WO2014200309A1 - 유기태양전지 및 이의 제조방법 - Google Patents
유기태양전지 및 이의 제조방법 Download PDFInfo
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- WO2014200309A1 WO2014200309A1 PCT/KR2014/005219 KR2014005219W WO2014200309A1 WO 2014200309 A1 WO2014200309 A1 WO 2014200309A1 KR 2014005219 W KR2014005219 W KR 2014005219W WO 2014200309 A1 WO2014200309 A1 WO 2014200309A1
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- WIPO (PCT)
- Prior art keywords
- layer
- electrode
- solar cell
- metal oxide
- organic solar
- Prior art date
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Images
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/80—Constructional details
- H10K30/81—Electrodes
- H10K30/82—Transparent electrodes, e.g. indium tin oxide [ITO] electrodes
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/10—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising heterojunctions between organic semiconductors and inorganic semiconductors
- H10K30/15—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/10—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising heterojunctions between organic semiconductors and inorganic semiconductors
- H10K30/15—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2
- H10K30/151—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2 the wide bandgap semiconductor comprising titanium oxide, e.g. TiO2
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/10—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising heterojunctions between organic semiconductors and inorganic semiconductors
- H10K30/15—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2
- H10K30/152—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2 the wide bandgap semiconductor comprising zinc oxide, e.g. ZnO
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/30—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising bulk heterojunctions, e.g. interpenetrating networks of donor and acceptor material domains
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2102/00—Constructional details relating to the organic devices covered by this subclass
- H10K2102/10—Transparent electrodes, e.g. using graphene
- H10K2102/101—Transparent electrodes, e.g. using graphene comprising transparent conductive oxides [TCO]
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- H—ELECTRICITY
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/50—Photovoltaic [PV] devices
-
- 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 specification relates to an organic solar cell and a method of manufacturing the same.
- Solar cells are devices that can directly convert solar energy into electrical energy by applying the photovoltaic effect.
- Solar cells can be divided into inorganic solar cells and organic solar cells according to the material constituting the thin film.
- Typical solar cells are made of p-n junctions by doping crystalline silicon (Si), an inorganic semiconductor. Electrons and holes generated by absorbing light diffuse to the p-n junction and are accelerated by the electric field to move to the electrode.
- the power conversion efficiency of this process is defined as the ratio of the power given to the external circuits and the solar power entered into the solar cell, and is now up to 24% when measured under standardized virtual solar irradiation conditions.
- the conventional inorganic solar cell has already shown a limit in the economic and material supply and demand, organic solar cells having easy processing, low cost and various functionalities are spotlighted as long-term alternative energy sources.
- the monomolecular organic material or the polymer material used in the organic solar cell has the advantage of being easy, fast and inexpensive and large area process.
- the organic solar cell has a disadvantage of low energy conversion efficiency. Therefore, efficiency improvement is very important to secure competitiveness with other solar cells at this time.
- the present specification is to provide an organic solar cell and a method of manufacturing the same.
- One embodiment of the present specification is a substrate; A first electrode provided on the substrate; A second electrode provided to face the first electrode; One or more organic material layers including a photoactive layer provided between the first electrode and the second electrode; And an electrode reformed layer provided between the first electrode and the photoactive layer, wherein the electrode reformed layer has a two-layer structure including a layer containing a metal oxide and a layer containing a halogenated alkali-based metal. And a layer comprising a halogenated alkali-based metal are provided in contact with each other, and the total thickness of the layer including the metal oxide is 15 from an interface between the layer including the metal oxide and the layer containing the halogenated alkali-based metal. It provides an organic solar cell in which the cation of the halogenated alkali metal is diffused to a thickness of less than or equal to%.
- One embodiment of the present specification is a substrate; A first electrode provided on the substrate; A second electrode provided to face the first electrode; One or more organic material layers including a photoactive layer provided between the first electrode and the second electrode; And an electrode reformed layer provided between the first electrode and the photoactive layer, wherein the electrode reformed layer has a single layer structure including a metal oxide and a halogenated alkali-based metal.
- One embodiment of the present specification comprises the steps of preparing a substrate; Forming a first electrode on the substrate; Forming an electrode reformed layer on the first electrode; Forming at least one organic material layer including a photoactive layer on the two electrode reformed layers; And forming a second electrode on the organic material layer, wherein the electrode reformed layer has a two-layer structure including a layer including a metal oxide and a layer including a halogenated alkali-based metal, and the layer including the metal oxide.
- a layer comprising a halogenated alkali-based metal is provided in contact with each other, the thickness of not more than 15% of the total thickness of the layer containing the metal oxide from the interface between the layer comprising the metal oxide and the layer comprising the halogenated alkali-based metal.
- a method of manufacturing an organic solar cell in which cations of the halogenated alkali-based metal are diffused.
- One embodiment of the present specification comprises the steps of preparing a substrate; Forming a first electrode on the substrate; Forming an electrode reformed layer on the first electrode; Forming at least one organic material layer including a photoactive layer on the two electrode reformed layers; And forming a second electrode on the organic material layer, wherein the electrode reformed layer has a single layer structure including a halogenated alkali metal and a metal oxide.
- the organic solar cell according to the exemplary embodiment of the present specification has excellent electron transfer capability, thereby realizing an increase in optical short-circuit current density J sc and an increase in efficiency.
- the organic solar cell according to the exemplary embodiment of the present specification may implement high efficiency by improving a fill factor (FF).
- FF fill factor
- the organic solar cell according to the exemplary embodiment of the present specification can improve the open contact property of the electrode and the organic material layer, and can lower the charge injection barrier through energy barrier control to prevent increase of charge collection and recombination of charge. .
- the organic solar cell according to the exemplary embodiment of the present specification may lower the heat treatment temperature at the time of manufacture, thereby lowering the unit cost.
- the organic solar cell according to the exemplary embodiment of the present specification can be manufactured at a low heat treatment temperature, there is an advantage that the substrate of the plastic material can be applied.
- 1 to 3 illustrate a laminated structure of an organic solar cell according to an exemplary embodiment of the present specification.
- One embodiment of the present specification is a substrate; A first electrode provided on the substrate; A second electrode provided to face the first electrode; One or more organic material layers including a photoactive layer provided between the first electrode and the second electrode; And an electrode reformed layer provided between the first electrode and the photoactive layer.
- the electrode reformed layer is a two-layer structure consisting of a layer containing a metal oxide and a layer containing a halogenated alkali-based metal,
- the layer containing the metal oxide and the layer containing a halogenated alkali-based metal are provided in contact with each other,
- Organic solar cell in which the cation of the halogenated alkali-based metal is diffused from the interface between the layer including the metal oxide and the layer containing the halogenated alkali-based metal to a thickness of 15% or less of the total thickness of the layer including the metal oxide.
- the halogenated alkali-based metal from the interface between the layer containing the metal oxide and the layer containing the halogenated alkali-based metal to a thickness of 10% or less of the total thickness of the layer including the metal oxide.
- the cation of can diffuse.
- a layer including the metal oxide may be provided on the first electrode, and a layer including the halogenated alkali metal may be provided on the layer including the metal oxide.
- a layer including the halogenated alkali metal may be provided on the first electrode, and a layer including the metal oxide may be provided on the layer including the halogenated alkali metal.
- FIGS. 1 and 2 illustrate a laminated structure of an organic solar cell according to an exemplary embodiment of the present specification.
- FIGS. 1 and 2 are provided with a first electrode 201 on a substrate 101 and a layer 401 including a metal oxide as a two-layer electrode modified layer on the first electrode 201.
- a layer 501 comprising a halogenated alkali-based metal a photoactive layer 601 is provided on the electrode reformed layer, a buffer layer 701 of the second electrode is provided on the photoactive layer,
- the stacked structure in which the second electrode is provided on the buffer layer 701 of the second electrode is illustrated.
- the organic solar cell according to the exemplary embodiment of the present specification is not limited to the stacked structure of FIGS. 1 and 2, and an additional layer may be further provided.
- the layer including the metal oxide may serve to modify the characteristics of the first electrode. Specifically, when the first electrode exhibits p-type semiconductor characteristics, a layer including a metal oxide having n-type semiconductor characteristics may be formed to change the characteristics of the first electrode.
- the layer containing the metal oxide can smooth the electron flow between the transparent electrode and the organic material layer.
- performance is low as an n type layer.
- the charging efficiency of the organic solar cell is not good due to poor interface characteristics with the organic layer applied on the layer including the metal oxide, and control of the thickness and planarization of the thin film is difficult.
- the layer containing the metal oxide has a problem that the use of a weak plastic substrate, such as heat is limited because the process of heat treatment at a high temperature for the production of nanostructures. Accordingly, the present inventors have developed an organic solar cell capable of realizing high performance even by lowering the heat treatment temperature of the layer including the metal oxide.
- the organic solar cell according to the exemplary embodiment of the present specification may further exhibit excellent performance even with low heat treatment by further including a layer containing a halogenated alkali-based metal in the layer including the metal oxide as an electrode reforming layer. Specifically, the organic solar cell according to the exemplary embodiment of the present specification may lower the charge injection barrier due to the dipole formed between the transparent electrode and the metal oxide or between the metal oxide and the photoactive layer. In addition, in the organic solar cell according to the exemplary embodiment of the present specification, the doping effect of the alkali-based metal by the layer including the halogenated alkali-based metal is generated, thereby improving charge collection and transport characteristics and increasing charge density. have.
- the layer containing the halogenated alkali-based metal may serve to modify the properties of the layer including the transparent electrode and / or the metal oxide.
- the layer containing the halogenated alkali-based metal can lower the interface barrier with the organic material layer, and there is an advantage of forming a layer containing a metal oxide even by low temperature heat treatment.
- the organic solar cell according to an embodiment of the present disclosure is also the low temperature heat treatment process of 150 °C or less It is possible to form a layer comprising a metal oxide.
- the organic solar cell according to the exemplary embodiment of the present specification may improve the disadvantage of the layer including the metal oxide due to the low temperature heat treatment, and thus there is an advantage in that various kinds of substrates may be applied. That is, there is an advantage in that an organic solar cell can be manufactured using a flexible substrate, particularly a plastic substrate, which is difficult to apply at high temperature.
- One embodiment of the present specification is a substrate; A first electrode provided on the substrate; A second electrode provided to face the first electrode; One or more organic material layers including a photoactive layer provided between the first electrode and the second electrode; And an electrode reformed layer provided between the first electrode and the photoactive layer.
- the electrode reformed layer provides an organic solar cell having a single layer structure including a metal oxide and a halogenated alkali metal.
- FIG. 3 illustrates a laminated structure of an organic solar cell according to an exemplary embodiment of the present specification.
- FIG. 3 is provided with a first electrode 201 on the substrate 101, an electrode reformed layer 801 having a single layer structure on the first electrode 201, and the electrode reformed layer (
- the photoactive layer 601 is provided on the 801
- the buffer layer 701 of the second electrode is provided on the photoactive layer
- the stacked structure is provided on the buffer layer 701 of the second electrode.
- the organic solar cell according to the exemplary embodiment of the present specification is not limited to the stacked structure of FIG. 3, and an additional layer may be further provided.
- the electrode reformed layer of the single layer structure may have a ratio of the cation of the metal oxide and the cation of the halogenated alkali-based metal is 100: 1 to 10: 2.
- the organic solar cell including the electrode reformed layer of the single layer structure may exhibit the same effect as the organic solar cell including the electrode reformed layer of the two-layer structure described above. That is, the organic solar cell including the electrode reformed layer having the single layer structure may realize excellent performance even at a low temperature heat treatment of 150 ° C. or less. Specifically, the charge transfer capability of the electrode reformed layer may be increased by the halogenated alkali metal, and thus a highly conductive metal oxide structure may be formed in the electrode reformed layer even through a low temperature heat treatment process. .
- the electrode reformed layer of the single layer structure can be easily implemented in a solution without using a dry process such as evaporation to form a halogenated alkali-based metal layer, there is an advantage that can be implemented at a low cost when large area .
- the electrode reformed layer may be provided in contact with the first electrode.
- the metal oxide is a group consisting of ZnO, TiO x NiO, RuO, V 2 O 5 , WO x , Cs 2 CO 3 , MoO 3 , ZrO 2 , Ta 2 O 3 , and MgO It may include one or two or more selected from.
- the layer including the halogenated alkali metal layer is LiF, NaF, KF, RbF, CsF, FrF, BeF 2, MgF 2, CaF 2, SrF 2, BaF 2 and RaF 2 It may include one or two or more selected from the group consisting of.
- the layer including the metal oxide may be doped with alkali metal ions.
- the thickness of the layer including the metal oxide may be 5 nm or more and 200 nm or less. Specifically, according to one embodiment of the present specification, the thickness of the layer containing the metal oxide may be 20 nm or more and 60 nm or less.
- the thickness of the layer including the halogenated alkali-based metal may be 0.1 nm or more and 15 nm or less. Specifically, according to one embodiment of the present specification, the thickness of the layer containing the halogenated alkali-based metal may be 1 nm or more and 7 nm or less.
- the thickness of the electrode reformed layer of the single layer structure may be 5 nm or more and 200 nm or less. Specifically, according to an exemplary embodiment of the present specification, the thickness of the electrode reformed layer of the single layer structure may be 20 nm or more and 60 nm or less.
- the electrode reformed layer may be a transparent electrode reformed layer.
- the first electrode may be a transparent electrode.
- the second electrode may be a metal electrode.
- the first electrode may be a transparent electrode
- the second electrode may be a metal electrode
- the first electrode and the second electrode may be a transparent electrode.
- the first electrode may be a metal electrode
- the second electrode may be a transparent electrode
- Transparent as used herein may mean that the transmittance of the visible line is 50% or more. Specifically, the “transparent” may mean that the transmittance of visible light is 75% or more and 100% or less.
- the transparent electrode may be a transparent conductive oxide layer.
- the transparent conductive oxide layer is in addition to glass and quartz plate, polyethylene terephthalate (PET), polyethylene naphthelate (PEN), polyperopylene (PP), polyimide (PI), polycarbornate (PC), polystyrene (PS), polyoxyethlene (POM) Doped with a conductive material on a flexible and transparent substrate such as a plastic, including an AS resin (acrylonitrile styrene copolymer), ABS resin (acrylonitrile butadiene styrene copolymer), triacetyl cellulose (TAC), and polyarylate (PAR).
- AS resin acrylonitrile styrene copolymer
- ABS resin acrylonitrile butadiene styrene copolymer
- TAC triacetyl cellulose
- PAR polyarylate
- the transparent conductive oxide layer is indium tin oxide (ITO), fluorine doped tin oxide (FTO), aluminum doped zinc oxide (AZO), indium zinc oxide (IZO), ZnO-Ga 2 O 3 , ZnO-Al 2 O 3, antimony tin oxide (ATO), and the like, and more specifically, ITO.
- the metal electrode is silver (Ag), aluminum (Al), platinum (Pt), platinum (Pt), tungsten (W), copper (Cu), molybdenum (Mo), It may include one or two or more selected from the group consisting of gold (Au), nickel (Ni) and palladium (Pd). More specifically, the metal electrode may be silver (Ag).
- the substrate may include one or more selected from the group consisting of glass, a polymer material, and a metal.
- the substrate may be a transparent substrate.
- the transparent substrate may be soda ash glass or transparent plastic, but is not limited thereto.
- the substrate may be a flexible substrate.
- the substrate may be a flexible substrate including a polymer material.
- the substrate may be a plastic substrate.
- the polymer material is polyimide (PI), polycarbonate (PC), polyether sulfone (PES), polyether ether ketone (PEEK), polybutylene terephthalate (PBT), polyethylene Terephthalate (PET), polyvinyl chloride (PVC), polyethylene (PE), ethylene copolymer, polypropylene (PP), propylene copolymer, poly (4-methyl-1-pentene) (TPX), polyarylate ( PAR), polyacetal (POM), polyphenylene oxide (PPO), polysulfone (PSF), polyphenylene sulfide (PPS), polyvinylidene chloride (PVDC), polyvinyl acetate (PVAC), polyvinyl alcohol ( PVAL), polyvinyl acetal, polystyrene (PS), AS resin, ABS resin, polymethyl methacrylate (PMMA), fluorine resin, phenol resin (PF), melamine resin (MF),
- PI polyimide
- PC poly
- the first electrode may be an anode, and the second electrode may be a cathode.
- the first electrode may be a cathode, and the second electrode may be an anode.
- the organic solar cell may have an inverted structure.
- the inverted structure means that the first electrode provided on the substrate is a cathode.
- the organic solar cell may have a normal structure.
- the normal structure means that the first electrode provided on the substrate is an anode.
- the organic solar cell may further include a buffer layer of a second electrode provided between the photoactive layer and the second electrode.
- the buffer layer of the second electrode may be located between the metal electrode and the photoactive layer, and the buffer layer controls the interfacial energy between the metal electrode and the photoactive layer to facilitate smooth charge flow. Can be induced.
- the buffer layer of the second electrode may include a conductive polymer and / or a metal oxide.
- the conductive polymer may be a conjugated polymer material, a dielectric polymer, graphene carbon nanotubes and a composite thereof.
- the conjugated polymer material is PEN (poly [(9,9-bis (30- (N, N-dimethylamino) propyl) -2,7-fluorene) -alt-2,7- (9,9-dioctylfluorene )]) And FPQ-Br (poly [9,9'-bis [6 ''-(N, N, N-trimethylammonium) hexyl] fluorene-co-alt-phenylene] dibromide).
- the dielectric polymer may be polyethylenimine (PEI), polyethylenimine ethoxylated (PEIE), or the like.
- the conductive polymer may include one or two or more selected from the group consisting of phthalocyanine derivatives, naphthalocyanine derivatives, aromatic amine compounds, polyethylenedioxythiophene (PEDOT: PSS) and polyaniline.
- the metal oxide included in the buffer layer of the second electrode may include V 2 O 5 , and / or MoO 3 .
- the photoactive layer may be a bulk heterojunction structure or a double layer junction structure.
- the bulk heterojunction structure may be a bulk heterojunction (BHJ) junction type
- the bilayer junction structure may be a bi-layer junction type.
- the bi-layer p-n junction photoactive unit includes a photoactive layer including two layers of a p-type semiconductor thin film and an n-type semiconductor thin film.
- the bulk heterojunction (BHJ) bonded photoactive unit includes a photoactive layer in which an n-type semiconductor and a p-type semiconductor are blended.
- the photoactive layer of the present specification forms an exciton in which a p-type semiconductor is paired with electrons and holes by photo excitation, and the exciton is separated into electrons and holes at the p-n junction.
- the separated electrons and holes move to the n-type semiconductor thin film and the p-type semiconductor thin film, respectively, and they are collected by the first electrode and the second electrode, respectively, so that they can be used as electrical energy from the outside.
- the photoactive layer includes an electron donor material and an electron acceptor material as a photoactive material.
- the photoactive material may mean the electron donor material and the electron acceptor material.
- the photoactive layer forms excitons in which the electron donor material pairs electrons and holes by photoexcitation, and the excitons are separated into electrons and holes at the interface of the electron donor / electron acceptor.
- the separated electrons and holes move to the electron donor material and the electron acceptor material, respectively, and are collected by the first electrode and the second electrode, respectively, so that they can be used as electrical energy from the outside.
- the mass ratio of the electron donor material and the electron acceptor material may be 1:10 to 10: 1.
- the mass ratio of the electron acceptor material and the electron donor material of the present specification may be 1: 0.5 to 1: 5.
- an electron donor material and an electron accepting material may form a bulk heterojunction (BHJ).
- the photoactive layer of the present specification may be annealed at 30 to 300 ° C. for 1 second to 24 hours to maximize properties after the electron donating material and the electron accepting material are mixed.
- the photoactive layer may include at least one electron donor material and at least one electron acceptor material.
- the photoactive layer may include at least two kinds of electron donor materials and at least one kind of electron acceptor material.
- the photoactive layer may include at least one electron donor material and at least two electron acceptor materials.
- the electron donor material is at least one electron donor; Or a polymer of at least one kind of electron acceptor and at least one kind of electron donor.
- the electron donor may include at least one kind of electron donor.
- the electron donor material may include a polymer of at least one kind of electron acceptor and at least one kind of electron donor.
- the electron donor material may be a copolymer including at least one of the electron acceptors represented by the following formula.
- R 2 to R 5 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Halogen group; Nitrile group; Nitro group; Imide group; Amide group; Hydroxyl group; Substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkylthioxy group; Substituted or unsubstituted arylthioxy group; Substituted or unsubstituted alkyl sulfoxy group; Substituted or unsubstituted aryl sulfoxy group; Substituted or unsubstituted alkenyl group; Substituted or unsubstituted silyl group; Substituted or unsubstituted boron group; Substi
- X 1 and X 2 are the same as or different from each other, and are each independently selected from the group consisting of CRR ', NR, O, SiRR', PR, S, GeRR 'and Se, Te, Y 1 to Y 4 are each other The same or different, each independently selected from the group consisting of CR, N, SiR, P, GeR and;
- R and R ' are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Halogen group; Nitrile group; Nitro group; Imide group; Amide group; Hydroxyl group; Substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkylthioxy group; Substituted or unsubstituted arylthioxy group; Substituted or unsubstituted alkyl sulfoxy group; Substituted or unsubstituted aryl sulfoxy group; Substituted or unsubstituted alkenyl group; Substituted or unsubstituted silyl group; Substituted or unsubstituted boron group; Substi
- the electron donating material may be a copolymer containing at least one of the electron donors represented by the following formula.
- R 2 and R 3 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Halogen group; Nitrile group; Nitro group; Imide group; Amide group; Hydroxyl group; Substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkylthioxy group; Substituted or unsubstituted arylthioxy group; Substituted or unsubstituted alkyl sulfoxy group; Substituted or unsubstituted aryl sulfoxy group; Substituted or unsubstituted alkenyl group; Substituted or unsubstituted silyl group; Substituted or unsubstituted boron group; Substi
- X 1 to X 3 are the same as or different from each other, and are each independently selected from the group consisting of CRR ', NR, O, SiRR', PR, S, GeRR ', Se and Te, Y 1 and Y 2 are each other The same or different, each independently selected from the group consisting of CR, N, SiR, P, and GeR,
- R and R ' are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Halogen group; Nitrile group; Nitro group; Imide group; Amide group; Hydroxyl group; Substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkylthioxy group; Substituted or unsubstituted arylthioxy group; Substituted or unsubstituted alkyl sulfoxy group; Substituted or unsubstituted aryl sulfoxy group; Substituted or unsubstituted alkenyl group; Substituted or unsubstituted silyl group; Substituted or unsubstituted boron group; Substi
- A may be an integer of 1 to 4
- b may be an integer of 1 to 6
- c may be an integer of 1 to 8
- d may be an integer of 1 to 3
- e is 1 to 3 It may be an integer of.
- the photoactive layer may further include an additive.
- the additive may be a material for controlling the movement of the charge and the density of the charge, specifically, Lewis acid material, F4-TCNQ, dihydrobenzoimidazole-based material, metallocene dimer Material and the like.
- the additive may be a material for controlling the miscibility and / or morphology of the photoactive layer, and specifically, 1,8-diidooctane (1,8-Diiodooctane) , 1,8-octandithiol (1,8-octanedithiol), triethyleneglycol, 1,8-dibromooctane, 1,4-diidobutane (1,4 -Diiodobutane, 1,6-Diiodohexane, Hexadecane, Diethyleneglycoldibutylether, 1-Chlorophthalene, Nitrobenzene ), 4-bromoanisole, N-methyl-2-pyrrolidone, 3-methylthiophene, 3-hexylthiophene 3-Hexylthiophene, Polydimethylsiloxane, 1-Methylnaphthalen
- the electron donor material is thiophene-based, fluorene-based, carbazole-based, etc. starting with MEH-PPV (poly [2-methoxy-5- (2'-ethyl-hexyloxy) -1,4-phenylene vinylene]) It can be a variety of high molecular and monomolecular materials.
- the monomolecular substance is copper (II) phthalocyanine, zinc phthalocyanine, tris [4- (5-dicynomethylidemethyl-2-thienyl) phenyl] Amine (tris [4- (5-dicyanomethylidenemethyl-2-thienyl) phenyl] amine), 2,4-bis [4- (N, N-dibenzylamino) -2,6-dihydroxyphenyl] squalane (2,4-bis [4- (N, N-dibenzylamino) -2,6-dihydroxyphenyl] squaraine), benz [b] anthracene, and pentacene It may include one or more materials.
- the polymer material is poly 3-hexyl thiophene (P3HT: poly 3-hexyl thiophene), PCDTBT (poly [N-9'-heptadecanyl-2,7-carbazole-alt-5,5- (4'-) 7'-di-2-thienyl-2 ', 1', 3'-benzothiadiazole)]), PCPDTBT (poly [2,6- (4,4-bis- (2-ethylhexyl) -4H-cyclopenta [2, 1-b; 3,4-b '] dithiophene) -alt-4,7- (2,1,3-benzothiadiazole)]), PFO-DBT (poly [2,7- (9,9-dioctyl-fluorene) ) -alt-5,5- (4,7-di 2-thienyl-2,1,3-benzothiadiazole)]), PTB7 (Poly [[4,8-bis [(2-a)
- the electron acceptor material may be a fullerene derivative or a nonfullerene derivative.
- the fullerene derivative is a fullerene derivative of C60 to C90.
- the fullerene derivative may be a C60 fullerene derivative or a C70 fullerene derivative.
- the C60 fullerene derivative or C70 fullerene derivative are each independently hydrogen; heavy hydrogen; Halogen group; Nitrile group; Nitro group; Imide group; Amide group; Hydroxyl group; Substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkylthioxy group; Substituted or unsubstituted arylthioxy group; Substituted or unsubstituted alkyl sulfoxy group; Substituted or unsubstituted aryl sulfoxy group; Substituted or unsubstituted alkenyl group; Substituted or unsubstituted silyl group; Substituted or unsubstituted or unsubstitute
- the fullerene derivative may be selected from the group consisting of C76 fullerene derivative, C78 fullerene derivative, C84 fullerene derivative, and C90 fullerene derivative.
- the C76 fullerene derivative, C78 fullerene derivative, C84 fullerene derivative and C90 fullerene derivative are each independently hydrogen; heavy hydrogen; Halogen group; Nitrile group; Nitro group; Imide group; Amide group; Hydroxyl group; Substituted or unsubstituted alkyl group; A substituted or unsubstituted cycloalkyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted aryloxy group; Substituted or unsubstituted alkylthioxy group; Substituted or unsubstituted arylthioxy group; Substituted or unsubstituted alkyl sulfoxy group; Substituted or unsubstituted aryl sulfoxy group; Substituted or unsubstituted alkenyl group; Substituted or unsubsti
- the fullerene derivative has an ability to separate electron-hole pairs (exciton, electron-hole pair) and charge mobility compared to the non-fullerene derivative, which is advantageous for efficiency characteristics.
- the photoactive layer is a poly 3-hexyl thiophene [P3HT: poly 3-hexyl thiophene] as an electron donor, [6,6] -phenyl-C 61 -butyl acid methyl ester (PC 61 BM) and / or [6,6] -phenyl-C 71 -butyl acid methyl ester (PC 71 BM) as the electron acceptor material.
- P3HT poly 3-hexyl thiophene
- the mass ratio of the electron donor material and the electron acceptor material may be 1: 0.4 to 1: 2, and specifically 1: 0.7.
- the photoactive layer is not limited to the above material.
- the photoactive materials are dissolved in an organic solvent and then the solution is introduced into the photoactive layer in a thickness ranging from 50 nm to 280 nm by spin coating or the like.
- the photoactive layer may be applied to a method such as dip coating, screen printing, spray coating, doctor blade, brush painting.
- the electron acceptor may include other fullerene derivatives such as C70, C76, C78, C80, C82, C84, including PC 61 BM, and the coated thin film may be heat-treated at 80 ° C. to 160 ° C. to determine the conductive polymer. It is good to increase the sex.
- the hole transport layer and / or the electron transport layer material of the present specification may be a material that increases the probability that the generated charge is transferred to the electrode by efficiently transferring electrons and holes to the photoactive layer, but is not particularly limited.
- the hole transport layer is PEDOT: PSS; Molybdenum oxide (MoO x ); Vanadium oxide (V 2 O 5 ); Nickel oxide (NiO); And tungsten oxide (WO x ) It may include one or more selected from the group consisting of.
- the hole transport layer may be an anode buffer layer.
- a hole transport layer may be introduced through spin coating, dip coating, inkjet printing, gravure printing, spray coating, doctor blade, bar coating, gravure coating, brush painting, thermal deposition, and the like.
- the hole transport layer may be formed to a thickness of 5 nm ⁇ 10 nm MoO 3 through a thermal deposition system.
- the organic solar cell may have a wound structure.
- the organic solar cell may be manufactured in the form of a flexible film, which may be rolled into a cylindrical shape to form a solar cell having a hollow structure. If the organic solar cell is a wound structure, it can be installed in a manner that is standing on the ground. In this case, while the sun at the position where the organic solar cell is installed is moved from east to west, it is possible to secure a portion where the incident angle of light is maximum. Therefore, there is an advantage to increase the efficiency by absorbing as much light as possible while the sun is floating.
- the organic solar cell includes a hole injection layer between the first electrode and the second electrode; Hole transport layer; Interlayers; Hole blocking layer; Charge generating layer; Electron blocking layer; And one or more organic material layers selected from the group consisting of electron transport layers.
- the hole transport layer and / or the electron transport layer material may be a material that increases the probability that the generated charge is transferred to the electrode by efficiently transferring electrons and holes to the photoactive layer, but is particularly limited. It doesn't work.
- the interlayer refers to a layer located between the hole injection layer and the hole transport layer.
- the charge generating layer is a layer in which holes and electrons are generated when a voltage is applied.
- the electron transport layer may include one or two or more selected from the group consisting of a conductive oxide and a metal.
- the conductive oxide of the electron transport layer may be electron-extracting metal oxides, specifically, titanium oxide (TiO x ); Zinc oxide (ZnO); And cesium carbonate (Cs 2 CO 3 ) It may include one or more selected from the group consisting of.
- the electron transport layer may be formed by being applied to one surface of the first electrode or coated in a film form using sputtering, E-Beam, thermal deposition, spin coating, screen printing, inkjet printing, doctor blade or gravure printing.
- the electron transport layer may be a cathode buffer layer.
- One embodiment of the present specification comprises the steps of preparing a substrate; Forming a first electrode on the substrate; Forming an electrode reformed layer on the first electrode; Forming at least one organic material layer including a photoactive layer on the two electrode reformed layers; And forming a second electrode on the organic material layer.
- the electrode reformed layer is a two-layer structure consisting of a layer containing a metal oxide and a layer containing a halogenated alkali-based metal,
- the layer containing the metal oxide and the layer containing a halogenated alkali-based metal are provided in contact with each other,
- Organic solar cell in which the cation of the halogenated alkali-based metal is diffused from the interface between the layer including the metal oxide and the layer containing the halogenated alkali-based metal to a thickness of 15% or less of the total thickness of the layer including the metal oxide. It provides a method of manufacturing.
- One embodiment of the present specification comprises the steps of preparing a substrate; Forming a first electrode on the substrate; Forming an electrode reformed layer on the first electrode; Forming at least one organic material layer including a photoactive layer on the two electrode reformed layers; And forming a second electrode on the organic material layer.
- the electrode reformed layer provides a method of manufacturing an organic solar cell having a single layer structure including a halogenated alkali metal and a metal oxide.
- the metal oxide layer may be formed by omitting a heat treatment process or may be formed using a heat treatment process of 50 ° C. or more and 250 ° C. or less.
- the electrode reformed layer of the single layer structure may be formed by omitting a heat treatment process, or may be formed using a heat treatment process of 50 ° C. or more and 250 ° C. or less.
- the electrode reformed layer may be formed by a solution process using halogenated alkali metal particles and metal oxide particles.
- the layer containing the metal oxide and the layer containing the halogenated alkali-based metal may be formed by a solution process, respectively.
- the layer containing the metal oxide is formed by a solution process, and the layer containing the halogenated alkali-based metal is formed by using a deposition process. Can be formed.
- the electrode reformed layer of the single layer structure may be formed using a sol-gel coating solution in which halogenated alkali metal particles and metal oxide particles are dispersed.
- the electrode reformed layer of the single layer structure may be formed by dispersing a halogenated alkali-based metal particle and a metal oxide particle in a solution.
- the ITO glass was washed with acetone and ethanol for 30 minutes using sonication, and surface treated for 15 minutes using UVO (uv / ozone).
- the ZnO solution was coated on the ITO glass, and then heat-treated at 200 ° C. for 10 minutes.
- a P3HT: PCBM solution mixed at a ratio of 1: 0.7 was formed to form a photoactive layer of about 220 nm, and then 110 ° C. Heat treatment for 10 minutes at.
- An organic solar cell was manufactured by depositing a MoO 3 / Ag electrode at 1 ⁇ 10 ⁇ 7 torr on the photoactive layer.
- An organic solar cell was manufactured in the same manner as in Example 1, except that LiF was deposited to a thickness of 3 kHz.
- An organic solar cell was manufactured in the same manner as in Example 1, except that LiF was deposited at a thickness of 5 kHz.
- An organic solar cell was manufactured in the same manner as in Example 1, without forming a LiF layer.
- V oc denotes an open voltage
- J sc denotes a short circuit current
- FF denotes a fill factor
- PCE denotes an energy conversion efficiency.
- the open-circuit and short-circuit currents are the X- and Y-axis intercepts in the four quadrants of the voltage-current density curve, respectively. The higher these two values, the higher the efficiency of the solar cell.
- the fill factor is the area of the rectangle drawn inside the curve divided by the product of the short circuit current and the open voltage. By dividing these three values by the intensity of the emitted light, the energy conversion efficiency can be obtained, and higher values are preferable.
- the ITO glass was washed with acetone and ethanol for 30 minutes using sonication, and surface treated for 15 minutes using UVO (uv / ozone). After coating the ZnO solution on the ITO glass and dried without heat treatment. After vacuum deposition of LiF on the ZnO layer at a thickness of 3 kPa at a vacuum degree of 1 ⁇ 10 -7 torr, a P3HT: PCBM solution mixed at a ratio of 1: 0.7 was formed to form a photoactive layer of about 220 nm, followed by 110 ° C. Heat treatment for 10 minutes at. An organic solar cell was manufactured by depositing a MoO 3 / Ag electrode at 1 ⁇ 10 ⁇ 7 torr on the photoactive layer.
- An organic solar cell was manufactured in the same manner as in Example 4, except that ZnO was heat-treated at 100 ° C. for 10 minutes.
- An organic solar cell was manufactured in the same manner as in Example 4, except that ZnO was heat-treated at 150 ° C. for 10 minutes.
- An organic solar cell was manufactured in the same manner as in Example 4, except that ZnO was heat-treated at 200 ° C. for 10 minutes.
- An organic solar cell was manufactured in the same manner as in Example 4, without forming a LiF layer.
- An organic solar cell was manufactured in the same manner as in Example 5, without forming a LiF layer.
- An organic solar cell was manufactured in the same manner as in Example 6, without forming a LiF layer.
- An organic solar cell was manufactured in the same manner as in Example 7, without forming a LiF layer.
- the ITO glass was washed with acetone and ethanol for 30 minutes using sonication, and surface treated for 15 minutes using UVO (UV / ozone).
- MgF 2 was vacuum deposited to a thickness of 1 kPa on the ITO glass at a vacuum degree of 1 ⁇ 10 ⁇ 7 torr, and then ZnO solution was coated and heat-treated at 200 ° C. for 10 minutes.
- PBDTTPD Poly (benzo [1,2-b: 4,5-b '] dithiophenealt-thieno [3,4-c] pyrrole-4,6-dione) and PC 61 BM on the ZnO layer were 1: 1.5 Coated with a 100 nm thick solution and then heat treated at 80 ° C. for 5 minutes to form a photoactive layer, and fabricating an organic solar cell by depositing a MoO 3 / Ag electrode at 1 ⁇ 10 ⁇ 7 torr on the photoactive layer. It was.
- An organic solar cell was manufactured in the same manner as in Example 8, except that the MgF 2 layer was formed to a thickness of 3 GPa.
- An organic solar cell was manufactured in the same manner as in Example 8, except that the MgF 2 layer was formed to a thickness of 5 mm 3.
- An organic solar cell was manufactured in the same manner as in Example 8, without forming the MgF 2 layer.
- 401 a layer comprising a metal oxide
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Abstract
Description
LiF 두께(Å) | Voc(V) | Jsc(mA/cm2) | FF | PCE(%) | |
비교예 1 | 0 | 0.628 | 8.48 | 0.575 | 3.06 |
실시예 1 | 1 | 0.622 | 7.92 | 0.52 | 2.56 |
실시예 2 | 3 | 0.634 | 8.86 | 0.6 | 3.37 |
실시예 3 | 5 | 0.636 | 8.57 | 0.598 | 3.26 |
열처리 온도(℃) | Voc(V) | Jsc(mA/cm2) | FF | PCE(%) | |
실시예 4 | 열처리 없음 | 0.518 | 0.015 | 0.564 | 4.46×10-3 |
실시예 5 | 100 | 0.598 | 0.063 | 0.423 | 0.016 |
실시예 6 | 150 | 0.612 | 10.98 | 0.607 | 4.08 |
실시예 7 | 200 | 0.61 | 10.91 | 0.598 | 3.98 |
비교예 2 | 열처리 없음 | 0.52 | 0.013 | 0.298 | 2.08×10-3 |
비교예 3 | 100 | 0.574 | 0.04 | 0.349 | 7.94×10-3 |
비교예 4 | 150 | 0.592 | 10.81 | 0.496 | 3.18 |
비교예 5 | 200 | 0.608 | 10.96 | 0.555 | 3.7 |
MgF2 두께(Å) | Voc(V) | Jsc(mA/cm2) | FF | PCE(%) | |
비교예 6 | 0 | 0.962 | 12.365 | 0.545 | 6.487 |
실시예 8 | 1 | 0.964 | 13.029 | 0.615 | 7.73 |
실시예 9 | 3 | 0.975 | 12.628 | 0.588 | 7.24 |
실시예 10 | 5 | 0.967 | 12.22 | 0.608 | 7.19 |
Claims (21)
- 기판;상기 기판 상에 구비된 제1 전극;상기 제1 전극에 대향하여 구비된 제2 전극;상기 제1 전극 및 상기 제2 전극 사이에 구비된 광활성층을 포함하는 1층 이상의 유기물층; 및상기 제1 전극과 상기 광활성층 사이에 구비된 전극 개질층을 포함하고,상기 전극 개질층은 금속 산화물을 포함하는 층 및 할로겐화 알칼리계 금속을 포함하는 층으로 이루어진 2층 구조이며,상기 금속 산화물을 포함하는 층 및 할로겐화 알칼리계 금속을 포함하는 층은 서로 접하여 구비되고,상기 금속 산화물을 포함하는 층과 상기 할로겐화 알칼리계 금속을 포함하는 층의 계면으로부터 상기 금속 산화물을 포함하는 층 전체 두께의 15 % 이하의 두께까지 상기 할로겐화 알칼리계 금속의 양이온이 확산되어 있는 유기태양전지.
- 청구항 1에 있어서,상기 제1 전극 상에 상기 금속 산화물을 포함하는 층이 구비되고, 상기 금속 산화물을 포함하는 층 상에 상기 할로겐화 알칼리계 금속을 포함하는 층이 구비되는 것인 유기태양전지.
- 청구항 1에 있어서,상기 제1 전극 상에 상기 할로겐화 알칼리계 금속을 포함하는 층이 구비되고, 상기 할로겐화 알칼리계 금속을 포함하는 층 상에 상기 금속 산화물을 포함하는 층이 구비되는 것인 유기태양전지.
- 기판;상기 기판 상에 구비된 제1 전극;상기 제1 전극에 대향하여 구비된 제2 전극;상기 제1 전극 및 상기 제2 전극 사이에 구비된 광활성층을 포함하는 1층 이상의 유기물층; 및상기 제1 전극과 상기 광활성층 사이에 구비된 전극 개질층을 포함하고,상기 전극 개질층은 금속 산화물 및 할로겐화 알칼리계 금속을 포함하는 단일층 구조인 유기태양전지.
- 청구항 4에 있어서,상기 전극 개질층은 상기 금속 산화물의 양이온과 상기 할로겐화 알칼리계 금속의 양이온의 비율이 100:1 내지 10:2 인 것인 유기태양전지.
- 청구항 1 또는 4에 있어서,상기 전극 개질층은 상기 제1 전극에 접하여 구비되는 것인 유기태양전지.
- 청구항 1 또는 4에 있어서,상기 제1 전극은 투명전극인 것인 유기태양전지.
- 청구항 1 또는 4에 있어서,상기 금속산화물은 ZnO, TiOx NiO, RuO, V2O5, WOx, Cs2CO3, MoO3, ZrO2, Ta2O3, 및 MgO로 이루어진 군에서 선택되는 1종 또는 2종 이상을 포함하는 것인 유기태양전지.
- 청구항 1 또는 4에 있어서,상기 할로겐화 알칼리계 금속을 포함하는 층은 층은 LiF, NaF, KF, RbF, CsF, FrF, BeF2, MgF2, CaF2, SrF2, BaF2 및 RaF2로 이루어진 군에서 선택되는 1종 또는 2종 이상을 포함하는 것인 유기태양전지.
- 청구항 1에 있어서,상기 금속 산화물을 포함하는 층의 두께는 5 ㎚ 이상 200 ㎚ 이하인 것인 유기태양전지.
- 청구항 1에 있어서,상기 알칼리토금속-불소화합물을 포함하는 층의 두께는 0.1 ㎚ 이상 15 ㎚ 이하인 것인 유기태양전지.
- 청구항 4에 있어서,상기 전극 개질층의 두께는 5 ㎚ 이상 200 ㎚ 이하인 것인 유기태양전지.
- 청구항 1 또는 4에 있어서,상기 기판은 유리, 고분자 물질 및 금속으로 이루어진 군에서 선택되는 1종 이상을 포함하는 것인 유기태양전지.
- 청구항 1 또는 4에 있어서,상기 기판은 플렉서블 기판인 것인 유기태양전지.
- 청구항 1 또는 4에 있어서,상기 광활성층은 벌크 이종 접합구조 또는 이중층 접합구조인 것인 유기 태양전지.
- 청구항 1 또는 4에 있어서,상기 제1 전극 및 상기 제2 전극 사이에 정공주입층; 정공수송층; 중간층(interlayer); 정공차단층; 전하발생층; 전자차단층; 및 전자수송층으로 이루어진 군에서 선택되는 1층 이상의 유기물층을 더 포함하는 것인 유기태양전지.
- 기판을 준비하는 단계;상기 기판 상에 제1 전극을 형성하는 단계;상기 제1 전극 상에 전극 개질층을 형성하는 단계;상기 2층의 전극 개질층 상에 광활성층을 포함하는 1층 이상의 유기물층을 형성하는 단계; 및상기 유기물층 상에 제2 전극을 형성하는 단계를 포함하고,상기 전극 개질층은 금속 산화물을 포함하는 층 및 할로겐화 알칼리계 금속을 포함하는 층으로 이루어진 2층 구조이며,상기 금속 산화물을 포함하는 층 및 할로겐화 알칼리계 금속을 포함하는 층은 서로 접하여 구비되고,상기 금속 산화물을 포함하는 층과 상기 할로겐화 알칼리계 금속을 포함하는 층의 계면으로부터 상기 금속 산화물을 포함하는 층 전체 두께의 15 % 이하의 두께까지 상기 할로겐화 알칼리계 금속의 양이온이 확산되어 있는 유기태양전지의 제조방법.
- 기판을 준비하는 단계;상기 기판 상에 제1 전극을 형성하는 단계;상기 제1 전극 상에 전극 개질층을 형성하는 단계;상기 2층의 전극 개질층 상에 광활성층을 포함하는 1층 이상의 유기물층을 형성하는 단계; 및상기 유기물층 상에 제2 전극을 형성하는 단계를 포함하고,상기 전극 개질층은 할로겐화 알칼리계 금속 및 금속 산화물을 포함하는 단일층 구조인 유기태양전지의 제조방법.
- 청구항 17에 있어서,상기 금속 산화물층은 열처리 공정을 생략하여 형성되거나, 50 ℃ 이상 250 ℃ 이하의 열처리 공정을 이용하여 형성되는 것인 유기태양전지의 제조방법.
- 청구항 18에 있어서,상기 전극 개질층은 열처리 공정을 생략하여 형성되거나, 50 ℃ 이상 250 ℃ 이하의 열처리 공정을 이용하여 형성되는 것인 유기태양전지의 제조방법.
- 청구항 17 또는 18에 있어서,상기 전극 개질층은 할로겐화 알칼리계 금속 입자 및 금속 산화물 입자를 이용한 용액 공정으로 형성되는 것인 유기태양전지의 제조방법.
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CN105409019B (zh) | 2018-04-17 |
KR20160002634A (ko) | 2016-01-08 |
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