CN103579389B - A kind of solar module and preparation method thereof - Google Patents
A kind of solar module and preparation method thereof Download PDFInfo
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- CN103579389B CN103579389B CN201210265682.XA CN201210265682A CN103579389B CN 103579389 B CN103579389 B CN 103579389B CN 201210265682 A CN201210265682 A CN 201210265682A CN 103579389 B CN103579389 B CN 103579389B
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- adhesive layer
- refractive index
- hot melt
- solar module
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- 238000002360 preparation method Methods 0.000 title claims abstract description 31
- 239000010410 layer Substances 0.000 claims abstract description 76
- 239000004831 Hot glue Substances 0.000 claims abstract description 39
- 239000012790 adhesive layer Substances 0.000 claims abstract description 36
- 229920006264 polyurethane film Polymers 0.000 claims abstract description 33
- 239000012528 membrane Substances 0.000 claims abstract description 11
- 238000007639 printing Methods 0.000 claims abstract description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 25
- 239000004611 light stabiliser Substances 0.000 claims description 24
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 20
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 20
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 17
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 17
- 239000004814 polyurethane Substances 0.000 claims description 16
- 229920002635 polyurethane Polymers 0.000 claims description 15
- -1 salicylic acid lipid Chemical class 0.000 claims description 14
- 239000002131 composite material Substances 0.000 claims description 12
- 239000003963 antioxidant agent Substances 0.000 claims description 11
- 239000012760 heat stabilizer Substances 0.000 claims description 11
- 239000012948 isocyanate Substances 0.000 claims description 11
- 238000005984 hydrogenation reaction Methods 0.000 claims description 10
- 230000003078 antioxidant effect Effects 0.000 claims description 9
- 239000011521 glass Substances 0.000 claims description 9
- 238000007731 hot pressing Methods 0.000 claims description 9
- GTACSIONMHMRPD-UHFFFAOYSA-N 2-[4-[2-(benzenesulfonamido)ethylsulfanyl]-2,6-difluorophenoxy]acetamide Chemical compound C1=C(F)C(OCC(=O)N)=C(F)C=C1SCCNS(=O)(=O)C1=CC=CC=C1 GTACSIONMHMRPD-UHFFFAOYSA-N 0.000 claims description 7
- 101710130081 Aspergillopepsin-1 Proteins 0.000 claims description 7
- 102100031007 Cytosolic non-specific dipeptidase Human genes 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 7
- 150000002513 isocyanates Chemical class 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 239000012964 benzotriazole Substances 0.000 claims description 4
- 150000003918 triazines Chemical class 0.000 claims description 4
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 3
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- KPTLPIAOSCGETM-UHFFFAOYSA-N benzene 1,2-diisocyanatoethane Chemical compound O=C=NCCN=C=O.c1ccccc1 KPTLPIAOSCGETM-UHFFFAOYSA-N 0.000 claims description 3
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 3
- 230000000149 penetrating effect Effects 0.000 claims description 3
- 150000008301 phosphite esters Chemical class 0.000 claims description 3
- 229930185605 Bisphenol Natural products 0.000 claims description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N Salicylic acid Natural products OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 2
- 239000012965 benzophenone Substances 0.000 claims description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 229960004889 salicylic acid Drugs 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 24
- 238000002834 transmittance Methods 0.000 abstract description 10
- 230000008569 process Effects 0.000 abstract description 9
- 230000003667 anti-reflective effect Effects 0.000 abstract description 7
- 238000006243 chemical reaction Methods 0.000 abstract description 6
- 230000005611 electricity Effects 0.000 abstract description 5
- 230000032683 aging Effects 0.000 abstract description 4
- 239000010408 film Substances 0.000 description 28
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 23
- 229910052710 silicon Inorganic materials 0.000 description 23
- 239000010703 silicon Substances 0.000 description 23
- 239000002313 adhesive film Substances 0.000 description 13
- 239000006117 anti-reflective coating Substances 0.000 description 9
- 239000012943 hotmelt Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 238000010030 laminating Methods 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical class CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000000306 component Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 238000003475 lamination Methods 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- 229910003978 SiClx Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- GLDOVTGHNKAZLK-UHFFFAOYSA-N n-octadecyl alcohol Natural products CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- YAXWOADCWUUUNX-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidine Chemical compound CC1CCCN(C)C1(C)C YAXWOADCWUUUNX-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 229920000305 Nylon 6,10 Polymers 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 235000008216 herbs Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920005591 polysilicon Polymers 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- JKQOXZANUWHVLY-UHFFFAOYSA-N (3,5-ditert-butyl-2-hydroxyphenyl) propanoate Chemical compound CCC(=O)OC1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1O JKQOXZANUWHVLY-UHFFFAOYSA-N 0.000 description 1
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical class OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 description 1
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-(1,1-dimethylethyl)-phenol Natural products CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- FMRHJJZUHUTGKE-UHFFFAOYSA-N Ethylhexyl salicylate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1O FMRHJJZUHUTGKE-UHFFFAOYSA-N 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 235000017858 Laurus nobilis Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229910004205 SiNX Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 244000125380 Terminalia tomentosa Species 0.000 description 1
- 235000005212 Terminalia tomentosa Nutrition 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229910021419 crystalline silicon Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000000686 essence Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 230000005622 photoelectricity Effects 0.000 description 1
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
- H01L31/0481—Encapsulation of modules characterised by the composition of the encapsulation material
-
- 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
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/10—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the pressing technique, e.g. using action of vacuum or fluid pressure
-
- 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
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/12—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by using adhesives
- B32B37/1207—Heat-activated adhesive
-
- 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
- B32B7/04—Interconnection of layers
- B32B7/10—Interconnection of layers at least one layer having inter-reactive properties
-
- 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
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/12—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by using adhesives
- B32B37/1207—Heat-activated adhesive
- B32B2037/1215—Hot-melt adhesive
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Electromagnetism (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Fluid Mechanics (AREA)
- Photovoltaic Devices (AREA)
Abstract
The invention provides a kind of solar module and preparation method thereof, this solar module includes hot melt adhesive layer/some solar battery sheet/adhesive layer/backboards of the printing opacity upper cover plate/adhesive layer/refractive index 1.6 1.7 stacked gradually, the polyurethane film that hot melt adhesive layer is refractive index 1.6 1.7 of described refractive index 1.6 1.7 and/or the modified polyorganosiloxane film of refractive index 1.6 1.7.The anti-reflective effect on solar battery sheet surface is good, and the electricity conversion of solar module is high, and solar battery sheet need not carry out the process of complexity, and hot melt adhesive layer is on solar battery sheet without impact simultaneously, and technique the most easily realizes, and thickness is easy to control.And the hot melt adhesive layer of the present invention is organic membrane, having good flexibility, the compatibility in solar module is good, also has certain cohesive force simultaneously, has the characteristics such as light transmittance is high, heat-resisting, cold-resistant, moisture-proof, ageing-resistant, mechanical strength is high.
Description
Technical field
The present invention relates to a kind of solar module and preparation method thereof.
Background technology
Along with the increasingly sharpening of day by day exhausted, problem of environmental pollution of traditional energy, the development and application of new forms of energy is
Through becoming the focus of human research.Solar energy inexhaustible, green non-pollution is the weight that new energy development utilizes
One of point.
Owing to the refractive index of silicon is 3.8, and the refractive index of air is 1.0, smooth silicon face to the reflectance of light up to
To about 30%, cause solar battery sheet relatively low to the absorption of light, therefore to the photoelectricity improving crystal silicon solar energy battery turns
Change efficiency, it usually needs reduce the luminous reflectance of silicon chip front surface, also need to be passivated surface of crystalline silicon processing, with fall simultaneously
Low surface defect is for the compound action of minority carrier.Prior art has research to use the texturing on surface to reduce a part
Reflection, generally by corrosion treatmentCorrosion Science, increases the roughness of silicon chip surface, but the reduction of reflectance inconspicuous, particularly
For polysilicon, using anisotropic acid system making herbs into wool, the black line of generation is easily destroyed PN junction, makes the electric leakage of solar battery sheet
Stream increases.What prior art commonly used is to cover, at silicon chip surface, the light transmission medium film that one layer of refractive index is moderate, thus reduces
Silicon chip surface reflects.One layer of silicon nitride film is prepared in being usually after removing removing oxide layer of existing technology, is a kind of excellent subtracting
Reflectance coating.Owing to silicon face has substantial amounts of dangling bonds, the nonequilibrium carrier for N type launch site has the strongest capture
Compound action, so that the short circuit current of cell piece and open-circuit voltage reduce.And hydrogeneous SiNx:H film has for silicon face
Passivation, decreases the undersaturated dangling bonds in surface, decreases surface energy level, be typically prepared one layer, the refraction of silicon nitride film
Rate is 1.9-2.1.Existing also have research to prepare, at silicon chip surface, the silicon nitride film antireflective coating that two-layer refractive index is different, such as, have
The surface being disclosed in solar battery sheet has the thick 155-65nm ground floor silicon nitride film and refractive index that refractive index is 2.3-2.6
Second layer silicon nitride film for the thick 85-110nm of 1.4-1.7;It is also disclosed employing multilamellar (such as seven layers) thickness difference, refraction
The multi-layer nano thin-film material superposition that rate changes in gradient, to prepare antireflective coating, is rolled over by the antireflective coating of contact silicon chip surface
Rate of penetrating is high, and the refractive index of the antireflective coating of solar battery sheet outer layer is little, reduces the silicon chip reflection to light further, increases light
Absorbance.But its for essentially modification to silicon chip, and silicon chip is the core component of solaode, it is desirable to high, table
Face modified technique is complicated, and other performances of solar battery sheet also can be existed impact, and film requires height, and preparation is difficult, and this
A little antireflective coatings are all inorganic material, and the low machinability of pliability is low, also increases difficulty prepared by follow-up solar module
Degree, the anti-reflective effect of the most existing silicon chip surface does not reaches ideal effect.
Summary of the invention
The present invention is to solve that the antireflective on the solar battery sheet surface in the solar module of prior art is imitated
The most undesirable and other performances of solar battery sheet are impacted, the technical problem of complex process, it is provided that a kind of solar energy
The anti-reflective effect on cell piece surface is good, and the absorption efficiency of light is high, solar module that electricity conversion is high and system thereof
Preparation Method.
First purpose of the present invention is to provide a kind of solar module, and this solar module includes layer successively
Hot melt adhesive layer/some solar battery sheet/adhesive layer/back ofs the body of folded printing opacity upper cover plate/adhesive layer/refractive index 1.6-1.7
Plate, the hot melt adhesive layer of described refractive index 1.6-1.7 is the polyurethane film of refractive index 1.6-1.7, and/or refractive index 1.6-1.7
Modified polyorganosiloxane film.
Second object of the present invention is to provide the preparation method of above-mentioned solar module, and step includes: by printing opacity
The hot melt adhesive layer of upper cover plate/adhesive layer/refractive index 1.6-1.7/some solar battery sheets/adhesive layer/backboard layer successively
Folded, after the most hot-forming the solar module.
The present inventor has been surprisingly found that subtracting of the solar battery sheet surface in the solar module of the present invention
Reflecting effect is significantly improved, and improves the utilization rate of light, improves the electricity conversion of battery.The present invention is the most sharp
Form composite film with composite hot melt glue-line on solar battery sheet surface, reflectance can be made minimum near centre wavelength,
So that the effective luminous flux entering silicon chip is maximum, improve the efficiency of battery.The film layer on solar battery sheet surface is from top to bottom
It is followed successively by hot melt adhesive layer/solar battery sheet (common process surface system of printing opacity upper cover plate/adhesive layer/refractive index 1.6-1.7
Have silicon nitride film), refractive index increases successively and advantageously reduces light line reflection.The present invention by compound special refractive index is
The hot melt adhesive layer of 1.6-1.7, thus form adhesive layer/refractive index 1.6-1.7 being followed successively by refractive index 1.4-1.5 from top to bottom
The surfaces nitrided silicon layer of solar battery sheet of hot melt adhesive layer/refractive index 1.9-2.1, define from EVA-polyurethane-carborundum
The refractive index of material increases successively, is also formed with effect ground refractive index match, and the effective luminous flux making entrance solaode is maximum,
Improve the efficiency of solaode, and solar battery sheet need not be carried out the process of complexity.Simultaneously because hot melt adhesive layer is not required to
Will prepare at silicon chip surface, after film forming can be manufactured separately, laying forms solar components, the therefore preparation process of hot melt adhesive layer
Solar battery sheet impact will not be produced, during lamination, laying the surface of solar battery sheet can be compounded in together with EVA layer,
Technique the most easily realizes.And the hot melt adhesive layer of the present invention is organic membrane, there is good flexibility, can be with solar battery sheet
Combine very well with adhesive layer, in the lamination process of solar module, can be one-body molded with adhesive layer, do not result in
Bubble, impurity etc., film surface is smooth, and the compatibility in solar module is good, also have simultaneously certain cohesive force,
There is the characteristics such as light transmittance is high, heat-resisting, cold-resistant, moisture-proof, ageing-resistant, mechanical strength is high, can obtain in solar module
Well application.
Detailed description of the invention
In order to make technical problem solved by the invention, technical scheme and beneficial effect clearer, below in conjunction with
Embodiment, is further elaborated to the present invention.Should be appreciated that specific embodiment described herein is only in order to explain
The present invention, is not intended to limit the present invention.
The invention provides a kind of solar module, this solar module includes the printing opacity upper cover stacked gradually
The hot melt adhesive layer of plate/adhesive layer/refractive index 1.6-1.7/some solar battery sheet/adhesive layer/backboards, described refractive index
The hot melt adhesive layer of 1.6-1.7 is polyurethane film and/or the modified polyorganosiloxane film of refractive index 1.6-1.7 of refractive index 1.6-1.7.
Wherein, the anti-reflective effect on solar battery sheet surface is good, and the absorption efficiency of light is high, the photoelectric conversion effect of solar module
Rate is high.
Preferably, the thickness of the hot melt adhesive layer of refractive index 1.6-1.7 is 20-300nm, more preferably 80-250nm, relatively
It is 200nm in the case of good.The center frequency-band of need light to be processed can be adjusted, so that anti-reflective effect is by regulation thickness
Good.
Preferably, the hot melt adhesive layer of refractive index 1.6-1.7 is the polyurethane film of refractive index 1.6-1.7, in solar battery group
Can laying hot pressing together with EVA layer in part, it is preferable that the polyurethane film of refractive index 1.6-1.7 is by by PEPA, isocyanide
Acid esters, light stabilizer and heat stabilizer react to obtain polyurethane solutions in a solvent, and rear film forming obtains polyurethane film, described isocyanates
In toluene di-isocyanate(TDI), isophorone diisocyanate or the hydrogenation of benzene dimethylene diisocyanate of hydrogenation one
Kind.Wherein, prepare polyurethane film ageing-resistant, that refractive index is unique by the isocyanates without phenyl ring, be applied to the present invention's
In solar module, optimize light transmittance the most further, and the service life of assembly can be improved.
Film forming is preferably and is coated in mould release membrance or release paper by polyurethane solutions, dries to obtain poly-ammonia through 60 DEG C-120 DEG C
Ester composite membrane, removes mould release membrance by polyurethane composite membrane or release paper is transferred on solar battery sheet and/or adhesive layer
Polyurethane film, preparation method is simple, simultaneously to the miscellaneous part in solar module such as solar battery sheet or bonding
Oxidant layer etc. are without impact.In the case of compare Jia, polyurethane composite membrane can be removed mould release membrance or release paper is transferred at 0-50 DEG C
Obtaining polyurethane film on adhesive layer, can process with adhesive layer integrated molding, technique is simple, saves the energy, reduces cost.
Printing opacity upper cover plate can be the upper cover plate that solar module is conventional, such as glass plate etc..
Backboard can be the backboard that solar module is conventional, such as TPT composite membrane, TPE composite membrane, BBF composite membrane,
Polyimide composite film, it is also possible to for glass or steel plate etc..
Adhesive layer can be selected for ethylene-vinyl acetate copolymer (EVA) layer or polyvinyl butyral resin (PVB) layer,
More preferably ethylene-vinyl acetate copolymer (EVA) layer, makes the tool between layers of the solar module of the present invention
There is preferably degree of laminating, improve the sealing of assembly, improve security intensity and water resistance, the thickness of adhesive layer of assembly
It is preferably 0.25-0.80mm, more preferably 0.4-0.5mm, optimizes the intensity of battery component, it is to avoid cell piece sliver,
The thickness of solar module is also optimized simultaneously.
The various solar battery sheets that solar battery sheet can be known to the skilled person, can be polysilicon or
Monocrystaline silicon solar cell sheet, it is also possible to for silicon film solar batteries sheet.Wherein solar battery sheet is usually silicon chip process
Technique → removal damage layer → making herbs into wool → diffusion technique → the periphery that deoils etches → goes removing oxide layer → silicon nitride film → silk screen processed
The printing back of the body, anelectrode → sintering → testing, sorting etc. prepare.When being assembled into solar module, solar battery sheet with
Silicon nitride anti-reflecting film is contained on the surface of the hot melt adhesive layer contact of refractive index 1.6-1.7, and silicon nitride anti-reflecting film is the present invention do not have
Limit, can be one layer, it is also possible to for multilamellar, the present invention is one layer, and the preferably refractive index of silicon nitride anti-reflecting film is 1.9-
2.1, form optimal refractive index gradient, improve light transmittance, can be prepared by the conventional method preparing silicon nitride anti-reflecting film,
Such as the silicon chip removing removing oxide layer is placed in SINA_XXL_PECVD technique storehouse, with SiH4And NH3For reaction source, at silicon chip table
Face deposited silicon nitride antireflective coating.
The number present invention of solar battery sheet does not limit, and it can also be multiple, according to the electricity of preparation for can being one
Cell voltage demand, can form array with the some solar battery sheets of serial or parallel connection.
Invention also provides the preparation method of above-mentioned solar module, step includes: by printing opacity upper cover plate/viscous
Knot oxidant layer/refractive index 1.6-1.7 hot melt adhesive layer/some solar battery sheet/adhesive layer/backboards stack gradually, after very
Hot-forming solar module under empty condition.The most hot-forming general by printing opacity upper cover plate/binding agent
The hot melt adhesive layer of layer/refractive index 1.6-1.7/some solar battery sheet/adhesive layer/backboards put into lamination after stacking gradually
In heating plate in machine, evacuation, simultaneously heating plate, realize the solar energy to stacking by the elastica on laminating machine top cover
The hot pressing of battery component, makes solar module molding, gets rid of the gas within solar module simultaneously.Preferably, heat
The temperature of pressure is 120-150 DEG C, and the time of hot pressing is 12-20min.
Preferably, the preparation method of the hot melt adhesive layer of refractive index 1.6-1.7 includes will be attached on release paper or mould release membrance
The hot melt adhesive layer of refractive index 1.6-1.7 removes release paper or mould release membrance is transferred on adhesive layer and/or solar battery sheet, side
Method the most easily realizes, and on solar battery sheet and adhesive layer etc. all without impact, the film surface of preparation is smooth.Preferably situation
Under, hot melt adhesive layer removal release paper or the mould release membrance that can will be attached to refractive index 1.6-1.7 on release paper or mould release membrance exist
Being transferred on adhesive layer at 0-50 DEG C, process with adhesive layer integrated molding, technique is simple, saves the energy, reduces cost.
Preferably, the preparation process of the hot melt adhesive layer being attached to refractive index 1.6-1.7 on release paper or mould release membrance include by
PEPA, isocyanates, light stabilizer and heat stabilizer react to obtain polyurethane solutions in a solvent, after by polyurethane solutions
It is coated in mould release membrance or release paper, through 60 DEG C-120 DEG C polyurethane films drying to be attached in release paper or mould release membrance;Institute
State isocyanates toluene di-isocyanate(TDI), isophorone diisocyanate or hydrogenation of benzene dimethylene two Carbimide. selected from hydrogenation
One in ester.
Preferably, the preparation process of the hot melt adhesive layer being attached to refractive index 1.6-1.7 on release paper or mould release membrance also includes
Be attached on the polyurethane film in release paper or mould release membrance be combined mould release membrance or release paper again at gained, described compound mould release membrance or
The temperature of release paper is 10-110 DEG C, and the polyurethane film of preparation easily shifts and transfers, easy to operate, with adhesive layer and solar energy
The adhesive property of cell piece is good, and stacking is more smooth, it is to avoid impurity etc..
Preferably, light stabilizer is steady selected from salicylic acid lipid light stabilizer, benzophenone light stabilizer, benzotriazole light
Determine agent, triazines as light stabilizer, replacement propylene fine class light stabilizer, oxamide light stabilizer, organo-nickel compounds class light steady
Determine one or more in agent, hindered amine light stabilizer or light shield class light stabilizer, preferably in the case of, be specifically as follows
ESCALOL 567,2-hydroxyl-4-octyloxy-benzophenone, 2-(2 '-hydroxyl-3 ', 5 '-diamyl benzene
Base) benzotriazole, 2-(2 '-hydroxyl-3 ' dodecyl-5 '-methyl)-benzotriazole, N-(2-ethoxyl phenenyl)-N '-(4-second
Base phenyl) oxalamide, 4 benzoic acid ethyl ester)-N ', N '-(methyl, phenyl) carbonamidine, double (2,2,6,6-tetramethyl piperidines
Base) sebacate, poly-[1-(2`-ethoxy)-2,2,6,6-tetramethyl-4-hydroxy piperidine succinate], poly-[6-[(1,1,
3,3 ,-tetramethyl butyl)-amido] 1,3,5 ,-triazine-2,4-diyl] [(2,2,6,6-tetramethyl-piperidyl)-imido grpup]-1,
6-hexane diyl-[(2,2,6,6-tetramethyl-piperidyl)-imido grpup] }, zinc oxide, one or more in titanium dioxide.Excellent
Choosing, relative to the PEPA of 100 weight portions, the amount of described light stabilizer is 0.1-1 weight portion, more preferably 0.1-
0.5 weight portion,
Described heat stabilizer resists selected from Hinered phenols antioxidant, amine antioxidants, phosphite ester kind antioxidant, monothioester class
One or more in oxygen agent, antioxidant of bisphenol monoacryate or triazines antioxidant, preferably in the case of, be specifically as follows
β-(4-hydroxyl-3,5-di-tert-butyl-phenyl) propanoic acid octadecyl alcohol ester, β-(4-hydroxyl-3,5-di-tert-butyl-phenyl) Ji Wusi
Alcohol ester, three (2,4-DI-tert-butylphenol compounds) phosphite ester, double stearyl alcohol pentaerythritol diphosphites, double (3,5-bis-uncle
Butyl phenyl) pentaerythritol diphosphites, 3,3 '-propane thioic acid Laurel alcohol ester, 3,3 '-propane thioic acid tristearin alcohol ester, sulfur generation
Second two supports double [3-(3,5-di-t-butyl tetrahydroxy phenyl) propionic ester], 2,4-(dimethylene octyl thioether)-6-methylbenzene
Phenol, N, one or more in N '-bis-[β (3,5-di-tert-butyl-hydroxy phenyl) propionyl]-1,6-hexamethylene diamine.Preferably, relatively
In the PEPA of 100 weight portions, the amount of described heat stabilizer is 0.1-1 weight portion, more preferably 0.1-0.5 weight
Part.
Described solvent is toluene or ethyl acetate.
The shape of solar module of preparation can use well known to a person skilled in the art variously-shaped, at solar energy
The week of battery component, along cladding bezel seal, installs connection rosette etc. on backboard and can be prepared as solaode.Solar energy
Other structures of battery and device all can use and well known to a person skilled in the art various structure and device, does not goes to live in the household of one's in-laws on getting married at this
State.
Unless stated otherwise, various solvent of the present invention and reagent are commercially available analytical reagent.
Below in conjunction with specific embodiment, the present invention is further described.
Embodiment 1
Hydrogenated toluene by the polyester diol (682#, hydroxyl value 13mgKOH/g are spun by Japan) of 100 mass parts Yu 3 mass parts
Diisocyanate (H6TDI), double 2,2,6, the 6 tetramethyl piperidine alcohol esters of the hindered amine light stabilizer decanedioic acid of 0.3 mass parts
(chisorb770) heat stabilizer β (3,5-di-tert-butyl-hydroxy phenyl) the propanoic acid octadecyl alcohol ester of and 0.3 mass parts
(chinox1076) it is blended in toluene, obtains polyurethane-hot melt sol solution.
Polyurethane-hot melt sol solution coating machine is coated on mould release membrance, dries at 120 DEG C and make about 200nm
Polyurethane film, in 50 DEG C of thermal transfers to EVA packaging adhesive film, according to glass/with the EVA adhesive film/solar-electricity of polyurethane film
The order stacking of pond sheet/EVA adhesive film/backboard, wherein, it is 2.0 nitrogen that one layer of refractive index is contained on the solar battery sheet surface of selection
SiClx antireflective coating, puts in laminating machine, in 138 DEG C of evacuation hot pressing 19min, carries out solar battery group laminated into type
Part.
The refractive index of the polyurethane film that employing abbe's refractometer records preparation is 1.62.
Embodiment 2
By the polyhexamethylene adipate glycol (PHA, hydroxyl value 35 mgKOH/g, Liming chemical Inst) of 100 mass parts;
The polyether polyol (PPG, hydroxyl value 56mgKOH/g, Liming chemical Inst) of 100 mass parts;The hydrogenation 4,4'-of 42 mass parts
Methyl diphenylene diisocyanate (H12MDI., purity 99.6%, Yantai Wanhua Polyurethane Co., Ltd);0.1 mass parts
Heat stabilizer β (3,5-di-tert-butyl-hydroxy phenyl) propionate (chinox1010), the sulfur of 0.2 mass parts
Double [3-(3,5-di-t-butyl tetrahydroxy phenyl) propionic ester] (chinox 1035), the hindered amines of 0.3 mass parts is supportted for second two
Light stabilizer poly-[1-(2 '-ethoxy)-2,2,6,6 tetramethyl piperidine succinates] (chisorb622) is blended in toluene,
Obtain polyurethane-hot melt sol solution.
Polyurethane-hot melt sol solution coating machine is coated on mould release membrance, dries at 120 DEG C and make about 200nm
Polyurethane film, in 50 DEG C of thermal transfers to EVA packaging adhesive film, according to glass/with the EVA adhesive film/solar-electricity of polyurethane film
The order stacking of pond sheet/EVA adhesive film/backboard, wherein, it is 2.0 nitrogen that one layer of refractive index is contained on the solar battery sheet surface of selection
SiClx antireflective coating, puts in laminating machine, in 138 DEG C of evacuation hot pressing 19min, carries out solar battery group laminated into type
Part.
The refractive index using the polyurethane film that method same as in Example 1 records preparation is 1.65.
Embodiment 3
By the polyether polyol (PPG, hydroxyl value 56mgKOH/g, Liming chemical Inst) of 100 mass parts;14.6 mass
The hydrogenation Asia xylylene diisocyanate (H6XDI, purity 99.6%, Yantai Wanhua Polyurethane Co., Ltd) of part; 0.5
Heat stabilizer 2-hydroxyl-4-octyloxybenzophenone (UV531) of mass parts, the tricresyl phosphite (nonyl phenyl) of 1 mass parts
(Naugard P), double 2,2,6, the 6 tetramethyl piperidine alcohol esters of the hindered amine light stabilizer decanedioic acid of 0.5 mass parts
(chisorb770) it is blended in toluene, obtains polyurethane-hot melt sol solution.
Polyurethane-hot melt sol solution coating machine is coated on mould release membrance, dries at 120 DEG C and make about 200nm
Polyurethane film, in 50 DEG C of thermal transfers to EVA packaging adhesive film, according to glass/with the EVA adhesive film/solar-electricity of polyurethane film
The order stacking of pond sheet/EVA adhesive film/backboard, wherein, it is 2.0 nitrogen that one layer of refractive index is contained on the solar battery sheet surface of selection
SiClx antireflective coating, puts in laminating machine, in 138 DEG C of evacuation hot pressing 19min, carries out solar battery group laminated into type
Part.
The refractive index using the polyurethane film that method same as in Example 1 records preparation is 1.63.
Embodiment 4
Using method same as in Example 1 to prepare solar module, except for the difference that the thickness of polyurethane film is
80nm。
Embodiment 5
Using method same as in Example 1 to prepare solar module, except for the difference that the thickness of polyurethane film is
250nm。
Embodiment 6
Using method same as in Example 1 to prepare solar module, except for the difference that the thickness of polyurethane film is
300nm。
Comparative example 1
According to the order stacking of glass/EVA adhesive film/solar battery sheet/EVA adhesive film/backboard, wherein, the sun of selection
It is 2.0 silicon nitride anti-reflecting films that one layer of refractive index is contained on energy cell piece surface, puts in laminating machine, in 138 DEG C of evacuation hot pressing
19min, carries out solar module laminated into type.
Performance test:
Use all band light transmittance tester testing example 1-6 glass/EVA adhesive film/polyurethane film light transmittance and
The light transmittance of the glass/EVA adhesive film of comparative example 1, test result such as table 1.
Table 1
Light transmittance | |
Embodiment 1 | 92.0 |
Embodiment 2 | 91.8 |
Embodiment 3 | 92.2 |
Embodiment 4 | 91.8 |
Embodiment 5 | 92.2 |
Embodiment 6 | 92.1 |
Comparative example 1 | 90.2 |
The light transmittance on the solar battery sheet surface of solar module prepared by the present invention is high, significantly improves the sun
The anti-reflective effect on energy cell piece surface, can improve the utilization rate of light, can improve the electricity conversion of battery.And need not be to too
Sun can carry out complicated process by cell piece, and hot melt adhesive layer is on solar battery sheet without impact simultaneously, can be fabricated separately, during lamination
Being compounded in the surface of solar battery sheet, technique the most easily realizes, and thickness is easy to control.And the hot melt adhesive layer of the present invention is organic
Film, has good flexibility, can be combined very well with solar battery sheet and adhesive layer, at the layer of solar module
During pressure, can be one-body molded with adhesive layer, do not result in bubble, impurity etc., film surface is smooth, in solar battery group
The compatibility in part is good, also have simultaneously certain cohesive force, have that light transmittance is high, heat-resisting, cold-resistant, moisture-proof, ageing-resistant, mechanical
The characteristics such as intensity is high, can well be applied in solar module.
The foregoing is only presently preferred embodiments of the present invention, not in order to limit the present invention, all essences in the present invention
Any amendment, equivalent and the improvement etc. made within god and principle, should be included within the scope of the present invention.
Claims (15)
1. a solar module, it is characterised in that described solar module includes the printing opacity upper cover stacked gradually
The hot melt adhesive layer of plate/adhesive layer/refractive index 1.6-1.7/some solar battery sheet/adhesive layer/backboards, described solar energy
Silicon nitride anti-reflecting film is contained on the surface that cell piece contacts with hot melt adhesive layer, and the hot melt adhesive layer of described refractive index 1.6-1.7 is folding
Penetrate the polyurethane film of rate 1.6-1.7 and/or the modified polyorganosiloxane film of refractive index 1.6-1.7;Described adhesive layer, hot melt adhesive layer
Increase successively with the refractive index of silicon nitride anti-reflecting film.
Solar module the most according to claim 1, it is characterised in that the PUR of described refractive index 1.6-1.7
The thickness of layer is 20-300nm.
Solar module the most according to claim 2, it is characterised in that the PUR of described refractive index 1.6-1.7
The thickness of layer is 80-250nm.
Solar module the most according to claim 1, it is characterised in that the PUR of described refractive index 1.6-1.7
Layer is the polyurethane film of refractive index 1.6-1.7, and the polyurethane film of described refractive index 1.6-1.7 is by by PEPA, isocyanide
Acid esters, light stabilizer and heat stabilizer react to obtain polyurethane solutions in a solvent, and rear film forming obtains polyurethane film, described isocyanates
In toluene di-isocyanate(TDI), isophorone diisocyanate or the hydrogenation of benzene dimethylene diisocyanate of hydrogenation one
Kind.
Solar module the most according to claim 4, it is characterised in that polyurethane solutions is coated in mould release membrance or
In release paper, dry to obtain polyurethane composite membrane through 60 DEG C-120 DEG C, polyurethane composite membrane is removed mould release membrance or release paper transfer
Solar battery sheet and/or adhesive layer obtain polyurethane film.
Solar module the most according to claim 5, it is characterised in that by polyurethane composite membrane remove mould release membrance or
Release paper is transferred on adhesive layer to obtain polyurethane film at 0-50 DEG C.
Solar module the most according to claim 1, it is characterised in that described solar battery sheet and refractive index
One layer of silicon nitride anti-reflecting film, the refractive index of described silicon nitride anti-reflecting film are contained in the surface of the hot melt adhesive layer contact of 1.6-1.7
For 1.9-2.1.
Solar module the most according to claim 1, it is characterised in that described printing opacity upper cover plate is glass;Described
Adhesive layer is ethylene-vinyl acetate copolymer layer.
9. the preparation method of a solar module as claimed in claim 1, it is characterised in that step includes: will be thoroughly
The hot melt adhesive layer of light upper cover plate/adhesive layer/refractive index 1.6-1.7/some solar battery sheet/adhesive layer/backboards are successively
Stacking, after the most hot-forming the solar module.
Preparation method the most according to claim 9, it is characterised in that the system of the hot melt adhesive layer of described refractive index 1.6-1.7
Preparation Method includes that the hot melt adhesive layer that will be attached to refractive index 1.6-1.7 on release paper or mould release membrance removes release paper or mould release membrance
It is transferred on adhesive layer and/or solar battery sheet.
11. preparation methoies according to claim 10, it is characterised in that the hot melt adhesive layer of described refractive index 1.6-1.7
Preparation method includes that the hot melt adhesive layer that will be attached to refractive index 1.6-1.7 on release paper or mould release membrance removes mould release membrance or release
Paper is transferred on adhesive layer at 0-50 DEG C.
12. preparation methoies according to claim 10, it is characterised in that described in be attached to the folding on release paper or mould release membrance
The preparation process of the hot melt adhesive layer penetrating rate 1.6-1.7 includes existing PEPA, isocyanates, light stabilizer and heat stabilizer
Solvent reacts to obtain polyurethane solutions, after polyurethane solutions is coated in mould release membrance or release paper, through 60 DEG C-120 DEG C drying
The polyurethane film on release paper or mould release membrance must be attached to;Described isocyanates is selected from the toluene di-isocyanate(TDI) of hydrogenation, different Buddhist
One in that ketone diisocyanate or hydrogenation of benzene dimethylene diisocyanate.
13. preparation methoies according to claim 12, it is characterised in that described in be attached to the folding on release paper or mould release membrance
The preparation process of the hot melt adhesive layer penetrating rate 1.6-1.7 is additionally included in gained and is attached on the polyurethane film on release paper or mould release membrance
Being combined mould release membrance or release paper again, the temperature of described compound mould release membrance or release paper is 10-110 DEG C.
14. preparation methoies according to claim 12, it is characterised in that described light stabilizer is steady selected from salicylic acid lipid light
Determine agent, benzophenone light stabilizer, benzotriazole light stabilizer, triazines as light stabilizer, replacement propylene fine class light stably
Agent, oxamide light stabilizer, organo-nickel compounds class light stabilizer, hindered amine light stabilizer or light shield class light are stable
One or more in agent;Described heat stabilizer selected from Hinered phenols antioxidant, amine antioxidants, phosphite ester kind antioxidant,
One or more in monothioester kind antioxidant, antioxidant of bisphenol monoacryate or triazines antioxidant;Described solvent is
Toluene or ethyl acetate;Relative to the PEPA of 100 weight portions, the amount of described light stabilizer is 0.1-1 weight portion, described
The amount of heat stabilizer is 0.1-1 weight portion.
15. preparation methoies according to claim 9, it is characterised in that the temperature of described hot pressing is 120-150 DEG C, hot pressing
Time be 12-20min.
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CN101933162A (en) * | 2007-12-03 | 2010-12-29 | 泰德里斯解决方案私人有限公司 | The flexible solar cell laminate that comprises semiconductor layer |
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