JPS61226931A - Manufacture of passivation glass and semiconductor device using the same - Google Patents
Manufacture of passivation glass and semiconductor device using the sameInfo
- Publication number
- JPS61226931A JPS61226931A JP60068686A JP6868685A JPS61226931A JP S61226931 A JPS61226931 A JP S61226931A JP 60068686 A JP60068686 A JP 60068686A JP 6868685 A JP6868685 A JP 6868685A JP S61226931 A JPS61226931 A JP S61226931A
- Authority
- JP
- Japan
- Prior art keywords
- oxide
- glass
- passivation
- arsenic
- semiconductor device
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Formation Of Insulating Films (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の属する技術分野〕
本発明は、ノヤッシペーション用ガラスおよびこれを用
いた半導体装置の製造方法に係シ、安定でかつ高耐圧の
半導体装置を形成するためのノやッシペーション用ガラ
スおよびこれを用いた半導体装置の製造方法に関する。[Detailed Description of the Invention] [Technical Field to which the Invention Pertains] The present invention relates to a glass for noyassipation and a method for manufacturing a semiconductor device using the same, and relates to a method for manufacturing a semiconductor device that is stable and has a high breakdown voltage. The present invention relates to a glass for insulation and a method of manufacturing a semiconductor device using the same.
半導体表面の電気的特性を安定化すると共に、外部雰囲
気の影響から素子を保護するためのパッシベーション膜
は、特に、集積度の高い超大型半導体集積回路(超LS
I)等、微細な回路・ぐターンを有する半導体装置では
、特に重要な存在となっている。Passivation films are used to stabilize the electrical characteristics of semiconductor surfaces and protect devices from the effects of the external atmosphere, especially in highly integrated ultra-large semiconductor integrated circuits (ultra LS).
It is particularly important in semiconductor devices having minute circuits such as I).
従来、半導体装置のパッシベーション用ガラスとしては
PSG (リン酸シリカ糸ガラス)が広く用いられてい
る。しかし、このPSGは流動化温度が1050℃と非
常に高い上、ガラス中に含まれているリン酸のために耐
水性が不充分であった。またPSG膜はCVD法によっ
て着膜されるため、生産性は良いが被膜の厚さは高々1
μm程度であった。このような欠点のため、低温化プロ
セスを必要とするデバイスには特に適用不可能であった
。Conventionally, PSG (phosphoric acid silica thread glass) has been widely used as passivation glass for semiconductor devices. However, this PSG had a very high fluidization temperature of 1050° C. and had insufficient water resistance due to the phosphoric acid contained in the glass. Furthermore, since the PSG film is deposited by the CVD method, productivity is good, but the film thickness is at most 1.
It was about μm. Because of these drawbacks, it has not been particularly applicable to devices requiring low-temperature processes.
本発明は、前記実情に鑑みてなされたもので、低温プロ
セスで流動化し被膜化し得ると共に、高抵抗であってか
つ高耐圧のパッシベーション膜を提供することを目的と
する。The present invention has been made in view of the above-mentioned circumstances, and an object of the present invention is to provide a passivation film that can be fluidized and formed into a film in a low-temperature process, has high resistance, and has a high breakdown voltage.
」二記目的を達成するため、本発明のパッシベーション
用ガラスは、重量比で酸化鉛(PbO) 30〜55%
、酸化シリコン(Sin2) 20〜45%、酸化ホウ
素(B203)5〜30%、酸化アルミニウム(Al2
O. ) 1〜7%、酸化ヒ素(As2o、) 0.0
1〜3係を含有すると共に、水又は水酸基(OH基)の
含有率が500 ppm以下となるようにしたものであ
る。In order to achieve the second object, the passivation glass of the present invention contains 30 to 55% lead oxide (PbO) by weight.
, silicon oxide (Sin2) 20-45%, boron oxide (B203) 5-30%, aluminum oxide (Al2)
O. ) 1-7%, arsenic oxide (As2o, ) 0.0
1 to 3, and the content of water or hydroxyl groups (OH groups) is 500 ppm or less.
また、本発明の半導体装置の製造方法は、重量比で酸化
鉛30〜55%、酸化シリコン20〜45%、酸化ホウ
素5〜30%、酸化アルミニウム1〜7%、酸化ヒ素0
.01〜3係を含有すると共に水又は水酸基(OH基)
の含有率が500 ppm以下であるようなガラスで半
導体装置を被覆し、酸化雰囲気中で流動化固化すること
によりパッシベーション膜を形成するものである。In addition, the method for manufacturing a semiconductor device of the present invention includes, by weight, 30 to 55% lead oxide, 20 to 45% silicon oxide, 5 to 30% boron oxide, 1 to 7% aluminum oxide, and 0 arsenic oxide.
.. Contains 01 to 3 groups and also contains water or hydroxyl group (OH group)
A passivation film is formed by coating a semiconductor device with glass having a content of 500 ppm or less and fluidizing and solidifying it in an oxidizing atmosphere.
ここで酸化鉛はガラスの流動化温度を下げる作用をする
が、30係以下ではその効果が少く、55係以上ではガ
ラスが失透傾向を生じる。Here, lead oxide has the effect of lowering the fluidization temperature of the glass, but if the coefficient is less than 30, the effect is small, and if it is more than 55, the glass tends to devitrify.
また、酸化シリコンはガラス形成酸化物であるが20係
以下ではガラス化することが不可能であり、45係以上
では流動化温度が900℃以上とガって事実上半導体デ
バイスには使用出来ないためである。In addition, silicon oxide is a glass-forming oxide, but it is impossible to vitrify at temperatures below 20%, and when it is above 45%, the fluidization temperature exceeds 900°C, making it practically unusable for semiconductor devices. It's for a reason.
酸化ホウ素はガラス化を助は耐酸性を上げる働きをする
ものであるが5係以下ではその効果が少く、30係以上
では流動化温度が上って半導体装置の被覆には事実上使
用できなくなる。Boron oxide helps with vitrification and increases acid resistance, but if it is less than 5 parts, its effect is small, and if it is more than 30 parts, the fluidization temperature increases and it becomes virtually unusable for coating semiconductor devices. .
更にまた、酸化アルミニウムは、失透防止剤であるが1
係以下ではその効果が少く、7係以上ではガラスの融点
が著しく上って溶融することが困難になるためである。Furthermore, aluminum oxide is an anti-devitrification agent, but 1
This is because if the temperature is lower than 7, the effect will be small, and if it is higher than 7, the melting point of the glass will rise significantly and it will be difficult to melt the glass.
また、酸化ヒ素は清澄剤であり、0.01係以下ではそ
の効果がなく、3係以上ではガラスの均質性および流動
性が悪くなる。Further, arsenic oxide is a clarifying agent, and if it is less than 0.01, it has no effect, and if it is more than 3, the homogeneity and fluidity of the glass will deteriorate.
更に、ガラス中の水分又は水酸基の含有率は5 n o
ppm以−ヒとなるとデバイスの耐圧が悪化する。従
って、耐圧を上げるにはガラス中の残留OH基が少いこ
とが必要であるが、これは酸化雰囲気中でメルトするか
又は溶融メルトの中へ乾燥空気を送り込んでバブリング
することによりOH基を500 ppm以下にすること
が可能である。Furthermore, the content of water or hydroxyl groups in the glass is 5 n o
If it exceeds ppm, the withstand voltage of the device deteriorates. Therefore, in order to increase the pressure resistance, it is necessary that the residual OH groups in the glass be small, but this can be done by melting in an oxidizing atmosphere or bubbling dry air into the molten melt. It is possible to reduce the amount to 500 ppm or less.
更にまた、酸化雰囲気中で該ガラスを流動化固化するこ
とにより/4?ッシベーシ、ン膜を形成するようにして
いるため、ガラス中の酸化鉛は、還元されて金属鉛とな
りガラスの抵抗率を低下せしめることなく、酸化鉛とし
てガラス中に残留し、高抵抗を維持することができる。Furthermore, by fluidizing and solidifying the glass in an oxidizing atmosphere, /4? As a result, the lead oxide in the glass is reduced to metallic lead and remains in the glass as lead oxide, maintaining high resistance without reducing the resistivity of the glass. be able to.
(還元性雰囲気で流動化固化すると酸化鉛が金属鉛と化
しパッシベーション膜としての機能を失ってしまう。)
〔発明の効果〕
本発明のパッジページ、ンガラスによれば、流動化温度
が低く低温プロセスで被膜化し得る上、高抵抗を有して
いる。(When fluidized and solidified in a reducing atmosphere, lead oxide turns into metallic lead and loses its function as a passivation film.)
[Effects of the Invention] According to the pad page and glass of the present invention, the fluidization temperature is low and it can be formed into a film in a low-temperature process, and it also has high resistance.
また、本発明の方法によれば、高耐圧のパッシベーショ
ン膜の形成が可能である。Further, according to the method of the present invention, it is possible to form a passivation film with a high breakdown voltage.
以下、本発明の実施例について、図面を参照しつつ詳細
に説明する。Embodiments of the present invention will be described in detail below with reference to the drawings.
図は、 N+N−P+型のダイオードを本発明のノJ?
ッシベーション用ガラス1で被覆した例を示す。2はN
+N””P+型のシリコン層、3はアノード、4はカソ
ードである。The figure shows an N+N-P+ type diode according to the present invention.
An example is shown in which the glass is coated with glass 1 for sewage. 2 is N
+N""P+ type silicon layer, 3 is an anode, and 4 is a cathode.
(実施例1)
重量比で酸化鉛44%、酸化シリコン35%、酸化ホウ
素15%、酸化アルミニウム5%、酸化ヒ素1.0係を
混合し、白金るつぼの中で加熱溶融せしめることによシ
がラスを形成する。(Example 1) By mixing 44% lead oxide, 35% silicon oxide, 15% boron oxide, 5% aluminum oxide, and 1.0% arsenic oxide by weight, the mixture was heated and melted in a platinum crucible. forms a lath.
この後、白金るつは中にモルキュラーシーブおよび酸化
アルミニウムパイプを介して乾燥空気を導入し、約30
分間バブリングを行なう。After this, dry air was introduced into the platinum melt through a molecular sieve and an aluminum oxide pipe, and the
Bubble for a minute.
このようにして形成されたガラスの流動化温度はTf=
600℃、比抵抗はρ=IX10””Ω”cmであった
0
このガラスを粉末にした後、溶媒を加えてイースト状に
し前記に一スト状のガラスを前記ダイオ−Pに塗布する
。The fluidization temperature of the glass thus formed is Tf=
The temperature was 600 DEG C., and the specific resistance was ρ=IX10""Ω"cm.0 This glass was powdered, and a solvent was added to make it yeast-like, and the glass in the form of a single stroke was applied to the Dio-P.
この後酸化性雰囲気中で650℃に加熱して該ガラスを
流動化固化せしめ膜厚約3μmのノやッシペーション膜
を形成する。Thereafter, the glass is heated to 650° C. in an oxidizing atmosphere to fluidize and solidify the glass to form a sintering film with a thickness of about 3 μm.
このようにして形成されたダイオード9の耐圧は900
vであった。The diode 9 formed in this way has a breakdown voltage of 900
It was v.
(実施例2)
重量比で酸化鉛35%、酸化シリコン33%、酸化ホウ
素26%、酸化アルミニウム4%、酸化ヒ素1.5係を
混合し、前記実施例1と同様に、加熱溶融せしめてガラ
ス化を行なった後30分間のバブリングを行なう。(Example 2) 35% lead oxide, 33% silicon oxide, 26% boron oxide, 4% aluminum oxide, and 1.5 parts arsenic oxide were mixed by weight, and heated and melted in the same manner as in Example 1. After vitrification, bubbling is performed for 30 minutes.
このようにして形成されたガラスの流動化温度はTf=
600℃、比抵抗はρ=5X10 Ω・鋸であった。The fluidization temperature of the glass thus formed is Tf=
At 600°C, the specific resistance was ρ=5×10 Ω·saw.
このガラスを、実施例1と同様に、ペースト状にして、
前記ダイオードに塗布した後、650℃の酸化性雰囲気
中で流動化し固化せしめて約2.5μmのパッシベーシ
ョン膜を形成する。This glass was made into a paste as in Example 1,
After being applied to the diode, it is fluidized and solidified in an oxidizing atmosphere at 650° C. to form a passivation film of about 2.5 μm.
このようにして形成されたダイオ−Pの耐圧は850v
であった。The diode P thus formed has a breakdown voltage of 850V.
Met.
(実施例3)
重量比で酸化鉛45%、酸化シリコン25%、酸化ホウ
素24%、酸化アルミニウム5%、酸化ヒ素1係を混合
し、前記実施例1および2と同様に加熱溶融せしめてガ
ラス化を行なった後、30分間のバブリングを行なう。(Example 3) 45% lead oxide, 25% silicon oxide, 24% boron oxide, 5% aluminum oxide, and 1 part arsenic oxide were mixed by weight and heated and melted in the same manner as in Examples 1 and 2 to form glass. After bubbling for 30 minutes.
このようにして形成されたガラスの流動化温度はTf=
560℃、比抵抗はρ=IX10 Ω・αであったO
このガラスを、前記実施例1および2と同様にペースト
状にしてダイオードに塗布した後、650℃の酸化性雰
囲気中で流動化固化せしめて約3.5μmのパッシベー
ション膜を形成した。The fluidization temperature of the glass thus formed is Tf=
560℃, the specific resistance was ρ = IX10 Ω・α. This glass was made into a paste and applied to the diode in the same manner as in Examples 1 and 2, and then fluidized and solidified in an oxidizing atmosphere at 650℃. A passivation film with a thickness of at least about 3.5 μm was formed.
□どのようにして形成されたダイオードの制圧は900
Vであった。□How is the suppression of the diode formed 900?
It was V.
なお、本発明のパッシベーション用ガラスは、水酸基が
少なく気泡も少ないため、通常のガラスに比べてリーク
が少なく、ダイオードの79ツシベーシ、ヨン膜のみな
らず、LSI用のセラミックスノやッケージの溶着ガラ
ス等にも使用できることは勿論である。The passivation glass of the present invention has fewer hydroxyl groups and fewer air bubbles, so it has less leakage than normal glass, and is suitable for use not only in diodes, but also in ceramic coatings for LSIs, welded glass for packages, etc. Of course, it can also be used.
図は、ノ千ッシペーション膜を有するデバイスの1例を
示す図である。
111.パッシベーション用ガラス、2・・・シリコン
層、3・・・アノード、4・・・カソード。The figure shows an example of a device having an insipation film. 111. Passivation glass, 2... silicon layer, 3... anode, 4... cathode.
Claims (2)
リコン(SiO_2)20〜45%、酸化ホウ素(B_
2O_3)5〜30%、酸化アルミニウム(Al_2O
_3)1〜7%、酸化ヒ素(As_2O_3)0.01
〜3%を含有すると共に、ガラス中に含有する水酸基(
OH基)又は水分が500ppm以下となるようにした
ことを特徴とするパッシベーション用ガラス。(1) Lead oxide (PbO) 30-55%, silicon oxide (SiO_2) 20-45%, boron oxide (B_
2O_3) 5-30%, aluminum oxide (Al_2O
_3) 1-7%, arsenic oxide (As_2O_3) 0.01
It contains ~3% of hydroxyl groups (
1. A passivation glass characterized by containing 500 ppm or less of water or OH groups.
リコン(SiO_2)20〜45%、酸化ホウ素(B_
2O_3)5〜30%、酸化アルミニウム(Al_2O
_3)1〜7%、酸化ヒ素(As_2O_3)0.01
〜3%を含有すると共に水酸基(OH基)又は水分が5
00ppm以下であるガラスによって半導体装置表面を
被覆する工程と、酸化雰囲気中で流動化し固化せしめる
工程とを含むことを特徴とする半導体装置の製造方法。(2) Lead oxide (PbO) 30-55%, silicon oxide (SiO_2) 20-45%, boron oxide (B_
2O_3) 5-30%, aluminum oxide (Al_2O
_3) 1-7%, arsenic oxide (As_2O_3) 0.01
~3% and hydroxyl group (OH group) or water content is 5%.
1. A method for manufacturing a semiconductor device, comprising the steps of: coating the surface of a semiconductor device with glass having a concentration of 00 ppm or less; and fluidizing and solidifying in an oxidizing atmosphere.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60068686A JPS61226931A (en) | 1985-04-01 | 1985-04-01 | Manufacture of passivation glass and semiconductor device using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60068686A JPS61226931A (en) | 1985-04-01 | 1985-04-01 | Manufacture of passivation glass and semiconductor device using the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61226931A true JPS61226931A (en) | 1986-10-08 |
JPH0260057B2 JPH0260057B2 (en) | 1990-12-14 |
Family
ID=13380869
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60068686A Granted JPS61226931A (en) | 1985-04-01 | 1985-04-01 | Manufacture of passivation glass and semiconductor device using the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61226931A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5863545A (en) * | 1981-10-12 | 1983-04-15 | Nissan Motor Co Ltd | Construction of radiator grill |
JPS58167263U (en) * | 1982-05-06 | 1983-11-08 | 富士重工業株式会社 | Lamp mounting structure of resin bumper |
JPS598911Y2 (en) * | 1978-08-16 | 1984-03-21 | 日産自動車株式会社 | Radiator grill structure |
-
1985
- 1985-04-01 JP JP60068686A patent/JPS61226931A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS598911Y2 (en) * | 1978-08-16 | 1984-03-21 | 日産自動車株式会社 | Radiator grill structure |
JPS5863545A (en) * | 1981-10-12 | 1983-04-15 | Nissan Motor Co Ltd | Construction of radiator grill |
JPS58167263U (en) * | 1982-05-06 | 1983-11-08 | 富士重工業株式会社 | Lamp mounting structure of resin bumper |
Also Published As
Publication number | Publication date |
---|---|
JPH0260057B2 (en) | 1990-12-14 |
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