JPH1112551A - Electroconductive resin paste and semiconductor device produced by using the same - Google Patents

Electroconductive resin paste and semiconductor device produced by using the same

Info

Publication number
JPH1112551A
JPH1112551A JP9167779A JP16777997A JPH1112551A JP H1112551 A JPH1112551 A JP H1112551A JP 9167779 A JP9167779 A JP 9167779A JP 16777997 A JP16777997 A JP 16777997A JP H1112551 A JPH1112551 A JP H1112551A
Authority
JP
Japan
Prior art keywords
resin
paste
silver powder
powder
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP9167779A
Other languages
Japanese (ja)
Other versions
JP3469432B2 (en
Inventor
Toshiro Takeda
敏郎 竹田
Yutaka Matsuda
豊 松田
Ryuichi Murayama
竜一 村山
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 JP16777997A priority Critical patent/JP3469432B2/en
Publication of JPH1112551A publication Critical patent/JPH1112551A/en
Application granted granted Critical
Publication of JP3469432B2 publication Critical patent/JP3469432B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L24/00Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
    • H01L24/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L24/26Layer connectors, e.g. plate connectors, solder or adhesive layers; Manufacturing methods related thereto
    • H01L24/28Structure, shape, material or disposition of the layer connectors prior to the connecting process
    • H01L24/29Structure, shape, material or disposition of the layer connectors prior to the connecting process of an individual layer connector
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/013Alloys
    • H01L2924/0132Binary Alloys
    • H01L2924/01322Eutectic Alloys, i.e. obtained by a liquid transforming into two solid phases
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/10Details of semiconductor or other solid state devices to be connected
    • H01L2924/102Material of the semiconductor or solid state bodies
    • H01L2924/1025Semiconducting materials
    • H01L2924/10251Elemental semiconductors, i.e. Group IV
    • H01L2924/10253Silicon [Si]
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/15Details of package parts other than the semiconductor or other solid state devices to be connected
    • H01L2924/151Die mounting substrate
    • H01L2924/156Material
    • H01L2924/15786Material with a principal constituent of the material being a non metallic, non metalloid inorganic material
    • H01L2924/15787Ceramics, e.g. crystalline carbides, nitrides or oxides

Abstract

PROBLEM TO BE SOLVED: To obtain the subject paste, excellent in electroconductivity and further heat radiating properties by including a specific spherical nickel powder, a specified silver powder, specific two kinds of (meth)acrylic resins and an organic peroxide in a specific proportion therein. SOLUTION: This paste is obtained by including (A) 10-90 wt.% of a spherical nickel powder having 5-30 μm average particle diameter, (B) 5-85 wt.% of a silver powder having 0.5-15 μm average particle diameter so as to provide 80-97 wt.% total amount of the components A and B, (C) a resin component composed of (i) an acrylic or a methacrylic resin represented by formula I or II R1 is CH2 , C(CH3 )2 , etc.; R2 is Cn H2n [(n) is >=4]; (X+Y) is >=4}, (ii) 0.1-50 wt.% (based on the total resin) of an acrylic or a methacrylic resin represented by formula III or IV I (a) is 0 or 1; (b) and (c) are each 1 or 2; [(b)+(c)] is 3}, (D) an organic peroxide (e.g. 1,1,3,3-tetramethylbutyl peroxy-2- ethylhexanate) and, as necessary, (E) an adhesion improving component such as another resin or a silane coupling agent, a pigment, a defoaming agent, etc.

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の基板に接着させる半導体素
子接着用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 substrate such as a metal frame.

【0002】[0002]

【従来の技術】半導体装置の組立において、半導体素子
を金属フレームに接着させる工程、いわゆるダイボンデ
ィング工程において用いられる接合方式は、これまで金
−シリコン共晶に始まり、半田、樹脂ペーストと推移し
てきた。現在では主にIC,LSIの組立においては導
電性樹脂ペーストを、トランジスタ、ダイオードなどの
ディスクリートにおいては通常半田を使用している。
2. Description of the Related Art In the process of assembling a semiconductor device, a bonding method used in a process of bonding a semiconductor element to a metal frame, that is, a so-called die bonding process has been changed from a gold-silicon eutectic to a solder and a resin paste. . At present, conductive resin paste is mainly used for assembling ICs and LSIs, and usually solder is used for discretes such as transistors and diodes.

【0003】IC、LSI等の半導体装置においてはそ
の半導体素子の面積が大きいことから半田に対してより
低応力性が高い樹脂ペーストを使用する方法が行われて
いる。この樹脂ペーストはエポキシ樹脂中にフレーク状
の銀粉が分散されている。しかし導電性樹脂ペーストを
用いる方法では近年の半導体装置において半導体素子と
金属フレームの間の導電性に関する要求は低くなってき
ている。なぜならば近年の半導体装置では半導体素子や
半導体装置のデザインの進歩に伴い、アースを取るため
に半導体素子の裏面から金属フレームに電気を流す構造
が必ずしも必要とされていない。また導電性樹脂ペース
トを通して電気を流すにしてもIC,LSIでは電流が
2〜3mA程度の微弱な電流である。この程度の電流で
は樹脂中に金属粉が分散している従来の導電性樹脂ペー
ストでも充分に対応が可能である。
[0003] In semiconductor devices such as ICs and LSIs, a method of using a resin paste having a lower stress property to solder has been used because the area of the semiconductor element is large. In this resin paste, flake silver powder is dispersed in an epoxy resin. However, in a method using a conductive resin paste, a requirement for conductivity between a semiconductor element and a metal frame in a semiconductor device in recent years has been reduced. This is because a recent semiconductor device does not necessarily require a structure for flowing electricity from the back surface of the semiconductor device to the metal frame in order to ground the semiconductor device along with the progress of the design of the semiconductor device. Even if electricity is passed through the conductive resin paste, the current is a very small current of about 2 to 3 mA in ICs and LSIs. With such a current, a conventional conductive resin paste in which metal powder is dispersed in a resin can sufficiently cope.

【0004】導電性樹脂ペースト対し半田は導電性や接
着性に優れ、価格も安価である。この半田を主に使用し
ているダイオード、トランジスタ等のディスクリートで
はその製品の構造上半導体素子と金属フレームの間で電
気を流す必要がある。ところが近年の環境問題から半田
に使用している鉛を使わない方向に各半導体メーカーが
動いており、更に半田を使用する際には必要なフラック
スの洗浄工程が減らすことによるコスト削減の意味から
IC,LSIに使用している導電性樹脂ペーストをディ
スクリート用に開発しているが、半導体装置に流れる電
流が2〜3A程度の大電流が流れる製品もあり、従来の
導電性樹脂ペーストでは満足する導電性を得ることがで
きなかった。この点に関しては金属皮膜を施したフィラ
ー(例えばカーボン、シリカ、ガラスビーズ、ポリマ
ー、その他無機フィラー)を配合することにより、大電
流をが流れる半導体製品においても満足な導電性を得る
ことは可能であった。
[0004] Solder to conductive resin paste has excellent conductivity and adhesiveness, and is inexpensive. In the case of discrete components such as diodes and transistors that mainly use this solder, it is necessary to flow electricity between the semiconductor element and the metal frame due to the structure of the product. However, due to recent environmental problems, each semiconductor maker is moving in a direction that does not use lead that is used for soldering. Furthermore, when solder is used, ICs are reduced in terms of cost reduction by reducing the necessary flux cleaning process. , The conductive resin paste used for LSI has been developed for discrete use, but there are products that have a large current of about 2 to 3 A flowing to the semiconductor device. I couldn't get the sex. In this regard, it is possible to obtain satisfactory conductivity even in a semiconductor product through which a large current flows by blending a filler coated with a metal film (for example, carbon, silica, glass beads, a polymer, and other inorganic fillers). there were.

【0005】しかし大電流を流す半導体製品ではこの電
流により、多量の熱を発生し、この発熱が生じることで
導電性樹脂ペーストの温度が高くなる。その場合熱抵抗
により電流が流れにくくなり、半導体製品としての信頼
性を低下させるという結果を招いている。従ってこの様
な導電性には優れるが、熱放散性に劣る導電性樹脂ペー
ストを使用する場合には充分な冷却機構を持った半導体
製品でなければならなかったが、コストアップにつなが
り実用的ではなかった。
[0005] However, in a semiconductor product in which a large current flows, a large amount of heat is generated by this current, and this heat is generated, thereby increasing the temperature of the conductive resin paste. In this case, the current becomes difficult to flow due to the thermal resistance, and the reliability of the semiconductor product is reduced. Therefore, when using a conductive resin paste that is excellent in such conductivity but inferior in heat dissipation, it must be a semiconductor product with a sufficient cooling mechanism, but it increases the cost and is not practical. Did not.

【0006】[0006]

【発明が解決しようとする課題】本発明は導電性に優
れ、更に熱放散性にも優れる導電性樹脂ペーストを提供
するものである。
SUMMARY OF THE INVENTION The present invention provides a conductive resin paste having excellent conductivity and heat dissipation.

【0007】[0007]

【課題を解決するための手段】本発明は(A)平均粒径
が5〜30μmの球状ニッケル粉、(B)平均粒径が
0.5〜15μmの銀粉、(C)下記(1)または
(2)の一般式からなるアクリル樹脂またはメタクリル
樹脂と、(3)または(4)に示されるアクリル樹脂ま
たはメタクリル樹脂からなり、(3)または(4)に示
される樹脂が全樹脂中0.1〜50重量%である樹脂成
分、並びに(D)有機過酸化物を必須成分として、該成
分中に球状ニッケル粉(A)が10〜90重量%、銀粉
(B)が5〜85重量%含まれており、尚かつ(A)+
(B)が80〜97重量%であることを特徴とする導電
性樹脂ペースト及び上記の導電性樹脂ペーストを用いて
製造された半導体装置に関するものである。
The present invention provides (A) a spherical nickel powder having an average particle size of 5 to 30 μm, (B) a silver powder having an average particle size of 0.5 to 15 μm, (C) the following (1) or The acrylic resin or methacrylic resin represented by the general formula (2) and the acrylic resin or methacrylic resin represented by (3) or (4), wherein the resin represented by (3) or (4) is 0.1% of the total resin. 1 to 50% by weight of a resin component, and (D) an organic peroxide as essential components, in which spherical nickel powder (A) is 10 to 90% by weight and silver powder (B) is 5 to 85% by weight. Included and (A) +
(B) is 80 to 97% by weight, and relates to a conductive resin paste and a semiconductor device manufactured using the conductive resin paste.

【0008】[0008]

【化1】 Embedded image

【0009】[0009]

【化2】 Embedded image

【0010】[0010]

【化3】 Embedded image

【0011】[0011]

【化4】 Embedded image

【0012】[0012]

【発明の実施の形態】本発明の様な半導体用導電性樹脂
ペーストは導電性を付与するために通常フィラーに銀粉
を用いるが、本発明では銀粉だけではなくニッケル粉が
必須である。銀粉にニッケル粉を併用した理由はより導
電性、熱放散性を向上させる場合、当然金属の比率を上
昇させるのが常套手段である。しかし銀粉のみでこの様
な高充填の導電性樹脂ペーストを作製しようとすると作
製時に使用する三本ロールにおけるロールの回転による
機械的な力で銀粉がつぶれてしまい、結果として銀粉が
造粒してしまうため十分に分散されず、導電性、熱放散
性、作業性を著しく低下させてしまう。そこで銀粉にく
らべ機械的に強いニッケル粉を添加することにより銀粉
のつぶれを防ぐものである。しかしつぶれやすい銀粉の
粒径がニッケル粉の粒径より大きいとロールによりつぶ
れる可能性が大きい。そこで本発明では銀粉の粒径はニ
ッケル粉の粒径よりも小さいものが好ましい。一方、ニ
ッケル粉だけで導電性を得ようとすると半導体製品での
信頼性試験における吸湿によりニッケル表面に酸化膜的
な絶縁層が生じるため抵抗が大きくなる。従ってニッケ
ルより化学的な銀を併用し、導電性を維持することが本
発明のポイントである。
BEST MODE FOR CARRYING OUT THE INVENTION In the conductive resin paste for semiconductors according to the present invention, silver powder is usually used as a filler for imparting conductivity. In the present invention, not only silver powder but also nickel powder is essential. The reason why nickel powder is used in combination with silver powder is that it is customary to increase the proportion of metal when improving conductivity and heat dissipation. However, when attempting to produce such a highly-filled conductive resin paste using only silver powder, the silver powder is crushed by mechanical force due to the rotation of the three rolls used in the production, and as a result, the silver powder is granulated. Therefore, they are not sufficiently dispersed and the conductivity, heat dissipation, and workability are significantly reduced. Therefore, the addition of nickel powder which is mechanically stronger than silver powder prevents the silver powder from being crushed. However, if the particle size of the silver powder that is easily crushed is larger than the particle size of the nickel powder, the possibility of crushing by the roll is large. Therefore, in the present invention, the particle size of the silver powder is preferably smaller than the particle size of the nickel powder. On the other hand, if an attempt is made to obtain conductivity only with nickel powder, the resistance increases because an insulating film-like insulating layer is formed on the nickel surface due to moisture absorption in a reliability test of a semiconductor product. Therefore, the point of the present invention is to maintain the conductivity by using chemical silver in combination with nickel.

【0013】本発明ではニッケル粉と銀粉の併せた量が
80〜97重量%で無ければならない。ニッケル粉と銀
粉を併せた量が80重量%より少ないと導電性と熱放散
性に劣る。また97重量%より多いと粘度が高くなり過
ぎ塗布作業性が著しく低下する。球状ニッケル粉が10
〜90重量%、銀粉が5〜85重量%であるのが望まし
い。球状ニッケル粉が10重量%を下回ると銀粉の造粒
が激しく分散性が著しく低下するため導電性が低下す
る。球状ニッケル粉が90重量%を越えると吸水後の導
電性が低下するので好ましくない。
In the present invention, the combined amount of nickel powder and silver powder must be 80 to 97% by weight. If the combined amount of the nickel powder and the silver powder is less than 80% by weight, the conductivity and the heat dissipation are poor. On the other hand, if it is more than 97% by weight, the viscosity becomes too high and the coating workability is remarkably reduced. 10 spherical nickel powder
It is desirable that the silver powder be 5 to 90% by weight and the silver powder be 5 to 85% by weight. If the content of the spherical nickel powder is less than 10% by weight, the silver powder is excessively granulated and the dispersibility is remarkably reduced. If the spherical nickel powder exceeds 90% by weight, the conductivity after absorbing water is undesirably reduced.

【0014】本発明で用いるニッケル粉は球状が望まし
い。本発明の様に高充填にする場合、粒子の形状は球状
の方が比表面積が小さくタップ密度が小さいためより多
くの粒子を充填することができるので好ましい。ニッケ
ル粉の平均粒径は5〜30μmが望ましい。粒径がこれ
より小さいと粘度が高くなり金属粉の高充填化は困難に
なる。またこれより大きいと塗布した場合のペースト厚
みが大きくなるため導電性が劣る。
The nickel powder used in the present invention is preferably spherical. In the case of high filling as in the present invention, spherical particles are preferable because more particles can be filled because the specific surface area is small and the tap density is small. The average particle size of the nickel powder is preferably 5 to 30 μm. If the particle size is smaller than this, the viscosity increases and it becomes difficult to highly fill the metal powder. On the other hand, if it is larger than this, the thickness of the paste when applied becomes large, resulting in poor conductivity.

【0015】本発明に用いる銀粉の平均粒径は0.5〜
15μmが望ましい。形状は球状の方がより高充填化が
可能ではあるが、本発明の様な比較的粒径の大きい球状
ニッケル粉を添加により粘度が低下するためフレーク状
の銀粉であっても良好な作業性が得られるため特に限定
するものではない。平均粒径が0.5μmより小さいと
球状ニッケル粉の添加でもロール混練が不可能、もしく
は混練が可能な場合でも粘度が高過ぎてディスペンスは
おろかスクリーン印刷による塗布も出来ない高い粘度に
なってしまう。逆に平均粒径が15μmより大きい粒径
を使用すると粒度分布が非常に狭くなり、流動性が低下
するため、塗れ広がり性が著しく低下するので好ましく
ない。
The silver powder used in the present invention has an average particle size of 0.5 to 0.5.
15 μm is desirable. Spherical shape allows higher filling, but the addition of spherical nickel powder having a relatively large particle size as in the present invention lowers the viscosity. Is not particularly limited because it is obtained. If the average particle size is smaller than 0.5 μm, roll kneading is impossible even with the addition of spherical nickel powder, or even if kneading is possible, the viscosity is too high and the dispensing becomes too viscous, not to mention coating by screen printing. . Conversely, if the average particle size is larger than 15 μm, the particle size distribution becomes extremely narrow, and the fluidity is reduced, so that the spreadability is remarkably reduced.

【0016】本発明に用いる式(1)または、(2)で
示されるアクリル樹脂 、または、メタクリル樹脂は、
低弾性率の特徴を有している。式中のR1はメチレン基
・イソプロピレン基のものが工業化されている。また、
式中のR2は、エチレン基、イソプロピレン基のものが
工業化されているが、イソプロピレン基のほうが好まし
い。エチレン基を導入した場合、親水性が高く、吸水率
増加の原因となる。また、X+Yは、m+nは4以上で
あることが好ましい。m+nが4未満であると接着後の
チップの反りが急激に大きくなり、低応力性の特徴がな
くなる。
The acrylic resin or methacrylic resin represented by the formula (1) or (2) used in the present invention is:
It has the characteristic of low elastic modulus. R1 in the formula is a methylene group / isopropylene group having been industrialized. Also,
R2 in the formula is an ethylene group or an isopropylene group, but an isopropylene group is more preferable. When an ethylene group is introduced, it has high hydrophilicity and causes an increase in water absorption. In addition, as for X + Y, m + n is preferably 4 or more. If m + n is less than 4, the warpage of the chip after bonding will increase sharply, and the characteristic of low stress will be lost.

【0017】全樹脂中に含まれる式(3)または(4)
のアクリル樹脂、または メタクリル樹脂は0.1〜5
0重量%が好ましい。0.1重量%未満では接着強度の
低下が起こり、また、50重量%以上では硬化時に発生
するアウトガスが増加、汚染性が低下して耐半田クラッ
ク性低下の原因となる。
Formula (3) or (4) contained in all resins
Of acrylic resin or methacrylic resin is 0.1 to 5
0% by weight is preferred. If the amount is less than 0.1% by weight, the adhesive strength is reduced. If the amount is more than 50% by weight, outgas generated at the time of curing is increased, the contamination is reduced, and the solder crack resistance is reduced.

【0018】本発明に用いられる有機過酸化物としては
特に限定されるものではなく、例えば1,1,3,3−
テトラメチルブチルパーオキシ−2−エチルヘキサネー
ト、t−ブチルパ−オキシ−2−エチルヘキサネート、
t−ヘキシルパ−オキシ−2−エトルヘキサネート、
1,1−ビス(t−ブチルパ−オキシ)−3,3,5−
トリメチルシクロヘキサン、1,1−ビス(t−ヘキシ
ルパ−オキシ)−3,3,5−トリメチルシクロヘキサ
ン、ビス(4−t−ブチルシクロヘキシル)パ−オキシ
ジカーボネート等が挙げられる。これら過酸化物は単独
あるいは硬化性をコントロールするため2種以上を混合
して用いることもできる。さらに、樹脂の保存性を向上
するために各種重合禁止剤を予め添加しておくことも可
能である。
The organic peroxide used in the present invention is not particularly limited. For example, 1,1,3,3-
Tetramethylbutyl peroxy-2-ethyl hexanate, t-butyl peroxy-2-ethyl hexanate,
t-hexylpa-oxy-2-ethorhexanate,
1,1-bis (t-butylperoxy) -3,3,5-
Trimethylcyclohexane, 1,1-bis (t-hexylperoxy) -3,3,5-trimethylcyclohexane, bis (4-t-butylcyclohexyl) peroxydicarbonate and the like can be mentioned. These peroxides can be used alone or in combination of two or more to control curability. Further, various polymerization inhibitors can be added in advance in order to improve the storage stability of the resin.

【0019】更に本発明の樹脂組成物には必要に応じて
他の樹脂やシランカップリング剤等の密着性向上成分や
顔料、消泡剤などの各種添加剤を配合することができ
る。本発明の製造方法は例えば各成分を予備混練した
後、三本ロールを用いて混練し、ペーストを得て真空下
脱泡する等の方法が用いられる。
Further, the resin composition of the present invention may optionally contain other resins, an adhesion improving component such as a silane coupling agent, and various additives such as a pigment and an antifoaming agent. In the production method of the present invention, for example, a method of pre-kneading each component, kneading using a three-roll mill, obtaining a paste, and defoaming under vacuum is used.

【0020】[0020]

【実施例】以下、本発明を実施例で具体的に説明する。 実施例1 ・式(1)に示すR1=C(CH32、R2=CH2CH
(CH3)O、X+Y=20を有するアクリル樹脂(C1
成分)、 ・式(2)に示すメタクリル樹脂(C2成分) ・式(3)に示すa=1、b=1、c=2を有するアク
リル樹脂(C3成分)、 ・1,1,3,3−テトラメチルブチルパーオキシ−2
−エチルヘキサネート(C5成分)、 更に平均粒径6、28μmの球状ニッケル粉及び平均粒
径1、13μmの球状銀粉と平均粒径13μmのフレー
ク状銀粉を表1及び表2に示す割合で配合し、3本ロー
ルで混練して導電性樹脂ペーストを得た。この導電性樹
脂ペーストを真空チャンバーにて2mmHgで30分脱
泡後、以下に示す方法により各種性能を評価した。評価
結果を表1に示す。
The present invention will be specifically described below with reference to examples. Example 1 R 1 CC (CH 3 ) 2 , R 2 CHCH 2 CH shown in formula (1)
Acrylic resin having (CH 3 ) O, X + Y = 20 (C1
Component), a methacrylic resin represented by the formula (2) (C2 component), an acrylic resin represented by the formula (3) having a = 1, b = 1, and c = 2 (a C3 component); 3-tetramethylbutylperoxy-2
-Ethylhexanate (C5 component), and a spherical nickel powder having an average particle diameter of 6,28 μm, a spherical silver powder having an average particle diameter of 1,13 μm, and a flaky silver powder having an average particle diameter of 13 μm, in the proportions shown in Tables 1 and 2. Then, the mixture was kneaded with three rolls to obtain a conductive resin paste. After defoaming the conductive resin paste in a vacuum chamber at 2 mmHg for 30 minutes, various performances were evaluated by the following methods. Table 1 shows the evaluation results.

【0021】[0021]

【表1】 [Table 1]

【0022】実施例2〜8 実施例1において、式(3)に示すアクリル樹脂に代え
て式(4)に示すa=1、b=1、c=2を有するメタ
クリル樹脂(C4成分)を表1に示す割合で用いる他は
全て実施例1と同様の方法で導電性ペーストを作成し、
各種性能を評価した。評価結果を表1に示す。
Examples 2 to 8 In Example 1, a methacrylic resin (a component C4) having a = 1, b = 1 and c = 2 shown in the formula (4) was used instead of the acrylic resin shown in the formula (3). Except for using the proportions shown in Table 1, a conductive paste was prepared in the same manner as in Example 1;
Various performances were evaluated. Table 1 shows the evaluation results.

【0023】粘度:E型粘度計(3°コーン)を用い、
25℃、2.5rpmでの測定値。 体積抵抗率:スライドガラス上にペーストを幅4mm、
厚み30μmに塗布し、120℃オーブン中で60分間
硬化した後の硬化物の体積抵抗率を測定した。 垂直体積抵抗率:銅フレーム上にペーストをペースト塗
布し、2X2mmの銅板を120℃オーブン中で60分
間硬化した後の銅板表面と銅フレームの間の電圧を求
め、そこから硬化物の垂直体積抵抗率を算出した。又温
度85℃、湿度85%の恒温糟に168時間放置した後
の垂直体積抵抗率も測定した。 350℃熱時接着強度:2mm角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180℃オーブ
ン中で60分間硬化した。硬化後、プッシュプルゲージ
を用い350℃での熱時ダイシェア強度を測定した。 拡がり性:銅フレームにペーストを塗布し、室温に1時
間放置してシリコンチップをマウントした時にチップの
端までペーストが広がるか評価した。 総合評価:粘度、体積抵抗率及び熱時接着強度の全てを
良好なものを○、1つでも不満足なものを×とした。
Viscosity: Using an E-type viscometer (3 ° cone),
Measured at 25 ° C. and 2.5 rpm. Volume resistivity: paste 4 mm wide on a glass slide,
The coating was applied to a thickness of 30 μm and cured in an oven at 120 ° C. for 60 minutes, and the volume resistivity of the cured product was measured. Vertical volume resistivity: After applying a paste on a copper frame and curing a 2 × 2 mm copper plate in a 120 ° C. oven for 60 minutes, the voltage between the copper plate surface and the copper frame is determined, and the vertical volume resistance of the cured product is determined therefrom. The rate was calculated. In addition, the vertical volume resistivity after standing in a thermostat at a temperature of 85 ° C. and a humidity of 85% for 168 hours was also measured. 350 ° C. hot adhesive strength: A 2 mm square silicon chip was mounted on a copper frame using a paste and cured in a 180 ° C. oven for 60 minutes. After curing, the die shear strength under heat at 350 ° C. was measured using a push-pull gauge. Spreadability: The paste was applied to a copper frame and left at room temperature for 1 hour to evaluate whether the paste spread to the edge of the chip when the silicon chip was mounted. Overall evaluation: Good for all of the viscosity, volume resistivity, and adhesive strength under heat was rated as Good, and even one that was unsatisfactory was rated as Poor.

【0024】比較例1〜9 表2に示す配合割合で実施例と全く同様にして導電性樹
脂ペーストを作製した。
Comparative Examples 1 to 9 Conductive resin pastes were prepared in exactly the same manner as in the examples with the mixing ratios shown in Table 2.

【0025】[0025]

【表2】 [Table 2]

【0026】表1及び表2の結果から明らかなように、
本発明に従えば導電性に優れる樹脂ペーストを得ること
ができる。
As is clear from the results of Tables 1 and 2,
According to the present invention, a resin paste having excellent conductivity can be obtained.

【0027】[0027]

【発明の効果】本発明の導電性樹脂ペーストは半導体素
子と金属フレーム間の導電性が良好で、尚かつダイボン
ディング時のペーストの濡れ拡がり性が良好で、銅、4
2合金等の金属フレーム、セラミック基板、ガラスエポ
キシ等の有機基板へのIC、LSI等の半導体素子の接
着に用いることができる。
The conductive resin paste of the present invention has good conductivity between the semiconductor element and the metal frame, and has good wet spreadability of the paste during die bonding.
It can be used for bonding a semiconductor element such as an IC or an LSI to an organic substrate such as a metal frame of two alloys, a ceramic substrate, or a glass epoxy.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C09J 171/00 C09J 171/00 B // H01L 21/52 H01L 21/52 E ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 6 Identification symbol FI C09J 171/00 C09J 171/00 B // H01L 21/52 H01L 21/52 E

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 (A)平均粒径が5〜30μmの球状ニ
ッケル粉、(B)平均粒径が0.5〜15μmの銀粉、
(C)下記(1)または(2)の一般式からなるアクリ
ル樹脂またはメタクリル樹脂と、(3)または(4)に
示されるアクリル樹脂またはメタクリル樹脂からなり、
(3)または(4)に示される樹脂が全樹脂中0.1〜
50重量%である樹脂成分、並びに(D)有機過酸化物
を必須成分として、該成分中に球状ニッケル粉(A)が
10〜90重量%、銀粉(B)が5〜85重量%含まれ
ており、尚かつ(A)+(B)が80〜97重量%であ
ることを特徴とする導電性樹脂ペースト。 【化1】 【化2】 【化3】 【化4】
(A) a spherical nickel powder having an average particle size of 5 to 30 μm, (B) a silver powder having an average particle size of 0.5 to 15 μm,
(C) An acrylic resin or methacrylic resin represented by the following general formula (1) or (2), and an acrylic resin or methacrylic resin represented by (3) or (4),
The resin shown in (3) or (4) is 0.1 to
50% by weight of a resin component and (D) an organic peroxide as essential components, the component containing 10 to 90% by weight of spherical nickel powder (A) and 5 to 85% by weight of silver powder (B). And (A) + (B) is 80 to 97% by weight. Embedded image Embedded image Embedded image Embedded image
【請求項2】 請求項1記載の導電性樹脂ペーストを用
いて製造された半導体装置。
2. A semiconductor device manufactured by using the conductive resin paste according to claim 1.
JP16777997A 1997-06-24 1997-06-24 Conductive resin paste and semiconductor device manufactured using the same Expired - Lifetime JP3469432B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16777997A JP3469432B2 (en) 1997-06-24 1997-06-24 Conductive resin paste and semiconductor device manufactured using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16777997A JP3469432B2 (en) 1997-06-24 1997-06-24 Conductive resin paste and semiconductor device manufactured using the same

Publications (2)

Publication Number Publication Date
JPH1112551A true JPH1112551A (en) 1999-01-19
JP3469432B2 JP3469432B2 (en) 2003-11-25

Family

ID=15855961

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Country Status (1)

Country Link
JP (1) JP3469432B2 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0569054A2 (en) * 1988-06-24 1993-11-10 Sony Corporation Magneto-optical recording apparatus
JPH11335630A (en) * 1998-05-27 1999-12-07 Sumitomo Bakelite Co Ltd Die attaching paste
JP2002012602A (en) * 2000-06-27 2002-01-15 Hitachi Chem Co Ltd Resin paste composition and semiconductor device using the same
JP2007308708A (en) * 2007-05-28 2007-11-29 Hitachi Chem Co Ltd Resin paste composition and semiconductor device using the same
US20120055978A1 (en) * 2010-09-03 2012-03-08 Heraeus Materials Technology Gmbh & Co. Kg Contacting Means and Method for Contacting Electrical Components
US20120153011A1 (en) * 2009-09-04 2012-06-21 Heraeus Materials Technology Gmbh & Co. Kg Metal paste with oxidizing agents
JP2017066407A (en) * 2013-11-27 2017-04-06 日東電工株式会社 Conductive adhesive tape, electronic member and adhesive
JP2018538381A (en) * 2015-10-15 2018-12-27 ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング Use of nickel and nickel-containing alloys as conductive fillers in adhesive formulations.

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0569054A2 (en) * 1988-06-24 1993-11-10 Sony Corporation Magneto-optical recording apparatus
JPH11335630A (en) * 1998-05-27 1999-12-07 Sumitomo Bakelite Co Ltd Die attaching paste
JP2002012602A (en) * 2000-06-27 2002-01-15 Hitachi Chem Co Ltd Resin paste composition and semiconductor device using the same
JP2007308708A (en) * 2007-05-28 2007-11-29 Hitachi Chem Co Ltd Resin paste composition and semiconductor device using the same
US20120153011A1 (en) * 2009-09-04 2012-06-21 Heraeus Materials Technology Gmbh & Co. Kg Metal paste with oxidizing agents
US8950652B2 (en) * 2009-09-04 2015-02-10 Heraeus Materials Technology Gmbh & Co. Kg Metal paste with oxidizing agents
US20120055978A1 (en) * 2010-09-03 2012-03-08 Heraeus Materials Technology Gmbh & Co. Kg Contacting Means and Method for Contacting Electrical Components
CN102386149A (en) * 2010-09-03 2012-03-21 贺利氏材料工艺有限及两合公司 Contacting means and method for contacting electrical components
US8925789B2 (en) * 2010-09-03 2015-01-06 Heraeus Materials Technology Gmbh & Co. Kg Contacting means and method for contacting electrical components
JP2017066407A (en) * 2013-11-27 2017-04-06 日東電工株式会社 Conductive adhesive tape, electronic member and adhesive
JP2018538381A (en) * 2015-10-15 2018-12-27 ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング Use of nickel and nickel-containing alloys as conductive fillers in adhesive formulations.

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