JPS59227052A - Photomagnetic recording medium - Google Patents
Photomagnetic recording mediumInfo
- Publication number
- JPS59227052A JPS59227052A JP9961383A JP9961383A JPS59227052A JP S59227052 A JPS59227052 A JP S59227052A JP 9961383 A JP9961383 A JP 9961383A JP 9961383 A JP9961383 A JP 9961383A JP S59227052 A JPS59227052 A JP S59227052A
- Authority
- JP
- Japan
- Prior art keywords
- film
- optical layer
- magnetic optical
- recording medium
- chip
- 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.)
- Pending
Links
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 4
- 239000010941 cobalt Substances 0.000 claims abstract description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 4
- 230000005415 magnetization Effects 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 abstract description 6
- 238000004544 sputter deposition Methods 0.000 abstract description 4
- 229910052771 Terbium Inorganic materials 0.000 abstract description 3
- 239000011521 glass Substances 0.000 abstract description 3
- 239000000919 ceramic Substances 0.000 abstract description 2
- 239000002131 composite material Substances 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 abstract description 2
- 230000003287 optical effect Effects 0.000 abstract 3
- 229910052692 Dysprosium Inorganic materials 0.000 abstract 1
- 229910052688 Gadolinium Inorganic materials 0.000 abstract 1
- 238000000151 deposition Methods 0.000 abstract 1
- 238000007733 ion plating Methods 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 12
- 239000010409 thin film Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910017061 Fe Co Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000005300 metallic glass Substances 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 230000005374 Kerr effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910002058 ternary alloy Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B11/00—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor
- G11B11/10—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor using recording by magnetic means or other means for magnetisation or demagnetisation of a record carrier, e.g. light induced spin magnetisation; Demagnetisation by thermal or stress means in the presence or not of an orienting magnetic field
- G11B11/105—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor using recording by magnetic means or other means for magnetisation or demagnetisation of a record carrier, e.g. light induced spin magnetisation; Demagnetisation by thermal or stress means in the presence or not of an orienting magnetic field using a beam of light or a magnetic field for recording by change of magnetisation and a beam of light for reproducing, i.e. magneto-optical, e.g. light-induced thermomagnetic recording, spin magnetisation recording, Kerr or Faraday effect reproducing
- G11B11/10582—Record carriers characterised by the selection of the material or by the structure or form
- G11B11/10586—Record carriers characterised by the selection of the material or by the structure or form characterised by the selection of the material
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B11/00—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor
- G11B11/10—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor using recording by magnetic means or other means for magnetisation or demagnetisation of a record carrier, e.g. light induced spin magnetisation; Demagnetisation by thermal or stress means in the presence or not of an orienting magnetic field
- G11B11/105—Recording on or reproducing from the same record carrier wherein for these two operations the methods are covered by different main groups of groups G11B3/00 - G11B7/00 or by different subgroups of group G11B9/00; Record carriers therefor using recording by magnetic means or other means for magnetisation or demagnetisation of a record carrier, e.g. light induced spin magnetisation; Demagnetisation by thermal or stress means in the presence or not of an orienting magnetic field using a beam of light or a magnetic field for recording by change of magnetisation and a beam of light for reproducing, i.e. magneto-optical, e.g. light-induced thermomagnetic recording, spin magnetisation recording, Kerr or Faraday effect reproducing
Landscapes
- Thin Magnetic Films (AREA)
Abstract
Description
【発明の詳細な説明】
一1刻転外野
本発明は光磁気記録媒体に用いられる非晶質磁気光学層
に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an amorphous magneto-optic layer used in a magneto-optical recording medium.
−vt迷−伐賀
従来、膜面と垂直な方向に磁化容易軸を有する強磁(2
+薄膜としては八・I n 13 iに代表される多粘
品金属薄膜、C,’= d −Co、(、d F’(
!などに代表される非晶質金属薄膜、GIGに代表され
る化合物’N−1+’i品薄膜か′知られている。これ
らの薄膜は種々の利点を有するが、M n B iはキ
ュリ一点が高いために書ぎ込みに大きなエネルギーを必
要としまた薄膜の作製が技術的に困何であるという欠点
かある。また、(id−Co、 Gd−Feの非晶質金
属薄膜は室温における保磁力か小さく(300〜50(
l Oe)記録された情報が不安定であるという欠点を
有している。そこで、上記のような従来の磁性薄膜記録
媒体の欠点を除去する新しい磁性薄膜記録媒体として、
それぞれG d ”I’ l) −Fe3元系合金薄
膜を有するもの(特開昭56−126907号公報参照
)およびコ゛l] D y Fe非晶質薄膜を有するも
の(特開昭57−169945号公報参照)か提案され
ている。しカルなか呟これらのものはキュリ一温度か比
較的小さく小さなレーザーパワーで書き込むことか可能
である等の利点を有するにもかかわらず、カー(Ker
r)回転角かf)、 20−0.35dcg と小さく
尤11j生特性の点て゛いまだr:ei足のいくもので
はない。-vtmaze-Sukiga Conventionally, ferromagnets (2
+ As a thin film, a multiviscous metal thin film represented by 8・I n 13 i, C,'= d −Co, (, d F'(
! Amorphous metal thin films such as those typified by the above, and compound 'N-1+'i thin films typified by GIG are known. Although these thin films have various advantages, M n B i requires a large amount of energy for writing due to its high Curie point, and also has the disadvantage that it is technically difficult to fabricate the thin film. In addition, (id-Co, Gd-Fe amorphous metal thin films have a small coercive force at room temperature (300-50(
l Oe) It has the disadvantage that the recorded information is unstable. Therefore, we developed a new magnetic thin film recording medium that eliminates the drawbacks of conventional magnetic thin film recording media as described above.
G d "I' l) - Fe having a ternary alloy thin film (see JP-A No. 56-126907) and G d "I' l) - Fe having an amorphous thin film (see JP-A-57-169945); Although these devices have advantages such as being able to write at Curie temperature, being relatively small and being able to write with a small laser power, Kerr (see publication) has been proposed.
The r) rotation angle (f) is small at 20-0.35 dcg, and the raw characteristics of r:ei are still not satisfactory.
1拍
本発明は上記現状に鑑みてなされたものであって、その
目的はキュリ一温度が低くしが乙カー回転角の大とい非
晶質磁気光学層を提供することである。The present invention has been made in view of the above-mentioned current situation, and its object is to provide an amorphous magneto-optical layer having a low Currency temperature and a large Curr rotation angle.
ち111な
本発明の非晶質磁気ソ0学層は膜面と垂直な方向に磁化
容易軸を有するTb−1’)y−Fe膜またはG(IT
b−Fe膜に少なくとも0.5原子%のコバルトを含む
ものである。本発明においてコバル1の含有11)、を
少なくとも0.5原子%と限定するのは、大きなカー回
転角を1))るためであり、0.5原子%未満では充分
なカー回転角か得られす本発明の効果が達成されない。The amorphous magnetic sonic layer of the present invention is a Tb-1')y-Fe film or a G(IT
The b-Fe film contains at least 0.5 at.% of cobalt. In the present invention, the content of Kobal-111) is limited to at least 0.5 at% in order to obtain a large Kerr rotation angle. Therefore, the effects of the present invention cannot be achieved.
一方、コバルトの含有量をあまり天外くするとキュリ一
温度か上かりすぎるので(1,5〜20原子%の範囲か
(l+’ましい。On the other hand, if the cobalt content is increased too much, the temperature will rise too much (1.5 to 20 atomic %) (l+' is preferable).
本発明の磁気光学R4はガラス、プラスティック、セラ
ミックなどからなる非磁性法板上に、又バッタ法、蒸着
法、イオンブレーティング法などにより、少なくとも0
.5原r−%のCoを含むTI+ −Dy −Fc膜ま
たは(id−Tb−Fe膜を形成させることにより作製
することができる。ターゲラ1は例えば゛コンポジット
法を用い、F″e0円板) 、J−ニ’rb、Dyt、
J:UCo+ ップマr、:1.tGd。The magneto-optical R4 of the present invention is produced on a non-magnetic plate made of glass, plastic, ceramic, etc., or by a batter method, vapor deposition method, ion blating method, etc.
.. It can be produced by forming a TI+-Dy-Fc film or (id-Tb-Fe film) containing 5 elements r-% of Co. Targetera 1 can be produced using, for example, a composite method using a F″e0 disk. , J-ni'rb, Dyt,
J: UCo+ puma r, :1. tGd.
TbおよびCoチップをのぜて構成しそして組成はター
ゲット表面の面積比でフントロールする。It is composed of Tb and Co chips, and the composition is determined by the area ratio of the target surface.
また、本発明の磁気光学層を尤磁気記#i !l!11
.体に使用する場合はそれを単独で用いてもよいしある
いは池の膜と一緒に用いてもよい。例えば保護膜は例え
ばSin、、5iO1Si、+N、などからなる膜をT
I+−1)y Fe−Co膜またはCi d −1”
l+Fe、Co膜の上にスパッタ法、蒸着法、イオン
ブレーティング法などにより設けることかでbる。In addition, the magneto-optic layer of the present invention may be used as a magneto-optical layer #i! l! 11
.. For body use, it may be used alone or in conjunction with pond membranes. For example, the protective film is a film made of, for example, Sin, 5iO1Si, +N, etc.
I+-1)y Fe-Co film or Ci d-1"
It can be provided on the l+Fe, Co film by sputtering, vapor deposition, ion blating, or the like.
実施例
以下に実施例をあげて本発明を具体的に説明するが、こ
れに限定されるものではない。EXAMPLES The present invention will be specifically explained with reference to Examples below, but the present invention is not limited thereto.
実施例1
この実施例では以下の作製条件でスライドガラス上に約
20旧)人の膜厚のTI]−Dy−Fe−Co膜を作製
し、Incの大きい補償組成(=1近のFe0.79”
Fbo、501)yO,50)0.2]′)組成におい
てFeの一部をCoで置換していく場合のカー回転角(
θk)およびキュリ一温度(Tc)の変化をみた。Example 1 In this example, a TI]-Dy-Fe-Co film with a film thickness of approximately 20 mm was prepared on a slide glass under the following manufacturing conditions, and a compensation composition with a large Inc (Fe0. 79”
Fbo, 501) yO, 50) 0.2]') Kerr rotation angle (
Changes in θk) and Curie temperature (Tc) were observed.
〈作製条件〉
残留ガス圧 ’、 rj X ] (,1−’ i”
orr)\f力゛ス圧 : 1.5xlO−2To
rr放電々力 : 、=l fl fl Wプレス
パッツ時間: (if1minメインスパッタ時間:
ff1lTlll力−回転角θ1(は^(板側がらl1
c−Neレーザ(λ= 6328 A )を照射してカ
ー効果により求めた1、また、キュリ一温度1゛cは振
動試料型磁化測定装置により測定した。<Production conditions> Residual gas pressure ', rj
orr)\fforce pressure: 1.5xlO-2To
rr discharge power: ,=l fl fl W press sputtering time: (if1min main sputtering time:
ff1lTllll force-rotation angle θ1(ha^(from the plate side l1
1, which was determined by the Kerr effect by irradiation with a c-Ne laser (λ = 6328 A), and the Curie temperature, 1°c, were measured using a vibrating sample type magnetization measuring device.
(1′″(+−XCoX)0.7g(i″l]0.50
1)yo、50)0.21中0C(l添加電×とθ1(
との関係を第1図に示す。これから明らかなように、c
o添加量Xを増すとθには0.2 o deHがら0.
31 de8まで増加するが、X−1,1、] (l
(・j近でほぼ飽和傾向を示しそれ以、J、 C。(1′″(+−XCoX)0.7g(i″l)0.50
1) yo, 50) 0C in 0.21 (l added charge × and θ1 (
Figure 1 shows the relationship between As is clear from this, c
When the amount of o added X increases, θ changes from 0.2 o deH to 0.
31 de8, but X-1,1, ] (l
(・It shows an almost saturated tendency near j, and after that, J, C.
を添加しても余り効果かない。一方、キュリ一温度′1
゛(は第2図に示したようにCo添加量Xを増1と9
+) ’Cがら1 り (1’C位まで直線的に」ユy
1する。i’ cか高すぎると記tiエネルギーが必要
となるので記録感度が悪くなる。本実施例ではθkかx
=0.1041近で飽和傾向を示していることからTc
が余り高くならないX=:o、]。Even if you add it, it won't be very effective. On the other hand, Curi one temperature'1
゛(As shown in Figure 2, increase the amount of Co added 1 and 9.
+) 'C-gara 1 ri (straight line to 1'C')
Do 1. If i'c is too high, more energy is required, resulting in poor recording sensitivity. In this example, θk or x
Since it shows a tendency to saturate near = 0.1041, Tc
is not too high.
伺近の値でθ1(が太きくTcが低い最適条件であると
結論できる。It can be concluded that the approximate value is the optimum condition where θ1 is large and Tc is low.
実施例2
この実施例では以下の作製条件で又ライト力゛ラス」−
に200 (l 〕\の膜厚のC1d−TI] Fe
−Co膜を作製し]−1cの大きい補償組成1;1近
のF”0.79” do、 50 ” ”0.50 )
0.21の組成においてFeの一部をCoで置換してい
く場合のカー回1j角(θk)およびキュリ一温度じ1
゛c)の変化をみた。Example 2 In this example, the following manufacturing conditions were used:
C1d-TI with a film thickness of 200 (l)\]Fe
-Co film was prepared] -1c large compensation composition 1;
The Kerr rotation angle 1j (θk) and the Curie temperature 1 when part of Fe is replaced with Co in a composition of 0.21
We looked at the changes in (c).
〈作製条件〉
残留ガス圧 : 8 x 11)−?TorrArガ
ス圧 : 1.5xlO−二i’orr放電々力
: 401) w
プレスバッフ時間:60m団
メインスパッタ時間: L3 III j IIシカ
−転角およびキュリ一温度の!flll定は実施例1と
同様にして測定した。(Fe膜−xCox)0.79(
Gdo、5oTIJo、5o)0.21中のCo添加量
Xとθにとの関係を第3図に示す。これから明らかなよ
うに、Co添加量×を増すとθには0.35deεから
0 、45 deBまで増加するか、x = 0 、1
. O[=l近でほぼ飽和傾向を示しそれ以j二coを
添加しても効果がない。一方、キュリ一温度]゛cは第
4図に示したようにCo添加量Xを増すと160 ’C
から240 ”C位まで直線的に上昇動る。Tcか高す
ぎると記録エネルギーか必要となるので記録感度が悪く
なる。以」−の結果から、CO添加量xの最適値は0.
08〜O、] (lであると結論できる。<Production conditions> Residual gas pressure: 8 x 11) -? TorrAr gas pressure: 1.5xlO-2i'orr discharge force
: 401) w Press buff time: 60m group Main sputter time: L3 III j II Deer turning angle and Curie temperature! The full constant was measured in the same manner as in Example 1. (Fe film-xCox) 0.79 (
The relationship between the Co addition amount X and θ in Gdo, 5oTIJo, 5o)0.21 is shown in FIG. As is clear from this, when the Co addition amount x is increased, θ increases from 0.35 deε to 0,45 deB, or x = 0, 1
.. It shows a tendency to saturation near O[=l, and beyond that point, there is no effect even if J2CO is added. On the other hand, the Curie temperature] ゛c becomes 160'C as the Co addition amount X is increased, as shown in Figure 4.
The temperature rises linearly from 240 to about 240"C. If Tc is too high, recording energy is required, resulting in poor recording sensitivity. From the following results, the optimum value for the amount of CO added x is 0.
08~O, ] (It can be concluded that l.
例來
本発明の非晶質磁気光学層はCoを含むことによりカー
回転角θ1(か′0.2O−(1,45deBまで火ト
くなり再生特性の良い光磁気記録媒体を提f共で・きる
。For example, since the amorphous magneto-optic layer of the present invention contains Co, the Kerr rotation angle θ1 (~'0.2O-(1.45 deB) can be reached, thereby providing a magneto-optical recording medium with good reproduction characteristics. ·Wear.
第1図ないし第4図は本発明の磁気光学層の最適条件を
決定するにあたっての組成変化にヌ1]するカー回1を
角とキュリ一温度との関係をそれぞれ示す図である。
Co3祭加量L
Co勇得カロ量工
Co>励口量Oつ
Co旅カロ量aつFIGS. 1 to 4 are diagrams showing the relationship between the Kerr cycle 1 and the Curie temperature, which are related to composition changes in determining the optimum conditions for the magneto-optic layer of the present invention. Co3 supplementary quantity L Co Yukari quantity Co > Excitation quantity Otsu Co travel quantity atsu
Claims (1)
Fe膜またはG d i” l+ F e膜に少な
くとも0.5原子%のコバルトを含むことを特徴とする
、非晶質磁気光学層。Tb-1)y- having an axis of easy magnetization in the direction perpendicular to the film surface
An amorphous magneto-optical layer comprising at least 0.5 atomic % of cobalt in the Fe film or the G d i "l+ Fe film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9961383A JPS59227052A (en) | 1983-06-06 | 1983-06-06 | Photomagnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9961383A JPS59227052A (en) | 1983-06-06 | 1983-06-06 | Photomagnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59227052A true JPS59227052A (en) | 1984-12-20 |
Family
ID=14251940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9961383A Pending JPS59227052A (en) | 1983-06-06 | 1983-06-06 | Photomagnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59227052A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6214350A (en) * | 1985-07-12 | 1987-01-22 | Hitachi Ltd | magneto-optical recording medium |
JPH05174437A (en) * | 1991-04-30 | 1993-07-13 | Canon Inc | Magneto-optical recording medium |
JPH05182265A (en) * | 1991-04-30 | 1993-07-23 | Canon Inc | Magneto-optical recording medium |
US5786078A (en) * | 1990-10-26 | 1998-07-28 | Teijin Limited | Magneto-optical recording medium |
-
1983
- 1983-06-06 JP JP9961383A patent/JPS59227052A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6214350A (en) * | 1985-07-12 | 1987-01-22 | Hitachi Ltd | magneto-optical recording medium |
US5786078A (en) * | 1990-10-26 | 1998-07-28 | Teijin Limited | Magneto-optical recording medium |
JPH05174437A (en) * | 1991-04-30 | 1993-07-13 | Canon Inc | Magneto-optical recording medium |
JPH05182265A (en) * | 1991-04-30 | 1993-07-23 | Canon Inc | Magneto-optical recording medium |
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