WO2011030797A1 - 半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 - Google Patents
半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 Download PDFInfo
- Publication number
- WO2011030797A1 WO2011030797A1 PCT/JP2010/065431 JP2010065431W WO2011030797A1 WO 2011030797 A1 WO2011030797 A1 WO 2011030797A1 JP 2010065431 W JP2010065431 W JP 2010065431W WO 2011030797 A1 WO2011030797 A1 WO 2011030797A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- semiconductor wafer
- spacer
- forming layer
- spacer forming
- outer peripheral
- Prior art date
Links
- 239000004065 semiconductor Substances 0.000 title claims abstract description 251
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 53
- 125000006850 spacer group Chemical group 0.000 claims abstract description 292
- 239000000758 substrate Substances 0.000 claims abstract description 130
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 38
- 238000011161 development Methods 0.000 claims abstract description 15
- 238000000059 patterning Methods 0.000 claims abstract description 7
- 229920005989 resin Polymers 0.000 claims description 108
- 239000011347 resin Substances 0.000 claims description 108
- 238000000034 method Methods 0.000 claims description 73
- 230000002093 peripheral effect Effects 0.000 claims description 64
- 230000008569 process Effects 0.000 claims description 56
- 238000003825 pressing Methods 0.000 claims description 49
- 239000000463 material Substances 0.000 claims description 43
- 239000003822 epoxy resin Substances 0.000 claims description 32
- 229920000647 polyepoxide Polymers 0.000 claims description 32
- 229920001187 thermosetting polymer Polymers 0.000 claims description 29
- 239000005011 phenolic resin Substances 0.000 claims description 10
- 239000003999 initiator Substances 0.000 claims description 9
- 230000001678 irradiating effect Effects 0.000 claims description 6
- 150000002989 phenols Chemical class 0.000 claims description 6
- 230000005855 radiation Effects 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 159
- 239000002585 base Substances 0.000 description 78
- 239000011342 resin composition Substances 0.000 description 27
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 21
- -1 polyethylene terephthalate Polymers 0.000 description 16
- 239000002313 adhesive film Substances 0.000 description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 14
- 229920003986 novolac Polymers 0.000 description 11
- 238000012545 processing Methods 0.000 description 11
- 239000000178 monomer Substances 0.000 description 10
- 238000002834 transmittance Methods 0.000 description 10
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 9
- 239000011256 inorganic filler Substances 0.000 description 9
- 229910003475 inorganic filler Inorganic materials 0.000 description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 239000000945 filler Substances 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 7
- 238000010586 diagram Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 238000003475 lamination Methods 0.000 description 7
- 229910000679 solder Inorganic materials 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 6
- 239000005020 polyethylene terephthalate Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 229920006241 epoxy vinyl ester resin Polymers 0.000 description 5
- 238000000227 grinding Methods 0.000 description 5
- 238000005304 joining Methods 0.000 description 5
- 238000010030 laminating Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 125000003700 epoxy group Chemical group 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 229930185605 Bisphenol Natural products 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 206010034972 Photosensitivity reaction Diseases 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 241000276425 Xiphophorus maculatus Species 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 150000002148 esters Chemical group 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 238000000016 photochemical curing Methods 0.000 description 2
- 230000036211 photosensitivity Effects 0.000 description 2
- 229920002577 polybenzoxazole Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- HHQAGBQXOWLTLL-UHFFFAOYSA-N (2-hydroxy-3-phenoxypropyl) prop-2-enoate Chemical compound C=CC(=O)OCC(O)COC1=CC=CC=C1 HHQAGBQXOWLTLL-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 description 1
- WMYINDVYGQKYMI-UHFFFAOYSA-N 2-[2,2-bis(hydroxymethyl)butoxymethyl]-2-ethylpropane-1,3-diol Chemical compound CCC(CO)(CO)COCC(CC)(CO)CO WMYINDVYGQKYMI-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- XLLXMBCBJGATSP-UHFFFAOYSA-N 2-phenylethenol Chemical compound OC=CC1=CC=CC=C1 XLLXMBCBJGATSP-UHFFFAOYSA-N 0.000 description 1
- CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical group C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical group CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 206010047571 Visual impairment Diseases 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 125000004018 acid anhydride group Chemical group 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- OJMOMXZKOWKUTA-UHFFFAOYSA-N aluminum;borate Chemical compound [Al+3].[O-]B([O-])[O-] OJMOMXZKOWKUTA-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- CSNNWDJQKGMZPO-UHFFFAOYSA-N benzoic acid;2-hydroxy-1,2-diphenylethanone Chemical compound OC(=O)C1=CC=CC=C1.C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 CSNNWDJQKGMZPO-UHFFFAOYSA-N 0.000 description 1
- SCNCICQTOSFGRB-UHFFFAOYSA-N benzoic acid;2-hydroxy-1-(2-methylphenyl)-2-phenylethanone Chemical compound OC(=O)C1=CC=CC=C1.CC1=CC=CC=C1C(=O)C(O)C1=CC=CC=C1 SCNCICQTOSFGRB-UHFFFAOYSA-N 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- 239000004842 bisphenol F epoxy resin Substances 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000004643 cyanate ester Substances 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate group Chemical group [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012765 fibrous filler Substances 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- JESXATFQYMPTNL-UHFFFAOYSA-N mono-hydroxyphenyl-ethylene Natural products OC1=CC=CC=C1C=C JESXATFQYMPTNL-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920005575 poly(amic acid) Polymers 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/16—Fillings or auxiliary members in containers or encapsulations, e.g. centering rings
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L27/00—Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate
- H01L27/14—Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components 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
- H01L27/144—Devices controlled by radiation
- H01L27/146—Imager structures
- H01L27/14601—Structural or functional details thereof
- H01L27/14618—Containers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L27/00—Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate
- H01L27/14—Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components 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
- H01L27/144—Devices controlled by radiation
- H01L27/146—Imager structures
- H01L27/14683—Processes or apparatus peculiar to the manufacture or treatment of these devices or parts thereof
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/31—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the arrangement or shape
- H01L23/3107—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the arrangement or shape the device being completely enclosed
- H01L23/3114—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the arrangement or shape the device being completely enclosed the device being a chip scale package, e.g. CSP
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/15—Details of package parts other than the semiconductor or other solid state devices to be connected
- H01L2924/151—Die mounting substrate
- H01L2924/153—Connection portion
- H01L2924/1531—Connection portion the connection portion being formed only on the surface of the substrate opposite to the die mounting surface
- H01L2924/15311—Connection portion the connection portion being formed only on the surface of the substrate opposite to the die mounting surface being a ball array, e.g. BGA
Definitions
- the present invention relates to a method for manufacturing a semiconductor wafer bonded body, a semiconductor wafer bonded body, and a semiconductor device.
- a semiconductor substrate As a semiconductor device typified by a light receiving device such as a CMOS image sensor or a CCD image sensor, a semiconductor substrate provided with a light receiving portion and a light receiving portion side with respect to the semiconductor substrate are formed so as to surround the light receiving portion. And a transparent substrate bonded to a semiconductor substrate through the spacer.
- a light receiving device such as a CMOS image sensor or a CCD image sensor
- a method for manufacturing such a semiconductor device includes a step of attaching a photosensitive adhesive film (spacer forming layer) to a semiconductor wafer provided with a plurality of light receiving portions, and a mask for the adhesive film.
- a step of dicing a joined body obtained by joining the substrate with a spacer for example, see Patent Document 1.
- the adhesive film before being stuck on a semiconductor wafer is provided on a sheet-like substrate. And this sheet-like base material is made to adsorb
- the outer diameters of the sheet-like base material and the adhesive film cut along the outer periphery of the pressing plate are each smaller than the outer diameter of the semiconductor wafer. Then, when the adhesive film is stuck on the semiconductor wafer while pressing the adhesive film through the sheet-like base material by the pressing plate, the outer peripheral edge of the adhesive film protrudes outward from the outer peripheral edge of the base material, and the protruding part is It is formed on a semiconductor wafer.
- the thickness of the part of the adhesive film that protrudes outside the outer peripheral edge of the sheet-like substrate becomes thicker than the other part (the part that has been pressed and thinned).
- the bonding of the semiconductor wafer and the transparent substrate has been performed using a transparent substrate having the same size as the semiconductor wafer or a slightly larger transparent substrate than the semiconductor wafer. Therefore, a transparent substrate will be joined ranging over the thick part and thin part of the adhesive film mentioned above. As a result, the adhesive film and the transparent substrate cannot be uniformly adhered, and there may be a partial bonding failure.
- An object of the present invention is to provide a method for manufacturing a semiconductor wafer bonded body capable of manufacturing a semiconductor wafer bonded body in which a semiconductor wafer and a transparent substrate are bonded uniformly and reliably through a spacer, and reliability.
- An object of the present invention is to provide a bonded semiconductor wafer and a semiconductor device.
- a step of preparing a spacer-forming film comprising a sheet-like support substrate and a photosensitive spacer-forming layer provided on the support substrate; Adhering the spacer forming layer to one surface of the semiconductor wafer; and Forming a spacer by exposing and developing the spacer forming layer and patterning, and removing the support substrate; and And a step of bonding a transparent substrate so as to be included inside the portion of the spacer that has been in contact with the support base material.
- the spacer forming layer is attached onto the semiconductor wafer in a state where the outer peripheral edge of the spacer forming layer is located outside the outer peripheral edge of the support base material. Said (1) The manufacturing method of the semiconductor wafer bonded body of Claim 1.
- the support base Before the step of adhering the spacer forming layer to the semiconductor wafer, the support base is adsorbed to the pressing surface of the pressing member including the pressing surface, and along the outer peripheral edge of the pressing surface.
- the transparent substrate is included inside the portion of the spacer that is in contact with the support base material in the step of bonding the transparent substrate.
- the semiconductor wafer has a chamfered portion at a corner of the outer peripheral edge, and in the step of attaching the spacer forming layer to the semiconductor wafer, the outer peripheral edge of the spacer forming layer is on or near the chamfered portion.
- the outer peripheral edge of the spacer forming layer coincides with the outer peripheral edge of the semiconductor wafer or is located outside the above (5) or The manufacturing method of the semiconductor wafer bonded body as described in (6).
- the outer peripheral edge of the spacer forming layer is located on the inner side of the outer peripheral edge of the semiconductor wafer.
- the exposure is performed by selectively irradiating the spacer forming layer with actinic radiation through the support base before the support base is removed, and the development is performed by removing the support base.
- thermosetting resin is an epoxy resin
- FIG. 1 is a cross-sectional view showing a semiconductor device according to an embodiment of the present invention.
- FIG. 2 is a longitudinal sectional view showing a semiconductor wafer bonded body according to an embodiment (first embodiment) of the present invention.
- FIG. 3 is a plan view showing the bonded semiconductor wafer shown in FIG. 4 is a process diagram showing an example of a method for manufacturing the semiconductor device shown in FIG. 1 (the semiconductor wafer bonded body shown in FIG. 2).
- FIG. 5 is a process diagram showing an example of a method for manufacturing the semiconductor device shown in FIG. 1 (the semiconductor wafer bonded body shown in FIG. 2).
- FIG. 6 is a diagram for explaining the attaching step shown in FIG.
- FIG. 7 is a view for explaining the sticking step shown in FIG. FIG.
- FIG. 8 is a longitudinal sectional view showing a semiconductor wafer bonded body according to an embodiment (second embodiment) of the present invention.
- FIG. 9 is a process diagram showing an example of a manufacturing method of the semiconductor wafer bonded body shown in FIG.
- FIG. 10 is a process diagram showing an example of a manufacturing method of the semiconductor wafer bonded body shown in FIG.
- FIG. 1 is a cross-sectional view showing a semiconductor device according to an embodiment of the present invention.
- the upper side in FIG. 1 is referred to as “upper” and the lower side is referred to as “lower”.
- a semiconductor device 100 shown in FIG. 1 is obtained by separating a semiconductor wafer bonded body 1000 of the present invention described later.
- such a semiconductor device (light receiving device) 100 is provided on a base substrate 101, a transparent substrate 102 disposed so as to face the base substrate 101, and a surface of the base substrate 101 on the transparent substrate 102 side.
- the base substrate 101 is a semiconductor substrate and is provided with a circuit (not shown) (an individual circuit included in a semiconductor wafer described later).
- the individual circuit 103 is provided over almost the entire surface.
- the individual circuit 103 including the light receiving unit has, for example, a configuration in which a light receiving element and a microlens array are stacked in this order on the base substrate 101.
- Examples of the light receiving element included in the individual circuit 103 including the light receiving unit include a charge coupled device (CCD), a complementary metal oxide semiconductor (CMOS) image sensor, and the like.
- the individual circuit 103 including the light receiving unit including such a light receiving element converts light received by the individual circuit 103 including the light receiving unit into an electric signal.
- the transparent substrate 102 is disposed so as to face one surface (upper surface) of the base substrate 101, and has substantially the same planar dimension as the planar dimension of the base substrate 101.
- Examples of the transparent substrate 102 include an acrylic resin substrate, a polyethylene terephthalate resin (PET) substrate, and a glass substrate.
- PET polyethylene terephthalate resin
- the spacer 104 is directly bonded to the individual circuit 103 including the light receiving unit and the transparent substrate 102, respectively. Thereby, the base substrate 101 and the transparent substrate 102 are bonded via the spacer 104.
- the spacer 104 has a frame shape so as to follow the outer peripheral edge portions of the individual circuit 103 including the light receiving portion and the transparent substrate 102.
- a gap portion 105 is formed between the individual circuit 103 including the light receiving portion and the transparent substrate 102.
- the spacer 104 is provided so as to surround the central portion of the individual circuit 103 including the light receiving portion. However, the spacer 104 is exposed to the portion surrounded by the spacer 104 in the individual circuit 103 including the light receiving portion, that is, the gap portion 105.
- the functioning part functions as a substantial light receiving part.
- the solder bump 106 has conductivity, and is electrically connected to the wiring provided on the base substrate 101 on the lower surface of the base substrate 101. As a result, an electrical signal converted from light by the individual circuit 103 including the light receiving portion is transmitted to the solder bump 106.
- FIG. 2 is a longitudinal sectional view showing a semiconductor wafer bonded body according to an embodiment of the present invention
- FIG. 3 is a plan view showing the semiconductor wafer bonded body shown in FIG.
- the semiconductor wafer bonded body 1000 is composed of a stacked body in which a semiconductor wafer 101 ', a spacer 104', and a transparent substrate 102 'are sequentially stacked. That is, in the semiconductor wafer bonded body 1000, the semiconductor wafer 101 'and the transparent substrate 102' are bonded via the spacer 104 '.
- the semiconductor wafer 101 ′ is a substrate that becomes the base substrate 101 of the semiconductor device 100 as described above by going through an individualization process as described later.
- the semiconductor wafer 101 ′ is provided with a plurality of individual circuits (not shown). On the one surface (upper surface) of the semiconductor wafer 101 ′, the individual circuit 103 as described above is formed corresponding to each individual circuit.
- the spacer 104 ′ is formed in a lattice shape so as to surround each individual circuit (the individual circuit 103 including the light receiving unit) on the semiconductor wafer 101 ′ when viewed in plan.
- the spacer 104 ′ forms a plurality of gaps 105 between the semiconductor wafer 101 ′ and the transparent substrate 102 ′.
- the plurality of gaps 105 are arranged corresponding to the plurality of individual circuits described above when viewed in plan.
- the spacer 104 ′ is a member that becomes the spacer 104 of the semiconductor device 100 as described above by undergoing an individualization process as described later.
- the transparent substrate 102 ' is bonded to the semiconductor wafer 101' via a spacer 104 '.
- the transparent substrate 102 ′ is a member that becomes the transparent substrate 102 of the semiconductor device 100 as described above by performing an individualization process as described later.
- a plurality of semiconductor devices 100 can be obtained by dividing such a semiconductor wafer bonded body 1000 into individual pieces as will be described later.
- FIG. 4 and FIG. 5 are process diagrams showing an example of a manufacturing method of the semiconductor device shown in FIG. 1 (semiconductor wafer assembly shown in FIG. 2), and FIGS. 6 and 7 are respectively shown in FIG. It is a figure for demonstrating the sticking process shown.
- the manufacturing method of the semiconductor device 100 includes [A] a process of manufacturing the semiconductor wafer bonded body 1000 and [B] a process of separating the semiconductor wafer bonded body 1000 into pieces.
- the manufacturing method of the semiconductor wafer bonded body 1000 includes the step of attaching the spacer forming layer 12 on the ⁇ A1 >> semiconductor wafer 101 'and the ⁇ A2 >> spacer forming layer 12 selectively. Removing the spacer 104 ′ to form, ⁇ A3 >> bonding the transparent substrate 102 'to the surface of the spacer 104' opposite to the semiconductor wafer 101 ', and ⁇ A4 >> on the lower surface of the semiconductor wafer 101'. And a predetermined process or process.
- the spacer forming film 1 has a supporting base 11 and a spacer forming layer 12 supported on the supporting base 11.
- Such a spacer-forming film 1 is cut along the outer peripheral edge of the pressing surface 301 of the pressing member 30 of a laminating apparatus (laminator apparatus) used in process A1-3 (laminating process) described later. .
- the support base material 11 ⁇ / b> A of the spacer forming film 1 ⁇ / b> A before cutting is adsorbed (held) on the pressing surface 301 of the pressing member 30.
- the spacer forming film 1 ⁇ / b> A is cut along the outer peripheral edge of the pressing surface 301 with the supporting base 11 ⁇ / b> A adsorbed to the pressing surface 301. Thereby, the film 1 for spacer formation is obtained.
- the spacer forming layer 12 can be sized to form the spacer 104 ′.
- the spacer forming layer 12A and the supporting base material 11A are cut in this way, the cutting is usually performed by applying a cutting tool or the like from the spacer forming layer 12 side. Therefore, the obtained spacer forming film 1 after cutting has a size slightly larger than the pressing surface 301. That is, the outer peripheral edges of the spacer forming layer 12 ⁇ / b> A and the support base material 11 ⁇ / b> A are positioned outside the outer peripheral edge of the pressing surface 301.
- the distance G 1 between the outer edge of the outer peripheral edge and the support base 11 of the pressing surface 301 (spacer formation layer 12) is not particularly limited, is preferably about 100 ⁇ 1000 .mu.m. Thereby, the part which is contacting the support base material 11 among the spacer formation layers 12 can be uniformly pressed with the pressing surface 301 in the sticking process mentioned later.
- the spacer forming layer 12 has the outer peripheral edge of the spacer forming layer 12 coincident with the outer peripheral edge of the semiconductor wafer 101 ′ in step A1-3 (lamination step) described later.
- the spacer forming layer 12 may have a dimension such that the outer peripheral edge of the spacer forming layer 12 is outside the outer peripheral edge of the semiconductor wafer 101 ′ in step A1-3 (lamination step) described later.
- the support substrate 11 has a sheet shape and has a function of supporting the spacer forming layer 12.
- This support base material 11 has optical transparency. Thereby, it is possible to irradiate the spacer forming layer 12 with exposure light through the support base material 11 while the support base material 11 is attached to the spacer forming layer 12 in the exposure process in the step ⁇ A2 >> described later.
- the constituent material of the support base 11 is not particularly limited as long as it has the function of supporting the spacer forming layer 12 and the light transmittance as described above.
- polyethylene terephthalate (PET), polypropylene (PP), polyethylene (PE), etc. are mentioned.
- PET polyethylene terephthalate
- PET polyethylene terephthalate
- PET is used as the constituent material of the support substrate 11 because it can make the balance between the light transmittance and the breaking strength of the support substrate 11 excellent. preferable.
- Such an average thickness of the support base 11 is preferably 5 to 100 ⁇ m, and more preferably 15 to 50 ⁇ m. Thereby, the handleability of the film for forming a spacer can be improved, and the thickness of the portion of the spacer forming layer that is in contact with the supporting substrate can be made uniform.
- the support substrate 11 cannot exhibit the function of supporting the spacer forming layer 12.
- the handleability of the spacer forming film 1 is lowered.
- the transmittance of the exposure light in the thickness direction of the support base 11 is not particularly limited, but is preferably 0.2 or more and 1 or less, and more preferably 0.4 or more and 1 or less. Thereby, in the exposure process mentioned later, exposure light can be reliably performed by irradiating exposure light to the spacer formation layer 12 via the support base material 11.
- the spacer forming layer 12 has adhesiveness to the surface of the semiconductor wafer 101 '. Thereby, the spacer forming layer 12 and the semiconductor wafer 101 ′ can be bonded (bonded).
- the spacer forming layer 12 has photocurability (photosensitivity). Accordingly, the spacer 104 ′ can be formed by patterning to have a desired shape by an exposure process and a development process in a process ⁇ A2 >> described later.
- the spacer forming layer 12 has thermosetting properties. Thereby, the spacer formation layer 12 can express adhesiveness by thermosetting even after photocuring by an exposure process in a process ⁇ A2 >> described later. Therefore, the spacer 104 ′ and the transparent substrate 102 ′ can be bonded by thermosetting in the step ⁇ A3 >> described later.
- Such a spacer forming layer 12 is not particularly limited as long as it has adhesiveness, photocurability, and thermosetting properties as described above, but an alkali-soluble resin, a thermosetting resin, and a photopolymerization initiator are used. It is preferably composed of a material (hereinafter referred to as “resin composition”).
- alkali-soluble resin examples include novolak resins such as cresol type, phenol type, bisphenol A type, bisphenol F type, catechol type, resorcinol type, pyrogallol type, phenol aralkyl resin, hydroxystyrene resin, methacrylic acid resin, and methacrylic acid ester.
- novolak resins such as cresol type, phenol type, bisphenol A type, bisphenol F type, catechol type, resorcinol type, pyrogallol type, phenol aralkyl resin, hydroxystyrene resin, methacrylic acid resin, and methacrylic acid ester.
- Acrylic resins such as resins, cyclic olefin resins containing hydroxyl groups and carboxyl groups, polyamide resins (specifically, having at least one of a polybenzoxazole structure and a polyimide structure and having hydroxyl groups in the main chain or side chain Resin having a carboxyl group, an ether group or an ester group, a resin having a polybenzoxazole precursor structure, a resin having a polyimide precursor structure, a resin having a polyamic acid ester structure, and the like. It can be used singly or in combination of two or more.
- the spacer forming layer 12 configured to include such an alkali-soluble resin has an alkali developability with less environmental load.
- alkali-soluble resins described above those having both an alkali-soluble group contributing to alkali development and a double bond are preferably used.
- alkali-soluble group examples include a hydroxyl group and a carboxyl group.
- the alkali-soluble group can contribute to alkali development and can also contribute to a thermosetting reaction.
- alkali-soluble resin can contribute to photocuring reaction by having a double bond.
- Examples of such a resin having an alkali-soluble group and a double bond include a curable resin that can be cured by both light and heat, and specifically, for example, an acryloyl group, a methacryloyl group, and a vinyl. And a thermosetting resin having a photoreactive group such as a group, and a photocurable resin having a thermoreactive group such as a phenolic hydroxyl group, an alcoholic hydroxyl group, a carboxyl group, and an acid anhydride group.
- the compatibility between the alkali-soluble resin and the thermosetting resin described later can be improved.
- the strength of the cured spacer forming layer 12, that is, the spacer 104 'can be increased.
- the photocurable resin having a thermally reactive group may further have another thermally reactive group such as an epoxy group, an amino group, or a cyanate group.
- the photocurable resin having such a structure include (meth) acryl-modified phenolic resins, (meth) acryloyl group-containing acrylic acid polymers, carboxyl group-containing (epoxy) acrylates, and the like.
- a thermoplastic resin such as a carboxyl group-containing acrylic resin may be used.
- the resins having an alkali-soluble group and a double bond as described above it is preferable to use a (meth) acryl-modified phenol resin.
- a (meth) acrylic modified phenolic resin it contains an alkali-soluble group. Therefore, when an unreacted resin is removed by a development process, instead of an organic solvent that is usually used as a developer, the load on the environment is reduced. Less alkaline solution can be applied.
- the double bond contributes to the curing reaction, and as a result, the heat resistance of the resin composition can be improved.
- the (meth) acryl-modified phenol resin is preferably used from the viewpoint that the warpage of the semiconductor wafer bonded body 1000 can be reliably reduced by using the (meth) acryl-modified phenol resin.
- the (meth) acryl-modified phenol resin for example, a (meth) acryloyl-modified bisphenol resin obtained by reacting a hydroxyl group of a bisphenol with an epoxy group of a compound having an epoxy group and a (meth) acryloyl group is used. Can be mentioned.
- examples of such a (meth) acryloyl-modified bisphenol resin include those shown in Chemical Formula 1 below.
- this (meth) acryloyl is included in the molecular chain of the (meth) acryloyl-modified epoxy resin in which (meth) acryloyl groups are introduced at both ends of the epoxy resin.
- a compound in which a dibasic acid is introduced by bonding a hydroxyl group in the molecular chain of the modified epoxy resin and one carboxyl group in the dibasic acid by an ester bond (in addition, the repetition of the epoxy resin in this compound) 1 or more units, and the number of dibasic acids introduced into the molecular chain is 1 or more).
- such a compound for example, first, by reacting an epoxy group at both ends of an epoxy resin obtained by polymerizing epichlorohydrin and a polyhydric alcohol and (meth) acrylic acid, at both ends of the epoxy resin.
- an epoxy resin obtained by polymerizing epichlorohydrin and a polyhydric alcohol and (meth) acrylic acid at both ends of the epoxy resin.
- a (meth) acryloyl-modified epoxy resin having a (meth) acryloyl group introduced By obtaining a (meth) acryloyl-modified epoxy resin having a (meth) acryloyl group introduced, and then reacting the hydroxyl group in the molecular chain of the obtained (meth) acryloyl-modified epoxy resin with an anhydride of a dibasic acid It is obtained by forming an ester bond with one carboxyl group of this dibasic acid.
- the modification rate (substitution rate) of the photoreactive group is not particularly limited, but 20% of the total reactive groups of the resin having an alkali-soluble group and a double bond. It is preferably about 80%, more preferably about 30-70%. By setting the modification amount of the photoreactive group within the above range, a resin composition having particularly excellent resolution can be provided.
- the modification rate (substitution rate) of the thermally reactive group is not particularly limited, but is 20 to 20% of the total reactive group of the resin having an alkali-soluble group and a double bond. It is preferably about 80%, more preferably about 30 to 70%.
- the weight average molecular weight of the resin is not particularly limited, but is preferably 30000 or less, more preferably about 5000 to 150,000. preferable. When the weight average molecular weight is within the above range, the film formability when the spacer forming layer 12 is formed on the support substrate 11 is particularly excellent.
- the weight average molecular weight of the alkali-soluble resin is, for example, G.P. P. C.
- the weight average molecular weight can be calculated from a calibration curve prepared in advance using a styrene standard substance. At that time, tetrahydrofuran (THF) is used as a measurement solvent, and measurement is performed at a temperature of 40 ° C.
- THF tetrahydrofuran
- the content of the alkali-soluble resin in the resin composition is not particularly limited, but is preferably about 15 to 50% by weight, and preferably about 20 to 40% by weight with respect to the entire resin composition. More preferred.
- the content of the alkali-soluble resin is about 10 to 80% by weight with respect to the resin components of the resin composition (all components except the filler). It is preferably about 15 to 70% by weight.
- the blending balance of the alkali-soluble resin and the thermosetting resin described later in the spacer forming layer 12 can be optimized. Therefore, while making the resolution and developability of the patterning of the spacer forming layer 12 excellent in the exposure process and the developing process in the step ⁇ A2 >> to be described later, the adhesiveness of the spacer forming layer 12, that is, the spacer 104 'thereafter Can be made good.
- the content of the alkali-soluble resin is less than the lower limit, there is an effect of improving the compatibility with other components (for example, a photocurable resin described later) in the resin composition using the alkali-soluble resin. May decrease.
- the content of the alkali-soluble resin exceeds the upper limit, the developability or resolution of patterning of the spacer 104 ′ formed by photolithography technology may be deteriorated.
- thermosetting resin examples include phenol novolak resins, cresol novolak resins, novolac type phenol resins such as bisphenol A novolak resin, phenol resins such as resol phenol resin, bisphenol type epoxy such as bisphenol A epoxy resin and bisphenol F epoxy resin.
- novolak epoxy resin novolak epoxy resin, cresol novolak epoxy resin, etc., novolak epoxy resin, biphenyl type epoxy resin, stilbene type epoxy resin, triphenolmethane type epoxy resin, alkyl-modified triphenolmethane type epoxy resin, triazine nucleus-containing epoxy resin, di Epoxy resins such as cyclopentadiene-modified phenolic epoxy resins, urea (urea) resins, resins having a triazine ring such as melamine resins, unsaturated polymers Examples include ester resins, bismaleimide resins, polyurethane resins, diallyl phthalate resins, silicone resins, resins having a benzoxazine ring, cyanate ester resins, epoxy-modified siloxanes, and the like. Can do.
- the spacer forming layer 12 including such a thermosetting resin exhibits adhesiveness even after being exposed to light and developed.
- the transparent substrate 102 can be thermocompression bonded to the spacer forming layer 12 (spacer 104 ′).
- thermosetting resin when a curable resin that can be cured by heat is used as the aforementioned alkali-soluble resin, a resin different from this resin is selected.
- thermosetting resins it is particularly preferable to use an epoxy resin. Thereby, the heat resistance of the spacer forming layer 12 (spacer 104 ′) after curing and the adhesion with the transparent substrate 102 can be further improved.
- the epoxy resin when used as the thermosetting resin, includes an epoxy resin that is solid at room temperature (particularly bisphenol type epoxy resin) and an epoxy resin that is liquid at room temperature (particularly a silicone-modified epoxy resin that is liquid at room temperature). It is preferable to use together. Thereby, it is possible to obtain the spacer forming layer 12 that is excellent in both flexibility and resolution while maintaining excellent heat resistance.
- the content of the thermosetting resin in the resin composition is not particularly limited, but is preferably about 10 to 40% by weight, more preferably about 15 to 35% by weight with respect to the entire resin composition. preferable. If the content of the thermosetting resin is less than the lower limit, the effect of improving the heat resistance of the spacer forming layer 12 by the thermosetting resin may be reduced. On the other hand, if the content of the thermosetting resin exceeds the upper limit, the effect of improving the toughness of the spacer forming layer 12 by the thermosetting resin may be reduced.
- thermosetting resin when used as the thermosetting resin, it is preferable that the thermosetting resin further contains a phenol novolac resin in addition to the epoxy resin.
- a phenol novolac resin By adding a phenol novolac resin to the epoxy resin, the developability of the resulting spacer forming layer 12 can be improved.
- thermosetting property of the epoxy resin is further improved, and the strength of the spacer 104 to be formed is further improved.
- Photopolymerization initiator examples include benzophenone, acetophenone, benzoin, benzoin isobutyl ether, methyl benzoin benzoate, benzoin benzoic acid, benzoin methyl ether, benzylfinyl sulfide, benzyl, dibenzyl, diacetyl and the like.
- the spacer forming layer 12 including such a photopolymerization initiator can be more efficiently patterned by photopolymerization.
- the content of the photopolymerization initiator in the resin composition is not particularly limited, but it is preferably about 0.5 to 5% by weight, and 0.8 to 3.0% by weight with respect to the entire resin composition. More preferably, it is about%. If the content of the photopolymerization initiator is less than the lower limit, the effect of initiating the photopolymerization of the spacer forming layer 12 may not be sufficiently obtained. On the other hand, when the content of the photopolymerization initiator exceeds the upper limit, the reactivity of the spacer forming layer 12 is increased, and the storage stability and resolution may be deteriorated.
- the resin composition constituting the spacer forming layer 12 preferably contains a photopolymerizable resin in addition to the above components. Thereby, the patternability of the spacer formation layer 12 obtained can be improved more.
- this photopolymerizable resin when a curable resin curable with light is used as the alkali-soluble resin described above, a resin different from this resin is selected.
- the photopolymerizable resin is not particularly limited.
- an unsaturated polyester an acrylic compound such as an acrylic monomer or oligomer having at least one acryloyl group or methacryloyl group in one molecule, or a vinyl type such as styrene.
- acrylic compound such as an acrylic monomer or oligomer having at least one acryloyl group or methacryloyl group in one molecule
- vinyl type such as styrene.
- examples thereof include compounds, and these can be used alone or in combination of two or more.
- an ultraviolet curable resin mainly composed of an acrylic compound is preferable.
- Acrylic compounds have a high curing rate when irradiated with light, and thus can pattern a resin with a relatively small amount of exposure.
- acrylic compound examples include monomers of acrylic acid ester or methacrylic acid ester, and specifically include ethylene glycol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, glycerin di (meth) acrylate.
- the spacer 104 obtained from the spacer formation layer 12 can exhibit excellent strength.
- the semiconductor device 100 including the spacer 104 is more excellent in shape retention.
- the acrylic polyfunctional monomer means a monomer of (meth) acrylic acid ester having a tri- or higher functional acryloyl group or methacryloyl group.
- acrylic polyfunctional monomers it is particularly preferable to use trifunctional (meth) acrylate or tetrafunctional (meth) acrylate. Thereby, the effect becomes more remarkable.
- an acrylic polyfunctional monomer as the photopolymerizable resin
- an acrylic polyfunctional monomer and epoxy vinyl ester resin carry out radical polymerization, the intensity
- the solubility with respect to the alkali developing solution of the part which is not exposed of the spacer formation layer 12 can be improved at the time of image development, the residue after image development can be reduced.
- Epoxy vinyl ester resins include 2-hydroxy-3-phenoxypropyl acrylate, Epolite 40E methacrylic adduct, Epolite 70P acrylic acid adduct, Epolite 200P acrylic acid adduct, Epolite 80MF acrylic acid adduct, Epolite 3002 methacrylic acid adduct.
- the content of the acrylic polyfunctional polymer in the resin composition is not particularly limited, but is about 1 to 50% by weight in the entire resin composition. It is preferably about 5% to 25% by weight.
- the photopolymerizable resin contains an epoxy vinyl ester resin in addition to the acrylic polyfunctional polymer
- the content of the epoxy vinyl ester resin is not particularly limited, but is 3 to 30 with respect to the entire resin composition. It is preferably about% by weight, more preferably about 5% to 15% by weight.
- the photopolymerizable resin as described above is preferably liquid at normal temperature.
- the curing reactivity by the light irradiation (for example, ultraviolet irradiation) of the spacer formation layer 12 can be improved more.
- work with the optical slave constituent resin and other compounding components (for example, alkali-soluble resin) in a resin composition can be made easy.
- the photopolymerizable resin that is liquid at normal temperature include, for example, an ultraviolet curable resin mainly composed of the acrylic compound described above.
- the weight average molecular weight of the photopolymerizable resin is not particularly limited, but is preferably 5,000 or less, and more preferably about 150 to 3,000. When the weight average molecular weight is within the above range, the sensitivity of the spacer forming layer 12 is particularly excellent. Furthermore, the resolution of the spacer formation layer 12 is also excellent.
- the weight average molecular weight of the photopolymerizable resin is, for example, G.P. P. C. And can be calculated using the same method as described above.
- the resin composition constituting the spacer forming layer 12 may contain an inorganic filler. Thereby, the strength of the spacer 104 formed by the spacer forming layer 12 can be further improved.
- the content of the inorganic filler in the resin composition is preferably 9% by weight or less with respect to the entire resin composition.
- the strength of the spacer 104 ′ formed by the spacer forming layer 12 can be sufficiently improved by the addition of the acrylic polyfunctional monomer. Therefore, the addition of the inorganic filler into the resin composition can be omitted.
- inorganic fillers include fibrous fillers such as alumina fibers and glass fibers, potassium titanate, wollastonite, aluminum borate, acicular magnesium hydroxide, acicular fillers such as whiskers, talc, and mica. , Sericite, glass flakes, flake graphite, platy fillers such as platy calcium carbonate, spherical fillers such as calcium carbonate, silica, fused silica, calcined clay, unfired clay, zeolite, silica gel And the like, and the like. These may be used alone or in combination. Among these, it is particularly preferable to use a porous filler.
- the average particle size of the inorganic filler is not particularly limited, but is preferably about 0.01 to 90 ⁇ m, and more preferably about 0.1 to 40 ⁇ m.
- the average particle diameter exceeds the upper limit, there is a risk that the appearance of the spacer forming layer 12 may be abnormal or the resolution may be poor. Further, if the average particle diameter is less than the lower limit value, there is a risk of poor adhesion when the spacer 104 is heated and pasted to the transparent substrate 102.
- the average particle size can be evaluated using, for example, a laser diffraction particle size distribution analyzer SALD-7000 (manufactured by Shimadzu Corporation).
- the average pore diameter of the porous filler is preferably about 0.1 to 5 nm, and more preferably about 0.3 to 1 nm.
- the resin composition constituting the spacer forming layer 12 can contain additives such as a plastic resin, a leveling agent, an antifoaming agent, and a coupling agent within the range not impairing the object of the present invention in addition to the above-described components. .
- the visible light transmittance of the spacer forming layer 12 can be made more suitable, and exposure defects in the exposure process can be more effectively prevented. can do. As a result, the semiconductor device 100 with higher reliability can be provided.
- the average thickness of the spacer forming layer 12 is not particularly limited, but is preferably 5 to 350 ⁇ m.
- the spacer 104 forms a gap portion 105 having a necessary size, and in the exposure process described later, the spacer forming layer 12 is irradiated with exposure light through the support base material 11 to perform exposure processing, and then support.
- the development processing performed by removing the base material 11 can be reliably performed.
- the gap portion 105 having a size required for the spacer 104 cannot be formed.
- the average thickness of the spacer forming layer 12 exceeds the upper limit, it is difficult to form the spacer 104 having a uniform thickness. Further, in the exposure process described later, it is difficult to reliably perform exposure processing by irradiating the spacer forming layer 12 with exposure light through the support base 11. Furthermore, when the average thickness of the spacer forming layer 12 exceeds the upper limit, it is difficult to reliably perform the development process.
- the transmittance of exposure light in the thickness direction of the spacer forming layer 12 is not particularly limited, but is preferably 0.1 or more and 0.9 or less. Thereby, in the exposure process mentioned later, exposure light can be reliably performed by irradiating exposure light to the spacer formation layer 12 via the support base material 11.
- the transmittance of exposure light in the thickness direction of the support substrate 11 and the spacer formation layer 12 is the peak wavelength of exposure light in the thickness direction of the support substrate 11 and the spacer formation layer 12. It refers to the transmittance (for example, 365 nm).
- the light transmittance in the thickness direction of the support base 11 and the spacer forming layer 12 can be measured using, for example, a transmittance measuring device (manufactured by Shimadzu Corporation, UV-160A). .
- the average thickness of the spacer forming film 1 is not particularly limited, but is preferably 5 to 350 ⁇ m. On the other hand, when the average thickness is less than 5 ⁇ m, the support base material 11 cannot exhibit the function of supporting the spacer forming layer 12 or the spacer 104 forms the gap 105 having a required size. I can't do it. On the other hand, when this average thickness exceeds 350 micrometers, the handleability of the film 1 for spacer formation falls.
- a plurality of individual circuits 103 are formed on one surface of the semiconductor wafer 101 ′. Specifically, a plurality of light receiving elements and a plurality of microlens arrays are stacked in this order on one surface of the semiconductor wafer 101 ′.
- the spacer formation layer 12 of the film 1 for spacer formation is affixed on the said one surface side of semiconductor wafer 101 '(lamination process).
- the spacer forming film 1 is received by the semiconductor wafer 101 ′ with the support base 11 being sucked and held on the pressing surface 301 of the pressing member 30 (see FIG. 6B). On the surface of the individual circuit 103 side including the portion.
- the surface opposite to the individual circuit 103 including the light receiving portion of the semiconductor wafer 101 ′ is placed on the pressing surface 401 of the pressing member 40.
- the pressing surface 301 of the pressing member 30 and the pressing surface 401 of the pressing member 40 are pressed (pressed) in the direction in which they approach. Thereby, the support base material 11 is pressed to the spacer forming layer 12 side by the pressing surface 301.
- the spacer forming layer 12 can be adhered to the semiconductor wafer 101 'while being in close contact with each other.
- the outer peripheral edge of the spacer forming layer 12 usually protrudes outside the outer peripheral edge of the support base 11, and the protruding part 121 is replaced with another part. It swells upward and becomes thicker than (the portion in contact with the support substrate 11).
- the spacer forming layer 12 is stuck so that the outer peripheral edge thereof coincides with the outer peripheral edge of the semiconductor wafer 101 ′.
- chamfering is performed on the corners of the outer peripheral edge of the semiconductor wafer 101 ′.
- a chamfered portion 1011 is provided above the outer peripheral edge of the semiconductor wafer 101 ′, and a chamfered portion 1012 is provided below the outer peripheral edge of the semiconductor wafer 101 ′.
- the spacer forming layer 12 is attached to the semiconductor wafer 101 ′ so that the outer peripheral edge of the spacer forming layer 12 coincides with (or substantially coincides with) the outer peripheral edge of the semiconductor wafer 101 ′.
- Affixing is performed with the periphery positioned on the chamfered portion (specifically, chamfered portion 1011) or in the vicinity thereof.
- chamfered portions 1011 and 1012 are formed by chamfering the upper and lower sides of the outer peripheral edge of the semiconductor wafer 101 ′.
- the shapes of the chamfered portions 1011 and 1012 are not limited to those described above, and may be various shapes formed by known chamfering. Even in that case, an effect of preventing or suppressing the protruding portion 121 as described above from rising can be obtained.
- the chamfered portions 1011 and 1012 may be formed by rounding the upper and lower sides of the outer peripheral edge of the semiconductor wafer 101 ′. Further, the upper side of the outer peripheral edge of the semiconductor wafer 101 ′ (the side on which the spacer forming layer 12 is attached) may be chamfered, and for example, the chamfered portion 1012 may be omitted.
- step ⁇ A3 (joining step) described later, the spacer 104 and the transparent substrate 102 'can be joined uniformly without forming a gap between them.
- ⁇ A2 Step of selectively removing the spacer formation layer 12 to form the spacer 104 ′ A2-1
- the spacer forming layer 12 is irradiated with exposure light (ultraviolet rays) to perform exposure processing (exposure process).
- the spacer forming layer 12 is irradiated with exposure light through a mask 20 including a light transmission portion 201 having a plan view shape corresponding to the plan view shape of the spacer 104.
- the light transmitting portion 201 has light transmittance, and the exposure light transmitted through the light transmitting portion 201 is applied to the spacer forming layer 12. Thereby, the spacer formation layer 12 is selectively exposed, and the portion irradiated with the exposure light is photocured.
- the spacer forming layer 12 is exposed to the spacer forming layer 12 with the support base 11 attached thereto, and the spacer forming layer 12 is exposed through the support base 11. Irradiate light.
- the support base 11 functions as a protective layer of the spacer forming layer 12, and it is possible to effectively prevent foreign matters such as dust from adhering to the surface of the spacer forming layer 12. Moreover, even if a foreign substance adheres on the support substrate 11, the foreign substance can be easily removed. Further, as described above, when the mask 20 is installed, the distance between the mask 20 and the spacer forming layer 12 can be further reduced without the mask 20 sticking to the spacer forming layer 12. As a result, it is possible to prevent the image formed by the exposure light applied to the spacer forming layer 12 through the mask 20 from being blurred, and to sharpen the boundary between the exposed portion and the unexposed portion. Can do. As a result, the spacer 104 ′ can be formed with excellent dimensional accuracy, and the gap portion 105 can be formed with a desired shape and size close to the design. Thereby, the reliability of the semiconductor device 100 can be improved.
- the alignment of the mask 20 with respect to the semiconductor wafer 101 ′ can be performed by aligning the alignment mark provided on the semiconductor wafer 101 ′ with the alignment mark provided on the mask 20. it can.
- the distance between the support substrate 11 and the mask 20 is preferably 0 to 100 ⁇ m, and more preferably 0 to 50 ⁇ m. Thereby, the image formed by the exposure light irradiated to the spacer formation layer 12 through the mask 20 can be made clearer, and the spacer 104 can be formed with excellent dimensional accuracy.
- the exposure process in a state where the support base 11 and the mask 20 are in contact with each other.
- the distance between the spacer formation layer 12 and the mask 20 can be stably kept constant over the whole area.
- the portion of the spacer forming layer 12 to be exposed can be uniformly exposed, and the spacer 104 ′ having excellent dimensional accuracy can be formed more efficiently.
- the distance between the spacer formation layer 12 and the mask 20 can be freely chosen by selecting the thickness of the support base material 11 suitably. Can be set accurately. Further, by reducing the thickness of the support substrate 11, the distance between the spacer formation layer 12 and the mask 20 is made smaller, and the support substrate 11 is formed by light irradiated to the spacer formation layer 12 through the mask 20. It is possible to prevent image blurring.
- the exposure of the spacer forming layer 12 can also be performed using a projection exposure apparatus in which the support base 11 and the mask 20 do not contact or a reduced projection exposure apparatus.
- the spacer forming layer 12 may be exposed after the support substrate 11 is peeled off.
- the light applied to the spacer forming layer 12 is preferably actinic rays (ultraviolet rays), and the wavelength thereof is preferably about 150 to 700 nm, and more preferably about 170 to 450 nm.
- the integrated light amount of the irradiated light is preferably about 200 to 3000 J / cm 2 , and more preferably about 300 to 2500 J / cm 2 .
- the spacer forming layer 12 may be subjected to a heat treatment at a temperature of about 40 to 80 ° C. as necessary (post-exposure heating step (PEB step)).
- PEB step post-exposure heating step
- the portion to be the spacer 104 of the spacer forming layer 12 can be more firmly bonded to the individual circuit 103 including the light receiving portion. Furthermore, the residual stress remaining in the spacer formation layer 12 can be relaxed.
- the temperature for heating the spacer forming layer 12 is preferably about 20 to 120 ° C., more preferably about 30 to 100 ° C.
- the time for heating the spacer forming layer 12 is preferably about 1 to 10 minutes, and more preferably about 2 to 7 minutes.
- the support base material 11 is removed (support base material removal process). That is, the support base material 11 is peeled from the spacer forming layer 12.
- the support base 11 is removed prior to development, thereby preventing the adhesion of foreign matters such as dust to the spacer formation layer 12 during the exposure as described above. Twelve patterning can be performed.
- the uncured portion of the spacer forming layer 12 is removed using a developer (development process). Thereby, the photocured portion of the spacer forming layer 12 remains, and the spacer 104 ′ and the gap portion 105 ′ are formed.
- an alkaline aqueous solution can be used as a developer.
- the bonding between the spacer 104 ′ and the transparent substrate 102 ′ can be performed, for example, by bonding the upper surface of the formed spacer 104 ′ and the transparent substrate 102 ′ and then thermocompression bonding.
- the pressing surface 601 is pressed (pressed) in the direction in which they approach.
- the transparent substrate 102 ′ is thermocompression bonded onto the spacer forming layer 12 (spacer 104).
- the transparent substrate 102 ′ is bonded to the portion of the spacer 104 that has been in contact with the support base 11 so as to be included inside the outer peripheral edge.
- the transparent substrate 102 ′ is bonded to the uniform thickness portion (flat surface) of the spacer 104, avoiding the convex portion (protrusion) portion 121 formed near the outer peripheral edge of the spacer 104.
- the spacer 104 and the transparent substrate 102 ′ can be bonded uniformly without forming a gap between them.
- the width of the transparent substrate 102 '(diameter) W 3 is equal to the width W 2 of the support base 11 described above.
- the transparent substrate 102 ′ is placed on the spacer 104 so that the outer peripheral edge of the portion of the spacer 104 that has been in contact with the support base 11 and the outer peripheral edge of the transparent substrate 102 ′ coincide.
- the spacer forming layer 12 is applied to the corner of the outer peripheral edge of the semiconductor wafer 101 ′ by being attached so that the outer peripheral edge of the spacer forming layer 12 matches (or substantially matches) the outer peripheral edge of the semiconductor wafer 111 ′.
- the chamfering (the chamfered portion 1011), it is possible to prevent or suppress the portion 121 that protrudes outside the outer peripheral edge of the support base material 11 from rising and becoming thicker in the vicinity of the outer peripheral edge of the spacer forming layer 12. (See FIG. 7).
- the width (diameter) W 4 of the transparent substrate 102 ′ can be made smaller than the width W 2 of the support base material 11.
- thermocompression bonding is preferably performed within a temperature range of 80 to 180 ° C. Accordingly, the spacer 104 ′ and the transparent substrate 102 ′ can be joined by thermocompression while suppressing the applied pressure during thermocompression. Therefore, the formed spacer 104 is suppressed from unintentional deformation and has excellent dimensional accuracy.
- ⁇ A4 Step of performing predetermined processing or processing on the lower surface of the semiconductor wafer 101 ′ A4-1
- the surface (lower surface) 111 opposite to the transparent substrate 102 of the semiconductor wafer 101 ′ is ground (back grinding process).
- the grinding of the surface 111 of the semiconductor wafer 101 ′ can be performed using, for example, a grinding device (grinder).
- the thickness of the semiconductor wafer 101 ′ varies depending on the electronic device to which the semiconductor device 100 is applied, but is usually set to about 100 to 600 ⁇ m and is applied to a smaller electronic device. Is set to about 50 ⁇ m.
- solder bumps 106 are formed on the surface 111 of the semiconductor wafer 101 ′.
- wiring is also formed on the surface 111 of the semiconductor wafer 101 '.
- the semiconductor wafer bonded body 1000 is separated into pieces for each individual circuit formed on the semiconductor wafer 101 ′, that is, for each gap portion 105.
- the semiconductor wafer bonded body 1000 is separated into individual pieces by first cutting incisions 21 along the lattice of the spacer 104 by a dicing saw from the semiconductor wafer 101 ′ side. It is performed by making a cut corresponding to the cut 21 with a dicing saw from the 102 'side.
- the semiconductor device 100 can be manufactured. In this way, by separating the semiconductor wafer bonded body 1000 into individual pieces and obtaining a plurality of semiconductor devices 100 in a lump, the semiconductor devices 100 can be mass-produced and productivity can be improved.
- the semiconductor device 100 thus obtained is mounted on, for example, a substrate on which wiring is patterned, and the wiring on the substrate and the wiring formed on the lower surface of the base substrate 101 are connected via the solder bumps 106. Are electrically connected.
- the semiconductor device 100 can be widely applied to electronic devices such as a mobile phone, a digital camera, a video camera, and a small camera while being mounted on a substrate as described above. (Second Embodiment) Next, a second embodiment of the present invention will be described.
- FIG. 8 is a longitudinal sectional view showing a semiconductor wafer bonded body according to an embodiment of the present invention
- FIGS. 9 and 10 are process diagrams showing an example of a method for manufacturing the semiconductor wafer bonded body shown in FIG. It is.
- the semiconductor wafer bonded body and the manufacturing method thereof according to the second embodiment will be described focusing on the differences from the above-described embodiment, and description of similar matters will be omitted.
- the same components as those in the above-described embodiment are denoted by the same reference numerals.
- the second embodiment is substantially the same as the first embodiment except that the spacer forming film, the pressing member, and the transparent substrate are different in size. ⁇ Semiconductor wafer assembly>
- the semiconductor wafer bonded body 1000C is composed of a laminated body in which a semiconductor wafer 101 ', a spacer 104C', and a transparent substrate 102C 'are sequentially laminated. That is, in the semiconductor wafer bonded body 1000C, the semiconductor wafer 101 'and the transparent substrate 102C' are bonded via the spacer 104C '.
- the spacer 104 ⁇ / b> C ′ has a lattice shape in plan view and is formed so as to surround each individual circuit (the individual circuit 103 including the light receiving unit) on the semiconductor wafer 101 ′. Further, the spacer 104 ⁇ / b> C ′ forms a plurality of gaps 105 between the semiconductor wafer 101 ′ and the transparent substrate 102 ⁇ / b> C ′. The plurality of gaps 105 are arranged corresponding to the plurality of individual circuits described above when viewed in plan.
- the spacer 104C ′ is a member that becomes the spacer 104 of the semiconductor device 100 as described above by going through an individualization process as described later.
- the transparent substrate 102C ' is bonded to the semiconductor wafer 101' via a spacer 104 '.
- the transparent substrate 102C ' is a member that becomes the transparent substrate 102 of the semiconductor device 100 as described above by going through an individualization process as described later.
- a plurality of semiconductor devices 100 can be obtained by dividing such a semiconductor wafer bonded body 1000C into individual pieces as will be described later.
- the manufacturing method of the semiconductor wafer bonded body 1000 includes a step of attaching the spacer forming layer 12C on the ⁇ C1 >> semiconductor wafer 101 'and a step of selectively removing the ⁇ C2 >> spacer forming layer 12C to form the spacer 104C'. And (C3) bonding the transparent substrate 102C ′ to the surface of the spacer 104C ′ opposite to the semiconductor wafer 101 ′, and (A4) performing predetermined processing or processing on the lower surface of the semiconductor wafer 101 ′.
- C3 bonding the transparent substrate 102C ′ to the surface of the spacer 104C ′ opposite to the semiconductor wafer 101 ′, and (A4) performing predetermined processing or processing on the lower surface of the semiconductor wafer 101 ′.
- ⁇ C1 Step of bonding spacer forming layer 12C on semiconductor wafer 101 ′ C1-1 First, as shown in FIG. 9A, a spacer forming film 1C is prepared.
- the spacer forming film 1C has a supporting base 11C and a spacer forming layer 12C supported on the supporting base 11C.
- Such a spacer forming film 1C is cut along the outer peripheral edge of the pressing surface 301C of the pressing member 30C of a laminating apparatus (laminator apparatus) used in process C1-3 (laminating process) described later. .
- the spacer forming film 1C is the same as the spacer forming film 1 described above.
- the dimension is such that the outer peripheral edge of the spacer forming layer 12C is positioned inside the outer peripheral edge of the semiconductor wafer 101 'in a process A1-3 (lamination process) described later.
- a plurality of individual circuits 103 are formed on one surface of the semiconductor wafer 101 ′. This step can be performed in the same manner as step A1-2 in the first embodiment described above.
- a spacer forming layer 12C of the spacer forming film 1C is attached to the one surface side of the semiconductor wafer 101 ′ (laminating). This step can be performed in the same manner as the step A1-3 of the first embodiment described above.
- the spacer forming layer 12C is stuck so that the outer peripheral edge thereof is located inside the outer peripheral edge of the semiconductor wafer 101 '.
- ⁇ C2 Step of selectively removing the spacer forming layer 12C to form the spacer 104 ′ C2-1
- the spacer forming layer 12C is irradiated with exposure light (ultraviolet rays) to perform exposure processing (exposure process). This step can be performed in the same manner as step A2-1 in the first embodiment described above.
- the support base material 11C is removed (support base material removal step). That is, the support base 11C is peeled from the spacer forming layer 12C. This step can be performed in the same manner as step A2-2 in the first embodiment described above.
- the uncured portion of the spacer forming layer 12C is removed using a developer (development process). As a result, the photocured portion of the spacer forming layer 12C remains, and the spacer 104C ′ and the portion 105 ′ serving as the gap are formed.
- This step can be performed in the same manner as step A2-3 in the first embodiment described above.
- ⁇ C3 The step of bonding the transparent substrate 102C 'to the surface of the spacer 104C' opposite to the semiconductor wafer 101 '.
- the upper surface of the formed spacer 104C 'and the transparent substrate 102C' are joined (joining step).
- a semiconductor wafer bonded body 1000C semiconductor wafer bonded body of the present invention in which the semiconductor wafer 101 'and the transparent substrate 102C' are bonded via the spacer 104C 'is obtained.
- This step can be performed in the same manner as the step ⁇ A3 >> of the first embodiment described above.
- ⁇ C4 Step of performing predetermined processing or processing on the lower surface of the semiconductor wafer 101 ′.
- the surface (lower surface) 111 opposite to the transparent substrate 102C of the semiconductor wafer 101 ′ is ground (back grinding process). This step can be performed in the same manner as step C4-1 in the first embodiment described above.
- solder bumps 106 are formed on the surface 111 of the semiconductor wafer 101 ′. This step can be performed in the same manner as step C4-2 in the first embodiment described above.
- the semiconductor wafer bonded body 1000C is singulated to obtain a plurality of semiconductor devices 100 (dicing step).
- This step can be performed in the same manner as the step [B] of the first embodiment described above.
- the semiconductor device 100 can be manufactured.
- one or two or more arbitrary steps may be added.
- PLB process post-lamination heating process
- the exposure is performed once has been described.
- the present invention is not limited to this.
- the exposure may be performed a plurality of times.
- each part of the semiconductor wafer bonded body and the semiconductor device of the present invention can be replaced with any configuration that exhibits the same function, and any configuration can be added.
- the method for producing a bonded semiconductor wafer according to the present invention comprises a step of preparing a spacer-forming film comprising a sheet-like support substrate and a spacer-forming layer having photosensitivity provided on the support substrate; A step of adhering the spacer forming layer to one surface side of the wafer, a step of exposing and developing the spacer forming layer to form a spacer, and removing the supporting substrate; And a step of bonding a transparent substrate to a portion of the spacer that has been in contact with the support base so as to be included inside.
- the semiconductor wafer bonded body in which the semiconductor wafer and the transparent substrate are bonded uniformly and reliably via the spacer can be manufactured.
- Such the present invention has industrial applicability.
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Electromagnetism (AREA)
- Solid State Image Pick-Up Elements (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
半導体ウエハーの一方の面側に、前記スペーサ形成層を貼着する工程と、
前記スペーサ形成層を露光・現像してパターンニングすることによりスペーサを形成するとともに、前記支持基材を除去する工程と、
前記スペーサの前記支持基材と接触していた部分に、その内側に包含されるように、透明基板を接合する工程とを有することを特徴とする半導体ウエハー接合体の製造方法。
(第1実施形態)
<半導体装置(イメージセンサ)>
まず、本発明の半導体装置を説明する。
次に、本発明の半導体ウエハー接合体を説明する。
そして、半導体ウエハー101’の一方の面(上面)上には、上記各個別回路毎に対応して、上述したような個別回路103が形成されている。
次に、本発明の半導体装置(半導体ウエハー接合体)の製造方法の好適な実施形態について説明する。なお、以下では、本発明の半導体ウエハー接合体の製造方法について、前述した半導体装置100および半導体ウエハー接合体1000を製造する場合を一例として説明する。
[A]半導体ウエハー接合体1000の製造工程
《A1》半導体ウエハー101’上にスペーサ形成層12を貼り付ける工程
A1-1
まず、図4(a)に示すように、スペーサ形成用フィルム1を用意する。
この支持基材11は、光透過性を有している。これにより、後述する工程《A2》における露光処理において、支持基材11をスペーサ形成層12に付けたまま、支持基材11を介してスペーサ形成層12に露光光を照射することができる。
(アルカリ可溶性樹脂)
アルカリ可溶性樹脂としては、例えば、クレゾール型、フェノール型、ビスフェノールA型、ビスフェノールF型、カテコール型、レゾルシノール型、ピロガロール型等のノボラック樹脂、フェノールアラルキル樹脂、ヒドロキシスチレン樹脂、メタクリル酸樹脂、メタクリル酸エステル樹脂等のアクリル系樹脂、水酸基およびカルボキシル基等を含む環状オレフィン系樹脂、ポリアミド系樹脂(具体的には、ポリベンゾオキサゾール構造およびポリイミド構造の少なくとも一方を有し、かつ主鎖または側鎖に水酸基、カルボキシル基、エーテル基またはエステル基を有する樹脂、ポリベンゾオキサゾール前駆体構造を有する樹脂、ポリイミド前駆体構造を有する樹脂、ポリアミド酸エステル構造を有する樹脂等)等が挙げられ、これらのうちの1種または2種以上を組み合わせて用いることができる。
熱硬化性樹脂としては、例えば、フェノールノボラック樹脂、クレゾールノボラック樹脂、ビスフェノールAノボラック樹脂等のノボラック型フェノール樹脂、レゾールフェノール樹脂等のフェノール樹脂、ビスフェノールAエポキシ樹脂、ビスフェノールFエポキシ樹脂等のビスフェノール型エポキシ樹脂、ノボラックエポキシ樹脂、クレゾールノボラックエポキシ樹脂等のノボラック型エポキシ樹脂、ビフェニル型エポキシ樹脂、スチルベン型エポキシ樹脂、トリフェノールメタン型エポキシ樹脂、アルキル変性トリフェノールメタン型エポキシ樹脂、トリアジン核含有エポキシ樹脂、ジシクロペンタジエン変性フェノール型エポキシ樹脂等のエポキシ樹脂、ユリア(尿素)樹脂、メラミン樹脂等のトリアジン環を有する樹脂、不飽和ポリエステル樹脂、ビスマレイミド樹脂、ポリウレタン樹脂、ジアリルフタレート樹脂、シリコーン樹脂、ベンゾオキサジン環を有する樹脂、シアネートエステル樹脂、エポキシ変性シロキサン等が挙げられ、これらのうち1種または2種以上を組み合わせて用いることができる。
光重合開始剤としては、例えば、ベンゾフェノン、アセトフェノン、ベンゾイン、ベンゾインイソブチルエーテル、ベンゾイン安息香酸メチル、ベンゾイン安息香酸、ベンゾインメチルエーテル、ベンジルフィニルサルファイド、ベンジル、ジベンジル、ジアセチル等が挙げられる。
スペーサ形成層12を構成する樹脂組成物は、上記成分の他、光重合性樹脂を含んでいるのが好ましい。これにより、得られるスペーサ形成層12のパターニング性をより向上させることができる。
なお、スペーサ形成層12を構成する樹脂組成物中には、無機充填材を含有していてもよい。これにより、スペーサ形成層12により形成されるスペーサ104の強度をより向上させることができる。
一方、図4(b)に示すように、半導体ウエハー101’の一方の面上に、複数の個別回路103を形成する。具体的には、半導体ウエハー101’の一方の面上に、複数の受光素子と複数のマイクロレンズアレイとをこの順で積層する。
次に、図4(c)に示すように、半導体ウエハー101’の前記一方の面側に、スペーサ形成用フィルム1のスペーサ形成層12を貼着する(ラミネート加工)。
本実施形態では、図7に示すように、半導体ウエハー101’の外周縁の上側および下側がそれぞれ角面取りされることにより、面取り部1011、1012が形成されている。
なお、面取り部1011、1012の形状は、それぞれ、上述したものに限定されず、公知の面取りにより形成される種々の形状であってもよい。その場合にも、前述したようなはみ出した部分121が盛り上がるのを防止または抑制する効果が得られる。例えば、面取り部1011、1012は、半導体ウエハー101’の外周縁の上側および下側がそれぞれ丸面取りされることにより形成されたものであってもよい。また、半導体ウエハー101’の外周縁の上側(スペーサ形成層12が貼着される面側)が面取りされていればよく、例えば、面取り部1012は、省略されていてもよい。
A2-1
次に、図4(d)に示すように、スペーサ形成層12に露光光(紫外線)を照射し、露光処理を行う(露光工程)。
次に、図4(e)に示すように、支持基材11を除去する(支持基材除去工程)。すなわち、支持基材11をスペーサ形成層12から剥離する。
次に、図4(f)に示すように、スペーサ形成層12の未硬化の部分を現像液を用いて除去する(現像工程)。これにより、スペーサ形成層12の光硬化した部分が残存して、スペーサ104’および空隙部105’が形成される。
次に、図5(g)に示すように、形成されたスペーサ104’の上面と透明基板102’とを接合する(接合工程)。これにより、半導体ウエハー101’と透明基板102’とがスペーサ104’を介して接合された半導体ウエハー接合体1000(本発明の半導体ウエハー接合体)が得られる。
A4-1
次に、図5(h)に示すように、半導体ウエハー101’の透明基板102とは反対側の面(下面)111を研削する(バックグラインド工程)。
次に、図5(i)に示すように、半導体ウエハー101’の面111上に、半田バンプ106を形成する。
次に、半導体ウエハー接合体1000を個片化することにより、複数の半導体装置100を得る(ダイシング工程)。
このように、半導体ウエハー接合体1000を個片化して、一括して複数の半導体装置100を得ることにより、半導体装置100を大量生産することができ、生産性の効率化を図ることができる。
(第2実施形態)
次に、本発明の第2実施形態を説明する。
である。
以下、第2実施形態の半導体ウエハー接合体およびその製造方法について、前述した実施形態との相違点を中心に説明し、同様の事項については、その説明を省略する。なお、図8~10では、前述した実施形態と同様の構成については、同一符号を付している。
第2実施形態は、スペーサ形成用フィルム、押圧部材および透明基板の大きさが異なる以外は、第1実施形態とほぼ同様である。
<半導体ウエハー接合体>
次に、本発明の半導体ウエハー接合体の製造方法について、半導体ウエハー接合体1000Cを製造する場合を一例として説明する。
C1-1
まず、図9(a)に示すように、スペーサ形成用フィルム1Cを用意する。
一方、図9(b)に示すように、半導体ウエハー101’の一方の面上に、複数の個別回路103を形成する。この工程は、前述した第1実施形態の工程A1-2と同様に行うことができる。
次に、図9(c)に示すように、半導体ウエハー101’の前記一方の面側に、スペーサ形成用フィルム1Cのスペーサ形成層12Cを貼着する(ラミネート加工)。この工程は、前述した第1実施形態の工程A1-3と同様に行うことができる。
C2-1
次に、図9(d)に示すように、スペーサ形成層12Cに露光光(紫外線)を照射し、露光処理を行う(露光工程)。この工程は、前述した第1実施形態の工程A2-1と同様に行うことができる。
次に、図9(e)に示すように、支持基材11Cを除去する(支持基材除去工程)。すなわち、支持基材11Cをスペーサ形成層12Cから剥離する。この工程は、前述した第1実施形態の工程A2-2と同様に行うことができる。
次に、図9(f)に示すように、スペーサ形成層12Cの未硬化の部分を現像液を用いて除去する(現像工程)。これにより、スペーサ形成層12Cの光硬化した部分が残存して、スペーサ104C’および空隙部となる部位105’が形成される。この工程は、前述した第1実施形態の工程A2-3と同様に行うことができる。
C4-1
次に、図10(h)に示すように、半導体ウエハー101’の透明基板102Cとは反対側の面(下面)111を研削する(バックグラインド工程)。この工程は、前述した第1実施形態の工程C4-1と同様に行うことができる。
次に、図10(i)に示すように、半導体ウエハー101’の面111上に、半田バンプ106を形成する。この工程は、前述した第1実施形態の工程C4-2と同様に行うことができる。
以上のような工程を経ることにより、半導体装置100を製造することができる。
Claims (16)
- シート状の支持基材と、該支持基材上に設けられた感光性を有するスペーサ形成層とを備えるスペーサ形成用フィルムを用意する工程と、
半導体ウエハーの一方の面側に、前記スペーサ形成層を貼着する工程と、
前記スペーサ形成層を露光・現像してパターンニングすることによりスペーサを形成するとともに、前記支持基材を除去する工程と、
前記スペーサの前記支持基材と接触していた部分に、その内側に包含されるように、透明基板を接合する工程とを有することを特徴とする半導体ウエハー接合体の製造方法。 - 前記スペーサ形成層を前記半導体ウエハーに貼着する工程では、前記スペーサ形成層の外周縁が前記支持基材の外周縁よりも外側に位置した状態で前記半導体ウエハー上に貼着される請求項1に記載の半導体ウエハー接合体の製造方法。
- 前記スペーサ形成層を前記半導体ウエハーに貼着する工程の前に、押圧面を備える押圧部材の前記押圧面に前記支持基材を吸着させた状態で、前記押圧面の外周縁に沿って前記スペーサ形成用フィルムを切断する工程を有する請求項2に記載の半導体ウエハー接合体の製造方法。
- 前記スペーサ形成層を前記半導体ウエハーに貼着する工程では、前記押圧面により前記支持基材を前記スペーサ形成層側に押圧する請求項3に記載の半導体ウエハー接合体の製造方法。
- 前記半導体ウエハーに前記スペーサ形成層を貼着する工程では、前記透明基板を接合する工程において前記透明基板が前記スペーサの前記支持基材と接触していた部分の内側に包含されるように、前記支持基材および前記スペーサ形成層が十分に大きく形成されている請求項1ないし4のいずれかに記載の半導体ウエハー接合体の製造方法。
- 前記半導体ウエハーは外周縁の角部に面取り部を有し、前記スペーサ形成層を前記半導体ウエハーに貼着する工程では、前記スペーサ形成層の外周縁が前記面取り部分上またはその近傍に位置した状態で貼着される請求項5に記載の半導体ウエハー接合体の製造方法。
- 前記スペーサ形成層を前記半導体ウエハーに貼着する工程では、前記スペーサ形成層の外周縁は、前記半導体ウエハーの外周縁と一致またはそれよりも外側に位置している請求項5または6に記載の半導体ウエハー接合体の製造方法。
- 前記スペーサ形成層を前記半導体ウエハーに貼着する工程では、前記スペーサ形成層の外周縁は、前記半導体ウエハーの外周縁よりも内側に位置している請求項1ないし4のいずれかに記載の半導体ウエハー接合体の製造方法。
- 前記透明基板を接合する工程では、前記透明基板の外周縁が前記スペーサ形成層の外周縁よりも内側に位置している請求項8に記載の半導体ウエハー接合体の製造方法。
- 前記露光は、前記支持基材の除去前に、前記支持基材を介して前記スペーサ形成層に化学線を選択的に照射することにより行い、前記現像は、前記支持基材の除去後に行う請求項1ないし9のいずれかに記載の半導体ウエハー接合体の製造方法。
- 前記支持基材の平均厚さは、5~100μmである請求項1ないし10のいずれかに記載の半導体ウエハー接合体の製造方法。
- 前記スペーサ形成層は、アルカリ可溶性樹脂と、熱硬化性樹脂と、光重合開始剤とを含む材料で構成されている請求項1ないし11のいずれかに記載の半導体ウエハー接合体の製造方法。
- 前記アルカリ可溶性樹脂は、(メタ)アクリル変性フェノール樹脂である請求項12に記載の半導体ウエハー接合体の製造方法。
- 前記熱硬化性樹脂は、エポキシ樹脂である請求項12または13に記載の半導体ウエハー接合体の製造方法。
- 請求項1ないし14のいずれかに記載の方法により製造されたことを特徴とする半導体ウエハー接合体。
- 請求項15に記載の半導体ウエハー接合体を個片化することにより得られることを特徴とする半導体装置。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/394,993 US20120187553A1 (en) | 2009-09-09 | 2010-09-08 | Method of manufacturing semiconductor wafer bonding product, semiconductor wafer bonding product and semiconductor device |
CN2010800404039A CN102696102A (zh) | 2009-09-09 | 2010-09-08 | 半导体晶片接合体的制造方法、半导体晶片接合体和半导体装置 |
JP2011530857A JPWO2011030797A1 (ja) | 2009-09-09 | 2010-09-08 | 半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009208705 | 2009-09-09 | ||
JP2009-208705 | 2009-09-09 | ||
JP2009215055 | 2009-09-16 | ||
JP2009-215055 | 2009-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011030797A1 true WO2011030797A1 (ja) | 2011-03-17 |
Family
ID=43732466
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2010/065431 WO2011030797A1 (ja) | 2009-09-09 | 2010-09-08 | 半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20120187553A1 (ja) |
JP (1) | JPWO2011030797A1 (ja) |
CN (1) | CN102696102A (ja) |
TW (1) | TW201118962A (ja) |
WO (1) | WO2011030797A1 (ja) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006040986A1 (ja) * | 2004-10-13 | 2006-04-20 | Sumitomo Bakelite Co., Ltd. | 受光装置 |
WO2008146936A1 (ja) * | 2007-05-30 | 2008-12-04 | Sumitomo Bakelite Co., Ltd. | 感光性接着剤樹脂組成物、接着フィルムおよび受光装置 |
WO2008155896A1 (ja) * | 2007-06-19 | 2008-12-24 | Sumitomo Bakelite Co., Ltd. | 電子装置の製造方法 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3801601B2 (ja) * | 2004-06-15 | 2006-07-26 | シャープ株式会社 | 蓋部を備えた半導体ウェハの製造方法及び半導体装置の製造方法 |
JP4310266B2 (ja) * | 2004-12-06 | 2009-08-05 | パナソニック株式会社 | 感光性硬化樹脂の塗布方法および接着方法 |
US7378724B2 (en) * | 2005-03-24 | 2008-05-27 | Taiwan Semiconductor Manufacturing Company, Ltd. | Cavity structure for semiconductor structures |
US8093092B2 (en) * | 2007-06-08 | 2012-01-10 | Flextronics Ap, Llc | Techniques for glass attachment in an image sensor package |
EP2400541A4 (en) * | 2009-02-23 | 2013-03-27 | Sumitomo Bakelite Co | SEMICONDUCTOR WAFER ASSEMBLY, METHOD FOR PRODUCING SEMICONDUCTOR WAFER ASSEMBLY, AND SEMICONDUCTOR DEVICE |
KR20110130462A (ko) * | 2009-03-12 | 2011-12-05 | 스미또모 베이크라이트 가부시키가이샤 | 스페이서 형성용 필름, 반도체 웨이퍼 및 반도체 장치 |
US8647463B2 (en) * | 2009-06-30 | 2014-02-11 | Dic Corporation | Method for forming transparent conductive layer pattern |
US20120168970A1 (en) * | 2009-09-16 | 2012-07-05 | Toshihiro Sato | Spacer formation film, method of manufacturing semiconductor wafer bonding product, semiconductor wafer bonding product and semiconductor device |
-
2010
- 2010-09-08 WO PCT/JP2010/065431 patent/WO2011030797A1/ja active Application Filing
- 2010-09-08 US US13/394,993 patent/US20120187553A1/en not_active Abandoned
- 2010-09-08 CN CN2010800404039A patent/CN102696102A/zh active Pending
- 2010-09-08 JP JP2011530857A patent/JPWO2011030797A1/ja not_active Withdrawn
- 2010-09-09 TW TW099130560A patent/TW201118962A/zh unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006040986A1 (ja) * | 2004-10-13 | 2006-04-20 | Sumitomo Bakelite Co., Ltd. | 受光装置 |
WO2008146936A1 (ja) * | 2007-05-30 | 2008-12-04 | Sumitomo Bakelite Co., Ltd. | 感光性接着剤樹脂組成物、接着フィルムおよび受光装置 |
WO2008155896A1 (ja) * | 2007-06-19 | 2008-12-24 | Sumitomo Bakelite Co., Ltd. | 電子装置の製造方法 |
Also Published As
Publication number | Publication date |
---|---|
TW201118962A (en) | 2011-06-01 |
JPWO2011030797A1 (ja) | 2013-02-07 |
US20120187553A1 (en) | 2012-07-26 |
CN102696102A (zh) | 2012-09-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20100164126A1 (en) | Resin composition, resin spacer film, and semiconductor device | |
WO2010113759A1 (ja) | 樹脂スペーサー用フィルム、受光装置及びその製造方法、並びにmemsデバイス及びその製造方法 | |
WO2011046181A1 (ja) | 樹脂組成物、半導体ウエハー接合体および半導体装置 | |
JP5338663B2 (ja) | 電子装置の製造方法 | |
WO2010095593A1 (ja) | 半導体ウエハー接合体、半導体ウエハー接合体の製造方法および半導体装置 | |
WO2009116258A1 (ja) | 感光性樹脂組成物、感光性樹脂スペーサ用フィルムおよび半導体装置 | |
WO2011034025A1 (ja) | スペーサ形成用フィルム、半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 | |
WO2010095592A1 (ja) | 半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 | |
KR20110015444A (ko) | 수광장치, 수광장치의 제조방법 | |
JP2011084658A (ja) | 樹脂組成物、半導体ウエハー接合体および半導体装置 | |
WO2011030797A1 (ja) | 半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 | |
JP2010008639A (ja) | 感光性樹脂組成物、接着フィルムおよび受光装置 | |
WO2011118600A1 (ja) | 半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 | |
JP2011066167A (ja) | スペーサ形成用フィルム、半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 | |
JP2010192628A (ja) | 半導体ウエハー接合体、半導体装置の製造方法および半導体装置 | |
JP2011066166A (ja) | スペーサ形成用フィルム、半導体ウエハー接合体の製造方法、半導体ウエハー接合体および半導体装置 | |
WO2010103903A1 (ja) | スペーサ形成用フィルム、半導体ウエハーおよび半導体装置 | |
JP2011086779A (ja) | 樹脂組成物、半導体ウエハー接合体および半導体装置 | |
KR20100027223A (ko) | 전자 장치의 제조 방법 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10815392 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011530857 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13394993 Country of ref document: US |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 10815392 Country of ref document: EP Kind code of ref document: A1 |