JPS63266651A - Magneto-optical recording medium - Google Patents

Magneto-optical recording medium

Info

Publication number
JPS63266651A
JPS63266651A JP32283987A JP32283987A JPS63266651A JP S63266651 A JPS63266651 A JP S63266651A JP 32283987 A JP32283987 A JP 32283987A JP 32283987 A JP32283987 A JP 32283987A JP S63266651 A JPS63266651 A JP S63266651A
Authority
JP
Japan
Prior art keywords
magneto
optical recording
layer
oxide
recording medium
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
JP32283987A
Other languages
Japanese (ja)
Other versions
JP2550118B2 (en
Inventor
Kiyoshi Chiba
潔 千葉
Tetsuo Sato
哲生 佐藤
Masahiko Sekiya
昌彦 関谷
Kazutomi Suzuki
鈴木 和富
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.)
Teijin Ltd
Original Assignee
Teijin Ltd
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Filing date
Publication date
Application filed by Teijin Ltd filed Critical Teijin Ltd
Priority to JP62322839A priority Critical patent/JP2550118B2/en
Publication of JPS63266651A publication Critical patent/JPS63266651A/en
Application granted granted Critical
Publication of JP2550118B2 publication Critical patent/JP2550118B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To form a magneto-optical recording medium having good durability by forming a transparent dielectric layer of a dielectric transparent oxide layer consisting of the oxide of at least one element selected from a group consisting of In and Sn and having specific electric resistivity or above. CONSTITUTION:The dielectric layer 2 of the magneto-optical recording medium provided with a magneto-optical recording layer 3 via the dielectric layer 2 and further a protective layer 4 at need on a transparent synthetic resin substrate 1 is the dielectric transparent oxide layer consisting of the oxide of at least one element selected from the group consisting of In and Sn and having >=1X10<-1>OMEGA.cm electric resistivity. Such oxide film is, for example, the indium oxide (In2 O3) film and/or tin oxide (SnOx) film which has a sufficiently high oxygen concn. and has a low carrier concn. by defects, etc. The magneto-optical recording medium having extremely high environmental resistance and excellent dynamic characteristics by the improved angle of Kerr rotation is thereby obtd.

Description

【発明の詳細な説明】 [利用分野] 本発明はレーザ等の光により情報の記録・再生・消去等
を行う光磁気記録媒体に関する。更に詳細には、透明合
成樹脂基板上に膜面に垂直な方向に磁化容易方向を有し
た金属薄膜よりなる記録層を形成し、磁気光学効果によ
り情報を記録再生する光磁気記録に用いられる耐環境性
の秀れた光磁気記録媒体に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Application] The present invention relates to a magneto-optical recording medium in which information is recorded, reproduced, erased, etc. using light such as a laser. More specifically, a recording layer made of a thin metal film with the direction of easy magnetization perpendicular to the film surface is formed on a transparent synthetic resin substrate, and information is recorded and reproduced using the magneto-optic effect. Concerning magneto-optical recording media with excellent environmental friendliness.

[従来技術] 光記録媒体は高密度・大容量の情報記録として種々の研
究開発が行なわれている。特に情報の消去可能な光磁気
記録媒体は応用分野が広く種々の材料・システムが発表
されており、その実用化が待望されている。
[Prior Art] Various research and developments are being conducted on optical recording media for high-density, large-capacity information recording. In particular, a wide variety of materials and systems have been announced for use in erasable magneto-optical recording media, and their practical application is eagerly awaited.

上述の光磁気記録材料としては、例えば、特開昭52−
31703号公報記載のFe Tb、特開昭56−12
6907号公報記載のFe rb Gd、特開昭58−
73746Q公報記載のFe rb Co、 re C
o Dy、特開昭61−165846号公報記載のre
 Nd等既に多くの提案がある。しかし、これらの情報
の消去可能な光磁気記録媒体の実用化には、記録・再生
特性のより一層の向上及びその記録層を構成覆る記憶材
料の大半は酸化等の腐蝕を起こしゃ覆い為、その耐酸化
性を含めた耐久性を向上させることが必要と言われてい
る。
As the above-mentioned magneto-optical recording material, for example, JP-A-52-
FeTb described in Publication No. 31703, JP-A-56-12
Ferb Gd described in Publication No. 6907, JP-A-58-
Ferb Co, re C described in 73746Q publication
o Dy, re described in JP-A-61-165846
There are already many proposals such as Nd. However, in order to put these information erasable magneto-optical recording media into practical use, it is necessary to further improve the recording and reproducing characteristics, and to protect the majority of the storage materials that make up the recording layer from corrosion such as oxidation. It is said that it is necessary to improve its durability including its oxidation resistance.

これに対して、例えば特開昭59110052 号公報
には、光メーしり素子の記録層を少なくとも一方が誘電
体層である2層の酸素を含有しない膜間に挟持すること
により記録層の酸化を防止することが提案されている。
On the other hand, for example, Japanese Patent Application Laid-Open No. 59110052 discloses that the recording layer of an optical metering element is sandwiched between two oxygen-free films, at least one of which is a dielectric layer, thereby preventing oxidation of the recording layer. It is proposed to prevent

またこのような基板と記録層との間に誘電体を設けてカ
ー回転角を向上させることが広く知られている。そして
この場合においては誘電体層は酸素を含有していないこ
とが必要であり、誘電体層としてはAi’N、 M[F
2 、7.n3. CcF:+ 、 Affil−+ 
 ・3NaF、 Si3N4等の窒化物、弗化物等で形
成されることが好ましいとされている。
Furthermore, it is widely known that a dielectric material is provided between such a substrate and a recording layer to improve the Kerr rotation angle. In this case, it is necessary that the dielectric layer does not contain oxygen, and the dielectric layer is made of Ai'N, M[F
2, 7. n3. CcF:+, Affil-+
- It is said that it is preferable to use nitride, fluoride, etc. such as 3NaF and Si3N4.

ところでこれらの中で耐環境性に秀れているといわれる
AI!N、 S!:+ N4等の窒化膜について検討し
たところ、その製膜速度が遅いこと、また膜中ヒズミが
大きく特にプラスチックス基板上に多層膜を形成した場
合、環境劣化試験によりグループに沿った剥離等が生じ
る問題があり、耐酸化性とは別の面での耐久性での問題
があること等より一層の改善が必要なことがわかった。
By the way, among these, AI is said to have excellent environmental resistance! N, S! :+ When we investigated nitride films such as N4, we found that the film formation speed was slow, and the distortion in the film was large, especially when a multilayer film was formed on a plastic substrate. It was found that further improvements were needed, including problems with durability in aspects other than oxidation resistance.

[発明の[1的] 本発明はかかる現状に鑑みなされたもので、透明合成樹
脂基板上に誘電体Mを介して記録層を有する耐久性の良
い光磁気記録媒体を目的とするものである。すなわら、
具体的には前記記録媒体の環境安定化をはかり特に基板
と誘電体層界面の劣化によるワレ、剥離を防止すること
を第1の目的とする。また誘電体層と光磁気合金層との
界面の安定化を第2の目的とする。また、プラスチック
基板よりあるいは基板を通し光磁気記録層界面に侵入す
る特に 112O等の劣化因子を抑制することを第3の
目的とする。
[Object 1 of the Invention] The present invention was made in view of the current situation, and its object is to provide a highly durable magneto-optical recording medium having a recording layer on a transparent synthetic resin substrate via a dielectric M. . In other words,
Specifically, the first objective is to stabilize the environment of the recording medium, and particularly to prevent cracking and peeling due to deterioration of the interface between the substrate and the dielectric layer. A second purpose is to stabilize the interface between the dielectric layer and the magneto-optical alloy layer. A third purpose is to suppress deterioration factors, particularly 112O, which enter the interface of the magneto-optical recording layer through or through the plastic substrate.

[発明の構成2作用] 上述の目的は、以下の本発明により達成される。[Configuration 2 of the invention] The above objects are achieved by the invention as follows.

すなわら本発明は透明合成樹脂基板上に誘電体層を介し
て光磁気記録層、更には必要に応じ保護層を設けた光磁
気記録媒体において、前記誘電体層がIn及びSnから
なる群から選ばれた少なくとも一つの元素の酸化物から
なり、電気抵抗率が1×10’ Q・cm以上の誘電性
の透明酸化物層であることを特徴とする光磁気記録媒体
である。なお、以下この本発明の光磁気記録媒体を本発
明媒体、透明酸化物層をIn及び/又はSnの酸化物層
という。
That is, the present invention provides a magneto-optical recording medium in which a magneto-optical recording layer and, if necessary, a protective layer are provided on a transparent synthetic resin substrate via a dielectric layer, wherein the dielectric layer is made of a group consisting of In and Sn. This is a magneto-optical recording medium characterized by a dielectric transparent oxide layer comprising an oxide of at least one element selected from the following, and having an electrical resistivity of 1×10' Q·cm or more. Hereinafter, the magneto-optical recording medium of the present invention will be referred to as the present invention medium, and the transparent oxide layer will be referred to as an In and/or Sn oxide layer.

本発明媒体において、In及び/又はsnの透明酸化物
からなる誘電体層は、物理的堆積(physrca+V
apor Deposition : P V D )
法により形成される。
In the inventive medium, the dielectric layer consisting of In and/or sn transparent oxide is formed by physical deposition (physrca+V
apor Deposition: PVD)
Formed by law.

また本発明媒体において酸化物膜と光磁気膜との間に金
属チタン膜からなる保護層を設けることが耐酸化性、耐
透湿性の向上面から好ましい。金属チタン膜の膜厚は記
録・再生面から50Å以下、更には2OÅ以下が好まし
い。
Further, in the medium of the present invention, it is preferable to provide a protective layer made of a metallic titanium film between the oxide film and the magneto-optical film in terms of improving oxidation resistance and moisture permeation resistance. The thickness of the metallic titanium film is preferably 50 Å or less, more preferably 20 Å or less from the recording/reproducing surface.

本発明媒体の誘電体層はIn及び/又はSnの誘電性の
酸化物層で誘電体層の作用を奏するものであれば良いが
、記録特性面から電気抵抗率が1×10−1Ωcm以上
の不良導電性の充分酸化された酸化物が好ましい。かか
る酸化物としては例えば酸素潤度が充分高く、かつ欠陥
等によるキャリアー濃度の少ない酸化インジウム(In
2O.+)膜及び/又は錫酸化物(SnOx )膜であ
る。またIn2O3及び/又はSnQ x酸化物中に不
純物としてTa、 sb、  F等を含んだものでも良
い。中でも、InQ3膜或いは錫酸化物を含む主として
Inz 03からなる酸化物膜が耐久t1面、読み取り
レーザー電力が低い面から好ましい。なお、この酸化物
の錫酸化物の含有量は30wt%以下、好ましくは7w
t%以下であり、屈折率の面から更に好ましくは3wt
%以下である。
The dielectric layer of the medium of the present invention may be a dielectric oxide layer of In and/or Sn, as long as it functions as a dielectric layer. Well-oxidized oxides with poor electrical conductivity are preferred. Examples of such oxides include indium oxide (In), which has a sufficiently high oxygen moisture content and a low carrier concentration due to defects, etc.
2O. +) film and/or a tin oxide (SnOx) film. Alternatively, In2O3 and/or SnQx oxide may contain Ta, sb, F, etc. as impurities. Among these, an InQ3 film or an oxide film mainly composed of Inz 03 containing tin oxide is preferable from the viewpoint of durability t1 and low reading laser power. Note that the content of tin oxide in this oxide is 30 wt% or less, preferably 7 wt%.
t% or less, more preferably 3wt in terms of refractive index
% or less.

これらのIn2O3及び/又はSnOxの層は前述の通
り、公知の真空蒸着法、スパッタリング法等のPVD法
で作られるが、高温高湿耐環境性試験で生じるハガレを
生じさせないためにプラスチック基板との接摺性が大ぎ
い条件で作製することが好ましい。この為にはスパッタ
リング法が好ましい。
As mentioned above, these In2O3 and/or SnOx layers are made by known PVD methods such as vacuum evaporation and sputtering. It is preferable to manufacture under conditions where the sliding property is large. For this purpose, sputtering is preferred.

なお、本発明の誘電体層を構成するIn及び/又はSn
金属を含む誘電性の酸化膜には以下の通り透明導電層と
して知られた膜例えば酸化インジウム膜、インジウム・
錫酸化物膜(ITO)等は含まれない。すなわら、透明
導電膜として知られている導電性の電気抵抗率が10−
2−10−4Ω・ciiのIn及び/又はSn金属を含
む酸化膜は熱伝導性も良く、レーザ光によりスポット状
に高温となる媒体記録部よりの導電性酸化膜側への熱の
散逸が起り、必要記録レーザパワーが高くなること、ま
たビット形状が乱れC/Nが低下する。更に、高湿度雰
囲気において鉄系合金層と導電性酸化物層との間に電気
化学的電流が流れ、光磁気記録媒体の環境劣化を促進す
る。このため、In及び/又はSnn行右導電性酸化物
層は光磁気記録媒体への適用は困難である。更に、電気
抵抗率が10−4Ω・cm稈度の導電性のIn又は/及
びsnを含む酸化物層はキX・リアー濃度が高くプラズ
マ振動による近赤外レーザ光に対する反射損失が生じる
Note that In and/or Sn constituting the dielectric layer of the present invention
Dielectric oxide films containing metal include films known as transparent conductive layers, such as indium oxide films, indium oxide films, etc.
It does not include a tin oxide film (ITO) or the like. In other words, the conductive electrical resistivity known as a transparent conductive film is 10-
The oxide film containing In and/or Sn metals with a resistance of 2-10-4Ω·cii has good thermal conductivity, and the heat dissipates from the medium recording area, which becomes hot in a spot shape due to laser light, to the conductive oxide film side. As a result, the required recording laser power increases, and the bit shape becomes disordered, resulting in a decrease in C/N. Furthermore, an electrochemical current flows between the iron-based alloy layer and the conductive oxide layer in a high humidity atmosphere, promoting environmental deterioration of the magneto-optical recording medium. Therefore, it is difficult to apply the In and/or Snn row right conductive oxide layer to magneto-optical recording media. Furthermore, the conductive oxide layer containing In and/or Sn and having an electrical resistivity of 10<-4 >[Omega].cm has a high concentration of x-rea, causing reflection loss to near-infrared laser light due to plasma vibration.

ざらにポリカーボネート、アクリル樹脂等の透明プラス
チックディスク基板に通常In及び/又はSn金属を含
む酸化膜を透明導電膜として形成するためには通常膜形
成時100℃程度の基板加熱が必要となり、この熱的因
子によりプラスチック基板表面のグループが乱れ良好な
媒体の実現は困難でおる。以上より本発明には上述の透
明導電膜は適用されない。
In order to form an oxide film containing In and/or Sn metal as a transparent conductive film on a transparent plastic disk substrate such as polycarbonate or acrylic resin, it is usually necessary to heat the substrate to about 100°C during film formation. Due to various factors, the groups on the surface of the plastic substrate are disordered, making it difficult to realize a good medium. From the above, the above-mentioned transparent conductive film is not applicable to the present invention.

本発明媒体においては、透明酸化物層はインジウムある
いは錫の酸化物、更にはこれらの両金属を含む酸化物か
らなる。
In the medium of the present invention, the transparent oxide layer is made of an oxide of indium or tin, or an oxide containing both of these metals.

本発明媒体において、錫酸化物層は誘電性具体的にはそ
の電気低効率がlXl0−1Ω・cm以上の錫の酸化物
であれば、いかなるものでも良い。好ましくは、記録・
再生に使用されるレーザー光の吸収が小さい点から1≦
X≦2のSnOXである。
In the medium of the present invention, the tin oxide layer may be any tin oxide as long as it has a dielectric property, specifically, an electrical efficiency of lXl0-1 Ω·cm or more. Preferably, recording
1≦ due to low absorption of laser light used for reproduction
It is SnOX with X≦2.

In及び/又はSnを含む酸化物からなる誘電体層の屈
折率は読み出しレーザー光の波長に対して1゜7以上で
なければならず、更にカー回転角を適当に増加させる而
からは1.9以上が好ましい。
The refractive index of the dielectric layer made of an oxide containing In and/or Sn must be 1.7 or more with respect to the wavelength of the readout laser beam, and in order to increase the Kerr rotation angle appropriately, the refractive index must be 1.7 or more. 9 or more is preferable.

次にIn及び/又はsn含有の酸化物層の効果を、従来
技術と対比しつつ説明する。
Next, the effect of the oxide layer containing In and/or sn will be explained in comparison with the conventional technology.

透明プラスチック基板を用い、膜面反射によるカー回転
角を大ぎくする為基板と光磁気記録層との間に誘電体膜
を設けた従来の光磁気記録媒体では、前述の通り誘電体
膜として代表的な公知のSiO,zns、MN、Si:
+ N4等を用イティスクを構成した場合、高温高湿及
び又はヒートリイクルによる耐久性試験を行うとディス
クに亀裂がはいり光磁気特性が急激に劣化することが観
察された。
In conventional magneto-optical recording media, a transparent plastic substrate is used, and a dielectric film is provided between the substrate and the magneto-optical recording layer in order to greatly increase the Kerr rotation angle due to film surface reflection. Known SiO, zns, MN, Si:
When a disk was constructed using +N4 or the like, it was observed that when a durability test was conducted under high temperature and high humidity conditions and/or heat recycling, cracks appeared in the disk and the opto-magnetic properties rapidly deteriorated.

これは本発明者らの研究によれば、主にプラスチック基
板界面での誘電体膜のはがれに起因する。
According to research conducted by the present inventors, this is mainly due to peeling of the dielectric film at the interface of the plastic substrate.

ところが本発明による誘電体層にIn及び/又はSn金
属の誘電性の酸化膜を用いたディスクではおどろくべき
ことにこの界面での劣化によるハクリは生じず、ディス
クの耐久性が著しく改善される作用があることを見出し
た。これは該In及び/又はSn金属の酸化膜とプラス
ブック界面、特にポリカーボネート基板との親和性が大
きいことによるものと思われる。これらの改良は通常の
環境下での長期安定性と共にヒートリイクル、ヒートシ
ョックに対して特に有効となる。また、さらに本発明の
酸化物膜の誘電体層と光磁気記録層との間にTiの薄膜
を設けることにより酸化物表面に吸着する02あるいは
H2Oをトラップする作用があり、酸素による光磁気記
録層の劣化を防ぎ、耐久性をより増すことができる。[
iの熱膨張率は誘電体層と記録層の鉄系合金の熱膨張率
の中間値となるので、そのインターフェースでの熱的シ
ョックに起因するストレスが減少し、媒体は安定化する
。保護層のチタンは酸化されるが、その屈折率は元々1
.8以上であり、その変化は小さい。チタンは屈折率の
酸化への依存性が上述の小さい範囲にある限り合金であ
っても良い。チタン保護層は記録・再生面から50Å以
下の厚さが好ましく、この場合のこの層により光吸収は
2O%以下となる。厚み2OA以下のチタン保護層が該
光吸収が5%以下である点で更に好ましい。
However, in the case of the disk in which a dielectric oxide film of In and/or Sn metal is used as the dielectric layer according to the present invention, surprisingly, peeling does not occur due to deterioration at this interface, and the durability of the disk is significantly improved. I found out that there is. This is thought to be due to the high affinity between the In and/or Sn metal oxide film and the interface between the plastic book and the polycarbonate substrate in particular. These improvements improve long-term stability under normal environments and are particularly effective against heat recycling and heat shock. Further, by providing a Ti thin film between the dielectric layer and the magneto-optical recording layer of the oxide film of the present invention, there is an effect of trapping O2 or H2O adsorbed on the oxide surface, and magneto-optical recording using oxygen is achieved. This prevents layer deterioration and increases durability. [
Since the coefficient of thermal expansion of i is an intermediate value between the coefficients of thermal expansion of the dielectric layer and the iron-based alloy of the recording layer, stress caused by thermal shock at the interface is reduced and the medium is stabilized. Titanium in the protective layer is oxidized, but its refractive index was originally 1.
.. 8 or more, and the change is small. Titanium may be an alloy as long as the dependence of the refractive index on oxidation is within the above-mentioned small range. The titanium protective layer preferably has a thickness of 50 Å or less from the recording/reproducing surface, and in this case, this layer provides light absorption of 20% or less. A titanium protective layer having a thickness of 2 OA or less is more preferable since the light absorption is 5% or less.

次に本発明媒体、すなわちIn及び/又は釦の誘電性透
明酸化物層の誘電体層を備えたもの、この誘電体層と記
録層との間にチタン保護層を備えたものにおける光磁気
配B層2合成樹脂基板、光磁気記録層の保護層について
説明する。
Next, the magneto-optical distribution in the medium of the present invention, that is, the one provided with a dielectric layer of In and/or dielectric transparent oxide layer, and the one provided with a titanium protective layer between this dielectric layer and the recording layer. The protective layer of the B layer 2 synthetic resin substrate and magneto-optical recording layer will be explained.

本発明の光磁気記録層としては、光磁気効果により記録
、再生できるものであれば良く、公知の膜面に垂直な方
向に磁化容易方向を有し任意の反転磁区を作ることによ
り光磁気効果に基いて情報の記録再生が可能な磁性金属
薄膜、例えばre rb金合金のFe Tb Co合金
、 F’e Tb Gd金合金、 ト’eCooyNd
、 FeCoDyNdTi等のre−Nd系の合金、F
e−Pr、re−3m、 Fe−Ce系の各合金等が適
用できる。
The magneto-optical recording layer of the present invention may be of any type as long as it can be recorded and reproduced by the magneto-optical effect, and the magneto-optical recording layer can be made to have an easy magnetization direction perpendicular to the known film surface and create arbitrary reversal magnetic domains. Magnetic metal thin films capable of recording and reproducing information based on
, re-Nd alloy such as FeCoDyNdTi, F
E-Pr, re-3m, Fe-Ce alloys, etc. can be used.

本発明における合成樹脂基板としてはポリカーボネート
樹脂、アクリル樹脂、エポキシ樹脂、4−メヂルーベン
テン樹脂などまたそれらの共重合体などが適用できるが
、機械強度、耐候性、耐熱性、透湿mの点でポリカーボ
ネート樹脂が好ましい。
As the synthetic resin substrate in the present invention, polycarbonate resin, acrylic resin, epoxy resin, 4-medylbentene resin, and copolymers thereof can be used, but polycarbonate is preferable in terms of mechanical strength, weather resistance, heat resistance, and moisture permeability. Resins are preferred.

本発明の光磁気記録層の基板と反対側に設ける保護膜と
しては、誘電体及び/又は金属等が用いられる。保護膜
の場合は酸化物膜と異なりプラスチック基板との接着性
は特に問題とならないため1[体としてはI’d!N、
 M(IF2 、 zns、 CeF:+ 。
As the protective film provided on the side opposite to the substrate of the magneto-optical recording layer of the present invention, dielectric material and/or metal is used. In the case of a protective film, unlike an oxide film, adhesion to the plastic substrate is not a particular problem; N,
M(IF2, zns, CeF:+.

Aif:3” 3NaF、 Si3N4 、 Sin、
 5iOz、 Ti0z。
Aif: 3” 3NaF, Si3N4, Sin,
5iOz, Ti0z.

Zr2O3. In2O3などの窒化物、弗化物、酸化
物などが適用できる。また金属としては熱伝導度の小さ
い物質、すなわらTi、 Zr等が好ましい。これらは
公知の真空蒸着法、スパッタリング法で作製で゛   
ぎる。
Zr2O3. Nitride, fluoride, oxide, etc. such as In2O3 can be applied. Further, the metal is preferably a substance with low thermal conductivity, such as Ti or Zr. These can be manufactured using the well-known vacuum evaporation method or sputtering method.
Giru.

以上の通り本発明はプラスチック基板上に誘電性のIn
及び/又はSn:&属の酸化膜を設けることにより耐環
境性が極めて秀れ且つカー回転角の向上により秀れた動
特性を有する光磁気媒体を実現したものである。
As described above, the present invention provides dielectric In on a plastic substrate.
By providing a Sn:& group oxide film, a magneto-optical medium is realized which has excellent environmental resistance and excellent dynamic characteristics due to an improved Kerr rotation angle.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

[実施例1] 直径2O0mm 、厚さ1.2mmの円板で2.5 μ
mピッチのグループを有するアクリル樹脂(PMMA)
のディスク基板を3ターゲツトの高周波マグネトロンス
パッタ装置くアネルバvIJ製5PF−430型) ノ
真空槽内に固定し、4 x 10−71orr以下にな
るまで排気する。なお、基板1は水冷し、15rpmで
回転させた。
[Example 1] A disc with a diameter of 200 mm and a thickness of 1.2 mm has a thickness of 2.5 μ.
Acrylic resin (PMMA) with m-pitch groups
The disk substrate was fixed in a vacuum chamber of a three-target high-frequency magnetron sputtering device (Model 5PF-430 manufactured by Anelva vIJ), and the vacuum chamber was evacuated to below 4 x 10-71 orr. Note that the substrate 1 was water-cooled and rotated at 15 rpm.

次にへr、Oz混合ガス(Oz 2OVo 1%)を真
空槽内に導入し、圧力1 X 10−2 Torrにな
るように混合ガスの流量を調整し、直径100mm 、
厚さ5開のInの円盤をターゲットとし、放電電力10
0Δ、 hIi電周波周波数136HIIzで高周波反
応性スパッタリングを行ない、誘電体層2としてIn2
O3膜を約800人堆積した。続いて、記録層3として
ターゲットをFe6.T b23  CO8合金(添数
字は組成(原子%)を示す)に変えAr(アルゴン)ガ
ス(5N)を真空槽に導入し上述と同様の放電条件でF
e Tb Co合金膜を約100OA堆積した。
Next, a mixed gas of Oz, Oz (Oz 2OVo 1%) was introduced into the vacuum chamber, the flow rate of the mixed gas was adjusted so that the pressure was 1 X 10-2 Torr, and the diameter was 100 mm.
Targeting an In disk with a thickness of 5 mm, the discharge power was 10 mm.
High-frequency reactive sputtering was performed at a radio frequency of 136HIIz, and In2 was used as the dielectric layer 2.
Approximately 800 people deposited O3 films. Subsequently, as the recording layer 3, a target of Fe6. Argon gas (5N) was introduced into the vacuum chamber instead of the T b23 CO8 alloy (the suffix indicates the composition (atomic %)), and F was heated under the same discharge conditions as above.
e A Tb Co alloy film of about 100 OA was deposited.

最1表に保護層4として誘電体層2と同様にIn2O3
膜を約800人堆積した。
In the first table, In2O3 is used as the protective layer 4 in the same way as the dielectric layer 2.
Approximately 800 people deposited films.

以上の順序で第1図(a)に示すPMMA/In;+ 
Ox/’rbFOco/Inz Owlの積層体ずなわ
ら光磁気記録媒体を得た。この媒体の1点A(第1図(
b)参照)の周囲を光学顕微鏡にて観察し、欠点、剥離
が無いことを確認した。
In the above order, PMMA/In shown in FIG. 1(a);+
A magneto-optical recording medium consisting of a laminate of Ox/'rbFOco/Inz Owl was obtained. One point A on this medium (Fig. 1 (
The surrounding area of (see b) was observed using an optical microscope, and it was confirmed that there were no defects or peeling.

この積層体を60℃、90%Rtlの恒温恒湿下に90
時間放置した。
This laminate was kept at constant temperature and humidity at 60°C and 90% RTL for 90 minutes.
I left it for a while.

その後、光学顕微鏡にて前述の媒体の1点Aの周囲をv
A察したが放置前と同様で欠点、剥離は無かった。 ま
た、同一・条件でIn2O3単独膜を作成し電気抵抗を
測定したところ表面抵抗は10)1Ω/sq以上、対応
する電気抵抗率の値はBxioΩ・cm以上の絶縁性膜
であった。
After that, the area around one point A on the medium was examined using an optical microscope.
I noticed that it was the same as before it was left and there were no defects or peeling. Further, when an In2O3 single film was prepared under the same conditions and its electrical resistance was measured, it was found to be an insulating film with a surface resistance of 10) 1Ω/sq or more and a corresponding electrical resistivity value of BxioΩ·cm or more.

[比較例1] 直径2O0mm 、厚さ1.2mmの円板で2.5 μ
mピッチのグループを有するアクリル樹脂(PMMA)
のディスク基板を3ターゲツトの高周波マグネト[1ン
スパツタ装置(アネルバ■製5PF−430型)の真空
槽内に固定し、4 X 10−7 TOrr以下になる
まで排気する。なお基板1は水冷し、15rpmで回転
させた。
[Comparative Example 1] 2.5μ in a disc with a diameter of 2O0mm and a thickness of 1.2mm
Acrylic resin (PMMA) with m-pitch groups
The disk substrate was fixed in a vacuum chamber of a three-target high-frequency magnet [one-instrument sputtering device (Model 5PF-430 manufactured by Anelva ■), and the vacuum chamber was evacuated until the pressure became below 4 X 10-7 Torr. Note that the substrate 1 was water-cooled and rotated at 15 rpm.

次に酊、 N2混合ガス(N250VOI%)を真空槽
内に導入し、圧力1X 10−2 TOrrになるよう
に混合ガスの流量を調整し、直径100mm 、厚さ5
mmのSiの円盤をターゲットとし、放電電力1oov
、放電周波数 13.56HtlZで高周波スパッタリ
ングを行ない、誘電体[I2としてSiN膜を約800
人堆積した。
Next, N2 mixed gas (N250 VOI%) was introduced into the vacuum chamber, and the flow rate of the mixed gas was adjusted so that the pressure was 1X 10-2 Torr.
Targeting a mm Si disk, the discharge power was 1oov.
, high-frequency sputtering was performed at a discharge frequency of 13.56 HtlZ, and a SiN film was deposited as the dielectric [I2] at a density of about 800 HtlZ.
People piled up.

続いて、記録83としてターゲラ1〜をFe6g’l1
)23Co3合金(添数字は組成(原子%)を示′1J
−)に変え上述と同様の放電条件でFe rb Co合
金膜を約1ooo入堆積した。
Next, as record 83, Targera 1 ~ Fe6g'l1
)23Co3 alloy (the suffix indicates the composition (atomic %)'1J
-), a Ferb Co alloy film was deposited to a thickness of about 100 mm under the same discharge conditions as described above.

最後に保護層4として誘電体層2と同様にSiN膜を約
800人堆積した。
Finally, about 800 SiN films were deposited as the protective layer 4 in the same manner as the dielectric layer 2.

以上の順序で第1図(a)に示すPMMA/SiN/ 
rbFecO/ S i Nの積層体すなわち光磁気記
録媒体を19だ。
In the above order, the PMMA/SiN/
19 is a rbFecO/S i N stack, that is, a magneto-optical recording medium.

実施例1と同様に、この媒体の1点A(第1図(b)参
照)の周囲を光学顕微鏡にて観察し、欠点。
As in Example 1, the area around point A (see FIG. 1(b)) of this medium was observed using an optical microscope to identify any defects.

剥離が無いことを確認した。It was confirmed that there was no peeling.

このvi層体を60℃、 90%RHの恒温恒湿下に9
0時間放置した。
This VI layer body was placed at constant temperature and humidity at 60°C and 90% RH.
It was left for 0 hours.

その後、光学顕微鏡にて前述の媒体の1点Aの周囲を観
察すると、グループに沿った剥離がll!察された。剥
離部分をX線マイクロアナライザー(XMA>により元
素の面分析を行なったところ誘電体層2の部分から剥離
が生じていることが確認された。
After that, when the area around point A of the medium mentioned above was observed using an optical microscope, peeling along the groups was observed! It was noticed. When the peeled portion was subjected to elemental surface analysis using an X-ray microanalyzer (XMA), it was confirmed that peeling occurred from the dielectric layer 2 portion.

実施例1.比較例1より本発明の有為性が示された。Example 1. Comparative Example 1 demonstrated the effectiveness of the present invention.

[実施例2] 直径2O0mm 、厚ざi、zmmの円板で1.6 μ
lllピッチのグループを有するポリカーボネート樹脂
(PC)のディスク基板を3ターゲツトの高周波マグネ
トロンスパッタ装置(アネルバ@製5PF−430型)
の真空槽内に固定し、4 X 10−7 Torr以下
になるまで排気する。なお、基板1は水冷し、15 p
pmで回転させた。
[Example 2] A disc with a diameter of 200 mm and a thickness of i and z mm is 1.6 μm.
A polycarbonate resin (PC) disk substrate with groups of 110 pitches was sputtered using a 3-target high-frequency magnetron sputtering device (5PF-430 model manufactured by ANELVA@).
The chamber was fixed in a vacuum chamber and evacuated until the pressure became 4 X 10-7 Torr or less. Note that the substrate 1 was water-cooled and heated at 15 p.
Rotated at pm.

次にAr、 02混合ガス(0210VOI%)を真空
槽内に導入し、圧力’1X10−2丁orrになるよう
にAr、 02混合fJ ス(7) 流ffi ラミ!
整し、直径100mm 、厚さ5mmのIn2O3焼結
体の円盤をターゲットとし、放電電力100W、放電周
波数13.56聞2で高周波スパッタリングを行ない、
誘電体層2としてIn2O3膜を約800人堆積した。
Next, Ar and 02 mixed gas (0210 VOI%) is introduced into the vacuum chamber, and the Ar and 02 mixed gas (7) Flow ffi Rami!
Using a disc of In2O3 sintered body with a diameter of 100 mm and a thickness of 5 mm as a target, high-frequency sputtering was performed at a discharge power of 100 W and a discharge frequency of 13.56/2.
About 800 people deposited an In2O3 film as the dielectric layer 2.

続いて第1の保護層5としてターゲットをTiに変え酊
ガス(5N)を真空槽内に導入し子連と同様の放電条イ
1でTi膜を約10人堆積した。
Subsequently, as the first protective layer 5, the target was changed to Ti, intoxicant gas (5N) was introduced into the vacuum chamber, and about 10 Ti films were deposited using the same discharge strip 1 as in the first layer.

更に記録層3としてターゲットをF’c6.Tb23C
oa合金(添数字は組成(原子%)を示す)に変えAr
ガス(5N)を真空槽内に導入し上述と同様の放電条件
でre Ib Co合金膜を約1000人堆積した。
Further, as the recording layer 3, a target of F'c6. Tb23C
Ar
Gas (5N) was introduced into the vacuum chamber and about 1000 re Ib Co alloy films were deposited under the same discharge conditions as described above.

なお、上述の各膜形成のとぎIn2O3膜、[1llQ
及びre rb Co合金膜は直径2O0mmの基板上
において中心から半径90mmまで堆積する様にマスク
が設置されている。
In addition, the In2O3 film, [1llQ
A mask was installed so that the Co alloy film was deposited on a substrate with a diameter of 200 mm to a radius of 90 mm from the center.

最後にこのマスクを取り外し基板全面に膜が堆積する様
にし、第2の保護層6として11ターゲツトに変え、−
1二連と同様の放電条件で11膜を約2O0人堆積した
Finally, this mask is removed and a film is deposited on the entire surface of the substrate, and the target is changed to 11 as the second protective layer 6.
Approximately 200 11 films were deposited under the same discharge conditions as in the first two series.

以、上の順序で第2図に示す第2の保護層6ににり記録
層3を含む全層の側面まで被覆したPC/Inz O:
+/Ti/FOrb CO/liの積層体ずなわら光磁
気記録媒体を得た。
Hereinafter, PC/Inz O was applied to the second protective layer 6 shown in FIG. 2 in the above order, and the sides of all layers including the recording layer 3 were coated:
A magneto-optical recording medium consisting of a laminate of +/Ti/FOrb CO/li was obtained.

この積層体のC/間 [なお、C/N=S/N+101
0(J (雑音帯域)/(分解能帯域幅)]を測定した
。この測定は光磁気記録再生装置(ナカミチ0H3−1
000TVpe (III ) )を用い、900rp
mでディスクを回転さt! 1.024HIIZの信号
を5.0−半導体レーザ光で記録したのら、0.8m−
の半導体レーザ光で読み出した。印加磁界は5000e
 (エルステッド)である。結果を表1の実施例2に示
す。
C/N of this laminate [Note: C/N=S/N+101
0(J (noise band)/(resolution bandwidth)]. This measurement was carried out using a magneto-optical recording/reproducing device (Nakamichi 0H3-1
000TVpe (III)), 900rp
Rotate the disc with m and t! If a signal of 1.024 HIIZ is recorded with a 5.0-semiconductor laser beam, then 0.8 m-
It was read out using a semiconductor laser beam. Applied magnetic field is 5000e
(Oersted). The results are shown in Example 2 in Table 1.

次にこの積層体を60℃、 90%RHの恒温、恒湿下
に500時間放置した。その後のC/間を測定した。
Next, this laminate was left at constant temperature and humidity at 60° C. and 90% RH for 500 hours. The subsequent C/interval was measured.

結果を表1の実施例2に示す。The results are shown in Example 2 in Table 1.

なお、1qられたIn2O3PAの表面抵抗は10ト1
Ω/sq以上で電気抵抗率は8×10Ω・cm以上の絶
縁性の膜であった。
In addition, the surface resistance of In2O3PA reduced by 1q is 10t1
It was an insulating film with an electrical resistivity of 8×10 Ω·cm or more at Ω/sq or more.

[比較例2] 直径2O0mm 、厚さ1.21の円盤で1.6 μm
ビッグのグループを有するポリカーボネート樹脂(PC
)のディスク基板を3ターゲツトの高周波マグネ1〜[
1ンスパツタ装置(アネルバ@製5PF−430型)の
真空槽内に固定し、4 X 10−7 T’Orr以下
になるまで排気する。なお、基板1は水冷し、15 p
pmで回転させた。
[Comparative Example 2] 1.6 μm in a disk with a diameter of 200 mm and a thickness of 1.21
Polycarbonate resin (PC) with big groups
) disk substrate with three targets of high frequency magnets 1 to [
The sample was fixed in a vacuum chamber of a 1-inch sputtering device (Model 5PF-430 manufactured by ANELVA@) and evacuated until the pressure became 4 x 10-7 T'Orr or less. Note that the substrate 1 was water-cooled and heated at 15 p.
Rotated at pm.

次に酊ガス(5N)を真空槽内に導入し、圧力i X 
10−2 rorrになるように^「ガスの流量を調整
し、直径100non 、厚さ5mmのZnSの円盤を
ターゲットとし、放電電力100W、放電周波数13.
56HH2で高周波スパッタリングを行ない、誘電体層
2として1口S膜を約800人堆積した。
Next, intoxication gas (5N) is introduced into the vacuum chamber, and the pressure i
10-2 rorr^ Adjust the gas flow rate, target a ZnS disk with a diameter of 100non and a thickness of 5mm, discharge power of 100W, and discharge frequency of 13.
Approximately 800 1-hole S films were deposited as the dielectric layer 2 by high-frequency sputtering using 56HH2.

続いて、記録層3としてターゲットをFe6gTb23
CoB合金(添数字は組成(原子%)を示す)に変え上
述と同様の放電条件でFe Tb C0合金膜を約10
00人堆積した。
Next, as the recording layer 3, the target was Fe6gTb23.
CoB alloy (the suffix indicates the composition (atomic %)) was replaced with about 10% of the FeTbC0 alloy film under the same discharge conditions as above.
00 people deposited.

最後に保護層4としてlnSターゲットに変え、上述と
同様の放電条件でZnS膜を約800人堆積した。
Finally, the protective layer 4 was changed to an lnS target, and about 800 ZnS films were deposited under the same discharge conditions as described above.

以上の順序で第1図(a)に示す積層構成で保護層4に
より記録層3を含む全層の側面まで被覆したPC/Zn
S/Te rb Co/ZnSの@周体プなわら光磁気
記録媒体を(qだ。
PC/Zn is coated with the protective layer 4 up to the side surfaces of all layers including the recording layer 3 in the laminated structure shown in FIG. 1(a) in the above order.
S/Te rb Co/ZnS @peripheral magneto-optical recording medium (q).

この積層体のC/間を実施例2と同じ条件で測定した。The C/distance of this laminate was measured under the same conditions as in Example 2.

結果を表1の比較例2に示す。The results are shown in Comparative Example 2 in Table 1.

次にこの積層体を60℃、 90%RHの恒温恒湿下に
500時間放置した。その後のC/間を測定した。
Next, this laminate was left at constant temperature and humidity at 60° C. and 90% RH for 500 hours. The subsequent C/interval was measured.

ディスクを観察したところ媒体面に多くのワレが観測さ
れた。結果を表1の比較例2に示す。
When the disk was observed, many cracks were observed on the media surface. The results are shown in Comparative Example 2 in Table 1.

表1から明らかなごとく本実施例2においてC/間及び
外観は全く変化していないのに対し、比較例2において
C/間は51 dBから44 dBへ減少し、外観も腐
蝕劣化と思われるシワが認められた。
As is clear from Table 1, in Example 2, the C/distance and appearance did not change at all, whereas in Comparative Example 2, the C/dimension decreased from 51 dB to 44 dB, and the appearance also appeared to be due to corrosion deterioration. Wrinkles were observed.

上述のごとく本発明の有為性が示された。As mentioned above, the effectiveness of the present invention was demonstrated.

[実施例3] 直径2O0111m 、厚さ1.2mmの円板で1.6
 μmピッチのグループを有するポリカーボネート樹脂
(PC)のディスク基板を3ターゲツトの高周波マグネ
ト1]ンスパツタ装置(アネルl<1dlJ製5PF−
430型)の真空槽内に固定し、4 X 10−7 T
Orr以下になるまで排気覆る。なお、基板1は水冷し
、15rpmで回転させた。
[Example 3] 1.6 for a disc with a diameter of 200111 m and a thickness of 1.2 mm.
A disk substrate of polycarbonate resin (PC) having groups with a μm pitch was sputtered using a three-target high-frequency magnet sputtering device (5PF-
430 type) in a vacuum chamber of 4 x 10-7 T.
Cover the exhaust until it is below Orr. Note that the substrate 1 was water-cooled and rotated at 15 rpm.

次に^「、O2混合ガス(022OVOI%)を真空槽
内に導入し、圧力2 X 10−2 rorrになるよ
うに^r、02混合ガスの流はを調整し、直径ioom
m 、厚さ5mmのsn□z焼結体の円盤をターゲラ1
〜とし、放電電力50W 、放電周波数13.56)I
n2で高周波スパッタリングを行い、誘電体層2として
5nOz膜を約800人堆積した。
Next, introduce O2 mixed gas (022 OVOI%) into the vacuum chamber, adjust the flow of O2 mixed gas so that the pressure is 2 x 10-2 rorr, and adjust the flow of O2 mixed gas (022 OVOI%) to a diameter of
m, a disk of sn□z sintered body with a thickness of 5 mm was placed in Targetera 1.
~, discharge power 50W, discharge frequency 13.56)I
High frequency sputtering was performed using n2 to deposit a 5nOz film as the dielectric layer 2 in a thickness of approximately 800.

続いて第1の保護層5としてターゲットを[iに変え^
「ガス(5N)を真空槽内に導入し上述と同様の放電条
件で[i膜を約10人堆積した。
Next, as the first protective layer 5, change the target to [i^
``Gas (5N) was introduced into the vacuum chamber and approximately 10 I films were deposited under the same discharge conditions as above.

更に記録層3としてターゲットをrbFeco複合ター
ゲットに変え^rガス(5N)を真空槽内に導入し上述
と同様の放電条件でFelbCO合金膜を約1000人
堆積した。
Furthermore, as the recording layer 3, the target was changed to an rbFeco composite target, ^r gas (5N) was introduced into the vacuum chamber, and about 1000 FelbCO alloy films were deposited under the same discharge conditions as described above.

最後に第2の保護層6としてTiターゲットに変え、上
述と同様の放電糸イ1で[i膜を約2O0人堆積しIこ
Finally, a Ti target was used as the second protective layer 6, and about 200 films were deposited using the same discharge thread 1 as described above.

以上の順序で第2図に示す第2の保護層6により記録層
3を含む仝層の側面まで被覆したPC/sn□x /T
i/FerbCo/Tiのv4Fff1体すなわち光磁
気記録媒体を1qた。
PC/sn□x/T with the second protective layer 6 shown in FIG. 2 covering the side surfaces of the remaining layers including the recording layer 3 in the above order.
One i/FerbCo/Ti v4Fff body, ie, 1 q of magneto-optical recording medium was prepared.

この積層体のC/N [なお、C/N=S/N+101
oa (雑音帯域)/(分解能帯域幅)]を測定した。
The C/N of this laminate [C/N=S/N+101
oa (noise band)/(resolution bandwidth)] was measured.

この測定は光磁気記録再生装置(すhミチ0H3−10
00丁VI)e (I[I ) )を用い、9oorp
mでディスクを回転させ1.024聞2の信号を7.5
mW半導体レーザ光で記録したのら、0.8mWの半導
体レーザ光で読み出した。印加磁界は5000e (エ
ルステッド)である。結果を表2の実施例3に示す。
This measurement was carried out using a magneto-optical recording/reproducing device (Shmichi 0H3-10).
00-cho VI) e (I [I ) ),
Rotate the disk at m and convert the signal of 1.024 to 2 to 7.5
After recording with mW semiconductor laser light, reading was performed with 0.8 mW semiconductor laser light. The applied magnetic field is 5000e (Oersted). The results are shown in Example 3 in Table 2.

次にこの積層体を60℃、90%Rt+の恒温、恒湿下
に500時間放置した。その後のC/Nを測定した。
Next, this laminate was left at constant temperature and humidity of 60° C. and 90% Rt+ for 500 hours. The C/N was then measured.

結果を表2の実施例3に示す。又ディスク面から観察し
たところ、腐蝕劣化で見られるシワ、シミ等は見られな
かった。表2には比較のため前述の比較例2の結果を併
記しである。
The results are shown in Example 3 in Table 2. Further, when observed from the disk surface, no wrinkles, stains, etc., which are caused by corrosion deterioration, were observed. Table 2 also includes the results of Comparative Example 2 described above for comparison.

なお、1qられた5nOz膜の表面抵抗は108Ω/S
Q以上で電気抵抗率は8×100・cm以上の絶縁性の
膜であった。更にぞの屈折率をエリプソメータ(溝尻光
学@製)を用いて測定したところ、この5n02膜は波
長8300mにおいて2.0の屈折率を持つことがわか
った。
In addition, the surface resistance of the 1q 5nOz film is 108Ω/S.
It was an insulating film with an electrical resistivity of Q or more and an electrical resistivity of 8×100 cm or more. Furthermore, when the refractive index of the film was measured using an ellipsometer (manufactured by Mizojiri Kogaku@), it was found that this 5n02 film had a refractive index of 2.0 at a wavelength of 8300 m.

表   2 表2から明らかなごとく本実施例3においてC/N及び
外観はほとんど変化していないのに対し、比較例2にお
いてC/Nは51 dBから44d8へ減少し、外観も
腐蝕劣化と思われるシワが認められた。
Table 2 As is clear from Table 2, in Example 3, the C/N and appearance hardly changed, whereas in Comparative Example 2, the C/N decreased from 51 dB to 44 d8, and the appearance also seemed to be due to corrosion deterioration. wrinkles were observed.

なお、実施例2よりも本例の方が半導体レーザによる出
き込みパワーが大きいのは、ln2OxtよりSnOx
層の屈折率が小さいことによると思われる。
The reason why the output power of the semiconductor laser is larger in this example than in Example 2 is that SnOx than ln2Oxt.
This is probably due to the low refractive index of the layer.

[実施例4] 耐食性評価の1つとして以下の検討を行なった。[Example 4] The following study was conducted as one of the corrosion resistance evaluations.

1000人の膜厚の誘電性のSnO2含有のIn2O3
薄膜を水冷した10x 2Omm角、 1.2mm厚の
ガラス基板上に実施例2と同様に高周波スパッタ法によ
り形成した。スパッタ条f[はAr10z混合ガス(0
2:2Ovo1%)でガス圧はl x 10−2 To
rr、ターゲットはIn−8n (Sn : 5wt%
)合金であった。形成されたSnO2含有の1112O
3膜は電気抵抗率が’1X10Ω−CIllで、表面抵
抗が100)1Ω/SQ以上で誘電体であった。
1000mm thick dielectric SnO2-containing In2O3
A thin film was formed on a water-cooled glass substrate of 10 x 2 Omm square and 1.2 mm thick by high frequency sputtering in the same manner as in Example 2. The sputtering strip f[ is Ar10z mixed gas (0
2:2 Ovo 1%) and the gas pressure is l x 10-2 To
rr, target is In-8n (Sn: 5wt%
) was an alloy. Formed SnO2-containing 1112O
The three films had an electrical resistivity of 1×10Ω-CIll, a surface resistance of 100)1Ω/SQ or more, and were dielectric.

光磁気膜は、同じ寸法の1.2mm厚のポリカーボネー
ト基板上に、実施例2と同様にFe6gC0B Tl)
23合金ターゲツトを用い高周波マグネトロンスパッタ
法でArガス雰囲気下、形成した。
The magneto-optical film was made of Fe6gC0B Tl) on a 1.2 mm thick polycarbonate substrate with the same dimensions as in Example 2.
It was formed by high frequency magnetron sputtering using a No. 23 alloy target in an Ar gas atmosphere.

このようにして形成した2つの膜を電極にして、5em
間隔で対向させて0.1 mol /1のNaα溶液に
浸し、12O分間で電極間に流れる電流を測定した。
Using the two films thus formed as electrodes, a 5em
The electrodes were immersed in a 0.1 mol/1 Naα solution while facing each other at an interval, and the current flowing between the electrodes was measured for 120 minutes.

電流はわずかに流れ、総H量は1.4X10−2クーロ
ンであった。
A slight current flowed and the total amount of H was 1.4×10 −2 coulombs.

[比較例3] 1000人の膜厚の導電性のSnO2含有の)n2O3
薄膜を実施例2と同じ装置を用い、高周波スパッタ法に
より実施例4と同じ寸法のガラス基板上に形成した。タ
ーゲットはInz 03−3nOz (5wt%5nO
z>焼結ターゲットでAr雰囲気中、”+ x 1o−
z rorrのガス圧で基板温度は130℃とした。形
成されたSnO2含右のIn2O3膜は電気抵抗率が5
X10−3Ω・cmで表面抵抗が500Ω/SQの透明
導電膜でめった。
[Comparative Example 3] Conductive (SnO2-containing) n2O3 with a film thickness of 1000 people
A thin film was formed on a glass substrate having the same dimensions as in Example 4 by high frequency sputtering using the same apparatus as in Example 2. The target is Inz 03-3nOz (5wt%5nO
z>Sintered target in Ar atmosphere, ``+ x 1o-
The substrate temperature was 130° C. with a gas pressure of z rorr. The formed In2O3 film containing SnO2 has an electrical resistivity of 5.
It was plated with a transparent conductive film having a surface resistance of 500 Ω/SQ and a width of 10 −3 Ω·cm.

実施例4と同じのポリカーボネート上に形成したrec
oTbの光磁気膜を対向する電極とし、実施例4と同じ
ようにして0.1 mol /1のNaα溶液に浸した
ところ電極間にかなりの電流が流れた。12O分の間の
電荷の総長は1.3クーロンであった。
rec formed on the same polycarbonate as in Example 4.
When oTb magneto-optical films were used as opposing electrodes and immersed in a 0.1 mol/1 Naα solution in the same manner as in Example 4, a considerable current flowed between the electrodes. The total charge during 120 minutes was 1.3 coulombs.

前述の実施例4との比較より、高湿度雰囲気下では比較
例3の如き導電性の前記In2O3膜上に形成した光磁
気膜では局部電池が形成され劣化の原因となることが確
認され、実施例4の如き誘電性の前記1n2O3膜では
かかる劣化が大rlJに改善されることが確認された。
From the comparison with the above-mentioned Example 4, it was confirmed that in a high humidity atmosphere, in the magneto-optical film formed on the conductive In2O3 film as in Comparative Example 3, a local battery is formed and causes deterioration. It was confirmed that in the dielectric 1n2O3 film as in Example 4, such deterioration was improved to a large rlJ.

[実施例5」 実施例2において、そのIn2O3層に替えてSnO2
を7wt%含右するIn2O3からなるターゲットを用
いて5002含有のIn2O3層を形成する以外は、実
施例2と全く同様にして媒体を作成した。(qられた媒
体はPC/ In2O3 (5nOz > / It/
 F’eTbCo/Tiの構成でめった。
[Example 5] In Example 2, SnO2 was used instead of the In2O3 layer.
A medium was prepared in exactly the same manner as in Example 2, except that an In2O3 layer containing 5002 was formed using a target made of In2O3 containing 7 wt% of . (The q medium is PC/ In2O3 (5nOz > / It/
This happened with the F'eTbCo/Ti configuration.

実施例2と同じテストをしたところ、実施例2と同様の
結果を得た。
When the same test as in Example 2 was conducted, the same results as in Example 2 were obtained.

[実施例6] 実施例2においてそのIn+ 03層に代えて、釦02
を30wt%含有するIn2O3からなるターゲットを
用いてSnO2含有のIn2O3層を形成した以外は、
実施例2と全く同様にして媒体を作成した。得られた媒
体はPC/ Tnz 03 (5no2 ) / Ti
/ FerbCo/ riの構成であった。実施例2と
同じテストをしたところ、実施例2と同様の結果を得た
[Example 6] In place of the In+ 03 layer in Example 2, button 02
Except that the In2O3 layer containing SnO2 was formed using a target made of In2O3 containing 30 wt% of
A medium was prepared in exactly the same manner as in Example 2. The obtained medium was PC/Tnz 03 (5no2)/Ti
/ FerbCo/ri. When the same test as in Example 2 was conducted, the same results as in Example 2 were obtained.

[実施例7] 直径2O0mm 、厚ざ1.2IIIIIlの円板で2
.5 μmピッチのグループを有するアクリル樹脂(P
MMA)のディスク基板を3ターゲツトの高周波マグネ
トロンスパッタ装置(アネルバ(11製5PF−430
型)の真空槽内に固定し、4 X 10−7 ’ror
r以下になるまで排気する。なお、基板1は水冷し、1
りrpmで回転させた。
[Example 7] 2 discs with a diameter of 200 mm and a thickness of 1.2 III
.. Acrylic resin (P
A disk substrate of MMA) was sputtered using a three-target high-frequency magnetron sputtering device (5PF-430 manufactured by ANELVA (11)).
4 x 10-7'ror
Exhaust until the temperature is below r. Note that the substrate 1 is water-cooled,
It was rotated at 100 rpm.

次にAr、 02混合ガス(022OVOI%)を真空
槽内に導入し、圧力I X 10−2 rorrになる
ように混合ガスの流量を調整し、直径ioomm 、厚
ざ5mmのInの円盤をターゲットとし、放電電力10
0W、放電周波数13.56)11Zで高周波反応性ス
パッタリングを行ない、誘電体層2としてIn2O3膜
を約800人堆積した。
Next, introduce Ar and 02 mixed gas (022 OVOI%) into the vacuum chamber, adjust the flow rate of the mixed gas so that the pressure is I x 10-2 rorr, and target an In disk with a diameter of iomm and a thickness of 5 mm. and the discharge power is 10
Approximately 800 In2O3 films were deposited as dielectric layer 2 by high frequency reactive sputtering at 0W and discharge frequency 13.56)11Z.

続いて、ターゲットを記録層3堆積用のターゲットすな
わちN’7.50”17.5[e52.5CO22,5
合金(添数字は組成(原子%)を示す)に変えAr(ア
ルボ、  ン)ガス(5N)を真空槽に導入し上述と同
様の放電条件でNdDVF’eCO合金膜を約1000
人堆積した。
Subsequently, the target was changed to a target for recording layer 3 deposition, that is, N'7.50"17.5[e52.5CO22,5
Argon (Arbon) gas (5N) was introduced into the vacuum chamber instead of the alloy (the suffix indicates the composition (atomic %)), and a NdDVF'eCO alloy film of about 1000% was heated under the same discharge conditions as above.
People piled up.

最後に保護層4として誘電体層2と同様にIn2O3膜
を約800人堆積した。
Finally, about 800 In2O3 films were deposited as the protective layer 4 in the same manner as the dielectric layer 2.

以上の順序で第1図(a)に示tPMMA/In2O3
/NdDVFeCO/Inz Owlの積層体すなわち
光磁気記録媒体を得た。この媒体の1点A(第1図(b
)参照)の周囲を光学顕微鏡にて観察し、欠点。
In the above order, tPMMA/In2O3 is shown in FIG. 1(a).
A laminate of /NdDVFeCO/Inz Owl, that is, a magneto-optical recording medium was obtained. One point A on this medium (Fig. 1(b)
)) Observe the surrounding area with an optical microscope to find any defects.

剥離が無いことを確認した。It was confirmed that there was no peeling.

この積層体を60℃、 90%曲の恒温恒湿下に2O0
時間放置した。
This laminate was heated to 200°C under constant temperature and humidity at 60°C and 90%
I left it for a while.

その後、光学顕微鏡にて上述の媒体の1点Aの周囲を観
察したが放置前と同様で欠点、剥離は無く、テスト前に
比し変化は無かった。
Thereafter, the area around point A of the above-mentioned medium was observed using an optical microscope, but it was the same as before being left, with no defects or peeling, and no changes compared to before the test.

また、同一条件でInz 03単独膜を作成し電気抵抗
を測定したところ表面抵抗は108Ω/SQ以上、対応
する電気抵抗率の値は8X100・cm以上の絶縁性膜
であった。
Furthermore, when a single Inz 03 film was prepared under the same conditions and its electrical resistance was measured, it was found to be an insulating film with a surface resistance of 108 Ω/SQ or more and a corresponding electrical resistivity value of 8×100 cm or more.

[比較例4] 実施例2と同じ装置でInz 03膜を作る時、基板温
石を100℃、ターゲットをIn2Ox (5wt%5
nOz)焼結体、スパッタガスを純^rガス(5N)と
覆る外は実施例2と同じ条件でディスクを作成した。
[Comparative Example 4] When making an Inz 03 film using the same equipment as in Example 2, the substrate was heated at 100°C and the target was In2Ox (5wt%5
A disk was produced under the same conditions as in Example 2, except that the sputtering gas was covered with pure^r gas (5N).

得られたfriz 03 (5nO2)膜は、表面抵抗
500Ω/sq、電気抵抗率4X10−3Ω・cmの透
明導電膜であった。このディスクを90Orpmで回転
させ、1、024)fllzの信号を5.0四半導体レ
ーザ光で記録した後、0.8m−半導体レーザ光で読み
出したところC/Nは44  dBであったa書き込み
レーザ光パワーを8.5mWにあげたところ49 dB
の値が得られた。
The obtained friz 03 (5nO2) film was a transparent conductive film with a surface resistance of 500 Ω/sq and an electrical resistivity of 4×10 −3 Ω·cm. This disk was rotated at 90 rpm, and a signal of 1,024)flz was recorded with a 5.04 semiconductor laser beam, and then read out with a 0.8 m semiconductor laser beam, and the C/N was 44 dB. When the laser light power was increased to 8.5mW, it was 49 dB.
The value of was obtained.

これより透明電極として用いられる導電性のInz 0
3 (5nOz )膜を同一構成の多層膜として用いた
媒体は、書き込みレーザパワーのエネルギー損失が大ぎ
く好ましくないことが判明した。
From this, conductive Inz 0 used as a transparent electrode
It has been found that a medium using a multilayer film having the same structure as a 3.3 (5 nOz) film has a large energy loss in the writing laser power, which is undesirable.

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

第1図(a)、 (b)は実施例における積層体の断面
図、平面図である。 第2図は伯の実施例における断面図である。 1:基板、2:誘電体層、3:記録層。 4.5.6:保護層
FIGS. 1(a) and 1(b) are a cross-sectional view and a plan view of a laminate in an example. FIG. 2 is a sectional view of Haku's embodiment. 1: Substrate, 2: Dielectric layer, 3: Recording layer. 4.5.6: Protective layer

Claims (1)

【特許請求の範囲】 1、透明合成樹脂基板上に透明誘電体層を介して光磁気
記録層、更に必要に応じて保護層を設けた光磁気記録媒
体において、前記透明誘電体層がIn及びSnからなる
群から選ばれた少なくとも一つの元素の酸化物からなる
電気抵抗率が1×10^−^1Ω・cm以上の誘電性の
透明酸化物層であることを特徴とする光磁気記録媒体。 2、前記透明酸化物層がIn_2O_3である特許請求
の範囲第1項記載の光磁気記録媒体。 3、前記透明酸化物層がインジウム酸化物を主成分とし
て錫酸化物を含む混合酸化物である特許請求の範囲第1
項記載の光磁気記録媒体。 4、前記インジウム酸化物がIn_2O_3であり錫酸
化物がSnO_2である特許請求の範囲第3項記載の光
磁気記録媒体。 5、前記錫酸化物の含有量が30wt%以下である特許
請求の範囲第3項若しくは第4項記載の光磁気記録媒体
。 6、前記錫酸化物の含有量が7wt%以下である特許請
求の範囲第5項記載の光磁気記録媒体。 7、前記錫酸化物の含有量が3wt%以下である特許請
求の範囲第6項記載の光磁気記録媒体。 8、前記透明酸化物層が1≦X≦2のSnO_Xからな
る特許請求の範囲第1項記載の光磁気記録媒体。 9、前記保護層として前記透明誘電体層と前記光磁気記
録層との間に金属チタン層を有する特許請求の範囲第1
項〜第8項記載の光磁気記録媒体。 10、前記金属チタン層は厚さが50Å以下である特許
請求の範囲第9項記載の光磁気記録媒体。 11、前記光磁気記録層の前記透明合成樹脂基板側と反
対側に第2の保護層を有する特許請求の範囲第1項〜第
10項記載の光磁気記録媒体。 12、前記第2の保護層がIn及びSnからなる群から
選ばれた少なくとも1つの元素の酸化物層からなる特許
請求の範囲第11項記載の光磁気記録媒体。 13、前記第2の保護層が金属チタン層である特許請求
の範囲第11項記載の光磁気記録媒体。
[Claims] 1. A magneto-optical recording medium in which a magneto-optical recording layer is provided on a transparent synthetic resin substrate via a transparent dielectric layer, and further a protective layer is provided as necessary, wherein the transparent dielectric layer is made of In and A magneto-optical recording medium characterized by a dielectric transparent oxide layer having an electrical resistivity of 1×10^-^1 Ωcm or more and made of an oxide of at least one element selected from the group consisting of Sn. . 2. The magneto-optical recording medium according to claim 1, wherein the transparent oxide layer is In_2O_3. 3. Claim 1, wherein the transparent oxide layer is a mixed oxide containing indium oxide as a main component and tin oxide.
Magneto-optical recording medium as described in . 4. The magneto-optical recording medium according to claim 3, wherein the indium oxide is In_2O_3 and the tin oxide is SnO_2. 5. The magneto-optical recording medium according to claim 3 or 4, wherein the content of the tin oxide is 30 wt% or less. 6. The magneto-optical recording medium according to claim 5, wherein the content of the tin oxide is 7 wt% or less. 7. The magneto-optical recording medium according to claim 6, wherein the content of the tin oxide is 3 wt% or less. 8. The magneto-optical recording medium according to claim 1, wherein the transparent oxide layer is made of SnO_X with 1≦X≦2. 9. Claim 1, wherein a metallic titanium layer is provided between the transparent dielectric layer and the magneto-optical recording layer as the protective layer.
9. A magneto-optical recording medium according to items 8 to 9. 10. The magneto-optical recording medium according to claim 9, wherein the metal titanium layer has a thickness of 50 Å or less. 11. The magneto-optical recording medium according to any one of claims 1 to 10, further comprising a second protective layer on a side of the magneto-optical recording layer opposite to the transparent synthetic resin substrate. 12. The magneto-optical recording medium according to claim 11, wherein the second protective layer comprises an oxide layer of at least one element selected from the group consisting of In and Sn. 13. The magneto-optical recording medium according to claim 11, wherein the second protective layer is a metallic titanium layer.
JP62322839A 1986-12-26 1987-12-22 Magneto-optical recording medium Expired - Lifetime JP2550118B2 (en)

Priority Applications (1)

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JP62322839A JP2550118B2 (en) 1986-12-26 1987-12-22 Magneto-optical recording medium

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP30852086 1986-12-26
JP61-308520 1986-12-26
JP050,527 1986-12-26
US5052787A 1987-05-13 1987-05-13
US050,527 1987-05-13
JP62322839A JP2550118B2 (en) 1986-12-26 1987-12-22 Magneto-optical recording medium

Publications (2)

Publication Number Publication Date
JPS63266651A true JPS63266651A (en) 1988-11-02
JP2550118B2 JP2550118B2 (en) 1996-11-06

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58215744A (en) * 1982-06-08 1983-12-15 Yoshifumi Sakurai Photothermal magnetic recording medium
JPS62209750A (en) * 1986-03-11 1987-09-14 Seiko Instr & Electronics Ltd Photomagnetic recording medium
JPS63149847A (en) * 1986-12-12 1988-06-22 Nippon Telegr & Teleph Corp <Ntt> Magneto-optical recording medium
JPS63195847A (en) * 1987-02-10 1988-08-12 Fujitsu Ltd Magneto-optical disk
JPS63197043A (en) * 1987-02-12 1988-08-15 Hitachi Ltd Optical disk

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58215744A (en) * 1982-06-08 1983-12-15 Yoshifumi Sakurai Photothermal magnetic recording medium
JPS62209750A (en) * 1986-03-11 1987-09-14 Seiko Instr & Electronics Ltd Photomagnetic recording medium
JPS63149847A (en) * 1986-12-12 1988-06-22 Nippon Telegr & Teleph Corp <Ntt> Magneto-optical recording medium
JPS63195847A (en) * 1987-02-10 1988-08-12 Fujitsu Ltd Magneto-optical disk
JPS63197043A (en) * 1987-02-12 1988-08-15 Hitachi Ltd Optical disk

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