explained in more detail with the aid of figures, test methods and non-limiting examples.
The differences in colour between the areas 8 and 9 shown in
a shows a dipping process for application of various substances to a layered body 2. For this, the desired substance 18, 19 which is to be applied to the layered body 2 is provided as a liquid in a bath 17. This can be, for example, a solution P1 19 or a solution Z1 18, depending on the step in which the dipping process is used. By using a dipping bath 17, a large amount of solution 18, 19 is required in order to wet the layered body 2 completely. Heating of such a dipping bath 17 is very expensive, since the entire solution 18, 19 must be heated. Furthermore, the production of a layered body 1 by means of the dipping process described here takes at least 1 to approx. 30 min in order to bring the part regions which are to be non-conducting to a surface resistance of 1010 ohm/square.
This process time can be reduced to 1 to 30 seconds if the following process, as shown in
By the process described; both the substrate 3 and the entire layered body 2 can be heated and/or wetted with solution 18 in part or in its entirety in a simple manner. By this combined heating and etching process, the conversion of the layered body 2 into the layered body 1 according to the invention can be carried out within a few seconds or even fractions of a second. Washing with ethanol in an ultrasound bath for 5 seconds (not shown in the diagram) forms the conclusion of this additional process step.
A further possibility of transferring the substance to be transferred to the layered body 2 in the form of a solution 18 is shown in
The layered body 2 is first brought into contact with at least a part of the layered body 2 with the first roll 15. In this context, the substrate 3 preferably points in the direction of the roll 15 (not shown here). The roll 15, for example in the form of a roller 15, can be heated. This can be effected, for example, by passing a hot gas or a hot liquid through the roll 15. The layered body 2 can be brought into contact with the roll 15 for different lengths of time. In this example it has been brought into contact with the roll 15 for 5 seconds. The contact time can be determined both by the speed of the moving layered body and/or by the contact area between the layered body 2 with the roll 15. The same also applies to the roll 16. The layered body can be brought to a temperature in a range of between 25 and 100° C. in this manner.
The layered body 1, 2 can subsequently or simultaneously be brought into contact with the second roll 16. This roll 16 has an absorbent surface 16a with which it can come into contact with the layered body 2, preferably on the opposite side to the first roll 15. The roll 16 can also be brought into contact with the layered body 2 on the same side as roll 15 (not shown here). Before contact with the layered body 2, the surface 16a is impregnated in a bath 17 which contains a solution 18. The solution 18 can be renewed continuously in the bath 17, so that the concentration of the substances in the solution 18 is always constant. After this, the layered body 2 can be passed through or over a washing station 22 in order to configure the layered body 1. The washing station 22 can be, for example, a bath or a spray unit for water or other wash solutions, for example alcohol, such as ethanol. In contrast to the dipping process, as has been shown in
Test Methods
Unless stated otherwise, the test methods and the Examples are carried out under standard conditions. Unless stated otherwise, % ranges are % by weight ranges.
Determination of the Surface Resistance
For determination of the surface resistance, Ag electrodes of 2.5 cm length are vapour-deposited via a shadow mask such that a resistance measurement is possible in each of the areas A and B. The surface resistance is determined with an electrometer (Keithly 614). The determination was carried out by means of the so-called “four point probe” measurement as is described, for example, in U.S. Pat. No. 6,943,571 B1.
Determination of the Colour Values L, a and b and the Transmission
The procedure for measurement of the transmission spectra of coated PET films is in accordance with ASTM 308-94a. For this, a 2-channel photospectrometer from Perkin Elmer, type Lambda 900 is used. The apparatus is equipped with a 15 cm photometer sphere. Proper functioning of the photospectrometer is ensured by regular checking of the wavelength calibration and the linearity of the detector in accordance with the manufacturer's recommendations and is documented.
For the transmission measurement, the film to be measured is fixed in front of the entry opening of the photometer sphere with the aid of a press-on holder, so that the measuring beam penetrates through the film without shadowing. The film is visually homogeneous in the region of the penetrating measuring beam. The film is orientated with the coated side towards the sphere. The transmission spectrum is recorded in the wavelength range of 320-780 nm in wavelength increments of 5 nm. In this context, there is no sample in the reference beam path, so that measurement is against air.
For evaluation of the colour of the transmission spectrum the “WinCol—version 1.2” software provided by the manufacturer of the apparatus is used. In this context, the CIE tristimulus values (standard colour values) X, Y and Z of the transmission spectrum in the wavelength range of 380-780 nm are calculated in accordance with ASTM 308-94a and DIN 5033. From the standard colour values, the standard colour value contents x and y and CIELAB coordinates L*, a* and b* are calculated in accordance with ASTM 308-94a and DIN 5033.
Climate Test
The layered body is stored at 85 C and 85% relative atmospheric humidity. The colour values L, a and b are measured beforehand and afterwards.
Preparation of the Solutions/Formulations:
Polymer P1
Clevios® FE-T (PEDOT/PSS dispersion obtainable from Heraeus Clevios GmbH) is used as composition Z2.
Sulphuric Acid Solution
An approx. 1 wt. % strength solution in water is prepared.
Composition Z1
10 g of sodium dichlorodiisocyanurate dihydrate are dissolved in 90 g of water at room temperature (approx. 22° C.), while stirring. This stock solution was diluted with water to a sodium dichlorodiisocyanurate dihydrate content of 10 wt. % and 5 wt. % respectively.
An electrically conductive layer 4 in the form of a PEDOT/PSS layer was coated from the Clevios® FE-T dispersion on to a substrate 3 consisting of a polyester film from DuPont Teijin—type Melinex 505—by means of a bar coater. The wet film thickness was in the range of 4-12 μm. Drying was carried out at 130° C. for 5 minutes. The surface resistance at a dry film thickness of 12 μm was approx. 180 ohm/sq.
The film obtained after the drying is laid under paper 12 (for example, as here, a Whatmann 602 filter paper) which was impregnated with a 10 wt. % strength sodium dichlorodiisocyanurate dihydrate solution 18. The paper has release areas 12a which project out of the surface of the paper. The release areas 12a come into contact with the electrically conductive layer 4. This step is also call an etching step. The film was treated at 60° C. for 15 seconds over a water bath or a hot-plate 11, for example a photo dryer, as in this example. This process was followed by washing under running, preferably distilled water for 10 s.
After these steps the film had a surface resistance of >1010 ohm/square on the etched regions Du and a surface resistance with the starting value of approx. 180 ohm/square on the non-etched regions Dd.
The procedure was as in Example 1, with the difference that a PET film A was used as the substrate, which was coated with a formulation which had a higher degree of crosslinking than the polyester film of DuPont (type Melinex 505).
The procedure was as in Example 1, with the difference that a PET film A was used as the substrate, which was coated with a formulation which had a higher degree of crosslinking than Clexios® FET (commercially available from Heraeus Precious Metals GmbH & Co. KG, Germany).
It can be seen from
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2011 107 459.0 | Jul 2011 | DE | national |
| 10 2012 009 176.1 | May 2012 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2012/002841 | 7/6/2012 | WO | 00 | 5/9/2014 |
| Number | Date | Country | |
|---|---|---|---|
| 61507239 | Jul 2011 | US | |
| 61658537 | Jun 2012 | US |
