JP5191247B2 - Thin film field effect transistor and display device using the same - Google Patents

Description

  The present invention relates to a thin film field effect transistor and a display device using the same. In particular, the present invention relates to a thin film field effect transistor using an amorphous oxide semiconductor as an active layer and a display device using the same.

2. Description of the Related Art In recent years, flat and thin image display devices (Flat Panel Displays: FPD) have been put into practical use due to advances in liquid crystal and electroluminescence (EL) technologies. In particular, an organic electroluminescent device using a thin film material that emits light when excited by passing an electric current (hereinafter sometimes referred to as “organic EL device”) can emit light with high luminance at a low voltage. Device thinning, lightening, miniaturization, and power saving are expected in a wide range of fields including mobile phone displays, personal digital assistants (PDAs), computer displays, automobile information displays, TV monitors, or general lighting. ing.
These FPDs are active field-effect thin film transistors (hereinafter referred to as “Thin Film Transistor” or “TFT”) that use an amorphous silicon thin film or a polycrystalline silicon thin film provided on a glass substrate as an active layer. It is driven by a matrix circuit.

On the other hand, in order to further reduce the thickness, weight, and breakage resistance of these FPDs, an attempt has been made to use a lightweight and flexible resin substrate instead of a glass substrate.
However, the manufacture of the transistor using the above-described silicon thin film requires a relatively high temperature thermal process and is generally difficult to form directly on a resin substrate having low heat resistance.

For example, a MOSFET (Metal-Oxide Field-Effect Transistor) in which a driving voltage of a transistor using a silicon thin film is reduced is disclosed, and indium tin oxide (ITO), tin oxide, or zinc oxide is used as a semiconductor material of an active layer. A configuration in which a dielectric material having a large relative dielectric constant is used for the gate insulating film is disclosed (for example, see Patent Document 3). It is disclosed that ITO, tin oxide, zinc oxide or the like is a crystalline metal oxide and has a carrier concentration of about 1 × 10 ¹⁹ / cm ³ . In the case of an active layer made of a crystalline metal oxide, in order to express desired semiconductor characteristics, a high-temperature heat treatment for crystallization control, such as post-annealing at 300 ° C. for 15 minutes, is performed after film formation by sputtering. A process is required (see, for example, paragraph number “0054” of Patent Document 3). Therefore, it is difficult to directly form such an active layer on a resin substrate having low heat resistance.

An amorphous oxide such as an In—Ga—Zn—O-based amorphous oxide can be formed at a low temperature, and has attracted attention as a material that can be formed on a plastic film at room temperature (for example, Non-Patent Document 1). reference.). However, when used for an active layer of a TFT using an amorphous oxide semiconductor, there is a problem that the OFF current is high and the ON / OFF ratio is low. For example, a structure of a TFT using IZO (In—Zn—O) having a carrier concentration of 2.1 × 10 ¹⁷ / cm ³ as an active layer as an amorphous oxide semiconductor is disclosed (for example, see Non-Patent Document 2). .) However, the OFF current is still high, and the current flows even when the TFT gate voltage is not applied, resulting in a “normally on” state, which requires an extra circuit and power consumption for the ON / OFF operation. There is.
As a means for improving this problem, the carrier concentration of the amorphous oxide semiconductor is reduced, for example, if it is less than 10 ¹⁸ / cm ³ , the TFT operates and has a good ON / OFF ratio at less than 10 ¹⁶ / cm ^3. It is disclosed that the carrier concentration is preferably less than 10 ¹⁶ / cm ^{3 in} order to obtain a TFT and to have good low off-current characteristics (see, for example, Patent Document 1).

  On the other hand, the gate insulating film of the TFT is usually formed by vapor deposition, but it is difficult to form a flat film surface. Therefore, when the active layer is formed directly on the gate insulating film, the thickness of the active layer varies locally. As a result, there is a problem that the TFT performance is deteriorated. As means for improving this problem, it has been proposed to dispose an electric resistance layer made of an amorphous oxide semiconductor between the gate insulating film and the active layer, and to planarize the surface unevenness of the gate insulating film by the electric resistance layer. (For example, refer to Patent Document 2).

However, TFTs that are practically used have a low OFF current and a high ON / OFF ratio, as well as their performance does not change even when continuously driven, and conditions such as the temperature and humidity of the operating environment. Even if it fluctuates, it is required to show stable performance, and many problems to be solved still remain.
JP 2006-186319 A JP 2007-73701 A JP 2006-121029 A NATURE, Vol. 432 (25 November, 2004), P.M. 488-492 APPLIED PHYSICS LETTERS, 89,062103 (2006)

  An object of the present invention is to provide a TFT using an amorphous oxide semiconductor, and in particular, an improvement in which the OFF performance is low, the ON / OFF ratio is high, and the TFT performance does not change even when the environmental temperature changes. It is to provide an improved TFT. It is another object of the present invention to provide a high-performance TFT that can be manufactured on a flexible resin substrate. Another object is to provide a display device using the TFT.

The above-described problems of the present invention have been solved by the following means.
<1> A thin film field effect transistor having at least a gate electrode, a gate insulating film, an active layer containing an amorphous oxide semiconductor, a source electrode and a drain electrode on a substrate, wherein the carrier concentration of the active layer is 3 × 10 ¹⁵ / cm ³ or more and 3 × 10 ¹⁸ / cm ³ or less, having a resistance layer between the active layer and the source electrode or the drain electrode, and the electrical resistivity of the resistance layer is 10 ⁵ Ω · A thin film field-effect transistor characterized by having a thickness of less than or equal to cm and less than or equal to 10 ¹³ Ω · cm and less than 20 nm.
<2> The thin film field effect transistor according to <1>, wherein at least one of the source electrode and the drain electrode is IZO.
<3> The thin film field effect transistor according to <1> or <2>, wherein the resistance layer is an amorphous oxide.
<4> The thin film field effect transistor according to any one of <1> to <3>, wherein the amorphous oxide semiconductor of the active layer contains In.
<5> The thin film field effect transistor according to <4>, wherein the amorphous oxide semiconductor of the active layer contains In and Ga or In and Zn.
<6> The thin film field effect transistor according to <4>, wherein the amorphous oxide semiconductor of the active layer contains In, Ga, and Zn.
<7> The thin film field effect transistor according to any one of <3> to <6>, wherein the amorphous oxide of the resistance layer contains In.
<8> The thin film field effect transistor according to <7>, wherein the amorphous oxide of the resistance layer contains In and Ga or In and Zn.
<9> The thin film field effect transistor according to <7>, wherein the amorphous oxide of the resistance layer contains In, Ga, and Zn.
<10> The thin film field effect transistor according to any one of <1> to <9>, wherein the substrate is a flexible substrate.
<11> A display device including a light-emitting element having a pair of electrodes and a light-emitting layer interposed between the electrodes, and a field-effect transistor for driving the light-emitting element, the field-effect transistor Is a thin film field effect transistor according to any one of <1> to <10>.

A TFT using an amorphous oxide semiconductor can be formed at room temperature and can be manufactured using a flexible plastic film as a substrate, and thus has attracted attention as a material for an active layer of a film (flexible) TFT. In particular, as disclosed in JP-A Nos. 2006-165529 and 2006-186319, an amorphous oxide semiconductor having a carrier concentration of less than 10 ¹⁸ / cm ³ is used as an active layer on a polyester film substrate. A TFT having an effective mobility of 10 cm ² / Vs and an ON / OFF ratio exceeding 10 ³ has been reported.
However, when this is used for a driving circuit of a display device, for example, the performance is still insufficient to operate the driving circuit from the viewpoint of mobility and ON / OFF ratio. The amorphous oxide semiconductor used for the active layer has a tendency that the electron mobility is lowered when the carrier concentration is lowered. Therefore, it is difficult to form a TFT having both good OFF characteristics and high mobility.
Furthermore, as a result of detailed analysis by the present inventors, when the carrier concentration is reduced to less than 10 ¹⁸ / cm ³ , the OFF current value changes or the threshold voltage of the TFT changes when the temperature of the operating environment of the TFT changes. The problem became clear. This variation of the threshold voltage fluctuations and TFT OFF current value as the carrier concentration decreases significantly, it has been found to cause practical problems and become change and decreases especially below ³ × 10 17 ^/ cm 3. It has also been found that the fluctuation of the OFF current value and the fluctuation of the threshold voltage of the TFT also occur when the TFT is continuously and repeatedly driven. Conventionally, when such a problem occurs in a semiconductor element, a temperature compensation circuit unit is generally introduced as a countermeasure. However, the circuit is complicated, the element volume increases, and the aperture ratio decreases. Accompanied by the evils. Therefore, this problem is a serious problem to be solved, and further improvements in environmental temperature dependency and durability have been demanded while achieving both OFF current characteristics and high mobility.

As a result of earnestly pursuing the development search, the present inventors have used a high concentration amorphous oxide semiconductor having a carrier concentration of 3 × 10 ¹⁵ / cm ³ or more and 3 × 10 ¹⁸ / cm ³ or less for the active layer, By arranging an electric resistance layer between the active layer and the source electrode or the drain electrode, and making the resistance layer a layer having an electric resistivity of 10 ⁵ Ω · cm or more and 10 ¹³ Ω · cm or less and a thickness of less than 20 nm The present inventors have found that the problem can be solved completely unexpectedly and have reached the present invention. That is, it has been found that even an amorphous oxide semiconductor having a high carrier concentration can be controlled to a sufficiently low OFF current.

  According to the present invention, a TFT having a low OFF current, a high ON / OFF ratio, and excellent temperature dependency and continuous drive stability is provided. In particular, a thin film field effect transistor useful as a film (flexible) TFT using a flexible substrate is provided. In addition, a display device using these TFTs is provided.

1. Thin film field effect transistor (TFT)
The TFT of the present invention has at least a gate electrode, a gate insulating film, an active layer, a source electrode, and a drain electrode in order, and controls the current flowing through the active layer by applying a voltage to the gate electrode, It is an active element having a function of switching a current between electrodes. As the TFT structure, either a staggered structure or an inverted staggered structure can be formed.

The carrier concentration of the active layer in the present invention is 3 × 10 ¹⁵ / cm ³ or more and 3 × 10 ¹⁸ / cm ³ or less. The carrier concentration is preferably 5 × 10 ¹⁵ / cm ³ or more and 2 × 10 ¹⁸ / cm ³ or less, and more preferably the carrier concentration is 1 × 10 ¹⁶ / cm ³ or more and 1 × 10 ¹⁸ / cm ³ or less.
The electrical resistance layer has an electrical resistivity of 10 ⁵ Ω · cm to 10 ¹³ Ω · cm and a thickness of less than 20 nm. Preferably, the electrical resistivity is 2 × 10 ⁵ Ω · cm to 5 × 10 ¹² Ω · cm and the thickness is 2 nm to 18 nm, and more preferably 5 × 10 ⁵ Ω · cm to 1 × 10 ¹² Ω. -It is cm or less and thickness is 5 nm or more and 15 nm or less. Within the above range, it is preferable that the thickness is relatively thin when the electrical resistivity is high, and the thickness is relatively thick when the electrical resistivity is low. The resistance layer of the present invention is controlled so that the carrier mobility is kept optimal.

  Preferably, the amorphous oxide semiconductor of the active layer contains at least In. An amorphous oxide semiconductor containing In and Ga or containing In and Zn is more preferable. More preferably, it is an amorphous oxide semiconductor containing In, Ga, and Zn.

Preferably, at least one of the source electrode and the drain electrode is IZO.
Preferably, the electrical resistance layer is made of an amorphous oxide. The amorphous oxide used for the electrical resistance layer contains at least In. More preferably, it is an amorphous oxide containing In and Ga or containing In and Zn. More preferably, it is an amorphous oxide containing In, Ga, and Zn.
Preferably, the substrate is a flexible resin substrate.
The TFT of the present invention will be described in more detail below.

1) Active layer An amorphous oxide semiconductor is used for the active layer used in the present invention. Since an amorphous oxide semiconductor can be formed at a low temperature, it can be formed on a flexible resin substrate such as a plastic. Good amorphous oxide semiconductors that can be produced at low temperatures include oxides containing at least In, oxides containing In and Ga, oxides containing In and Zn, and oxides containing In, Ga, and Zn. As the composition structure, it is known that InGaO ₃ (ZnO) _m (m is a natural number of less than 6) is preferable. These are n-type semiconductors whose carriers are electrons. Of course, a p-type oxide semiconductor such as ZnO.Rh ₂ O ₃ , CuGaO ₂ , or SrCu ₂ O ₂ may be used for the active layer. An oxide semiconductor disclosed in JP-A-2006-165529 can also be used.

Specifically, the amorphous oxide semiconductor according to the present invention includes In—Ga—Zn—O, and the composition in the crystalline state is represented by InGaO ₃ (ZnO) _m (m is a natural number of less than 6). A physical semiconductor is preferred. In particular, InGaZnO ₄ is more preferable. As an amorphous oxide semiconductor having this composition, the electron mobility tends to increase as the electrical conductivity increases. Further, the electric conductivity can be controlled by the oxygen partial pressure during film formation. Of course, the active layer can be applied not only to oxide semiconductors but also to inorganic semiconductors such as Si and Ge, compound semiconductors such as GaAs, organic semiconductor materials such as pentacene and polythiophene, and carbon nanotubes.

<Carrier concentration>
The carrier concentration of the active layer in the present invention can be adjusted to a desired value by various means.

Examples of the means for adjusting the carrier concentration of the active layer include the following means.
(1) Adjustment by oxygen defect It is known that when an oxygen defect is formed in an oxide semiconductor, the carrier concentration in the active layer increases and the electrical conductivity increases. Therefore, the carrier concentration of the oxide semiconductor can be controlled by adjusting the amount of oxygen defects. Specific methods for controlling the amount of oxygen defects include oxygen partial pressure during film formation, oxygen concentration and treatment time during post-treatment after film formation, and the like. Specific examples of post-treatment include heat treatment at 100 ° C. or higher, oxygen plasma, and UV ozone treatment. Among these methods, a method of controlling the oxygen partial pressure during film formation is preferable from the viewpoint of productivity. By adjusting the oxygen partial pressure during film formation, the carrier concentration of the oxide semiconductor can be controlled.
(2) Adjustment by composition ratio It is known that the carrier concentration is changed by changing the metal composition ratio of the oxide semiconductor. For example, in InGaZn _1-X Mg _X O ₄ , the carrier concentration decreases as the Mg ratio increases. In the (In ₂ O ₃ ) _1-X (ZnO) _X oxide system, when the Zn / In ratio is 10% or more, the carrier concentration decreases as the Zn ratio increases. As specific methods for changing these composition ratios, for example, in a film formation method by sputtering, targets having different composition ratios are used. Alternatively, it is possible to change the composition ratio of the film by co-sputtering with a multi-target and adjusting the sputtering rate individually.
(3) Adjustment by impurities It is possible to reduce the carrier concentration by adding elements such as Li, Na, Mn, Ni, Pd, Cu, Cd, C, N, and P to the oxide semiconductor as impurities. . As a method for adding an impurity, an oxide semiconductor and an impurity element are co-evaporated, an ion of the impurity element is added to the formed oxide semiconductor film by an ion doping method, or the like.
(4) Adjustment by oxide semiconductor material In the above (1) to (3), the method for adjusting the carrier concentration in the same oxide semiconductor system has been described. Of course, the carrier concentration can be changed by changing the oxide semiconductor material. Can be changed. For example, it is generally known that a SnO ₂ oxide semiconductor has a lower carrier concentration than an In ₂ O ₃ oxide semiconductor. Thus, the carrier concentration can be adjusted by changing the oxide semiconductor material.
As means for adjusting the carrier concentration, the above methods (1) to (4) may be used alone or in combination.

<Method for forming active layer>
As a method for forming the active layer, a vapor phase film forming method is preferably used with a polycrystalline sintered body of an oxide semiconductor as a target. Among vapor deposition methods, sputtering and pulsed laser deposition (PLD) are suitable. Furthermore, the sputtering method is preferable from the viewpoint of mass productivity.

For example, the film is formed by controlling the degree of vacuum and the oxygen flow rate by RF magnetron sputtering deposition. The greater the oxygen flow rate, the smaller the electrical conductivity.
The active layer in the present invention is an extremely thin layer, and in order to exhibit excellent TFT performance in such a thin layer region, the uniformity of the interface between the active layer and the adjacent layer on which the active layer is placed is required. is important. For example, in the case of a bottom gate type TFT, an active layer is usually provided on the gate insulating film, but the interface between the gate insulating film and the active layer is smooth, preferably the interface roughness is less than 2 nm. Is desirable. More preferably, it is less than 1 nm. For this purpose, it is preferable to execute the film formation rate of the gate insulating film and the active layer by controlling the sputtering rate and vapor deposition rate of each film component and finding the conditions for forming the film uniformly.

  The formed film can be confirmed to be an amorphous film by a known X-ray diffraction method. The composition ratio can be determined by an RBS (Rutherford backscattering) analysis method.

<Thickness of active layer>
The thickness of the active layer in the present invention is preferably 2 nm or more and 100 nm or less. More preferably, it is 5 nm or more and 70 nm or less.
The film thickness of the active layer in the present invention can be measured by HRTEM (High Resolution TEM) photography of the cross section of the produced element.

By using the active layer having the above-described structure, a transistor characteristic having a high mobility of 10 cm ² / (V · sec) or more and an ON / OFF ratio of 10 ⁶ or more can be realized.

2) Electrical resistance layer The electrical resistance layer is disposed between the active layer and at least one of the gate electrode or the source electrode. The electrical resistance layer used in the present invention has an electrical resistivity of 10 ⁵ Ω · cm to 10 ¹³ Ω · cm and a thickness of less than 20 nm. Preferably, it is 2 × 10 ⁵ Ω · cm or more and 5 × 10 ¹² Ω · cm or less, and the thickness is 2 nm or more and 18 nm or less, more preferably 5 × 10 ⁵ Ω · cm or more and 1 × 10 ¹² Ω · cm or less. The thickness is 5 nm or more and 15 nm or less.
Preferably, the electrical resistance layer is made of an amorphous oxide. The amorphous oxide used for the electrical resistance layer contains at least In. More preferably, it is an amorphous oxide containing In and Ga or containing In and Zn. More preferably, it is an amorphous oxide containing In, Ga, and Zn.

  The amorphous oxide used for the electrical resistance layer can be selected and used from the materials described for the material of the active layer. The electrical resistivity can be adjusted by the same means as described for the carrier concentration control means in the active layer.

3) Gate electrode Examples of the gate electrode in the present invention include metals such as Al, Mo, Cr, Ta, Ti, Au, and Ag, alloys such as Al-Nd and APC, tin oxide, zinc oxide, indium oxide, and oxide. Preferable examples include metal oxide conductive films such as indium tin (ITO) and indium zinc oxide (IZO), organic conductive compounds such as polyaniline, polythiophene, and polypyrrole, or mixtures thereof.
The thickness of the gate electrode is preferably 10 nm or more and 1000 nm or less.

  The electrode film formation method is not particularly limited, and may be a printing method, a wet method such as a coating method, a physical method such as a vacuum deposition method, a sputtering method, or an ion plating method, a CVD method, a plasma CVD method, or the like. It can be formed on the substrate according to a method appropriately selected in consideration of suitability with the material from among chemical methods. For example, when ITO is selected, it can be performed according to a direct current or high frequency sputtering method, a vacuum deposition method, an ion plating method, or the like. When an organic conductive compound is selected as the material for the gate electrode, it can be performed according to a wet film forming method.

4) Gate insulating film As the gate insulating film, at least two or more insulators such as SiO ₂ , SiN _x , SiON, Al ₂ O ₃ , Y ₂ O ₃ , Ta ₂ O ₅ , and HfO ₂ are used. A mixed crystal compound is used. A polymer insulator such as polyimide can also be used as the gate insulating film.

The thickness of the gate insulating film is preferably 10 nm to 10 μm. The gate insulating film needs to be thickened to some extent in order to reduce leakage current and increase voltage resistance. However, increasing the thickness of the gate insulating film results in an increase in the driving voltage of the TFT. Therefore, it is more preferable that the film thickness of the gate insulating film is 50 nm to 1000 nm for an inorganic insulator and 0.5 μm to 5 μm for a polymer insulator. In particular, it is particularly preferable to use a high dielectric constant insulator such as HfO ₂ for the gate insulating film because TFT driving at a low voltage is possible even if the film thickness is increased.

5) Source electrode and drain electrode Examples of the source electrode and drain electrode materials in the present invention include metals such as Al, Mo, Cr, Ta, Ti, Au, and Ag, alloys such as Al-Nd and APC, tin oxide, and oxidation. Preferable examples include metal oxide conductive films such as zinc, indium oxide, indium tin oxide (ITO), and zinc indium oxide (IZO), organic conductive compounds such as polyaniline, polythiophene, and polypyrrole, or mixtures thereof. Particularly preferred is IZO.
The thickness of the source electrode and the drain electrode is preferably 10 nm or more and 1000 nm or less.

  The electrode film formation method is not particularly limited, and may be a printing method, a wet method such as a coating method, a physical method such as a vacuum deposition method, a sputtering method, or an ion plating method, a CVD method, a plasma CVD method, or the like. It can be formed on the substrate according to a method appropriately selected in consideration of suitability with the material from among chemical methods. For example, when ITO is selected, it can be performed according to a direct current or high frequency sputtering method, a vacuum deposition method, an ion plating method, or the like. Further, when an organic conductive compound is selected as a material for the source electrode and the drain electrode, it can be performed according to a wet film forming method.

6) Substrate The substrate used in the present invention is not particularly limited. For example, YSZ (zirconia stabilized yttrium), inorganic materials such as glass, polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate Synthetic resins such as polyester such as polyester, polystyrene, polycarbonate, polyethersulfone, polyarylate, allyl diglycol carbonate, polyimide, polycycloolefin, norbornene resin, poly (chlorotrifluoroethylene), etc. Organic materials, and the like. In the case of the organic material, it is preferable that the organic material is excellent in heat resistance, dimensional stability, solvent resistance, electrical insulation, workability, low air permeability, low moisture absorption, and the like.

  In the present invention, a flexible substrate is particularly preferably used. The material used for the flexible substrate is preferably an organic plastic film having a high transmittance. For example, polyesters such as polyethylene terephthalate, polybutylene phthalate, polyethylene naphthalate, polystyrene, polycarbonate, polyethersulfone, polyarylate, polyimide, polycyclo Plastic films such as olefin, norbornene resin, and poly (chlorotrifluoroethylene) can be used. In addition, if the insulating property is insufficient for the film-like plastic substrate, the insulating layer, the gas barrier layer for preventing the transmission of moisture and oxygen, the flatness of the film-like plastic substrate and the adhesion with the electrode and active layer It is also preferable to provide an undercoat layer or the like for improvement.

  Here, the thickness of the flexible substrate is preferably 50 μm or more and 500 μm or less. This is because it is difficult for the substrate itself to maintain sufficient flatness when the thickness of the flexible substrate is less than 50 μm. Further, when the thickness of the flexible substrate is more than 500 μm, it is difficult to bend the substrate itself freely, that is, the flexibility of the substrate itself is poor.

7) Structure Next, the structure of the TFT in the present invention will be described in detail with reference to the drawings.
FIG. 1 is a schematic view showing an example of the TFT of the present invention. When the substrate 1 is a flexible substrate such as a plastic film, an insulating layer 6 is disposed on at least one surface of the substrate 1, and a gate electrode 2, a gate insulating film 3, an active layer 4, and a resistance layer 7 are stacked thereon. The source electrode 5-1 and the drain electrode 5-2 are provided on the surface.

According to this configuration, the carrier concentration of the active layer 4 is as high as 3 × 10 ¹⁵ / cm ³ or more and 3 × 10 ¹⁸ / cm ³ or less, and a high ON current can be provided. On the other hand, the OFF current value is suppressed and kept low while the high ON current is maintained by the resistance layer 7. Therefore, according to this configuration, an excellent TFT can be obtained with a high ON / OFF ratio. In particular, since a high current can be generated, a TFT suitable for driving control of the organic EL element can be obtained.

  FIG. 2 is a schematic diagram of an equivalent circuit of an active matrix driving type organic EL display device using the TFT element of the present invention. The circuit of the organic EL display device in the present invention is not particularly limited to that shown in FIG. 2, and a conventionally known circuit can be applied as it is.

2. Display Device The field effect thin film transistor of the present invention is preferably used for an image display device using liquid crystal or an EL element, in particular, a flat panel display (FPD). More preferably, it is used for a flexible display device using a flexible substrate such as an organic plastic film as the substrate. In particular, the field effect thin film transistor of the present invention is most preferably used for a display device using an organic EL element and a flexible organic EL display device because of its high mobility.

(Organic EL display device)
The organic EL display device used in the present invention includes an organic EL element having at least a lower electrode on the substrate, an organic layer including at least a light emitting layer, and an upper electrode in sequence, and at least a gate electrode, a gate insulating film on the upper electrode, The TFT has an active layer containing an oxide semiconductor, a source electrode, and a drain electrode, and drives the organic EL element. Since TFT is arrange | positioned at the back surface of an organic EL element, the opening part which takes out light emission of an organic EL element can be taken large. Preferably, a protective insulating film is provided between the TFT and the organic EL element, and the upper electrode of the organic EL element and the source electrode or the drain electrode of the TFT are connected via a contact hole formed in the protective insulating film. Electrically connected. Preferably, the lower electrode is a light transmissive electrode, and the upper electrode is a light reflective electrode.

Hereinafter, the organic EL device of the present invention will be described in detail.
The light-emitting element of the present invention has a cathode and an anode on a substrate, and an organic compound layer including an organic light-emitting layer (hereinafter sometimes simply referred to as “light-emitting layer”) between both electrodes. In view of the properties of the light emitting element, at least one of the anode and the cathode is preferably transparent.

In the present invention, the organic compound layer is preferably laminated in the order of the hole transport layer, the light emitting layer, and the electron transport layer from the anode side. Further, a hole injection layer is provided between the hole transport layer and the anode, and / or an electron transporting intermediate layer is provided between the light emitting layer and the electron transport layer. Further, a hole transporting intermediate layer may be provided between the light emitting layer and the hole transport layer, and similarly, an electron injection layer may be provided between the cathode and the electron transport layer.
Each layer may be divided into a plurality of secondary layers.

  Each layer constituting the organic compound layer can be suitably formed by any of dry film forming methods such as vapor deposition and sputtering, transfer methods, printing methods, coating methods, ink jet methods, and spray methods.

  Next, elements constituting the organic EL element will be described in detail.

(substrate)
The substrate used in the present invention is preferably a substrate that does not scatter or attenuate light emitted from the organic compound layer. Specific examples include zirconia-stabilized yttrium (YSZ), inorganic materials such as glass, polyesters such as polyethylene terephthalate, polybutylene phthalate, and polyethylene naphthalate, polystyrene, polycarbonate, polyethersulfone, polyarylate, polyimide, and polycycloolefin. , Norbornene resins, and organic materials such as poly (chlorotrifluoroethylene).
For example, when glass is used as the substrate, alkali-free glass is preferably used as the material in order to reduce ions eluted from the glass. Moreover, when using soda-lime glass, it is preferable to use what gave barrier coatings, such as a silica. In the case of an organic material, it is preferable that it is excellent in heat resistance, dimensional stability, solvent resistance, electrical insulation, and workability.

  There is no restriction | limiting in particular about the shape of a board | substrate, a structure, a magnitude | size, It can select suitably according to the use, purpose, etc. of a light emitting element. In general, the shape of the substrate is preferably a plate shape. The structure of the substrate may be a single layer structure, a laminated structure, may be formed of a single member, or may be formed of two or more members.

  The substrate may be colorless and transparent or colored and transparent, but is preferably colorless and transparent in that it does not scatter or attenuate light emitted from the organic light emitting layer.

The substrate can be provided with a moisture permeation preventing layer (gas barrier layer) on the front surface or the back surface.
As a material for the moisture permeation preventive layer (gas barrier layer), inorganic materials such as silicon nitride and silicon oxide are preferably used. The moisture permeation preventing layer (gas barrier layer) can be formed by, for example, a high frequency sputtering method.
When a thermoplastic substrate is used, a hard coat layer, an undercoat layer, or the like may be further provided as necessary.

(anode)
The anode usually has a function as an electrode for supplying holes to the organic compound layer, and there is no particular limitation on the shape, structure, size, etc., depending on the use and purpose of the light-emitting element. , Can be appropriately selected from known electrode materials. As described above, the anode is usually provided as a transparent anode.

  Suitable examples of the material for the anode include metals, alloys, metal oxides, conductive compounds, and mixtures thereof. Specific examples of the anode material include conductive metals such as tin oxide doped with antimony and fluorine (ATO, FTO), tin oxide, zinc oxide, indium oxide, indium tin oxide (ITO), and indium zinc oxide (IZO). Metals such as oxides, gold, silver, chromium, nickel, and mixtures or laminates of these metals and conductive metal oxides, inorganic conductive materials such as copper iodide and copper sulfide, polyaniline, polythiophene, polypyrrole, etc. Organic conductive materials, and a laminate of these and ITO. Among these, conductive metal oxides are preferable, and ITO is particularly preferable from the viewpoints of productivity, high conductivity, transparency, and the like.

  The anode is composed of, for example, a wet method such as a printing method and a coating method, a physical method such as a vacuum deposition method, a sputtering method, and an ion plating method, and a chemical method such as a CVD and a plasma CVD method. It can be formed on the substrate according to a method appropriately selected in consideration of suitability with the material to be processed. For example, when ITO is selected as the anode material, the anode can be formed according to a direct current or high frequency sputtering method, a vacuum deposition method, an ion plating method, or the like.

  In the organic electroluminescent element of the present invention, the formation position of the anode is not particularly limited and can be appropriately selected according to the use and purpose of the light emitting element. Is preferably formed on the substrate. In this case, the anode may be formed on the entire one surface of the substrate, or may be formed on a part thereof.

  The patterning for forming the anode may be performed by chemical etching such as photolithography, or may be performed by physical etching such as laser, or vacuum deposition or sputtering with a mask overlapped. It may be performed by a lift-off method or a printing method.

  The thickness of the anode can be appropriately selected depending on the material constituting the anode and cannot be generally defined, but is usually about 10 nm to 50 μm, and preferably 50 nm to 20 μm.

The resistance value of the anode is preferably 10 ³ Ω / □ or less, and more preferably 10 ² Ω / □ or less. When the anode is transparent, it may be colorless and transparent or colored and transparent. In order to take out light emission from the transparent anode side, the transmittance is preferably 60% or more, and more preferably 70% or more.

  The transparent anode is described in detail in the book “New Development of Transparent Electrode Films” published by CMC (1999), supervised by Yutaka Sawada, and the matters described here can be applied to the present invention. In the case of using a plastic substrate having low heat resistance, a transparent anode formed using ITO or IZO at a low temperature of 150 ° C. or lower is preferable.

(cathode)
The cathode usually has a function as an electrode for injecting electrons into the organic compound layer, and there is no particular limitation on the shape, structure, size, etc., depending on the use and purpose of the light-emitting element, It can select suitably from well-known electrode materials.

  Examples of the material constituting the cathode include metals, alloys, metal oxides, electrically conductive compounds, and mixtures thereof. Specific examples include alkali metals (eg, LI, Na, K, Cs, etc.), alkaline earth metals (eg, Mg, Ca, etc.), gold, silver, lead, aluminum, sodium-potassium alloys, lithium-aluminum alloys, magnesium. -Rare earth metals such as silver alloys, indium and ytterbium. These may be used alone, but two or more can be suitably used in combination from the viewpoint of achieving both stability and electron injection.

Among these, as a material constituting the cathode, an alkali metal or an alkaline earth metal is preferable from the viewpoint of electron injecting property, and a material mainly composed of aluminum is preferable from the viewpoint of excellent storage stability.
The material mainly composed of aluminum is aluminum alone, an alloy of aluminum and 0.01% by mass to 10% by mass of alkali metal or alkaline earth metal, or a mixture thereof (for example, lithium-aluminum alloy, magnesium-aluminum alloy). Etc.).

  The materials for the cathode are described in detail in JP-A-2-15595 and JP-A-5-121172, and the materials described in these public relations can also be applied in the present invention.

  There is no restriction | limiting in particular about the formation method of a cathode, According to a well-known method, it can carry out. For example, the cathode described above is configured from a wet method such as a printing method or a coating method, a physical method such as a vacuum deposition method, a sputtering method, or an ion plating method, or a chemical method such as CVD or plasma CVD method. It can be formed according to a method appropriately selected in consideration of suitability with the material. For example, when a metal or the like is selected as the cathode material, one or more of them can be simultaneously or sequentially performed according to a sputtering method or the like.

  Patterning when forming the cathode may be performed by chemical etching such as photolithography, physical etching by laser, or the like, or by vacuum deposition or sputtering with the mask overlaid. It may be performed by a lift-off method or a printing method.

In the present invention, the cathode formation position is not particularly limited, and may be formed on the entire organic compound layer or a part thereof.
Further, a dielectric layer made of an alkali metal or alkaline earth metal fluoride or oxide may be inserted between the cathode and the organic compound layer with a thickness of 0.1 nm to 5 nm. This dielectric layer can also be regarded as a kind of electron injection layer. The dielectric layer can be formed by, for example, a vacuum deposition method, a sputtering method, an ion plating method, or the like.

The thickness of the cathode can be appropriately selected depending on the material constituting the cathode and cannot be generally defined, but is usually about 10 nm to 5 μm, and preferably 50 nm to 1 μm.
Further, the cathode may be transparent or opaque. The transparent cathode can be formed by depositing a thin cathode material to a thickness of 1 nm to 10 nm and further laminating a transparent conductive material such as ITO or IZO.

(Organic compound layer)
The organic compound layer in the present invention will be described.
The organic EL device of the present invention has at least one organic compound layer including a light emitting layer, and as the organic compound layer other than the light emitting layer, as described above, a hole transport layer, an electron transport layer, a charge Examples of the layer include a block layer, a hole injection layer, and an electron injection layer.

  In the organic EL device of the present invention, each layer constituting the organic compound layer is preferably formed by any of dry film forming methods such as vapor deposition and sputtering, wet coating methods, transfer methods, printing methods, and ink jet methods. Can do.

(Light emitting layer)
The organic light emitting layer receives holes from the anode, the hole injection layer, or the hole transport layer when an electric field is applied, receives electrons from the cathode, the electron injection layer, or the electron transport layer, and recombines holes and electrons. It is a layer having a function of providing a field to emit light.
The light emitting layer in the present invention may be composed only of a light emitting material, or may be a mixed layer of a host material and a light emitting dopant. The luminescent dopant may be a fluorescent material or a phosphorescent material, and may be two or more kinds. The host material is preferably a charge transport material. The host material may be one type or two or more types, and examples thereof include a configuration in which an electron transporting host material and a hole transporting host material are mixed. Further, the light emitting layer may include a material that does not have charge transporting properties and does not emit light.
Further, the light emitting layer may be a single layer or two or more layers, and each layer may emit light in different emission colors.

  As the luminescent dopant in the present invention, any of phosphorescent luminescent materials and fluorescent luminescent materials can be used as the dopant.

  The light emitting layer in the present invention can contain two or more kinds of light emitting dopants in order to improve color purity and to broaden the light emission wavelength region. The luminescent dopant in the present invention is a dopant that satisfies the relationship of 1.2 eV> ΔIp> 0.2 eV and / or 1.2 eV> ΔEa> 0.2 eV with the host compound. This is preferable from the viewpoint of driving durability.

《Phosphorescent dopant》
In general, examples of the phosphorescent light-emitting dopant include complexes containing a transition metal atom or a lanthanoid atom.
For example, the transition metal atom is not particularly limited, but preferably includes ruthenium, rhodium, palladium, tungsten, rhenium, osmium, iridium, gold, silver, copper, and platinum, and more preferably rhenium, iridium. And platinum, more preferably iridium and platinum.
Examples of lanthanoid atoms include lanthanum, cerium, praseodymium, neodymium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium. Among these lanthanoid atoms, neodymium, europium, and gadolinium are preferable.

  Examples of the ligand of the complex include G.I. Wilkinson et al., Comprehensive Coordination Chemistry, Pergamon Press, 1987, H.C. Examples include ligands described in Yersin's "Photochemistry and Photophysics of Coordination Compounds" published by Springer-Verlag 1987, Akio Yamamoto "Organic Metal Chemistry-Fundamentals and Applications-" .

  The specific ligand is preferably a halogen ligand (preferably a chlorine ligand) or an aromatic carbocyclic ligand (for example, preferably 5 to 30 carbon atoms, more preferably 6 to 6 carbon atoms). 30, more preferably 6 to 20 carbon atoms, particularly preferably 6 to 12 carbon atoms, such as a cyclopentadienyl anion, a benzene anion, or a naphthyl anion), a nitrogen-containing heterocyclic ligand (for example, preferably Has 5 to 30 carbon atoms, more preferably 6 to 30 carbon atoms, still more preferably 6 to 20 carbon atoms, particularly preferably 6 to 12 carbon atoms, and phenylpyridine, benzoquinoline, quinolinol, bipyridyl, or phenanthroline. Etc.), diketone ligand (for example, acetylacetone, etc.), carboxylic acid ligand (for example, preferably 2-30 carbon atoms, and more) Preferably, it has 2 to 20 carbon atoms, more preferably 2 to 16 carbon atoms, such as an acetic acid ligand), an alcoholate ligand (for example, preferably 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms). More preferably, it has 6 to 20 carbon atoms, such as phenolate ligand), silyloxy ligand (for example, preferably 3 to 40 carbon atoms, more preferably 3 to 30 carbon atoms, still more preferably 3 to 3 carbon atoms). 20 such as trimethylsilyloxy ligand, dimethyl-tert-butylsilyloxy ligand, triphenylsilyloxy ligand), carbon monoxide ligand, isonitrile ligand, cyano ligand, Phosphorus ligand (preferably having 3 to 40 carbon atoms, more preferably 3 to 30 carbon atoms, still more preferably 3 to 20 carbon atoms, and particularly preferably 6 to 20 carbon atoms. A rephenylphosphine ligand), a thiolato ligand (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, still more preferably 6 to 20 carbon atoms, such as a phenylthiolato ligand) ), A phosphine oxide ligand (preferably having 3 to 30 carbon atoms, more preferably 8 to 30 carbon atoms, still more preferably 18 to 30 carbon atoms, such as a triphenylphosphine oxide ligand). More preferably, it is a nitrogen-containing heterocyclic ligand.

  The complex may have one transition metal atom in the compound, or may be a so-called binuclear complex having two or more. Different metal atoms may be contained at the same time.

Among these, specific examples of the luminescent dopant include, for example, US6303238B1, US6097147, WO00 / 57676, WO00 / 70655, WO01 / 08230, WO01 / 39234A2, WO01 / 41512A1, WO02 / 02714A2, WO02 / 15645A1, WO02 / 44189A1. , WO 05/19373 A2, JP 2001-247859, JP 2002-302671, JP 2002-117978, JP 2003-133074, JP 2002-235076, JP 2003-123982, JP 2002-170684, EP 12112257, Special JP 2002-226495, JP 2002-234894, JP 2001247478, JP 2001-298470, JP 2002 73674, JP 2002-203678, JP 2002-203679, JP 2004-357799, JP 2006-256999, JP 2007-19462, JP 2007-84635, JP 2007-96259, and the like. Phosphorescent compounds and the like are mentioned. Among them, more preferable luminescent dopants include Ir complex, Pt complex, Cu complex, Re complex, W complex, Rh complex, Ru complex, Pd complex, Os complex, Eu complex, Tb complex. , Gd complex, Dy complex, and Ce complex.
Particularly preferred is an Ir complex, a Pt complex, or a Re complex, among which an Ir complex or a Pt complex containing at least one coordination mode of a metal-carbon bond, a metal-nitrogen bond, a metal-oxygen bond, and a metal-sulfur bond. Or a Re complex. Furthermore, from the viewpoints of luminous efficiency, driving durability, chromaticity, etc., an Ir complex, a Pt complex, or a Re complex containing a tridentate or higher polydentate ligand is particularly preferable.

《Fluorescent luminescent dopant》
As the fluorescent light-emitting dopant, generally, benzoxazole, benzimidazole, benzothiazole, styrylbenzene, polyphenyl, diphenylbutadiene, tetraphenylbutadiene, naphthalimide, coumarin, pyran, perinone, oxadiazole, aldazine, Pyraridin, cyclopentadiene, bisstyrylanthracene, quinacridone, pyrrolopyridine, thiadiazolopyridine, cyclopentadiene, styrylamine, aromatic dimethylidin compounds, condensed polycyclic aromatic compounds (anthracene, phenanthroline, pyrene, perylene, rubrene, or pentacene, etc. ), 8-quinolinol metal complexes, various metal complexes represented by pyromethene complexes and rare earth complexes, polythiophene, polyphenylene, polyphenylene Polymeric compounds such as vinylene, organic silane, and the like, and their derivatives.

  Among these, specific examples of the luminescent dopant include the following, but are not limited thereto.

  The light-emitting dopant in the light-emitting layer is contained in an amount of 0.1% by mass to 50% by mass with respect to the total compound mass generally forming the light-emitting layer in the light-emitting layer. To 1 mass% to 50 mass%, and more preferably 2 mass% to 40 mass%.

  Although the thickness of the light emitting layer is not particularly limited, it is usually preferably 2 nm to 500 nm, more preferably 3 nm to 200 nm, and more preferably 5 nm to 100 nm from the viewpoint of external quantum efficiency. More preferably.

<Host material>
As the host material used in the present invention, a hole transporting host material excellent in hole transportability (sometimes referred to as a hole transportable host) and an electron transporting host compound excellent in electron transportability (electron transportability) May be described as a host).

《Hole-transporting host》
Specific examples of the hole transporting host used in the present invention include the following materials.
Pyrrole, indole, carbazole, azaindole, azacarbazole, triazole, oxazole, oxadiazole, pyrazole, imidazole, thiophene, polyarylalkane, pyrazoline, pyrazolone, phenylenediamine, arylamine, amino-substituted chalcone, styrylanthracene, fluorenone, hydrazone , Stilbene, silazane, aromatic tertiary amine compounds, styrylamine compounds, aromatic dimethylidin compounds, porphyrin compounds, polysilane compounds, poly (N-vinylcarbazole), aniline copolymers, thiophene oligomers, polythiophenes, etc. Conductive polymer oligomers, organic silanes, carbon films, and derivatives thereof.
Preferred are indole derivatives, carbazole derivatives, aromatic tertiary amine compounds, and thiophene derivatives, and more preferred are those having a carbazole group in the molecule. In particular, a compound having a t-butyl substituted carbazole group is preferable.

《Electron transporting host》
The electron transporting host in the light emitting layer used in the present invention preferably has an electron affinity Ea of 2.5 eV or more and 3.5 eV or less from the viewpoint of improving durability and lowering driving voltage. More preferably, it is 0.4 eV or less, and further preferably 2.8 eV or more and 3.3 eV or less. Further, from the viewpoint of improving durability and reducing driving voltage, the ionization potential Ip is preferably 5.7 eV or more and 7.5 eV or less, more preferably 5.8 eV or more and 7.0 eV or less, and 5.9 eV or more. More preferably, it is 6.5 eV or less.

Specific examples of such an electron transporting host include the following materials.
Pyridine, pyrimidine, triazine, imidazole, pyrazole, triazole, oxazole, oxadiazol, fluorenone, anthraquinodimethane, anthrone, diphenylquinone, thiopyran dioxide, carbodiimide, fluorenylidenemethane, distyrylpyrazine, Fluorine-substituted aromatic compounds, heterocyclic tetracarboxylic anhydrides such as naphthaleneperylene, phthalocyanines, and derivatives thereof (may form condensed rings with other rings), metal complexes and metals of 8-quinolinol derivatives Examples thereof include various metal complexes represented by metal complexes having phthalocyanine, benzoxazole or benzothiazol as a ligand.

Preferred examples of the electron transporting host include metal complexes, azole derivatives (benzimidazole derivatives, imidazopyridine derivatives, etc.), and azine derivatives (pyridine derivatives, pyrimidine derivatives, triazine derivatives, etc.). To metal complex compounds are preferred. The metal complex compound (A) is more preferably a metal complex having a ligand having at least one nitrogen atom, oxygen atom or sulfur atom coordinated to the metal.
The metal ion in the metal complex is not particularly limited, but is preferably beryllium ion, magnesium ion, aluminum ion, gallium ion, zinc ion, indium ion, tin ion, platinum ion, or palladium ion, more preferably beryllium ion, Aluminum ion, gallium ion, zinc ion, platinum ion, or palladium ion, and more preferably aluminum ion, zinc ion, or palladium ion.

  There are various known ligands contained in the metal complex. For example, “Photochemistry and Photophysics of Coordination Compounds”, Springer-Verlag, H.C. Examples include the ligands described in Yersin, published in 1987, “Organometallic Chemistry: Fundamentals and Applications”, Sakai Hanafusa, Yamamoto Akio, published in 1982, and the like.

The ligand is preferably a nitrogen-containing heterocyclic ligand (preferably having 1 to 30 carbon atoms, more preferably 2 to 20 carbon atoms, particularly preferably 3 to 15 carbon atoms, and a monodentate ligand. Alternatively, it may be a bidentate or higher ligand, preferably a bidentate or higher and a hexadentate or lower ligand, or a bidentate or higher and lower 6 or lower ligand and a monodentate mixed ligand. preferable.
Examples of the ligand include an azine ligand (for example, pyridine ligand, bipyridyl ligand, terpyridine ligand, etc.), a hydroxyphenylazole ligand (for example, hydroxyphenylbenzimidazole coordination). And a hydroxyphenyl benzoxazole ligand, a hydroxyphenyl imidazole ligand, a hydroxyphenylimidazopyridine ligand, etc.), an alkoxy ligand (preferably having 1 to 30 carbon atoms, more preferably 1 carbon atom). To 20, particularly preferably 1 to 10 carbon atoms, such as methoxy, ethoxy, butoxy, 2-ethylhexyloxy), aryloxy ligands (preferably 6 to 30 carbon atoms, more preferably 6-20 carbon atoms, particularly preferably 6-12 carbon atoms, for example phenyl Carboxymethyl, 1-naphthyloxy, 2-naphthyloxy, 2,4,6-trimethylphenyl oxy, and 4-biphenyloxy and the like.),

Heteroaryloxy ligand (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, and examples thereof include pyridyloxy, pyrazyloxy, pyrimidyloxy, and quinolyloxy. ), An alkylthio ligand (preferably having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, such as methylthio and ethylthio), arylthio ligands (Preferably 6 to 30 carbon atoms, more preferably 6 to 20 carbon atoms, particularly preferably 6 to 12 carbon atoms, such as phenylthio), heteroarylthio ligand (preferably 1 carbon atom) To 30, more preferably 1 to 20 carbon atoms, particularly preferably 1 to 12 carbon atoms, such as pyridylthio , 2-benzimidazolylthio, 2-benzoxazolylthio, 2-benzthiazolylthio, etc.), a siloxy ligand (preferably having 1 to 30 carbon atoms, more preferably 3 to 25 carbon atoms). Particularly preferably, it has 6 to 20 carbon atoms, and examples thereof include a triphenylsiloxy group, a triethoxysiloxy group, and a triisopropylsiloxy group.), An aromatic hydrocarbon anion ligand (preferably having 6 carbon atoms) To 30, more preferably 6 to 25 carbon atoms, particularly preferably 6 to 20 carbon atoms, such as a phenyl anion, a naphthyl anion, an anthranyl anion, etc.), an aromatic heterocyclic anion ligand (preferably Has 1 to 30 carbon atoms, more preferably 2 to 25 carbon atoms, and particularly preferably 2 to 20 carbon atoms. Pyrrole anion, pyrazole anion, pyrazole anion, triazole anion, oxazole anion, benzoxazole anion, thiazole anion, benzothiazole anion, thiophene anion, benzothiophene anion, etc.), indolenine anion ligand, etc. , Preferably a nitrogen-containing heterocyclic ligand, aryloxy ligand, heteroaryloxy group, or siloxy ligand, more preferably a nitrogen-containing heterocyclic ligand, aryloxy ligand, siloxy coordination Or an aromatic hydrocarbon anion ligand or an aromatic heterocyclic anion ligand.

  Examples of the metal complex electron transporting host are described in, for example, JP-A No. 2002-235076, JP-A No. 2004-214179, JP-A No. 2004-221106, JP-A No. 2004-221665, JP-A No. 2004-221068, JP-A No. 2004-327313, and the like. The compound of this is mentioned.

  In the light emitting layer of the present invention, it is preferable in terms of color purity, light emission efficiency, and driving durability that the triplet lowest excitation level (T1) of the host material is higher than T1 of the phosphorescent light emitting material.

  Further, the content of the host compound in the present invention is not particularly limited, but from the viewpoint of light emission efficiency and driving voltage, it is 15% by mass to 95% by mass with respect to the total compound mass forming the light emitting layer. Preferably there is.

(Hole injection layer, hole transport layer)
The hole injection layer and the hole transport layer are layers having a function of receiving holes from the anode or the anode side and transporting them to the cathode side. The hole injection material and the hole transport material used for these layers may be a low molecular compound or a high molecular compound.
Specifically, pyrrole derivatives, carbazole derivatives, triazole derivatives, oxazole derivatives, oxadiazole derivatives, imidazole derivatives, polyarylalkane derivatives, pyrazoline derivatives, pyrazolone derivatives, phenylenediamine derivatives, arylamine derivatives, amino-substituted chalcone derivatives, styryl Anthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives, aromatic tertiary amine compounds, styrylamine compounds, aromatic dimethylidin compounds, phthalocyanine compounds, porphyrin compounds, thiophene derivatives, organosilane derivatives, carbon, And the like.

  An electron-accepting dopant can be contained in the hole injection layer or the hole transport layer of the organic EL device of the present invention. As the electron-accepting dopant introduced into the hole-injecting layer or the hole-transporting layer, an inorganic compound or an organic compound can be used as long as it has an electron-accepting property and oxidizes an organic compound.

  Specifically, examples of the inorganic compound include metal halides such as ferric chloride, aluminum chloride, gallium chloride, indium chloride, and antimony pentachloride, metal oxides such as vanadium pentoxide, and molybdenum trioxide.

  In the case of an organic compound, a compound having a nitro group, halogen, cyano group, trifluoromethyl group or the like as a substituent, a quinone compound, an acid anhydride compound, fullerene, or the like can be preferably used. In addition, JP-A-6-212153, JP-A-11-111463, JP-A-11-251067, JP-A-2000-196140, JP-A-2000-286054, JP-A-2000-315580, JP-A-2001-102175, JP-A-2001-2001. -160493, JP2002-252085, JP2002-56985, JP2003-157981, JP2003-217862, JP2003-229278, JP2004-342614, JP2005-72012, JP20051666667 The compounds described in JP-A-2005-209643 and the like can be preferably used.

  Among these, hexacyanobutadiene, hexacyanobenzene, tetracyanoethylene, tetracyanoquinodimethane, tetrafluorotetracyanoquinodimethane, p-fluoranyl, p-chloranil, p-bromanyl, p-benzoquinone, 2,6-dichlorobenzoquinone, 2 , 5-dichlorobenzoquinone, 1,2,4,5-tetracyanobenzene, 1,4-dicyanotetrafluorobenzene, 2,3-dichloro-5,6-dicyanobenzoquinone, p-dinitrobenzene, m-dinitrobenzene, o-dinitrobenzene, 1,4-naphthoquinone, 2,3-dichloronaphthoquinone, 1,3-dinitronaphthalene, 1,5-dinitronaphthalene, 9,10-anthraquinone, 1,3,6,8-tetranitrocarbazole, 2,4,7-trinitro-9- Luenone, 2,3,5,6-tetracyanopyridine or fullerene C60 is preferred, and hexacyanobutadiene, hexacyanobenzene, tetracyanoethylene, tetracyanoquinodimethane, tetrafluorotetracyanoquinodimethane, p-fluoranyl, p- Chloranil, p-bromanyl, 2,6-dichlorobenzoquinone, 2,5-dichlorobenzoquinone, 2,3-dichloronaphthoquinone, 1,2,4,5-tetracyanobenzene, 2,3-dichloro-5,6-dicyano Benzoquinone or 2,3,5,6-tetracyanopyridine is more preferred, and tetrafluorotetracyanoquinodimethane is particularly preferred.

  These electron-accepting dopants may be used alone or in combination of two or more. Although the usage-amount of an electron-accepting dopant changes with kinds of material, it is preferable that it is 0.01 mass%-50 mass% with respect to hole transport layer material, and it is 0.05 mass%-20 mass%. It is further more preferable and it is especially preferable that it is 0.1 mass%-10 mass%.

The thicknesses of the hole injection layer and the hole transport layer are each preferably 500 nm or less from the viewpoint of lowering the driving voltage.
The thickness of the hole transport layer is preferably 1 nm to 500 nm, more preferably 5 nm to 200 nm, and still more preferably 10 nm to 100 nm. In addition, the thickness of the hole injection layer is preferably 0.1 nm to 200 nm, more preferably 0.5 nm to 100 nm, and still more preferably 1 nm to 100 nm.
The hole injection layer and the hole transport layer may have a single-layer structure composed of one or more of the materials described above, or may have a multilayer structure composed of a plurality of layers having the same composition or different compositions. .

(Electron injection layer, electron transport layer)
The electron injection layer and the electron transport layer are layers having a function of receiving electrons from the cathode or the cathode side and transporting them to the anode side. The electron injection material and the electron transport material used for these layers may be a low molecular compound or a high molecular compound.
Specifically, pyridine derivatives, quinoline derivatives, pyrimidine derivatives, pyrazine derivatives, phthalazine derivatives, phenanthroline derivatives, triazine derivatives, triazole derivatives, oxazole derivatives, oxadiazole derivatives, imidazole derivatives, fluorenone derivatives, anthraquinodimethane derivatives, anthrone Derivatives, diphenylquinone derivatives, thiopyran dioxide derivatives, carbodiimide derivatives, fluorenylidenemethane derivatives, distyrylpyrazine derivatives, naphthalene, perylene and other aromatic ring tetracarboxylic acid anhydrides, phthalocyanine derivatives, 8-quinolinol derivative metal complexes, Metal phthalocyanines, various metal complexes represented by metal complexes with benzoxazole and benzothiazole as ligands, organosilane derivatives represented by siloles Body, or the like is preferably a layer containing.

The electron injection layer or the electron transport layer of the organic EL device of the present invention can contain an electron donating dopant. The electron donating dopant introduced into the electron injecting layer or the electron transporting layer only needs to have an electron donating property and a property of reducing an organic compound, such as an alkali metal such as Li or an alkaline earth metal such as Mg. Transition metals including rare earth metals and reducing organic compounds are preferably used. As the metal, a metal having a work function of 4.2 eV or less can be preferably used. Specifically, Li, Na, K, Be, Mg, Ca, Sr, Ba, Y, Cs, La, Sm, Gd , And Yb. Examples of the reducing organic compound include nitrogen-containing compounds, sulfur-containing compounds, and phosphorus-containing compounds.
In addition, materials described in JP-A-6-212153, JP-A-2000-196140, JP-A-2003-68468, JP-A-2003-229278, JP-A-2004-342614, and the like can be used.

  These electron donating dopants may be used alone or in combination of two or more. The amount of the electron donating dopant varies depending on the type of material, but is preferably 0.1% by mass to 99% by mass, and 1.0% by mass to 80% by mass with respect to the electron transport layer material. Is more preferable, and 2.0 mass% to 70 mass% is particularly preferable.

The thicknesses of the electron injection layer and the electron transport layer are each preferably 500 nm or less from the viewpoint of lowering the driving voltage.
The thickness of the electron transport layer is preferably 1 nm to 500 nm, more preferably 5 nm to 200 nm, and still more preferably 10 nm to 100 nm. In addition, the thickness of the electron injection layer is preferably 0.1 nm to 200 nm, more preferably 0.2 nm to 100 nm, and still more preferably 0.5 nm to 50 nm.
The electron injection layer and the electron transport layer may have a single layer structure composed of one or more of the above-described materials, or may have a multilayer structure composed of a plurality of layers having the same composition or different compositions.

(Hole blocking layer)
The hole blocking layer is a layer having a function of preventing holes transported from the anode side to the light emitting layer from passing through to the cathode side. In the present invention, a hole blocking layer can be provided as an organic compound layer adjacent to the light emitting layer on the cathode side.
Examples of the compound constituting the hole blocking layer include aluminum complexes such as BAlq, triazole derivatives, phenanthroline derivatives such as BCP, and the like.
The thickness of the hole blocking layer is preferably 1 nm to 500 nm, more preferably 5 nm to 200 nm, and still more preferably 10 nm to 100 nm.
The hole blocking layer may have a single layer structure composed of one or more of the above-described materials, or may have a multilayer structure composed of a plurality of layers having the same composition or different compositions.

(Electronic block layer)
The electron blocking layer is a layer having a function of preventing electrons transported from the cathode side to the light emitting layer from passing through to the anode side. In the present invention, an electron blocking layer can be provided as the organic compound layer adjacent to the light emitting layer on the anode side. As examples of the compound constituting the electron blocking layer, for example, those mentioned as the hole transport material described above can be applied.
The thickness of the electron blocking layer is preferably 1 nm to 500 nm, more preferably 5 nm to 200 nm, and even more preferably 10 nm to 100 nm.
The electron blocking layer may have a single layer structure composed of one or more of the above-described materials, or may have a multilayer structure composed of a plurality of layers having the same composition or different compositions.

(Protective layer)
In the present invention, the entire organic EL element may be protected by a protective layer.
As a material contained in the protective layer, any material may be used as long as it has a function of preventing materials that promote device deterioration such as moisture and oxygen from entering the device.
Specific _{examples, MgO, SiO, SiO 2,} Al 2 O 3, GeO, NiO, CaO, BaO, Fe 2 O 3, Y 2 O 3, TiO metal oxides such as _{2, SiN x,} SiN x O metal nitrides such as _y , metal fluorides such as MgF ₂ , LiF, AlF ₃ , and CaF ₂ , polyethylene, polypropylene, polymethyl methacrylate, polyimide, polyurea, polytetrafluoroethylene, polychlorotrifluoroethylene, polydichlorodifluoroethylene , A copolymer of chlorotrifluoroethylene and dichlorodifluoroethylene, a copolymer obtained by copolymerizing a monomer mixture containing tetrafluoroethylene and at least one comonomer, and a copolymer main chain containing a cyclic structure. Fluorine copolymer, water-absorbing substance with water absorption of 1% or more, water absorption Examples include moisture-proof substances having a rate of 0.1% or less.

  The method for forming the protective layer is not particularly limited, and for example, vacuum deposition, sputtering, reactive sputtering, MBE (molecular beam epitaxy), cluster ion beam, ion plating, plasma polymerization (high frequency) Excited ion plating method), plasma CVD method, laser CVD method, thermal CVD method, gas source CVD method, coating method, printing method, transfer method can be applied.

(Sealing)
Furthermore, the organic electroluminescent element of this invention may seal the whole element using a sealing container.
Further, a moisture absorbent or an inert liquid may be sealed in a space between the sealing container and the light emitting element. Although it does not specifically limit as a moisture absorber, For example, barium oxide, sodium oxide, potassium oxide, calcium oxide, sodium sulfate, calcium sulfate, magnesium sulfate, phosphorus pentoxide, calcium chloride, magnesium chloride, copper chloride Cesium fluoride, niobium fluoride, calcium bromide, vanadium bromide, molecular sieve, zeolite, magnesium oxide, and the like. The inert liquid is not particularly limited, and examples thereof include paraffins, liquid paraffins, fluorinated solvents such as perfluoroalkane, perfluoroamine, and perfluoroether, chlorinated solvents, and silicone oils. Can be mentioned.

Moreover, the method of sealing with the resin sealing layer shown below is also used suitably.
(Resin sealing layer)
The functional element of the present invention preferably suppresses deterioration of element performance due to oxygen or moisture by contact with the atmosphere by the resin sealing layer.
<Material>
The resin material for the resin sealing layer is not particularly limited, and an acrylic resin, an epoxy resin, a fluorine resin, a silicon resin, a rubber resin, an ester resin, or the like can be used. An epoxy resin is preferable from the viewpoint of the prevention function. Among the epoxy resins, a thermosetting epoxy resin or a photocurable epoxy resin is preferable.
<Production method>
The method for producing the resin sealing layer is not particularly limited, and examples thereof include a method of applying a resin solution, a method of pressure bonding or thermocompression bonding of a resin sheet, and a method of dry polymerization by vapor deposition or sputtering.
<Film thickness>
The thickness of the resin sealing layer is preferably 1 μm or more and 1 mm or less. More preferably, they are 5 micrometers or more and 100 micrometers or less, Most preferably, they are 10 micrometers or more and 50 micrometers or less. If it is thinner than this, the inorganic film may be damaged when the second substrate is mounted. On the other hand, if the thickness is larger than this, the thickness of the electroluminescent element itself is increased, and the thin film property that is characteristic of the organic electroluminescent element is impaired.

(Sealing adhesive)
The sealing adhesive used in the present invention has a function of preventing intrusion of moisture and oxygen from the end portion.
<Material>
As the material of the sealing adhesive, the same material as that used for the resin sealing layer can be used. Among these, epoxy adhesives are preferable from the viewpoint of moisture prevention, and among them, a photocurable adhesive or a thermosetting adhesive is preferable.

It is also preferable to add a filler to the above material.
The filler added to the sealant is preferably an inorganic material such as SiO ₂ , SiO (silicon oxide), SiON (silicon oxynitride) or SiN (silicon nitride). Addition of the filler increases the viscosity of the sealant, improves processing suitability, and improves moisture resistance.

<Drying agent>
The sealing adhesive may contain a desiccant. As the desiccant, barium oxide, calcium oxide, or strontium oxide is preferable.
The amount of the desiccant added to the sealing adhesive is preferably 0.01% by mass or more and 20% by mass or less, and more preferably 0.05% by mass or more and 15% by mass or less. If the amount is less than this, the effect of adding the desiccant is diminished. On the other hand, when it is more than this, it becomes difficult to uniformly disperse the desiccant in the sealing adhesive, which is not preferable.
<Prescription of sealing adhesive>
・ Polymer composition, concentration,
It does not specifically limit as a sealing adhesive agent, The said thing can be used. For example, XNR5516 manufactured by Nagase Chemtech Co., Ltd. can be cited as a photo-curable epoxy adhesive. What is necessary is just to add and disperse | distribute the said desiccant directly there.
-Thickness The coating thickness of the sealing adhesive is preferably 1 μm or more and 1 mm or less. If it is thinner than this, the sealing adhesive cannot be applied uniformly, which is not preferable. On the other hand, if it is thicker than this, the route through which moisture invades becomes wide, which is not preferable.
<Sealing method>
In the present invention, a functional element can be obtained by applying an arbitrary amount of the sealing adhesive containing the desiccant with a dispenser or the like, and stacking and curing the second substrate after application.

(Drive)
The organic electroluminescence device of the present invention emits light by applying a direct current (which may include an alternating current component as necessary) voltage (usually 2 to 15 volts) or a direct current between the anode and the cathode. Can be obtained.
The driving method of the organic electroluminescence device in the present invention is described in JP-A-2-148687, JP-A-6-301355, JP-A-5-29080, JP-A-7-134558, JP-A-8-234585, and JP-A-8-2441047. The driving method described in each publication, Japanese Patent No. 2784615, US Pat. Nos. 5,828,429, 6023308, and the like can be applied.

  The organic EL light emitting device of the present invention can improve the light extraction efficiency by various known devices. For example, by processing the substrate surface shape (for example, forming a fine concavo-convex pattern), controlling the refractive index of the substrate / ITO layer / organic layer, controlling the film thickness of the substrate / ITO layer / organic layer, etc. It is possible to improve light extraction efficiency and external quantum efficiency.

  The light emitting element in the present invention may be a so-called top emission method in which light emission is extracted from the anode side.

The organic EL device of the present invention can have a structure in which a charge generation layer is provided between a plurality of light emitting layers in order to improve the light emission efficiency.
The charge generation layer is a layer having a function of generating charges (holes and electrons) when an electric field is applied and a function of injecting the generated charges into a layer adjacent to the charge generation layer.

The material for forming the charge generation layer may be any material having the above functions, and may be formed of a single compound or a plurality of compounds.
Specifically, it may be a conductive material, a semiconductive material such as a doped organic layer, or an electrically insulating material. 11-329748, Unexamined-Japanese-Patent No. 2003-272860, and the material of Unexamined-Japanese-Patent No. 2004-39617 are mentioned.
More specifically, transparent conductive materials such as ITO and IZO (indium zinc oxide), fullerenes such as C60, conductive organic materials such as oligothiophene, metal phthalocyanines, metal-free phthalocyanines, metal porphyrins, metal-free Conductive organic materials such as porphyrins, metal materials such as Ca, Ag, Al, Mg: Ag alloy, Al: Li alloy, Mg: Li alloy, hole conductive material, electron conductive material, and a mixture thereof May be used.
The hole conductive material is, for example, a material in which a hole transporting organic material such as 2-TNATA or NPD is doped with an oxidant having an electron withdrawing property such as F4-TCNQ, TCNQ, or FeCl ₃ , or a P-type conductive material. The electron conductive material includes an electron transporting organic material doped with a metal or a metal compound having a work function of less than 4.0 eV, an N type conductive polymer, N type Type semiconductors. Examples of the N-type semiconductor include N-type Si, N-type CdS, and N-type ZnS. Examples of the P-type semiconductor include P-type Si, P-type CdTe, and P-type CuO.
Further, an electrically insulating material such as V ₂ O ₅ can be used for the charge generation layer.

  The charge generation layer may be a single layer or a stack of a plurality of layers. A structure in which a plurality of layers are stacked includes a conductive material such as a transparent conductive material and a metal material and a hole conductive material, or a structure in which an electron conductive material is stacked, and the above hole conductive material and electron conductive And a layer having a structure in which a functional material is laminated.

In general, it is preferable to select a film thickness and a material for the charge generation layer so that the visible light transmittance is 50% or more. The film thickness is not particularly limited, but is preferably 0.5 to 200 nm, more preferably 1 to 100 nm, still more preferably 3 to 50 nm, and particularly preferably 5 to 30 nm.
The method for forming the charge generation layer is not particularly limited, and the above-described method for forming the organic compound layer can be used.

The charge generation layer is formed between the two or more light emitting layers. The charge generation layer may include a material having a function of injecting charges into adjacent layers on the anode side and the cathode side. In order to improve the electron injection property to the layer adjacent to the anode side, for example, an electron injection compound such as BaO, SrO, Li ₂ O, LiCl, LiF, MgF ₂ , MgO, and CaF _{2 is} added to the anode side of the charge generation layer. May be laminated.
In addition to the contents mentioned above, the material for the charge generation layer should be selected based on the descriptions in JP-A-2003-45676, US Pat. Nos. 6,337,492, 6,107,734, 6,872,472, and the like. Can do.

The organic EL element in the present invention may have a resonator structure. For example, a multilayer mirror made of a plurality of laminated films having different refractive indexes, a transparent or translucent electrode, a light emitting layer, and a metal electrode are superimposed on a transparent substrate. The light generated in the light emitting layer resonates repeatedly with the multilayer mirror and the metal electrode as a reflection plate.
In another preferred embodiment, a transparent or translucent electrode and a metal electrode each function as a reflector on a transparent substrate, and light generated in the light emitting layer repeats reflection and resonates between them.
In order to form a resonant structure, the optical path length determined from the effective refractive index of the two reflectors and the refractive index and thickness of each layer between the reflectors is adjusted to an optimum value to obtain the desired resonant wavelength. Is done.
The calculation formula in the case of the first embodiment is described in JP-A-9-180883. The calculation formula in the case of the second aspect is described in Japanese Patent Application Laid-Open No. 2004-127795.

For example, as described in “Monthly Display”, September 2000 issue, pages 33 to 37, the organic EL display can be a full color type, as described in the three primary colors (blue (B), green ( G), a three-color light emission method in which organic EL elements that emit light corresponding to red (R)) are arranged on a substrate, and a white method in which white light emission by an organic EL element for white light emission is divided into three primary colors through a color filter In addition, a color conversion method that converts blue light emission by an organic EL element for blue light emission into red (R) and green (G) through a fluorescent dye layer is known.
Moreover, the planar light source of a desired luminescent color can be obtained by using combining the organic EL element of the different luminescent color obtained by the said method. For example, a white light-emitting light source that combines blue and yellow light-emitting elements, a white light-emitting light source that combines blue, green, and red light-emitting elements.

4). Protective insulating film In the organic EL display device of the present invention, the entire organic EL element is protected by a protective insulating film. The protective insulating film has a function of reducing damage to the organic EL element when a TFT is formed on the organic EL element, and a function of electrically insulating the organic EL element and the TFT. Further, it is more preferable that the protective insulating film has a function of preventing a substance that promotes element deterioration such as moisture and oxygen from entering the element.

Specific _{examples, MgO, SiO, SiO 2,} Al 2 O 3, GeO, NiO, CaO, BaO, Fe 2 O 3, Y 2 O 3, TiO metal oxides such as _{2, SiN x,} SiN x O metal nitrides such as _y , metal fluorides such as MgF ₂ , LiF, AlF ₃ , and CaF ₂ , polyethylene, polypropylene, polymethyl methacrylate, polyimide, polyurea, polytetrafluoroethylene, polychlorotrifluoroethylene, polydichlorodifluoroethylene , A copolymer of chlorotrifluoroethylene and dichlorodifluoroethylene, a copolymer obtained by copolymerizing a monomer mixture containing tetrafluoroethylene and at least one comonomer, and a copolymer main chain containing a cyclic structure. Fluorine copolymer, water-absorbing substance with water absorption of 1% or more, water absorption Examples include moisture-proof substances having a rate of 0.1% or less.

  The method for forming the protective insulating film is not particularly limited. For example, a vacuum deposition method, a sputtering method, a reactive sputtering method, an MBE (molecular beam epitaxy) method, a cluster ion beam method, an ion plating method, a plasma polymerization method ( High frequency excitation ion plating method), plasma CVD method, laser CVD method, thermal CVD method, gas source CVD method, coating method, printing method, transfer method can be applied.

  Since the upper electrode of the organic EL element and the source or drain electrode of the driving TFT need to be electrically connected, it is necessary to make a contact hole in the protective insulating film. As a method for forming the contact hole, there are a wet etching method using an etchant, a dry etching method using plasma, an etching method using a laser, and the like.

5. Pixel Circuit Configuration of Organic EL Display Device FIG. 3 is a schematic diagram of a pixel circuit of an active matrix organic EL display device using a TFT element used in the present invention. The circuit of the display device in the present invention is not particularly limited to that shown in FIG. 3, and a conventionally known circuit can be applied as it is.

(application)
The TFT of the present invention can be used as an image display device using liquid crystal or an EL element, particularly as an FPD switching element or driving element. In particular, it is suitable for use as a switching element and a driving element of a flexible FPD device. Further, the display device using the field effect thin film transistor of the present invention is applied in a wide range of fields including a mobile phone display, a personal digital assistant (PDA), a computer display, an automobile information display, a TV monitor, or general lighting. The
In addition to the display device, the TFT of the present invention can be widely applied to IC cards and ID tags by forming the field effect thin film transistor of the present invention on a flexible substrate such as an organic plastic film. .

  Hereinafter, the thin film field effect transistor of the present invention will be described with reference to examples, but the present invention is not limited to these examples.

Example 1
1. Production of active layer (production of IGZO semiconductors with different carrier concentrations)
<Condition 1>
A polycrystalline sintered body having a composition of InGaZnO ₄ was used as a target, and an RF magnetron sputtering vacuum deposition method was used under the conditions of an Ar flow rate of 12 sccm, an O ₂ flow rate of 0.4 sccm, an RF power of 200 W, and a total pressure of 0.4 Pa.
<Condition 2>
As in Condition 1, except that the O ₂ flow rate was changed to 1.3 sccm.
<Condition 3>
As in Condition 1, except that the O ₂ flow rate was changed to 1.5 sccm.

  A sample for measuring physical properties was prepared in which these layers were directly provided in a thickness of 100 nm on an alkali-free glass substrate (Corning, product number: No. 1737) under the same conditions as in the above conditions 1 to 3. As a result of analyzing these physical property measurement samples by a well-known X-ray diffraction method, it was confirmed that these films were amorphous films. The carrier concentration of these physical property measurement samples was measured by the following Hall measurement method.

-Carrier concentration measurement by Hall effect measurement method-
The carrier concentration of the sample for measuring physical properties was measured by performing Hall effect measurement using ResiTest 8300 type (manufactured by Toyo Technica Co., Ltd.). Hall effect measurement was performed in an environment of 20 ° C. By measuring the Hall effect, not only the carrier concentration but also the hole mobility of the carrier can be obtained. A stylus type surface shape measuring machine DekTak-6M (manufactured by ULBAC) was used for measuring the film thickness of the sample for measuring physical properties.

2. Preparation of resistance layer <Condition 4>
A polycrystalline sintered body having a composition of InGaZnO ₄ was used as a target, and an RF magnetron sputtering vacuum deposition method was used under the conditions of an Ar flow rate of 12 sccm, an O ₂ flow rate of 1.5 sccm, an RF power of 200 W, and a total pressure of 0.4 Pa.

A sample for measuring physical properties was prepared directly on a non-alkali glass substrate (Corning, product number NO. 1737) at a thickness of 100 nm under the same conditions as in the above condition 4. As a result of analyzing these physical property measurement samples by a well-known X-ray diffraction method, it was confirmed that these films were amorphous films. Further, the carrier concentration of these physical property measurement samples was measured by the hole measurement method. Moreover, the electrical resistivity was measured by the following.
-Measurement method of electrical resistivity-
The electrical conductivity of the sample for measuring physical properties was calculated from the measured sheet resistance and film thickness of the sample. Here, when the sheet resistance is ρ (Ω / □) and the film thickness is d (cm), the electrical conductivity σ (Scm ⁻¹ ) is calculated as σ = 1 / (ρ * d).
In this example, (manufactured by Mitsubishi Chemical Corporation) Loresta -GP in sheet resistance 10 ⁷ Ω / □ of less than area of the sample for measuring physical properties, high tester -UP (manufactured by Mitsubishi Chemical Corporation in sheet resistance 10 ⁷ Ω / □ or more regions ) In an environment of 20 ° C. A stylus type surface shape measuring device DekTak-6M (manufactured by ULVAC) was used for measuring the film thickness of the sample for measuring physical properties.

  The obtained results are shown in Table 1.

3. Fabrication of TFT Element The present invention and a comparative TFT element were fabricated using the above-described amorphous semiconductor material and amorphous oxide.
As the substrate, an alkali-free glass substrate (Corning, product number No. 1737) was used.

<Gate electrode>
Using an indium zinc oxide (IZO, manufactured by Idemitsu Kosan Co., Ltd.) target having a ZnO content of 10 mass%, RF magnetron sputtering (conditions: film formation temperature 43 ° C., sputtering gas Ar = 96 sccm, RF power 200 W) Then, an IZO thin film (thickness: 200 nm) as a gate electrode was formed at a film forming pressure of 0.4 Pa. The gate electrode IZO was patterned by using a shadow mask during sputtering.

<Gate insulation film>
Next, the following gate insulating film was formed on the gate electrode.
Gate insulating film: SiO ₂ by RF magnetron sputtering vacuum deposition method (conditions: target SiO ₂ , film forming temperature 54 ° C., sputtering gas Ar / O ₂ = 12/2 sccm, RF power 400 W, film forming pressure 0.4 Pa) The gate insulating film was provided with a thickness of 200 nm. Patterning of the gate insulating film SiO ₂ was performed by using a shadow mask during sputtering.

<Active layer>
On this, an active layer was provided using any of the above-mentioned active layer manufacturing conditions. The deposition time was adjusted by adjusting the sputtering time. The conditions used and the deposition thickness are shown in Table 2. The active layer was patterned by using a shadow mask during sputtering.

<Resistance layer>
On top of this, a resistance layer was provided using any of the resistance layer manufacturing conditions. The deposition time was adjusted by adjusting the sputtering time. The conditions used and the deposition thickness are shown in Table 2.

  Subsequently, aluminum (Al) was vapor-deposited as a source electrode and a drain electrode on the resistance layer by resistance heating vapor deposition (film formation temperature: 25 ° C.) to a thickness of 360 nm. The source electrode and the drain electrode were patterned by using a shadow mask at the time of sputtering. As described above, the TFT element of the present invention having a channel length L = 200 μm and a channel width W = 1000 μm and a comparative TFT element were manufactured.

4). Performance Evaluation For each of the obtained TFT elements, the TFT transfer characteristics were measured at a saturation region drain voltage Vd = 10 V (gate voltage−10 V ≦ Vg ≦ 15 V), and the TFT performance was evaluated. The measurement of TFT transfer characteristics was performed using a semiconductor parameter analyzer 4156C (manufactured by Agilent Technologies). Each parameter and its definition in the present invention are as follows.
TFT threshold voltage (Vth): a gate voltage at a current value of 50 nA.
OFF current (Ioff): A drain current value at a gate voltage 5 V lower than the threshold voltage. The unit is [A].
ON current (Ion): drain current at a gate voltage 5 V higher than the threshold voltage.
Carrier mobility: Field effect mobility was measured.
The field effect mobility μ in the saturation region can be obtained from the TFT transfer characteristic by the following equation.
μ = (2L / W * C _ox ) * (∂Id ^1/2 / ∂Vg)
Here, L is the channel length, W is the channel width, Cox is the capacitance of the gate insulating film, Id is the drain current, and Vg is the gate voltage.

The TFT characteristics obtained from the above measurement results are shown in Table 2. From the results in Table 2, the TFT elements of Inventions 1 to 2 according to the present invention unexpectedly have extremely high on-current and low off-current value, and have excellent performance suitable for driving an organic EL display device. Indicated.
Particularly preferably, provided InGaZnO ₄ Condition 2 to the thickness 50nm in the active layer, the present invention 2 of the TFT element of InGaZnO ₄ was placed in a thickness of 10nm conditions 4 to the resistor layer showed the best performance.

On the other hand, in the TFT element of the comparative example, the comparative example 1 in which InGaZnO ₄ of the condition 1 was installed in the active layer at a film thickness of 50 nm had a defect that the Ion was high but the Ioff was high. Established the InGaZnO ₄ Condition 2 to the thickness 50nm in the active layer, although the InGaZnO ₄ conditions 4 to the resistive layer Comparative Example 3 was placed in a thickness of 70nm is Ioff is low, Ion also had low drawbacks.

Example 2
In place of the alkali-free glass substrate in Example 1, a film with a barrier having an insulating layer having the following barrier function on both sides of a polyethylene naphthalate film (thickness: 100 μm) was used, and the other elements were the same as in Example 1 Was made.

Insulating layer: SiON was deposited to a thickness of 500 nm. For the deposition of SiON, an RF magnetron sputtering deposition method (sputtering conditions: target Si ₃ N ₄ , RF power 400 W, gas flow rate Ar / O ₂ = 12/3 sccm, film forming pressure 0.45 Pa) was used.

  As a result of evaluating the performance of the obtained element in the same manner as in Example 1, as in Example 1, the on-current was unexpectedly extremely high and the off-current value was low, which was excellent for driving an organic EL display device. Showed performance.

Example 3
1. Production of organic EL display device (production of organic EL element part)
1) Formation of lower electrode A film with a barrier having an insulating layer having the following barrier function on both sides of a polyethylene naphthalate film was used for the substrate. Indium tin oxide (hereinafter abbreviated as ITO) was deposited on the substrate to a thickness of 150 nm to form an anode.

2) Formation of organic layer After washing, a hole injection layer, a hole transport layer, a light emitting layer, a hole blocking layer, an electron transport layer, and an electron injection layer were sequentially provided.

The configuration of each layer is as follows. Each layer was provided by resistance heating vacuum deposition.
Hole injection layer: 4,4 ′, 4 ″ -tris (2-naphthylphenylamino) triphenylamine (abbreviated as 2-TNATA) and 2,3,5,6-tetrafluoro-7,7,8, A layer containing 1% by mass of 8-tetracyanoquinodimethane (abbreviated as F4-TCNQ) with respect to 2-TNATA, a thickness of 160 nm.
Hole transport layer: N, N′-dinaphthyl-N, N′-diphenyl- [1,1′-biphenyl] -4,4′-diamine (abbreviated as α-NPD), thickness 10 nm.
Light-emitting layer: a layer containing 13% by mass of 1,3-bis (carbazol-9-yl) benzone (abbreviated as mCP) and platinum complex Pt-1 with respect to mCP, thickness 60 nm.
Hole blocking layer: bis- (2-methyl-8-quinonylphenolate) aluminum (abbreviated as BAlq), thickness 40 nm.
Electron transport layer: Tris (8-hydroxyquinoninate) aluminum (abbreviated as Alq3), thickness 10 nm.
Electron injection layer: LiF, thickness 1 nm.

3) Upper electrode It patterned by the shadow mask so that element size might be set to 2 mm x 2 mm, and Al was vapor-deposited in thickness of 100 nm, and it was set as the cathode.

(Protective insulating film)
A 500 nm SiON film was formed on the upper electrode as a protective insulating film by an ion plating method. After film formation, contact holes were formed by laser.

  The structures of the compounds used in the examples are shown below.

(Driving test)
An equivalent circuit was configured by combining the obtained organic EL element and the TFT fabricated in Example 1, and a driving test was performed under various conditions.
As a result, when the TFT of the present invention was used, stable light emission was obtained even when driven at a high temperature and continuously for a long time.

It is a schematic diagram which shows the TFT element structure of this invention. It is a schematic diagram of an equivalent circuit of an active matrix driving type organic EL display device using the TFT element of the present invention.

Explanation of symbols

1: Substrate 2: Gate electrode 3: Gate insulating film 4: Active layer 5-1: Source electrode 5-2: Drain electrode 6: Insulating layer 7: Resistance layer 200: Switching TFT
300: Organic EL element 400: Signal electrode line 500: Scan electrode line 600: Capacitor 700: Drive TFT
800: Common wire

Claims (11)

A thin film field effect transistor having at least a gate electrode, a gate insulating film, an active layer containing an amorphous oxide semiconductor, a source electrode and a drain electrode on a substrate, wherein the carrier concentration of the active layer is 3 × 10 ^15. / Cm ³ or more and 3 × 10 ¹⁸ / cm ³ or less, and has a resistance layer between the active layer and the source electrode or the drain electrode, and the electrical resistivity of the resistance layer is 10 ⁵ Ω · cm or more and 10 A thin film field-effect transistor having a thickness of less than ¹³ Ω · cm and less than 20 nm.   2. The thin film field effect transistor according to claim 1, wherein at least one of the source electrode and the drain electrode is IZO.   The thin film field effect transistor according to claim 1, wherein the resistance layer is an amorphous oxide.   The thin film field effect transistor according to any one of claims 1 to 3, wherein the amorphous oxide semiconductor of the active layer contains In.   5. The thin film field effect transistor according to claim 4, wherein the amorphous oxide semiconductor of the active layer contains In and Ga or In and Zn.   5. The thin film field effect transistor according to claim 4, wherein the amorphous oxide semiconductor of the active layer contains In, Ga, and Zn.   The thin film field effect transistor according to any one of claims 3 to 6, wherein the amorphous oxide of the resistance layer contains In.   8. The thin film field effect transistor according to claim 7, wherein the amorphous oxide of the resistance layer contains In and Ga or In and Zn.   8. The thin film field effect transistor according to claim 7, wherein the amorphous oxide of the resistance layer contains In, Ga, and Zn.   The thin film field effect transistor according to claim 1, wherein the substrate is a flexible substrate.   A display device comprising a light emitting element having a pair of electrodes and a light emitting layer interposed between the electrodes, and a field effect transistor for driving the light emitting element, wherein the field effect transistor is claimed. A display device comprising the thin film field effect transistor according to claim 1.