TW202239036A - Workpiece handling sheet and device manufacturing method - Google Patents
Workpiece handling sheet and device manufacturing method Download PDFInfo
- Publication number
- TW202239036A TW202239036A TW111101970A TW111101970A TW202239036A TW 202239036 A TW202239036 A TW 202239036A TW 111101970 A TW111101970 A TW 111101970A TW 111101970 A TW111101970 A TW 111101970A TW 202239036 A TW202239036 A TW 202239036A
- Authority
- TW
- Taiwan
- Prior art keywords
- workpiece
- interface
- ablation
- ablation layer
- mentioned
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 24
- 238000002679 ablation Methods 0.000 claims abstract description 163
- 239000000758 substrate Substances 0.000 claims abstract description 34
- 238000002835 absorbance Methods 0.000 claims abstract description 21
- 239000010410 layer Substances 0.000 claims description 149
- 238000012545 processing Methods 0.000 claims description 81
- 239000000853 adhesive Substances 0.000 claims description 80
- 230000001070 adhesive effect Effects 0.000 claims description 78
- 239000000463 material Substances 0.000 claims description 37
- 239000003999 initiator Substances 0.000 claims description 36
- 239000012790 adhesive layer Substances 0.000 claims description 24
- 239000004065 semiconductor Substances 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 9
- 238000010521 absorption reaction Methods 0.000 claims description 5
- 239000003522 acrylic cement Substances 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 39
- 239000000178 monomer Substances 0.000 description 34
- 229920000642 polymer Polymers 0.000 description 31
- 235000012431 wafers Nutrition 0.000 description 31
- 238000000034 method Methods 0.000 description 30
- -1 dichlorodiphenyl ketone Chemical class 0.000 description 29
- 125000000524 functional group Chemical group 0.000 description 25
- 238000000926 separation method Methods 0.000 description 23
- 239000000203 mixture Substances 0.000 description 21
- 229920006243 acrylic copolymer Polymers 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 18
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 13
- 229920001577 copolymer Polymers 0.000 description 13
- 238000000576 coating method Methods 0.000 description 12
- 238000005259 measurement Methods 0.000 description 11
- 239000011248 coating agent Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 9
- 229910052710 silicon Inorganic materials 0.000 description 9
- 239000010703 silicon Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 230000001681 protective effect Effects 0.000 description 8
- 125000003277 amino group Chemical group 0.000 description 7
- 239000003431 cross linking reagent Substances 0.000 description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 238000005227 gel permeation chromatography Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000013329 compounding Methods 0.000 description 5
- 239000000470 constituent Substances 0.000 description 5
- 230000001678 irradiating effect Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 230000002950 deficient Effects 0.000 description 4
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 230000001747 exhibiting effect Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- NJWGQARXZDRHCD-UHFFFAOYSA-N 2-methylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3C(=O)C2=C1 NJWGQARXZDRHCD-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 125000004069 aziridinyl group Chemical group 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
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- RBQRWNWVPQDTJJ-UHFFFAOYSA-N methacryloyloxyethyl isocyanate Chemical compound CC(=C)C(=O)OCCN=C=O RBQRWNWVPQDTJJ-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000011112 polyethylene naphthalate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- CVBWTNHDKVVFMI-LBPRGKRZSA-N (2s)-1-[4-[2-[6-amino-8-[(6-bromo-1,3-benzodioxol-5-yl)sulfanyl]purin-9-yl]ethyl]piperidin-1-yl]-2-hydroxypropan-1-one Chemical compound C1CN(C(=O)[C@@H](O)C)CCC1CCN1C2=NC=NC(N)=C2N=C1SC(C(=C1)Br)=CC2=C1OCO2 CVBWTNHDKVVFMI-LBPRGKRZSA-N 0.000 description 1
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- GIMQKKFOOYOQGB-UHFFFAOYSA-N 2,2-diethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)(OCC)C(=O)C1=CC=CC=C1 GIMQKKFOOYOQGB-UHFFFAOYSA-N 0.000 description 1
- BTJPUDCSZVCXFQ-UHFFFAOYSA-N 2,4-diethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC(CC)=C3SC2=C1 BTJPUDCSZVCXFQ-UHFFFAOYSA-N 0.000 description 1
- LCHAFMWSFCONOO-UHFFFAOYSA-N 2,4-dimethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC(C)=C3SC2=C1 LCHAFMWSFCONOO-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- UMLWXYJZDNNBTD-UHFFFAOYSA-N 2-(dimethylamino)-1-phenylethanone Chemical compound CN(C)CC(=O)C1=CC=CC=C1 UMLWXYJZDNNBTD-UHFFFAOYSA-N 0.000 description 1
- PUBNJSZGANKUGX-UHFFFAOYSA-N 2-(dimethylamino)-2-[(4-methylphenyl)methyl]-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=C(C)C=C1 PUBNJSZGANKUGX-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- DZZAHLOABNWIFA-UHFFFAOYSA-N 2-butoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCCCC)C(=O)C1=CC=CC=C1 DZZAHLOABNWIFA-UHFFFAOYSA-N 0.000 description 1
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 1
- BQBSIHIZDSHADD-UHFFFAOYSA-N 2-ethenyl-4,5-dihydro-1,3-oxazole Chemical compound C=CC1=NCCO1 BQBSIHIZDSHADD-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- SJEBAWHUJDUKQK-UHFFFAOYSA-N 2-ethylanthraquinone Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3C(=O)C2=C1 SJEBAWHUJDUKQK-UHFFFAOYSA-N 0.000 description 1
- YJQMXVDKXSQCDI-UHFFFAOYSA-N 2-ethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC=C3SC2=C1 YJQMXVDKXSQCDI-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 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
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 1
- JEHFRMABGJJCPF-UHFFFAOYSA-N 2-methylprop-2-enoyl isocyanate Chemical compound CC(=C)C(=O)N=C=O JEHFRMABGJJCPF-UHFFFAOYSA-N 0.000 description 1
- MYISVPVWAQRUTL-UHFFFAOYSA-N 2-methylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3SC2=C1 MYISVPVWAQRUTL-UHFFFAOYSA-N 0.000 description 1
- YTPSFXZMJKMUJE-UHFFFAOYSA-N 2-tert-butylanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(C(C)(C)C)=CC=C3C(=O)C2=C1 YTPSFXZMJKMUJE-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- WHNPOQXWAMXPTA-UHFFFAOYSA-N 3-methylbut-2-enamide Chemical compound CC(C)=CC(N)=O WHNPOQXWAMXPTA-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- JKTORXLUQLQJCM-UHFFFAOYSA-N 4-phosphonobutylphosphonic acid Chemical compound OP(O)(=O)CCCCP(O)(O)=O JKTORXLUQLQJCM-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 241001050985 Disco Species 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 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
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- LOCXTTRLSIDGPS-UHFFFAOYSA-N [[1-oxo-1-(4-phenylsulfanylphenyl)octan-2-ylidene]amino] benzoate Chemical compound C=1C=C(SC=2C=CC=CC=2)C=CC=1C(=O)C(CCCCCC)=NOC(=O)C1=CC=CC=C1 LOCXTTRLSIDGPS-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- HXBPYFMVGFDZFT-UHFFFAOYSA-N allyl isocyanate Chemical compound C=CCN=C=O HXBPYFMVGFDZFT-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000001541 aziridines Chemical class 0.000 description 1
- 238000007611 bar coating method Methods 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000004532 chromating Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- MAWOHFOSAIXURX-UHFFFAOYSA-N cyclopentylcyclopentane Chemical group C1CCCC1C1CCCC1 MAWOHFOSAIXURX-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000007607 die coating method Methods 0.000 description 1
- KIQKWYUGPPFMBV-UHFFFAOYSA-N diisocyanatomethane Chemical class O=C=NCN=C=O KIQKWYUGPPFMBV-UHFFFAOYSA-N 0.000 description 1
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- GFJVXXWOPWLRNU-UHFFFAOYSA-N ethenyl formate Chemical compound C=COC=O GFJVXXWOPWLRNU-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- WUDNUHPRLBTKOJ-UHFFFAOYSA-N ethyl isocyanate Chemical compound CCN=C=O WUDNUHPRLBTKOJ-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 238000000227 grinding Methods 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
- 150000002429 hydrazines Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 238000000608 laser ablation Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 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
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002918 oxazolines Chemical class 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006290 polyethylene naphthalate film Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000013464 silicone adhesive Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
Images
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
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/385—Acrylic polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/16—Layered products comprising a layer of synthetic resin specially treated, e.g. irradiated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/02—Physical, chemical or physicochemical properties
- B32B7/023—Optical properties
-
- 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
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/062—Copolymers with monomers not covered by C09J133/06
- C09J133/066—Copolymers with monomers not covered by C09J133/06 containing -OH groups
-
- 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
-
- 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
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21S—NON-PORTABLE LIGHTING DEVICES; SYSTEMS THEREOF; VEHICLE LIGHTING DEVICES SPECIALLY ADAPTED FOR VEHICLE EXTERIORS
- F21S2/00—Systems of lighting devices, not provided for in main groups F21S4/00 - F21S10/00 or F21S19/00, e.g. of modular construction
-
- G—PHYSICS
- G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
- G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
- G09F9/00—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements
-
- 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
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Theoretical Computer Science (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Engineering & Computer Science (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Laser Beam Processing (AREA)
- Laminated Bodies (AREA)
Abstract
Description
本發明是關於一種可使用在用以操作半導體組件、半導體裝置等的工件小片的工件處理片,以及使用該工件處理片的裝置製造方法,尤其是關於一種可使用在用以操作微發光二極體(micro light emitting diode)、功率元件(power device)、MEMS(Micro Electro Mechanical Systems)等的工件小片的工件處理片,以及使用該工件處理片的裝置製造方法。The present invention relates to a workpiece processing chip that can be used to manipulate semiconductor components, semiconductor devices, etc. A workpiece processing chip for small workpieces such as micro light emitting diodes, power devices, and MEMS (Micro Electro Mechanical Systems), and a device manufacturing method using the workpiece processing chip.
近年來,使用微發光二極體的顯示器的開發正在進展當中。該顯示器為一個個的畫素由微發光二極體所構成,各個微發光二極體的發光獨立地受到控制。在該顯示器的製造中,一般而言,必須將配置在藍寶石(sapphire)、玻璃等的供給基板上的微發光二極體組裝在設置有配線的配線基板上。In recent years, the development of displays using micro light emitting diodes is progressing. In the display, each pixel is composed of micro-light-emitting diodes, and the light emission of each micro-light-emitting diode is controlled independently. In the manufacture of such a display, generally, micro light emitting diodes arranged on a supply substrate such as sapphire or glass must be assembled on a wiring substrate provided with wiring.
在上述組裝時,配置在供給基板上的複數個微發光二極體,必須正確地載置在配線基板的特定位置。此時,必須從複數個微發光二極體當中選擇特定者,使其載置在配線基板上,而且複數個微發光二極體必須同時載置。During the above-mentioned assembly, the plurality of micro light-emitting diodes arranged on the supply substrate must be accurately placed on a specific position of the wiring substrate. In this case, a specific one must be selected from among a plurality of micro light emitting diodes and placed on the wiring board, and the plurality of micro light emitting diodes must be placed at the same time.
從良好地進行此類組裝的觀點而言,利用雷射光的照射受到研究。例如,將複數個微發光二極體,透過特定的層維持在支撐體上之後,藉由對該層照射雷射光,在此照射的位置上使該層的燒蝕發生,藉此將從支撐體進行分離(雷射剝離(laser lift-off))的微發光二極體,載置到配線基板上的方法獲得研究(專利文獻1)。雷射光由於指向性(directivity)以及收斂性(convergence)佳,容易控制照射的位置,可良好地進行選擇性地載置。 [先前技術文獻] [專利文獻] Irradiation with laser light has been studied from the viewpoint of performing such assembly satisfactorily. For example, after a plurality of micro light-emitting diodes are maintained on a support body through a specific layer, by irradiating the layer with laser light, the ablation of the layer occurs at the irradiated position, whereby the Research has been conducted on a method of placing micro-light emitting diodes that are separated (laser lift-off) on a wiring board (Patent Document 1). Since laser light has good directivity and convergence, it is easy to control the position of irradiation, and it can perform selective placement well. [Prior Art Literature] [Patent Document]
專利文獻1:日本特許6546278號公報Patent Document 1: Japanese Patent No. 6546278
[發明所欲解決的問題][Problem to be solved by the invention]
然而,當微發光二極體的進一步微小化、微發光二極體的更高密度的組裝推進時,對應此等,尋求相較於專利文獻1之類的過去的手段,更有效率地操作多數個微發光二極體等的微小的工件小片的手段。However, as micro-light emitting diodes are further miniaturized and micro-light-emitting diodes are assembled at a higher density, in response to these, more efficient operations are sought compared to conventional means such as
本發明為鑒於此種情形而完成者,其目的為提供一種即使是微小的工件小片仍可良好地操作的工件處理片,以及使用該工件處理片的裝置製造方法。 [用以解決問題的手段] The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a workpiece processing sheet that can handle well even a small workpiece, and a device manufacturing method using the workpiece processing sheet. [means used to solve a problem]
為了達成上述目的,首先,本發明提供一種工件處理片,其具備:基材,及積層在上述基材中的單面側的可用以維持工件小片,並且藉由雷射光的照射進行界面燒蝕的界面燒蝕層,上述界面燒蝕層含有光聚合起始劑,上述工件處理片的波長355nm的光線的吸光度為1.5以上(發明1)。In order to achieve the above object, firstly, the present invention provides a workpiece processing sheet, which includes: a base material, and a small piece laminated on one side of the base material, which can be used to maintain the workpiece, and the interface is ablated by irradiation of laser light The interface ablation layer contains a photopolymerization initiator, and the absorbance of light with a wavelength of 355 nm of the workpiece treatment sheet is 1.5 or more (Invention 1).
上述發明(發明1)相關的工件處理片,藉由界面燒蝕層含有光聚合起始劑,波長355nm的光線的吸光度於上述範圍,照射雷射光時有效地進行界面燒蝕,藉此可將工件小片朝著對象物良好地進行分離。In the workpiece processing sheet related to the above invention (Invention 1), the interface ablation layer contains a photopolymerization initiator, the absorbance of light with a wavelength of 355 nm is within the above range, and the interface ablation is effectively performed when irradiated with laser light. The workpiece small pieces are well separated toward the object.
在上述發明(發明1)中,上述光聚合起始劑以在200nm以上,400nm以下的波長的範圍中具有吸收峰值為佳(發明2)。In the above invention (Invention 1), it is preferable that the photopolymerization initiator has an absorption peak in a wavelength range of not less than 200 nm and not more than 400 nm (Invention 2).
在上述發明(發明1、2)中,以上述界面燒蝕層為黏著劑層為佳(發明3)。In the above inventions (
在上述發明(發明3)中,以構成上述黏著劑層的黏著劑為活性能量線硬化性黏著劑為佳(發明4)。In the above invention (Invention 3), it is preferable that the adhesive constituting the adhesive layer is an active energy ray-curable adhesive (Invention 4).
在上述發明(發明3、4)中,以構成上述黏著劑層的黏著劑為丙烯酸系黏著劑為佳(發明5)。In the above inventions (
在上述發明(發明1~5)中,以上述雷射光具有紫外線區域的波長者為佳(發明6)。In the above inventions (
在上述發明(發明1~6)中,在上述界面燒蝕層使界面燒蝕發生時,以在該界面燒蝕發生的位置上形成膨泡(blister)為佳(發明7)。In the above inventions (
在上述發明(發明1~7)中,以使用在藉由在上述界面燒蝕層使其局部地發生界面燒蝕,將維持在上述界面燒蝕層中的與上述基材相反的面上的複數個工件小片當中的任意的工件小片,從上述界面燒蝕層選擇性地進行分離者為佳(發明8)。In the above-mentioned inventions (
在上述發明(發明8)中,以上述工件小片為將維持在上述界面燒蝕層中的與基材相反的面上的工件,在該面上進行個片化可獲得者為佳(發明9)。In the above invention (Invention 8), it is preferable that the workpiece small pieces are to be maintained on the surface of the above-mentioned interface ablation layer opposite to the base material, and the pieces can be obtained on this surface (Invention 9 ).
在上述發明(發明8、9)中,上述工件小片以選自半導體組件以及半導體裝置當中的至少1種為佳(發明10)。In the above inventions (Inventions 8 and 9), it is preferable that the workpiece chip is at least one selected from a semiconductor package and a semiconductor device (Invention 10).
在上述發明(發明8~10)中,上述工件小片以選自迷你發光二極體以及微發光二極體當中的發光二極體為佳(發明11)。In the above inventions (Inventions 8-10), the workpiece chip is preferably a light-emitting diode selected from miniature light-emitting diodes and micro-light-emitting diodes (invention 11).
第二,本發明提供一種裝置製造方法,具備:準備具備基材,及積層在上述基材中的單面側的含有光聚合起始劑的界面燒蝕層,波長355nm的光線的吸光度為1.5以上的工件處理片,在上述界面燒蝕層側的面上維持有複數個工件小片而成的積層體的準備步驟;對於可容納上述工件小片的對象物,以面對上述積層體中的上述工件小片側的面的方式,配置上述積層體的配置步驟;對於上述積層體中的上述界面燒蝕層中的貼附有至少1個上述工件小片的位置,照射雷射光,藉由使上述界面燒蝕層中的上述被照射的位置上發生的界面燒蝕,將存在於該界面燒蝕發生的位置的上述工件小片,從上述工件處理片分離,將上述工件小片載置於上述對象物上的分離步驟(發明12)。Second, the present invention provides a device manufacturing method comprising: preparing a base material, and an interface ablation layer containing a photopolymerization initiator laminated on one side of the base material, and having an absorbance of 1.5 for light with a wavelength of 355 nm. In the above workpiece processing sheet, a preparation step of a laminate formed by maintaining a plurality of workpiece small pieces on the surface of the above-mentioned interface ablation layer side; A method of arranging the layered body on the surface of the workpiece small piece side; a step of arranging the above-mentioned laminated body; for the position where at least one of the above-mentioned workpiece small pieces is attached in the above-mentioned interface ablation layer in the above-mentioned laminated body, laser light is irradiated, and the above-mentioned interface is The interface ablation that occurs at the above-mentioned irradiated position in the ablation layer, the above-mentioned workpiece small piece existing at the position where the interface ablation occurs, is separated from the above-mentioned workpiece processing piece, and the above-mentioned workpiece small piece is placed on the above-mentioned object The separation step (invention 12).
在上述發明(發明12)中,以藉由在上述準備步驟中,將維持在上述界面燒蝕層中的與上述基材相反的面上的工件,於該面上進行個片化,可獲得上述工件小片為佳(發明13)。In the above invention (Invention 12), by performing individualization on the surface of the workpiece maintained on the surface of the interface ablation layer opposite to the above-mentioned substrate in the above-mentioned preparatory step, it is possible to obtain The above workpiece small pieces are preferable (Invention 13).
在上述發明(發明12、13)中,以上述工件小片為選自半導體組件以及半導體裝置當中的至少1種為佳(發明14)。In the above inventions (
在上述發明(發明12~14)中,以使用選自迷你發光二極體以及微發光二極體當中的發光二極體,作為上述工件小片,製造具備複數個上述發光二極體的發光裝置為佳(發明15)。In the above-mentioned inventions (
在上述發明(發明15)中,以上述發光裝置為顯示器為佳(發明16)。 [發明功效] In the above invention (Invention 15), it is preferable that the above-mentioned light-emitting device is a display (Invention 16). [Efficacy of the invention]
本發明相關的工件處理片,即使為微小的工件小片,仍可良好地操作,此外,根據本發明相關的裝置製造方法,可製造具有優異性能的裝置。The workpiece processing sheet related to the present invention can be handled well even if it is a minute workpiece piece, and furthermore, according to the device manufacturing method related to the present invention, a device having excellent performance can be manufactured.
[用以實施發明的形態][Mode for Carrying Out the Invention]
以下,針對本發明的實施形態加以說明。
圖1中,表示一實施形態相關的工件處理片的剖面圖。如圖1所示的工件處理片1,具備:基材12,及積層在基材12中的單面側的界面燒蝕層11。
Embodiments of the present invention will be described below.
FIG. 1 shows a cross-sectional view of a workpiece processing sheet according to an embodiment. The
在本實施形態相關的工件處理片1中,界面燒蝕層11可用以維持工件小片。亦即,本實施形態相關的工件處理片1,為積層在界面燒蝕層11中的與基材12相反的面上的工件小片,能夠維持其狀態的原樣。In the
上述維持的具體的態樣雖然未限定,作為較佳例,可列舉,界面燒蝕層11藉由發揮對於工件小片的黏著性而維持。此時,界面燒蝕層11如下述,作為構成其的成分之一,以包含黏著劑,換言之,為黏著劑層為佳。Although the specific aspect of the above-mentioned maintenance is not limited, as a preferable example, the
此外,本實施形態中的界面燒蝕層11,為藉由雷射光的照射進行界面燒蝕者。亦即,界面燒蝕層11為在受到上述雷射光的照射的區域上,局部地進行界面燒蝕者。且,作為上述雷射光,只要能夠使界面燒蝕發生的話,並未特別限定,可以是具有紫外線區域、可見光區域以及紅外區域的任一波長的雷射光,其中以具有紫外線區域的波長的雷射光為佳。In addition, the
在本說明書中,界面燒蝕是指藉由上述雷射光的能量,將構成界面燒蝕層11的成分的一部份蒸發或揮發,藉此所產生的氣體在界面燒蝕層11與基材12之間的界面滯留而產生空隙(膨泡)。此時,藉由膨泡使界面燒蝕層11的形狀變化,工件小片由界面燒蝕層11剝落,而將工件小片分離。In this specification, interfacial ablation refers to evaporating or volatilizing a part of the components constituting the
然後,本實施形態中的界面燒蝕層11含有光聚合起始劑,本實施形態相關的工件處理片1為波長355nm的光線的吸光度為1.5以上。如此一來,藉由在界面燒蝕層11中有光聚合起始劑存在,且,工件處理片1顯示上述吸光度,界面燒蝕層11接收來自雷射光的能量的效率獲得提升。藉此,有效地發生界面燒蝕,可將所維持的工件小片從界面燒蝕層11良好地分離。尤其是用以使工件小片充分地分離所必須的雷射光的照射量降低,可降低雷射光的照射裝置的運作成本,同時只有作為目標的工件小片可良好地容易分離的準確度獲得提升,再者,可防止由於過度雷射光照射所引起的裝置等的損傷。Then, the
從更加提升接收來自雷射光的能量的效率的觀點而言,上述光吸光度以2.0以上為佳,以2.2以上為更佳,尤其以2.5以上為佳,進一步以3.0以上為佳。且,針對上述吸光度的上限值,並未特別限定,例如,可以是6.0以下。此外,上述吸光度的測定方法的詳情,如下述試驗例中所記載。From the viewpoint of further improving the efficiency of receiving energy from laser light, the light absorbance is preferably 2.0 or higher, more preferably 2.2 or higher, particularly preferably 2.5 or higher, and further preferably 3.0 or higher. In addition, the upper limit of the above-mentioned absorbance is not particularly limited, and may be, for example, 6.0 or less. In addition, the detail of the measuring method of the said absorbance is as described in the following test example.
1.界面燒蝕層
本實施形態中的界面燒蝕層11的具體的構成、組成,只要是可用以維持工件小片,連同具有藉由雷射光的照射進行界面燒蝕之類的性質之外,只要含有光聚合起始劑,同時,可達成作為工件處理片1的上述吸光度,並未特別限定。
1. Interface ablation layer
The specific composition and composition of the
從易於良好地發揮可用以維持工件小片之類的性質的觀點而言,界面燒蝕層11以含有如上述作為構成其的構成成分之一的黏著劑為佳。界面燒蝕層11包含黏著劑時,界面燒蝕層11以由含有光聚合起始劑的黏著性組合物所形成者為佳。From the viewpoint of easily exhibiting properties such as being able to maintain workpiece chips, the
(1) 光聚合起始劑 本實施形態中的光聚合起始劑的種類並未特別限定。作為較佳的光聚合起始劑的例子,以使用2-二甲基胺基-2-(4-甲基苯甲基)-1-(4-嗎啉基-苯基)丁烷-1-酮、乙酮、1-[9-乙基-6-(2-甲基苯甲醯基)-9H-咔唑-3-基],1-(0-乙醯肟)、1,2-辛二酮、1-[4-(苯硫基)苯基],2-(鄰-苯甲醯肟)、2-苯甲基-2-二甲基胺基-1-(4-嗎啉基苯基)-丁酮、2-甲基-1-[4-(甲硫基)苯基]-2-嗎啉基丙烷-1-酮的至少1種為佳。 (1) Photopolymerization initiator The kind of photopolymerization initiator in this embodiment is not specifically limited. As an example of a preferable photopolymerization initiator, 2-dimethylamino-2-(4-methylbenzyl)-1-(4-morpholinyl-phenyl)butane-1 -ketone, ethyl ketone, 1-[9-ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl], 1-(0-acetyloxime), 1,2 -octanedione, 1-[4-(phenylthio)phenyl], 2-(o-benzoyl oxime), 2-benzyl-2-dimethylamino-1-(4-morphoxime Preferably at least one of olinophenyl)-butanone and 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one.
連同上述光聚合起始劑,可併用其他光聚合起始劑。作為可併用的光聚合起始劑的例子,苯偶姻(benzoin)、苯偶姻甲醚、苯偶姻乙醚、苯偶姻異丙醚、苯偶姻正丁醚、苯偶姻異丁醚、乙醯苯(acetophenone)、二甲基胺基乙醯苯、2,2-二甲氧基-1,2-二苯乙烷-1-酮、2,2-二乙氧基-2-苯基乙醯苯、2-羥基-2-甲基-1-苯基丙烷-1-酮、1-羥環己基苯基酮、4-(2-羥乙氧基)苯基-2-(羥基-2-丙基)酮、1-[4-(2-羥乙氧基)-苯基]-2-羥基-甲基丙酮、二苯基酮(benzophenone)、對-苯基二苯基酮、4,4’-二乙基胺基二苯基酮、二氯二苯基酮、2-甲基蒽醌、2-乙基蒽醌、2-三級丁基蒽醌、2-胺基蒽醌、2-甲基噻噸酮、2-乙基噻噸酮、2-氯噻噸酮、2,4-二甲基噻噸酮、2,4-二乙基噻噸酮、苯甲基二甲基縮酮(benzil dimethyl ketal)、乙醯苯二甲基縮酮、對-二甲基胺基安息香酸酯、寡聚[2-羥基-2-甲基-1[4-(1-甲基乙烯基)苯基]丙酮]、2,4,6-三甲基苯甲醯基-二苯基-氧化膦等。Along with the photopolymerization initiator described above, other photopolymerization initiators may be used in combination. Examples of photopolymerization initiators that can be used in combination include benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzoin n-butyl ether, and benzoin isobutyl ether. , acetophenone, dimethylaminoacetylbenzene, 2,2-dimethoxy-1,2-diphenylethane-1-one, 2,2-diethoxy-2- Phenylacetylbenzene, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, 4-(2-hydroxyethoxy)phenyl-2-( Hydroxy-2-propyl)ketone, 1-[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-methylacetone, benzophenone, p-phenyldiphenyl Ketone, 4,4'-diethylaminodiphenyl ketone, dichlorodiphenyl ketone, 2-methylanthraquinone, 2-ethylanthraquinone, 2-tertiary butylanthraquinone, 2-amine Anthraquinone, 2-methylthioxanthone, 2-ethylthioxanthone, 2-chlorothioxanthone, 2,4-dimethylthioxanthone, 2,4-diethylthioxanthone, benzene Methyl dimethyl ketal (benzil dimethyl ketal), acetyl xylylene dimethyl ketal, p-dimethylamino benzoate, oligo[2-hydroxy-2-methyl-1[4-( 1-methylvinyl)phenyl]acetone], 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, etc.
本實施形態中的光聚合起始劑,以在200nm以上,400nm以下的波長範圍中具有吸收高峰者為佳。如此一來,界面燒蝕層11有效率地吸收雷射光,藉此變得易於良好地進行界面燒蝕。由此觀點而言,上述範圍的下限值,尤其以300nm以上為佳,進一步以330nm以上為佳。此外,上述範圍的上限值,尤其以380nm以下為佳,進一步以370nm以下為佳。The photopolymerization initiator in this embodiment preferably has an absorption peak in the wavelength range of 200 nm to 400 nm. In this way, the
且,上述吸收峰值根據以下的方法可進行指定。首先,將光聚合起始劑溶解於作為溶媒的甲醇或乙腈中,調製濃度0.01質量%的測定溶液。接著,針對該測定溶液,藉由分光光度計(例如,島津製作所公司製,「UV-3600」)測定吸光度,獲得吸收光譜。然後,從所得的吸收光譜,可將吸收峰值(nm)的波長的範圍進行指定。In addition, the above-mentioned absorption peak can be specified by the following method. First, a photopolymerization initiator was dissolved in methanol or acetonitrile as a solvent to prepare a measurement solution having a concentration of 0.01% by mass. Next, the absorbance of this measurement solution is measured with a spectrophotometer (for example, "UV-3600" manufactured by Shimadzu Corporation) to obtain an absorption spectrum. Then, from the obtained absorption spectrum, the wavelength range of the absorption peak (nm) can be specified.
此外,本實施形態中的光聚合起始劑,在濃度0.01質量%的溶液中的波長355nm的吸光度,以0.5以上為佳,尤其以0.75以上為佳,進一步以1.0以上為佳。藉由上述吸光度為0.5以上,界面燒蝕層11有效率地吸收雷射光,藉此變得易於良好地進行界面燒蝕。且,上述吸光度的上限值雖然未特別限定,例如,可以是4.0以下。In addition, the photopolymerization initiator in this embodiment preferably has an absorbance at a wavelength of 355 nm in a solution having a concentration of 0.01% by mass of 0.5 or more, especially 0.75 or more, and further preferably 1.0 or more. When the above-mentioned absorbance is 0.5 or more, the
且,上述吸光度為調製光聚合起始劑的濃度0.01質量%的甲醇溶液(光聚合起始劑不溶於甲醇中時,為乙腈溶液),在此溶液中的波長200~500nm的範圍的吸光度,使用紫外線可見光近紅外(UV-Vis-NIR)分光光度計(島津製作所公司製,製品名「UV-3600」,光徑長10mm)所測定者。In addition, the above-mentioned absorbance is a methanol solution (when the photopolymerization initiator is insoluble in methanol, it is an acetonitrile solution) in which the concentration of the photopolymerization initiator is adjusted to 0.01% by mass, and the absorbance in the range of a wavelength of 200 to 500 nm in this solution, Measured using an ultraviolet-visible-near-infrared (UV-Vis-NIR) spectrophotometer (manufactured by Shimadzu Corporation, product name "UV-3600", optical path length: 10 mm).
本實施形態中的界面燒蝕層11中的光聚合起始劑的含量,以1.8質量%以上為佳,尤其以3.0質量%以上為佳,進一步以5.0質量%以上為佳。藉由光聚合起始劑的含量為1.8質量%以上,界面燒蝕層11有效率地吸收雷射光,藉此變得易於良好地進行界面燒蝕。此外,本實施形態中的界面燒蝕層11中的光聚合起始劑的含量,以40.0質量%以下為佳,尤其以30.0質量%以下為佳,進一步以25.0質量%以下為佳。藉由光聚合起始劑的含量為40.0質量%以下,用以形成界面燒蝕層11的材料的黏度成為適當者,易於確保良好的造膜性。The content of the photopolymerization initiator in the
此外,本實施形態中的界面燒蝕層11為由下述黏著性組合物所形成時,光聚合起始劑亦可調配在此黏著性組合物中。尤其是光聚合起始劑隨著下述活性能量線硬化型聚合物(A)調配於黏著性組合物中時,黏著性組合物中的光聚合起始劑的調配量,相對於下述活性能量線硬化型聚合物(A)100質量份,以1.8質量份以上為佳,尤其以3.0質量份以上為佳,進一步以5.0質量份以上為佳。藉由光聚合起始劑的調配量為1.8質量份以上,界面燒蝕層11有效率地吸收雷射光,藉此易於良好的進行界面燒蝕。此外,上述黏著性組合物中的光聚合起始劑的調配量,相對於活性能量線硬化型聚合物(A)100質量份,以40.0質量份以下為佳,尤其以30.0質量份以下為佳,進一步以25.0質量份以下為佳。藉由光聚合起始劑的調配量為40.0質量份以下,所獲得的黏著劑成為易於發揮期望的黏著力者。In addition, when the
(2) 黏著劑
如前述,本實施形態中的界面燒蝕層11,加上光聚合起始劑,亦可為含有黏著劑者。此時,以界面燒蝕層11為由含有光聚合起始劑的黏著性組合物所形成者為佳。
(2) Adhesive
As mentioned above, the
作為上述黏著劑,只要能夠發揮對於工件小片等的被附著物充分的維持力(黏著力),並未特別限定。作為上述黏著劑的例子,可列舉,丙烯酸系黏著劑、橡膠系黏著劑、矽酮系黏著劑、氨酯系黏著劑、聚酯系黏著劑、聚乙烯醚系黏著劑等。此等當中,從易於發揮期望的黏著力的觀點而言,以使用丙烯酸系黏著劑為佳。The above-mentioned adhesive is not particularly limited as long as it can exhibit sufficient maintaining force (adhesive force) with respect to adherends such as workpiece chips. Examples of the above adhesives include acrylic adhesives, rubber adhesives, silicone adhesives, urethane adhesives, polyester adhesives, and polyvinyl ether adhesives. Among these, it is preferable to use an acrylic adhesive from the viewpoint of easily exhibiting a desired adhesive force.
此外,上述黏著劑雖然可以是未具有活性能量線硬化性的黏著劑,但以具有活性能量線硬化性的黏著劑(以下,有時稱為「活性能量線硬化性黏著劑」)者為佳。界面燒蝕層11為由活性能量線硬化性黏著劑所構成時,藉由活性能量線的照射,使界面燒蝕層11硬化,可易於使工件處理片1的對於被附著物的黏著力降低。In addition, although the above-mentioned adhesive may be an adhesive that does not have active energy ray-curable properties, it is preferably an adhesive that has active energy ray-curable properties (hereinafter, sometimes referred to as "active energy ray-curable adhesive"). . When the
尤其是藉由活性能量線的照射使黏著力的降低,藉由與如上述界面燒蝕配合進行,變得易於從工件處理片1將工件小片的分離。換言之,藉由在使上述界面燒蝕發生之前,或與上述界面燒蝕同時,藉由活性能量線的照射使密附性降低,可確實地進行從本實施形態相關的工件處理片1將工件小片的分離。此外,使工件小片的充分的分離發生所必要的雷射光的照射量可進一步減少。In particular, the reduction of the adhesive force by the irradiation of active energy rays is carried out in conjunction with the above-mentioned interface ablation, and it becomes easy to separate the workpiece small pieces from the
作為上述活性能量線硬化性黏著劑,可以是以具有活性能量線硬化性的聚合物當作主成分者,也可以是活性能量線非硬化性聚合物(未具有活性能量線硬化性的聚合物)與具有至少1個以上的活性能量線硬化性基的單體及/或寡聚物的混合物當作主成分者。此外,活性能量線硬化性黏著劑,可以是具有活性能量線硬化性的聚合物,與具有至少1個以上的活性能量線硬化性基的單體及/或寡聚物的混合物。The active energy ray-curable adhesive may be a polymer having active energy ray-curable properties as a main component, or an active energy ray non-curable polymer (polymer not curable by active energy ray). ) and a mixture of monomers and/or oligomers having at least one active energy ray-curable group as the main component. In addition, the active energy ray-curable adhesive may be a mixture of an active energy ray-curable polymer and a monomer and/or oligomer having at least one active energy ray-curable group.
上述具有活性能量線硬化性的聚合物,以在側鏈被導入具有能量線硬化性的官能基(活性能量線硬化性基)的(甲基)丙烯酸酯(共)聚合物(A)(以下,有時稱為「活性能量線硬化型聚合物(A)」者為佳。此活性能量線硬化型聚合物(A),以使具有含官能基的單體單元的丙烯酸系共聚合物(a1),與具有鍵結在此官能基的官能基的含不飽和基的化合物(a2)反應所獲得者為佳。且,在本說明書中,所謂(甲基)丙烯酸酯,是指丙烯酸酯及甲基丙烯酸酯兩者的意思。其他類似用語亦相同。再者,「聚合物」亦包括「共聚合物」的概念。The aforementioned active energy ray curable polymer is a (meth)acrylate (co)polymer (A) (hereinafter , sometimes called "active energy ray-curable polymer (A)". This active energy ray-curable polymer (A) is such that the acrylic copolymer ( a1), preferably obtained by reacting with an unsaturated group-containing compound (a2) having a functional group bonded to this functional group. And, in this specification, the so-called (meth)acrylate refers to acrylate and methacrylate. Other similar terms are also the same. Furthermore, "polymer" also includes the concept of "copolymer".
丙烯酸系共聚合物(a1)以含有來自含官能基的單體所導出的構成單元,及來自(甲基)丙烯酸酯單體或其衍生物所導出的構成單元為佳。The acrylic copolymer (a1) preferably contains a structural unit derived from a functional group-containing monomer and a structural unit derived from a (meth)acrylate monomer or a derivative thereof.
作為丙烯酸系共聚合物(a1)的構成單元的含官能基的單體,以在分子內具有聚合性的雙鍵,及羥基、羧基、胺基、取代胺基、環氧基等的官能基的單體為佳。The functional group-containing monomer as a constituent unit of the acrylic copolymer (a1) has a polymerizable double bond in the molecule, and a functional group such as a hydroxyl group, a carboxyl group, an amino group, a substituted amino group, an epoxy group, etc. The monomer is better.
作為含羥基的單體,可列舉,例如,(甲基)丙烯酸2-羥乙酯、(甲基)丙烯酸2-羥丙酯、(甲基)丙烯酸3-羥丙酯、(甲基)丙烯酸2-羥丁酯、(甲基)丙烯酸3-羥丁酯、(甲基)丙烯酸4-羥丁酯等,此等可單獨或組合2種以上使用。Examples of hydroxyl-containing monomers include 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, (meth)acrylic acid 2-Hydroxybutyl, 3-hydroxybutyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate etc. can be used individually or in combination of 2 or more types.
作為含羧基的單體,可列舉,例如,丙烯酸、甲基丙烯酸、丁烯酸、順丁烯二酸、衣康酸、檸康酸等的乙烯性不飽和羧酸。此等可單獨使用,亦可組合2種以上使用。Examples of the carboxyl group-containing monomer include ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid, and citraconic acid. These may be used individually or in combination of 2 or more types.
作為含胺基的單體或含取代胺基的單體,可列舉,例如,(甲基)丙烯酸胺基乙酯、(甲基)丙烯酸正丁基胺基乙酯等。此等可單獨使用,亦可組合2種以上使用。Examples of the amino group-containing monomer or substituted amino group-containing monomer include aminoethyl (meth)acrylate, n-butylaminoethyl (meth)acrylate, and the like. These may be used individually or in combination of 2 or more types.
作為構成丙烯酸系共聚合物(a1)的(甲基)丙烯酸酯單體,烷基的碳數為1~20的(甲基)丙烯酸烷基酯之外,較佳還可使用,例如,在分子內具有脂環式構造的單體(含脂環式構造的單體)。As the (meth)acrylate monomer constituting the acrylic copolymer (a1), other than alkyl (meth)acrylates having an alkyl group having 1 to 20 carbon atoms are preferably used, for example, in A monomer having an alicyclic structure in the molecule (monomer containing an alicyclic structure).
作為(甲基)丙烯酸烷基酯,尤其是烷基的碳數為1~18的(甲基)丙烯酸烷基,較佳可使用例如,(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸丙酯、(甲基)丙烯酸正丁酯、(甲基)丙烯酸2-乙基己酯等。此等可單獨1種使用,亦可組合2種以上使用。As the alkyl (meth)acrylate, especially the alkyl (meth)acrylate whose alkyl group has 1 to 18 carbon atoms, for example, methyl (meth)acrylate, ethyl (meth)acrylate, ester, propyl (meth)acrylate, n-butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, etc. These may be used alone or in combination of two or more.
作為含脂環式構造的單體,較佳可使用例如,(甲基)丙烯酸環己酯、(甲基)丙烯酸二環戊酯、(甲基)丙烯酸金剛烷酯、(甲基)丙烯酸異莰酯、(甲基)丙烯酸二環戊烯酯、(甲基)丙烯酸二環戊烯基氧乙酯等。此等可使用單獨1種,亦可組合2種以上使用。As monomers containing an alicyclic structure, for example, cyclohexyl (meth)acrylate, dicyclopentyl (meth)acrylate, adamantyl (meth)acrylate, Camphenyl, dicyclopentenyl (meth)acrylate, dicyclopentenyloxyethyl (meth)acrylate, and the like. These may be used alone or in combination of two or more.
丙烯酸系共聚合物(a1)含有來自上述含官能基的單體所導出的構成單元的比例,較佳為1質量%以上,尤其以5質量%以上為佳,進一步以10質量%以上為佳。此外,丙烯酸系共聚合物(a1)含有來自上述含官能基的單體所導出的構成單元的比例,較佳為35質量%以下,尤其以30質量%以下為佳,進一步以25質量%以下為佳。The proportion of the acrylic copolymer (a1) containing the structural unit derived from the above-mentioned functional group-containing monomer is preferably at least 1% by mass, particularly preferably at least 5% by mass, and more preferably at least 10% by mass . In addition, the proportion of the acrylic copolymer (a1) containing the structural unit derived from the above-mentioned functional group-containing monomer is preferably at most 35% by mass, particularly preferably at most 30% by mass, and further preferably at most 25% by mass. better.
再者,丙烯酸系共聚合物(a1)含有來自(甲基)丙烯酸酯單體或其衍生物所導出的構成單元的比例,較佳為50質量%以上,尤其以60質量%以上為佳,進一步以70質量%以上為佳。此外,丙烯酸系共聚合物(a1)含有來自(甲基)丙烯酸酯單體或其衍生物所導出的構成單元的比例,較佳為99質量%以下,尤其以95質量%以下為佳,進一步以90質量%以下為佳。Furthermore, the proportion of the acrylic copolymer (a1) containing the constituent units derived from (meth)acrylate monomers or derivatives thereof is preferably 50% by mass or more, especially 60% by mass or more, Furthermore, it is more preferably 70% by mass or more. In addition, the proportion of the acrylic copolymer (a1) containing structural units derived from (meth)acrylate monomers or derivatives thereof is preferably at most 99% by mass, particularly preferably at most 95% by mass, and further It is preferably 90% by mass or less.
丙烯酸系共聚合物(a1)可藉由使如上述的含官能基的單體,與(甲基)丙烯酸酯單體或其衍生物,以常用方法進行共聚合而獲得,然而,亦可使此等單體之外的二甲基丙烯醯胺、甲酸乙烯酯、乙酸乙烯酯、苯乙烯等共聚合。The acrylic copolymer (a1) can be obtained by copolymerizing the above-mentioned functional group-containing monomer with a (meth)acrylate monomer or its derivatives by a common method. However, it can also be obtained by Copolymerization of dimethylacrylamide, vinyl formate, vinyl acetate, styrene, etc. other than these monomers.
藉由使上述具有含官能基的單體單元的丙烯酸系共聚合物(a1),與具有鍵結在此官能基的官能基的含不飽和基的化合物(a2)反應,可獲得活性能量線硬化型聚合物(A)。Active energy rays can be obtained by reacting the above-mentioned acrylic copolymer (a1) having a functional group-containing monomer unit with an unsaturated group-containing compound (a2) having a functional group bonded to the functional group. Hardening type polymer (A).
含不飽和基的化合物(a2)所具有的官能基,可對應丙烯酸系共聚合物(a1)所具有的含官能基的單體單元的官能基的種類,而適當選擇。例如,丙烯酸系共聚合物(a1)所具有的官能基為羥基、胺基或取代胺基時,作為含不飽和基的化合物(a2)所具有的官能基,以異氰酸酯基或環氧基為佳,丙烯酸系共聚合物(a1)所具有的官能基為環氧基時,作為含不飽和基的化合物(a2)所具有的官能基,以胺基、羧基或氮丙啶基(aziridinyl)為佳。The functional group which the unsaturated group containing compound (a2) has can be selected suitably according to the kind of the functional group of the functional group containing monomeric unit which the acrylic-type copolymer (a1) has. For example, when the functional group that the acrylic copolymer (a1) has is a hydroxyl group, an amino group, or a substituted amino group, the functional group that the unsaturated group-containing compound (a2) has is an isocyanate group or an epoxy group. Preferably, when the functional group of the acrylic copolymer (a1) is an epoxy group, the functional group of the unsaturated group-containing compound (a2) may be an amine group, a carboxyl group or an aziridinyl group (aziridinyl) better.
此外,上述含不飽和基的化合物(a2)中,以1分子中至少包含1個能量線聚合性的碳-碳雙鍵為佳,較佳為1~6個,又更佳為1~4個。作為此類含不飽和基的化合物(a2)的具體例,可列舉,例如,異氰酸2-甲基丙烯醯氧乙基酯、間-異丙烯基-α,α-二甲基苯甲基異氰酸酯、甲基丙烯醯基異氰酸酯、烯丙基異氰酸酯、1,1-(雙丙烯醯基氧甲基)乙基異氰酸酯;二異氰酸酯化合物或聚異氰酸酯化合物,與(甲基)丙烯酸羥乙酯的反應所獲得的丙烯醯基單異氰酸酯化合物;二異氰酸酯化合物或聚異氰酸酯化合物,與多元醇化合物,與(甲基)丙烯酸羥乙酯的反應所獲得的丙烯醯基單異氰酸酯化合物;(甲基)丙烯酸環氧丙酯;(甲基)丙烯酸、(甲基)丙烯酸2-(1-氮丙啶基)乙酯、2-乙烯基-2-噁唑啉、2-異丙烯基-2-噁唑啉等。In addition, in the above-mentioned unsaturated group-containing compound (a2), it is preferable that one molecule contains at least one energy-ray polymerizable carbon-carbon double bond, preferably 1 to 6, and more preferably 1 to 4. indivual. Specific examples of such an unsaturated group-containing compound (a2) include, for example, 2-methacryloxyethyl isocyanate, m-isopropenyl-α,α-dimethylbenzyl methacryl isocyanate, methacryl isocyanate, allyl isocyanate, 1,1-(bisacryloxymethyl)ethyl isocyanate; diisocyanate compound or polyisocyanate compound, with hydroxyethyl (meth)acrylate Acryl monoisocyanate compound obtained by reaction; diisocyanate compound or polyisocyanate compound, polyol compound, and acryl monoisocyanate compound obtained by reaction of hydroxyethyl (meth)acrylate; (meth)acrylic acid Glycidyl ester; (meth)acrylic acid, 2-(1-aziridinyl)ethyl (meth)acrylate, 2-vinyl-2-oxazoline, 2-isopropenyl-2-oxazole phylloline etc.
使用上述含不飽和基的化合物(a2)的比例,相對於上述丙烯酸系共聚合物(a1)的含官能基的單體莫耳數,較佳為50莫耳%以上,尤其以60莫耳%以上為佳,進一步以70莫耳%以上為佳。此外,使用上述含不飽和基的化合物(a2)的比例,相對於上述丙烯酸系共聚合物(a1)的含官能基的單體莫耳數,較佳為95莫耳%以下,尤其以93莫耳%以下為佳,進一步以90莫耳%以下為佳。The proportion of the above-mentioned unsaturated group-containing compound (a2) relative to the number of moles of the functional group-containing monomer of the above-mentioned acrylic copolymer (a1) is preferably 50 mole % or more, especially 60 mole % or more is preferable, and further preferably more than 70 mole %. In addition, the proportion of the above-mentioned unsaturated group-containing compound (a2) relative to the number of moles of the functional group-containing monomer of the above-mentioned acrylic copolymer (a1) is preferably 95 mole % or less, especially 93 It is preferably not more than mol%, more preferably not more than 90 mol%.
在丙烯酸系共聚合物(a1)與含不飽和基的化合物(a2)的反應中,對應丙烯酸系共聚合物(a1)所具有的官能基與含不飽和基的化合物(a2)所具有的官能基的組合,可適當選擇反應的溫度、壓力、溶媒、時間、有無觸媒、觸媒的種類。如此一來,存在於丙烯酸系共聚合物(a1)中的官能基,與含不飽和基的化合物(a2)中的官能基進行反應,將不飽和基導入至丙烯酸系共聚合物(a1)中的側鏈,可獲得活性能量線硬化型聚合物(A)。In the reaction between the acrylic copolymer (a1) and the unsaturated group-containing compound (a2), the functional groups corresponding to the acrylic copolymer (a1) and the unsaturated group-containing compound (a2) have The combination of functional groups can appropriately select the reaction temperature, pressure, solvent, time, presence or absence of a catalyst, and the type of catalyst. In this way, the functional group present in the acrylic copolymer (a1) reacts with the functional group in the unsaturated group-containing compound (a2) to introduce the unsaturated group into the acrylic copolymer (a1). In the side chain, the active energy ray-curable polymer (A) can be obtained.
藉此所獲得的活性能量線硬化型聚合物(A)的重量平均分子量(Mw),以1萬以上為佳,尤其以5萬以上為佳,進一步以10萬以上為佳。此外,該重量平均分子量(Mw)以300萬以下為佳,尤其以200萬以下為佳,進一步以150萬以下為佳。且,本說明書中的重量平均分子量(Mw),為藉由凝膠滲透層析法(GPC法)所測定的換算標準聚苯乙烯的值。The weight average molecular weight (Mw) of the active energy ray-curable polymer (A) thus obtained is preferably at least 10,000, particularly preferably at least 50,000, and further preferably at least 100,000. In addition, the weight average molecular weight (Mw) is preferably at most 3 million, particularly preferably at most 2 million, and further preferably at most 1.5 million. In addition, the weight average molecular weight (Mw) in this specification is the value measured by gel permeation chromatography (GPC method) in conversion of standard polystyrene.
即使是活性能量線硬化性黏著劑以活性能量線硬化型聚合物(A)之類的具有活性能量線硬化性的聚合物當作主成分的情況時,活性能量線硬化性黏著劑亦可進一步含有能量線硬化性的單體及/或寡聚物(B)。Even when the active energy ray-curable adhesive contains an active energy ray-curable polymer such as the active energy ray-curable polymer (A) as a main component, the active energy ray-curable adhesive can further Contains energy ray curable monomers and/or oligomers (B).
作為活性能量線硬化性的單體及/或寡聚物(B),例如,可使用多元醇及(甲基)丙烯酸的酯等。As the active energy ray-curable monomer and/or oligomer (B), for example, a polyhydric alcohol, an ester of (meth)acrylic acid, or the like can be used.
作為相關的活性能量線硬化性的單體及/或寡聚物(B),可列舉,例如,(甲基)丙烯酸環己酯、(甲基)丙烯酸異莰酯等的單官能性丙烯酸酯類、三羥甲基丙烷三(甲基)丙烯酸酯、新戊四醇三(甲基)丙烯酸酯、新戊四醇四(甲基)丙烯酸酯、二新戊四醇六(甲基)丙烯酸酯、1,4-丁二醇二(甲基)丙烯酸酯、1,6-己二醇二(甲基)丙烯酸酯、聚乙二醇二(甲基)丙烯酸酯、二羥甲基三環癸烷二(甲基)丙烯酸酯等的多官能性丙烯酸酯類、聚酯寡聚(甲基)丙烯酸酯、聚氨酯寡聚(甲基)丙烯酸酯等。Examples of the relevant active energy ray-curable monomers and/or oligomers (B) include monofunctional acrylates such as cyclohexyl (meth)acrylate and isobornyl (meth)acrylate. trimethylolpropane tri(meth)acrylate, neopentylthritol tri(meth)acrylate, neopentylthritol tetra(meth)acrylate, dipenteoerythritol hexa(meth)acrylate ester, 1,4-butanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, polyethylene glycol di(meth)acrylate, dimethylol tricyclic Polyfunctional acrylates such as decane di(meth)acrylate, polyester oligo(meth)acrylate, urethane oligo(meth)acrylate, and the like.
對於活性能量線硬化型聚合物(A),調配活性能量線硬化性的單體及/或寡聚物(B)時,活性能量線硬化性黏著劑中的活性能量線硬化性的單體及/或寡聚物(B)的含量,相對於活性能量線硬化型聚合物(A)100質量份,以超過0質量份為佳,尤其以60質量份以上為佳。此外,該含量相對於活性能量線硬化型聚合物(A)100質量份,以250質量份以下為佳,尤其以200質量份以下為佳。For the active energy ray-curable polymer (A), when the active energy ray-curable monomer and/or oligomer (B) is formulated, the active energy ray-curable monomer and the active energy ray-curable adhesive in the active energy ray-curable adhesive The content of/or the oligomer (B) is preferably more than 0 parts by mass, particularly preferably 60 parts by mass or more, based on 100 parts by mass of the active energy ray-curable polymer (A). In addition, the content is preferably at most 250 parts by mass, particularly preferably at most 200 parts by mass, based on 100 parts by mass of the active energy ray-curable polymer (A).
接著,針對活性能量線硬化性黏著劑,以活性能量線非硬化性聚合物成分與具有至少1個以上的活性能量線硬化性基的單體及/或寡聚物的混合物當作主成分的情況,於以下進行說明。Next, for the active energy ray-curable adhesive, a mixture of an active energy ray non-curable polymer component and a monomer and/or oligomer having at least one active energy ray-curable group as a main component The situation is described below.
作為活性能量線非硬化性聚合物成分,例如,可使用與上述丙烯酸系共聚合物(a1)相同的成分。As the active energy ray non-curable polymer component, for example, the same component as the above-mentioned acrylic copolymer (a1) can be used.
作為具有至少1個以上的活性能量線硬化性基的單體及/或寡聚物,可選擇與上述成分(B)相同者。活性能量線非硬化性聚合物成分與具有至少1個以上的活性能量線硬化性基的單體及/或寡聚物的調配比,相對於活性能量線非硬化性聚合物成分100質量份,具有至少1個以上的活性能量線硬化性基的單體及/或寡聚物,以1質量份以上為佳,尤其以60質量份以上為佳。此外,該調配比,以相對於活性能量線非硬化性聚合物成分100質量份,具有至少1個以上的活性能量線硬化性基的單體及/或寡聚物,為200質量份以下為佳,尤其以160質量份以下為佳。As the monomer and/or oligomer having at least one active energy ray-curable group, the same ones as those for the above-mentioned component (B) can be selected. The compounding ratio of the active energy ray non-curable polymer component to the monomer and/or oligomer having at least one active energy ray-curable group is based on 100 parts by mass of the active energy ray non-curable polymer component, The monomer and/or oligomer having at least one active energy ray-curable group is preferably at least 1 part by mass, particularly preferably at least 60 parts by mass. In addition, the compounding ratio is 200 parts by mass or less of the monomer and/or oligomer having at least one active energy ray-curable group relative to 100 parts by mass of the active energy ray non-curable polymer component. Preferably, especially less than 160 parts by mass.
(3) 其他成分 上述黏著性組合物中,亦可調配適當的其他成分。作為其他成分,可列舉,例如,活性能量線非硬化性聚合物成分或寡聚物成分(D)、交聯劑(E)等。 (3) Other ingredients In the above-mentioned adhesive composition, other appropriate components can also be compounded. Examples of other components include active energy ray non-curable polymer components or oligomer components (D), crosslinking agents (E) and the like.
作為活性能量線非硬化性聚合物成分或寡聚物成分(D),可列舉,例如,聚丙烯酸酯、聚酯、聚氨酯、聚碳酸酯、聚烯烴等,以重量平均分子量(Mw)為3000~250萬的聚合物或寡聚物為佳。藉由將該成分(D)調配於能量線硬化性黏著劑中,可改善在硬化前的黏著性以及剝離性、硬化後的強度、與其他層的接著性、保存穩定性等。該成分(D)的調配量並未特別限定,相對於能量線硬化型共聚合物(A)100質量份,在超過0質量份,50質量份以下的範圍適當決定。As the active energy ray non-hardening polymer component or oligomer component (D), for example, polyacrylate, polyester, polyurethane, polycarbonate, polyolefin, etc., the weight average molecular weight (Mw) is 3000 ~2.5 million polymers or oligomers are preferred. By blending this component (D) into an energy ray-curable adhesive, the adhesiveness and peelability before curing, the strength after curing, the adhesiveness with other layers, the storage stability, and the like can be improved. The compounding quantity of this component (D) is not specifically limited, It is determined suitably within the range of more than 0 mass part and 50 mass parts or less with respect to 100 mass parts of energy ray hardening type copolymers (A).
從易於將界面燒蝕層11的儲存模數(storage modulus)調整至期望的範圍內的觀點而言,以使用交聯劑(E)為佳。作為交聯劑(E),可使用與活性能量線硬化型共聚合物(A)等所具有的官能基具有反應性的多官能性化合物。作為此種多官能性化合物的例子,可列舉,異氰酸酯化合物、環氧化合物、胺化合物、三聚氰胺化合物、氮丙啶(aziridine)化合物、肼(hydrazine)化合物、醛(aldehyde)化合物、噁唑啉化合物、金屬醇鹽(metal alkoxide)化合物、金屬螯合化合物、金屬鹽、銨鹽、反應性苯酚樹脂等。From the viewpoint of easy adjustment of the storage modulus of the
交聯劑(E)的調配量,相對於活性能量線硬化型共聚合物(A)100質量份,以0.001質量份以上為佳,尤其以0.1質量份以上為佳,進一步以0.2質量份以上為佳。此外,交聯劑(E)的調配量,相對於活性能量線硬化型共聚合物(A)100質量份,以20質量份以下為佳,尤其以10質量份以下為佳,進一步以5質量份以下為佳。The compounded amount of the crosslinking agent (E) is preferably at least 0.001 parts by mass, particularly preferably at least 0.1 parts by mass, and further preferably at least 0.2 parts by mass, based on 100 parts by mass of the active energy ray-curable copolymer (A). better. In addition, the compounded amount of the crosslinking agent (E) is preferably not more than 20 parts by mass, particularly preferably not more than 10 parts by mass, and further preferably not more than 5 parts by mass relative to 100 parts by mass of the active energy ray-curable copolymer (A). Servings or less are preferred.
此外,作為上述黏著性組合物中可調配的其他成分,可列舉,增黏劑、染料、顏料等的著色材料、阻燃劑、填料、抗靜電劑等的添加劑。且,上述黏著性組合物,從易於使工件小片的分離良好的發生的觀點而言,以不含有氣體產生劑為佳。當使用氣體產生劑時,會在界面燒蝕層11全區域產生氣體。此時,難以只在想要的位置使界面燒蝕發生,難以只有使位在該位置的工件小片分離,工件小片的分離無法良好地進行。In addition, examples of other components that can be formulated in the above-mentioned adhesive composition include additives such as thickeners, coloring materials such as dyes and pigments, flame retardants, fillers, and antistatic agents. In addition, it is preferable that the above-mentioned adhesive composition does not contain a gas generating agent from the viewpoint of making separation of the workpiece small pieces easy to occur favorably. When a gas generating agent is used, gas is generated in the entire area of the
(4) 界面燒蝕層的厚度
本實施形態中的界面燒蝕層11的厚度,以3μm以上為佳,尤其以20μm以上為佳,進一步以25μm以上為佳。此外,界面燒蝕層11的厚度,以100μm以下為佳,尤其以50μm以下為佳,進一步以40μm以下為佳。藉由界面燒蝕層11的厚度為上述範圍,變得易於兼顧在界面燒蝕層11上的工件小片的維持,及藉由界面燒蝕使工件小片分離。
(4) The thickness of the interface ablation layer
The thickness of the
2.基材
本實施形態中的基材12,針對其組成、物性並未特別限定。從易於發揮工件處理片1所期望的機能的觀點而言,基材12以由樹脂所構成為佳。當基材12為由樹脂所構成時,作為該樹脂的例子,可列舉,聚對苯二甲酸乙二酯、聚對苯二甲酸丁二酯、聚萘二甲酸乙二酯等的聚酯系樹脂;聚乙烯、聚丙烯、聚丁烯、聚丁二烯、聚甲基戊烯、乙烯-降莰烯(norbornene)共聚合物、降莰烯樹脂等的聚烯烴系樹脂;乙烯-乙酸乙烯酯共聚合物;乙烯-(甲基)丙烯酸共聚合物、乙烯-(甲基)丙烯酸甲酯共聚合物、其他的乙烯-(甲基)丙烯酸酯共聚合物等的乙烯系共聚合樹脂;聚氯乙烯、氯乙烯共聚合物等的聚氯乙烯系樹脂;(甲基)丙烯酸酯共聚合物;聚氨酯;聚醯亞胺;聚苯乙烯;聚碳酸酯;氟樹脂等。此外,構成基材12的樹脂,可以是將上述樹脂進行交聯者,也可以是上述樹脂的離子聚合物(ionomer)之類進行改質者。此外,基材12可以是由上述樹脂所形成的單層的膜,或者,將該膜積層複數層所形成的積層膜。在此積層膜中,構成各層的材料可以相同,也可相異。
2. Substrate
The composition and physical properties of the
本實施形態中的基材12的表面上,以提升對於界面燒蝕層11的密附性為目的,亦可實施氧化法、凹凸化法等的表面處理,或者底塗(primer)處理。作為上述氧化法,可列舉,例如,電暈放電處理、電漿放電處理、鉻酸化處理(濕式)、火焰處理、熱風處理、臭氧、紫外線照射處理等,此外,作為凹凸化法,可列舉,例如,噴砂法、熔噴處理法等。The surface of the
本實施形態中的基材12,亦可含有著色劑、阻燃劑、塑化劑、抗靜電劑、潤滑劑、填料等的各種添加劑。此外,界面燒蝕層11含有藉由活性能量線進行硬化的材料時,以基材12對於活性能量線具有穿透性為佳。The
本實施形態中的基材12的製造方法,只要是由樹脂製造基材12者即可,並未特別限定。例如,可藉由T模法、圓模法等的熔融擠出法;壓延法;乾式法、濕式法等的溶液法等,將樹脂成形為片材狀而製造。The manufacturing method of the
本實施形態中的基材12的厚度,以10μm以上為佳,尤其以30μm以上為佳,進一步以50μm以上為佳。此外,基材12厚度以500μm以下為佳,以300μm以下為更佳,尤其以200μm以下為佳,進一步以150μm以下為佳,以100μm以下為最佳。藉由基材12的厚度為上述範圍,工件處理片1成為以特定的平衡具備剛性及柔軟性者,而成為易於進行工件小片的良好的處理者。The thickness of the
3.剝離片
本實施形態中界面燒蝕層11含有黏著劑作為構成其的成分之一時,亦可在界面燒蝕層11中的與基材12相反側的面貼附至工件小片為止的期間,以保護該面為目的,在該面積層剝離片。
3. Peeling sheet
In this embodiment, when the
上述剝離片的構成可以是任意,可舉例,塑膠膜藉由剝離劑等實施剝離處理者。作為該塑膠膜的具體例,可列舉,聚對苯二甲酸乙二酯、聚對苯二甲酸丁二酯、聚萘二甲酸乙二酯等的聚酯膜,以及聚丙烯、聚乙烯等的聚烯烴膜。作為上述剝離劑,可使用矽酮系、氟系、長鏈烷系等,此等當中,以便宜且可獲得穩定性能的矽酮系為佳。The structure of the above-mentioned release sheet may be arbitrary, and for example, a plastic film is subjected to a release treatment with a release agent or the like. Specific examples of the plastic film include polyester films such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate, and polyester films such as polypropylene and polyethylene. Polyolefin film. As the release agent, silicone-based, fluorine-based, long-chain alkane-based, etc. can be used. Among them, silicone-based ones that are inexpensive and can provide stable performance are preferable.
關於上述剝離片的厚度並未特別限制,例如,可以是20μm以上,250μm以下。The thickness of the release sheet is not particularly limited, and may be, for example, not less than 20 μm and not more than 250 μm.
4.其他的構成
本實施形態相關的工件處理片1,亦可在界面燒蝕層11中的與基材12相反側的面積層接著劑層。該片材藉由在接著劑層中的與界面燒蝕層11相反側的面上貼附工件,切割該工件連同接著劑層,可獲得積層有經個片化的接著劑層的工件小片。該晶片透過此經個片化的接著劑層,變得容易固定在搭載有該工件小片的對象上。作為構成上述接著劑層的材料,以使用含有熱可塑性樹脂及低分子量的熱硬化性接著成分者、含有B階段(B stage,半硬化狀)的熱硬化型接著成分者等為佳等。
4. Other components
In the
此外,本實施形態相關的工件處理片1,亦可在界面燒蝕層11中的與基材12相反側的面上積層保護膜形成層。此類片材藉由將保護膜形成層中的與界面燒蝕層11相反側的面貼附至工件,切割該工件連同保護膜形成層,可獲得積層有經個片化的保護膜形成層的工件小片。作為該工件,以使用在單面形成有迴路者為佳,此時,通常會在與該形成有迴路的面相反側的面上積層保護膜形成層。經個片化的保護膜形成層,藉由在特定時機使其硬化,可將具有充分耐久性的保護膜形成於工件小片上。保護膜形成層以由未硬化的硬化性接著劑所形成為佳。In addition, in the
5.工件處理片的物性
本實施形態相關的工件處理片1,對於矽晶圓的鏡面的黏著力,以10mN/25mm以上為佳,尤其以100mN/25mm以上為佳,進一步以200mN/25mm以上為佳。藉由上述黏著力為10mN/25mm以上,變得易於在工件處理片1上良好地固定工件小片等的被附著物,成為操作性優異者。此外,上述黏著力以30000mN/25mm以下為佳,尤其以15000mN/25mm以下為佳,進一步以10000mN/25mm以下為佳。藉由上述黏著力為30000mN/25mm以下,變得易於良好地進行藉由雷射光照射使工件小片的分離。
5. Physical properties of the workpiece processing sheet
The
此外,本實施形態中的界面燒蝕層11為由上述活性能量線硬化性黏著劑所構成的黏著劑層時,關於在紫外線照射後的黏著力,以滿足以下條件為佳。換言之,將界面燒蝕層11中的與基材12相反側的面貼附於矽晶圓的鏡面上,對於界面燒蝕層11,使用高壓水銀燈,照射紫外線,使界面燒蝕層11硬化後,對於矽晶圓的鏡面的黏著力,以2000mN/25mm以下為佳,尤其以1000mN/25mm以下為佳,進一步以200mN/25mm以下為佳。藉由上述黏著力為2000mN/25mm以下,藉由隨後的界面燒蝕,變得易於良好地使工件小片分離。且,作為上述黏著力的下限值並未特別限定,例如,可以是5mN/25mm以上,尤其可以是10mN/25mm以上,再者可以是20mN/25mm以上。In addition, when the
且,此等黏著力的測定方法的詳細情況,如下述試驗例中所記載。In addition, the detail of the measuring method of these adhesive forces is as described in the following test example.
6.工件處理片的製造方法
本實施形態相關的工件處理片1的製造方法並未特別限定。例如,可在基材12上直接形成界面燒蝕層11,或者,製程片(processing sheet)上形成界面燒蝕層11後,將該界面燒蝕層11轉印至基材12上。
6. Manufacturing method of workpiece handling sheet
The method of manufacturing the
界面燒蝕層11含有黏著劑作為構成其的成分之一時,該界面燒蝕層11的形成,可藉由已知的方法進行。例如,調製含有用以形成界面燒蝕層11的黏著性組合物,以及根據需要的溶媒或分散媒的塗佈液。然後,在基材的單面或剝離片具有剝離性的面(以下,有時稱為「剝離面」)上,塗佈上述塗佈液。接著,藉由使所獲得的塗膜乾燥,可形成界面燒蝕層11。When the
上述塗佈液的塗佈可藉由已知的方法進行,例如,桿塗佈法、刀式塗佈法、輥塗佈法、翼片塗佈法、模具塗佈法、凹版塗佈法等進行。且,塗佈液只要是可進行塗佈,其性質並未特別限定,用以形成界面燒蝕層11的成分,有時作為溶質而含有,有時作為分散質而含有。此外,在剝離片上形成界面燒蝕層11時,該剝離片亦可作為製程材料進行剝離,亦可在貼附至被附著物為止的期間,保護界面燒蝕層11。Coating of the above-mentioned coating liquid can be performed by a known method, for example, a bar coating method, a knife coating method, a roll coating method, a blade coating method, a die coating method, a gravure coating method, etc. conduct. Further, the properties of the coating liquid are not particularly limited as long as it can be applied, and components for forming the
用以形成界面燒蝕層11的黏著性組合物含有上述交聯劑時,藉由改變上述乾燥的條件(溫度、時間等),或藉由額外設置加熱處理,使塗膜內的聚合物成分與交聯劑間的交聯反應進行,可在界面燒蝕層11內以期望的存在密度形成交聯構造為佳。再者,為了使上述交聯反應充分進行,工件處理片1的完成後,例如,亦可在23℃,相對溼度50%的環境中靜置數日期間,進行所謂的熟成。When the adhesive composition for forming the
7.工件處理片的使用方法
本實施形態相關的工件處理片1,可適合使用在工件小片的操作。如上述,本實施形態相關的工件處理片1,由於界面燒蝕層11為藉由雷射光的照射有效率地進行界面燒蝕者,維持在界面燒蝕層11上的工件小片,能夠以高精準度針對特定位置進行分離。
7. How to use the workpiece processing sheet
The
作為本實施形態相關的工件處理片1的使用方法的一例,可列舉,藉由使界面燒蝕層11局部地發生界面燒蝕,將維持在界面燒蝕層11中的與基材12相反的面上的複數個工件小片當中的任意的工件小片,從界面燒蝕層11選擇性地進行分離之類的使用方法。As an example of the method of using the
在上述使用方法中,維持在界面燒蝕層11上的複數個工件小片,可以是將維持在界面燒蝕層11中的與基材12相反的面上的工件(成為工件小片的材料者),在該面上進行個片化所獲得者。換言之,工件小片也可以是在界面燒蝕層11上將工件進行切割所獲得者。或者,工件小片也可以是將本實施形態相關的工件處理片1獨立地所形成者,而後載置於界面燒蝕層11上者。In the above method of use, the plurality of workpiece small pieces maintained on the
且,本實施形態相關的工件處理片1具備上述接著劑層、保護膜形成層時,以將此等的層與工件在界面燒蝕層11上進行切割為佳。如此一來,可獲得積層有此等的層經個片化而成者的工件小片。Furthermore, when the
雖然關於本實施形態中的工件小片的形狀、尺寸並未特別限定,然而,關於尺寸,工件小片以平視時的面積為10μm
2以上為佳,尤其以100μm
2以上為佳。此外,工件小片以平視時的面積為1mm
2以下為佳,尤其以0.25mm
2以下為佳。此外,作為工件小片的維度,當工件小片為矩形時,以工件小片的最小的一邊為2μm以上為佳,尤其以5μm以上為佳,進一步以10μm以上為佳。此外,以上述最小的一邊為1mm以下為佳,尤其以0.5mm以下為佳。作為矩形的工件小片的維度的具體例,可列舉,2μm×5μm、10μm×10μm、0.5mm×0.5mm、1mm×1mm等。本實施形態相關的工件處理片1,此類微小的工件小片,尤其是即使是不易從如針尖般的片材的分離的微小的工件小片,仍可良好地操作。另一方面,本實施形態相關的工件處理片1,針對面積超過1mm
2者(例如,1mm
2~2000mm
2)、厚度為1~10000μm者(例如,10~1000μm)之類尺寸比較大的工件小片,仍可良好地操作。
Although the shape and size of the workpiece piece in this embodiment are not particularly limited, the size of the workpiece piece is preferably 10 μm 2 or more in plan view, especially 100 μm 2 or more. In addition, the area of the small piece of workpiece is preferably less than 1mm 2 , especially less than 0.25mm 2 . In addition, as the dimensions of the workpiece piece, when the workpiece piece is rectangular, the smallest side of the workpiece piece is preferably 2 μm or more, especially 5 μm or more, and further preferably 10 μm or more. In addition, the above-mentioned smallest side is preferably 1 mm or less, especially preferably 0.5 mm or less. Specific examples of the dimensions of the rectangular workpiece piece include 2 μm×5 μm, 10 μm×10 μm, 0.5 mm×0.5 mm, 1 mm×1 mm, and the like. The
作為工件小片,可列舉,半導體組件、半導體裝置等,更具體而言,可列舉,微發光二極體、功率元件、MEMS(Micro Electro Mechanical Systems)等。此等當中,以工件小片為發光二極體為合適,尤其以選自迷你發光二極體以及微發光二極體的發光二極體為佳。近年來,研究以高密度配置有迷你發光二極體、微發光二極體的裝置的開發,在此類裝置的製造中,非常適合能夠以高精準度操作此等發光二極體的本實施形態相關的工件處理片1。Examples of workpiece chips include semiconductor modules, semiconductor devices, and more specifically, micro light emitting diodes, power elements, MEMS (Micro Electro Mechanical Systems), and the like. Among them, it is suitable for the workpiece small pieces to be light emitting diodes, especially light emitting diodes selected from mini light emitting diodes and micro light emitting diodes. In recent years, research has been conducted on the development of devices in which miniature light-emitting diodes and micro-light-emitting diodes are arranged at a high density. In the manufacture of such devices, it is very suitable for this implementation that can operate these light-emitting diodes with high precision. Morphology-related
以下,作為工件處理片1的具體使用例,裝置製造方法根據圖2加以說明。該裝置製造方法至少具備:準備步驟(圖2(a))、配置步驟(圖2(b))以及分離步驟(圖2(c)以及(d))等的3個步驟。Hereinafter, as a specific usage example of the
在準備步驟中,如圖2(a)所示,在本實施形態相關的工件處理片1中,準備一在界面燒蝕層11側的面上維持有複數個工件小片2而成的積層體。該積層體可藉由將另外製作的工件小片2載置於工件處理片1上而準備,或者,亦可將維持在界面燒蝕層11側的面上的工件在該面上進行個片化(亦即,進行切割)而準備。該切割可藉由已知的方法進行。In the preparatory step, as shown in FIG. 2(a), in the
工件小片2的形狀、尺寸如上述,並未特別限定,較佳尺寸亦如上述。關於工件小片2的具體例,亦如上述,可列舉,半導體組件、半導體裝置等,尤其是可列舉,迷你發光二極體以及微發光二極體之類的發光二極體。The shape and size of the
在接續的配置步驟中,如圖2(b)所示,對於可容納工件小片2的對象物3,以面向上述積層體中的工件小片2側的面的方式配置上述積層體。對象物3的例子,雖然是對應製造的裝置而適當決定,但以工件小片2為發光二極體而言,作為對象物3的具體例,可列舉,基板、片材、捲盤(reel)等,尤其適合設置有配線的配線基板。In the subsequent arranging step, as shown in FIG. 2( b ), the laminate is arranged so as to face the surface of the laminate on the workpiece
之後,在分離步驟中,首先,如圖2(c)所示,在上述積層體中的界面燒蝕層11,對於貼附有至少1個工件小片2的位置,照射雷射光。該照射亦可對於貼附有工件小片2的複數個位置同時進行,或者對於此等位置依序進行。作為雷射光的照射條件,只要能夠使界面燒蝕發生並未限定。作為用以照射的裝置,可使用已知者。After that, in the separation step, first, as shown in FIG. 2( c ), the
藉由上述照射,如圖2(d)所示,可以在界面燒蝕層11中被照射的位置上使界面燒蝕發生。具體而言,藉由雷射光的照射,在界面燒蝕層11中靠近基材12的區域,構成該區域的成分蒸發或揮發,成為反應區域13。然後,藉由上述蒸發或揮發所產生的氣體滯留在基材11與反應區域13之間,形成膨泡5。藉由該膨泡5的形成,在工件小片2’的位置,局部的界面燒蝕層11變形,以從界面燒蝕層11剝落的方式,將工件小片2’進行分離。藉由以上,可將存在於該界面燒蝕發生位置的工件小片2’載置於對象物3。By the above irradiation, as shown in FIG. 2( d ), interface ablation can occur at the irradiated position in the
且,藉由雷射光的照射所產生的反應區域13以及膨泡5,通常在工件小片2’的分離後仍然殘存。圖3中,顯示依序照射雷射光進行工件小片2的分離的狀態,尤其是顯示分離後的狀態(左側2個),分離中的狀態(中央),以及分離前的狀態(右側2個)。如圖示,通常,分離後的膨泡5,相較於分離中的膨泡5,呈現稍微洩氣的狀態。Moreover, the
且,本實施形態中的界面燒蝕層11,為上述由活性能量線硬化性黏著劑所構成的黏著劑層時,上述裝置製造方法亦可具備接下來的硬化步驟。換言之,亦可具備藉由對於由維持在界面燒蝕層11側的面上的複數個工件小片2而成的積層體中的界面燒蝕層11的全體,或對於上述積層體中的界面燒蝕層11中的貼附有至少1個工件小片2的位置,照射活性能量線,使界面燒蝕層11全體或局部地硬化的硬化步驟。此硬化步驟可在上述分離步驟之前進行,或亦可與上述分離步驟同時進行。In addition, when the
如上述,藉由活性能量線的照射,使界面燒蝕層11全體或局部硬化,可以使工件處理片1中對於工件小片2的黏著力降低,在界面燒蝕發生時,易於良好地將工件小片2分離。在硬化步驟中的活性能量線的照射,可使用已知的手法進行,例如,使用具備作為光源的高壓水銀燈、紫外線LED的紫外線照射裝置,在分離步驟亦可使用的雷射光照射裝置。同時進行硬化步驟及分離步驟時,以將使用雷射光照射裝置的雷射光4的照射,兼作為活性能量線的照射進行為佳。As mentioned above, the whole or part of the
上述裝置製造方法,亦可具備準備步驟、配置步驟、硬化步驟以及分離步驟以外的步驟。例如,在準備步驟及分離步驟之間的任意時間點,亦可進行磨光(grind)、固晶(die bonding)、打線(wire bonding)、成型(molding)、檢測(examination)、轉印(transfer)步驟。The above device manufacturing method may include steps other than the preparation step, arrangement step, hardening step, and separation step. For example, at any point in time between the preparation step and the separation step, grinding, die bonding, wire bonding, molding, examination, transfer ( transfer) steps.
根據以上說明的裝置製造方法,藉由適當選擇所使用的工件小片2、對象物3,可製造各種裝置。例如,作為工件小片2,使用選自迷你發光二極體以及微發光二極體的發光二極體時,可製造具備複數個此種發光二極體的發光裝置,更具體而言,可製造顯示器。尤其是,可製造具備微發光二極體當作畫素的顯示器、具備複數個迷你發光二極體作為背光的顯示器。According to the device manufacturing method described above, various devices can be manufactured by appropriately selecting the
此外,本實施形態相關的工件處理片1,亦可使用在設置在該片材上的複數個工件小片2當中,選擇性去除特定的工件小片2的方法中。In addition, the
例如,在本實施形態相關的工件處理片1上製造複數個發光二極體等後,在該片材上進行發光二極體的檢測。可在該處僅針對被確認為不良品的發光二極體,使界面燒蝕發生而從工件處理片1予以脫離而去除。For example, after manufacturing a plurality of light-emitting diodes and the like on the
再者,可將此等良品的集合,從工件處理片1轉印至運送用片材。此時,界面燒蝕層11為由上述活性能量線硬化性黏著劑所構成時,藉由對於該界面燒蝕層11照射活性能量線,使工件處理片1對於發光二極體的黏著力降低,可良好地將良品的集合轉印至運送用片材。之後,藉由在不良品被去除的位置上,再配置另外製作的良品,可獲得僅設置有良品的工件處理片1。Furthermore, a collection of such good products can be transferred from the
如上述,藉由界面燒蝕去除不良品的方法,由於沒有必要進行片材的延展以及不良品的撿拾,不易發生發光二極體的間隔的改變、位置的偏移。因此,成為易於對於運送用片材進行轉印者。As mentioned above, in the method of removing defective products by interface ablation, since there is no need to stretch the sheet and pick up defective products, it is not easy to change the spacing of the light emitting diodes and shift the position. Therefore, it becomes easy to transfer to the sheet|seat for conveyance.
以上說明的實施形態,為用以易於理解本發明所記載者,並非用以限定本發明所記載。因此,上述實施形態所揭示的各元件,其主旨包括本發明所屬技術領域中所有的設計變更、均等物。The embodiments described above are described for easy understanding of the present invention, and are not described for limiting the present invention. Therefore, the gist of each element disclosed in the above embodiments includes all design changes and equivalents in the technical field to which the present invention pertains.
例如,在本實施形態相關的工件處理片1中的界面燒蝕層11與基材12之間,或在基材12中的與界面燒蝕層11相反側的面上,亦可積層其他的層。作為該其他的層的具體例,可列舉,黏著劑層。此時,能夠以將該黏著劑層側的面貼附在支撐台(玻璃板等的透明基板)上的狀態,進行上述分離步驟等。For example, between the
作為構成上述黏著劑層的黏著劑,並未特別限定,但以不易吸收活性能量線且不遮蔽活性能量線者為佳。此時,隔著該黏著劑層,照射雷射光時,該雷射光易於到達界面燒蝕層11,可良好地使界面燒蝕發生。具體而言,作為構成上述黏著劑層的黏著劑,以使用不具有活性能量線硬化性的黏著劑為佳,尤其是以使用不含有活性能量線硬化性成分的黏著劑為佳。藉由使用不具有活性能量線硬化性的黏著劑,即使是照射上述雷射光的場合,上述黏著劑層不會硬化,如此一來,變得可防止來自透明基板的工件處理片1非意圖的剝離。作為上述黏著劑層的厚度,雖然並未特別限定,但例如,以5~50μm為佳。
[實施例]
The adhesive constituting the adhesive layer is not particularly limited, but is preferably one that does not easily absorb active energy rays and does not shield active energy rays. At this time, when the laser light is irradiated through the adhesive layer, the laser light easily reaches the
以下,雖然藉由實施例等進一步具體說明本發明,但本發明的範圍並不限定於此等實施例等。Hereinafter, although an Example etc. demonstrate this invention more concretely, the scope of the present invention is not limited to these Examples etc.
[實施例1] (1) 黏著性組合物的調製 使丙烯酸2-乙基己酯70質量份,與丙烯酸2-羥乙酯30質量份藉由溶劑聚合法使其聚合,獲得(甲基)丙烯酸酯聚合物。對於此(甲基)丙烯酸酯聚合物,使其與相對於此丙烯酸2-羥乙酯90莫耳%的異氰酸甲基丙烯醯氧乙基酯(MOI)反應,獲得在側鏈上導入有活性能量線硬化性基的(甲基)丙烯酸酯共聚合物(活性能量線硬化型聚合物(A))。此活性能量線硬化型聚合物(A)的重量平均分子量(Mw)藉由上述方法進行測定,為80萬。 [Example 1] (1) Preparation of adhesive composition 70 mass parts of 2-ethylhexyl acrylate and 30 mass parts of 2-hydroxyethyl acrylate were polymerized by the solvent polymerization method, and the (meth)acrylate polymer was obtained. For this (meth)acrylate polymer, react it with 90 mole % of methacryloxyethyl isocyanate (MOI) relative to the 2-hydroxyethyl acrylate to obtain A (meth)acrylate copolymer having an active energy ray-curable group (active energy ray-curable polymer (A)). The weight average molecular weight (Mw) of this active energy ray curable polymer (A) was measured by the above-mentioned method, and it was 800,000.
將如上述所獲得的活性能量線硬化型聚合物(A)100質量份(固形分換算,以下相同),與作為交聯劑的三羥甲基丙烷改質甲伸苯基二異氰酸酯(東曹股份有限公司製,商品名「Coronate L」)2.5質量份,與作為光聚合起始劑的乙酮,1-[9-乙基-6-(2-甲基苯甲醯基)-9H-咔唑-3基]-,1-(0-乙醯肟)(BASF公司製,製品名「Irugacure OXE02」)4質量份,在溶媒中混合,獲得固形分濃度為30質量%的黏著性組合物的塗佈液。100 parts by mass (in terms of solid content, the same below) of the active energy ray-curable polymer (A) obtained above was mixed with trimethylolpropane-modified methylene diisocyanate (Tosoh Co., Ltd., trade name "Coronate L") 2.5 parts by mass, and ethyl ketone as a photopolymerization initiator, 1-[9-ethyl-6-(2-methylbenzoyl)-9H- Carbazole-3-yl]-, 1-(O-acetyloxime) (manufactured by BASF Corporation, product name "Irugacure OXE02") 4 parts by mass were mixed in a solvent to obtain an adhesive composition with a solid content concentration of 30% by mass Coating solution for objects.
(2) 工件處理片的製作 對於作為基材的單面經易接著處理的聚對苯二甲酸乙二酯膜(東洋紡製,製品名「COSMOSHINE A4100」,厚度:50μm)中的易接著處理面,塗佈上述步驟(1)所獲得的黏著性組合物的塗佈液,藉由加熱所獲得的塗膜使其乾燥。如此一來,在基材上形成厚度30μm的界面燒蝕層(黏著劑層)。 (2) Production of workpiece handling sheet On the easy-adhesive side of a polyethylene terephthalate film (manufactured by Toyobo Co., Ltd., product name "COSMOSHINE A4100", thickness: 50 μm) that has been easily-adhesively treated on one side as a base material, apply the above-mentioned step (1) The obtained coating liquid of the adhesive composition is dried by heating the obtained coating film. In this way, an interface ablation layer (adhesive layer) with a thickness of 30 μm was formed on the substrate.
接著,將界面燒蝕層中的與基材相反的面側,與厚度38μm的聚對苯二甲酸乙二酯膜的單面上由矽酮系的剝離劑層形成的剝離片(LINTEC Corporation製,製品名「SP-PET381031」)的剝離面貼合。如此一來,獲得由依序積層剝離片、界面燒蝕層以及基材而成的工件處理片。Next, a release sheet (manufactured by LINTEC Corporation) formed of a silicone-based release agent layer was placed on the side of the interface ablation layer opposite to the substrate, and one side of a polyethylene terephthalate film with a thickness of 38 μm. , product name "SP-PET381031") peeling side bonding. In this way, the workpiece processing sheet is obtained by sequentially laminating the release sheet, the interface ablation layer and the base material.
(3) 重量平均分子量的測定方法 上述重量平均分子量(Mw)為使用凝膠滲透層析儀(GPC),根據以下的條件所測定(GPC測定)的換算標準聚苯乙烯的重量平均分子量。 <測定條件> .測定裝置:東曹股份有限公司製,HLC-8320 .GPC管柱(依以下的順序通過):東曹股份有限公司製 TSK gel super H-H TSK gel super HM-H TSK gel super H2000 .測定溶媒:四氫呋喃 .測定溫度:40℃。 (3) Determination method of weight average molecular weight The said weight average molecular weight (Mw) is the weight average molecular weight of the conversion standard polystyrene measured (GPC measurement) under the following conditions using the gel permeation chromatography (GPC). <Measurement conditions> . Measuring device: Tosoh Co., Ltd., HLC-8320 . GPC column (pass through in the following order): manufactured by Tosoh Co., Ltd. TSK gel super H-H TSK gel super HM-H TSK gel super H2000 . Determination of solvent: tetrahydrofuran . Measurement temperature: 40°C.
[實施例2~3以及比較例1~3] 將光聚合起始劑的種類及含量變更如表1所示以外,其餘與實施例1同樣地製造工件處理片。且,比較例1為未使用光聚合起始劑的例子。 [Examples 2-3 and Comparative Examples 1-3] Except having changed the kind and content of a photoinitiator as shown in Table 1, it carried out similarly to Example 1, and manufactured the workpiece processing sheet. In addition, Comparative Example 1 is an example in which no photopolymerization initiator was used.
[試驗例1](紫外線吸光度的測定) 從在實施例以及比較例所製造的工件處理片將剝離片加以剝離,使界面燒蝕層露出。針對此工件處理片,使用紫外線.可見光.近紅外分光光度計(島津製作所公司製,製品名「UV-3600」)以及附屬的大型樣品艙(島津製作所公司製,製品名「MPC-3100」),測定紫外線吸光度。該測定為藉由使用上述大型樣品艙中內建的積分球,以狹縫寬度20nm,將波長355nm的光線面對界面燒蝕層側的面照射而進行。結果如表1所示。 [Test Example 1] (Measurement of Ultraviolet Absorbance) The release sheet was peeled off from the workpiece processing sheets produced in the examples and comparative examples to expose the interface ablation layer. For this workpiece treatment sheet, use ultraviolet light. Visible light. The ultraviolet absorbance was measured with a near-infrared spectrophotometer (manufactured by Shimadzu Corporation, product name "UV-3600") and an attached large sample chamber (manufactured by Shimadzu Corporation, product name "MPC-3100"). This measurement was carried out by irradiating the surface of the interface ablation layer side with light having a wavelength of 355 nm with a slit width of 20 nm using the integrating sphere built in the above-mentioned large sample chamber. The results are shown in Table 1.
[試驗例2](黏著力的測定) 在實施例以及比較例所製造的工件處理片,裁斷成25mm寬的短條狀。從所得的短條狀的工件處理片將剝離片剝離,將所露出的界面燒蝕層的露出面,對於進行鏡面加工而成的矽晶圓的該鏡面(mirror surface),在溫度23℃,相對溼度50%的環境下,使用2kg橡膠滾輪(rubber roller)進行貼附,靜置20分鐘,作為黏著力測定用樣品。 [Test Example 2] (Measurement of Adhesive Force) The workpiece processing sheets manufactured in Examples and Comparative Examples were cut into short strips with a width of 25 mm. The peeling sheet was peeled off from the obtained strip-shaped workpiece processing sheet, and the exposed surface of the exposed interface ablation layer was subjected to a temperature of 23° C. In an environment with a relative humidity of 50%, use a 2kg rubber roller (rubber roller) for attachment, and let it stand for 20 minutes as a sample for adhesion measurement.
之後,使用萬能拉伸試驗機(ORIENTEC Corporation製,製品名「TENSILON UTM-4-100」),從矽晶圓,以剝離速度300mm/min,剝離角度180°將工件處理片剝離,藉由以JIS Z0237:2009為準則的180°拉剝法,測定對於矽晶圓的鏡面的黏著力(mN/25mm)。其結果作為紫外線照射前的黏著力表示於表1中。Thereafter, using a universal tensile testing machine (manufactured by ORIENTEC Corporation, product name "TENSILON UTM-4-100"), the workpiece handling sheet was peeled from the silicon wafer at a peeling speed of 300 mm/min and a peeling angle of 180°. JIS Z0237:2009 is the standard 180° peeling method to measure the adhesion (mN/25mm) to the mirror surface of the silicon wafer. The results are shown in Table 1 as the adhesive force before ultraviolet irradiation.
此外,對於與上述同樣所獲得的黏著力測定用樣品中的界面燒蝕層,隔著基材,使用具備作為光源的高壓水銀燈的紫外線照射裝置(LINTEC Corporation製,製品名「RAD-2000」),照射紫外線(照度:230mW/cm 2,光量:190mJ/cm 2),使界面燒蝕層硬化。針對此紫外線照射後的黏著力測定用樣品,與上述同樣地測定對於矽晶圓的鏡面的黏著力(mN/25mm)。此結果作為紫外線照射後的黏著力表示於表1中。 In addition, for the interface ablation layer in the sample for adhesion measurement obtained in the same manner as above, an ultraviolet irradiation device (manufactured by LINTEC Corporation, product name "RAD-2000") equipped with a high-pressure mercury lamp as a light source was used through the substrate. , and irradiate ultraviolet rays (illuminance: 230mW/cm 2 , light intensity: 190mJ/cm 2 ) to harden the interface ablation layer. The adhesive force (mN/25mm) to the mirror surface of a silicon wafer was measured similarly to the above about the sample for adhesive force measurement after this ultraviolet-ray irradiation. The results are shown in Table 1 as adhesive force after ultraviolet irradiation.
[試驗例3](雷射剝離適合性的評價) (1) 工件處理片上的晶片的準備(準備步驟) 在矽晶圓(#2000,厚度:350μm)的單面,貼附切割片(LINTEC Corporation製,製品名「D-485H」)的黏著面。接著,在該切割片上的上述黏著面的周緣部位(未與矽晶圓重疊的位置),附著切割用環形框架。進一步,配合環形框架的外徑將切割片裁斷。之後,使用切割裝置(Disco Corporation製,製品名「DFD6362」),將矽晶圓切割成具有300μm×300μm的尺寸的晶片。之後,對於切割片,照射紫外線(照度230mW/cm 2,光量190mJ/cm 2),如此一來,獲得在切割片上設置有複數個晶片而成的積層體。 [Test Example 3] (Evaluation of suitability for laser peeling) (1) Preparation of wafer on workpiece handling sheet (preparation step) On one side of a silicon wafer (#2000, thickness: 350 μm), a dicing sheet (LINTEC Corporation, product name "D-485H") adhesive surface. Next, a ring frame for dicing is attached to the peripheral portion (the position not overlapping the silicon wafer) of the above-mentioned adhesive surface on the dicing sheet. Further, the cutting pieces are cut according to the outer diameter of the ring frame. Thereafter, the silicon wafer was diced into wafers having a size of 300 μm×300 μm using a dicing device (manufactured by Disco Corporation, product name “DFD6362”). Thereafter, ultraviolet rays (illuminance: 230 mW/cm 2 , light intensity: 190 mJ/cm 2 ) were irradiated on the dicing sheet to obtain a laminate in which a plurality of wafers were placed on the dicing sheet.
接著,從在實施例以及比較例所製造的工件處理片將剝離片剝離,將藉此所露出的露出面,與如上述所獲得的積層體中有複數個晶片存在的面貼合。之後,從複數個晶片將切割片剝離。如此一來,將複數個晶片從切割片轉印至工件處理片,獲得在工件處理片上設置有複數個晶片而成的積層體。Next, the peeling sheet was peeled off from the workpiece handling sheets produced in Examples and Comparative Examples, and the exposed surface exposed by this was bonded to the surface of the laminate obtained above where a plurality of wafers existed. Thereafter, the diced sheets are peeled off from the plurality of wafers. In this way, the plurality of wafers are transferred from the dicing sheet to the workpiece processing sheet, and a laminate in which the plurality of wafers are provided on the workpiece processing sheet is obtained.
(2) 藉由雷射光照射的晶片的分離(分離步驟) 針對在上述步驟(1)所獲得的在工件處理片上設置複數個晶片而成的積層體,使用雷射光照射裝置,穿過工件處理片對晶片照射雷射光。 (2) Separation of wafers irradiated with laser light (separation step) With respect to the laminate obtained in the above step (1) in which a plurality of wafers are placed on a workpiece processing sheet, a laser light irradiation device is used to irradiate the wafer with laser light through the workpiece processing sheet.
具體而言,使用雷射光照射裝置(KEYENCE Corporation製,製品名「MD-U1000C」),穿過工件處理片,對於晶片照射波長355nm的雷射光。該照射為對於晶片中央,將雷射光點以劃圓的方式依序照射而進行。此時,以雷射光點的直徑為25μm,作為照射的軌跡所產生的環形的內徑為65μm的方式進行。作為其他照射條件,頻率:40kHz,掃描速度:500mm/s,照射量:50μJ/shot。此外,照射為從複數個晶片當中選擇100個晶片(縱10個×橫10個的晶片的總數),對此進行。Specifically, using a laser light irradiation device (manufactured by KEYENCE Corporation, product name "MD-U1000C"), the wafer was irradiated with laser light having a wavelength of 355 nm through the workpiece processing sheet. This irradiation is performed by sequentially irradiating laser spots in a circle to the center of the wafer. At this time, the diameter of the laser spot was 25 μm, and the inner diameter of the ring formed as the trajectory of irradiation was 65 μm. As other irradiation conditions, frequency: 40 kHz, scanning speed: 500 mm/s, irradiation amount: 50 μJ/shot. In addition, irradiation was performed by selecting 100 wafers (total number of 10 vertically x 10 horizontally) from among a plurality of wafers.
(3) 膨泡以及晶片分離的確認 針對進行以上照射的工件處理片以及晶片,確認在工件處理片中的基材與界面燒蝕層的界面上有無膨泡的發生,以及有無從工件處理片的晶片的脫離,根據以下的基準,評價雷射剝離適合性。結果如表1所示。 ◎…在100個全部晶片的位置上發生膨泡,且,100個全部晶片脫離。 ○…膨泡的發生以及產生脫離的晶片的數目為80個以上,未達100個。 ×…膨泡的發生以及產生脫離的晶片的數目未達80個。 (3) Confirmation of foaming and wafer separation For the workpiece processing sheet and the wafer subjected to the above irradiation, it was confirmed whether there is bubble generation at the interface between the base material and the interface ablation layer in the workpiece processing sheet, and whether there is detachment of the wafer from the workpiece processing sheet, according to the following criteria, Evaluation of suitability for laser ablation. The results are shown in Table 1. ◎...Bubbles occurred at the positions of all 100 wafers, and all 100 wafers were detached. ◯...The number of wafers in which bubbles occurred and detachment occurred was 80 or more and less than 100. ×...The number of wafers in which bubbles occurred and detachment occurred was less than 80 pieces.
且,表1中所記載的簡稱等的詳情如以下。 IrugacureOXE02:乙酮,1-[9-乙基-6-(2-甲基苯甲醯基)-9H-咔唑-3-基]-,1-(0-乙醯肟)(BASF公司製,製品名「IrugacureOXE02」) Omnirad379:2-二甲基胺基-2-(4-甲基苯甲基)-1-(4-嗎啉基-苯基)丁烷-1-酮(IGM Resins公司製,製品名「Omnirad379」) Omnirad651:2,2-二甲氧基-1,2-二苯乙烷-1-酮(IGM Resins公司製,製品名「Omnirad651」) In addition, details such as the abbreviations described in Table 1 are as follows. IrugacureOXE02: Ethanone, 1-[9-ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]-, 1-(0-acetyloxime) (manufactured by BASF Corporation , product name "IrugacureOXE02") Omnirad379: 2-Dimethylamino-2-(4-methylbenzyl)-1-(4-morpholino-phenyl)butan-1-one (manufactured by IGM Resins, product name "Omnirad379 」) Omnirad651: 2,2-dimethoxy-1,2-diphenylethane-1-one (manufactured by IGM Resins, product name "Omnirad651")
[表1]
由表1可清楚得知,實施例所製造的工件處理片,其雷射剝離適合性優異。 [產業利用性] It can be clearly seen from Table 1 that the workpiece processing sheets manufactured in the examples have excellent suitability for laser stripping. [Industrial Utilization]
本發明的工件處理片,可適當使用在具備微發光二極體作為畫素的顯示器等的製造中。The workpiece processing sheet of the present invention can be suitably used in the manufacture of displays and the like having micro light emitting diodes as pixels.
1:工件處理片
11:界面燒蝕層
12:基材
13:反應區域
2,2’:工件小片
3:對象物
4:雷射光
5:膨泡
6:雷射光照射點
1: Workpiece handling sheet
11: Interface ablation layer
12: Substrate
13:
[圖1] 為本發明的一實施形態相關的工件處理片的剖面圖。 [圖2] 為說明使用本發明一實施形態相關的工件處理片的裝置製造方法的剖面圖。 [圖3] 為說明藉由雷射光的照射所產生的膨泡以及反應區域的狀態的剖面圖。 [ Fig. 1 ] is a cross-sectional view of a workpiece processing sheet according to an embodiment of the present invention. [ Fig. 2] Fig. 2 is a cross-sectional view illustrating a method of manufacturing a device using a workpiece processing sheet according to an embodiment of the present invention. [FIG. 3] It is a cross-sectional view explaining the state of the bubble and reaction area which generate|occur|produce by irradiation of laser light.
1:工件處理片 1: Workpiece handling sheet
11:界面燒蝕層 11: Interface ablation layer
12:基材 12: Substrate
Claims (16)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2021-053427 | 2021-03-26 | ||
JP2021053427 | 2021-03-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW202239036A true TW202239036A (en) | 2022-10-01 |
Family
ID=83396741
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW111101970A TW202239036A (en) | 2021-03-26 | 2022-01-18 | Workpiece handling sheet and device manufacturing method |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP7325634B2 (en) |
KR (1) | KR20230161411A (en) |
CN (1) | CN116368003A (en) |
TW (1) | TW202239036A (en) |
WO (1) | WO2022201766A1 (en) |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5444798B2 (en) | 2009-04-10 | 2014-03-19 | ソニー株式会社 | Device transfer method |
KR101963420B1 (en) | 2011-04-11 | 2019-03-28 | 엔디에스유 리서치 파운데이션 | Selective laser-assisted transfer of discrete components |
WO2016183845A1 (en) | 2015-05-21 | 2016-11-24 | Goertek.Inc | Transferring method, manufacturing method, device and electronic apparatus of micro-led |
KR20240130146A (en) * | 2017-06-12 | 2024-08-28 | 쿨리케 & 소파 네덜란드 비.브이. | Parallel assembly of discrete components onto a substrate |
WO2019207920A1 (en) * | 2018-04-26 | 2019-10-31 | Jsr株式会社 | Mounting method and mounting device for semiconductor elements |
JP2021024991A (en) | 2019-08-08 | 2021-02-22 | 日東電工株式会社 | Detachment method of adherend and adhesive composition |
-
2022
- 2022-01-13 WO PCT/JP2022/000964 patent/WO2022201766A1/en active Application Filing
- 2022-01-13 CN CN202280007251.5A patent/CN116368003A/en active Pending
- 2022-01-13 KR KR1020237005270A patent/KR20230161411A/en active Search and Examination
- 2022-01-13 JP JP2022530951A patent/JP7325634B2/en active Active
- 2022-01-18 TW TW111101970A patent/TW202239036A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CN116368003A (en) | 2023-06-30 |
KR20230161411A (en) | 2023-11-27 |
JP7325634B2 (en) | 2023-08-14 |
WO2022201766A1 (en) | 2022-09-29 |
JPWO2022201766A1 (en) | 2022-09-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3784202B2 (en) | Double-sided adhesive sheet and method of using the same | |
JP5603757B2 (en) | Laser dicing adhesive sheet and method for manufacturing semiconductor device | |
JP5901422B2 (en) | Semiconductor wafer dicing method and semiconductor processing dicing tape used therefor | |
JP5607847B1 (en) | Adhesive tape for semiconductor processing | |
JP5379919B1 (en) | Adhesive tape for semiconductor processing | |
TWI494226B (en) | Adhesive tape for semiconductor wafer protection | |
WO2015132852A1 (en) | Adhesive tape for semiconductor processing | |
CN109937469A (en) | Mask material for plasma dicing, mask-integrated surface protection tape, and manufacturing method of semiconductor chip | |
JP2014082344A (en) | Adhesive tape for semiconductor processing | |
TW201729276A (en) | Mask-integrated surface protection tape | |
US20240274460A1 (en) | Back grinding adhesive film and method for manufacturing electronic device | |
JP7325403B2 (en) | Work processing sheet | |
US20240258172A1 (en) | Method for manufacturing electronic device | |
TW202239036A (en) | Workpiece handling sheet and device manufacturing method | |
JP2007250790A (en) | Manufacturing method of semiconductor chip | |
TW202302346A (en) | Workpiece handling sheet and device manufacturing method | |
US20240258150A1 (en) | Method for manufacturing electronic device | |
US20240258152A1 (en) | Method for manufacturing electronic device | |
TW202239021A (en) | Workpiece handling sheet and device manufacturing method | |
US20240379403A1 (en) | Back grinding adhesive film and method for manufacturing electronic device | |
US20240249967A1 (en) | Method for manufacturing electronic device | |
JP7588226B2 (en) | Manufacturing method of electronic device | |
US20240266203A1 (en) | Method for manufacturing electronic device | |
US20240290648A1 (en) | Back grinding adhesive film and method for manufacturing electronic device | |
TW202244239A (en) | Workpiece handling sheet, method for handling small workpiece item, device manufacturing method, and use of workpiece handling sheet |