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JP3029702B2 - AlN substrate - Google Patents
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JP3029702B2 - AlN substrate - Google Patents

AlN substrate

Info

Publication number
JP3029702B2
JP3029702B2 JP3146050A JP14605091A JP3029702B2 JP 3029702 B2 JP3029702 B2 JP 3029702B2 JP 3146050 A JP3146050 A JP 3146050A JP 14605091 A JP14605091 A JP 14605091A JP 3029702 B2 JP3029702 B2 JP 3029702B2
Authority
JP
Japan
Prior art keywords
layer
metal
substrate
thin film
aln substrate
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
Application number
JP3146050A
Other languages
Japanese (ja)
Other versions
JPH04287953A (en
Inventor
恭章 安本
晃司 山川
靖 五代儀
馨 小岩
暢男 岩瀬
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.)
Toshiba Corp
Original Assignee
Toshiba Corp
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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP3146050A priority Critical patent/JP3029702B2/en
Publication of JPH04287953A publication Critical patent/JPH04287953A/en
Application granted granted Critical
Publication of JP3029702B2 publication Critical patent/JP3029702B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/52Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00844Uses not provided for elsewhere in C04B2111/00 for electronic applications

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Ceramic Products (AREA)
  • Manufacturing Of Printed Wiring (AREA)
  • Parts Printed On Printed Circuit Boards (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】この発明は、薄膜回路基板等に用
いられるAlN基板に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an AlN substrate used for a thin film circuit board or the like.

【0002】[0002]

【従来の技術】従来、薄膜配線実装モジュ―ルの基板と
して主にアルミナが使われている。しかし、能動素子
は、性能の向上に伴い稼働時の発熱量が増大する傾向に
あり、アルミナの熱伝導率では能動素子の実装個数に制
約を受ける。このため、モジュ―ルの実装密度が熱的な
理由から低レベルとなってしまう。
2. Description of the Related Art Conventionally, alumina has been mainly used as a substrate of a thin-film wiring mounting module. However, the amount of heat generated during operation of the active element tends to increase with the improvement in performance, and the thermal conductivity of alumina is limited by the number of mounted active elements. For this reason, the mounting density of the module becomes low due to thermal reasons.

【0003】このようなことから、アルミナに代わり高
熱伝導率をもつBeOを基板材料として使用することが
試みられてきたが、BeOは加工や研磨時における毒性
のため基板としての応用範囲が限定される。
For this reason, attempts have been made to use BeO, which has a high thermal conductivity, as a substrate material instead of alumina, but BeO has a limited range of application as a substrate due to toxicity during processing and polishing. You.

【0004】このような問題点を有するBeOの代替材
料として、近時、AlNが用いられつつある。AlNは
無毒であり、その中に含まれる酸素濃度の低下や緻密化
を促進する焼結助材の開発などにより、BeOを上回る
熱伝導率を達成している。このため、AlNの薄膜回路
基板への応用も徐々に始まっており、高熱伝導率を生か
した高密度実装基板として薄膜導体の配線化が具体化し
つつある。このようなものとして、AlN基体上に、T
i/Ni/Au、Ti/Pt/Au、Cr/Cu/A
u、又はTiN/Ni/Auを形成した回路基板があ
る。しかしながら、このような回路基板は、薄膜導体と
AlN基体との密着強度が不十分なため、基体表面から
薄膜導体により形成された配線層が剥離したり、断線す
る欠点を有している。さらに、AlNは結晶方位により
エッチング速度が異なるので、AlN基体では結晶方位
の異なる粒界に段差を生じる。この結果、薄膜導体と基
体との密着強度が不十分であると、配線層は段差上で断
線を生じ、信頼性が充分でないという問題を有してい
る。このため、薄膜導体を密着性よく安定的にAlN基
体上に形成することができる回路基板が望まれている。
AlN has recently been used as an alternative to BeO having such problems. AlN is non-toxic, and has achieved a thermal conductivity higher than that of BeO by reducing the concentration of oxygen contained therein and developing a sintering aid that promotes densification. For this reason, the application of AlN to a thin film circuit board has begun gradually, and wiring of a thin film conductor is being embodied as a high-density mounting board utilizing high thermal conductivity. As such, on an AlN substrate, T
i / Ni / Au, Ti / Pt / Au, Cr / Cu / A
There is a circuit board formed with u or TiN / Ni / Au. However, such a circuit board has a drawback that a wiring layer formed by the thin film conductor is peeled off or disconnected from the surface of the substrate due to insufficient adhesion strength between the thin film conductor and the AlN substrate. Further, since the etching rate of AlN differs depending on the crystal orientation, a step occurs at the grain boundary having a different crystal orientation in the AlN substrate. As a result, if the adhesion strength between the thin film conductor and the base is insufficient, the wiring layer has a problem of disconnection on a step, resulting in insufficient reliability. For this reason, a circuit board capable of stably forming a thin film conductor on an AlN substrate with good adhesion is desired.

【0005】[0005]

【発明が解決しようとする課題】この発明は、このよう
な従来技術の問題点を解決するためになされたものであ
って、AlN基体と薄膜導体との密着強度が高く、また
信頼性の優れたAlN基板を提供することを目的とす
る。
SUMMARY OF THE INVENTION The present invention has been made to solve such problems of the prior art, and has a high adhesion strength between an AlN substrate and a thin-film conductor and a high reliability. It is an object of the present invention to provide an AlN substrate.

【0006】[0006]

【課題を解決するための手段及び作用】第1の発明に係
るAlN基板は、AlN基体と、該基体上に設けられ、
Ti,Cr,Ta,Zr,Hfの中から選択される少な
くとも一種の元素M1とAlとNとをAlx
100-x :M1:M1y 100-y =u:v:w(ただ
し、x,yは原子%、u,v,wは分子%を示し、u+
v+w= 100であり、夫々25≦x≦90、40≦y≦70、40
≦u≦98、 0.2≦v≦40、1≦w≦40の範囲である)の
割合になるように含む金属・窒化物層と、該金属・窒化
物層の上に積層され前記M1を含有する接合層と、該接
合層の上に積層されW,Nb,Ta,Mo,Ni,P
t,Pd,NiCrの中から選択される少なくとも一種
を主体とするバリア層と、該バリア層の上に積層されA
u,Cu,Alのうち少なくとも一種を主体とする薄膜
導体層とを有し、該薄膜導体層の所定位置に金属面を有
する部品が接合されることを特徴とする。
The AlN substrate according to the first invention is provided on an AlN substrate and provided on the substrate.
At least one element M1 selected from Ti, Cr, Ta, Zr, and Hf, and Al and N are converted to Al x M
1 100-x : M1: M1 y N 100-y = u: v: w (where x and y indicate atomic%, u, v and w indicate molecular%, and u +
v + w = 100, 25 ≦ x ≦ 90, 40 ≦ y ≦ 70, 40
≤ u ≤ 98, 0.2 ≤ v ≤ 40, and 1 ≤ w ≤ 40) and a metal / nitride layer containing the M1 laminated on the metal / nitride layer. Bonding layer, and W, Nb, Ta, Mo, Ni, P laminated on the bonding layer
a barrier layer mainly composed of at least one selected from t, Pd, and NiCr;
and a thin-film conductor layer mainly composed of at least one of u, Cu, and Al, and a component having a metal surface is bonded to a predetermined position of the thin-film conductor layer.

【0007】また、第2の発明に係るAlN基板は、A
lN基体と、該基体上に設けられ、AlとNとをAlt
100-t (ただしtは原子%を示し50<t< 100の範囲
である)の割合になるように含む窒素・アルミニウム層
と、該窒素・アルミニウム層の上に積層されTi,C
r,Ta,Zr,Hfの中から選択される少なくとも一
種の元素M1とAlとをAlx ' M1100-x ' (ただし
x' は原子%を示し10≦x' ≦90の範囲である)の割合
になるように含む金属層と、該金属層の上に積層され、
前記M1を含有する接合層と、該接合層の上に積層され
W,Nb,Ta,Mo,Ni,Pt,Pd,NiCrの
中から選択される少なくとも一種を主体とするバリア層
と、該バリア層の上に積層されAu,Cu,Alのうち
少なくとも一種を主体とする薄膜導体層とを有し、該薄
膜導体層の所定位置に金属面を有する部品が接合される
ことを特徴とする。
Further, the AlN substrate according to the second invention is characterized in that
and lN substrate, provided on said substrate, Al and N Al t
A nitrogen / aluminum layer containing N 100-t (where t represents atomic% and in the range of 50 <t <100), and Ti, C laminated on the nitrogen / aluminum layer.
At least one element M1 and Al selected from r, Ta, Zr, and Hf are represented by Al x ' M1 100-x' (where x 'represents atomic% and in the range of 10 ≦ x ′ ≦ 90) A metal layer containing so as to have a ratio of, and laminated on the metal layer,
A bonding layer containing the M1, a barrier layer laminated on the bonding layer and mainly composed of at least one selected from W, Nb, Ta, Mo, Ni, Pt, Pd, and NiCr; A thin film conductor layer mainly composed of at least one of Au, Cu, and Al laminated on the layer, and a component having a metal surface is bonded to a predetermined position of the thin film conductor layer.

【0008】本発明で使用されるAlN基体は、必要に
応じて適宜の焼結助剤を伴う焼結体であり、酸素含有量
が 0.005〜10原子%のものを用いることが望ましい。こ
れは、基板中の酸素含有量が 0.005原子%未満であると
金属・窒化物層の密着強度を十分に高めることが困難と
なり、一方10原子%を超えるとAlN基体の熱伝導率が
アルミナと同程度の値まで低下して高熱伝導性の利点が
損なわれる恐れがあるからである。第1の発明における
AlN基体上には、以下に詳細に説明する金属・窒化物
層と、接合層と、バリア層と、薄膜導体層とが設けられ
ている。
The AlN substrate used in the present invention is a sintered body with an appropriate sintering aid, if necessary, and preferably has an oxygen content of 0.005 to 10 atomic%. This is because if the oxygen content in the substrate is less than 0.005 atomic%, it is difficult to sufficiently increase the adhesion strength of the metal / nitride layer, while if it exceeds 10 atomic%, the thermal conductivity of the AlN substrate is lower than that of alumina. This is because the value may be reduced to a similar value and the advantage of high thermal conductivity may be lost. On the AlN substrate in the first invention, a metal / nitride layer, a bonding layer, a barrier layer, and a thin-film conductor layer, which will be described in detail below, are provided.

【0009】金属・窒化物層はAlN基体を被覆する層
であり、接合層を基体に接合するための層として作用す
る。こ金属・窒化物層は、上記M1で、表される元素と
AlとMとで構成された層であり、一定組成のAl−M
1合金とM1とM1の窒化物とを所定の割合で含有して
いる。この層は、金属成分と窒化物とが膜厚方向に濃度
勾配を有していてもよく、基体側が金属成分リッチ、接
合層側が窒化物リッチであっても構わない。この層の構
成成分であるAl,N,M1は、AlN基体とM1を主
体とする接合層との密着強度を向上させる作用を有し、
NはさらにAlN基体と接合層との間の格子定数を整合
化する作用、及び熱膨脹係数を緩和する作用を有する。
The metal / nitride layer covers the AlN substrate and functions as a layer for bonding the bonding layer to the substrate. The metal / nitride layer is a layer composed of the element represented by M1 and Al and M, and has a constant composition of Al-M
One alloy, M1 and a nitride of M1 are contained at a predetermined ratio. In this layer, the metal component and the nitride may have a concentration gradient in the film thickness direction, and the base side may be rich in the metal component and the bonding layer side may be rich in the nitride. Al, N, and M1, which are components of this layer, have an effect of improving the adhesion strength between the AlN substrate and the bonding layer mainly composed of M1.
N further has the effect of matching the lattice constant between the AlN substrate and the bonding layer, and the effect of reducing the coefficient of thermal expansion.

【0010】金属・窒化物層は、M1,Al,Nを、A
x M1100-x :M1:M1y 100-y =u:v:w
(ただし、x,y,vは原子%、u,wは分子%を示
し、u+v+w= 100であり、夫々25≦x≦90、40≦y
≦70、40≦u≦98、 0.2≦v≦40、1≦w≦40の範囲で
ある)を満たすような割合で含んでいる。M1の種類、
並びに各構成元素及び成分の比率をこの範囲に限定した
理由を以下に説明する。
The metal / nitride layers are represented by M1, Al, N and A
l x M1 100-x : M1: M1 y N 100-y = u: v: w
(Where x, y, and v indicate atomic%, u and w indicate molecular%, u + v + w = 100, and 25 ≦ x ≦ 90 and 40 ≦ y, respectively)
≤ 70, 40 ≤ u ≤ 98, 0.2 ≤ v ≤ 40, and 1 ≤ w ≤ 40). The type of M1,
The reason why the ratio of each constituent element and component is limited to this range will be described below.

【0011】Alx M1100-x におけるAlを25原子%
未満とすると、AlN基体との間の密着強度を十分に高
めることができず、一方この量が90原子%を超えると金
属・窒化物層中のAl量が多くなって、回路形成等のパ
タ―ニングに際し、エッチングが不十分となり、配線間
の抵抗低下、短絡等を招く。従って、Alの量は25〜90
原子%、好ましくは30〜85重量%である。ただし、Al
は金属・窒化物層中ではM1との合金又は化合物として
存在する。
[0011] The Al in Al x M1 100-x 25 atomic%
If the amount is less than 90%, the amount of Al in the metal / nitride layer increases, and if the amount exceeds 90 atomic%, the amount of patterning, such as circuit formation, increases. When etching, the etching becomes insufficient, causing a decrease in resistance between wirings, a short circuit, and the like. Therefore, the amount of Al is 25-90.
Atomic%, preferably 30-85% by weight. Where Al
Exists as an alloy or compound with M1 in the metal / nitride layer.

【0012】M1はTi,Cr,Ta,Zr,Hfの中
から選択される元素である。これらの元素は窒素、Al
との反応性が高いので、合金、窒化物の形成に好適であ
り、この層の機能を果たす上で好適である。
M1 is an element selected from Ti, Cr, Ta, Zr, and Hf. These elements are nitrogen, Al
It is suitable for the formation of alloys and nitrides, and is suitable for fulfilling the function of this layer.

【0013】M1y 100-y におけるM1を40原子%未
満にすると、AlN基体の含有窒素がガス化し、薄膜の
膨れ剥離をもたらし、一方70原子%を超えるとM1窒化
物の生成量が少なくなり、この層の上に形成された接合
層中のM1がこの金属・窒化物層中に容易に移動し、こ
の濃度が過剰となる。この結果、AlM1の組成比がこ
の発明の範囲から逸脱し、AlN基体と薄膜導体層との
密着強度を十分に高めることができなくなる。このた
め、M1の量は40〜70原子%の範囲、好ましくは45〜70
原子%の範囲とする。
When M1 in M1 y N 100-y is less than 40 atomic%, the nitrogen contained in the AlN substrate is gasified, causing swelling of the thin film. On the other hand, when it exceeds 70 atomic%, the amount of M1 nitride formed is small. Therefore, M1 in the bonding layer formed on this layer easily moves into this metal / nitride layer, and its concentration becomes excessive. As a result, the composition ratio of AlM1 deviates from the range of the present invention, and the adhesion strength between the AlN substrate and the thin film conductor layer cannot be sufficiently increased. For this reason, the amount of M1 is in the range of 40 to 70 atomic%, preferably 45 to 70 atomic%.
Atomic% range.

【0014】この層を構成するAlM1、M1、及びM
lは高密着強度化、及びこの層の安定化に適している。
AlM1が40分子%未満の場合、高温下での密着強度が
低下し、ろう付けする場合に薄膜とAlN基体との剥離
を生じ、一方98分子%を超えると界面での内部応力が大
きくなって安定的な密着強度を得ることが困難である。
このため、AlM1の分子%(すなわちuの値)の範囲
は40〜98であり、より好ましくは42〜95である。また、
M1Nが1分子%未満の場合、この層と接合層との反応
を防止することが困難であり、接合層を形成するM1が
AlM1を不安定にし、高温下での密着強度が低下す
る。一方、M1Nが40分子%を超えると、この金属・窒
化物層の内部応力が大きくなり、安定的に密着強度を得
ることが困難である。このためM1Nの分子%(すなわ
ちwの値)は1〜40の範囲であり、より好ましくは2〜
37の範囲である。さらに、M1が 0.2原子%未満では金
属・窒化物層形成の際の未反応Nがガス化し、薄膜にふ
くれを生じる。また、M1が40原子%を超えると高温下
での密着強度が低下する。このためM1の原子%(すな
わちvの値)は 0.2〜40の範囲であり、より好ましくは
0.5〜38の範囲である。
The AlM1, M1, and M constituting this layer
l is suitable for increasing the adhesion strength and stabilizing this layer.
If AlM1 is less than 40% by mole, the adhesion strength at high temperature is reduced, and the thin film and the AlN substrate are separated when brazing. On the other hand, if over 98% by mole, the internal stress at the interface becomes large. It is difficult to obtain a stable adhesion strength.
For this reason, the range of the molecular% (that is, the value of u) of AlM1 is 40 to 98, and more preferably 42 to 95. Also,
If M1N is less than 1 mol%, it is difficult to prevent the reaction between this layer and the bonding layer, and M1 forming the bonding layer destabilizes AlM1 and lowers the adhesive strength at high temperatures. On the other hand, when M1N exceeds 40% by mole, the internal stress of the metal / nitride layer increases, and it is difficult to stably obtain the adhesion strength. For this reason, the molecular% of M1N (that is, the value of w) is in the range of 1 to 40, more preferably 2 to 40.
It is in the range of 37. Further, when M1 is less than 0.2 atomic%, unreacted N gas at the time of forming the metal / nitride layer is gasified, causing blisters in the thin film. On the other hand, if M1 exceeds 40 atomic%, the adhesion strength at high temperatures decreases. For this reason, the atomic% of M1 (that is, the value of v) is in the range of 0.2 to 40, more preferably
It is in the range of 0.5 to 38.

【0015】このような金属・窒化物層の厚さは3nm
以上にすることが望ましい。これは、この層の厚さが3
nm未満の場合には、AlN基体と薄膜導体層との間の
密着強度を安定的に向上させることが困難となるからで
ある。この層が厚すぎると、回路基板の薄膜化及びエッ
チングによる除去に長時間を要し、パタ―ン精度等の条
件設定が困難なものとなる。より好ましい金属・窒化物
層の厚さの範囲は、10〜 500nmである。
The thickness of such a metal / nitride layer is 3 nm.
It is desirable to make the above. This means that the thickness of this layer is 3
If the thickness is less than nm, it is difficult to stably improve the adhesion strength between the AlN substrate and the thin film conductor layer. If this layer is too thick, it will take a long time to make the circuit board thinner and remove it by etching, and it will be difficult to set conditions such as pattern accuracy. A more preferable range of the thickness of the metal / nitride layer is 10 to 500 nm.

【0016】接合層は、上述したように、Ti,Cr,
Ta,Zr,Hfの中から選択される少なくとも一種の
元素M1を主体とするものである。この接合層は金属・
窒化物層に対する密着強度をた高める作用を有する。ま
た、この接合層の上に形成されたバリア層の構成元素が
成膜時のインタ―ミキシングや熱処理によって、接合層
の元素と混合しても密着強度に与える影響は小さい。
As described above, the bonding layer is made of Ti, Cr,
At least one element M1 selected from Ta, Zr, and Hf is mainly used. This bonding layer is made of metal
It has the effect of increasing the adhesion strength to the nitride layer. Further, even if the constituent elements of the barrier layer formed on the bonding layer are mixed with the elements of the bonding layer by intermixing or heat treatment during film formation, the effect on the adhesion strength is small.

【0017】また、接合層中に窒素又は酸素が含有され
ていてもよい。このとき窒素又は酸素は固溶している又
は化合物を形成している。特に窒素が含有されていると
きにはM1と薄膜導体層を構成する元素の相互拡散を防
ぐバリアとしても有効である。そのためにはM1とNと
がM1Z 100-z (ただしzは原子%を示し1≦z≦40
の範囲である)の割合になるように含まれるのがよい。
また均一に含まれていても傾斜をもっていてもよい。
Further, nitrogen or oxygen may be contained in the bonding layer. At this time, nitrogen or oxygen is forming a solid solution or a compound. In particular, when nitrogen is contained, it is also effective as a barrier for preventing mutual diffusion of M1 and the elements constituting the thin film conductor layer. As M1 and the N is M1 Z N 100-z (although z is for the 1 ≦ z ≦ represent atomic% 40
).
Further, they may be uniformly contained or may have a slope.

【0018】接合層の厚さは1nm〜1μmであること
が好ましい。これは、その厚さが1nm未満の場合には
金属・窒化物層との接合が不十分で、高い密着強度を達
成することが困難となり、一方この厚さが1μmを超え
ると内部応力のために接合層、バリア層及び導体層が剥
離しやすくなるからである。好ましい厚さは3〜 900n
m,より好ましい厚さの範囲は10〜 500nmである。
The thickness of the bonding layer is preferably from 1 nm to 1 μm. This is because if the thickness is less than 1 nm, the bonding with the metal / nitride layer is insufficient and it is difficult to achieve high adhesion strength. On the other hand, if the thickness exceeds 1 μm, internal stress is caused. This is because the bonding layer, the barrier layer, and the conductor layer are easily peeled off. Preferred thickness is 3 to 900n
m, a more preferable thickness range is 10 to 500 nm.

【0019】バリア層は、上述したように、W,Nb,
Ta,Mo,Ni,Pt,Pd,NiCrの中から選択
される少なくとも1種を主体とするものである。この層
は、接合層を構成するM1と導体層を構成するAu,C
u,Alのうち少なくとも一種とが相互に拡散すること
を阻止する作用を有する。このバリア層の厚さは5nm
〜5μmの範囲であることが好ましい。これは、バリア
層の厚さを5nm未満にすると上述のバリア効果を十分
に達成することが困難となり、一方5μmを超えるとこ
の層の内部応力のためにこの層及び導体層が剥離した
り、パタ―ニングに際してのエッチングにおいてサイド
エッチング度合が大きくなって信頼性の高い薄膜導体の
形成が困難となるからである。より好ましい厚さの範囲
は10nm〜2μmである。
As described above, the barrier layer is made of W, Nb,
The main component is at least one selected from Ta, Mo, Ni, Pt, Pd, and NiCr. This layer is composed of M1 forming the bonding layer and Au, C forming the conductor layer.
It has an action of preventing at least one of u and Al from mutually diffusing. The thickness of this barrier layer is 5 nm
It is preferably in the range of 5 to 5 μm. This is because if the thickness of the barrier layer is less than 5 nm, it is difficult to sufficiently achieve the above-mentioned barrier effect. On the other hand, if the thickness exceeds 5 μm, the layer and the conductor layer are separated due to internal stress of the layer, This is because the degree of side etching becomes large in the etching at the time of patterning, and it becomes difficult to form a highly reliable thin film conductor. A more preferable thickness range is 10 nm to 2 μm.

【0020】薄膜導体層はAu,Cu又はAlを主体と
するものであり、その厚さは50nm〜20μmであること
が望ましい。50nm未満にすると配線抵抗が高くなり、
パタ―ンの微細化に不適当となり、一方、20μmを超え
ると内部応力のために剥離が生じてしまう。より好まし
くは70nm〜15μmがよい。この様にして、AlN基
体,金属・窒化物層,接合層,バリア層,薄膜導体層か
ら成るAlN基板が構成される。
The thin film conductor layer is mainly composed of Au, Cu or Al, and its thickness is desirably 50 nm to 20 μm. If it is less than 50 nm, the wiring resistance increases,
The pattern becomes unsuitable for miniaturization of the pattern. On the other hand, if it exceeds 20 μm, peeling will occur due to internal stress. More preferably, the thickness is 70 nm to 15 μm. Thus, an AlN substrate including the AlN substrate, the metal / nitride layer, the bonding layer, the barrier layer, and the thin film conductor layer is formed.

【0021】第2の発明におけるAlN基体上には、以
下に詳細に説明する窒素・アルミニウム層と、金属層と
第1の発明と同様の接合層とバリア層と薄膜導体層が設
けられている。
On the AlN substrate of the second invention, a nitrogen / aluminum layer, a metal layer, a bonding layer, a barrier layer and a thin film conductor layer similar to those of the first invention are provided in detail. .

【0022】アルミニウム・窒素層は金属層との密着性
向上に効果があり、Alの原子%(すなわちtの値)が
50以下では密着強度が向上せず、 100になると基板表面
の抵抗率が低下し、基板上に配線パタ―ンを形成できな
くなる。このため、アルミニウム・窒素層は原子比で50
<t< 100の範囲が望ましく、さらに好ましくは51≦t
≦90の範囲である。尚、この組成範囲はアルミニウム・
窒素層の平均組成であり、層内は均一であっても傾斜を
持っていても良い。アルミニウム・窒素層の厚さは1n
mから50μmの範囲とすることが好ましく、この理由は
1nm未満の膜厚では薄膜導体と基板との密着強度を安
定的に保持することがむづかしくなり、50μm以上では
膜の内部応力のため剥離するためである。前記した基板
に含有される酸素を上記化合物層中に含有しても、密着
強度におよぼす影響は小さい。さらにより好ましくは1
nmから30μmの範囲である。
The aluminum / nitrogen layer is effective for improving the adhesion to the metal layer, and the atomic% of Al (that is, the value of t) is reduced.
If it is less than 50, the adhesion strength will not be improved, and if it is 100, the resistivity of the substrate surface will decrease, and it will not be possible to form a wiring pattern on the substrate. Therefore, the aluminum / nitrogen layer has an atomic ratio of 50%.
<T <100, more preferably 51 ≦ t
≦ 90. In addition, this composition range is aluminum
This is the average composition of the nitrogen layer, and the inside of the layer may be uniform or may have a slope. Aluminum / nitrogen layer thickness is 1n
It is preferable that the thickness be in the range of m to 50 μm. The reason for this is that if the film thickness is less than 1 nm, it becomes difficult to stably maintain the adhesion strength between the thin film conductor and the substrate. This is for peeling. Even if oxygen contained in the above-mentioned substrate is contained in the above-mentioned compound layer, the influence on the adhesion strength is small. Even more preferably 1
The range is from nm to 30 μm.

【0023】金属層はAlとM1から成る。このとき、
層内に窒素若しくは酸素が固溶若しくは化合物を形成し
ていても良く、また、それが均一であっても傾斜を持っ
ていても良い。例えば、基板側が上記窒化物層リッチ、
接合層側が金属層リッチとなっても問題ない。この層の
構成成分であるAl、M1はAlN基体と該基体側に配
置される接合層のM1層との密着強度を向上する作用を
有する。かかる金属層の各構成成分の比率(原子比)、
M1の種類を限定したのは以下の理由によるものであ
る。
The metal layer is composed of Al and M1. At this time,
Nitrogen or oxygen may form a solid solution or form a compound in the layer, and it may be uniform or have a gradient. For example, the substrate side is rich in the nitride layer,
There is no problem even if the bonding layer side becomes rich in the metal layer. Al and M1, which are constituents of this layer, have an effect of improving the adhesion strength between the AlN substrate and the M1 layer of the bonding layer disposed on the substrate side. The ratio (atomic ratio) of each component of the metal layer,
The reason for limiting the type of M1 is as follows.

【0024】Alt M1100-t におけるAlの原子比を
10未満にすると、AlN基板と薄膜導体層間との密着強
度を十分に高めることができず、一方この原子比が90を
越えると金属層中のAl量が多くなって、回路形成等の
パタ―ニングに際しエッチングが不十分となり、配線間
の抵抗低下、短絡等を招く。Alの原子比にて表される
好ましい量は10〜90の範囲でより好ましい量は15〜88の
範囲である。
The atomic ratio of Al in Al t M1 100-t is
If it is less than 10, the adhesion strength between the AlN substrate and the thin-film conductor layer cannot be sufficiently increased, while if this atomic ratio exceeds 90, the amount of Al in the metal layer increases and the pattern for circuit formation and the like increases. Insufficient etching at the time of thinning causes a decrease in resistance between wirings, a short circuit, and the like. The preferred amount represented by the atomic ratio of Al is in the range of 10 to 90, and the more preferred amount is in the range of 15 to 88.

【0025】またM1はTi,Cr,To,Zr,Hf
のうちから選ばれる一種の元素から構成される。これら
の元素はAlとの反応性が高く、合金形成に好適であ
る。なお、このような金属層中に含有されるM1元素
は、一部がAlと合金を形成せず、金属単体または金属
窒化物として存在していてもよい。
M1 is Ti, Cr, To, Zr, Hf
It is composed of a kind of element selected from the above. These elements have high reactivity with Al and are suitable for alloy formation. In addition, the M1 element contained in such a metal layer may not exist partially as an alloy with Al, and may exist as a simple metal or a metal nitride.

【0026】金属層の厚さは、1nmから1μmの範囲
にすることが望ましい。この理由は化合物層の厚さを1
nm未満にするとAlN基板と薄膜導体層の密着強度を
安定的に向上することが困難となる。1μm以上の膜厚
では、回路基板の薄膜化およびエッチングによる除去に
時間を要し、パタ―ン精度等の条件設定が困難なものと
なる。より好ましい化合物層の厚さは、3〜1μmの範
囲である。この様な金属層上に、第1の発明と同様の接
合層,バリア層,導体層が形成される。さらに、第1及
び第2の発明のAlN基板上の所望の位置に金属面を有
する部品が接合される。
It is desirable that the thickness of the metal layer be in the range of 1 nm to 1 μm. This is because the thickness of the compound layer is 1
If it is less than nm, it is difficult to stably improve the adhesion strength between the AlN substrate and the thin film conductor layer. If the film thickness is 1 μm or more, it takes time to make the circuit board thinner and remove it by etching, and it is difficult to set conditions such as pattern accuracy. A more preferred thickness of the compound layer is in the range of 3 to 1 μm. On such a metal layer, the same bonding layer, barrier layer, and conductor layer as in the first invention are formed. Further, components having a metal surface are joined at desired positions on the AlN substrates of the first and second inventions.

【0027】金属面を有する部品としては、AlN基板
の用途に応じて種々のものを採用することができるが、
回路基板として用いる場合には、電極端子、封止用接合
金属、基板支持用部品、冷却フィン付き接合金属など、
ろう材又ははんだと接合可能なものであればよい。
As the component having a metal surface, various components can be adopted according to the use of the AlN substrate.
When used as a circuit board, electrode terminals, joining metal for sealing, parts for substrate support, joining metal with cooling fins, etc.
Any material can be used as long as it can be joined to a brazing material or solder.

【0028】以上説明したAlN基体及び各層は、成膜
やアニ―ルの際に、互いに相互拡散、インタ―ミキシン
グしたり、傾斜構造を生じるなどしても、各々の組成が
本発明の範囲内である限り、基板の機能が劣化すること
はなく、問題は生じない。次に、本発明のAlN基板の
製造方法の例について説明する。
The above-described AlN substrate and each layer have the respective compositions falling within the scope of the present invention even if they are mutually diffused, intermixed, or have a gradient structure during film formation or annealing. As long as, the function of the substrate does not deteriorate, and no problem occurs. Next, an example of the method for manufacturing an AlN substrate of the present invention will be described.

【0029】先ず、表面粗さが例えば薄膜回路を形成す
るために十分な値を有するAlN基体を用意する。表面
粗さの調整は焼結基板の研磨によって行うことができる
が、サブミクロン粒子原料を用いた焼結基板を使用すれ
ば焼結のままで所望の表面粗さを得ることができる。
First, an AlN substrate having a surface roughness sufficient for forming, for example, a thin film circuit is prepared. The surface roughness can be adjusted by polishing the sintered substrate. However, if a sintered substrate using a submicron particle material is used, a desired surface roughness can be obtained without sintering.

【0030】次に、第1の発明においては、薄膜層であ
る金属・窒化物層、接合層、バリア層、薄膜導体層を順
次形成する。また、第2の発明においては、薄膜層であ
る窒素・アルミニウム層,金属層,接合層,バリア層,
薄膜導体層を順次形成する。これらの層の薄膜形成方法
としては真空蒸着法、スパッタ、クラスタイオンビ―
ム、イオンプレ―ティング、イオン注入法などの一般的
薄膜形成法を用いることができ、基板温度、雰囲気、真
空度、成膜速度を適宜調整する。薄膜形成に先立ち、基
板表面を湿式洗浄法、逆スパッタ法などで十分洗浄を行
うが、AlNは強酸、強アルカリに対して不安定なた
め、洗浄液の選定に注意が必要である。洗浄液としては
中性のものを使用することが好ましい。金属・窒化物層
若しくは窒素・アルミニウム層及び金属層を上述の薄膜
形成法のうちの適宜の方法で形成した後、真空を破らず
に連続的に、接合層を成膜する。基板温度は成膜に支障
のない範囲であればよく室温から 800℃程度までが使用
される。このようにして成膜した接合層の上に、真空を
破らずに連続的にバリア層を成膜する。次いでバリア層
の上に薄膜導体層を形成する。この場合に、この層を真
空を破らずに連続的に形成してもよいし、湿式メッキに
より形成してもよい。
Next, in the first aspect, a metal / nitride layer, a bonding layer, a barrier layer, and a thin film conductor layer, which are thin film layers, are sequentially formed. Further, in the second invention, a nitrogen / aluminum layer as a thin film layer, a metal layer, a bonding layer, a barrier layer,
Thin-film conductor layers are sequentially formed. Methods for forming thin films of these layers include vacuum deposition, sputtering, and cluster ion beam.
A general thin film forming method such as ion implantation, ion plating, or ion implantation can be used, and the substrate temperature, atmosphere, degree of vacuum, and film formation rate are appropriately adjusted. Prior to the formation of the thin film, the substrate surface is sufficiently cleaned by a wet cleaning method, a reverse sputtering method, or the like. However, since AlN is unstable to strong acids and strong alkalis, care must be taken in selecting a cleaning solution. It is preferable to use a neutral cleaning solution. After forming a metal / nitride layer or a nitrogen / aluminum layer and a metal layer by an appropriate method among the above-described thin film formation methods, a bonding layer is continuously formed without breaking vacuum. The substrate temperature may be within a range that does not hinder film formation, and is used from room temperature to about 800 ° C. On the bonding layer thus formed, a barrier layer is continuously formed without breaking vacuum. Next, a thin film conductor layer is formed on the barrier layer. In this case, this layer may be formed continuously without breaking vacuum, or may be formed by wet plating.

【0031】このようにして形成されたAlN基板は、
基体に対する薄膜導体層の密着強度が高く、薄膜導体層
の剥離を防止することができ、さらにその上に金属面を
有する部品を高い密着強度で接合することができる。従
って、ろう付け部品の剥離や断線等を防止することがで
き、能動素子等の高密度実装が可能な、半導体モジュ―
ルに有用な高信頼性の回路基板を得ることができる。
The AlN substrate thus formed is:
The adhesive strength of the thin-film conductor layer to the base is high, the peeling of the thin-film conductor layer can be prevented, and a component having a metal surface thereon can be joined with high adhesive strength. Therefore, it is possible to prevent the peeling or disconnection of the brazed parts, and to realize a semiconductor module capable of high-density mounting of active elements and the like.
Thus, it is possible to obtain a highly reliable circuit board that is useful for a device.

【0032】本発明のAlN基板を回路基板として使用
する場合には、配線部のパタ―ンニングは薄膜導体層形
成後又は部品接合後に行われるが、一般に前者の方法が
作業上便利である。所望のパタ―ンはポジ又はネガレジ
ストにより薄膜導体層上に形成し、湿式法又はドライ法
のエッチング、イオンミリングをこれら各層に行い、配
線パタ―ンを形成する。また、薄膜導体層の接合が必要
な部分にAg−Cu、Ag、Ag−Au、Pb−Sn、
Au−Sn、Au−Siのうち1種のろう材又ははんだ
層を形成することが好ましい。この場合、薄膜導体層に
プリフォ―ムする金属パタ―ン上に厚膜印刷又は薄膜形
成するなどの方法を用いればよい。金属面を有する部品
との接合条件は、ろう材又ははんだの作業範囲内であれ
ば問題なく、例えば、Ag−Cuでは 800〜 850℃、3
分間である。なお、このような回路基板では、必要に応
じて、薄膜抵抗、薄膜コンデンサを形成してもよい。
When the AlN substrate of the present invention is used as a circuit board, the patterning of the wiring portion is performed after the formation of the thin film conductor layer or after the joining of the components, but the former method is generally more convenient in operation. A desired pattern is formed on the thin film conductor layer by using a positive or negative resist, and etching or ion milling is performed on each of these layers by a wet method or a dry method to form a wiring pattern. In addition, Ag-Cu, Ag, Ag-Au, Pb-Sn,
It is preferable to form a brazing material or a solder layer of one of Au-Sn and Au-Si. In this case, a method such as printing a thick film or forming a thin film on a metal pattern preformed on the thin film conductor layer may be used. The joining condition with the component having the metal surface is not problematic as long as it is within the working range of the brazing material or the solder.
Minutes. In such a circuit board, a thin film resistor and a thin film capacitor may be formed as necessary.

【0033】[0033]

【実施例】以下、本発明の実施例について説明する。実
施例1
Embodiments of the present invention will be described below. Example 1

【0034】表1に示す条件でAlN基体上に金属・窒
化物層(Alx M1100-x :M1:M1y 100-y
u:v:w、ただしx,y,vは原子%、u,wは分子
%)、接合層M1,バリア層,導体層,ろう材層を形成
し、必要に応じて薄膜コンデンサ及び薄膜抵抗を接合
し、No1〜10の回路基板を作成した。
Under the conditions shown in Table 1, a metal / nitride layer (Al x M1 100-x : M1: M1 y N 100-y =
u: v: w, where x, y, and v are atomic%, and u and w are molecular%), a bonding layer M1, a barrier layer, a conductor layer, and a brazing material layer are formed, and if necessary, a thin film capacitor and a thin film resistor are formed. Were bonded to form No. 1 to No. 10 circuit boards.

【0035】先ず夫々表1に示す熱伝導率及び酸素含有
量を有するAlN基体を、焼成のままで、あるいは必要
に応じてラッピング、研磨を行った後、その表面を湿式
洗浄し、逆スパッタを行い、表1に示す条件で金属・窒
化物層,接合層,バリア層,薄膜導体層を形成した。そ
の後、ポジレジストにより配線パタ―ンを形成後、金属
の種類に応じて、AuはKI+I2 +脱イオン水のエッ
チャントで、NiはCuSO4 +HCl+エチルアルコ
―ル+脱イオン水のエッチャントで、Wは過酸化水素+
純水エッチャントで、TiはHF+純水エッチャント
で、Nb,Ta,Mo,Zrは硝酸+HF+純水エッチ
ャントでエッチングした。なお、金属・窒化物層はTi
及びTaエッチャントによりエッチングが可能であっ
た。この後、必要に応じて薄膜抵抗、薄膜コンデンサを
基板表面に設けた回路基板を作成した。
First, an AlN substrate having a thermal conductivity and an oxygen content shown in Table 1 is baked, or lapping and polishing is performed as necessary, and the surface is wet-cleaned and reverse sputtered. Then, a metal / nitride layer, a bonding layer, a barrier layer, and a thin film conductor layer were formed under the conditions shown in Table 1. Thereafter, after a wiring pattern is formed with a positive resist, Au is an etchant of KI + I 2 + deionized water, Ni is an etchant of CuSO 4 + HCl + ethyl alcohol + deionized water, and W is an etchant of Deionized water according to the type of metal. Hydrogen peroxide +
With a pure water etchant, Ti was etched with a HF + pure water etchant, and Nb, Ta, Mo, and Zr were etched with a nitric acid + HF + pure water etchant. The metal / nitride layer is Ti
And etching was possible with a Ta etchant. Thereafter, a circuit board having a thin film resistor and a thin film capacitor provided on the substrate surface as necessary was prepared.

【0036】又、比較例1,2として、表1に示すよう
な組成のものを、実施例1と同様にして作成した。さら
に、比較例3〜6として表3に示す熱伝導率及び酸素含
有量を有するAlN基体を、焼成ラッピング,研磨後、
表3に示す条件で接合層,バリア層,薄膜導体層を形成
し、実施例1と同様にして回路基板を作成した。
Further, as Comparative Examples 1 and 2, compositions having the compositions shown in Table 1 were prepared in the same manner as in Example 1. Further, AlN substrates having thermal conductivity and oxygen content shown in Table 3 as Comparative Examples 3 to 6 were fired, lapped and polished.
A bonding layer, a barrier layer, and a thin-film conductor layer were formed under the conditions shown in Table 3, and a circuit board was prepared in the same manner as in Example 1.

【0037】回路基板を作成後、密着強度、1000サイク
ルの温度サイクル試験(TCT:−50〜 150℃、30分保
持)、1000時間のプレッシャ―クッカ―試験(PCT:
121℃、2atm)後の剥離の有無、 500℃・5分間の
耐熱試験を行った後、導体間(間隔60μm)の絶縁抵
抗,密着強度,はんだ接合後の密着強度を評価した。そ
の結果を表2及び表4に示す。
After preparing the circuit board, adhesion strength, temperature cycle test of 1000 cycles (TCT: -50 to 150 ° C., holding for 30 minutes), pressure cooker test of 1000 hours (PCT:
After performing a heat resistance test at 500 ° C. for 5 minutes, the insulation resistance between the conductors (interval: 60 μm), the adhesion strength, and the adhesion strength after soldering were evaluated. The results are shown in Tables 2 and 4.

【0038】その結果、No1〜10においては、配線パ
タ―ンの基板との密着強度が20MPa以上と十分であ
り、温度サイクル試験、プレッシャ―クッカ―試験後も
剥離がなく、密着性が良好であり、耐熱試験後の絶縁抵
抗も490GΩと十分実用的であることが確認された。ま
た、ろう付温度 300〜1000℃においても剥離なく良好で
あることが確認された。
As a result, in Nos. 1 to 10, the adhesion strength of the wiring pattern to the substrate was sufficient at 20 MPa or more, and there was no peeling even after the temperature cycle test and the pressure cooker test, and the adhesion was good. It was confirmed that the insulation resistance after the heat resistance test was 490 GΩ, which was sufficiently practical. In addition, it was confirmed that even at a brazing temperature of 300 to 1000 ° C., the film was good without peeling.

【0039】これに対し表2,4に示すようにNo1〜
6は、いずれも密着強度が実施例のものより低く、温度
サイクル試験、プレッシャ―クッカ―試験、耐熱試験
後、配線パタ―ンに剥離が見られた。また、配線間抵抗
も低く、エッチングが不十分であることが確認された。
実施例2
On the other hand, as shown in Tables 2 and 4,
In No. 6, the adhesion strength was lower than that of the example, and peeling was observed in the wiring pattern after the temperature cycle test, the pressure cooker test, and the heat resistance test. Further, it was confirmed that the inter-wiring resistance was low and the etching was insufficient.
Example 2

【0040】表5に示す条件で、AlN基体上に金属・
窒化物層(Alx M1100-x :M1:M1y 100-y
u,v,w、ただしx,y,vは原子%、u,wは分子
%),接合層(M1z 100-z ,ただしzは原子%),
バリア層,薄膜導体層,ろう材層を形成し、実施例1と
同様にしてNo11〜24の回路基板を作成し、実施例1と
同様に評価した。その結果、表6に示すように良好な特
性であり、また実施例1よりもさらに密着性が強いこと
が確認された。これに対し、同様に作成された表7に示
す組成の比較例No7〜9は表8に示すように比較例1
〜6と同様に十分な特性が得られなかった。実施例3
Under the conditions shown in Table 5, a metal
Nitride layer (Al x M1 100-x : M1: M1 y N 100-y =
u, v, w, where x, y, and v are atomic%, u and w are molecular%, a bonding layer (M1 z N 100-z , where z is atomic%),
A barrier layer, a thin film conductor layer, and a brazing material layer were formed. Circuit boards Nos. 11 to 24 were prepared in the same manner as in Example 1, and evaluated in the same manner as in Example 1. As a result, it was confirmed that the characteristics were good as shown in Table 6, and that the adhesion was stronger than that of Example 1. On the other hand, Comparative Examples Nos. 7 to 9 having the compositions shown in Table 7 and prepared in the same manner as Comparative Example 1 as shown in Table 8
Sufficient characteristics could not be obtained as in the cases of Nos. 6 to 6. Example 3

【0041】表9に示す条件で、AlN基体上にアルミ
ニウム・窒素層(Alt 100-t ,ただしtは原子
%),金属層(Alx' M1100-x ' ,ただしx' は原
子%),接合層M1,バリア層,導体層,ろう材層を形
成し、実施例1と同様にして、No25〜41の回路基板を
作成し、実施例1と同様に評価した。その結果、表10に
示すように良好な特性であり、また実施例1よりも密着
性が強いことが確認された。これに対し、同様に作成さ
れた表11に示す組成の比較例No10,11は表12に示すよ
うに比較例1〜9と同様に十分な特性が得られなかっ
た。
Under the conditions shown in Table 9, an aluminum / nitrogen layer (Al t M 100-t , where t is atomic%) and a metal layer (Al x ′ M1 100-x ′ , where x ′ %), A bonding layer M1, a barrier layer, a conductor layer, and a brazing material layer were formed, and circuit boards Nos. 25 to 41 were prepared in the same manner as in Example 1, and evaluated in the same manner as in Example 1. As a result, as shown in Table 10, it was confirmed that the characteristics were good and the adhesion was stronger than that of Example 1. On the other hand, Comparative Examples Nos. 10 and 11 having the compositions shown in Table 11 similarly prepared did not have sufficient characteristics as in Comparative Examples 1 to 9 as shown in Table 12.

【0042】[0042]

【表1】 [Table 1]

【0043】[0043]

【表2】 [Table 2]

【0044】[0044]

【表3】 [Table 3]

【0045】[0045]

【表4】 [Table 4]

【0046】[0046]

【表5】 [Table 5]

【0047】[0047]

【表6】 [Table 6]

【0048】[0048]

【表7】 [Table 7]

【0049】[0049]

【表8】 [Table 8]

【0050】[0050]

【表9】 [Table 9]

【0051】[0051]

【表10】 [Table 10]

【0052】[0052]

【表11】 [Table 11]

【0053】[0053]

【表12】 [Table 12]

【0054】[0054]

【発明の効果】この発明によれば、薄膜導体層とAlN
基体との密着強度が高いAlN基板を提供することがで
きる。
According to the present invention, the thin-film conductor layer and the AlN
An AlN substrate having a high adhesion strength to a substrate can be provided.

フロントページの続き (72)発明者 小岩 馨 神奈川県川崎市幸区柳町70番地 株式会 社東芝 柳町工場内 (72)発明者 岩瀬 暢男 神奈川県川崎市幸区柳町70番地 株式会 社東芝 柳町工場内 (56)参考文献 特開 平4−218950(JP,A) 特許2664744(JP,B2) 特許2685806(JP,B2) (58)調査した分野(Int.Cl.7,DB名) H05K 1/03 H05K 1/09 H05K 3/38 Continued on the front page (72) Inventor Kaoru Koiwa 70, Yanagimachi, Yukicho, Kawasaki-shi, Kanagawa Prefecture Inside the Toshiba Yanagimachi Plant Co., Ltd. (56) References JP-A-4-218950 (JP, A) Patent 2664744 (JP, B2) Patent 2685806 (JP, B2) (58) Fields investigated (Int. Cl. 7 , DB name) H05K 1/03 H05K 1/09 H05K 3/38

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 AlN基体と、該基体上に設けられ、T
i,Cr,Ta,Zr,Hfの中から選択される少なく
とも一種の元素M1とAlとNとをAlx M1100-x
M1:M1y 100-y =u:v:w(ただし、x,y,
vは原子%、u,wは分子%を示し、u+v+w= 100
であり、夫々25≦x≦90、40≦y≦70、40≦u≦98、
0.2≦v≦40、1≦w≦40の範囲である)の割合になる
ように含む金属・窒化物層と、該金属・窒化物層の上に
積層され前記M1を含有する接合層と、該接合層の上に
積層されW,Nb,Ta,Mo,Ni,Pt,Pd,N
iCrの中から選択される少なくとも一種を主体とする
バリア層と、該バリア層の上に積層されAu,Cu,A
lのうち少なくとも一種を主体とする薄膜導体層とを有
し、該薄膜導体層の所定位置に金属面を有する部品が接
合されることを特徴とするAlN基板。
An AlN substrate and a TN provided on the substrate,
At least one kind of element M1 selected from i, Cr, Ta, Zr and Hf, Al and N are represented by Al x M1 100-x :
M1: M1 y N 100-y = u: v: w (where x, y,
v indicates atomic%, u and w indicate molecular%, and u + v + w = 100
25 ≦ x ≦ 90, 40 ≦ y ≦ 70, 40 ≦ u ≦ 98, respectively.
0.2 ≦ v ≦ 40, 1 ≦ w ≦ 40), and a bonding layer laminated on the metal / nitride layer and containing the M1. W, Nb, Ta, Mo, Ni, Pt, Pd, N
a barrier layer mainly composed of at least one selected from iCr, and Au, Cu, A laminated on the barrier layer
An AlN substrate comprising: a thin-film conductor layer mainly composed of at least one of the following: 1. A component having a metal surface is bonded to a predetermined position of the thin-film conductor layer.
【請求項2】 AlN基体と、該基体上に設けられ、A
lとNとをAlt 100-t (ただしtは原子%を示し50
<t< 100の範囲である)の割合になるように含む窒素
・アルミニウム層と、該窒素・アルミニウム層の上に積
層されTi,Cr,Ta,Zr,Hfの中から選択され
る少なくとも一種の元素M1とAlとをAlx ' M1
100-x ' (ただしx' は原子%を示し10≦x' ≦90の範
囲である)の割合になるように含む金属層と、該金属層
の上に積層され、前記M1を含有する接合層と、該接合
層の上に積層されW,Nb,Ta,Mo,Ni,Pt,
Pd,NiCrの中から選択される少なくとも一種を主
体とするバリア層と、該バリア層の上に積層されAu,
Cu,Alのうち少なくとも一種を主体とする薄膜導体
層とを有し、該薄膜導体層の所定位置に金属面を有する
部品が接合されることを特徴とするAlN基板。
2. An AlN substrate and an AlN substrate provided on the substrate.
l and N are represented by Al t N 100-t (where t represents atomic% and 50
<T <100) and at least one selected from Ti, Cr, Ta, Zr, and Hf laminated on the nitrogen / aluminum layer. The elements M1 and Al are converted to Al x ' M1
A metal layer containing 100-x ′ (where x ′ represents atomic% and in the range of 10 ≦ x ′ ≦ 90), and a junction laminated on the metal layer and containing the M1 And W, Nb, Ta, Mo, Ni, Pt,
A barrier layer mainly composed of at least one selected from Pd and NiCr; and Au, laminated on the barrier layer.
An AlN substrate comprising: a thin-film conductor layer mainly composed of at least one of Cu and Al; and a component having a metal surface bonded to a predetermined position of the thin-film conductor layer.
JP3146050A 1990-09-28 1991-06-18 AlN substrate Expired - Lifetime JP3029702B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3146050A JP3029702B2 (en) 1990-09-28 1991-06-18 AlN substrate

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2-259042 1990-09-28
JP25904290 1990-09-28
JP3146050A JP3029702B2 (en) 1990-09-28 1991-06-18 AlN substrate

Publications (2)

Publication Number Publication Date
JPH04287953A JPH04287953A (en) 1992-10-13
JP3029702B2 true JP3029702B2 (en) 2000-04-04

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ID=26476992

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Country Link
JP (1) JP3029702B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6936040B2 (en) * 2016-04-28 2021-09-15 三ツ星ベルト株式会社 Metallized substrate and its manufacturing method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2664744B2 (en) 1988-11-02 1997-10-22 株式会社東芝 Aluminum nitride thin film circuit board
JP2685806B2 (en) 1988-05-30 1997-12-03 株式会社東芝 Multilayer wiring circuit board

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2685806B2 (en) 1988-05-30 1997-12-03 株式会社東芝 Multilayer wiring circuit board
JP2664744B2 (en) 1988-11-02 1997-10-22 株式会社東芝 Aluminum nitride thin film circuit board

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Publication number Publication date
JPH04287953A (en) 1992-10-13

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