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JP2000344864A - Resin paste for semiconductor and semiconductor device sealed therewith - Google Patents

Resin paste for semiconductor and semiconductor device sealed therewith

Info

Publication number
JP2000344864A
JP2000344864A JP11162121A JP16212199A JP2000344864A JP 2000344864 A JP2000344864 A JP 2000344864A JP 11162121 A JP11162121 A JP 11162121A JP 16212199 A JP16212199 A JP 16212199A JP 2000344864 A JP2000344864 A JP 2000344864A
Authority
JP
Japan
Prior art keywords
resin
epoxy resin
resin paste
semiconductor
paste
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.)
Pending
Application number
JP11162121A
Other languages
Japanese (ja)
Inventor
Shingo Ito
慎吾 伊藤
Hikari Okubo
光 大久保
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP11162121A priority Critical patent/JP2000344864A/en
Publication of JP2000344864A publication Critical patent/JP2000344864A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a resin paste capable of rapid curing by curing in an oven and exhibiting high hot adhesive strength and giving bonding having excellent stress relaxation and high reliability by including an epoxy resin with a latent curing agent, an imidazole compound, and an inorganic filler. SOLUTION: An epoxy resin (100 pts.wt.) prepared by mixing a liquid epoxy resin having a structure of the formula (wherein n>=0) with an epoxy-containing reactive diluent in a weight ratio of 60/40 to 90/10 is mixed with 0.5-5 pts.wt. latent curing agent such as adipic hydrazide or dicyandiamide, 0.5-10 pts.wt. imidazole compound, and an inorganic filler such as a silver powder or a silica filler. The obtained mixture is kneaded with a three-roll mill, and deaerated in a vacuum to obtain a resin paste for semiconductors. This resin paste is suited for bonding of a large chip such as an IC to a copper frame and can give a semiconductor device made proof against malfunction due to chip crack and warpage and having high reliability.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明はIC、LSI等の半
導体素子を金属フレーム等に接着する樹脂ペーストに関
するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin paste for bonding a semiconductor element such as an IC or an LSI to a metal frame or the like.

【0002】[0002]

【従来の技術】エレクトロニクス業界の最近の著しい発
展により、トランジスター、IC、LSI、超LSIと進化して
きており、これら半導体素子に於ける回路の集積度が急
激に増大すると共に大量生産が可能となり、これらを用
いた半導体製品の普及に伴って、その量産に於ける作業
性の向上並びにコストダウンが重要な問題となってき
た。従来は半導体素子を金属フレームなどの導体にAu-S
i共晶法により接合し、次いでハーメチックシールによ
って封止して、半導体製品とするのが普通であった。し
かし量産時の作業性、コストの面より、樹脂封止法が開
発され、現在は一般化されている。これに伴い、マウン
ト工程に於けるAu-Si共晶法の改良としてハンダ材料や
樹脂ペースト即ちマウント用樹脂による方法が取り上げ
られるようになった。
2. Description of the Related Art Recent remarkable developments in the electronics industry have evolved into transistors, ICs, LSIs, and ultra-LSIs. The integration of circuits in these semiconductor devices has rapidly increased, and mass production has become possible. With the spread of semiconductor products using these, improvement in workability and cost reduction in mass production have become important issues. Conventionally, semiconductor elements were replaced with Au-S
In general, they were joined by an eutectic method and then sealed by a hermetic seal to obtain a semiconductor product. However, in view of workability and cost during mass production, a resin encapsulation method has been developed and is now generally used. Along with this, a method using a solder material or a resin paste, that is, a mounting resin has come to be taken up as an improvement of the Au-Si eutectic method in the mounting step.

【0003】しかし、ハンダ法では信頼性が低いこと、
素子の電極の汚染を起こし易いこと等が欠点とされ、高
熱伝導性を要するパワートランジスター、パワーICの素
子に使用が限られている。これに対しマウント用樹脂は
ハンダ法に較べ、作業性に於いても信頼性等に於いても
優れており、その需要が急激に増大している。
However, the solder method has low reliability,
The disadvantage is that the electrodes of the element are liable to be contaminated, and the use thereof is limited to power transistors and power IC elements that require high thermal conductivity. On the other hand, the mounting resin is superior in workability and reliability as compared with the soldering method, and the demand thereof is rapidly increasing.

【0004】更に近年、IC等の集積度の高密度化によ
り、チップが大型化してきており、一方従来用いられて
きたリードフレームである42合金フレームが高価なこと
より、コストダウンの目的から銅フレームが用いられる
ようになってきた。ここでIC等のチップの大きさが約4
〜5mm角より大きくなると、IC等の組立工程での加熱に
より、マウント法としてAu-Si共晶法を用いると、チッ
プの熱膨張率と銅フレームの熱膨張率との差からチップ
のクラックや反りによる特性不良が問題となってきてい
る。
Further, in recent years, the chip has been increased in size due to the increase in the degree of integration of ICs and the like. On the other hand, since the 42 alloy frame, which has been conventionally used, is expensive, copper is used for cost reduction purposes. Frames have come to be used. Here, the size of the chip such as IC is about 4
When the size is larger than ~ 5 mm square, chip cracking or cracking may occur due to the difference between the coefficient of thermal expansion of the chip and the coefficient of thermal expansion of the copper frame when Au-Si eutectic method is used as the mounting method due to heating during the assembly process of ICs and the like. Defective characteristics due to warpage have become a problem.

【0005】即ちこれは、チップの材料であるシリコン
等の熱膨張率が3×10-6/℃であるのに対し、42合金フレ
ームでは8×10-6/℃であるが、銅フレームでは20×10-6
/℃と大きくなる為である。これに対し、マウント法と
してマウント用樹脂を用いることが考えられるが、従来
のエポキシ樹脂系ペーストでは、熱硬化性樹脂で三次元
硬化する為、弾性率が高く、チップと銅フレームとの歪
を吸収するには至らなかった。
That is, the thermal expansion coefficient of silicon or the like as a chip material is 3 × 10 −6 / ° C., whereas that of a 42 alloy frame is 8 × 10 −6 / ° C. 20 × 10 -6
/ ° C. On the other hand, it is conceivable to use a mounting resin as the mounting method.However, with a conventional epoxy resin-based paste, since the thermosetting resin is three-dimensionally cured, the elastic modulus is high, and the distortion between the chip and the copper frame is reduced. Did not absorb.

【0006】また、硬化時に架橋密度を小さくするよう
なエポキシ樹脂、例えばエポキシモノマーを多量に含む
ものを使用すれば弾性率を低くできるが、接着強度が低
下するという欠点があった。更に通常のエポキシ樹脂は
粘度が高く、これに無機フィラーを配合すると粘度が高
くなりすぎ、ディスペンス時の糸ひきが発生し作業性が
悪くなる。作業性を改良するために多量の溶剤を添加す
るとボイドが発生するという問題があった。また従来の
マウント用樹脂は硬化に150〜200℃のオーブンで1〜2時
間加熱処理する必要があった。最近では半導体組立工程
の合理化のため、オーブンで30分以内に硬化するイン
ライン化の要求が高まっている。速硬化にするために
は、硬化促進剤を多量に添加する方法があるが、常温ま
たは低温での保存性、すなわちポットライフやシェルラ
イフが短くなり、1液タイプでは実用性がなく、熱時の
接着強度も低いという欠点があった。
If an epoxy resin which reduces the crosslink density during curing, for example, a resin containing a large amount of an epoxy monomer, is used, the modulus of elasticity can be lowered, but there is a disadvantage that the adhesive strength is reduced. Furthermore, a normal epoxy resin has a high viscosity, and if an inorganic filler is added thereto, the viscosity becomes too high, and threading occurs during dispensing, resulting in poor workability. When a large amount of solvent is added to improve workability, there is a problem that voids are generated. Further, the conventional mounting resin had to be heat-treated in an oven at 150 to 200 ° C. for 1 to 2 hours for curing. Recently, there has been an increasing demand for in-line curing in an oven within 30 minutes in order to streamline the semiconductor assembly process. There is a method of adding a large amount of a curing accelerator to achieve rapid curing, but the storage stability at room temperature or low temperature, that is, the pot life and the shell life is shortened, and the one-pack type is not practical and Had a disadvantage that the adhesive strength was low.

【0007】[0007]

【発明が解決しようとする課題】本発明の目的は、熱時
接着強度を低下させないで、IC等の大型チップと銅フ
レーム等の組合せでもチップクラックや反りによるIC
等の特性不良が起こらず、速硬化でかつボイドの発生の
ない樹脂ペーストを提供することにある。
SUMMARY OF THE INVENTION It is an object of the present invention to provide an IC which is not affected by chip cracks or warpage even in a combination of a large chip such as an IC and a copper frame without lowering the adhesive strength when heated.
It is an object of the present invention to provide a resin paste which does not cause poor properties such as the above, is fast-curing, and does not generate voids.

【0008】[0008]

【課題を解決するための手段】本発明は、熱時接着強度
を低下させないで硬化物の低弾性率化を計ったもので、
一般式(1)の構造を有する液状エポキシ樹脂とエポキ
シ基を有する反応性希釈剤の重量比が60:40〜9
0:10である(A)エポキシ樹脂、(B)潜在性硬化
剤、(C)イミダゾール化合物、(D)無機フィラーか
らなり、成分(A)100重量部に対し、成分(B)が
0.5〜5重量部、成分(C)が0.5〜10重量部で
ある半導体用樹脂ペーストである。また、上記の半導体
用樹脂ペーストを用いて製作された半導体装置である。
SUMMARY OF THE INVENTION The present invention aims at lowering the elastic modulus of a cured product without lowering the adhesive strength during heating.
The weight ratio of the liquid epoxy resin having the structure of the general formula (1) to the reactive diluent having an epoxy group is 60:40 to 9
0:10, comprising (A) an epoxy resin, (B) a latent curing agent, (C) an imidazole compound, and (D) an inorganic filler. It is a resin paste for a semiconductor containing 5 to 5 parts by weight and 0.5 to 10 parts by weight of the component (C). Further, the present invention is a semiconductor device manufactured using the above-mentioned resin paste for a semiconductor.

【0009】[0009]

【化1】 Embedded image

【0010】[0010]

【発明の実施の形態】本発明に用いるエポキシ樹脂
(A)は、一般式(1)の構造を有する液状エポキシ樹
脂とエポキシ基を有する反応性希釈剤の重量比が60:
40〜90:10である液状のエポキシ樹脂である。一
般式(1)で示されるものは分子量により各種のものが
あるが、分子量が小さく常温で液状のものが、配合する
ときの作業性及び配合後の粘度の点から好ましい。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The epoxy resin (A) used in the present invention has a weight ratio of a liquid epoxy resin having a structure of the general formula (1) to a reactive diluent having an epoxy group of 60:
It is a liquid epoxy resin having a ratio of 40 to 90:10. The compound represented by the general formula (1) has various types depending on the molecular weight. However, a compound having a small molecular weight and being liquid at ordinary temperature is preferable in view of workability at the time of compounding and viscosity after compounding.

【0011】一般式(1)で示される液状エポキシ樹脂
と混合するエポキシ基を有する反応性希釈剤には、例え
ば、n−ブチルグリシジルエーテル、バーサティック酸
グリシジルエステル、スチレンオサイド、エチルヘキシ
ルグリシジルエーテル、フェニルグリシジルエーテル、
クレジルグリシジルエーテル、ブチルフェニルグリシジ
ルエーテル等があり、これらの内の1種類あるいは複数
種と併用可能である。
The reactive diluent having an epoxy group to be mixed with the liquid epoxy resin represented by the general formula (1) includes, for example, n-butyl glycidyl ether, glycidyl versatate, styrene oside, ethylhexyl glycidyl ether, Phenylglycidyl ether,
There are cresyl glycidyl ether, butylphenyl glycidyl ether and the like, and one or more of these can be used in combination.

【0012】一般式(1)で示される液状エポキシ樹脂
とエポキシ基を有する反応性希釈剤の重量比は60:4
0〜90:10であることが好ましい。反応性希釈剤の
重量比が40を越えると接着強度が弱く、10未満では
樹脂ペーストとしたときに粘度が高くなり作業性が低下
する。
The weight ratio of the liquid epoxy resin represented by the general formula (1) to the reactive diluent having an epoxy group is 60: 4.
It is preferably 0 to 90:10. When the weight ratio of the reactive diluent exceeds 40, the adhesive strength is weak, and when it is less than 10, the viscosity becomes high when the resin paste is used, and the workability is reduced.

【0013】本発明においては他のエポキシ樹脂を混合
して用いてもよい。上記エポキシ樹脂と混合する場合の
他のエポキシ樹脂としては,例えばビスフェノールA、
ビスフェノールF、フェノールノボラック、クレゾール
ノボラック類とエピクロルヒドリンとの反応により得ら
れるポリグリシジルエーテル、ブタンジオールジグリシ
ジルエーテル、ネオペンチルグリコールジグリシジルエ
ーテル等の脂肪族エポキシ、ジグリシジルヒダントイン
等の複素環式エポキシ、ビニルシクロヘキセンジオキサ
イド、ジシクロペンタジエンジオキサイド、アリサイク
リックジエポキシーアジペイトのような脂環式エポキシ
があり、これらの内の1種類あるいは複数種と併用可能
である。
In the present invention, other epoxy resins may be mixed and used. As other epoxy resins when mixed with the above epoxy resin, for example, bisphenol A,
Bisphenol F, phenol novolak, aliphatic epoxy such as polyglycidyl ether, butanediol diglycidyl ether, neopentyl glycol diglycidyl ether obtained by reaction of cresol novolaks with epichlorohydrin, heterocyclic epoxy such as diglycidyl hydantoin, vinyl There are alicyclic epoxies such as cyclohexene dioxide, dicyclopentadiene dioxide, and alicyclic diepoxy-adipate, which can be used in combination with one or more of these.

【0014】本発明に用いる潜在性硬化剤(B)は、エ
ポキシ樹脂の硬化剤として用いられ、例えばアジピン酸
ジヒドラジド、ドデカン酸ジヒドラジド、イソフタル酸
ジヒドラジド、P-オキシ安息香酸ジヒドラジド等のカル
ボン酸ジヒドラジドやジシアンジアミド等の潜在性硬化
剤である。潜在性硬化剤を用いるとフェノール硬化剤単
独で硬化した場合に比べ著しく熱時接着強度が高くな
る。又潜在性硬化剤はフェノール硬化剤よりも当量が小
さいため、併用することにより粘度がそれ程高くなく、
又潜在性であるため保存性にも優れたペーストを得るこ
とができる。潜在性硬化剤(B)の配合量は全エポキシ
樹脂に対し、0.5〜5重量%使用するのが好ましい。0.5
重量%未満では熱時接着強度が弱く、5重量%を越える
と低応力性が低下する。
The latent curing agent (B) used in the present invention is used as a curing agent for epoxy resins, for example, carboxylic acid dihydrazide such as adipic acid dihydrazide, dodecanoic acid dihydrazide, isophthalic acid dihydrazide, P-oxybenzoic acid dihydrazide and the like. It is a latent curing agent such as dicyandiamide. When a latent curing agent is used, the adhesive strength when heated becomes significantly higher than when cured with a phenol curing agent alone. Also, since the latent curing agent has a smaller equivalent weight than the phenolic curing agent, the viscosity is not so high when used in combination,
In addition, since it is latent, a paste having excellent storage stability can be obtained. The amount of the latent curing agent (B) is preferably 0.5 to 5% by weight based on the total epoxy resin. 0.5
If the amount is less than 5% by weight, the adhesive strength at the time of heating is weak, and if it exceeds 5% by weight, the low stress property is reduced.

【0015】本発明においては,速硬化を可能とするた
めイミダゾール化合物(C)を使用することを必須とし
ている。一般にイミダゾール化合物は,目的とする温度
170〜250℃で硬化時間が短いことが知られてい
る。イミダゾール化合物としては,例えば2−メチルイ
ミダゾール,2−エチルイミダゾール,2−フェニルイ
ミダゾール,2−フェニル−4−メチルイミダゾール,
2−フェニル−4−メチル−5−ヒドロキシメチルイミ
ダゾール,2−フェニル−4,5−ジヒドロキシメチル
イミダゾール,2−C1123−イミダゾール等の一般的
なイミダゾールやトリアジンやイソシアヌル酸を付加
し,保存安定性を付与した2,4−ジアミノ−6−{2
−メチルイミダゾール−(1)}−エチル−S−トリア
ジン,またそのイソシアネート付加物等があり,これら
の内の1種類あるいは複数種と併用可能である。イミダ
ゾール化合物の配合量は、全エポキシ樹脂に対し、0.
5〜10重量%使用するのが好ましい。0.5重量%未
満では熱時接着強度が弱く、10重量%を越えるとポッ
トライフ著しく短くなる。
In the present invention, it is essential to use an imidazole compound (C) to enable rapid curing. Generally, it is known that an imidazole compound has a short curing time at a target temperature of 170 to 250 ° C. Examples of the imidazole compound include 2-methylimidazole, 2-ethylimidazole, 2-phenylimidazole, 2-phenyl-4-methylimidazole,
2-phenyl-4-methyl-5-hydroxymethylimidazole, 2-phenyl-4,5-dihydroxy methyl imidazole, 2-C 11 H 23 - adds a generic imidazole or triazine and isocyanuric acid such as imidazole, save 2,4-diamino-6- {2} with stability
-Methylimidazole- (1)}-ethyl-S-triazine and its isocyanate adducts, etc., and can be used in combination with one or more of these. The compounding amount of the imidazole compound is 0.1% with respect to all epoxy resins.
It is preferable to use 5 to 10% by weight. If it is less than 0.5% by weight, the adhesive strength under heat is weak, and if it exceeds 10% by weight, the pot life becomes extremely short.

【0016】本発明に用いる無機フィラー(D)として
は銀粉、シリカフィラー等がある。
The inorganic filler (D) used in the present invention includes silver powder and silica filler.

【0017】銀粉は導電性を付与するために用いられ、
ハロゲンイオン、アルカリ金属イオン等のイオン性不純
物の含有量は10ppm以下であることが好ましい。又銀粉
の形状としてはフレーク状、樹脂状や球状等が用いられ
る。必要とするペーストの粘度により、使用する銀粉の
粒径は異なるが、通常平均粒径は2〜10μm、最大粒径
は50μm程度のものが好ましい。又比較的粗い銀粉と細
かい銀粉とを混合して用いることもでき、形状について
も各種のものを適宜混合してもよい。
Silver powder is used for imparting conductivity,
The content of ionic impurities such as halogen ions and alkali metal ions is preferably 10 ppm or less. The shape of the silver powder may be flake, resin, sphere or the like. The particle size of the silver powder to be used varies depending on the required viscosity of the paste, but usually the average particle size is preferably 2 to 10 μm, and the maximum particle size is preferably about 50 μm. In addition, a mixture of relatively coarse silver powder and fine silver powder can be used, and various shapes may be appropriately mixed.

【0018】本発明に用いるシリカフィラーは平均粒径
1〜20μmで最大粒径50μm以下のものである。平均粒
径が1μm以下だと粘度が高くなり、20μm以上だと塗
布又は硬化時に樹脂分が流出するのでブリードが発生す
るため好ましくない。最大粒径が50μmを越えるとディ
スペンサーでペーストを塗布するときに、ニードルの出
口を塞ぎ長時間の連続使用ができない。又比較的粗いシ
リカフィラーと細かいシリカフィラーとを混合して用い
ることもでき、形状についても各種のものを適宜混合し
てもよい。
The silica filler used in the present invention has an average particle size.
It has a maximum particle size of 50 μm or less with a size of 1 to 20 μm. If the average particle size is 1 μm or less, the viscosity increases, and if the average particle size is 20 μm or more, bleeding occurs because the resin component flows out during coating or curing, which is not preferable. If the maximum particle size exceeds 50 μm, the outlet of the needle is blocked when applying the paste with a dispenser, so that long-time continuous use cannot be performed. Further, a mixture of a relatively coarse silica filler and a fine silica filler may be used, and various shapes may be appropriately mixed.

【0019】又、必要とされる特性を付与するために本
発明以外の無機フィラーを添加してもよい。
Further, an inorganic filler other than the present invention may be added to impart required properties.

【0020】本発明における樹脂ペーストには、必要に
より用途に応じた特性を損なわない範囲内で、シランカ
ップリング剤、チタネートカップリング剤、顔料、染
料、消泡剤、界面活性剤、溶剤等の添加剤を用いること
ができる。本発明の製造法としては、例えば各成分を予
備混合して三本ロール等を用いて、ペーストを得て、真
空下脱泡すること等がある。
The resin paste according to the present invention may contain a silane coupling agent, a titanate coupling agent, a pigment, a dye, a defoaming agent, a surfactant, a solvent, etc., as long as the properties according to the intended use are not impaired. Additives can be used. As the production method of the present invention, for example, there is a method in which each component is premixed, a paste is obtained using a three-roll or the like, and the paste is defoamed under vacuum.

【0021】本発明の半導体用樹脂ペーストを用いて製
作された半導体装置は、オーブン硬化での速硬化が可能
で、熱時接着強度の低下がなく、大型チップと銅フレー
ム等の組み合わせでも反りがないため、信頼性の高い半
導体装置を得ることが出来る。半導体用樹脂ペーストを
用いて半導体装置を製作する方法は公知の方法を用いる
ことが出来る。
A semiconductor device manufactured by using the resin paste for a semiconductor of the present invention can be quickly cured by oven curing, has no decrease in adhesive strength when heated, and has warpage even in a combination of a large chip and a copper frame. Therefore, a highly reliable semiconductor device can be obtained. A known method can be used for manufacturing a semiconductor device using a resin paste for a semiconductor.

【0022】[0022]

【実施例】本発明を実施例で具体的に説明する。各成分
の配合割合は重量部とする。
EXAMPLES The present invention will be specifically described with reference to Examples. The mixing ratio of each component is part by weight.

【0023】<実施例1〜7及び比較例1〜8>表1に
示した組成の各成分と無機フィラーを配合し、三本ロー
ルで混練して樹脂ペーストを得た。この樹脂ペーストを
真空チャンバーにて2mmHgで30分間脱泡した後、以下の
方法により各種の性能を評価した。評価結果を表1に示
す。
<Examples 1 to 7 and Comparative Examples 1 to 8> Each component having the composition shown in Table 1 and an inorganic filler were blended and kneaded with a three-roll mill to obtain a resin paste. After defoaming the resin paste at 2 mmHg for 30 minutes in a vacuum chamber, various performances were evaluated by the following methods. Table 1 shows the evaluation results.

【0024】<用いる原料成分> ・一般式(1)で示される液状エポキシ樹脂:粘度5000
mPa・s、エポキシ当量190
<Raw materials used> Liquid epoxy resin represented by general formula (1): Viscosity 5000
mPas, epoxy equivalent 190

【0025】・ビスフェノールA型エポキシ樹脂(BP
A):粘度9000mPa・s、エポキシ当量185 ・ビスフェノールF型エポキシ樹脂(BPF):粘度50
00mPa・s、エポキシ当量170 ・反応性希釈剤 :フェニルグリシジルエーテル ・潜在性硬化剤(B):ジシアンジアミド(DDA) ・イミダゾール化合物(C):2−フェニル−4−メチ
ル−5−ヒドロキシメチルイミダゾール(2P4MH
Z) ・ 無機フィラー(D): 銀粉 :粒径が0.1〜50μmで平均粒径3μmのフレーク状 シリカフィラー:平均粒径5μmで最大粒径20μmのシ
リカフィラー
Bisphenol A type epoxy resin (BP
A): viscosity 9000 mPas, epoxy equivalent 185 bisphenol F type epoxy resin (BPF): viscosity 50
00 mPa · s, epoxy equivalent 170 • Reactive diluent: phenylglycidyl ether • Latent curing agent (B): dicyandiamide (DDA) • Imidazole compound (C): 2-phenyl-4-methyl-5-hydroxymethylimidazole ( 2P4MH
Z)-Inorganic filler (D): Silver powder: Flake-like silica filler with particle size of 0.1 to 50 m and average particle size of 3 m: Silica filler with average particle size of 5 m and maximum particle size of 20 m

【0026】<評価方法> 粘度 :E型粘度計(3°コーン)を用い25
℃、2.5rpmでの値を測定し粘度とした。 弾性率 :テフロンシート上にペーストを幅10m
m長さ約150mm厚さ100μmに塗布し、200℃
オーブン中30分間硬化した後、引っ張り試験機で試験
長100mm、引っ張り速度1mm/分にて測定し得ら
れた応力―ひずみ曲線の初期勾配より弾性率を算出し
た。 接着強度 :2×2mmのシリコンチップをペースト
を用いて銅フレームにマウントし200℃中30分間オ
ーブン中で硬化した。硬化後マウント強度測定装置でを
用い25℃,250℃での熱時ダイシェア強度を測定し
た。 反り量 :6×15×0.3mmシリコンチップを
銅フレーム(200μm厚さ)に樹脂ペーストでマウン
トし、200℃20分間硬化した後、チップの反りを表
面粗さ計(測定長13mm)で測定した。 ポットライフ:25℃の恒温槽内に樹脂ペーストを放置
した時の粘度が初期粘度の1.2倍以上増粘するまでの
日数を測定した。
<Evaluation Method> Viscosity: 25 using an E-type viscometer (3 ° cone)
The viscosity was measured at a temperature of 2.5 ° C. and a temperature of 2.5 ° C., and the viscosity was determined. Elastic modulus: Paste 10m width on Teflon sheet
m length about 150mm thickness 100μm, 200 ℃
After curing in an oven for 30 minutes, the modulus of elasticity was calculated from the initial gradient of the stress-strain curve obtained by measuring with a tensile tester a test length of 100 mm and a tensile speed of 1 mm / min. Adhesive strength: A silicon chip of 2 × 2 mm was mounted on a copper frame using a paste and cured in an oven at 200 ° C. for 30 minutes. After curing, the die shear strength under heat at 25 ° C. and 250 ° C. was measured using a mount strength measuring device. Warpage amount: A 6 × 15 × 0.3 mm silicon chip is mounted on a copper frame (200 μm thick) with a resin paste, cured at 200 ° C. for 20 minutes, and then the warpage of the chip is measured with a surface roughness meter (measuring length 13 mm). did. Pot life: The number of days until the viscosity when the resin paste was allowed to stand in a thermostat at 25 ° C. increased to 1.2 times or more the initial viscosity was measured.

【0027】[0027]

【表1】 [Table 1]

【0028】[0028]

【表2】 [Table 2]

【0029】実施例1〜7では熱時接着強度、低応力性
(低弾性率、低反り量)及びポットライフに優れたペー
ストが得られるが、比較例1はビスフェノールA型エポ
キシ樹脂を使用したため低応力性が悪く、反り量が大き
くなりチップクラックが発生した。比較例2はビスフェ
ノールF型エポキシ樹脂を使用したため低応力性が悪
く、反り量が大きくなりチップクラックが発生した。比
較例3は反応性希釈剤の配合量が多く、接着強度が著し
く低下した。比較例4は反応性希釈剤の配合量が少な
く、粘度が著しく高くなり作業性が低下した。比較例5
は潜在性硬化剤の配合量が少なく、接着強度が著しく低
下した。比較例6は潜在性硬化剤の配合量が多く、反り
量が大きくなりチップクラックが発生した。比較例7は
イミダゾール化合物の配合量が少なく、接着強度が著し
く低下した。比較例8はイミダゾール化合物の配合量が
多く、ポットライフが著しく短くなった。
In Examples 1 to 7, pastes excellent in hot adhesive strength, low stress property (low elastic modulus, low warpage) and pot life were obtained, but Comparative Example 1 used a bisphenol A type epoxy resin. Poor low stress properties, large warpage, and chip cracks. In Comparative Example 2, since the bisphenol F type epoxy resin was used, the low stress property was poor, the amount of warpage was large, and chip cracks occurred. In Comparative Example 3, the content of the reactive diluent was large, and the adhesive strength was significantly reduced. In Comparative Example 4, the amount of the reactive diluent was small, the viscosity was significantly increased, and the workability was reduced. Comparative Example 5
The amount of the latent curing agent was small, and the adhesive strength was significantly reduced. In Comparative Example 6, the amount of the latent curing agent was large, the amount of warpage was large, and chip cracks occurred. In Comparative Example 7, the amount of the imidazole compound was small, and the adhesive strength was significantly reduced. In Comparative Example 8, the amount of the imidazole compound was large, and the pot life was significantly shortened.

【0030】[0030]

【発明の効果】本発明の半導体用樹脂ペーストは、オー
ブン硬化での速硬化が可能で、熱時接着強度が高く、か
つ応力緩和性に優れているため、IC等の大型チップと銅
フレームとの接着に適しており、IC組立工程でのチップ
クラックやチップ歪みによるIC等の特性不良を防止で
き、信頼性の高い半導体装置を得ることができる。
The resin paste for semiconductors of the present invention can be rapidly cured by oven curing, has a high adhesive strength when heated, and has excellent stress relaxation properties. It is suitable for bonding, and it is possible to prevent a characteristic failure of an IC or the like due to a chip crack or a chip distortion in an IC assembling process, and to obtain a highly reliable semiconductor device.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 一般式(1)の構造を有する液状エポキ
シ樹脂とエポキシ基を有する反応性希釈剤の重量比が6
0:40〜90:10である(A)エポキシ樹脂、
(B)潜在性硬化剤、(C)イミダゾール化合物、及び
(D)無機フィラーからなり、成分(A)100重量部
に対し、成分(B)が0.5〜5重量部、成分(C)が
0.5〜10重量部であることを特徴とする半導体用樹
脂ペースト。 【化1】
A weight ratio of a liquid epoxy resin having a structure of the general formula (1) to a reactive diluent having an epoxy group is 6:
(A) an epoxy resin having a ratio of 0:40 to 90:10,
(B) a latent curing agent, (C) an imidazole compound, and (D) an inorganic filler, wherein component (B) is 0.5 to 5 parts by weight and component (C) is 100 parts by weight of component (A). Is 0.5 to 10 parts by weight. Embedded image
【請求項2】 請求項1記載の半導体用樹脂ペーストを
用いて製作された半導体装置。
2. A semiconductor device manufactured using the resin paste for a semiconductor according to claim 1.
JP11162121A 1999-06-09 1999-06-09 Resin paste for semiconductor and semiconductor device sealed therewith Pending JP2000344864A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11162121A JP2000344864A (en) 1999-06-09 1999-06-09 Resin paste for semiconductor and semiconductor device sealed therewith

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11162121A JP2000344864A (en) 1999-06-09 1999-06-09 Resin paste for semiconductor and semiconductor device sealed therewith

Publications (1)

Publication Number Publication Date
JP2000344864A true JP2000344864A (en) 2000-12-12

Family

ID=15748448

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11162121A Pending JP2000344864A (en) 1999-06-09 1999-06-09 Resin paste for semiconductor and semiconductor device sealed therewith

Country Status (1)

Country Link
JP (1) JP2000344864A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017126307A1 (en) * 2016-01-19 2017-07-27 三菱ケミカル株式会社 Epoxy resin composition, prepreg for fiber-reinforced composite material, and fiber-reinforced composite material
CN114502619A (en) * 2020-08-31 2022-05-13 东芝三菱电机产业系统株式会社 Method for preparing resin and method for preparing insulation structure

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017126307A1 (en) * 2016-01-19 2017-07-27 三菱ケミカル株式会社 Epoxy resin composition, prepreg for fiber-reinforced composite material, and fiber-reinforced composite material
JPWO2017126307A1 (en) * 2016-01-19 2018-02-01 三菱ケミカル株式会社 Epoxy resin composition, prepreg for fiber reinforced composite material, and fiber reinforced composite material
US10577455B2 (en) 2016-01-19 2020-03-03 Mitsubishi Chemical Corporation Epoxy resin composition, prepreg for fiber-reinforced composite material, and fiber-reinforced composite material
CN114502619A (en) * 2020-08-31 2022-05-13 东芝三菱电机产业系统株式会社 Method for preparing resin and method for preparing insulation structure
CN114502619B (en) * 2020-08-31 2024-03-08 东芝三菱电机产业系统株式会社 Method for preparing resin and method for preparing insulating structure
EP4206261A4 (en) * 2020-08-31 2024-09-11 Toshiba Mitsubishi-Electric Industrial Systems Corporation RESIN PRODUCTION METHOD AND INSULATING STRUCTURE PRODUCTION METHOD
US12168722B2 (en) 2020-08-31 2024-12-17 Tmeic Corporation Method of producing resin and method of producing insulating structure

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