JPH0319706B2 - - Google Patents
Info
- Publication number
- JPH0319706B2 JPH0319706B2 JP57000861A JP86182A JPH0319706B2 JP H0319706 B2 JPH0319706 B2 JP H0319706B2 JP 57000861 A JP57000861 A JP 57000861A JP 86182 A JP86182 A JP 86182A JP H0319706 B2 JPH0319706 B2 JP H0319706B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- epoxy resin
- semiconductor device
- cured product
- epoxy
- 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.)
- Expired - Lifetime
Links
- 239000003822 epoxy resin Substances 0.000 claims description 37
- 229920000647 polyepoxide Polymers 0.000 claims description 37
- 239000004065 semiconductor Substances 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 21
- 229920003986 novolac Polymers 0.000 claims description 16
- 239000011256 inorganic filler Substances 0.000 claims description 7
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 7
- 125000000962 organic group Chemical group 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 239000004593 Epoxy Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical group [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052787 antimony Inorganic materials 0.000 claims description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical group [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052785 arsenic Inorganic materials 0.000 claims description 3
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical group [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 229910052797 bismuth Inorganic materials 0.000 claims description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical group [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000010680 novolac-type phenolic resin Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 229910052711 selenium Inorganic materials 0.000 claims description 3
- 239000011669 selenium Chemical group 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Chemical group 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 238000012360 testing method Methods 0.000 description 12
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 9
- 238000007789 sealing Methods 0.000 description 9
- 239000012778 molding material Substances 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 229920001568 phenolic resin Polymers 0.000 description 6
- 239000005011 phenolic resin Substances 0.000 description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 230000007547 defect Effects 0.000 description 5
- 238000001721 transfer moulding Methods 0.000 description 5
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical class O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 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
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 238000004566 IR spectroscopy Methods 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 239000006087 Silane Coupling Agent Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- 229910002026 crystalline silica Inorganic materials 0.000 description 2
- XYWMKGIIJHMCDU-UHFFFAOYSA-N dimethylstiborylmethane Chemical compound C[Sb](C)(C)=O XYWMKGIIJHMCDU-UHFFFAOYSA-N 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 239000005007 epoxy-phenolic resin Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- ZFVJLNKVUKIPPI-UHFFFAOYSA-N triphenyl(selanylidene)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=[Se])C1=CC=CC=C1 ZFVJLNKVUKIPPI-UHFFFAOYSA-N 0.000 description 2
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 2
- VYNGFCUGSYEOOZ-UHFFFAOYSA-N triphenylphosphine sulfide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=S)C1=CC=CC=C1 VYNGFCUGSYEOOZ-UHFFFAOYSA-N 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- QSSXJPIWXQTSIX-UHFFFAOYSA-N 1-bromo-2-methylbenzene Chemical compound CC1=CC=CC=C1Br QSSXJPIWXQTSIX-UHFFFAOYSA-N 0.000 description 1
- YTWBFUCJVWKCCK-UHFFFAOYSA-N 2-heptadecyl-1h-imidazole Chemical compound CCCCCCCCCCCCCCCCCC1=NC=CN1 YTWBFUCJVWKCCK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- GGECNORVQSLCLI-UHFFFAOYSA-N bis(chloromethyl)phosphoryl-chloromethane Chemical compound ClCP(=O)(CCl)CCl GGECNORVQSLCLI-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000005465 channeling Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- IWQIEVOJUWFMSB-UHFFFAOYSA-N dihexylphosphane Chemical compound CCCCCCPCCCCCC IWQIEVOJUWFMSB-UHFFFAOYSA-N 0.000 description 1
- LRMLWYXJORUTBG-UHFFFAOYSA-N dimethylphosphorylmethane Chemical compound CP(C)(C)=O LRMLWYXJORUTBG-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- ZTEHTGMWGUKFNE-UHFFFAOYSA-N methyl 3-[[2-(diaminomethylideneamino)-1,3-thiazol-4-yl]methylsulfanyl]propanimidate Chemical compound COC(=N)CCSCC1=CSC(N=C(N)N)=N1 ZTEHTGMWGUKFNE-UHFFFAOYSA-N 0.000 description 1
- OPYUUGSDSYNKGN-UHFFFAOYSA-N methyl(oxo)bismuthane Chemical compound C[Bi]=O OPYUUGSDSYNKGN-UHFFFAOYSA-N 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000001225 nuclear magnetic resonance method Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- WKGDNXBDNLZSKC-UHFFFAOYSA-N oxido(phenyl)phosphanium Chemical compound O=[PH2]c1ccccc1 WKGDNXBDNLZSKC-UHFFFAOYSA-N 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000005143 pyrolysis gas chromatography mass spectroscopy Methods 0.000 description 1
- 238000000275 quality assurance Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000005480 straight-chain fatty acid group Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- PDXFZIWCZNAGOE-UHFFFAOYSA-N triethyl(sulfanylidene)-$l^{5}-arsane Chemical compound CC[As](=S)(CC)CC PDXFZIWCZNAGOE-UHFFFAOYSA-N 0.000 description 1
- WTNQHMJTIHJURG-UHFFFAOYSA-N triethyl(sulfanylidene)-$l^{5}-phosphane Chemical compound CCP(=S)(CC)CC WTNQHMJTIHJURG-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- WFSHMSGJALVRMK-UHFFFAOYSA-N trimethyl(sulfanylidene)-$l^{5}-stibane Chemical compound C[Sb](C)(C)=S WFSHMSGJALVRMK-UHFFFAOYSA-N 0.000 description 1
- JWOWJQPAYGEFFK-UHFFFAOYSA-N trimethylarsine oxide Chemical compound C[As](C)(C)=O JWOWJQPAYGEFFK-UHFFFAOYSA-N 0.000 description 1
- PFHNKLAITHQAMD-UHFFFAOYSA-N triphenyl(sulfanylidene)-$l^{5}-arsane Chemical compound C=1C=CC=CC=1[As](C=1C=CC=CC=1)(=S)C1=CC=CC=C1 PFHNKLAITHQAMD-UHFFFAOYSA-N 0.000 description 1
- VLSAAACBQLMOTB-UHFFFAOYSA-N triphenyl(sulfanylidene)-$l^{5}-stibane Chemical compound C=1C=CC=CC=1[Sb](C=1C=CC=CC=1)(=S)C1=CC=CC=C1 VLSAAACBQLMOTB-UHFFFAOYSA-N 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
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
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)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
Description
本発明はエポキシ樹脂系組成物の硬化物によつ
て封止された高信頼性の樹脂封止型半導体装置に
関する。
エポキシ樹脂は電気特性、機械特性、耐薬品性
などが優れているため信頼性の高い電気絶縁材料
として半導体装置の封止に広く用いられている。
最近では従来のセラミツクスを用いたハーメチツ
ク封止にかわつて、ほとんどの半導体装置たとえ
ば集積回路、大規模集積回路、トランジスタ、ダ
イオードなどが低圧成形用のエポキシ樹脂系組成
物を用いて封止されている。
半導体封止用エポキシ樹脂系組成物としては、
信頼性、成形性などの点を考慮してエポキシ樹
脂、ノボラツク型フエノール樹脂硬化剤、イミダ
ゾール硬化促進剤から成るエポキシ樹脂系組成物
が広く用いられている。
しかし従来のエポキシ樹脂系封止樹脂を用い、
トランスフア成形して得られる樹脂封止型半導体
装置は次のような欠点があつた。
(1) 樹脂封止型半導体装置に要求される信頼性の
レベルの高さに較べ耐湿性が劣ること
(2) 樹脂封止型半導体装置に要求される信頼性の
レベルの高さに較べ高温時の電気特性が劣るこ
と
上記耐湿性について説明すると、樹脂封止型半
導体装置は高温高湿雰囲気下で使用または保存す
ることがあるので、そのような条件においても信
頼性を保証しなければならない。耐湿性の品質保
証のための評価試験としては、85℃または120℃
の飽和水蒸気中に暴露する加速評価法が行なわれ
ており、最近では電圧を印加して更に加速性を高
めたバイアス印加型の評価試験も実施されてい
る。
しかし封止したエポキシ樹脂系組成物の硬化物
は吸湿性、透湿性があるため、このような高温高
湿状態下では外部から水分が封止樹脂硬化物層を
通つて内部に浸透し、または封止樹脂とリードフ
レームとの界面を通つて内部に入り、半導体素子
の表面にまで到達する。この水分と封止樹脂中に
存在している不純物イオンなどの作用の結果とし
て、樹脂封止型半導体装置は絶縁性の低下、リー
ク電流の増加、アルミニウム電極、配線などの腐
食を主体とした不良を発生する。またバイアス電
圧を印加した場合にはその電気化学的作用によつ
てアルミニウム電極、配線の腐食による不良が特
に著しく多発する。
従来の樹脂封止型半導体装置は上記耐湿性に関
し充分に満足できるものではなく、耐湿性の向上
が求められていた。
次に高温時の電気特性について説明すると、樹
脂封止型半導体装置は高温条件下で使用すること
があるので、そのような条件においても信頼性を
保証しなければならない。そのための評価試験と
しては80℃〜150℃でバイアス電圧を印加して信
頼性を評価する加速試験が一般的である。
このような試験において表面が鋭敏なMOS構
造をもつ素子や、逆バイアスが印加されたPN接
合をもつ素子に特に著しく多発する不良として、
チヤンネリングによるリーク電流の増加する現象
があることはよく知られている。この現象は電圧
が印加された素子の表面に接している樹脂層に電
界が作用することによつて発生すると考えられて
いる。
従来の樹脂封止型半導体装置は上記高温時の電
気特性に関し充分に満足できるものではなく、改
良が求められていた。
本発明の目的はこのような従来の樹脂封止型半
導体装置の難点を改良し、優れた耐湿性と高温電
気特性を有するエポキシ樹脂系組成物によつて封
止された信頼性の高い樹脂封止型半導体装置を提
供することにある。
上記目的を達成すべく、本発明者らが鋭意研究
を重ねた結果、硬化促進剤などが上記難点を形成
する主要因であることを解明し、更に以下の化学
式[1]で示す化合物を含んでなる硬化物が、半
導体封止用樹脂として従来のものに較べ、優れた
耐湿性と高温電気特性を有することを見出し、こ
れを用いることによつて従来のものに較べ、耐湿
性や高温電気特性などの信頼性に優れた樹脂封止
型半導体装置が得られることを見出した。
すなわち本発明は、
半導体装置がエポキシ樹脂系組成物の硬化物に
よつて封止されて成る樹脂封止型半導体装置にお
いて、該硬化物が
(a) エポキシ当量170〜300のノボラツク型エポキ
シ樹脂、
(b) 軟化点60℃〜120℃のノボラツク型フエノー
ル樹脂、
(c) 化学式[1]
において、Mはリン、ヒ素、アンチモン、ビス
マスから選ばれ、Xは酸素、イオウ、セレンか
ら選ばれ、R1は有機基の中から選ばれ、R2、
R3は有機基または水素から選ばれる化合物の
少なくとも1種、
および
(d) 無機質充てん剤、
を含むことを特徴とする樹脂封止型半導体装置で
ある。
本発明に係る硬化物を構成する第1の成分であ
るエポキシ樹脂は、エポキシ当量170〜300のノボ
ラツク型エポキシ樹脂であつて、たとえばフエノ
ールノボラツク型エポキシ樹脂、クレゾールノボ
ラツク型エポキシ樹脂、ハロゲン化フエノールノ
ボラツク型エポキシ樹脂などである。これらエポ
キシ樹脂は1種もしくは2種以上の混合系で用い
てもよい。またこれらエポキシ樹脂は塩素イオン
の含有量が10ppm以下、加水分解性塩素の含有量
が0.1重量%以下のものが望ましい。
本発明に係る硬化物を構成する第2の成分であ
るノボラツク型フエノール樹脂硬化剤としてはフ
エノールノボラツク樹脂、クレゾールノボラツク
樹脂、test−ブチルフエノールノボラツク樹脂、
ノニルフエノールノボラツク樹脂などが挙げられ
る。これらのフエノール樹脂の軟化点は60℃〜
120℃の範囲内になければならない。その理由は
60℃未満、また120℃を越えた場合には本発明の
効果が充分に得られないためである。また常温に
おける水に可溶性のフエノール樹脂成分が3%以
下であることが好ましい。しかしてこれらの硬化
剤は1種もしくは2種以上の混合系で使用するこ
とができる。
エポキシ樹脂と硬化剤の配合比については、ノ
ボラツク型フエノール樹脂のフエノール性水酸基
の数とエポキシ樹脂のエポキシ基の数の比が0.5
〜1.5の範囲内にあることが望ましい。その理由
は0.5未満あるいは1.5を超えると反応が充分にお
こりにくくなり、硬化物の特性が劣化するためで
ある。
本発明に係る硬化物を構成する第3の成分であ
る硬化促進剤は、化学式〔1〕
において、Mはリン、ヒ素、アンチモン、ビスマ
スから選ばれ、Xは酸素、イオウ、セレンから選
ばれ、R1は有機基の中から選ばれ、R2、R3は有
機基または水素から選ばれる化合物の少くとも1
種である。有機基としては、アルキル基、アリー
ル基、シクロアルキル基、アルカリル基、アラル
キル基などが挙げられる。化学式〔1〕の化合物
を具体的に例示すると、酸化トリフエニルホスフ
イン、硫化トリフエニルホスフイン、セレン化ト
リフエニルホスフイン、酸化トリメチルホスフイ
ン、硫化トリエチルホスフイン、酸化トリス(ク
ロルメチル)ホスフイン、酸化ジヘキシルホスフ
イン、酸化フエニルホスフイン、硫化ジメエニル
メチルホスフイン、酸化トリメチルアルシン、硫
化トリエチルアルシン、酸化トリフエニルアルシ
ン、硫化トリフエニルアルシン、酸化トリメチル
スチビン、硫化トリメチルスチビン、硫化トリフ
エニルスチビン、酸化メチルビスマス、などであ
る。配合量は樹脂成分(エポキシ樹脂とフエノー
ル樹脂)に対し、0.01〜20重量%の範囲内にある
ことが好ましい。
本発明に係る硬化物を構成する第4の成分であ
る無機質充てん剤としては、石英ガラス粉末、結
晶性シリカ粉末、ガラス繊維、タルク、アルミナ
粉末、ケイ酸カルシウム粉末、炭酸カルシウム粉
末、硫酸バリウム粉末、マグネシア粉末などであ
るが、これらの中で石英ガラス粉末や、結晶性シ
リカ粉末が、高純度と低熱膨張係数の点で最も好
ましい。しかしてこれら無機質充てん剤の配合量
はエポキシ樹脂、フエノール樹脂硬化剤および無
機質充てん剤の種類によつても異るが、たとえば
トランスフア成形に用いる場合にはエポキシ樹脂
とフエノール樹脂硬化剤の総量に対し重量比で
1.5倍〜4倍程度でよい。無機質充てん剤の粒度
分布については、粗い粒子と細い粒子を組み合せ
て分布を均一にすることによつて成形性を改善す
ることができる。
本発明に係るエポキシ樹脂系組成物は必要に応
じて、例えば天然ワツクス類、合成ワツクス類、
直鎖脂肪酸の金属塩、酸アミド類、エステル類も
しくはパラフイン類などの離型剤、塩素化パラフ
イン、ブロムトルエン、ヘキサブロムベンゼン、
三酸化アンチモンなどの難燃剤、カーボンブラツ
クなどの着色剤、シランカツプリング剤などを適
宜添加配合しても差しつかえない。
本発明に係るエポキシ樹脂系組成物を成形材料
として調製する場合の一般的な方法としては、所
定の組成比に選んだ原料組成分を例えばミキサー
によつて充分混合後、さらに熱ロールによる溶融
混合処理、またはニーダーなどによる混合処理を
加えることにより容易にエポキシ樹脂系成形材料
を得ることができる。
本発明の樹脂封止型半導体装置は、上記エポキ
シ樹脂系組成物乃至成形材料を用いて半導体装置
を封止することにより容易に製造することができ
る。封止の最も一般的な方法としては低圧トラン
スフア成形法があるが、インジエクシヨン成形、
圧縮成形、注型などによる封止も可能である。
エポキシ樹脂系組成物乃至成形材料は封止の際
に加熱して硬化させ、最終的にはこの組成物乃至
成形材料の硬化物によつて封止された樹脂封止型
半導体装置を得ることができる。硬化に際しては
150℃以上に加熱することが特に望ましい。
本発明でいう半導体装置とは集積回路、大規模
集積回路、トランジスタ、サイリスタ、ダイオー
ドなどであつて特に限定されるものではない。
次に本発明の実施例を説明する。
実施例 1〜4
エポキシ当量220のクレゾールノボラツク型エ
ポキシ樹脂(エポキシ樹脂A)、エポキシ当量290
の臭素化エポキシノボラツク樹脂(エポキシ樹脂
B)、軟化点80℃のフエノールノボラツク樹脂硬
化剤、硫化トリフエニルホスフイン、酸化トレフ
エニルアルシン、酸化トリメチルスチビン、セレ
ン化トリフエニルホスフイン、2−ヘプタデシル
イミダゾール、カルナバワツクス、石英ガラス粉
末、三酸化アンチモン、カーボンブラツク、シラ
ンカツプリング剤(γ−グリシドキシプロピルト
リメトキシシラン)を第1表に示す組成比(重量
部)に選び、各組成物をミキサーによる混合、加
熱ロールによる混練を行うことによつてトランス
フア成形材料を調製した。
このようにして得た成形材料を用いてトランス
フア成形することにより、MOS型集積回路を樹
脂封止した。封止は高周波予熱器で90℃に加熱し
た成形材料を195℃で10分間モールドし、更に180
℃で10時間アフタキユアすることにより行つた。
上記樹脂封止型半導体装置各100個について次
の試験を行つた。
(1) 120℃、2気圧の水蒸気中で10V印加してア
ルミニウム配線の腐食による断線不良を調べる
耐湿試験(バイアスPCT)を行い、その結果
を第2表に示した。
(2) 100℃のオーブン中でオフセツトゲート
MOSFET回路にドレイン電圧5Vオフセツトゲ
ート電圧5Vを印加して電気特性の劣化による
リーク電流不良を調べる試験(NOS−BT試
験)を行い、リーク電流が初期値の100倍以上
に増加した場合を不良と判定してその結果を第
3表に示した。
The present invention relates to a highly reliable resin-encapsulated semiconductor device sealed with a cured product of an epoxy resin composition. Epoxy resin has excellent electrical properties, mechanical properties, chemical resistance, etc., and is therefore widely used as a highly reliable electrical insulating material for encapsulating semiconductor devices.
Recently, most semiconductor devices, such as integrated circuits, large-scale integrated circuits, transistors, diodes, etc., have been encapsulated using epoxy resin compositions for low-pressure molding, instead of conventional hermetic encapsulation using ceramics. As an epoxy resin composition for semiconductor encapsulation,
Epoxy resin compositions comprising an epoxy resin, a novolac-type phenolic resin curing agent, and an imidazole curing accelerator are widely used in consideration of reliability, moldability, and the like. However, using conventional epoxy resin sealing resin,
Resin-sealed semiconductor devices obtained by transfer molding have the following drawbacks. (1) Moisture resistance is inferior to the high level of reliability required for resin-encapsulated semiconductor devices. (2) High temperature resistance is inferior to the high level of reliability required for resin-encapsulated semiconductor devices. Regarding the moisture resistance mentioned above, resin-sealed semiconductor devices are sometimes used or stored in high-temperature, high-humidity environments, so reliability must be guaranteed even under such conditions. . Evaluation tests for moisture resistance quality assurance include 85°C or 120°C.
An accelerated evaluation method has been conducted in which the material is exposed to saturated water vapor, and recently, a bias application type evaluation test in which a voltage is applied to further improve acceleration has also been conducted. However, the cured product of the encapsulated epoxy resin composition is hygroscopic and moisture permeable, so under such high temperature and high humidity conditions, moisture from the outside can penetrate into the interior through the cured epoxy resin layer, or It enters the interior through the interface between the sealing resin and the lead frame and reaches the surface of the semiconductor element. As a result of the action of this moisture and impurity ions existing in the sealing resin, resin-sealed semiconductor devices exhibit defects mainly due to decreased insulation, increased leakage current, and corrosion of aluminum electrodes, wiring, etc. occurs. Further, when a bias voltage is applied, defects due to corrosion of aluminum electrodes and wiring occur particularly frequently due to its electrochemical action. Conventional resin-sealed semiconductor devices are not fully satisfied with the above-mentioned moisture resistance, and there has been a demand for improved moisture resistance. Next, electric characteristics at high temperatures will be explained. Since resin-sealed semiconductor devices are sometimes used under high temperature conditions, reliability must be guaranteed even under such conditions. A typical evaluation test for this purpose is an accelerated test in which reliability is evaluated by applying a bias voltage at 80°C to 150°C. In such tests, defects that occur particularly frequently in devices with MOS structures with sensitive surfaces or devices with PN junctions to which reverse bias is applied are as follows:
It is well known that there is a phenomenon in which leakage current increases due to channeling. This phenomenon is thought to occur when an electric field acts on the resin layer that is in contact with the surface of the element to which a voltage is applied. Conventional resin-sealed semiconductor devices are not fully satisfactory with respect to the above-mentioned electrical characteristics at high temperatures, and improvements have been sought. The purpose of the present invention is to improve the drawbacks of conventional resin-sealed semiconductor devices, and to provide a highly reliable resin-sealed semiconductor device that is encapsulated with an epoxy resin composition that has excellent moisture resistance and high-temperature electrical properties. An object of the present invention is to provide a static semiconductor device. In order to achieve the above object, the present inventors have conducted extensive research and have found that curing accelerators and the like are the main factors contributing to the above-mentioned difficulties, and furthermore, the present inventors have found that curing accelerators and the like are the main factors contributing to the above-mentioned difficulties, and furthermore, they have found that curing accelerators, etc. It has been discovered that a cured product made from It has been discovered that a resin-sealed semiconductor device with excellent characteristics and reliability can be obtained. That is, the present invention provides a resin-encapsulated semiconductor device in which a semiconductor device is sealed with a cured product of an epoxy resin composition, wherein the cured product comprises (a) a novolac type epoxy resin having an epoxy equivalent of 170 to 300; (b) Novolac-type phenolic resin with a softening point of 60°C to 120°C, (c) Chemical formula [1] , M is selected from phosphorus, arsenic, antimony, bismuth, X is selected from oxygen, sulfur, selenium, R 1 is selected from organic groups, R 2 ,
R 3 is a resin-sealed semiconductor device characterized by containing at least one compound selected from an organic group or hydrogen, and (d) an inorganic filler. The epoxy resin which is the first component constituting the cured product according to the present invention is a novolak type epoxy resin having an epoxy equivalent of 170 to 300, such as a phenol novolak type epoxy resin, a cresol novolak type epoxy resin, a halogenated Examples include phenol novolac type epoxy resin. These epoxy resins may be used alone or in a mixed system of two or more. Further, these epoxy resins desirably have a chlorine ion content of 10 ppm or less and a hydrolyzable chlorine content of 0.1% by weight or less. Examples of the novolak-type phenolic resin curing agent, which is the second component constituting the cured product according to the present invention, include phenol novolak resin, cresol novolak resin, test-butylphenol novolak resin,
Examples include nonylphenol novolak resin. The softening point of these phenolic resins is 60℃ ~
Must be within 120℃. The reason is
This is because if the temperature is lower than 60°C or higher than 120°C, the effects of the present invention cannot be sufficiently obtained. Further, it is preferable that the phenol resin component soluble in water at room temperature is 3% or less. These curing agents can be used alone or in a mixed system of two or more. Regarding the compounding ratio of epoxy resin and curing agent, the ratio of the number of phenolic hydroxyl groups in the novolak type phenolic resin to the number of epoxy groups in the epoxy resin is 0.5.
It is desirable that it be within the range of ~1.5. The reason for this is that if it is less than 0.5 or more than 1.5, the reaction will be sufficiently difficult to occur and the properties of the cured product will deteriorate. The curing accelerator, which is the third component constituting the cured product according to the present invention, has the chemical formula [1] , M is selected from phosphorus, arsenic, antimony, and bismuth, X is selected from oxygen, sulfur, and selenium, R 1 is selected from organic groups, and R 2 and R 3 are selected from organic groups or hydrogen. at least one of the compounds
It is a seed. Examples of the organic group include an alkyl group, an aryl group, a cycloalkyl group, an alkaryl group, and an aralkyl group. Specific examples of the compound of chemical formula [1] include triphenylphosphine oxide, triphenylphosphine sulfide, triphenylphosphine selenide, trimethylphosphine oxide, triethylphosphine sulfide, tris(chloromethyl)phosphine oxide, and triphenylphosphine oxide. Dihexylphosphine, phenylphosphine oxide, dimenylmethylphosphine sulfide, trimethylarsine oxide, triethylarsine sulfide, triphenylarsine oxide, triphenylarsine sulfide, trimethylstibine oxide, trimethylstibine sulfide, triphenylstibine sulfide , methyl bismuth oxide, etc. The blending amount is preferably within the range of 0.01 to 20% by weight based on the resin components (epoxy resin and phenolic resin). Examples of the inorganic filler, which is the fourth component constituting the cured product according to the present invention, include quartz glass powder, crystalline silica powder, glass fiber, talc, alumina powder, calcium silicate powder, calcium carbonate powder, and barium sulfate powder. , magnesia powder, etc., but among these, quartz glass powder and crystalline silica powder are most preferred in terms of high purity and low coefficient of thermal expansion. However, the blending amount of these inorganic fillers varies depending on the type of epoxy resin, phenolic resin curing agent, and inorganic filler, but for example, when used in transfer molding, the total amount of epoxy resin and phenolic resin curing agent by weight ratio
It may be about 1.5 times to 4 times. Regarding the particle size distribution of the inorganic filler, moldability can be improved by making the distribution uniform by combining coarse particles and fine particles. The epoxy resin composition according to the present invention can be used as necessary, for example, natural waxes, synthetic waxes,
Mold release agents such as metal salts of straight chain fatty acids, acid amides, esters or paraffins, chlorinated paraffins, bromotoluene, hexabromobenzene,
Flame retardants such as antimony trioxide, colorants such as carbon black, silane coupling agents, etc. may be appropriately added and blended. A general method for preparing the epoxy resin composition according to the present invention as a molding material is to thoroughly mix the raw material components selected at a predetermined composition ratio using, for example, a mixer, and then melt-mix using hot rolls. An epoxy resin molding material can be easily obtained by processing or mixing using a kneader or the like. The resin-sealed semiconductor device of the present invention can be easily manufactured by sealing the semiconductor device using the epoxy resin composition or molding material. The most common method for sealing is low-pressure transfer molding, but injection molding,
Sealing by compression molding, casting, etc. is also possible. The epoxy resin composition or molding material is heated and cured at the time of sealing, and a resin-sealed semiconductor device can finally be obtained which is encapsulated with the cured product of this composition or molding material. can. When curing
Heating to 150°C or higher is particularly desirable. The semiconductor device referred to in the present invention includes an integrated circuit, a large-scale integrated circuit, a transistor, a thyristor, a diode, etc., and is not particularly limited. Next, embodiments of the present invention will be described. Examples 1 to 4 Cresol novolac type epoxy resin with epoxy equivalent weight 220 (epoxy resin A), epoxy equivalent weight 290
Brominated epoxy novolac resin (epoxy resin B), phenol novolac resin curing agent with a softening point of 80°C, triphenylphosphine sulfide, trephenylarsine oxide, trimethylstibine oxide, triphenylphosphine selenide, 2- Heptadecylimidazole, carnauba wax, quartz glass powder, antimony trioxide, carbon black, and silane coupling agent (γ-glycidoxypropyltrimethoxysilane) were selected in the composition ratios (parts by weight) shown in Table 1, and each A transfer molding material was prepared by mixing the composition with a mixer and kneading with a heated roll. The MOS type integrated circuit was resin-sealed by transfer molding using the molding material thus obtained. For sealing, the molding material was heated to 90℃ using a high-frequency preheater, then molded at 195℃ for 10 minutes, and then heated to 180℃ for 10 minutes.
This was done by after-curing at ℃ for 10 hours. The following tests were conducted on 100 of each of the above resin-sealed semiconductor devices. (1) A moisture resistance test (bias PCT) was conducted in water vapor at 120°C and 2 atm to check for disconnection defects due to corrosion of the aluminum wiring by applying 10V, and the results are shown in Table 2. (2) Offset gate in oven at 100℃
A test (NOS-BT test) is performed to check for leakage current defects due to deterioration of electrical characteristics by applying a drain voltage of 5V and an offset gate voltage of 5V to the MOSFET circuit.If the leakage current increases to more than 100 times the initial value, it is determined to be defective. The results are shown in Table 3.
【表】【table】
【表】【table】
【表】
なお、本発明に係るエポキシ樹脂系組成物の硬
化物中の各成分の分析は次のようにして行なうこ
とができる。すなわち、第1の成分であるノボラ
ツク型エポキシ樹脂と第2の成分であるノボラツ
ク型フエノール樹脂については、赤外分光光度法
(熱分解法)、熱分解ガスクロマトグラフ−質量分
析法、核磁気共鳴法等により分析することができ
る。また、第3の成分である化学式[1]の化合
物については、硬化物を微粉砕して溶剤で摘出し
たものについて、赤外分光光度法、ガスクロマト
グラフ−質量分析法、核磁気共鳴法等により分析
することができる。一方、第4の成分である無機
質充てん剤については、硬化物中の有機成分を酸
化させて除去した後に化学分析することによつて
確認することができる。
これらの方法で、半導体装置を封止した6種類
のエポキシ樹脂系組成物の硬化物(分析例1〜
6)の分析を行つた結果を第4表に示した。な
お、これら6種類の分析例のうち、分析例1〜4
は本発明の組成成分を有する硬化物であり、一方
分析例5、6は従来の封止樹脂を同様にして分析
したものである。これらの結果を以下の第4表に
示す。[Table] Incidentally, each component in the cured product of the epoxy resin composition according to the present invention can be analyzed as follows. That is, for the novolak type epoxy resin which is the first component and the novolak type phenol resin which is the second component, infrared spectrophotometry (pyrolysis method), pyrolysis gas chromatography-mass spectrometry method, and nuclear magnetic resonance method are used. It can be analyzed by etc. Regarding the compound of chemical formula [1], which is the third component, the cured product was finely pulverized and extracted with a solvent, and was analyzed by infrared spectrophotometry, gas chromatography-mass spectrometry, nuclear magnetic resonance, etc. can be analyzed. On the other hand, the fourth component, the inorganic filler, can be confirmed by chemical analysis after oxidizing and removing the organic components in the cured product. Cured products of six types of epoxy resin compositions that encapsulated semiconductor devices using these methods (Analysis Examples 1 to 3)
The results of analysis 6) are shown in Table 4. Of these six types of analysis examples, analysis examples 1 to 4
is a cured product having the compositional components of the present invention, while Analysis Examples 5 and 6 are results in which conventional sealing resins were analyzed in the same manner. These results are shown in Table 4 below.
【表】
○:含有している
×: 〃 していない
さらに、これら分析例1〜6の組成物により封
止された半導体装置に対して、先の実施例1〜4
及び比較例1〜2と同様に耐湿試験(バイアス
PCT)と電気特性試験(MOS−BT試験)とを
行なつた結果を、それぞれ以下の第5表及び第6
表に示す。[Table] ○: Contains ×: Does not contain In addition, for the semiconductor devices sealed with the compositions of these analysis examples 1 to 6, the compositions of the previous examples 1 to 4
And the same humidity test (bias) as in Comparative Examples 1 and 2.
PCT) and electrical characteristics test (MOS-BT test) are shown in Tables 5 and 6 below, respectively.
Shown in the table.
【表】【table】
【表】
以上のように、本発明に係る樹脂封止型半導体
装置は、すぐれた耐湿性および電気特性を有する
ことが確認された。[Table] As described above, it was confirmed that the resin-sealed semiconductor device according to the present invention has excellent moisture resistance and electrical properties.
Claims (1)
によつて封止されて成る樹脂封止型半導体装置に
おいて、該硬化物が、 (a) エポキシ当量170〜300のノボラツク型エポキ
シ樹脂、 (b) 軟化点60℃〜120℃のノボラツク型フエノー
ル樹脂、 (c) 化学式[1] において、Mはリン、ヒ素、アンチモン、ビス
マスから選ばれ、Xは酸素、イオウ、セレンか
ら選ばれ、R1は有機基の中から選ばれ、R2、
R3は有機基または水素から選ばれる化合物の
少なくとも1種、 および (d) 無機質充てん剤、 を含むことを特徴とする樹脂封止型半導体装置。[Scope of Claims] 1. A resin-encapsulated semiconductor device in which a semiconductor device is encapsulated with a cured product of an epoxy resin composition, wherein the cured product is (a) a novolak type having an epoxy equivalent of 170 to 300; Epoxy resin, (b) Novolac type phenolic resin with a softening point of 60℃ to 120℃, (c) Chemical formula [1] , M is selected from phosphorus, arsenic, antimony, bismuth, X is selected from oxygen, sulfur, selenium, R 1 is selected from organic groups, R 2 ,
A resin-encapsulated semiconductor device characterized in that R 3 contains at least one compound selected from an organic group or hydrogen, and (d) an inorganic filler.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57000861A JPS58119656A (en) | 1982-01-08 | 1982-01-08 | Resin sealed type semiconductor device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57000861A JPS58119656A (en) | 1982-01-08 | 1982-01-08 | Resin sealed type semiconductor device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58119656A JPS58119656A (en) | 1983-07-16 |
JPH0319706B2 true JPH0319706B2 (en) | 1991-03-15 |
Family
ID=11485442
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57000861A Granted JPS58119656A (en) | 1982-01-08 | 1982-01-08 | Resin sealed type semiconductor device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58119656A (en) |
-
1982
- 1982-01-08 JP JP57000861A patent/JPS58119656A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS58119656A (en) | 1983-07-16 |
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