JPH0793330B2 - Semiconductor element - Google Patents
Semiconductor elementInfo
- Publication number
- JPH0793330B2 JPH0793330B2 JP26553486A JP26553486A JPH0793330B2 JP H0793330 B2 JPH0793330 B2 JP H0793330B2 JP 26553486 A JP26553486 A JP 26553486A JP 26553486 A JP26553486 A JP 26553486A JP H0793330 B2 JPH0793330 B2 JP H0793330B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- epoxy resin
- parts
- chip
- semiconductor element
- 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
- 239000004065 semiconductor Substances 0.000 title claims description 27
- 229920005989 resin Polymers 0.000 claims description 26
- 239000011347 resin Substances 0.000 claims description 26
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 18
- 239000003822 epoxy resin Substances 0.000 claims description 17
- 229920000647 polyepoxide Polymers 0.000 claims description 17
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 13
- 239000011342 resin composition Substances 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 9
- 239000005062 Polybutadiene Substances 0.000 claims description 8
- 229920002857 polybutadiene Polymers 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 claims description 7
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 description 16
- 230000001070 adhesive effect Effects 0.000 description 16
- 238000000034 method Methods 0.000 description 11
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229910000679 solder Inorganic materials 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 229910015365 Au—Si Inorganic materials 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000005496 eutectics Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 3
- 239000004843 novolac epoxy resin Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229920003319 Araldite® Polymers 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-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
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000011156 evaluation Methods 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
- 150000002500 ions Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- OTARVPUIYXHRRB-UHFFFAOYSA-N diethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](C)(OCC)CCCOCC1CO1 OTARVPUIYXHRRB-UHFFFAOYSA-N 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- -1 glycidyl ester Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-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
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
- Die Bonding (AREA)
- Conductive Materials (AREA)
Description
【発明の詳細な説明】 [発明の目的] (産業上の利用分野) 本発明は、大形ICなどチップを樹脂で封止した半導体素
子に関し、特に耐湿性、耐加水分解性、接着性に優れた
半導体素子に係るものである。DETAILED DESCRIPTION OF THE INVENTION Object of the Invention (Field of Industrial Application) The present invention relates to a semiconductor element such as a large IC in which a chip is sealed with a resin, and particularly to moisture resistance, hydrolysis resistance and adhesiveness. It relates to an excellent semiconductor device.
(従来の技術) 金属薄板(リードフレーム)上の所定部分にIC、LSI等
の半導体チップを接続する工程は、素子の長期信頼性に
影響を与える重要な工程の1つである。従来からこの接
続方法としてチップのシリコン面をリードフレーム上の
金メッキ面に加熱圧着するというAu−Si共晶法が主流で
あった。しかし、近年の貴金属、特に金の高騰を契機と
して、樹脂封止形半導体装置では、Au−Si共晶法から、
半田を使用する方法、導電性接着剤を使用する方法等に
急速に移行しつつある。(Prior Art) The process of connecting a semiconductor chip such as an IC or LSI to a predetermined portion on a thin metal plate (lead frame) is one of the important processes that affect the long-term reliability of the device. In the past, the Au-Si eutectic method, in which the silicon surface of the chip was thermocompression bonded to the gold-plated surface on the lead frame, was the mainstream connection method. However, in recent years, with the rise of precious metals, especially gold, in resin-sealed semiconductor devices, Au-Si eutectic method
The method of using solder, the method of using a conductive adhesive, etc. are rapidly shifting.
しかし、半田を使用する方法は、一部実用化されている
が半田や半田ボールが飛散して電極等に付着し、腐食断
線の原因となることが指摘されている。一方、導電性接
着剤を使用する方法では、通常、銀粉末を配合したエポ
キシ樹脂が用いられ、数10年程前から一部実用化されて
きたが、信頼性の面でAu−Si共晶法に比較して満足すべ
きものが得られなかった。導電性接着剤を使用する場合
は、半田法に比べて耐熱性に優れる等の長所を有してい
るが、その反面、樹脂や硬化剤が半導体素子接着用とし
て作られたものでないため、ボイドの発生や、耐湿性、
耐加水分解性に劣り、アルミニウム電極の腐食を促進
し、断線不良の原因となることが多く、素子の信頼性は
Au−Si共晶法に比べて劣っていた。また近年、IC/LSIや
LED等の半導体チップの大形化に伴い、チップクラック
の発生や接着力の低下が起こり、問題となってきた。However, although the method using solder has been partially put into practical use, it has been pointed out that solder or solder balls scatter and adhere to electrodes or the like, which causes corrosion breakage. On the other hand, in the method using a conductive adhesive, an epoxy resin mixed with silver powder is usually used, and it has been partially put into practical use for several decades, but in terms of reliability, the Au-Si eutectic We were not able to obtain satisfactory results in comparison with the law. When using a conductive adhesive, it has advantages such as superior heat resistance compared to the solder method, but on the other hand, since the resin and curing agent are not made for bonding semiconductor elements, voids Generation, moisture resistance,
Inferior in hydrolysis resistance, it promotes corrosion of aluminum electrodes and often causes disconnection failure.
It was inferior to the Au-Si eutectic method. In recent years, IC / LSI and
With the increase in the size of semiconductor chips such as LEDs, chip cracks have occurred and the adhesive strength has decreased, which has become a problem.
(発明が解決しようとする問題点) 本発明は、上記の事情・欠点に鑑みてなされたもので、
半導体チップの大形化に対応した耐湿性、耐加水分解
性、接着性に優れ、特に接着チップの反りを低減した信
頼性の高い半導体素子を提供しようとするものである。(Problems to be Solved by the Invention) The present invention has been made in view of the above circumstances and drawbacks.
It is an object of the present invention to provide a highly reliable semiconductor element which is excellent in moisture resistance, hydrolysis resistance and adhesiveness corresponding to an increase in size of a semiconductor chip, and in particular has reduced warpage of the adhesive chip.
[発明の構成] (問題点を解決するための手段と作用) 本発明者らは、上記の目的を達成しようと鋭意研究を重
ねた結果、後述する樹脂組成物を用いることによって、
耐湿性、耐加水分解性、接着性に優れ、ボイドの発生が
なく、またチップの反りが少ない高信頼性の半導体素子
が得られることを見いだし、本発明を完成したものであ
る。すなわち、本発明は、 (A)固形エポキシ樹脂 (B)低粘度液状エポキシ樹脂 (C)ノルボネン環を有する樹脂 (D)アクリロニトリル基を有するポリブタジエン系液
状樹脂 (E)イミダゾール系触媒および (F)導電性粉末 を含む樹脂組成物を用い、半導体チップとリードフレー
ムとを接着固定してなることを特徴とする半導体素子で
ある。[Structure of the Invention] (Means and Actions for Solving Problems) As a result of intensive studies to achieve the above-mentioned object, the present inventors have found that by using a resin composition described below,
The inventors have found that a highly reliable semiconductor element which is excellent in moisture resistance, hydrolysis resistance, and adhesiveness, does not generate voids, and has less chip warpage, and has completed the present invention. That is, the present invention provides (A) a solid epoxy resin, (B) a low-viscosity liquid epoxy resin, (C) a resin having a norbornene ring, (D) a polybutadiene liquid resin having an acrylonitrile group, (E) an imidazole catalyst, and (F) a conductive material. A semiconductor element characterized in that a semiconductor chip and a lead frame are bonded and fixed to each other using a resin composition containing a conductive powder.
本発明に用いる(A)固形エポキシ樹脂としては、工業
生産されており、かつ本発明に効果的に使用し得るもの
として、例えば次のようなビスフェノール類のジエポキ
シドがある。シェル化学社製エピコート1001,1002,100
4,1007,1009、ダウケミカル社製DER660,661,662,667,66
8,669、チバガイギー社製アラルダイトGY6071,6084,609
7,6099、大日本インキ化学工業社製エピクロン1010,301
0や旭電化社製EPシリーズ・EP−5100,5400,5700,5900
(以上いずれも商品名)等がある。さらに固形エポキシ
樹脂として、例えば平均エポキシ基数3以上のノボラッ
ク・エポキシ樹脂を使用することにより、熱時(350
℃)の接着強度を更に向上させることができ、このノボ
ラック・エポキシ樹脂としては、分子量500以上のもの
が適している。このようなノボラック・エポキシ樹脂で
工業生産されているものとしては、例えば次のようなも
のがある。チバガイギー社製アラルダイトEPN1138,113
9、ECN1273,1280,1299、ダウケミカル社製DEN431,438、
シェル化学社製エピコート152,154、ユニオンカーバイ
ト社製ERR−0100,ERRB−0447,ERLB−0488、日本化薬社
製EOCNシリーズ、山陽国策パルプ社製DER400(以上いず
れも商品名)等が挙げられ、これらは単独又は2種以上
の混合系として用いる。The solid epoxy resin (A) used in the present invention is industrially produced and can be effectively used in the present invention, for example, the following bisphenol diepoxides. Shell Chemical Co. Epicoat 1001,1002,100
4,1007,1009, DER660,661,662,667,66 made by Dow Chemical Company
8,669, Ciba Geigy Araldite GY6071,6084,609
7,6099, Dainippon Ink and Chemicals, Inc. Epicron 1010,301
0 and Asahi Denka EP series EP-5100,5400,5700,5900
(All of the above are trade names) etc. Furthermore, as a solid epoxy resin, for example, by using a novolac epoxy resin having an average number of epoxy groups of 3 or more, it is possible to reduce the heat (350
It is possible to further improve the adhesive strength at (° C.), and as this novolac epoxy resin, one having a molecular weight of 500 or more is suitable. Examples of industrially manufactured novolac epoxy resins include the following. Ciba Geigy Araldite EPN1138,113
9, ECN1273,1280,1299, DEN431,438 made by Dow Chemical Co.,
Shell Chemical Co., Ltd. Epicoat 152,154, Union Carbide Co. ERR-0100, ERRB-0447, ERLB-0488, Nippon Kayaku Co., Ltd. EOCN series, Sanyo Kokusaku Pulp Co., Ltd. DER400 (all above are trade names), etc. These are used alone or as a mixed system of two or more kinds.
本発明に用いる(B)低粘度液状エポキシ樹脂として
は、例えばβ−(3,4エポキシシクロヘキシル)エチル
トリメトキシシラン,γ−グリシドキシプロピルトリメ
トキシシラン,γ−グリシドキシプロピルメチルジエト
キシシラン等のシラン系モノマーおよびビスフェノール
形低粘度液状エポキシ樹脂,脂環式低粘度液状エポキシ
樹脂,グリシジルエーテル形エポキシ樹脂,グリシジル
エステル形エポキシ樹脂等が挙げられ、これらは単独も
しくは2種以上混合して用いる。Examples of the low viscosity liquid epoxy resin (B) used in the present invention include β- (3,4 epoxycyclohexyl) ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane. And other silane monomers and bisphenol type low-viscosity liquid epoxy resins, alicyclic low-viscosity liquid epoxy resins, glycidyl ether type epoxy resins, glycidyl ester type epoxy resins, and the like. These are used alone or in combination of two or more. .
(A)固形エポキシ樹脂と(B)低粘度液状エポキシ樹
脂とは重量比で5:95〜40:60の範囲で配合される。固形
エポキシ樹脂が5重量%未満では必要とする接着強度が
得られず、また40重量%を超えると導電性ペーストにし
た場合の作業性が極めて悪くなり好ましくない。The solid epoxy resin (A) and the low viscosity liquid epoxy resin (B) are blended in a weight ratio of 5:95 to 40:60. If the solid epoxy resin is less than 5% by weight, the required adhesive strength cannot be obtained, and if it exceeds 40% by weight, the workability of the conductive paste becomes extremely poor, which is not preferable.
本発明に用いる(C)ノルボネン環を有する樹脂として
は、石油樹脂などがあり、石油のC5〜C9留分から得られ
る汎用の樹脂である。例えば市販されているものとし
て、セロキサイド4000(ダイセル化学社製、商品名)、
タッキロール1000(住友化学工業社製、商品名)、クイ
ントン1500,1000,1300,1700(日本ゼオン社製、商品
名)等が挙げられる。そして、これらは単独又は2種以
上混合して用いる。ノルボネン環を有する樹脂の配合割
合は、前述した(A)固形エポキシ樹脂と(B)低粘度
液状エポキシ樹脂との合計量に対して0.5〜30重量%配
合することが望ましい。配合量が0.5重量%末端の場合
は、接着強度の向上に効果なく、また30重量%を超える
と反応性が劣る傾向にあり好ましくない。The resin having a norbornene ring (C) used in the present invention includes a petroleum resin and the like, which is a general-purpose resin obtained from a C 5 to C 9 fraction of petroleum. For example, as a commercially available product, Celoxide 4000 (trade name, manufactured by Daicel Chemical Co., Ltd.),
Tacky Roll 1000 (manufactured by Sumitomo Chemical Co., Ltd., trade name), Quinton 1500, 1000, 1300, 1700 (manufactured by Nippon Zeon Co., Ltd., trade name) and the like. And these are used individually or in mixture of 2 or more types. The proportion of the resin having a norbornene ring is preferably 0.5 to 30% by weight based on the total amount of the above-mentioned (A) solid epoxy resin and (B) low-viscosity liquid epoxy resin. When the compounding amount is 0.5% by weight at the end, there is no effect in improving the adhesive strength, and when it exceeds 30% by weight, the reactivity tends to be poor, which is not preferable.
本発明に用いる(D)アクリロニトリル基を有するポリ
ブタジエン系液状樹脂としては、例えばCTBN1300,2000
(宇部興産社製、商品名)等が挙げられ、1種又は2種
以上混合して使用する。このポリブタジエン系液状樹脂
の配合割合は、(A)固形エポキシ樹脂と(B)低粘度
液状エポキシ樹脂との合計量に対して0.5〜30重量%配
合することが望ましい。配合量が0.5重量%未満の場合
は、低応力に効果がなく、また30重量%を超えると接着
力が低下する傾向にあり好ましくない。Examples of the (A) acrylonitrile group-containing polybutadiene liquid resin used in the present invention include CTBN1300 and 2000.
(Manufactured by Ube Industries, Ltd.) and the like, and one kind or a mixture of two or more kinds is used. The mixing ratio of the polybutadiene liquid resin is preferably 0.5 to 30% by weight based on the total amount of the (A) solid epoxy resin and the (B) low viscosity liquid epoxy resin. If the blending amount is less than 0.5% by weight, there is no effect on low stress, and if the blending amount exceeds 30% by weight, the adhesive force tends to decrease, which is not preferable.
本発明に用いる(E)イミダゾール系触媒としては、例
えば四国化成工業社製の2PZ−OK,2PZ−CN,2MZ−OK(以
上いずれも商品名)等がある。イミダゾール系触媒は、
通常、(A)固形エポキシ樹脂と(B)低粘度液状エポ
キシ樹脂との合計量に対して0.01〜8重量%配合する。Examples of the (E) imidazole catalyst used in the present invention include 2PZ-OK, 2PZ-CN, 2MZ-OK (all of which are trade names) manufactured by Shikoku Chemicals. The imidazole-based catalyst is
Usually, 0.01 to 8% by weight is blended with respect to the total amount of (A) solid epoxy resin and (B) low-viscosity liquid epoxy resin.
本発明に用いる(A)固形エポキシ樹脂,(B)低粘度
液状エポキシ樹脂,(C)ノルボネン環を有する樹脂,
(D)アクリロニトリル基を有するポリブタジエン系液
状樹脂および(E)イミダゾール系触媒を配合する場合
は、全成分に溶剤を加えて混合溶解させてもよいが、最
初にノルボネン環を有する樹脂およびアクリロニトリル
基を有するポリブタジエン系液状樹脂を溶剤に溶解させ
た後、これに固形エポキシ樹脂と低粘度液状エポキシ樹
脂とを溶解混合したものを、添加混合することが望まし
い。ここで用いる粘度調整用の溶剤類としては、ジオキ
サン,ヘキサノン,ベンゼン,トルエン,ソルベントナ
フサ,工業用ガソリン,酢酸セロソルブ,エチルセロソ
ルブ,ブチルセロソルブアセテート,ブチルカルビトー
ルアセテート,ジメチルホルムアミド,ジメチルアセト
アミド,N−メチルピロリドン等が挙げられ、これらは単
独もしくは2種以上混合して使用することができる。(A) solid epoxy resin used in the present invention, (B) low viscosity liquid epoxy resin, (C) resin having norbornene ring,
When (D) a polybutadiene-based liquid resin having an acrylonitrile group and (E) an imidazole-based catalyst are blended, a solvent may be added to all components and mixed and dissolved, but first, a resin having a norbonene ring and an acrylonitrile group are first added. It is desirable to dissolve the polybutadiene-based liquid resin that is contained in a solvent and then add and mix a mixture of the solid epoxy resin and the low-viscosity liquid epoxy resin. Examples of the viscosity adjusting solvent used here include dioxane, hexanone, benzene, toluene, solvent naphtha, industrial gasoline, cellosolve acetate, ethyl cellosolve, butyl cellosolve acetate, butyl carbitol acetate, dimethylformamide, dimethylacetamide, N-methyl. Examples thereof include pyrrolidone, and these can be used alone or in combination of two or more.
本発明に用いる(F)導電性粉末としては、例えば銀粉
末等が使用される。As the conductive powder (F) used in the present invention, for example, silver powder or the like is used.
本発明に用いる樹脂組成物は、固形エポキシ樹脂,低粘
度液状エポキシ樹脂,ノルボネン環を有する樹脂,アク
リロニトリル基を有する液状ポリブタジエン樹脂,イミ
ダゾール系触媒,導電性粉末を含むが、必要に応じて消
泡剤,カップリング剤その他の添加剤を加えることがで
きる。そして、この樹脂組成物は、常法に従い各原料成
分を充分混合した後、更に例えば三本ロールによる混練
処理をし、その後、減圧脱泡して製造することができ
る。こうして製造した樹脂組成物を用いて半導体チップ
とリードフレームを接着固定した後、ワイヤボンディン
グを行い、次いで樹脂で封止して半導体素子を製造す
る。この半導体素子は、200℃で樹脂組成物を加熱硬化
させても、大型チップの反り変形が少なく、接着力は半
導体チップの接着に必要な強度を有し、ワイヤボンディ
ング強度も同じく4〜5gの値以上の強度を得ることがで
きる。The resin composition used in the present invention contains a solid epoxy resin, a low-viscosity liquid epoxy resin, a resin having a norbornene ring, a liquid polybutadiene resin having an acrylonitrile group, an imidazole-based catalyst, and a conductive powder. Agents, coupling agents and other additives can be added. Then, this resin composition can be produced by sufficiently mixing the respective raw material components according to a conventional method, further kneading with, for example, three rolls, and then defoaming under reduced pressure. After the semiconductor chip and the lead frame are bonded and fixed using the resin composition thus manufactured, wire bonding is performed, and then the semiconductor chip is manufactured by sealing with a resin. This semiconductor element has little warp deformation of a large chip even when a resin composition is heated and cured at 200 ° C., has an adhesive strength required for bonding a semiconductor chip, and a wire bonding strength of 4 to 5 g. It is possible to obtain a strength equal to or higher than the value.
(実施例) 次に本発明を実施例によって説明するが、本発明はこれ
らの実施例によって限定されるものではない。実施例お
よび比較例において「部」とは特に説明のない限り「重
量部」を意味する。(Examples) Next, the present invention will be described with reference to examples, but the present invention is not limited to these examples. In the examples and comparative examples, "parts" means "parts by weight" unless otherwise specified.
実施例 1 固形エポキシ樹脂EOCN103S(日本化薬社製、商品名)9.
6部、液状エポキシ樹脂EX201(長瀬化成社製、商品名)
9.6部、ノルボネン環を有する樹脂セロキサイド4000
(ダイセル社製、商品名)3.0部、ポリブタジエン系樹
脂CTBN1300(宇部興産社製、商品名)3.0部およびジエ
チレングリコールジエチルエーテル1.8部を混合溶解
し、粘稠な褐色の樹脂を得た。この樹脂29部に触媒とし
て2PZ−OK(四国化成工業社製、商品名)1.2部と銀粉末
70部とを混合して樹脂組成物Aを製造した。Example 1 Solid epoxy resin EOCN103S (trade name, manufactured by Nippon Kayaku Co., Ltd.) 9.
6 parts, liquid epoxy resin EX201 (product name, manufactured by Nagase Kasei Co., Ltd.)
9.6 parts, resin Celoxide 4000 having norbornene ring
(Daicel Co., Ltd., trade name) 3.0 parts, polybutadiene-based resin CTBN1300 (Ube Industries, trade name) 3.0 parts and diethylene glycol diethyl ether 1.8 parts were mixed and dissolved to obtain a viscous brown resin. To 29 parts of this resin, 1.2 parts of 2PZ-OK (manufactured by Shikoku Kasei Kogyo Co., Ltd.) as a catalyst and silver powder
70 parts were mixed to prepare a resin composition A.
実施例 2 EOCN103S(前出)5.0部、EP1001(シェル化学社製、商
品名)4.6部、EX201(前出)9.6部、クイントン1700
(日本ゼオン社製、商品名)3.0部、およびジエチレン
グリコールジエチルエーテル1.8部を混合溶解し、粘稠
な褐色の樹脂を得た。この樹脂29部に触媒として2PZ−O
K(前出)1.2部と銀粉末70部を混合して樹脂組成物Bを
製造した。Example 2 EOCN103S (supra) 5.0 parts, EP1001 (Shell Chemical Co., trade name) 4.6 parts, EX201 (supra) 9.6 parts, Quinton 1700
(Nippon Zeon Co., Ltd., trade name) 3.0 parts and diethylene glycol diethyl ether 1.8 parts were mixed and dissolved to obtain a viscous brown resin. 2PZ-O as a catalyst was added to 29 parts of this resin.
A resin composition B was manufactured by mixing 1.2 parts of K (described above) and 70 parts of silver powder.
実施例 3 DEC400(山陽国策パルプ社製、商品名)9.6部、EX201
(前出)9.6部、クイントン1700(前出)3.0部、CTBN13
00(前出)3.0部、およびジエチレングリコールジエチ
ルエーテル1.8部を混合溶解し、粘稠な黄色の樹脂を得
た。この樹脂29部に触媒として2PZ−OK(前出)1.2部と
銀粉末70部とを加えて十分混合して樹脂組成物Cを製造
した。Example 3 DEC400 (manufactured by Sanyo Kokusaku Pulp Company, trade name) 9.6 parts, EX201
(Previously) 9.6 copies, Quinton 1700 (previously) 3.0 copies, CTBN13
3.0 parts of 00 (described above) and 1.8 parts of diethylene glycol diethyl ether were mixed and dissolved to obtain a viscous yellow resin. To 29 parts of this resin, 1.2 parts of 2PZ-OK (mentioned above) as a catalyst and 70 parts of silver powder were added and sufficiently mixed to produce a resin composition C.
比較例 市販のエポキシ樹脂ベースの溶剤型半導体用導電性接着
剤Dを入手した。Comparative Example A commercially available epoxy resin-based conductive adhesive D for solvent type semiconductors was obtained.
実施例1〜3および比較例で得た樹脂組成物A,B,Cおよ
び導電性接着剤Dを用いて半導体チップとリードフレー
ムとを接着硬化して半導体素子を製造した。これらの半
導体素子について接着強度、加水分解性、耐湿性、チッ
プの反りの試験を行った。その結果を第1表に示したが
いずれも本発明の顕著な効果が認められた。Using the resin compositions A, B, C and the conductive adhesive D obtained in Examples 1 to 3 and Comparative Example, a semiconductor chip and a lead frame were adhesively cured to produce a semiconductor element. These semiconductor devices were tested for adhesive strength, hydrolyzability, moisture resistance and chip warpage. The results are shown in Table 1, and in all cases, the remarkable effect of the present invention was recognized.
接着強度は、200μm厚のリードフレーム(銅系)上に
4×12mmのシリコンチップを接着し、それぞれの温度で
プッシュプルゲージを用いて測定した。加水分解性Clイ
オンは、半導体素子接着条件で硬化させた後、100メッ
シュに粉砕して、180℃で2時間加熱抽出を行ったClイ
オンの量を測定した。耐湿性試験は、温度121℃,圧力
2気圧の水蒸気中における耐湿試験(PCT)および温度1
20℃,圧力2気圧の水蒸気中印加電圧直流15Vを通電し
て耐湿試験(バイアス−PCT)を各半導体素子について
行い評価した。この試験に供した半導体素子数は各々60
個で、時間の経過に伴う不良発生数を第1表に示した。
なお、評価の方法は半導体素子を構成するアルミニウム
電極の腐食によるオープン又はリーク電流が許容値の50
0%以上への上昇をもって不良と判定した。チップの反
りは、硬化後のチップ表面を表面あらさ計で測定し、チ
ップ中央部と末端との距離で示した。The adhesive strength was measured by sticking a 4 × 12 mm silicon chip on a 200 μm thick lead frame (copper-based) and using a push-pull gauge at each temperature. The hydrolyzable Cl ion was cured under the conditions for adhering to a semiconductor device, then pulverized into 100 mesh, and heated and extracted at 180 ° C. for 2 hours to measure the amount of Cl ion. Humidity resistance test is conducted at a temperature of 121 ° C and a pressure of 2 atm in water vapor (PCT) and a temperature of 1
A moisture resistance test (bias-PCT) was conducted on each semiconductor element by applying an applied voltage of 15 V DC in water vapor at 20 ° C. and a pressure of 2 atm for evaluation. The number of semiconductor devices used in this test is 60 each.
Table 1 shows the number of defects generated with the passage of time.
The evaluation method is that the open or leak current due to the corrosion of the aluminum electrode that constitutes the semiconductor element is 50% of the allowable value.
It was judged to be defective when it increased to 0% or more. The warp of the chip was measured by measuring the surface of the chip after curing with a surface roughness meter and indicated by the distance between the center of the chip and the end.
[発明の効果] 以上の説明および第1表からも明らかなように本発明の
半導体素子は、樹脂組成物を接着剤として用いたことに
よって、優れた耐湿性、耐加水分解性を示し、その結果
アルミニウム電極の腐食による断線不良等が起こらず、
ボイドの発生もなく、接着チップの反りが少なく、また
接着性、特に熱時の接着性に優れた、高信頼性の製品を
得ることができる。 [Effects of the Invention] As is clear from the above description and Table 1, the semiconductor element of the present invention exhibits excellent moisture resistance and hydrolysis resistance by using the resin composition as an adhesive. As a result, there is no disconnection failure due to corrosion of the aluminum electrode,
It is possible to obtain a highly reliable product in which voids do not occur, the adhesive chip warps little, and the adhesiveness is excellent, especially when heated.
Claims (1)
状樹脂 (E)イミダゾール系触媒および (F)導電性粉末 を含む樹脂組成物を用い、半導体チップとリードフレー
ムとを接着固定してなることを特徴とする半導体素子。1. (A) Solid epoxy resin (B) Low-viscosity liquid epoxy resin (C) Resin having norbornene ring (D) Acrylonitrile group-containing polybutadiene liquid resin (E) Imidazole catalyst and (F) Conductivity A semiconductor element comprising a resin composition containing powder, and a semiconductor chip and a lead frame bonded and fixed to each other.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26553486A JPH0793330B2 (en) | 1986-11-10 | 1986-11-10 | Semiconductor element |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26553486A JPH0793330B2 (en) | 1986-11-10 | 1986-11-10 | Semiconductor element |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63120432A JPS63120432A (en) | 1988-05-24 |
| JPH0793330B2 true JPH0793330B2 (en) | 1995-10-09 |
Family
ID=17418460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP26553486A Expired - Lifetime JPH0793330B2 (en) | 1986-11-10 | 1986-11-10 | Semiconductor element |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0793330B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4690714B2 (en) * | 2004-12-09 | 2011-06-01 | 積水化学工業株式会社 | Epoxy curable composition and electronic component mounting structure |
| JP6388202B2 (en) * | 2014-08-07 | 2018-09-12 | パナソニックIpマネジメント株式会社 | Insulating resin sheet, and circuit board and semiconductor package using the same |
-
1986
- 1986-11-10 JP JP26553486A patent/JPH0793330B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63120432A (en) | 1988-05-24 |
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