JPS61215259A - Manufacture of silicon nitride target for sputtering - Google Patents
Manufacture of silicon nitride target for sputteringInfo
- Publication number
- JPS61215259A JPS61215259A JP60053277A JP5327785A JPS61215259A JP S61215259 A JPS61215259 A JP S61215259A JP 60053277 A JP60053277 A JP 60053277A JP 5327785 A JP5327785 A JP 5327785A JP S61215259 A JPS61215259 A JP S61215259A
- Authority
- JP
- Japan
- Prior art keywords
- silicon nitride
- target
- sputtering
- manufacture
- silicon
- 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
Landscapes
- Physical Vapour Deposition (AREA)
- Ceramic Products (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はスパッタリングにより保護膜を形成する場合等
に使用される窒化ケイ素ターゲットの製法に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for manufacturing a silicon nitride target used when forming a protective film by sputtering.
(従来の技術)
従来、窒化ケイ素ターゲットは焼結して製造されるが、
焼結性を持たせるためにイツトリアや酸化カルシウムを
数%添加して焼結することを一般としている。(Prior art) Conventionally, silicon nitride targets are manufactured by sintering.
In order to provide sinterability, it is common to add several percent of ittria or calcium oxide for sintering.
(発明が解決しようとする問題点)゛
前記のようにイツトリア等を添加したターゲラトラスパ
ッタリングして基板に保護膜管形成するに使用すると、
保護膜が色彩を帯びたり或は密着性が不良にな・る欠点
が発生ずる。またイツトリアは高価であり安価な窒化ケ
イ素ターゲットヲ得らnない欠点がある。(Problems to be Solved by the Invention) ゛When used to form a protective film tube on a substrate by sputtering a target layer containing yttoria, etc. as described above,
Disadvantages such as the protective film becoming colored or poor adhesion occur. Furthermore, itria is expensive and has the disadvantage that a cheap silicon nitride target cannot be obtained.
こうした欠点の改善のために反応焼結法により該ターゲ
ットを製造することも提案さnたが、未反応のケイ素が
保護膜の形成を阻害する欠点がなお存Tる。In order to improve these drawbacks, it has been proposed to manufacture the target by a reactive sintering method, but the drawback still remains that unreacted silicon inhibits the formation of a protective film.
本発明はこうした欠点を解決し安価で成膜性の良い窒化
ケイ素ターゲットヲ得る製法を提供Tることを目的とす
るものである。The object of the present invention is to solve these drawbacks and provide a manufacturing method for obtaining a silicon nitride target that is inexpensive and has good film formation properties.
(問題点を解決するための手段)
本発明では、窒化ケイ素と二酸化ケイ素の粉末を、重量
比で70=30乃至9585の割合で混合したのち焼成
するよう(した。(Means for Solving the Problems) In the present invention, silicon nitride and silicon dioxide powders are mixed in a weight ratio of 70=30 to 9585, and then fired.
(作用)
窒化ケイ素と共通の元素(シリコン)f:有する二酸化
ケイ素はバインダーとして作用し、両者t?70:30
乃至95:5の割合で混合して焼成して得らnた窒化ケ
イ素ターゲットは、窒化ケイ素にイツトリア又は酸化カ
ルシウムを添加して焼成した従来のターゲットよりも密
度は低いが反応焼結法によるターゲットとほぼ同等の密
度が得らn比較的焼結性が良好であった。(Function) Silicon dioxide, which has a common element (silicon) f: silicon nitride, acts as a binder, and both t? 70:30
The silicon nitride target obtained by mixing and firing at a ratio of 95:5 has a lower density than the conventional target made by adding itria or calcium oxide to silicon nitride and firing it, but it is a target made by the reaction sintering method. Almost the same density was obtained, and the sinterability was relatively good.
また本発明による窒化ケイ素ターゲットはスパッタ電力
も十分にと01スパツタリングレートも満足するもので
あった。さらに形成さnた薄膜は着色がなく、保護膜と
しての性能も従来のイツトリア等を混入したターゲット
によるものと変りがなかった。Furthermore, the silicon nitride target according to the present invention had sufficient sputtering power and a satisfactory 01 sputtering rate. Furthermore, the thin film formed was not colored, and its performance as a protective film was the same as that of a conventional target mixed with itria or the like.
(実施例) 本発明の実施例は次の通りである。(Example) Examples of the invention are as follows.
実施例1
窒化ケイ素粉末70部に対し二酸化ケイ素粉末30部を
混合し、こnを金型く入nて焼結成形した。これによっ
て得たテストピースについて密度を測定した結果2表1
に示すようにLsF/iで、後記の比較例1による従来
の製法くよるテストピースよりも密度は小さいが比較例
2による従来の製法によるテストピースの密度と略同等
であった。Example 1 70 parts of silicon nitride powder and 30 parts of silicon dioxide powder were mixed, and the mixture was put into a mold and sintered. Results of measuring the density of the test piece thus obtained Table 1
As shown in FIG. 2, the density of LsF/i was lower than that of the conventionally manufactured test piece according to Comparative Example 1, which will be described later, but was approximately equal to the density of the conventionally manufactured test piece according to Comparative Example 2.
さらに直径4インチ、厚さ6Mのターゲット疋ついて、
一定条件下でメタルボンデングを行なった後、膜形成率
を測定し、形成膜の密着性、着色の具合を肉眼で観察し
た結果1表2に示すヨ’31c膜形成率はαa (am
/ h )/ (V−A/d )で密着性も良く無色
の保護膜が得られた。Furthermore, a target of 4 inches in diameter and 6M in thickness was attached.
After metal bonding was carried out under certain conditions, the film formation rate was measured and the adhesion and coloring of the formed film were observed with the naked eye.
/h)/(VA/d), a colorless protective film with good adhesion was obtained.
実施例2
窒化ケイ素粉末80部に対し、二酸化ケイ素粉末り0部
全混合し、こnt−金型に入れ焼結成形した。こnによ
って得たテストピースの密度を測定した結果、表1に示
すようにz2り/c!tで後記の比較例2の場合と余り
変わりがなかった。さらに直径4インチ厚さ6IIJl
のターゲットについて一定条件下でのメタルボンディン
グ金石なった後、膜形成率を測定し、形成膜の密着性及
び着色の具合を肉眼で観察したところ表2に示すように
実施例1と同様であった。Example 2 80 parts of silicon nitride powder and 0 parts of silicon dioxide powder were mixed together, and the mixture was placed in a mold and sintered. As a result of measuring the density of the test piece obtained by this method, as shown in Table 1, z2/c! t was not much different from the case of Comparative Example 2 described later. Furthermore, the diameter is 4 inches and the thickness is 6IIJl.
After metal bonding of the target under certain conditions, the film formation rate was measured, and the adhesion and coloring of the formed film were observed with the naked eye. As shown in Table 2, it was the same as in Example 1. Ta.
実施例3
窒化ケイ素粉末95部に対し、二酸化ケイ素粉末5部を
混合し、金型に入n焼結成形した。Example 3 95 parts of silicon nitride powder and 5 parts of silicon dioxide powder were mixed and sintered into a mold.
こELKよって得たテストピースについての密度の測定
の結果は表1の如くであり、直径4インチ、厚さ61m
のターゲットについて一定条件下でメタルボンディング
を行なった後、膜形成率を測定し、密着性、着色の具合
を肉眼で観察した結果は表2の通り実施例1と同様であ
った。The density measurement results for the test piece obtained by this ELK are shown in Table 1, and it has a diameter of 4 inches and a thickness of 61 m.
After metal bonding was performed on the target under certain conditions, the film formation rate was measured, and the adhesion and coloring were observed with the naked eye. The results were the same as in Example 1 as shown in Table 2.
比較例1
窒化ケイ素粉末95部酸化力ルシウム粉末3部イツトリ
ア粉末2部を混合し、金型に入n焼結成形する従来の製
法によりテストピースを形成し、こnの密度を測定した
結果を表1に示す。Comparative Example 1 A test piece was formed by the conventional manufacturing method of mixing 95 parts of silicon nitride powder, 3 parts of oxidizing lucium powder, and 2 parts of ittria powder, and sintering the mixture into a mold.The density of the test piece was measured. It is shown in Table 1.
さら〈直径4インチ、厚さ6鴎のターゲットについて、
一定条件下でのメタルボンディングを行なった後、膜形
成率を測定し、形成膜の密着性や着色の具合を肉眼で観
察した結果は表2の通りである。Sara〈About a target with a diameter of 4 inches and a thickness of 6 mm,
After metal bonding was performed under certain conditions, the film formation rate was measured, and the adhesion and coloring of the formed film were observed with the naked eye. The results are shown in Table 2.
比較例2
金属ケイ素粉末を金型に入れ、高温条件下で窒素ガスを
反応させる従来公知の反応焼結法により製作したテスト
ピースの密度は表1に示Tように2.4り/dであり、
比較例1と同様に直径4インチ、厚さ61のターゲラト
ラ製作してこnf一定条件下でメタルボンディングを行
なった径、膜形成率を測定し、形成膜の密着性、着色の
具合全肉眼で観察した結果は表2の通りである。Comparative Example 2 The density of a test piece manufactured by a conventionally known reaction sintering method in which metal silicon powder is placed in a mold and reacted with nitrogen gas under high temperature conditions is 2.4 r/d as shown in Table 1. can be,
Similar to Comparative Example 1, a target rattler with a diameter of 4 inches and a thickness of 61 mm was prepared, and the diameter and film formation rate of the metal bonding were measured under constant nf conditions, and the adhesion and coloring of the formed film were observed with the naked eye. The results are shown in Table 2.
表−1窒化ケイ素テストピースの密度
表−2窒化ケイ素ターゲットによる膜形成率、薄膜の特
性及び着色の具合
(発明の効果)
このように本発明に於ては、窒化ケイ素と二酸化ケイ素
の粉末を重量比で70:30乃至95:5の割合で混合
したのち焼成してスパッタリング用窒化ケイ素ターゲッ
トを製作するようにしたので、安価で焼結性の良いター
ゲットが得られ、こnf使用して形成した保護膜は無色
で遊離ケイ素の突起などが無く、さらに膜形成率も良く
、良好な保護膜を迅速に形成出来る等の効果がある。Table 1 Density table of silicon nitride test piece Table 2 Film formation rate, thin film characteristics and coloring by silicon nitride target (effects of the invention) As described above, in the present invention, silicon nitride and silicon dioxide powders are Since the silicon nitride target for sputtering is produced by mixing at a weight ratio of 70:30 to 95:5 and then firing, a target with good sintering properties is obtained at low cost. The resulting protective film is colorless and free of free silicon protrusions, and has a good film formation rate, allowing for rapid formation of a good protective film.
Claims (1)
0乃至95:5の割合で混合したのち焼成することを特
徴とするスパッタリング用窒化ケイ素ターゲットの製法
。Silicon nitride and silicon dioxide powder at a weight ratio of 70:3
A method for producing a silicon nitride target for sputtering, which comprises mixing at a ratio of 0 to 95:5 and then firing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60053277A JPS61215259A (en) | 1985-03-19 | 1985-03-19 | Manufacture of silicon nitride target for sputtering |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60053277A JPS61215259A (en) | 1985-03-19 | 1985-03-19 | Manufacture of silicon nitride target for sputtering |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61215259A true JPS61215259A (en) | 1986-09-25 |
JPH04948B2 JPH04948B2 (en) | 1992-01-09 |
Family
ID=12938241
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60053277A Granted JPS61215259A (en) | 1985-03-19 | 1985-03-19 | Manufacture of silicon nitride target for sputtering |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61215259A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0283261A (en) * | 1988-09-21 | 1990-03-23 | Shin Etsu Chem Co Ltd | Silicon nitride-based target material for sputtering |
JP2009280832A (en) * | 2008-05-19 | 2009-12-03 | Dainippon Printing Co Ltd | Raw powder for ion plating evaporation source material, ion plating evaporation source material and method for producing the same, gas barrier sheet and method for producing the same |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54123110A (en) * | 1978-03-17 | 1979-09-25 | Tokyo Shibaura Electric Co | Production of siliconee ceramics |
JPS56141153A (en) * | 1980-04-03 | 1981-11-04 | Toshiba Corp | Target for x-ray tube |
JPS56169773A (en) * | 1980-05-30 | 1981-12-26 | Sharp Corp | Target for spattering by plenar magnetron |
JPS5774177A (en) * | 1980-10-29 | 1982-05-10 | Toshiba Corp | Thin film thermal head |
JPS5874585A (en) * | 1981-10-26 | 1983-05-06 | 三菱マテリアル株式会社 | Surface clad silicon nitride base sintered member for high speed cutting |
JPS58118273A (en) * | 1982-01-06 | 1983-07-14 | Hitachi Ltd | Heat-sensitive recording head |
JPS58161975A (en) * | 1982-03-16 | 1983-09-26 | 日本特殊陶業株式会社 | Manufacture of silicon nitride sintered body |
JPS58204451A (en) * | 1982-05-21 | 1983-11-29 | Seiko Epson Corp | X-ray generator |
-
1985
- 1985-03-19 JP JP60053277A patent/JPS61215259A/en active Granted
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54123110A (en) * | 1978-03-17 | 1979-09-25 | Tokyo Shibaura Electric Co | Production of siliconee ceramics |
JPS56141153A (en) * | 1980-04-03 | 1981-11-04 | Toshiba Corp | Target for x-ray tube |
JPS56169773A (en) * | 1980-05-30 | 1981-12-26 | Sharp Corp | Target for spattering by plenar magnetron |
JPS5774177A (en) * | 1980-10-29 | 1982-05-10 | Toshiba Corp | Thin film thermal head |
JPS5874585A (en) * | 1981-10-26 | 1983-05-06 | 三菱マテリアル株式会社 | Surface clad silicon nitride base sintered member for high speed cutting |
JPS58118273A (en) * | 1982-01-06 | 1983-07-14 | Hitachi Ltd | Heat-sensitive recording head |
JPS58161975A (en) * | 1982-03-16 | 1983-09-26 | 日本特殊陶業株式会社 | Manufacture of silicon nitride sintered body |
JPS58204451A (en) * | 1982-05-21 | 1983-11-29 | Seiko Epson Corp | X-ray generator |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0283261A (en) * | 1988-09-21 | 1990-03-23 | Shin Etsu Chem Co Ltd | Silicon nitride-based target material for sputtering |
JP2009280832A (en) * | 2008-05-19 | 2009-12-03 | Dainippon Printing Co Ltd | Raw powder for ion plating evaporation source material, ion plating evaporation source material and method for producing the same, gas barrier sheet and method for producing the same |
Also Published As
Publication number | Publication date |
---|---|
JPH04948B2 (en) | 1992-01-09 |
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