JP2013138253A - Solar battery backside sealing sheet - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a solar battery backside sealing sheet which is arranged to prevent the deterioration of material accompanied by hydrolysis, allows a solar battery to retain its electricity output property, and has an excellent weather resistance.SOLUTION: The solar battery backside sealing sheet is composed of a laminate which comprises: a polyurethane-based adhesive agent B-2; and two or more layers B-1 of base material put together by the adhesive agent. The polyurethane-based adhesive agent is an adhesive composition which includes 1-50 pts.wt. of at least one compound selected from the group consisting of a carbodiimide compound, an oxazoline compound and an epoxy compound to 100 pts.wt. of the composition produced by blending polyol with a crosslinking agent. The polyol comprises one of a polycarbonate polyol and a polycarbonate urethane polyol chain-lengthened by a bifunctional or more isocyanate compound, or a mixture thereof. The polyurethane-based adhesive agent has hydrolysis resistance satisfying predetermined conditions.

Description

  The present invention relates to a sheet for sealing a back surface of a solar cell that is excellent in hydrolysis resistance, and more specifically, is laminated using an adhesive that is particularly excellent in hydrolysis resistance, and prevents deterioration of the material accompanying hydrolysis, The present invention relates to a solar cell back surface sealing sheet that can maintain not only the appearance defect due to delamination but also the barrier characteristics as a back surface sealing sheet and the electrical output characteristics as a solar cell.

  In recent years, various efforts have been made to suppress carbon dioxide emissions while interest from various countries both inside and outside Japan has increased. Increasing fossil fuel consumption leads to an increase in atmospheric carbon dioxide, and the greenhouse effect raises the Earth's temperature, significantly affecting the global environment. Various studies have been carried out to solve this global problem, and in particular, solar power generation is highly expected in terms of cleanliness and non-pollution. Solar cells constitute the heart of a photovoltaic power generation system that directly converts sunlight energy into electricity, and are made of single crystal, polycrystalline, or amorphous silicon semiconductors. As a structure thereof, a single solar cell element (cell) is not used as it is, and generally several to several tens of solar cell elements are wired in series and in parallel, for a long time (about 20 years). In order to protect the cell, various packaging is performed and unitized. The unit incorporated in this package is called a solar cell module, and the surface that is generally exposed to sunlight is covered with a glass surface, and the gap is filled with a filler made of a thermoplastic (especially ethylene-vinyl acetate copolymer), The back surface is protected by a sealing sheet (FIG. 1).

  Since these solar cell modules are mainly used outdoors, sufficient durability and weather resistance are required in the configuration and material structure thereof. In particular, the back surface sealing sheet is required to have a weather resistance and a low water vapor transmission rate (excellent moisture barrier property). This is because if the filler is peeled off or discolored due to the permeation of moisture or the wiring is corroded, the module output itself may be affected.

  Conventionally, as this solar cell back surface sealing sheet, a “fluorine-based resin having weather resistance, flame retardancy, and an ethylene-vinyl acetate copolymer often used as a filler for solar cell modules and good adhesiveness” Is used (Patent Documents 1, 2, etc.). In addition, a sheet for solar cell backside sealing using a polyester film such as polyethylene terephthalate having excellent electrical insulation has been developed, and in order to improve the weather resistance mentioned as a disadvantage of using a polyester film, There are many disclosures such as a system containing a UV absorber (Patent Document 3 etc.), the amount of cyclic oligomer in polyester (Patent Documents 4 and 5 etc.), and the molecular weight of polyester (Patent Document 6 etc.). I can see it.

  As described above, the solar cell needs to maintain its performance for about 20 years, and an accelerated test at high temperature and high humidity (85 ° C.-85% relative humidity) is performed to evaluate its durability. In particular, when a polyester film is used, the film base material causes hydrolysis in this accelerated test environment, and the strength physical properties are remarkably reduced. Therefore, as described in the above-mentioned patent document, the reduction in the strength physical properties should be compensated. The actual situation has been through various studies. However, there is a problem newly found by improving the weather resistance (hydrolysis resistance) of the film substrate. It is a delamination due to hydrolysis of the adhesive that bonds the film substrate. In general, these film bases use polyurethane adhesives based on polyester polyols, taking into account heat resistance and stability, but these polyester polyols themselves have a low molecular weight due to hydrolysis, and the accelerated test environment. Underlying problems such as a significant drop in bond strength emerged. Of course, this problem is also seen in the above-described fluororesin, and when the above accelerated test is performed, floating due to delamination occurs over time, and not only a poor appearance but also a barrier required as a sheet for backside sealing. As a result, the electrical output characteristics of the solar cell may be affected.

  From the above points, not only the weather resistance (hydrolysis resistance) as a film base material but also the adhesive for bonding it is required to have hydrolysis resistance, but at present it has not yet been solved. Is the current situation.

JP-T 8-500214 Japanese translation of PCT publication No. 2002-520820 JP 2001-1111073 A Japanese Patent Laid-Open No. 2002-100788 JP 2002-134771 A JP 2002-26354 A

  The present invention has been made in consideration of the technical background described above, and is not limited to an environment actually used as a solar cell module, but also under a high temperature and high humidity which is considered when evaluating a solar cell module. Even in accelerated evaluation, it is excellent in weather resistance (hydrolysis resistance) that can prevent deterioration of the material due to hydrolysis and maintain not only the poor appearance due to delamination but also the electrical output characteristics as a solar cell. It aims at providing the sheet | seat for solar cell backside sealing.

The present invention provides a solar cell back surface sealing sheet comprising a laminate in which at least two layers of substrates are bonded together with a polyurethane adhesive, wherein the polyurethane adhesive is a composition in which a polyol is blended with a crosslinking agent. Is an adhesive composition in which at least one compound selected from the group consisting of a carbodiimide compound, an oxazoline compound and an epoxy compound is blended in an amount of 1 to 50 parts by weight, and the polyol is polycarbonate polyol or bifunctional Any one or a mixture (hereinafter referred to as polyol B) of polycarbonate urethane polyol chain-extended with the above isocyanate compound is included, and the polyurethane adhesive has hydrolysis resistance satisfying the following conditions.
-It has a laminate strength of 1 N / 15 mm or more in a high pressure cooker (accelerated evaluation device using pressurized steam) at least at 105 ° C. to 168 h.
-In storage evaluation with a high pressure cooker (accelerated evaluation device using pressurized steam), there is no floating between substrates due to delamination.

The polyol may be a polyol composition in which 50 to 99% by weight of the polyol B is blended with respect to the following polyol A of 1 to 50% by weight.
The polyol may be a copolymer polyol obtained by subjecting the polyol B to 50 to 99% by weight and the following polyol A to 1 to 50% by weight to chain extension with a bifunctional or higher isocyanate compound.
Polyol A: A polyester polyol or a polyester urethane polyol chain-extended with a bifunctional or higher functional isocyanate compound, either alone or as a mixture.

  The crosslinking agent is 2,4- or 2,6-tolylene diisocyanate, xylylene diisocyanate, 4,4′-diphenylmethane diisocyanate, methylene diisocyanate, isopropylene diisocyanate, lysine diisocyanate, 2,2,4-- or 2, Isocyanate selected from the group consisting of 4,4-trimethylhexamethylene diisocyanate, 1,6-hexamethylene diisocyanate, methylcyclohexane diisocyanate, isophorone diisocyanate, 4,4′-dicyclohexylmethane diisocyanate, isopropylidene dicyclohexyl-4,4′-diisocyanate Any of an adduct body, a burette body, and an isocyanurate body derived from a compound may be used.

  The base material is a polyester base material selected from polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), polycyclohexanedimethanol-terephthalate (PCT), polycarbonate base material, polyvinyl fluoride ( PVF), polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), polyethylene tetrafluoroethylene (ETFE), polytetrafluoroethylene (PTFE), tetrafluoroethylene perfluoroalkyl vinyl ether copolymer (PFA), tetra You may select from the fluorine-type base material chosen from a fluoroethylene-hexafluoropropylene copolymer (FEP), or an acrylic base material.

  The base material may be a polyester base material having hydrolysis resistance, particularly having a number average molecular weight in the range of 18,000 to 40,000, a cyclic oligomer content of 1.5 wt% or less, and an intrinsic viscosity of 0.5 dl / g or more. Good.

  You may further interpose the vapor deposition base material which vapor-deposited inorganic compounds, such as an aluminum foil base material, metal aluminum, a silica, and an alumina, as a gas barrier layer in the said laminated body.

  Since the solar cell back surface sealing sheet of the present invention is composed of a laminate laminated with an adhesive having excellent hydrolysis resistance, not only the environment actually used as a solar cell module, but also the solar Even in accelerated evaluation under high temperature and high humidity, which is considered when evaluating battery modules, it prevents deterioration of materials due to hydrolysis, and not only poor appearance due to delamination but also barrier properties as a sheet for backside sealing. And a solar cell back surface sealing sheet capable of maintaining electrical output characteristics as a solar cell.

It is a schematic diagram which shows an example of a solar cell module. It is a schematic cross section which shows an example of the solar cell back surface sealing sheet of this invention. It is a schematic cross section which interposed the barrier layer as another example of the solar cell backside sealing sheet of this invention. It is a schematic explanatory drawing which shows an example of the manufacturing process of a solar cell module.

  Hereinafter, a preferred embodiment as an example of the present invention will be described in detail. The solar cell back surface sealing sheet according to the present invention is characterized in that the polyurethane adhesive used when bonding two or more kinds of base materials constituting the solar cell back surface sealing sheet is an adhesive having excellent hydrolysis resistance or An adhesive composition is provided. Here, the definition of being excellent in hydrolysis resistance is based on the influence of hydrolysis of the adhesive as an index, and promoted evaluation by a high pressure cooker (accelerated evaluation apparatus using pressurized steam JIS C 60068-2-66). Etc.) having a laminate strength of 1 N / 15 mm or more at a storage state of at least 105 ° C. and 168 h, and not accompanied by floating between substrates due to delamination.

  Hereinafter, the adhesive or adhesive composition having excellent hydrolysis resistance will be described. First, as a polyurethane-based adhesive used in the solar cell backside sealing sheet of the present invention, either a polyester polyol or a polyester urethane polyol chain-extended with a bifunctional or higher functional isocyanate compound, or a mixture (hereinafter, polyol A and 1) to 50 parts by weight of a compound selected from at least one kind selected from a carbodiimide compound, an oxazoline compound, and an epoxy compound with respect to 100 parts by weight of the composition in which a crosslinking agent is blended in (described).

  The characteristics of this adhesive composition are the point of initial laminate strength between two or more kinds of base materials used for the solar cell back surface sealing sheet, and the point of heat resistance considering an accelerated test in a high temperature environment. Polyol A is used. However, a urethane-based adhesive composed of polyol A and a crosslinking agent is a preferable bonding mode in terms of hydrolysis of urethane bonds, but there is a concern about hydrolysis of ester bonds. In addition, the ester bond site that has undergone hydrolysis in an accelerated environment under high temperature and high humidity is cleaved into a carboxyl group and a hydroxyl group. Since this carboxyl group acts as an acid catalyst, hydrolysis of the ester bond site is further promoted. Therefore, in order to block the carboxyl group generated by the hydrolysis, at least one compound selected from a carbodiimide compound, an oxazoline compound, and an epoxy compound is added to 100 parts by weight of a composition in which a crosslinking agent is added to polyol A. In contrast, 1 to 50 parts by weight is blended.

  Polyester polyols used in the present invention include aliphatic systems such as succinic acid, glutaric acid, adipic acid, pimelic acid, speric acid, azelaic acid, sebacic acid and brassic acid, isophthalic acid, terephthalic acid, naphthalenedicarboxylic acid, etc. One or more aromatic dibasic acids, and aliphatics such as ethylene glycol, propylene glycol, butanediol, neopentyl glycol, methylpentanediol, hexanediol, heptanediol, octanediol, nonanediol, decanediol, dodecanediol It can be obtained by using one or more of alicyclic diols such as cyclohexanediol and hydrogenated xylylene glycol, and aromatic diols such as xylylene glycol. Further, the hydroxyl groups at both ends of this polyester polyol are, for example, 2,4- or 2,6-tolylene diisocyanate, xylylene diisocyanate, 4,4'-diphenylmethane diisocyanate, methylene diisocyanate, isopropylene diisocyanate, lysine diisocyanate, 2 , 2,4-- or 2,4,4-trimethylhexamethylene diisocyanate, 1,6-hexamethylene diisocyanate, methylcyclohexane diisocyanate, isophorone diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, isopropylidene dicyclohexyl-4,4 ' -A single isocyanate compound selected from diisocyanates, etc., or at least one isocyanate compound selected from the above Adducts consisting of biuret body, such as a polyester urethane polyol chain extension with isocyanurate products thereof.

  Moreover, as said crosslinking agent which bridge | crosslinks these polyols A, it is possible to use the said isocyanate compound, and it is not restricted to these, A crosslinker which has reactivity with an active hydrogen group will not ask | require a kind.

  The carbodiimide compound to be blended in order to block the carboxyl group produced when hydrolysis occurs in an accelerated environment under high temperature and high humidity, N, N′-di-o-toluylcarbodiimide, N , N′-diphenylcarbodiimide, N, N′-di-2,6-dimethylphenylcarbodiimide, N, N′-bis (2,6-diisopropylphenyl) carbodiimide, N, N′-dioctyldecylcarbodiimide, N-triyl -N'-cyclohexylcarbodiimide, N, N'-di-2,2-di-tert. -Butylphenylcarbodiimide, N-triyl-N'-phenylcarbodiimide, N, N'-di-p-nitrophenylcarbodiimide, N, N'-di-p-aminophenylcarbodiimide, N, N'-di-p- Examples include hydroxyphenyl carbodiimide, N, N′-di-cyclohexylcarbodiimide, and N, N′-di-p-toluylcarbodiimide.

  Examples of the oxazoline compound having the same action include 2-oxazoline, 2-methyl-2-oxazoline, 2-phenyl-2-oxazoline, 2,5-dimethyl-2-oxazoline, and 2,4-diphenyl-2-oxazoline. Monooxazoline compounds such as 2,2 ′-(1,3-phenylene) -bis (2-oxazoline), 2,2 ′-(1,2-ethylene) -bis (2-oxazoline), 2,2 ′ Examples thereof include dioxazoline compounds such as-(1,4-butylene) -bis (2-oxazoline) and 2,2 '-(1,4-phenylene) -bis (2-oxazoline).

  Similarly, epoxy compounds include diglycidyl ethers of aliphatic diols such as 1,6-hexanediol, neopentyl glycol, polyalkylene glycol, sorbitol, sorbitan, polyglycerol, pentaerythritol, diglycerol, glycerol, trimethylol. Polyglycidyl ether of aliphatic polyol such as propane, polyglycidyl ether of alicyclic polyol such as cyclohexanedimethanol, aliphatic, aromatic such as terephthalic acid, isophthalic acid, naphthalene dicarboxylic acid, trimellitic acid, adipic acid, sebacic acid Diglycidyl ester or polyglycidyl ester, resorcinol, bis- (p-hydroxyphenyl) methane, 2,2-bis- (p-hydroxyphenyl) Dipanidyl or polyglycidyl ether of polyphenol such as lopan, tris- (p-hydroxyphenyl) methane, 1,1,2,2-tetrakis (p-hydroxyphenyl) ethane, N, N-diglycidylaniline, N-glycidyl derivatives of amines such as N, N-diglycidyl toluidine, N, N, N ′, N′-tetraglycidyl-bis- (p-aminophenyl) methane, triglycidyl derivatives of aminofail, triglycidyl tris (2-Hydroxyethyl) isocyanurate, triglycidyl isocyanurate, orthocresol type epoxy, phenol novolac type epoxy.

  The compound capable of blocking these carboxyl groups is blended in an amount of 1 to 50 parts by weight with respect to 100 parts by weight of the composition obtained by blending polyol A with a crosslinking agent. If it is less than 1 part by weight, the hydrolysis resistance is poor. A larger amount is preferable in terms of blocking the carboxyl group produced by hydrolysis, but the polyurethane component that apparently contributes to adhesion is reduced, and the adhesion function may be lowered. In consideration of the coating handling property of the polyurethane adhesive, it is preferably 50 parts by weight or less.

  Moreover, you may mix | blend the compound which forms a crosslinking reaction from the hydroxyl group produced by hydrolysis. Examples of such compounds include phosphorus compounds such as tris (2,4-di-t-butylphenyl) phosphite and tetrakis (2,4-di-t-butylphenyl) 4,4′-biphenylene phosphor. Knight, bis (2,4-di-t-butylphenyl) pentaerythritol-di-phosphite, bis (2,6-di-t-butyl-4-methylphenyl) pentaerythritol-di-phosphite, 2, 2-methylenebis (4,6-di-t-butylphenyl) octyl phosphite, 4,4′-butylidene-bis (3-methyl-6-tert-butylphenyl-di-tridecyl) phosphite, 1,1, 3-tris (2-methyl-4-ditridecyl phosphite-5-tert-butyl-phenyl) butane, tris (mixed mono and di-nonylphenyl) Sufaito, tris (nonylphenyl) phosphite, 4,4'-isopropylidene-bis (phenyl - dialkyl phosphite) can be used. However, in terms of inhibiting hydrolysis of the polyester compound, it is essential to block the carboxyl group that acts as an acid catalyst for hydrolysis rather than further crosslinking the hydroxyl group once generated by hydrolysis with a phosphorus compound. Therefore, the carbodiimide compound, the oxazoline compound, and the epoxy compound are preferable, and the most preferable compound is a carbodiimide compound.

  The polyurethane-based adhesive using the polyol A described above suppresses the hydrolyzed adhesive by using a carbodiimide compound, an oxazoline compound, an epoxy compound, or the like. Therefore, it is possible to design so that the polyurethane adhesive itself is not hydrolyzed. As the polyol component considered as a polyurethane-based material, polyether polyol, polycarbonate polyol, acrylic polyol, and the like can be considered, and those containing these components as the main component can be used. And acrylic polyol are preferred.

  The polycarbonate polyol can be obtained, for example, by reacting a carbonate compound and a diol. As the carbonate compound, dimethyl carbonate, diphenyl carbonate, ethylene carbonate and the like can be used. Diols include ethylene glycol, propylene glycol, butanediol, neopentyl glycol, methylpentanediol, hexanediol, heptanediol, octanediol, nonanediol, decanediol, dodecanediol and other aliphatic diols, cyclohexanediol, hydrogenated xylylene Polycarbonate polyol using a mixture of one or more aromatic diols such as alicyclic diol such as reel, xylylene glycol, or the like, or polycarbonate urethane polyol subjected to chain extension by the isocyanate compound described above (hereinafter referred to as polyol) B) can be used, and it is more preferable to use an aliphatic polycarbonate-based polyol B in consideration of the performance as an adhesive.

  As the acrylic polyol, a hydroxyl group-containing monomer such as 2-hydroxyethyl (meth) acrylate and 2-hydroxypropyl (meth) acrylate is essential, and (meth) acrylic acid, alkyl group as methyl group, ethyl group, n-propyl A polymer based on an alkyl (meth) acrylate monomer that is a group, i-propyl group, n-butyl group, i-butyl group, t-butyl group, 2-ethylhexyl group, cyclohexyl group, (Meth) acrylamide, N-alkyl (meth) acrylamide, N, N-dialkyl (meth) acrylamide (As the alkyl group, methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, i -Butyl group, t-butyl group, 2-ethylhexyl group, cyclohexyl group, etc.), N Alkoxy (meth) acrylamide, N, N-dialkoxy (meth) acrylamide (as alkoxy groups, methoxy group, ethoxy group, butoxy group, isobutoxy group, etc.), N-methylol (meth) acrylamide, N-phenyl (meta ) Copolymerized amide group-containing monomers such as acrylamide and glycidyl group-containing monomers such as glycidyl (meth) acrylate and allyl glycidyl ether can be used. Furthermore, vinyl isocyanate, allyl isocyanate, styrene, α-methyl styrene, vinyl methyl ether, vinyl ethyl ether, maleic acid, alkyl maleic acid monoester, fumaric acid, alkyl fumaric acid monoester, itaconic acid, alkyl itaconic acid monoester, It is possible to use a product obtained by copolymerizing monomers such as (meth) acrylonitrile, vinylidene chloride, ethylene, propylene, vinyl chloride, vinyl acetate, butadiene (hereinafter, polyol C).

  These polyols B and C may be a blend with polyol A, for example, a combination composition such as polyol B + polyol A, polyol C + polyol A (hereinafter this blend is referred to as polyol D). Polyols B and C are a chain-extended copolymer using polyol A and the above-described bifunctional or higher isocyanate compound, for example, a main chain block copolymer of polyol B-polyol A, polyol C-polyol A side It may be a chain block copolymer (hereinafter referred to as polyol E). Furthermore, polyol B and polyol C are also mixtures or chain extenders, and may be blends or copolymers of these with polyol A. In other words, it is a combination of polyols B and C, which are hydrolysis-resistant skeletons, and polyol A, which exhibits hydrolysis properties. For polyols D and E, 50 of polyols B and C, which are hydrolysis-resistant skeletons, are used. For example, the polyol A having hydrolyzability may be set to 1 to 50% by weight with respect to ˜99% by weight. The effect of blending or copolymerizing will be described later.

  About these polyols B-E, the carbodiimide compound mentioned above, an oxazoline compound, an epoxy compound, Preferably it is possible to mix | blend a carbodiimide compound. Since these compounds having a carboxyl group-blocking function are not essential components, 0 to 50 parts by weight may be added to 100 parts by weight of a composition in which a crosslinking agent is added to polyols B to E. Therefore, it is preferable to add to these compounds.

  These polyurethane-based adhesives described above are used for bonding substrates used as solar cell back surface sealing sheets. As the substrates at that time, polyethylene terephthalate (PET), polyethylene naphthalate (PEN), poly Polyester base selected from butylene terephthalate (PBT), polycyclohexanedimethanol-terephthalate (PCT), polycarbonate base, polyvinyl fluoride (PVF), polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), Polyethylenetetrafluoroethylene (ETFE), polytetrafluoroethylene (PTFE), tetrafluoroethylene perfluoroalkyl vinyl ether copolymer (PFA), tetrafluoroethylene-hexafluoropro Fluorine-based base material selected from alkylene copolymer (FEP), or the like to be selected from an acrylic substrate. Moreover, it is not limited to these, It can select suitably considering heat resistance, an intensity | strength physical property, electrical insulation, etc., such as polyolefin resin, polyamide-type resin, polyarylate-type resin.

  When a polyester base material is used, it is obtained by using a polybasic acid or an ester-forming derivative thereof and a polyol or an ester-forming derivative thereof. As the polybasic acid component, terephthalic acid, isophthalic acid, phthalic acid, phthalic anhydride Two or more acid components such as 2,6-naphthalenedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, adipic acid, sebacic acid, trimellitic acid, pyromellitic acid, dimer acid, maleic acid, itaconic acid, and As the polyol component, ethylene glycol, 1,4-butanediol, diethylene glycol, dipropylene glycol, 1,6-hexanediol, 1,4-cyclohexanedimethanol, trimethylolpropane, pentaerythritol, xylene glycol, dimethylolpropane, poly (Echile Oxide) glycol, poly (tetramethylene oxide) glycol, and polyester obtained by using one or more polyol components containing carboxylic acid groups, sulfonic acid groups, amino groups, or salts thereof. However, polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), and polycyclohexanedimethanol-terephthalate (PCT) are generally used.

  However, polyester base materials, particularly polyethylene terephthalate, are materials that are likely to be hydrolyzed, like the polyurethane adhesives described above. Therefore, when a polyester base material such as polyethylene terephthalate is used, hydrolysis resistance with a number average molecular weight in the range of 18000 to 40000, a cyclic oligomer content of 1.5 wt% or less, and an intrinsic viscosity of 0.5 dl / g or more. It is preferable that it is the polyester base material which has this. Like the polyol A described above, when the molecular terminal is a carboxylic acid group, such a polyester base material acts as heat, water, and further as an acid catalyst and is most affected by hydrolysis. A solid phase polymerization method that can increase the number average molecular weight without increasing the amount may be used, or the terminal carboxylic acid group may be sealed with a carbodiimide compound, an epoxy compound, or an oxazoline compound. In addition, when there is a concern about the effect of shrinkage due to heat when manufacturing a solar cell module, a polyester base material having a heat shrinkage rate of 1% or less, preferably 0.5% or less by performing an annealing treatment is used. It is possible to use. When weather resistance is required, UV absorbers such as benzophenone, benzotriazole, and triazine, hindered phenol-based, phosphorus-based, sulfur-based, tocopherol-based antioxidants, hindered amine-based light stabilizers are also appropriately used. It is possible to mix.

  Although the polyester base material used for the solar cell backside sealing sheet may be transparent, it is preferable to use a white polyester film from the viewpoint of improving the power generation efficiency of the solar cell element. In particular, when the solar cell back surface sealing sheet has a multilayer structure, it is also possible to provide a white polyester film on at least the base material bonded to the filler. The white polyester film used at this time is a “pigment dispersion type” in which white additives such as titanium oxide, silica, alumina, calcium carbonate, and barium sulfate are added. It is possible to use a “fine foam type” or the like that is whitened by forming voids at the blend interface during stretching. In the “fine foaming type”, the polymer incompatible with the polyester is preferably a polyolefin resin such as polyethylene, polypropylene, polybutene, polymethylpentene. If necessary, polyalkylene glycol or a copolymer thereof can be used as a compatibilizing agent. Specific examples of the fine particles include organic particles and inorganic particles. Silicon particles, polyimide particles, crosslinked styrene-divinylbenzene copolymer particles, crosslinked polyester particles, fluorine-based particles, and the like are used. As the inorganic particles, calcium carbonate, silicon dioxide, barium sulfate or the like is used.

  The schematic diagram of the structure which bonded together the base material of the said content with the polyurethane-type adhesive using polyol AE is shown in FIG. FIG. 2 shows the simplest structure, in which two base materials (B-1) are bonded with a polyurethane adhesive (B-2). However, when actually used as a solar cell back surface sealing sheet, it is necessary to interpose a gas barrier layer (B-3) against moisture and oxygen, and finally the gas barrier layer (B -3) is interposed. Examples of such a gas barrier layer include a metal foil base material, a metal vapor deposition film base material, an aluminum foil base material, and an inorganic compound vapor deposition film base material. The metal foil is typically an aluminum foil, and the metal vapor deposition film is typically an aluminum vapor deposition film obtained by depositing aluminum on a polyester or polyolefin stretched film. Examples of the inorganic compound vapor-deposited film base material include a film base material obtained by vapor-depositing aluminum oxide, silicon oxide, tin oxide, magnesium oxide, indium oxide or a composite oxide thereof on a polyester base material. Any material having gas barrier properties such as water vapor may be used. Among them, aluminum oxide and silicon oxide are particularly preferable. The optimum conditions of the thickness vary depending on the type and configuration of the inorganic oxide used, but generally the thickness is preferably in the range of 5 to 300 nm, and the value is appropriately selected. If the film thickness is less than 5 nm, a uniform film cannot be obtained, and the film thickness is not sufficient for exhibiting the barrier function. When the film thickness is larger than 300 nm, the film is subjected to flexibility, and there is a possibility that a crack is easily generated due to external stress. Preferably, it exists in the range of 10-150 nm. As a method of providing these vapor deposition layers, it can be formed by a normal vacuum vapor deposition method, but other thin film formation methods such as sputtering, ion plating, and plasma vapor deposition (CVD) are used. Is also possible. Further, if necessary, an overcoat layer composed of a part of ethylene-vinyl acetate copolymer or a completely saponified product and a silane compound is provided on the vapor deposition layer of the inorganic compound from the viewpoint of further improving the gas barrier property. It doesn't matter.

  The gas barrier layer (B-3) is preferably an inorganic compound vapor deposition film substrate rather than an aluminum foil substrate or an aluminum vapor deposition film substrate from the viewpoint of electrical insulation. Moreover, when using as a sheet | seat for solar cell backside sealing, it is necessary to use the base material which this gas barrier layer is excellent also in hydrolysis resistance. From such points, it is possible to obtain an inorganic compound vapor-deposited film using the above-mentioned substrate, particularly a polyester substrate, but the substrate usually used for the inorganic compound vapor-deposited film has a thickness in the range of about 10 to 40 μm. It is common to use a polyethylene terephthalate film. The polyethylene terephthalate film having this thickness is manufactured by forming a film of a polyester resin melted by a T-die casting method, and heat-fixing the film after in-line simultaneous or sequential biaxial stretching. At this time, in order to improve workability, there are many cases of using a polyester resin having an intrinsic viscosity in the range of 0.2 to 0.5 dl / g. That is, a film substrate, particularly a polyester substrate, generally used for an inorganic compound vapor-deposited film is inferior in hydrolysis resistance. Therefore, even if the hydrolysis resistance of the substrate (B-1) or the polyurethane adhesive (B-2) is improved, the gas barrier layer (B-3) corresponding to the intermediate layer in FIG. 3 causes hydrolysis. There is a fear.

  That is, the design intention of polyols D and E, and further the intention of blending polyols B to E with a carbodiimide compound, an oxazoline compound, an epoxy compound, preferably a carbodiimide compound, suppresses hydrolysis of the gas barrier layer (B-3). There is. The basic principle is as follows.

  First, regarding the effect of adding a carbodiimide compound or the like when using an adhesive main agent having excellent hydrolysis resistance such as polyols B and C, the gas barrier layer is not added to suppress hydrolysis of the adhesive. (B-3) is blended for inhibiting hydrolysis. That is, the polyurethane-based adhesive using polyol A protects the gas barrier layer (B-3) instead of lowering the function as an adhesive. In other words, the gas barrier layer (B-3) is hydrolyzed. The idea is that the moisture to be added is supplemented at the expense of polyol A. Polyols B and C are less likely to be hydrolyzed by the polyurethane adhesive itself, and moisture that causes hydrolysis when polyol A is used permeates through the polyurethane adhesive composed of polyols B and C to form a gas barrier layer ( B-3) is consumed for hydrolysis. Therefore, addition of a carbodiimide compound or the like is effective in order to suppress hydrolysis of the gas barrier layer (B-3). On the other hand, the intention of blending a hydrolysis-resistant main ingredient and a hydrolyzable main ingredient like polyols D and E is to provide an adhesive function in the hydrolysis-resistant main ingredient, and at the same time, a hydrolyzable main ingredient ( (Corresponding to polyol A) is an idea that water that hydrolyzes the base material of the gas barrier layer (B-3) is consumed for hydrolysis of polyol A. Further, the purpose of blending these polyols D and E with a carbodiimide compound or the like is to blend these carboxyl groups of the hydrolyzed polyol A. Thus, as a polyurethane-based adhesive composition, it is possible to impart the adhesion function and hydrolysis resistance necessary for a solar cell back surface sealing sheet by clearly sharing the function of each additive. .

As a manufacturing method of the sheet | seat for solar cell backside sealing mentioned above, 0.1-10 g / m < ² > as dry solid content using techniques, such as a gravure coat, a roll coat, a bar coat, a reverse coat, on the base material mentioned above. In the range described above, the polyurethane adhesive is applied and laminated using a known method such as dry lamination. At this time, the substrate side can be subjected to surface treatment for improving adhesion such as corona treatment, flame treatment, plasma treatment, etc., especially when a fluororesin is used as the substrate. Plasma treatment or the like is preferable. In addition to the dry process, an easy-adhesion coat layer made of, for example, polyester, polyurethane, acrylic, or a mixture thereof may be provided on the substrate side.

A solar cell module is manufactured using the laminate thus obtained as a solar cell back surface sealing sheet. This process is the following (1) to (4) (FIG. 4).
(1) A glass plate, a filler, a cell, a filler, and a back surface sealing sheet are set on a heated top plate (approximately 120 to 160 ° C.).
(2) The chambers 1 and 2 are evacuated.
(3) The chamber 1 is opened to the atmosphere, and a rubber sheet having heat resistance is brought into close contact with the module. (4) The filler is melted ethylene vinyl acetate copolymer, cell embedding, glass plate / Adhesion with cell / backside sealing sheet, crosslinking / solidification of filler.

  At this time, the step (4) is classified into a case where a cross-linking reaction is performed in an oven provided in another line after lamination and a case where a cross-linking reaction is performed inside the laminator. The former is a type called standard cure, and the latter is a type called fast cure. Usually, the material used as the filler for the solar cell module is an ethylene-vinyl acetate copolymer having a vinyl acetate content of 10 to 40% by weight in order to ensure the heat resistance and physical strength of the solar cell. The ethylene-vinyl acetate copolymer is crosslinked by heat or light.

  In the case of performing thermal crosslinking, an organic peroxide is usually used, and one that decomposes at a temperature of 70 ° C. or higher to generate radicals is used. Usually, those having a decomposition temperature of 50 ° C. or more with a half-life of 10 hours are used, and 2,5-dimethylhexane-2,5-dihydroxyperoxide, 2,5-dimethyl-2,5-di (t-butyl) Peroxy) hexyne-3, di-t-butyl peroxide, t-butylcumyl peroxide, 2,5-dimethyl-2,5-di (t-butylperoxy) hexane, dicumyl peroxide, α, α '-Bis (t-butylperoxyisopropyl) benzene, n-butyl-4,4-bis- (t-butylperoxy) valerate, t-butylperoxybenzoate, benzoyl peroxide and the like are used.

  In the case of photocuring, a photosensitizer is used, and hydrogen abstraction type (bimolecular reaction type) such as benzophenone, methyl orthobenzoylbenzoate, 4-benzoyl-4′-methyldiphenyl sulfide, isopropylthioxanthone, etc. As the internal cleavage type initiator, α-hydroxyalkylphenone type such as benzoin ether, benzyldimethyl ketal, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexyl, etc. Phenyl ketone, alkylphenyl glyoxylate, diethoxyacetophenone and the like can be used. Further, as α-aminoalkylphenone type, 2-methyl-1- [4 (methylthio) phenyl] -2-morpholinopropane-1,2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) -Butanone-1 and the like, and acylphosphine oxide and the like are also used.

  A silane coupling agent is also blended in consideration of adhesion to the glass plate constituting the solar cell module, and vinyltriethoxysilane, vinyltris (β-methoxyethoxy) silane, γ-methacryloxypropyltrimethoxysilane, Vinyltriacetoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyltriethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-chloropropylmethoxysilane, vinyltrichlorosilane , Γ-mercaptopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-β (aminoethyl) -γ-aminopropyltrimethoxysilane, and the like.

  Furthermore, an epoxy group-containing compound may be blended for the purpose of promoting adhesion and curing. Examples of the epoxy group-containing compound include triglycidyl tris (2-hydroxyethyl) isocyanurate, neopentyl glycol diglycidyl ether, 1,6-hexanediol diglycidyl ether, acrylic glycidyl ether, 2-ethylhexyl glycidyl ether, phenyl glycidyl ether, phenol glycidyl ether, pt-butylphenyl glycidyl ether, adipic acid diglycidyl ester, o-phthalic acid diglycidyl ester , Glycidyl methacrylate, butyl glycidyl ether and other compounds, oligomers containing an epoxy group with a molecular weight of several hundred to several thousand, and polymers with a weight average molecular weight of several thousand to several hundred thousand. Some cases are there.

  Furthermore, for the purpose of improving the crosslinking, adhesion, mechanical strength, heat resistance, moist heat resistance, weather resistance, etc. of the filler, an acryloxy group, methacryloxy group or allyl group-containing compound is added, and (meth) acrylic is added. Acid derivatives such as their alkyl esters and amides are most common. In this case, as the alkyl group, in addition to an alkyl group such as methyl, ethyl, dodecyl, stearyl, lauryl, cyclohexyl group, tetrahydrofurfuryl group, aminoethyl group, 2-hydroxyethyl group, 3-hydroxypropyl group, A 3-chloro-2-hydroxypropyl group and the like can be mentioned. Further, esters of (meth) acrylic acid and polyfunctional alcohols such as ethylene glycol, triethylene glycol, polyethylene glycol, glycerin, trimethylolpropane, pentaerythritol and the like are also used. A typical amide is acrylamide. Further, as the allyl group-containing compound, triallyl cyanurate, triallyl isocyanurate, diallyl phthalate, diallyl isophthalate, diallyl maleate and the like are blended.

  Furthermore, an inorganic compound for imparting flame retardancy, an ultraviolet absorber for imparting weather resistance, and an antioxidant for preventing oxidative degradation are variously blended. That is, it can be mentioned that the ethylene-vinyl acetate copolymer constituting the solar cell module is a resin composition in which various additives are blended in order to satisfy the functions required for the solar cell module.

  Therefore, in order to improve the adhesion between the composition of the ethylene-vinyl acetate copolymer obtained by blending such various additives and the sheet for sealing the back surface of the solar cell, a substrate is used as necessary. An easy-adhesion coat layer made of an acrylic, epoxy, phenol, polyester, urethane, styrene resin, or a modified product thereof may be provided on the side to be bonded to the filler (B-1).

  By providing the solar cell back surface sealing sheet having the above-described configuration, it is possible to obtain a solar cell back surface sealing sheet having good hydrolysis resistance and good solar cell module protection.

  Although the Example of this invention is shown below, it is not necessarily limited to this.

[Polyester substrate]
<Base material: 1>
A “fine foam type” white polyethylene terephthalate film having a thickness of 188 μm was used. This polyethylene terephthalate has an oligomer content of 0.5 wt%, a number average molecular weight of 19,500, and an intrinsic viscosity of 0.7 dl / g. This base material is a multilayer film of two types and three layers in which a fine foam layer is provided on the intermediate layer, and the intermediate layer occupies 80%. This white polyethylene terephthalate film was untreated.
<Substrate: 2>
A polyvinylidene fluoride (PVDF) type two-layer two-layer multilayer film having a thickness of 40 μm was used. This material is an alloy composed of PVDF and acrylic resin. One layer has PVDF / acryl = 80/20, and the other layer has PVDF / acryl = 20/80. The layer side of PVDF / acryl = 20/80 was used as the adhesive bonding surface, and the bonding surface side was previously subjected to plasma treatment.
<Base material: 3>
Solvent-gel reaction of hydrolyzate of alkoxysilane to a complete saponified product of ethylene-vinyl acetate copolymer as an overcoat layer on an alumina vapor deposition layer of 20 nm by PVD method on a normal biaxially stretched polyethylene terephthalate film with a thickness of 12 μm The coating layer was 0.5 μm. This substrate was used as a gas barrier substrate.

The following adhesives were used.
<Adhesive: 1>
A polyurethane-based adhesive in which a curing agent composed of a mixture of xylylene diisocyanate (adduct body) and hexamethylene diisocyanate (burette body) was blended at a solid content ratio of 3: 1 with a main component composed of polyester polyol was used.
<Adhesive: 2>
A polyurethane-based adhesive in which 10 parts by weight of N, N′-diphenylcarbodiimide was blended with 100 parts by weight of the adhesive 1 was used.
<Adhesive: 3>
A polyurethane-based adhesive in which a curing agent composed of isophorone diisocyanate (trimer) was blended at a solid content ratio of 3: 1 to an aliphatic polycarbonate-based main component subjected to chain extension with isophorone diisocyanate (monomer) was used.
<Adhesive: 4>
A polyurethane adhesive in which 30 parts by weight of N, N′-diphenylcarbodiimide was blended with 100 parts by weight of the adhesive 3 was used.
<Adhesive: 5>
A polyurethane-based adhesive in which a curing agent composed of hexamethylene diisocyanate (burette) was blended at a solid content ratio of 3: 1 to an acrylic polyol-based main component obtained by copolymerizing hydroxyethyl methacrylate in the skeleton was used. .
<Adhesive: 6>
A hardener consisting of isophorone diisocyanate (trimer) in a solid content ratio is blended into a mixed main agent blended to a base of 70/30 with an aliphatic polycarbonate main agent subjected to chain extension with isophorone diisocyanate (monomer) and a polyester polyol. A polyurethane adhesive containing 30 parts by weight of N, N′-diphenylcarbodiimide was used with respect to 100 parts by weight of the polyurethane adhesive compounded to 3: 1.
<Adhesive: 7>
A main component of a copolymer type in which a main component composed of an aliphatic polycarbonate main component and a polyester polyol blended so as to be 70/30 is subjected to chain extension with isophorone diisocyanate (monomer), and is composed of isophorone diisocyanate (trimer). A polyurethane adhesive in which 30 parts by weight of N, N′-diphenylcarbodiimide was added to 100 parts by weight of the polyurethane adhesive in which the solid content ratio was 3: 1 was used.

[Creation of solar cell back surface sealing sheet]
<Substrate: 1> to <Substrate: 3> were laminated by the dry lamination method using the above <Adhesive: 1> to <Adhesive: 8>. The coating amount of the adhesive was adjusted to 5 g / m ² in terms of dry. The aging temperature is 50 ° C.-5 days. The configurations actually made as trials are the following <configuration: 1> to <configuration: 4>.
<Constitution: 1>: <Base material: 1> / Adhesive / <Base material: 1>
<Constitution: 2>: <Base material: 2> / Adhesive / <Base material: 2>
<Constitution: 3>: <Base material: 1> / Adhesive / <Base material: 3> / Adhesive / <Base material: 1>
<Constitution: 4>: <Base material: 2> / Adhesive / <Base material: 3> / Adhesive / <Base material: 2>
However, the adhesive (underline) in <Configuration: 3> and <Configuration: 4> is the side in contact with the vapor deposition layer in <Base Material: 3>.

[Evaluation method of evaluation sample]
The above configuration was evaluated by an accelerated evaluation test using pressurized steam. The sample having the above configuration was cut into A4 size, set in a high pressure cooker (accelerated evaluation apparatus using pressurized steam), and evaluated for laminate strength and peeling behavior over time in an environment of 105 ° C. The laminate strength was a T-type peeling method using Tensilon and a 15 mm wide crosshead speed of 300 mm / min. The strength at was measured. The solar cell back surface sealing sheet usually needs to be stored for 2000 hours or more in an 85 ° C.-85% RH environment as an accelerated evaluation. By using this evaluation method, the accelerated evaluation can be shortened, and the 85 ° C. It has been confirmed that the physical property values in the −85% RH environment 2000 h correspond to the physical property values stored at 105 ° C. to 168 h.

  Based on the above evaluation method, the basic performance of the adhesive was evaluated for the samples prototyped in the following examples. The evaluation results are shown in Tables 1-3.

[Example 1]
Using <Adhesive: 1>, a sample composed of the above <Structure: 1-4> was made as an experiment.

[Example 2]
Using <Adhesive: 2>, a sample composed of the above <Constitution: 1-4> was made as an experiment.

[Example 3]
Using <Adhesive: 3>, a sample composed of the above <Constitution: 1-4> was made as an experiment.

[Example 4]
Using <Adhesive: 4>, a sample composed of the above <Constitution: 1-4> was made as an experiment.

[Example 5]
Using <Adhesive: 5>, a sample composed of the above <Constitution: 1-4> was made as an experiment.

[Example 6]
Using <Adhesive: 6>, a sample composed of the above <Constitution: 1-4> was made as an experiment.

[Example 7]
Using <Adhesive: 7>, a sample composed of the above <Constitution: 1-4> was made as an experiment.

  From Tables 1 to 3, from configurations 1 and 2, the polyester polyol polyurethane resin to which carbodiimide is not added shows a decrease in strength at an acceleration rating of 168 h or more, and the floating due to delamination is confirmed visually. By adding carbodiimide, it is confirmed that the cohesive strength is maintained and the hydrolysis resistance is excellent. It is confirmed that those using a polycarbonate-based or acrylic-based main agent are less affected by hydrolysis even if carbodiimide is not blended, and show a good laminate strength over time. On the other hand, as for the constitution 3 and constitution 4 in which a layer composed of a normal biaxially stretched polyester film is provided in the intermediate layer as a constitution, those using a polycarbonate-based or acrylic main component not containing a carbodiimide are intermediate layer polyesters. The tendency which cannot be used as a solar cell back surface sealing sheet is confirmed by hydrolysis of the base material. However, by blending carbodiimide, it is possible to impart an effect of suppressing hydrolysis of not only the adhesive layer but also the polyester layer of the intermediate layer.

  From the above, the solar cell back surface sealing sheet of the configuration of the present invention is not only in an environment actually used as a solar cell module, but also in accelerated evaluation under high temperature and high humidity that is considered when evaluating solar cell modules. However, it is possible to prevent deterioration of the material due to hydrolysis and maintain not only the appearance defect due to delamination but also the barrier property as the back surface sealing sheet and the electrical output property as the solar cell.

A: Solar cell module A-1: Solar cell A-2: Filler A-3: Glass plate B: Back surface sealing sheet B-1: Substrate B-2: Polyurethane adhesive B-3: Barrier layer C: Laminator C-1: Top plate C-2: Chamber 1
C-3: Chamber 2
C-4: Rubber sheet

Claims (7)

In the solar cell back surface sealing sheet comprising a laminate in which at least two layers of base materials are bonded together with a polyurethane adhesive,
1 to 50 parts by weight of at least one compound selected from the group consisting of a carbodiimide compound, an oxazoline compound, and an epoxy compound is blended with 100 parts by weight of the polyurethane-based adhesive blended with a polyol and a crosslinking agent. An adhesive composition;
The polyol includes a polycarbonate polyol or a polycarbonate urethane polyol that is chain-extended with a bifunctional or higher functional isocyanate compound, or a mixture (hereinafter, polyol B).
A sheet for sealing a back surface of a solar cell, wherein the polyurethane-based adhesive has hydrolysis resistance satisfying the following conditions.
-It has a laminate strength of 1 N / 15 mm or more in a high pressure cooker (accelerated evaluation device using pressurized steam) at least at 105 ° C. to 168 h.
-In storage evaluation with a high pressure cooker (accelerated evaluation device using pressurized steam), there is no floating between substrates due to delamination. 2. The solar cell back surface sealing sheet according to claim 1, wherein the polyol is a polyol-based composition in which 50 to 99 wt% of the polyol B is blended with respect to 1 to 50 wt% of the following polyol A. 3.
Polyol A: A polyester polyol or a polyester urethane polyol chain-extended with a bifunctional or higher functional isocyanate compound, either alone or as a mixture. 2. The polyol according to claim 1, wherein the polyol is a copolymer-type polyol obtained by subjecting the polyol B to 50 to 99 wt% and the following polyol A to 1 to 50 wt% to chain extension with a bifunctional or higher isocyanate compound. Solar cell back surface sealing sheet.
Polyol A: A polyester polyol or a polyester urethane polyol chain-extended with a bifunctional or higher functional isocyanate compound, either alone or as a mixture.   The cross-linking agent is 2,4- or 2,6-tolylene diisocyanate, xylylene diisocyanate, 4,4'-diphenylmethane diisocyanate, methylene diisocyanate, isopropylene diisocyanate, lysine diisocyanate, 2,2,4-- or 2, Isocyanate selected from the group consisting of 4,4-trimethylhexamethylene diisocyanate, 1,6-hexamethylene diisocyanate, methylcyclohexane diisocyanate, isophorone diisocyanate, 4,4′-dicyclohexylmethane diisocyanate, isopropylidene dicyclohexyl-4,4′-diisocyanate 4. An adduct body, a burette body, or an isocyanurate body derived from a compound. A rear surface of a solar cell sealing sheet according to an item or.   The substrate is a polyester substrate selected from polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polybutylene terephthalate (PBT), polycyclohexanedimethanol-terephthalate (PCT), polycarbonate substrate, polyvinyl fluoride ( PVF), polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), polyethylene tetrafluoroethylene (ETFE), polytetrafluoroethylene (PTFE), tetrafluoroethylene perfluoroalkyl vinyl ether copolymer (PFA), tetra The fluorocarbon base material selected from fluoroethylene-hexafluoropropylene copolymer (FEP) or an acrylic base material is selected. Sealing a rear surface of a solar cell sheet according to the deviation or claim.   The base material is a polyester base material having hydrolysis resistance, in particular, having a number average molecular weight in the range of 18,000 to 40,000, a cyclic oligomer content of 1.5 wt% or less, and an intrinsic viscosity of 0.5 dl / g or more. The solar cell back surface sealing sheet according to any one of claims 1 to 5, wherein the solar cell back surface sealing sheet is provided.   7. The laminate according to claim 1, further comprising an aluminum foil base material as a gas barrier layer and a vapor deposition base material on which an inorganic compound such as metal aluminum, silica, and alumina is vapor-deposited. The sheet | seat for solar cell back surface sealing of description.