JPS584914A - Sputter target for forming magnetic thin film with oxide - Google Patents

Sputter target for forming magnetic thin film with oxide

Info

Publication number
JPS584914A
JPS584914A JP56103065A JP10306581A JPS584914A JP S584914 A JPS584914 A JP S584914A JP 56103065 A JP56103065 A JP 56103065A JP 10306581 A JP10306581 A JP 10306581A JP S584914 A JPS584914 A JP S584914A
Authority
JP
Japan
Prior art keywords
oxide
magnetic
thin film
substrate
fe3o4
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
Application number
JP56103065A
Other languages
Japanese (ja)
Other versions
JPH0430171B2 (en
Inventor
Kozo Nishimoto
西本 幸三
Masamichi Tagami
勝通 田上
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.)
NEC Corp
Original Assignee
NEC Corp
Nippon Electric Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NEC Corp, Nippon Electric Co Ltd filed Critical NEC Corp
Priority to JP56103065A priority Critical patent/JPS584914A/en
Publication of JPS584914A publication Critical patent/JPS584914A/en
Publication of JPH0430171B2 publication Critical patent/JPH0430171B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/62Record carriers characterised by the selection of the material
    • G11B5/64Record carriers characterised by the selection of the material comprising only the magnetic material without bonding agent
    • G11B5/65Record carriers characterised by the selection of the material comprising only the magnetic material without bonding agent characterised by its composition
    • G11B5/658Record carriers characterised by the selection of the material comprising only the magnetic material without bonding agent characterised by its composition containing oxygen, e.g. molecular oxygen or magnetic oxide

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Compounds Of Iron (AREA)
  • Physical Vapour Deposition (AREA)
  • Manufacturing Of Magnetic Record Carriers (AREA)
  • Thin Magnetic Films (AREA)

Abstract

PURPOSE:To effectively provide uniform and stable oxide magnetic thin film on the entire surface of a substrate by using, as a sputter target for the magnetic recording medium, Fe3O4 sinter obtained by containing a 0.5-10wt% of Cu and/or a 0.5-5wt% of Co each as an oxide in metal iron. CONSTITUTION:Using a magnetic oxide comprising Fe3O4 sinter obtained by containing in metal iron a 0.5-10wt% of Cu and/or a 0.5-5wt% of Co each as an oxide, a magnetic recording medium such as a magnetic disk is produced as follows : Poweders of Fe3O4, Co2O3 and CuO are sufficiently mixed at the specified weight ratio and grained into uniform particles into which some binders are mixed. They are then pressed into the specified shape, and heat treated for several hours at 1,250-1,300 deg.C in the inert gas environment. The treatment temperature necessary for changing to gamma-Fe2O3 is lowered and thus a load on the substrate is relieved.

Description

【発明の詳細な説明】 本発明は磁気ディスク装置等において磁気記録媒体とし
て用いられる酸化物磁性薄膜形成に使用するスバ、り・
ターゲットに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for forming a thin oxide magnetic thin film used as a magnetic recording medium in a magnetic disk drive, etc.
Regarding the target.

磁気記録装置における紀録密匿の向上は斯界の変らぬ趨
勢であ、す、これを災現する為には峰気紀録媒体の薄膜
化、薄膜化が不可欠であるOそこで島性能蜂気記録媒体
として、薄膜化がd易な連続薄膜媒体、特に酸化@両性
薄膜が注目を集めている。その理由は、(1)残留磁束
密度が小さい、(2)機械的強度と化学的安定性に富み
、金属薄膜に必要とされる保護膜を必要とせず、その結
果、(a)@気ヘッドー媒体間がより小さく出来、高密
度と低価格化に適しているという・点にある。
Improving the secrecy of records in magnetic recording devices is a constant trend in this field.In order to prevent this from happening, it is essential to make the record media thinner and thinner. As such, continuous thin film media that can be easily thinned, especially oxidized and amphoteric thin films, are attracting attention. The reasons for this are (1) low residual magnetic flux density, (2) high mechanical strength and chemical stability, and no protective film required for metal thin films. The advantage is that the space between media can be made smaller, making it suitable for high density and low cost.

酸化物磁性薄膜としては、その形成が容易であることか
ら酸化鉄薄膜が専ら用いられ、その製造方法としては種
々あるが、マグネタイード(Th5Ck )をターゲッ
トとしてスパッタリングすることによリマグネタイを主
成分とする強磁性酸化鉄薄膜を直接基板上に形成する簡
便で再現性のよい方法が提案されている(特開昭51−
8200号公報参照)bこの方法において磁気特性の制
御のためコバルトを添加物として用いればスパッタされ
たマグネタイト膜の保磁力を任意に制御出来る。形成さ
れた膜はその後磁気特性の向上及び膜の安定化のため比
較的高い装置でr化処理(peaQn 2sらr−p6
2Uaにする処理)が施される。通常基板としてはアル
マイト被覆を施こしたアブレミニウム合金基板が使用さ
れるが、この種の基板は高温にさらされた場合、表面の
平面層が損なわnたり被板されたアルマイト層に基体ア
ルミニウム合金との熱膨張率の差からクラックが発生す
るなどの問題が生じる為、γ比処理温度は出来るだけ低
い方が好ましい。しかるに、上記方法で形成したマクネ
タイト膜はγ比処理温度を基板に負担がかからない温度
まで低くすることが峻しく、特にコバルトを添加したマ
クネタイト膜は一層γ化処理温度が筒くなる傾向がある
Iron oxide thin films are used exclusively as oxide magnetic thin films because they are easy to form, and there are various methods for manufacturing them, but by sputtering using magnetide (Th5Ck) as a target, it is possible to make remagnetide as the main component. A simple and highly reproducible method for forming a ferromagnetic iron oxide thin film directly on a substrate has been proposed (Japanese Unexamined Patent Application Publication No. 1986-1999).
(See Japanese Patent Application No. 8200) b In this method, if cobalt is used as an additive to control the magnetic properties, the coercive force of the sputtered magnetite film can be arbitrarily controlled. The formed film was then subjected to R treatment (peaQn 2s et al. r-p6) using relatively expensive equipment to improve magnetic properties and stabilize the film.
2Ua processing) is performed. Normally, an alumite-coated alumite alloy substrate is used as a substrate, but when this type of substrate is exposed to high temperatures, the surface plane layer may be damaged, or the coated alumite layer may become invisible to the base aluminum alloy. Since problems such as cracks occur due to the difference in the coefficient of thermal expansion, it is preferable that the γ ratio treatment temperature be as low as possible. However, for the macnetite film formed by the above method, it is difficult to lower the γ ratio treatment temperature to a temperature that does not impose a burden on the substrate, and in particular, the macnetite film to which cobalt is added tends to have a further γ ratio treatment temperature.

かかる点を解決する方法として本発明者らは先にマグネ
タイトをターゲットとして中性ガスもしくは中性ガスと
酸化性ガスとの混合亦囲気中においてスパッタリングす
ることにより基板上に直接形成されるマグネタイトを主
成分とする酸化q#磁性薄膜において、添加剤として銅
を含有していることを特徴とし、磁気特性制御の必要上
、場合により添加剤として更にコバルトも含有している
酸化@磁性薄膜を用いることを提案した。
As a method to solve this problem, the present inventors first focused on magnetite, which is formed directly on a substrate by sputtering in a neutral gas or a mixture of a neutral gas and an oxidizing gas using magnetite as a target. The oxidized q# magnetic thin film as a component is characterized by containing copper as an additive, and in order to control the magnetic properties, an oxide@magnetic thin film may also be used that further contains cobalt as an additive. proposed.

本発明は上記発明において使用するに適した酸化物磁性
薄膜形成用スパッタ・ターゲットを提供するものである
り 本発明にかかわる磁性酸化物薄膜形成用スパッタ・ター
ゲットは例えば次のような方法によって製作することが
できる。所定重敏比のk”e 304 、 Go 2−
03及びCuOの粉末を十分混合、粉砕し、均一な粒子
サイズとした後、バインダーを混ぜて所定の形にプレス
成型する。この成型体を不活性ガス雰囲気中において制
御された加熱、冷却過程と最高1.250〜1,300
℃数時間の熱処理を施こすことによって割れのない堅牢
なCt+、Cu添加Fe 304焼結体が得られる。
The present invention provides a sputter target for forming a magnetic oxide thin film suitable for use in the above invention, and the sputter target for forming a magnetic oxide thin film according to the present invention can be manufactured, for example, by the following method. be able to. k”e 304 of the predetermined gravity ratio, Go 2-
After the powders of 03 and CuO are sufficiently mixed and pulverized to have a uniform particle size, a binder is mixed therein and press-molded into a predetermined shape. This molded body is subjected to a controlled heating and cooling process in an inert gas atmosphere to a maximum temperature of 1.250 to 1,300
By performing heat treatment at ℃ for several hours, a crack-free and robust Ct+, Cu-added Fe 304 sintered body can be obtained.

以下実施例によって本発明の慧義を詳細に説明する。The merits of the present invention will be explained in detail with reference to Examples below.

実施例1゜ 上記例示した製造法によって金属鉄比1.Q 、 4.
0 。
Example 1゜The metal iron ratio was 1. Q, 4.
0.

6.0重量−のCuを酸化物として含むl+’eaQ4
焼結体を作製し、これらをターゲットとしてアルコン圧
力(PAr) 8 x 10−”Torr、 ターゲ、
 )M板id距Ill D= 30wa 、付着速度(
8、R) 250A/minにおいてR,Fスパ、タリ
ングを行ないアルマイト核種したA1合金基板上に1.
5 、4.0 、6.0重tqbのCuを含むFe+0
4膜を形成した。これらの膜を大気中、1時間の酸化処
理を行なったところ、いずれの膜も250〜275℃で
の酸化処理によりγ−に’e 203膜に変換されてい
ることを確認した。これに対して比較例としてeuを添
加しない純Fe5O4焼結体をターゲットとして同じ条
件で形成したk”e304膜をr−FezOa膜とする
為には320℃以上でのば化処理を要した。
l+'eaQ4 containing 6.0 wt- Cu as oxide
Prepare sintered bodies and use them as targets at an arcon pressure (PAr) of 8 x 10-” Torr,
) M plate id distance Ill D = 30wa, adhesion speed (
8.R) 1. On an A1 alloy substrate which was subjected to R, F spacing and taring at 250 A/min and anodized with anodized nuclide.
Fe+0 containing Cu of 5, 4.0, 6.0 tqb
Four films were formed. When these films were subjected to oxidation treatment for 1 hour in the air, it was confirmed that all the films were converted into γ-'e 203 films by the oxidation treatment at 250 to 275°C. On the other hand, as a comparative example, a k"e304 film formed under the same conditions using a pure Fe5O4 sintered body without adding eu as a target required an aggregation treatment at 320 DEG C. or higher in order to form an r-FezOa film.

更にCu添添加−ル゛e203膜では純γ−Fe 20
3膜に比してHc減少があったがこれはCu添加量の多
いものほど顕老であった(表参照)。
Furthermore, in the case of Cu-added Rue203 film, pure γ-Fe 20
There was a decrease in Hc compared to the 3 films, but this was more pronounced as the amount of Cu added increased (see table).

実施例2゜ 同様の製造法によって金属鉄比−2,0〜3.0重蓋チ
(1) Co 、 2.2〜4.4重′klk% 0)
 Cuを酸化物として含むFeast焼結体を作値しこ
れをターゲットとしてアルゴン雰囲気中Phr = 2
 X 10−3〜5 X 10−”Torr、D = 
30m、 8 、ルー 1.200A/1nin (1
)条゛件でマグネトロンスパッタ法により実施例1と同
じくアルマイト被板したアルミ合金基板上に1,500
〜1.70OAの厚さに種々組成のCo 、Cu含有F
eaO4膜を形成した。これらの膜は250〜300’
Cでの空気中酸化処理によって容易にCo、Cu會有γ
FezO3膜に変換できた。更にそれらの磁気特性はB
s3ρOOU。
Example 2゜By the same manufacturing method, metal iron ratio -2.0 to 3.0 weight (1) Co, 2.2 to 4.4 weight'klk% 0)
A Feast sintered body containing Cu as an oxide was prepared and used as a target in an argon atmosphere at Phr = 2.
X 10-3~5 X 10-”Torr, D =
30m, 8, Roux 1.200A/1nin (1
1,500 particles were deposited on an aluminum alloy substrate coated with alumite in the same manner as in Example 1 using the magnetron sputtering method under the following conditions.
~1.70OA thick with various compositions of Co, Cu-containing F
An eaO4 film was formed. These membranes are 250-300'
Co, Cu association γ can be easily formed by in-air oxidation treatment with C.
It was possible to convert it to FezO3 film. Furthermore, their magnetic properties are B
s3ρOOU.

80.7.S(抗磁力矩形性)0.8.Hc500−8
000eであり密度記録媒体に追わしいものであった(
表参照)0このようにCo 、 Cuを同時に硲加する
ことはHc増加とrFe zos化促進を行える利点が
あった。
80.7. S (coercive force rectangularity) 0.8. Hc500-8
000e, which was inferior to density recording media (
(See table) 0 Simultaneously adding Co and Cu in this manner had the advantage of increasing Hc and promoting rFezos formation.

実施例3゜ 先と同様の製法によって4゜0〜5.01(i%のCo
Example 3 By the same manufacturing method as above, 4°0 to 5.01 (i% Co
.

5〜7.5重IkLlbのCuを酸化物として含むpe
 304焼結体を作製し、それらをターゲットとしてp
ar= 6 X 10−’〜8 X 10−”Torr
、 D = 130m。
pe containing 5 to 7.5 times IkLlb of Cu as oxide
304 sintered bodies and used them as targets.
ar = 6 x 10-'~8 x 10-''Torr
, D = 130m.

S、几=100〜1000A/mtn(7)9に件で先
ト同シ基板上にCo 、 Cu合金1’6sQ4膜を形
成した0これらの膜を275−300℃において空気中
酸化処理することによってHc90G−1,3000e
の高抗磁力媒体を得た(表参照)。
S, 几=100-1000A/mtn (7) In the case of 9, a Co, Cu alloy 1'6sQ4 film was formed on the same substrate as before. These films were oxidized in air at 275-300°C. by Hc90G-1,3000e
A high coercive force medium was obtained (see table).

実施例2に示したターゲット、スパッタ条件によって外
径210mのアルマイトt6にしたアルミ合金ディスク
基板にCo 、 Cu含有Fe 304 m f形成し
、これを酸化してGo、Cu含含有−Fe2es膜峰気
デイスクを試作した。このディスクをディスク1%V試
 ′験機に装着しトラック鴨20μm1記録黴度24,
00 (JFRPlにおける丹生出力/、!:献測した
ところ、ディスク全面に亘り円周方向に勾−な再生出力
かイ4すられることを確認したり 以上のように本発明にかかる低注改化物薄杉成用スパッ
タ・ターゲットを用いl’Lば磁気ディスク媒体等に用
いる眩化物口正注薄挨であって、便米のものよりr−に
’e2g3化処理温度が低く基板への負担を軽減し、且
つ基板全面に亘っ”C均−安寛に効率よく広範囲の低気
符性を有する酸化物両性薄膜を形成することが可能にな
る。
Using the target and sputtering conditions shown in Example 2, Co and Cu-containing Fe 304 mf were formed on an aluminum alloy disk substrate made of alumite T6 with an outer diameter of 210 m, and this was oxidized to form a Go and Cu-containing -Fe2es film. I made a prototype disk. This disk was installed in a disk 1%V tester, and the track size was 20 μm, the recording hardness was 24,
00 (Nyu output in JFRPl/,!: When we measured it, we confirmed that there was a sloped playback output in the circumferential direction over the entire surface of the disc. It is a direct injection thin powder used for magnetic disk media etc. using a sputter target for thin cedar formation, and has a lower R-'E2G3 processing temperature than that of Binmai, which reduces the burden on the substrate. It becomes possible to efficiently form an oxide amphoteric thin film having a wide range of low-temperature properties over the entire surface of the substrate.

゛h゛h

Claims (1)

【特許請求の範囲】[Claims] 金属鉄に対して0.5〜10重倉パ重上パーセント又は
さらに0.5〜5重波パーセントのCoをそnぞれ酸化
物として含むFe30a焼結体からなる磁性酸化物薄膜
形成用スパッタ・ターゲット。
Sputtering for forming a magnetic oxide thin film consisting of a Fe30a sintered body containing Co as an oxide in an amount of 0.5 to 10 percent Co or further 0.5 to 5 percent Co based on metal iron. target.
JP56103065A 1981-07-01 1981-07-01 Sputter target for forming magnetic thin film with oxide Granted JPS584914A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56103065A JPS584914A (en) 1981-07-01 1981-07-01 Sputter target for forming magnetic thin film with oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56103065A JPS584914A (en) 1981-07-01 1981-07-01 Sputter target for forming magnetic thin film with oxide

Publications (2)

Publication Number Publication Date
JPS584914A true JPS584914A (en) 1983-01-12
JPH0430171B2 JPH0430171B2 (en) 1992-05-21

Family

ID=14344261

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56103065A Granted JPS584914A (en) 1981-07-01 1981-07-01 Sputter target for forming magnetic thin film with oxide

Country Status (1)

Country Link
JP (1) JPS584914A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57143161U (en) * 1981-03-03 1982-09-08

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57143161U (en) * 1981-03-03 1982-09-08

Also Published As

Publication number Publication date
JPH0430171B2 (en) 1992-05-21

Similar Documents

Publication Publication Date Title
JPH0670858B2 (en) Magneto-optical recording medium and its manufacturing method
JPS584914A (en) Sputter target for forming magnetic thin film with oxide
JPH04297572A (en) Co-cr-pt series target for magnetic recording medium
JPS62114124A (en) Production of magnetic disk
US5560786A (en) Magnetic thin film material for magnetic recording
JPS6313256B2 (en)
JPS61216125A (en) Production of magnetic recording medium
JPS60109215A (en) Spatter target for forming iron oxide magnetic thin film
JPH0628088B2 (en) Magnetic recording medium
JPS61139919A (en) Magnetic recording medium
JPS63266066A (en) Alloy target and production thereof
JPH1092640A (en) Ultra-high density magnetic recording medium and manufacturing method
JPS62120627A (en) Magnetic recording medium
JPS5820732A (en) Preparation of magnetic thin film of oxide
JPS62275315A (en) Magnetic recording medium and its production
JPS61276115A (en) Magnetic recording medium and its production
JPH03173915A (en) Production of magnetic recording medium
JPH0785296B2 (en) Magnetic recording medium
JPS59119530A (en) Magnetic recording medium for vertical magnetization recording
JPS5957412A (en) Manufacture of magnetic recording medium
JPS62120625A (en) Magnetic recording medium
JPS61224125A (en) Magnetic recording medium
JPS6126131B2 (en)
JPS6177128A (en) Magnetic recording medium
JPH0365650B2 (en)