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WO2016031962A1 - Procédé de production d'un élément semi-conducteur organique, et élément semi-conducteur organique - Google Patents

Procédé de production d'un élément semi-conducteur organique, et élément semi-conducteur organique Download PDF

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Publication number
WO2016031962A1
WO2016031962A1 PCT/JP2015/074425 JP2015074425W WO2016031962A1 WO 2016031962 A1 WO2016031962 A1 WO 2016031962A1 JP 2015074425 W JP2015074425 W JP 2015074425W WO 2016031962 A1 WO2016031962 A1 WO 2016031962A1
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organic semiconductor
semiconductor element
organic
layer
element according
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Japanese (ja)
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敏則 松島
有 江崎
安達　千波矢
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Kyushu University NUC
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Kyushu University NUC
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    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/10—Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10D—INORGANIC ELECTRIC SEMICONDUCTOR DEVICES
    • H10D30/00—Field-effect transistors [FET]
    • H10D30/60—Insulated-gate field-effect transistors [IGFET]
    • H10D30/67—Thin-film transistors [TFT]
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
    • H10K10/40—Organic transistors
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00—Energy generation through renewable energy sources
    • Y02E10/50—Photovoltaic [PV] energy
    • Y02E10/549—Organic PV cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50—Manufacturing or production processes characterised by the final manufactured product

Definitions

  • the present invention relates to a method for manufacturing an organic semiconductor element and an organic semiconductor element.
  • Organic semiconductor materials are mechanically flexible compared to inorganic semiconductor materials such as silicon, which are mainly used today, and can be produced at low cost by printing methods, and their characteristics can be changed in various ways through molecular design. It has the advantage of being able to do so. For this reason, organic electroluminescence elements, organic solar cells, and organic transistors have been actively developed as electronic devices (organic semiconductor elements) using organic semiconductor materials.
  • These organic semiconductor elements are configured to have a base material and at least one organic semiconductor layer formed on the base material.
  • the organic semiconductor layer is usually formed by a vapor deposition method such as a vapor deposition method, or a wet film formation method such as a spin coating method or an ink jet method.
  • a vapor deposition method such as a vapor deposition method
  • a wet film formation method such as a spin coating method or an ink jet method.
  • the cold isostatic pressurization method is a processing method for densifying a sample by isotropically pressurizing a sample contained in a metal syringe through a pressure medium such as water or a rubber mold. It is often used as a method of forming an inorganic powder such as carbon or ceramic.
  • Patent Document 1 discloses that a phthalocyanine vapor-deposited film formed on a glass substrate is a polyethylene polymer bag having a thickness of 0.05 mm. And by applying cold isostatic pressing through an aqueous medium, the thickness of the phthalocyanine vapor-deposited film was reduced from 1050 nm to 630 nm, and its hardness, elastic modulus, and bending strength were increased. Yes. Further, in Non-Patent Document 1, the film thickness was reduced by about 40% by placing a vapor deposited phthalocyanine film in a 0.1 mm thick polyester polymer bag and performing cold isostatic pressing. It is described.
  • the present inventors can manufacture an organic semiconductor element in which the density of the organic semiconductor layer is high and a high carrier mobility and a long carrier diffusion length can be obtained. Studies have been conducted for the purpose of providing a method for producing a semiconductor element and an organic semiconductor element capable of obtaining excellent device characteristics.
  • the present inventors have found that in the isotropic pressure pressing of the organic semiconductor layer, the polymer bag used in the isotropic pressure pressing for the density and carrier mobility obtained.
  • the thickness of the organic semiconductor layer is greatly affected, and the density of the organic semiconductor layer obtained is significantly increased by applying isotropic pressure using a bag body that is thinner than the conventional one, and the carrier mobility is dramatically increased.
  • hot isostatic pressing is extremely effective for densification and improvement of crystallinity, thereby diffusing carriers generated by light absorption. It has been found for the first time that the length is increased and high photoelectric conversion efficiency is realized.
  • the present invention has the following configuration.
  • a laminate having a base material and a crystalline material film formed on the base material is accommodated in a bag made of a sheet having a thickness of 0.1 to 40 ⁇ m, and a gas in the bag is contained.
  • An organic semiconductor element comprising: a laminate housing step for sealing the bag body after exhausting air; and a pressurizing step for isotropically pressurizing the laminate body through the bag body. Production method.
  • the base material is an electrode, and the crystalline material film is directly formed on the electrode, or the crystalline material film is formed on another crystalline material film formed on the electrode. It is formed, The manufacturing method of the organic-semiconductor element as described in [1] characterized by the above-mentioned.
  • An organic semiconductor device manufactured by the method for manufacturing an organic semiconductor device according to any one of [1] to [18].
  • An organic semiconductor element comprising at least one crystalline material film, wherein the density of at least one layer of the crystalline material film is within a range of ⁇ 20% of the single crystal density of the crystalline material.
  • An organic semiconductor element characterized by being.
  • the manufacturing method of the present invention it is possible to manufacture an organic semiconductor element in which the crystalline material film has a high density and high carrier mobility and a long carrier diffusion length can be obtained. Moreover, according to this invention, the organic-semiconductor element from which the outstanding device characteristic is acquired can be provided.
  • FIG. 1 It is a schematic sectional drawing which shows the layer structural example of an organic electroluminescent element.
  • An organic electroluminescent element (Example 1) subjected to cold isostatic pressing using a bag having a thickness of 30 ⁇ m and an organic electroluminescent element (Comparative Example 2) not subjected to cold isostatic pressing Is a graph showing a current density-voltage characteristic.
  • Organic electroluminescent element (Comparative Example 1) subjected to cold isostatic pressing using a bag body having a thickness of 75 ⁇ m and Organic electroluminescent element (Comparative Example 2) not subjected to cold isostatic pressing Is a graph showing a current density-voltage characteristic.
  • An organic electroluminescent element (Example 1) subjected to cold isostatic pressing using a bag having a thickness of 30 ⁇ m and an organic electroluminescent element (Comparative Example 2) not subjected to cold isostatic pressing ) Is a graph showing the external quantum efficiency-current density characteristics.
  • Organic electroluminescent element (Comparative Example 1) subjected to cold isostatic pressing using a bag body having a thickness of 75 ⁇ m and Organic electroluminescent element (Comparative Example 2) not subjected to cold isostatic pressing ) Is a graph showing the external quantum efficiency-current density characteristics. Drain current of an organic transistor (Example 2) subjected to cold isostatic pressing using a bag having a thickness of 30 ⁇ m and an organic transistor (Comparative Example 4) not subjected to cold isostatic pressing -A graph showing the gate voltage characteristics.
  • 6 is a graph showing drain current-drain voltage characteristics of an organic transistor (Example 2) subjected to cold isostatic pressing using a bag having a thickness of 30 ⁇ m. It is a graph which shows the drain current-drain voltage characteristic of the organic transistor (comparative example 3) which performed cold isostatic pressing using the bag body whose thickness is 75 micrometers.
  • FIG. 5 is a graph in which I P / I A is plotted with respect to thickness for a perovskite layer provided with a spiro-OMeTAD layer.
  • 7 is a graph showing current density-voltage characteristics of an organic / inorganic perovskite solar cell (Comparative Example 7).
  • 6 is a graph showing the voltage-current density characteristics of a single layer element (Example 5) subjected to cold isostatic pressing and a single layer element (Comparative Example 8) not subjected to cold isostatic pressing.
  • a numerical range expressed using “to” means a range including numerical values described before and after “to” as a lower limit value and an upper limit value.
  • a laminate having a base material and a crystalline material film formed on the base material is placed in a bag made of a sheet having a thickness of 0.1 to 40 ⁇ m. After containing and exhausting the gas in the bag body, it has at least a laminate housing step for sealing the bag body and a pressurizing step for isostatically pressing the laminate through the bag body.
  • the laminated body is isostatically pressed through a bag made of a sheet having a thickness of 0.1 to 40 ⁇ m, whereby the grain boundary of the crystalline material film included in the laminated body is obtained.
  • the crystalline material film has a high density, the contact resistance between the crystalline material film and the base material, and the contact resistance between the crystalline material films are low, and high carrier mobility is obtained. be able to.
  • a bag composed of a sheet of 0.1 to 40 ⁇ m is used for isotropic pressure pressurization, and the mold thickness is thinner than that of the conventional cold isostatic pressurization method. Therefore, it is considered that the pressure applied to the bag body is efficiently transmitted to the crystalline material film, and the voids are efficiently compressed. For this reason, the density of the crystalline material film of the obtained organic semiconductor element is significantly higher than that of the conventional organic semiconductor element by cold isostatic pressing, and the carrier mobility can be drastically improved. it can.
  • each process of the manufacturing method of the organic-semiconductor element of this invention is demonstrated in detail.
  • Laminate housing step In the laminate housing step, a bag composed of a base material and a laminate having a crystalline material film formed on the base material with a sheet having a thickness of 0.1 to 40 ⁇ m. After accommodating in the body and exhausting the gas in the bag, the bag is sealed.
  • a laminated body to be accommodated in a bag is prepared.
  • the laminate has a base material and at least one crystalline material film formed on the base material.
  • the base material used for the laminate any of those conventionally used for organic semiconductor elements can be used.
  • the organic semiconductor element is an organic electroluminescence element or an organic solar battery
  • an electrode plate made of a conductive material or an electrode substrate having an electrode film formed on the substrate hereinafter referred to as an electrode plate
  • the electrode substrate may be collectively referred to as “electrode”.
  • the conductive material for the electrode plate and the electrode film cathode and anode materials exemplified in the column of the organic electroluminescence element below can be used.
  • substrate used for an electrode substrate or a board
  • substrate of an organic transistor what consists of glass, transparent plastic, quartz, silicon etc. can be used, for example.
  • the electrode plate, electrode film, and substrate may have a single layer configuration or a multilayer configuration.
  • the crystalline material film is a functional film that contributes to the operation of the organic semiconductor element to be manufactured.
  • the “crystalline material film” means “a material film having a crystal structure” and “an amorphous film capable of forming a crystal structure” by some treatment.
  • the material film having a crystal structure can be confirmed by observing a peak corresponding to the crystal plane in the X-ray diffraction spectrum.
  • the material film having a crystal structure may be entirely crystalline, a part thereof may be crystalline, and the other part may be amorphous.
  • the crystalline crystal structure may be a polycrystalline structure or a single crystal structure.
  • “Amorphous film capable of forming a crystal structure by treatment” can be confirmed by observing a peak corresponding to the crystal plane in the X-ray diffraction spectrum of the material film after the treatment. it can.
  • Examples of the “treatment” of “amorphous film capable of forming a crystal structure by treatment” include a treatment of heating to a temperature higher than the crystallization temperature of the material contained in the amorphous film.
  • the description of the crystal structure after the processing of “amorphous film capable of forming a crystal structure by processing” the description of “material film having crystal structure” can be referred to.
  • the crystalline material film is preferably a “material film having a crystal structure”, and the crystal structure is more preferably a polycrystalline structure. Since the effect of the present invention is to improve the carrier mobility by reducing the voids existing in the crystal grain boundaries and the like, a remarkable effect can be obtained when the crystalline material film has a polycrystalline structure.
  • an organic semiconductor material usually used as a functional film material of an organic semiconductor element can be used, which may be a low molecular material or a polymer material. Good.
  • the organic semiconductor material specifically, it is usually used in the material of each organic layer exemplified in the column of the organic electroluminescence element below, the photoelectric conversion layer of an organic solar cell, or the organic semiconductor layer of an organic transistor. Examples thereof include p-type organic semiconductor materials, n-type organic semiconductor materials, and light-absorbing materials. Among them, it is preferable to contain at least one of phthalocyanine, phthalocyanine derivatives, metal complexes of phthalocyanines, and metal complexes of phthalocyanine derivatives.
  • Organic / inorganic perovskite compounds can also be preferably used as the crystalline material of the crystalline material film.
  • the organic / inorganic perovskite compound is a crystalline material represented by ABX 3 (A represents an organic cation, B represents a metal cation, and X represents a halogen ion), and forms a perovskite structure.
  • the organic / inorganic perovskite compound used in the present invention is preferably a perovskite compound represented by the following general formula (1).
  • General formula (1) R 1 NH 3 MX 3 R 1 represents a hydrogen atom or an alkyl group constituting an ammonium ion together with a nitrogen atom (N) and a hydrogen atom (H).
  • the number of carbon atoms of the alkyl group is not particularly limited, but is preferably 1 to 20, more preferably 1 to 10, and still more preferably 1. That is, R 1 is most preferably a methyl group.
  • M represents a divalent metal ion. Examples of the divalent metal ion include Cu 2+ , Ni 2+ , Mn 2+ , Fe 2+ , Co 2+ , Pd 2+ , Ge 2+ , Sn 2+ , Pb 2+ , Eu 2+, and the like, such as Cu 2+ , Ni 2+ , Co 2+ , Sn 2+ and Pb 2+ are preferred, Sn 2+ and Pb 2+ are more preferred, and Pb 2+ is even more preferred.
  • X represents a halogen ion, and examples thereof include F, Cl, Br, and I ions.
  • X is Cl -, I -, Br - is preferably in, I - is more preferable.
  • the halogen ions represented by a plurality of X may be the same or different from each other, but are preferably the same.
  • R 1 of the perovskite compound represented by the general formula (1) is a mixture of a plurality of alkyl groups (for example, two types of alkyl groups represented by R 1 and R 2 ). Also good. That is, R 1 in the general formula (1) may be replaced with, for example, R 1 a R 2 (1-a) .
  • a is a number from 0 to 1.
  • M of the perovskite compound represented by the general formula (1) is a plurality of divalent metal ions (for example, a divalent metal ion represented by M 1 and a divalent metal ion represented by M 2). 2 types) may be mixed. That is, M in the general formula (1) may be replaced with, for example, M 1 b M 2 (1-b) .
  • b is a number from 0 to 1.
  • Specific examples of the organic / inorganic perovskite compound include CH 3 NH 3 PbCl 3 , CH 3 NH 3 PbI 3 , and CH 3 NH 3 PbBr 3 , and CH 3 NH 3 PbI 3 is preferable.
  • the organic / inorganic perovskite compounds that can be used in the present invention are not limitedly interpreted by these compounds.
  • the density of the crystalline material film is preferably 0.1 to 7 g / cm 3 , and is preferably 0.5 to 5 g / cm 3. Is more preferably 0.5 to 4 g / cm 3 .
  • the thickness of the crystalline material film is preferably 10 to 100,000 nm, more preferably 30 to 30,000 nm, and more preferably 50 to More preferably, it is 10,000 nm.
  • the thickness of the crystalline material film can be measured by a profilometer, and the density of the crystalline material film is the same as the measuring method of “The density of the crystalline material film after isotropic pressurization” described later. Can be measured.
  • One layer may be sufficient as the number of layers of the crystalline material film in a laminated body, and two or more layers may be sufficient as it.
  • the crystalline material film included in the stacked body may be a crystalline material film corresponding to all layers formed in the organic semiconductor element, or a crystallinity corresponding to some layers formed in the organic semiconductor element. Only the material film may be used.
  • the crystalline material film is a film made of a material that can be crystallized, and includes an amorphous film as described above.
  • the laminate may have an amorphous material film, but when the substrate is an electrode, the layer directly formed on the electrode is a crystalline material film. A membrane is preferred. Since the present invention has the effect of reducing the gap at the interface between the crystalline material film and the base material, the contact resistance is effectively reduced by forming the crystalline material film directly on the electrode. An organic semiconductor element having excellent electrical characteristics can be obtained.
  • a method for forming a crystalline material film for example, a vapor deposition method such as an evaporation method, a coating method such as a spin coating method or a dip coating method, an ink jet printing method (droplet discharge method), or a screen printing method can be used. Such a printing method can be used.
  • the crystalline material film may be formed entirely on the base material, or may be formed in a predetermined pattern.
  • the crystalline material film may be formed continuously using a roll-to-roll method, or may be performed in a batch type or a single wafer type, but an organic semiconductor element is produced at an industrial level.
  • a roll-to-roll method is used to continuously form a crystalline material film, and by constructing a production line that transports the resulting laminate to an isotropic pressurization apparatus in a flow operation, Production efficiency can be obtained.
  • the above laminate is accommodated in a bag made of a sheet having a thickness of 0.1 to 40 ⁇ m, and the gas in the bag is exhausted. Thereby, the inner surface of the bag body comes into close contact with the laminated body in the bag body.
  • the bag body that accommodates the laminated body is constituted by a sheet formed in a bag shape, and at least one of the bags is an open portion for carrying the laminated body.
  • the thickness of the sheet constituting the bag is preferably 0.1 to 40 ⁇ m, more preferably 0.1 to 30 ⁇ m, and even more preferably 1 to 30 ⁇ m.
  • the thickness of the bag can be measured with a profilometer, an optical microscope, or the like.
  • an elastic material or a flexible material that does not transmit the pressure medium used in the isotropic pressure pressing performed in the next process is used, and the laminated body is accommodated in the bag body. It is preferable to have sufficient strength so as not to be broken when the gas is exhausted or when isotropic pressure is applied in the next step [2].
  • resin materials such as polyolefin resins such as polyethylene, polyester resins, fluororesins such as polytetrafluoroethylene, and polyamide resins such as nylon (registered trademark) can be suitably used.
  • a known additive such as a heat stabilizer, an ultraviolet stabilizer, an antioxidant, or an antiblocking agent may be added to the sheet material as necessary.
  • the layer structure of the sheet is not particularly limited, and may be a single layer structure or a multilayer structure in which a plurality of layers having different compositions are laminated.
  • the gas in the bag can be exhausted by using a vacuum pump usually used for a vacuum pack.
  • the gas exhaust rate is not particularly limited, but is preferably 1 to 100 L / min, more preferably 10 to 100 L / min, and further preferably 50 to 100 L / min.
  • the total amount of gas and moisture remaining in the bag after exhaust is preferably 0.1 ppm or less, more preferably 0.01 ppm or less, and further preferably 0.001 ppm or less.
  • the total amount of gas and moisture remaining in the bag can be measured with an oximeter or moisture meter.
  • the opening of the bag is sealed.
  • the opening portion can be sealed by, for example, heat sealing.
  • the above series of steps may be performed in the atmosphere, but is preferably performed in an atmosphere containing an inert gas such as nitrogen gas or argon gas. Thereby, an organic semiconductor element having more excellent characteristics can be manufactured.
  • the substrate is damaged when the pressure is increased, so that the applied pressure is limited to some extent.
  • the base material is not easily damaged even if the pressure is increased, so that the crystalline material film can be densified using a relatively high pressure.
  • isotropic pressurization the grain boundary of the crystalline material film, voids existing at the interface between the crystalline material film and the base material, and, if the crystalline material film has a multilayer structure, The void existing at the interface between the material films is uniformly compressed, and the volume of the void is reduced. For this reason, the occurrence of anisotropy in the film quality of the crystalline material film can be suppressed.
  • the isotropic pressure transmitted from the pressure medium to the bag body is efficiently transmitted to the laminated body, particularly because the thickness of the bag body is as thin as 0.1 to 40 ⁇ m. It is considered that the existing voids are efficiently compressed. For this reason, the obtained organic semiconductor element has reduced contact resistance between the crystalline material film and the base material and contact resistance between the crystalline material films compared to the conventional organic semiconductor element by cold isostatic pressing. Thus, carrier mobility and carrier diffusion length can be dramatically improved.
  • the isotropic pressure pressurization may be cold isostatic pressurization (CIP) in which isotropic pressure pressurization is performed using a normal pressure medium, or isotropic pressurization is performed using a heated pressure medium. It may be hot isostatic pressing (HIP) in which pressure is applied.
  • hot isostatic pressing depending on the crystalline material film, the film may be softened by the action of heat from the pressure medium, which may favor the compression of the voids.
  • hot isostatic pressing depending on the crystalline material film, the film may be softened by the action of heat from the pressure medium, which may favor the compression of the voids.
  • hot isostatic pressing is performed on a laminate having a crystalline material film containing an organic / inorganic perovskite compound, the crystalline material film is softened by heat from the pressure medium.
  • isotropic pressure is applied to the crystalline material film, so that pinholes and voids in crystal grain boundaries existing in the crystalline material film are effectively compressed, and a functional film having
  • the pressure medium a liquid such as water or oil usually used for isotropic pressure pressurization, or an inert gas such as argon can be used, and water is particularly preferable.
  • the pressure applied to the laminate by isotropic pressure is preferably 0.2 to 2000 MPa, more preferably 0.2 to 1000 MPa, and even more preferably 1 to 1000 MPa.
  • the temperature of the pressure medium at the isotropic pressure is not particularly limited, but is preferably ⁇ 200 to 500 ° C., more preferably 0 to 300 ° C., and preferably 20 to 200 ° C. Further preferred.
  • the temperature of the pressure medium when performing cold isostatic pressing is not particularly limited, but is preferably ⁇ 200 to 300 ° C., more preferably 0 to 300 ° C., and 0 to 100 ° C. More preferably.
  • the temperature of the pressure medium at the time of hot isostatic pressing is preferably 20 to 500 ° C., more preferably 20 to 300 ° C., and further preferably 20 to 200 ° C. .
  • the temperature of the pressure medium is preferably 20 to 150 ° C.
  • the density of the crystalline material film after isotropic pressure pressing is preferably in the range of ⁇ 20% of the single crystal density of the crystal material, more preferably in the range of ⁇ 18% of the single crystal density, More preferably, it is in the range of ⁇ 15% of the single crystal density.
  • the “single crystal density” is a density measured by an X-ray structural analysis method.
  • the density of the crystalline material film can be generally measured by the X-ray structure analysis method, the crystal oscillator method, the solution method, or the spectroscopic ellipsometry, but the “density of the crystalline material film” in the present invention is the X-ray structure analysis. Density measured by the method.
  • This isotropic pressure pressurization may be performed only once, or may be performed a plurality of times on the same laminate. Further, after forming another crystalline material film on the laminate subjected to isotropic pressure pressurization, further isotropic pressure pressurization may be performed.
  • an organic semiconductor element is completed by forming another functional film as necessary. In the manufactured organic semiconductor element, the density of the crystalline material film is high, so that carriers easily move in the crystalline material film. In addition to this, the contact resistance between the crystalline material film and the substrate and the crystalline material film Since the contact resistance between them is low, high carrier mobility and long carrier diffusion length can be obtained.
  • an organic-semiconductor element is an organic electroluminescent element
  • a drive voltage can be made low. It is also possible to provide organic semiconductor elements with high luminous efficiency, organic solar cells with high photoelectric conversion efficiency, and organic transistors with excellent input / output characteristics.
  • the organic semiconductor element of the present invention includes a base material and at least one crystalline material film formed on the base material, and the density of the at least one crystalline material film is a single crystal of the crystalline material. It is characterized by being in the range of ⁇ 20% of the density.
  • the definitions of “single crystal density” and “density of crystalline material film” in the method of manufacturing an organic semiconductor element can be referred to.
  • the crystalline material having a density close to the single crystal density has no voids in the inside or has a very low porosity, thereby obtaining a high carrier mobility and a long carrier diffusion length. Can do. For this reason, for example, when the organic semiconductor element is an organic electroluminescence element, high emission efficiency and low driving voltage can be obtained, and when the organic semiconductor element is an organic solar cell, high photoelectric conversion efficiency can be obtained. In the case of an organic transistor, excellent input / output characteristics can be obtained.
  • the explanation and preferred range of the crystalline material film and the substrate the explanation and preferred range of the crystalline material film and the substrate used in the method for producing an organic semiconductor element can be referred to.
  • the method for producing the organic semiconductor element of the present invention is not particularly limited. If the above-described method for producing an organic semiconductor element of the present invention is used, the conventional organic semiconductor element production process includes a laminate housing process and a pressurizing process. An organic semiconductor element can be manufactured by a simple process such as addition of That is, by using the method for producing an organic semiconductor element of the present invention, an organic semiconductor element having excellent characteristics can be efficiently produced by a simple process.
  • the organic electroluminescence element has a structure in which at least an anode, a cathode, and an organic layer are formed between the anode and the cathode.
  • the organic layer includes at least a light emitting layer, and may consist of only the light emitting layer, or may have one or more organic layers in addition to the light emitting layer. Examples of such other organic layers include a hole transport layer, a hole injection layer, an electron blocking layer, a hole blocking layer, an electron injection layer, an electron transport layer, and an exciton blocking layer.
  • the hole transport layer may be a hole injection / transport layer having a hole injection function
  • the electron transport layer may be an electron injection / transport layer having an electron injection function.
  • FIG. 1 A specific example of the structure of an organic electroluminescence element is shown in FIG.
  • 1 is a substrate
  • 2 is an anode
  • 3 is a hole injection layer
  • 4 is a hole transport layer
  • 5 is a light emitting layer
  • 6 is an electron transport layer
  • 7 is a cathode.
  • the organic electroluminescence device to which the present invention is applied at least one of these organic layers forms a crystalline material film, and the density of the organic layer is within a range of ⁇ 20% of the single crystal density of the organic material. It is configured to be.
  • the organic layer having a density close to the single crystal density does not have voids inside or has a very low void ratio, whereby high carrier mobility can be obtained. For this reason, this organic electroluminescent element can obtain high luminous efficiency and low driving voltage.
  • the hole injection layer 3, the hole transport layer 4, the light emitting layer 5, and the electron transport layer 6 are formed on the electrode substrate having the substrate 1 and the anode 2.
  • a crystalline material film corresponding to at least one of them is formed to produce a laminated body, and the laminated body accommodation process and pressurizing process of the present invention are performed on this laminated body.
  • the density of the crystalline material film included in the stacked body is increased, and the contact resistance between the crystalline material film (organic layer) and the electrode substrate and the contact resistance between the crystalline material films (organic layer) are reduced.
  • the crystalline material film constituting the laminate may be a crystalline material film corresponding to all of the organic layers constituting the organic electroluminescence element, or may be a crystalline material film corresponding to a part thereof.
  • the laminate preferably includes at least a crystalline material film corresponding to the electrode substrate and the hole injection layer 3.
  • the laminated body accommodation process and pressurization process of this invention formed the remaining organic layer and the cathode. It is preferable to carry out later. At this time, you may perform the laminated body accommodation process and pressurization process of this invention with respect to the laminated body before forming the remaining organic layer and a cathode. Below, each member and each layer of an organic electroluminescent element are demonstrated.
  • the organic electroluminescence device of the present invention is preferably supported on a substrate.
  • the substrate is not particularly limited and may be any substrate conventionally used for organic electroluminescence elements.
  • a substrate made of glass, transparent plastic, quartz, silicon, or the like can be used.
  • an electrode material made of a metal, an alloy, an electrically conductive compound, or a mixture thereof having a high work function (4 eV or more) is preferably used.
  • electrode materials include metals such as Au, and conductive transparent materials such as CuI, indium tin oxide (ITO), SnO 2 and ZnO.
  • conductive transparent materials such as CuI, indium tin oxide (ITO), SnO 2 and ZnO.
  • an amorphous material such as IDIXO (In 2 O 3 —ZnO) capable of forming a transparent conductive film may be used.
  • a thin film may be formed by vapor deposition or sputtering of these electrode materials, and a pattern of a desired shape may be formed by photolithography, or when pattern accuracy is not so high (about 100 ⁇ m or more) ), A pattern may be formed through a mask having a desired shape at the time of vapor deposition or sputtering of the electrode material.
  • wet film-forming methods such as a printing system and a coating system, can also be used.
  • the transmittance be greater than 10%, and the sheet resistance as the anode is preferably several hundred ⁇ / ⁇ or less.
  • the film thickness depends on the material, it is usually selected in the range of 10 to 1000 nm, preferably 10 to 200 nm.
  • cathode a material having a low work function (4 eV or less) metal (referred to as an electron injecting metal), an alloy, an electrically conductive compound, and a mixture thereof as an electrode material is used.
  • electrode materials include sodium, sodium-potassium alloy, magnesium, lithium, magnesium / copper mixture, magnesium / silver mixture, magnesium / aluminum mixture, magnesium / indium mixture, aluminum / aluminum oxide (Al 2 O 3 ) Mixtures, indium, lithium / aluminum mixtures, rare earth metals and the like.
  • a mixture of an electron injecting metal and a second metal which is a stable metal having a larger work function value than this for example, a magnesium / silver mixture, Magnesium / aluminum mixtures, magnesium / indium mixtures, aluminum / aluminum oxide (Al 2 O 3 ) mixtures, lithium / aluminum mixtures, aluminum and the like are preferred.
  • the cathode can be produced by forming a thin film of these electrode materials by a method such as vapor deposition or sputtering.
  • the sheet resistance as the cathode is preferably several hundred ⁇ / ⁇ or less, and the film thickness is usually selected in the range of 10 nm to 5 ⁇ m, preferably 50 to 200 nm.
  • the emission luminance is advantageously improved.
  • a transparent or semi-transparent cathode can be produced. By applying this, an element in which both the anode and the cathode are transparent is used. Can be produced.
  • the light emitting layer is a layer that emits light after excitons are generated by recombination of holes and electrons injected from each of the anode and the cathode, and the light emitting material may be used alone for the light emitting layer. , Preferably including a luminescent material and a host material.
  • the light emitting material may be a fluorescent material or a phosphorescent material.
  • the fluorescent material may emit delayed fluorescence.
  • an organic compound in which at least one of excited singlet energy and excited triplet energy has a value higher than that of the light-emitting material can be used.
  • singlet excitons and triplet excitons generated in the light emitting material can be confined in the molecule of the light emitting material, and the light emission efficiency can be sufficiently extracted.
  • high luminous efficiency can be obtained, so that host materials that can achieve high luminous efficiency are particularly limited. And can be used in the present invention.
  • light emission is generated from the light emitting material contained in the light emitting layer.
  • This luminescence may include both fluorescence and delayed fluorescence, or may be phosphorescence.
  • light emission from the host material may be partly or partly emitted.
  • the amount of the light emitting material contained in the light emitting layer is preferably 0.1% by weight or more, more preferably 1% by weight or more, and 50% by weight or less. Preferably, it is 20% by weight or less, more preferably 10% by weight or less.
  • the host material in the light-emitting layer is preferably an organic compound that has a hole transporting ability and an electron transporting ability, prevents the emission of longer wavelengths, and has a high glass transition temperature.
  • the injection layer is a layer provided between the electrode and the organic layer for lowering the driving voltage and improving the luminance of light emission.
  • the injection layer can be provided as necessary.
  • the blocking layer is a layer that can prevent diffusion of charges (electrons or holes) and / or excitons existing in the light emitting layer to the outside of the light emitting layer.
  • the electron blocking layer can be disposed between the light emitting layer and the hole transport layer and blocks electrons from passing through the light emitting layer toward the hole transport layer.
  • a hole blocking layer can be disposed between the light emitting layer and the electron transporting layer to prevent holes from passing through the light emitting layer toward the electron transporting layer.
  • the blocking layer can also be used to block excitons from diffusing outside the light emitting layer. That is, each of the electron blocking layer and the hole blocking layer can also function as an exciton blocking layer.
  • the term “electron blocking layer” or “exciton blocking layer” as used herein is used in the sense of including a layer having the functions of an electron blocking layer and an exciton blocking layer in one layer.
  • the hole blocking layer has a function of an electron transport layer in a broad sense.
  • the hole blocking layer has a role of blocking holes from reaching the electron transport layer while transporting electrons, thereby improving the recombination probability of electrons and holes in the light emitting layer.
  • the material for the hole blocking layer the material for the electron transport layer described later can be used as necessary.
  • the electron blocking layer has a function of transporting holes in a broad sense.
  • the electron blocking layer has a role to block electrons from reaching the hole transport layer while transporting holes, thereby improving the probability of recombination of electrons and holes in the light emitting layer. .
  • the exciton blocking layer is a layer for preventing excitons generated by recombination of holes and electrons in the light emitting layer from diffusing into the charge transport layer. It becomes possible to efficiently confine in the light emitting layer, and the light emission efficiency of the device can be improved.
  • the exciton blocking layer can be inserted on either the anode side or the cathode side adjacent to the light emitting layer, or both can be inserted simultaneously.
  • the layer when the exciton blocking layer is provided on the anode side, the layer can be inserted adjacent to the light emitting layer between the hole transport layer and the light emitting layer, and when inserted on the cathode side, the light emitting layer and the cathode Between the luminescent layer and the light-emitting layer.
  • a hole injection layer, an electron blocking layer, or the like can be provided between the anode and the exciton blocking layer adjacent to the anode side of the light emitting layer, and the excitation adjacent to the cathode and the cathode side of the light emitting layer can be provided.
  • an electron injection layer, an electron transport layer, a hole blocking layer, and the like can be provided.
  • the blocking layer is disposed, at least one of the excited singlet energy and the excited triplet energy of the material used as the blocking layer is preferably higher than the excited singlet energy and the excited triplet energy of the light emitting material.
  • the hole transport layer is made of a hole transport material having a function of transporting holes, and the hole transport layer can be provided as a single layer or a plurality of layers.
  • the hole transport material has any one of hole injection or transport and electron barrier properties, and may be either organic or inorganic.
  • hole transport materials that can be used include, for example, triazole derivatives, oxadiazole derivatives, imidazole derivatives, carbazole derivatives, indolocarbazole derivatives, polyarylalkane derivatives, pyrazoline derivatives and pyrazolone derivatives, phenylenediamine derivatives, arylamine derivatives, Examples include amino-substituted chalcone derivatives, oxazole derivatives, styrylanthracene derivatives, fluorenone derivatives, hydrazone derivatives, stilbene derivatives, silazane derivatives, aniline copolymers, and conductive polymer oligomers, particularly thiophene oligomers.
  • An aromatic tertiary amine compound and an styrylamine compound are preferably used, and an aromatic tertiary amine compound is more preferably used.
  • the electron transport layer is made of a material having a function of transporting electrons, and the electron transport layer can be provided as a single layer or a plurality of layers.
  • the electron transport material (which may also serve as a hole blocking material) may have a function of transmitting electrons injected from the cathode to the light emitting layer.
  • Examples of the electron transport layer that can be used include nitro-substituted fluorene derivatives, diphenylquinone derivatives, thiopyran dioxide oxide derivatives, carbodiimides, fluorenylidenemethane derivatives, anthraquinodimethane and anthrone derivatives, oxadiazole derivatives, and the like.
  • a thiadiazole derivative in which the oxygen atom of the oxadiazole ring is substituted with a sulfur atom, and a quinoxaline derivative having a quinoxaline ring known as an electron withdrawing group can also be used as an electron transport material.
  • a polymer material in which these materials are introduced into a polymer chain or these materials are used as a polymer main chain can also be used.
  • the film forming method of these layers is not particularly limited, and may be produced by either a dry process or a wet process.
  • the preferable material which can be used for an organic electroluminescent element is illustrated concretely.
  • the material that can be used in the present invention is not limited to the following exemplary compounds.
  • R, R ′, and R 1 to R 10 in the structural formulas of the following exemplary compounds each independently represent a hydrogen atom or a substituent.
  • X represents a carbon atom or a hetero atom forming a ring skeleton
  • n represents an integer of 3 to 5
  • Y represents a substituent
  • m represents an integer of 0 or more.
  • the organic electroluminescence device produced by the above method emits light by applying an electric field between the anode and the cathode of the obtained device. At this time, if the light is emitted by excited singlet energy, light having a wavelength corresponding to the energy level is confirmed as fluorescence emission and delayed fluorescence emission. In addition, in the case of light emission by excited triplet energy, a wavelength corresponding to the energy level is confirmed as phosphorescence. Since normal fluorescence has a shorter fluorescence lifetime than delayed fluorescence, the emission lifetime can be distinguished from fluorescence and delayed fluorescence.
  • the organic electroluminescence element of the present invention can be applied to any of a single element, an element having a structure arranged in an array, and a structure in which an anode and a cathode are arranged in an XY matrix. According to the present invention, an organic electroluminescence device having greatly improved luminous efficiency can be obtained.
  • the organic electroluminescence device of the present invention can be further applied to various uses. For example, it is possible to produce an organic electroluminescence display device using the organic electroluminescence element of the present invention. For details, see “Organic EL Display” (Ohm Co., Ltd.) written by Shizushi Tokito, Chiba Adachi and Hideyuki Murata. ) Can be referred to. In particular, the organic electroluminescence device of the present invention can be applied to organic electroluminescence illumination and backlights that are in great demand.
  • the organic electroluminescence element has been described as an example of the organic semiconductor element to which the present invention is applied.
  • the organic semiconductor element to which the present invention is applied only needs to have a substrate and a crystalline material film. It is not limited to a luminescence element.
  • the present invention can also be applied to organic solar cells, organic transistors, and the like.
  • the organic solar cell includes a pair of electrodes, an organic semiconductor layer containing a p-type organic semiconductor material and an n-type organic semiconductor material, and a substrate that supports each electrode and the organic semiconductor layer. Configured.
  • An organic / inorganic perovskite solar cell includes a pair of electrodes, a layer containing an organic / inorganic perovskite compound and a carrier transport layer provided between the electrodes, and a substrate supporting each electrode and each layer.
  • the organic transistor is provided with a source electrode and a drain electrode provided separately from each other, an organic semiconductor layer provided between the source electrode and the drain electrode, and a gate insulating layer on the organic semiconductor layer.
  • a semiconductor substrate that supports each electrode and the organic semiconductor layer is provided.
  • at least a crystalline material film that becomes an organic semiconductor layer is formed on a substrate to form a stacked body, and the stacked body includes A pressure process is performed. Thereby, a crystalline material film (organic semiconductor layer) having a high density is obtained, and an organic solar cell excellent in photoelectric conversion characteristics and an organic thin film transistor excellent in input / output characteristics can be obtained.
  • the evaluation of the light emission characteristics is as follows: source meter (manufactured by Keithley: 2400 series), semiconductor parameter analyzer (manufactured by Agilent Technologies: E5273A), optical power meter measuring device (manufactured by Newport: 1930C), optical spectrometer (Ocean Optics, USB2000), spectroradiometer (Topcon, SR-3) and streak camera (Hamamatsu Photonics C4334) were used.
  • the transistor characteristics were evaluated using a semiconductor parameter analyzer (manufactured by Agilent Technologies: B1500A).
  • the carrier mobility ( ⁇ ) and the threshold voltage (V th ) were obtained from the plot of drain current square root vs. gate voltage (V g ) using the following formula.
  • Example 1 ⁇ Production and evaluation of organic electroluminescence device> (Example 1) Each thin film was laminated at a vacuum degree of 10 ⁇ 4 Pa by a vacuum deposition method on a glass substrate on which an anode made of indium tin oxide (ITO) having a thickness of 100 nm was formed. First, H 2 Pc is deposited on ITO to a thickness of 200 nm to form an H 2 PC layer, then ⁇ -NPD is formed to a thickness of 50 nm, and Alq 3 is further formed to a thickness of 50 nm. A light emitting layer was formed.
  • ITO indium tin oxide
  • lithium fluoride (LiF) was vacuum-deposited at 0.8 nm, and then aluminum (Al) was evaporated at a thickness of 100 nm to form a cathode to obtain a laminate.
  • the density of the formed H 2 Pc layer was 0.81 g / cm 3 .
  • This laminated body was accommodated in a bag made of a polymer sheet having a thickness of 30 ⁇ m in a nitrogen glove box and the gas in the bag was exhausted, and then the bag was vacuum packed. Next, the bag body in which the laminate was vacuum-packed was set in a cold isostatic pressurizer filled with water (pressure medium), and pressurized at a temperature of 20 ° C. and a pressurization pressure of 200 MPa for 1 hour.
  • the thickness of the H 2 PC layer was reduced to 134 nm.
  • Density of H 2 PC layer after the pressure treatment is 1.23 g / cm 3, was 85.4% of the single crystal densities of H 2 Pc (1.44g / cm 3 ).
  • the emission spectrum of the produced organic electroluminescence device is shown in FIG. 2, the current density-voltage characteristic is shown in FIG. 3, and the external quantum efficiency-current density characteristic is shown in FIG.
  • Example 1 (Comparative Example 1) Example 1 except that a bag made of a polymer sheet having a thickness of 75 ⁇ m was used instead of a bag made of a polymer sheet having a thickness of 30 ⁇ m when cold isostatic pressing was performed on the laminate. In the same manner, an organic electroluminescence device was produced.
  • FIG. 4 shows the current density-voltage characteristics of the produced organic electroluminescence device
  • FIG. 6 shows the external quantum efficiency-current density characteristics.
  • Example 2 An organic electroluminescent element was produced in the same manner as in Example 1 except that cold isostatic pressing was not performed on the laminate.
  • the emission spectrum of the produced organic electroluminescence device is shown in FIG. 2, the current density-voltage characteristics are shown in FIGS. 3 and 4, and the external quantum efficiency-current density characteristics are shown in FIGS.
  • the organic electroluminescence device of Example 1 in which cold isostatic pressing was performed using a bag body having a thickness of 30 ⁇ m was compared without performing cold isostatic pressing.
  • the voltage at 100 mA / cm 2 was reduced by about 2 V (9.79 V ⁇ 7.59 V), and the external quantum efficiency was also high.
  • the current density-voltage curve (FIG. 4) of the organic electroluminescence element of Comparative Example 1 in which cold isostatic pressing was performed using a bag body having a thickness of 75 ⁇ m shows the organic density of Comparative Example 2.
  • the current density-voltage curve of the electroluminescence element was shifted to a higher voltage side, and the external quantum efficiency was low.
  • Example 2 A silicon oxide (SiO 2 ) layer having a thickness of 300 nm was formed on a silicon substrate, and hexamethyldisilazane (HMDS) treatment was performed. On this silicon substrate, each thin film was laminated at a vacuum degree of 10 ⁇ 4 Pa by a vacuum deposition method. First, H 2 Pc was deposited to a thickness of 50 nm on a silicon oxide layer that had been subjected to HMDS treatment to form an H 2 Pc layer. On top of that, gold (Au) was formed to a thickness of 200 nm to form a gate electrode to obtain a laminate.
  • HMDS hexamethyldisilazane
  • FIG. 7 shows the drain current-gate voltage characteristics of the manufactured organic transistor
  • FIG. 9 shows the drain current-drain voltage characteristics.
  • the voltage values shown above and below the curve represent the gate voltage.
  • Table 1 shows the carrier mobility of the thin film transistor obtained from the measured value.
  • Example 3 Comparative Example 3 except that a bag made of a polymer sheet with a thickness of 75 ⁇ m was used instead of a bag made of a polymer sheet with a thickness of 30 ⁇ m when cold isostatic pressing was performed on the laminate.
  • an organic transistor was produced.
  • the drain current-gate voltage characteristics of the fabricated organic transistor are shown in FIG. 8, and the drain current-drain voltage characteristics are shown in FIG. In FIG. 10, the voltage values shown above and below the curve represent the gate voltage.
  • Table 2 shows the carrier mobility of the thin film transistor obtained from the measured value.
  • Example 4 An organic transistor was produced in the same manner as in Example 2 except that cold isostatic pressing was not applied to the laminate.
  • the drain current-gate voltage characteristics of the fabricated organic transistor are shown in FIGS. 7 and 8, and the drain current-gate voltage characteristics are shown in FIGS. In FIGS. 11 and 12, the voltage values shown above and below the curve represent the gate voltage.
  • required from the measured value is shown to Table 1,2.
  • the organic transistor of Comparative Example 4 shown in FIGS. 7 and 11 and Table 1 corresponds to the organic transistor before performing cold isostatic pressing in Example 2, and the comparison shown in FIGS.
  • the organic transistor of Example 4 corresponds to the organic transistor before performing the cold isostatic pressing of Comparative Example 3.
  • the organic thin film transistor of Example 2 in which cold isostatic pressing was performed using a bag having a thickness of 30 ⁇ m was a comparative example in which cold isostatic pressing was not performed. About 16 times the carrier mobility could be obtained for the four organic transistors.
  • the carrier mobility of the organic transistor of Comparative Example 3 subjected to cold isostatic pressing using a 75 ⁇ m thick bag was lower than the carrier mobility of the organic transistor of Comparative Example 4. It was.
  • Example 3 Each thin film was laminated at a vacuum degree of 10 ⁇ 4 Pa by a vacuum deposition method on a glass substrate on which an anode made of indium tin oxide (ITO) having a thickness of 100 nm was formed.
  • ITO indium tin oxide
  • H 2 Pc was deposited on ITO to a thickness of 40 nm to form an H 2 Pc layer
  • C60 fullerene was formed to a thickness of 30 nm
  • BCP was formed to a thickness of 10 nm thereon.
  • silver (Ag) was vacuum-deposited with a thickness of 100 nm to form a cathode to obtain a laminate.
  • FIG. 13 shows current density-voltage characteristics of the manufactured organic solar battery under irradiation with pseudo sunlight (AM 1.5, 100 mA / cm 2 ), and Table 3 shows measured battery characteristics.
  • Example 5 An organic solar cell was produced in the same manner as in Example 3 except that cold isotropic pressure was not applied to the laminate.
  • FIG. 13 shows the current density-voltage characteristics of the produced organic solar cell, and Table 3 shows the measured battery characteristics.
  • Example 3 the organic solar cell of Example 3 in which cold isostatic pressing was performed using a bag body having a thickness of 30 ⁇ m was Comparative Example 5 in which cold isostatic pressing was not performed. As compared with the organic solar cell, a photoelectric conversion efficiency of about 1.5 times could be obtained.
  • a glass substrate on which an anode made of indium tin oxide (ITO) having a thickness of 150 nm was formed was prepared.
  • ITO indium tin oxide
  • PEDOT: PSS was spin-coated at 3000 rpm for 60 seconds to form a 25 nm thick coating film, and heated on a hot plate at 200 ° C. for 10 minutes to form a PEDOT: PSS layer.
  • a perovskite layer was formed in a nitrogen atmosphere glove box and hot isostatic pressing was performed.
  • a solution (370 mg / mL) was prepared by dissolving PbCl 2 and CH 3 NH 3 I in a molar ratio of 1: 3 in N, N-dimethylformamide, and the solution was added to the PEDOT: PSS layer at 4000 rpm.
  • the precursor layer was formed by spin coating for 30 seconds.
  • the precursor layer was heated on a hot plate at 60 ° C. for 30 minutes, followed by heating at 100 ° C. for 90 minutes.
  • the yellow precursor was converted into brown perovskite (CH 3 NH 3 PbI 3-x Cl x ) to obtain a perovskite layer having a thickness of 0.151 ⁇ m.
  • the comparative element 1 prepared in the same manner as the evaluation element 1 except that hot isostatic pressing is not performed, and non-hot isostatic pressing instead of performing hot isostatic pressing.
  • a comparative element 2 produced in the same manner as the above-described evaluation element 1 was prepared except that an annealing treatment at 90 ° C. was performed for 1 hour under pressure.
  • the perovskite layer of the evaluation element 1 subjected to hot isostatic pressing has a peak intensity increased by about 2.5 times that of the untreated perovskite layer of the comparative element 1, and the half width is about It was found that the crystal structure was further developed, and the perovskite layer of the comparative element 2 that was annealed under no pressure also showed an increase in peak intensity and a decrease in half-value width. Therefore, it was suggested that heating is advantageous for improving the crystallinity of the perovskite layer. From these results, it was confirmed that when hot isostatic pressing was performed on the perovskite layer, pinholes and voids between crystal grains were effectively compressed, and crystallinity was significantly improved.
  • L represents a carrier diffusion length of the perovskite layer
  • d represents the thickness of the perovskite layer
  • I P denotes the PL intensity when provided with the PC 71 BM layer or spiro over OMeTAD layer perovskite layer
  • I A represents the PL intensity when the PC 71 BM layer and the spiro-OMeTAD layer are not provided in the perovskite layer.
  • the element used for the measurement was produced as follows. A plurality of quartz glass substrates were prepared, and a perovskite layer was formed on each quartz glass substrate by changing the thickness by spin coating in a glove box in a nitrogen atmosphere. When performing spin coating, the rotation speed was 3000 rpm, 5000 rpm, or 8000 rpm, and the solution concentration was 295 mg / mL or 481 mg / mL. Next, a PC 71 BM layer having a thickness of 10 nm or a spiro-OMeTAD layer having a thickness of 20 nm was formed on the formed perovskite layer by a spin coating method to obtain a laminate.
  • the PC 71 BM layer is spin-coated with a chlorobenzene solution in which PC 71BM is dissolved at a concentration of 10 mg / mL for 30 seconds at 2000 rpm in a nitrogen atmosphere glove box, and then heated on a hot plate at 90 ° C. for 15 minutes.
  • the spiro-OMeTAD layer was formed by spin-coating a chlorobenzene solution in which spiro-OMeTAD was dissolved at a concentration of 0.02M for 30 seconds at 2000 rpm, and then allowing it to stand overnight.
  • the produced laminate is housed in a bag made of a polymer sheet having a thickness of 30 ⁇ m and subjected to hot isostatic pressing under the same conditions as used in (Evaluation of Perovskite Layer Form and Crystallinity).
  • various evaluation elements were produced.
  • various comparative elements prepared in the same manner as the above-described various evaluation elements except that hot isostatic pressing is not performed, and non-pressurizing instead of hot isostatic pressing.
  • Various comparison elements prepared in the same manner as the above-described various evaluation elements were prepared except that the annealing treatment at 90 ° C. was performed under pressure.
  • the element for evaluation subjected to hot isostatic pressing was able to obtain a longer diffusion length for both electrons and holes than the comparative element that was not treated.
  • the comparison element that has been annealed under non-pressurization has a longer electron and hole diffusion length because many pinholes and crystal grains exist in the perovskite layer. It is thought that this is because PC 71 BM and spiro-OMeTAD easily permeate, thereby quenching electrons, holes, and excitons.
  • the results in Table 5 seen with the comparative element annealed under no pressure means an extension of the apparent carrier diffusion length, and there are many pinholes and voids between particles. It is presumed that it is derived from.
  • Example 4 On a quartz glass substrate on which an anode made of indium tin oxide (ITO) having a thickness of 150 nm is formed under the same conditions as those used in the above (evaluation of the form and crystallinity of the perovskite layer), PEDOT: A PSS layer and a perovskite layer were formed. Further, a chlorobenzene solution in which PC 71 BM was dissolved at a concentration of 10 mg / mL was spin-coated at 2000 rpm for 30 seconds, and then heated on a hot plate at 90 ° C. for 15 minutes to form a PC 71 BM layer.
  • ITO indium tin oxide
  • each thin film was laminated on the PC 71 BM layer at a vacuum degree of 10 ⁇ 4 Pa by a vacuum deposition method.
  • the C 60 is formed in a thickness of 10nm on the PC 71 BM layer, was formed thereon the BCP to a thickness of 10nm.
  • a cathode was formed by vapor-depositing Ag to a thickness of 200 nm to obtain a laminate.
  • the produced laminate is housed in a bag made of a polymer sheet having a thickness of 30 ⁇ m and subjected to hot isostatic pressing under the same conditions as used in (Evaluation of Perovskite Layer Form and Crystallinity).
  • FIG. 18 shows the current density-voltage characteristics of the produced organic solar battery under simulated sunlight (AM1.5G, 100 mW / cm 2 ), and Table 6 shows the measured battery characteristics.
  • FIG. 18 shows the current density-voltage characteristics of the produced organic solar battery under simulated sunlight (AM1.5G, 100 mW / cm 2 ), and Table 6 shows the measured battery characteristics.
  • FIG. 18 shows the current density-voltage characteristics of the produced organic solar battery under simulated sunlight (AM1.5G, 100 mW / cm 2 ), and Table 6 shows the measured battery characteristics.
  • Example 5 As shown in Table 6, the organic solar cell of Example 5 in which hot isostatic pressing was performed using a bag body having a thickness of 30 ⁇ m was approximately the same as the untreated Comparative Example 6 solar cell. A photoelectric conversion efficiency of 1.5 times could be obtained.
  • Example 5 A toluene solution of F8BT (concentration 20 mg / mL) was prepared. The prepared F8BT toluene solution was applied on a glass substrate on which an anode made of indium tin oxide (ITO) having a film thickness of 100 nm was formed by spin coating at 3000 rpm for 30 seconds, and then at 10O 0 C at 100 ° C. The F8BT layer was formed by baking for minutes.
  • ITO indium tin oxide
  • the preparation of the toluene solution, spin coating, and baking were performed in a glove box in a nitrogen atmosphere. Further, the thickness of the formed F8BT layer was 90 nm.
  • a cathode was formed on the F8BT layer by vacuum deposition of Al with a thickness of 100 nm under a vacuum degree of 10 ⁇ 4 Pa.
  • the obtained laminate made of ITO substrate / F8BT layer / Al cathode is accommodated in a bag made of a 30 ⁇ m polymer sheet and subjected to cold isostatic pressing under the same conditions as in Example 1 to obtain a single layer element. Obtained.
  • the thickness of the F8BT layer after the pressure treatment was 0.09 ⁇ m.
  • FIG. 19 shows the voltage-current density characteristics of the fabricated single layer element.
  • FIG. 19 shows the voltage-current density characteristics of the fabricated single layer element. From FIG. 19, the single layer element of Example 5 subjected to cold isostatic pressing has a current density several times that of the single layer element of Comparative Example 8 not subjected to cold isostatic pressing. It can be seen that it has improved. Then, when the driving voltage at a current density of 50 mA / cm 2 was compared, it was found that the driving voltage decreased by about 1 V (13.2 ⁇ 12.3 V) on average due to cold isostatic pressing. This result indicates that the contact between the electrode and the F8BT layer is improved, considering that no change in film thickness was observed before and after isotropic pressure application.
  • an organic semiconductor element capable of obtaining high carrier mobility can be manufactured by a simple process. For this reason, if the manufacturing method of this invention is used, the organic electroluminescent element, organic solar cell, and organic transistor which have the outstanding characteristic can be manufactured efficiently, and industrial applicability is high.

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Abstract

Selon la présente invention, la production d'un élément semi-conducteur organique consiste à : placer un stratifié, qui comprend un substrat et un film de matériau cristallin formé sur le substrat, dans un sac constitué d'une feuille ayant une épaisseur de 0,1 à 40 µm; évacuer un gaz du sac et sceller le sac; et pressuriser de manière isotrope le stratifié à travers le sac. De cette façon, il est possible de fournir un élément semi-conducteur organique dans lequel la densité du film de matériau cristallin est élevée et qui a une grande mobilité de porteurs de charge et une grande longueur de diffusion des porteurs de charge.
PCT/JP2015/074425 2014-08-29 2015-08-28 Procédé de production d'un élément semi-conducteur organique, et élément semi-conducteur organique Ceased WO2016031962A1 (fr)

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