JP2816151B2 - Method for manufacturing perpendicular magnetic recording medium - Google Patents
Method for manufacturing perpendicular magnetic recording mediumInfo
- Publication number
- JP2816151B2 JP2816151B2 JP63056078A JP5607888A JP2816151B2 JP 2816151 B2 JP2816151 B2 JP 2816151B2 JP 63056078 A JP63056078 A JP 63056078A JP 5607888 A JP5607888 A JP 5607888A JP 2816151 B2 JP2816151 B2 JP 2816151B2
- Authority
- JP
- Japan
- Prior art keywords
- heat treatment
- recording medium
- magnetic recording
- oxide film
- perpendicular magnetic
- 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 - Fee Related
Links
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明はCoを主成分とする金属の部分酸化物より成る
垂直磁気記録媒体に係り、特に磁気特性の優れた上記垂
直磁気記録媒体を提供するものである。Description: BACKGROUND OF THE INVENTION The present invention relates to a perpendicular magnetic recording medium comprising a partial oxide of a metal containing Co as a main component, and particularly to the perpendicular magnetic recording medium having excellent magnetic properties. Is what you do.
磁気記録の分野における記録密度の向上は著しいもの
がある。特に垂直磁気記録方式は現在実用化されている
面内記録方式と異なり、記録密度が高くなるほど自己減
磁作用が小さくなる特徴を有し、将来の高密度磁気記録
方式として注目を集め精力的に研究がなされている。There is a remarkable improvement in recording density in the field of magnetic recording. In particular, the perpendicular magnetic recording method has the characteristic that the self-demagnetization effect decreases as the recording density increases, unlike the in-plane recording method currently in practical use. Research is being done.
垂直磁気記録媒体としては岩崎らによってCo−Cr合金
が発表されている〔岩崎,大内;アイ・イー・イー・イ
ー・,トランザクション オンマクネチックス,エムエ
ージー14,849(1987年)(S.Iwasaki and K.Ouchi:IEEE
Trans.Magn.,MAG−14,849(1987))〕。CoCr合金は磁
気異方性,飽和磁化ともに大きく、垂直磁気記録媒体と
して優れた特性を備えている。ところが、金属であり摩
耗に弱い点がある。このような観点から例えばCoの部分
酸化膜が検討され磁気異方性の大きな垂直磁化膜が得ら
れている。〔吉田他:特開昭59−140629号,および中村
ら:ジャパニーズ・ジャーナル・オブ・アプライド・フ
ィジックス,23巻,No.6,L397(1984年)(K.Nakamura e
t.al.:Jpn.J.Appl.Phys.Vol.23,No.6,L397(198
4))〕。As a perpendicular magnetic recording medium, a Co-Cr alloy has been announced by Iwasaki et al. [Iwasaki, Ouchi; .Ouchi: IEEE
Trans. Magn., MAG-14, 849 (1987)). The CoCr alloy has large magnetic anisotropy and saturation magnetization, and has excellent characteristics as a perpendicular magnetic recording medium. However, it is a metal and is vulnerable to wear. From such a viewpoint, for example, a partial oxide film of Co has been studied, and a perpendicular magnetization film having a large magnetic anisotropy has been obtained. [Yoshida et al .: JP-A-59-140629, and Nakamura et al .: Japanese Journal of Applied Physics, Vol. 23, No. 6, L397 (1984) (K. Nakamura e
t.al.:Jpn.J.Appl.Phys.Vol.23,No.6,L397(198
Four))〕.
しかし,上記Co系部分酸化膜磁性薄膜では、飽和磁化
(以下Msと略す)が10×105A/m以下の範囲で垂直磁化膜
が実現するものの、実際に記録再生を行うと、再生出力
が低く、磁気記録媒体としては不十分な特性しか得られ
ない。However, in the Co-based partial oxide film magnetic thin film, although a perpendicular magnetization film is realized with a saturation magnetization (hereinafter abbreviated as Ms) in a range of 10 × 10 5 A / m or less, when the recording and reproduction are actually performed, the reproduction output is reduced. , And only insufficient characteristics for a magnetic recording medium can be obtained.
本発明の目的はCo系部分酸化膜の磁気特性を改善し、
記録再生出力の高い実用に供する垂直磁気記録体を提供
することにある。An object of the present invention is to improve the magnetic properties of a Co-based partial oxide film,
An object of the present invention is to provide a perpendicular magnetic recording medium which has a high recording / reproducing output and is practically used.
尚、ここでCo系部分酸化膜とは従来の技術の欄に示し
た文献等に示されたCo系部分酸化膜であり、CoCx(0<
X<1)で表わされる非化学量論的組成をもつものであ
る。微視的には金属Coと一酸化コバルト(CoOけの混在
した状態と推論している。Here, the Co-based partial oxide film is a Co-based partial oxide film shown in the literature and the like described in the section of the prior art, and CoCx (0 <
It has a non-stoichiometric composition represented by X <1). Microscopically, it is inferred that metal Co and cobalt monoxide (CoO are mixed).
上記目的は、従来技術により形成したCo系部分酸化膜
を、好ましくは100℃以上300℃以下の温度で加熱処理す
ることにより達成できる。熱処理時における雰囲気は大
気中でも真空中でもよく、また処理時間は所定温度にお
いて30分以上あれば十分である。The above object can be achieved by subjecting a Co-based partial oxide film formed by a conventional technique to a heat treatment at a temperature of preferably 100 ° C. or more and 300 ° C. or less. The atmosphere during the heat treatment may be in the air or in a vacuum, and the treatment time may be 30 minutes or more at a predetermined temperature.
加熱処理により記録再生特性が向上する明確な理由は
明らかではないが、以下の様に考えられる。The clear reason why the recording / reproducing characteristics are improved by the heat treatment is not clear, but is considered as follows.
第2図にCo部分酸化膜の空気中熱処理前後における磁
化曲線の変化を示した。熱処理前の磁化曲線6に比較
し、熱処理を行うことにより磁化ヒステリシス曲線7の
肩の部分の角形性が大幅に改善されていることが分か
る。このことは、熱処理を行うことによって磁化反転が
急峻に起こる様になることを示している。このような磁
気特性の改善が実際に記録再生を行った時の記録分解能
や再生出力の向上をもたらしたものと考えられる。FIG. 2 shows the change of the magnetization curve before and after the heat treatment in the air of the Co partial oxide film. Compared with the magnetization curve 6 before the heat treatment, it can be seen that the heat treatment significantly improves the squareness of the shoulder portion of the magnetization hysteresis curve 7. This indicates that the magnetization reversal occurs sharply by performing the heat treatment. It is considered that such an improvement in the magnetic characteristics resulted in an improvement in the recording resolution and the reproduction output when the recording and reproduction were actually performed.
また、このように磁化ヒステリシス曲線の形が変化し
たのは次の様に考えられる。従来技術で作製したCo部分
酸化膜は金属Coの微結晶がCoO酸化酸化物で覆われた構
造であるが、金属Coの微結晶中に過飽和の酸素が存在
し、微結晶に大きな歪を与え、一様性が悪いと思われ
る。そのために膜中の金属Coの磁化反転が一様に行れな
いと考えられる。一方、この様な膜に100℃以上、300℃
以下の加熱処理を施すと、金属Co中の過飽和の酸素が拡
散し、金属Co微結晶表面で安定なCoO酸化物を形成する
と思われる。また、その結果として、金属Co中の酸素濃
度が減少し、Co微結晶の結晶性が改善され、膜中でのCo
微結晶の磁化反転が一様に行われると考えられる。The change in the shape of the magnetization hysteresis curve is considered as follows. The Co partial oxide film produced by the conventional technology has a structure in which microcrystals of metal Co are covered with CoO oxide oxide, but supersaturated oxygen exists in the microcrystals of metal Co, causing a large strain on the microcrystals. It seems that the uniformity is bad. Therefore, it is considered that the magnetization reversal of the metal Co in the film cannot be performed uniformly. On the other hand, such a film should
It is considered that when the following heat treatment is performed, supersaturated oxygen in the metal Co diffuses to form a stable CoO oxide on the surface of the metal Co microcrystal. As a result, the oxygen concentration in the metal Co decreases, the crystallinity of the Co microcrystals is improved, and the Co
It is considered that the magnetization reversal of the microcrystal is performed uniformly.
以下、本発明の一実施例を第1図および第2図により
説明する。An embodiment of the present invention will be described below with reference to FIGS. 1 and 2.
第1図に示した真空蒸着装置を用いて、ポリイミド基
板1上に周知技術を用いてCoの部分酸化膜を形成した。
Coは電子ビーム加熱法(電子ビーム加熱源2を使用)に
より溶解し、蒸着を行った。また、部分酸化を行うため
の酸素の導入量はニードルバルブ5により調整した。Using a vacuum deposition apparatus shown in FIG. 1, a Co partial oxide film was formed on the polyimide substrate 1 using a known technique.
Co was melted by an electron beam heating method (using an electron beam heating source 2), and vapor deposition was performed. The amount of oxygen introduced for performing partial oxidation was adjusted by the needle valve 5.
蒸着条件は基板温度を30℃、Coの蒸着速度を0.3nm/
s、酸素分圧を9×10-3Paとした。このような条件で膜
の厚さが240nmのCo部分酸化膜を作製し、大気中で215℃
の温度で1時間加熱処理で施して熱処理前後の磁気特性
を比較した。The deposition conditions were a substrate temperature of 30 ° C and a Co deposition rate of 0.3 nm /
s and the oxygen partial pressure were 9 × 10 −3 Pa. Under these conditions, a Co partial oxide film with a thickness of 240 nm was formed and
The magnetic properties before and after the heat treatment at a temperature of 1 hour were compared.
第2図は、熱処理前後における磁化ヒステリシス曲線
の第1象限を示したものであり、いずれも膜面に垂直な
方向に磁界を印加したものである。FIG. 2 shows the first quadrant of the magnetization hysteresis curve before and after the heat treatment, in which a magnetic field was applied in a direction perpendicular to the film surface.
熱処理前のCo部分酸化膜のMsは5.16×105A/mであり、
保磁力(以下Hc⊥と略す)は9.71×104A/mである。熱処
理後のCo部分酸化膜のMsは4.92×105A/m、Hc⊥は9.51×
104A/mである。熱処理後に見られる0.2%程度のMsの減
少は、部分酸化膜中の過飽和の酸素が金属Coと反応し、
CoO酸化物を形成し、実質的に部分酸化膜中の金属Coの
密度が減少したためと思われる。なお、このようなMsの
減少は、1.3×10-4Paの圧力の真空中における加熱処理
においても見られた。The Ms of the Co partial oxide film before the heat treatment is 5.16 × 10 5 A / m,
Coercive force (hereinafter referred to as Hc ⊥) is 9.71 × 10 4 A / m. Ms of the Co partial oxide film after the heat treatment is 4.92 × 10 5 A / m, Hc⊥ is 9.51 ×
10 4 A / m. The decrease in Ms of about 0.2% observed after heat treatment is due to the supersaturated oxygen in the partial oxide film reacting with metal Co,
This is probably because a CoO oxide was formed and the density of metal Co in the partial oxide film was substantially reduced. Note that such a decrease in Ms was also observed in the heat treatment in a vacuum at a pressure of 1.3 × 10 −4 Pa.
第2図の磁化ヒステリシス曲線における加熱処理前後
の大きな違いは図中に矢印で示したヒステリシス曲線の
肩の部分である。熱処理前ではこの肩の部分がなだらか
であり、この領域での磁界変化に対する磁化反転が一様
でないことを示している。これに対し、熱処理後は肩の
部分が鋭く、この領域での磁界の変化に対して磁化反転
が一様でかつ急峻であることを示している。The major difference between the magnetization hysteresis curve in FIG. 2 before and after the heat treatment is the shoulder portion of the hysteresis curve indicated by the arrow in the figure. Before the heat treatment, the shoulder portion is gentle, indicating that the magnetization reversal to the magnetic field change in this region is not uniform. On the other hand, the shoulder portion is sharp after the heat treatment, which indicates that the magnetization reversal is uniform and steep with respect to the change in the magnetic field in this region.
このようにして作製した加熱処理前後のCo部分酸化膜
の記録再生特性をギャップ長0.3μmの磁気ヘッドを用
いて、線記録密度80kFCIにおいて測定した。加熱処理前
における出力が1.5μVpp(巻線1ターン、相対速度1m/s
における値)であったのが熱処理後の試料においては3
μVppとなり、再生出力は2倍に向上した。The recording / reproducing characteristics of the Co partial oxide film before and after the heat treatment thus manufactured were measured at a linear recording density of 80 kFCI using a magnetic head having a gap length of 0.3 μm. Output before heat treatment is 1.5μV pp (winding 1 turn, relative speed 1m / s
Was 3) in the sample after the heat treatment.
μV pp , and the reproduction output was doubled.
なお、本実施例で用いたCo部分酸化膜では加熱処理温
度が150℃以上で第2図に示した磁化ヒステリシス曲線
の変化が見られ、そのような磁化曲線の変化が起った試
料ではいずれも記録再生特性が向上することが確認され
た。また、本実施例においてはCo部分酸化膜をとりあげ
たが、Ti、Mn,Zr,Cr,Al,Pt,Nb,Ru,Re,Feの元素の中から
1種あるいは2種類の元素を総量で、0.1原子%から15
原子%含んだCo部分酸化膜においても、第2図に示した
磁化ヒステリシス曲線と同様な変化が見られた。In the case of the Co partial oxide film used in this example, the change in the magnetization hysteresis curve shown in FIG. 2 was observed at a heat treatment temperature of 150 ° C. or higher. It was also confirmed that the recording / reproducing characteristics were improved. In the present embodiment, the Co partial oxide film is taken up, but one or two of the elements of Ti, Mn, Zr, Cr, Al, Pt, Nb, Ru, Re, and Fe are used in total. , 0.1 atomic% to 15
A change similar to the magnetization hysteresis curve shown in FIG. 2 was also observed in the Co partial oxide film containing atomic%.
本発明による垂直磁化膜は製造方法が簡単であり、原
料としては金属Coと酸素ガスだけですみ、しかも簡単な
加熱処理により特性の良好な垂直磁気記録媒体を得るこ
とができるので実用上の利点は大きい。The perpendicular magnetization film according to the present invention is simple in manufacturing method, requires only metal Co and oxygen gas as raw materials, and can obtain a perpendicular magnetic recording medium having good characteristics by a simple heat treatment, and thus has a practical advantage. Is big.
第1図は本発明のCo部分酸化膜の作製に用いた電子ビー
ム加熱蒸着装置の概略断面図、第2図は本発明で作製し
たCo部分酸化膜の熱処理前後における磁化ヒステリシス
曲線の第1象限を表した図であり、実線は熱処理前、破
線は熱処理後のものである。 符号の説明 1……基板,2……電子ビーム加熱蒸着源, 3……Co蒸気流,4……O2ガス流, 5……ニードルバルブ, 6……加熱処理前のCo部分酸化膜の磁化ヒステリシス曲
線, 7……加熱処理後のCo部分酸化膜の磁化ヒステリシス曲
線。FIG. 1 is a schematic cross-sectional view of an electron beam heating evaporation apparatus used for producing a Co partial oxide film of the present invention, and FIG. 2 is a first quadrant of a magnetization hysteresis curve before and after heat treatment of a Co partial oxide film produced by the present invention. Where the solid line is before heat treatment and the dashed line is after heat treatment. DESCRIPTION OF SYMBOLS 1... Substrate, 2... Electron beam heating evaporation source, 3... Co vapor flow, 4... O 2 gas flow, 5... Needle valve, 6. Magnetization hysteresis curve, 7: Magnetization hysteresis curve of Co partial oxide film after heat treatment.
フロントページの続き (72)発明者 吉田 和悦 東京都国分寺市東恋ケ窪1丁目280番地 株式会社日立製作所中央研究所内 (56)参考文献 特開 昭62−214522(JP,A) 特開 昭62−103851(JP,A)Continuation of the front page (72) Inventor Kazuyoshi Yoshida 1-280 Higashi Koikebo, Kokubunji-shi, Tokyo Inside the Central Research Laboratory, Hitachi, Ltd. (56) References JP-A-62-214522 (JP, A) JP-A-62-103851 ( JP, A)
Claims (2)
酸化物より成る磁性層を形成した垂直磁気記録媒体の製
造方法において、上記磁性層を形成したのち、加熱処理
を施すことを特徴とする垂直磁気記録媒体の製造方法。In a method for manufacturing a perpendicular magnetic recording medium in which a magnetic layer composed of a partial oxide containing metal Co as a main component is formed on a non-magnetic substrate, a heat treatment is performed after forming the magnetic layer. A method for manufacturing a perpendicular magnetic recording medium.
媒体の製造方法において、上記加熱処理の温度は100℃
以上300℃以下である垂直磁気記録媒体の製造方法。2. A method for manufacturing a perpendicular magnetic recording medium according to claim 1, wherein the temperature of said heat treatment is 100 ° C.
A method for producing a perpendicular magnetic recording medium at a temperature of not less than 300 ° C.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63056078A JP2816151B2 (en) | 1988-03-11 | 1988-03-11 | Method for manufacturing perpendicular magnetic recording medium |
US07/321,081 US5244751A (en) | 1988-03-11 | 1989-03-09 | Perpendicular magnetic recording medium, its fabrication method and read-write machine using it |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63056078A JP2816151B2 (en) | 1988-03-11 | 1988-03-11 | Method for manufacturing perpendicular magnetic recording medium |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01232536A JPH01232536A (en) | 1989-09-18 |
JP2816151B2 true JP2816151B2 (en) | 1998-10-27 |
Family
ID=13017051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63056078A Expired - Fee Related JP2816151B2 (en) | 1988-03-11 | 1988-03-11 | Method for manufacturing perpendicular magnetic recording medium |
Country Status (1)
Country | Link |
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JP (1) | JP2816151B2 (en) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62103851A (en) * | 1985-10-31 | 1987-05-14 | Toray Ind Inc | Production of vertical magnetic recording medium |
JPS62214522A (en) * | 1986-03-14 | 1987-09-21 | Canon Inc | Production of magnetic recording medium |
-
1988
- 1988-03-11 JP JP63056078A patent/JP2816151B2/en not_active Expired - Fee Related
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Publication number | Publication date |
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JPH01232536A (en) | 1989-09-18 |
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