TW201840689A - Encapsulant for solar cells and solar cell module comprising the same - Google Patents
Encapsulant for solar cells and solar cell module comprising the same Download PDFInfo
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- TW201840689A TW201840689A TW107108871A TW107108871A TW201840689A TW 201840689 A TW201840689 A TW 201840689A TW 107108871 A TW107108871 A TW 107108871A TW 107108871 A TW107108871 A TW 107108871A TW 201840689 A TW201840689 A TW 201840689A
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- ethylene
- solar cell
- vinyl acetate
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- 239000008393 encapsulating agent Substances 0.000 title abstract 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 71
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 68
- 230000009467 reduction Effects 0.000 claims abstract description 10
- 239000005022 packaging material Substances 0.000 claims description 86
- 239000000395 magnesium oxide Substances 0.000 claims description 58
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 58
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 53
- 239000000463 material Substances 0.000 claims description 39
- 239000004594 Masterbatch (MB) Substances 0.000 claims description 20
- 238000002156 mixing Methods 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 17
- 238000004132 cross linking Methods 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 239000003431 cross linking reagent Substances 0.000 claims description 9
- 239000000758 substrate Substances 0.000 claims description 8
- 230000001681 protective effect Effects 0.000 claims description 7
- 238000005538 encapsulation Methods 0.000 claims description 6
- 230000000977 initiatory effect Effects 0.000 claims description 5
- 150000001451 organic peroxides Chemical class 0.000 claims description 5
- 238000001125 extrusion Methods 0.000 claims description 4
- 238000005520 cutting process Methods 0.000 claims description 3
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims description 2
- UPZFLZYXYGBAPL-UHFFFAOYSA-N 2-ethyl-2-methyl-1,3-dioxolane Chemical compound CCC1(C)OCCO1 UPZFLZYXYGBAPL-UHFFFAOYSA-N 0.000 claims 1
- 229920001567 vinyl ester resin Polymers 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract description 45
- -1 carbodiimide compound Chemical class 0.000 description 9
- 239000002245 particle Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- AZQWKYJCGOJGHM-UHFFFAOYSA-N para-benzoquinone Natural products O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 6
- 239000006087 Silane Coupling Agent Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical group C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000655 anti-hydrolysis Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- NALFRYPTRXKZPN-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane Chemical compound CC1CC(C)(C)CC(OOC(C)(C)C)(OOC(C)(C)C)C1 NALFRYPTRXKZPN-UHFFFAOYSA-N 0.000 description 1
- HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 description 1
- ZNCDSAZBKYUMAB-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)octane Chemical compound CCCCCCCC(OOC(C)(C)C)OOC(C)(C)C ZNCDSAZBKYUMAB-UHFFFAOYSA-N 0.000 description 1
- HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 description 1
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
- JGBAASVQPMTVHO-UHFFFAOYSA-N 2,5-dihydroperoxy-2,5-dimethylhexane Chemical compound OOC(C)(C)CCC(C)(C)OO JGBAASVQPMTVHO-UHFFFAOYSA-N 0.000 description 1
- OXYZDRAJMHGSMW-UHFFFAOYSA-N 3-chloropropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCl OXYZDRAJMHGSMW-UHFFFAOYSA-N 0.000 description 1
- MIHQWNKDHBLQEZ-UHFFFAOYSA-N 3-tert-butyl-2-methylphenol Chemical compound CC1=C(O)C=CC=C1C(C)(C)C MIHQWNKDHBLQEZ-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- BRQMAAFGEXNUOL-LLVKDONJSA-N [(2R)-2-ethylhexyl] (2-methylpropan-2-yl)oxy carbonate Chemical compound CCCC[C@@H](CC)COC(=O)OOC(C)(C)C BRQMAAFGEXNUOL-LLVKDONJSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 229960003328 benzoyl peroxide Drugs 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 1
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003902 salicylic acid esters Chemical class 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
- 230000001568 sexual effect Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- DLSMLZRPNPCXGY-UHFFFAOYSA-N tert-butylperoxy 2-ethylhexyl carbonate Chemical compound CCCCC(CC)COC(=O)OOOC(C)(C)C DLSMLZRPNPCXGY-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- JPMBLOQPQSYOMC-UHFFFAOYSA-N trimethoxy(3-methoxypropyl)silane Chemical compound COCCC[Si](OC)(OC)OC JPMBLOQPQSYOMC-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 238000004383 yellowing Methods 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
-
- 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
- H01L31/0488—Double glass encapsulation, e.g. photovoltaic cells arranged between front and rear glass sheets
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
- H01L31/049—Protective back sheets
-
- 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
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- 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)
- Photovoltaic Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Laminated Bodies (AREA)
Abstract
Description
發明領域 實施例有關一種用於太陽能電池的封裝材料,其具有優異的耐久性及防潮性,因此可使該太陽能電池之輸出功率的降低減至最小,以及一種包含該封裝材料之太能電池模組。FIELD OF THE INVENTION Embodiments relate to a packaging material for a solar cell, which has excellent durability and moisture resistance, so that a reduction in output power of the solar cell can be minimized, and a solar cell mold including the packaging material. group.
發明背景 乙烯-醋酸乙烯酯共聚物廣泛地用作為太陽能電池模組的封裝材料。然而,乙烯-醋酸乙烯酯共聚物具有因長時間曝露於外部時水解產生醋酸之問題。特別是,由此產生之醋酸會引起太陽能電池模組之電極腐蝕的問題,從而縮短了太陽能電池模組之使用期限。因此,研發人員致力於控制從乙烯-醋酸乙烯酯共聚物產生醋酸。BACKGROUND OF THE INVENTION Ethylene-vinyl acetate copolymers are widely used as packaging materials for solar cell modules. However, the ethylene-vinyl acetate copolymer has a problem that acetic acid is generated by hydrolysis when exposed to the outside for a long time. In particular, the resulting acetic acid will cause the electrode corrosion problem of the solar cell module, thereby shortening the lifetime of the solar cell module. As a result, researchers are working to control the production of acetic acid from ethylene-vinyl acetate copolymers.
作為最根本的解決方案,提出了一種用聚烯烴取代乙烯-醋酸乙烯酯共聚物作為太陽能電池模組的封裝材料之方法(韓國早期專利公開案第2009-0096487號)。然而,聚烯烴之耐熱性低於乙烯-醋酸乙烯酯共聚物,且聚烯烴封裝材料價格昂貴,因而限制了其之商業化。As the most fundamental solution, a method of replacing the ethylene-vinyl acetate copolymer as a packaging material for a solar cell module with a polyolefin (Korea Early Patent Publication No. 2009-0096487) has been proposed. However, polyolefins have lower heat resistance than ethylene-vinyl acetate copolymers, and polyolefin packaging materials are expensive, which limits their commercialization.
此外,日本專利案第5819159號及第5820132號揭示一種混合乙烯-醋酸乙烯酯共聚物與乙烯甲基丙烯酸共聚物之方法。然而,此無法確保抑制醋酸產生之作用,且二或多種樹脂之混合會增加製程之困難度。In addition, Japanese Patent Nos. 5619159 and 5820132 disclose a method of mixing an ethylene-vinyl acetate copolymer and an ethylene methacrylic acid copolymer. However, this cannot ensure the effect of suppressing the production of acetic acid, and the mixing of two or more resins will increase the difficulty of the process.
再者,日本專利案第4863812號揭示一種使用碳二亞胺化合物作為抗水解劑,以便抑制從乙烯-醋酸乙烯酯共聚物產生醋酸之方法。然而,該抗水解劑涉及封裝材料發生黃化之問題。Furthermore, Japanese Patent No. 4863812 discloses a method of using a carbodiimide compound as an anti-hydrolysis agent in order to suppress the production of acetic acid from an ethylene-vinyl acetate copolymer. However, the anti-hydrolysis agent involves the problem of yellowing of the packaging material.
技術問題 據此,一實施例目的在於提供一種用於太陽能電池的封裝材料,其憑藉著抑制從乙烯-醋酸乙烯酯共聚物產生醋酸而具有優異的耐久性,以致於有可能使該太陽能電池之輸出功率的降低及使用期限的縮短減至最小,及提供一種包含該封裝材料之太陽能電池模組。解決問題之方法 Technical Problem Accordingly, an embodiment aims to provide a packaging material for a solar cell, which has excellent durability by suppressing the production of acetic acid from an ethylene-vinyl acetate copolymer, so that it is possible to make the solar cell The reduction of the output power and the shortening of the service life are minimized, and a solar cell module including the packaging material is provided. Solutions to problems
用以達到以上目的之實施例提供一種用於太陽能電池的封裝材料,其包含:乙烯-醋酸乙烯酯共聚物及氧化鎂,其中以該乙烯-醋酸乙烯酯共聚物為100重量份計,該氧化鎂之含量為0.001至0.20重量份且具有50至200m2 /g之比表面積。The embodiment for achieving the above purpose provides a packaging material for a solar cell, comprising: an ethylene-vinyl acetate copolymer and magnesium oxide, wherein the oxide is based on 100 parts by weight of the ethylene-vinyl acetate copolymer, and the oxide The content of magnesium is 0.001 to 0.20 parts by weight and has a specific surface area of 50 to 200 m 2 / g.
另一實施例提供一種太陽能電池模組,其包含一透明保護基材、一第一封裝材料板、連接至一電極之至少一種太陽能電池、一第二封裝材料板及一背板,其等按此順序層壓,其中該第一封裝材料板及該第二封裝材料板中之至少一者包含乙烯-醋酸乙烯酯共聚物及氧化鎂,及以該乙烯-醋酸乙烯酯共聚物為100重量份計,該氧化鎂之含量為0.001至0.20重量份且具有50至200m2 /g之比表面積。Another embodiment provides a solar cell module including a transparent protective substrate, a first encapsulating material plate, at least one solar cell connected to an electrode, a second encapsulating material plate, and a back plate. This sequential lamination, wherein at least one of the first encapsulating material plate and the second encapsulating material plate comprises an ethylene-vinyl acetate copolymer and magnesium oxide, and the ethylene-vinyl acetate copolymer is 100 parts by weight The content of the magnesium oxide is 0.001 to 0.20 parts by weight and has a specific surface area of 50 to 200 m 2 / g.
又另一實施例提供一種用於製備一用於太陽能電池的封裝材料之方法,其包含:(1)混合乙烯-醋酸乙烯酯共聚合與氧化鎂,製得一母料;(2)混合該母料與乙烯-醋酸乙烯酯共聚物,製得一封裝材料組成物;及(3)熔融-擠壓該封裝材料組成物,其中以該乙烯-醋酸乙烯酯共聚物為100重量份計,該封裝材料組成物中之該氧化鎂的含量為0.001至0.20重量份且具有50至200m2 /g之比表面積。本發明之有利作用 Yet another embodiment provides a method for preparing a packaging material for a solar cell, comprising: (1) mixing ethylene-vinyl acetate copolymerization with magnesium oxide to obtain a master batch; (2) mixing the A masterbatch and an ethylene-vinyl acetate copolymer to obtain an encapsulation material composition; and (3) melting-extrusion the encapsulation material composition, wherein the ethylene-vinyl acetate copolymer is 100 parts by weight, the The content of the magnesium oxide in the packaging material composition is 0.001 to 0.20 parts by weight and has a specific surface area of 50 to 200 m 2 / g. Advantageous effects of the invention
根據該實施例之用於太陽能電池的封裝材料具優異的防潮性及耐久性,因為其會吸收從乙烯-醋酸乙烯酯共聚物產生之醋酸。因此,包含該用於太陽能電池的封裝材料之太陽能電池模組,即使長時間曝露於外部,亦可使功率輸出的降低減至最小。The packaging material for a solar cell according to this embodiment has excellent moisture resistance and durability because it absorbs acetic acid generated from an ethylene-vinyl acetate copolymer. Therefore, even if the solar cell module including the packaging material for a solar cell is exposed to the outside for a long time, the reduction in power output can be minimized.
進行本發明之最佳實施例 在下文中,將參照範例詳細說明本發明。該等實施例不限於以下所述的,且只要不改變本發明之要旨,可被修改成各種形式。 BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail with reference to examples. These embodiments are not limited to those described below, and may be modified into various forms as long as the gist of the present invention is not changed.
在整個實施例之說明中,提到各膜、視窗、板、層或類似物形成在另一膜、視窗、板、層或類似物之“上”或“下”時,其不僅意指一元件直接形成在另一元件上或下,且亦指一元件間接形成在另一元件上或下,其間插入其它元件。且,針對各元件之術語“上”或“下”,可參考圖式。為方便說明起見,在隨附的圖式中,個別元件之尺寸可能誇張描述,而不是指出實際的尺寸。再者,在整個說明書中,相同的符號意指相同的元件。Throughout the description of the embodiment, when it is mentioned that each film, window, plate, layer or the like is formed "on" or "under" another film, window, plate, layer or the like, it means not only a An element is directly formed on or under another element, and also means that one element is indirectly formed on or under another element with other elements interposed therebetween. And, for the terms “up” or “down” of each element, reference may be made to the drawings. For convenience of explanation, in the accompanying drawings, the dimensions of individual components may be described exaggerated, rather than indicating the actual dimensions. Moreover, throughout the specification, the same symbols mean the same elements.
在此說明書中,當稱一部件“包含”一元件時,除非有特別指示,否則應了解該部件亦可包含其它元件。In this specification, when a component is referred to as "containing" an element, it should be understood that the component may also include other elements unless specifically instructed otherwise.
再者,在此所使用之所有與組份之數量、反應條件等等相關之數字與詞語,除非有特別指出,否則應理解為經“約”之術語修飾過的。用於太陽能電池的封裝材料 Furthermore, all numbers and words related to the number of components, reaction conditions, etc. used herein should be understood as modified by the term "about" unless specifically stated otherwise. Packaging materials for solar cells
根據一實施例,提供有一種用於太陽能電池的封裝材料,其包含乙烯-醋酸乙烯酯共聚物及氧化鎂,其中以該乙烯-醋酸乙烯酯共聚物為100重量份計,該氧化鎂之含量為0.001至0.20重量份且具有50至200m2 /g之比表面積。 乙烯-醋酸乙烯酯共聚物According to an embodiment, there is provided a packaging material for a solar cell, comprising an ethylene-vinyl acetate copolymer and magnesium oxide, wherein the content of the magnesium oxide is based on 100 parts by weight of the ethylene-vinyl acetate copolymer. It is 0.001 to 0.20 parts by weight and has a specific surface area of 50 to 200 m 2 / g. Ethylene-vinyl acetate copolymer
以該共聚物之總重量計,該乙烯-醋酸乙烯酯共聚物可包含20至35重量%之醋酸乙烯酯。具體地,以該共聚物之總重量計,該乙烯-醋酸乙烯酯共聚物可包含20至33重量%、25至33重量%或26至33重量%之醋酸乙烯酯。假如醋酸乙烯酯之含量落在以上之範圍內,則該共聚物具有優異的可加工成薄板之作用,且在作為太陽能電池的封裝材料以保護電池方面具優異的性能。The ethylene-vinyl acetate copolymer may include 20 to 35% by weight of vinyl acetate based on the total weight of the copolymer. Specifically, the ethylene-vinyl acetate copolymer may include 20 to 33% by weight, 25 to 33% by weight, or 26 to 33% by weight of vinyl acetate based on the total weight of the copolymer. If the content of vinyl acetate falls within the above range, the copolymer has an excellent effect of being processed into a thin plate, and has excellent performance as a packaging material for a solar cell to protect the battery.
該乙烯-醋酸乙烯酯共聚物在190°C、2.16kg之荷重下,可具有5至30g/10min之熔流速率(MFR)。具體地,該乙烯-醋酸乙烯酯共聚物在190°C、2.16kg之荷重下,可具有5至25g/10min、5至20g/10min或10至20g/10min之熔流速率(MFR)。假如該乙烯-醋酸乙烯酯共聚物之熔流速率落在以上之範圍內,則有可能在沒有因低流動性而不易進行該共聚物之擠壓,以及因流動性過高使得該共聚物在層壓步驟中流出而污染設備之問題的情況下,穩定地形成薄板。The ethylene-vinyl acetate copolymer may have a melt flow rate (MFR) of 5 to 30 g / 10 min under a load of 2.16 kg at 190 ° C. Specifically, the ethylene-vinyl acetate copolymer may have a melt flow rate (MFR) of 5 to 25 g / 10 min, 5 to 20 g / 10 min, or 10 to 20 g / 10 min under a load of 2.16 kg at 190 ° C. If the melt flow rate of the ethylene-vinyl acetate copolymer falls within the above range, it is possible that the copolymer is not easily extruded due to low fluidity, and the copolymer is not suitable for high fluidity. In the case where the problem arises during the lamination step and the equipment is contaminated, a thin plate is stably formed.
該乙烯-醋酸乙烯酯共聚物可具有10,000至100,000克/莫耳之重量平均分子量。具體地,該共聚物可具有20,000至60,000克/莫耳、30,000至60,000克/莫耳或50,000至60,000克/莫耳之重量平均分子量。 氧化鎂The ethylene-vinyl acetate copolymer may have a weight average molecular weight of 10,000 to 100,000 g / mole. Specifically, the copolymer may have a weight average molecular weight of 20,000 to 60,000 g / mole, 30,000 to 60,000 g / mole, or 50,000 to 60,000 g / mole. Magnesium oxide
以該乙烯-醋酸乙烯酯共聚物為100重量份計,該氧化鎂之含量為0.001至0.20重量份。具體地,以該乙烯-醋酸乙烯酯共聚物為100重量份計,該氧化鎂之含量可為0.005至0.10重量份、0.009至0.07重量份、0.01至0.20重量份或0.01至0.15重量份。假如氧化鎂之含量落在以上之範圍內,則該氧化鎂可均勻地分散於封裝材料中,從而容易吸收醋酸,且有可能防止因削弱該封裝材料之透光性而降低太陽能電池模組之功率輸出之問題,以及因延遲該乙烯-醋酸乙烯酯共聚物之交聯反應而降低該封裝材料之交聯程度之問題。The content of the magnesium oxide is 0.001 to 0.20 parts by weight based on 100 parts by weight of the ethylene-vinyl acetate copolymer. Specifically, based on 100 parts by weight of the ethylene-vinyl acetate copolymer, the content of the magnesium oxide may be 0.005 to 0.10 parts by weight, 0.009 to 0.07 parts by weight, 0.01 to 0.20 parts by weight, or 0.01 to 0.15 parts by weight. If the content of magnesium oxide falls within the above range, the magnesium oxide can be evenly dispersed in the packaging material, so that it can easily absorb acetic acid, and it is possible to prevent the solar cell module from being reduced by weakening the light transmission of the packaging material. The problem of power output and the problem of reducing the degree of cross-linking of the packaging material by delaying the cross-linking reaction of the ethylene-vinyl acetate copolymer.
此外,該氧化鎂具有50至200m2 /g之比表面積。具體地,該氧化鎂可具有70至200m2 /g、90至200m2 /g或100至200m2 /g之比表面積。該氧化鎂視其比表面積,在吸收醋酸方面可具有不同的能力。假如該氧化鎂之比表面積落在以上之範圍內,則有可能防止因阻礙其之反應性而降低吸收醋酸之能力之問題,以及因延遲該乙烯-醋酸乙烯酯共聚物之交聯反應而降低該封裝材料之交聯程度之問題。特別是,如上所述,因為該實施例之氧化鎂具有大比表面積,所以即使用量小,亦可達到所需要之吸收醋酸的能力。因此,有可能藉由抑制醋酸的形成而改善如此製得之用於太陽能電池的封裝材料之耐久性,同時可降低因氧化鎂過量使用可能發生之副作用。In addition, the magnesium oxide has a specific surface area of 50 to 200 m 2 / g. Specifically, the magnesium oxide may have a specific surface area of 70 to 200 m 2 / g, 90 to 200 m 2 / g, or 100 to 200 m 2 / g. Depending on its specific surface area, the magnesium oxide may have different abilities in absorbing acetic acid. If the specific surface area of the magnesium oxide falls within the above range, it is possible to prevent the problem of reducing the ability to absorb acetic acid by hindering its reactivity, and to reduce it by delaying the crosslinking reaction of the ethylene-vinyl acetate copolymer. The degree of cross-linking of the packaging material. In particular, as described above, since the magnesium oxide of this embodiment has a large specific surface area, the required ability to absorb acetic acid can be achieved even in a small amount. Therefore, it is possible to improve the durability of the packaging material for solar cells thus prepared by suppressing the formation of acetic acid, and to reduce the side effects that may occur due to the excessive use of magnesium oxide.
除了以上所提及之氧化鎂外,大部分會吸收酸之物質亦具有吸收濕氣之特徵。例如,沸石或二氧化矽與氧化鎂相似具有吸收酸之特性。因此,假如將其用於太陽能電池的封裝材料,則可能會產生吸收醋酸之相似的作用。但其有吸收濕氣以及醋酸之缺點。因此,假如在封裝材料中使用沸石或二氧化矽而不是氧化鎂,則在嚴荷的條件下該封裝材料會吸收濕氣,導致該封裝材料之容積電阻率減低以及其對濕洩漏的耐受性變差之問題。相反的,因為氧化鎂不會吸收濕氣,所以即使在嚴荷的條件下,其不會引發以上之問題。In addition to the magnesium oxide mentioned above, most substances that can absorb acids also have the characteristics of absorbing moisture. For example, zeolite or silica has similar acid absorption properties as magnesium oxide. Therefore, if it is used as a packaging material for solar cells, it may have a similar effect of absorbing acetic acid. However, it has the disadvantages of absorbing moisture and acetic acid. Therefore, if zeolite or silica instead of magnesium oxide is used in the packaging material, the packaging material will absorb moisture under severe loading conditions, resulting in a reduction in the volume resistivity of the packaging material and its resistance to wet leakage Sexual deterioration. In contrast, because magnesium oxide does not absorb moisture, it does not cause the above problems even under severe loading conditions.
該氧化鎂可具有1至20μm之平均直徑。具體地,該氧化鎂可具有2至20μm、2至15μm或2至10μm之平均直徑。The magnesium oxide may have an average diameter of 1 to 20 μm. Specifically, the magnesium oxide may have an average diameter of 2 to 20 μm, 2 to 15 μm, or 2 to 10 μm.
該氧化鎂可具有適當的粒度分佈。例如,該氧化鎂可含有比平均粒徑小2.5μm或更小之粒徑且以該氧化鎂之總重量計數量為5至15重量%之粒子。此外,該氧化鎂可含有比平均粒徑大6.5μm或更大且以該氧化鎂之總重量計數量為5至15重量%之粒子。假如該氧化鎂具有如上述之粒度分佈,則可改善因此製得之用於太陽能電池的封裝材料之耐久性。 交聯劑The magnesium oxide may have an appropriate particle size distribution. For example, the magnesium oxide may contain particles having a particle diameter smaller than the average particle diameter by 2.5 μm or less, and 5 to 15% by weight of the total weight of the magnesium oxide. In addition, the magnesium oxide may contain particles larger than the average particle diameter by 6.5 μm or more and in an amount of 5 to 15% by weight based on the total weight of the magnesium oxide. If the magnesium oxide has a particle size distribution as described above, the durability of the encapsulating material for a solar cell thus obtained can be improved. Crosslinker
該用於太陽能電池的封裝材料可包含有機過氧化物作為交聯劑。該有機過氧化物用來改善該用於太陽能電池的封裝材料之耐候性。The packaging material for a solar cell may include an organic peroxide as a crosslinking agent. The organic peroxide is used to improve the weather resistance of the packaging material for solar cells.
該交聯劑沒有特別的限制,只要其是在100°C或更高之溫度下能夠產生自由基的有機過氧化物即可。但考慮到化合期間之安定性,其較佳地具有10個小時或更長之半衰期以及70°C或更高之分解溫度。半衰期溫度愈低,反應愈快。半衰期溫度愈高,反應愈慢。The crosslinking agent is not particularly limited as long as it is an organic peroxide capable of generating radicals at a temperature of 100 ° C or higher. However, considering the stability during the compounding period, it preferably has a half-life of 10 hours or longer and a decomposition temperature of 70 ° C or higher. The lower the half-life temperature, the faster the reaction. The higher the half-life temperature, the slower the reaction.
具體地,該有機過氧化物可為至少一種選自於由下列所構成之群組:2,5-二甲基己烷-2,5-二氫過氧化物、2,5-二甲基-2,5-二(叔丁基過氧基)己烷、二叔丁基過氧化物、α,α'-雙(叔丁基過氧基異丙基)苯、正丁基-4,4-雙(叔丁基過氧基)丁烷、2,2-雙(叔丁基過氧基)丁烷、1,1-雙(叔丁基過氧基)環己烷、1,1-雙(叔丁基過氧基)-3,3,5-三甲基環己烷、過氧化苯甲酸叔丁酯、過氧化苯甲醯及叔丁基過氧基碳酸-2-乙己酯。Specifically, the organic peroxide may be at least one selected from the group consisting of: 2,5-dimethylhexane-2,5-dihydroperoxide, 2,5-dimethyl -2,5-di (t-butylperoxy) hexane, di-t-butyl peroxide, α, α'-bis (t-butylperoxyisopropyl) benzene, n-butyl-4, 4-bis (t-butylperoxy) butane, 2,2-bis (t-butylperoxy) butane, 1,1-bis (t-butylperoxy) cyclohexane, 1,1 -Bis (tert-butylperoxy) -3,3,5-trimethylcyclohexane, tert-butyl peroxybenzoate, benzoylperoxide and t-butylperoxy-2-ethylhexyl carbonate .
以該乙烯-醋酸乙烯酯共聚物為100重量份計,該交聯劑之含量可為5重量份或更少。具體地,以該乙烯-醋酸乙烯酯共聚物為100重量份計,該交聯劑之含量可為0.3至5重量份或0.3至2重量份。 交聯助劑The content of the crosslinking agent may be 5 parts by weight or less based on 100 parts by weight of the ethylene-vinyl acetate copolymer. Specifically, based on 100 parts by weight of the ethylene-vinyl acetate copolymer, the content of the crosslinking agent may be 0.3 to 5 parts by weight or 0.3 to 2 parts by weight. Crosslinking Auxiliaries
該用於太陽能電池的封裝材料可包含交聯助劑。該交聯助劑用來改善該乙烯-醋酸乙烯酯共聚物之凝膠分率及改善該封裝材料之耐久性。The encapsulating material for a solar cell may include a crosslinking auxiliary. The crosslinking assistant is used to improve the gel fraction of the ethylene-vinyl acetate copolymer and improve the durability of the packaging material.
以該乙烯-醋酸乙烯酯共聚物為100重量份計,該交聯助劑之含量可為10重量份或更少。具體地,以該乙烯-醋酸乙烯酯共聚物為100重量份計,該交聯助劑之含量可為0.1至10重量份、0.1至5重量份或0.1至3重量份。The content of the crosslinking assistant may be 10 parts by weight or less based on 100 parts by weight of the ethylene-vinyl acetate copolymer. Specifically, based on 100 parts by weight of the ethylene-vinyl acetate copolymer, the content of the crosslinking assistant may be 0.1 to 10 parts by weight, 0.1 to 5 parts by weight, or 0.1 to 3 parts by weight.
該交聯助劑之例子包括具有三個諸如三烯丙基異氰脲酸酯、三烯丙基異氰酸酯等等之官能基團之化合物及具有一個諸如酯等等之官能基團之化合物。 添加物Examples of the crosslinking assistant include compounds having three functional groups such as triallyl isocyanurate, triallyl isocyanate, and the like and compounds having one functional group such as ester and the like. Additives
該用於太陽能電池的封裝材料可進一步包含選自於由下列所構成之群組之添加物:矽烷偶合劑、醌類化合物、紫外線吸收劑、抗氧化劑及變色抑制劑。The packaging material for a solar cell may further include an additive selected from the group consisting of a silane coupling agent, a quinone compound, an ultraviolet absorber, an antioxidant, and a discoloration inhibitor.
該矽烷偶合劑用來改善該封裝材料與該太陽能電池間之黏著性。該矽烷偶合劑可為,例如,γ-氯丙基三甲氧基矽烷、乙烯基三氯矽烷、乙烯-三-(β-甲氧乙氧基)矽烷、γ-甲氧丙基三甲氧基矽烷、β-(3,4-乙氧基環己基)乙基三甲氧基矽烷、γ-巰基丙基三甲氧基矽烷或類似物。The silane coupling agent is used to improve the adhesion between the packaging material and the solar cell. The silane coupling agent may be, for example, γ-chloropropyltrimethoxysilane, vinyltrichlorosilane, ethylene-tri- (β-methoxyethoxy) silane, γ-methoxypropyltrimethoxysilane , Β- (3,4-ethoxycyclohexyl) ethyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, or the like.
以該乙烯-醋酸乙烯酯共聚物為100重量份計,該矽烷偶合劑之含量可為5重量份或更少。具體地,以該乙烯-醋酸乙烯酯共聚物為100重量份計,該矽烷偶合劑之含量可為0.1至5重量份、0.1至3重量份或0.1至2重量份。The content of the silane coupling agent may be 5 parts by weight or less based on 100 parts by weight of the ethylene-vinyl acetate copolymer. Specifically, based on 100 parts by weight of the ethylene-vinyl acetate copolymer, the content of the silane coupling agent may be 0.1 to 5 parts by weight, 0.1 to 3 parts by weight, or 0.1 to 2 parts by weight.
該醌類化合物用來改善該乙烯-醋酸乙烯酯共聚物之安定性。該醌類化合物可為,例如,氫醌、氫醌甲乙基、對-苯醌、甲基氫醌等等。此外,以該乙烯-醋酸乙烯酯共聚物為100重量份計,該醌類化合物之含量可為5重量份或更少。具體地,以該乙烯-醋酸乙烯酯共聚物為100重量份計,該醌類化合物之含量可為0.1至5重量份。The quinone compound is used to improve the stability of the ethylene-vinyl acetate copolymer. The quinoid compound may be, for example, hydroquinone, hydroquinone methylethyl, p-benzoquinone, methylhydroquinone, and the like. In addition, the content of the quinone compound may be 5 parts by weight or less based on 100 parts by weight of the ethylene-vinyl acetate copolymer. Specifically, based on 100 parts by weight of the ethylene-vinyl acetate copolymer, the content of the quinone compound may be 0.1 to 5 parts by weight.
該紫外線吸收劑可為,例如,二苯基酮化合物,諸如2-羥基-4-辛氧基二苯基酮、2-羥基-4-甲氧基-5-碸二苯基酮等等;苯並三唑化合物,諸如2-(2'-羥基-5-甲基苯基)苯並三唑等等;及水楊酸酯化合物,諸如水楊酸苯酯、水楊酸對叔丁基苯酯等等。The ultraviolet absorber may be, for example, a diphenyl ketone compound such as 2-hydroxy-4-octyloxydiphenyl ketone, 2-hydroxy-4-methoxy-5-fluorendiphenyl ketone, and the like; Benzotriazole compounds, such as 2- (2'-hydroxy-5-methylphenyl) benzotriazole, etc .; and salicylate compounds, such as phenyl salicylate, p-tert-butyl salicylate Phenyl esters and more.
該抗氧化劑可為,例如,胺類、酚類或聯苯類抗氧化劑。具體地,該抗氧化劑可為叔丁基甲酚、雙-(2,2,6,6-四甲基-4-哌嗪)癸二酸酯等等。 用於太陽能電池的封裝材料The antioxidant may be, for example, an amine-based, phenol-based or biphenyl-based antioxidant. Specifically, the antioxidant may be tert-butylcresol, bis- (2,2,6,6-tetramethyl-4-piperazine) sebacate, and the like. Packaging materials for solar cells
該用於太陽能電池的封裝材料可通過將包含乙烯-醋酸乙烯酯共聚物及氧化鎂之封裝材料組成物擠壓成未固化或半固化薄板而製得。The packaging material for a solar cell can be prepared by extruding a packaging material composition containing an ethylene-vinyl acetate copolymer and magnesium oxide into an uncured or semi-cured sheet.
將該用於太陽能電池的封裝材料施用於一太陽能電池模組,然後固化以便完成該封裝材料之功能。將在下面描述之該用於太陽電池之封裝材料之容積電阻率及霧度,是在該用於太陽能電池的封裝材料固化後測量的。The packaging material for a solar cell is applied to a solar cell module, and then cured to complete the function of the packaging material. The volume resistivity and haze of the packaging material for solar cells, which will be described below, are measured after the packaging material for solar cells is cured.
該用於太陽能電池的封裝材料可具有在1,000V電壓、25°C下測得之容積電阻率為1×1016 至1×1017 Ω·cm。具體地,該用於太陽能電池的封裝材料可具有在1,000V電壓、25°C下測得之容積電阻率為1×1016 至5×1016 Ω·cm、1×1016 至4×1016 Ω·cm或1×1016 至3×1016 Ω·cm。The packaging material for a solar cell may have a volume resistivity of 1 × 10 16 to 1 × 10 17 Ω · cm measured at a voltage of 1,000 V at 25 ° C. Specifically, the packaging material for a solar cell may have a volume resistivity of 1 × 10 16 to 5 × 10 16 Ω · cm, 1 × 10 16 to 4 × 10 measured at a voltage of 1,000 V and 25 ° C. 16 Ω · cm or 1 × 10 16 to 3 × 10 16 Ω · cm.
該用於太陽能電池的封裝材料在置於120°C、100%相對濕度下72個小時後,可具有在1,000V電壓下測得之容積電阻率為1×1015 Ω·cm或更高。具體地,該用於太陽能電池的封裝材料在置於120°C、100%相對濕度下72個小時後,可具有在1,000V電壓下測得之容積電阻率為1×1015 至1×1017 Ω·cm、1×1015 至1×1016 Ω·cm、1×1015 至8×1015 Ω·cm或1×1015 至5×1015 Ω·cm。特別地,假如該用於太陽能電池的封裝材料之容積電阻率小於1×1015 Ω·cm,則可能有對濕洩漏的耐受性變差之問題。The packaging material for a solar cell may have a volume resistivity of 1 × 10 15 Ω · cm or higher measured at 1,000 V after 72 hours at 120 ° C and 100% relative humidity. Specifically, the packaging material for a solar cell may have a volume resistivity of 1 × 10 15 to 1 × 10 measured at 1,000V after being placed at 120 ° C and 100% relative humidity for 72 hours. 17 Ω · cm, 1 × 10 15 to 1 × 10 16 Ω · cm, 1 × 10 15 to 8 × 10 15 Ω · cm, or 1 × 10 15 to 5 × 10 15 Ω · cm. In particular, if the volume resistivity of the packaging material for a solar cell is less than 1 × 10 15 Ω · cm, there may be a problem that the resistance to wet leakage is deteriorated.
然而,因為一實施例之用於太陽能電池的封裝材料具優異的防潮性,所以即使在置於120°C及100%相對濕度之條件下72個小時後,其仍具有1×1015 Ω·cm或更高之容積電阻率,從而產生該封裝材料之電阻不會變差之作用。However, because the packaging material for a solar cell of one embodiment has excellent moisture resistance, even after being placed at 120 ° C and 100% relative humidity for 72 hours, it still has 1 × 10 15 Ω · The volume resistivity of cm or higher, so that the resistance of the packaging material does not deteriorate.
該用於太陽能電池的封裝材料在將該封裝材料之尺寸從1,000mm×200mm×0.5mm (寬×長×厚)切割成100mm×100mm (寬×長)而獲得之樣本上,可具有在25°C下測得之平均霧度為2至8%,其中該樣本之霧度的標準差可為0.1至0.5%。具體地,該用於太陽能電池的封裝材料在將該封裝材料之尺寸從1,000mm×200mm×0.5mm (寬×長×厚)切割成100mm×100mm (寬×長)而獲得之樣本上,可具有在25°C下測得之平均霧度為3至8%、4至7%或5至6%,其中該樣本之霧度的標準差可為0.1至0.4%或0.1至0.3%。The packaging material for a solar cell may have a size of 25 mm on a sample obtained by cutting the size of the packaging material from 1,000 mm × 200 mm × 0.5 mm (width × length × thickness) to 100 mm × 100 mm (width × length). The average haze measured at ° C is 2 to 8%, and the standard deviation of the haze of the sample can be 0.1 to 0.5%. Specifically, the packaging material for a solar cell can be obtained from a sample obtained by cutting a size of the packaging material from 1,000 mm × 200 mm × 0.5 mm (width × length × thickness) into 100 mm × 100 mm (width × length). The average haze measured at 25 ° C is 3 to 8%, 4 to 7%, or 5 to 6%, and the standard deviation of the haze of the sample may be 0.1 to 0.4% or 0.1 to 0.3%.
該用於太陽能電池的封裝材料可具有以流變計在150°C下測得之固化反應的引發時間為3分鐘或更短。具體地,該用於太陽能電池的封裝材料可具有以流變計在150°C下測得之固化反應的引發時間為1至3分鐘。The encapsulating material for a solar cell may have an initiation time of a curing reaction measured at 150 ° C. in a rheometer of 3 minutes or less. Specifically, the packaging material for a solar cell may have an initiation time of a curing reaction measured at 150 ° C. in a rheometer of 1 to 3 minutes.
該用於太陽能電池的封裝材料可具有200至800μm之平均厚度。具體地,該用於太陽能電池的封裝材料可具有300至700μm之平均厚度。太陽能電池模組 The packaging material for a solar cell may have an average thickness of 200 to 800 μm. Specifically, the packaging material for a solar cell may have an average thickness of 300 to 700 μm. Solar battery module
根據一實施例,提供有一種太陽能電池模組,其包含一透明保護基材、一第一封裝材料板、至少一種太陽能電池連接至一電極、一第二封裝材料板及一背板,其全部按此順序層壓,其中該第一封裝材料板及該第二封裝材料板中之至少一者包含乙烯-醋酸乙烯酯共聚物及氧化鎂,及以該乙烯-醋酸乙烯酯共聚物為100重量份計,該氧化鎂之含量為0.001至0.20重量份且具有50至200m2 /g之比表面積。According to an embodiment, a solar cell module is provided, which includes a transparent protective substrate, a first packaging material plate, at least one solar cell connected to an electrode, a second packaging material plate, and a back plate, all of which Laminate in this order, wherein at least one of the first encapsulating material plate and the second encapsulating material plate comprises an ethylene-vinyl acetate copolymer and magnesium oxide, and the ethylene-vinyl acetate copolymer is 100 weight The magnesium oxide has a content of 0.001 to 0.20 parts by weight and has a specific surface area of 50 to 200 m 2 / g.
圖1及2圖例說明太陽能電池模組之配置(即,分別為展開視圖及組合視圖)。太陽能電池模組(10)包含透明保護基材(14)、第一封裝材料板(12)、至少一種太陽能電池(11)連接至電極、第二封裝材料板(12')及背板(13),其等全部按此順序層壓。第一封裝材料板(12)及第二封裝材料板(12')中之至少一者包含乙烯-醋酸乙烯酯共聚物及氧化鎂。1 and 2 illustrate the configuration of the solar cell module (ie, an expanded view and a combined view, respectively). The solar cell module (10) includes a transparent protective substrate (14), a first encapsulating material plate (12), at least one solar cell (11) connected to an electrode, a second encapsulating material plate (12 '), and a back plate (13). ), And all of them are laminated in this order. At least one of the first packaging material plate (12) and the second packaging material plate (12 ') includes an ethylene-vinyl acetate copolymer and magnesium oxide.
太陽能電池模組(10)之製備,可通過按順序層壓包含太陽能電池(11)及封裝材料板(12及12')之組合層,然後加工處理(如,熱及壓制)其等。在此,第一封裝材料板(12)及第二封裝材料板(12')中之至少一者可採用如上所述之用於太陽能電池的封裝材料。The solar cell module (10) can be prepared by sequentially laminating the combined layers including the solar cell (11) and the packaging material plates (12 and 12 '), and then processing (such as heating and pressing) them. Here, at least one of the first encapsulating material plate (12) and the second encapsulating material plate (12 ') may use the encapsulating material for a solar cell as described above.
構成太陽能電池模組(10)之太陽能電池(11)、背板(13)及透明保護基材(14),可從常規使用的材料中適當地選取。特別是,該透明保護基材及該背板二者可為玻璃基材。The solar cell (11), the back plate (13), and the transparent protective substrate (14) constituting the solar cell module (10) can be appropriately selected from conventionally used materials. In particular, both the transparent protective substrate and the back sheet may be glass substrates.
該太陽能電池模組在置於85°C、85%相對濕度下3,000個小時後,可具有5%或更少之輸出功率的降低。具體地,該太陽能電池模組在置於85°C、85%相對濕度下3,000個小時後,可具有0.1至5%、1至5%、2至5%、2至4.8%、2.5至3%之輸出功率的降低。用於製備一用於太陽能電池的封裝材料之方法 The solar cell module can reduce output power by 5% or less after being placed at 85 ° C and 85% relative humidity for 3,000 hours. Specifically, the solar cell module may have 0.1 to 5%, 1 to 5%, 2 to 5%, 2 to 4.8%, 2.5 to 3 after being placed at 85 ° C and 85% relative humidity for 3,000 hours. % Reduction in output power. Method for preparing a packaging material for solar cells
根據另一實施例,提供有一種用於製備一用於太陽能電池的封裝材料之方法,其包含(1)混合乙烯-醋酸乙烯酯共聚物與氧化鎂,製得一母料;(2)混合該母料與乙烯-醋酸乙烯酯共聚物,製得一封裝材料組成物;及(3)熔融-擠壓該封裝材料組成物,其中以該乙烯-醋酸乙烯酯共聚物為100重量份計,該封裝材料組成物中該氧化鎂的含量為0.001至0.20重量份且具有50至200m2 /g之比表面積。 步驟(1)According to another embodiment, there is provided a method for preparing an encapsulating material for a solar cell, comprising (1) mixing an ethylene-vinyl acetate copolymer with magnesium oxide to obtain a master batch; (2) mixing The master batch and the ethylene-vinyl acetate copolymer are used to prepare a packaging material composition; and (3) the packaging material composition is melt-extruded, wherein the ethylene-vinyl acetate copolymer is 100 parts by weight, The content of the magnesium oxide in the packaging material composition is 0.001 to 0.20 parts by weight and has a specific surface area of 50 to 200 m 2 / g. step 1)
在此步驟中,乙烯-醋酸乙烯酯共聚物與氧化鎂混合製得一母料。In this step, an ethylene-vinyl acetate copolymer is mixed with magnesium oxide to prepare a masterbatch.
該乙烯-醋酸乙烯酯共聚物與該氧化鎂,與針對該用於太陽能電池的封裝材料所描述的一樣。The ethylene-vinyl acetate copolymer and the magnesium oxide are the same as described for the encapsulation material for a solar cell.
以該乙烯-醋酸乙烯酯共聚物為100重量份計,該母料可包含0.3至5重量份之氧化鎂。具體地,以該乙烯-醋酸乙烯酯共聚物為100重量份計,該母料可包含0.3至4重量份、0.3至3重量份或0.4至1重量份之氧化鎂。The master batch may include 0.3 to 5 parts by weight of magnesium oxide based on 100 parts by weight of the ethylene-vinyl acetate copolymer. Specifically, based on 100 parts by weight of the ethylene-vinyl acetate copolymer, the master batch may include 0.3 to 4 parts by weight, 0.3 to 3 parts by weight, or 0.4 to 1 part by weight of magnesium oxide.
此步驟中之混合可在80至160°C下進行。具體地,此步驟中之混合可在80至150°C、100至140°C或120至140°C下進行。 步驟(2)The mixing in this step can be performed at 80 to 160 ° C. Specifically, the mixing in this step may be performed at 80 to 150 ° C, 100 to 140 ° C, or 120 to 140 ° C. Step (2)
在此步驟中,該母料與乙烯-醋酸乙烯酯共聚物混合製得一封裝材料組成物。In this step, the master batch is mixed with an ethylene-vinyl acetate copolymer to obtain a packaging material composition.
該母料對該乙烯-醋酸乙烯酯共聚物之混合重量比可為1:5至1:100。具體地,該母料對該乙烯-醋酸乙烯酯共聚物之混合重量比可為1:5至1:50、1:5至1:30或1:5至1:20。The mixing weight ratio of the master batch to the ethylene-vinyl acetate copolymer may be 1: 5 to 1: 100. Specifically, the mixing weight ratio of the master batch to the ethylene-vinyl acetate copolymer may be 1: 5 to 1:50, 1: 5 to 1:30, or 1: 5 to 1:20.
當該母料中氧化鎂之含量增加時,可增加該乙烯-醋酸乙烯酯共聚物相對於該母料之進料率。此外,該母料對該乙烯-醋酸乙烯酯共聚物之混合比,可由該母料對該乙烯-醋酸乙烯酯共聚物之進料率之比控制。When the content of magnesium oxide in the master batch is increased, the feed rate of the ethylene-vinyl acetate copolymer relative to the master batch can be increased. In addition, the mixing ratio of the master batch to the ethylene-vinyl acetate copolymer can be controlled by the ratio of the feed rate of the master batch to the ethylene-vinyl acetate copolymer.
此步驟中之混合可在70至120°C下進行。具體地,此步驟中之混合可在75至120°C、75至100°C或75至95°C下進行。範例 The mixing in this step can be performed at 70 to 120 ° C. Specifically, the mixing in this step may be performed at 75 to 120 ° C, 75 to 100 ° C, or 75 to 95 ° C. example
在下文中,將參照下列範例詳細說明本發明。然而,下列範例是用來進一步描述本發明。本發明之範疇不僅限於此。Hereinafter, the present invention will be described in detail with reference to the following examples. However, the following examples are used to further describe the present invention. The scope of the present invention is not limited to this.
以下之範例及比較例中所使用之組份如下。 -乙烯-醋酸乙烯酯共聚物:含28重量%之醋酸乙烯酯,重量平均分子量為54,000克/莫耳及在190°C、2.16kg荷重下之熔流速率(MFR)為15g/10 min。 -交聯劑:Arkema之Luperox TBEC (叔丁基過氧基碳酸-2-乙己酯)。 -交聯助劑:Evonik之TAICROS (三烯丙基異氰脲酸酯)。 -氧化鎂A:比表面積100m2 /g。 -氧化鎂B:比表面積150m2 /g。 -氧化鎂C:比表面積200m2 /g。 -氧化鎂D:比表面積30m2 /g。 -氧化鎂E:比表面積250m2 /g。範例 1 :封裝材料之製備 The components used in the following examples and comparative examples are as follows. -Ethylene-vinyl acetate copolymer: 28% by weight of vinyl acetate, with a weight average molecular weight of 54,000 g / mole and a melt flow rate (MFR) of 15 g / 10 min at 190 ° C and a load of 2.16 kg. -Crosslinking agent: Luperox TBEC (tert-butylperoxycarbonate-2-ethylhexyl) from Arkema. -Crosslinking aid: TAICROS (triallyl isocyanurate) from Evonik. -Magnesium oxide A: The specific surface area is 100 m 2 / g. -Magnesium oxide B: specific surface area 150 m 2 / g. -Magnesium oxide C: specific surface area of 200 m 2 / g. -Magnesium oxide D: The specific surface area is 30 m 2 / g. -Magnesium oxide E: specific surface area is 250 m 2 / g. Example 1 : Preparation of packaging materials
使0.01重量份的氧化鎂A與100重量份的乙烯-醋酸乙烯酯共聚物化合,以製得一混合物。之後,使1.0重量份的交聯劑和1.0重量份的交聯助劑與其化合,製得一封裝材料組成物。0.01 parts by weight of magnesium oxide A was combined with 100 parts by weight of an ethylene-vinyl acetate copolymer to prepare a mixture. After that, 1.0 part by weight of a crosslinking agent and 1.0 part by weight of a crosslinking assistant are combined therewith to prepare a packaging material composition.
使該封裝材料組成物經過100°C下T模頭擠壓步驟之處理,製得具有厚500μm之封裝材料。範例 2 至 9 及比較例 1 至 4 The packaging material composition is subjected to a T-die extrusion step at 100 ° C. to obtain a packaging material having a thickness of 500 μm. Examples 2 to 9 and Comparative Examples 1 to 4
除了氧化鎂之種類與含量改成以下表1中所示的外,用與範例1中相同的方法製備各封裝材料。範例 10 Each packaging material was prepared in the same manner as in Example 1 except that the type and content of magnesium oxide were changed to those shown in Table 1 below. Example 10
使0.5重量份的氧化鎂B與100重量份的乙烯-醋酸乙烯酯共聚物在130°C化合,以製得一母料。將該母料與該乙烯-醋酸乙烯酯共聚物以1:10之重量比例一起饋入並在85°C下混合,製得一混合物。之後,於其中加入1.0重量份的交聯劑及1.0重量份的交聯助劑,接著將其混合,以製得一封裝材料組成物。0.5 parts by weight of magnesium oxide B and 100 parts by weight of an ethylene-vinyl acetate copolymer were combined at 130 ° C. to prepare a master batch. The master batch and the ethylene-vinyl acetate copolymer were fed together at a weight ratio of 1:10 and mixed at 85 ° C to prepare a mixture. After that, 1.0 part by weight of a cross-linking agent and 1.0 part by weight of a cross-linking assistant are added thereto, and then they are mixed to obtain a packaging material composition.
使該封裝材料組成物經過100°C下T模頭擠壓步驟之處理,製得具有厚500μm之封裝材料。 [表1]
以下列方法測量範例1至10及比較例1至4之封裝材料之特性,結果示於以下表2至4中。 (1)容積電阻率The characteristics of the packaging materials of Examples 1 to 10 and Comparative Examples 1 to 4 were measured by the following methods, and the results are shown in Tables 2 to 4 below. (1) Volume resistivity
使用真空層壓機(NPC),在1大氣壓及150°C下加熱封裝材料15分鐘,然後根據ASTM D257,測量在25°C下之起始容積電阻率。此時,施加1,000V之電壓歷時120秒。A vacuum laminator (NPC) was used to heat the packaging material at 1 atmosphere and 150 ° C for 15 minutes, and then the initial volume resistivity at 25 ° C was measured according to ASTM D257. At this time, a voltage of 1,000 V was applied for 120 seconds.
之後,在將封裝材料置於120°C、100%相對濕度之壓力鍋測試室中72個小時後,測量容積電阻率之變化。 (2)霧度After that, the packaging material was placed in a pressure cooker test room at 120 ° C and 100% relative humidity for 72 hours, and then the change in volume resistivity was measured. (2) Haze
將封裝材料切成50mm×50mm×0.5mm (寬×長×厚)之大小,製備樣本,然後依照ASTM D1003測量其於25°C下之霧度。 (3)固化反應之引發時間(ts1)The packaging material was cut into a size of 50mm × 50mm × 0.5mm (width × length × thickness), a sample was prepared, and then its haze at 25 ° C was measured according to ASTM D1003. (3) Initiation time of curing reaction (ts1)
使用流變計測量封裝材料在150°C下之固化反應的引發時間。 (4)太陽能電池模組之製備及輸出功率的減低之評估A rheometer was used to measure the initiation time of the curing reaction of the packaging material at 150 ° C. (4) Preparation of solar cell modules and evaluation of reduction of output power
按照玻璃/封裝材料/太陽能電池(製造商:JSPV,商品名稱:JSCM3186)/封裝材料/玻璃之順序(即,G (玻璃)對G (玻璃)之結構)層壓,產生太陽能電池模組。在此使用各個於範例1至10及比較例1至4中製得之封裝材料。Laminated in the order of glass / encapsulation material / solar cell (manufacturer: JSPV, trade name: JSCM3186) / encapsulation material / glass (ie, G (glass) to G (glass) structure) to produce a solar cell module. Here, each of the packaging materials prepared in Examples 1 to 10 and Comparative Examples 1 to 4 was used.
使用一個太陽能電池之太陽能電池模組具有200mm×200mm (寬×長)之大小。該層壓係使用NPC製造之50×50層壓器,在溫度160°C真空下進行5分鐘以及於1大氣壓力下進行20分鐘,而製得該太陽能電池模組。A solar cell module using one solar cell has a size of 200 mm × 200 mm (width × length). The lamination system uses a 50 × 50 laminator manufactured by NPC, and is performed under a temperature of 160 ° C for 5 minutes under vacuum and for 1 minute under an atmospheric pressure to obtain the solar cell module.
使用歸在JIS C8912等級A下之太陽光模擬器(其中使用氖燈作為光源),測量太陽能電池模組之起始輸出功率。在將太陽能電池模組置於85°C、85%相對濕度下3,000個小時後,以上述相同的方式測量輸出功率(即,濕熱測試)。之後,在濕熱測試後,計算相對於起始輸出功率之輸出功率的降低百分比。 [表2]
如表2及3所示,範例1至10之封裝材料具有1×1015 Ω·cm或更高之起始容積電阻率、8%或更小之霧度及1×1015 Ω·cm或更高之壓力鍋測試後的容積電阻率。該封裝材料在置於85°C及85%相對濕度下3,000個小時後之輸出功率的降低小於5%。特別是,範例10之封裝材料具有2.1×1016 Ω·cm之極高的起始容積電阻率。As shown in Tables 2 and 3, the packaging materials of Examples 1 to 10 have an initial volume resistivity of 1 × 10 15 Ω · cm or higher, a haze of 8% or less, and 1 × 10 15 Ω · cm or Higher volume resistivity after pressure cooker test. The output power of this packaging material is less than 5% after 3,000 hours at 85 ° C and 85% relative humidity. In particular, the packaging material of Example 10 has an extremely high initial volume resistivity of 2.1 × 10 16 Ω · cm.
相反的,不含氧化鎂之比較例1之封裝材料在置於嚴苛的條件後,具有較大之輸出功率的降低,而含過量的氧化鎂之比較例2之封裝材料具高霧度。因此,其等不適合用於太陽能電池。 (5)霧度之標準差In contrast, the packaging material of Comparative Example 1 without magnesium oxide has a large reduction in output power after being placed under severe conditions, while the packaging material of Comparative Example 2 with excessive magnesium oxide has a high haze. Therefore, they are not suitable for use in solar cells. (5) Standard deviation of haze
將範例10之封裝材料切成1,000mm×200mm×0.5mm (寬×長×厚)之大小,之後再將其切成100mm×100mm (寬×長)之大小,製備20個樣本。然後依照ASTM D1003測量各樣本於25°C下之霧度,以及計算該20個樣本之平均霧度及標準差。 [表4]
範例10之封裝材料的樣本之平均霧度為5.6%,且霧度之標準差為0.207%,意味著非常均勻的分佈。The sample of the packaging material of Example 10 has an average haze of 5.6% and a standard deviation of haze of 0.207%, which means a very uniform distribution.
10‧‧‧太陽能電池模組10‧‧‧solar battery module
11‧‧‧太陽能電池11‧‧‧solar battery
12‧‧‧第一封裝材料板12‧‧‧The first packaging material board
12’‧‧‧第二封裝材料板12’‧‧‧Second package material board
13‧‧‧背板13‧‧‧ back plate
14‧‧‧透明保護基材14‧‧‧ transparent protective substrate
圖1及2按圖描述根據一實施例之太陽能電池模組之配置(即,分別為展開視圖及組合視圖),其包含太陽能電池及封裝材料板。Figures 1 and 2 describe the configuration of a solar cell module according to an embodiment (ie, an expanded view and a combined view, respectively) according to an embodiment, which includes a solar cell and a packaging material plate.
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