WO2007015364A1 - 薄膜トランジスタの製造方法 - Google Patents
薄膜トランジスタの製造方法 Download PDFInfo
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- WO2007015364A1 WO2007015364A1 PCT/JP2006/314145 JP2006314145W WO2007015364A1 WO 2007015364 A1 WO2007015364 A1 WO 2007015364A1 JP 2006314145 W JP2006314145 W JP 2006314145W WO 2007015364 A1 WO2007015364 A1 WO 2007015364A1
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- electrode
- thin film
- plating
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- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 229940001496 tribasic sodium phosphate Drugs 0.000 description 1
- PYJJCSYBSYXGQQ-UHFFFAOYSA-N trichloro(octadecyl)silane Chemical compound CCCCCCCCCCCCCCCCCC[Si](Cl)(Cl)Cl PYJJCSYBSYXGQQ-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000003960 triphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C3=CC=CC=C3C12)* 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/80—Constructional details
- H10K10/82—Electrodes
- H10K10/84—Ohmic electrodes, e.g. source or drain electrodes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
- H10K71/60—Forming conductive regions or layers, e.g. electrodes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/40—Organic transistors
- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/464—Lateral top-gate IGFETs comprising only a single gate
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/40—Organic transistors
- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/466—Lateral bottom-gate IGFETs comprising only a single gate
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K19/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic element specially adapted for rectifying, amplifying, oscillating or switching, covered by group H10K10/00
- H10K19/10—Integrated devices, or assemblies of multiple devices, comprising at least one organic element specially adapted for rectifying, amplifying, oscillating or switching, covered by group H10K10/00 comprising field-effect transistors
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
- H10K71/60—Forming conductive regions or layers, e.g. electrodes
- H10K71/611—Forming conductive regions or layers, e.g. electrodes using printing deposition, e.g. ink jet printing
Definitions
- the present invention relates to a method for manufacturing an organic thin film transistor used in electronics, photo-tus, bioelectronics, and the like, and particularly relates to a technique effective for easily forming a low-resistance electrode.
- Devices using organic semiconductors have milder film forming conditions than conventional inorganic semiconductor devices, and semiconductor thin films can be formed on various substrates or formed at room temperature. Expected to be low cost and flexible by forming a thin film on polymer film.
- polyacene compounds such as anthracene, tetracene, and pentacene have been studied as well as conjugated polymers and oligomers such as polyphenylene vinylene, polypyrrole, polythiophene, and oligogophene.
- polyacene compounds have high crystallinity due to their strong intermolecular cohesion, and are reported to exhibit high V carrier mobility and excellent semiconductor device characteristics. It is. For example, “Science” by Siyon et al., 2000, 289 ⁇ , p559, “Nature” by Siyon et al., 2000, 403 ⁇ , p408, “Transaction 'on' Electron. Device”, 1999, 46 ⁇ , ⁇ 1258, isotropic.
- conjugated polymers such as polythiophene compounds can be coated with this solution to form a thin film. Therefore, it is expected to form a pattern by printing and create a device at low cost. (See, for example, “Science” by Shillinows et al., 2000, 290 ⁇ , P2123).
- a method of forming an electrode pattern by etching or lift-off of a uniformly formed metal thin film (first method), or a paint containing a metal filler is used.
- the first method has a problem that the pattern formation process is complicated because it is necessary to form a resist layer for forming a pattern and to remove the resist layer.
- the second and third methods have a problem that the resistance of the electrode is increased by the influence of the contained binder!].
- Patent Document 1 describes that an electroless plating is used to easily form a low-resistance electrode. This is achieved by simply forming an electrode pattern by combining a catalyst that generates electroless plating, a plating agent, and a pattern thereof. As a result, it is possible to form an electrode pattern without going through complicated steps.
- the organic semiconductor layer comes into contact with the plating catalyst solution or the plating agent, the organic semiconductor layer changes, and the transistor performance is greatly deteriorated.
- the conventional electroless plating method has problems such as low pattern accuracy. The present invention greatly improves this.
- Patent Document 1 Japanese Unexamined Patent Application Publication No. 2004-158805
- an object of the present invention is to obtain a method for manufacturing a thin film transistor with high production efficiency and high resolution and good pattern accuracy, and the semiconductor performance is deteriorated during the plating process in the electrode formation.
- the object is to obtain a method for producing a prevented thin film transistor.
- a protective film is formed on an organic semiconductor layer according to a manufacturing method of a thin film transistor having an organic semiconductor layer, and a source or drain electrode in contact with the organic semiconductor layer formed by an electroless plating method. Then, after supplying a liquid containing a plating catalyst to form a plating catalyst pattern, a source electrode or a drain electrode is formed by bringing a plating agent into contact with the pattern.
- the electrode is patterned by electroless plating, thereby easily forming a high-performance organic thin film transistor that does not deteriorate the organic semiconductor layer. It becomes possible to do.
- FIG. 1 is a diagram showing a configuration example of an organic thin film transistor element of the present invention.
- FIG. 2 is a schematic equivalent circuit diagram of an example of an organic thin film transistor element sheet.
- FIG. 3 is a view showing a resin substrate provided with a gate electrode, a gate insulating layer, an organic semiconductor layer, and a protective film pattern.
- FIG. 4 is a diagram showing a production example of a TFT sheet using the thin film transistor production method of the present invention.
- FIG. 5 is a diagram showing a production example of a TFT sheet using the thin film transistor production method of the present invention.
- FIG. 6 is a diagram showing a production example of a TFT sheet using the thin film transistor production method of the present invention.
- FIG. 7 is a diagram showing a production example of a TFT sheet using the thin film transistor production method of the present invention.
- FIG. 8 is a diagram showing a production example of a TFT sheet using the thin film transistor production method of the present invention.
- the present invention forms a protective film on the organic semiconductor layer after the organic semiconductor layer is formed in order to avoid deterioration of the organic semiconductor layer. This prevents deterioration of the organic semiconductor layer due to the plating catalyst and the plating agent.
- the electrode is formed after the protective film pattern is formed. As a result, the deterioration of the organic semiconductor layer is greatly improved, and a high-performance organic thin film transistor and organic semiconductor element can be obtained.
- a catalyst that acts on the plating agent to generate the electroless plating is disposed on the portion where the electrode is provided, and then the plating agent is contacted. As a result, the catalyst and the plating agent come into contact with each other, and an electroless plating is applied to the portion to form an electrode.
- a protective film is formed on the organic semiconductor layer in a region protected from the plating catalyst solution, and the plating film is in contact with the protective film so that unnecessary portions are not exposed to the plating catalyst solution.
- a liquid containing a catalyst is supplied, and first, a catalyst catalyst pattern is formed.
- the formation of the plating catalyst pattern can be performed by patterning the protective film.
- the protective film can be patterned by forming a resist on the protective film with a photosensitive resin layer or an overlay layer. By using a resist, accurate patterning can be performed.
- a plating catalyst solution pattern By patterning the protective film, a plating catalyst solution pattern can be formed.
- the application of the plating catalyst liquid can be performed by a printing method, an ink jet method, or the like, but can also be performed by immersing or coating the plating catalyst solution.
- electroless plating is possible by applying a plating agent.
- the application of the plating agent can also be performed by a printing method, an ink jet method, or the like, and can also be performed by dipping or coating.
- a region (layer) that repels the liquid containing the catalyst catalyst in the protective film or a region in contact with the protective film it is preferable to provide a region (layer) that repels the liquid containing the catalyst catalyst in the protective film or a region in contact with the protective film.
- a specific method there is a method in which a surface of the protective layer is provided with a repellent layer for the plating catalyst solution or the plating agent.
- a catalyst that acts on the plating agent to generate an electroless plating may be disposed on the portion where the electrode is provided, and then the plating agent may be contacted, or the plating catalyst and the plating agent.
- a plating agent may be disposed on the portion where the electrode is provided, and a catalyst that acts on the plating agent to generate electroless plating may be contacted later.
- the catalyst that acts on the plating agent to generate electroless plating is composed of at least one compound selected from Pd, Rh, Pt, Ru, Os, Ir and their ions or metal fine particles.
- halides such as chlorides, bromides, and fluorides of the above elements
- inorganic salts or composite salts such as sulfates, nitrates, phosphates, borates, cyanides, and carboxylic acids Salts, organic sulfonates, organic phosphates, alkyl complexes, alkane complexes, alkene complexes, cyclopentagen complexes, porphyrins, phthalocyanines, and other organic complex salt powers selected or mixtures of these, ions of these elements, these Metal fine particles of these elements are applicable. It is also possible to apply a solution or dispersion containing a surfactant or a resin binder to a catalyst made of an organic complex salt.
- the plating agent for example, a solution in which metal ions deposited as an electrode are uniformly dissolved is used, and a reducing agent is contained together with the metal salt.
- a solution in which metal ions deposited as an electrode are uniformly dissolved is used, and a reducing agent is contained together with the metal salt.
- the metal salt includes at least one metal halide, nitrate, sulfate, phosphate, borate selected from Au, Ag, Cu, Ni, Co, and Fe. , Acetate, tartaric acid, kenate, etc. are applicable.
- the reducing agent hydrazine, hydrazine salt, borohalide salt, hypophosphite, hyposulfite, alcohol, aldehyde, carboxylic acid, carboxylate and the like are applicable.
- elements such as boron, phosphorus, and nitrogen contained in these reducing agents may be contained in the deposited electrode.
- an alloy may be formed using a mixture of these metal salts.
- a mixture of the metal salt and the reducing agent may be applied, or the metal salt and the reducing agent may be applied separately.
- the metal salt and the reducing agent may be applied separately.
- a metal salt is arranged, and then a reducing agent is arranged, so that a more stable electrode pattern can be formed.
- the plating agent can contain additives such as a buffer for adjusting pH and a surfactant.
- additives such as a buffer for adjusting pH and a surfactant.
- organic solvents such as alcohols, ketones and esters may be added as the solvent used in the solution.
- the composition of the plating agent is composed of a metal salt of the metal to be deposited, a reducing agent, and, if necessary, an additive and an organic solvent, and the concentration and composition are adjusted according to the deposition rate.
- the deposition rate can be adjusted by adjusting the temperature of the plating agent.
- the temperature adjusting method include a method of adjusting the temperature of the plating agent, and a method of adjusting the temperature by heating and cooling the substrate before immersion, for example, when immersed in the plating agent.
- the patterning of the catalyst or the plating agent is not particularly limited! However, it is preferable that the patterning of the protective film is performed.
- a method for bringing a plating catalyst (or a plating agent) into contact with a catalyst pattern patterned with a resist or the like is not particularly limited.
- the immersion in a plating agent (or catalyst) is a plating agent (or a catalyst).
- Spraying or printing such as ink-jet printing, screen printing, intaglio, lithographic and letterpress. This is preferred because the protective film prevents the catalyst solution and the plating agent from penetrating into unnecessary areas.
- the electrode provided by applying electroless plating is formed from the metal salt Au, Ag, Cu,
- At least one metal selected from Ni, Co, Fe or their alloy strength At least one metal selected from Ni, Co, Fe or their alloy strength
- the metal includes an intermetallic compound.
- the protective film formed on the organic semiconductor layer seals the action of the plating catalyst, the metal salt in the plating agent, the reducing agent, etc. If it is an inert material that does not affect organic semiconductor materials.
- a photosensitive composition such as a photosensitive resin layer is formed on the organic semiconductor protective layer, it is not affected by the coating process, and the photosensitive resin layer is not affected. Preference is given to materials that are not affected by patterning.
- Examples of such materials include the following polymer materials, particularly materials containing a hydrophilic polymer, and more preferred are aqueous solutions or aqueous dispersions of hydrophilic polymers.
- the hydrophilic polymer is a polymer that is soluble or dispersible in water or an acidic aqueous solution, an alkaline aqueous solution, an alcohol aqueous solution, or an aqueous solution of various surfactants.
- polybulal alcohol, homopolymers and copolymers having component power such as HEMA, acrylic acid, and acrylamide can be suitably used.
- materials containing inorganic oxides and inorganic nitrides are also preferable because they do not affect the organic semiconductor and do not affect other coating processes.
- the material of the gate insulating layer described later can also be used.
- the organic semiconductor protective layer containing an inorganic oxide or inorganic nitride as the gate insulating layer material is preferably formed by an atmospheric pressure plasma method.
- a method for forming a thin film by a plasma method under atmospheric pressure is a process in which a thin film is formed on a substrate by discharging under atmospheric pressure or a pressure near atmospheric pressure, exciting a reactive gas into plasma, and
- the method is as follows: JP 11-61406, 11-133205, 2000-121804, 2000-147209, 2000-185362, etc. (hereinafter referred to as atmospheric pressure plus) , Also called ma method).
- atmospheric pressure plus also called ma method
- a photoresist when patterning the protective film.
- the photoresist layer it is preferable to use a force laser sensitive material which can use a known positive or negative material.
- a photoresist material (1) dye-sensitized photopolymerization photosensitivity as disclosed in JP-A-11-271969, JP-A-2001-117219, JP-A-11-311859, JP-A-11-352691 Materials, (2) Infrared lasers such as JP-A-9 179292, US Patent No.
- Examples of the solvent for forming the coating solution of the photosensitive resin include propylene glycol monomethylenoateolene, propyleneglycolenomonoethylenoatenore, methinorecellosonoleb, methinorecerosonoleb acetate, ethinorecerosonoleb, Examples include ethyl acetate sorb acetate, dimethylformamide, dimethyl sulfoxide, dioxane, acetone, cyclohexanone, trichloroethylene, and methyl ethyl ketone. These solvents are used alone or in combination of two or more.
- Methods for forming the photosensitive resin layer include coating methods such as spray coating, spin coating, blade coating, dip coating, casting, roll coating, bar coating, and die coating. Etc., as described in the patterning of the protective film.
- patterning exposure is performed by an Ar laser, a semiconductor laser, a He—Ne laser, a YAG laser, a carbon dioxide gas laser, or the like.
- a semiconductor laser having an oscillation wavelength in the infrared is preferable.
- the output is suitably 50 mW or more, preferably 1 OO mW or more.
- a water-based alkaline developer is suitable as the developer used for developing the photosensitive resin layer.
- the aqueous alkaline developer include alkalis such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium metasilicate, potassium metasilicate, dibasic sodium phosphate, and tribasic sodium phosphate.
- Metal salt aqueous solution ammonia, ethylamine, n-propylamine, jetylamine, di-n-propylamine, triethylamine, methyljetylamine, dimethylethanolamine, triethanolamine, tetramethylammonium hydroxide, tetraethylammonium hydroxide, choline, Alkaline compounds such as pyrrole, pyribeline, 1,8-diazabicyclo [5,4,0] -7-undecene, 1,5-diazabicyclo [4,3,0] -5-nonane were dissolved. Can mention aqueous solution .
- the concentration of the alkaline compound in the present invention in the alkaline developer is usually 1 to 10% by mass, preferably 2 to 5% by mass.
- an organic solvent such as an ionic surfactant, an amphoteric surfactant, and alcohol can be added as necessary.
- an organic solvent propylene glycol, ethylene glycol monophenyl ether, benzyl alcohol, n -propyl alcohol, and the like are useful.
- an abrasion layer which is another photosensitive resin layer, may be used for forming a thick catalyst pattern of the protective film, that is, for forming an electrode pattern.
- the abrasion layer used in the present invention can also constitute an energy light absorber, a binder resin, and various additive powers added as necessary.
- the energy light absorber various organic and inorganic materials that absorb energy light to be irradiated can be used.
- the laser light source is an infrared laser
- a pigment, a dye, a metal
- Use ferromagnetic metal powder such as metal magnetic powder mainly composed of metal oxide, metal nitride, metal carbide, metal boride, graphite, carbon black, titanium black, Al, Fe, Ni, Co, etc.
- carbon black, cyanine dyes, and Fe ferromagnetic metal powder are preferable.
- the content of the energy light absorbing agent is about 30 to 95% by mass, preferably 40 to 80% by mass, of the abrasion layer forming component.
- the nodding resin of the abrasion layer can be used without particular limitation as long as it can sufficiently retain the coloring material fine particles.
- the polyurethane resin, the polyester resin, and the salt resin resin can be used. Examples thereof include a system resin, a polyvinylacetal resin, a cellulose resin, an acrylic resin, a phenoxy resin, a polycarbonate, a polyamide resin, a phenol resin, and an epoxy resin.
- the content of Noinda rosin is about 5 to 70% by mass, preferably 20 to 60% by mass, of the abrasion layer forming component.
- the ablation layer in the present specification refers to a layer that is ablated by irradiation with high-density energy light, and the ablation referred to here is one in which the ablation layer is completely scattered by physical or chemical changes. This includes a phenomenon in which a physical or chemical change occurs only in the vicinity of an interface with an adjacent layer, where a part is destroyed or scattered. Use this ablate To form a resist image and form electrodes.
- the high-density energy light is not particularly limited as long as it is active light that generates ablation.
- flash exposure using a xenon lamp, a halogen lamp, a mercury lamp, or the like may be performed through a photomask, or scanning exposure may be performed by converging laser light or the like.
- An infrared laser, particularly a semiconductor laser, whose output per laser beam is 20 to 200 mW is most preferably used.
- the energy density preferably 50 ⁇ 500MjZcm 2, more preferably Ru 100 ⁇ 300MjZcm 2 der.
- an electrode material repellent layer having a thickness of about 0.5 ⁇ m on the photosensitive resin layer (ablation layer) by solvent coating.
- the electrode material repellent layer uses a silicone rubber layer, a silane coupling agent, a titanate coupling agent, or the like to form an electrode material on the surface of the photosensitive layer, and in the present invention, the plating catalyst solution or the plating agent solution. It is a layer that imparts repellent properties.
- an electrode material repellent layer By coating an electrode material repellent layer on the photosensitive layer and exposing or developing the photosensitive layer, buttering can be performed in combination with the photosensitive layer.
- an abrasion layer or a photopolymerizable photosensitive material is preferred.
- the formed photosensitive layer and electrode material repellent layer are exposed to a pattern such as a source electrode and a source bus line with a semiconductor laser or the like, and then the exposed electrode material repellent layer (silicone rubber layer) is brushed. Remove. Since the adhesiveness between the photosensitive layer and the silicone rubber layer changes with exposure, the silicone rubber layer can be easily removed by brush treatment.
- the effect of the protective layer can be enhanced, and only the portion where the electrode is to be formed can be accurately patterned, and the electrode material can be patterned with a simple process.
- the resist image may be removed.
- Photoresists such as alcohols, ethers, esters, ketones, glycol ethers, etc. are used for resist images. These are appropriately selected from a wide range of organic solvents used as coating solvents. The organic semiconductor layer is not eroded and the solvent is preferred.
- various condensed polycyclic aromatic compounds and conjugated compounds are applicable.
- Examples of the condensed polycyclic aromatic compound include anthracene, tetracene, pentacene, hexacene, heptacene, taricene, picene, fluorene, pyrene, peropyrene, perylene, terylene, kuterite terylene, coronene, talenene And compounds such as musantracene, bisanthene, zeslen, heptazethrene, pyranslen, violanthene, isoviolanthene, sacobiphenyl, phthalocyanine, porphyrin, and derivatives thereof.
- Examples of the conjugated compound include polythiophene and its oligomer, polypyrrole and its oligomer, polyaniline, polyphenylene and its oligomer, polyphenylene vinylene and its oligomer, polyphenylene vinylene and its oligomer, polyacetylene, Examples include polydiacetylenes, tetrathiafulvalene compounds, quinone compounds, cyan compounds such as tetracyanoquinodimethane, fullerenes, and derivatives or mixtures thereof.
- thiophene hexamer ⁇ -sectiophene e, ⁇ -dihexinore a-secciothiophene, e, ⁇ -dihexinore a-quinketiophene, ⁇ , ⁇ Oligomers such as —bis (3-butoxypropyl) -a-secciothiophene can be preferably used.
- copper phthalocyanine is a metal phthalocyanine such as fluorine-substituted copper phthalocyanine described in JP-A-11-251601, naphthalene 1, 4, 5, 8-tetracarboxylic acid diimide, N, N'-bis (4 Trifluoromethylbenzyl) naphthalene 1, 4, 5, 8-tetracarboxylic acid diimide, N, N'-bis (1H, 1H-perfluorooctyl), N, N'-bis (1H , 1H perfluorobutyl) and N, N'-dioctylnaphthalene 1,4,5,8-tetracarboxylic diimide derivatives, naphthalene 2, 3, 6, 7 naphthalene tetracarboxylic diimides such as tetracarboxylic diimide And anthracene 2, 3, 6, 7-tetracyclic diimides such as tetracarbox
- dyes such as notube, merocyanine dyes, and hemicyanine dyes.
- At least one selected from the group consisting of condensed polycyclic aromatic compounds such as pentacene, fullerenes, condensed ring tetracarboxylic acid diimides, and metal phthalocyanines Preferred.
- examples of the organic semiconductor material according to the present invention include silylethyl-pentacene compounds described in Adv. Mater. 2003, 15, No. 23, December 3 (2009-2011), and J. Am. Chem. Soc., 2005, 127, 4986 to 4987
- the compounds having acene and heteroacene as the mother nucleus are also preferred, such as silylethynylpentacene, trisalkylsilylethylpentacene, triisopropyl silylethylpentacene, etc. It can be suitably used.
- organic semiconductor materials include tetrathiafulvalene (TTF) -tetracyanoquinodimethane (TCNQ) complex, bisethylenetetrathiafulvalene (BEDTTTF) -perchlorate complex, BEDTTTF-iodine complex, TCNQ-iodine complex
- TTF tetrathiafulvalene
- BEDTTTF bisethylenetetrathiafulvalene
- TCNQ-iodine complex TCNQ-iodine complex
- Organic molecular complexes such as can also be used.
- ⁇ -conjugated polymers such as polysilane and polygermane can also be used as organic'inorganic hybrid materials described in JP-A-2000-260999.
- thiophene oligomers represented by the following general formula (1) are preferred.
- R represents a substituent
- the thiophene oligomer represented by the general formula (1) will be described.
- examples of the substituent represented by R include an alkyl group (for example, a methyl group, an ethyl group, a propyl group, an isopropyl group, a tert-butyl group, a pentyl group, Xyl group, octyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, etc.), cycloalkyl group (eg, cyclopentyl group, cyclohexyl group, etc.), alkenyl group (eg, bur group, allyl group, etc.) , Alkyl groups (eg, ethynyl group, propargyl group, etc.), aryl groups (eg, phenol group, p-chlorophenol group, mesityl group, tolyl group, xylyl group, naphthyl group, anthryl group) Group, a
- a preferable substituent is an alkyl group, more preferably an alkyl group having 2 to 20 carbon atoms, and particularly preferably an alkyl group having 6 to 12 carbon atoms.
- the terminal group of the thiophene oligomer used in the present invention will be described.
- the terminal group of the thiophene oligomer used in the present invention does not have a chael group.
- an aryl group for example, a phenyl group, p-Chlorofuryl group, mesityl group, tolyl group, xylyl group, naphthyl group, anthryl group, azulyl group, acenaphthyl group, fluoro group, phenanthryl group, indenyl group, pyrenyl group, biphenyl group Etc.
- alkyl group for example, methyl group, ethyl group, propyl group, isopropyl group, tert-butyl group, pentyl group, hexyl group, octyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, etc.
- the thiophene oligomer used in the present invention preferably has no head-to-head structure in the structure, and more preferably, the structure has a head-to-tail structure, or It preferably has a tail-to-tail structure.
- head-to-head structure for example, " ⁇ -electron organic solids” (1998, published by the Japan Society for Publishing Press, Japan This can be referred to on pages 27-32 and Adv. Mater. 1998, 10, No. 2, pages 93-116, etc.
- specific structural features are shown below.
- R has the same meaning as R in the general formula (1).
- the organic semiconductor layer may be formed of a material having a functional group such as acrylic acid, acetamide, dimethylamino group, cyano group, carboxyl group, nitro group, benzoquinone derivative, tetra Cyanethylene and tetracyanoquinodimethane and their Materials that accept electrons, such as derivatives, materials having functional groups such as amino, triphenyl, alkyl, hydroxyl, alkoxy, and phenyl groups, substituted amines such as phenylenediamine , Anthracene, benzoanthracene, substituted benzoanthracene, pyrene, substituted pyrene, force rubazole and its derivatives, tetrathiofulvalene and its derivatives, etc. Processing may be performed.
- a functional group such as acrylic acid, acetamide, dimethylamino group, cyano group, carboxyl group, nitro group, benzoquinone derivative, tetra Cyanethylene and
- the doping means introducing an electron donating molecule (acceptor) or an electron donating molecule (donor) into the thin film as a dopant. Therefore, the doped thin film is a thin film containing the condensed polycyclic aromatic compound and the dopant.
- a well-known thing can be employ
- these organic semiconductor layers can be formed by a known method, for example, vacuum deposition, MBE (Molecular Beam Epitaxy), ion cluster beam method, low energy ion beam method, ion plate. Coating, sputtering, CVD (chemical vapor deposition), laser deposition, electron beam deposition, electrodeposition, spin coating, dip coating, bar coating, die coating, spray coating, LB, etc., and screen printing , Inkjet printing, blade coating, etc.
- MBE Molecular Beam Epitaxy
- ion cluster beam method low energy ion beam method
- ion plate ion plate.
- Coating sputtering, CVD (chemical vapor deposition), laser deposition, electron beam deposition, electrodeposition, spin coating, dip coating, bar coating, die coating, spray coating, LB, etc., and screen printing , Inkjet printing, blade coating, etc.
- the precursor film formed by coating is heat-treated. A thin film of the desired organic material may be formed.
- the film thickness of these organic semiconductor layers is not particularly limited, but the characteristics of the obtained transistor are largely influenced by the film thickness of the organic semiconductor layer. Different forces depending on the conductor Generally 1 ⁇ m or less, particularly 10 to 300 nm is preferred.
- At least one of the gate electrode and the source Z drain electrode is formed by the method for manufacturing an organic semiconductor device of the present invention. Therefore, it is possible to form a low resistance electrode without causing deterioration of characteristics of the organic semiconductor layer material layer.
- the source electrode or the drain electrode is a force formed by the electroless plating method
- one of the source electrode and the drain electrode is an electrode that does not depend on the electroless plating together with the gate electrode. It's okay.
- One of the gate electrode and the source and drain electrodes is formed by a known method and electrode material.
- the electrode material is not particularly limited as long as it is a conductive material.
- conductive polymers whose conductivity has been improved by doping or the like, for example, conductive polyarlin, conductive polypyrrole, conductive polythiophene (polyethylenedioxythiophene and polystyrenesulfonic acid complex, etc.) are also suitable. Used.
- materials with low electrical resistance at the contact surface with the semiconductor layer are preferred as materials for forming the source electrode or drain electrode.
- ⁇ materials with low electrical resistance at the contact surface with the semiconductor layer are preferred.
- the electrode is formed using a fluid electrode material such as a solution, paste, ink, or dispersion liquid containing the above-described conductive material, in particular, a conductive polymer, Alternatively, a fluid electrode material containing fine metal particles containing platinum, gold, silver, and copper is preferable.
- the solvent or dispersion medium is preferably a solvent or dispersion medium containing 60% or more, preferably 90% or more of water in order to suppress damage to the organic semiconductor.
- a known conductive paste may be used as the fluid electrode material containing metal fine particles.
- metal fine particles having a particle diameter of 1 to 50 nm, preferably 1 to: LOnm are used. It is a material dispersed in a dispersion medium that is water or any organic solvent using a dispersion stabilizer as required.
- Materials for the metal fine particles include platinum, gold, silver, nickel, chromium, copper, iron, tin, antimony lead, tantalum, indium, palladium, tellurium, rhenium, iridium, aluminum, ruthenium, germanium, Molybdenum, tungsten, zinc, or the like can be used.
- a metal phase in a liquid phase such as a physical generation method such as a gas evaporation method, a sputtering method or a metal vapor synthesis method, a colloid method or a coprecipitation method is used.
- a chemical production method include reducing metal ions to produce fine metal particles, but preferred are JP-A-11-76800, JP-A-11-80647, JP-A-11-319538, and JP-A-2000-239853. Colloidal method, JP 2001-254185, 2001-53028, 2001-352 55, 2000-124157, 2000-123634, etc. It is.
- An electrode is formed using these metal fine particle dispersions, the solvent is dried, and then heated to a shape in the range of 100 to 300 ° C, preferably 150 to 200 ° C, as necessary. Fine particles are thermally fused to form an electrode pattern having a desired shape.
- a method for forming an electrode a method of forming an electrode using a known photolithographic method or a lift-off method using a conductive thin film formed by a method such as vapor deposition or sputtering using the above as a raw material, aluminum, copper, or the like
- a conductive polymer solution, a dispersion liquid, or a dispersion liquid containing metal fine particles may be directly patterned by an ink jet method, or may be formed from a coating film by lithography, laser abrasion, or the like.
- a method of patterning a conductive ink or conductive paste containing a conductive polymer or metal fine particles by a printing method such as relief printing, intaglio printing, planographic printing, or screen printing can also be used.
- the source electrode and the drain electrode are particularly preferably formed using a photolithographic method.
- a photosensitive resin solution is applied to the entire surface of the layer in contact with the organic semiconductor protective layer. And forming a photosensitive resin layer.
- the same positive and negative photosensitive resins used for patterning the protective layer can be used.
- the solvent for forming the light-sensitive resin coating solution, the method for forming the light-sensitive resin layer, and the like are as described in the patterning of the protective film.
- an abrasion layer which is another photosensitive resin layer, may be used for electrode formation.
- the abrasion layer the same ones as those used for patterning the protective layer can be mentioned.
- Inorganic oxides include silicon oxide, acid aluminum, acid tantalum, titanium oxide, tin oxide, vanadium oxide, barium strontium titanate, barium zirconate titanate, and zirconate zirconate titanate.
- Inorganic nitrides such as silicon nitride and aluminum nitride can also be suitably used.
- Examples of the method for forming the film include vacuum deposition, molecular beam epitaxy, ion cluster beam, low energy ion beam, ion plating, CVD, sputtering, and atmospheric pressure plasma. Dry process, spray coating method, spin coating method, blade coating method, dip coating method, casting method, roll coating method, bar coating method, die coating method and other coating methods, printing and ink jet patterning methods, etc. Can be used depending on the material.
- the wet process includes a method of applying and drying a liquid in which inorganic oxide fine particles are dispersed in an arbitrary organic solvent or water using a dispersion aid such as a surfactant as required, or an oxide precursor. A so-called sol-gel method in which a solution of a body, for example, an alkoxide body is applied and dried is used.
- the atmospheric pressure plasma method described above is preferable.
- the gate insulating layer is composed of an anodic acid film or the anodic acid film and an insulating film.
- the anodized film is preferably sealed.
- the anodized film is formed by anodizing a metal that can be anodized by a known method.
- Examples of the metal that can be treated with anodic acid include aluminum and tantalum, and a known method with no particular limitation can be used for the method of anodic oxidation treatment.
- An oxide film is formed by anodizing.
- any electrolyte solution can be used as long as it can form a porous acid film, and generally, sulfuric acid, phosphoric acid, oxalic acid, chromic acid, boric acid.
- sulfamic acid, benzene sulfonic acid, etc. are mixed acids in which two or more of these are combined, and salts thereof are used.
- the treatment conditions for anodization vary depending on the electrolyte used, and therefore cannot be specified.
- the electrolyte concentration is 1 to 80% by mass
- the electrolyte temperature is 5 to 70 ° C
- the current is Density 0.5-60AZdm 2
- electrolysis time 10 seconds to 5 minutes are appropriate.
- a preferred anodizing treatment is a method in which an aqueous solution of sulfuric acid, phosphoric acid or boric acid is used as the electrolytic solution and the treatment is performed with a direct current, but an alternating current can also be used.
- the concentration of these acids is preferably 5 to 45% by weight.
- Electrolytic treatment with an electrolyte temperature of 20 to 50 ° C and a current density of 0.5 to 20 AZdm 2 is preferred for 20 to 250 seconds! / ,.
- organic compound film polyimide, polyamide, polyester, polyacrylate, photo-radical polymerization system, photopower thione polymerization system photocurable resin, or copolymer containing acrylonitrile component, polybule Phenolic alcohol, polybutyl alcohol, novolac resin, cyano ethyl pullulan and the like can also be used.
- the wet process is preferable.
- the inorganic oxide film and the organic oxide film can be laminated and used together.
- the thickness of these insulating films is generally 50 nm to 3 ⁇ m, preferably 100 nm to 1 ⁇ m.
- an arbitrary surface treatment may be performed on the surface of the gate insulating layer.
- Silane coupling agents such as octadecyltrichlorosilane, trichloromethylsilazane, self-organizing films such as alkane phosphoric acid, alkanesulfonic acid, and alkanecarboxylic acid are preferably used.
- the support material constituting the substrate can be used as ceramic substrates such as glass, quartz, aluminum oxide, sapphire, silicon nitride, and silicon carbide, silicon, germanium, and gallium arsenide.
- a semiconductor substrate such as gallium phosphide or gallium nitrogen, paper, non-woven fabric or the like can be used.
- the support is preferably made of a resin, for example, a plastic film sheet can be used.
- plastic films examples include polyethylene terephthalate (PET), polyethylene naphthalate (PE N), polyether sulfone (PES), polyether imide, polyether ether ketone, poly-phenylene sulfide, polyarylate, polyimide, polycarbonate (PC ), Cellulose triacetate (TAC), cellulose acetate propionate (CAP), and other films.
- PET polyethylene terephthalate
- PE N polyethylene naphthalate
- PES polyether sulfone
- polyether imide polyether ether ketone
- poly-phenylene sulfide polyarylate
- polyimide polyimide
- PC polycarbonate
- TAC Cellulose triacetate
- CAP cellulose acetate propionate
- An element protective layer may be provided on the organic thin film transistor element of the present invention.
- the protective layer include the inorganic oxides or inorganic nitrides described above, and it is preferable to form the protective layer by the atmospheric pressure plasma method described above. This improves the durability of the organic thin film transistor element.
- the support when the support is a plastic film, it has at least one of an undercoat layer containing a compound selected from inorganic oxides and inorganic nitrides, and an undercoat layer containing a polymer. It is preferable.
- Inorganic oxides contained in the undercoat layer include silicon oxide, acid aluminum, acid tantalum, titanium oxide, tin oxide, vanadium oxide, barium strontium titanate, zirconium Barium titanate titanate, lead zirconate titanate, lead lanthanum titanate, strontium titanate, barium titanate, barium magnesium fluoride, bismuth titanate Strontium bismuth titanate, strontium bismuth tantalate, tantalate bismuth butanoate, trioxide yttrium and the like.
- Examples of the inorganic nitride include nitride nitride and aluminum nitride.
- silicon oxide aluminum oxide, tantalum oxide, titanium oxide, and silicon nitride.
- the lower bow I layer containing a compound selected from inorganic oxides and inorganic nitride forces is formed by the atmospheric pressure plasma method described above.
- polyester resin polycarbonate resin, cellulose resin, acrylic resin, polyurethane resin, polyethylene resin, polypropylene resin, polystyrene resin, Phenoxy resin, norbornene resin, epoxy resin, vinyl chloride-vinyl acetate copolymer, vinyl chloride resin, vinyl acetate resin, copolymer of vinyl acetate and vinyl alcohol, partially water-decomposed vinyl chloride -Ruacetate butyl copolymer, salt-bule monosalt-biurydene copolymer, salt butyl-acrylonitrile copolymer, ethylene vinyl alcohol copolymer, polybulu alcohol, chlorinated polysulphated butyl, ethylene Bile monochloride copolymer, ethylene-vinyl acetate copolymer and other vinyl polymers, polyamide resin, ethylene butadiene Down ⁇ , butadiene - Atari port - DOO drill ⁇ rubber such
- FIG. 1 is a diagram showing a configuration example of an organic thin film transistor element of the present invention.
- a source electrode 52 and a drain electrode 53 are formed on a support 56 by a metal foil or the like, and an organic semiconductor layer 51 made of the organic semiconductor material of the present invention is formed between the two electrodes.
- An organic thin film transistor element is formed by forming an insulating layer 55 and further forming a gate electrode 54 thereon.
- FIG. 4B shows the organic semiconductor layer 51 formed between the electrodes in FIG. 5A so as to cover the entire surface of the electrode and the support using a coating method or the like.
- (C) shows that the organic semiconductor layer 51 is first formed on the support 56 using a coating method or the like, and then the source electrode 52, the drain electrode 53, the insulating layer 55, and the gate electrode 54 are formed.
- FIG. 2 shows an organic thin film transistor in which a plurality of organic thin film transistor elements of the present invention are arranged.
- 1 is a schematic equivalent circuit diagram of an example of an element sheet 10.
- the organic thin film transistor sheet 10 has a large number of organic thin film transistor elements 14 arranged in a matrix.
- 11 is a gate bus line of the gate electrode of each organic thin film transistor element 14, and 12 is a source bus line of the source electrode of each organic thin film transistor element 14.
- An output element 16 is connected to the drain electrode of each organic thin film transistor element 14, and the output element 16 is, for example, a liquid crystal, an electrophoretic element or the like, and constitutes a pixel in the display device.
- a liquid crystal is shown as the output element 16 in an equivalent circuit having resistance and capacitor power.
- 15 is a storage capacitor
- 17 is a vertical drive circuit
- 18 is a horizontal drive circuit.
- Fig. 3 shows an example of an actual TFT element sheet arrangement according to the above equivalent circuit.
- an organic thin film transistor sheet TFT
- it is an additional capacitor type.
- 9 ' is the output electrode and 10' is the additional capacitor.
- the semiconductor layer is applied and formed on the entire surface.
- an electrode ⁇ is formed on the 10 additional capacitor portions in the same manner as the gate electrode.
- FIG. 4 (1) shows a resin substrate provided with a gate electrode, a gate insulating layer, an organic semiconductor layer, and a protective film pattern.
- a gate electrode 8 is formed on a resin substrate 1 provided with an undercoat layer 2 which also serves as an insulating layer, and an anodized layer 9 is formed on the electrode surface for increasing the dielectric constant. 7 (for example, an silicon oxide layer), an organic semiconductor layer 6, and a protective film 3 patterned on the organic semiconductor layer.
- Patterning of the protective film is possible by an ink jet method or a printing method.
- a method of applying a photosensitive resin layer, performing pattern exposure to form a resist, and selectively leaving a protective film by washing or the like is preferable.
- the laser (LD) exposure is performed, the abrasion is performed, and the protective layer is removed by development.
- the photosensitive resin layer and the resist formed thereby are directly used as a protective film. It ’s good.
- the electroless plating catalyst solution is ejected by the ink jet (piezo type) method, and the plating catalyst solution is patterned to form the plating catalyst layer Ml (Fig. 4 (2), ( 3)).
- the protective layer covers the portion of the organic semiconductor material film where the channel is formed.
- the resin substrate film is immersed in a plating bath to form a metal thin film M2 on the plating catalyst portion to obtain source and drain electrodes (FIG. 4 (4)).
- the organic semiconductor element manufacturing method of the present invention protects the organic semiconductor protective layer except the electrode formation region, thereby having a low-resistance electrode by an electroless plating method, and It is possible to form a high-performance TFT sheet (organic thin film transistor sheet) without deteriorating the organic semiconductor layer.
- the organic thin film transistor element it is particularly effective to prevent the characteristic change in the region of the organic semiconductor layer constituting the channel.
- (1) in FIG. 5 shows a state in which the gate electrode is formed on the substrate.
- These gate bus lines and gate electrodes were produced as follows.
- As the substrate a PE S (polyether sulfone) resin film was used.
- a coating solution having the following composition was applied to a dry film thickness of 2 m, dried at 90 ° C for 5 minutes, and then cured for 4 seconds from a distance of 10 cm under a 60 WZcm high-pressure mercury lamp.
- an atmospheric pressure plasma treatment was performed on the layer under the following conditions to provide an oxide silicon film having a thickness of 50 nm. These layers were used as the undercoat layer 2.
- Inert gas helium 98.25 volume 0/0
- Reactive gas Oxygen gas 1.5% by volume
- Reactive gas Tetraethoxysilane vapor (published with helium gas) 0.25 vol% (discharge conditions)
- the electrode is coated with lmm of alumina by ceramic spraying on a stainless jacket roll base material having cooling means with cooling water, and then a solution obtained by diluting tetramethoxysilane with ethyl acetate is applied and dried, and then sealed by ultraviolet irradiation.
- This is a roll electrode that has a dielectric (relative permittivity of 10) with a smooth surface and an Rmax of 5 ⁇ m.
- the application electrode a hollow rectangular stainless steel pipe was covered with the same dielectric material under the same conditions.
- Photosensitive resin composition composition 1 On the undercoat layer 2 described above, a photosensitive resin composition solution 1 having the following composition was applied, and 1 at 100 ° C. By drying for 2 minutes, a photosensitive resin layer having a thickness of 2 m was formed. (Photosensitive resin composition composition 1)
- the gate line and gate electrode patterns were exposed with a semiconductor laser having an oscillation wavelength of 830 nm and an output power of lOOmW at an energy density of 200 nijZcm, and then developed with an alkaline aqueous solution to obtain a resist image.
- an anodized film was formed on the gate electrode as an auxiliary insulating film for smoothing and improving insulation.
- a silicon oxide layer having a thickness of 30 nm is provided by the atmospheric pressure plasma method described above, and the above-described anodized aluminum layer is combined to form a gate insulating layer 7 having a thickness of 150 nm. ((2) in FIG. 5).
- an organic semiconductor layer was formed over the gate insulating layer. That is, the Chiofu N'origoma one ⁇ 2> in hexane cyclo a (0.5 mass 0/0) is prepared and by using an ink jet method piezo method, discharged into region for forming a channel, in nitrogen gas The organic semiconductor layer 6 was formed on the substrate by drying at 50 ° C for 3 minutes (Fig. 5 (3)). At this time, the thickness of the semiconductor layer is 20 nm.
- organic semiconductor layer 6 On this organic semiconductor layer 6, a polybutyl alcohol that has been sufficiently purified is applied using an aqueous solution that has been dissolved in water that has been purified by an ultrapure manufacturing apparatus, and at 100 ° C in a nitrogen gas atmosphere. After thoroughly drying, an organic semiconductor protective layer 3 of polyvinyl alcohol having a thickness of 1 ⁇ m was formed ((1) in FIG. 6).
- composition 1 was kneaded and dispersed, and then 5.90 parts of polyisocyanate compound (Nippon Polyurethane Industry Co., Ltd., Coronate 3041; active ingredient 50%) was added and stirred with a dissolver. Coating solution 1 was prepared.
- Salt-bulb-based resin manufactured by Nippon Zeon Co., Ltd., MR-110) 10.0 parts Polyurethane resin (manufactured by Toyobo Co., Ltd., Byron UR-8200) 5.0 parts Phosphate ester (Toho Chemical Industries) Phosphanol RE610, manufactured by Co., Ltd.] 3.0 parts Methyl ethyl cane 105.0 parts
- Composition 1 was applied on protective layer 3 and treated at 100 ° C. for 5 minutes to form a photosensitive layer 3 ′ having a thickness of 0.3 m.
- the adhesion between the photosensitive layer 3 ′ and the electrode material repellent layer 3 mm is changed, and the exposed silicone rubber layer is brushed. Removed by processing.
- hydrochloric acid solution of palladium chloride (palladium chloride 1 wt%, hydrochloric acid 10 mass 0/0, isopropyl alcohol 20 wt 0/0, poly Bulle alcohol 1 wt% aqueous solution) was used.
- a source solution and a drain electrode were formed by a thin metal film M2 having a thickness of lOnm. After forming the electrode, it was thoroughly washed and dried to form a thin film transistor (Fig. 8).
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Thin Film Transistor (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
Description
Claims
Priority Applications (3)
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US11/989,912 US7816263B2 (en) | 2005-08-03 | 2006-07-18 | Method for manufacturing thin film transistor |
JP2007529202A JPWO2007015364A1 (ja) | 2005-08-03 | 2006-07-18 | 薄膜トランジスタの製造方法 |
GB0801632A GB2443577B (en) | 2005-08-03 | 2008-01-30 | Method for manufacturing thin film transistor |
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JP2005225288 | 2005-08-03 | ||
JP2005-225288 | 2005-08-03 |
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US (1) | US7816263B2 (ja) |
JP (1) | JPWO2007015364A1 (ja) |
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WO (1) | WO2007015364A1 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008258592A (ja) * | 2007-03-09 | 2008-10-23 | Hiroshima Univ | 電界効果トランジスタ |
JP2010525587A (ja) * | 2007-04-25 | 2010-07-22 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 電子装置の製造方法 |
JP2011187626A (ja) * | 2010-03-08 | 2011-09-22 | Sony Corp | 薄膜トランジスタおよび電子機器 |
JP2016051758A (ja) * | 2014-08-29 | 2016-04-11 | 国立大学法人 東京大学 | 電極形成方法 |
Families Citing this family (3)
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US8410600B2 (en) | 2009-10-02 | 2013-04-02 | Arkansas Power Electronics International, Inc. | Semiconductor device with protecting film and method of fabricating the semiconductor device with protecting film |
TWI692546B (zh) * | 2013-11-21 | 2020-05-01 | 日商尼康股份有限公司 | 佈線圖案之製造方法及電晶體之製造方法 |
JP6926939B2 (ja) * | 2017-10-23 | 2021-08-25 | 東京エレクトロン株式会社 | 半導体装置の製造方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004158805A (ja) * | 2002-11-08 | 2004-06-03 | Asahi Kasei Corp | 有機半導体素子の製造方法及び有機半導体素子 |
JP2004221573A (ja) * | 2002-12-26 | 2004-08-05 | Konica Minolta Holdings Inc | 電気回路の製造方法、有機薄膜トランジスタ素子の製造方法、これらの製造方法で製造された電気回路、有機薄膜トランジスタ素子及び有機薄膜トランジスタ素子シート |
Family Cites Families (4)
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US6452207B1 (en) * | 2001-03-30 | 2002-09-17 | Lucent Technologies Inc. | Organic semiconductor devices |
JP2004221334A (ja) * | 2003-01-15 | 2004-08-05 | Seiko Epson Corp | 金属素子形成方法、半導体装置の製造方法及び電子デバイスの製造方法、半導体装置及び電子デバイス、並びに電子機器 |
JP4415653B2 (ja) * | 2003-11-19 | 2010-02-17 | セイコーエプソン株式会社 | 薄膜トランジスタの製造方法 |
US7732330B2 (en) * | 2005-06-30 | 2010-06-08 | Semiconductor Energy Laboratory Co., Ltd. | Semiconductor device and manufacturing method using an ink-jet method of the same |
-
2006
- 2006-07-18 WO PCT/JP2006/314145 patent/WO2007015364A1/ja active Application Filing
- 2006-07-18 US US11/989,912 patent/US7816263B2/en not_active Expired - Fee Related
- 2006-07-18 JP JP2007529202A patent/JPWO2007015364A1/ja active Pending
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2004158805A (ja) * | 2002-11-08 | 2004-06-03 | Asahi Kasei Corp | 有機半導体素子の製造方法及び有機半導体素子 |
JP2004221573A (ja) * | 2002-12-26 | 2004-08-05 | Konica Minolta Holdings Inc | 電気回路の製造方法、有機薄膜トランジスタ素子の製造方法、これらの製造方法で製造された電気回路、有機薄膜トランジスタ素子及び有機薄膜トランジスタ素子シート |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008258592A (ja) * | 2007-03-09 | 2008-10-23 | Hiroshima Univ | 電界効果トランジスタ |
JP2010525587A (ja) * | 2007-04-25 | 2010-07-22 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 電子装置の製造方法 |
KR101475097B1 (ko) * | 2007-04-25 | 2014-12-23 | 메르크 파텐트 게엠베하 | 전자 디바이스의 제조 방법 |
JP2011187626A (ja) * | 2010-03-08 | 2011-09-22 | Sony Corp | 薄膜トランジスタおよび電子機器 |
JP2016051758A (ja) * | 2014-08-29 | 2016-04-11 | 国立大学法人 東京大学 | 電極形成方法 |
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US20100105161A1 (en) | 2010-04-29 |
GB2443577B (en) | 2011-02-23 |
GB2443577A (en) | 2008-05-07 |
GB0801632D0 (en) | 2008-03-05 |
US7816263B2 (en) | 2010-10-19 |
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