JPH01171232A - Semiconductor device - Google Patents
Semiconductor deviceInfo
- Publication number
- JPH01171232A JPH01171232A JP62331845A JP33184587A JPH01171232A JP H01171232 A JPH01171232 A JP H01171232A JP 62331845 A JP62331845 A JP 62331845A JP 33184587 A JP33184587 A JP 33184587A JP H01171232 A JPH01171232 A JP H01171232A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- semiconductor device
- resin
- bond pad
- die bond
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000004065 semiconductor Substances 0.000 title claims abstract description 42
- 239000003822 epoxy resin Substances 0.000 claims abstract description 42
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 41
- 239000005011 phenolic resin Substances 0.000 claims abstract description 23
- 239000004642 Polyimide Substances 0.000 claims abstract description 18
- 239000000203 mixture Substances 0.000 claims abstract description 18
- 229920001721 polyimide Polymers 0.000 claims abstract description 18
- 239000011256 inorganic filler Substances 0.000 claims abstract description 5
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 5
- 229920001568 phenolic resin Polymers 0.000 claims description 12
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 10
- 239000000945 filler Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims 2
- 229920005989 resin Polymers 0.000 abstract description 18
- 239000011347 resin Substances 0.000 abstract description 18
- 238000007789 sealing Methods 0.000 abstract description 18
- 229910000679 solder Inorganic materials 0.000 abstract description 9
- 230000000694 effects Effects 0.000 abstract description 3
- 238000004806 packaging method and process Methods 0.000 abstract description 2
- -1 benzophenone diamines Chemical class 0.000 description 16
- 229920003986 novolac Polymers 0.000 description 16
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 11
- 238000000576 coating method Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 9
- 230000001070 adhesive effect Effects 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 150000004985 diamines Chemical class 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- KZTYYGOKRVBIMI-UHFFFAOYSA-N S-phenyl benzenesulfonothioate Natural products C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 5
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- BUZMJVBOGDBMGI-UHFFFAOYSA-N 1-phenylpropylbenzene Chemical compound C=1C=CC=CC=1C(CC)C1=CC=CC=C1 BUZMJVBOGDBMGI-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical group C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 2
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 2
- LJCFOYOSGPHIOO-UHFFFAOYSA-N antimony pentoxide Chemical compound O=[Sb](=O)O[Sb](=O)=O LJCFOYOSGPHIOO-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 2
- 238000005476 soldering Methods 0.000 description 2
- 238000001721 transfer moulding Methods 0.000 description 2
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 1
- NUIURNJTPRWVAP-UHFFFAOYSA-N 3,3'-Dimethylbenzidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 description 1
- UENRXLSRMCSUSN-UHFFFAOYSA-N 3,5-diaminobenzoic acid Chemical compound NC1=CC(N)=CC(C(O)=O)=C1 UENRXLSRMCSUSN-UHFFFAOYSA-N 0.000 description 1
- NBAUUNCGSMAPFM-UHFFFAOYSA-N 3-(3,4-dicarboxyphenyl)phthalic acid Chemical compound C1=C(C(O)=O)C(C(=O)O)=CC=C1C1=CC=CC(C(O)=O)=C1C(O)=O NBAUUNCGSMAPFM-UHFFFAOYSA-N 0.000 description 1
- JFEXPVDGVLNUSC-UHFFFAOYSA-N 3-(3-aminophenyl)sulfanylaniline Chemical compound NC1=CC=CC(SC=2C=C(N)C=CC=2)=C1 JFEXPVDGVLNUSC-UHFFFAOYSA-N 0.000 description 1
- FQVFHZDGFYPWSX-UHFFFAOYSA-N 3-(3-methylcyclohex-2-en-1-yl)oxolane-2,5-dione Chemical compound C1CCC(C)=CC1C1C(=O)OC(=O)C1 FQVFHZDGFYPWSX-UHFFFAOYSA-N 0.000 description 1
- ZBMISJGHVWNWTE-UHFFFAOYSA-N 3-(4-aminophenoxy)aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(N)=C1 ZBMISJGHVWNWTE-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- CKOFBUUFHALZGK-UHFFFAOYSA-N 3-[(3-aminophenyl)methyl]aniline Chemical compound NC1=CC=CC(CC=2C=C(N)C=CC=2)=C1 CKOFBUUFHALZGK-UHFFFAOYSA-N 0.000 description 1
- DVXYMCJCMDTSQA-UHFFFAOYSA-N 3-[2-(3-aminophenyl)propan-2-yl]aniline Chemical compound C=1C=CC(N)=CC=1C(C)(C)C1=CC=CC(N)=C1 DVXYMCJCMDTSQA-UHFFFAOYSA-N 0.000 description 1
- ICNFHJVPAJKPHW-UHFFFAOYSA-N 4,4'-Thiodianiline Chemical compound C1=CC(N)=CC=C1SC1=CC=C(N)C=C1 ICNFHJVPAJKPHW-UHFFFAOYSA-N 0.000 description 1
- MITHMOYLTXMLRB-UHFFFAOYSA-N 4-(4-aminophenyl)sulfinylaniline Chemical compound C1=CC(N)=CC=C1S(=O)C1=CC=C(N)C=C1 MITHMOYLTXMLRB-UHFFFAOYSA-N 0.000 description 1
- ZYEDGEXYGKWJPB-UHFFFAOYSA-N 4-[2-(4-aminophenyl)propan-2-yl]aniline Chemical compound C=1C=C(N)C=CC=1C(C)(C)C1=CC=C(N)C=C1 ZYEDGEXYGKWJPB-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical group C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- TUQQUUXMCKXGDI-UHFFFAOYSA-N bis(3-aminophenyl)methanone Chemical compound NC1=CC=CC(C(=O)C=2C=C(N)C=CC=2)=C1 TUQQUUXMCKXGDI-UHFFFAOYSA-N 0.000 description 1
- MYMCSQDRHUQQDW-UHFFFAOYSA-N bis(4-amino-3-methylphenyl)methanone Chemical compound C1=C(N)C(C)=CC(C(=O)C=2C=C(C)C(N)=CC=2)=C1 MYMCSQDRHUQQDW-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- RLDQYSHDFVSAPL-UHFFFAOYSA-L calcium;dithiocyanate Chemical compound [Ca+2].[S-]C#N.[S-]C#N RLDQYSHDFVSAPL-UHFFFAOYSA-L 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- KADGVXXDDWDKBX-UHFFFAOYSA-N naphthalene-1,2,4,5-tetracarboxylic acid Chemical compound OC(=O)C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC(C(O)=O)=C21 KADGVXXDDWDKBX-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920005575 poly(amic acid) Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
- H01L23/293—Organic, e.g. plastic
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/01—Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
- H01L2224/26—Layer connectors, e.g. plate connectors, solder or adhesive layers; Manufacturing methods related thereto
- H01L2224/31—Structure, shape, material or disposition of the layer connectors after the connecting process
- H01L2224/32—Structure, shape, material or disposition of the layer connectors after the connecting process of an individual layer connector
- H01L2224/321—Disposition
- H01L2224/32151—Disposition the layer connector connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive
- H01L2224/32221—Disposition the layer connector connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked
- H01L2224/32245—Disposition the layer connector connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/01—Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
- H01L2224/42—Wire connectors; Manufacturing methods related thereto
- H01L2224/47—Structure, shape, material or disposition of the wire connectors after the connecting process
- H01L2224/48—Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
- H01L2224/481—Disposition
- H01L2224/48151—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive
- H01L2224/48221—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked
- H01L2224/48245—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic
- H01L2224/48247—Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic connecting the wire to a bond pad of the item
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/73—Means for bonding being of different types provided for in two or more of groups H01L2224/10, H01L2224/18, H01L2224/26, H01L2224/34, H01L2224/42, H01L2224/50, H01L2224/63, H01L2224/71
- H01L2224/732—Location after the connecting process
- H01L2224/73251—Location after the connecting process on different surfaces
- H01L2224/73265—Layer and wire connectors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L24/00—Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
- H01L24/73—Means for bonding being of different types provided for in two or more of groups H01L24/10, H01L24/18, H01L24/26, H01L24/34, H01L24/42, H01L24/50, H01L24/63, H01L24/71
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/15—Details of package parts other than the semiconductor or other solid state devices to be connected
- H01L2924/181—Encapsulation
Landscapes
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Encapsulation Of And Coatings For Semiconductor Or Solid State Devices (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、表面実装時におけるパッケージクラックの
発生の少ない半導体装置に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a semiconductor device in which package cracks are less likely to occur during surface mounting.
トランジスタ、IC,LSI等の半導体素子は、外部環
境の保護の観点および素子のハンドリングを可能にする
観点から、プラスチックパッケージ等により封止され半
導体装置化されている。この種のパッケージの代表例と
しては、デュアルインラインパッケージ(D I F)
がある。このDrPは、ピン挿入型のものであり、実装
基板に対してピンを挿入することにより半導体装置を取
り付けるようになっている。2. Description of the Related Art Semiconductor elements such as transistors, ICs, and LSIs are sealed in plastic packages or the like to form semiconductor devices from the viewpoint of protecting the external environment and enabling handling of the elements. A typical example of this type of package is the dual inline package (DIF).
There is. This DrP is a pin insertion type, and a semiconductor device is attached by inserting a pin into a mounting board.
最近は、LSIチップ等の半導体装置の高集積化と高速
化が進んでおり、加えて電子装置を小形で高機能にする
要求から、実装の高密度化が進んでいる。このような観
点からDIPのようなピン挿入型のパッケージに代えて
、表面実装用パッケージが主流になってきている。この
種のパッケージを用いた半導体装置においては、平面的
にピンを取り出し、これを実装基板表面に直接半田等に
よって固定するようになっている。このような表面実装
型半導体装置は、平面的にピンが取り出せるようになっ
ており、薄い、軽い、小さいという利点を備えており、
したがって実装基板に対する占有面積が小さくてすむと
いう利点を備え゛ている他、基板に対する両面実装も可
能であるという長所も有している。Recently, the integration and speed of semiconductor devices such as LSI chips have been increasing, and in addition, the demand for smaller and more highly functional electronic devices has led to higher density packaging. From this point of view, surface mount packages have become mainstream instead of pin insertion type packages such as DIP. In a semiconductor device using this type of package, pins are taken out in a plane and fixed directly to the surface of the mounting board by soldering or the like. These surface-mounted semiconductor devices have pins that can be taken out on a flat surface, and have the advantages of being thin, light, and small.
Therefore, it has the advantage that it occupies only a small area on the mounting board, and also has the advantage that it can be mounted on both sides of the board.
ところが、上記のような表面実装用パッケージを用いた
半導体装置において表面実装前にパッケージ自体が吸湿
している場合には、半田実装時に水分の蒸気圧によって
、パッケージにクラックが生じるという問題がある。す
なわち、第3図に示すような表面実装型半導体装置にお
いて、水分は矢印Aのように封止樹脂1を通って、また
リードフレーム2と封止樹脂1との隙間を通ってパッケ
ージ3内に侵入し、主としてリードフレーム2のグイボ
ンドパット4の裏面に滞溜する。そして、ペーパーフェ
ーズソルダリング等の半田表面実装を行う際に、上記滞
溜水分が、上記半田実装における加熱により気化し、そ
の蒸気圧により、第4図に示すようにグイボンドバット
4の裏面の樹脂部分を下方に押しやり、そこに空隙5を
つくると同時にパッケージ3にクラック6を生じさせる
。However, in a semiconductor device using a surface mount package as described above, if the package itself absorbs moisture before surface mounting, there is a problem that cracks occur in the package due to the vapor pressure of moisture during solder mounting. That is, in the surface-mounted semiconductor device as shown in FIG. It invades and accumulates mainly on the back surface of the Guibond pad 4 of the lead frame 2. Then, when performing solder surface mounting such as paper phase soldering, the accumulated moisture is vaporized by the heating during the solder mounting, and its vapor pressure causes the back surface of the Guibond batt 4 to be heated as shown in FIG. The resin portion is pushed downward, creating a gap 5 there and at the same time creating a crack 6 in the package 3.
第3図および第4図において、7は半導体素子。In FIGS. 3 and 4, 7 is a semiconductor element.
8はワイヤーボンディングである。8 is wire bonding.
このような問題に対する解決策として、半導体素子をパ
ッケージで封止した後、得られる半導体装置全体を密封
し、表面実装の直前に開封して使用する方法や、表面実
装の直前に上記半導体装置を100°Cで24時間乾燥
させ、その後半田実装を行うという方法が提案され、す
でに実施されている。しかしながら、このような前処理
方法によれば、製造工程が長くなる上、手間がかかると
いう問題がある。As a solution to such problems, there are methods in which the semiconductor element is sealed in a package, the entire semiconductor device obtained is sealed, and the package is opened and used immediately before surface mounting, or the semiconductor device is sealed in a package immediately before surface mounting. A method of drying at 100° C. for 24 hours and then performing solder mounting has been proposed and has already been implemented. However, such a pretreatment method has the problem that the manufacturing process is long and labor-intensive.
この発明はこのような事情に鑑みなされたもので、電子
機器への実装に際して前処理を要することなく、しかも
半田実装時の加熱に耐えうる半導体装置の提供をその目
的とする。The present invention was made in view of the above circumstances, and it is an object of the present invention to provide a semiconductor device that does not require pretreatment when mounted on electronic equipment and can withstand heat during solder mounting.
上記の目的を達成するため、この発明の半導体装置は、
少なくとも一部が下記の一般式(I)で表されるエポキ
シ樹脂からなるエポキシ樹脂主剤成分と、少なくとも一
部が下記の一般式(n)で表されるフェノール樹脂から
なるフェノール樹脂硬化剤成分と、無機質充填剤を主要
成分とするエポキシ樹脂組成物を用い、リードフレーム
のダイボンドパッド上に取着された半導体素子を封止し
てなる半導体装置であって、ダイボンドパッド裏面がポ
リイミドで被覆処理されているという構成をとる。In order to achieve the above object, the semiconductor device of the present invention includes:
An epoxy resin main component consisting of an epoxy resin at least partially represented by the following general formula (I); and a phenolic resin curing agent component consisting of a phenol resin at least partially represented by the following general formula (n). , a semiconductor device in which a semiconductor element mounted on a die bond pad of a lead frame is encapsulated using an epoxy resin composition containing an inorganic filler as a main component, the back surface of the die bond pad being coated with polyimide. The structure is that
(n−0〜10)
(以下余白)
(n= 0〜10)
なお、上記式(I)、(n)において繰り返し数nは、
重量平均分子量Mw値から求めたものである。(n-0 to 10) (blank below) (n = 0 to 10) In addition, in the above formulas (I) and (n), the number of repetitions n is
It is determined from the weight average molecular weight Mw value.
パッケージクラックの発生を防止する方法としては、■
封止樹脂に対する吸湿を抑制する、■グイボンドバット
の裏面および半導体素子の表面と封止樹脂との間の接着
力を高める、■封止樹脂自体の強度を高めるの三つの方
法が考えられる。この発明は、上記■のダイボンドバッ
トの裏面および半導体素子の表面と封止樹脂との間の接
着力を高めることと上記■の封止樹脂自体の強度を高め
ることにより、パッケージクラックの発生を防止するも
のであり、上記−形式(1)で表される特殊なエポキシ
樹脂と、上記−形式(II)で表される特殊なフェノー
ル樹脂とを用いることにより、半田実装におけるような
筋温下での封止樹脂の強度を現状の樹脂に比較して、約
3〜4倍に一向上させるようにするものである。さらに
、第1図に示すように、ダイボンドパッド4の裏面がポ
リイミド薄膜9で被覆されているため、封止樹脂1とダ
イボンドパッド4との間に優れた接着力が生じるように
なる。As a method to prevent the occurrence of package cracks, ■
Three methods can be considered: suppressing moisture absorption into the sealing resin; (1) increasing the adhesive force between the back surface of the Guibond bat and the surface of the semiconductor element and the sealing resin; and (2) increasing the strength of the sealing resin itself. This invention prevents the occurrence of package cracks by increasing the adhesive strength between the back side of the die bonding bat and the surface of the semiconductor element and the sealing resin as described in (■) above, and increasing the strength of the sealing resin itself as described in (■) above. By using the special epoxy resin represented by type (1) above and the special phenol resin represented by type (II) above, The strength of the sealing resin is improved by about 3 to 4 times compared to the current resin. Furthermore, as shown in FIG. 1, since the back surface of the die bond pad 4 is covered with the polyimide thin film 9, excellent adhesive force is generated between the sealing resin 1 and the die bond pad 4.
この発明の半導体装置は、ダイボンドパッドの裏面がポ
リイミドで被覆処理されているリードフレームに取着さ
れている半導体素子を対象とし、全部もしくは一部が前
記−形式(I)で表される特殊なエポキシ樹脂からなる
エポキシ樹脂主剤成分と、全部もしくは一部が前記−形
式(II)で表される特殊なフェノール樹脂からなるフ
ェノール樹脂硬化剤成分と、無機質充填剤とを主成分と
するエポキシ樹脂組成物とを用いて得られるものである
。そして、通常、上記エポキシ樹脂組成物は粉末状もし
くはそれを打錠したタブレット状になっている。The semiconductor device of the present invention is directed to a semiconductor element attached to a lead frame in which the back surface of the die bond pad is coated with polyimide, and all or part of which is a special semiconductor device represented by the above-mentioned type (I). An epoxy resin composition whose main components are an epoxy resin main component made of an epoxy resin, a phenolic resin curing agent component made of a special phenol resin whose whole or part is represented by the above-mentioned form (II), and an inorganic filler. It is something that can be obtained using things. The epoxy resin composition is usually in the form of a powder or a tablet formed by compressing it.
上記エポキシ樹脂主剤成分の全部もしくは一部を構成す
る前記−形式(I)の特殊なエポキシ樹脂は、ノボラッ
ク型エポキシ樹脂の主鎖のメチレン基にフェニルグリシ
ジルエーテルを結合させた構造のものである。このよう
な分子構造にすることにより、架橋点が増え、架橋密度
の高い構造物が得られるようになる。なお′、上記特殊
なエポキシ樹脂のみでエポキシ樹脂主剤成分を構成して
もよいし、それ以外の通常用いられるエポキシ樹脂と併
用するようにしてもよい。通常用いられるエポキシ樹脂
としては、タレゾールノボラック型。The special epoxy resin of type (I) that constitutes all or part of the epoxy resin base component has a structure in which phenyl glycidyl ether is bonded to a methylene group in the main chain of a novolac type epoxy resin. By adopting such a molecular structure, the number of crosslinking points increases and a structure with high crosslinking density can be obtained. Note that the epoxy resin base component may be composed only of the above-mentioned special epoxy resin, or may be used in combination with other commonly used epoxy resins. The commonly used epoxy resin is Talesol novolac type.
フェノールノボラック型やビスフェノールA型等の各種
のエポキシ樹脂があげられる。これらの樹脂の中でも、
融点が室温を超えており、室温下では固形状もしくは高
粘度の溶液状を呈するものを用いることが好結果をもた
らす。ノボラック型エポキシ樹脂としては、通常、エポ
キシ当量150〜250.軟化点50〜130°Cのも
のが用いられ、タレゾールノボラック型エポキシ樹脂と
しては、エポキシ当量180〜210.軟化点60〜1
10°Cのものが一般に用いられる。このように両者を
併用する場合には、上記−形式(1)で表される特殊な
エポキシ樹脂と、上記通常のエポキシ樹脂とは、前者1
00重量部(以下「部」と略す)に対して後者0〜10
0部の範囲内に設定することが好適である。Examples include various epoxy resins such as phenol novolac type and bisphenol A type. Among these resins,
Good results can be obtained by using a material having a melting point above room temperature and exhibiting a solid state or a highly viscous solution state at room temperature. The novolac type epoxy resin usually has an epoxy equivalent of 150 to 250. A Talesol novolac type epoxy resin with a softening point of 50 to 130°C is used, and an epoxy equivalent of 180 to 210. Softening point 60-1
A temperature of 10°C is generally used. In this way, when both are used together, the special epoxy resin represented by the above-mentioned form (1) and the above-mentioned ordinary epoxy resin are the former 1.
The latter 0 to 10 parts by weight (hereinafter abbreviated as "parts")
It is preferable to set it within the range of 0 copies.
フェノール樹脂硬化剤成分の全部もしくは一部を構成す
る上記−形式(II)で表される特殊なフェノール樹脂
は、フェノールノボラックの主鎖のメチレン基にフェノ
ールを結合させた構造のものであり、このような分子構
造によって架橋点が増加し、それによって架橋密度の貰
い三次元構造体が得られるようになる。上記特殊なフェ
ノール樹脂は、それ自体でフェノール樹脂硬化剤成分を
構成してもよいし、通常用いられているその他のフェノ
ール樹脂と併用しても差支えはない。その他のフェノー
ル樹脂としては、フェノールノボラック、クレゾールノ
ボラック、アルキル化フェノールノボラック等があげら
れる。これらのノボラック樹脂は、軟化点が50〜11
0°C2水酸基当量が70〜150のものを用いること
が望ましい。The special phenolic resin represented by form (II) above, which constitutes all or part of the phenolic resin curing agent component, has a structure in which phenol is bonded to the methylene group in the main chain of phenol novolac. Such a molecular structure increases the number of crosslinking points, thereby increasing the crosslinking density and making it possible to obtain a three-dimensional structure. The above-mentioned special phenolic resin may constitute the phenolic resin curing agent component by itself, or may be used in combination with other commonly used phenolic resins. Examples of other phenolic resins include phenol novolak, cresol novolak, and alkylated phenol novolak. These novolac resins have a softening point of 50 to 11
It is desirable to use one having a 0°C2 hydroxyl equivalent of 70 to 150.
特に上記ノボラック樹脂の中でも、タレゾールノボラッ
クを用いることが好結果をもたらす。上記−形式(ff
)で表される特殊なフェノール樹脂と、このような通常
のフェノール樹脂を併用する場合における両者の割合は
、前者100部に対して後者0〜100部の範囲内に設
定することが効果の点で好ましい。Particularly, among the above-mentioned novolac resins, use of Talesol novolac brings about good results. Above - Format (ff
) When using a special phenolic resin represented by ( ) and such a normal phenolic resin, the effective point is to set the ratio of both in the range of 0 to 100 parts to 100 parts of the former. It is preferable.
上記エポキシ樹脂主剤成分およびフェノール樹脂硬化剤
成分とともに用いられる無機質充填剤としては、結晶性
および溶融性フィラーはもちろんのこと、酸化アルミニ
ウム、酸化ベリリウム、炭化ケイ素、窒化ケイ素等があ
げられる。Examples of the inorganic filler used together with the epoxy resin base component and the phenolic resin curing agent component include crystalline and meltable fillers, as well as aluminum oxide, beryllium oxide, silicon carbide, silicon nitride, and the like.
上記ダイボンドパッド裏面の被覆処理に用いられるポリ
イミドとしては、従来公知のものがあげられ、通常、有
機テトラカルボン酸二無水物と有機ジアミンとから合成
される。The polyimide used for coating the back surface of the die bond pad includes conventionally known polyimides, and is usually synthesized from an organic tetracarboxylic dianhydride and an organic diamine.
上記有機テトラカルボン酸二無水物としては、下記の一
般式で表されるものがあげられる。Examples of the organic tetracarboxylic dianhydride include those represented by the following general formula.
(余 白 ) 1、、−CH2−C(CHり 2−CH2−等である。(Left white) 1, -CH2-C (CHri 2-CH2-, etc.).
ヲこのような有機テトラカルボン酸二無
水物の具体例としては、例えば、3.3’、4.4’
−ブタンテトラカルボン酸二無水物、シクロペンクンテ
トラカルボン酸二無水物や、下記の式(a)で表される
5−(2,5−ジオキソテトラヒドロフリル)−3−メ
チル−3−シクロヘキセン−1゜2−ジカルボキシリッ
クアンハイドライドおよび下記の式(b)で表されるビ
シクロ[2,2,2]オクテン−(7)−2,3,5,
6−テトラカルボン酸二無水物、
等の脂肪族テトラカルボン酸二無水物、ピロメリット酸
二無水物、3.3’、4.4’−ビフェニルテトラカル
ボン酸二無水物、2,3.3’、4’−ビフェニルテト
ラカルボン酸二無水物、21.3.6.7−ナフタリン
テトラカルボン酸二無水物、1,2,4.5−ナフタリ
ンテトラカルボン酸二無水物、1,2,5.6−ナフタ
リンテトラカルボン酸二無水物、3.3’、4.4’−
ベンゾフェノンテトラカルボン酸二無水物、2,2−ビ
ス[4−(2,3−ジカルボキシフェノキシ)フェニル
〕プロパンニ無水物、4.4’−ビス(2,3−ジカル
ボキシフェノキシ)ジフェニルエーテルニ無水物等の芳
香族テトラカルボン酸二無水物があげられ、単独もしく
は併せて用いることができる。また、有機テトラカルボ
ン酸二無水物の誘導体としては、上記テトラカルボン酸
二無水物のテトラカルボン酸化物、低級アルキルエステ
ル化物、多価アルコールエステル化物等があげられる。Specific examples of such organic tetracarboxylic dianhydrides include, for example, 3.3', 4.4'
-Butanetetracarboxylic dianhydride, cyclopenkune tetracarboxylic dianhydride, and 5-(2,5-dioxotetrahydrofuryl)-3-methyl-3-cyclohexene represented by the following formula (a) -1゜2-dicarboxylic anhydride and bicyclo[2,2,2]octene-(7)-2,3,5, represented by the following formula (b),
6-tetracarboxylic dianhydride, aliphatic tetracarboxylic dianhydride such as pyromellitic dianhydride, 3.3', 4.4'-biphenyltetracarboxylic dianhydride, 2,3.3 ',4'-Biphenyltetracarboxylic dianhydride, 21.3.6.7-naphthalenetetracarboxylic dianhydride, 1,2,4.5-naphthalenetetracarboxylic dianhydride, 1,2,5 .6-Naphthalene tetracarboxylic dianhydride, 3.3', 4.4'-
Benzophenone tetracarboxylic dianhydride, 2,2-bis[4-(2,3-dicarboxyphenoxy)phenyl]propanihydride, 4,4'-bis(2,3-dicarboxyphenoxy)diphenyl ether dianhydride These aromatic tetracarboxylic dianhydrides can be used alone or in combination. Examples of derivatives of organic tetracarboxylic dianhydrides include tetracarboxylic oxides, lower alkyl esters, and polyhydric alcohol esters of the above-mentioned tetracarboxylic dianhydrides.
つぎに、上記有機ジアミンとしては、下記の−形式で表
されるものがあげられる。Next, examples of the above-mentioned organic diamine include those represented by the following format.
HzN Rs NHz
上記有機ジアミンの具体例としては、例えば、1.2−
エチレンジアミン、1,6−へキサメチレンジアミン、
キシリレンジアミン、イソホロンジアミン、p−シクロ
へキシルジアミン、3,9−ビス(3−アミノプロピル
)−2,4,8,10−テトラオキサスピロ−(5,5
)−ウンデカン等の脂肪族ジアミン、4,4′−ジアミ
ノジフェニルエーテル、3,3′−ジメチル−4,4′
−ジアミノジフエニルエーテル、3,3′−ジメトキシ
−4,4′−ジアミノジフェニルエーテル、3.3′−
ジアミノジフェニルエーテル、3.4′−ジアミノジフ
ェニルエーテル等のジフェニルエーテル系ジアミン、4
,4′−ジアミノジフェニルチオエーテル、3,3′−
ジメチル−4,4′−ジアミノジフェニルチオエーテル
、3,3′−ジメトキシ−4,4′−ジアミノジフェニ
ルチオエーテル、3.3′−ジアミノジフェニルチオエ
ーテル等のジフェニルチオエーテル系ジアミン、4.4
′−ジアミノベンゾフェノン、3.3’−ジメチル−4
,4′−ジアミノベンゾフェノン、3.3′−ジアミノ
ベンゾフェノン等のベンゾフェノン系ジアミン、3,3
′−ジアミノジフェニルメタン、4.4′−ジアミノジ
フェニルメタン、3.3′−ジメトキシ−4,4′−ジ
アミノジフェニルメタン、3,3′−ジメチル−4,4
’−ジアミノジフェニルメタン等のジフェニルメタン系
ジアミン、2,2−ビス(4−アミノフェニル)プロパ
ン、2,2−ビス(3−アミノフェニル)プロパン等の
ビスフェニルプロパン系ジアミン、4.4’−ジアミノ
ジフェニルスルホキシド、3.3′−ジアミノジフェニ
ルスルホキシド等のジフェニルスルホキシド系ジアミン
、4.4’−ジアミノジフェニルスルホン、3.3’−
ジアミノジフェニルスルホン等のジフェニルスルホン系
ジアミン、ベンチジン、3.3’ −ジメチルベンチジ
ン、3,3′−ジメトキシベンチジン、3゜3′−ジア
ミノビフェニル等のビフェニル系ジアミン、2,6−ジ
アミノピリジン、3.6−ジアミノピリジン、2,5−
ジアミノピリジン、3゜4−ジアミノピリジン等のピリ
ジン系ジアミン、o−、m−またはp−ジアミノベンゼ
ン、3,5−ジアミノ安息香酸等、4.4′−ジ(m−
アミノフェノキシ)ジフェニルスルホン、4.4’ −
ジ(p−アミノフェノキシ)ジフェニルスルホン、4.
4’−ジ(m−アミノフェノキシ)ジフェニルエーテル
、4.4’−ジ(p−アミノフェノキシ)ジフェニルエ
ーテル、4.4′−ジ(m−アミノフェノキシ)ジフェ
ニルプロパン、4.4′−ジ(p−アミノフェノキシ)
ジフェニルプロパン、4.4’−ジ(m−アミノフェニ
ルスルホニル)ジフェニルエーテル、4,4′−ジ(p
−アミノフェニルスルホニル)ジフェニルエーテル、
4.4’−ジ(m−アミノフェニルチオエーテル)ジフ
ェニルスルフィド、4.4’−ジ(p−アミノフェニル
チオエーテル)ジフェニルスルフィド、4,4′−ジ(
m−アミノフェノキシ)ジフェニルケトン、4,4′−
ジ(p−アミノフエノキシ)ジフェニルケトン、4.4
′−ジ(m−アミノフェノキシ)ジフェニルメタン、4
.4′−ジ(p−アミノフェノキシ)ジフェニルメタン
等の芳香族ジアミンがあげられる。HzNRs NHz Specific examples of the above organic diamine include 1.2-
Ethylenediamine, 1,6-hexamethylenediamine,
Xylylenediamine, isophoronediamine, p-cyclohexyldiamine, 3,9-bis(3-aminopropyl)-2,4,8,10-tetraoxaspiro-(5,5
)-Aliphatic diamines such as undecane, 4,4'-diaminodiphenyl ether, 3,3'-dimethyl-4,4'
-diaminodiphenyl ether, 3,3'-dimethoxy-4,4'-diaminodiphenyl ether, 3,3'-
Diphenyl ether diamines such as diaminodiphenyl ether and 3,4′-diaminodiphenyl ether, 4
, 4'-diaminodiphenylthioether, 3,3'-
Diphenylthioether diamines such as dimethyl-4,4'-diaminodiphenylthioether, 3,3'-dimethoxy-4,4'-diaminodiphenylthioether, 3.3'-diaminodiphenylthioether, 4.4
'-Diaminobenzophenone, 3,3'-dimethyl-4
, 4'-diaminobenzophenone, benzophenone diamines such as 3,3'-diaminobenzophenone, 3,3
'-Diamino diphenylmethane, 4.4'-diaminodiphenylmethane, 3.3'-dimethoxy-4,4'-diaminodiphenylmethane, 3,3'-dimethyl-4,4
Diphenylmethane diamines such as '-diaminodiphenylmethane, bisphenylpropane diamines such as 2,2-bis(4-aminophenyl)propane, 2,2-bis(3-aminophenyl)propane, 4,4'-diaminodiphenyl sulfoxide, diphenyl sulfoxide diamines such as 3.3'-diaminodiphenylsulfoxide, 4.4'-diaminodiphenylsulfone, 3.3'-
Diphenylsulfone diamines such as diaminodiphenylsulfone, benzidine, 3,3'-dimethylbenzidine, 3,3'-dimethoxybenzidine, biphenyl diamines such as 3°3'-diaminobiphenyl, 2,6-diaminopyridine, 3,6-diaminopyridine, 2,5-
Pyridine diamines such as diaminopyridine, 3゜4-diaminopyridine, o-, m- or p-diaminobenzene, 3,5-diaminobenzoic acid, 4,4'-di(m-
aminophenoxy) diphenyl sulfone, 4.4'-
Di(p-aminophenoxy)diphenylsulfone, 4.
4'-di(m-aminophenoxy)diphenyl ether, 4.4'-di(p-aminophenoxy)diphenyl ether, 4.4'-di(m-aminophenoxy)diphenylpropane, 4.4'-di(p- aminophenoxy)
Diphenylpropane, 4,4'-di(m-aminophenylsulfonyl)diphenyl ether, 4,4'-di(p
-aminophenylsulfonyl) diphenyl ether,
4.4'-di(m-aminophenylthioether) diphenyl sulfide, 4.4'-di(p-aminophenylthioether) diphenyl sulfide, 4,4'-di(
m-aminophenoxy)diphenylketone, 4,4'-
Di(p-aminophenoxy)diphenylketone, 4.4
'-di(m-aminophenoxy)diphenylmethane, 4
.. Examples include aromatic diamines such as 4'-di(p-aminophenoxy)diphenylmethane.
また、シリコン系ジアミンとしては、例えば、下記の式
(イ)〜(ト)で表されるもの等があげられる。Furthermore, examples of silicon-based diamines include those represented by the following formulas (a) to (g).
CH3CH3
イ) nzN+cHz→TSi−0−Si+CH,−)
−r−NH2CH3CHi
CbHs Ci、H5
l
CH3CHi
CHs 0CHz CH:I
Il+
このような有機ジアミンは、単独でもしくは併せて用い
ることができる。CH3CH3 a) nzN+cHz→TSi-0-Si+CH,-)
-r-NH2CH3CHi CbHs Ci, H5 l CH3CHi CHs 0CHz CH:I Il+ Such organic diamines can be used alone or in combination.
上記ポリイミドでのダイボンドパッドの被覆処理は、例
えばポリアミド酸溶液の状態で少なくともリードフレー
ムのダイボンドパッド裏面に、従来公知の処理方法であ
るスピンコード法、スクリーン印刷法、吹き付は法、塗
布法およびディッピング法等により塗布した後、温度2
50°Cで5時間程度の熱処理を行いポリイミド薄膜を
得ることにより行われる。熱処理による硬化条件として
は、ポリイミドの種類により適切な条件に差異があるが
、通常、温度200°Cで3時間のキュアーにより塗布
面に対して充分な接着力が得られる。被覆ポリイミドの
厚みは、1〜200μm1より好ましくは5〜30μm
に設定すれば好結果が得られる。なお、ポリイミドでの
被覆処理は、ダイボンドパッドの裏面だけでなく、ダイ
ボンドパッドの側面、半導体素子外周面9 リードフレ
ーム表面に行ってもよい。また、ダイボンドパッドの裏
面の全体でなく、部分的に行われていてもよい。The coating treatment of the die bond pad with the above-mentioned polyimide can be carried out by coating at least the back side of the die bond pad of the lead frame in the state of a polyamic acid solution using conventionally known treatment methods such as spin cord method, screen printing method, spraying method, coating method, etc. After applying by dipping method etc., temperature 2
This is done by performing heat treatment at 50°C for about 5 hours to obtain a polyimide thin film. Appropriate conditions for curing by heat treatment vary depending on the type of polyimide, but usually sufficient adhesive strength to the coated surface can be obtained by curing at a temperature of 200° C. for 3 hours. The thickness of the coating polyimide is 1 to 200 μm, preferably 5 to 30 μm.
Good results can be obtained by setting it to . Note that the coating treatment with polyimide may be performed not only on the back surface of the die bond pad, but also on the side surface of the die bond pad, the outer peripheral surface 9 of the semiconductor element, and the surface of the lead frame. Furthermore, the coating may be applied not only to the entire back surface of the die bond pad but also to a portion thereof.
なお、この発明に用いるエポキシ樹脂組成物には、必要
に応じて上記の成分以外に難燃化剤、カップリング剤、
硬化促進剤、ワックス等が用いられる。In addition, the epoxy resin composition used in this invention may contain flame retardants, coupling agents,
A curing accelerator, wax, etc. are used.
上記難燃化剤としては、ノボラック型ブロム化エポキシ
もしくは、ビスAタイプエポキシ、三酸化アンチモンお
よび五酸化アンチモン等の化合物を適宜単独でもしくは
併せて使用することが行われる。As the flame retardant, compounds such as novolac type brominated epoxy, bis A type epoxy, antimony trioxide, and antimony pentoxide may be used alone or in combination as appropriate.
上記カップリング剤としては、グリシジルエーテルタイ
プ、アミンタイプ、チオシアンタイプ。The above-mentioned coupling agents include glycidyl ether type, amine type, and thiocyan type.
ウレアタイプ等のメトキシないしはエトキシシランが、
適宜に単独でもしくは併せて用いられる。Methoxy or ethoxysilane such as urea type,
They may be used alone or in combination as appropriate.
その使用方法としては、充填剤に対して、トライブレン
ドしたり、もしくは予備加熱反応させたり、さらには有
機成分原料に対する予備混合等自由である。It can be used in any manner, such as by triblending or preheating the filler, or by premixing the organic component raw material.
上記硬化促進剤としては、アミン系(三級アミン、四級
アンモニウム塩、イミダゾール類)、リン系、ホウ素系
等の硬化促進剤があげられ、単独でもしくは併せて使用
される。Examples of the curing accelerator include amine-based (tertiary amines, quaternary ammonium salts, imidazoles), phosphorus-based, boron-based curing accelerators, etc., which may be used alone or in combination.
上記ワックスとしては、高級脂肪酸、高級脂肪酸エステ
ル、高級脂肪酸カルシウム等の化合物があげられ、単独
でもしくは併せて使用される。Examples of the wax include compounds such as higher fatty acids, higher fatty acid esters, and higher fatty acid calcium, which may be used alone or in combination.
この発明に用いられるエポキシ樹脂組成物は、例えばつ
ぎのようにして製造することができる。The epoxy resin composition used in this invention can be produced, for example, as follows.
すなわち、上記の成分原料を適宜配合し予備混合した後
、ミキシングロール機等の混練機にかけ加熱状態で混練
して溶融混合し、これを室温に冷却した後、公知の手段
によって粉砕し、必要に応じて打錠するという一連の工
程により製造することができる。That is, after suitably blending and pre-mixing the above-mentioned component raw materials, they are kneaded and melt-mixed in a heated state using a kneading machine such as a mixing roll machine, and after cooling this to room temperature, it is pulverized by known means, and as necessary. It can be manufactured by a series of steps of tabletting according to the appropriate conditions.
この発明の半導体装置は、上記のようなエポキシ樹脂組
成物を用い、例えばつぎのようにして製造することがで
きる。すなわち、まず封止すべきリードフレームのダイ
ボンドパッド裏面に対してポリイミドで被覆処理したの
ち、このリードフレームに半導体素子を取り付け、上記
エポキシ樹脂組成物によって封止することにより得るこ
とができる。上記の封止は、特に限定するものではなく
、通常のトランスファー成形等の公知のモールド方法に
より行うことができる。The semiconductor device of the present invention can be manufactured using the epoxy resin composition as described above, for example, in the following manner. That is, it can be obtained by first coating the back surface of the die bond pad of a lead frame to be sealed with polyimide, then attaching a semiconductor element to this lead frame, and sealing it with the above-mentioned epoxy resin composition. The above sealing is not particularly limited, and can be performed by a known molding method such as normal transfer molding.
このようにして得られる半導体装置は、エポキシ樹脂組
成物中に含まれる上記−形式(I)で表される特殊なエ
ポキシ樹脂および、−形式(1)で表される特殊なフェ
ノール樹脂の作用により、封止樹脂の強度、特に高温時
における強度が従来のものの3〜4倍と高くなっている
ため、半田実装に際しても、パッケージクラック等が生
ずることがない。また、リードフレームのダイボンドパ
ッドの裏面がポリイミドで被覆処理されているため、封
止樹脂とリードフレームとの接着力が極めて優れている
。The semiconductor device thus obtained is produced by the action of the special epoxy resin represented by the above-mentioned form (I) and the special phenol resin represented by form (1) contained in the epoxy resin composition. Since the strength of the sealing resin, especially the strength at high temperatures, is three to four times higher than that of conventional ones, package cracks do not occur even during solder mounting. Furthermore, since the back surface of the die bond pad of the lead frame is coated with polyimide, the adhesive strength between the sealing resin and the lead frame is extremely excellent.
この発明の半導体装置は、上記のような特殊なエポキシ
樹脂およびフェノール樹脂を含有する特殊なエポキシ樹
脂組成物を用いて半導体素子が樹脂封止されているため
、半田実装におけるような過酷な条件下においてもパッ
ケージクラックが生ずることがない。さらに、リードフ
レームのダイボンドパッドの裏面がポリイミドで被覆処
理されているため、封止樹脂とリードフレームとの接着
力が向上し極めて優れた耐湿信頼性を有している。特に
、上記特殊なエポキシ樹脂組成物による封止により、8
ピン以上、特に16ピン以上もしくはチップの長辺が4
mm以上の大形の半導体装置において上記のような高信
軌度が得られるようになるのであり、これが大きな特徴
である。In the semiconductor device of the present invention, the semiconductor element is resin-sealed using a special epoxy resin composition containing the above-mentioned special epoxy resin and phenol resin, so it can withstand harsh conditions such as solder mounting. No package cracks will occur even in this case. Furthermore, since the back surface of the die bond pad of the lead frame is coated with polyimide, the adhesive strength between the sealing resin and the lead frame is improved, and the lead frame has extremely excellent moisture resistance reliability. In particular, by sealing with the above-mentioned special epoxy resin composition, 8
Pins or more, especially 16 pins or more or the long side of the chip is 4
This makes it possible to obtain high reliability orbits as described above in large-sized semiconductor devices of mm or more, and this is a major feature.
つぎに、実施例について比較例と併せて説明する。Next, examples will be described together with comparative examples.
〔実施例1〜10、比較例1〜5〕
まず、実施例および比較例で使用した成分原料は下記の
通りである。[Examples 1 to 10, Comparative Examples 1 to 5] First, the component raw materials used in the Examples and Comparative Examples are as follows.
(主剤)
Aニー形式(I)成分 (n=3)
B:エポキシクレゾールノボラック(n=4)(nはG
PCポリエチレン換算データの重量平均分子量より計算
した。)
(硬化剤)
C: mAII)成分 (n=3)D:フェノー
ルノボラック(n=4)
(nはGPCポリエチレン換算データの重量平均分子量
より計算した。)
〈充填剤〉
E:最大粒径= 150 u m、平均粒径=20μm
。(Main agent) A knee format (I) component (n = 3) B: Epoxy cresol novolac (n = 4) (n is G
Calculated from the weight average molecular weight of PC polyethylene conversion data. ) (Curing agent) C: mAII) component (n = 3) D: Phenol novolac (n = 4) (n was calculated from the weight average molecular weight of GPC polyethylene conversion data.) <Filler> E: Maximum particle size = 150 um, average particle size = 20 μm
.
破砕型溶融SiO□
〈難燃化剤)
F:ノボラック型Br化エポキシ
G:二酸化ニアンチモン
〈硬化触媒)
Hニジメチルイミダゾール ゛
(離型剤〉
■:ポリエチレンwax
(添加剤〉
Jニトリメトキシシラングリシジルエーテル(ポリイミ
ド合成材料)
〈酸無水物〉
〈アミン〉
CH。Crushed type molten SiO□ (Flame retardant) F: Novolac type Br epoxy G: Niantimony dioxide (curing catalyst) H Nidimethylimidazole (Release agent) ■: Polyethylene wax (Additive) J Nitrimethoxysilane glycidyl Ether (polyimide synthetic material) <Acid anhydride><Amine> CH.
C!o)H2N−()−0りFC−Q−0−Q−NH4
I
CH。C! o) H2N-()-0riFC-Q-0-Q-NH4
ICH.
(C) H2N+0eNH2
(ポリイミドの塗布方法)
(d) 刷毛塗り
(e) ディッピングコート
げ) スピンコート
(熱処理による硬化条件)
(樽 温度200°C,3時間
(5)温度250’C,5時間
(i) 温度250°C920時間
後記の第1表に示す原料を同表に示す割合で配合し、ミ
キシングロール機にかけて100°Cで10分間混練し
、シート状組成物を得た。ついで、得られたシート状組
成物を粉砕し、目的とする粉末状のエポキシ樹脂組成物
を得た。(C) H2N+0eNH2 (Polyimide application method) (d) Brush coating (e) Dipping coating) Spin coating (curing conditions by heat treatment) (Cask temperature 200°C, 3 hours (5) Temperature 250'C, 5 hours ( i) Temperature: 250°C, 920 hours The raw materials shown in Table 1 below were blended in the proportions shown in the same table, and kneaded using a mixing roll machine at 100°C for 10 minutes to obtain a sheet-like composition. The sheet composition was pulverized to obtain the desired powdered epoxy resin composition.
(以下余白)
以上の実施例および比較例で得られた粉末状のエポキシ
樹脂組成物を用い、半導体素子をトランスファー成形で
モールドすることにより、半導体装置を得た。この半導
体装置は、80ビンQFPのパッケージ(20X 14
mm、厚み2.25mm)のものであり、7X7mmの
チップサイズを存するものである。(The following is a blank space) A semiconductor device was obtained by molding a semiconductor element by transfer molding using the powdered epoxy resin composition obtained in the above Examples and Comparative Examples. This semiconductor device is packaged in an 80-bin QFP package (20×14
mm, thickness 2.25 mm), and has a chip size of 7 x 7 mm.
このようにして得られた半導体装置について、測定試験
を行った。その結果を下記の第2表に示す。なお、ダイ
ポンドパッドと封止樹脂との接着力は、第2図に示すよ
うに封止樹脂成形物5とダイボンドパッドと同様の材質
板(実施例は板上に予めポリイミドの被覆処理を施しで
ある)4a間の剪断接着力を矢印Bの方向に応力をかけ
て測定した。Measurement tests were conducted on the semiconductor device thus obtained. The results are shown in Table 2 below. Note that the adhesive force between the die bond pad and the sealing resin is as shown in FIG. ) The shear adhesive force between 4a was measured by applying stress in the direction of arrow B.
(以下余白)
第2表の結果から実施例品は、各特性、特に曲げ物性が
室温については、比較測高と大差はないものの、215
°Cのような高温においては、比較測高よりも著しく優
れた結果が得られており、高温時におけるパッケージの
強度が大幅に向上していることがわかる。さらに、実施
例品はパッケージクラック発生数が極めて少なく耐湿信
頼性が著しく向上していることがわかる。(Margins below) From the results in Table 2, the properties of the example product, especially the bending properties at room temperature, are not significantly different from those of the comparative height measurement, but the 215
At high temperatures such as °C, the results are significantly better than the comparative height measurements, and it can be seen that the strength of the package at high temperatures is significantly improved. Furthermore, it can be seen that the number of package cracks occurring in the example products is extremely small, and the moisture resistance reliability is significantly improved.
第1図はこの発明における実施例の説明図、第2図はダ
イボンドパッドと封止樹脂との接着力測定方法の説明図
、第3図および第4図は、従来例の説明図である。
1・・・封止樹脂 2・・・リードフレーム 3・・・
パッケージ 4・・・ダイボンドパッド 7・・・半導
体素子8・・・ワイヤーボンディング 9・・・ポリイ
ミド薄膜
特許出願人 日東電気工業株式会社代理人 弁
理士 西 藤 征 彦第2図FIG. 1 is an explanatory diagram of an embodiment of the present invention, FIG. 2 is an explanatory diagram of a method for measuring adhesive force between a die bond pad and a sealing resin, and FIGS. 3 and 4 are explanatory diagrams of a conventional example. 1... Sealing resin 2... Lead frame 3...
Package 4...Die bond pad 7...Semiconductor element 8...Wire bonding 9...Polyimide thin film patent applicant Nitto Electric Industry Co., Ltd. Representative Patent attorney Yukihiko Nishifuji Figure 2
Claims (1)
るエポキシ樹脂からなるエポキシ樹脂主剤成分と、少な
くとも一部が下記の一般式(II)で表されるフェノール
樹脂からなるフェノール樹脂硬化剤成分と、無機質充填
剤を主要成分とするエポキシ樹脂組成物を用い、リード
フレームのダイボンドパッド上に取着された半導体素子
を封止してなる半導体装置であって、ダイボンドパッド
裏面がポリイミドで被覆処理されていることを特徴とす
る半導体装置。 ▲数式、化学式、表等があります▼……( I ) (n=0〜10) ▲数式、化学式、表等があります▼……(II) (n=0〜10)(1) Curing of a phenolic resin consisting of an epoxy resin main component, at least a part of which is an epoxy resin represented by the following general formula (I), and a phenol resin, at least a part of which is a phenol resin represented by the following general formula (II). A semiconductor device in which a semiconductor element attached to a die bond pad of a lead frame is encapsulated using an epoxy resin composition whose main components are a filler and an inorganic filler, and the back surface of the die bond pad is made of polyimide. A semiconductor device characterized by being coated. ▲There are mathematical formulas, chemical formulas, tables, etc.▼...(I) (n=0-10) ▲There are mathematical formulas, chemical formulas, tables, etc.▼...(II) (n=0-10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62331845A JP2587074B2 (en) | 1987-12-25 | 1987-12-25 | Semiconductor device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62331845A JP2587074B2 (en) | 1987-12-25 | 1987-12-25 | Semiconductor device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01171232A true JPH01171232A (en) | 1989-07-06 |
JP2587074B2 JP2587074B2 (en) | 1997-03-05 |
Family
ID=18248298
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62331845A Expired - Lifetime JP2587074B2 (en) | 1987-12-25 | 1987-12-25 | Semiconductor device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2587074B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03195722A (en) * | 1989-12-25 | 1991-08-27 | Sumitomo Bakelite Co Ltd | Epoxy resin composition |
CN1080931C (en) * | 1995-07-31 | 2002-03-13 | 三星电子株式会社 | Technology for production of frame for enclosing semi-conductor leadwire |
WO2014122892A1 (en) * | 2013-02-06 | 2014-08-14 | 三菱電機株式会社 | Semiconductor module |
-
1987
- 1987-12-25 JP JP62331845A patent/JP2587074B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03195722A (en) * | 1989-12-25 | 1991-08-27 | Sumitomo Bakelite Co Ltd | Epoxy resin composition |
CN1080931C (en) * | 1995-07-31 | 2002-03-13 | 三星电子株式会社 | Technology for production of frame for enclosing semi-conductor leadwire |
WO2014122892A1 (en) * | 2013-02-06 | 2014-08-14 | 三菱電機株式会社 | Semiconductor module |
Also Published As
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