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JPH035642B2 - - Google Patents
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JPH035642B2 - - Google Patents

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Publication number
JPH035642B2
JPH035642B2 JP58013953A JP1395383A JPH035642B2 JP H035642 B2 JPH035642 B2 JP H035642B2 JP 58013953 A JP58013953 A JP 58013953A JP 1395383 A JP1395383 A JP 1395383A JP H035642 B2 JPH035642 B2 JP H035642B2
Authority
JP
Japan
Prior art keywords
film
gas pressure
argon gas
magnetic
torr
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
JP58013953A
Other languages
Japanese (ja)
Other versions
JPS59139616A (en
Inventor
Masahide Suenaga
Toshihiro Yoshida
Masayuki Takagi
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP1395383A priority Critical patent/JPS59139616A/en
Publication of JPS59139616A publication Critical patent/JPS59139616A/en
Publication of JPH035642B2 publication Critical patent/JPH035642B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F41/00Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
    • H01F41/14Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates
    • H01F41/18Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates by cathode sputtering

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  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Physical Vapour Deposition (AREA)
  • Thin Magnetic Films (AREA)

Description

【発明の詳細な説明】 〔発明の利用分野〕 本発明は磁性薄膜の製造方法に係り、特にマグ
ネトロンスパツタ法により保磁力の小さい磁性薄
膜を製造する方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Application of the Invention] The present invention relates to a method of manufacturing a magnetic thin film, and particularly to a method of manufacturing a magnetic thin film with a low coercive force by a magnetron sputtering method.

〔従来技術〕[Prior art]

第1図に、薄膜磁気ヘツドの一種である磁気抵
抗効果型磁気ヘツドの媒体対向面近傍の構造を示
す。
FIG. 1 shows the structure of a magnetoresistive magnetic head, which is a type of thin film magnetic head, near the medium facing surface.

磁気抵抗効果型磁気ヘツドは、一般に、セラミ
ツク基板1上にスパツタ法などの薄膜形成技術を
用いて、薄膜1μm以上の磁性膜である下部シー
ルド膜2、膜厚500Å以下の磁性膜である磁気抵
抗膜3、導体膜4、膜厚1μmの以上の磁性膜で
ある上部シールド膜5を積層して形成される。
A magnetoresistive magnetic head generally uses a thin film forming technique such as sputtering on a ceramic substrate 1 to form a lower shield film 2, which is a magnetic film with a thickness of 1 μm or more, and a magnetoresistive film, which is a magnetic film with a film thickness of 500 Å or less. It is formed by laminating a film 3, a conductor film 4, and an upper shield film 5 which is a magnetic film with a thickness of 1 μm or more.

下部シールド膜2と磁気抵抗膜3、磁気抵抗膜
3と上部シールド膜5の間には、それぞれギヤツ
プを形成するための絶縁膜6,7が形成されてい
る。
Insulating films 6 and 7 are formed between the lower shield film 2 and the magnetoresistive film 3, and between the magnetoresistive film 3 and the upper shield film 5, respectively, for forming gaps.

このような薄膜磁気ヘツドの特性は、磁場中蒸
着あるいはスパツタ法により形成されるパーマロ
イよりなる前記磁気膜2,3,5の磁気特性に著
しく左右される。磁性薄膜の磁気特性をもつとも
端的に表す量は保磁力であるが、良好なヘツド特
性を得るためには、シールド膜(磁性膜)2,5
の磁化容易軸方向の保磁力を少なくとも1.0O¨e以
下に、磁気抵抗膜3の容易軸方向の保磁力を
2.5O¨以下に抑えなければならない。
The characteristics of such a thin film magnetic head are significantly influenced by the magnetic characteristics of the magnetic films 2, 3, and 5 made of permalloy formed by evaporation in a magnetic field or sputtering method. The coercive force is the quantity that directly represents the magnetic properties of a magnetic thin film, but in order to obtain good head characteristics, the shielding film (magnetic film) 2, 5
The coercive force in the easy axis direction of the magnetoresistive film 3 is at least 1.0 O¨e or less, and the coercive force in the easy axis direction of the magnetoresistive film 3 is at least 1.0 O¨e or less.
Must be kept below 2.5O¨.

パーマロイ膜をスパツタ法で形成する場合、保
磁力に影響をおよぼす因子としてアルゴンガス圧
力があり、保磁力を小さくするためには、アルゴ
ンガス圧力を装置の能力範囲内でなるべく低くす
る方が望ましい。これは、スパツタ中に膜中に吸
蔵される活性な不純物ガス(例えば酸素)の量が
アルゴンガス圧の減少に伴つて少なくなるため、
不純物ガスによる磁気特性の劣化が防止されるか
らである。
When forming a permalloy film by sputtering, argon gas pressure is a factor that affects coercive force, and in order to reduce coercive force, it is desirable to lower the argon gas pressure as much as possible within the capability of the apparatus. This is because the amount of active impurity gas (e.g. oxygen) occluded in the film during sputtering decreases as the argon gas pressure decreases.
This is because deterioration of magnetic properties due to impurity gas is prevented.

ところで、通常の2極スパツタ装置では、1×
10-2Torr以上のアルゴンガス圧力下でないと安
定して放電が持続しないため、油拡散ポンプがダ
ウンしないように主弁をほとんど閉じて排気速度
が小さい状態で使用しなければならず、残留ガス
(酸素等の活性な不純物ガス)による保磁力の増
大が避けられない。すなわち、1μm以上の膜の
保磁力は通常1.0〜3.0O¨eとなり、このような高保
磁力の膜は薄膜磁気ヘツド用磁性膜として使用す
ることはできない。
By the way, in a normal two-pole sputtering device, 1×
Since the discharge will not continue stably unless the argon gas pressure is 10 -2 Torr or higher, the main valve must be mostly closed and the pumping speed must be kept low to prevent the oil diffusion pump from going down. An increase in coercive force due to (active impurity gas such as oxygen) is unavoidable. That is, the coercive force of a film of 1 μm or more is usually 1.0 to 3.0 O¨e, and a film with such a high coercive force cannot be used as a magnetic film for a thin film magnetic head.

このような問題を解決するため、2極スパツタ
装置において基板にバイアス電圧を印加し、基板
表面をスパツタエツチしながらスパツタを行う方
法も知られているが、この方法は膜厚が不均一に
なりやすく、特に、基板周辺部の膜厚が極端に薄
くなりやすいという大きな欠点があるため、現在
のところ実用化されるに至つていない。
To solve this problem, a method is known in which sputtering is performed by applying a bias voltage to the substrate using a two-pole sputtering device and sputtering the substrate surface, but this method tends to result in non-uniform film thickness. In particular, it has a major drawback in that the film thickness tends to become extremely thin around the substrate, so it has not been put into practical use at present.

2極スパツタのようような欠点を除去し、1×
10-3Torr以下の低アルゴンガス圧下でもスパツ
タできる方法としては、イオンビームスパツタ
法、3極あるいは4極スパツタ法が知られてい
る。このうち、イオンビームスパツタ法は、ター
ゲツトにイオンビームを照射してスパツタを行う
方法であり、(1)プラズマフリーの状態で膜を形成
できるため、膜形成中の基板表面温度を低く抑え
ることができる、(2)膜形成条件の精密な制御が可
能などの特徴を有するため、スパツタ現象の解明
や分析装置において大きな役割を果してきた。し
かしながら、大電流イオン源の開発が困難なため
膜形成速度が怠く、膜形成への応用はプラズマス
パツタ法に比べて著しく遅れている。
Removes defects such as 2-pole spatter, 1x
Ion beam sputtering, three-pole sputtering, or four-pole sputtering are known as methods that allow sputtering even under low argon gas pressures of 10 -3 Torr or less. Among these, the ion beam sputtering method is a method in which sputtering is performed by irradiating a target with an ion beam.(1) It is possible to form a film in a plasma-free state, so it is possible to keep the substrate surface temperature low during film formation. (2) It is possible to precisely control the film formation conditions, so it has played a major role in elucidating the spatter phenomenon and in analytical equipment. However, because it is difficult to develop a high-current ion source, the film formation rate is slow, and its application to film formation is significantly slower than the plasma sputtering method.

一方、プラズマ生成用電子供給源として熱電子
放出用の第3電極を付加した3極あるいは4極ス
パツタ法は、(1)フイラメントの寿命が短いため、
装置の連続運転の障害となる、(2)フイラメントか
ら出る不純物が膜中に混入し、膜の特性を変化さ
せるという問題があり、今日ではほとんど採用さ
れていない。
On the other hand, the three-pole or four-pole sputtering method, in which a third electrode for thermionic emission is added as an electron supply source for plasma generation, (1) has a short filament life;
This method is rarely used today because of the problem that (2) impurities from the filament get mixed into the membrane and change the characteristics of the membrane, which impedes the continuous operation of the device.

マグネトロンスパツタ法は、ターゲツト表面に
平行な磁界を印加することによりターゲツトから
放出される高速電子を偏向させ、基板衝突による
基板加熱などの悪影響を抑制すると同時に、アル
ゴンガスのイオン化に積極的に利用する。そのた
め、5×10-3Torr程度の低アルゴンガス圧下で
も、ホトレジストなどの有機絶縁膜上に高速で膜
を形成することができ、薄膜磁気ヘツド用磁性膜
形成方法としてもつとも適した方法といえる。し
かしながら、発明者等が行つた実験によると、通
常のマグネトロンスパツタ法で放電が持続する限
界である1×10-3Torrのアルゴンガス圧下でス
パツタと行つても、膜厚1μm以上のパーマロイ
膜の保磁力は0.3〜1.2O¨eの範囲で変動し、保磁力
を常に薄膜磁気ヘツド用磁性膜の実用的限界値で
ある1.0O¨e以下にすることは困難であることが判
明した。
The magnetron sputtering method deflects high-speed electrons emitted from the target by applying a magnetic field parallel to the target surface, suppressing adverse effects such as substrate heating due to substrate collision, and at the same time actively using it to ionize argon gas. do. Therefore, it is possible to form a film on an organic insulating film such as a photoresist at high speed even under a low argon gas pressure of about 5×10 -3 Torr, making it an extremely suitable method for forming a magnetic film for a thin-film magnetic head. However, according to experiments conducted by the inventors, even when sputtering is performed under an argon gas pressure of 1×10 -3 Torr, which is the limit for sustaining discharge in the normal magnetron sputtering method, permalloy films with a thickness of 1 μm or more The coercive force varies in the range of 0.3 to 1.2 O¨e, and it has been found difficult to always keep the coercive force below 1.0 O¨e, which is the practical limit for magnetic films for thin film magnetic heads.

〔発明の目的〕[Purpose of the invention]

本発明の目的は、上記の如き従来の欠点を改善
するため、1×10-3Torr以下のアルゴンガス圧
下でマグネトロンスパツタを行うことにより、
1.0エルステツド以下の保磁力を有する磁性膜を
再現性よく得ることのできる磁性薄膜の製造方法
を提供することにある。
The purpose of the present invention is to improve the above-mentioned conventional drawbacks by performing magnetron sputtering under an argon gas pressure of 1×10 -3 Torr or less.
The object of the present invention is to provide a method for producing a magnetic thin film that can produce a magnetic film having a coercive force of 1.0 oersted or less with good reproducibility.

〔発明の概要〕[Summary of the invention]

上記目的を達成するため、本発明は、マグネト
ロンスパツタ法により磁性膜を形成する際に、1
×10-3Torr以上のアルゴンガス圧下で放電を開
始し、その後前記アルゴンガス圧を1×
10-3Torr以下にして10-4Torr台で放電を持続さ
せることを特徴とする。
In order to achieve the above object, the present invention provides a method for forming a magnetic film by a magnetron sputtering method.
Discharge is started under an argon gas pressure of ×10 -3 Torr or more, and then the argon gas pressure is increased to 1 ×
It is characterized by sustaining discharge at 10 -4 Torr level at 10 -3 Torr or less.

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

以下、本発明の一実施例を第2〜6図を参照し
て説明する。
Hereinafter, one embodiment of the present invention will be described with reference to FIGS. 2 to 6.

第2図は本実施例に用いるマグネトロン型スパ
ツタリング装置の概略図、第3図は、第1図に示
すような磁気抵抗効果型薄膜磁気ヘツド用シール
ド膜(パーマロイ膜)2,5を第2図に示したマ
グネトロン型スパツタリング装置により形成した
時のベルジヤー8内ガス圧力の経時変化示す。
FIG. 2 is a schematic diagram of the magnetron type sputtering apparatus used in this example, and FIG. 2 shows the change over time in the gas pressure inside the bell gear 8 when formed by the magnetron type sputtering device shown in FIG.

磁性膜2,5を形成するには、まず洗浄済の基
板15をベルジヤー(真空溝)8内の所定の場所
に設置し、拡散ポンプ10により1×10-5Torr
まで排気する。その後、基板15をヒーター16
により350℃まで加熱して、トラツプ12により
残留ガスを排出し、ベルジヤー8内のガス圧が1
×10-6Torrに達した時点で基板15の温度を300
℃まで降下させ、ベルジヤー8内のガス圧が1×
10-3Torr以上(本実施例においては第3図に示
したように5×10-3Torr)になるようにフロー
メータ18を監視しつつアルゴンガスをガス導入
口11から導入する(T1)。
To form the magnetic films 2 and 5, first, a cleaned substrate 15 is placed in a predetermined location in a bell gear (vacuum groove) 8, and a diffusion pump 10 is used to heat the substrate 15 to 1×10 -5 Torr.
exhaust to. After that, the substrate 15 is placed on the heater 16
The gas is heated to 350℃ by the trap 12, and the residual gas is discharged by the trap 12, and the gas pressure in the bell gear 8 is reduced to 1.
When the temperature reaches ×10 -6 Torr, the temperature of the substrate 15 is increased to 300
℃, and the gas pressure inside the bell gear 8 is 1×
Argon gas is introduced from the gas inlet 11 while monitoring the flow meter 18 so that the pressure is 10 -3 Torr or higher (5×10 -3 Torr as shown in FIG . 3 in this embodiment) (T 1 ).

次にターゲツト14表面を清浄化するため基板
15表面に膜が被着しないようにシヤツター17
を閉じたままでプリスパツタを行う。従来は第3
図に破線aで示したように、プリスパツタ後も同
じアルゴンガス圧力下で放電を持続させたまま、
コイル13により基板15表面に100O¨eの磁場を
印加しながらシヤツター17開いて本スパツタに
移行していた。本実施例においては、第2図に実
線bで示すように、シヤツター17を開く前に、
放電を持続させたままニードルバルブ19をを操
作してアルゴンガス圧を減少させ、1×
10-3Torr以下(本実施例においては第3図に示
したように2×10-4Torr)の圧力以下で基板1
5表面にコイル13より100O¨eの磁場を印加しな
がらシヤツター17を開いて本スパツタを開始し
(T2)、膜厚1μmのパーマロイ膜を形成した。本
スパツタ終了後(H3)は、ベルジヤー8内を排
気しながら、基板15の冷却を行い、基板温度が
50℃以下になつた時点でベルジヤー8外へ取出し
た。
Next, in order to clean the surface of the target 14, a shutter 17 is used to prevent the film from adhering to the surface of the substrate 15.
Perform Puri Spatsuta while keeping it closed. Previously, the third
As shown by the broken line a in the figure, even after presputtering, the discharge was continued under the same argon gas pressure.
While applying a magnetic field of 100 O¨e to the surface of the substrate 15 by the coil 13, the shutter 17 was opened and the main sputtering began. In this embodiment, as shown by the solid line b in FIG. 2, before opening the shutter 17,
While maintaining the discharge, operate the needle valve 19 to reduce the argon gas pressure to 1×
The substrate 1 is heated under a pressure of 10 -3 Torr or less (2×10 -4 Torr in this example as shown in FIG. 3).
The main sputtering was started by opening the shutter 17 while applying a magnetic field of 100 O¨e from the coil 13 to the surface of the sample (T 2 ), and a permalloy film with a thickness of 1 μm was formed. After the main sputtering (H 3 ), the substrate 15 is cooled while the inside of the bell gear 8 is evacuated, and the substrate temperature is lowered.
When the temperature dropped to below 50°C, it was taken out of the Belgear 8.

なお、本実施例のように放電しやすいアルゴン
ガス圧下(1×10-3Torr以上)で一旦放電を起
こさせれば、その後アルゴンガス圧を低下させて
も放電は持続することができことが判明した。
It should be noted that, as in this example, it has been found that once a discharge is caused under argon gas pressure (1×10 -3 Torr or more), where discharge is easy to occur, the discharge can be sustained even if the argon gas pressure is subsequently lowered. did.

第4図は、81Ni−19Feパーマロイ薄膜を形成
する際の本スパツタ中のアルゴンガス圧力と、形
成された当該薄膜の容易軸保磁力との関係を示
す。第4図中aは従来のアルゴンガス圧力下で、
bは本実施例のアルゴンガス圧力下で形成したパ
ーマロイ膜の特性を示す。第4図より、本実施例
の如く、1×10-3Torr以下のアルゴンガス圧下
で形成したパーマロイ膜厚のの容易軸保磁力は小
さく、基板間の特性バラツキ幅Cを考慮しても常
に1.0O¨e以下になること、またバラツキ幅Cが小
さいことがかる。一方、従来のように、1×
10-3Torr以上のアルゴンガス圧下で形成したパ
ーマロイ薄膜の容易軸保磁力は大きく、基板間の
バラツキ幅dも大きいため、すべての膜の保磁力
を1.0O¨e以下に抑えることは困難であることがわ
かる。
FIG. 4 shows the relationship between the argon gas pressure in the present sputtering when forming an 81Ni-19Fe permalloy thin film and the easy axis coercive force of the formed thin film. In Fig. 4, a is under conventional argon gas pressure;
b shows the characteristics of the permalloy film formed under argon gas pressure in this example. From FIG. 4, the easy-axis coercive force of the permalloy film formed under argon gas pressure of 1×10 -3 Torr or less as in this example is small, and even when considering the property variation width C between substrates, it is always It can be seen that it is less than 1.0O¨e and that the variation width C is small. On the other hand, as before, 1×
The easy axis coercive force of permalloy thin films formed under argon gas pressure of 10 -3 Torr or more is large, and the variation width d between substrates is also large, so it is difficult to suppress the coercive force of all films to less than 1.0 O¨e. I understand that there is something.

第5図は、第4図に示したパーマロイ膜におけ
る異方性分散角(α90)とアルゴンガス圧力の関
係を示す。第5図中aは、従来のアルゴンガス圧
力下で、bは本実施例のアルゴンガス圧力下で形
成したパーマロイ膜の異方性分散角を示す。
FIG. 5 shows the relationship between the anisotropic dispersion angle (α90) and argon gas pressure in the permalloy film shown in FIG. In FIG. 5, a shows the anisotropic dispersion angle of the permalloy film formed under the conventional argon gas pressure, and b shows the permalloy film formed under the argon gas pressure of this example.

第5図より、本実施例による方法で形成したパ
ーマロイ膜の異方性分散角は、従来法により形成
されたパーマロイ膜の異方性分散角と比較して小
さく、かつ基板間の異方性分散角のバラツキ幅e
も従来法によるバラツキ幅fに比べて小さく、磁
気特性の良好な磁性膜を再現性よく得らることが
わかる。
From FIG. 5, the anisotropic dispersion angle of the permalloy film formed by the method according to this example is smaller than that of the permalloy film formed by the conventional method, and the anisotropic dispersion angle between the substrates is small. Dispersion angle variation width e
It can be seen that the variation width f is smaller than that of the conventional method, and a magnetic film with good magnetic properties can be obtained with good reproducibility.

第6図は、SiO2によりなる1μmの磁気ギヤツ
プ6,7と膜厚0.05μmのパーマロイ磁気抵抗膜
3、膜厚0.2μmのAl導体膜4、膜厚1μmのシー
ルド膜2,5をを備えた磁気抵抗効果型薄膜磁気
ヘツドで磁気デイスク上に記録した孤立反転磁化
状態を再生した波形の半値幅(相対値)と、前記
膜厚1μmのシールド膜2,5の容易軸保磁力と
の関係を示す。第6図より、容易軸保磁力の大き
さが1.0O¨e以下では再生波形の半値幅に大差は見
られないが、1.0O¨e以上では半値幅が増大し、シ
ールド膜の機能が十分に発揮されていないことが
わかる。このような半値幅の増大は、高密度記録
された情報を再生する際にヘツド出力の低下、従
つてS/N比の低下をもたらすもので好ましくな
いことが確認された。
FIG. 6 shows a device comprising a magnetic gap 6, 7 of 1 μm made of SiO 2 , a permalloy magnetoresistive film 3 of 0.05 μm thick, an Al conductor film 4 of 0.2 μm thick, and shield films 2, 5 of 1 μm thick. Relationship between the half-width (relative value) of a waveform reproduced from an isolated reversed magnetization state recorded on a magnetic disk using a magnetoresistive thin-film magnetic head and the easy-axis coercive force of the shield films 2 and 5 with a thickness of 1 μm. shows. From Figure 6, there is no significant difference in the half-width of the reproduced waveform when the easy-axis coercive force is less than 1.0 O¨e, but when it is more than 1.0 O¨e, the half-width increases and the shielding film has sufficient function. It can be seen that they are not fully utilized. It has been confirmed that such an increase in half-width is undesirable because it causes a decrease in the head output and therefore a decrease in the S/N ratio when reproducing information recorded at high density.

なお、上記実施例においては、高透磁率磁性材
料よりなるシールド膜としてFe−Ni合金(パー
マロイ)膜を形成する場合において述べたが、同
様の効果は高透磁率材料として知られているFe
−Ni−Mo、Fe−Al−Si、Fe−B、Co−Ti、お
よびCo−Fe−Bなどのの非晶質合金膜において
も認めめられることが確認された。
In the above example, the case was described in which an Fe-Ni alloy (permalloy) film was formed as a shield film made of a high magnetic permeability material, but the same effect can be obtained by forming an Fe-Ni alloy (permalloy) film as a shield film made of a high magnetic permeability material.
-It was confirmed that this phenomenon was also observed in amorphous alloy films such as -Ni-Mo, Fe-Al-Si, Fe-B, Co-Ti, and Co-Fe-B.

また、上記実施例においては磁気抵抗効果型薄
膜磁気ヘツドについて述べたが、同様の効果は誘
導型薄膜磁気ヘツドにおいても認められることが
確認された。
Further, although the above embodiments have described a magnetoresistive type thin film magnetic head, it has been confirmed that similar effects can also be observed in an inductive type thin film magnetic head.

このように、マグネトロン型スパツタリング装
置を用いて1×10-3Torr以下のアルゴンガス圧
力下で形成された磁性薄膜は、保磁力が常に
1.0O¨e以下であるばかりでなく分散角も小さい。
更に、同方法により形成された磁性膜を有する薄
膜磁気ヘツドを用いると、高密度記録された情報
をもS/N比を低下させることなく再生すること
ができる。
In this way, a magnetic thin film formed using a magnetron sputtering device under an argon gas pressure of 1×10 -3 Torr or less has a constant coercive force.
Not only is it less than 1.0O¨e, but the dispersion angle is also small.
Furthermore, by using a thin film magnetic head having a magnetic film formed by the same method, even information recorded at high density can be reproduced without reducing the S/N ratio.

〔発明の効果〕〔Effect of the invention〕

以上説明したように、本発明によれば、1×
10-3Torr以下のアルゴンガス圧力下でマグネト
ロンスパツタを行うことができ、保磁力の小さい
磁性膜を再現性よく製造することができ、製造歩
留りを向上させることができる。
As explained above, according to the present invention, 1×
Magnetron sputtering can be performed under argon gas pressure of 10 -3 Torr or less, making it possible to manufacture magnetic films with low coercive force with good reproducibility, and improving manufacturing yield.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は磁気抵抗効果型薄膜磁気ヘツドの媒体
対向面近傍の構造を示す斜視図、第2図は本発明
に用いるマグネトロン型スパツタ装置の構成概略
を示す図、第3図は本発明の一実施例におけるベ
ルジヤー内ガス圧力の経時変化を示す図、第4図
はベルジヤー内のアルゴンガス圧力と該アルゴン
ガス圧力下で形成されるパーマロイ薄膜の容易軸
保磁力との関係を示す図、第5図はベルジヤー内
のアルゴンガス圧力と該アルゴンガス圧力下で形
成されるパーマロイ薄膜の分散角との関係を示す
図、第6図は磁気抵抗効果型薄膜磁気ヘツドのシ
ールド膜の容易軸保磁力と、該ヘツドにおける再
生波形の半値幅との関係を示す図である。 a:従来法におけるアルゴンガス圧力、b:本
発明におけるアルゴンガス圧力、T1:アルゴン
ガス導入時間、T2:本スパツタ開始時間、T3
本スパツタ終了時間。
FIG. 1 is a perspective view showing the structure of a magnetoresistive thin film magnetic head in the vicinity of the medium facing surface, FIG. 2 is a diagram showing a schematic configuration of a magnetron type sputtering device used in the present invention, and FIG. FIG. 4 is a diagram showing the change over time in the gas pressure inside the bell jar in Examples; FIG. The figure shows the relationship between the argon gas pressure in the bell gear and the dispersion angle of the permalloy thin film formed under the argon gas pressure. , is a diagram showing the relationship between the half-width of the reproduced waveform in the head. a: Argon gas pressure in the conventional method, b: Argon gas pressure in the present invention, T 1 : Argon gas introduction time, T 2 : Main sputtering start time, T 3 :
End time of this spatuta.

Claims (1)

【特許請求の範囲】[Claims] 1 マグネトロンスパツタ法により磁性薄膜を形
成する際に、1×10-3Torr以上のアルゴンガス
圧力下で放電を開始し、その後、前記アルゴンガ
ス圧力を1×10-3Torr以下にして、10-4Torr台
で前記放電を持続させることを特徴とする磁性薄
膜の製造方法。
1 When forming a magnetic thin film by the magnetron sputtering method, discharge is started under an argon gas pressure of 1 × 10 -3 Torr or more, and then the argon gas pressure is reduced to 1 × 10 -3 Torr or less, and 10 - A method for producing a magnetic thin film, characterized in that the discharge is sustained on a 4 Torr stand.
JP1395383A 1983-01-31 1983-01-31 Manufacture of magnetic thin film Granted JPS59139616A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1395383A JPS59139616A (en) 1983-01-31 1983-01-31 Manufacture of magnetic thin film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1395383A JPS59139616A (en) 1983-01-31 1983-01-31 Manufacture of magnetic thin film

Publications (2)

Publication Number Publication Date
JPS59139616A JPS59139616A (en) 1984-08-10
JPH035642B2 true JPH035642B2 (en) 1991-01-28

Family

ID=11847569

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1395383A Granted JPS59139616A (en) 1983-01-31 1983-01-31 Manufacture of magnetic thin film

Country Status (1)

Country Link
JP (1) JPS59139616A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4684454A (en) * 1983-05-17 1987-08-04 Minnesota Mining And Manufacturing Company Sputtering process for making magneto optic alloy
JPS62195109A (en) * 1986-02-21 1987-08-27 Hitachi Ltd sputtering device
US4950556A (en) * 1987-10-26 1990-08-21 Minnesota Mining And Manufacturing Company Magneto-optic recording medium
GB0210660D0 (en) * 2002-05-10 2002-06-19 Trikon Technologies Ltd Shutter

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56118321A (en) * 1980-02-22 1981-09-17 Nippon Hoso Kyokai <Nhk> Forming method for preliminary protecting film

Also Published As

Publication number Publication date
JPS59139616A (en) 1984-08-10

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