JP2707808B2 - Method for manufacturing magneto-optical recording medium - Google Patents

Method for manufacturing magneto-optical recording medium

Info

Publication number
JP2707808B2
JP2707808B2 JP2159118A JP15911890A JP2707808B2 JP 2707808 B2 JP2707808 B2 JP 2707808B2 JP 2159118 A JP2159118 A JP 2159118A JP 15911890 A JP15911890 A JP 15911890A JP 2707808 B2 JP2707808 B2 JP 2707808B2
Authority
JP
Japan
Prior art keywords
dielectric layer
recording medium
film
sin
optical recording
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP2159118A
Other languages
Japanese (ja)
Other versions
JPH0449548A (en
Inventor
英嗣 苅屋田
薫 土岐
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NEC Corp
Original Assignee
NEC Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NEC Corp filed Critical NEC Corp
Priority to JP2159118A priority Critical patent/JP2707808B2/en
Publication of JPH0449548A publication Critical patent/JPH0449548A/en
Application granted granted Critical
Publication of JP2707808B2 publication Critical patent/JP2707808B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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、光磁気記録媒体に関する。Description: TECHNICAL FIELD The present invention relates to a magneto-optical recording medium.

〔従来の技術〕[Conventional technology]

光ディスクは、大容量のファイルメモリの一つとして
注目されている。中でも光磁気ディスクは、記録情報の
書換えが可能であると言う利点を持っていることから、
コードデータファイルメモリを始め、画像ファイルメモ
リ等広範囲な応用が各所で盛んに研究されている。
Optical discs are receiving attention as one of large-capacity file memories. Above all, magneto-optical disks have the advantage that recorded information can be rewritten,
A wide range of applications including code data file memories and image file memories are being actively studied in various places.

記録媒体としては、ポリカーボネイト等の樹脂基体上
に、SiNからなる第一の誘電体層、希土類金属と鉄族遷
移金属との組合せによって作成されるTbFeCoの様な非晶
質磁性合金膜からなる記録層、SiNからなる第二の誘電
体層の順に成膜された三層構成、もしくはさらにAl等の
反射膜を形成した4層構成が知られている。これらを用
いた光磁気ディスクは、パソコンのコードデータファイ
ルメモリ分野を始めとして、既に、実用レベルにあり、
用途拡大が期待されている。用途の拡大に伴い、更に過
酷な環境下に於いても安定に動作する高い信頼性が要求
されている。
As the recording medium, a first dielectric layer made of SiN, a recording made of an amorphous magnetic alloy film such as TbFeCo formed by a combination of a rare earth metal and an iron group transition metal on a resin substrate such as polycarbonate. There is known a three-layer configuration in which a layer and a second dielectric layer made of SiN are formed in this order, or a four-layer configuration in which a reflective film such as Al is further formed. Magneto-optical disks using these are already at a practical level, including in the field of code data file memory for personal computers.
The application is expected to expand. With the expansion of applications, high reliability is required to operate stably even in harsh environments.

当初、第一誘電体層のSiNはポリカーボネイト基板へ
の付着力が弱いため、高温高湿環境下では、剥離を生じ
る事があった。これに対して、SiNの膜ストレスを低減
等の改善が図られた結果、付着力が向上し、高温高湿環
境下でも問題の無い信頼性の高いディスクが得られるこ
とが知られている。
Initially, the SiN of the first dielectric layer had a weak adhesive force to the polycarbonate substrate, and thus sometimes peeled off in a high-temperature and high-humidity environment. On the other hand, it has been known that, as a result of improving the film stress of SiN and the like, the adhesive force is improved, and a highly reliable disk with no problem can be obtained even in a high-temperature and high-humidity environment.

近年、更に付着力を向上するものとしてSiNとポリカ
ーボネイト基板との間にTaの酸化物(TaOx)を形成する
方法が提案されている(特開昭64−189049)。
In recent years, a method of forming an oxide of Ta (TaOx) between SiN and a polycarbonate substrate has been proposed to further improve the adhesive force (Japanese Patent Application Laid-Open No. 64-189049).

この方法は、酸化物の焼結体Ta2O5ターゲットを用
い、Arガスをスパッタガスとして、ポリカーボネイト等
の樹脂基体上にTaOxを成膜している。
The method using a sintered body Ta 2 O 5 targets oxides, the Ar gas as the sputtering gas, and forming a TaOx on a resin substrate such as polycarbonate.

〔発明が解決しようとする課題〕[Problems to be solved by the invention]

しかしながら、このような上述した従来の光磁気記録
媒体は、TaOxの成膜において、ターゲットが焼結体であ
り、ターゲットへ大きな電力を投入するとターゲットが
割れる恐れがあるため、あまり大きな電力を投入するこ
とができないので膜堆積速度が非常に遅い。(数A/分程
度)これに対して、Taターゲットを用いて、ArとO2の混
合ガスをスパッタガスとした反応性スパッタを行った場
合、ターゲットに大きな電力を投入することが可能とな
り、膜堆積速度が速くなり(100〜200A/分)、媒体の量
産に適していることが判った。ただし、Taターゲットを
用い、ArとO2の混合ガスをスパッタガスとした反応性ス
パッタによりTaOxを成膜する場合、成膜条件の選定を誤
ると、透明性が損なわれたメタリックな膜が得られた
り、かえって付着力が低下するという問題が生じた。
However, in the above-described conventional magneto-optical recording medium, in forming a film of TaOx, the target is a sintered body, and when a large power is applied to the target, the target may be broken. Film deposition rate is very slow. On the other hand, when reactive sputtering is performed using a Ta target and a mixed gas of Ar and O 2 as a sputtering gas, a large electric power can be applied to the target. The film deposition rate was increased (100 to 200 A / min), which proved to be suitable for mass production of media. However, using a Ta target, when forming the TaOx by reactive sputtering and the sputtering gas, a mixed gas of Ar and O 2, Improper selection of deposition conditions, resulting transparency is compromised metallic film Or the adhesive strength is reduced.

本発明の目的は、Taターゲットに対して、ArとO2の混
合ガスをスパッタガスとした反応性スパッタにより成膜
されるTaOxの成膜条件を選定することにより、樹脂基板
への付着力が強いTaOxを形成し、耐剥離性に優れた記録
媒体を提供することにある。
An object of the present invention is to select a film forming condition of TaOx formed by reactive sputtering using a mixed gas of Ar and O 2 as a sputtering gas with respect to a Ta target, so that an adhesive force to a resin substrate is reduced. An object of the present invention is to provide a recording medium which forms strong TaOx and has excellent peel resistance.

〔課題を解決するための手段〕[Means for solving the problem]

本発明の光磁気記録媒体は、基体上に、少なくとも、
Taの酸化物(TaOx)からなる第一の誘電体層、SiNから
なる第二の誘電体層、希土類金属と鉄族遷移金属との組
合せによって作成される非晶質磁性合金からなる記録
層、SiNからなる第三の誘電体層の順に成膜された光磁
気記録媒体において、前記第一の誘電体層が、Taターゲ
ットに対して、酸素分圧が0.045〜0.09Paの範囲のArとO
2の混合ガスをスパッタガスとした反応性スパッタによ
り成膜されるように構成される。
The magneto-optical recording medium of the present invention, at least on the substrate,
A first dielectric layer composed of an oxide of Ta (TaOx), a second dielectric layer composed of SiN, a recording layer composed of an amorphous magnetic alloy formed by a combination of a rare earth metal and an iron group transition metal, In a magneto-optical recording medium formed in the order of a third dielectric layer made of SiN, the first dielectric layer has a partial oxygen pressure of 0.045 to 0.09 Pa relative to a Ta target.
A film is formed by reactive sputtering using the mixed gas of 2 as a sputtering gas.

〔実施例〕 次に、本発明の実施例について、図面を参照して説明
する。
Embodiment Next, an embodiment of the present invention will be described with reference to the drawings.

第1図は本発明の一実施例を示す部分断面図である。
第1図に示す光磁気記録媒体は、厚さ1.2mm,直径、130m
mのポリカーボネイトの基板1上にタンタルTaの酸化物
(TaOx)からなる厚さ300Åの第一の誘電体層2、窒化
シリコンSiNからなる厚さ600Åの第二の誘電体層3、鉄
コバルトテルビウムTbFeCoからなる厚さ700Åの記録層
4、窒化シリコンSiNからなる厚さ800Åの第三の誘電体
層5の順に、形成されている。
FIG. 1 is a partial sectional view showing one embodiment of the present invention.
The magneto-optical recording medium shown in FIG. 1 has a thickness of 1.2 mm, a diameter of 130 m.
a first dielectric layer 2 having a thickness of 300 mm made of a tantalum Ta oxide (TaOx), a second dielectric layer 3 having a thickness of 600 mm made of silicon nitride SiN, and iron-cobalt terbium The recording layer 4 is made of TbFeCo and has a thickness of 700 、, and the third dielectric layer 5 is made of silicon nitride SiN and has a thickness of 800 順 に.

タンタルTaの酸化物(TaOx)からなる厚さ300Åの誘
電体層2は、タンタルTaターゲットを用い、アルゴンAr
と酸素O2の混合ガス(30%O2)をスパッタガスとした反
応性スパッタによりパワー密度9.6w/cm2で作成される。
The dielectric layer 2 made of a tantalum Ta oxide (TaOx) and having a thickness of 300 mm was formed using a tantalum Ta target using argon Ar.
It is formed at a power density of 9.6 w / cm 2 by reactive sputtering using a mixed gas of oxygen and oxygen O 2 (30% O 2 ) as a sputtering gas.

実験によれば、TaOx膜堆積速度は、第2図に膜堆積速
度曲線vとに示すように、スパッタガス圧の増加に伴
い、0.15Pa近傍でピークを示し、その後単調に減少す
る。そして、TaOxは、0.15Paより大きいスパッタガス圧
において、屈折率が、第2図に屈折率曲線nとして示す
ように2.07〜2.1の透明な膜となるが0.15Paより小さい
スパッタガス圧では、透明性が損なわれたメタリックな
膜となる。
According to the experiment, the TaOx film deposition rate shows a peak near 0.15 Pa with the increase of the sputtering gas pressure and then monotonously decreases as shown by the film deposition rate curve v in FIG. At a sputtering gas pressure of more than 0.15 Pa, TaOx becomes a transparent film having a refractive index of 2.07 to 2.1 as shown as a refractive index curve n in FIG. It becomes a metallic film with impaired properties.

ここでは、0.15Paより大きいスパッタガス圧の範囲で
作成される透明なTaOxを有する6種類の媒体サンプルA
〜Fを次の第1表に示す。
Here, six types of media samples A having transparent TaOx prepared in the range of the sputtering gas pressure greater than 0.15 Pa
To F are shown in Table 1 below.

これらの媒体サンプルにおいて、SiN膜からなる第二
および第四の誘電体層およびTbFeCoからなる記録層は、
すべて以下に示す同一構成とした。
In these media samples, the second and fourth dielectric layers made of a SiN film and the recording layer made of TbFeCo are:
All had the same configuration as shown below.

すなわち、SiN膜からなる第二および第四の誘電体層
3および5は、Siターゲットを用い、ArとN2の混合ガス
(50%N2)をスパッタガスとした反応性スパッタによ
り、パワー密度8w/cm2、スパッタガス圧2.5×10-Paで作
成される。
That is, the power density of the second and fourth dielectric layers 3 and 5 made of a SiN film is increased by reactive sputtering using a Si target and a mixed gas of Ar and N 2 (50% N 2 ) as a sputtering gas. 8w / cm 2, the sputtering gas pressure 2.5 × 10 - is created in Pa.

また、TbFeCoからなる厚さ700Åの記録層4は、Tbタ
ーゲットとFeCoターゲットを用いた2元DCマグネトロン
スパッタ法により、基板を回転しながら、Arガス圧0.08
Pa、TbターゲットおよびFeCoターゲットのパワー密度、
それぞれ、1.5w/cm2および3.0w/cm2で作成される。
Further, the recording layer 4 of TbFeCo having a thickness of 700 mm was formed by a binary DC magnetron sputtering method using a Tb target and an FeCo target while rotating the substrate to an Ar gas pressure of 0.08.
Power density of Pa, Tb target and FeCo target,
Each of which is created by the 1.5 w / cm 2 and 3.0 w / cm 2.

上述した6種類の媒体各2枚を、それぞれホットメル
ト法により密着貼り合わせした後、80℃90%RHの温湿度
条件で、1000時間、環境試験を行った。基板とSiN層と
の間にTaOxが成膜されていない従来の媒体サンプルにつ
いても同時に環境試験を行った。
After two sheets of each of the above-described six types of media were closely adhered to each other by a hot melt method, an environmental test was performed for 1000 hours under the temperature and humidity conditions of 80 ° C. and 90% RH. An environmental test was also performed on a conventional medium sample in which TaOx was not formed between the substrate and the SiN layer.

その結果、媒体サンプルE、Fおよび従来の媒体サン
プルには、膜の剥離がみられたが、媒体サンプルA〜D
には、なんら異常は忍められなかった。
As a result, peeling of the film was observed in the media samples E and F and the conventional media sample, but the media samples A to D
Did not endure any abnormalities.

媒体サンプルA〜DのTaOxは、Taターゲットに対し
て、ArとO2の混合ガス(30%O2)を用い、スパッタガス
圧0.15〜0.30Paの範囲の反応性スパッタで製作された物
である。この場合、スパッタ中の酸素量は、第2図に酸
素分圧範囲wで示すように、おおよそ0.045〜0.09Paの
範囲にある。さらに、TaOx成膜時のArとO2の混合ガスと
して、異なる酸素濃度の物を用いた場合も、酸素分圧で
表すと、ほぼ同様の範囲において付着力の強い良好な膜
が得られることを確認した。
TaOx media samples A~D, to the Ta target, a mixed gas of Ar and O 2 (30% O 2) , those which have been produced by reactive sputtering of a range of sputtering gas pressure 0.15~0.30Pa is there. In this case, the amount of oxygen during sputtering is in the range of approximately 0.045 to 0.09 Pa, as indicated by the oxygen partial pressure range w in FIG. Furthermore, when using a mixed gas of Ar and O 2 as a mixed gas of Ar and O 2 during TaOx film formation, a good film with strong adhesive force can be obtained in almost the same range when expressed in terms of oxygen partial pressure. It was confirmed.

なお、媒体構成としては上述のものに限定されるもの
ではなく、SiNからなる第三の誘電体層の上にさらにAl
等の反射膜を形成した媒体構成に対しても同様の効果が
あることはいうまでもない。
Note that the medium configuration is not limited to the above-described one, and an Al layer is further formed on the third dielectric layer made of SiN.
It is needless to say that the same effect can be obtained for a medium configuration having a reflective film formed thereon.

〔発明の効果〕〔The invention's effect〕

本発明の光磁気記録媒体は、従来より樹脂基板への付
着力が強い光磁気記録媒体を実現できるので、耐剥離性
に優れた信頼性の高い光磁気記録媒体を提供できる。
Since the magneto-optical recording medium of the present invention can realize a magneto-optical recording medium having a stronger adhesive force to a resin substrate than ever, a highly reliable magneto-optical recording medium having excellent peel resistance can be provided.

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

第1図は本発明の一実施例を示す部分断面図、第2図は
第1図に示す実施例の特性図である。 1……基板、2,3,5……誘電体層、4……記録層、v…
…膜堆積速度曲線、n……屈折率曲線、w……酸素分圧
範囲。
FIG. 1 is a partial sectional view showing an embodiment of the present invention, and FIG. 2 is a characteristic diagram of the embodiment shown in FIG. 1 ... substrate, 2, 3, 5 ... dielectric layer, 4 ... recording layer, v ...
... film deposition rate curve, n ... refractive index curve, w ... oxygen partial pressure range.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】基体上に少なくともTaの酸化物(TaOx)か
らなる第一の誘電体層と、 前記第一の誘電体層の上に成膜されたSiNからなる第二
の誘電体層と、 前記第二の誘電体層の上に成膜された希土類金属と鉄族
遷移金属との組合せによって作成される非晶質磁性合金
膜からなる記録層と、 前記記録層の上に成膜されたSiNからなる第三の誘電体
層とを含む光磁気記録媒体の製造方法において、 前記第一の誘電体層はTaターゲットに対して酸素分圧が
0.045〜0.09(Pa)の範囲のArとO2の混合ガスをスパッ
タガスとした反応性スパッタにより成膜することで作成
し、 しかる後に前記第二の誘電体層、前記記録層、前記第三
の誘電体層を順次成膜することを特徴とする光磁気記録
媒体の製造方法。
1. A first dielectric layer made of at least Ta oxide (TaO x ) on a substrate, and a second dielectric layer made of SiN formed on the first dielectric layer A recording layer made of an amorphous magnetic alloy film formed by a combination of a rare earth metal and an iron group transition metal formed on the second dielectric layer; and a film formed on the recording layer A third dielectric layer made of SiN, wherein the first dielectric layer has an oxygen partial pressure relative to a Ta target.
It is formed by forming a film by reactive sputtering using a mixed gas of Ar and O 2 in a range of 0.045 to 0.09 (Pa) as a sputtering gas, and thereafter, the second dielectric layer, the recording layer, and the third A method of manufacturing a magneto-optical recording medium, wherein the dielectric layers are sequentially formed.
JP2159118A 1990-06-18 1990-06-18 Method for manufacturing magneto-optical recording medium Expired - Lifetime JP2707808B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2159118A JP2707808B2 (en) 1990-06-18 1990-06-18 Method for manufacturing magneto-optical recording medium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2159118A JP2707808B2 (en) 1990-06-18 1990-06-18 Method for manufacturing magneto-optical recording medium

Publications (2)

Publication Number Publication Date
JPH0449548A JPH0449548A (en) 1992-02-18
JP2707808B2 true JP2707808B2 (en) 1998-02-04

Family

ID=15686634

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2159118A Expired - Lifetime JP2707808B2 (en) 1990-06-18 1990-06-18 Method for manufacturing magneto-optical recording medium

Country Status (1)

Country Link
JP (1) JP2707808B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0714231A (en) * 1993-06-29 1995-01-17 Sharp Corp Magneto-optical disk, optical pickup, and magneto-optical disk device

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62222453A (en) * 1986-03-24 1987-09-30 Seiko Epson Corp Optical recording medium
JPH01189049A (en) * 1988-01-22 1989-07-28 Nec Corp Magneto-optical recording medium

Also Published As

Publication number Publication date
JPH0449548A (en) 1992-02-18

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