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JPH0455153B2 - - Google Patents
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JPH0455153B2 - - Google Patents

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Publication number
JPH0455153B2
JPH0455153B2 JP9878886A JP9878886A JPH0455153B2 JP H0455153 B2 JPH0455153 B2 JP H0455153B2 JP 9878886 A JP9878886 A JP 9878886A JP 9878886 A JP9878886 A JP 9878886A JP H0455153 B2 JPH0455153 B2 JP H0455153B2
Authority
JP
Japan
Prior art keywords
aln
powder
silicate
substrate
metal film
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
Application number
JP9878886A
Other languages
Japanese (ja)
Other versions
JPS62256781A (en
Inventor
Hirozo Matsumoto
Shizuyasu Yoshida
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.)
Fuji Electric Co Ltd
Original Assignee
Fuji Electric 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 Fuji Electric Co Ltd filed Critical Fuji Electric Co Ltd
Priority to JP9878886A priority Critical patent/JPS62256781A/en
Publication of JPS62256781A publication Critical patent/JPS62256781A/en
Publication of JPH0455153B2 publication Critical patent/JPH0455153B2/ja
Granted legal-status Critical Current

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  • Chemically Coating (AREA)

Description

【発明の詳細な説明】 (発明の属する技術分野〕 この発明は、半導体用基板として用いられる窒
化アルミニウムセラミツクの表面に、ハンダ付お
よび硬ろう付が可能な金属被膜を形成する方法に
関する。
DETAILED DESCRIPTION OF THE INVENTION (Technical Field to Which the Invention Pertains) The present invention relates to a method for forming a metal film that can be soldered and hard brazed on the surface of an aluminum nitride ceramic used as a semiconductor substrate.

〔従来技術とその問題点〕[Prior art and its problems]

ここ数年、電子機器に対する小形・軽量化(高
密度実装),高速化、高出力化、高信頼化の要請
がますます強まつており、用いられる半題導体は
高集積化、チツプサイズの増大、マルチチツプ・
モジユール化あるいは高出力化の方向に進んでい
る。このような半導体の動向に伴つて以下のよう
な問題が発生しつつある。
In recent years, there has been an increasing demand for electronic devices to be smaller, lighter (higher density packaging), faster, higher output, and more reliable. , multi-chip
The trend is toward modularization or higher output. With these trends in semiconductors, the following problems are occurring.

(1) 高集積・高密度化によつて素子の単体体積当
り発熱量が多くなつて半導体素子の信頼性に悪
影響を与える。
(1) High integration and density increase the amount of heat generated per unit volume of the device, which adversely affects the reliability of semiconductor devices.

(2) チツプの高速化に基板またはパツケージ部分
が対応できない(信号の遅引)。
(2) The board or package cannot cope with the increase in chip speed (signal slowdown).

(3) チツプサイズの増大によりチツプと基板との
熱膨張差が大きくなつて応力が発生しやすくな
り、接合の信頼性が低下する。
(3) As the chip size increases, the difference in thermal expansion between the chip and the substrate increases, making stress more likely to occur and reducing bonding reliability.

(4) 高電力用チツプでは使用電圧がますます増加
傾向にあるので基板の絶縁破壊が生じやすい。
(4) As the operating voltage of high-power chips continues to increase, dielectric breakdown of the substrate is likely to occur.

このため、半導体を支持する役目をもつ基板や
パツケージ材料にも種々の責務が課せられるよう
になつてきた。そして、素子の高集積・高密度化
を可能とする基板およびパツケージ材料は以下の
性能を保持することが必要となる。
For this reason, various responsibilities have come to be placed on substrates and package materials that play a role in supporting semiconductors. Substrate and package materials that enable high integration and high density of devices are required to maintain the following properties.

(1) 熱伝導率が大きいこと。(1) High thermal conductivity.

(2) 電気絶縁性が優れていること。(2) Excellent electrical insulation.

(3) 熱膨張係数(μ)がSiと同程度であること。(3) The coefficient of thermal expansion (μ) is comparable to that of Si.

(4) 誘電率,誘電損失が小さいこと。(4) Low dielectric constant and low dielectric loss.

(5) 機械的強度が大きいこと。(5) High mechanical strength.

(6) メタライス性が優れていること。(6) Excellent metallization properties.

(7) 加工性が良いこと。(7) Good workability.

(8) 化学的に安定であること。(8) Be chemically stable.

(9) 耐熱性があること。(9) Must be heat resistant.

(10) 低コストであること。(10) Low cost.

従来、半導体素子塔載用のセラミツク基板とし
ては、アルミナ(以下、Al2O3)が最も幅広く用
いられており、安価で技術完成度も高い。しか
し、Al2O3はその熱伝導率が小さいため、素子発
熱が問題となる高密度実装用基板としては不向き
である。Al2O3に変る高熱伝導性セラミツク基板
として、最近注目されているのが、酸化イツトリ
ウム(Y2O3)あるいは酸化カルシウム(CaO)
を焼結助剤に用いた窒化アルミニウム(以下
AlNという)と酸化ベリウム(BeO)を1〜2
重量%含有した炭化けい素(以下SiCという)の
2つである。後者のSiC基板は熱伝導率が高く、
熱膨張係数もSiに近いなどの優れた特徴をもつて
いるが、誘電率が大きく、耐電圧も低いなどの半
導体用基板としての問題も有している。
Conventionally, alumina (hereinafter referred to as Al 2 O 3 ) has been most widely used as a ceramic substrate for mounting semiconductor devices, and is inexpensive and has a high degree of technological perfection. However, since Al 2 O 3 has a low thermal conductivity, it is not suitable as a substrate for high-density packaging where element heat generation is a problem. Yttrium oxide (Y 2 O 3 ) or calcium oxide (CaO) has recently been attracting attention as a highly thermally conductive ceramic substrate to replace Al 2 O 3 .
Aluminum nitride (hereinafter referred to as
(AlN) and beryum oxide (BeO) 1-2
There are two types of silicon carbide (hereinafter referred to as SiC) containing % by weight. The latter SiC substrate has high thermal conductivity,
Although it has excellent characteristics such as a coefficient of thermal expansion close to that of Si, it also has problems as a substrate for semiconductors, such as a high dielectric constant and low withstand voltage.

一方、AlN基板はAl2O3と同様の高い体積抵抗
率、高い絶縁耐圧、低誘電率をもち、かつ高熱伝
導率(Ai2O3の5〜8倍)、低熱膨張率(Siに近
い)および高強度(Al2O3の約2倍)を有する材
料であるので、今後の高熱伝導性セラミツク基板
としてとくに有望とされている。
On the other hand, AlN substrates have high volume resistivity, high dielectric strength voltage, and low dielectric constant similar to Al 2 O 3 , and also have high thermal conductivity (5 to 8 times that of Al 2 O 3 ) and low coefficient of thermal expansion (close to that of Si). ) and high strength (approximately twice that of Al 2 O 3 ), it is considered particularly promising as a future highly thermally conductive ceramic substrate.

ところで、基板に半導体素子を塔載する際はハ
ンダ付あるいはろう付などの手法が採用される。
このため、セラミツク基板にあつてはその表面に
導体回路のための金属被膜層(メタライズ層)を
形成せしめる必要がある。AlN基板表面に金属
被膜を形成する方法としてはこれまでに次の2つ
が知られている。
Incidentally, when mounting semiconductor elements on a substrate, methods such as soldering or brazing are employed.
For this reason, it is necessary to form a metal coating layer (metalized layer) for conductor circuits on the surface of the ceramic substrate. The following two methods are known so far for forming a metal film on the surface of an AlN substrate.

(1) AlNの表面を1000〜1400℃で酸化しして
Al2O3層を形成した後、AlN上に銅板を配置
し、配素分圧、温度をCu−O系の共晶温度に
精密にコントロールした電気炉中で接合する方
法。
(1) Oxidize the surface of AlN at 1000-1400℃
After forming the Al 2 O 3 layer, a copper plate is placed on the AlN and bonded in an electric furnace with the partial pressure and temperature precisely controlled to the eutectic temperature of the Cu-O system.

(2) AlNの表面にAu,Ag−Pb,Cuなどのペー
ストを塗布した後、焼成する方法。
(2) A method in which a paste of Au, Ag-Pb, Cu, etc. is applied to the surface of AlN and then fired.

上記(1)の方法はDBC(Direct Bond Copper)
基板として知られているが、酸素分圧および温度
のわずかな違いで接合強度および気密性などにバ
ラツキを生じやすいという問題がある。(2)はいわ
ゆる厚膜法として知られ、簡便な方法であるが、
その接合強さは1.2〜2.0Kg/mm2のレベルである。
したがつて、高集積、高密度実装用途の半導体基
板としてAlNを実用化していくには信頼性の高
い金属被膜の形成方法を確立していくのが課題で
ある。
Method (1) above is DBC (Direct Bond Copper)
Although it is known as a substrate, there is a problem in that slight differences in oxygen partial pressure and temperature tend to cause variations in bonding strength and airtightness. (2) is known as the so-called thick film method and is a simple method, but
Its bonding strength is at the level of 1.2-2.0Kg/ mm2 .
Therefore, in order to put AlN into practical use as a semiconductor substrate for high-integration, high-density packaging applications, it is necessary to establish a method for forming a highly reliable metal film.

〔発明の目的〕[Purpose of the invention]

この発明の目的は、気密性と接合強度に優れた
金属被膜をAlN基板上に形成させめる新規な方
法を提供することにある。
An object of the present invention is to provide a novel method for forming a metal film with excellent airtightness and bonding strength on an AlN substrate.

〔発明の要点〕[Key points of the invention]

前記目的は、モリブデン粉末もしくはタングス
テン粉末に硅酸マンガンまたは硅酸鉄またそれら
を主成分とする硅酸塩の粉末を15〜40重量%加え
た混合粉末をAlN表面に塗布し、その後弱酸化
性雰囲気で1250℃から1400℃の温度範囲に加熱し
て焼結を行なうことにより達成することができ
る。
The above purpose was to apply a mixed powder of molybdenum powder or tungsten powder to which 15 to 40% by weight of manganese silicate, iron silicate, or silicate powder containing these as main components was applied to the AlN surface, and then apply a weakly oxidizing powder to the AlN surface. This can be achieved by sintering by heating to a temperature range of 1250°C to 1400°C in an atmosphere.

〔発明の実施例〕[Embodiments of the invention]

高融点金属粉末であるモリブデン粉末あるいは
タングステン粉末とマンガン粉末およびチタン粉
末を用いセラミツクの接合部を予め金属化し、セ
ラミツクと金属をろう付によつて気密接合するこ
とは公知であり、とくにアルミニウムセラミツク
ではMo−MnあるいはMo−Mn−Ti法として広
く用いられている。本発明者らは、このMo−
Mn法をAlNに適用して金属被膜を得ようと試み
たが、所期の目的を達成することができなかつ
た。そこで、高融点のモリブデンおよびタングス
テン粉末に対する添加元素を種々検討したとこ
ろ、高融点金属粉末にマンガンもしくは鉄を硅酸
塩の化合物の形で添加した混合粉末を用いると
AlN表面上において良好な金属被膜が形成でき
るという知見を得た。
It is known to metallize the joints of ceramics in advance using molybdenum powder, tungsten powder, manganese powder, and titanium powder, which are high-melting point metal powders, and to hermetically bond the ceramic and metal together by brazing, especially for aluminum ceramics. It is widely used as the Mo-Mn or Mo-Mn-Ti method. The present inventors discovered that this Mo-
An attempt was made to apply the Mn method to AlN to obtain a metal coating, but the intended purpose could not be achieved. Therefore, we investigated various additive elements for high-melting-point molybdenum and tungsten powders, and found that it is possible to use a mixed powder in which manganese or iron is added in the form of a silicate compound to high-melting-point metal powders.
We obtained the knowledge that a good metal film can be formed on the AlN surface.

モリブデン、タングステンの高融点金属粉末に
添加する硅酸塩粉末の割合は15〜40重量%の範囲
が最適である。これは、15重量%以下ではAlN
に対する高融点金属粉末の結合性が低下し、逆に
40重量%以上では金属被膜形成後に高融点金属上
へ施すメツキの付着性およびろう付あるいはハン
ダ付の接合強度が劣化して、半導体用基板として
の信頼性が保証できなくなるためである。また、
本発明によればAlN表面に金属被膜を形成せし
める際の温度は1250゜〜1450℃の範囲およびその
雰囲気は弱酸化性であることが必要である。これ
は、1250℃以下の温度ではAlNと高融点金属−
硅酸塩混合粉末がよく反応せず、さらに硅酸塩粉
末が高融点金属粉末粒子よく濡らさないため、接
合強度に問題を生じるためである。また1450℃以
上になると、硅酸塩が一部ガラス化してAlNの
結晶粒界に拡散し、その強度と誘電特性を劣化さ
せるため不可である。1250〜1450℃の範囲であれ
ば硅酸塩がAlNと高融点金属粉末の双方をよく
濡らしAlNとの結合が強固でかつ微密な金属被
膜を得ることができる。
The optimal proportion of silicate powder added to high melting point metal powders such as molybdenum and tungsten is in the range of 15 to 40% by weight. This means that below 15% by weight AlN
The bonding properties of high melting point metal powder to
This is because if it exceeds 40% by weight, the adhesion of plating applied to the high-melting point metal after the formation of the metal film and the bonding strength of brazing or soldering deteriorate, making it impossible to guarantee reliability as a semiconductor substrate. Also,
According to the present invention, the temperature when forming the metal film on the AlN surface must be in the range of 1250° to 1450°C, and the atmosphere must be weakly oxidizing. At temperatures below 1250°C, AlN and high melting point metals -
This is because the silicate mixed powder does not react well, and furthermore, the silicate powder does not wet the high melting point metal powder particles well, causing problems in bonding strength. Furthermore, if the temperature exceeds 1450°C, some of the silicate becomes vitrified and diffuses into the grain boundaries of AlN, degrading its strength and dielectric properties, so this is not possible. If the temperature is in the range of 1250 to 1450°C, the silicate will wet both the AlN and the high melting point metal powder well, and a finely dense metal coating with a strong bond to the AlN can be obtained.

一方、加熱時の雰囲気が還元性であると硅酸塩
中に酸化物の形で存在するマンガンまたはFeが
還元されてしまうため、AlNとの結合層を形成
できなくなつてしまう。他方、雰囲気の酸化性が
強いとAlNおよび高融点金属が酸化されて金属
被膜を形成できなくなる。このため、本発明では
弱酸化性雰囲気を使用するのであるが、この場合
酸化性の下限は還元性となる直前まで許容でき
る。弱い酸化剤としてはとくに水蒸気が有効であ
り、加温した水中に素ガスをバブリングし、その
水温によつて雰囲気中の酸素濃度を調整するのが
良い。
On the other hand, if the atmosphere during heating is reducing, manganese or Fe present in the form of oxides in the silicate will be reduced, making it impossible to form a bonding layer with AlN. On the other hand, if the atmosphere is strongly oxidizing, AlN and the high melting point metal will be oxidized, making it impossible to form a metal film. Therefore, in the present invention, a weakly oxidizing atmosphere is used, and in this case, the lower limit of oxidizing property can be tolerated up to just before reducing property. Water vapor is particularly effective as a weak oxidizing agent, and it is best to bubble elementary gas into heated water and adjust the oxygen concentration in the atmosphere depending on the temperature of the water.

なお、本発明の方法で得た高融点金属の金属被
膜は、ハンダおよび硬ろうに対して濡れ性が悪く
酸化されやすいので、金属被膜を形成後、ニツケ
ル等のメツキを施す必要がある。以下に、この発
明を実施例に基づき説明する。
It should be noted that the metal film of the high melting point metal obtained by the method of the present invention has poor wettability with solder and hard solder and is easily oxidized, so after forming the metal film, it is necessary to perform plating with nickel or the like. The present invention will be explained below based on examples.

実施例 1 モリブデン粉末80重量%、硅酸マンガン粉末20
重量%の混合粉末を有機溶剤中でよく懸濁してペ
ースト状とし、これをスクリーン印刷法でAlN
の表面上に18μmの厚さに塗布した。これを電気
炉に挿入し、炉内には50℃の水温でバブリングし
た水素ガスを流しながら時間当り300℃の速度で
1400℃まで昇温し、1400℃で1時間保持して
AlN表面に10μm厚の金属被膜を形成した。この
後、金属被膜に無電解ニツケルメツキ法で厚さ
4μmのニツケルメツキを施した。これを水素と窒
素ガスの混合雰囲気で820℃×15minの熱処理を
行つたメツキの剥離、ふくれなどの有無を検査し
たが、それらの欠陥は一切観察されなかつた。次
にメツキ処理したAlN基板と鉄−ニツケル合金
について銀ろう(BAg−8)を用いて820℃の水
素雰囲気でろう付し、その接合部の気密性を調べ
た。その接合部のヘリウムソーワ量は1×10-5
atmml/sec以下であり、その気密性は良好であ
ることを確認した。さらに、メツキ処理した
AlN基板上に直径が0.5mmの銅線を共晶ハンダ
(40%pd−60%Sn)ハンダ付して、その引張試験
を行つた。この試験では全てが銅線部分で破断
し、金属被膜とメツキ界面およびAlNと金属被
膜の界面などで破損は認められなかつた。そし
て、銅線が破断した時の引張強さは25Kg/mm2であ
り、本発明の方法によるAlN基板上の金属被膜
はこれ以上の強度に耐えることを示した。
Example 1 Molybdenum powder 80% by weight, manganese silicate powder 20%
% by weight of the mixed powder is well suspended in an organic solvent to form a paste, which is then printed with AlN using a screen printing method.
It was applied to a thickness of 18 μm on the surface of This was inserted into an electric furnace, and hydrogen gas bubbled at a water temperature of 50°C was flowed through the furnace at a rate of 300°C per hour.
Raise the temperature to 1400℃ and hold at 1400℃ for 1 hour.
A 10 μm thick metal film was formed on the AlN surface. After this, the metal coating is coated with an electroless nickel plating method.
A nickel plating of 4 μm was applied. This was heat-treated at 820°C for 15 minutes in a mixed atmosphere of hydrogen and nitrogen gas, and the plating was inspected for peeling, blistering, etc., but no defects were observed. Next, the plated AlN substrate and the iron-nickel alloy were brazed using silver solder (BAg-8) in a hydrogen atmosphere at 820°C, and the airtightness of the joint was examined. The amount of helium saw at the joint is 1×10 -5
Atmml/sec or less, and it was confirmed that the airtightness was good. In addition, it was treated with plating
A copper wire with a diameter of 0.5 mm was soldered onto an AlN substrate using eutectic solder (40% PD - 60% Sn), and a tensile test was performed on the wire. In this test, all of the wires broke at the copper wire part, and no damage was observed at the interface between the metal coating and the plating, or the interface between the AlN and metal coating. The tensile strength of the copper wire at breakage was 25 Kg/mm 2 , indicating that the metal coating on the AlN substrate produced by the method of the present invention can withstand even higher strength.

実施例 2 モリブデン粉末80重量%、硅酸鉄20重量%の混
合粉末を実施例1と同様にAlN表面上に塗布し、
1350℃で1時間保持して金属被膜を形成した。こ
れについても、実施例1と同条件で評価したが、
そ気密性、接合強度は実施例1と同等の結果であ
つた。
Example 2 A mixed powder of 80% by weight of molybdenum powder and 20% by weight of iron silicate was applied onto the AlN surface in the same manner as in Example 1,
A metal film was formed by holding at 1350°C for 1 hour. This was also evaluated under the same conditions as Example 1, but
The airtightness and bonding strength were the same as in Example 1.

なお、実施例1,2において、高融点金属粉末
としてモリブデン粉末を用いても前記のモリブデ
ン粉末の場合と同様の結果であることが実験的に
確認できた。
In addition, in Examples 1 and 2, it was experimentally confirmed that even if molybdenum powder was used as the high melting point metal powder, the same results as in the case of the molybdenum powder described above were obtained.

〔発明の効果〕〔Effect of the invention〕

以上説明したごとく、本発明によればモリブデ
ン粉末もしくはタングステン粉末に硅酸マンガン
または硅酸鉄またはそれらを主成分として含む硅
酸塩の粉末を15〜40重量%加えた混合粉をAlN
表面に塗布した後、弱残化性の雰囲気で1250℃か
ら1450℃の温度で焼結することにより、従来知ら
れている方法に比べてAlNとの結合が強固でか
つ緻密な金属被膜が得られるので、気密性と接合
強度にすぐれかつ電子機器の小形、軽量化、高速
化、高出力化、高信頼化を可能とする半導体素子
塔載用基板を提供できるという効果を有する。
As explained above, according to the present invention, a mixed powder in which 15 to 40% by weight of manganese silicate, iron silicate, or silicate powder containing these as main components is added to molybdenum powder or tungsten powder is AlN.
After being applied to the surface, it is sintered at a temperature of 1250°C to 1450°C in a mildly residual atmosphere, resulting in a dense metal coating with a stronger bond with AlN than conventional methods. Therefore, it is possible to provide a substrate for mounting a semiconductor element, which has excellent airtightness and bonding strength, and which enables electronic devices to be made smaller, lighter, faster, higher output, and more reliable.

Claims (1)

【特許請求の範囲】[Claims] 1 窒化アルミニウムセラミツクの表面に、モリ
ブデン粉末もしくはタングステン粉末に硅酸マン
ガンまたは硅酸鉄またはそれらを主成分として含
む硅酸塩の粉末を15〜40重量%加えた混合粉末を
塗布した後、弱酸化性の雰囲気で1250℃から1450
℃の温度に加熱して焼結することを特徴とする金
属被膜の形成方法。
1 After applying a mixed powder of molybdenum powder or tungsten powder to 15 to 40% by weight of manganese silicate, iron silicate, or silicate powder containing these as main components on the surface of aluminum nitride ceramic, weak oxidation is applied. 1250℃ to 1450℃ in a sexual atmosphere
A method for forming a metal film, characterized by heating and sintering to a temperature of °C.
JP9878886A 1986-04-28 1986-04-28 Formation of metal coating Granted JPS62256781A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9878886A JPS62256781A (en) 1986-04-28 1986-04-28 Formation of metal coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9878886A JPS62256781A (en) 1986-04-28 1986-04-28 Formation of metal coating

Publications (2)

Publication Number Publication Date
JPS62256781A JPS62256781A (en) 1987-11-09
JPH0455153B2 true JPH0455153B2 (en) 1992-09-02

Family

ID=14229109

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9878886A Granted JPS62256781A (en) 1986-04-28 1986-04-28 Formation of metal coating

Country Status (1)

Country Link
JP (1) JPS62256781A (en)

Also Published As

Publication number Publication date
JPS62256781A (en) 1987-11-09

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