JP3128232B2 - Magneto-optical recording medium - Google Patents
Magneto-optical recording mediumInfo
- Publication number
- JP3128232B2 JP3128232B2 JP02234372A JP23437290A JP3128232B2 JP 3128232 B2 JP3128232 B2 JP 3128232B2 JP 02234372 A JP02234372 A JP 02234372A JP 23437290 A JP23437290 A JP 23437290A JP 3128232 B2 JP3128232 B2 JP 3128232B2
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- Prior art keywords
- film
- magneto
- optical recording
- recording medium
- oxygen
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Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、基板上に光磁気記録膜として希土類−遷移
金属系非晶質合金膜が担持された光磁気記録媒体に係
り、特に、希土類−遷移金属系非晶質合金膜の組成に関
する。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a magneto-optical recording medium in which a rare earth-transition metal-based amorphous alloy film is supported as a magneto-optical recording film on a substrate, and more particularly to a rare earth element. -It relates to the composition of the transition metal based amorphous alloy film.
[従来の技術] 従来より、光磁気記録膜として、希土類−遷移金属系
非晶質合金膜を基板の片面に成膜してなる光磁気記録媒
体が知られている。[Prior Art] Conventionally, as a magneto-optical recording film, a magneto-optical recording medium in which a rare earth-transition metal based amorphous alloy film is formed on one surface of a substrate has been known.
前記光磁気記録膜の成膜に当っては、例えばスバッタ
リングやイオンプレーティングそれに真空蒸着など、真
空中もしくは低圧雰囲気中でガス化した成膜材料を基板
表面に付着し、膜状に成長させる、いわゆる真空成膜法
がとられるが、成膜開始前の真空容器内の排気(真空引
き)が不十分であると、真空容器内に残留した空気中の
窒素および酸素と反応して光磁気記録膜中の活性な希土
類が窒化および酸化しやすく、過度にその反応が進行す
ると、カー回転角が低下して再生信号出力が低下した
り、垂直磁気異方性エネルギーが低下して垂直磁気記録
ができなくなるといった現象を生じる。In the formation of the magneto-optical recording film, a film-forming material gasified in a vacuum or a low-pressure atmosphere, such as sputtering, ion plating, and vacuum deposition, is attached to the substrate surface and grown into a film. However, if the evacuation (vacuum evacuation) in the vacuum vessel before the start of film formation is insufficient, the film reacts with nitrogen and oxygen in the air remaining in the vacuum vessel to form a light. Active rare earths in the magnetic recording film are easily nitrided and oxidized, and if the reaction proceeds excessively, the Kerr rotation angle decreases and the output of the read signal decreases, or the perpendicular magnetic anisotropy energy decreases and the perpendicular magnetic anisotropy decreases. A phenomenon occurs in which recording cannot be performed.
かかる不都合があるため、従来は光磁気記録膜内に混
入した窒素および酸素は不純物であると認識されてお
り、光磁気記録膜内への窒素および酸素の混入を防止す
る方向で技術的な検討が行われている。その一例として
は、真空容器内に残留する空気量を極力減少するため、
真空引きを可能な限り高度に行うことが検討されている
が、高度の真空引きを行うほど量産性が劣化してしまう
ため、記録/再生特性と量産性とを比較衡量して、例え
ば10-5〔Pa〕オーダーまで真空引きを行うといった方法
が提案されている。Due to such inconvenience, nitrogen and oxygen mixed in the magneto-optical recording film have conventionally been recognized as impurities, and technical studies have been conducted in the direction of preventing nitrogen and oxygen from being mixed in the magneto-optical recording film. Has been done. As an example, to minimize the amount of air remaining in the vacuum vessel,
Although as much as possible evacuation be performed highly has been studied, since the higher the productivity for advanced vacuuming is deteriorated, and balanced against the recording / reproducing characteristics and productivity, for example, 10 - A method has been proposed in which evacuation is performed to the order of 5 [Pa].
[発明が解決しようとする課題] ところが、前記の方法によって作製され、窒素あるい
は酸素の混入率が低レベルに調整された希土類−遷移金
属系非晶質合金膜は、逆に垂直磁気異方性エネルギーが
高くなり過ぎ、ひいては磁壁エネルギーが高くなり過ぎ
て、情報の記録および消去に大きな外部磁界(例えば、
コイル)が必要になるという問題がある。[Problems to be Solved by the Invention] However, a rare earth-transition metal based amorphous alloy film produced by the above-described method and in which the mixing ratio of nitrogen or oxygen is adjusted to a low level is inversely perpendicular magnetic anisotropy. The energy becomes too high, and thus the domain wall energy becomes too high, so that a large external magnetic field (for example,
Coil) is required.
大型の外部磁界を備えると、(1)消費電力が増加す
る、(2)外部磁界の設定スペースが大きくなり、記録
/再生装置が大型化する、(3)記録/再生ヘッドが重
量化し、記録/再生ヘッドの動特性が悪くなる、といっ
た各種の不都合を生じるため、記録/再生装置の設計
上、情報の記録および消去を小さな外部磁界で行いうる
光磁気記録媒体が嘱望されている。When a large external magnetic field is provided, (1) power consumption increases, (2) a space for setting the external magnetic field increases, and a recording / reproducing apparatus becomes large. Due to various inconveniences such as deterioration of the dynamic characteristics of the read / write head, a magneto-optical recording medium capable of recording and erasing information with a small external magnetic field has been demanded in designing a recording / reproducing apparatus.
本願発明者らは、希土類−遷移金属系非晶質合金膜中
に混入される窒素および酸素の混入率と残留カー回転角
との関係、前記混入率と垂直磁気異方性定数との関係、
前記混入率とC/N比との関係等について研究した結果、
カー回転角を低下することなく、垂直磁気異方性エネル
ギーのみを低下できる領域があるという事実を知得し
た。The inventors of the present invention have a relationship between the mixing ratio of nitrogen and oxygen mixed into the rare earth-transition metal based amorphous alloy film and the residual Kerr rotation angle, a relationship between the mixing ratio and the perpendicular magnetic anisotropy constant,
As a result of studying the relationship between the mixing ratio and the C / N ratio,
We have learned that there is a region where only the perpendicular magnetic anisotropy energy can be reduced without reducing the Kerr rotation angle.
本発明は、前記の知見に基づいてなされたものであっ
て、希土類−遷移金属系非晶質合金膜中に混入される窒
素および酸素の混入率を調整することによって、カー回
転角が高く、かつ垂直磁気異方性エネルギーが小さな光
磁気記録媒体を提供することを目的とするものである。The present invention has been made based on the above-described findings, and has a high Kerr rotation angle by adjusting the mixing ratio of nitrogen and oxygen mixed in a rare earth-transition metal-based amorphous alloy film. It is another object of the present invention to provide a magneto-optical recording medium having a small perpendicular magnetic anisotropy energy.
[課題を解決するための手段] 本発明は、前記の目的を達成するため、第1に、基板
上に、クロム、チタンまたはニオブが添加された希土類
−遷移金属系の非晶質合金からなる光磁気記録膜と、シ
リコン、アルミニウム、ジルコニウム、チタンまたはタ
ンタルの窒化物もしくは酸化物からなる無機誘電体膜を
担持してなる光磁気記録媒体において、前記光磁気記録
膜中に、前記非晶質合金に対して総量で0.1〜5.0〔原子
%〕の窒素および酸素を含有するという構成にした。Means for Solving the Problems In order to achieve the above object, the present invention firstly comprises a rare earth-transition metal based amorphous alloy to which chromium, titanium or niobium is added on a substrate. In a magneto-optical recording medium comprising a magneto-optical recording film and an inorganic dielectric film made of a nitride or oxide of silicon, aluminum, zirconium, titanium or tantalum, The alloy was configured to contain 0.1 to 5.0 [atomic%] of nitrogen and oxygen in total with respect to the alloy.
また、第2に、基板上に、クロム、チタンまたはニオ
ブが添加された希土類−遷移金属系の非晶質合金からな
る光磁気記録膜と、シリコン、アルミニウム、ジルコニ
ウム、チタンまたはタンタルの窒化物もしくは酸化物か
らなる無機誘電体膜を担持してなる光磁気記録媒体にお
いて、前記光磁気記録膜中に、前記非晶質合金に対して
総量で0.1〜5.0〔原子%〕の窒素および酸素を含有し、
当該光磁気記録媒体の飽和記録磁界および/または消去
磁界を200〔Oe〕以下にするという構成にした。Second, a magneto-optical recording film made of a rare earth-transition metal based amorphous alloy to which chromium, titanium, or niobium is added, and a nitride of silicon, aluminum, zirconium, titanium, or tantalum or In a magneto-optical recording medium carrying an inorganic dielectric film made of an oxide, the magneto-optical recording film contains nitrogen and oxygen in a total amount of 0.1 to 5.0 [atomic%] with respect to the amorphous alloy. And
The saturation recording magnetic field and / or the erasing magnetic field of the magneto-optical recording medium is set to 200 [Oe] or less.
[作用] 本願発明者らの研究によると、希土類−遷移金属系非
晶質合金膜中に、窒素および酸素を0.1〜5.0〔原子%〕
含有すると、カー回転角を低下することなく、垂直磁気
異方性エネルギーのみを低下することができる。よっ
て、外部磁界を小型かつ軽量化することができ、消費電
力の低減、記録/再生装置の小型化、それに記録、消去
動作の高速化などを図ることができる。[Action] According to the study of the present inventors, nitrogen and oxygen are contained in the rare earth-transition metal based amorphous alloy film in an amount of 0.1 to 5.0 [atomic%].
When contained, only the perpendicular magnetic anisotropy energy can be reduced without reducing the Kerr rotation angle. Therefore, the external magnetic field can be reduced in size and weight, and power consumption can be reduced, the size of the recording / reproducing device can be reduced, and the speed of recording and erasing operations can be increased.
[実施例] 以下、本発明の実施例を図に基づいて説明する。Embodiment An embodiment of the present invention will be described below with reference to the drawings.
第1図は、本発明に係る光磁気記録媒体の膜構造の一
例を示す断面図であって、透明基板1の信号パターン形
成面2に、第1の多重干渉膜3と、光磁気記録膜4と、
第2の多重干渉膜5と、熱拡散膜6とが順次積層されて
いる。FIG. 1 is a cross-sectional view showing an example of a film structure of a magneto-optical recording medium according to the present invention, wherein a first multiple interference film 3 and a magneto-optical recording film are formed on a signal pattern forming surface 2 of a transparent substrate 1. 4 and
The second multiple interference film 5 and the thermal diffusion film 6 are sequentially laminated.
透明基板1は、例えばポリカーボネート、ポリメチル
メタクリレート、ポリオレフイン、エポキシなどのプラ
スチック材料や、ガラスなどの透明材料をもって、ディ
スク状もしくはカード状など、所望の形状に形成され
る。The transparent substrate 1 is formed of a plastic material such as polycarbonate, polymethyl methacrylate, polyolefin, or epoxy, or a transparent material such as glass into a desired shape such as a disk shape or a card shape.
信号パターン面2には、記録/再生用光ビームスポッ
トを案内するための案内溝やヘッダー信号を表すブリビ
ット列などの信号パターンが微細な凹凸状に形成され
る。なお、第1図においては、透明基板1の片面に信号
パターンが直接形成されているが、平板状に形成された
透明基板の片面に、当該透明基板と屈折率が近似した光
硬化性樹脂層を設け、この光硬化性樹脂層の表面に前記
信号パターンを転写することもできる。A signal pattern such as a guide groove for guiding a recording / reproducing light beam spot and a bribit string representing a header signal is formed on the signal pattern surface 2 in a fine uneven shape. In FIG. 1, a signal pattern is directly formed on one surface of the transparent substrate 1. However, a photocurable resin layer having a refractive index similar to that of the transparent substrate is formed on one surface of the transparent substrate formed in a plate shape. And the signal pattern can be transferred to the surface of the photocurable resin layer.
第1の多重干渉膜3は、光磁気記録膜4と透明基板1
との間で再生用光ビームを多重干渉させ、見掛け上のカ
ー回転角を大きくするために設けられるものであって、
シリコン、アルミニウム、ジルコニウム、チタン、タン
タルの窒化物や酸化物など、屈折率が前記透明基板1よ
りも大きな無機誘電体からなり、600〜1000Åの膜厚に
形成される。該膜3の成膜手段としては、スバッタリン
グが特に好適である。The first multiple interference film 3 includes a magneto-optical recording film 4 and a transparent substrate 1.
Is provided in order to cause a reproduction light beam to cause multiple interference between them and increase an apparent Kerr rotation angle,
It is made of an inorganic dielectric material such as silicon, aluminum, zirconium, titanium, or tantalum nitride or oxide having a refractive index larger than that of the transparent substrate 1, and is formed to a thickness of 600 to 1000 °. As a means for forming the film 3, sputtering is particularly preferable.
光磁気記録膜4は、膜中に窒素と酸素の双方が総量で
0.1〜5.0〔原子%〕混入された希土類−遷移金属系非晶
質合金膜からなり、200〜500Åの膜厚に形成される。希
土類−遷移金属系非晶質合金膜としては、希土類(例え
ば、テルビウム、ガドリウム、ネオジム、ジスプロシウ
ム).と、遷移金属(例えば、鉄、コバルト、ニツ1ケ
ル)と、添加元素(例えば、クロム、チタン、ニオブ)
とを含む3元合金系が特に好ましい。The magneto-optical recording film 4 has a total amount of both nitrogen and oxygen in the film.
It is composed of a rare earth-transition metal based amorphous alloy film mixed with 0.1 to 5.0 [at%], and is formed to a thickness of 200 to 500 °. As the rare earth-transition metal based amorphous alloy film, rare earth (for example, terbium, gadolinium, neodymium, dysprosium). , Transition metals (eg, iron, cobalt, nickel) and additional elements (eg, chromium, titanium, niobium)
Particularly, a ternary alloy system containing
以下に、この光磁気記録膜4の形成方法を列挙する。 The method of forming the magneto-optical recording film 4 will be described below.
(1)前記第1の多重干渉膜3を成膜した後、希土類−
遷移金属系非晶質合金膜を適宜の方法で成膜し、次い
で、第2の多重干渉膜5を当該希土類−遷移金属系非晶
質合金膜上に積層する以前に、前記希土類−遷移金属系
非晶質合金膜を、真空度が1.0×10-5〜1.0×10-3〔Pa〕
に調整された真空容器中で、5〜90〔分間〕、20〜120
〔℃〕に保持し、希土類−遷移金属系非晶質合金膜を窒
化または酸化して所望の光磁気記録膜4とする。(1) After forming the first multiple interference film 3, the rare earth
A transition metal-based amorphous alloy film is formed by an appropriate method, and then, before the second multiple interference film 5 is laminated on the rare earth-transition metal-based amorphous alloy film, the rare earth-transition metal System amorphous alloy film, the degree of vacuum is 1.0 × 10 −5 to 1.0 × 10 −3 (Pa)
In a vacuum vessel adjusted to 5 to 90 minutes, 20 to 120
While maintaining the temperature at [° C.], the rare earth-transition metal based amorphous alloy film is nitrided or oxidized to obtain a desired magneto-optical recording film 4.
(2)前記第1の多重干渉膜3を成膜した後、希土類−
遷移金属系非晶質合金膜を0.1〜5.0〔%〕の分圧の窒素
と酸素の混合ガスを含む雰囲気中で成膜し、この成膜過
程で希土類−遷移金属系非晶質合金膜を窒化および酸化
して所望の光磁気記録膜4とする。(2) After forming the first multiple interference film 3, the rare earth
A transition metal-based amorphous alloy film is formed in an atmosphere containing a mixed gas of nitrogen and oxygen at a partial pressure of 0.1 to 5.0 [%], and a rare earth-transition metal-based amorphous alloy film is formed in this film forming process. The desired magneto-optical recording film 4 is obtained by nitriding and oxidizing.
前記(2)に挙げた0.1〜5.0〔%〕の分圧の窒素と酸
素の混合ガスを含む雰囲気を作る方法としては、以下の
ような方法がある。As a method for creating an atmosphere containing a mixed gas of nitrogen and oxygen at a partial pressure of 0.1 to 5.0% described in the above (2), the following method is available.
(a)真空容器を10-5〔Pa〕オーダーの高真空度まで真
空引きした後、当該真空容器中に窒素と酸素の混合ガス
を供給し、成膜工程中の真空容器内の窒素と酸素の混合
ガスの分圧を0.1〜5.0〔%〕に調整する。(A) After evacuating the vacuum container to a high degree of vacuum of the order of 10 -5 [Pa], a mixed gas of nitrogen and oxygen is supplied into the vacuum container, and nitrogen and oxygen in the vacuum container during the film forming process are supplied. Is adjusted to 0.1-5.0%.
(b)希土類−遷移金属系非晶質合金膜の成膜に先立っ
て行われる真空引きで、真空容器中の真空度を1.0×10
-4〜5.0×10-4〔Pa〕に調整し、真空容器中に0.1〜5.0
〔%〕の分圧の空気を残留させる。(B) The degree of vacuum in the vacuum vessel is reduced to 1.0 × 10 5 by evacuation performed before the formation of the rare earth-transition metal amorphous alloy film.
-4 to 5.0 × 10 -4 (Pa), and 0.1 to 5.0 in a vacuum vessel
[%] Partial pressure of air is left.
なお、希土類−遷移金属系非晶質合金膜を成膜する方
法としては、スバッタリング、イオンプレーティング、
真空蒸着など、任意の真空成膜法を適用することができ
る。In addition, as a method of forming a rare earth-transition metal based amorphous alloy film, sputtering, ion plating,
Any vacuum film formation method such as vacuum evaporation can be applied.
第2の多重干渉膜5は、前記第1の多重干渉膜3と同
様の無機誘電体からなり、50〜500Åの膜厚に形成され
る。形成方法についても、前記第1の多重干渉膜3と同
様の方法がとられる。The second multiple interference film 5 is made of the same inorganic dielectric as the first multiple interference film 3, and is formed to a thickness of 50 to 500 °. Regarding the forming method, the same method as that of the first multiple interference film 3 is used.
熱拡散膜6は、金、銀、鋼、アルミニウムなどの金属
材料、あるいはこれらにチタン、ニッケル、タンタルな
どの添加元素を加えた合金からなり、300〜1000Åの膜
厚に形成される。この熱拡散膜6は、スバッタリング、
イオンプレーティング、真空蒸着など、任意の真空成膜
法によって形成することができるが、製造工程を簡略化
するため、前記各膜3,4,5と同一の真空成膜法によって
形成することが特に好ましい。The thermal diffusion film 6 is made of a metal material such as gold, silver, steel, or aluminum, or an alloy obtained by adding an additional element such as titanium, nickel, or tantalum, and is formed to a thickness of 300 to 1000 mm. This thermal diffusion film 6 is formed by sputtering,
Ion plating, vacuum deposition, etc., can be formed by any vacuum film forming method, but in order to simplify the manufacturing process, it can be formed by the same vacuum film forming method as the films 3, 4, 5 described above. Particularly preferred.
第2図に光磁気記録膜4中の窒素混入率および酸素混
入率と垂直磁気異方性定数との関係を、また第3図に光
磁気記録膜4中の窒素混入率および酸素混入率と残留カ
ー回転角との関係を示す。FIG. 2 shows the relationship between the nitrogen mixing ratio and oxygen mixing ratio in the magneto-optical recording film 4 and the perpendicular magnetic anisotropy constant, and FIG. 3 shows the nitrogen mixing ratio and oxygen mixing ratio in the magneto-optical recording film 4. This shows the relationship with the remaining Kerr rotation angle.
第2図に示すように、光磁気記録膜の垂直磁気異方性
定数Kuは、窒素または酸素の混入によって敏感に減少
し、窒素または酸素の混入率が大きくなるに従って漸次
減少する。そして、窒素または酸素の混入率が5.0〔原
子%〕を超えると、反磁界以下となり、磁気モーメント
が面内に傾くようになる。As shown in FIG. 2, the perpendicular magnetic anisotropy constant Ku of the magneto-optical recording film decreases sensitively with the incorporation of nitrogen or oxygen, and gradually decreases as the incorporation rate of nitrogen or oxygen increases. When the mixing ratio of nitrogen or oxygen exceeds 5.0 [atomic%], the magnetic field becomes equal to or less than the demagnetizing field, and the magnetic moment tilts in the plane.
一方、第3図に示すように、残留カー回転角は窒素お
よび酸素の混入に対して比較的安定であり、混入率が0
〜5.0〔原子%〕の範囲では、ほとんど低下しない。混
入率が5.0〔原子%〕を超えると、残留カー回転角が急
激に低下するが、これは第2図に見られる垂直磁気異方
性の消失によるものである。なお、残留カー回転角の低
下の程度は、窒素混入率を増加したときよりも酸素混入
率を増加したときの方が急激に起こる。On the other hand, as shown in FIG. 3, the residual Kerr rotation angle is relatively stable against the mixing of nitrogen and oxygen, and the mixing rate is 0%.
In the range of -5.0 [atomic%], it hardly decreases. When the mixing ratio exceeds 5.0 [atomic%], the residual Kerr rotation angle sharply decreases, which is due to the disappearance of the perpendicular magnetic anisotropy shown in FIG. The degree of decrease in the residual Kerr rotation angle occurs more rapidly when the oxygen mixing rate is increased than when the nitrogen mixing rate is increased.
第2図および第3図から、光磁気記録膜中の窒素混入
率および酸素混入率を0〜5.0〔原子%〕に調整するこ
とによって、信号出力レベルを低下することなく、情報
の記録および消去に要する外部磁界を小型化できること
がわかる。From FIGS. 2 and 3, it can be seen that by adjusting the nitrogen mixing ratio and oxygen mixing ratio in the magneto-optical recording film to 0 to 5.0 [atomic%], recording and erasing of information can be performed without lowering the signal output level. It can be understood that the external magnetic field required for (1) can be reduced.
第5図、第6図、第7図に、光磁気記録膜4中の窒素
混入率および酸素混入率と、再生出力信号のC/N、飽和
記録磁界、消去比が−40dBとなる外部磁界の大きさ、す
なわち消去磁界との関係を示す。ただし、試料として
は、第4図の膜構造を有するディスク状光磁気記録媒体
を用いた。FIGS. 5, 6, and 7 show the nitrogen mixing ratio and oxygen mixing ratio in the magneto-optical recording film 4, the C / N of the reproduction output signal, the saturation recording magnetic field, and the external magnetic field at which the erasure ratio becomes -40 dB. , Ie, the relationship with the erasing magnetic field. However, a disk-shaped magneto-optical recording medium having the film structure shown in FIG. 4 was used as a sample.
第5図に示すように、窒素混入率とC/Nとの関係で
は、混入率を0〜5.0〔原子%〕の範囲で変化させても
ほとんどC/Nは変化しないが、5.0〔原子%〕を超えた当
りから徐々にC/Nが低下し、6.0〔原子%〕を超えると急
速にC/Nが低下する。一方、酸素混入率とC/Nとの関係で
は、混入率を0〜3.5〔原子%〕の範囲で変化させても
ほとんどC/Nは変化しないが、3.5〔原子%〕を超えた当
りから徐々にC/Nが低下し、5.5〔原子%〕を超えると急
速にC/Nが低下する。As shown in FIG. 5, in the relationship between the nitrogen mixing ratio and C / N, the C / N hardly changes even if the mixing ratio is changed within the range of 0 to 5.0 [at. ], The C / N gradually decreases when the amount exceeds 6.0 [atomic%]. On the other hand, in the relationship between the oxygen mixing ratio and C / N, even if the mixing ratio is changed in the range of 0 to 3.5 [at%], the C / N hardly changes, but from around 3.5 [at%]. C / N gradually decreases, and when it exceeds 5.5 [atomic%], C / N decreases rapidly.
第6図に示すように、蝕和記録磁界、すなわち充分に
大きな外部磁界を加えたときのレベルに搬送波および雑
音が達する最小の磁界については、窒素混入率を変化さ
せた場合および酸素混入率を変化させた場合とも同一の
傾向を示す。そして、窒素混入率を増加するほど、また
酸素混入率を増加するほど飽和記録磁界を低下すること
ができ、0.1〔原子%〕以上の窒素または酸素を混入す
れば、飽和記録磁界を200〔Oe〕以下にすることができ
る。また、ISO規格にあるように、現状では飽和記録磁
界を225〔Oe〕以下にすることが目標になっており、窒
素混入率または酸素混入率を0.1〔原子%〕以上とする
ことによって、この目標をクリアすることができる。As shown in FIG. 6, the erosion recording magnetic field, that is, the minimum magnetic field at which the carrier and the noise reach a level when a sufficiently large external magnetic field is applied, is obtained by changing the nitrogen mixing rate and the oxygen mixing rate. It shows the same tendency even when it is changed. The saturation recording magnetic field can be reduced by increasing the nitrogen mixing rate and the oxygen mixing rate. If nitrogen or oxygen of 0.1 atomic% or more is mixed, the saturation recording magnetic field can be reduced by 200 [Oe ] Can be as follows. At present, the target is to set the saturation recording magnetic field to 225 [Oe] or lower, as specified in the ISO standard. By setting the nitrogen mixing rate or oxygen mixing rate to 0.1 [at. You can clear your goals.
また、第7図に示すように、消去磁界(本例では、消
去比、すなわち記録時の搬送波レベルに対する消去後の
雑音レベルが−40dBとなる外部磁界とした)について
も、窒素混入率を変化させた場合および酸素混入率を変
化させた場合とも同一の傾向を示す。そして、窒素混入
率を増加するほど、また酸素混入率を増加するほど消去
磁界を低下することができ、0.1〔原子%〕以上の窒素
または酸素を混入すれば、消去磁界を200〔Oe〕以下に
することができる。Also, as shown in FIG. 7, the nitrogen mixing rate of the erasing magnetic field (in this example, the erasing ratio, that is, the external magnetic field where the noise level after erasing was −40 dB with respect to the carrier level at the time of recording) was changed. The same tendency is exhibited in both cases where the oxygen concentration is changed and when the oxygen mixing ratio is changed. The erasing magnetic field can be lowered as the nitrogen mixing rate increases and the oxygen mixing rate increases. If nitrogen or oxygen of 0.1 atomic% or more is mixed, the erasing magnetic field can be reduced to 200 Oe or less. Can be
かように、第5図、第6図、第7図のデータは、第2
図、第3図に示したデータと対応している。Thus, the data in FIGS. 5, 6 and 7 are
This corresponds to the data shown in FIGS.
以下に、本発明の実験例および比較例を挙げ、各例の
光磁気記録媒体のC/N、蝕和記録磁界、消去磁界、それ
に光磁気記録膜4中の窒素混入率および酸素混入率を示
す。Hereinafter, experimental examples and comparative examples of the present invention will be described, and the C / N, erosion recording magnetic field, erasing magnetic field, and nitrogen mixing rate and oxygen mixing rate in the magneto-optical recording film 4 of each example of the magneto-optical recording medium will be described. Show.
〈実験例1〉 ポリカーボネート基板の信号パターン面に、第1の多
重干渉膜としてAlSiONを800Åの厚さにスバッタリング
した後、この基板が収められた真空容器内を5×10
-5〔Pa〕まで真空引きし、次いで、この真空容器内にス
バッタガスとして純アルゴンガスを供給して真空容器内
のガス圧を所定の値に調整し、このガス圧条件のもとで
TbFeCo膜を250Åの厚さにスバッタリングした。<Experimental example 1> After sputtering AlSiON to a thickness of 800 mm as a first multiple interference film on the signal pattern surface of a polycarbonate substrate, the inside of a vacuum vessel containing the substrate was 5x10.
-5 [Pa], and then supply pure argon gas as a sputtering gas into the vacuum vessel to adjust the gas pressure in the vacuum vessel to a predetermined value.
The TbFeCo film was sputtered to a thickness of 250 mm.
TbFeCo膜形成後、この真空容器内を再度5×10-5〔P
a〕まで真空引きし、この中で前記TbFeCo膜を15〔分
間〕、80〔℃〕に加熱した。After the formation of the TbFeCo film, the inside of the vacuum vessel was again filled with 5 × 10 −5 [P
a), and the TbFeCo film was heated to 80 ° C. for 15 minutes in this.
加熱後、このTbFeCo膜上に、第2の多重干渉膜として
AlSiONを800Åの厚さにスバッタリングし、さらにこのA
lSiON膜上に、熱拡散膜としてAlCrを750Åの厚さにスバ
ッタリングして、ディスク状光磁気記録媒体とした。After heating, a second multiple interference film is formed on this TbFeCo film.
AlSiON is sputtered to a thickness of 800 mm, and this A
On the lSiON film, AlCr was sputtered to a thickness of 750 mm as a thermal diffusion film to obtain a disk-shaped magneto-optical recording medium.
〈実験例2〉 ポリカーボネート基板の信号パターン面に、第1の多
重干渉膜としてAlSiONを800Åの厚さにスバッタリング
した後、この基板が収められた真空容器内を2×10
-5〔Pa〕まで真空引きし、次いで、この真空容器内にス
バッタガスとしてアルゴン99〔原子%〕、窒素1〔原子
%〕の混合ガスを供給して真空容器内のガス庄を所定の
値に調整し、このガス圧条件のもとでTbFeCo膜を250Å
の厚さにスバッタリングした。<Experimental Example 2> AlSiON was sputtered to a thickness of 800 mm as a first multiple interference film on the signal pattern surface of a polycarbonate substrate, and then the inside of a vacuum vessel containing the substrate was 2 × 10 4.
-5 [Pa], and a gas mixture of 99 [at%] of argon and 1 [at%] of nitrogen is supplied as a sputtering gas into the vacuum vessel to adjust the gas pressure in the vacuum vessel to a predetermined value. The TbFeCo film was adjusted to 250 ガ ス under this gas pressure condition.
Was sputtered to a thickness of
TbFeCo膜形成後、加熱処理を施すことなく、直ちに、
このTbFeCo膜上に、第2の多重干渉膜と熱拡散膜とを形
成してディスク状光磁気記録媒体とした。第2の多重干
渉膜および熱拡散膜の組成、膜厚、成膜方法は、前記実
験例1と同じである。Immediately after forming the TbFeCo film, without performing heat treatment,
A second multiple interference film and a heat diffusion film were formed on the TbFeCo film to obtain a disk-shaped magneto-optical recording medium. The composition, film thickness, and film forming method of the second multiple interference film and the thermal diffusion film are the same as those in Experimental Example 1.
〈実験例3〉 ポリカーボネート基板の信号パターン面に、第1の多
重干渉膜としてAlSiONを800Åの厚さにスパツ久リング
した後、この基板が収められた真空容器内を2×10
-4〔Pa〕まで真空引きし、次いで、この真空容器内にス
バッタガスとして純アルゴンガスを供給して真空容器内
のガス圧を所定の値に調整し、このガス圧条件のもとで
TbFeCo膜を250Åの厚さにスバッタリングした。<Experimental Example 3> After a sputtered AlSiON layer having a thickness of 800 mm was formed as a first multiple interference film on the signal pattern surface of a polycarbonate substrate, the inside of a vacuum vessel containing the substrate was 2 × 10 4.
-4 (Pa), and then supply pure argon gas as a sputtering gas into the vacuum vessel to adjust the gas pressure in the vacuum vessel to a predetermined value.
The TbFeCo film was sputtered to a thickness of 250 mm.
TbFeCo膜形成後、この真空容器内の真空度を3×10-4
〜5×10-5〔Pa〕に調整し、この中に前記TbFeCo膜を30
〔分間〕放置した。このときのTbFeCo膜の温度は、40
〔℃〕であった。After forming the TbFeCo film, the degree of vacuum in the vacuum vessel is reduced to 3 × 10 -4
55 × 10 −5 [Pa], and the TbFeCo film was 30
[Minute] Left. At this time, the temperature of the TbFeCo film is 40
[° C].
放置後、このTbFeCo膜上に、第2の多重干渉膜と熱拡
散膜とを形成してディスク状光磁気記録媒体とした。第
2の多重干渉膜および熱拡散膜の組成、膜厚、成膜方法
は、前記実験例1と同じである。After the standing, a second multiple interference film and a heat diffusion film were formed on the TbFeCo film to obtain a disk-shaped magneto-optical recording medium. The composition, film thickness, and film forming method of the second multiple interference film and the thermal diffusion film are the same as those in Experimental Example 1.
〈実験例4〉 ポリカーボネート基板の信号パターン面に、第1の多
重干渉膜としてAlSiONを800Åの厚さにスバッタリング
した後、この基板が収められた真空容器内を2×10
-5〔Pa〕まで真空引きし、次いで、この真空容器内にス
バッタガスとしてアルゴン99.5〔原子%〕、窒素0.5
〔原子%〕の混合ガスを供給して真空容器内のガス圧を
所定の値に調整し、このガス圧条件のもとでTbFeCo膜を
250Åの厚さにスバッタリングした。<Experimental Example 4> After sputtering AlSiON to a thickness of 800 mm as a first multiple interference film on the signal pattern surface of a polycarbonate substrate, the inside of a vacuum vessel containing the substrate was 2 × 10 4.
-5 [Pa] and then 99.5 [at.%] Of argon and 0.5
[Atomic%] gas mixture is supplied to adjust the gas pressure in the vacuum vessel to a predetermined value, and the TbFeCo film is formed under the gas pressure conditions.
Sputtered to a thickness of 250 mm.
TbFeCo膜形成後、加熱処理を施すことなく、直ちに、
このTbFeCo膜上に、第2の多重干渉膜と熱拡散膜とを形
成してディスク状光磁気記録媒体とした。第2の多重干
渉膜および熱拡散膜の組成、膜厚、成膜方法は、前記実
験例1と同じである。Immediately after forming the TbFeCo film, without performing heat treatment,
A second multiple interference film and a heat diffusion film were formed on the TbFeCo film to obtain a disk-shaped magneto-optical recording medium. The composition, film thickness, and film forming method of the second multiple interference film and the thermal diffusion film are the same as those in Experimental Example 1.
〈実験例5〉 ポリカーボネート基板の信号パターン面に、第1の多
重干渉膜としてAlSiONを800Åの厚さたスバッタリング
した後、この基板が収められた真空容器内を2×10
-5〔Pa〕まで真空引きし、次いで、この真空容器内にス
バッタガスとしてアルゴン99.5〔原子%〕、窒素0.4
〔原子%〕、酸素0.1〔原子%〕の混合ガスを供給して
真空容器内のガス圧を所定の値に調整し、このガス圧条
件のもとで前記AlSiON膜上にTbFeCo膜を250Åの厚さに
スバッタリングした。<Experimental Example 5> AlSiON was sputtered to a thickness of 800 ° as a first multiple interference film on the signal pattern surface of a polycarbonate substrate, and then the inside of a vacuum vessel containing the substrate was 2 × 10 4.
-5 [Pa] and then 99.5 [at.%] Of argon and 0.4
A gas mixture of [atomic%] and oxygen 0.1 [atomic%] was supplied to adjust the gas pressure in the vacuum vessel to a predetermined value. Under this gas pressure condition, a TbFeCo film was formed on the AlSiON film by 250 ° C. Sputtered to thickness.
TbFeCo膜形成後、加熱処理を施すことなく、直ちに、
このTbFeCo膜上に、第2の多重干渉膜と熱拡散膜とを順
次積層してディスク状光磁気記録媒体とした。第2の多
重干渉膜および熱拡散膜の組成、膜厚、成膜方法は、前
記実験例1と同じである。Immediately after forming the TbFeCo film, without performing heat treatment,
On this TbFeCo film, a second multiple interference film and a heat diffusion film were sequentially laminated to obtain a disk-shaped magneto-optical recording medium. The composition, film thickness, and film forming method of the second multiple interference film and the thermal diffusion film are the same as those in Experimental Example 1.
〈比較例〉 ポリカーボネート基板の信号パターン面に、第1の多
重干渉膜としてAlSiONを800Åの厚さにスバッタリング
した後、この基板が収められた真空容器内を5×10
-5〔Pa〕まで真空引きし、次いで、この真空容器内にス
バッタガスとして純アルゴンガスを供給して真空容器内
のガス圧を所定の値に調整し、このガス圧条件のもとで
前記AlSiON膜上にTbFeCo膜を250Åの厚さにスバッタリ
ングした。<Comparative Example> After sputtering AlSiON to a thickness of 800 mm as a first multiple interference film on the signal pattern surface of a polycarbonate substrate, the inside of a vacuum vessel containing the substrate was 5x10.
-5 [Pa], and then pure argon gas was supplied as a sputtering gas into the vacuum vessel to adjust the gas pressure in the vacuum vessel to a predetermined value. A TbFeCo film was sputtered to a thickness of 250 mm on the film.
TbFeCo膜形成後、加熱処理を施すことなく、直ちに、
このTbFeCo膜上に、第2の多重干渉膜と熱拡散膜とを順
次積層してディスク状光磁気記録媒体とした。第2の多
重干渉膜および熱拡散膜の組成、膜厚、成膜方法は、前
記実験例1と同じである。Immediately after forming the TbFeCo film, without performing heat treatment,
On this TbFeCo film, a second multiple interference film and a heat diffusion film were sequentially laminated to obtain a disk-shaped magneto-optical recording medium. The composition, film thickness, and film forming method of the second multiple interference film and the thermal diffusion film are the same as those in Experimental Example 1.
第8図に、前記各実験例および比較例に係る光磁気記
録媒体の製造方法の概略と、各方法によって製造された
光磁気記録媒体のC/N、飽和記録磁界、消去磁界、それ
に光磁気記録膜4中の窒素混入率および酸素混入率を示
す。FIG. 8 shows the outline of the method of manufacturing the magneto-optical recording medium according to each of the experimental examples and the comparative examples, the C / N, the saturation recording magnetic field, the erasing magnetic field, and the magneto-optical properties of the magneto-optical recording medium manufactured by each method. The nitrogen mixing rate and the oxygen mixing rate in the recording film 4 are shown.
この図から明らかなように、実験例1〜5の光磁気記
録媒体は、再生出力信号のC/Nが比較例(従来例)の光
磁気記録媒体と同程度であるのに対し、蝕和紀録磁界は
従来例の50%程度に低下し、消去磁界は従来例の40%に
低下している。従って、情報の記録および消去に必要な
外部磁界の小型化、軽量化を図ることができ、マグネッ
ト電源部の簡素化、消費電力の低減、記録/再生装置の
小型化、それに記録、消去動作の高速化などを図ること
ができる。また、媒体側から見れば、外部磁界と光磁気
記録媒体との距離変動や発熱による磁場の変動に対して
大きな余裕をもたせることができ、信頼性に優れた光磁
気記録媒体とすることができる。As is clear from this figure, the magneto-optical recording media of Experimental Examples 1 to 5 have the same C / N of the reproduction output signal as the magneto-optical recording media of the comparative example (conventional example), but The recorded magnetic field is reduced to about 50% of the conventional example, and the erase magnetic field is reduced to 40% of the conventional example. Therefore, the external magnetic field required for recording and erasing information can be reduced in size and weight, and the magnet power supply unit can be simplified, the power consumption can be reduced, the recording / reproducing device can be downsized, and the recording and erasing operations can be performed. Higher speed can be achieved. Further, when viewed from the medium side, a large margin can be provided for the fluctuation in the distance between the external magnetic field and the magneto-optical recording medium and the fluctuation in the magnetic field due to heat generation, and a highly reliable magneto-optical recording medium can be obtained. .
なお、前記実施例においては、基板の信号パターン面
に第1の多重干渉膜と、光磁気記録膜と、第2の多重干
渉膜と、熱拡散膜とが積層された光磁気記録媒体を例に
とって説明したが、本発明の要旨がこれに限定されるも
のではなく、少なくとも光磁気記録膜を有するものであ
れば、任意の膜構造を有する光磁気記録媒体に応用する
ことができる。In the above embodiment, a magneto-optical recording medium in which a first multiple interference film, a magneto-optical recording film, a second multiple interference film, and a heat diffusion film are laminated on a signal pattern surface of a substrate is taken as an example. However, the gist of the present invention is not limited to this, and the invention can be applied to a magneto-optical recording medium having an arbitrary film structure as long as it has at least a magneto-optical recording film.
[発明の効果] 以上説明したように、本発明の光磁気記録媒体は、基
板上に、クロム、チタンまたはニオブが添加された希土
類−遷移金属系の非晶質合金からなる光磁気記録膜と、
シリコン、アルミニウム、ジルコニウム、チタンまたは
タンタルの窒化物もしくは酸化物からなる無機誘電体膜
を担持してなる光磁気記録媒体において、前記光磁気記
録膜中に、前記非晶質合金に対して総量で0.1〜5.0〔原
子%〕の窒素および酸素を含有するという構成にしたの
で、再生信号出力レベルを低下することなく、情報の記
録および消去に必要な外部磁界の小型化を図ることがで
きる。[Effects of the Invention] As described above, the magneto-optical recording medium of the present invention has a magneto-optical recording film made of a rare earth-transition metal based amorphous alloy to which chromium, titanium, or niobium is added. ,
In a magneto-optical recording medium carrying an inorganic dielectric film made of silicon, aluminum, zirconium, titanium or tantalum nitride or oxide, the magneto-optical recording film contains a total amount of the amorphous alloy. Since the composition contains 0.1 to 5.0 [atomic%] of nitrogen and oxygen, it is possible to reduce the external magnetic field required for recording and erasing information without lowering the output level of the reproduction signal.
第1図は光磁気記録媒体の膜構造の一例を模式的に示す
要部断面図、第2図は窒素混入率および酸素混入率と垂
直磁気異方性定数との関係を示すグラフ図、第3図は窒
素混入率および酸素混入率と残留カー回転角との関係を
示すグラフ図、第4図は光磁気記録媒体に積層された各
膜の組成と膜厚の一例を示す表図、第5図は第4図の光
磁気記録媒体を用いて測定した窒素混入率および酸素混
入率と再生出力信号のC/Nとの関係を示すグラフ図、第
6図は第4図の光磁気記録媒体を用いて測定した窒素混
入率および酸素混入率と飽和記録磁界との関係を示すグ
ラフ図、第7図は第4図の光磁気記録媒体を用いて測定
した窒素混入率および酸素混入率と消去磁界との関係を
示すグラフ図、第8図は実験例および比較例に係る光磁
気記録媒体の製造法とC/Nと飽和記録磁界と消去磁界と
窒素混入率と酸素混入率とを示す表図である。 1……透明基板、2……信号パターン面、3……第1の
多重干渉膜、4……光磁気記録膜、5……第2の多重干
渉膜、6……熱拡散膜。FIG. 1 is a cross-sectional view of a principal part schematically showing an example of a film structure of a magneto-optical recording medium, FIG. 2 is a graph showing a relationship between a nitrogen mixing ratio and an oxygen mixing ratio and a perpendicular magnetic anisotropy constant, FIG. 3 is a graph showing the relationship between the nitrogen mixing ratio and oxygen mixing ratio and the residual Kerr rotation angle. FIG. 4 is a table showing an example of the composition and thickness of each film laminated on the magneto-optical recording medium. FIG. 5 is a graph showing the relationship between the nitrogen mixing ratio and oxygen mixing ratio measured using the magneto-optical recording medium of FIG. 4 and the C / N of the reproduced output signal, and FIG. 6 is the magneto-optical recording of FIG. FIG. 7 is a graph showing the relationship between the nitrogen mixing rate and oxygen mixing rate measured using the medium and the saturation recording magnetic field. FIG. 7 shows the nitrogen mixing rate and oxygen mixing rate measured using the magneto-optical recording medium of FIG. FIG. 8 is a graph showing a relationship with an erasing magnetic field, and FIG. 8 is a method for manufacturing a magneto-optical recording medium according to an experimental example and a comparative example. Is a table showing a C / N and saturated recording magnetic field and the erasing magnetic field and the nitrogen incorporation rate and oxygen mixture ratio. 1 ... transparent substrate, 2 ... signal pattern surface, 3 ... first multiple interference film, 4 ... magneto-optical recording film, 5 ... second multiple interference film, 6 ... thermal diffusion film.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 大貫 悟 大阪府茨木市丑寅1丁目1番88号 日立 マクセル株式会社内 (72)発明者 荻原 典之 大阪府茨木市丑寅1丁目1番88号 日立 マクセル株式会社内 (56)参考文献 特開 平2−302949(JP,A) 特開 平3−66048(JP,A) 特開 平1−208749(JP,A) 特開 平1−133240(JP,A) 特開 平1−311438(JP,A) 特開 昭62−132254(JP,A) 特開 昭61−87306(JP,A) 特開 昭61−84803(JP,A) 特開 昭61−144743(JP,A) 特開 昭63−66746(JP,A) ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Satoru Onuki 1-1-88 Ushitora, Ibaraki-shi, Osaka Hitachi Maxell Co., Ltd. (72) Noriyuki Ogihara 1-1-88 Ushitora, Ibaraki-shi, Osaka Hitachi Maxell (56) References JP-A-2-302949 (JP, A) JP-A-3-66048 (JP, A) JP-A-1-208749 (JP, A) JP-A-1-133240 (JP, A A) JP-A 1-311438 (JP, A) JP-A 62-132254 (JP, A) JP-A 61-87306 (JP, A) JP-A 61-84803 (JP, A) JP-A 61 -144743 (JP, A) JP-A-63-66746 (JP, A)
Claims (2)
添加された希土類−遷移金属系の非晶質合金からなる光
磁気記録膜と、シリコン、アルミニウム、ジルコニウ
ム、チタンまたはタンタルの窒化物もしくは酸化物から
なる無機誘電体膜を担持してなる光磁気記録媒体におい
て、前記光磁気記録膜中に、前記非晶質合金に対して総
量で0.1〜5.0〔原子%〕の窒素および酸素を含有したこ
とを特徴とする光磁気記録媒体。1. A magneto-optical recording film comprising a rare earth-transition metal based amorphous alloy to which chromium, titanium or niobium is added, and a nitride or oxide of silicon, aluminum, zirconium, titanium or tantalum on a substrate. In the magneto-optical recording medium carrying an inorganic dielectric film made of a material, the magneto-optical recording film contained nitrogen and oxygen in a total amount of 0.1 to 5.0 [atomic%] with respect to the amorphous alloy. A magneto-optical recording medium characterized by the above-mentioned.
添加された希土類−遷移金属系の非晶質合金からなる光
磁気記録膜と、シリコン、アルミニウム、ジルコニウ
ム、チタンまたはタンタルの窒化物もしくは酸化物から
なる無機誘電体膜を担持してなる光磁気記録媒体におい
て、前記光磁気記録膜中に、前記非晶質合金に対して総
量で0.1〜5.0〔原子%〕の窒素および酸素を含有し、当
該光磁気記録媒体の飽和記録磁界および/または消去磁
界を200〔Oe〕以下にしたことを特徴とする光磁気記録
媒体。2. A magneto-optical recording film comprising a rare earth-transition metal based amorphous alloy to which chromium, titanium or niobium is added, and a nitride or oxide of silicon, aluminum, zirconium, titanium or tantalum on a substrate. In a magneto-optical recording medium carrying an inorganic dielectric film made of a material, the magneto-optical recording film contains nitrogen and oxygen in a total amount of 0.1 to 5.0 [atomic%] with respect to the amorphous alloy. A magneto-optical recording medium, wherein a saturation recording magnetic field and / or an erasing magnetic field of the magneto-optical recording medium is set to 200 [Oe] or less.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP02234372A JP3128232B2 (en) | 1990-09-06 | 1990-09-06 | Magneto-optical recording medium |
| DE69130441T DE69130441T2 (en) | 1990-08-07 | 1991-08-05 | Magneto-optical recording medium |
| EP91113129A EP0470546B1 (en) | 1990-08-07 | 1991-08-05 | Magneto-optical recording medium |
| US08/247,119 US5639563A (en) | 1990-08-07 | 1994-05-20 | Magneto-optical recording medium |
| US08/794,349 US5965286A (en) | 1990-08-07 | 1997-02-03 | Magneto-optical recording medium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP02234372A JP3128232B2 (en) | 1990-09-06 | 1990-09-06 | Magneto-optical recording medium |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04117647A JPH04117647A (en) | 1992-04-17 |
| JP3128232B2 true JP3128232B2 (en) | 2001-01-29 |
Family
ID=16969977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP02234372A Expired - Lifetime JP3128232B2 (en) | 1990-08-07 | 1990-09-06 | Magneto-optical recording medium |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3128232B2 (en) |
-
1990
- 1990-09-06 JP JP02234372A patent/JP3128232B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04117647A (en) | 1992-04-17 |
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