WO2015088282A1 - 다이싱 필름 점착층 형성용 조성물 및 다이싱 필름 - Google Patents
다이싱 필름 점착층 형성용 조성물 및 다이싱 필름 Download PDFInfo
- Publication number
- WO2015088282A1 WO2015088282A1 PCT/KR2014/012283 KR2014012283W WO2015088282A1 WO 2015088282 A1 WO2015088282 A1 WO 2015088282A1 KR 2014012283 W KR2014012283 W KR 2014012283W WO 2015088282 A1 WO2015088282 A1 WO 2015088282A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- adhesive layer
- dicing
- composition
- film
- Prior art date
Links
- 239000012790 adhesive layer Substances 0.000 title claims abstract description 57
- 239000000203 mixture Substances 0.000 title claims abstract description 55
- 239000000853 adhesive Substances 0.000 claims abstract description 76
- 230000001070 adhesive effect Effects 0.000 claims abstract description 76
- 150000001875 compounds Chemical class 0.000 claims abstract description 57
- 239000011230 binding agent Substances 0.000 claims abstract description 49
- 239000004065 semiconductor Substances 0.000 claims abstract description 43
- 125000000524 functional group Chemical group 0.000 claims abstract description 42
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 40
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 47
- -1 polydimethylsiloxane Polymers 0.000 claims description 28
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 239000004593 Epoxy Substances 0.000 claims description 17
- 239000012948 isocyanate Substances 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 15
- 239000002952 polymeric resin Substances 0.000 claims description 15
- 229920003002 synthetic resin Polymers 0.000 claims description 15
- 125000003277 amino group Chemical group 0.000 claims description 13
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 11
- 229920001577 copolymer Polymers 0.000 claims description 8
- 239000003960 organic solvent Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 239000004925 Acrylic resin Substances 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 claims description 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 5
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 4
- 230000001678 irradiating effect Effects 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 244000028419 Styrax benzoin Species 0.000 claims description 3
- 235000000126 Styrax benzoin Nutrition 0.000 claims description 3
- 235000008411 Sumatra benzointree Nutrition 0.000 claims description 3
- 150000008062 acetophenones Chemical class 0.000 claims description 3
- 150000005215 alkyl ethers Chemical class 0.000 claims description 3
- 150000004056 anthraquinones Chemical class 0.000 claims description 3
- 229960002130 benzoin Drugs 0.000 claims description 3
- 239000012965 benzophenone Substances 0.000 claims description 3
- 150000008366 benzophenones Chemical class 0.000 claims description 3
- 239000013522 chelant Substances 0.000 claims description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 3
- 235000019382 gum benzoic Nutrition 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000003700 epoxy group Chemical group 0.000 claims description 2
- 238000007781 pre-processing Methods 0.000 claims description 2
- 235000012431 wafers Nutrition 0.000 claims 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- HEQOJEGTZCTHCF-UHFFFAOYSA-N 2-amino-1-phenylethanone Chemical class NCC(=O)C1=CC=CC=C1 HEQOJEGTZCTHCF-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 45
- 229940048053 acrylate Drugs 0.000 description 36
- 229920005989 resin Polymers 0.000 description 29
- 239000011347 resin Substances 0.000 description 29
- 238000001723 curing Methods 0.000 description 28
- 239000003822 epoxy resin Substances 0.000 description 28
- 229920000647 polyepoxide Polymers 0.000 description 28
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 24
- 239000010410 layer Substances 0.000 description 19
- 150000002513 isocyanates Chemical class 0.000 description 14
- 239000000178 monomer Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 10
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 10
- 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 8
- 229920000098 polyolefin Polymers 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- 239000011254 layer-forming composition Substances 0.000 description 6
- 239000000523 sample Substances 0.000 description 6
- 238000003848 UV Light-Curing Methods 0.000 description 5
- 238000005520 cutting process Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002313 adhesive film Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- 230000001588 bifunctional effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- CQOZJDNCADWEKH-UHFFFAOYSA-N 2-[3,3-bis(2-hydroxyphenyl)propyl]phenol Chemical compound OC1=CC=CC=C1CCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O CQOZJDNCADWEKH-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 150000001298 alcohols Chemical group 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 239000004843 novolac epoxy resin Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- NFPLJTNXOKFJRO-UHFFFAOYSA-N 1-ethenylpyridin-2-one Chemical compound C=CN1C=CC=CC1=O NFPLJTNXOKFJRO-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- 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 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920012753 Ethylene Ionomers Polymers 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- 239000004842 bisphenol F epoxy resin Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 description 1
- 229920005680 ethylene-methyl methacrylate copolymer Polymers 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 125000004356 hydroxy functional group Polymers O* 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012858 packaging process Methods 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/08—Macromolecular additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/683—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere for supporting or gripping
- H01L21/6835—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support
- H01L21/6836—Wafer tapes, e.g. grinding or dicing support tapes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/326—Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2483/00—Presence of polysiloxane
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2221/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof covered by H01L21/00
- H01L2221/67—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere
- H01L2221/683—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping
- H01L2221/68304—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support
- H01L2221/68327—Apparatus for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support used during dicing or grinding
Definitions
- Dicing film adhesive layer forming composition and dicing film
- the present invention relates to a composition for forming a dichroic film adhesion layer and a dicing film.
- the manufacturing process of the semiconductor chip includes a process of forming a fine pattern on the wafer and a process of polishing and packaging the wafer to meet the specifications of the final device.
- the packaging process includes a wafer inspection process for inspecting a defect of a semiconductor chip; Dicing process which cuts a wafer and isolates into individual chips; Separated chips .
- the wafer is cut to a predetermined thickness using a diamond wheel or the like.
- the dicing film is laminated on the wafer back side under appropriate conditions, and then the process is performed.
- a die bonding film adheresive film
- the dicing process includes cutting a semiconductor wafer with a dicing blade, and irradiating ultraviolet rays to the base film of the semiconductor wafer, and picking up individual chips separated by cutting the semiconductor wafer.
- the present invention is a dicing for providing a dicing die-bonding film that can prevent the sticking between the films in the dicing process to increase the pick-up success rate and exhibit a relatively high die share strength to prevent the peeling phenomenon due to the adhesive force degradation It is to provide a composition for forming a film adhesion layer.
- this invention is providing the dicing film using the composition for dicing film adhesion layer formation mentioned above.
- the present invention is to provide a dicing die-bonding film containing the dicing film.
- this invention is providing the dicing method of the semiconductor wafer using the said dicing film.
- the silicone compound oil containing at least one semi-active functional group Adhesive binders; And a photoinitiator; wherein the increase ratio of the silicone compound oil containing at least one semi-aung functional group to the adhesive binder is 0.01% to 4.5%, and a composition for forming a dicing film adhesive layer is provided.
- the reactive functional group may include at least one functional group selected from the group consisting of a hydroxyl group, a carbinol, an epoxy, an amino group, a thile group, and a carboxyl group.
- the silicone compound oil containing at least one semi-functional functional group may include at least one silicone compound selected from the group consisting of a silicone compound represented by Formula 1, a silicone compound represented by Formula 2, and a polyether modified hydroxy functional polydimethylsiloxane; And organic solvents.
- 3 ⁇ 4 is alkyl having 1 to 3 carbon atoms
- R 2 is a hydroxy group, alkylene alcohol having 1 to 10 carbon atoms, epoxy, amino group, thiol group or carboxyl group
- m is an integer of 0 to 500
- 3 ⁇ 4 is alkyl having 1 to 3 carbon atoms
- at least one of R 4 is alkyl having 1 to 3 carbon atoms
- the other is a hydroxy group, an alkylene alcohol having 1 to 10 carbon atoms, epoxy, amino group, or thiol group.
- a carboxyl group, or 3 ⁇ 4 and 3 ⁇ 4 are each a hydroxy group, an alkylene alcohol having 1 to 10 carbon atoms, an epoxy, an amino group, a thiol group or a carboxyl group
- p is an integer of 0 to 500.
- the organic solvent is alcohols, ethers, acetates or ketones.
- Silicone compound oil containing one or more reactive functional groups may have a viscosity of 10 iniiiVs to 20, 000 ⁇ 2 / s at 25 ° C.
- the adhesive binder is a hydroxyl group, an isocyanate group, a vinyl group and
- One or more functional groups selected from the group consisting of (meth) acrylate groups may include a (meth) acrylate polymer or a (meth) acrylate copolymer having one or more substituted or unsubstituted groups.
- the adhesive binder may include an intrinsic adhesive binder in which an acrylate having a carbon-carbon double bond is added to the main chain of the (meth) acrylate resin.
- an intrinsic adhesive binder in which an acrylate having a carbon-carbon double bond is added to the main chain of the (meth) acrylate resin.
- a polymer resin in which 1 w t% to 45 wt% of a (meth) acrylate functional group is added to the main chain of the (meth) acrylate base resin as a side chain may be used as the internal adhesive binder.
- the adhesive binder may include a polymer resin having a weight average molecular weight of 100, 000 to 1, 500, 000.
- the photoinitiator is a group consisting of benzoin and its alkyl ethers, acetophenones, anthraquinones, thioxanthones, ketals, benzophenones, a-aminoacetophenones, acylphosphine oxides, and oxime esters. It may include one or more selected from.
- the composition for forming a dicing film adhesive layer may further include a curing agent.
- the curing agent may include one or more selected from the group consisting of an isocyanate compound, an aziridine compound, an epoxy compound, and a metal chelate compound.
- the dicing film adhesive layer-forming composition may include 0.01 to 30 parts by weight of the curing agent relative to 100 parts by weight of the adhesive binder.
- a base film and an adhesive layer formed on at least one surface of the base film, wherein the adhesive layer comprises a dicing film adhesive layer-forming composition of claim 1, a dicing film may be provided have.
- the thickness of the base film is from 10 to 200, the thickness of the adhesive layer is 0.5 ⁇ to 50 im.
- the dicing film; And an adhesive layer formed on at least one surface of the dicing film, a dicing die bonding film may be provided.
- Dicing film adhesive layer for providing a dicing die-bonding film that can prevent the sticking between the films in the dicing process to increase the pick-up success rate and exhibit a relatively high die share strength to prevent the peeling phenomenon due to the decrease in adhesion Dicing comprising a composition for forming and a pressure-sensitive adhesive layer comprising the composition
- a dicing method of a semiconductor wafer using a dicing die bonding film and an additive dicing die bonding film, comprising a film and the dicing film, is provided.
- silicone compound oil containing one or more reactive functional groups containing one or more reactive functional groups
- Adhesive binders Adhesive binders
- a photoinitiator wherein the weight ratio of the silicone compound oil including at least one reactive functional group to the pressure-sensitive adhesive binder is 0.01% to 4.5%, and a composition for forming a dicing film adhesive layer may be provided.
- the inventors of the present invention when using a dicing film containing a tackifier formed from the dicing film adhesive layer-forming composition containing a silicone compound oil containing at least one reactive functional group in a specific content, prevents sticking between the films And lowering the peel strength between the films to improve the pick-up success rate of the chips, exhibiting a relatively high die share strength to prevent the delamination due to the adhesion loss, and improve the reliability of the semiconductor manufacturing process It confirmed through experiment and completed invention.
- the silicone compound containing at least one reactive functional group contained in the silicone compound oil containing at least one reactive functional group has a releasability to an organic material or an inorganic material, and an alkyl device having a dimethyl siloxane structure acts as a nonpolar molecule to the surface of the adherend.
- an alkyl device having a dimethyl siloxane structure acts as a nonpolar molecule to the surface of the adherend.
- the dicing film adhesive layer-forming composition may provide higher release properties and slip properties to the adhesive layer (die bonding film) to facilitate peeling after UV curing.
- the weight ratio of the silicone compound oil including one or more of the semi-ungseong functional groups relative to the adhesive binder may be 0.01% to 4.5%, or 0.01% to 2%.
- the pressure-sensitive adhesive layer of the dicing film prepared from the composition for forming during dicing film adhesion of the above embodiment is subjected to peel strength, for example, 180 degree peel force and tack strength and SUS strength before and after UV irradiation.
- peel strength for example, 180 degree peel force and tack strength and SUS strength before and after UV irradiation.
- the peeling force against can be greatly increased.
- the peel strength of the adhesive layer of the dicing film prepared from the composition for forming a die-like film adhesion layer of the embodiment is to some extent although it may be lowered, the die share strength of the pressure-sensitive adhesive layer may be significantly lowered, thereby causing a peeling phenomenon due to a decrease in adhesive strength, and thus, reliability may be lowered in a semiconductor manufacturing process.
- the silicone contained in the silicone compound oil may contain or substitute one or more semi-functional functional groups, specific examples of the reactive functional group is a group consisting of hydroxy group, carbinol, epoxy, amino group, thiol group and carboxyl group One or more functional groups selected from the above can be mentioned.
- Silicone compound oil containing at least one reactive functional group includes a silicone compound and at least one organic solvent comprising at least one reactive functional group.
- the silicone compound oil containing at least one semi-functional functional group may include at least one silicone compound selected from the group consisting of a silicone compound of Formula 1, a silicone compound of Formula 2, and a polyether modified hydroxy functional polydimethylsiloxane; And an organic solvent. .
- 3 ⁇ 4 is alkyl having 1 to 3 carbon atoms, is a hydroxy group, an alkylene alcohol having 1 to 10 carbon atoms, an epoxy, an amino group, a thiol group or a carboxyl group, m is an integer of 0 to 500, n is 1 To an integer from 500.
- R 3 and R 4 are each alkyl having 1 to 3 carbon atoms, at least one of R 3 and R 4 is alkyl having 1 to 3 carbon atoms, the other is a hydroxy group, alkylene alcohol having 1 to 10 carbon atoms, epoxy, amino group, thiol Or 3 ⁇ 4 and R4 are each a hydroxy group, an alkylene alcohol having 1 to 10 carbon atoms, an epoxy, an amino group, a thiol group or a carboxyl group, and p is an integer of 0 to 500.
- polyether-modified hydroxy functional polydimethylsiloxanes examples include commercial products such as BYK s l l ean 3720, but specific examples are not limited thereto.
- organic solvent included in the silicone compound oil including one or more semi-functional functional groups are not limited.
- the organic solvent may be alcohols, ethers, acetates or ketones.
- Silicone compound oil containing one or more reactive functional groups may have a viscosity (vi scos i ty) of 10 miiiVs to 20, 000 ⁇ 7s at 25 ° C.
- the adhesive binder can be used without limitation, a polymer resin known to be used to form the adhesive layer of the dicing film, for example, of the main chain containing a polymer resin or a semi-functional group substituted with a predetermined reactive functional group A polymer resin can be used.
- the adhesive binder has at least one functional group selected from the group consisting of a hydroxyl group, an isocyanate group, a vinyl group and a (meth) acrylate group.
- It may contain a (meth) acrylate copolymer.
- the pressure-sensitive adhesive may be an internal pressure-sensitive adhesive binder in which an acrylate having a carbon-carbon double bond is added to the main chain of the (meth) acrylate resin.
- the intrinsic pressure-sensitive adhesive binder is a polymer in which 1 wt% to 45 wt% of a (meth) acrylate functional group is added to the main chain of the (meth) acrylate base resin as a side chain. Resin can be used
- the adhesive binder may include a polymer resin having an increased average molecular weight of 100, 000 to 1, 500, 000.
- At least one functional group selected from the group consisting of the hydroxyl group, the isocyanate group, the vinyl group, and the (meth) acrylate group is a (meth) acrylate-based polymer or a (meth) acrylate-based
- the copolymer may have a weight average molecular weight of 100, 000 to 1, 500, 000.
- (meth) acrylate is meant to include both acrylate [acryl ate] and (meth) acrylate [(meth) acryl ate].
- Such a (meth) acrylate polymer or a (meth) acrylate copolymer may be, for example, a polymer or copolymer of a (meth) acrylic acid ester monomer and a crosslinkable functional group-containing monomer.
- examples of the (meth) acrylic acid ester monomer include alkyl (meth) acrylate, and more specifically, monomers having an alkyl group having 1 to 12 carbon atoms, such as pentyl (meth) acrylate and n-butyl (meth).
- alkyl (meth) acrylate and more specifically, monomers having an alkyl group having 1 to 12 carbon atoms, such as pentyl (meth) acrylate and n-butyl (meth).
- Acrylate ethyl (meth) acrylate, methyl (meth) acrylate, nuclear chamber (meth) acrylate, n-octyl (meth) acrylate, isobutyl (meth) acrylate, 2-ethylnuclear chamber (meth) acrylic And a mixture of one or more kinds of dodecyl (meth) acrylate or decyl (meth) acrylate. Since the higher the carbon number of the alky
- examples of the crosslinkable functional group-containing monomer include one or more kinds of hydroxy group-containing monomers, carboxyl group-containing monomers, or nitrogen-containing monomers.
- examples of the hydroxyl group-containing compound include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, and the like.
- examples of the carboxyl group-containing compound include (meth) acrylic acid.
- examples of the nitrogen-containing monomer include (meth) acrylonitrile ⁇ N—vinyl pyridone or N-vinyl caprolactam, but are not limited thereto. remind
- the (meth) acrylate resin also contains a vinyl acetate, styrene or acrylonitrile carbon-carbon double bond-containing low molecular weight compound in view of other functionalities such as compatibility. And the like may further be included.
- the intrinsic pressure-sensitive adhesive binder to which the acrylate having a carbon-carbon double bond is added to the main chain of the (meth) acrylate resin may have a weight average molecular weight of 100, 000 to 1, 500, 000.
- the coating property or cohesion of the dicing film adhesive layer-forming composition of the embodiment may be lowered, and when peeling the adhesive layer formed from the composition of the embodiment Residual fire may remain on the adherend or the 3 ⁇ 4 bond layer may be destroyed.
- the weight average molecular weight of the polymer resin included in the adhesive binder is too high, ultraviolet curing of the composition for forming a dicing film adhesive layer of the embodiment may not sufficiently occur, whereby the adhesive layer formed from the composition has a peel force This may not be low enough so that the pick-up success rate may be lowered.
- the dicing film adhesive layer-forming composition may further comprise an ultraviolet curable compound.
- the type of the UV-curable compound is not particularly limited, and for example, a polyfunctional compound having a weight average molecular weight of about 500 to 300, 000 (ex. Polyfunctional urethane acrylate, polyfunctional acrylate monomer or oligomer, etc.) Can be used.
- a polyfunctional compound having a weight average molecular weight of about 500 to 300, 000 ex. Polyfunctional urethane acrylate, polyfunctional acrylate monomer or oligomer, etc.
- the average person skilled in the art can easily select the appropriate compound according to the intended use.
- the content of the ultraviolet curable compound may be 5 parts by weight to 400 parts by weight, preferably 10 parts by weight to 200 parts by weight, based on 100 parts by weight of the above-mentioned adhesive binder. If the content of the ultraviolet curable compound is less than 5 parts by weight, there is a risk that the lowering of the adhesive strength after curing, the pick-up property may be degraded. If the content of the ultraviolet curable compound exceeds 400 parts by weight, the cohesive strength of the adhesive before UV irradiation is insufficient, or peeling with a release film or the like There is a possibility that it may not be easily performed.
- photoinitiator included in the composition for forming a dicing film adhesive layer of the above embodiment is not limited, and conventionally known photoinitiators may be used without particular limitation O.
- photoinitiator benzoin and its alkyl ethers, acetophenones, anthraquinones, thioxanthones, ketals, benzophenones, d-aminoacetophenones, acylphosphine oxides, and oximes Esters or two kinds thereof The above mixture can be used.
- the amount of the photoinitiator may be determined in consideration of the physical properties and properties of the adhesive layer to be prepared and the type and properties of the adhesive binder used, for example, the composition for forming a dicing film adhesive layer of the embodiment is 100 weight of the adhesive binder. It may include 0.01 to 5 parts by weight of the photoinitiator relative to parts.
- the composition for forming a dicing film adhesion layer of the embodiment may further comprise a curing agent.
- the curing agent may form crosslinking by reacting at a temperature of 30 to 50 ° C. with the reaction of the adhesive binder.
- the predetermined reactor included in the curing agent may remain in an unreacted state, and further crosslinking may proceed through UV irradiation before pickup, thereby lowering the adhesive force of the adhesive layer.
- the curing agent may include one or more selected from the group consisting of an isocyanate compound, an aziridine compound, an epoxy compound, and a metal chelate compound.
- the amount of the curing agent may be determined in consideration of the physical properties and properties of the adhesive layer to be prepared and the type and characteristics of the adhesive binder used, for example, the composition for forming a dicing film adhesive layer of the embodiment is 100 weight of the adhesive binder.
- the amount of the curing agent may include 0.1 to 30 parts by weight of the curing agent.
- a base film and a pressure-sensitive adhesive layer formed on at least one surface of the base film, the pressure-sensitive adhesive layer is dicing comprising the composition for forming a dicing film pressure-sensitive adhesive layer of the above-described embodiment Films can be provided.
- the type of the base film is not particularly limited, and for example, a plastic film or a metal foil known in the art may be used.
- the base film may be low density polyethylene, linear polyethylene, medium density polyethylene, high density polyethylene, ultra low density polyethylene, random copolymer of polypropylene, block copolymer of polypropylene, homopolypropylene, polymethylpentene, Ethylene-vinyl acetate co-polymer, ethylene-methacrylic acid copolymer, ethylene-methyl methacrylate copolymer, ethylene-ionomer copolymer ⁇ ethylene-vinyl alcohol copolymer, polybutene, copolymer of styrene or 2 or more types of these combinations are mentioned.
- the meaning of the base film including a mixture of two or more polymers in the above means that a film having a structure in which two or more layers of films including each of the aforementioned polymers are laminated or a single layer containing two or more of the aforementioned polymers includes both films. do.
- the thickness of the base film is not particularly limited, and is usually formed in a thickness of 10 to 200 m, preferably 50 to 180. If the thickness is less than 10, and there is a possibility to be the control of the cutting depth (cu t depth) unstable in the binary process, when it is more than 200, or the large amount of the burr (burr) generated in the dicing step, the elongation is off IX There is a fear that the holding process may not be accurate.
- the base film may be subjected to conventional physical or chemical treatments such as matt treatment, corona discharge treatment, primer treatment or crosslinking treatment, as necessary.
- the adhesive layer may have a thickness of 0.5 to 50, or 5 m to 30.
- Information on the dicing film, adhesive layer, forming composition contained in the pressure-sensitive adhesive layer includes all of the above-described information with respect to the one embodiment.
- the dicing film according to another embodiment of the invention, the dicing film; And a bonding layer formed on at least one surface of the dicing film.
- the adhesive layer may include an epoxy resin, a low elastic high molecular weight resin, and a curing agent for an adhesive layer.
- the epoxy resin may include a general adhesive epoxy resin known in the art, for example, an epoxy resin containing two or more epoxy groups in the molecule, the weight average molecular weight of 100 to 5,000.
- the epoxy resin may form a hard crosslinked structure through a curing process, and may exhibit excellent adhesion, heat resistance, and mechanical strength.
- the epoxy resin it is particularly preferable to use an epoxy resin having an average epoxy equivalent of 100 to 1,000.
- the epoxy equivalent of the said epoxy resin is less than 100, a crosslinking density will become high too much, and an adhesive film will There exists a possibility of exhibiting a hard property as a whole, and when the epoxy equivalent of the said epoxy resin exceeds 1,000, there exists a possibility that heat resistance may fall.
- Bifunctional epoxy resin such as a bisphenol A epoxy resin or a bisphenol F epoxy resin; Or cresol novolac epoxy resins; phenol novolac epoxy resins, tetrafunctional epoxy resins, biphenyl epoxy resins, triphenol methane epoxy resins, alkyl modified triphenol methane epoxy resins, naphthalene epoxy resins, dicyclopentadiene
- polyfunctional epoxy resins having three or more functional groups such as a type epoxy resin or a dicyclopentadiene modified phenol type epoxy resin, are not limited thereto.
- Said "polyfunctional epoxy resin” means the epoxy resin which has 3 or more functional groups. That is, in general, bifunctional epoxy resins have excellent flexibility and flowability in silver, but heat resistance and curing rate are poor, whereas polyfunctional epoxy resins having three or more functional groups have a high curing rate and excellent crosslink density. Heat resistance, but flexibility and flowability is poor. Therefore, by appropriately using the above two kinds of resins, the elastic modulus and the t ack characteristics of the adhesive layer can be controlled while suppressing chip scattering and burr generation during the dicing process.
- the low elastic high molecular weight resin may serve to impart a soft segment in the adhesive to impart stress relaxation characteristics at high temperature.
- the high molecular weight resin it may be blended with the epoxy resin to cause viscoelasticity after formation of a crosslinked structure without causing breakage during film formation, and any resin component may be used as long as it has excellent compatibility with other components and storage stability. Can be.
- the specific kind of the low elastic high molecular weight resin is not particularly limited as long as it satisfies the above-described characteristics, for example, polyimide, polyetherimide, polyesterimide, polyamide, polyether sulfone, polyether ketone, polyolefin , Polyvinyl chloride , phenoxy , reactive acrylonitrile butadiene rubber or
- (meth) acrylate resin One kind or a mixture of two or more kinds such as (meth) acrylate resin can be used.
- Specific examples of the (meth) acrylate resins include (meth) acrylic acid and And acrylic copolymers containing the derivatives thereof.
- Examples of (meth) acrylic acid and derivatives thereof include (meth) acrylic acid; Methyl (meth) acrylate or ethyl
- Alkyl (meth) acrylate containing a C1-C12 alkyl group such as (meth) acrylate; (Meth) acrylonitrile or (meth) acrylamide; And other copolymerizable monomers.
- the (meth) acrylate resin may also include one or more functional groups such as glycidyl group, hydroxy group, carboxyl group and amine group, and such functional group may be glycidyl (meth) acrylate) hydroxy ( It can introduce
- the curing agent that can be included in the adhesive composition is not particularly limited as long as it can react with the epoxy resin and / or the low elastic high molecular weight resin to form a crosslinked structure.
- a curing agent capable of reacting with the two components simultaneously to form a crosslinked structure may be used.
- Such a curing agent forms a crosslinked structure with the soft and hard segments in the adhesive, respectively, to improve heat resistance, and at the same time, the interface between the two components. It can act as a cross-linking agent of two segments in to improve the reliability of the semiconductor package.
- the thickness of the adhesive layer is not particularly limited, but may be, for example, in the range of 1 / im to 100 im or 3 m to 50.
- a semiconductor wafer in which the adhesive layer of the dicing die bonding film is attached to one side of the wafer, the base film of the dicing die bonding film is fixed to the wafering frame may be provided. have.
- the semiconductor wafer as described above may be manufactured by attaching (laminating) the adhesive portion of the dicing die bonding film to the back surface of the wafer at a temperature of 0 ° C. to 180 ° C. and fixing the base film to the wafer ring frame. Can be.
- a wiring board An adhesive layer formed on the chip mounting surface of the wiring board and including the adhesive film for semiconductors described above; And said A semiconductor device including a semiconductor wafer mounted on an adhesive layer.
- the semiconductor device as described above may be manufactured through the following process. That is, the semiconductor wafer with the above-described die-die die-bonding film is completely cut using a dicing apparatus and divided into individual chips.
- the pressure sensitive adhesive portion is cured by means such as ultraviolet irradiation or heat application.
- cured by ultraviolet-ray or heat falls, and the adhesive force of an adhesive falls and it becomes easy to pick up a chip in a post process.
- an expanding process of tensioning the dicing die-bonding film may be performed to determine the gap between the chips, and may cause a shift in the interface between the adhesive portion and the adhesive portion to facilitate pickup.
- Adhesion temperature of the chip is typically a 100 ° C to 180 ° C
- adhesion time is from 0.5 seconds to 3 seconds
- the attachment pressure is 0.5 kgf / cuf to 2 kgf / cuf.
- the semiconductor device is obtained through the wire bonding and molding process.
- the wire bonding is performed without performing the wire curing process after the die bonding, in particular through optimization of the strength of the die bonding adhesive. Alternatively, peeling, pushing or tipping of chips in the molding process may be suppressed.
- the manufacturing method of a semiconductor device is not limited to the said process, Arbitrary process may be included, and the order of process may be changed.
- UV curing ⁇ dicing ⁇ expanding may be performed, or dicing ⁇ expanding ⁇ ultraviolet curing may also be performed. It may further include a heating or engraving process after the chip attaching process.
- the dicing die bonding film And a wafer stacked on at least one surface of the dicing die-bonding film; a preprocessing step of partially or partially dividing the semiconductor wafer; Expanding the semiconductor wafer after the pretreatment step; And irradiating ultraviolet rays to the base film of the expanded semiconductor wafer, and picking up individual chirps separated by the division of the semiconductor wafer.
- a method may be provided.
- Example 1 By using a dicing die-bonding film including the dicing film, it is possible to minimize the burr phenomenon that may occur during the dicing process of the semiconductor wafer to prevent contamination of the semiconductor chip and improve the reliability and life of the semiconductor chip. Can be. Specific embodiments of the present invention are described in more detail in the following examples. However, the following examples are merely to illustrate specific embodiments of the invention, the content of the present invention is not limited by the following examples. Example 1
- isocyanate-based curing agent polyfunctional isocyanate oligomer
- photocurable adhesive binder resin 100 parts by weight of photocurable adhesive binder resin
- silicone compound oil X— 22-4039 silicone compound oil X— 22-4039 (Shin-Etsu Co., Ltd.)
- taroker ⁇ 1 part by weight of taroker ⁇ as photoinitiator.
- the photocurable adhesive binder resin a polymer resin (Mw 300,000) in which 20 wt% of an acrylate functional group was added to the main chain of the acrylic base resin as a side chain was used.
- the UV-curable pressure-sensitive adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a dicing film including an adhesive layer of 10 ⁇ s.
- Example 2 The UV-curable pressure-sensitive adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a dicing film including an adhesive layer of 10 ⁇ s.
- UV curable pressure-sensitive adhesive composition by mixing 2 parts by weight of isocyanate-based curing agent (polyfunctional isocyanate oligomer), 0.5 parts by weight of silicone compound oil KF-1001 (Shin-Etsu Co.) and 1 part by weight of Darocer TP0 as a photoinitiator to 100 parts by weight of the photocurable adhesive binder resin.
- the photocurable adhesive binder resin a polymer resin (Mw 300, 000) in which 20 wt% of an acrylate functional group was added to the main chain of the acrylic base resin as a side chain was used.
- the UV-curable adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a dicing film including an adhesive layer of 100 ⁇ m.
- UV curable adhesive composition 2 parts by weight of isocyanate-based curing agent (polyfunctional isocyanate oligomer), 0.5 parts by weight of silicone compound oil X-KF-8008 (Shin-Etsu Co.) and 1 part by weight of polylocker TPO as photoinitiator
- a UV curable adhesive composition was prepared.
- the photocurable adhesive binder resin a polymer resin (Mw 300, 000) in which 20 wt% of an acrylate functional group was added to the main chain of the acrylic base resin as a side chain was used.
- the UV-curable adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a dicing film including an adhesive layer of 100 ⁇ m.
- Example 4 The UV-curable adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a dicing film including an adhesive layer of 100 ⁇ m.
- UV curable pressure-sensitive adhesive composition was prepared by mixing 2 parts by weight of isocyanate-based curing agent (polyfunctional isocyanate oligomer) with 0.5 parts by weight of silicone compound oil byk si lc 3720 and 1 part by weight of taroker TPO as photoinitiator. It was.
- As the photocurable adhesive binder resin a polymer resin (Mw 300, 000) in which 20 wt% of an acrylate functional group was added to the main chain of the acrylic base resin as a side chain was used.
- the UV curable pressure-sensitive adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a die film including an adhesive layer of 100 ⁇ m. Comparative Example 1
- isocyanate-based curing agent polyfunctional isocyanate oligomer
- the UV cure adhesive composition was prepared.
- an acrylate functional group is formed as a side chain in the main chain of the acrylic base resin.
- isocyanate-based curing agent polyfunctional isocyanate oligomer
- silicone compound oil X-22-4039 silicone compound oil X-22-4039
- Daroker TP0 a photoinitiator
- the photocurable adhesive binder resin a polymer resin (Mw 300, 000) in which 20 wt% of an acrylate functional group was added to the main chain of the acrylic base resin as a side chain was used.
- the UV-curable pressure-sensitive adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a die film including a pressure-sensitive adhesive layer of 100 ⁇ m. Comparative Example 3
- UV curable pressure-sensitive adhesive composition 2 parts by weight of isocyanate-based curing agent (polyfunctional isocyanate oligomer), 0.5 parts by weight of silicone compound oil L-7500 (Si 1 wet), and 1 part by weight of polylocker TP0 as a photoinitiator to 100 parts by weight of the photocurable adhesive binder resin. was prepared.
- the UV-curable pressure-sensitive adhesive composition was coated on one side of a polyolefin film of 100 ⁇ m and dried to prepare a dicing film including an adhesive layer of 100 ⁇ m.
- a dimming film of 25 mm width was prepared, and SUS 304 was made to adhere and adhered. After hardening for 1 hour after adhesion, the 90 degree peeling strength was measured at the speed of 300 kPa / min. The measurement was performed three or more times per sample to describe the average value.
- the tack strength was measured using a 1 inch diameter ball type probe with the adhesive layer of the dicing film facing upwards on the plate. At this time, the force applied to the probe was 800gf, the contact time was 0.01 seconds, the measurement speed of detaching the probe was 1 ⁇ / s, and the instrument used for the measurement was Texture An lyzer.
- the dicing die-bonding film and wafer prepared from the dicing film prepared according to the above examples and comparative examples were laminated at 7 (rc conditions. Then, the die was subjected to the following conditions using a dicing apparatus (manufactured by NEON). Ultraviolet irradiation was carried out on the dicing film surface under the number of the dicing process, and then 200 chips were picked up by a die bonder (Shinkawa Co., Ltd.) and the number of unpicked was measured and expressed in percentage. .
- Blade rotation speed 40, 000rpm
- Chip size 10 ⁇ X 10mm
- Lamp metal hal ide type Illuminance : 70mW / cm 2 (Illuminance measurement: UV meter)
- the dicing film prepared in Examples 1 to 4 exhibits a relatively high die share strength compared to the dicing film fabricated in Comparative Examples 1 to 3 can prevent the peeling phenomenon due to the adhesive force degradation and thus ripple It has been shown that low cracks can be suppressed and the reliability of the semiconductor manufacturing process can be improved.
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Abstract
Description
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US14/781,507 US9540547B2 (en) | 2013-12-13 | 2014-12-12 | Composition for forming adhesive layer of dicing film, and dicing film |
JP2016559139A JP6309108B2 (ja) | 2013-12-13 | 2014-12-12 | ダイシングフィルム粘着層形成用組成物およびダイシングフィルム |
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