WO2020100792A1 - Paste composition - Google Patents
Paste composition Download PDFInfo
- Publication number
- WO2020100792A1 WO2020100792A1 PCT/JP2019/044065 JP2019044065W WO2020100792A1 WO 2020100792 A1 WO2020100792 A1 WO 2020100792A1 JP 2019044065 W JP2019044065 W JP 2019044065W WO 2020100792 A1 WO2020100792 A1 WO 2020100792A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- paste composition
- inorganic
- oxide
- aluminum
- silicon
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 67
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000000843 powder Substances 0.000 claims abstract description 31
- 239000011521 glass Substances 0.000 claims abstract description 30
- 238000002161 passivation Methods 0.000 claims abstract description 13
- 229910052806 inorganic carbonate Inorganic materials 0.000 claims abstract description 9
- 229910001959 inorganic nitrate Inorganic materials 0.000 claims abstract description 8
- 229910052809 inorganic oxide Inorganic materials 0.000 claims abstract description 8
- 229910052920 inorganic sulfate Inorganic materials 0.000 claims abstract description 8
- 150000004767 nitrides Chemical class 0.000 claims abstract description 8
- 150000004703 alkoxides Chemical class 0.000 claims abstract description 6
- 229910052751 metal Inorganic materials 0.000 claims abstract description 6
- 239000002184 metal Substances 0.000 claims abstract description 6
- 238000010304 firing Methods 0.000 claims description 12
- 150000002823 nitrates Chemical class 0.000 claims description 5
- 150000001247 metal acetylides Chemical class 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 20
- 229910052710 silicon Inorganic materials 0.000 abstract description 19
- 239000010703 silicon Substances 0.000 abstract description 19
- 229910052782 aluminium Inorganic materials 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- 239000000758 substrate Substances 0.000 description 13
- -1 ester compounds Chemical class 0.000 description 12
- 239000004065 semiconductor Substances 0.000 description 11
- 101001073212 Arabidopsis thaliana Peroxidase 33 Proteins 0.000 description 9
- 101001123325 Homo sapiens Peroxisome proliferator-activated receptor gamma coactivator 1-beta Proteins 0.000 description 9
- 102100028961 Peroxisome proliferator-activated receptor gamma coactivator 1-beta Human genes 0.000 description 9
- 239000002245 particle Substances 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 235000012431 wafers Nutrition 0.000 description 4
- 229910052581 Si3N4 Inorganic materials 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 235000010216 calcium carbonate Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000007561 laser diffraction method Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- 229910021364 Al-Si alloy Inorganic materials 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 239000001856 Ethyl cellulose Substances 0.000 description 2
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229910000676 Si alloy Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 2
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- NLSCHDZTHVNDCP-UHFFFAOYSA-N caesium nitrate Chemical compound [Cs+].[O-][N+]([O-])=O NLSCHDZTHVNDCP-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- PPQREHKVAOVYBT-UHFFFAOYSA-H dialuminum;tricarbonate Chemical compound [Al+3].[Al+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O PPQREHKVAOVYBT-UHFFFAOYSA-H 0.000 description 2
- KQTXIZHBFFWWFW-UHFFFAOYSA-L disilver;carbonate Chemical compound [Ag]OC(=O)O[Ag] KQTXIZHBFFWWFW-UHFFFAOYSA-L 0.000 description 2
- 229920001249 ethyl cellulose Polymers 0.000 description 2
- 235000019325 ethyl cellulose Nutrition 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 2
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 description 2
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- RVDLHGSZWAELAU-UHFFFAOYSA-N 5-tert-butylthiophene-2-carbonyl chloride Chemical compound CC(C)(C)C1=CC=C(C(Cl)=O)S1 RVDLHGSZWAELAU-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229910000521 B alloy Inorganic materials 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- 229910015902 Bi 2 O 3 Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 229910002601 GaN Inorganic materials 0.000 description 1
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 description 1
- 229910000003 Lead carbonate Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Chemical class 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000004931 aggregating effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- DJPURDPSZFLWGC-UHFFFAOYSA-N alumanylidyneborane Chemical compound [Al]#B DJPURDPSZFLWGC-UHFFFAOYSA-N 0.000 description 1
- CAVCGVPGBKGDTG-UHFFFAOYSA-N alumanylidynemethyl(alumanylidynemethylalumanylidenemethylidene)alumane Chemical compound [Al]#C[Al]=C=[Al]C#[Al] CAVCGVPGBKGDTG-UHFFFAOYSA-N 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- JPUHCPXFQIXLMW-UHFFFAOYSA-N aluminium triethoxide Chemical compound CCO[Al](OCC)OCC JPUHCPXFQIXLMW-UHFFFAOYSA-N 0.000 description 1
- 229940118662 aluminum carbonate Drugs 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- GYIWFHXWLCXGQO-UHFFFAOYSA-N barium(2+);ethanolate Chemical compound [Ba+2].CC[O-].CC[O-] GYIWFHXWLCXGQO-UHFFFAOYSA-N 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- ZBUQRSWEONVBES-UHFFFAOYSA-L beryllium carbonate Chemical compound [Be+2].[O-]C([O-])=O ZBUQRSWEONVBES-UHFFFAOYSA-L 0.000 description 1
- 229910000023 beryllium carbonate Inorganic materials 0.000 description 1
- 229910000416 bismuth oxide Inorganic materials 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 1
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 1
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 1
- 229910000024 caesium carbonate Inorganic materials 0.000 description 1
- KOPBYBDAPCDYFK-UHFFFAOYSA-N caesium oxide Chemical compound [O-2].[Cs+].[Cs+] KOPBYBDAPCDYFK-UHFFFAOYSA-N 0.000 description 1
- 229910001942 caesium oxide Inorganic materials 0.000 description 1
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical compound [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 description 1
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- JHLCADGWXYCDQA-UHFFFAOYSA-N calcium;ethanolate Chemical compound [Ca+2].CC[O-].CC[O-] JHLCADGWXYCDQA-UHFFFAOYSA-N 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 229910000009 copper(II) carbonate Inorganic materials 0.000 description 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000011646 cupric carbonate Substances 0.000 description 1
- 235000019854 cupric carbonate Nutrition 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- AJNVQOSZGJRYEI-UHFFFAOYSA-N digallium;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Ga+3].[Ga+3] AJNVQOSZGJRYEI-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 229910001195 gallium oxide Inorganic materials 0.000 description 1
- 238000009689 gas atomisation Methods 0.000 description 1
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 1
- RXPAJWPEYBDXOG-UHFFFAOYSA-N hydron;methyl 4-methoxypyridine-2-carboxylate;chloride Chemical compound Cl.COC(=O)C1=CC(OC)=CC=N1 RXPAJWPEYBDXOG-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000011656 manganese carbonate Substances 0.000 description 1
- 235000006748 manganese carbonate Nutrition 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical compound C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 229910000008 nickel(II) carbonate Inorganic materials 0.000 description 1
- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 description 1
- 229910000484 niobium oxide Inorganic materials 0.000 description 1
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical compound [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- SJLOMQIUPFZJAN-UHFFFAOYSA-N oxorhodium Chemical compound [Rh]=O SJLOMQIUPFZJAN-UHFFFAOYSA-N 0.000 description 1
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 229910003445 palladium oxide Inorganic materials 0.000 description 1
- JQPTYAILLJKUCY-UHFFFAOYSA-N palladium(ii) oxide Chemical compound [O-2].[Pd+2] JQPTYAILLJKUCY-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- BSPSZRDIBCCYNN-UHFFFAOYSA-N phosphanylidynetin Chemical compound [Sn]#P BSPSZRDIBCCYNN-UHFFFAOYSA-N 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910003450 rhodium oxide Inorganic materials 0.000 description 1
- WPFGFHJALYCVMO-UHFFFAOYSA-L rubidium carbonate Chemical compound [Rb+].[Rb+].[O-]C([O-])=O WPFGFHJALYCVMO-UHFFFAOYSA-L 0.000 description 1
- 229910000026 rubidium carbonate Inorganic materials 0.000 description 1
- 229910001952 rubidium oxide Inorganic materials 0.000 description 1
- CWBWCLMMHLCMAM-UHFFFAOYSA-M rubidium(1+);hydroxide Chemical compound [OH-].[Rb+].[Rb+] CWBWCLMMHLCMAM-UHFFFAOYSA-M 0.000 description 1
- 229910001925 ruthenium oxide Inorganic materials 0.000 description 1
- WOCIAKWEIIZHES-UHFFFAOYSA-N ruthenium(iv) oxide Chemical compound O=[Ru]=O WOCIAKWEIIZHES-UHFFFAOYSA-N 0.000 description 1
- HYXGAEYDKFCVMU-UHFFFAOYSA-N scandium oxide Chemical compound O=[Sc]O[Sc]=O HYXGAEYDKFCVMU-UHFFFAOYSA-N 0.000 description 1
- NYMLCLICEBTBKR-UHFFFAOYSA-H scandium(3+);tricarbonate Chemical compound [Sc+3].[Sc+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O NYMLCLICEBTBKR-UHFFFAOYSA-H 0.000 description 1
- DFCYEXJMCFQPPA-UHFFFAOYSA-N scandium(3+);trinitrate Chemical compound [Sc+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O DFCYEXJMCFQPPA-UHFFFAOYSA-N 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- LKZMBDSASOBTPN-UHFFFAOYSA-L silver carbonate Substances [Ag].[O-]C([O-])=O LKZMBDSASOBTPN-UHFFFAOYSA-L 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910001936 tantalum oxide Inorganic materials 0.000 description 1
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- GXMNGLIMQIPFEB-UHFFFAOYSA-N tetraethoxygermane Chemical compound CCO[Ge](OCC)(OCC)OCC GXMNGLIMQIPFEB-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- WOZZOSDBXABUFO-UHFFFAOYSA-N tri(butan-2-yloxy)alumane Chemical compound [Al+3].CCC(C)[O-].CCC(C)[O-].CCC(C)[O-] WOZZOSDBXABUFO-UHFFFAOYSA-N 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/22—Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/02—Details
- H01L31/0224—Electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/06—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers
- H01L31/068—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices characterised by potential barriers the potential barriers being only of the PN homojunction type, e.g. bulk silicon PN homojunction solar cells or thin film polycrystalline silicon PN homojunction solar cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/547—Monocrystalline silicon PV cells
Definitions
- the present invention relates to a paste composition.
- a paste composition containing aluminum is applied to the back surface of the solar cell and the paste composition is baked to form an electrode.
- Patent Document 1 As such a paste composition, in Patent Document 1, 30 to 70 cation mole percent of lead (Pb 2+ ), 1 to 40 cation mole percent of silicon (Si 4+ ) and 10 to 65 cation mole percent of boron (B 3+ ) are disclosed. And a paste composition using a glass frit containing 1 to 25 cation mole percent of aluminum (Al 3+ ) is disclosed.
- Patent Document 2 discloses a paste composition containing aluminum powder, aluminum-silicon alloy powder, silicon powder, glass powder, and an organic vehicle.
- Patent Document 3 proposes a method of suppressing warpage of a cell by using a paste composition containing an alkaline earth metal compound and Patent Document 4 containing silica.
- the conversion efficiency of a solar cell is defined as the efficiency with which a solar cell converts light energy into electrical energy.
- an object of the present invention is to provide a paste composition for PERC solar cells, which has a small warpage after firing and a low electric resistance value.
- the ratio of the aluminum powder contained in the paste composition is within a predetermined numerical range, and the paste composition contains an inorganic carbonate and silica.
- the present invention provides the following paste composition for PERC solar cells.
- Item 1 A paste composition for a backside passivation solar cell, The paste composition contains a silicon-free glass powder, an organic vehicle, and an aluminum powder, The content of the aluminum powder in 100% by mass of the paste composition is 65 to 75% by mass, The paste composition is characterized in that, in addition to the silicon-free glass powder, it does not contain any of inorganic oxides, inorganic carbides, inorganic nitrides, inorganic nitrates, inorganic sulfates and organic metal alkoxides. .. Item 2. A back surface passivation type solar cell having an electrode obtained by firing the paste composition according to Item 1.
- the paste composition for a PERC solar cell of the present invention has a small warpage after firing the paste composition and a low electric resistance value.
- the PERC solar cell is configured using, for example, a silicon semiconductor substrate 1 having a thickness of 140 to 170 ⁇ m. Then, as shown in FIG. 1B, the n-type impurity layer 2 and the antireflection film 3 are preferably laminated in this order on the light-receiving surface side of the silicon semiconductor substrate 1.
- a passivation film 4 is preferably provided on the back surface of the silicon semiconductor substrate 1 opposite to the light receiving surface.
- a contact hole 5 is provided in the passivation film 4 by a method such as laser irradiation.
- a layer made of the paste composition 6 is provided by a method such as coating so as to cover the passivation film 4 and the contact holes 5.
- the back electrode 9 is formed by baking the paste composition at a high temperature, for example, 700 to 1000 ° C.
- the aluminum contained in the paste composition 6 diffuses into the silicon semiconductor substrate 1 during firing, so that Al ⁇ is formed between the back electrode 9 and the silicon semiconductor substrate 1.
- An alloy layer 7 of Si is formed.
- a p + layer (BSF layer: BackSurface Field layer) 8 is formed as an impurity layer by diffusion of aluminum atoms.
- the paste composition of the present invention is a paste composition for a backside passivation solar cell, wherein the paste composition contains a silicon-free glass powder, an organic vehicle, and an aluminum powder, and the paste composition
- the content of the aluminum powder in 100% by mass of the product is 65 to 75% by mass
- the paste composition contains an inorganic oxide, an inorganic carbide, an inorganic nitride, an inorganic nitrate, in addition to the silicon-free glass powder. It is characterized by containing neither an inorganic sulfate nor an organic metal alkoxide.
- the paste composition of the present invention contains a silicon-free glass powder.
- a silicon-free glass powder is defined as a glass powder that does not contain or contains substantially no silica (SiO 2 ) component.
- the silicon-free glass powder is not particularly limited as long as it is a glass powder that does not contain or contains substantially no silica (SiO 2 ) component.
- SiO 2 silica
- one or more oxides selected from the group consisting of lead (Pb), bismuth (Bi), vanadium (V), boron (B), tin (Sn), phosphorus (P), zinc (Zn) and the like can be used. It may be the glass powder contained.
- the silicon-free glass powder it is possible to use lead-containing glass powder or lead-free glass powder such as bismuth-based, vanadium-based or tin-phosphorus-based glass powder. Particularly, considering the influence on the human body, it is preferable to use lead-free glass powder.
- the silicon-free glass powder in the paste composition preferably has an average particle size calculated by a laser diffraction method of 1 to 10 ⁇ m in order to reduce the risk of mask clogging during screen printing. Is more preferable.
- the content of the silicon-free glass powder contained in the paste composition is 0.1% by mass or more in 100% by mass of the paste composition in order to secure the adhesion between the electrode and the silicon wafer after firing. It is preferably present, and more preferably 0.5% by mass or more.
- the content of the silicon-free glass powder is preferably 10% by mass or less in 100% by mass of the paste composition, and 5% by mass is preferable. The above is more preferable.
- Organic vehicle As the organic vehicle, a solvent prepared by dissolving various additives and a resin in a solvent may be used.
- solvent known ones can be used, and specific examples thereof include diethylene glycol monobutyl ether, diethylene glycol monobutyl ether acetate, dipropylene glycol monomethyl ether and the like.
- an antioxidant for example, an antioxidant, a corrosion inhibitor, an antifoaming agent, a thickener, a tackfire, a coupling agent, an electrostatic imparting agent, a polymerization inhibitor, a thixotropic agent, an antisettling agent, etc.
- an antioxidant for example, an antioxidant, a corrosion inhibitor, an antifoaming agent, a thickener, a tackfire, a coupling agent, an electrostatic imparting agent, a polymerization inhibitor, a thixotropic agent, an antisettling agent, etc.
- polyethylene glycol ester compounds polyethylene glycol ether compounds, polyoxyethylene sorbitan ester compounds, sorbitan alkyl ester compounds, aliphatic polycarboxylic acid compounds, phosphoric acid ester compounds, amide amine salts of polyester acids, polyethylene oxide compounds. , Fatty acid amide wax and the like can be used.
- inorganic carbonate and silica are not included as such additives.
- Known resins can be used as the resin, ethyl cellulose, nitrocellulose, polyvinyl butyral, phenol resin, melanin resin, urea resin, xylene resin, alkyd resin, unsaturated polyester resin, acrylic resin, polyimide resin, furan resin, Thermosetting resin such as urethane resin, isocyanate compound, cyanate compound, polyethylene, polypropylene, polystyrene, ABS resin, polymethylmethacrylate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polyvinyl alcohol, polyacetal, polycarbonate, polyethylene terephthalate, One or more selected from the group consisting of polybutylene terephthalate, polyphenylene oxide, polysulfone, polyimide, polyether sulfone, polyarylate, polyether ether ketone, polytetrafluoroethylene, and silicone resin can be used.
- the content ratio of the organic vehicle contained in the paste composition of the present invention is not particularly limited, but is preferably 30 parts by mass or more and 60 parts by mass or less with respect to 100 parts by mass of aluminum powder described later. When the content ratio of the organic vehicle is within such a numerical range, good adhesiveness can be obtained when the paste composition is applied to the passivation film.
- the shape of the aluminum particles constituting the aluminum powder is not particularly limited, and may be, for example, spherical, elliptical, amorphous, scale-like, or fibrous. Among them, if it has a spherical shape, the filling property of aluminum in the formed electrode can be improved, and the electric resistance of the electrode can be lowered, and as a result, the conversion efficiency of the solar cell can be improved. You can
- the average particle size of the aluminum particles constituting the aluminum powder is measured by a laser diffraction method in order to prevent the aluminum powders from aggregating with each other and to improve the dispersibility of the aluminum powder in the paste composition.
- the average particle diameter is preferably 0.1 ⁇ m or more, more preferably 1 ⁇ m or more.
- the average particle diameter of the aluminum powder particles measured by the laser diffraction method is preferably 20 ⁇ m or less, and more preferably 15 ⁇ m or less.
- the aluminum powder may be composed only of aluminum (preferably high-purity aluminum) or may contain an aluminum alloy.
- Examples of the aluminum alloy include aluminum-silicon alloy and aluminum-boron alloy.
- the content of the aluminum powder contained in the paste composition is 65 to 75% by mass, preferably 71 to 74% by mass based on 100% by mass of the paste composition. If the content of the aluminum powder is less than 65% by mass, the conversion efficiency will decrease. On the other hand, when the content of the aluminum powder exceeds 75% by mass, the warp of the solar battery cell becomes large when the paste composition is fired to form the electrode.
- the paste composition of the present invention contains a silicon-free glass powder, an organic vehicle, and an aluminum powder as described above, in addition to the silicon-free glass powder, an inorganic carbonate, an inorganic oxide, an inorganic carbide, an inorganic nitride. It is characterized in that it does not contain any of a substance, an inorganic nitrate, an inorganic sulfate and an organic metal alkoxide.
- the inorganic carbonate here means all known inorganic carbonates. Specifically, calcium carbonate, sodium carbonate, magnesium carbonate, barium carbonate, aluminum carbonate, potassium carbonate, scandium carbonate, zinc carbonate, silver (I) carbonate, potassium hydrogen carbonate, calcium hydrogen carbonate, strontium carbonate, cesium carbonate, carbonate Examples are iron (II), copper (II) carbonate, sodium carbonate, lead (II) carbonate, nickel (II) carbonate, beryllium carbonate, manganese (II) carbonate, lithium carbonate and rubidium carbonate.
- the inorganic oxides here mean all known inorganic oxides. Specifically, sodium oxide, magnesium oxide, aluminum oxide, silicon oxide, potassium oxide, calcium oxide, scandium oxide, titanium oxide, vanadium oxide, chromium oxide, manganese oxide, iron oxide, cobalt oxide, nickel oxide, copper oxide, Zinc oxide, gallium oxide, germanium oxide, rubidium oxide, strontium oxide, yttrium oxide, zirconium oxide, niobium oxide, molybdenum oxide, ruthenium oxide, rhodium oxide, palladium oxide, silver oxide, cadmium oxide, indium oxide, tin oxide, antimony oxide
- rare earth oxides such as tellurium oxide, cesium oxide, barium oxide, tantalum oxide, tungsten oxide, lead oxide, bismuth oxide, lanthanum oxide and cerium oxide.
- inorganic carbide means all known inorganic carbides, and specific examples thereof include silicon carbide, boron carbide, and aluminum carbide.
- inorganic nitrides are all known inorganic nitrides, and specific examples thereof include aluminum nitride, silicon nitride, gallium nitride, and boron nitride.
- inorganic nitrates means inorganic nitrates, specifically, sodium nitrate, magnesium nitrate, aluminum nitrate, potassium nitrate, calcium nitrate, scandium nitrate, copper nitrate, zinc nitrate, strontium nitrate, cesium nitrate, barium nitrate, nitric acid.
- Lead and bismuth nitrate can be exemplified.
- inorganic sulfates are all known inorganic sulfates, and specific examples thereof include aluminum sulfate, barium sulfate, and magnesium sulfate.
- organometallic alkoxide means all organometallic alkoxides, specifically, aluminum isopropoxide, aluminum butoxide, aluminum ethoxide, barium ethoxide, calcium ethoxide, magnesium ethoxide, germanium ethoxide and titanium ethoxy. Can be illustrated.
- the paste composition of the present invention in addition to the silicon-free glass powder, inorganic carbonate, inorganic oxides, inorganic carbides, inorganic nitrides, inorganic nitrates, inorganic sulfates and organic metal alkoxide does not contain any of the composition By adopting this, warpage of the fired product after firing the paste composition is small and the electric resistance value can be lowered.
- the paste composition of the present invention can be manufactured by a conventional method, and can be manufactured by an appropriate method such as kneading the above-mentioned silicon-free glass powder, organic vehicle, and aluminum powder.
- the vehicle dissolved in was mixed in 100 mass% of the paste composition at a ratio shown in Table 1 below and made into a paste using a known dispersing device (disper) to obtain a paste composition.
- a paste composition As shown in Table 1, in addition to the above three components, calcium carbonate was added for Comparative Example 5 and silica was added for Comparative Example 6 to obtain a paste composition.
- a fired substrate which is a solar cell for evaluation, was manufactured as follows. First, a semiconductor substrate made of p-type single crystal silicon shown in FIG. 1A was prepared (substrate: 6 inches, thickness 160 ⁇ m, resistivity 2 ⁇ ⁇ cm). Subsequently, as shown in FIG. 1B, a sheet having a thickness of 0.3 to 1 ⁇ m and a thickness of 40 to 200 ⁇ / ⁇ by a vapor layer thermal diffusion method using a gasified POCl 3 (phosphorus oxychloride). The n + layer 2 was formed so as to have resistance.
- a semiconductor substrate made of p-type single crystal silicon shown in FIG. 1A was prepared (substrate: 6 inches, thickness 160 ⁇ m, resistivity 2 ⁇ ⁇ cm).
- FIG. 1B a sheet having a thickness of 0.3 to 1 ⁇ m and a thickness of 40 to 200 ⁇ / ⁇ by a vapor layer thermal diffusion method using a gasified POCl 3 (phosphorus oxy
- an antireflection film 3 containing silicon nitride as a main component was formed by a plasma CVD method, and a passivation film 4 made of aluminum oxide and silicon nitride was formed on the opposite surface.
- an IR laser having a wavelength of 1064 nm is used as a laser oscillator to form a contact hole 5 having a width D of 30 ⁇ m and a depth of 1 ⁇ m on the surface of the silicon semiconductor substrate 1 (aluminum paste printing). Part).
- each paste composition 6 obtained in each of the above Examples and Comparative Examples covers the entire back surface (the surface on the side where the contact holes 9 are formed).
- the silicon semiconductor substrate 1 was printed on the surface of the silicon semiconductor substrate 1 using a screen printer so as to be 0.8-0.9 g / pc. Then, it baked using the infrared belt furnace set to 800 degreeC. By this firing, as shown in FIG. 1E, the electrode layer 9 is formed, and during this firing, aluminum diffuses into the silicon semiconductor substrate 1, so that the electrode layer 9 and the silicon semiconductor substrate are diffused.
- the Al--Si alloy layer 7 and the Al--Si alloy layer 7 were formed at the same time, and at the same time, the p + layer (BSF layer) 8 was formed as an impurity layer by diffusion of aluminum atoms.
- the resistance of the electrode in the obtained solar battery cell was measured using a sheet resistance machine (manufactured by Napson Corporation, model number RT-70V). The amount of warpage was measured using a laser displacement meter. Also, as a performance evaluation of the BSF layer, which is the main function of the aluminum electrode, the obtained cell was immersed in hydrochloric acid heated to 50 ° C., the aluminum electrode was etched (see FIG. 1 (F)), and manufactured by Sinton Instruments. Implied Voc measurement was carried out using the Lifetime measuring instrument (WCT-120) of.
- the electrodes of the solar battery cells manufactured using the paste compositions of the respective examples have a high Implied Voc and a sufficiently high implied Voc, as compared with those using the paste compositions of the respective comparative examples.
- a low resistance value was obtained, and the amount of warpage could be suppressed to a low value of 2.0 mm or less.
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Abstract
Provided is a paste composition for a rear surface passivation type solar battery characterized in that: the paste composition comprises a silicon free glass powder, an organic vehicle, and an aluminum powder; the content of the aluminum powder relative to 100 mass% of the paste composition is 65 to 75 mass%; and other than the silicon free glass powder, the paste composition does not contain any of inorganic carbonate, inorganic oxide, inorganic carbide, inorganic nitride, inorganic nitrate, inorganic sulfate, or organic metal alkoxide.
Description
本発明は、ペースト組成物に関する。
The present invention relates to a paste composition.
従来より、結晶系太陽電池セルの変換効率及び生産効率等を向上させるために、種々の開発が行われている。特にかかる目的に適した太陽電池として、裏面パッシベーション(Passivated Emitter and Rear Cell;以下、単にPERCともいう。)型太陽電池が提案されている。
Conventionally, various developments have been made to improve the conversion efficiency and production efficiency of crystalline solar cells. As a solar cell particularly suitable for such a purpose, a backside passivation (Passivated Emitter and Rear Cell; hereinafter also simply referred to as PERC) type solar cell has been proposed.
一般的に、PERC型太陽電池を製造する際には、太陽電池セルの裏面にアルミニウムを含むペースト組成物を塗布し、該ペースト組成物を焼成して電極を形成する。
Generally, when manufacturing a PERC solar cell, a paste composition containing aluminum is applied to the back surface of the solar cell and the paste composition is baked to form an electrode.
このようなペースト組成物として、特許文献1には、鉛(Pb2+)30~70カチオンモルパーセントと、ケイ素(Si4+)1~40カチオンモルパーセントとホウ素(B3+)10~65カチオンモルパーセントと、アルミニウム(Al3+)1~25カチオンモルパーセントとを含むガラスフリットを使用したペースト組成物が開示されている。
As such a paste composition, in Patent Document 1, 30 to 70 cation mole percent of lead (Pb 2+ ), 1 to 40 cation mole percent of silicon (Si 4+ ) and 10 to 65 cation mole percent of boron (B 3+ ) are disclosed. And a paste composition using a glass frit containing 1 to 25 cation mole percent of aluminum (Al 3+ ) is disclosed.
特許文献2には、アルミニウム粉末、アルミニウム-シリコン合金粉末、シリコン粉末、ガラス粉末及び有機ビヒクルを含むペースト組成物が開示されている。
Patent Document 2 discloses a paste composition containing aluminum powder, aluminum-silicon alloy powder, silicon powder, glass powder, and an organic vehicle.
また、近年では、太陽電池セルの主原料となるシリコン価格の高騰及び太陽電池の市場価格の下落に伴い、シリコンウエハの薄型化の流れが加速している。最近では、厚さ140~170μmのシリコンウエハを使用が検討されている。
Also, in recent years, the trend of thinning silicon wafers has accelerated with the rise in the price of silicon, the main raw material for solar cells, and the drop in the market price of solar cells. Recently, the use of a silicon wafer having a thickness of 140 to 170 μm has been considered.
一方、上記のようなシリコンウエハの薄型化が進むと、電極を構成するためにペースト組成物を焼成した際に、アルミニウム(~23×10-6/K)とシリコン(~3×10-6/K)との熱膨張差により生じるセルの反りが大きくなり、その結果、太陽電池モジュール組立て時における、セルの割れや欠けに伴う歩留まり低下が問題となる。
On the other hand, as the silicon wafer becomes thinner as described above, when the paste composition is fired to form the electrode, aluminum (up to 23 × 10 −6 / K) and silicon (up to 3 × 10 −6) are formed. / K), the warp of the cell caused by the difference in thermal expansion becomes large, and as a result, a decrease in yield due to cracking or chipping of the cell during assembly of the solar cell module becomes a problem.
そこで、特許文献3ではアルカリ土類金属の化合物を、特許文献4ではシリカを、含有するペースト組成物を使用することにより、セルの反りを抑制する方法が提案されている。
Therefore, Patent Document 3 proposes a method of suppressing warpage of a cell by using a paste composition containing an alkaline earth metal compound and Patent Document 4 containing silica.
しかし、特許文献3及び4に記載されたペースト組成物では、焼成後のセルの反りは抑制される一方で、電極の電気抵抗が高くなり、その結果、太陽電池自体の変換効率が悪くなってしまう。尚、本明細書において太陽電池の変換効率とは、太陽電池が光エネルギーを電気エネルギーに変換する効率のことであると、定義される。
However, in the paste compositions described in Patent Documents 3 and 4, the warp of the cell after firing is suppressed, but the electric resistance of the electrode is increased, and as a result, the conversion efficiency of the solar cell itself is deteriorated. I will end up. In this specification, the conversion efficiency of a solar cell is defined as the efficiency with which a solar cell converts light energy into electrical energy.
上記のような事情に鑑み、本発明の目的とするところは、焼成後の反りが小さく、且つ、電気抵抗値の低い、PERC型太陽電池用のペースト組成物を提供することにある。
In view of the above circumstances, an object of the present invention is to provide a paste composition for PERC solar cells, which has a small warpage after firing and a low electric resistance value.
本発明者らは上記目的を達成すべく鋭意研究を重ねた結果、ペースト組成物中に含まれるアルミニウム粉末の割合を所定の数値範囲内とし、且つ、ペースト組成物が無機炭酸塩及びシリカを含有しないようにすることで、ペースト組成物焼成後の反りが小さく、且つ、電気抵抗値が低い、PERC型太陽電池用のペースト組成物を提供できることを見出した。本発明者らは、かかる知見に基づきさらに研究を重ね、本発明を完成するに至った。
As a result of intensive studies conducted by the inventors to achieve the above object, the ratio of the aluminum powder contained in the paste composition is within a predetermined numerical range, and the paste composition contains an inorganic carbonate and silica. By not doing so, it has been found that it is possible to provide a paste composition for PERC solar cells, which has a small warpage after firing the paste composition and has a low electric resistance value. The present inventors have conducted further research based on such findings and completed the present invention.
即ち、本発明は、以下のPERC型太陽電池用のペースト組成物を提供する。
項1.
裏面パッシベーション型太陽電池用のペースト組成物であって、
前記ペースト組成物は、ケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を含有し、
前記ペースト組成物100質量%中における前記アルミニウム粉末の含有量は65~75質量%であり、
前記ペースト組成物は、前記ケイ素非含有ガラス粉末以外に、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないことを特徴とする、ペースト組成物。
項2.
項1に記載のペースト組成物が焼成された電極を有する、裏面パッシベーション型太陽電池。 That is, the present invention provides the following paste composition for PERC solar cells.
Item 1.
A paste composition for a backside passivation solar cell,
The paste composition contains a silicon-free glass powder, an organic vehicle, and an aluminum powder,
The content of the aluminum powder in 100% by mass of the paste composition is 65 to 75% by mass,
The paste composition is characterized in that, in addition to the silicon-free glass powder, it does not contain any of inorganic oxides, inorganic carbides, inorganic nitrides, inorganic nitrates, inorganic sulfates and organic metal alkoxides. ..
Item 2.
A back surface passivation type solar cell having an electrode obtained by firing the paste composition according to Item 1.
項1.
裏面パッシベーション型太陽電池用のペースト組成物であって、
前記ペースト組成物は、ケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を含有し、
前記ペースト組成物100質量%中における前記アルミニウム粉末の含有量は65~75質量%であり、
前記ペースト組成物は、前記ケイ素非含有ガラス粉末以外に、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないことを特徴とする、ペースト組成物。
項2.
項1に記載のペースト組成物が焼成された電極を有する、裏面パッシベーション型太陽電池。 That is, the present invention provides the following paste composition for PERC solar cells.
Item 1.
A paste composition for a backside passivation solar cell,
The paste composition contains a silicon-free glass powder, an organic vehicle, and an aluminum powder,
The content of the aluminum powder in 100% by mass of the paste composition is 65 to 75% by mass,
The paste composition is characterized in that, in addition to the silicon-free glass powder, it does not contain any of inorganic oxides, inorganic carbides, inorganic nitrides, inorganic nitrates, inorganic sulfates and organic metal alkoxides. ..
Item 2.
A back surface passivation type solar cell having an electrode obtained by firing the paste composition according to Item 1.
本発明のPERC型太陽電池用のペースト組成物は、該ペースト組成物焼成後の反りが小さく、且つ、電気抵抗値が低い。
The paste composition for a PERC solar cell of the present invention has a small warpage after firing the paste composition and a low electric resistance value.
1.PERC型太陽電池セル
図1(A)に示すように、PERC型太陽電池セルは、例えば、厚みが140~170μmのシリコン半導体基板1を用いて構成される。そして、図1(B)のように、シリコン半導体基板1の受光面側には、n型不純物層2と、反射防止膜3とが、この順に積層されることが好ましい。 1. PERC Solar Cell As shown in FIG. 1 (A), the PERC solar cell is configured using, for example, a silicon semiconductor substrate 1 having a thickness of 140 to 170 μm. Then, as shown in FIG. 1B, the n-type impurity layer 2 and theantireflection film 3 are preferably laminated in this order on the light-receiving surface side of the silicon semiconductor substrate 1.
図1(A)に示すように、PERC型太陽電池セルは、例えば、厚みが140~170μmのシリコン半導体基板1を用いて構成される。そして、図1(B)のように、シリコン半導体基板1の受光面側には、n型不純物層2と、反射防止膜3とが、この順に積層されることが好ましい。 1. PERC Solar Cell As shown in FIG. 1 (A), the PERC solar cell is configured using, for example, a silicon semiconductor substrate 1 having a thickness of 140 to 170 μm. Then, as shown in FIG. 1B, the n-type impurity layer 2 and the
そして、図1(B)のように、シリコン半導体基板1の受光面と反対側の裏面には、パッシベーション膜4が設けられることが好ましい。パッシベーション膜4には、その後図1(C)にあるように、例えばレーザー照射等の方法により、コンタクト孔5が設けられる。
Then, as shown in FIG. 1B, a passivation film 4 is preferably provided on the back surface of the silicon semiconductor substrate 1 opposite to the light receiving surface. After that, as shown in FIG. 1C, a contact hole 5 is provided in the passivation film 4 by a method such as laser irradiation.
次いで、図1(D)に示すように、パッシベーション膜4及びコンタクト孔5を覆うように、ペースト組成物6からなる層が塗布等の方法により設けられる。前記ペースト組成物を高温、例えば700~1000℃で焼成することにより、裏面電極9が形成される。図1(E)にあるように、焼成の際にペースト組成物6中に含まれるアルミニウムがシリコン半導体基板1の内部に拡散することにより、裏面電極9とシリコン半導体基板1との間にAl-Siの合金層7が形成される。併せて、アルミニウム原子の拡散による不純物層としてp+層(BSF層:BackSurface Field層)8が形成される。
Next, as shown in FIG. 1D, a layer made of the paste composition 6 is provided by a method such as coating so as to cover the passivation film 4 and the contact holes 5. The back electrode 9 is formed by baking the paste composition at a high temperature, for example, 700 to 1000 ° C. As shown in FIG. 1 (E), the aluminum contained in the paste composition 6 diffuses into the silicon semiconductor substrate 1 during firing, so that Al− is formed between the back electrode 9 and the silicon semiconductor substrate 1. An alloy layer 7 of Si is formed. At the same time, a p + layer (BSF layer: BackSurface Field layer) 8 is formed as an impurity layer by diffusion of aluminum atoms.
2.ペースト組成物
本発明のペースト組成物は、裏面パッシベーション型太陽電池用のペースト組成物であって、前記ペースト組成物は、ケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を含有し、前記ペースト組成物100質量%中における前記アルミニウム粉末の含有量は65~75質量%であり、前記ペースト組成物は、前記ケイ素非含有ガラス粉末以外に、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないことを特徴とする。 2. Paste composition The paste composition of the present invention is a paste composition for a backside passivation solar cell, wherein the paste composition contains a silicon-free glass powder, an organic vehicle, and an aluminum powder, and the paste composition The content of the aluminum powder in 100% by mass of the product is 65 to 75% by mass, and the paste composition contains an inorganic oxide, an inorganic carbide, an inorganic nitride, an inorganic nitrate, in addition to the silicon-free glass powder. It is characterized by containing neither an inorganic sulfate nor an organic metal alkoxide.
本発明のペースト組成物は、裏面パッシベーション型太陽電池用のペースト組成物であって、前記ペースト組成物は、ケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を含有し、前記ペースト組成物100質量%中における前記アルミニウム粉末の含有量は65~75質量%であり、前記ペースト組成物は、前記ケイ素非含有ガラス粉末以外に、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないことを特徴とする。 2. Paste composition The paste composition of the present invention is a paste composition for a backside passivation solar cell, wherein the paste composition contains a silicon-free glass powder, an organic vehicle, and an aluminum powder, and the paste composition The content of the aluminum powder in 100% by mass of the product is 65 to 75% by mass, and the paste composition contains an inorganic oxide, an inorganic carbide, an inorganic nitride, an inorganic nitrate, in addition to the silicon-free glass powder. It is characterized by containing neither an inorganic sulfate nor an organic metal alkoxide.
(ケイ素非含有ガラス粉末)
本発明のペースト組成物は、ケイ素非含有ガラス粉末を含む。本明細書において、ケイ素非含有ガラス粉末とは、シリカ(SiO2)成分を全く含有しない、或いは、実質的に含有しないガラス粉末であると定義される。 (Silicon-free glass powder)
The paste composition of the present invention contains a silicon-free glass powder. In the present specification, a silicon-free glass powder is defined as a glass powder that does not contain or contains substantially no silica (SiO 2 ) component.
本発明のペースト組成物は、ケイ素非含有ガラス粉末を含む。本明細書において、ケイ素非含有ガラス粉末とは、シリカ(SiO2)成分を全く含有しない、或いは、実質的に含有しないガラス粉末であると定義される。 (Silicon-free glass powder)
The paste composition of the present invention contains a silicon-free glass powder. In the present specification, a silicon-free glass powder is defined as a glass powder that does not contain or contains substantially no silica (SiO 2 ) component.
ケイ素非含有ガラス粉末は、シリカ(SiO2)成分を全く含有しない、或いは、実質的に含有しないガラス粉末であれば特に限定はない。例えば、鉛(Pb)、ビスマス(Bi)、バナジウム(V)、ホウ素(B)、スズ(Sn)、リン(P)及び亜鉛(Zn)等からなる群より選択される一種以上の酸化物を含有するガラス粉末であってよい。
The silicon-free glass powder is not particularly limited as long as it is a glass powder that does not contain or contains substantially no silica (SiO 2 ) component. For example, one or more oxides selected from the group consisting of lead (Pb), bismuth (Bi), vanadium (V), boron (B), tin (Sn), phosphorus (P), zinc (Zn) and the like can be used. It may be the glass powder contained.
また、ケイ素非含有ガラス粉末として、鉛を含むガラス粉末、または、ビスマス系、バナジウム系、スズ-リン系等の無鉛のガラス粉末を用いることができる。特に人体への影響を考慮すると、無鉛のガラス粉末を用いることが好ましい。
Further, as the silicon-free glass powder, it is possible to use lead-containing glass powder or lead-free glass powder such as bismuth-based, vanadium-based or tin-phosphorus-based glass powder. Particularly, considering the influence on the human body, it is preferable to use lead-free glass powder.
ペースト組成物中のケイ素非含有ガラス粉末は、スクリーン印刷時のマスク目詰まりのリスクを低減するために、レーザー回折法により算出される平均粒子径が1~10μmであることが好ましく、1~3μmであることがより好ましい。
The silicon-free glass powder in the paste composition preferably has an average particle size calculated by a laser diffraction method of 1 to 10 μm in order to reduce the risk of mask clogging during screen printing. Is more preferable.
ペースト組成物中に含まれるケイ素非含有ガラス粉末の含有量は、焼成後の電極とシリコンウエハとの密着性を確保するために、ペースト組成物100質量%中に、0.1質量%以上であることが好ましく、0.5質量%以上であることがより好ましい。一方、焼成後の電極抵抗値が高くなり過ぎないようにするために、ケイ素非含有ガラス粉末の含有量は、ペースト組成物100質量%中に10質量%以下であることが好ましく、5質量%以上であることがより好ましい。
The content of the silicon-free glass powder contained in the paste composition is 0.1% by mass or more in 100% by mass of the paste composition in order to secure the adhesion between the electrode and the silicon wafer after firing. It is preferably present, and more preferably 0.5% by mass or more. On the other hand, in order to prevent the electrode resistance value after firing from becoming too high, the content of the silicon-free glass powder is preferably 10% by mass or less in 100% by mass of the paste composition, and 5% by mass is preferable. The above is more preferable.
(有機ビヒクル)
有機ビヒクルとしては、溶剤に、必要に応じて各種添加剤および樹脂を溶解したものを使用してもよい。 (Organic vehicle)
As the organic vehicle, a solvent prepared by dissolving various additives and a resin in a solvent may be used.
有機ビヒクルとしては、溶剤に、必要に応じて各種添加剤および樹脂を溶解したものを使用してもよい。 (Organic vehicle)
As the organic vehicle, a solvent prepared by dissolving various additives and a resin in a solvent may be used.
溶剤としては公知のものが使用可能であり、具体的には、ジエチレングリコールモノブチルエーテル、ジエチレングリコールモノブチルエーテルアセテート、ジプロピレングリコールモノメチルエーテル等が挙げられる。
As the solvent, known ones can be used, and specific examples thereof include diethylene glycol monobutyl ether, diethylene glycol monobutyl ether acetate, dipropylene glycol monomethyl ether and the like.
各種添加剤としては、たとえば、酸化防止剤、腐食抑制剤、消泡剤、増粘剤、タックファイヤー、カップリング剤、静電付与剤、重合禁止剤、チキソトロピー剤、沈降防止剤等を使用することができる。具体的には、ポリエチレングリコールエステル化合物、ポリエチレングリコールエーテル化合物、ポリオキシエチレンソルビタンエステル化合物、ソルビタンアルキルエステル化合物、脂肪族多価カルボン酸化合物、燐酸エステル化合物、ポリエステル酸のアマイドアミン塩、酸化ポリエチレン系化合物、脂肪酸アマイドワックス等を使用することができる。但し、本発明において、かかる添加剤として、無機炭酸塩及びシリカは含まれない。
As various additives, for example, an antioxidant, a corrosion inhibitor, an antifoaming agent, a thickener, a tackfire, a coupling agent, an electrostatic imparting agent, a polymerization inhibitor, a thixotropic agent, an antisettling agent, etc. are used. be able to. Specifically, polyethylene glycol ester compounds, polyethylene glycol ether compounds, polyoxyethylene sorbitan ester compounds, sorbitan alkyl ester compounds, aliphatic polycarboxylic acid compounds, phosphoric acid ester compounds, amide amine salts of polyester acids, polyethylene oxide compounds. , Fatty acid amide wax and the like can be used. However, in the present invention, inorganic carbonate and silica are not included as such additives.
樹脂としては公知のものが使用可能であり、エチルセルロース、ニトロセルロース、ポリビニールブチラール、フェノール樹脂、メラニン樹脂、ユリア樹脂、キシレン樹脂、アルキッド樹脂、不飽和ポリエステル樹脂、アクリル樹脂、ポリイミド樹脂、フラン樹脂、ウレタン樹脂、イソシアネート化合物、シアネート化合物等の熱硬化樹脂、ポリエチレン、ポリプロピレン、ポリスチレン、ABS樹脂、ポリメタクリル酸メチル、ポリ塩化ビニル、ポリ塩化ビニリデン、ポリ酢酸ビニル、ポリビニルアルコール、ポリアセタール、ポリカーボネート、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリフェニレンオキサイド、ポリスルフォン、ポリイミド、ポリエーテルスルフォン、ポリアリレート、ポリエーテルエーテルケトン、ポリ4フッ化エチレン、及びシリコン樹脂からなる群より選択される1種以上を用いることができる。本発明のペースト組成物に含められる有機ビヒクルとして、溶剤に溶解させないで樹脂を用いてもよい。
Known resins can be used as the resin, ethyl cellulose, nitrocellulose, polyvinyl butyral, phenol resin, melanin resin, urea resin, xylene resin, alkyd resin, unsaturated polyester resin, acrylic resin, polyimide resin, furan resin, Thermosetting resin such as urethane resin, isocyanate compound, cyanate compound, polyethylene, polypropylene, polystyrene, ABS resin, polymethylmethacrylate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polyvinyl alcohol, polyacetal, polycarbonate, polyethylene terephthalate, One or more selected from the group consisting of polybutylene terephthalate, polyphenylene oxide, polysulfone, polyimide, polyether sulfone, polyarylate, polyether ether ketone, polytetrafluoroethylene, and silicone resin can be used. As the organic vehicle included in the paste composition of the present invention, a resin may be used without being dissolved in a solvent.
本発明のペースト組成物中に含まれる有機ビヒクルの含有比率は、特に限定されないが、後述するアルミニウム粉末100質量部に対して、30質量部以上60質量部以下であることが好ましい。有機ビヒクルの含有比率がかかる数値範囲内であることにより、ペースト組成物をパッシベーション膜に塗布する際の良好な付着性を得ることができる。
The content ratio of the organic vehicle contained in the paste composition of the present invention is not particularly limited, but is preferably 30 parts by mass or more and 60 parts by mass or less with respect to 100 parts by mass of aluminum powder described later. When the content ratio of the organic vehicle is within such a numerical range, good adhesiveness can be obtained when the paste composition is applied to the passivation film.
(アルミニウム粉末)
アルミニウム粉末を構成するアルミニウム粒子の形状は、特に限定されず、例えば、球状、楕円状、不定形状、鱗片状及び繊維状のいずれでもよい。中でも、球状の形状を有していれば、形成される電極におけるアルミニウムの充填性が向上し、電極の電気抵抗を低くすることが可能であり、その結果、太陽電池の変換効率を向上させることができる。 (Aluminum powder)
The shape of the aluminum particles constituting the aluminum powder is not particularly limited, and may be, for example, spherical, elliptical, amorphous, scale-like, or fibrous. Among them, if it has a spherical shape, the filling property of aluminum in the formed electrode can be improved, and the electric resistance of the electrode can be lowered, and as a result, the conversion efficiency of the solar cell can be improved. You can
アルミニウム粉末を構成するアルミニウム粒子の形状は、特に限定されず、例えば、球状、楕円状、不定形状、鱗片状及び繊維状のいずれでもよい。中でも、球状の形状を有していれば、形成される電極におけるアルミニウムの充填性が向上し、電極の電気抵抗を低くすることが可能であり、その結果、太陽電池の変換効率を向上させることができる。 (Aluminum powder)
The shape of the aluminum particles constituting the aluminum powder is not particularly limited, and may be, for example, spherical, elliptical, amorphous, scale-like, or fibrous. Among them, if it has a spherical shape, the filling property of aluminum in the formed electrode can be improved, and the electric resistance of the electrode can be lowered, and as a result, the conversion efficiency of the solar cell can be improved. You can
アルミニウム粉末を構成するアルミニウム粒子の平均粒子径は、アルミニウム粉末同士が凝集することを防止し、ペースト組成物中におけるアルミニウム粉末の分散性を良好なものとするために、レーザー回折法により測定される平均粒子径が0.1μm以上とすることが好ましく、1μm以上とすることがより好ましい。一方、スクリーン印刷時のマスク目詰まりのリスクを低減するために、レーザー回折法により測定されるアルミニウム粉末粒子の平均粒子径は、20μm以下とすることが好ましく、15μm以下とすることがより好ましい。
The average particle size of the aluminum particles constituting the aluminum powder is measured by a laser diffraction method in order to prevent the aluminum powders from aggregating with each other and to improve the dispersibility of the aluminum powder in the paste composition. The average particle diameter is preferably 0.1 μm or more, more preferably 1 μm or more. On the other hand, in order to reduce the risk of mask clogging during screen printing, the average particle diameter of the aluminum powder particles measured by the laser diffraction method is preferably 20 μm or less, and more preferably 15 μm or less.
アルミニウム粉末は、アルミニウム(好ましくは、高純度のアルミニウム)のみから構成されてもよく、アルミニウム合金を含んでいてもよい。例えば、アルミニウム合金としては、アルミニウム-シリコン合金、アルミニウム-ボロン合金等を例示することができる。
The aluminum powder may be composed only of aluminum (preferably high-purity aluminum) or may contain an aluminum alloy. Examples of the aluminum alloy include aluminum-silicon alloy and aluminum-boron alloy.
ペースト組成物中に含まれるアルミニウム粉末の含有量は、ペースト組成物100質量%中に、65~75質量%であり、71~74質量%であることが好ましい。アルミニウム粉末の含有量が65質量%未満であると、変換効率が低下してしまう。一方、アルミニウム粉末の含有量が75質量%を超えると、電極を形成するためにペースト組成物を焼成した際に、太陽電池セルの反りが大きくなってしまう。
The content of the aluminum powder contained in the paste composition is 65 to 75% by mass, preferably 71 to 74% by mass based on 100% by mass of the paste composition. If the content of the aluminum powder is less than 65% by mass, the conversion efficiency will decrease. On the other hand, when the content of the aluminum powder exceeds 75% by mass, the warp of the solar battery cell becomes large when the paste composition is fired to form the electrode.
(無機炭酸塩及びシリカ)
本発明のペースト組成物は、上述の通りケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を含む一方で、前記ケイ素非含有ガラス粉末以外に、無機炭酸塩、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないことを特徴とする。 (Inorganic carbonate and silica)
While the paste composition of the present invention contains a silicon-free glass powder, an organic vehicle, and an aluminum powder as described above, in addition to the silicon-free glass powder, an inorganic carbonate, an inorganic oxide, an inorganic carbide, an inorganic nitride. It is characterized in that it does not contain any of a substance, an inorganic nitrate, an inorganic sulfate and an organic metal alkoxide.
本発明のペースト組成物は、上述の通りケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を含む一方で、前記ケイ素非含有ガラス粉末以外に、無機炭酸塩、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないことを特徴とする。 (Inorganic carbonate and silica)
While the paste composition of the present invention contains a silicon-free glass powder, an organic vehicle, and an aluminum powder as described above, in addition to the silicon-free glass powder, an inorganic carbonate, an inorganic oxide, an inorganic carbide, an inorganic nitride. It is characterized in that it does not contain any of a substance, an inorganic nitrate, an inorganic sulfate and an organic metal alkoxide.
ここでの無機炭酸塩は、公知の無機炭酸塩全般を意味する。具体的には、炭酸カルシウム、炭酸ナトリウム、炭酸マグネシウム、炭酸バリウム、炭酸アルミニウム、炭酸カリウム、炭酸スカンジウム、炭酸亜鉛、炭酸銀(I)、炭酸水素カリウム、炭酸水素カルシウム、炭酸ストロンチウム、炭酸セシウム、炭酸鉄(II)、炭酸銅(II)、炭酸ナトリウム、炭酸鉛(II)、炭酸ニッケル(II)、炭酸ベリリウム、炭酸マンガン(II)、炭酸リチウム及び炭酸ルビジウムを例示することができる。
The inorganic carbonate here means all known inorganic carbonates. Specifically, calcium carbonate, sodium carbonate, magnesium carbonate, barium carbonate, aluminum carbonate, potassium carbonate, scandium carbonate, zinc carbonate, silver (I) carbonate, potassium hydrogen carbonate, calcium hydrogen carbonate, strontium carbonate, cesium carbonate, carbonate Examples are iron (II), copper (II) carbonate, sodium carbonate, lead (II) carbonate, nickel (II) carbonate, beryllium carbonate, manganese (II) carbonate, lithium carbonate and rubidium carbonate.
ここでの無機酸化物も、公知の無機酸化物全般を意味する。具体的には、酸化ナトリウム、酸化マグネシウム、酸化アルミニウム、酸化ケイ素、酸化カリウム、酸化カルシウム、酸化スカンジウム、酸化チタン、酸化バナジウム、酸化クロム、酸化マンガン、酸化鉄、酸化コバルト、酸化ニッケル、酸化銅、酸化亜鉛、酸化ガリウム、酸化ゲルマニウム、酸化ルビジウム、酸化ストロンチウム、酸化イットリウム、酸化ジルコニウム、酸化ニオブ、酸化モリブデン、酸化ルテニウム、酸化ロジウム、酸化パラジウム、酸化銀、酸化カドミウム、酸化インジウム、酸化スズ、酸化アンチモン、酸化テルル、酸化セシウム、酸化バリウム、酸化タンタル、酸化タングステン、酸化鉛、酸化ビスマス、酸化ランタン及び酸化セリウム等の希土類酸化物を例示することができる。
The inorganic oxides here mean all known inorganic oxides. Specifically, sodium oxide, magnesium oxide, aluminum oxide, silicon oxide, potassium oxide, calcium oxide, scandium oxide, titanium oxide, vanadium oxide, chromium oxide, manganese oxide, iron oxide, cobalt oxide, nickel oxide, copper oxide, Zinc oxide, gallium oxide, germanium oxide, rubidium oxide, strontium oxide, yttrium oxide, zirconium oxide, niobium oxide, molybdenum oxide, ruthenium oxide, rhodium oxide, palladium oxide, silver oxide, cadmium oxide, indium oxide, tin oxide, antimony oxide Examples thereof include rare earth oxides such as tellurium oxide, cesium oxide, barium oxide, tantalum oxide, tungsten oxide, lead oxide, bismuth oxide, lanthanum oxide and cerium oxide.
同様に、無機炭化物も公知の無機炭化物全般を意味し、具体的には、炭化ケイ素、炭化ホウ素、炭化アルミニウムを例示することができる。
Similarly, inorganic carbide means all known inorganic carbides, and specific examples thereof include silicon carbide, boron carbide, and aluminum carbide.
無機窒化物としても公知の無機窒化物全般を意味し、具体的には、窒化アルミニウム、窒化ケイ素、窒化ガリウム及び窒化ホウ素を例示することができる。
Also known as inorganic nitrides are all known inorganic nitrides, and specific examples thereof include aluminum nitride, silicon nitride, gallium nitride, and boron nitride.
無機硝酸塩としても公知の無機硝酸塩を意味し、具体的には、硝酸ナトリウム、硝酸マグネシウム、硝酸アルミニウム、硝酸カリウム、硝酸カルシウム、硝酸スカンジウム、硝酸銅、硝酸亜鉛、硝酸ストロンチウム、硝酸セシウム、硝酸バリウム、硝酸鉛、硝酸ビスマスを例示することができる。
Also known as inorganic nitrates means inorganic nitrates, specifically, sodium nitrate, magnesium nitrate, aluminum nitrate, potassium nitrate, calcium nitrate, scandium nitrate, copper nitrate, zinc nitrate, strontium nitrate, cesium nitrate, barium nitrate, nitric acid. Lead and bismuth nitrate can be exemplified.
無機硫酸塩としても公知の無機硫酸塩全般を意味し、具体的には、硫酸アルミニウム、硫酸バリウム及び硫酸マグネシウムを例示することができる。
Also known as inorganic sulfates are all known inorganic sulfates, and specific examples thereof include aluminum sulfate, barium sulfate, and magnesium sulfate.
有機金属アルコキシドとしても公知の有機金属アルコキシド全般を意味し、具体的には、アルミニウムイソプロポキシド、アルミニウムブトキシド、アルミニウムエトキシド、バリウムエトキシド、カルシウムエトキシド、マグネシウムエトキシド、ゲルマニウムエトキシド及びチタニウムエトキシドを例示することができる。
Also known as organometallic alkoxide means all organometallic alkoxides, specifically, aluminum isopropoxide, aluminum butoxide, aluminum ethoxide, barium ethoxide, calcium ethoxide, magnesium ethoxide, germanium ethoxide and titanium ethoxy. Can be illustrated.
本発明のペースト組成物は、ケイ素非含有ガラス粉末以外には、無機炭酸塩、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないという構成を採用することにより、ペースト組成物焼成後の焼成物の反りが小さく、且つ、電気抵抗値を低くすることができる。
The paste composition of the present invention, in addition to the silicon-free glass powder, inorganic carbonate, inorganic oxides, inorganic carbides, inorganic nitrides, inorganic nitrates, inorganic sulfates and organic metal alkoxide does not contain any of the composition By adopting this, warpage of the fired product after firing the paste composition is small and the electric resistance value can be lowered.
また、本発明のペースト組成物は、常法により製造可能であり、上述したケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を混錬する等の適宜の方法で製造することが可能である。
Also, the paste composition of the present invention can be manufactured by a conventional method, and can be manufactured by an appropriate method such as kneading the above-mentioned silicon-free glass powder, organic vehicle, and aluminum powder.
以上、本発明の実施形態について説明したが、本発明はこうした例に何ら限定されるものではなく、本発明の要旨を逸脱しない範囲において種々なる形態で実施し得ることは勿論である。
Although the embodiments of the present invention have been described above, the present invention is not limited to these examples, and it is needless to say that the present invention can be implemented in various forms without departing from the scope of the present invention.
以下、実施例に基づき、本発明の実施形態をより具体的に説明するが、本発明がこれらに限定されるものではない。
Hereinafter, embodiments of the present invention will be described more specifically based on examples, but the present invention is not limited thereto.
(実施例及び比較例)
ガスアトマイズ法により生成したアルミニウム粉末、B2O3-Bi2O3-SrO-BaO-Sb2O3=40/40/10/5/5 (mol%)のガラス粉末、及びエチルセルロースをブチルジグリコールに溶解したビヒクルを、ペースト組成物100質量%中に下記表1に示される割合で配合し、既知の分散装置(ディスパー)を用いてペースト化し、ペースト組成物を得た。尚、表1に示すとおり、上記3成分以外にも、比較例5に関しては炭酸カルシウムを、比較例6に関してはシリカを加えてペースト組成物を得た。 (Examples and comparative examples)
Aluminum powder produced by gas atomization method, glass powder of B 2 O 3 —Bi 2 O 3 —SrO—BaO—Sb 2 O 3 = 40/40/10/5/5 (mol%), and ethyl cellulose with butyl diglycol The vehicle dissolved in was mixed in 100 mass% of the paste composition at a ratio shown in Table 1 below and made into a paste using a known dispersing device (disper) to obtain a paste composition. As shown in Table 1, in addition to the above three components, calcium carbonate was added for Comparative Example 5 and silica was added for Comparative Example 6 to obtain a paste composition.
ガスアトマイズ法により生成したアルミニウム粉末、B2O3-Bi2O3-SrO-BaO-Sb2O3=40/40/10/5/5 (mol%)のガラス粉末、及びエチルセルロースをブチルジグリコールに溶解したビヒクルを、ペースト組成物100質量%中に下記表1に示される割合で配合し、既知の分散装置(ディスパー)を用いてペースト化し、ペースト組成物を得た。尚、表1に示すとおり、上記3成分以外にも、比較例5に関しては炭酸カルシウムを、比較例6に関してはシリカを加えてペースト組成物を得た。 (Examples and comparative examples)
Aluminum powder produced by gas atomization method, glass powder of B 2 O 3 —Bi 2 O 3 —SrO—BaO—Sb 2 O 3 = 40/40/10/5/5 (mol%), and ethyl cellulose with butyl diglycol The vehicle dissolved in was mixed in 100 mass% of the paste composition at a ratio shown in Table 1 below and made into a paste using a known dispersing device (disper) to obtain a paste composition. As shown in Table 1, in addition to the above three components, calcium carbonate was added for Comparative Example 5 and silica was added for Comparative Example 6 to obtain a paste composition.
(太陽電池セルの作製)
得られた各実施例及び比較例のペースト組成物を使用し、評価用の太陽電池セルである焼成基板を次のように製作した。
まず、図1の(A)に示す、p型の単結晶シリコンからなる半導体基板を準備した(基板:6inch、厚み160μm、抵抗率2Ω・cm)。
続いて、図1の(B)に示すように、ガス状にしたPOCl3(オキシ塩化リン)を用いた気層熱拡散法によって0.3~1μmの厚み、及び40~200Ω/□のシート抵抗を有するようにn+層2を形成した。
次にプラズマCVD法によって、窒化ケイ素を主成分とする反射防止膜3を形成し、反対側の面には、酸化アルミニウムと窒化ケイ素をからなるパッシベーション膜4を形成した。次いで、図1の(C)に示すように、レーザー発振器として波長が1064nmのIRレーザーを用いて、幅Dが30μm、深さが1μmのコンタクト孔5をシリコン半導体基板1の表面(アルミニウムペースト印刷部分)に形成した。
次に、図1の(D)に示すように、裏面全体(コンタクト孔9が形成されている側の面)を覆うように、上記各実施例及び比較例で得られた各ペースト組成物6を、シリコン半導体基板1の表面上に、スクリーン印刷機を用いて、0.8-0.9g/pcになるように印刷した。
その後、800℃に設定した赤外ベルト炉を用いて焼成した。この焼成により、図1の(E)に示すように、電極層9を形成し、また、この焼成の際にアルミニウムがシリコン半導体基板1の内部に拡散することにより、電極層9とシリコン半導体基板1との間にAl-Siの合金層7が形成されると同時に、アルミニウム原子の拡散による不純物層としてp+層(BSF層)8が形成された。 (Production of solar cells)
Using the obtained paste compositions of Examples and Comparative Examples, a fired substrate, which is a solar cell for evaluation, was manufactured as follows.
First, a semiconductor substrate made of p-type single crystal silicon shown in FIG. 1A was prepared (substrate: 6 inches, thickness 160 μm, resistivity 2 Ω · cm).
Subsequently, as shown in FIG. 1B, a sheet having a thickness of 0.3 to 1 μm and a thickness of 40 to 200 Ω / □ by a vapor layer thermal diffusion method using a gasified POCl 3 (phosphorus oxychloride). The n + layer 2 was formed so as to have resistance.
Next, anantireflection film 3 containing silicon nitride as a main component was formed by a plasma CVD method, and a passivation film 4 made of aluminum oxide and silicon nitride was formed on the opposite surface. Then, as shown in FIG. 1C, an IR laser having a wavelength of 1064 nm is used as a laser oscillator to form a contact hole 5 having a width D of 30 μm and a depth of 1 μm on the surface of the silicon semiconductor substrate 1 (aluminum paste printing). Part).
Next, as shown in FIG. 1D, each paste composition 6 obtained in each of the above Examples and Comparative Examples covers the entire back surface (the surface on the side where the contact holes 9 are formed). Was printed on the surface of the silicon semiconductor substrate 1 using a screen printer so as to be 0.8-0.9 g / pc.
Then, it baked using the infrared belt furnace set to 800 degreeC. By this firing, as shown in FIG. 1E, the electrode layer 9 is formed, and during this firing, aluminum diffuses into the silicon semiconductor substrate 1, so that the electrode layer 9 and the silicon semiconductor substrate are diffused. The Al--Si alloy layer 7 and the Al--Si alloy layer 7 were formed at the same time, and at the same time, the p + layer (BSF layer) 8 was formed as an impurity layer by diffusion of aluminum atoms.
得られた各実施例及び比較例のペースト組成物を使用し、評価用の太陽電池セルである焼成基板を次のように製作した。
まず、図1の(A)に示す、p型の単結晶シリコンからなる半導体基板を準備した(基板:6inch、厚み160μm、抵抗率2Ω・cm)。
続いて、図1の(B)に示すように、ガス状にしたPOCl3(オキシ塩化リン)を用いた気層熱拡散法によって0.3~1μmの厚み、及び40~200Ω/□のシート抵抗を有するようにn+層2を形成した。
次にプラズマCVD法によって、窒化ケイ素を主成分とする反射防止膜3を形成し、反対側の面には、酸化アルミニウムと窒化ケイ素をからなるパッシベーション膜4を形成した。次いで、図1の(C)に示すように、レーザー発振器として波長が1064nmのIRレーザーを用いて、幅Dが30μm、深さが1μmのコンタクト孔5をシリコン半導体基板1の表面(アルミニウムペースト印刷部分)に形成した。
次に、図1の(D)に示すように、裏面全体(コンタクト孔9が形成されている側の面)を覆うように、上記各実施例及び比較例で得られた各ペースト組成物6を、シリコン半導体基板1の表面上に、スクリーン印刷機を用いて、0.8-0.9g/pcになるように印刷した。
その後、800℃に設定した赤外ベルト炉を用いて焼成した。この焼成により、図1の(E)に示すように、電極層9を形成し、また、この焼成の際にアルミニウムがシリコン半導体基板1の内部に拡散することにより、電極層9とシリコン半導体基板1との間にAl-Siの合金層7が形成されると同時に、アルミニウム原子の拡散による不純物層としてp+層(BSF層)8が形成された。 (Production of solar cells)
Using the obtained paste compositions of Examples and Comparative Examples, a fired substrate, which is a solar cell for evaluation, was manufactured as follows.
First, a semiconductor substrate made of p-type single crystal silicon shown in FIG. 1A was prepared (substrate: 6 inches, thickness 160 μm, resistivity 2 Ω · cm).
Subsequently, as shown in FIG. 1B, a sheet having a thickness of 0.3 to 1 μm and a thickness of 40 to 200 Ω / □ by a vapor layer thermal diffusion method using a gasified POCl 3 (phosphorus oxychloride). The n + layer 2 was formed so as to have resistance.
Next, an
Next, as shown in FIG. 1D, each paste composition 6 obtained in each of the above Examples and Comparative Examples covers the entire back surface (the surface on the side where the contact holes 9 are formed). Was printed on the surface of the silicon semiconductor substrate 1 using a screen printer so as to be 0.8-0.9 g / pc.
Then, it baked using the infrared belt furnace set to 800 degreeC. By this firing, as shown in FIG. 1E, the electrode layer 9 is formed, and during this firing, aluminum diffuses into the silicon semiconductor substrate 1, so that the electrode layer 9 and the silicon semiconductor substrate are diffused. The Al--Si alloy layer 7 and the Al--Si alloy layer 7 were formed at the same time, and at the same time, the p + layer (BSF layer) 8 was formed as an impurity layer by diffusion of aluminum atoms.
(電気抵抗及び反り量の評価)
シート抵抗機(ナプソン株式会社製、型番RT―70V)を用いて、得られた太陽電池セルにおける電極の抵抗を測定した。反り量の測定は、レーザー変位計を用いて実施した。
また、アルミニウム電極の主たる機能であるBSF層の性能評価として、得られたセルを、50℃に加熱した塩酸中に浸漬し、アルミニウム電極をエッチングし(図1(F)参照)、Sinton Instruments製のLifetime測定器 (WCT-120)を用いて、Implied Voc測定を実施した。 (Evaluation of electric resistance and warpage)
The resistance of the electrode in the obtained solar battery cell was measured using a sheet resistance machine (manufactured by Napson Corporation, model number RT-70V). The amount of warpage was measured using a laser displacement meter.
Also, as a performance evaluation of the BSF layer, which is the main function of the aluminum electrode, the obtained cell was immersed in hydrochloric acid heated to 50 ° C., the aluminum electrode was etched (see FIG. 1 (F)), and manufactured by Sinton Instruments. Implied Voc measurement was carried out using the Lifetime measuring instrument (WCT-120) of.
シート抵抗機(ナプソン株式会社製、型番RT―70V)を用いて、得られた太陽電池セルにおける電極の抵抗を測定した。反り量の測定は、レーザー変位計を用いて実施した。
また、アルミニウム電極の主たる機能であるBSF層の性能評価として、得られたセルを、50℃に加熱した塩酸中に浸漬し、アルミニウム電極をエッチングし(図1(F)参照)、Sinton Instruments製のLifetime測定器 (WCT-120)を用いて、Implied Voc測定を実施した。 (Evaluation of electric resistance and warpage)
The resistance of the electrode in the obtained solar battery cell was measured using a sheet resistance machine (manufactured by Napson Corporation, model number RT-70V). The amount of warpage was measured using a laser displacement meter.
Also, as a performance evaluation of the BSF layer, which is the main function of the aluminum electrode, the obtained cell was immersed in hydrochloric acid heated to 50 ° C., the aluminum electrode was etched (see FIG. 1 (F)), and manufactured by Sinton Instruments. Implied Voc measurement was carried out using the Lifetime measuring instrument (WCT-120) of.
下記表1に示される通り、各実施例のペースト組成物を使用して作製した太陽電池セルの電極は、各比較例のペースト組成物を使用したものと比較して、高いImplied Vocと十分に低い抵抗値とが得られ、且つ、反り量も2.0mm以下という低値に抑えることができた。
As shown in Table 1 below, the electrodes of the solar battery cells manufactured using the paste compositions of the respective examples have a high Implied Voc and a sufficiently high implied Voc, as compared with those using the paste compositions of the respective comparative examples. A low resistance value was obtained, and the amount of warpage could be suppressed to a low value of 2.0 mm or less.
1 シリコン半導体基板
2 n型不純物層
3 反射防止膜
4 パッシベーション膜
5 コンタクト孔
6 ペースト組成物
7 合金層
8 p+層
9 裏面電極 1 Silicon Semiconductor Substrate 2 n-type Impurity Layer 3 Antireflection Film 4 Passivation Film 5 Contact Hole 6 Paste Composition 7 Alloy Layer 8 p + Layer 9 Backside Electrode
2 n型不純物層
3 反射防止膜
4 パッシベーション膜
5 コンタクト孔
6 ペースト組成物
7 合金層
8 p+層
9 裏面電極 1 Silicon Semiconductor Substrate 2 n-
Claims (2)
- 裏面パッシベーション型太陽電池用のペースト組成物であって、
前記ペースト組成物は、ケイ素非含有ガラス粉末、有機ビヒクル、及びアルミニウム粉末を含有し、
前記ペースト組成物100質量%中における前記アルミニウム粉末の含有量は65~75質量%であり、
前記ペースト組成物は、前記ケイ素非含有ガラス粉末以外に、無機炭酸塩、無機酸化物、無機炭化物、無機窒化物、無機硝酸塩、無機硫酸塩及び有機金属アルコキシドのいずれも含有しないことを特徴とする、ペースト組成物。 A paste composition for a backside passivation solar cell,
The paste composition contains a silicon-free glass powder, an organic vehicle, and an aluminum powder,
The content of the aluminum powder in 100% by mass of the paste composition is 65 to 75% by mass,
The paste composition is characterized in that, in addition to the silicon-free glass powder, it does not contain any of inorganic carbonates, inorganic oxides, inorganic carbides, inorganic nitrides, inorganic nitrates, inorganic sulfates and organic metal alkoxides. , Paste composition. - 請求項1に記載のペースト組成物が焼成された電極を有する、裏面パッシベーション型太陽電池。 A backside passivation solar cell having an electrode obtained by firing the paste composition according to claim 1.
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JP2016213284A (en) * | 2015-05-01 | 2016-12-15 | 東洋アルミニウム株式会社 | Aluminum paste composition for PERC type solar cell |
JP2017218335A (en) * | 2016-06-03 | 2017-12-14 | 旭硝子株式会社 | Glass, conductive paste and solar battery |
JP2017222543A (en) * | 2016-06-16 | 2017-12-21 | 旭硝子株式会社 | Glass powder, conductive paste, and solar battery |
CN107673623A (en) * | 2017-08-28 | 2018-02-09 | 广州市儒兴科技开发有限公司 | A kind of two-sided PERC aluminium pastes glass dust and preparation method thereof |
JP2018074078A (en) * | 2016-11-02 | 2018-05-10 | 東洋アルミニウム株式会社 | Paste composition |
WO2018180441A1 (en) * | 2017-03-27 | 2018-10-04 | 東洋アルミニウム株式会社 | Paste composition for solar battery |
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JP2017218335A (en) * | 2016-06-03 | 2017-12-14 | 旭硝子株式会社 | Glass, conductive paste and solar battery |
JP2017222543A (en) * | 2016-06-16 | 2017-12-21 | 旭硝子株式会社 | Glass powder, conductive paste, and solar battery |
JP2018074078A (en) * | 2016-11-02 | 2018-05-10 | 東洋アルミニウム株式会社 | Paste composition |
WO2018180441A1 (en) * | 2017-03-27 | 2018-10-04 | 東洋アルミニウム株式会社 | Paste composition for solar battery |
CN107673623A (en) * | 2017-08-28 | 2018-02-09 | 广州市儒兴科技开发有限公司 | A kind of two-sided PERC aluminium pastes glass dust and preparation method thereof |
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