WO1999010939A9 - A method of manufacturing a field-effect transistor substantially consisting of organic materials - Google Patents

A method of manufacturing a field-effect transistor substantially consisting of organic materials

Info

Publication number
WO1999010939A9
WO1999010939A9 PCT/IB1998/001144 IB9801144W WO9910939A9 WO 1999010939 A9 WO1999010939 A9 WO 1999010939A9 IB 9801144 W IB9801144 W IB 9801144W WO 9910939 A9 WO9910939 A9 WO 9910939A9
Authority
WO
WIPO (PCT)
Prior art keywords
layer
organic
electrically insulating
electrode layer
electrode
Prior art date
Application number
PCT/IB1998/001144
Other languages
French (fr)
Other versions
WO1999010939A3 (en
WO1999010939A2 (en
Inventor
Cornelis Marcus Johan Mutsaers
Leeuw Dagobert Michel De
Christopher John Drury
Original Assignee
Koninkl Philips Electronics Nv
Philips Svenska Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Koninkl Philips Electronics Nv, Philips Svenska Ab filed Critical Koninkl Philips Electronics Nv
Priority to EP98932464A priority Critical patent/EP0968537B1/en
Priority to JP51409999A priority patent/JP4509228B2/en
Publication of WO1999010939A2 publication Critical patent/WO1999010939A2/en
Publication of WO1999010939A3 publication Critical patent/WO1999010939A3/en
Publication of WO1999010939A9 publication Critical patent/WO1999010939A9/en

Links

Classifications

    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/10Organic polymers or oligomers
    • H10K85/111Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K10/00Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having a potential-jump barrier or a surface barrier
    • H10K10/40Organic transistors
    • H10K10/46Field-effect transistors, e.g. organic thin-film transistors [OTFT]
    • H10K10/462Insulated gate field-effect transistors [IGFETs]
    • H10K10/468Insulated gate field-effect transistors [IGFETs] characterised by the gate dielectrics
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/10Organic polymers or oligomers
    • H10K85/111Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
    • H10K85/113Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K10/00Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having a potential-jump barrier or a surface barrier
    • H10K10/40Organic transistors
    • H10K10/46Field-effect transistors, e.g. organic thin-film transistors [OTFT]
    • H10K10/462Insulated gate field-effect transistors [IGFETs]
    • H10K10/464Lateral top-gate IGFETs comprising only a single gate
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/10Organic polymers or oligomers

Definitions

  • a method of manufacturing a field-effect transistor substantially consisting of organic materials is a method of manufacturing a field-effect transistor substantially consisting of organic materials.
  • the invention relates to a method of manufacturing a field-effect transistor substantially consisting of organic materials.
  • the invention also relates to a field-effect transistor substantially consisting of organic materials.
  • the invention further relates to an integrated circuit (IC) comprising such a field-effect transistor (FET).
  • IC integrated circuit
  • FET field-effect transistor
  • An integrated circuit comprising field-effect transistors substantially consisting of organic materials, in short organic field-effect transistors, is well suited for those electronic applications where using an integrated circuit manufactured using silicon technology would be prohibitively expensive. Examples include electronic bar codes.
  • each individual field-effect transistor must be operated in a saturated regime, which is the regime where the channel transconductance exceeds the channel conductance.
  • a method of the type mentioned in the opening paragraph, which provides an organic FET satisfying said condition for voltage amplification is known from an article by Gamier et al. published in Science, vol. 265 (1994), pp. 1684-1686.
  • a 1.5 ⁇ m thick polyester film is framed and is printed on both sides with a graphite- filled polymer ink, so as to form a 10 ⁇ m thick gate electrode on the one side and a source and drain electrode on the other side.
  • a 40 nm semiconducting sexithiophene layer is then deposited using flash evaporation.
  • a disadvantage of the known method is that the organic FETs provided by the method satisfy the condition for voltage amplification only at rather high (negative) source drain voltages. Typically, the difference is 30 V or higher. For many electronic applications, such as battery operated applications, such a voltage is too high. Also, the method is not very practical, not least because it involves framing and printing on a layer of only 1.5 ⁇ m. Such a thin film is very fragile and easily ruptures while being handled, leading to a defective device.
  • An object of the invention is, inter alia, to provide a novel method of manufacturing a field-effect transistor substantially consisting of organic materials. The novel method should enable, in a practical manner, the manufacture of an organic FET satisfying the condition of voltage amplification at a source drain voltage difference significantly less than 30 V, in particular less than 10 V.
  • the object of the invention is achieved by a method of manufacturing a field-effect transistor substantially consisting of organic materials on a substrate surface, said method comprising the steps of: - providing an electrically insulating substrate surface,
  • the invention is based on the insight that a very thin electrically insulating layer, that is a layer having a thickness of 0.3 ⁇ m or less, is required if an organic FET is to satisfy the condition of voltage amplification at a source drain voltage difference of less than 10 V. It is further based on the insight that such a thin insulating layer can only be obtained in a practical manner if (in contrast to the known method in which the insulating layer is used as a substrate for depositing the electrodes) the thin insulating layer is supported by a substrate throughout the manufacture of the FET. Most conveniently, the insulating layer is applied to a surface which is substantially planar.
  • the first electrode layer in the form of a patchwork pattern of electrically insulating and conducting areas provides a substantially planar surface (the difference in thickness between the insulating and conducting areas being 0.05 ⁇ m or less).
  • the method in accordance with the invention is simple and cost effective.
  • the first and second electrode layer, as well as the insulating and semiconducting layer, can be, and preferably are, all applied from solution using coating techniques known per se, such as spin-coating, dip-coating, spray-coating, curtain-coating, silkscreen-printing, offset-printing, Langmuir Blodgett and the doctor blade technique.
  • the field-effect transistor obtained by employing the method in accordance with the invention operates in the usual manner.
  • the semiconducting layer comprises an area, the channel, which interconnects the source and the drain electrode.
  • the gate electrode is electrically insulated from the channel by means of the insulating layer and overlaps the channel. If a voltage is applied between the source and drain electrode, a current, i.e.
  • the source drain current will flow through the channel.
  • a gate voltage By applying a gate voltage, an electric field is established across the semiconducting layer which will, depending on the polarity of both the gate voltage and the charge carriers, modify the free charge carrier distribution in the channel, thereby changing the resistivity of the channel and the source drain current. If the source drain voltage is increased while the gate voltage is kept constant, the source drain current will begin to saturate and at some point the condition of voltage amplification, i.e. the channel transconductance exceeding the channel conductance, is satisfied.
  • the first electrode layer comprises electrically insulating and conducting areas, which may be of any convenient shape.
  • the source and drain electrode are accommodated by separate conducting areas. In order to increase the channel width, thus allowing more current between source and drain, the source and drain electrode are preferably interdigitated.
  • the sheet resistance of the insulating areas needs to be as high as possible.
  • a suitable sheet resistance exceeds 10 10 ⁇ /square, or better 10 12 ⁇ /square or better still 10 13 ⁇ /square.
  • the specific conductivity of the conducting areas of the electrode layer is chosen such that the source drain current is substantially determined by the resistivity of the channel.
  • a suitable specific conductivity of the conducting areas is 0.1 S/cm or better 1 S/cm or better still more than 10 S/cm.
  • Applying the patchwork patterned first electrode layer is for example done by applying a semiconducting polymer in an insulating state from solution, applying and patterning a photoresist layer photolithographically and introducing conducting areas by selective indiffusion of a dopant which converts locally the polymer from its insulating to a conducting state.
  • the patchwork patterned first electrode layer is applied without using the elaborate technique of photolithography.
  • the organic first electrode is applied by performing the method steps of
  • a radiation-sensitive layer comprising an electrically conducting polyaniline and a photochemical radical initiator.
  • a layer may be rendered radiation insensitive by a simple heat treatment at for example 110 0 C. This property is very advantageous if an IC is to be manufactured, especially if multi level interconnects are required, for it allows the second (and any further) electrode layer to be patchwork patterned employing the same radiation-sensitive composition and method steps without the pattern of the first electrode layer being affected by the radiation employed in providing said second electrode layer.
  • Suitable semiconducting layers comprise organic compounds having an extensive conjugated system of double and/or triple bonds such as conjugated polymers (in the context of the invention, the term polymer includes oligomer) and fused (heterosubstituted) polycyclic hydrocarbons. Examples include polypyrroles, polypheny lenes, polythiophenes, polyphenylenevinylenes, poly(di)acetylenes, polyfuranes and polyanilines. As known by those skilled in the art, such compounds may be rendered semiconducting by doping with an oxidizing agent, reducing agent and/or (Bronsted) acid. It may happen that the method of preparing the semiconducting compound is such that the compound is obtained in the semiconducting state without explicitly adding a dopant, in which case the compound is said to be unintentionally doped.
  • the semiconducting layer may swell or even, dissolve into the subsequent layer before the solvent is removed, thus ruining the definition of the interface.
  • an insoluble semiconducting compound obtainable from a soluble precursor compound. Examples of such compounds, viz. a polythienylenevinylene and a pentacene, are described in a publication by Brown et al. in Science, vol. 270, (1995), pp. 972-974.
  • an organic electrically insulating layer is applied which electrically insulates the gate electrode from the semiconducting layer.
  • the electrically insulating layer preferably has a high capacitance so as to induce a large current between source and drain using a low gate voltage which is accomplished by using a material with a large dielectric constant and/ or a small layer thickness.
  • the thickness of the insulating layer is preferably more than 0.05 ⁇ m.
  • a preferred embodiment of the method in accordance with the invention is therefore characterized in that the organic electrically insulating layer comprises a cross-linked polymer.
  • a cross-linkable polymer which has been found very effective is a polyvinylphenol. It can be cross-linked by adding a cross-linking agent such as hexamethoxymethylenernelamine and heating.
  • the organic FET is completed by applying a second electrode layer accommodating a gate electrode.
  • the insulating layer already being in place, the (variation in) layer thickness and the deposition process is less critical.
  • the second electrode layer can be suitably applied using the method disclosed in the article by Garnier et al. cited hereinabove, that is, printing of a graphite filled polymer ink.
  • a method of manufacturing the organic FET which is more economical and allows a higher resolution, results if the second electrode is applied in the same manner as the first electrode layer.
  • the method involves providing an electrically insulating substrate surface.
  • the surface should be planar and smooth.
  • Suitable substrates are ceramics, glass, silica or, preferably, (laminated) polymer foils such as polystyrene, polyamide, polyamide and polyester foils. If a first electrode layer comprising conductive polyaniline and a photochemical radical initiator is applied, the substrate surface preferably comprises (cross- linked) polyvinylphenol or polyvinylalcohol.
  • a preferred embodiment of the method in accordance with the invention is the method according to Claim 5.
  • This method has been found particularly suitable in that each time a subsequent layer is applied from solution, swelling or dissolution of the preceding layer does not occur.
  • the method moreover allows FETs having a channel length as small as 1 to 2 ⁇ m to be produced in a reliable and practical manner.
  • a field-effect transistor manufactured using the method in accordance the invention is operated for a long time (for minutes to hours) at high source drain voltage differences, there is a risk that the performance of the FET deteriorates to the extent that it does no longer satisfy the condition for voltage amplification at voltages below 10 V.
  • a preferred embodiment of the method in accordance with the invention is characterized in that before the semiconducting layer is applied, the electrically insulating areas of the first electrode layer are removed, thereby forming a first electrode layer demonstrating a relief pattern of conducting areas.
  • the first electrode layer comprises polyaniline
  • removal can be achieved, for example, by dissolving selectively the electrically insulating areas in N- methylpyrrolidone .
  • the presence of a relief pattern does not lead to a dramatic increase in leakage current or short circuits between the source (drain) and gate electrode. At least this is found to be the case if the thickness of the first electrode layer is chosen to be smaller than the thickness of the insulating layer.
  • a relief pattern satisfying this criterion provides a surface which is more or less planar from the viewpoint of the capability of said surface to serve as a substrate surface onto which a very thin insulating layer can be applied in a practical manner.
  • the FET obtained by employing (preferred embodiments of) the method in accordance with the invention is a top gate field-effect transistor.
  • the method in accordance with the invention is simply modified in that the gate electrode is accommodated by the first and the source and drain electrodes are accommodated by the second electrode layer, and the semiconducting and electrically insulating layer are applied in reverse order.
  • Yet another bottom gate FET is obtained if the method of manufacturing the bottom gate FET is modified in that the second electrode and semiconducting layer are applied in reverse order.
  • the invention also relates to a field-effect transistor substantially consisting of organic materials, that is a field-effect transistor comprising a stack of: an organic first electrode layer accommodating a source and drain electrode and demonstrating a relief pattern of electrically conducting areas, an organic semiconducting layer, an organic electrically insulating layer, and an organic second electrode layer accommodating a gate electrode.
  • the field-effect transistor is therefore characterized in that the thickness of the electrically insulating layer is greater than the thickness of the first and/or second electrode layer and less than 0.3 ⁇ m. It is clear that applying a 0.3 ⁇ m layer on a 0.3 ⁇ m topography results in an insulating layer which is neither planar nor planarized. Surprisingly, the use of planarised insulating layers appears to be superfluous.
  • Short circuits are substantially absent if the surface defined by the first and/or second electrode layer has a topography smaller than the layer thickness of the insulating layer to be applied to that surface.
  • the insulating layer should have a thickness less than 0.3 ⁇ m. Since the insulating layer may be far from planar, the layer thickness is defined as the thickness that would have been obtained if, using the same method, it had been applied onto a planar surface.
  • a field-effect transistor substantially consisting of organic materials is disclosed.
  • Said document does not disclose a method of manufacturing such a device, let alone a practical method producing a field-effect transistor which satisfies the condition for voltage amplification below a source drain voltage of 10 V.
  • the known field-effect transistor does not have a patchwork patterned electrode layer and the thickness of the planarized insulating layer is not specified.
  • the invention also relates to an integrated circuit comprising a field-effect transistor in accordance with the invention or a field-effect transistor obtainable by a method in accordance with the invention.
  • Changing the pattern of the first and second electrode layer is all that needs to be done if not just one but a plurality of organic FETs is to be produced on a single substrate surface.
  • Fig. 1 schematically shows a transparent plan view of a field-effect transistor manufactured using the method in accordance with the invention
  • Fig. 2 schematically shows a cross-sectional view taken on the line I-I in Fig. 1, and
  • Fig. 3 shows a graph of the relationship between the source drain voltage V sd (in V) and the source drain current I sd (in iiA) at specified gate voltages V g (in V) of a field-effect transistor manufactured using the method in accordance with the invention when subjected to a source drain voltage sweep from 0 to -10 V and back.
  • Fig. 1 schematically shows (not drawn to scale) a transparent plan view of a (part of a) field-effect transistor 1 manufactured using the method in accordance with the invention.
  • Fig. 2 schematically shows (not drawn to scale) the field-effect transistor 1 in a cross-sectional view taken on the line I-I in Fig. 1.
  • the field-effect transistor 1 comprises an electrically insulating substrate 2 on which is provided an organic first electrode layer 3 demonstrating a patchwork pattern of electrically insulating areas 31 and conducting areas 32 and 33.
  • the conductive area 32 accommodates the source and the area 33 the drain electrode.
  • the organic semiconducting layer 4 comprises a channel 41 (drawn so as to indicate the definition of channel length and width), of which the channel length L is indicated by reference number 411 and the channel width W by reference number 412. Covering the layer 4 and thus the channel 41 is the organic electrically insulating layer 5. It electrically insulates the gate electrode from the channel 41, said gate electrode being accommodated by the electrically conducting area 62 of the second electrode layer 6.
  • the layer 6 is a layer demonstrating a patchwork pattern of electrically insulating areas 61 and conducting areas 62.
  • the field- effect transistor 1 may be manufactured as follows: A) preparation of a conducting polyaniline solution
  • Emeraldine base polyaniline (Neste) (0.7 g, 7.7 mmol) and camphor sulphonic acid (Janssen) (0.8 g, 3.4 mmol) are ground together with a mortar and pestle in a nitrogen-filled glove box.
  • the mixture is split in two and placed in two 30 ml polyethylene bottles each containing 30 g m-cresol and three agate balls (0.9 mm diameter). These are placed in a shaker (Retsch MM2) operating at full speed for 14 to 18 hours.
  • the contents of the bottles are combined and then sonified for 5 minutes.
  • the mixture is cooled to room temperature and then the sonification process is repeated. This mixture is then centrifuged at 12500 rpm for 2 hours.
  • the conducting polyaniline solution thus obtained is pipetted off leaving any solids at the bottom of the centrifuge tubes.
  • a quantity of 10.0 g (0.028 mol) 2,5-thienylenedimethylene- bis(tetrahydrothiophenium chloride) (supplier Syncom BV, Groningen, The Netherlands) is dissolved in 100 ml of a 2/1 v/v mixture of methanol and demineralised water and cooled to -22 0 C in a nitrogen environment.
  • Pentane (120 ml) is added and then sodium hydroxide (1.07 g, 0.0268 mol) dissolved in 100 ml of a 2/1 v/v mixture of methanol and demineralised water and cooled to -22 0 C is added instantaneously to the stirred monomer solution kept at -22 0 C.
  • a 65 ⁇ m polyamide foil (supplier Sellotape) is secured on a 3 inch silicon wafer.
  • the photochemical radical initiator 1 -hydroxy cyclohexyl phenyl ketone (tradename Irgacure 184, Ciba Geigy) is added 6 g of the conducting polyaniline solution prepared under A. After mixing well and sonifying twice for 1 min and cooling in between, the radiation- sensitive solution thus obtained is cooled and filtered (Millex FA, 1 ⁇ m). A radiation-sensitive layer is then formed by spin-coating (3 s/500 rpm, 7 s/2000 rpm) 1 ml of the radiation-sensitive solution on the polyvinylphenol coated surface of the substrate 2, and drying on a hotplate (2 min at 90 0 C).
  • the wafer is placed in a Karl Suss MJB3 aligner equipped with a 500 W Xe lamp and flushed with nitrogen for 3 min.
  • the radiation-sensitive layer is irradiated via the mask with deep XJV light (60 s, 20 mW/cm 2 at 240 nm), thereby forming a first electrode layer 3 demonstrating a patchwork pattern of irradiated areas 31 and non- irradiated areas 32 and 33.
  • the wafer is then heated on a hotplate (3 min at 110 0 C, 1 min at 15O 0 C) so as to remove the unreacted photochemical radical initiator.
  • the layer 3 is now insensitive to the deep UV light used in the irradiation and substantially planar, the thickness of the irradiated areas being 0.25 ⁇ m, and of the non-irradiated areas 0.22 ⁇ m.
  • the sheet resistance of the area 31 is 4 x 10 13 ⁇ /square (conductivity 10 "9 S/cm), of the areas 32 and 33 it is 760 ⁇ /square (conductivity 60 S/cm).
  • 3 ml precursor polythienylenevinylene solution prepared under B is spin-coated (3 s/500 rpm, 7 s/1000 rpm) on the layer 3.
  • This precursor layer is then heated on a hot plate at 150 0 C for 10 min in a nitrogen atmosphere containing HCl gas at a partial pressure of 2.3 x 10 '3 bar, thus converting the precursor layer into a 50 nm thick semiconducting layer 4 comprising a polythienylenevinylene.
  • a cross-linkable composition consisting of 4.0 g (0.034 mol) polyvinylphenol (Polysciences Inc., cat #6527) and 0.65 g (1.66 mmol) hexamethoxymethylenemelamine (Cymel 300 from Cyanamid) dissolved in 36 g propylene glycol methyl ether acetate (Aldrich), is spin-coated (3 s/500 rpm, 27 s/2500rpm) on the layer 4 and dried at 110 0 C for 1 min on a hotplate.
  • a cross-linkable composition consisting of 4.0 g (0.034 mol) polyvinylphenol (Polysciences Inc., cat #6527) and 0.65 g (1.66 mmol) hexamethoxymethylenemelamine (Cymel 300 from Cyanamid) dissolved in 36 g propylene glycol methyl ether acetate (Aldrich), is spin-coated (3 s/500 rpm, 27 s/2500r
  • the dielectric constant of the cross-linked polyvinylphenol is 4.78 and its conductivity (at 1 kHz) 4.4 x 10 "11 S/cm.
  • a second electrode layer 6 is applied on the layer 5.
  • the second electrode layer 6 demonstrates a patchwork pattern of irradiated electrically insulating areas 61 and non-irradiated electrically conducting areas 62 (only one area shown), the latter areas accommodating the gate electrodes.
  • FET 1 is covered by a 0.5 ⁇ n encapsulation layer obtained by spin-coating (3 s/500 rpm, 7 s/2000 rpm) a filtered (Millex LS 5 ⁇ m) solution of 1.5 g (0.028 mol) polyacrylonitrile (Polysciences Inc., cat# 3914) in 38.5 g N-methylpyrrolidone and drying at 110 0 C for 1 min.
  • a solution of 25 g polyvinylidenefluoride (Polysciences Inc, cat #15190) in 25 g N-methylpyrrolidone may be used.
  • Fig. 3 shows a graph of the relationship between the source drain voltage V sd (in V) and the source drain current I sd (in nA) at specified gate voltages V g (in V) of a field-effect transistor 1, manufactured using the method of exemplary embodiment 1, when subjected to a source drain voltage sweep from 0 to -10 V and back.
  • the channel length L equals 2 ⁇ m and the channel width W equals 1 mm.
  • the channel transconductance exceeds the channel conductance, thus satisfying the condition for voltage amplification.
  • the voltage sweep shows a substantially negligible hysteresis.
  • the FET mobility is 10 "4 cm 2 /Vs.
  • the method of exemplary embodiment 1 is repeated, with this difference that the patchwork patterned first electrode layer 3 is replaced by an electrode layer demonstrating a relief pattern.
  • the relief pattern consists of 0.25 ⁇ m thick gold areas obtained by means of vacuum deposition using a shadow mask. The gold areas which accommodate the source and drain electrode are located such that the channel width is 10 mm and the channel length is 10 ⁇ m.
  • the field-effect transistor obtained in this embodiment does not substantially consist of organic materials, and as such is not a FET in accordance with the invention, it does demonstrate that, in accordance with the invention, a FET may satisfy the condition for voltage amplification below 10 V if a relief pattern is used which has a topography (in casu 0.25 ⁇ m) less than the thickness of the insulating layer (in casu 0.27 ⁇ m).

Abstract

A practical method of manufacturing an organic field-effect transistor is disclosed. By applying the insulating layer having a thickness of 0.3 νm or less to a substantially planar electrode layer, an organic field-effect transistor can be made having a channel length down to 2 νm, satisfying the condition for voltage amplification at voltages well below 10 V, and having an on/off ratio of about 25.

Description

A method of manufacturing a field-effect transistor substantially consisting of organic materials.
The invention relates to a method of manufacturing a field-effect transistor substantially consisting of organic materials.
The invention also relates to a field-effect transistor substantially consisting of organic materials. The invention further relates to an integrated circuit (IC) comprising such a field-effect transistor (FET).
An integrated circuit comprising field-effect transistors substantially consisting of organic materials, in short organic field-effect transistors, is well suited for those electronic applications where using an integrated circuit manufactured using silicon technology would be prohibitively expensive. Examples include electronic bar codes.
As is well known by those skilled in the art, if an IC is to perform its task, it is imperative that the integrated logic gates, such as invertors, NOR and NAND gates, attain voltage amplification at the operating voltage. In order to attain voltage amplification, each individual field-effect transistor must be operated in a saturated regime, which is the regime where the channel transconductance exceeds the channel conductance.
A method of the type mentioned in the opening paragraph, which provides an organic FET satisfying said condition for voltage amplification is known from an article by Gamier et al. published in Science, vol. 265 (1994), pp. 1684-1686. In said known method a 1.5 μm thick polyester film is framed and is printed on both sides with a graphite- filled polymer ink, so as to form a 10 μm thick gate electrode on the one side and a source and drain electrode on the other side. Between the source and drain a 40 nm semiconducting sexithiophene layer is then deposited using flash evaporation.
A disadvantage of the known method is that the organic FETs provided by the method satisfy the condition for voltage amplification only at rather high (negative) source drain voltages. Typically, the difference is 30 V or higher. For many electronic applications, such as battery operated applications, such a voltage is too high. Also, the method is not very practical, not least because it involves framing and printing on a layer of only 1.5 μm. Such a thin film is very fragile and easily ruptures while being handled, leading to a defective device. An object of the invention is, inter alia, to provide a novel method of manufacturing a field-effect transistor substantially consisting of organic materials. The novel method should enable, in a practical manner, the manufacture of an organic FET satisfying the condition of voltage amplification at a source drain voltage difference significantly less than 30 V, in particular less than 10 V.
The object of the invention is achieved by a method of manufacturing a field-effect transistor substantially consisting of organic materials on a substrate surface, said method comprising the steps of: - providing an electrically insulating substrate surface,
- applying an organic first electrode layer accommodating a source and drain electrode and demonstrating a patchwork pattern of electrically insulating and conducting areas,
- applying an organic semiconducting layer,
- applying an organic electrically insulating layer having a thickness less than 0.3 μm, - applying an organic second electrode layer accommodating a gate electrode.
Using the method in accordance with the invention, it is possible to manufacture FETs satisfying the condition of voltage amplification at source drain voltages below 10 V, for example, about 2.5 V.
The invention is based on the insight that a very thin electrically insulating layer, that is a layer having a thickness of 0.3 μm or less, is required if an organic FET is to satisfy the condition of voltage amplification at a source drain voltage difference of less than 10 V. It is further based on the insight that such a thin insulating layer can only be obtained in a practical manner if (in contrast to the known method in which the insulating layer is used as a substrate for depositing the electrodes) the thin insulating layer is supported by a substrate throughout the manufacture of the FET. Most conveniently, the insulating layer is applied to a surface which is substantially planar. Manufacturing the first electrode layer in the form of a patchwork pattern of electrically insulating and conducting areas provides a substantially planar surface (the difference in thickness between the insulating and conducting areas being 0.05 μm or less). The method in accordance with the invention is simple and cost effective.
It involves few steps. The first and second electrode layer, as well as the insulating and semiconducting layer, can be, and preferably are, all applied from solution using coating techniques known per se, such as spin-coating, dip-coating, spray-coating, curtain-coating, silkscreen-printing, offset-printing, Langmuir Blodgett and the doctor blade technique. The field-effect transistor obtained by employing the method in accordance with the invention operates in the usual manner. The semiconducting layer comprises an area, the channel, which interconnects the source and the drain electrode. The gate electrode is electrically insulated from the channel by means of the insulating layer and overlaps the channel. If a voltage is applied between the source and drain electrode, a current, i.e. the source drain current, will flow through the channel. By applying a gate voltage, an electric field is established across the semiconducting layer which will, depending on the polarity of both the gate voltage and the charge carriers, modify the free charge carrier distribution in the channel, thereby changing the resistivity of the channel and the source drain current. If the source drain voltage is increased while the gate voltage is kept constant, the source drain current will begin to saturate and at some point the condition of voltage amplification, i.e. the channel transconductance exceeding the channel conductance, is satisfied.
The first electrode layer comprises electrically insulating and conducting areas, which may be of any convenient shape. The source and drain electrode are accommodated by separate conducting areas. In order to increase the channel width, thus allowing more current between source and drain, the source and drain electrode are preferably interdigitated.
In order to minimize the leakage current and the voltage drop between separate conducting areas, in particular between the source and drain electrodes, the sheet resistance of the insulating areas needs to be as high as possible. A suitable sheet resistance exceeds 1010 Ω/square, or better 1012 Ω/square or better still 1013 Ω/square.
The specific conductivity of the conducting areas of the electrode layer is chosen such that the source drain current is substantially determined by the resistivity of the channel. A suitable specific conductivity of the conducting areas is 0.1 S/cm or better 1 S/cm or better still more than 10 S/cm.
Applying the patchwork patterned first electrode layer is for example done by applying a semiconducting polymer in an insulating state from solution, applying and patterning a photoresist layer photolithographically and introducing conducting areas by selective indiffusion of a dopant which converts locally the polymer from its insulating to a conducting state.
Preferably, the patchwork patterned first electrode layer is applied without using the elaborate technique of photolithography. This is achieved by an embodiment of the method in accordance with the invention which is characterized in that the organic first electrode is applied by performing the method steps of
- applying an organic radiation-sensitive layer,
- irradiating said radiation-sensitive layer according to a desired pattern, thereby forming an organic first electrode layer accommodating a source and drain electrode and demonstrating a patchwork pattern of irradiated electrically insulating and non-irradiated conducting areas.
Examples of radiation-sensitive layers which have been found effective in the context of the present invention, are disclosed in United States patent specifications US 5,620,800 and US 5,447,824.
Within the context of the present invention, use is preferably made of a radiation-sensitive layer comprising an electrically conducting polyaniline and a photochemical radical initiator. Surprisingly, it has been found that such a layer may be rendered radiation insensitive by a simple heat treatment at for example 110 0C. This property is very advantageous if an IC is to be manufactured, especially if multi level interconnects are required, for it allows the second (and any further) electrode layer to be patchwork patterned employing the same radiation-sensitive composition and method steps without the pattern of the first electrode layer being affected by the radiation employed in providing said second electrode layer.
Onto the first electrode layer an organic semiconducting layer is applied. Suitable semiconducting layers comprise organic compounds having an extensive conjugated system of double and/or triple bonds such as conjugated polymers (in the context of the invention, the term polymer includes oligomer) and fused (heterosubstituted) polycyclic hydrocarbons. Examples include polypyrroles, polypheny lenes, polythiophenes, polyphenylenevinylenes, poly(di)acetylenes, polyfuranes and polyanilines. As known by those skilled in the art, such compounds may be rendered semiconducting by doping with an oxidizing agent, reducing agent and/or (Bronsted) acid. It may happen that the method of preparing the semiconducting compound is such that the compound is obtained in the semiconducting state without explicitly adding a dopant, in which case the compound is said to be unintentionally doped.
In case a subsequent layer is to be provided from solution using a solvent, the semiconducting layer may swell or even, dissolve into the subsequent layer before the solvent is removed, thus ruining the definition of the interface. In order to prevent this from happening, use is preferably made of an insoluble semiconducting compound obtainable from a soluble precursor compound. Examples of such compounds, viz. a polythienylenevinylene and a pentacene, are described in a publication by Brown et al. in Science, vol. 270, (1995), pp. 972-974.
Onto the semiconducting layer an organic electrically insulating layer is applied which electrically insulates the gate electrode from the semiconducting layer.
The electrically insulating layer preferably has a high capacitance so as to induce a large current between source and drain using a low gate voltage which is accomplished by using a material with a large dielectric constant and/ or a small layer thickness.
In order to reduce the risk of short circuits and/or the leakage current between gate. and source/drain, the thickness of the insulating layer is preferably more than 0.05 μm.
Examples of suitable organic electrically insulating materials are disclosed in United States patent specification US 5,347,144.
If a subsequent layer is applied from solution onto the electrically insulating layer, there is a risk that it swells, dissolves or mixes with the subsequent layer before the solvent has evaporated from the solution. In order to reduce this risk it has been found favourable to employ an insulating material which can be rendered insoluble by cross- linking. A preferred embodiment of the method in accordance with the invention is therefore characterized in that the organic electrically insulating layer comprises a cross-linked polymer. A cross-linkable polymer which has been found very effective is a polyvinylphenol. It can be cross-linked by adding a cross-linking agent such as hexamethoxymethylenernelamine and heating.
The organic FET is completed by applying a second electrode layer accommodating a gate electrode. The insulating layer already being in place, the (variation in) layer thickness and the deposition process is less critical. For example, the second electrode layer can be suitably applied using the method disclosed in the article by Garnier et al. cited hereinabove, that is, printing of a graphite filled polymer ink. However, a method of manufacturing the organic FET, which is more economical and allows a higher resolution, results if the second electrode is applied in the same manner as the first electrode layer. The method involves providing an electrically insulating substrate surface.
The surface should be planar and smooth. Suitable substrates are ceramics, glass, silica or, preferably, (laminated) polymer foils such as polystyrene, polyamide, polyamide and polyester foils. If a first electrode layer comprising conductive polyaniline and a photochemical radical initiator is applied, the substrate surface preferably comprises (cross- linked) polyvinylphenol or polyvinylalcohol.
A preferred embodiment of the method in accordance with the invention is the method according to Claim 5.
This method has been found particularly suitable in that each time a subsequent layer is applied from solution, swelling or dissolution of the preceding layer does not occur. The method moreover allows FETs having a channel length as small as 1 to 2 μm to be produced in a reliable and practical manner.
The inventors have observed that if a field-effect transistor manufactured using the method in accordance the invention is operated for a long time (for minutes to hours) at high source drain voltage differences, there is a risk that the performance of the FET deteriorates to the extent that it does no longer satisfy the condition for voltage amplification at voltages below 10 V. In order to reduce this risk, a preferred embodiment of the method in accordance with the invention is characterized in that before the semiconducting layer is applied, the electrically insulating areas of the first electrode layer are removed, thereby forming a first electrode layer demonstrating a relief pattern of conducting areas.
In case the first electrode layer comprises polyaniline, removal can be achieved, for example, by dissolving selectively the electrically insulating areas in N- methylpyrrolidone . Surprisingly, the presence of a relief pattern does not lead to a dramatic increase in leakage current or short circuits between the source (drain) and gate electrode. At least this is found to be the case if the thickness of the first electrode layer is chosen to be smaller than the thickness of the insulating layer. Apparently, a relief pattern satisfying this criterion provides a surface which is more or less planar from the viewpoint of the capability of said surface to serve as a substrate surface onto which a very thin insulating layer can be applied in a practical manner.
The FET obtained by employing (preferred embodiments of) the method in accordance with the invention is a top gate field-effect transistor. However, it will be obvious to those skilled in the art that if a bottom gate field-effect transistor is desired, the method in accordance with the invention is simply modified in that the gate electrode is accommodated by the first and the source and drain electrodes are accommodated by the second electrode layer, and the semiconducting and electrically insulating layer are applied in reverse order. Yet another bottom gate FET is obtained if the method of manufacturing the bottom gate FET is modified in that the second electrode and semiconducting layer are applied in reverse order.
The invention also relates to a field-effect transistor substantially consisting of organic materials, that is a field-effect transistor comprising a stack of: an organic first electrode layer accommodating a source and drain electrode and demonstrating a relief pattern of electrically conducting areas, an organic semiconducting layer, an organic electrically insulating layer, and an organic second electrode layer accommodating a gate electrode.
The remarkable observation, described hereinabove, that the presence of a relief patterned first electrode layer does not lead to large leakage currents between the source (drain) and gate electrode if the thickness of this layer is less than that of the insulating layer, remains valid regardless of the method of preparing the relief pattern. In accordance with the invention, the field-effect transistor is therefore characterized in that the thickness of the electrically insulating layer is greater than the thickness of the first and/or second electrode layer and less than 0.3 μm. It is clear that applying a 0.3 μm layer on a 0.3 μm topography results in an insulating layer which is neither planar nor planarized. Surprisingly, the use of planarised insulating layers appears to be superfluous. Short circuits are substantially absent if the surface defined by the first and/or second electrode layer has a topography smaller than the layer thickness of the insulating layer to be applied to that surface. In order to satisfy the condition for voltage amplification at a source drain voltage difference below 10 V, the insulating layer should have a thickness less than 0.3 μm. Since the insulating layer may be far from planar, the layer thickness is defined as the thickness that would have been obtained if, using the same method, it had been applied onto a planar surface. In the Japanese Patent Application JP-A-1-259563, a field-effect transistor substantially consisting of organic materials is disclosed. Said document does not disclose a method of manufacturing such a device, let alone a practical method producing a field-effect transistor which satisfies the condition for voltage amplification below a source drain voltage of 10 V. The known field-effect transistor does not have a patchwork patterned electrode layer and the thickness of the planarized insulating layer is not specified.
The invention also relates to an integrated circuit comprising a field-effect transistor in accordance with the invention or a field-effect transistor obtainable by a method in accordance with the invention. Changing the pattern of the first and second electrode layer is all that needs to be done if not just one but a plurality of organic FETs is to be produced on a single substrate surface.
These and other aspects of the invention will be apparent from and elucidated with reference to the embodiments described hereinafter.
In the drawings:
Fig. 1 schematically shows a transparent plan view of a field-effect transistor manufactured using the method in accordance with the invention,
Fig. 2 schematically shows a cross-sectional view taken on the line I-I in Fig. 1, and
Fig. 3 shows a graph of the relationship between the source drain voltage Vsd (in V) and the source drain current Isd (in iiA) at specified gate voltages Vg (in V) of a field-effect transistor manufactured using the method in accordance with the invention when subjected to a source drain voltage sweep from 0 to -10 V and back.
Exemplary embodiment 1
Fig. 1 schematically shows (not drawn to scale) a transparent plan view of a (part of a) field-effect transistor 1 manufactured using the method in accordance with the invention. Fig. 2 schematically shows (not drawn to scale) the field-effect transistor 1 in a cross-sectional view taken on the line I-I in Fig. 1. The field-effect transistor 1 comprises an electrically insulating substrate 2 on which is provided an organic first electrode layer 3 demonstrating a patchwork pattern of electrically insulating areas 31 and conducting areas 32 and 33. The conductive area 32 accommodates the source and the area 33 the drain electrode. The organic semiconducting layer 4 comprises a channel 41 (drawn so as to indicate the definition of channel length and width), of which the channel length L is indicated by reference number 411 and the channel width W by reference number 412. Covering the layer 4 and thus the channel 41 is the organic electrically insulating layer 5. It electrically insulates the gate electrode from the channel 41, said gate electrode being accommodated by the electrically conducting area 62 of the second electrode layer 6. In this particular example, but this is not essential, the layer 6 is a layer demonstrating a patchwork pattern of electrically insulating areas 61 and conducting areas 62.
As an example of the method in accordance with the invention, the field- effect transistor 1 may be manufactured as follows: A) preparation of a conducting polyaniline solution
Emeraldine base polyaniline (Neste) (0.7 g, 7.7 mmol) and camphor sulphonic acid (Janssen) (0.8 g, 3.4 mmol) are ground together with a mortar and pestle in a nitrogen-filled glove box. The mixture is split in two and placed in two 30 ml polyethylene bottles each containing 30 g m-cresol and three agate balls (0.9 mm diameter). These are placed in a shaker (Retsch MM2) operating at full speed for 14 to 18 hours. The contents of the bottles are combined and then sonified for 5 minutes. The mixture is cooled to room temperature and then the sonification process is repeated. This mixture is then centrifuged at 12500 rpm for 2 hours. The conducting polyaniline solution thus obtained is pipetted off leaving any solids at the bottom of the centrifuge tubes.
B) preparation of a precursor polythienylenevinylene solution
A quantity of 10.0 g (0.028 mol) 2,5-thienylenedimethylene- bis(tetrahydrothiophenium chloride) (supplier Syncom BV, Groningen, The Netherlands) is dissolved in 100 ml of a 2/1 v/v mixture of methanol and demineralised water and cooled to -22 0C in a nitrogen environment. Pentane (120 ml) is added and then sodium hydroxide (1.07 g, 0.0268 mol) dissolved in 100 ml of a 2/1 v/v mixture of methanol and demineralised water and cooled to -22 0C is added instantaneously to the stirred monomer solution kept at -22 0C. That temperature is maintained for 2 hours and the mixture is then neutralised using 1.5 ml 2 N HCl. After having stored the mixture in a flask for 2 days, the liquid part is decanted off, and the remaining solid precursor poly(2,5-thienylenevinylene) is washed three times with methanol and dried in a vacuum. The precursor polymer is then dissolved in dichloromethane and concentrated to obtain a solution which after filtration (Millex LS 5 μm and Millex SR 0.5 μm) would give a 0.05 μm film if spin-coated (3 s/500 rpm, 7 s/1000 rpm) onto a glass substrate.
C) manufacture of the field-effect transistor 1
A 65 μm polyamide foil (supplier Sellotape) is secured on a 3 inch silicon wafer. A solution of 10. Og (0.083 mol) polyvinylphenol (Poly sciences Inc., cat #6527) and 1.625 g (4.17 mmol) hexamethoxymethylenernelamine (Cymel 300 from Cyanamid) in 36 g propylene glycol methyl ether acetate (Aldrich) is spin-coated (3 s/500 rpm, 27 s/2000rpm) on the foil and then dried at 110 0C for 1 min on a hotplate. Cross-linking at 125 0C in a nitrogen atmosphere containing 5 % v/v HCl for 5 min affords a 1.47 μm cross-linked polyvinylphenol film. The laminate thus obtained serves as the substrate 2 of which the polyvinylphenol coated side serves as the substrate surface on which subsequent layers are to be applied.
To 145 mg of the photochemical radical initiator 1 -hydroxy cyclohexyl phenyl ketone (tradename Irgacure 184, Ciba Geigy) is added 6 g of the conducting polyaniline solution prepared under A. After mixing well and sonifying twice for 1 min and cooling in between, the radiation- sensitive solution thus obtained is cooled and filtered (Millex FA, 1 μm). A radiation-sensitive layer is then formed by spin-coating (3 s/500 rpm, 7 s/2000 rpm) 1 ml of the radiation-sensitive solution on the polyvinylphenol coated surface of the substrate 2, and drying on a hotplate (2 min at 90 0C). The wafer is placed in a Karl Suss MJB3 aligner equipped with a 500 W Xe lamp and flushed with nitrogen for 3 min. A mask defining a plurality of interdigitated source and drain electrode patterns with channel lengths of 10, 5, 3, 2 μm at channel widths of 1 and 3mm respectively (opaque areas of the mask corresponding to areas 32 and 33), is brought into contact with the radiation- sensitive layer. While continuously flushing with nitrogen, the radiation-sensitive layer is irradiated via the mask with deep XJV light (60 s, 20 mW/cm2 at 240 nm), thereby forming a first electrode layer 3 demonstrating a patchwork pattern of irradiated areas 31 and non- irradiated areas 32 and 33. The wafer is then heated on a hotplate (3 min at 1100C, 1 min at 15O0C) so as to remove the unreacted photochemical radical initiator. The layer 3 is now insensitive to the deep UV light used in the irradiation and substantially planar, the thickness of the irradiated areas being 0.25 μm, and of the non-irradiated areas 0.22 μm. The sheet resistance of the area 31 is 4 x 1013 Ω/square (conductivity 10"9 S/cm), of the areas 32 and 33 it is 760 Ω/square (conductivity 60 S/cm).
Immediately after having been filtered (Millex SR 0.5 μm), 3 ml precursor polythienylenevinylene solution prepared under B is spin-coated (3 s/500 rpm, 7 s/1000 rpm) on the layer 3. This precursor layer is then heated on a hot plate at 150 0C for 10 min in a nitrogen atmosphere containing HCl gas at a partial pressure of 2.3 x 10'3 bar, thus converting the precursor layer into a 50 nm thick semiconducting layer 4 comprising a polythienylenevinylene.
Subsequently, 3 ml of a cross-linkable composition, consisting of 4.0 g (0.034 mol) polyvinylphenol (Polysciences Inc., cat #6527) and 0.65 g (1.66 mmol) hexamethoxymethylenemelamine (Cymel 300 from Cyanamid) dissolved in 36 g propylene glycol methyl ether acetate (Aldrich), is spin-coated (3 s/500 rpm, 27 s/2500rpm) on the layer 4 and dried at 110 0C for 1 min on a hotplate. Cross-linking at 125 0C in a nitrogen atmosphere containing 5 % v/v HCl for 5 min affords a 0.27 μm cross-linked polyvinylphenol electrically insulating layer 5. The dielectric constant of the cross-linked polyvinylphenol is 4.78 and its conductivity (at 1 kHz) 4.4 x 10"11 S/cm.
Following the same procedure as used for applying the first electrode layer 3, except that a different mask is used, a second electrode layer 6 is applied on the layer 5. The second electrode layer 6 demonstrates a patchwork pattern of irradiated electrically insulating areas 61 and non-irradiated electrically conducting areas 62 (only one area shown), the latter areas accommodating the gate electrodes.
The manufacture of the field-effect transistor 1 substantially consisting of organic materials is now complete. In order to (mechanically) protect the FET 1 from the environment, the
FET 1 is covered by a 0.5 μτn encapsulation layer obtained by spin-coating (3 s/500 rpm, 7 s/2000 rpm) a filtered (Millex LS 5 μm) solution of 1.5 g (0.028 mol) polyacrylonitrile (Polysciences Inc., cat# 3914) in 38.5 g N-methylpyrrolidone and drying at 110 0C for 1 min. Alternatively, a solution of 25 g polyvinylidenefluoride (Polysciences Inc, cat #15190) in 25 g N-methylpyrrolidone may be used.
Exemplary embodiment 2
Fig. 3 shows a graph of the relationship between the source drain voltage Vsd (in V) and the source drain current Isd (in nA) at specified gate voltages Vg (in V) of a field-effect transistor 1, manufactured using the method of exemplary embodiment 1, when subjected to a source drain voltage sweep from 0 to -10 V and back. In this embodiment, the channel length L equals 2 μm and the channel width W equals 1 mm. At a source drain voltage difference of approximately 2.5 V, the channel transconductance exceeds the channel conductance, thus satisfying the condition for voltage amplification. The voltage sweep shows a substantially negligible hysteresis. The ratio of the current Isd(Vsd = -10 V, Vg = -10 V) and Isd(Vsd = -10 V, Vg = 0 V), in short the on/off ratio, is 25. The FET mobility is 10"4 cm2/Vs.
Similar results are obtained with FETs having a channel length of 3, 5 or 10 μm.
Exemplary embodiment 3 (not according to the invention)
The method of exemplary embodiment 1 is repeated, with this difference that the patchwork patterned first electrode layer 3 is replaced by an electrode layer demonstrating a relief pattern. The relief pattern consists of 0.25 μm thick gold areas obtained by means of vacuum deposition using a shadow mask. The gold areas which accommodate the source and drain electrode are located such that the channel width is 10 mm and the channel length is 10 μm.
By performing similar voltage sweeps as shown in Fig. 3, it is found that the condition for voltage amplification is satisfied at source drain voltage differences below 10 V.
Although the field-effect transistor obtained in this embodiment does not substantially consist of organic materials, and as such is not a FET in accordance with the invention, it does demonstrate that, in accordance with the invention, a FET may satisfy the condition for voltage amplification below 10 V if a relief pattern is used which has a topography (in casu 0.25 μm) less than the thickness of the insulating layer (in casu 0.27 μm).

Claims

CLAIMS:
1. A method of manufacturing a field-effect transistor substantially consisting of organic materials on a substrate surface, said method comprising the steps of:
- providing an electrically insulating substrate surface,
- applying an organic first electrode layer accommodating a source and drain electrode and demonstrating a patchwork pattern of electrically insulating and conducting areas,
- applying an organic semiconducting layer,
- applying an organic electrically insulating layer having a thickness less than 0.3 μm,
- applying an organic second electrode layer accommodating a gate electrode.
2. A method as claimed in Claim 1, characterized in that the organic first electrode layer is applied by performing the steps of
- applying an organic radiation-sensitive layer,
- irradiating said radiation-sensitive layer according to a desired pattern, thereby forming an organic first electrode layer accommodating a source and drain electrode and demonstrating a patchwork pattern of irradiated electrically insulating and non-irradiated conducting areas.
3. A method as claimed in Claim 2, characterized in that a radiation- sensitive layer is applied which comprises an electrically conducting polyaniline and a photochemical radical initiator.
4. A method as claimed in Claim 1, characterized in that the organic electrically insulating layer comprises a cross-linked polymer.
5. A method as claimed in Claim 1, comprising the steps of:
- providing an electrically insulating substrate surface,
- applying, from solution, a first organic radiation-sensitive layer comprising a conductive polyaniline and a photochemical radical initiator,
- irradiating said first radiation-sensitive layer according to a desired pattern, thereby forming an organic first electrode layer accommodating a source and drain electrode and demonstrating a patchwork pattern of irradiated electrically insulating and non-irradiated conducting areas,
- heating the first electrode layer at a temperature sufficient to render said first electrode layer radiation-insensitive, - applying, from solution, a second organic semiconducting layer comprising a polythienylenevinylene,
- applying, from solution, a cross-linkable polymer composition,
- cross-linking the cross-linkable polymer composition, thereby forming an organic electrically insulating layer comprising a cross-linked polymer composition,
- applying, from solution, a second organic radiation-sensitive layer comprising a conductive polyaniline and a photochemical radical initiator,
- irradiating said second radiation- sensitive layer according to a desired pattern, thereby forming an organic second electrode layer accommodating a gate electrode and demonstrating a patchwork pattern of irradiated electrically insulating and non -irradiated conducting areas.
6. A method as claimed in Claim 1, characterized in that before the semiconducting layer is applied, the electrically insulating areas of the first electrode layer are removed, thereby forming a first electrode layer demonstrating a relief pattern of conducting areas.
7. A method as claimed in Claim 1, modified in that the gate electrode is accommodated by the first and the source and drain electrodes are accommodated by the second electrode layer, and the semiconducting and electrically insulating layer are applied in reverse order.
8. A method as claimed in Claim 7, modified in that the semiconducting and second electrode layer are applied in reverse order.
9. A field-effect transistor comprising a stack of: an organic first electrode layer accommodating a source and drain electrode and demonstrating a relief pattern of electrically conducting areas, an organic semiconducting layer, an organic electrically insulating layer, and an organic second electrode layer accommodating a gate electrode, characterized in that the thickness of the electrically insulating layer is greater than the thickness of the First and/or second electrode layer and less than 0.3 μm.
10. An integrated circuit comprising a field-effect transistor as claimed in Claim 9 or a field-effect transistor obtainable by a method as claimed in Claim 1.
PCT/IB1998/001144 1997-08-22 1998-07-27 A method of manufacturing a field-effect transistor substantially consisting of organic materials WO1999010939A2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP98932464A EP0968537B1 (en) 1997-08-22 1998-07-27 A method of manufacturing a field-effect transistor substantially consisting of organic materials
JP51409999A JP4509228B2 (en) 1997-08-22 1998-07-27 Field effect transistor made of organic material and method of manufacturing the same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP97202587.8 1997-08-22
EP97202587 1997-08-22

Publications (3)

Publication Number Publication Date
WO1999010939A2 WO1999010939A2 (en) 1999-03-04
WO1999010939A3 WO1999010939A3 (en) 1999-06-10
WO1999010939A9 true WO1999010939A9 (en) 2006-05-26

Family

ID=8228663

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB1998/001144 WO1999010939A2 (en) 1997-08-22 1998-07-27 A method of manufacturing a field-effect transistor substantially consisting of organic materials

Country Status (4)

Country Link
US (2) US6429450B1 (en)
EP (1) EP0968537B1 (en)
JP (1) JP4509228B2 (en)
WO (1) WO1999010939A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9577016B2 (en) 2001-11-09 2017-02-21 Semiconductor Energy Laboratory Co., Ltd. Light emitting device

Families Citing this family (122)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1187793C (en) * 1998-01-28 2005-02-02 薄膜电子有限公司 Method for generation of electrical conducting or semicnducting structures in three dimensionsand methods for earasure of the same structures
AU768085B2 (en) * 1999-04-28 2003-12-04 E.I. Du Pont De Nemours And Company Flexible organic electronic device with improved resistance to oxygen and moisture degradation
GB9914489D0 (en) * 1999-06-21 1999-08-25 Univ Cambridge Tech Transistors
CN100461486C (en) 1999-06-21 2009-02-11 剑桥企业有限公司 Polymerase alignes for organic TFT
JP2003508807A (en) 1999-08-31 2003-03-04 イー−インク コーポレイション Electronically driven display transistors
JP4972260B2 (en) * 1999-08-31 2012-07-11 イー インク コーポレイション Method for forming patterned semiconductor film
EP1727220A3 (en) 1999-09-10 2008-07-16 Polymer Vision Limited Conductive structure based on poly-3,4-alkenedioxythiophene (PEDOT) and polystyrenesulfonic acid (PSS)
EP1085319B1 (en) * 1999-09-13 2005-06-01 Interuniversitair Micro-Elektronica Centrum Vzw A device for detecting an analyte in a sample based on organic materials
EP1085320A1 (en) * 1999-09-13 2001-03-21 Interuniversitair Micro-Elektronica Centrum Vzw A device for detecting an analyte in a sample based on organic materials
JP4587539B2 (en) * 1999-09-13 2010-11-24 アイメック Apparatus for detecting analytes in samples based on organic materials
WO2001027998A1 (en) 1999-10-11 2001-04-19 Koninklijke Philips Electronics N.V. Integrated circuit
BR0016661B1 (en) * 1999-12-21 2013-11-26 METHODS FOR FORMATION OF AN ELECTRONIC DEVICE, ELECTRONIC DEVICE AND DISPLAY DEVICE
BR0016660A (en) 1999-12-21 2003-02-25 Plastic Logic Ltd Method for forming a transistor, transistor, and logic circuit and display or memory device
CN1245769C (en) * 1999-12-21 2006-03-15 造型逻辑有限公司 Solution processing
GB9930217D0 (en) * 1999-12-21 2000-02-09 Univ Cambridge Tech Solutiion processed transistors
DE10037391A1 (en) 2000-08-01 2002-02-14 Covion Organic Semiconductors Structurable materials, processes for their production and their use
DE10057502A1 (en) * 2000-11-20 2002-05-29 Siemens Ag Organic field effect transistor has at least two current channels and/or one vertical current channel transverse to surface of substrate formed by field effect when voltage applied
EP1310004A2 (en) * 2000-08-18 2003-05-14 Siemens Aktiengesellschaft Organic field-effect transistor (ofet), a production method therefor, an integrated circuit constructed from the same and their uses
US7875975B2 (en) * 2000-08-18 2011-01-25 Polyic Gmbh & Co. Kg Organic integrated circuit completely encapsulated by multi-layered barrier and included in RFID tag
DE10043204A1 (en) * 2000-09-01 2002-04-04 Siemens Ag Organic field-effect transistor, method for structuring an OFET and integrated circuit
DE10044842A1 (en) * 2000-09-11 2002-04-04 Siemens Ag Organic rectifier, circuit, RFID tag and use of an organic rectifier
DE10045192A1 (en) 2000-09-13 2002-04-04 Siemens Ag Organic data storage, RFID tag with organic data storage, use of an organic data storage
US20040026121A1 (en) * 2000-09-22 2004-02-12 Adolf Bernds Electrode and/or conductor track for organic components and production method thereof
DE10061297C2 (en) * 2000-12-08 2003-05-28 Siemens Ag Procedure for structuring an OFET
DE10061299A1 (en) * 2000-12-08 2002-06-27 Siemens Ag Device for determining and / or forwarding at least one environmental influence, production method and use thereof
DE10063721A1 (en) * 2000-12-20 2002-07-11 Merck Patent Gmbh Organic semiconductor, manufacturing process therefor and uses
GB2371910A (en) * 2001-01-31 2002-08-07 Seiko Epson Corp Display devices
DE10105914C1 (en) * 2001-02-09 2002-10-10 Siemens Ag Organic field effect transistor with photo-structured gate dielectric and a method for its production
US7439096B2 (en) * 2001-02-21 2008-10-21 Lucent Technologies Inc. Semiconductor device encapsulation
SE520339C2 (en) * 2001-03-07 2003-06-24 Acreo Ab Electrochemical transistor device, used for e.g. polymer batteries, includes active element having transistor channel made of organic material and gate electrode where voltage is applied to control electron flow
US7012306B2 (en) 2001-03-07 2006-03-14 Acreo Ab Electrochemical device
CN1224862C (en) * 2001-03-07 2005-10-26 阿克里奥公司 Electrochemical pixel device
US6707063B2 (en) * 2001-03-22 2004-03-16 Hewlett-Packard Development Company, L.P. Passivation layer for molecular electronic device fabrication
EP1374138A2 (en) * 2001-03-26 2004-01-02 Siemens Aktiengesellschaft Device with at least two organic electronic components and method for producing the same
DE10120520A1 (en) * 2001-04-26 2002-11-14 Infineon Technologies Ag Semiconductor device and manufacturing process
CN1292496C (en) 2001-05-23 2006-12-27 造型逻辑有限公司 Laser parrering of devices
WO2003030278A2 (en) * 2001-10-01 2003-04-10 Koninklijke Philips Electronics N.V. Composition, method and electronic device
DE10151036A1 (en) * 2001-10-16 2003-05-08 Siemens Ag Isolator for an organic electronic component
DE10151440C1 (en) 2001-10-18 2003-02-06 Siemens Ag Organic electronic component for implementing an encapsulated partially organic electronic component has components like a flexible foil as an antenna, a diode or capacitor and an organic transistor.
DE10160732A1 (en) * 2001-12-11 2003-06-26 Siemens Ag OFET used e.g. in RFID tag, comprises an intermediate layer on an active semiconductor layer
US6620657B2 (en) * 2002-01-15 2003-09-16 International Business Machines Corporation Method of forming a planar polymer transistor using substrate bonding techniques
WO2003067333A1 (en) 2002-02-05 2003-08-14 Koninklijke Philips Electronics N.V. Photo-sensitive composition
EP1487935A1 (en) 2002-03-07 2004-12-22 Acreo AB Electrochemical device
ATE544092T1 (en) * 2002-03-07 2012-02-15 Acreo Ab ELECTROCHEMICAL DEVICE
DE10212639A1 (en) * 2002-03-21 2003-10-16 Siemens Ag Device and method for laser structuring functional polymers and uses
DE10212640B4 (en) * 2002-03-21 2004-02-05 Siemens Ag Logical components made of organic field effect transistors
DE10226370B4 (en) * 2002-06-13 2008-12-11 Polyic Gmbh & Co. Kg Substrate for an electronic component, use of the substrate, methods for increasing the charge carrier mobility and organic field effect transistor (OFET)
WO2004017439A2 (en) * 2002-07-29 2004-02-26 Siemens Aktiengesellschaft Electronic component comprising predominantly organic functional materials and method for the production thereof
US20060079327A1 (en) * 2002-08-08 2006-04-13 Wolfgang Clemens Electronic device
US6784017B2 (en) * 2002-08-12 2004-08-31 Precision Dynamics Corporation Method of creating a high performance organic semiconductor device
JP2004140333A (en) * 2002-08-22 2004-05-13 Yamanashi Tlo:Kk Organic field effect transistor and manufacturing method thereof
WO2004021256A1 (en) 2002-08-23 2004-03-11 Siemens Aktiengesellschaft Organic component for overvoltage protection and associated circuit
EP1416004A1 (en) * 2002-11-02 2004-05-06 MERCK PATENT GmbH Polymerizable amine mixtures, amine polymer materials and their use
US20040094761A1 (en) * 2002-11-02 2004-05-20 David Sparrowe Polymerizable amine mixtures, amine polymer materials and their use
CN1726604A (en) * 2002-11-05 2006-01-25 波尔伊克两合公司 Organic electronic component with high-resolution structuring and method for the production thereof
DE10253154A1 (en) * 2002-11-14 2004-05-27 Siemens Ag Biosensor, used to identify analyte in liquid sample, has test field with detector, where detector registers field changes as electrical signals for evaluation
US7442954B2 (en) * 2002-11-19 2008-10-28 Polyic Gmbh & Co. Kg Organic electronic component comprising a patterned, semi-conducting functional layer and a method for producing said component
WO2004047194A2 (en) * 2002-11-19 2004-06-03 Polyic Gmbh & Co.Kg Organic electronic component comprising the same organic material for at least two functional layers
GB0229191D0 (en) 2002-12-14 2003-01-22 Plastic Logic Ltd Embossing of polymer devices
US7078261B2 (en) * 2002-12-16 2006-07-18 The Regents Of The University Of California Increased mobility from organic semiconducting polymers field-effect transistors
DE10300521A1 (en) * 2003-01-09 2004-07-22 Siemens Ag Organoresistive memory
WO2004066348A2 (en) * 2003-01-21 2004-08-05 Polyic Gmbh & Co. Kg Organic electronic component and method for producing organic electronic devices
DE10302149A1 (en) * 2003-01-21 2005-08-25 Siemens Ag Use of conductive carbon black / graphite blends for the production of low-cost electronics
EP1590721B1 (en) * 2003-01-28 2007-04-11 Koninklijke Philips Electronics N.V. Electronic device
JP2006519483A (en) * 2003-01-29 2006-08-24 ポリアイシー ゲーエムベーハー ウント コー、 カーゲー Organic memory device and driver circuit therefor
DE10330064B3 (en) * 2003-07-03 2004-12-09 Siemens Ag Organic logic gate has load field effect transistor with potential-free gate electrode in series with switching field effect transistor
DE10330062A1 (en) * 2003-07-03 2005-01-27 Siemens Ag Method and device for structuring organic layers
DE10338277A1 (en) * 2003-08-20 2005-03-17 Siemens Ag Organic capacitor with voltage controlled capacity
DE10339036A1 (en) 2003-08-25 2005-03-31 Siemens Ag Organic electronic component with high-resolution structuring and manufacturing method
JP2005072528A (en) * 2003-08-28 2005-03-17 Shin Etsu Chem Co Ltd Thin film field effect transistor and its manufacturing method
GB0320491D0 (en) 2003-09-02 2003-10-01 Plastic Logic Ltd Multi-level patterning
WO2005022664A2 (en) 2003-09-02 2005-03-10 Plastic Logic Limited Production of electronic devices
DE10340643B4 (en) * 2003-09-03 2009-04-16 Polyic Gmbh & Co. Kg Printing method for producing a double layer for polymer electronics circuits, and thereby produced electronic component with double layer
DE10340644B4 (en) * 2003-09-03 2010-10-07 Polyic Gmbh & Co. Kg Mechanical controls for organic polymer electronics
DE10340711A1 (en) 2003-09-04 2005-04-07 Covion Organic Semiconductors Gmbh Electronic device containing organic semiconductors
GB0321383D0 (en) 2003-09-12 2003-10-15 Plastic Logic Ltd Polymer circuits
DE102004002024A1 (en) * 2004-01-14 2005-08-11 Siemens Ag Self-aligning gate organic transistor and method of making the same
JP4501444B2 (en) * 2004-02-04 2010-07-14 ソニー株式会社 Method of forming wiring structure in transistor and method of manufacturing field effect transistor
EP1564827A1 (en) * 2004-02-10 2005-08-17 Université Libre De Bruxelles Method for the manufacturing of multilayer mesogenic components
DE102004021989A1 (en) 2004-05-04 2005-12-15 Covion Organic Semiconductors Gmbh Organic electronic devices
US7449758B2 (en) * 2004-08-17 2008-11-11 California Institute Of Technology Polymeric piezoresistive sensors
DE102004040831A1 (en) * 2004-08-23 2006-03-09 Polyic Gmbh & Co. Kg Radio-tag compatible outer packaging
US8030124B2 (en) * 2004-11-05 2011-10-04 Creator Technology B.V. Method for patterning an organic material to concurrently form an insulator and a semiconductor and device formed thereby
JP4792781B2 (en) * 2004-12-06 2011-10-12 凸版印刷株式会社 Thin film transistor manufacturing method
WO2006061658A1 (en) 2004-12-06 2006-06-15 Plastic Logic Limited Electrode patterning
DE102004059467A1 (en) * 2004-12-10 2006-07-20 Polyic Gmbh & Co. Kg Gate made of organic field effect transistors
DE102004059464A1 (en) * 2004-12-10 2006-06-29 Polyic Gmbh & Co. Kg Electronic component with modulator
DE102004059465A1 (en) * 2004-12-10 2006-06-14 Polyic Gmbh & Co. Kg recognition system
DE102004063435A1 (en) 2004-12-23 2006-07-27 Polyic Gmbh & Co. Kg Organic rectifier
DE102005009820A1 (en) * 2005-03-01 2006-09-07 Polyic Gmbh & Co. Kg Electronic assembly with organic logic switching elements
DE102005009819A1 (en) 2005-03-01 2006-09-07 Polyic Gmbh & Co. Kg electronics assembly
GB0506895D0 (en) 2005-04-05 2005-05-11 Plastic Logic Ltd Ablation threshold adjustment by electroless plating
GB0506899D0 (en) 2005-04-05 2005-05-11 Plastic Logic Ltd Multiple conductive layer TFT
DE102005017655B4 (en) * 2005-04-15 2008-12-11 Polyic Gmbh & Co. Kg Multilayer composite body with electronic function
GB0518105D0 (en) 2005-09-06 2005-10-12 Plastic Logic Ltd Step-and-repeat laser ablation of electronic devices
WO2007029028A1 (en) 2005-09-06 2007-03-15 Plastic Logic Limited Laser ablation of electronic devices
GB0511132D0 (en) 2005-06-01 2005-07-06 Plastic Logic Ltd Layer-selective laser ablation patterning
DE102005031448A1 (en) 2005-07-04 2007-01-11 Polyic Gmbh & Co. Kg Activatable optical layer
GB0515175D0 (en) 2005-07-25 2005-08-31 Plastic Logic Ltd Flexible resistive touch screen
DE102005035590A1 (en) * 2005-07-29 2007-02-01 Polyic Gmbh & Co. Kg Electronic component has flexible substrate and stack of layers including function layer on substratesurface
DE102005035589A1 (en) 2005-07-29 2007-02-01 Polyic Gmbh & Co. Kg Manufacturing electronic component on surface of substrate where component has two overlapping function layers
EP1752480A1 (en) * 2005-08-12 2007-02-14 Merck Patent GmbH Polymerizable dielectric material
US20070034842A1 (en) * 2005-08-12 2007-02-15 Merck Patent Gesellschaft Mit Beschrankter Haftung Polymerizable dielectric material
DE102005042166A1 (en) * 2005-09-06 2007-03-15 Polyic Gmbh & Co.Kg Organic device and such a comprehensive electrical circuit
DE102005044306A1 (en) 2005-09-16 2007-03-22 Polyic Gmbh & Co. Kg Electronic circuit and method for producing such
WO2007110671A2 (en) 2006-03-29 2007-10-04 Plastic Logic Limited Techniques for device fabrication with self-aligned electrodes
GB0611032D0 (en) 2006-06-05 2006-07-12 Plastic Logic Ltd Multi-touch active display keyboard
JP2008041960A (en) 2006-08-07 2008-02-21 Nissan Chem Ind Ltd Manufacturing method of electronic circuit component
FI20070063A0 (en) * 2007-01-24 2007-01-24 Ronald Oesterbacka Organic field effect transistor
US8003980B2 (en) * 2007-01-30 2011-08-23 Hewlett-Packard Development Company, L.P. Layered electro-organic devices with crosslinked polymer and methods of preparing the same
WO2008144762A2 (en) * 2007-05-21 2008-11-27 Plextronics, Inc. Organic electrodes and electronic devices
WO2008144759A2 (en) * 2007-05-21 2008-11-27 Plextronics, Inc. Organic electrodes and electronic devices
WO2009053088A1 (en) 2007-10-24 2009-04-30 Merck Patent Gmbh Optoelectronic device
DE102008045664A1 (en) 2008-09-03 2010-03-04 Merck Patent Gmbh Optoelectronic device, useful e.g. as organic or polymer light-emitting diode, organic field-effect-transistor, organic constituent, organic field-quench element, comprises a layer comprising a polymer with fluorine-containing group
DE102008045662A1 (en) 2008-09-03 2010-03-04 Merck Patent Gmbh Optoelectronic device useful as white light emitting organic light-emitting diode in display, comprises first layer comprising electrode material, second layer comprising polymer material on substrate, and polymer layers having emitter
US7879678B2 (en) * 2008-02-28 2011-02-01 Versatilis Llc Methods of enhancing performance of field-effect transistors and field-effect transistors made thereby
DE102008045663A1 (en) 2008-09-03 2010-03-04 Merck Patent Gmbh Fluorine-bridged associates for opto-electronic applications
KR101491714B1 (en) * 2008-09-16 2015-02-16 삼성전자주식회사 Semiconductor devices and method of fabricating the same
GB0819274D0 (en) 2008-10-21 2008-11-26 Plastic Logic Ltd Method and apparatus for the formation of an electronic device
IT1392069B1 (en) * 2008-11-27 2012-02-09 St Microelectronics Srl METHOD FOR REALIZING AN ORGANIC ELECTRONIC DEVICE WITH THIN AND CORRESPONDING FILM
US20140097003A1 (en) * 2012-10-05 2014-04-10 Tyco Electronics Amp Gmbh Electrical components and methods and systems of manufacturing electrical components
TWI628803B (en) * 2017-09-15 2018-07-01 友達光電股份有限公司 Organic thin film transistor device and method for fabricating the same

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8715959D0 (en) * 1987-07-07 1987-08-12 British Petroleum Co Plc Field effect transistors
JPH01259563A (en) 1988-04-08 1989-10-17 Mitsubishi Electric Corp Field effect transistor
WO1990008402A1 (en) * 1989-01-10 1990-07-26 Mitsubishi Denki Kabushiki Kaisha Fet transistor and liquid crystal display device obtained by using the same
US5892244A (en) * 1989-01-10 1999-04-06 Mitsubishi Denki Kabushiki Kaisha Field effect transistor including πconjugate polymer and liquid crystal display including the field effect transistor
JP2813428B2 (en) * 1989-08-17 1998-10-22 三菱電機株式会社 Field effect transistor and liquid crystal display device using the field effect transistor
FR2664430B1 (en) * 1990-07-04 1992-09-18 Centre Nat Rech Scient THIN FILM FIELD EFFECT TRANSISTOR WITH MIS STRUCTURE, IN WHICH THE INSULATION AND THE SEMICONDUCTOR ARE MADE OF ORGANIC MATERIALS.
JP3224829B2 (en) * 1991-08-15 2001-11-05 株式会社東芝 Organic field effect device
ATE171560T1 (en) 1993-03-09 1998-10-15 Koninkl Philips Electronics Nv PROCESS FOR PRODUCING A PATTERN OF AN ELECTRICALLY CONDUCTIVE POLYMER ON A SUBSTRATE SURFACE AND METALIZATION OF SUCH A PATTERN
US5427841A (en) 1993-03-09 1995-06-27 U.S. Philips Corporation Laminated structure of a metal layer on a conductive polymer layer and method of manufacturing such a structure
US5567550A (en) * 1993-03-25 1996-10-22 Texas Instruments Incorporated Method of making a mask for making integrated circuits
JP3246189B2 (en) * 1994-06-28 2002-01-15 株式会社日立製作所 Semiconductor display device
EP1271669A3 (en) * 1994-09-06 2005-01-26 Koninklijke Philips Electronics N.V. Electroluminescent device comprising a transparent structured electrode layer made from a conductive polymer
TW293172B (en) * 1994-12-09 1996-12-11 At & T Corp
US5625199A (en) * 1996-01-16 1997-04-29 Lucent Technologies Inc. Article comprising complementary circuit with inorganic n-channel and organic p-channel thin film transistors

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9577016B2 (en) 2001-11-09 2017-02-21 Semiconductor Energy Laboratory Co., Ltd. Light emitting device

Also Published As

Publication number Publication date
US20020151117A1 (en) 2002-10-17
JP2001505002A (en) 2001-04-10
EP0968537A2 (en) 2000-01-05
WO1999010939A3 (en) 1999-06-10
JP4509228B2 (en) 2010-07-21
EP0968537B1 (en) 2012-05-02
US6429450B1 (en) 2002-08-06
WO1999010939A2 (en) 1999-03-04
US7402834B2 (en) 2008-07-22

Similar Documents

Publication Publication Date Title
EP0968537B1 (en) A method of manufacturing a field-effect transistor substantially consisting of organic materials
JP5060695B2 (en) Method for constructing electronic circuit from electronic element array and electronic circuit formed by the method
KR100973811B1 (en) Thin film transistor array panel using organic semiconductor and manufacturing method thereof
EP1243033B1 (en) Solution processing
KR100832873B1 (en) Self-aligned organic thin film transistor and fabrication method thereof
JP5073141B2 (en) Internal connection formation method
JP5658789B2 (en) Solution-treated device
US8089065B2 (en) Organic thin film transistors
US7834352B2 (en) Method of fabricating thin film transistor
US6635406B1 (en) Method of producing vertical interconnects between thin film microelectronic devices and products comprising such vertical interconnects
US20030059975A1 (en) Solution processed devices
JP2000505249A (en) Patterns of conductive polymers and their application as electrodes or electrical contacts
JP5055719B2 (en) Method for forming laminated structure comprising insulating layer and organic semiconductor layer, organic field effect transistor and method for manufacturing the same
JP5137296B2 (en) Field effect transistor
EP1604409B1 (en) Method of manufacturing an electronic arrangement
EP0966758B1 (en) A method of providing a vertical interconnect between thin film microelectronic devices
KR20090045884A (en) Self-aligned organic thin film transistor and fabrication method thereof
WO2009085599A1 (en) Organic semiconductor device and method of manufacturing same
JP4085420B2 (en) Field effect semiconductor device and manufacturing method thereof
JP4501444B2 (en) Method of forming wiring structure in transistor and method of manufacturing field effect transistor

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): JP

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

ENP Entry into the national phase

Ref country code: JP

Ref document number: 1999 514099

Kind code of ref document: A

Format of ref document f/p: F

WWE Wipo information: entry into national phase

Ref document number: 1998932464

Country of ref document: EP

121 Ep: the epo has been informed by wipo that ep was designated in this application
AK Designated states

Kind code of ref document: A3

Designated state(s): JP

AL Designated countries for regional patents

Kind code of ref document: A3

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

WWP Wipo information: published in national office

Ref document number: 1998932464

Country of ref document: EP

COP Corrected version of pamphlet

Free format text: PAGE 19, DESCRIPTION, REPLACED BY CORRECT PAGE 19