WO2022102128A1 - 多層接合型光電変換素子およびその製造方法 - Google Patents
多層接合型光電変換素子およびその製造方法 Download PDFInfo
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- WO2022102128A1 WO2022102128A1 PCT/JP2020/042625 JP2020042625W WO2022102128A1 WO 2022102128 A1 WO2022102128 A1 WO 2022102128A1 JP 2020042625 W JP2020042625 W JP 2020042625W WO 2022102128 A1 WO2022102128 A1 WO 2022102128A1
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- electrode
- photoactive
- silicon
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- VJYJJHQEVLEOFL-UHFFFAOYSA-N thieno[3,2-b]thiophene Chemical class S1C=CC2=C1C=CS2 VJYJJHQEVLEOFL-UHFFFAOYSA-N 0.000 description 1
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- HLLICFJUWSZHRJ-UHFFFAOYSA-N tioxidazole Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)SC2=C1 HLLICFJUWSZHRJ-UHFFFAOYSA-N 0.000 description 1
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/068—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN homojunction type, e.g. bulk silicon PN homojunction solar cells or thin film polycrystalline silicon PN homojunction solar cells
- H01L31/0687—Multiple junction or tandem solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022466—Electrodes made of transparent conductive layers, e.g. TCO, ITO layers
- H01L31/022475—Electrodes made of transparent conductive layers, e.g. TCO, ITO layers composed of indium tin oxide [ITO]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0224—Electrodes
- H01L31/022408—Electrodes for devices characterised by at least one potential jump barrier or surface barrier
- H01L31/022425—Electrodes for devices characterised by at least one potential jump barrier or surface barrier for solar cells
- H01L31/022441—Electrode arrangements specially adapted for back-contact solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/072—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN heterojunction type
- H01L31/0725—Multiple junction or tandem solar cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/18—Processes or apparatus specially adapted for the manufacture or treatment of these devices or of parts thereof
- H01L31/186—Particular post-treatment for the devices, e.g. annealing, impurity gettering, short-circuit elimination, recrystallisation
- H01L31/1868—Passivation
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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
- H10K30/50—Photovoltaic [PV] devices
- H10K30/57—Photovoltaic [PV] devices comprising multiple junctions, e.g. tandem PV cells
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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
- H10K30/80—Constructional details
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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
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- H—ELECTRICITY
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K39/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic radiation-sensitive element covered by group H10K30/00
- H10K39/10—Organic photovoltaic [PV] modules; Arrays of single organic PV cells
- H10K39/15—Organic photovoltaic [PV] modules; Arrays of single organic PV cells comprising both organic PV cells and inorganic PV cells
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K39/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic radiation-sensitive element covered by group H10K30/00
- H10K39/10—Organic photovoltaic [PV] modules; Arrays of single organic PV cells
- H10K39/18—Interconnections, e.g. terminals
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/50—Organic perovskites; Hybrid organic-inorganic perovskites [HOIP], e.g. CH3NH3PbI3
-
- 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
Definitions
- An embodiment of the present invention relates to a semiconductor device having high efficiency, a large area, and high durability.
- semiconductor devices such as photoelectric conversion elements or light emitting elements have generally been manufactured by a relatively complicated method such as a chemical vapor deposition method (CVD method).
- CVD method chemical vapor deposition method
- these semiconductor devices can be produced by a simpler method, for example, a coating method, a printing method, or a physical vapor deposition method (PVD method), they can be easily manufactured at low cost. Is being sought.
- semiconductor devices such as solar cells, sensors, or light emitting devices, which are made of organic materials or are made of combinations of organic materials and inorganic materials, are being actively researched and developed. These studies aim to find a device with high photoelectric conversion efficiency. Further, as a target of such research, an element using a perovskite semiconductor can be manufactured by a coating method or the like, and high efficiency can be expected, so that it has been attracting attention in recent years.
- An object of the present embodiment is to provide a semiconductor device capable of generating electricity with high efficiency and having high durability and a method for manufacturing the same.
- the multilayer junction type photoelectric conversion element is With the first electrode, The first photoactive layer containing the perovskite semiconductor, The first passivation layer, the first dope layer, A second photoactive layer containing silicon, With the second electrode, In this order, the multilayer junction type photoelectric conversion element is provided. Further, a light scattering layer composed of a plurality of silicon alloy layers separated from each other, which penetrates a part of the passivation layer and electrically joins the first photoactive layer and the first doped layer, is further provided. It is equipped.
- the method for manufacturing the multilayer junction type photoelectric conversion element includes the following steps: (A) A step of forming a first passivation layer on one surface of a silicon wafer constituting the first photoactive layer. (B) A step of forming an opening in the formed first passivation layer, (C) A step of applying a metal paste on a passivation layer in which an opening is formed. (D) A step of heating a silicon wafer coated with a metal paste to form a silicon alloy layer and a first doped layer. (E) A step of forming and piercing a second electrode on the back surface of a silicon wafer on which the first passivation layer is formed. (F) A step of forming a first photoactive layer containing perovskite on the first passivation layer by a coating method, and (g) a first electrode on the first photoactive layer. The process of forming.
- a multilayer junction type photoelectric conversion element having a large amount of light absorption, suppressed carrier recombination, high efficiency, high generated current amount, and high durability, and manufacturing thereof. The method is provided.
- FIG. 1 The conceptual diagram which shows the structure of the multilayer junction type photoelectric conversion element by one Embodiment of this invention.
- FIG. 1 The conceptual diagram which shows the structure of the multilayer junction type photoelectric conversion element by the comparative example 1.
- the photoelectric conversion element means both an element such as a solar cell or a sensor that converts light into electricity and an element that converts electricity into light.
- the basic structure of these is the same, although there is a difference in whether the active layer functions as a power generation layer or a light emitting layer.
- the constituent members of the multilayer junction type photoelectric conversion element according to the embodiment will be described by taking a solar cell as an example, but the embodiment can also be applied to other photoelectric conversion elements having a common structure.
- FIG. 1 is a schematic diagram showing an example of the configuration of a solar cell, which is one aspect of the multilayer junction type photoelectric conversion element according to the embodiment.
- the first electrode 101 and the second electrode 110 serve as an anode or a cathode, from which electrical energy generated by the element is extracted.
- the photoelectric conversion element has a first photoactive layer 103 containing a perovskite semiconductor, a first passivation layer 106, and a first doped layer between the first electrode 101 and the second electrode 110. And a second photoactive layer 109 containing silicon are provided in this order.
- the first passivation layer 106 has a plurality of openings, and the plurality of silicon alloy layers 107 penetrating the plurality of openings each form the first photoactive layer 103 and the first dope layer 108. It is electrically joined.
- the first photoactive layer 103 and the second photoactive layer 109 are excited by incident light to generate electrons or holes in the first electrode 101 and the second electrode 110.
- each photoactive layer is a layer containing a material that produces light when electrons and holes are injected from the first electrode and the second electrode.
- the first buffer layer 102 is arranged between the first electrode and the first photoactive layer, and the first photoactive layer 103 and the first passivation layer 106
- a second buffer layer 104 and an intermediate transparent electrode 105 are arranged between the two, and a second dope layer 110 and a second passivation layer 111 are arranged on the back surface of the second photoactive layer 109.
- the device according to the embodiment preferably includes these layers.
- the element illustrated in FIG. 1 includes two photoactive layers, the unit including the photoactive layer containing a perovskite semiconductor is a top cell, and the unit including a photoactive layer containing silicon is a bottom cell. It is a tandem solar cell having a structure connected in series by an intermediate transparent electrode.
- the first electrode 101 is arranged on the light incident surface side.
- the first electrode 101 is a complex of a first metal electrode 101a and a first transparent electrode 101b. Since the metal electrode and the transparent electrode have different characteristics, either one or a combination thereof may be used depending on the characteristics.
- the metal electrode can be selected from any conventionally known metal electrode as long as it has conductivity. Specifically, conductive materials such as gold, silver, copper, platinum, aluminum, titanium, iron, and palladium can be used.
- the first metal electrode can be formed by any method. For example, it can be formed by applying a paste-like composition containing a metal material on a substrate or a film and then heat-treating it. It is also possible to form a metal electrode by physical vapor deposition (PVD) using a mask pattern. Further, a vacuum heating vapor deposition method, an electron beam vapor deposition method, a resistance heating vapor deposition method and the like can be used. According to these methods, the conversion efficiency and durability of the solar cell can be improved because the damage to the underlying layer, for example, the perovskite semiconductor layer is less than that of the sputter film formation. A screen printing method using a metal paste is also preferable. The metal paste may contain a glass frit or an organic solvent. In addition, light induced plating (LIP) can be used. LIP is a method capable of selectively forming an electrode in a portion where silicon is exposed. In this case, Ni, Ag, Cu or the like can be used as the plating metal.
- the first electrode is generally formed on a laminate of other layers and then on top of it, for example, on the first buffer layer.
- it can be formed by applying a paste-like composition containing a metal as described above and heating the composition.
- the temperature is preferably lower than the annealing temperature of the perovskite-containing active layer described later.
- the temperature of the element is controlled, a surface different from the electrode forming surface is brought into contact with a stage having a cooling mechanism, and the atmosphere is evacuated. It becomes possible to control by setting.
- this heating step can be performed at the same time as the heating step in the formation of the second electrode, which will be described later. That is, heating in the manufacturing process of the first metal electrode and the second electrode can be performed at the same time.
- the first metal electrode has a shape in which a plurality of metal wires are arranged substantially in parallel.
- the thickness of the first metal electrode is preferably 30 to 300 nm, and the width is preferably 10 to 1000 ⁇ m. If the thickness of the metal electrode is thinner than 30 nm, the conductivity tends to decrease and the resistance tends to increase. If the resistance becomes high, it may cause a decrease in photoelectric conversion efficiency. When the thickness of the metal electrode is 100 nm or less, it has light transmittance and is preferable because it can improve power generation efficiency and luminous efficiency.
- the sheet resistance of the metal electrode is preferably as low as possible, preferably 10 ⁇ / ⁇ or less.
- the metal electrode may have a single-layer structure or a multi-layer structure in which layers composed of different materials are laminated.
- the first transparent electrode 101b is a transparent or translucent conductive layer.
- the first electrode 101b may have a structure in which a plurality of materials are laminated. Further, since the transparent electrode transmits light, it can be formed on the entire surface of the laminated body.
- Examples of the material of such a transparent electrode include a conductive metal oxide film and a translucent metal thin film. Specifically, indium oxide, zinc oxide, tin oxide, and their composites, indium tin oxide (ITO), indium zinc oxide (IZO), fluorine-doped tin oxide (FTO), and indium zinc.
- -A film made of conductive glass made of oxide or the like, aluminum, gold, platinum, silver, copper or the like is used.
- metal oxides such as ITO or IZO are preferred.
- a transparent electrode made of such a metal oxide can be formed by a generally known method. Specifically, it is formed by sputtering in an atmosphere rich in a reaction gas such as oxygen.
- the thickness of the first transparent electrode is preferably 30 to 300 nm when the electrode material is ITO. If the thickness of the electrode is thinner than 30 nm, the conductivity tends to decrease and the resistance tends to increase. If the resistance becomes high, it may cause a decrease in photoelectric conversion efficiency. On the other hand, when the thickness of the electrode is thicker than 300 nm, the flexibility of the ITO film tends to be low. As a result, when the film thickness is thick, it may crack when stress is applied.
- the sheet resistance of the electrode is preferably as low as possible, and preferably 10 ⁇ / ⁇ or less.
- the electrode may have a single-layer structure or a multi-layer structure in which layers composed of materials having different work functions are laminated.
- the first photoactive layer (photoelectric conversion layer) 103 formed by the method of the embodiment has a perovskite structure at least in a part thereof.
- This perovskite structure is one of the crystal structures and refers to the same crystal structure as the perovskite.
- the perovskite structure consists of ions A, B, and X, which may take a perovskite structure when ion B is smaller than ion A.
- the chemical composition of this crystal structure can be represented by the following general formula (1). ABX 3 (1)
- A can utilize a primary ammonium ion.
- CH 3 NH 3+ (hereinafter sometimes referred to as MA), C 2 H 5 NH 3+ , C 3 H 7 NH 3+ , C 4 H 9 NH 3+ , and HC (NH 2 ) 2+ (hereinafter, FA).
- CH 3 NH 3+ is preferable, but the present invention is not limited to this.
- A is preferably Cs, 1,1,1-trifluoro-ethylammonium iodide (FEAI), but is not limited thereto.
- B is a divalent metal ion, preferably Pb 2- or Sn 2- , but is not limited thereto.
- X is preferably a halogen ion.
- the ions A, B, or X may be single or mixed.
- the constituent ions can function without necessarily matching the stoichiometric ratio of ABX 3 .
- the ion A constituting the perovskite of the first photoactive layer is composed of an atomic weight or a total atomic weight (molecular weight) constituting the ion of 45 or more. More preferably, it contains 133 or less ions. Since ion A under these conditions has low stability by itself, it may be mixed with general MA (molecular weight 32), but when MA is mixed, it approaches the silicon bandgap of 1.1 eV and is divided into wavelengths. As a tandem to improve efficiency, the overall characteristics are reduced. In addition, the refractive index with respect to the light wavelength is also affected, and the effect of the light scattering layer is reduced.
- the ion A is a combination of a plurality of ions and contains Cs
- the ratio of the number of Cs to the total number of ions A is more preferably 0.1 to 0.9.
- This crystal structure has a unit cell of cubic, tetragonal, rectangular, etc., with A at each vertex, B at the body center, and X at each face center of the cube centered on this.
- the octahedron consisting of one B and six Xs contained in the unit cell is easily distorted by the interaction with A and undergoes a phase transition to a symmetric crystal. It is presumed that this phase transition dramatically changes the physical characteristics of the crystal, causing electrons or holes to be released outside the crystal, resulting in power generation.
- the thickness of the first photoactive layer is preferably 30 nm to 1000 nm, more preferably 60 to 600 nm.
- the device according to the embodiment can realize higher conversion efficiency than a general device under a low illuminance condition of about 200 lux.
- the first photoactive layer can be formed by any method. However, it is preferable to form the first photoactive layer by the coating method from the viewpoint of cost. That is, a coating liquid containing a precursor compound having a perovskite structure and an organic solvent capable of dissolving the precursor compound is applied onto a substrate, for example, a first passivation layer, an intermediate transparent electrode, or a second buffer layer. To form a coating film. At this time, the surface of the base layer with which the first photoactive layer comes into contact is substantially a smooth surface. That is, the interlayer interface existing between the first photoactive layer and the adjacent layer on the second photoactive layer side is a substantially smooth surface. By forming the base layer in such a shape, the thickness of the first photoactive layer can be made uniform, and the formation of a short-circuit structure can be prevented.
- the solvent used in the coating liquid for example, N, N-dimethylformamide (DMF), ⁇ -butyrolactone, dimethyl sulfoxide (DMSO) and the like are used.
- the solvent is not restricted as long as it can dissolve the material, and may be mixed.
- the first photoactive layer can be formed by applying a single coating solution in which all the raw materials forming the perovskite structure are dissolved in one solution. Further, a plurality of raw materials forming a perovskite structure may be individually prepared as a plurality of solutions, or a plurality of coating liquids may be prepared and coated sequentially.
- a spin coater, a slit coater, a bar coater, a dip coater, or the like can be used for coating.
- the coating liquid may further contain additives.
- additives 1,8-diiodooctane (DIO) and N-cyclohexyl-2-pyrrolidone (CHP) are preferable.
- the element structure includes a mesoporous structure
- the leakage current between the electrodes can be suppressed even if pinholes, cracks, voids, etc. occur in the photoactive layer.
- the element structure does not have a mesoporous structure, it is difficult to obtain such an effect.
- the coating liquid contains a plurality of raw materials having a perovskite structure
- the volume shrinkage at the time of forming the active layer is small, so that a film having less pinholes, cracks and voids can be easily obtained.
- MAI methylammonium iodide
- a metal halide compound and the like coexist during the formation of the perovskite structure, the reaction with the unreacted metal halide compound proceeds, and a film having few pinholes, cracks and voids can be easily obtained. Therefore, it is preferable to add MAI or the like to the coating liquid or to apply a solution containing MAI or the like on the coating film after coating.
- the coating liquid containing the precursor of the perovskite structure may be applied twice or more.
- the active layer formed by the first coating tends to be a lattice mismatch layer, so it is preferable to coat the active layer so as to have a relatively thin thickness.
- the conditions for the second and subsequent applications are that the rotation speed of the spin coater is relatively fast, the slit width of the slit coater or bar coater is relatively narrow, and the pulling speed of the dip coater is relatively fast. It is preferable that the conditions are such that the solute concentration in the coating solution is relatively thin and the film thickness is thinned.
- the perovskite structure formation reaction After the perovskite structure formation reaction is completed, it is preferable to perform annealing to dry the solvent. Since this annealing is performed to remove the solvent contained in the perovskite layer, it is preferable to perform this annealing before forming the next layer, for example, a buffer layer on the first photoactive layer.
- the annealing temperature is 50 ° C. or higher, more preferably 90 ° C. or higher, and the upper limit is 200 ° C. or lower, more preferably 150 ° C. or lower. It should be noted that if the annealing temperature is low, the solvent may not be sufficiently removed, and if the annealing temperature is too high, the smoothness of the surface of the first photoactive layer may be lost.
- the surface other than the coated surface for example, the surface of the second electrode may be contaminated. Since perovskite contains a corrosive halogen element, it is preferable to remove the contamination.
- the method for removing the contamination is not particularly limited, but a method of colliding ions with the passivation layer, laser treatment, etching paste treatment, and solvent cleaning are preferable. It is preferable that the contamination is removed before the first electrode is formed.
- the first buffer layer 102 and the second buffer layer 104 are between the first electrode and the first photoactive layer, or between the first photoactive layer and the tunnel insulating film, respectively. It is a layer that exists. It is a layer that preferentially extracts electrons or holes.
- the second buffer layer becomes a base layer of the first photoactive layer when present, it is preferable that the surface thereof is substantially smooth.
- the first buffer layer and the second buffer layer may have a laminated structure of two or more layers.
- the first buffer layer can be a layer containing an organic semiconductor and a layer containing a metal oxide.
- the layer containing the metal oxide can play a function of protecting the active layer when forming the first transparent electrode.
- the first transparent electrode has an effect of suppressing deterioration of the first electrode. In order to fully exert such an effect, the first transparent electrode is preferably a denser layer than the first buffer layer.
- one of the first buffer layer and the second buffer layer functions as a hole transport layer, and the other functions as an electron transport layer. It is preferable that the semiconductor device is provided with these layers in order to achieve better conversion efficiency, but it is not always essential in the embodiment, and even if one or both of them are not provided. good.
- the electron transport layer has a function of efficiently transporting electrons.
- the buffer layer functions as an electron transport layer, it preferably contains either a halogen compound or a metal oxide.
- Suitable examples of the halogen compound include LiF, LiCl, LiBr, LiI, NaF, NaCl, NaCl, NaI, KF, KCl, KBr, KI, or CsF. Of these, LiF is particularly preferable.
- the elements constituting the metal oxide are titanium, molybdenum, vanadium, zinc, nickel, lithium, potassium, cesium, aluminum, niobium, tin and barium.
- Composite oxides containing a plurality of metal elements are also preferred.
- aluminum-doped zinc oxide (AZO), niobium-doped titanium oxide, and the like are preferable.
- Titanium oxide is more preferable among these metal oxides.
- As the titanium oxide amorphous titanium oxide obtained by hydrolyzing titanium alkoxide by the sol-gel method is preferable.
- an inorganic material such as metallic calcium can be used for the electron transport layer.
- an n-type semiconductor can also be used for the electron transport layer.
- the n-type organic semiconductor is preferably fullerene and its derivatives, but is not particularly limited. Specific examples thereof include derivatives having C60, C70, C76, C78, C84 and the like as a basic skeleton.
- the carbon atom in the fullerene skeleton may be modified with an arbitrary functional group, and the functional groups may be bonded to each other to form a ring.
- Fullerene derivatives include fullerene-bound polymers. A fullerene derivative having a functional group having a high affinity for the solvent and having a high solubility in the solvent is preferable.
- Examples of the functional group in the fullerene derivative include a hydrogen atom; a hydroxyl group; a halogen atom such as a fluorine atom and a chlorine atom; an alkyl group such as a methyl group and an ethyl group; an alkenyl group such as a vinyl group; a cyano group; a methoxy group and an ethoxy group.
- a hydrogen atom such as C60H36 and C70H36, oxide fullerenes such as C60 and C70, and fullerene metal complexes.
- PCBM [6,6] -phenylC61 butyrate methyl ester
- PCBM [6,6] -phenylC71 butyrate methyl ester
- n-type organic semiconductor a small molecule compound that can be formed by vapor deposition can be used.
- the small molecule compound referred to here is one in which the number average molecular weight Mn and the weight average molecular weight Mw match. Either is 10,000 or less.
- BCP 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline
- TpPyPB (1,3,5-tri (p-pyridine-) 3-Il-phenyl) benzene
- DPPS diphenyl-bis (4-pyridin-3-yl) phenyl) silane
- the thickness of the electron transport layer is preferably 20 nm or less. This is because the film resistance of the electron transport layer can be lowered and the conversion efficiency can be increased. On the other hand, the thickness of the electron transport layer can be 5 nm or more.
- the hole transport layer has a function of efficiently transporting holes.
- the layer can include a p-type organic semiconductor material or an n-type organic semiconductor material.
- the p-type organic semiconductor material and the n-type organic semiconductor material referred to here are materials that can function as an electron donor material and an electron acceptor material when a heterojunction or a bulk heterojunction is formed.
- a p-type organic semiconductor can be used as the material of the hole transport layer.
- the p-type organic semiconductor preferably contains, for example, a copolymer composed of a donor unit and an acceptor unit.
- a donor unit fluorene, thiophene, or the like can be used.
- acceptor unit benzothiadiazole or the like can be used.
- polythiophene and its derivatives polypyrrole and its derivatives, pyrazoline derivatives, arylamine derivatives, stilben derivatives, triphenyldiamine derivatives, oligothiophene and its derivatives, polyvinylcarbazole and its derivatives, polysilane and its derivatives, side chains or Polysiloxane derivatives with aromatic amines in the main chain, polyaniline and its derivatives, phthalocyanine derivatives, porphyrin and its derivatives, polyphenylene vinylene and its derivatives, polythienylene vinylene and its derivatives, benzodithiophene derivatives, thieno [3,2- b] A thiophene derivative or the like can be used.
- These materials may be used in combination for the hole transport layer, or a copolymer composed of comonomers constituting these materials may be used.
- a copolymer composed of comonomers constituting these materials may be used.
- polythiophene and its derivatives are preferable because they have excellent stereoregularity and have relatively high solubility in a solvent.
- poly [N-9'-heptadecanyl-2,7-carbazole-alto-5,5- (4', 7), which is a copolymer containing carbazole, benzothiadiazole and thiophene, is used as a material for the hole transport layer.
- Derivatives such as'-di-2-thienyl-2', 1', 3'-benzothiadiazole)] (hereinafter, may be referred to as PCDTBT) may be used.
- poly [[4,8-bis [(2-ethylhexyl) oxy] benzo [1,2-b: 4,5-b'] dithiophene-2,6-diyl] [3-fluoro-2-[(2). -Ethylhexyl) carbonyl] thorium [3,4-b] thiopheneyl]] (hereinafter sometimes referred to as PTB7), PTB7-Th (PCE10, or PBDTTT) in which a thienyl group having a weaker electron donating property than the alkoxy group of PTB7 is introduced. -Sometimes called EFT) and the like are also preferable.
- a metal oxide can be used as the material of the hole transport layer.
- metal oxide examples include titanium oxide, molybdenum oxide, vanadium oxide, zinc oxide, nickel oxide, lithium oxide, calcium oxide, cesium oxide and aluminum oxide. These materials have the advantage of being inexpensive. Further, thiocyanate such as copper thiocyanate may be used as the material of the hole transport layer.
- dopants can be used for transport materials such as spiro-OMeTAD and the p-type organic semiconductor.
- Dopants include oxygen, 4-tert-butylpyridine, lithium-bis (trifluoromethanesulfonyl) imide (Li-TFSI), acetonitrile, tris [2- (1H-pyrazole-1-yl) pyridine] cobalt (III) tris. (Hexafluorophosphate) salt (commercially available under the trade name "FK102”), Tris [2- (1H-pyrazole-1-yl) pyrimidine] Cobalt (III) Tris [bis (trisfluoromethylsulfonyl) imide] (MY11) Etc. can be used.
- a conductive polymer compound such as polyethylene dioxythiophene can be used as the hole transport layer.
- a conductive polymer compound those listed in the section of electrodes can be used.
- a polythiophene-based polymer such as PEDOT
- another material such as PEDOT
- the first buffer layer is preferably an electron transport layer. Further, it is preferably an oxide layer of a metal selected from the group consisting of zinc, titanium, aluminum, tin and tungsten. This oxide layer may be a composite oxide layer containing two or more kinds of metals. This is because the light soaking effect improves the electrical conductivity, so that the electric power generated in the active layer can be efficiently extracted. By arranging this layer on the first electrode side of the active layer, light soaking becomes possible especially with UV light.
- the first buffer layer preferably has a structure in which a plurality of layers are laminated. In such a case, it is preferable to contain the oxide of the above metal. With such a structure, when a new type of metal oxide is newly formed by sputtering, the active layer and the metal oxide adjacent to the active layer are less likely to be damaged by sputtering.
- the first buffer layer has a structure including voids. More specifically, a buffer layer composed of a deposit of nanoparticles and having voids between the nanoparticles, a structure composed of a conjugate of nanoparticles and having voids between the bound nanoparticles, and the like. Is preferable.
- the first buffer layer contains a metal oxide film
- the film functions as a barrier layer.
- the barrier layer is provided between the second electrode and the second buffer layer in order to suppress corrosion of the second electrode by a substance penetrating from another layer.
- the material constituting the perovskite layer tends to have a high vapor pressure at high temperatures.
- halogen gas, hydrogen halide gas, and methylammonium gas are likely to be generated in the perovskite layer.
- the device When these gases are confined by the barrier layer, the device may be damaged from the inside due to the increase in internal pressure. In such a case, peeling of the layer interface is particularly likely to occur. Therefore, when the second buffer layer contains voids, the increase in internal pressure is alleviated, and it becomes possible to provide high durability.
- the first electrode that is, the metal layer is structurally isolated from the first photoactive layer by the metal oxide film
- the first electrode is less likely to be corroded by substances penetrating from the other layers.
- the first photoactive layer comprises a perovskite semiconductor. It is generally known that halogen ions such as iodine and bromine diffuse into the device from the photoactive layer containing the perovskite semiconductor, and the component reaching the metal electrode causes corrosion.
- a metal oxide film it is considered that the diffusion of such a substance can be efficiently blocked. It preferably contains indium tin oxide (ITO), fluorine-doped tin oxide (FTO), and aluminum-doped zinc oxide (AZO).
- the thickness is preferably 5 to 100 nm, more preferably 10 to 70 nm.
- the same metal oxide as that generally used for the transparent electrode can be used, but the one having physical properties different from the general metal oxide layer used for the transparent electrode is used. It is preferable to use it. That is, it is not only characterized by its constituent materials, but also its crystallinity or oxygen content.
- the crystallinity or oxygen content of the metal oxide film contained in the first buffer layer is lower than that of the metal oxide layer formed by sputtering, which is generally used as an electrode.
- the oxygen content is preferably 62.1 to 62.3 atomic%.
- the metal oxide film functions as a permeation prevention layer for corrosive substances can be confirmed by elemental analysis in the cross-sectional direction after the durability test.
- a time-of-flight secondary ion mass spectrometry TOF-SIMS
- the peak of the deteriorated substance is detected by dividing it into two or more so as to sandwich the material indicating the prevention of penetration of the corrosive substance, and the peak area on the first electrode side is the total area of the other peaks. Is smaller than. When the penetration is completely prevented, the peak on the first electrode side cannot be confirmed.
- the peak on the first electrode side is so small that it cannot be confirmed, but even if most of the peak is shielded, the durability of the device is greatly improved. That is, even if a part of the first electrode is deteriorated, the characteristics such as the overall electric resistance of the first electrode do not change significantly, so that the conversion efficiency of the solar cell does not change significantly. On the other hand, if the permeation is not sufficiently prevented and the corrosive substance reacts with the first electrode, the characteristics such as the electric resistance of the first electrode change significantly, so that the conversion efficiency of the solar cell changes greatly. (Decrease in conversion efficiency).
- the peak area on the first electrode side is 0.007 with respect to the total area of the other peaks.
- the method for forming such a metal oxide film is not particularly limited, but it can be formed by sputtering under specific conditions.
- the intermediate transparent electrode 105 has a function of electrically connecting the top cell and the bottom cell while isolating them, and guiding the light not absorbed by the top cell to the bottom cell. Therefore, the material can be selected from transparent or translucent conductive materials. Such a material can be selected from the same materials as the first transparent electrode.
- the thickness of the intermediate bright electrode is preferably 10 nm to 70 nm. If it is thinner than 10 nm, there are many membrane defects, and the separation of the layer adjacent to the intermediate transparent electrode becomes insufficient. If it is thicker than 70 nm, the light transmittance may cause a decrease in the amount of power generation of the bottom cell, for example, a silicon cell due to the diffraction effect.
- the first passivation layer 106 is arranged between the first photoactive layer 103 and the first dope layer 108 or the second photoactive layer 109.
- the first passivation layer electrically insulates the first photoactive layer and the second photoactive layer 109, but has an opening, and through the opening, the second photoactive layer and the second photoactive layer. An electrical connection is secured between the dope layer and the dope layer. Therefore, since the area where the carrier can move is limited, the carrier can be efficiently collected.
- the carrier recombination rate at the interface between the second photoactive layer (silicon layer) and the adjacent layer on the first photoactive layer side is as fast as about 107 cm / s, and the conversion efficiency is high. Although it causes a decrease, it can be suppressed by arranging the first passivation layer in between.
- dangling bonds are generally present on the silicon surface, which may also act as a recombination center. This dangling bond can also be reduced by the first passivation layer.
- the thickness of the passivation layer is preferably 0.1 nm to 20 nm.
- the material used to form the first passivation film is preferably a material capable of reducing dangling bonds on the silicon surface, and is not particularly limited.
- AlOx formed by a silicon oxide film formed by thermally oxidizing the surface of a silicon material plasma-enhanced chemical vapor deposition (PECVD), plasma-assisted atomic layer deposition (PEALD), or the like.
- PECVD plasma-enhanced chemical vapor deposition
- PEALD plasma-assisted atomic layer deposition
- Examples include a film such as SiNx.
- the silicon oxide film is formed by thermal oxidation, either dry oxidation in which oxidation is performed in an oxygen atmosphere or wet oxidation in which participation is performed in a water vapor atmosphere can be used.
- a wet oxide film is suitable for efficiently obtaining an oxide film having a uniform thickness.
- the first passivation film is preferably 100 nm to 100 ⁇ m.
- the first passivation layer is formed over the entire surface of the second photoactive layer, but in order to obtain an electrical connection between the second photoactive layer and the first photoactive layer. , A part has been removed to form an opening.
- the opening can be formed by removing a part of the first passivation layer by, for example, a wet treatment.
- the first passivation layer is a silicon nitride film
- hydrogen contained in the silicon nitride film is diffused into the silicon crystal when the alloy layer described later is formed, and the crystal lattice end is terminated by hydrogen to improve the electrical characteristics. Will be done.
- the device according to the embodiment has a first passivation layer and a light scattering layer between the second photoactive layer and the first photoactive layer.
- This structure is similar to the generally known backside passivation type solar cell (PERC type solar cell).
- the opening and the alloy layer 107 can be formed, for example, as follows. After forming the first passivation layer on the surface of the second photoactive layer, a part of the first passivation layer is removed by using a laser or an etching paste to form an opening. A metal paste is applied to the opening and fired to form an alloy layer. The firing is preferably carried out at a temperature of 600 to 1000 ° C. for several seconds. The metal paste preferably contains silver or aluminum. As another method, after forming the first passivation layer on the surface of the second photoactive layer, the paste for Fire light is applied to the portion where the alloy layer is to be formed, and the paste and the paste are fired. It reacts with one passivation layer to form an alloy layer.
- the opening is not formed in advance, but the first passivation layer is denatured when the alloy layer is formed. Therefore, in the embodiment, the denatured portion of the first passivation layer is referred to as an opening for convenience.
- the metal layer formed by these methods typically has a dome-shaped structure.
- a screen printing method using a metal paste containing silver or aluminum is preferable.
- the metal paste may further contain a glass frit or an organic solvent.
- a p + layer in which aluminum is diffused at a high concentration
- a silicon alloy layer in which aluminum and silicon are alloyed are formed.
- the plurality of silicon alloy layers 107 formed in this way form a light scattering layer.
- the first dope layer in which aluminum is diffused at a high concentration can form a backside electric field (BSF) and reduce carrier recombination.
- BSF backside electric field
- the openings Since the carrier flow between the first photoactive layer and the first dope layer is restricted by the openings, the openings relative to the area of each opening or the total area of the entire first passivation layer. It is preferable that the ratio of the total area occupied by the parts is within a specific range. Specifically, the ratio of the area is preferably 50 to 95%.
- the shape of the opening is a groove shape (straight line shape)
- the grooves are arranged substantially in parallel.
- the width of the grooves is preferably 10 to 500,000 nm, and the average spacing between the grooves is preferably 10 to 5,000,000 nm.
- the width and spacing of the grooves do not have to be constant, but it is preferable to make them substantially constant because the production becomes easy.
- the average spacing of the plurality of metal wires constituting the linearly formed first metal electrode is set to a plurality of openings formed in a groove shape in the intermediate passivation layer. It is preferable that the interval is shorter than the average interval of.
- the shape of the opening is hole-shaped, the shape is not particularly limited, but is generally circular, but may be irregular.
- the area of each opening is preferably included in the range of 0.01 to 40,000 ⁇ m 2 .
- the radius of curvature of the interface between the alloy layer formed on the back surface side of the device and the first dope layer is not constant. That is, the interface has a different radius of curvature for each position, which is suitable for scattering light.
- the reflectance of the light scattering layer composed of the alloy layer is preferably 80 to 96% in the visible light region. A light scattering layer having such a reflectance can realize effective light reflection with respect to a second photoactive layer (silicon layer) having a reflectance of 30 to 50%.
- the silicon layer has a high refractive index of 4.2 to 3.5 in the wavelength region of 500 to 1500 nm, whereas the refractive index of the light scattering layer is small, and effective light reflection can be realized from this viewpoint as well. .. Specifically, the refractive index of the light scattering layer is preferably 1.4 to 1.8.
- the interface between the silicon alloy layer and the first dope layer has few flat parts, that is, parts where the radius of curvature of the boundary line corresponding to the sea surface is infinite in the cross section in order to enable light reflection. Is preferable.
- the radius of curvature of the boundary line corresponding to the interface between the silicon alloy layer and the first dope layer in the cross section parallel to the stacking direction of the first photoactive layer and the second photoactive layer is concrete. It is preferably in the range of 1 to 100 ⁇ m, and more preferably in the range of 1 to 50 ⁇ m. Most preferably, all of the boundaries have such a radius of curvature, but some may include straight lines.
- the total length of the boundary line between the silicon alloy layer and the first dope layer in the cross section parallel to the stacking direction of the first photoactive layer and the second photoactive layer (vertical direction on the paper surface in FIG. 1).
- the length of the portion having a radius of curvature within the range of 1 to 100 ⁇ m is preferably 40% or more, and more preferably 80% or more.
- the boundary line can be confirmed by observing the cross-sectional sample of the device.
- a thin section sample is collected from the element by an ultrathin section method (microtome method), a focused ion beam (FIB), or the like, and can be measured by a transmission electron microscope (TEM), a scanning electron microscope (SEM), or the like.
- the distance from the alloy layer (light scattering layer) to the second photoactive layer is preferably 100 to 400 ⁇ m.
- the radius of curvature at the interface has such a range, it is possible to efficiently absorb light whose optical path has changed in a complicated manner. By adopting such a configuration, it is possible to maximize the amount of current that can be taken out from the element according to the embodiment.
- the radius of curvature becomes larger as the portion closer to the apex.
- Such a shape can be realized by increasing the removal range of the passivation layer and reducing the depth at which the alloy is formed when the alloy layer is formed.
- the carrier generation region can be further limited, so that the amount of current generated can be further increased.
- the thickness of the first dope layer is preferably 1 to 10 nm, more preferably 2 to 4 nm.
- the first dope layer can be formed at the same time as the alloy layer by the above method, it may be manufactured by the same method using the same material as the second dope layer described later.
- the second photoactive layer 109 contains silicon.
- the silicon contained in the second photoactive layer can adopt the same structure as the silicon generally used for a photovoltaic cell. Specific examples thereof include crystalline silicon containing crystalline silicon such as single crystal silicon, polysilicon, and heterojunction silicon, and thin film silicon containing amorphous silicon. Further, the silicon may be a thin film cut out from a silicon wafer. As the silicon wafer, an n-type silicon crystal doped with phosphorus or the like and a p-type silicon crystal doped with boron or the like can also be used. The electrons in the p-type silicon crystal have a long diffusion length, which is preferable.
- the thickness of the second photoactive layer is preferably 100 to 300 ⁇ m.
- the second photoactive layer may have a uniform thickness, but in order to increase the utilization efficiency of the incident light, a texture may be formed on one surface.
- a texture may be formed on the incident surface side of light, but in the embodiment, the light incident surface of the second photoactive layer uses the light transmitted through the top cell. It is preferable to smooth the light incident surface and form a texture on the opposite side surface.
- the second dope layer 110 is a layer arranged between the second photoactive layer 109 and the second electrode 112, respectively.
- an n-type layer, a p-type layer, a p + type layer, a p ++ type layer, etc. are combined according to the purpose, such as improvement of carrier collection efficiency, according to the characteristics of the second photoactive layer. be able to.
- the first dope layer can be combined with a phosphorus-doped silicon film (n layer), and the second dope layer can be combined with a p + layer.
- p + layers, p ++ layers, etc. can be formed by introducing a required dopant into, for example, amorphous silicon (a-Si).
- a-Si amorphous silicon
- silicon can be deposited by a PECVD method or the like to form an a—Si layer, and a part of the a—Si layer can be crystallized by an annealing treatment to form a layer having high carrier transportability.
- the doped amorphous silicon can also be formed by forming a film using silane and diborane, or silane and phosphine as raw materials at a low temperature.
- the a—Si layer can be doped with phosphorus.
- the method of doping phosphorus is not particularly limited.
- phosphorus-containing compounds such as POCl 3 and PH 3 can be used.
- Phosphorus silicate glass (PSG) is widely used as a diffusion source of phosphorus. More specifically, PSG is deposited on the surface of a silicon substrate by utilizing the reaction between POCl 3 and oxygen, and then heat treatment is performed at 800 to 950 ° C., and phosphorus is doped into the silicon substrate by thermal diffusion. be able to. After the doping treatment, PSG can also be removed with acid.
- the a—Si layer can be doped with boron.
- the method of doping Poron is not particularly limited.
- a compound containing boron such as BBr 3 , B 2 H 6 , and BN can be used.
- Borosilicate glass (BSG) is widely used as a diffusion source of boron. More specifically, BSG is deposited on the surface of the substrate by utilizing the reaction between BBr 3 and oxygen, and then heat treatment is performed at, for example, 800 to 1000 ° C, preferably 850 to 950 ° C, and the silicon substrate is thermally diffused. Boron can be doped into. After the doping treatment, BSG can be removed with acid.
- a dopant such as phosphorus or boron
- a laser Such a method can also be used to form a selective emitter.
- the bottom cell corresponds to a silicon solar cell.
- a general silicon solar cell has a textured structure on the surface, but when such a battery is adopted as a bottom cell, the thickness of the perovskite layer formed on it becomes non-uniform, and a short-circuit structure is formed in the thin portion. And deteriorates the characteristics of the solar cell.
- the texture structure of the surface is eliminated to make the surface smooth, the light reflection on the surface is reduced, the amount of light taken into the silicon layer having a large refractive index is reduced, and as a result, the amount of current is reduced. It ends up.
- the amount of light uptake can be increased by arranging the light scattering layer between the second photoactive layer and the first photoactive layer.
- the light scattering layer By providing a texture structure on the back surface side of the second photoactive layer as shown in FIG. 1, it is possible to increase light scattering inside the second photoactive layer and increase the amount of light uptake. can.
- the thickness of the second dope layer is preferably 1 to 100 nm.
- the second passivation layer 111 is arranged on the back surface side of the second photoactive layer 109. For example, it is arranged on the back surface of the second photoactive layer or on the surface of the second dope layer arranged on the back surface of the second photoactive layer.
- the second passivation layer has a function of reducing dangling bonds of the silicon layer like the first passivation layer, and can be formed by the same method as the first passivation layer.
- the light reflecting layer also has the effect of increasing the amount of light taken up by the first and second photoactive layers.
- the thickness of such a second passivation layer is preferably 0.01 to 1000 ⁇ m.
- the second electrode 112 can be formed by using any conventionally known material as long as it has conductivity. Further, the forming method thereof is not particularly limited. Specifically, it can be formed in the same manner as the above-mentioned first metal electrode. Further, in FIG. 1, the second electrode 112 has a plurality of electrodes arranged apart from each other on the back surface of the element, but may be formed along the entire back surface of the element. In this case, the light that could not be absorbed by the first and second photoactive layers can be reflected by the second electrode and used again for photoelectric conversion in the first and second photoactive layers.
- the thickness of the second electrode is preferably 30 to 300 nm. If the thickness of the electrode is thinner than 30 nm, the conductivity tends to decrease and the resistance tends to increase. If the resistance becomes high, it may cause a decrease in photoelectric conversion efficiency. When it is 100 nm or less, even a metal has light transmission property, which is preferable for improving power generation efficiency and luminous efficiency.
- the sheet resistance of the electrode is preferably as low as possible, and preferably 10 ⁇ / ⁇ or less.
- the electrode may have a single-layer structure or a multi-layer structure in which layers composed of different materials are laminated.
- the thickness of the second electrode is thinner than the above range, the resistance may become too large and the generated charge may not be sufficiently transmitted to the external circuit.
- the film thickness is thick, it takes a long time to form an electrode, so that the material temperature rises, which may damage other materials and deteriorate the performance. Further, since a large amount of material is used, the occupancy time of the film forming apparatus becomes long, which may lead to an increase in cost.
- an antireflection layer may be provided on the outermost layer of the device, that is, the interface with the atmosphere.
- Such an antireflection film can be used as a generally known material such as SnNx or MgF 2 . These materials can be formed into a film by a PECVD method, a vapor deposition method, or the like.
- the first electrode and the second electrode need to obtain an electrical connection with the outside in order to draw a current from the device. Therefore, it is preferable to remove a part of the antireflection film so as not to obstruct the electrical connection.
- a wet etching treatment method, a method using an etching paste, a method using a laser, or the like can be used.
- the element illustrated in FIG. 1 includes two photoactive layers, the unit including the photoactive layer containing a perovskite semiconductor is a top cell, and the unit including a photoactive layer containing silicon is a bottom cell. It is a tandem solar cell having a structure connected in series by an intermediate transparent electrode. Generally, the bandgap of a silicon solar cell is about 1.1 eV, but by combining it with a photovoltaic cell containing a perovskite semiconductor having a relatively wide bandgap, light in a wider wavelength range can be efficiently emitted. It becomes possible to absorb.
- the open circuit voltage of a silicon solar cell is 0.6 to 0.75 V
- the open circuit voltage of a perovskite solar cell is 0.9 to 1.3 V.
- the tandem solar cell that combines these, by increasing the amount of power generated by the perovskite solar cell, it is possible to obtain electric power having a higher voltage than that of the silicon solar cell alone. That is, the output obtained by the tandem solar cell can exceed that of the silicon solar cell alone. Since the tandem solar cell is a series circuit of the top cell and the bottom cell, the voltage can be obtained to be close to the total of the top cell and the bottom cell.
- the current is rate-determined by the lower current of the top cell and the bottom cell.
- the material of the active layer is selected to change the wavelength range of the absorbed light, or the thickness of the photoactive layer is adjusted to change the amount of absorbed light. Is done. Since a silicon solar cell generally has a short-circuit current density of about 40 mA / cm 2 alone, it is preferable to adjust the tandem solar cell so that the top cell and the bottom cell have a short-circuit current density of about 20 mA / cm 2 .
- the multilayer junction type photoelectric conversion element according to the embodiment can be manufactured by laminating the above-mentioned layers in an appropriate order.
- the stacking order is not particularly limited as long as a desired structure can be obtained, but for example, it can be manufactured in the following order.
- Manufacturing method of multilayer junction type photoelectric conversion element including the following steps: (A) A step of forming a first passivation layer on one surface of a silicon wafer constituting the second photoactive layer. (B) A step of forming an opening in the formed first passivation layer, (C) A step of applying a metal paste on a passivation layer in which an opening is formed.
- (D) A step of heating a silicon wafer coated with a metal paste to form a silicon alloy layer and a first doped layer.
- (E) A step of forming a second electrode on the back surface of the silicon wafer on which the first passivation layer is formed.
- (F) A step of forming a first photoactive layer containing perovskite on the first passivation layer by a coating method, and (g) a first electrode on the first photoactive layer. The process of forming.
- step (A0) A step of forming a texture structure on one side surface of a silicon wafer.
- any of the following steps can be combined between the steps (d) and (e).
- (D1) A step of forming a second dope layer on the back surface of the silicon wafer on which the first passivation layer is formed, if necessary.
- (D2) A step of forming a second passivation layer on the back surface of the silicon wafer on which the first passivation layer is formed or on the second dope layer, if necessary.
- any of the following steps can be combined between the steps (e) and (f).
- (E1) A step of forming an intermediate transparent electrode on the surface of the first passivation layer, if necessary.
- (E2) A step of forming a second buffer layer on the first passivation layer or the intermediate electrode, if necessary.
- step (F1) A step of forming a first buffer layer on the first photoactive layer, Can also be combined.
- the bottom cell containing the second photoactive layer is formed first, and the top cell containing the first photoactive layer is formed later.
- the step (e) of heating at a high temperature is performed before the step (f)
- the first photoactive layer is less likely to be damaged by heat.
- the first electrode is formed by the step (g)
- the first photoactive layer is heated, but when it is heated in the step (g), it is heated in the step (f). It is preferable to adopt a temperature lower than the temperature.
- Example 1 A multilayer junction type photoelectric conversion element having the structure shown in FIG. 1 is manufactured.
- the (111) plane can be selectively left by etching the silicon crystal (100) plane.
- a pyramid-shaped uneven structure can be formed on the surface.
- the opposite side can be flattened by polishing.
- phosphorus can be doped on the surface on which the texture structure is formed to form an n-layer.
- Phosphorus can be doped into silicon by depositing PSG on the surface of the substrate using the reaction of POCl 3 and oxygen and then performing a heat treatment at 900 ° C. PSG can be removed by acid treatment.
- AlOx: H layer and SnNx: H layer can be formed by PECVD on the opposite side surface of the surface on which the second dope layer is formed as the first passivation layer. Part of the first passivation layer can be removed with a 532 nm laser. An aluminum paste is applied to the removed portion by screen printing and fired in an oven at 950 ° C. to form a first dope layer and a silicon alloy layer (light scattering layer). Further, a silicon oxide film can be formed on the second dope layer as a second passivation film.
- Part of the silicon oxide film can be opened by laser, and then part of the second passivation layer can be removed by etching.
- a second electrode can be formed on the exposed second dope layer by Electron beam evolution to form a second electrode containing silver as a main component, which can be used as an electron extraction electrode.
- ITO can be formed by sputtering as an intermediate transparent electrode so that it can be electrically connected to the light scattering layer.
- the thickness can be adjusted to 20 nm.
- an alcohol dispersion of TiOx particles can be formed by spin coating. After film formation, annealing is performed at 150 ° C.
- the first photoactive layer is a precursor solution in which the precursor of Cs 0.17 FA 0.83 Pb (Br 0.17 I 0.83 ) 3 is dissolved in a mixed solvent of DMF and DMSO (DMSO is 10 Vol%). It can be formed by coating. After film formation, annealing is performed at 150 ° C. for 5 minutes.
- the first buffer layer can be formed by spin-coating Spiro-OMeTAD at 100 nm.
- IZO can be formed into a film by spatter as the first transparent electrode.
- a tandem solar cell can be formed by depositing silver as the first metal electrode with a vapor deposition machine.
- the amount of light absorption can be increased by forming the top cell containing the photoactive layer containing perovskite on the bottom cell having the silicon layer, and as a result, the photoelectric flow rate can be increased. To increase. Further, by forming the scattering layer, the light that could not be absorbed by the first and second photoactive layers and silicon can be scattered and reflected and reused for the photocurrent.
- the passivation layer is arranged between the first photoactive layer and the second photoactive layer, the effect of preventing carrier recombination at the electrode interface can be obtained.
- the amount of current can be increased by the light scattering effect and the carrier recombination prevention effect.
- Comparative Example 1 An element having the structure shown in FIG. 2 is formed.
- the device was manufactured by the same method as in Example 1 except that the light scattering layer and the first dope layer were not formed.
- the device according to Comparative Example 1 has a smooth interface existing between the first photoactive layer and the second photoactive layer, but has a top cell containing a perovskite semiconductor, so that the second photoactive layer is provided.
- Light absorption to is relatively high.
- the light that could not be absorbed by each photoactive layer is reflected by the texture structure, but is not sufficiently scattered.
- the distribution of the amount of light incident on the first and second photoactive layers becomes non-uniform.
- the generated carrier concentration also becomes non-uniform, and where the amount of light is high, the carrier concentration becomes high, the carrier recombination loss increases, and the amount of current decreases.
- Multilayer junction type photoelectric conversion element (multilayer junction type photoelectric conversion element of Example 1) 101 ... First electrode 101a ... First metal electrode 101b ... First transparent electrode 102 ... First buffer layer 103 ... First photoactive layer 104 containing perovskite semiconductor ... Second buffer layer 105 ... Intermediate transparent Electrode 106 ... First passivation layer 107 ... Alloy layer 108 ... First dope layer 109 ... Second photoactive layer 110 ... Second dope layer 111 ... Second passivation layer 112 ... Second electrode 200 ... Comparison Multilayer junction type photoelectric conversion element of Example 1
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Abstract
Description
第一の電極と、
ペロブスカイト半導体を含む第一の光活性層と、
第一のパッシベーション層と
第一のドープ層と、
シリコンを含む第二の光活性層と、
第二の電極と、
を、この順に具備する多層接合型光電変換素子であって、
さらに、前記パッシベーション層の一部分を貫通して、前記第一の光活性層と前記第一のドープ層とを電気的に接合する、相互に離間した複数のシリコン合金層からなる光散乱層をさらに具備するものである。
(a)第一の光活性層を構成するシリコンウェハーの一面に、第一のパッシベーション層を形成する工程、
(b)形成された第一のパッシベーション層に開口部を形成する工程、
(c)開口部が形成されたパッシベーション層の上に、金属ペーストを塗布する工程、
(d)金属ペーストが塗布されたシリコンウェハーを加熱して、シリコン合金層、第一のドープ層を形成させる工程、
(e)前記第一のパッシベーション層が形成されたシリコンウェハーの裏面に、第二の電極を形成刺さる工程、
(f)前記第一のパッシベーション層の上に、塗布法により、ペロブスカイトを含む第一の光活性層を形成する工程、および
(g)前記第一の光活性層の上に、第一の電極を形成する工程。
(第一の電極)
本実施形態においては、第一の電極101は光入射面側に配置される。
図1において、第一の電極101は、第一の金属電極101aと第一の透明電極101bとの複合体である。金属電極と透明電極は、それぞれ特性が異なるので、特性に応じて、いずれか一方を用いても、組み合わせて用いてもよい。
実施形態の方法により形成される第一の光活性層(光電変換層)103はペロブスカイト構造を少なくとも一部に有するものである。このペロブスカイト構造とは、結晶構造のひとつであり、ペロブスカイトと同じ結晶構造をいう。典型的には、ペロブスカイト構造はイオンA、B、およびXからなり、イオンBがイオンAに比べて小さい場合にペロブスカイト構造をとる場合がある。この結晶構造の化学組成は、下記一般式(1)で表すことができる。
ABX3 (1)
図1において、第一のバッファー層102と第二のバッファー層104は、第一の電極と第一の光活性層との間、または第一の光活性層とトンネル絶縁膜との間にそれぞれ存在する層である。電子またはホールを輸送する優先的に取り出す層である。ここで、第二のバッファー層は、存在する場合には第一の光活性層の下地層となるので、その表面は実質的に平滑面であることが好ましい。
中間透明電極105は、トップセルとボトムセルとを隔絶しながら電気的に連結し、かつトップセルで吸収されなかった光をボトムセルへ導く機能を有するものである。したがって、その材料は透明または半透明の導電性を有する材料から選択することができる。このような材料としては、第一の透明電極と同じものから選択することができる。
中間明電極の厚さは、10nm~70nmであることが好ましい。10nmよりも薄いと膜欠損が多く、中間透明電極に隣接する層の隔絶が不十分になる。70nmよりも厚いと、光透過性は回折効果により、ボトムセル、例えばシリコンセルの発電量の低下を招くことがある。
第一のパッシベーション層106は、第一の光活性層103と第一のドープ層108または第二の光活性層109との間に配置されている。第一のパッシベーション層は、第一の光活性層と第二の光活性層109とを電気的に絶縁するが、開口部を有しており、その開口部を通じて、第二の光活性層と第一のドープ層との間を、電気的接続を確保している。このため、キャリア移動が可能な領域が限定されるので、効率的にキャリアを収集することができる。
また合金層(光散乱層)から第二の光活性層までの距離が100~400μmであることが好ましい。界面における曲率半径がこのような範囲を有する場合、光路が複雑に変化した光を効率的に吸収することができる。このような構成を採用することで、実施形態による素子から取り出せる電流量を最大化することが可能である。
図1において、第二の光活性層109は、シリコンを含む。第二の光活性層に含まれるシリコンは、一般的に光電池に用いられるシリコンと同様の構成を採用することができる。具体的には、単結晶シリコン、多結晶シリコン、ヘテロ接合型シリコンなどの結晶シリコンを含む結晶シリコン、アモルファスシリコンを含む薄膜シリコンなどが挙げられる。また、シリコンはシリコンウェハーから切り出した薄膜であってもよい。シリコンウェハーとしては、リンなどをドープしたn型シリコン結晶、ボロンなどをドーピングしたp型シリコン結晶も使用できる。p型シリコン結晶中の電子は長い拡散長を有しているので好ましい。なお、第二の光活性層の厚さは、100~300μmであることが好ましい。
図1において、第二のドープ層110は、第二の光活性層109と第二の電極112との間にそれぞれ配置される層である。
第二のパッシベーション層111は、第二の光活性層109の裏面側に配置されている。例えば、第二の光活性層の裏面側表面、あるいは第二の光活性層の裏面側表面に配置された第二のドープ層の表面に配置される。この第二のパッシベーション層は第一のパッシベーション層と同様にシリコン層のダングリングボンドを低減する機能を有するものであり、第一のパッシベーション層と同様の方法で形成させることができる。また、光反射層として、第一および第二の光活性層の光取り込み量を増大させる効果もある。このような第二のパッシベーション層の厚さは0.01~1000μmであることが好ましい。
第二の電極112は導電性を有するものであれば、従来知られている任意の材料を用いて形成させることができる。またその形成方法も特に限定されない。具体的には、上記した第一の金属電極と同様にして形成させることができる。また、図1において、第二の電極112は、複数の電極が素子の裏面に離間して配置されているが、素子の裏面全体に沿うとして形成されていてもよい。この場合、第一および第二の光活性層で吸収できなかった光を、第二の電極で反射させ、再び第一および第二の光活性層において光電変換に利用することができる。
外部からの光取り込み量を増やすため、素子の最外層、つまり大気との界面部分に反射防止層を設けてもよい。このような反射防止膜は、一般的に知られている材料、例えばSnNx、やMgF2など材料として用いることができる。これらの材料をPECVD法、蒸着法等で成膜することができる。素子の最外層に反射防止膜を設ける場合、素子から電流を取り出すためには、第一の電極、および第二の電極は、外部と電気的接続を得る必要がある。このため反射防止膜が電気的接続を阻害しないように、その一部を除去することが好ましい。このような除去方法としては、湿式エッチング処理方法、エッチングペーストを用いた方法、レーザーを用いた方法などを用いることができる。
図1に例示されている素子は、光活性層を2つ具備しており、ペロブスカイト半導体を含む光活性層を具備する単位をトップセル、シリコンを含む光活性層を具備する単位をボトムセルとして、中間透明電極によりに直列に接続した構造を有するタンデム太陽電池である。一般的に、シリコン太陽電池のバンドギャップは1.1eV程度であるが、これに対して相対的にバンドギャップが広いペロブスカイト半導体を含む光電池を組み合わせることで、より広い波長域の光を効率的に吸収することが可能となる。
実施形態による多層接合型光電変換素子は、上記した各層を、適切な順序で積層することで製造することができる。積層順序は、所望の構造を得ることができれば特に制限されないが、例えば以下の順序で製造することができる。
下記の工程を含む、多層接合型光電変換素子の製造方法:
(a)第二の光活性層を構成するシリコンウェハーの一面に、第一のパッシベーション層を形成させる工程、
(b)形成された第一のパッシベーション層に開口部を形成させる工程、
(c)開口部が形成されたパッシベーション層の上に、金属ペーストを塗布する工程、
(d)金属ペーストが塗布されたシリコンウェハーを加熱して、シリコン合金層、第一のドープ層を形成させる工程、
(e)前記第一のパッシベーション層が形成されたシリコンウェハーの裏面に、第二の電極を形成させる工程、
(f)前記第一のパッシベーション層の上に、塗布法により、ペロブスカイトを含む第一の光活性層を形成させる工程、および
(g)前記第一の光活性層の上に、第一の電極を形成させる工程。
(a0)シリコンウェハーの片側表面にテクスチャ構造を形成させる工程。
(d1)必要に応じて、前記第一のパッシベーション層が形成されたシリコンウェハーの裏面に、第二のドープ層を形成させる工程、
(d2)必要に応じて、前記第一のパッシベーション層が形成されたシリコンウェハーの裏面、または第二のドープ層の上に、第二のパッシベーション層を形成させる工程。
(e1)必要に応じて、第一のパッシベーション層の表面に、中間透明電極を形成させる工程、
(e2)必要に応じて、第一のパッシベーション層または中間電極の上に、第二のバッファー層を形成させる工程。
(f1)第一の光活性層の上に、第一のバッファー層を形成させる工程、
を組み合わせることもできる。
図1に示される構造を有する多層接合型光電変換素子を作製する。p型ウェハーをアルカリ溶液を用いたエッチングを行うと、シリコン結晶(100)面のエッチングにより(111)面を選択的に残すことができる。これにより表面にピラミッド状の凹凸構造(テクスチャ構造)を形成できる。反対側面は研磨すれば平面化することができる。テクスチャ構造を形成した面に、第二のドープ層として、リンをドープしてn層を形成できる。POCl3と酸素の反応を利用して基板表面にPSGを堆積させ、その後、900℃で熱処理を行うことで、シリコン中にリンをドープすることができる。PSGは酸処理で取り除くことができる。
図2に示した構造を有する素子を形成する。光散乱層および第一のドープ層を形成しないことの他は、実施例1と同一の方法により素子を作製した。
101…第一の電極
101a…第一の金属電極
101b…第一の透明電極
102…第一のバッファー層
103…ペロブスカイト半導体を含む第一の光活性層
104…第二のバッファー層
105…中間透明電極
106…第一のパッシベーション層
107…合金層
108…第一のドープ層
109…第二の光活性層
110…第二のドープ層
111…第二のパッシベーション層
112…第二の電極
200…比較例1の多層接合型光電変換素子
Claims (8)
- 第一の電極と、
ペロブスカイト半導体を含む第一の光活性層と、
第一のパッシベーション層と
第一のドープ層と、
シリコンを含む第二の光活性層と、
第二の電極と、
を、この順に具備する多層接合型光電変換素子であって、
さらに、前記パッシベーション層の一部分を貫通して、前記第一の光活性層と前記第一のドープ層とを電気的に接合する、相互に離間した複数のシリコン合金層からなる光散乱層をさらに具備する、多層接合型光電変換素子。 - 第一の光活性層及び第二の光活性層の積層方向に平行な断面における前記シリコン合金層と前記第一のドープ層との境界線の曲率半径が一定でない、請求項1に記載の多層接合型光電変換素子。
- 前記境界線の総長に対して、前記曲率半径が1~100μmの範囲内である部分の長さが40%以上である、請求項2に記載の多層接合型光電変換素子。
- 前記第一の光活性層と、前記光散乱層と間に中間透明電極をさらに具備する、請求項1~3のいずれか1項に記載の多層接合型光電変換素子。
- 前記第一の光活性層と、第二の光活性層側の隣接層との間に存在する界面が実質的に平滑面である、請求項1~3のいずれか1項に記載の多層接合型光電変換素子。
- 前記第一の電極が、複数の金属線が実質的に平行に配置された第一の金属電極層を具備し、前記光散乱層が、複数の金属線が実質的に平行に配置されたシリコン合金層を具備し、前記複数の金属線の平均間隔が、前記複数のシリコン合金層の平均間隔よりも狭い、請求項1~5のいずれか1項に記載の多層接合型光電変換素子。
- 下記の工程を含む、多層接合型光電変換素子の製造方法:
(a)第二の光活性層を構成するシリコンウェハーの一面に、第一のパッシベーション層を形成させる工程、
(b)形成された第一のパッシベーション層に開口部を形成させる工程、
(c)開口部が形成されたパッシベーション層の上に、金属ペーストを塗布する工程、
(d)金属ペーストが塗布されたシリコンウェハーを加熱して、シリコン合金層、第一のドープ層を形成させる工程、
(e)前記第一のパッシベーション層が形成されたシリコンウェハーの裏面に、第二の電極を形成させる工程、
(f)前記第一のパッシベーション層の上に、塗布法により、ペロブスカイトを含む第一の光活性層を形成する工程、および
(g)前記第一の光活性層の上に、第一の電極を形成させる工程。 - 工程(g)における温度が、工程(f)における温度よりも低い、請求項7に記載の多層接合型光電変換素子の製造方法。
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