WO2015053314A1 - 太陽電池封止用シートセットおよび太陽電池モジュール - Google Patents
太陽電池封止用シートセットおよび太陽電池モジュール Download PDFInfo
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- WO2015053314A1 WO2015053314A1 PCT/JP2014/076948 JP2014076948W WO2015053314A1 WO 2015053314 A1 WO2015053314 A1 WO 2015053314A1 JP 2014076948 W JP2014076948 W JP 2014076948W WO 2015053314 A1 WO2015053314 A1 WO 2015053314A1
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- WIPO (PCT)
- Prior art keywords
- solar cell
- sheet
- sealing material
- sealing
- ethylene
- Prior art date
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- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- FRGPKMWIYVTFIQ-UHFFFAOYSA-N triethoxy(3-isocyanatopropyl)silane Chemical compound CCO[Si](OCC)(OCC)CCCN=C=O FRGPKMWIYVTFIQ-UHFFFAOYSA-N 0.000 description 1
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000008096 xylene Substances 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
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
- B32B17/10697—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer being cross-linked
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
- B32B17/10788—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing ethylene vinylacetate
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
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- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/02—Physical, chemical or physicochemical properties
- B32B7/022—Mechanical properties
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- H—ELECTRICITY
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- 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
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
- H01L31/0481—Encapsulation of modules characterised by the composition of the encapsulation material
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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
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
- H01L31/049—Protective back sheets
-
- 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
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/05—Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells
- H01L31/0504—Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells specially adapted for series or parallel connection of solar cells in a module
-
- 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
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/05—Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells
- H01L31/0504—Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells specially adapted for series or parallel connection of solar cells in a module
- H01L31/0508—Electrical interconnection means between PV cells inside the PV module, e.g. series connection of PV cells specially adapted for series or parallel connection of solar cells in a module the interconnection means having a particular shape
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02S—GENERATION OF ELECTRIC POWER BY CONVERSION OF INFRARED RADIATION, VISIBLE LIGHT OR ULTRAVIOLET LIGHT, e.g. USING PHOTOVOLTAIC [PV] MODULES
- H02S50/00—Monitoring or testing of PV systems, e.g. load balancing or fault identification
- H02S50/10—Testing of PV devices, e.g. of PV modules or single PV cells
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2457/00—Electrical equipment
- B32B2457/12—Photovoltaic modules
-
- 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
- Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
- Y02B10/00—Integration of renewable energy sources in buildings
- Y02B10/10—Photovoltaic [PV]
-
- 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
Definitions
- the present invention relates to a solar cell sealing sheet set and a solar cell module.
- solar cells are attracting attention as a means of generating energy that is clean and free from depletion.
- a solar cell When a solar cell is used outdoors such as a roof portion of a building, it is generally used in the form of a solar cell module.
- the above solar cell module is generally manufactured by the following procedure. First, a crystalline solar cell element (hereinafter sometimes referred to as a power generation element or a cell) formed of polycrystalline silicon, single crystal silicon, or the like, or amorphous silicon or crystalline silicon is placed on a substrate such as glass. A thin film solar cell element or the like obtained by forming a very thin film of several ⁇ m is manufactured. Next, in order to obtain a crystalline solar cell module, a solar cell module protective sheet (light-receiving surface side protective member) / solar cell sealing material / crystalline solar cell element / solar cell sealing material / protection for solar cell module The sheets (back side protective member) are laminated in this order.
- a solar cell module protective sheet light-receiving surface side protective member
- the thin film type solar cell element / solar cell sealing material / solar cell module protective sheet (back surface side protective member) are laminated in this order. Then, a solar cell module is manufactured by utilizing the lamination method etc. which vacuum-suck these and heat-press them.
- the solar cell module manufactured in this way has weather resistance and is suitable for outdoor use such as a roof portion of a building.
- Patent Document 1 discloses a sealing film that is made of an EVA composition containing a cross-linking agent and trimellitic acid ester and that is excellent in both adhesiveness and film-forming properties.
- the present invention has been made in view of the above circumstances, and suppresses bending and fatigue of the wiring material of the solar cell module, and thus can avoid disconnection of the wiring material, and the solar cell sealing
- the solar cell module using the sheet set for a vehicle is provided.
- the present inventors diligently studied design guidelines for achieving the above-mentioned problems. As a result, the present inventors have a common logarithm of the ratio of storage elastic modulus at a high temperature between the first sealing material sheet disposed on the light receiving surface side and the second sealing material sheet disposed on the back surface side. However, the inventors have found that this is effective as a design guideline for achieving the above-mentioned problems, and have reached the present invention.
- the following sheet set for solar cell sealing and solar cell module are provided.
- the first sealing material sheet and the back surface which are disposed between the light receiving surface side protection member and the back surface side protection member, are used for sealing the solar cell element and the wiring material, and are disposed on the light receiving surface side. It is a sheet set for solar cell sealing provided with a second sealing material sheet disposed on the side, The first sealing material before the crosslinking treatment at 120 ° C. when the solid viscoelasticity is measured under the conditions of a measurement temperature range of 25 ° C. to 180 ° C., a frequency of 1.0 Hz, a heating rate of 10 ° C./min, and a shear mode.
- the storage modulus of the sheet (P 1) and the crosslinking pretreatment of the second sealing member storage modulus of the sheet (P 2) is, for sealing a solar cell sheet set to satisfy the relation of the following equation (1).
- the first sealing material after the crosslinking treatment at 90 ° C. when the solid viscoelasticity is measured under the conditions of a measurement temperature range of 25 ° C. to 180 ° C., a frequency of 1.0 Hz, a heating rate of 10 ° C./min, and a shear mode The storage elastic modulus (G 1 ) of the sheet;
- At least one of the first sealing material sheet and the second sealing material sheet is selected from the group consisting of an ethylene / ⁇ -olefin copolymer and an ethylene / vinyl acetate copolymer as a crosslinkable resin, or The sheet set for sealing a solar cell according to any one of the above [1] to [3], including two or more kinds.
- At least one of the first sealing material sheet and the second sealing material sheet contains an organic peroxide, and the content of the organic peroxide is 0. 0 parts by mass relative to 100 parts by mass of the crosslinkable resin.
- the sheet set for sealing a solar cell according to the above [4] which is 1 part by mass or more and 1.2 parts by mass or less.
- the storage elastic modulus (P 1 ) is 1.0 ⁇ 10 ⁇ 1 Pa to 1.2 ⁇ 10 6 Pa and the storage elastic modulus (P 2 ) is 8.0 ⁇ 10 ⁇ 2 Pa to 1.
- the solar cell module which uses the sheet
- the solar cell module has a sealing layer between the light receiving surface side protection member and the back surface side protection member, and the solar cell element is sealed in the sealing layer,
- the sealing layer is formed by the solar cell sealing sheet set,
- the sealing layer has a first sealing layer and a second sealing layer,
- the first sealing layer is formed by crosslinking the first sealing material sheet
- the second sealing layer is formed by crosslinking the second sealing material sheet
- the first sealing layer is provided between the light-receiving surface side protection member and the solar cell element
- the solar cell module in which the second sealing layer is provided between the back surface side protective member and the solar cell element.
- a solar cell sealing sheet set capable of suppressing stress applied to a solar cell element and a wiring material at the time of manufacturing a solar cell module, and further suppressing cracking of the solar cell element and disconnection of the wiring material. Can do. Furthermore, according to the present invention, it is possible to provide a solar cell module that is not easily affected by the temperature cycle.
- FIG. 1 is a cross-sectional view schematically showing one embodiment of a solar cell module 10 of the present invention.
- the solar cell module 10 of the present embodiment includes a pair of solar cell sealing sheet sets including a first sealing material sheet 11 disposed on the light receiving surface side and a second sealing material sheet 12 disposed on the back surface side.
- the sealing layer 1 which becomes, the light-receiving surface side protection member 14, the back surface side protection member 13, the solar cell element 16, and the wiring material 15 (interconnector) are provided.
- the first sealing material sheet 11 and the second sealing material sheet 12 are collectively referred to as “first and second sealing material sheets”.
- the sheet set for sealing a solar cell of the present embodiment is disposed between the light-receiving surface side protection member 14 and the back surface side protection member 13, and is used to seal the solar cell element 16 and the wiring material 15.
- positioned at a back surface side are provided. Measure the solid viscoelasticity of the first sealing material sheet 11 and the second sealing material sheet 12 under the conditions of a measurement temperature range of 25 ° C.
- each storage elastic modulus (P 1 ) and storage elastic modulus (P 2 ) at 120 ° C. satisfies the relationship of the formula (1). It is more preferable to satisfy
- Measurement temperature range of the first encapsulant sheet 11 before cross-linking treatment is 25 ° C. to 180 ° C., frequency 1.0 Hz, temperature rising rate 10 ° C./min, 120 ° C. when the solid viscoelasticity is measured under shear mode conditions.
- the storage elastic modulus (P 1 ) is preferably 1.0 ⁇ 10 ⁇ 1 to 1.2 ⁇ 10 6 Pa, more preferably 1.0 ⁇ 10 0 to 1.2 ⁇ 10 5 Pa. More preferably, it is 1.0 ⁇ 10 0 to 1.2 ⁇ 10 4 Pa.
- the load which a 1st, 2nd sealing material sheet gives to a solar cell element and wiring material is further suppressed at the time of solar cell module manufacture, and also the crack of a solar cell element and the disconnection of wiring material are more. It is possible to provide a solar cell module that is further suppressed and is less susceptible to the influence of the temperature cycle.
- the storage elastic modulus (P 2 ) is preferably 8.0 ⁇ 10 ⁇ 2 to 1.0 ⁇ 10 6 Pa, more preferably 8.0 ⁇ 10 ⁇ 1 to 1.0 ⁇ 10 5 Pa. More preferably 1.0 ⁇ 10 0 to 1.0 ⁇ 10 4 Pa.
- the load which a 1st, 2nd sealing material sheet gives to a solar cell element and wiring material is further suppressed at the time of solar cell module manufacture, and also the crack of a solar cell element and the disconnection of wiring material are more. It is possible to provide a solar cell module that is further suppressed and that is less susceptible to the influence of the temperature cycle.
- the sheet set for sealing a solar cell of the present embodiment has a measurement temperature range of 25 ° C. to 180 ° C., a frequency of 1.0 Hz, and a temperature rising rate of the first sealing material sheet 11 after the crosslinking treatment arranged on the light receiving surface side.
- the linear expansion coefficient ( ⁇ 1 ) and the linear expansion coefficient ( ⁇ 2 ) of the first sealing material sheet 11 after the crosslinking treatment at 50 ° C. to 90 ° C. satisfy Expression (2).
- the formula (2c) is satisfied.
- the load which a 1st, 2nd sealing material sheet gives to a solar cell element and wiring material is further suppressed at the time of solar cell module manufacture, and also the crack of a solar cell element and the disconnection of wiring material are more. It is possible to provide a solar cell module that is further suppressed and is less susceptible to the effects of temperature cycling.
- the storage elastic modulus (G 1 ) at ° C. is preferably 1.0 ⁇ 10 3 to 1.0 ⁇ 10 9 Pa, more preferably 1.0 ⁇ 10 4 to 1.0 ⁇ 10 8 Pa, More preferably, it is 1.0 ⁇ 10 4 to 1.0 ⁇ 10 7 Pa.
- the linear expansion coefficient ( ⁇ 1 ) of the first sealing material sheet 11 after the crosslinking treatment at ⁇ 40 ° C. to 0 ° C. is preferably 1 ⁇ 10 ⁇ 6 to 5000 ⁇ 10 ⁇ 6 / ° C., more preferably It is 10 ⁇ 10 ⁇ 6 to 1000 ⁇ 10 ⁇ 6 / ° C., more preferably 10 ⁇ 10 ⁇ 6 to 500 ⁇ 10 ⁇ 6 / ° C.
- the linear expansion coefficient ( ⁇ 2 ) of the first sealing material sheet 11 after the crosslinking treatment at 50 ° C. to 90 ° C. is preferably 1 ⁇ 10 ⁇ 6 to 5000 ⁇ 10 ⁇ 6 / ° C., preferably 10 ⁇ .
- the solar cell module which suppresses the crack of a solar cell element and the disconnection of wiring material much more, and is much less susceptible to the influence of a temperature cycle can be provided.
- the storage elastic modulus (P 1 ), storage elastic modulus (P 2 ), storage elastic modulus (G 1 ), linear expansion coefficient ( ⁇ 1 ), and linear expansion coefficient ( ⁇ 2 ) are, for example, first, first The types and blending ratios of the crosslinkable resin, crosslinker and crosslinking aid contained in the two encapsulant sheets, the molecular weight and MFR and density of the crosslinkable resin, the porosity P of the first and second encapsulant sheets, etc. It is possible to control by adjusting each.
- the sheet set for solar cell sealing in this embodiment includes a first sealing material sheet 11 disposed on the light receiving surface side and a second sealing material sheet 12 disposed on the back surface side.
- the first and second sealing material sheets usually contain a crosslinkable resin. Conventionally known resins can be used as the crosslinkable resin.
- ethylene / ⁇ -olefin copolymer containing ethylene and ⁇ -olefin having 3 to 20 carbon atoms, high density ethylene resin, low density ethylene resin, medium density ethylene resin, ultra low density ethylene resin, propylene (Co) polymer, 1-butene (co) polymer, 4-methylpentene-1 (co) polymer, ethylene / cyclic olefin copolymer, ethylene / ⁇ -olefin / cyclic olefin copolymer, ethylene / ⁇ -Olefin resins such as olefin / non-conjugated polyene copolymer, ethylene / ⁇ -olefin / conjugated polyene copolymer, ethylene / aromatic vinyl copolymer, ethylene / ⁇ -olefin / aromatic vinyl copolymer; ethylene -Ethylene / carboxylic anhydrides such as unsaturated carboxylic anhydr
- an ethylene / ⁇ -olefin copolymer composed of ethylene and an ⁇ -olefin having 3 to 20 carbon atoms, which can be crosslinked with an organic peroxide, a low density ethylene resin, a medium density ethylene resin, Low-density ethylene resin, ethylene / cyclic olefin copolymer, ethylene / ⁇ -olefin / cyclic olefin copolymer, ethylene / ⁇ -olefin / non-conjugated polyene copolymer, ethylene / ⁇ -olefin / conjugated polyene copolymer Olefin resins such as ethylene / aromatic vinyl copolymer, ethylene / ⁇ -olefin / aromatic vinyl copolymer; ethylene / unsaturated carboxylic anhydride copolymer, ethylene / ⁇ -olefin / unsaturated carboxylic anhydride Ethylene
- an ethylene / ⁇ -olefin copolymer comprising ethylene and an ⁇ -olefin having 3 to 20 carbon atoms, a low density ethylene resin, an ultra low density ethylene resin, an ethylene / ⁇ -olefin / non-conjugated polyene copolymer, Ethylene / ⁇ -olefin / conjugated polyene copolymer, ethylene / unsaturated carboxylic anhydride copolymer, ethylene / ⁇ -olefin / unsaturated carboxylic anhydride copolymer, ethylene / epoxy-containing unsaturated compound copolymer, ethylene
- an ethylene / ⁇ -olefin copolymer comprising ethylene and an ⁇ -olefin having 3 to 20 carbon atoms, a low density ethylene resin, an ultra low density ethylene resin, an ethylene / ⁇ -olefin / non-conjugated polyene copolymer, It is preferable to use one or more selected from ethylene / ⁇ -olefin / conjugated polyene copolymers, ethylene / vinyl acetate copolymers, ethylene / acrylic acid copolymers, and ethylene / methacrylic acid copolymers. . Among these, at least one selected from ethylene / ⁇ -olefin copolymers and ethylene / vinyl acetate copolymers is particularly preferably used. In the present embodiment, the above-described resins may be used alone or blended.
- the crosslinkable resin contains at least one selected from an ethylene / ⁇ -olefin copolymer and an ethylene / vinyl acetate copolymer
- the content of the resin selected from the ethylene / vinyl acetate copolymer is preferably 80% by mass or more when the total resin component contained in the first and second sealing material sheets is 100% by mass, More preferably, it is 90 mass% or more, More preferably, it is 95 mass% or more, and Preferably it is 100 mass%.
- ⁇ -olefin of the ethylene / ⁇ -olefin copolymer composed of ethylene and an ⁇ -olefin having 3 to 20 carbon atoms used as the crosslinkable resin usually one kind of ⁇ -olefin having 3 to 20 carbon atoms is used. It can be used alone or in combination of two or more. Among these, ⁇ -olefins having 10 or less carbon atoms are preferable, and ⁇ -olefins having 3 to 8 carbon atoms are particularly preferable.
- ⁇ -olefins include propylene, 1-butene, 1-pentene, 1-hexene, 3-methyl-1-butene, 3,3-dimethyl-1-butene, 4-methyl-1- Examples include pentene, 1-octene, 1-decene, and 1-dodecene. Among these, it is preferable to use one or more selected from propylene, 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene and 1-octene in view of availability.
- the ethylene / ⁇ -olefin copolymer may be a random copolymer or a block copolymer, but a random copolymer is preferred from the viewpoint of flexibility.
- the polymerization of the ethylene / ⁇ -olefin copolymer can be carried out by any of the conventionally known gas phase polymerization methods, and liquid phase polymerization methods such as slurry polymerization methods and solution polymerization methods.
- Metallocene catalysts, Ziegler-Natta catalysts, Polymerization can be performed using a conventionally known olefin polymerization catalyst such as a vanadium catalyst.
- the ethylene / ⁇ -olefin copolymer may be a copolymer comprising ethylene, an ⁇ -olefin having 3 to 20 carbon atoms, and a non-conjugated polyene.
- the ⁇ -olefin is the same as described above, and examples of the non-conjugated polyene include 5-ethylidene-2-norbornene (ENB), 5-vinyl-2-norbornene (VNB), and dicyclopentadiene (DCPD). These non-conjugated polyenes can be used alone or in combination of two or more.
- the ethylene / ⁇ -olefin copolymer preferably further satisfies the following requirements a1 and a2.
- the density of the ethylene / ⁇ -olefin copolymer measured according to ASTM D1505 is preferably 0.865 to 0.884 g / cm 3 , more preferably 0.866 to 0.883 g / cm 3. 3 , more preferably 0.866 to 0.880 g / cm 3 , and particularly preferably 0.867 to 0.880 g / cm 3 .
- the density of the ethylene / ⁇ -olefin copolymer can be adjusted by a balance between the content ratio of ethylene units and the content ratio of ⁇ -olefin units.
- the density of the ethylene / ⁇ -olefin copolymer is not more than the above upper limit, the crystallinity is lowered and the transparency can be increased. Furthermore, extrusion molding at low temperature becomes easy, and for example, extrusion molding can be performed at 130 ° C. or lower. For this reason, even if an organic peroxide is kneaded into the ethylene / ⁇ -olefin copolymer, the crosslinking reaction in the extruder is prevented from progressing, the generation of gel-like foreign matters on the sheet is suppressed, and the appearance of the sheet is improved. Deterioration can also be suppressed.
- the density of the ethylene / ⁇ -olefin copolymer is not less than the above lower limit, the crystallization speed of the ethylene / ⁇ -olefin copolymer can be increased, so that the sheet extruded from the extruder is not sticky, and cooling Peeling with a roll becomes easy, and the first and second sealing material sheets can be easily obtained. Further, since stickiness is less likely to occur in the sheet, the occurrence of blocking can be suppressed, and the sheet feedability can be improved. Moreover, since it can fully bridge
- Requirement a2 The melt flow rate (MFR) of the ethylene / ⁇ -olefin copolymer measured in accordance with ASTM D1238 and at a temperature of 190 ° C. and a load of 2.16 kg is usually 0.1 to 50 g / 10 min. Yes, preferably 2 to 40 g / 10 min, more preferably 2 to 30 g / 10 min, and still more preferably 5 to 10 g / 10 min.
- the MFR of the ethylene / ⁇ -olefin copolymer can be adjusted by adjusting the polymerization temperature during the polymerization reaction, the polymerization pressure, and the molar ratio between the ethylene and ⁇ -olefin monomer concentrations and the hydrogen concentration in the polymerization system. can do.
- a sheet can be produced by calendar molding.
- the MFR is 0.1 g / 10 min or more and less than 10 g / 10 min, since the fluidity of the resin composition containing the ethylene / ⁇ -olefin copolymer is low, the melted out when the sheet is laminated with the battery element This is preferable in that the laminating apparatus can be prevented from being soiled by the resin.
- the MFR is 2 g / 10 min or more, preferably the MFR is 10 g / 10 min or more, the fluidity of the resin composition containing the ethylene / ⁇ -olefin copolymer is improved, and the productivity at the time of sheet extrusion molding is improved. Can be improved.
- the MFR is 50 g / 10 min or less, the molecular weight increases, and therefore, adhesion to a roll surface such as a chill roll can be suppressed. Therefore, peeling is unnecessary, and a sheet having a uniform thickness can be formed. Furthermore, since it becomes a resin composition with “koshi”, a thick sheet of 0.1 mm or more can be easily formed.
- the crosslinking characteristic at the time of laminate molding of the solar cell module is improved, it is possible to sufficiently crosslink and suppress a decrease in heat resistance.
- the MFR is 27 g / 10 min or less, the draw-down during sheet forming can be suppressed, a wide sheet can be formed, the cross-linking characteristics and heat resistance are further improved, and the best first and second sealing are achieved. A stopping material sheet can be obtained.
- the influence of decomposition of the organic peroxide is small in the melt extrusion process, so that the MFR is 0.1 g / 10 min or more.
- a sheet can also be obtained by extrusion molding using a resin composition of less than 10 g / 10 minutes, preferably 0.5 g / 10 minutes or more and less than 8.5 g / 10 minutes.
- a resin composition having an MFR of 0.1 g / 10 min or more and less than 10 g / 10 min is used.
- a sheet can also be produced by extrusion molding at a molding temperature of 170 to 250 ° C. while performing a fine crosslinking treatment. When the MFR is within this range, it is preferable in that the laminating apparatus can be prevented from being soiled by the molten resin that protrudes when the sheet is laminated with the solar cell element.
- the ethylene / ⁇ -olefin copolymer preferably further satisfies the following requirement a3.
- Requirement a3 The content of structural units derived from ethylene (hereinafter also referred to as “ethylene units”) contained in the ethylene / ⁇ -olefin copolymer is 80 mol% or more and 90 mol% or less, preferably 80 mol% or more and 88 mol % Or less, more preferably 82 mol% or more and 88 mol% or less, and still more preferably 82 mol% or more and 87 mol% or less.
- ethylene units structural units derived from ethylene
- the content of a structural unit derived from an ⁇ -olefin having 3 to 20 carbon atoms (hereinafter also referred to as “ ⁇ -olefin unit”) contained in the ethylene / ⁇ -olefin copolymer is 10 mol% or more and 20 mol% or less.
- ⁇ -olefin unit a structural unit derived from an ⁇ -olefin having 3 to 20 carbon atoms contained in the ethylene / ⁇ -olefin copolymer.
- ⁇ -olefin unit a structural unit derived from an ⁇ -olefin having 3 to 20 carbon atoms
- the obtained first and second sealing material sheets are excellent in transparency. Further, extrusion molding at a low temperature can be easily performed, and for example, extrusion molding at 130 ° C. or lower is possible. For this reason, even when an organic peroxide is kneaded into the ethylene / ⁇ -olefin copolymer, it is possible to suppress the progress of the crosslinking reaction in the extruder, and the first and second sealing material sheets are gelled. It can prevent that a foreign material generate
- the content of the ⁇ -olefin unit contained in the ethylene / ⁇ -olefin copolymer is not more than the above upper limit value, the crystallization rate of the ethylene / ⁇ -olefin copolymer becomes appropriate, and therefore the ethylene / ⁇ -olefin copolymer is extruded from an extruder.
- the sheet is not sticky and can be easily peeled off by a cooling roll, so that the first and second sealing material sheets can be obtained efficiently. Further, since no stickiness is generated on the sheet, blocking can be prevented, and the sheet feeding property is good. Moreover, the fall of the heat resistance of a 1st, 2nd sealing material sheet can also be prevented.
- the melt flow rate (MFR) of the ethylene / vinyl acetate copolymer used as the crosslinkable resin is preferably 5 to 50 g / 10 minutes, more preferably 5 to 30 g / 10 minutes, still more preferably 5 to 25 g / 10. Minutes.
- MFR of the ethylene / vinyl acetate copolymer is within the above range, the extrusion moldability is excellent.
- the MFR of the ethylene / vinyl acetate copolymer can be adjusted by adjusting the polymerization temperature during the polymerization reaction, the polymerization pressure, and the molar ratio between the monomer concentration and the hydrogen concentration of the polar monomer in the polymerization system. .
- the MFR of the ethylene / vinyl acetate copolymer is measured under conditions of 190 ° C. and a load of 2.16 kg in accordance with ASTM D1238.
- the content of vinyl acetate in the ethylene / vinyl acetate copolymer is preferably 10% by mass to 47% by mass, and more preferably 13% by mass to 35% by mass.
- the content of vinyl acetate is in this range, the balance between the adhesiveness, weather resistance, transparency, and mechanical properties of the first and second sealing material sheets is further improved.
- the film formability is good.
- the vinyl acetate content can be measured according to JIS K7192: 1999.
- the vinyl acetate content was determined by dissolving the sample in xylene, hydrolyzing the acetate group with an alcohol solution of potassium hydroxide, adding excess sulfuric acid or hydrochloric acid, and adding dropwise with a standard sodium hydroxide solution. It can be measured by quantification.
- the ethylene / vinyl acetate copolymer is not particularly limited, and can be produced by a known method. For example, in the presence of a radical generator, at 500 to 4000 atm and 100 to 300 ° C., in the presence or absence of a solvent or a chain transfer agent, ethylene, vinyl acetate, and other copolymerization components as necessary are copolymerized. It can be produced by polymerization.
- an ethylene / ⁇ -olefin copolymer or an ethylene / vinyl acetate copolymer may be used alone, or may be blended.
- the total amount of ethylene / ⁇ -olefin copolymer and ethylene / vinyl acetate copolymer is 100 parts by mass.
- the ethylene / ⁇ -olefin copolymer is preferably 50 to 99 parts by mass, the ethylene / vinyl acetate copolymer is preferably 1 to 50 parts by mass, the ethylene / ⁇ -olefin copolymer is preferably 50 to 98 parts by mass,
- the ethylene / vinyl acetate copolymer is more preferably 2 to 50 parts by mass, the ethylene / ⁇ -olefin copolymer is 50 to 95 parts by mass, and the ethylene / vinyl acetate copolymer is 5 to 50 parts by mass. More preferably, the ethylene / ⁇ -olefin copolymer is 75 to 95 parts by mass, and the ethylene / vinyl acetate copolymer is particularly preferably 5 to 25 parts by mass.
- the MFR of the crosslinkable resin contained in the first encapsulant sheet 11 is smaller than the MFR of the crosslinkable resin contained in the second encapsulant sheet 12.
- the MFR ratio represented by (MFR of crosslinkable resin contained in first sealing material sheet 11) / (MFR of crosslinkable resin contained in second sealing material sheet 12) is 1.0. Is preferably less than 0.8, more preferably 0.8 or less, and even more preferably 0.6 or less.
- the MFR ratio is in the above range, the relationship between the storage elastic modulus (P 1 ) and the storage elastic modulus (P 2 ) at 120 ° C. satisfies the relationship of the above-described formula (1), and the first and second Deflection and stress concentration of the interconnector of the solar cell module installed between the sealing material sheets are further less likely to occur.
- the first sealing material sheet 11 The vinyl acetate content is preferably smaller than that of the second sealing material sheet 12.
- the VA ratio represented by (vinyl acetate content of first sealing material sheet 11) / (vinyl acetate content of second sealing material sheet 12) is preferably less than 1.0. Is more preferably 0.9 or less, and further preferably 0.8 or less.
- the ratio of the vinyl acetate content is in the above range, the relationship between the storage elastic modulus (P 1 ) and the storage elastic modulus (P 2 ) at 120 ° C. satisfies the relationship of the above formula (1), and the first Further, the deflection and stress concentration of the interconnector of the solar cell module installed between the second sealing material sheets are more difficult to occur.
- the first sealing material sheet 11 includes an ethylene / vinyl acetate copolymer
- the second sealing material sheet 12 includes an ethylene / ⁇ -olefin copolymer
- the first sealing material sheet 11 includes Examples include an embodiment including an ethylene / ⁇ -olefin copolymer and the second sealing material sheet 12 including an ethylene / vinyl acetate copolymer. It is preferable that the first sealing material sheet 11 includes an ethylene / vinyl acetate copolymer and the second sealing material sheet 12 includes an ethylene / ⁇ -olefin copolymer.
- the first sealing material sheet 11 includes an ethylene / vinyl acetate copolymer
- the second sealing material sheet 12 includes an ethylene / ⁇ -olefin copolymer
- the MFR ratio is less than 1.0. It is particularly preferred.
- the first sealing material sheet 11 contains an ethylene / ⁇ -olefin copolymer
- the second sealing material sheet 12 contains an ethylene / vinyl acetate copolymer
- the MFR ratio is less than 1.0.
- the MFR of the ethylene / ⁇ -olefin copolymer constituting the first sealing material sheet 11 is particularly preferably 10 g / 10 min or less, and further preferably 8 g / 10 min or less.
- the first and second sealing material sheets may contain a silane coupling agent. By containing this silane coupling agent, the adhesive strength between the first and second sealing material sheets and other members can be made excellent.
- the content of the silane coupling agent in the first and second sealing material sheets is preferably 0.1 to 2 parts by mass, more preferably 0.1 to 1.8 parts with respect to 100 parts by mass of the crosslinkable resin. Part by mass, particularly preferably 0.1 to 1.5 parts by mass. When the content of the silane coupling agent is within the above range, bubbles are more reliably generated in the first and second sealing material sheets while improving the adhesiveness of the first and second sealing material sheets. Can be suppressed.
- silane coupling agent examples include vinyltriethoxysilane, vinyltrimethoxysilane, vinyltris ( ⁇ -methoxyethoxysilane), 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, and 3-glycidoxypropylmethyl.
- the first and second sealing material sheets preferably contain an organic peroxide.
- the organic peroxide preferably has a one-minute half-life temperature of 100 to 170 ° C. of the organic peroxide from the balance between productivity in extrusion sheet molding and crosslinking rate at the time of lamination of the solar cell module.
- the one-minute half-life temperature of the organic peroxide is 100 ° C. or higher, sheet molding can be facilitated and the appearance of the first and second sealing material sheets can be improved.
- the dielectric breakdown voltage can be prevented from being lowered, moisture permeability can be prevented from being lowered, and adhesiveness is further improved.
- the one-minute half-life temperature of the organic peroxide is 170 ° C.
- Organic peroxides having a 1 minute half-life temperature in the range of 100 to 170 ° C. include dilauroyl peroxide, 1,1,3,3-tetramethylbutylperoxy-2-ethylhexanoate, and dibenzoylperoxide.
- Oxide t-amylperoxy-2-ethylhexanoate, t-butylperoxy-2-ethylhexanoate, t-butylperoxyisobutyrate, t-butylperoxymaleic acid, 1,1-di (T-amylperoxy) -3,3,5-trimethylcyclohexane, 1,1-di (t-amylperoxy) cyclohexane, t-amylperoxyisononanoate, t-amylperoxynormal octoate, 1 , 1-Di (t-butylperoxy) -3,3,5-trimethylcyclohexane, 1,1-di (t-butylpero C) Cyclohexane, t-butylperoxyisopropyl carbonate, t-butylperoxy-2-ethylhexyl carbonate, 2,5-dimethyl-2,5-di (benzoy
- dilauroyl peroxide t-butyl peroxyisopropyl carbonate, t-butyl peroxyacetate, t-butyl peroxyisononanoate, t-butyl peroxy-2-ethylhexyl carbonate, t-butyl peroxybenzoate It is preferable to use 1 type, or 2 or more types selected from.
- the first and second encapsulant sheets have excellent cross-linking properties by containing an organic peroxide, so there is no need to go through a two-step bonding process of a vacuum laminator and a cross-linking furnace, and high temperatures Can be completed in a short time.
- the content of the organic peroxide in the first and second sealing material sheets is preferably 0.1 to 1.2 parts by mass, more preferably 0.2 to 1. 0 parts by mass, more preferably 0.2 to 0.8 parts by mass.
- the content of the organic peroxide is not less than the above lower limit value, the deterioration of the crosslinking characteristics of the first and second sealing material sheets is suppressed, and the graft reaction of the silane coupling agent to the main chain of the crosslinkable resin is performed. It is possible to improve the heat resistance and adhesiveness.
- the content of the organic peroxide is not more than the above upper limit value, the generation amount of the decomposition product of the organic peroxide is further reduced, and the bubbles in the first and second sealing material sheets are more surely produced. Can be suppressed.
- the first and second sealing material sheets contain at least one additive selected from the group consisting of an ultraviolet absorber, a light stabilizer, and a heat stabilizer, and at least two additives It is more preferable to contain an agent, and it is even more preferable that all of the above three types are contained.
- the contents of the three additives in the first and second sealing material sheets are each preferably 0.005 to 5 parts by mass with respect to 100 parts by mass of the crosslinkable resin. By making it within this range, the effect of improving resistance to constant temperature and humidity, heat cycle resistance, weather resistance stability, and heat stability is sufficiently ensured, and the first and second encapsulant sheets are transparent. Deterioration of adhesiveness and adhesiveness can be prevented.
- Examples of the ultraviolet absorber include 2-hydroxy-4-normal-octyloxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2,2-dihydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4- Benzophenone ultraviolet absorbers such as carboxybenzophenone and 2-hydroxy-4-N-octoxybenzophenone; 2- (2-hydroxy-3,5-di-t-butylphenyl) benzotriazole, 2- (2-hydroxy- Benzotriazole ultraviolet absorbers such as 5-methylphenyl) benzotriazole; one or more selected from salicylic acid ester ultraviolet absorbers such as phenyl salicylate and p-octylphenyl salicylate may be used. it can.
- Examples of the light stabilizer include bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, poly [ ⁇ 6- (1,1,3,3-tetramethylbutyl) amino-1, 3,5-triazine-2,4-diyl ⁇ ⁇ (2,2,6,6-tetramethyl-4-piperidyl) imino ⁇ hexamethylene ⁇ (2,2,6,6-tetramethyl-4-piperidyl)
- One or more selected from hindered amine compounds such as imino ⁇ ], hindered piperidine compounds, and the like can be used.
- heat stabilizers examples include tris (2,4-di-tert-butylphenyl) phosphite, bis [2,4-bis (1,1-dimethylethyl) -6-methylphenyl] ethyl ester phosphorous acid Tetrakis (2,4-di-tert-butylphenyl) [1,1-biphenyl] -4,4′-diylbisphosphonite, bis (2,4-di-tert-butylphenyl) pentaerythritol diphos Phosphite heat stabilizers such as phyto; Lactone heat stabilizers such as the reaction product of 3-hydroxy-5,7-di-tert-butyl-furan-2-one and o-xylene; 3,3 ′ , 3 ", 5,5 ', 5" -hexa-tert-butyl-a, a', a "-(methylene-2,4,6-triyl) tri-p-cresol
- the first and second sealing material sheets preferably contain a crosslinking aid.
- the content of the crosslinking aid in the first and second sealing material sheets is preferably 0.05 to 5 parts by mass with respect to 100 parts by mass of the crosslinkable resin.
- a compound having two or more double bonds in the molecule can be used.
- t-butyl acrylate, lauryl acrylate, cetyl acrylate, stearyl acrylate, 2-methoxyethyl acrylate, ethyl carbitol acrylate Monoacrylates such as methoxytripropylene glycol acrylate; monomethacrylates such as t-butyl methacrylate, lauryl methacrylate, cetyl methacrylate, stearyl methacrylate, methoxyethylene glycol methacrylate, methoxypolyethylene glycol methacrylate; 1,4-butanediol diacrylate, 1, 6-hexanediol diacrylate, 1,9-nonanediol diacrylate, neopentyl glycol diacrylate, Diacrylates such as ethylene glycol diacrylate, tetraethylene glycol diacrylate, polyethylene glycol diacrylate
- Triacrylate Triacrylate; trimethacrylate such as trimethylolpropane trimethacrylate and trimethylolethane trimethacrylate; tetraacrylate such as pentaerythritol tetraacrylate and tetramethylolmethane tetraacrylate; divinyl aromatic compound such as divinylbenzene and di-i-propenylbenzene; Cyanurates such as triallyl cyanurate and triallyl isocyanurate; diallyl compounds such as diallyl phthalate; triallyl compounds; oximes such as p-quinonedioxime and pp′-dibenzoylquinonedioxime; maleimides such as phenylmaleimide One kind or two or more kinds selected can be used.
- various components other than the components described in detail above can be appropriately contained as long as the object of the present invention is not impaired.
- examples include various polyolefins other than the crosslinkable resin, styrene-based, ethylene-based block copolymers, and propylene-based polymers. These can be contained in an amount of 0.0001 to 50 parts by weight, preferably 0.001 to 40 parts by weight, based on 100 parts by weight of the crosslinkable resin.
- various resins other than polyolefins and / or one or more additives selected from various rubbers, plasticizers, fillers, pigments, dyes, antistatic agents, antibacterial agents, antifungal agents, flame retardants, dispersants, etc. can be contained appropriately.
- the thicknesses of the first and second sealing material sheets after the crosslinking treatment are each preferably 0.01 to 2 mm, more preferably 0.05 to 1.5 mm, still more preferably 0.1 to 1.2 mm, and more More preferably, it is 0.2 to 1 mm, particularly preferably 0.3 to 0.9 mm, and particularly preferably 0.3 to 0.8 mm.
- the thickness is within this range, damage to the light-receiving surface side protective member, solar cell element, thin film electrode, etc. in the laminating step can be suppressed, and a high amount of photovoltaic power can be obtained by ensuring sufficient light transmittance. be able to.
- the solar cell module can be laminated at a low temperature.
- the manufacturing method of a 1st, 2nd sealing material sheet Although the method normally used can be utilized as a manufacturing method of a 1st, 2nd sealing material sheet, It is preferable to manufacture by melt-blending with a calender roll, a kneader, a Banbury mixer, an extruder, etc. In particular, the production with an extruder capable of continuous production is preferred.
- a crosslinkable resin and various additives such as a silane coupling agent, an organic peroxide, an ultraviolet absorber, a light stabilizer, a heat stabilizer, a crosslinking aid, and other additives, for example, a plastic bag In a bag, etc., it is blended by human power, or mixed by a stirring mixer such as a Henschel mixer, tumbler mixer, or super mixer.
- a stirring mixer such as a Henschel mixer, tumbler mixer, or super mixer.
- the first and second sealing material sheets are obtained by putting the obtained composition into an extruded sheet molding hopper and performing extrusion sheet molding while performing melt kneading.
- the extrusion temperature range is preferably 100 to 130 ° C. By setting it as this range, the 1st, 2nd sealing material sheet
- a crosslinkable resin is mixed with additives, such as an organic peroxide, with a Henschel mixer or a tumbler mixer, is supplied to an extruder, and is sheet-like The method of shape
- the crosslinkable resin and the additive may be separately supplied to the extruder and melt-mixed in the extruder. Further, the crosslinkable resin may be once melt-kneaded to prepare mixed pellets, and the pellets may be supplied again to the extruder to form a sheet.
- the surface of the first and second sealing material sheets may be embossed.
- the embossing may be performed on one side or both sides of the first and second sealing material sheets.
- the porosity P (%) is preferably 10 to 50%, more preferably 10 to 40%, and still more preferably 15 to 40%.
- the apparent volume VA of the first and second sealing material sheets is obtained by multiplying the unit area by the maximum thickness of the first and second sealing material sheets.
- the porosity P is 10% or more, the elastic modulus of the first and second sealing material sheets can be sufficiently lowered, so that sufficient cushioning properties can be obtained. For this reason, even when a large pressure is locally applied to the solar cell element at the time of laminating, it is possible to prevent the solar cell element from being broken.
- the porosity P is 80% or less, air can be satisfactorily degassed at the time of laminating pressurization, thereby preventing deterioration of the appearance of the solar cell module and corrosion of the electrode. Adhesive area between the sheet and the adherend increases, and sufficient adhesive strength can be obtained.
- the porosity P can be obtained by the following calculation.
- V A (mm 3 ) t max (mm) ⁇ 10 6 (mm 2 ) (A)
- the actual volume V 0 (mm 3 ) of the first and second sealing material sheets of this unit area is equal to the specific gravity ⁇ (g / mm 3 ) of the resin constituting the first and second sealing material sheets.
- the actual weight W (g) of the first and second sealing material sheets per unit area (1 m 2 ) is calculated by applying the following formula (B).
- V 0 (mm 3 ) W / ⁇ (B)
- the total volume V H (mm 3 ) of the recesses per unit area of the first and second sealing material sheets is expressed as “apparent of the first and second sealing material sheets” as shown in the following formula (C). It is calculated by subtracting “actual volume V 0 ” from “volume V A ”.
- the porosity P (%) can be obtained by the above formula, but the actual first and second encapsulant sheet cross-sections and embossed surfaces should be microscopically photographed and subjected to image processing, etc. Can also be obtained.
- the first sealing material sheet and the second sealing material that are not cross-linked at the time of manufacturing.
- the storage elastic modulus is important in the temperature environment of 90 ° C. to 160 ° C. applied to the sheet, particularly in the environment of 120 ° C. where the resin becomes flexible, and it is important to satisfy the above-described (Equation 1).
- the storage elastic modulus and the linear expansion coefficient of the first sealing material sheet after the crosslinking treatment Suppresses the stress applied to the solar cell elements and wiring materials by the first and second encapsulant sheets when manufacturing the battery module, further suppresses cracking of the solar cell elements and disconnection of the wiring materials, and is less susceptible to temperature cycles.
- a battery module can be provided.
- the 1st sealing material sheet 11 with a some sealing material sheet.
- the storage elastic modulus (P 1 ) of the first sealing material sheet 11 before the crosslinking treatment, the storage elastic modulus (G 1 ) after the crosslinking treatment, the linear expansion coefficient ( ⁇ 1 ), and the linear expansion coefficient ( ⁇ 2). ) Can obtain the values of Formula 1 and Formula 2 from the respective measured values and sheet thicknesses of the individual sheets constituting the first sealing material sheet 11.
- the relationship between the storage elastic modulus (P 1 ) before the cross-linking treatment and the storage elastic modulus (P 2 ) before the cross-linking treatment of the second sealing material sheet in the case of Di is expressed by the following equation (3 ) Can be expressed as:
- FIG. 1 one Embodiment of the solar cell module 10 of this invention is typically shown.
- the solar cell module 10 of the present embodiment is obtained using the above-described solar cell sealing sheet set of the present embodiment.
- the solar cell module 10 includes, for example, a solar cell element 16 formed of polycrystalline silicon or the like, a pair of light-receiving surface side first sealing material sheets 11 that are sealed with the solar cell element 16 interposed therebetween, and a back surface side of the first sealing material sheet 11.
- seat) 13 are provided.
- the solar cell module 10 of the present embodiment includes a solar cell module protective sheet (light-receiving surface side protective member 14) / first sealing material sheet 11 / solar cell element 16 / second sealing material sheet 12 / solar cell.
- the module protective sheet (back surface side protective member 13) is configured.
- the solar cell module 10 of the present embodiment is not limited to the above-described configuration, and a part of each of the above layers is appropriately omitted or a layer other than the above is appropriately provided as long as the object of the present invention is not impaired. be able to.
- the layer other than the above include an adhesive layer, a shock absorbing layer, a coating layer, an antireflection layer, a back surface rereflection layer, and a light diffusion layer.
- the interconnector (wiring material 15) that connects the plurality of solar cell elements 16 may exist on the first sealing material sheet 11 side, or the second sealing material. It may exist in the sheet 12 or may exist over both sealing materials.
- seat set for solar cell sealing which concerns on this embodiment is a sealing layer
- crosslinking the 1st sealing material sheet 11 is a 1st sealing layer
- a 2nd sealing material sheet A layer formed by crosslinking 12 is also referred to as a second sealing layer.
- solar cell element 16 examples include silicon systems such as single crystal silicon, polycrystalline silicon, and amorphous silicon, and III-V and II-VI compound semiconductor systems such as gallium-arsenic, copper-indium-selenium, and cadmium-tellurium Various solar cell elements such as can be used.
- the plurality of solar cell elements 16 are electrically connected in series via a wiring material 15 having a conducting wire and a solder joint.
- Examples of the light receiving surface side protection member 14 include a glass plate; a resin plate formed of acrylic resin, polycarbonate, polyester, fluorine-containing resin, or the like.
- back surface side protection member 13 examples include single or multilayer sheets such as metals and various thermoplastic resin films. Examples thereof include metals such as tin, aluminum, and stainless steel; inorganic materials such as glass; various thermoplastic resin films formed of polyester, inorganic material-deposited polyester, fluorine-containing resin, polyolefin, and the like.
- the back surface side protection member 13 may be a single layer or a multilayer.
- a glass plate is used as the light-receiving surface side protection member 14 and a thermoplastic resin film is used as the back surface side protection member 13
- bending, fatigue, disconnection, or the like of the wiring material in the solar cell module is likely to occur. Therefore, when a glass plate is used as the light-receiving surface side protection member 14 and a thermoplastic resin film is used as the back surface side protection member 13, the solar cell sealing sheet set according to the present embodiment is used as a sealing layer. It is particularly effective.
- the wiring material 15 is usually an interconnector that connects a plurality of solar cell elements.
- Examples of the wiring material 15 include metal foils such as aluminum foil and copper foil.
- the manufacturing method of the solar cell module 10 of this embodiment is not specifically limited, For example, the following method is mentioned.
- a plurality of solar cell elements 16 electrically connected using the wiring material 15 are sandwiched between the first sealing material sheet 11 and the second sealing material sheet 12, and further, these first sealing material sheet 11 and second
- the sealing material sheet 12 is sandwiched between the light receiving surface side protection member 14 and the back surface side protection member 13 to produce a laminate.
- the laminated body is heated, and the first sealing material sheet 11 and the second sealing material sheet 12, the first sealing material sheet 11 and the light receiving surface side protection member 14, the second sealing material sheet 12 and the back surface side.
- the protective member 13 is bonded.
- the organic peroxide may be heated at a half-life temperature of one minute for 5 to 10 minutes. For example, if the one-minute half-life temperature of the organic peroxide is 160 ° C., the laminate may be heated at 160 ° C. for 5 to 10 minutes.
- MFR Based on ASTM D1238, MFR of ethylene / ⁇ -olefin copolymer and ethylene / vinyl acetate copolymer was measured under the conditions of 190 ° C. and 2.16 kg load.
- the cross-linking treatment of the encapsulant sheet is performed by laminating the encapsulant sheet into a size of 10 cm ⁇ 10 cm, and then laminating under conditions of 150 ° C., vacuum pressure 250 Pa for 3 minutes, and pressurization pressure 100 kPa for 15 minutes.
- the measurement was performed using an apparatus (LM-110X160S manufactured by NPC).
- the cross-linking treatment of the encapsulant sheet is performed by laminating the encapsulant sheet into a size of 10 cm ⁇ 10 cm, and then laminating under conditions of 150 ° C., vacuum pressure 250 Pa for 3 minutes, and pressurization pressure 100 kPa for 15 minutes.
- the measurement was performed using an apparatus (LM-110X160S manufactured by NPC).
- FIG. 2 is a cross-sectional view schematically showing the laminate 20 used for the evaluation of the deflection amount.
- the glass 22 a 3.2 mm thick blue plate glass manufactured by Asahi Glass Fabricate Co., Ltd. cut to 12 ⁇ 7.5 cm was used.
- As an element for evaluating deflection two pieces of 0.3 mm thick aluminum plate 23 (3 cm ⁇ 2 cm) are provided on a 0.1 mm thick PET film 24 cut to 4.2 cm ⁇ 3 cm with a spacing of 2 mm. What was bonded and produced was used.
- the first sealing material sheet 11 and the second sealing material sheet 12 are arranged on the glass 22 so as to sandwich the element for evaluating the deflection, and cut into 13 ⁇ 8 cm as a back sheet (back side protection member).
- a 25 mm PET film 21 was laminated on the upper surface of the second sealing material sheet 12.
- the resulting laminate 20 was laminated with the glass 22 side down using a vacuum laminator (NPC: LM-110x160-S) at a hot platen temperature of 150 ° C., a vacuum time of 3 minutes, and a pressurization time of 15 minutes. . Then, the 1st sealing material sheet 11, the 2nd sealing material sheet 12, and the PET film 21 which protruded from the glass 22 were cut.
- NPC vacuum laminator
- the laminate 20 was cut in a cross section where the deflection of the 2 mm PET film 24 between the aluminum plates 23 could be confirmed, and the amount of deflection of the PET film 24 was measured with a microscope. The amount of deflection was based on the plane of the aluminum plate 23, and the maximum value when the PET film 24 was pressed between the aluminum plates 23 was measured.
- FIG. 3 is a cross-sectional view schematically showing a pseudo module 30A used in the temperature cycle test in Examples and Comparative Examples.
- FIG. 4 is a front view schematically showing the pseudo module 30A used in the temperature cycle test in Examples and Comparative Examples.
- Laminate 30A obtained was laminated with the glass 22 side down using a vacuum laminator (NPC: LM-110x160-S) at a hot platen temperature of 150 ° C., a vacuum time of 3 minutes, and a pressurization time of 15 minutes. did.
- the obtained pseudo module was put into a temperature cycle test tank having a cycle of ⁇ 40 ° C. ⁇ 1 hour, temperature increase of 2 hours, and 90 ° C.
- Ethylene / vinyl acetate copolymer (EVA) As the ethylene / vinyl acetate copolymer (EVA) used in Examples and Comparative Examples, a vinyl acetate content of 27% by mass and MFR of 16.8 g / 10 min was used.
- the ethylene / ⁇ -olefin copolymer normal hexane / toluene mixed solution produced in the polymerization vessel is continuously discharged through a discharge port provided at the bottom of the polymerization vessel, and the ethylene / ⁇ -olefin copolymer solution is discharged.
- the jacket portion was led to a connecting pipe heated with 3 to 25 kg / cm 2 steam so that the normal hexane / toluene mixed solution had a temperature of 150 to 190 ° C.
- a supply port for injecting methanol, which is a catalyst deactivator, is attached, and methanol is injected at a rate of about 0.75 L / hr.
- the mixture was merged into a combined normal hexane / toluene mixed solution.
- the normal hexane / toluene mixed solution of the ethylene / ⁇ -olefin copolymer kept at about 190 ° C. in the connection pipe with steam jacket is subjected to pressure provided at the end of the connection pipe so as to maintain about 4.3 MPaG.
- the liquid was continuously fed to the flash tank by adjusting the opening of the control valve. In the transfer to the flash tank, the solution temperature and the pressure adjustment valve opening are set so that the pressure in the flash tank is about 0.1 MPaG and the temperature of the vapor part in the flash tank is maintained at about 180 ° C. It was broken.
- the strand was cooled in a water tank through a single screw extruder set at a die temperature of 180 ° C., and the strand was cut with a pellet cutter to obtain an ethylene / ⁇ -olefin copolymer as pellets.
- the yield was 2.2 kg / hr.
- the physical properties are shown in Table 1.
- Various evaluation results of the obtained sealing material sheet are shown in Table 2.
- the present invention includes the following aspects.
- Appendix 1 The solar cell element and the wiring material arranged between the light receiving surface side protection member and the back surface side protection member, and the first sealing after the crosslinking treatment disposed on the light receiving side used for sealing them It is a sheet set for sealing a solar cell consisting of a second sealing material after crosslinking treatment arranged on the material and the back surface side, Storage of the first sealing material before cross-linking treatment at 120 ° C. when the solid viscoelasticity is measured under conditions of a measurement temperature range of 25 to 150 ° C., a frequency of 1.0 Hz, a heating rate of 10 ° C./min, and a shear mode.
- a sheet set for sealing a solar cell wherein the elastic modulus (P 1 ) and the storage elastic modulus (P 2 ) of the second sealing material before the crosslinking treatment are in the relationship of the following formula (1).
- (Appendix 2) Storage of the first sealing material after the crosslinking treatment at 90 ° C. when the solid viscoelasticity is measured under the conditions of a measurement temperature range of 25 to 150 ° C., a frequency of 1.0 Hz, a heating rate of 10 ° C./min, and a shear mode. modulus and (G 1), the linear expansion coefficient at -40 ° C. ⁇ 0 ° C.
- the sheet set for sealing a solar cell according to appendix 1. (Appendix 3) 3.
- Appendix 4 A solar cell module comprising the solar cell sealing sheet set according to any one of appendices 1 to 3.
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Abstract
Description
次に、結晶型太陽電池モジュールを得るには、太陽電池モジュール用保護シート(受光面側保護部材)/太陽電池封止材/結晶型太陽電池素子/太陽電池封止材/太陽電池モジュール用保護シート(裏面側保護部材)の順に積層する。
一方、薄膜型太陽電池モジュールを得るには、薄膜型太陽電池素子/太陽電池封止材/太陽電池モジュール用保護シート(裏面側保護部材)の順に積層する。
その後、これらを真空吸引して加熱圧着するラミネーション法等を利用することにより、太陽電池モジュールが製造される。このようにして製造される太陽電池モジュールは、耐候性を有し、建物の屋根部分等の屋外での使用にも適したものとなっている。
また、比較的短時間で架橋して十分な接着力を有し、剛性と架橋特性のバランスに優れるエチレン・α-オレフィン共重合体を用いた太陽電池封止材用樹脂組成物も提案されている(例えば、特許文献3参照)。
受光面側保護部材と裏面側保護部材との間に配置させて、太陽電池素子および配線材料を封止するために用いられ、かつ、受光面側に配置される第一封止材シートと裏面側に配置される第二封止材シートとを備える太陽電池封止用シートセットであって、
測定温度範囲25℃~180℃、周波数1.0Hz、昇温速度10℃/分、ずりモードの条件での固体粘弾性を測定したときの120℃における、架橋処理前の上記第一封止材シートの貯蔵弾性率(P1)と架橋処理前の上記第二封止材シートの貯蔵弾性率(P2)が、下式(1)の関係を満たす太陽電池封止用シートセット。
測定温度範囲25℃~180℃、周波数1.0Hz、昇温速度10℃/分、ずりモードの条件での固体粘弾性を測定したときの90℃における、架橋処理後の上記第一封止材シートの貯蔵弾性率(G1)と、
架橋処理後の上記第一封止材シートの-40℃~0℃における線膨張係数(α1)と、
架橋処理後の上記第一封止材シートの50℃~90℃における線膨張係数(α2)と、
が下式(2)を満たす上記[1]に記載の太陽電池封止用シートセット。
架橋処理後の上記第一封止材シートおよび架橋処理後の上記第二封止材シートの厚みがそれぞれ0.2~1mmである、上記[1]または[2]に記載の太陽電池封止用シートセット。
[4]
上記第一封止材シートおよび上記第二封止材シートの少なくとも一方が、架橋性樹脂として、エチレン・α-オレフィン共重合体およびエチレン・酢酸ビニル共重合体からなる群から選択される一種または二種以上を含む上記[1]乃至[3]いずれか一つに記載の太陽電池封止用シートセット。
[5]
上記第一封止材シートおよび上記第二封止材シートの少なくとも一方が、有機過酸化物を含み、上記有機過酸化物の含有量が、上記架橋性樹脂100質量部に対して、0.1質量部以上1.2質量部以下である上記[4]に記載の太陽電池封止用シートセット。
[6]
上記貯蔵弾性率(P1)が1.0×10-1Pa以上1.2×106Pa以下であり、上記貯蔵弾性率(P2)が、8.0×10-2Pa以上1.0×106Pa以下である上記[1]乃至[5]いずれか一つに記載の太陽電池封止用シートセット。
[7]
上記受光面側保護部材がガラス板であり、上記裏面側保護部材が熱可塑性樹脂フィルムである上記[1]乃至[6]いずれか一つに記載の太陽電池封止用シートセット。
[8]
上記[1]乃至[7]いずれか一つに記載の太陽電池封止用シートセットを用いてなる太陽電池モジュール。
[9]
上記[8]に記載の太陽電池モジュールにおいて、
受光面側保護部材と裏面側保護部材との間に封止層を有し、該封止層内に太陽電池素子が封止されてなり、
上記封止層が上記太陽電池封止用シートセットにより形成されたものであり、
上記封止層は、第一封止層と第二封止層とを有し、
上記第一封止層が、上記第一封止材シートを架橋させてなり、
上記第二封止層が、上記第二封止材シートを架橋させてなり、
上記第一封止層が上記受光面側保護部材と上記太陽電池素子との間に設けられており、
上記第二封止層が上記裏面側保護部材と上記太陽電池素子との間に設けられている太陽電池モジュール。
[10]
上記受光面側保護部材がガラス板であり、上記裏面側保護部材が熱可塑性樹脂フィルムである上記[9]に記載の太陽電池モジュール。
さらに、本発明によれば、温度サイクルの影響を受けにくい太陽電池モジュールを提供することができる。
本実施形態の太陽電池モジュール10は、受光面側に配置される第一封止材シート11と、裏面側に配置される第二封止材シート12の一対の太陽電池封止用シートセットからなる封止層1、受光面側保護部材14、裏面側保護部材13、太陽電池素子16、および配線材料15(インターコネクタ)を備える。
なお、本実施形態において、第一封止材シート11および第二封止材シート12をまとめて「第一、第二封止材シート」とも呼ぶ。
<太陽電池封止用シートセット>
本実施形態の太陽電池封止用シートセットは、受光面側保護部材14と裏面側保護部材13との間に配置させて、太陽電池素子16および配線材料15を封止するために用いられ、かつ、受光面側に配置される第一封止材シート11と裏面側に配置される第二封止材シート12とを備える。第一封止材シート11と第二封止材シート12の、測定温度範囲25℃~180℃、周波数1.0Hz、昇温速度10℃/分、ずりモードの条件での固体粘弾性を測定したときの120℃での各々の貯蔵弾性率(P1)と貯蔵弾性率(P2)の関係が式(1)の関係を満たす。式(1a)の関係を満たすことがより好ましく、式(1b)の関係を満たすことがさらに好ましい。
50℃~90℃における、架橋処理後の第一封止材シート11の線膨張係数(α2)は、好ましくは1×10-6~5000×10-6/℃であり、好ましくは10×10-6~1000×10-6/℃であり、さらに好ましくは10×10-6~500×10-6/℃である。上記範囲にあることにより、太陽電池素子の割れや配線材料の断線をより一層抑制し、温度サイクルの影響をより一層受け難い太陽電池モジュールを提供することができる。
本実施形態における太陽電池封止用シートセットは受光面側に配置される第一封止材シート11と、裏面側に配置される第二封止材シート12とを備える。第一、第二封止材シートは、通常、架橋性樹脂を含有する。
上記架橋性樹脂としては、従来公知の樹脂を用いることができる。例えば、エチレンおよび炭素数3~20のα-オレフィンを含むエチレン・α-オレフィン共重合体、高密度エチレン系樹脂、低密度エチレン系樹脂、中密度エチレン系樹脂、超低密度エチレン系樹脂、プロピレン(共)重合体、1-ブテン(共)重合体、4-メチルペンテン-1(共)重合体、エチレン・環状オレフィン共重合体、エチレン・α-オレフィン・環状オレフィン共重合体、エチレン・α-オレフィン・非共役ポリエン共重合体、エチレン・α-オレフィン・共役ポリエン共重合体、エチレン・芳香族ビニル共重合体、エチレン・α-オレフィン・芳香族ビニル共重合体等のオレフィン系樹脂;エチレン・不飽和無水カルボン酸共重合体、エチレン・α-オレフィン・不飽和無水カルボン酸共重合体等のエチレン・無水カルボン酸系共重合体;エチレン・エポキシ含有不飽和化合物共重合体、エチレン・α-オレフィン・エポキシ含有不飽和化合物共重合体等のエチレン・エポキシ系共重合体;エチレン・酢酸ビニル共重合体等のエチレン・ビニルエステル共重合体;エチレン・アクリル酸共重合体、エチレン・メタアクリル酸共重合体等のエチレン・不飽和カルボン酸共重合体;エチレン・アクリル酸エチル共重合体、エチレン・メタアクリル酸メチル共重合体等のエチレン・不飽和カルボン酸エステル共重合体;(メタ)アクリル酸エステル(共)重合体等の不飽和カルボン酸エステル(共)重合体;エチレン・アクリル酸金属塩共重合体、エチレン・メタアクリル酸金属塩共重合体等のアイオノマー樹脂;ウレタン系樹脂;シリコーン系樹脂;アクリル酸系樹脂;メタアクリル酸系樹脂;環状オレフィン(共)重合体;α-オレフィン・芳香族ビニル化合物・芳香族ポリエン共重合体;エチレン・α-オレフィン・芳香族ビニル化合物・芳香族ポリエン共重合体;エチレン・芳香族ビニル化合物・芳香族ポリエン共重合体;スチレン系樹脂;アクリロニトリル・ブタジエン・スチレン共重合体、スチレン・共役ジエン共重合体、アクリロニトリル・スチレン共重合体、アクリロニトリル・エチレン・α-オレフィン・非共役ポリエン・スチレン共重合体、アクリロニトリル・エチレン・α-オレフィン・共役ポリエン・スチレン共重合体、メタアクリル酸・スチレン共重合体等のスチレン系共重合体樹脂;エチレンテレフタレート樹脂;フッ素樹脂;ポリエステルカーボネート;ポリ塩化ビニル、ポリ塩化ビニリデン等の塩素系樹脂;ポリオレフィン系熱可塑性エラストマー、ポリスチレン系熱可塑性エラストマー、ポリウレタン系熱可塑性エラストマー、1,2-ポリブタジエン系熱可塑性エラストマー、トランスポリイソプレン系熱可塑性エラストマー、塩素化ポリエチレン系熱可塑性エラストマー等の熱可塑性エラストマー;液晶性ポリエステル;ポリ乳酸等から選択される一種または二種以上を用いることができる。
上記架橋性樹脂として用いられる、エチレンおよび炭素数3~20のα-オレフィンからなるエチレン・α-オレフィン共重合体のα-オレフィンとしては、通常、炭素数3~20のα-オレフィンを1種類単独でまたは2種類以上を組み合わせて用いることができる。中でも好ましいのは、炭素数が10以下であるα-オレフィンであり、とくに好ましいのは炭素数が3~8のα-オレフィンである。このようなα-オレフィンの具体例としては、プロピレン、1-ブテン、1-ペンテン、1-ヘキセン、3-メチル-1-ブテン、3,3-ジメチル-1-ブテン、4-メチル-1-ペンテン、1-オクテン、1-デセン、1-ドデセン等を挙げることができる。これらの中でも、入手の容易さからプロピレン、1-ブテン、1-ペンテン、1-ヘキセン、4-メチル-1-ペンテンおよび1-オクテンから選択される一種または二種以上を用いることが好ましい。なお、エチレン・α-オレフィン共重合体はランダム共重合体であっても、ブロック共重合体であってもよいが、柔軟性の観点からランダム共重合体が好ましい。
上記エチレン・α-オレフィン共重合体は、以下の要件a1およびa2をさらに満たすことが好ましい。
エチレン・α-オレフィン共重合体の密度は、エチレン単位の含有割合とα-オレフィン単位の含有割合とのバランスにより調整することができる。すなわち、エチレン単位の含有割合を高くすると結晶性が高くなり、密度の高いエチレン・α-オレフィン共重合体を得ることができる。一方、エチレン単位の含有割合を低くすると結晶性が低くなり、密度の低いエチレン・α-オレフィン共重合体を得ることができる。
エチレン・α-オレフィン共重合体のMFRは、重合反応の際の重合温度、重合圧力、並びに重合系内のエチレンおよびα-オレフィンのモノマー濃度と水素濃度のモル比率等を調整することにより、調整することができる。
太陽電池モジュールのラミネート工程において第一、第二封止材シートの架橋処理を行わない場合は、溶融押出工程において有機過酸化物の分解の影響が小さいため、MFRが0.1g/10分以上10g/10分未満、好ましくは0.5g/10分以上8.5g/10分未満の樹脂組成物を用い、押出成形によってシートを得ることもできる。樹脂組成物の有機過酸化物の含有量が0.15質量部以下である場合には、MFRが0.1g/10分以上10g/10分未満の樹脂組成物を用い、シラン変性処理、または微架橋処理を行いつつ170~250℃の成形温度で押出成形によってシートを製造することもできる。MFRがこの範囲にあるとシートを太陽電池素子とラミネートする際にはみ出した溶融樹脂によるラミネート装置の汚れを防止できる点で好ましい。
上記架橋性樹脂として用いられるエチレン・酢酸ビニル共重合体のメルトフローレ-ト(MFR)は好ましくは5~50g/10分、より好ましくは5~30g/10分、さらに好ましくは5~25g/10分である。エチレン・酢酸ビニル共重合体のMFRが上記範囲であると、押出成形性が優れる。エチレン・酢酸ビニル共重合体のMFRは、重合反応の際の重合温度、重合圧力、並びに重合系内の極性モノマーのモノマー濃度と水素濃度のモル比率等を調整することにより、調整することができる。
本実施形態において、エチレン・酢酸ビニル共重合体のMFRは、ASTM D1238に準拠し、190℃、2.16kg荷重の条件で測定されるものである。
本実施形態の太陽電池封止用シートセットにおいて、第一封止材シート11に含まれる架橋性樹脂のMFRが、第二封止材シート12に含まれる架橋性樹脂のMFRよりも小さいことが好ましい。具体的には、(第一封止材シート11に含まれる架橋性樹脂のMFR)/(第二封止材シート12に含まれる架橋性樹脂のMFR)で表されるMFR比が1.0未満であることが好ましく、0.8以下であることがより好ましく、0.6以下であることがさらに好ましい。
MFR比が上記範囲であることにより、120℃での各々の貯蔵弾性率(P1)と貯蔵弾性率(P2)の関係が上述した式(1)の関係を満たし、第一、第二封止材シート間に設置される太陽電池モジュールのインターコネクタのたわみや応力集中がより一層起きにくくなる。
本実施形態の太陽電池封止用シートセットにおいて、第一封止材シート11および第二封止材シート12の双方にエチレン・酢酸ビニル共重合体を用いる場合、第一封止材シート11の酢酸ビニル含量が、第二封止材シート12のそれよりも小さいことが好ましい。
具体的には、(第一封止材シート11の酢酸ビニル含量)/(第二封止材シート12の酢酸ビニル含量)で表されるVA比が1.0未満であることが好ましく、0.9以下であることがより好ましく、0.8以下であることがさらに好ましい。
酢酸ビニル含量の比が上記範囲であることにより、120℃での各々の貯蔵弾性率(P1)と貯蔵弾性率(P2)の関係が上述した式(1)の関係を満たし、第一、第二封止材シート間に設置される太陽電池モジュールのインターコネクタのたわみや応力集中がより一層起きにくくなる。
第一封止材シート11がエチレン・酢酸ビニル共重合体を含み、第二封止材シート12がエチレン・α-オレフィン共重合体を含み、かつ、上記したMFR比が1.0未満であることが特に好ましい。
第一封止材シート11がエチレン・α-オレフィン共重合体を含み、第二封止材シート12がエチレン・酢酸ビニル共重合体を含み、かつ、上記したMFR比が1.0未満であり、さらに第一封止材シート11を構成するエチレン・α-オレフィン共重合体のMFRが10g/10min以下、さらには8g/10min以下であることが特に好ましい。
第一、第二封止材シートは、シランカップリング剤を含有してもよい。このシランカップリング剤を含有することにより、第一、第二封止材シートと他の部材との接着強度を優れたものにすることができる。第一、第二封止材シート中のシランカップリング剤の含有量は、架橋性樹脂100質量部に対して、好ましくは0.1~2質量部、より好ましくは0.1~1.8質量部、特に好ましくは0.1~1.5質量部である。シランカップリング剤の含有量が上記範囲内であると、第一、第二封止材シートの接着性を向上させつつ、より確実に第一、第二封止材シート中に気泡が発生するのを抑制することができる。
これらの中でも、接着性向上の観点から、3-グリシドキシプロピルトリメトキシシラン、3-グリシドキシプロピルトリエトキシシラン、3-アミノプロピルトリエトキシシラン、3-メタクリロキシプロピルトリメトキシシラン、3-メタクリロキシプロピルトリエトキシシラン、3-アクリロキシプロピルトリメトキシシラン、ビニルトリエトキシシランから選択される一種または二種以上を用いることが好ましい。
第一、第二封止材シートは有機過酸化物を含有することが好ましい。上記有機過酸化物は、押出シート成形での生産性と太陽電池モジュールのラミネート成形時の架橋速度のバランスから、有機過酸化物の1分間半減期温度が100~170℃であるものが好ましい。有機過酸化物の1分間半減期温度が100℃以上であると、シート成形を容易にし、かつ、第一、第二封止材シートの外観を良好にすることができる。また、絶縁破壊電圧の低下を防ぐことができ、透湿性の低下も防止でき、さらに接着性も向上する。有機過酸化物の1分間半減期温度が170℃以下であると、太陽電池モジュールのラミネート成形時の架橋速度の低下を抑制できるため、太陽電池モジュールの生産性の低下を防ぐことができる。また、第一、第二封止材シートの耐熱性、接着性の低下を防ぐこともできる。
これらの中でも、ジラウロイルパーオキサイド、t-ブチルパーオキシイソプロピルカーボネート、t-ブチルパーオキシアセテート、t-ブチルパーオキシイソノナノエート、t-ブチルパーオキシ-2-エチルヘキシルカーボネート、t-ブチルパーオキシベンゾエートから選択される一種または二種以上を用いることが好ましい。
第一、第二封止材シートには、紫外線吸収剤、光安定化剤、および耐熱安定剤からなる群より選択される少なくとも一種の添加剤が含有されることが好ましく、少なくとも二種の添加剤を含有することがより好ましく、上記三種の全てが含有されていることがさらに好ましい。
第一、第二封止材シートは架橋助剤を含有することが好ましい。第一、第二封止材シート中の架橋助剤の含有量は、架橋性樹脂100質量部に対して、好ましくは0.05~5質量部である。これにより、第一、第二封止材シートを適度な架橋構造とすることができ、第一、第二封止材シートの耐熱性、機械物性、および接着性を向上できる。
これらの架橋助剤の中でも、ジアクリレート;ジメタクリレート;ジビニル芳香族化合物;トリメチロールプロパントリアクリレート、テトラメチロールメタントリアクリレート、ペンタエリスリトールトリアクリレート等のトリアクリレート;トリメチロールプロパントリメタクリレート、トリメチロールエタントリメタクリレート等のトリメタクリレート;ペンタエリスリトールテトラアクリレート、テトラメチロールメタンテトラアクリレート等のテトラアクリレート;トリアリルシアヌレート、トリアリルイソシアヌレート等のシアヌレート;ジアリルフタレート等のジアリル化合物;トリアリル化合物;p-キノンジオキシム、p-p'-ジベンゾイルキノンジオキシム等のオキシム;フェニルマレイミド等のマレイミドから選択される一種または二種以上を用いることが好ましい。さらにこれらの中でも、第一、第二封止材シート中の気泡の発生をより抑制できるとともに、架橋特性に優れる点から、トリアリルイソシアヌレートが特に好ましい。
第一、第二封止材シートには、以上詳述した諸成分以外の各種成分を、本発明の目的を損なわない範囲において、適宜含有させることができる。例えば、上記架橋性樹脂以外の各種ポリオレフィン、スチレン系やエチレン系ブロック共重合体、プロピレン系重合体等が挙げられる。これらは,架橋性樹脂100質量部に対して、0.0001~50質量部、好ましくは0.001~40質量部含有させることができる。また、ポリオレフィン以外の各種樹脂、および/または各種ゴム、可塑剤、充填剤、顔料、染料、帯電防止剤、抗菌剤、防黴剤、難燃剤、および分散剤等から選ばれる一種以上の添加剤を適宜含有することができる。
第一、第二封止材シートの製造方法としては通常用いられている方法が利用できるが、カレンダーロール、ニーダー、バンバリミキサー、押出機等により溶融ブレンドすることにより製造することが好ましい。とくに、連続生産が可能な押出機での製造が好ましい。
VA(mm3)=tmax(mm)×106(mm2) (A)
一方、この単位面積の第一、第二封止材シートの実際の体積V0(mm3)は、第一、第二封止材シートを構成する樹脂の比重ρ(g/mm3)と単位面積(1m2)当りの第一、第二封止材シートの実際の重さW(g)と、を下記式(B)に当てはめることにより算出される。
V0(mm3)=W/ρ (B)
第一、第二封止材シートの単位面積当りの凹部の合計体積VH(mm3)は、下記式(C)に示されるように、「第一、第二封止材シートの見掛けの体積VA」から「実際の体積V0」を差し引くことによって算出される。
VH(mm3)=VA-V0=VA-(W/ρ) (C)
したがって、空隙率P(%)は次のようにして求めることができる。
空隙率P(%)=VH/VA×100
=(VA-(W/ρ))/VA×100
=1-W/(ρ・VA)×100
=1-W/(ρ・tmax・106)×100
図1に、本発明の太陽電池モジュール10の一実施形態を模式的に示す。
本実施形態の太陽電池モジュール10は、上記した本実施形態の太陽電池封止用シートセットを用いて得られる。太陽電池モジュール10は、例えば、多結晶シリコン等により形成された太陽電池素子16と、太陽電池素子16を挟んで封止する一対の受光面側の第一封止材シート11および裏面側の第二封止材シート12と、受光面側保護部材14と、裏面側保護部材(バックシート)13とを備える。
すなわち、本実施形態の太陽電池モジュール10は、太陽電池モジュール用保護シート(受光面側保護部材14)/第一封止材シート11/太陽電池素子16/第二封止材シート12/太陽電池モジュール用保護シート(裏面側保護部材13)という構成になっている。ただし、本実施形態の太陽電池モジュール10は、上記の構成には限定されず、本発明の目的を損なわない範囲で、上記の各層の一部を適宜省略し、または上記以外の層を適宜設けることができる。上記以外の層としては、例えば接着層、衝撃吸収層、コーティング層、反射防止層、裏面再反射層、光拡散層等を挙げることができる。これらの層は、とくに限定はされないが、各層を設ける目的や特性を考慮して、適切な位置に設けることができる。本実施形態の太陽電池モジュール10においては、複数の太陽電池素子16を連結するインターコネクタ(配線材料15)は、第一封止材シート11側に存在してもよいし、第二封止材シート12に存在してもよいし、両封止材にまたがって存在してもよい。
なお、本実施形態に係る太陽電池封止用シートセットにより形成された層を封止層、第一封止材シート11を架橋させてなる層を第一封止層、第二封止材シート12を架橋させてなる層を第二封止層とも呼ぶ。
太陽電池素子16としては、単結晶シリコン、多結晶シリコン、アモルファスシリコン等のシリコン系、ガリウム-砒素、銅-インジウムーセレン、カドミウム-テルル等のIII-V族やII-VI族化合物半導体系等の各種太陽電池素子を用いることができる。
太陽電池モジュール10においては、複数の太陽電池素子16は、導線および半田接合部を備えた配線材料15を介して電気的に直列に接続されている。
受光面側保護部材14としては、ガラス板;アクリル樹脂、ポリカーボネート、ポリエステル、フッ素含有樹脂等により形成された樹脂板;等が挙げられる。
裏面側保護部材13としては、金属や各種熱可塑性樹脂フィルム等の単体もしくは多層のシートが挙げられる。例えば、錫、アルミ、ステンレススチール等の金属;ガラス等の無機材料;ポリエステル、無機物蒸着ポリエステル、フッ素含有樹脂、ポリオレフィン等により形成された各種熱可塑性樹脂フィルム等が挙げられる。
裏面側保護部材13は、単層であってもよく、複層であってもよい。
ここで、受光面側保護部材14としてガラス板を使用し、裏面側保護部材13として熱可塑性樹脂フィルムを使用した場合、太陽電池モジュールにおける配線材料のたわみや疲労、断線等が起こりやすい。そのため、受光面側保護部材14としてガラス板を使用し、裏面側保護部材13として熱可塑性樹脂フィルムを使用した場合、本実施形態に係る太陽電池封止用シートセットを封止層として用いることが特に効果的である。
配線材料15は、通常、複数の太陽電池素子を連結するインターコネクタである。
配線材料15としては、アルミ箔、銅箔等の金属箔が挙げられる。
本実施形態の太陽電池モジュール10の製造方法は特に限定されないが、例えば、以下の方法が挙げられる。
まず、配線材料15を用いて電気的に接続した複数の太陽電池素子16を第一封止材シート11と第二封止材シート12で挟み、さらにこれら第一封止材シート11と第二封止材シート12を受光面側保護部材14と裏面側保護部材13とで挟んで積層体を作製する。次いで、積層体を加熱して、第一封止材シート11と第二封止材シート12、第一封止材シート11と受光面側保護部材14、第二封止材シート12と裏面側保護部材13とを接着する。
なお、積層体を加熱する際の条件としては、有機過酸化物の一分間半減期温度にて5~10分間に亘って加熱すればよい。例えば、有機過酸化物の一分間半減期温度が160℃であれば、160℃にて5~10分間に亘って積層体を加熱すればよい。
[エチレン・α-オレフィン共重合体のエチレン単位およびα-オレフィン単位の含有割合]
試料0.35gをヘキサクロロブタジエン2.0mlに加熱溶解させて得られた溶液をグラスフィルター(G2)濾過した後、重水素化ベンゼン0.5mlを加え、内径10mmのNMRチューブに装入した。日本電子社製のJNM GX-400型NMR測定装置を使用し、120℃で13C-NMR測定を行った。積算回数は8000回以上とした。得られた13C-NMRスペクトルより、共重合体中のエチレン単位の含有割合、およびα-オレフィン単位の含有割合を定量した。
ASTM D1238に準拠し、190℃、2.16kg荷重の条件にてエチレン・α-オレフィン共重合体およびエチレン・酢酸ビニル共重合体のMFRを測定した。
ASTM D1505に準拠して、エチレン・α-オレフィン共重合体の密度を測定した。
封止材シートのサンプルを、ずりモードでの固体粘弾性装置(ReoStress、HAAKE製)で、25℃(室温)~180℃まで1.0Hzの周波数、10℃/分の昇温速度にて測定した。なお、プレートは20mmφのディスポータブルのパラレルプレートを用い、ひずみ制御は0.01で行った。これにより、架橋処理前の封止材シートの120℃における貯蔵弾性率(P)および架橋処理後の封止材シートの90℃における貯蔵弾性率(G1)をそれぞれ算出した。
ここで、封止材シートの架橋処理は、封止材シートをそれぞれ10cm×10cmのサイズに裁断した後、150℃、真空圧250Paで3分、加圧圧力100kPaで15分の条件下、ラミネート装置(NPC社製、LM-110X160S)を用いておこなった。
エス・エス・アイナノテクノロジー社製の熱機械分析測定装置TMA-SS6100を使用し、窒素雰囲気下、試験荷重3gf、昇温速度5℃/分、温度範囲-40℃から90℃、フィルム伸長モードの条件にて、架橋処理後の封止材シートの線膨張係数を測定した。これにより、-40℃~0℃における架橋処理後の封止材シートの線膨張係数および50℃~90℃における架橋処理後の封止材シートの線膨張係数をそれぞれ算出した。
ここで、封止材シートの架橋処理は、封止材シートをそれぞれ10cm×10cmのサイズに裁断した後、150℃、真空圧250Paで3分、加圧圧力100kPaで15分の条件下、ラミネート装置(NPC社製、LM-110X160S)を用いておこなった。
図2は、たわみ量の評価に用いた積層体20を模式的に示した断面図である。
ガラス22としては、12×7.5cmにカットした旭硝子ファブリテック社製の3.2mm厚みの青板ガラスを用いた。
たわみを評価する素子としては、4.2cm×3cmにカットした0.1mm厚みのPETフィルム24上に、0.3mm厚みのアルミ板23(3cm×2cm)を、2mmの間隔を設けて2枚貼り合わせて作製したものを用いた。
ガラス22上に、たわみを評価する素子を挟むように第一封止材シート11および第二封止材シート12を配置し、バックシート(裏面側保護部材)として13×8cmにカットした0.25mmのPETフィルム21を第二封止材シート12の上面に積層した。得られた積層体20を、ガラス22側を下にして真空ラミネーター(NPC製:LM-110x160-S)を用いて熱盤温度150℃、真空時間3分、加圧時間15分にてラミネートした。その後、ガラス22からはみ出した第一封止材シート11、第二封止材シート12、PETフィルム21をカットした。
○:たわみ量 ≦ 0.160mm
△:0.160mm < たわみ量 ≦ 0.165mm
×:たわみ量 > 0.165mm
図3は、実施例および比較例における温度サイクル試験に用いた擬似モジュール30Aを模式的に示した断面図である。図4は、実施例および比較例における温度サイクル試験に用いた擬似モジュール30Aを模式的に示した正面図である。
ガラス22としては、20×20cmにカットした旭硝子ファブリテック社製の3.2mm厚みの青板ガラスを用いた。
評価用素子として、0.3mm厚みのアルミ板23(4cm×4cm)をそれぞれ2mm間隔で4列×4列並べ、それぞれのアルミ板23の間に、0.05mm厚、1×3cmのアルミ箔31をカプトンテープ32で固定したものを用いた。
ガラス22上に、この評価用素子を挟むように第一封止材シート11および第二封止材シート12を配置し、バックシート(裏面側保護部材)としてPETフィルム21を第二封止材シート12の上面に積層した。
得られた積層体30Aを、ガラス22側を下にして真空ラミネーター(NPC社製:LM-110x160-S)を用いて熱盤温度150℃、真空時間3分、加圧時間15分にてラミネートした。
得られた擬似モジュールを-40℃×1時間、昇温2時間、90℃×1時間を1サイクルとする温度サイクル試験槽に投入し、上記サイクルを2000回おこなった。次いで、2000サイクル後の擬似モジュールの外観を観察した。
○:外観変化無し
△:外観にわずかな変化が認められる(アルミ箔31の変形等)
×:外観変化有り(アルミ箔31の顕著な変形または破断)
測定不能:封止材シートの溶融等の発生により、形状保持困難
(2-1)エチレン・酢酸ビニル共重合体(EVA)
実施例および比較例で用いるエチレン・酢酸ビニル共重合体(EVA)としては、酢酸ビニル含量27質量%、MFR16.8g/10分のものを使用した。
(合成例1)
撹拌羽根を備えた内容積50Lの連続重合器の一つの供給口に、共触媒としてメチルアルミノキサンのトルエン溶液を8.0mmol/hr、主触媒としてビス(1,3-ジメチルシクロペンタジエニル)ジルコニウムジクロライドのヘキサンスラリーを0.025mmol/hr、トリイソブチルアルミニウムのヘキサン溶液を0.5mmol/hrの割合で供給し、触媒溶液と重合溶媒として用いる脱水精製したノルマルヘキサンの合計が20L/hrとなるように脱水精製したノルマルヘキサンを連続的に供給した。同時に重合器の別の供給口に、エチレンを3kg/hr、1-ブテンを15kg/hr、水素を5NL/hrの割合で連続供給し、重合温度90℃、全圧3MPaG、滞留時間1.0時間の条件下で連続溶液重合を行った。重合器で生成したエチレン・α-オレフィン共重合体のノルマルヘキサン/トルエン混合溶液は、重合器の底部に設けられた排出口を介して連続的に排出させ、エチレン・α-オレフィン共重合体のノルマルヘキサン/トルエン混合溶液が150~190℃となるように、ジャケット部が3~25kg/cm2スチームで加熱された連結パイプに導いた。なお、連結パイプに至る直前には、触媒失活剤であるメタノールが注入される供給口が付設されており、約0.75L/hrの速度でメタノールを注入してエチレン・α-オレフィン共重合体のノルマルヘキサン/トルエン混合溶液に合流させた。スチームジャケット付き連結パイプ内で約190℃に保温されたエチレン・α-オレフィン共重合体のノルマルヘキサン/トルエン混合溶液は、約4.3MPaGを維持するように、連結パイプ終端部に設けられた圧力制御バルブの開度の調整によって連続的にフラッシュ槽に送液された。なお、フラッシュ槽内への移送においては、フラッシュ槽内の圧力が約0.1MPaG、フラッシュ槽内の蒸気部の温度が約180℃を維持するように溶液温度と圧力調整バルブ開度設定が行われた。その後、ダイス温度を180℃に設定した単軸押出機を通し、水槽にてストランドを冷却し、ペレットカッターにてストランドを切断し、ペレットとしてエチレン・α-オレフィン共重合体を得た。収量は2.2kg/hrであった。物性を表1に示す。
合成例1の条件を元に、原料供給量等を調整し、表1に示すエチレン・α-オレフィン共重合体を得た。
(製造例1)
エチレン・酢酸ビニル共重合体(EVA)100質量部に対し、シランカップリング剤として3-メタクリロキシプロピルトリメトキシシランを0.5質量部、有機過酸化物として1分間半減期温度が166℃のt-ブチルパーオキシ-2-エチルヘキシルカーボネートを1.0質量部、架橋助剤としてトリアリルイソシアヌレートを1.2質量部、紫外線吸収剤として2-ヒドロキシ-4-ノルマル-オクチルオキシベンゾフェノンを0.3質量部、光安定化剤としてビス(2,2,6,6-テトラメチル-4-ピペリジル)セバケートを0.2質量部、耐熱安定剤1としてトリス(2,4-ジ-tert-ブチルフェニル)ホスファイト0.1質量部、耐熱安定剤2としてオクタデシル-3-(3,5-ジ-tert-ブチル-4-ヒドロキシフェニル)プロピオネート0.1質量部を配合した。
表2に示す配合としたこと以外は、前述の製造例1と同様にしてエンボスシート(封止材シート)を得た。得られたシートの空隙率はいずれも28%であった。得られた封止材シートの各種評価結果を表2に示す。
ガラス22側の第一封止材シート11およびPETフィルム21側の第二封止材シート12の組み合わせを表3の組み合わせとし、上記たわみ量の評価および温度サイクル試験をそれぞれおこなった。得られた結果を表3に示す。
(付記1)
受光面側保護部材と裏面側保護部材との間に配置された、太陽電池素子および配線材料と、これらを封止するために用いられる、受光側に配される架橋処理後の第一封止材と裏面側に配される架橋処理後の第二封止材からなる太陽電池封止用シートセットであって、
測定温度範囲25~150℃、周波数1.0Hz、昇温速度10℃/分、ずりモードの条件での固体粘弾性を測定したときの120℃における、架橋処理前の第一封止材の貯蔵弾性率(P1)と架橋処理前の第二封止材の貯蔵弾性率(P2)が、下式(1)の関係にあることを特徴とする太陽電池封止用シートセット。
測定温度範囲25~150℃、周波数1.0Hz、昇温速度10℃/分、ずりモードの条件での固体粘弾性を測定したときの90℃における、架橋処理後の第一封止材の貯蔵弾性率(G1)と、-40℃~0℃における線膨張係数(α1)と、50℃~90℃における線膨張係数(α2)が下式(2)を満たすことを特徴とする付記1に記載の太陽電池封止用シートセット。
架橋処理後の第一封止材および架橋処理後の第二封止材の厚みが0.2~1mmである、付記1または2に記載の太陽電池封止用シートセット。
(付記4)
付記1~3のいずれか1つに記載の太陽電池封止用シートセットを用いてなる太陽電池モジュール。
Claims (10)
- 架橋処理後の前記第一封止材シートおよび架橋処理後の前記第二封止材シートの厚みがそれぞれ0.2~1mmである、請求項1または2に記載の太陽電池封止用シートセット。
- 前記第一封止材シートおよび前記第二封止材シートの少なくとも一方が、架橋性樹脂として、エチレン・α-オレフィン共重合体およびエチレン・酢酸ビニル共重合体からなる群から選択される一種または二種以上を含む請求項1または2に記載の太陽電池封止用シートセット。
- 前記第一封止材シートおよび前記第二封止材シートの少なくとも一方が、有機過酸化物を含み、前記有機過酸化物の含有量が、前記架橋性樹脂100質量部に対して、0.1質量部以上1.2質量部以下である請求項4に記載の太陽電池封止用シートセット。
- 前記貯蔵弾性率(P1)が1.0×10-1Pa以上1.2×106Pa以下であり、前記貯蔵弾性率(P2)が、8.0×10-2Pa以上1.0×106Pa以下である請求項1または2に記載の太陽電池封止用シートセット。
- 前記受光面側保護部材がガラス板であり、前記裏面側保護部材が熱可塑性樹脂フィルムである請求項1または2に記載の太陽電池封止用シートセット。
- 請求項1または2に記載の太陽電池封止用シートセットを用いてなる太陽電池モジュール。
- 請求項8に記載の太陽電池モジュールにおいて、
受光面側保護部材と裏面側保護部材との間に封止層を有し、該封止層内に太陽電池素子が封止されてなり、
前記封止層が前記太陽電池封止用シートセットにより形成されたものであり、
前記封止層は、第一封止層と第二封止層とを有し、
前記第一封止層が、前記第一封止材シートを架橋させてなり、
前記第二封止層が、前記第二封止材シートを架橋させてなり、
前記第一封止層が前記受光面側保護部材と前記太陽電池素子との間に設けられており、
前記第二封止層が前記裏面側保護部材と前記太陽電池素子との間に設けられている太陽電池モジュール。 - 前記受光面側保護部材がガラス板であり、前記裏面側保護部材が熱可塑性樹脂フィルムである請求項9に記載の太陽電池モジュール。
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WO2017150217A1 (ja) * | 2016-02-29 | 2017-09-08 | 三井化学東セロ株式会社 | 樹脂シート、合わせガラスおよび太陽電池モジュール |
CN117375528A (zh) * | 2023-10-12 | 2024-01-09 | 天合光能股份有限公司 | 组件测试方法 |
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US20210082634A1 (en) * | 2018-02-14 | 2021-03-18 | Lg Electronics Inc. | Solar cell module comprising perovskite solar cell and manufacturing method thereof |
JP6897621B2 (ja) * | 2018-03-30 | 2021-06-30 | 株式会社オートネットワーク技術研究所 | ワイヤハーネス |
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