JPH0366012A - Magneto-resistance effect type head - Google Patents
Magneto-resistance effect type headInfo
- Publication number
- JPH0366012A JPH0366012A JP20120389A JP20120389A JPH0366012A JP H0366012 A JPH0366012 A JP H0366012A JP 20120389 A JP20120389 A JP 20120389A JP 20120389 A JP20120389 A JP 20120389A JP H0366012 A JPH0366012 A JP H0366012A
- Authority
- JP
- Japan
- Prior art keywords
- film
- layer
- soft magnetic
- amorphous soft
- head
- 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
Links
- 230000000694 effects Effects 0.000 title abstract description 4
- 230000005291 magnetic effect Effects 0.000 claims abstract description 69
- 239000004020 conductor Substances 0.000 claims abstract description 28
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims abstract description 7
- 230000005294 ferromagnetic effect Effects 0.000 claims abstract description 5
- 238000010438 heat treatment Methods 0.000 abstract description 22
- 230000006866 deterioration Effects 0.000 abstract description 7
- 238000009792 diffusion process Methods 0.000 abstract description 6
- 238000000034 method Methods 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract 5
- 239000010408 film Substances 0.000 description 68
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 15
- 230000005415 magnetization Effects 0.000 description 11
- 238000004458 analytical method Methods 0.000 description 8
- 229910000889 permalloy Inorganic materials 0.000 description 7
- 239000010936 titanium Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000009826 distribution Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000000696 magnetic material Substances 0.000 description 4
- 238000004544 sputter deposition Methods 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 229910001030 Iron–nickel alloy Inorganic materials 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 238000000992 sputter etching Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Magnetic Heads (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は磁気記憶媒体に書き込まれた磁気的情報を、磁
気抵抗効果を利用して読み出す強磁性磁気抵抗効果素子
(以下、MR素子と略記する〉を具備した磁気抵抗効果
ヘッド(以下、MRヘッドと略記する〉に関するもので
ある。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a ferromagnetic magnetoresistive element (hereinafter abbreviated as MR element) that reads magnetic information written on a magnetic storage medium using the magnetoresistive effect. The present invention relates to a magnetoresistive head (hereinafter abbreviated as MR head) equipped with a magnetoresistive head (hereinafter abbreviated as MR head).
[従来の技術]
周知の如く、MR素子を磁気記憶媒体に書き込まれた磁
気的情報に対して線形応答性を呈する高効率の再生専用
磁気ヘッドとして使用する場合には、MR素子に流すセ
ンス電流IとMR素子の磁化Mのなす角度θ(以下、バ
イアス角度と呼ぶ〉を所定の値(望ましくは45度〉に
設定するバイアス手段を具備しなければならない。[Prior Art] As is well known, when an MR element is used as a highly efficient read-only magnetic head that exhibits linear response to magnetic information written on a magnetic storage medium, a sense current flowing through the MR element is required. A bias means must be provided for setting the angle θ (hereinafter referred to as bias angle) between I and the magnetization M of the MR element to a predetermined value (preferably 45 degrees).
上述のバイアス手段としては、種々の方法が開示されて
いるが、この中で実願昭59−048201号あるいは
特願昭62−072054@に開示されたMRヘッドに
おいては、MR素子上に非磁性導体層と非晶質軟磁性体
層(例えばCOZrMO膜)とを順次積層した構造によ
り良好なバイアス角度θが得られ、線形応答性に優れた
MRヘッドが実現できることが示されている。Various methods have been disclosed as the above-mentioned bias means, but among these, in the MR head disclosed in Utility Model Application No. 59-048201 or Japanese Patent Application No. 62-072054@, a non-magnetic material is used on the MR element. It has been shown that a structure in which a conductor layer and an amorphous soft magnetic layer (for example, a COZrMO film) are sequentially laminated can provide a good bias angle θ and realize an MR head with excellent linear response.
即ち、第4図に示すように、ガラス、フェライト等から
なる表面の滑らかな絶縁性基板(図示せず〉上に、スパ
ッタ法ないしは蒸着法により、強磁性体薄膜からなるM
R素子1(例えば膜厚200〜500A(7)N i
Fe合金)を形成し、前記MR素子1上にTi、MO,
Cr等の非磁性導体層2を同様の方法で形成し、さらに
前記非磁性導体層2上に非晶質軟磁性体層5を同様な方
法で形成した構造を有するMRヘッドを開示している。That is, as shown in FIG. 4, M made of a ferromagnetic thin film is deposited on an insulating substrate (not shown) with a smooth surface made of glass, ferrite, etc. by sputtering or vapor deposition.
R element 1 (for example, film thickness 200 to 500A (7) Ni
Ti, MO,
An MR head is disclosed having a structure in which a non-magnetic conductor layer 2 made of Cr or the like is formed by a similar method, and an amorphous soft magnetic material layer 5 is further formed on the non-magnetic conductor layer 2 by a similar method. .
ここで、6はMR素子1、非磁性導体@2および非晶質
軟磁性体層5の積層体に通電するための端子である。Here, 6 is a terminal for supplying current to the laminate of the MR element 1, the nonmagnetic conductor @2, and the amorphous soft magnetic layer 5.
このようなMRヘッドにおいては、端子6から供給され
るセンス電流■は、MR素子1にのみならず非磁性導体
層2および非晶質軟磁性体@5にも分流する。従って、
このような構造においては、MR素子1および非磁性導
体層2に分流したセンス電流■により、非晶質軟磁性体
層5の面内を通りかつセンス電流Iの方向と垂直方向の
磁界が発生し、この磁界により非晶質軟磁性体層5の磁
化方向が回転する。このため、非晶質軟磁性体層5にお
ける磁化は、非晶質軟磁性体層5の周囲に前記磁化の方
向とは逆方向の磁界を生じ、その一部はMR素子1に印
加される。一方、非晶質軟磁性体層5および非磁性導体
層2に分流したセンス電流■により、MR素子1の面内
を通りセンス電流Iと垂直方向の磁界が生じ、この磁界
の方向は前述の非晶質軟磁性体層5の磁化によって発生
する磁界の方向と一致する。つまり、非晶質軟磁性体層
5の磁化によって発生する磁界とセンス電流Iによって
生じる磁界が、MR素子にバイアス磁界として印加され
る。このバイアス磁界は、MR素子1の磁化をセンス電
流Iに対して回転させ、MR素子のバイアス角度θを所
定の値(理想的には45度)とし、線形応答性に優れた
MRヘッドを実現する。In such an MR head, the sense current (2) supplied from the terminal 6 is shunted not only to the MR element 1 but also to the nonmagnetic conductor layer 2 and the amorphous soft magnetic material @5. Therefore,
In such a structure, the sense current (IV) shunted to the MR element 1 and the non-magnetic conductor layer 2 generates a magnetic field that passes within the plane of the amorphous soft magnetic layer 5 and is perpendicular to the direction of the sense current I. However, the magnetization direction of the amorphous soft magnetic layer 5 is rotated by this magnetic field. Therefore, the magnetization in the amorphous soft magnetic layer 5 generates a magnetic field around the amorphous soft magnetic layer 5 in a direction opposite to the direction of the magnetization, a part of which is applied to the MR element 1. . On the other hand, the sense current {circle around (2)} which is shunted into the amorphous soft magnetic layer 5 and the nonmagnetic conductor layer 2 generates a magnetic field in the plane of the MR element 1 in a direction perpendicular to the sense current I, and the direction of this magnetic field is as described above. This coincides with the direction of the magnetic field generated by the magnetization of the amorphous soft magnetic layer 5. That is, the magnetic field generated by the magnetization of the amorphous soft magnetic layer 5 and the magnetic field generated by the sense current I are applied to the MR element as a bias magnetic field. This bias magnetic field rotates the magnetization of the MR element 1 with respect to the sense current I, sets the bias angle θ of the MR element to a predetermined value (ideally 45 degrees), and realizes an MR head with excellent linear response. do.
[発明が解決しようとする課題]
ところで1.前述の構造、即ちMR素子1、非磁性導体
層2および非晶質軟磁性体層5を積層した構造を有する
MRヘッドにおいては、非磁性導体層2をTi膜、MO
膜ないしはC「膜とした場合、製造プロセ゛ス中の加熱
工程(300〜350’C)で非晶質軟磁性体層5ある
いはMR素子1の磁気特性が劣化し、MRヘッドの再生
効率が低下するという問題点があった。[Problems to be solved by the invention] By the way, 1. In the MR head having the above-mentioned structure, that is, a structure in which the MR element 1, the nonmagnetic conductor layer 2, and the amorphous soft magnetic layer 5 are laminated, the nonmagnetic conductor layer 2 is made of a Ti film, an MO film, etc.
In the case of a film or C film, the magnetic properties of the amorphous soft magnetic layer 5 or the MR element 1 deteriorate during the heating step (300 to 350'C) during the manufacturing process, and the reproduction efficiency of the MR head decreases. There was a problem.
製造プロセス中の加熱工程は、非晶質軟磁性体層5の磁
気特性を改善するため、および非晶質軟磁性体層5の磁
化容易軸方向とMR素子1の磁化容易軸方向を同一方向
に揃えて良好なバイアスレベルを実現するために必要な
工程で、MRヘッドの製造プロセスでは必須の工程であ
る。従って、加熱によって磁気特性が劣化することのな
いMRヘッドであることが必要である。The heating step during the manufacturing process is performed in order to improve the magnetic properties of the amorphous soft magnetic layer 5 and to align the easy axis of magnetization of the amorphous soft magnetic layer 5 and the easy axis of magnetization of the MR element 1 in the same direction. This is a necessary step to achieve a good bias level in line with the MR head, and is an essential step in the MR head manufacturing process. Therefore, it is necessary to provide an MR head whose magnetic properties do not deteriorate due to heating.
本発明は、以上述べたような従来の課題を解決するため
になされたもので、加熱工程でのMR素子1および非晶
質軟磁性体層5の磁気特性の劣化の生じない磁気抵抗効
果ヘッドを提供することを目的とする。The present invention has been made to solve the conventional problems as described above, and provides a magnetoresistive head that does not cause deterioration of the magnetic properties of the MR element 1 and the amorphous soft magnetic layer 5 during the heating process. The purpose is to provide
[課題を解決するための手段]
本発明は、強磁性磁気抵抗効果素子と非晶質軟磁性体層
とが非磁性導体層を介して積層され、かつ前記非磁性導
体層が窒化チタニウム膜からなることを特徴とする磁気
抵抗効果ヘッドである。[Means for Solving the Problems] The present invention provides a structure in which a ferromagnetic magnetoresistive element and an amorphous soft magnetic layer are laminated with a nonmagnetic conductor layer interposed therebetween, and the nonmagnetic conductor layer is made of a titanium nitride film. This is a magnetoresistive head characterized by the following.
[作用]
本発明者の検討によれば、加熱工程にあける特性の劣化
の原因は、前述のMRヘッド製造プロセスの加熱工程で
、非磁性導体層2とMR素子1との界面、あるいは非磁
性導体層2と非晶質軟磁性体層5との界面で拡散が生じ
るためであることがわかった。以下、この点に関して詳
細に言及する。[Function] According to the inventor's study, the cause of the deterioration of characteristics during the heating process is the interface between the non-magnetic conductor layer 2 and the MR element 1, or the non-magnetic It was found that this is due to diffusion occurring at the interface between the conductor layer 2 and the amorphous soft magnetic layer 5. This point will be discussed in detail below.
第3図は、Sil板上に約500AのN i Fe膜(
MR素子1に対応する〉および約30OAのT膜(非磁
性導体層2に対応する〉を、この順序に積層した試料の
加熱処理前後のオージェ分析装置による深さ方向の分析
結果の例である。ここで、加熱処理条件は、300℃、
1時間であり、加熱処理は真空中(真空度: 2 X
10−6 丁orr)で行った。Figure 3 shows an approximately 500A N i Fe film (
This is an example of analysis results in the depth direction by an Auger analyzer before and after heat treatment of a sample in which a T film (corresponding to MR element 1) and a T film (corresponding to nonmagnetic conductor layer 2) of approximately 30 OA were laminated in this order. Here, the heat treatment conditions are 300°C,
1 hour, and the heat treatment was performed in a vacuum (degree of vacuum: 2X
10-6 tons orr).
第3図(a)は、加熱処理前のオージェ分析結果である
が、各元素の分布は深さ約300Aを境にして明瞭であ
り、NiFe膜とli膜はほとんど拡散していないと言
える。一方、第3図(b)は加熱処理後の分析結果であ
るが、第3図(a)に比較して各元素の分布は深さ方向
に広く分布しており、特にTiは深さ600A程度まで
拡散している。FIG. 3(a) shows the results of Auger analysis before heat treatment, and it can be said that the distribution of each element is clear at a depth of about 300 A, and that there is almost no diffusion in the NiFe film and the Li film. On the other hand, FIG. 3(b) shows the analysis results after heat treatment, and compared to FIG. 3(a), the distribution of each element is wider in the depth direction, especially Ti at a depth of 600A. It has spread to some extent.
また、膜厚約30OAのTi膜上に膜厚約500AのC
OZrMO膜(非晶質軟磁性体層5に対応する)を積層
した試料を上記と同様に300 ’C11時問、真空中
(真空度:2X10−6Torr)で加熱処理したあと
においても同様なT1の拡散が認められた。In addition, a C film with a thickness of about 500A was applied on a Ti film with a thickness of about 30OA.
The same T1 was obtained after the sample in which the OZrMO film (corresponding to the amorphous soft magnetic material layer 5) was laminated was heat treated in vacuum (degree of vacuum: 2X10-6 Torr) for 300' C11 hours in the same manner as above. The spread of was observed.
以上のように、オージェ分析結果によれば、MRヘッド
の製造プロセス中の加熱工程により、非磁性導体層2と
MR素子1ないしは非磁性導体層2と非晶質軟磁性体層
5との間に拡散が生じ、これによりMR素子1あるいは
非晶質軟磁性体層5の磁気特性、例えば飽和磁化、異方
性磁界、抵抗変化率等が劣化したと考えられる。As described above, according to the Auger analysis results, the heating process during the manufacturing process of the MR head causes the gap between the nonmagnetic conductor layer 2 and the MR element 1 or the nonmagnetic conductor layer 2 and the amorphous soft magnetic layer 5 to Diffusion occurs, and this is considered to have deteriorated the magnetic properties of the MR element 1 or the amorphous soft magnetic layer 5, such as saturation magnetization, anisotropic magnetic field, and rate of change in resistance.
Ti膜の代わりにMO膜やCr膜を用いた試料において
も、はぼ同様な分析結果が得られており、これらの材料
を非磁性導体層2として用いた場合の特性劣化も拡散が
原因と考えられる。Almost similar analysis results were obtained for samples using MO films or Cr films instead of Ti films, indicating that diffusion is the cause of characteristic deterioration when these materials are used as the nonmagnetic conductor layer 2. Conceivable.
一方、第2図は3i基板上に約50OAのNiFe膜(
MR素子1に対応する)および約30OAのTiN膜(
非磁性導体層2に対応する)を、この順序に積層した試
料の加熱処理後のオージェ分析装置による深さ方向の分
析結果の例である。ここで、加熱処理条件は、350℃
、2時間であり、加熱処理は真空中(真空度: 2 X
10−6 Torr)で行った。第2図から明らかな
通り、加熱処理後においても各元素の分布は深さ約30
OAを境にして明瞭であり、N i Fe膜とTiN膜
はほとんど拡散していない。また、膜厚約300Aの丁
IN膜上に膜厚約5()OAのCoZrMo膜を積層し
た試料を350℃、2時間、真空中(真空度: 2 X
10−6 Torr)で加熱処理したあとにおいても
、はぼ同様な結果が得られた。On the other hand, Fig. 2 shows a NiFe film (approximately 50 OA) on a 3i substrate.
) and a TiN film of approximately 30OA (corresponding to MR element 1)
This is an example of an analysis result in the depth direction by an Auger analyzer after heat treatment of a sample in which layers (corresponding to the non-magnetic conductor layer 2) were laminated in this order. Here, the heat treatment conditions are 350°C
, 2 hours, and the heat treatment was performed in vacuum (degree of vacuum: 2
10-6 Torr). As is clear from Figure 2, even after heat treatment, the distribution of each element is approximately 30 mm deep.
It is clear with OA as the boundary, and the Ni Fe film and TiN film are hardly diffused. In addition, a sample in which a CoZrMo film with a film thickness of about 5 () OA was laminated on a DIN film with a film thickness of about 300 A was heated at 350° C. for 2 hours in a vacuum (vacuum degree: 2
Similar results were obtained even after heat treatment at 10-6 Torr).
このように、TiN膜を非磁性導体層として用いること
により、非磁性導体層とMR素子ないしは非磁性導体層
と非晶質軟磁性体層との間の拡散が防止でき、その結果
、MRヘッド作製プロセス中の加熱工程でのMR素子あ
るいは非晶質軟磁性体層の特性劣化を、回避することが
できる。In this way, by using the TiN film as the nonmagnetic conductor layer, diffusion between the nonmagnetic conductor layer and the MR element or the nonmagnetic conductor layer and the amorphous soft magnetic layer can be prevented, and as a result, the MR head Deterioration of the characteristics of the MR element or the amorphous soft magnetic layer during the heating step during the manufacturing process can be avoided.
[実施例] 次に、本発明の実施例について説明する。[Example] Next, examples of the present invention will be described.
実施例 第1図は本発明の一実施例の構成図である。Example FIG. 1 is a block diagram of an embodiment of the present invention.
第1図において、ガラス等の非磁性基板(図示せず〉上
に八「ガス雰囲気中でのスパッタ法を用いてMR素子1
となる膜厚400Aのパーマロイ(Ni82%−101
8%、重量%)膜を成膜した。なお、蒸着時には100
0eの磁界を永久磁石で印加し、パーマロイ膜に一軸異
方性を付与した。In FIG. 1, an MR element 1 is placed on a non-magnetic substrate (not shown) such as glass using a sputtering method in a gas atmosphere.
Permalloy (Ni82%-101) with a film thickness of 400A
8%, weight %) film was formed. In addition, at the time of vapor deposition, 100
A magnetic field of 0e was applied using a permanent magnet to impart uniaxial anisotropy to the permalloy film.
次いで、Arガスと窒素ガスの混合雰囲気中(流量換算
でA r : 100 SCCm 、 N2 :
6sccm)でスパッタ法を用いて非磁性導体層となる
膜厚300AのTiN膜7を前記パーマロイ膜上に成膜
した。なお、成膜時には基板側に一80Vのバイアス電
圧を印加し、TiN膜中の不純物、特に酸素を除去して
TiN膜の比抵抗を小ざくした。成膜したTiN膜の比
抵抗は約110μΩ・cmであった。Next, in a mixed atmosphere of Ar gas and nitrogen gas (in terms of flow rate, Ar: 100 SCCm, N2:
A TiN film 7 having a thickness of 300 Å and serving as a non-magnetic conductive layer was formed on the permalloy film using a sputtering method (6 sccm). Note that during film formation, a bias voltage of -80 V was applied to the substrate side to remove impurities, particularly oxygen, in the TiN film, thereby reducing the specific resistance of the TiN film. The specific resistance of the TiN film formed was about 110 μΩ·cm.
ざらに、非晶質軟磁性体層5として膜厚300A、異方
性磁界(口k)50eのCoZrMo膜からなる非晶質
軟磁性体層7(膜組成はCo82%−・Zr6%−MO
12%、原子%〉を前述のTiN膜7上にA「ガス雰囲
気中でのスパッタ法により成膜した。Roughly speaking, the amorphous soft magnetic layer 7 is made of a CoZrMo film with a thickness of 300 A and an anisotropic magnetic field (k) of 50 e as the amorphous soft magnetic layer 5 (film composition is Co82%-Zr6%-MO).
12%, atomic %> was formed on the TiN film 7 by sputtering in a gas atmosphere.
その後、非晶質軟磁性体層5(CoZrMo膜〉に−軸
異方性を付与するため、前述したパーマロイ膜、TiN
膜、CoZrMo膜の積層体に対して、350℃、2時
間、4800eの磁界をパーマロイ膜の磁化容易軸方向
と同一方向に印加しながら、真空中で加熱処理を行った
。After that, in order to impart −axis anisotropy to the amorphous soft magnetic layer 5 (CoZrMo film), the above-mentioned permalloy film, TiN
The film and the laminate of the CoZrMo film were heat-treated in vacuum at 350° C. for 2 hours while applying a magnetic field of 4800 e in the same direction as the easy axis of magnetization of the permalloy film.
次いで、この積層体上に所定形状のフォトレジストパタ
ーンを形成し、Arガス雰囲気中でイオンエツチングを
行い、長さ50jJIr1、幅5iiInの矩形状のパ
ターンに加工した。ここで、エツチング条件は、加速電
圧: 500V、Arガス圧カニ0.1mTorrで
ある。Next, a photoresist pattern of a predetermined shape was formed on this laminate, and ion etching was performed in an Ar gas atmosphere to form a rectangular pattern with a length of 50jJIr1 and a width of 5iiIn. Here, the etching conditions are an acceleration voltage of 500 V and an Ar gas pressure of 0.1 mTorr.
次いで、前述の積層体にセンス電流■を供給する端子6
を集積化薄膜技術を用いて形成し、MRヘッドを作製し
た。なお、端子6はTiとAuの積層蒸着膜を使用し、
膜厚は各々50 A、0.5間とした。Next, a terminal 6 for supplying the sense current ■ to the above-mentioned multilayer body
was formed using integrated thin film technology to produce an MR head. Note that the terminal 6 uses a laminated vapor deposited film of Ti and Au.
The thickness of each film was 50 A and 0.5 mm.
以上のような構成を持つ本実施例によるMRヘッドにお
いては、センス電流■が5〜15mAでMR素子1のバ
イアス角度θがほぼ45度に設定できることが確認され
、良好な線形応答性と高い再生効率を有するMRヘッド
が実現された。In the MR head according to this example having the above configuration, it was confirmed that the bias angle θ of the MR element 1 can be set to approximately 45 degrees when the sense current ■ is 5 to 15 mA, and it has good linear response and high reproduction. An efficient MR head has been realized.
なお、上記実施例においては、MR素子(パーマロイ膜
>、’rrN膜層、非晶質軟磁性体層をこの順序で積層
する例のみについて言及したが、非晶質軟磁性体層、T
iN膜層、MR素子の順序で積層したMRヘッドにおい
ても優れた線形応答性と高い再生効率が得られた。また
、非晶質軟磁性体層をなす材料はCOZrMO膜に限定
されるものではなく、例えばCOTaMO膜、Cozr
Ta膜等を使用しても構わない。In the above embodiments, only the example in which the MR element (permalloy film>, 'rrN film layer, and amorphous soft magnetic layer are laminated in this order) has been described, but the amorphous soft magnetic layer, the T
Even in the MR head in which the iN film layer and the MR element were laminated in this order, excellent linear response and high reproduction efficiency were obtained. Furthermore, the material forming the amorphous soft magnetic layer is not limited to the COZrMO film, but may include, for example, a COTaMO film, a CozrMO film, and a COZrMO film.
A Ta film or the like may be used.
更に、実施例中のTiN膜の成膜方法・成膜条件は一例
であり、他の方法・条件を用いても構わない。勿論この
場合、TiN膜の比抵抗が極端に大きいと導電性が損な
われたり、ジュール熱による発熱の問題が生じるため、
成膜したTiN膜の比抵抗の値に注意すべきである。T
iN膜の比抵抗値については、本発明の適用されるMR
ヘッドの設計・仕様やヒートシンクの状態に大きく依存
するため一概に言えないが、200μΩ・cm以下の比
抵抗であることが望ましい。Further, the method and conditions for forming the TiN film in the examples are merely examples, and other methods and conditions may be used. Of course, in this case, if the specific resistance of the TiN film is extremely high, the conductivity will be impaired and the problem of heat generation due to Joule heat will occur.
Care should be taken regarding the resistivity value of the TiN film formed. T
Regarding the specific resistance value of the iN film, MR to which the present invention is applied
Although it is difficult to make a general statement because it largely depends on the design and specifications of the head and the condition of the heat sink, it is desirable that the resistivity be 200 μΩ·cm or less.
比較例
TiN膜を11膜とした以外は実施例と全く同様にして
MRヘッドを作製した。Comparative Example An MR head was manufactured in the same manner as in the example except that 11 TiN films were used.
このMRヘッドにおいては、非晶質軟磁性体層に一軸異
方性を付与する350℃、2時間の加熱工程でMR素子
1となるパーマロイ膜あるいは非晶質軟磁性体層2とな
るCOZrMO膜の磁気特性が劣化したため、センス電
流を35〜40mA程度流しても十分なバイアスがMR
素子に印加されず、本発明によるMRヘッドに比較して
、再生効率が30〜50%程度小さく、実用に供し得な
いことが明らかとなった。In this MR head, a permalloy film that becomes the MR element 1 or a COZrMO film that becomes the amorphous soft magnetic layer 2 is heated at 350°C for 2 hours to impart uniaxial anisotropy to the amorphous soft magnetic layer. Because the magnetic properties of the MR have deteriorated, even if a sense current of about 35 to 40 mA is applied, sufficient bias is not applied to the MR.
It became clear that the reproduction efficiency was about 30 to 50% lower than that of the MR head according to the present invention because no voltage was applied to the element, and it could not be put to practical use.
また、Cr膜、MO膜をTiN膜の代わりとして用いた
MRヘッドも作製したが、本比較例で述べたMRヘッド
と同様に十分なバイアスレベルが得られず、やはり本発
明の実施例で述べたMRヘッドに比較して再生効率が小
・さがった。In addition, an MR head using a Cr film or an MO film in place of the TiN film was also fabricated, but as with the MR head described in this comparative example, a sufficient bias level could not be obtained. The reproduction efficiency was lower than that of the MR head.
[発明の効果]
以上説明したように、本発明によれば拡散性の低いTi
N膜を非磁性導体層とする゛構成により、MRヘッド!
l!造プロセス中の加熱工程におけるMR素子あるいは
非晶質軟磁性体層の特性劣化を回避でき、優れた線形応
答性と高い再生効率を持つ磁気抵抗効果ヘッドが実現さ
れる。[Effects of the Invention] As explained above, according to the present invention, Ti with low diffusivity
MR head!
l! It is possible to avoid characteristic deterioration of the MR element or the amorphous soft magnetic layer during the heating step during the manufacturing process, and to realize a magnetoresistive head with excellent linear response and high reproduction efficiency.
第1図は本発明の一実施例の構成図、第2図はNiFe
膜とTiN膜を積層した試料の加熱処理後のオージェ分
析による深さ方向の濃度分布を示す図、第3図はNiF
e膜とTi膜を積層した試料の加熱処理前後のオージェ
分析による深さ方向の濃度分布を示す図、第4図はMR
ヘッドを説明するための説明図である。
1・・・MR素子 2・・・非磁性導体層5
・・・非晶質軟磁性体層 6・・・端子、7・・・窒
化チタニウム層
第1図
工・・ノナニジ・り・・深で=+!)
第2図Figure 1 is a block diagram of one embodiment of the present invention, Figure 2 is a NiFe
Figure 3 shows the concentration distribution in the depth direction by Auger analysis after heat treatment of a sample in which a film and a TiN film are laminated.
Figure 4 shows the concentration distribution in the depth direction by Auger analysis before and after heat treatment of a sample in which an e-film and a Ti film are laminated.
FIG. 3 is an explanatory diagram for explaining a head. 1...MR element 2...Nonmagnetic conductor layer 5
...Amorphous soft magnetic material layer 6...Terminal, 7...Titanium nitride layer 1st drawing...Nonaniji...Deep =+! ) Figure 2
Claims (1)
非磁性導体層を介して積層され、かつ前記非磁性導体層
が窒化チタニウム膜からなることを特徴とする磁気抵抗
効果ヘッド。(1) A magnetoresistive head characterized in that a ferromagnetic magnetoresistive element and an amorphous soft magnetic layer are laminated with a nonmagnetic conductor layer interposed therebetween, and the nonmagnetic conductor layer is made of a titanium nitride film. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1201203A JP2560482B2 (en) | 1989-08-04 | 1989-08-04 | Magnetoresistive head |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1201203A JP2560482B2 (en) | 1989-08-04 | 1989-08-04 | Magnetoresistive head |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0366012A true JPH0366012A (en) | 1991-03-20 |
| JP2560482B2 JP2560482B2 (en) | 1996-12-04 |
Family
ID=16437058
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1201203A Expired - Fee Related JP2560482B2 (en) | 1989-08-04 | 1989-08-04 | Magnetoresistive head |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2560482B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5485333A (en) * | 1993-04-23 | 1996-01-16 | Eastman Kodak Company | Shorted DMR reproduce head |
| KR100439143B1 (en) * | 2000-09-26 | 2004-07-05 | 마쯔시다덴기산교 가부시키가이샤 | Magnetic resistance element and magnetic device using the same |
| KR20110013350A (en) | 2008-05-26 | 2011-02-09 | 테이진 카세이 가부시키가이샤 | Flame Retardant Polycarbonate Resin Composition |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6352492A (en) * | 1986-08-22 | 1988-03-05 | Hitachi Ltd | Magnetoresistive element |
| JPS6370584A (en) * | 1986-09-12 | 1988-03-30 | Hitachi Ltd | Magnetoresistance effect type element of shunt type |
| JPS63237204A (en) * | 1987-03-25 | 1988-10-03 | Nec Corp | Magneto-resistance effect head |
-
1989
- 1989-08-04 JP JP1201203A patent/JP2560482B2/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6352492A (en) * | 1986-08-22 | 1988-03-05 | Hitachi Ltd | Magnetoresistive element |
| JPS6370584A (en) * | 1986-09-12 | 1988-03-30 | Hitachi Ltd | Magnetoresistance effect type element of shunt type |
| JPS63237204A (en) * | 1987-03-25 | 1988-10-03 | Nec Corp | Magneto-resistance effect head |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5485333A (en) * | 1993-04-23 | 1996-01-16 | Eastman Kodak Company | Shorted DMR reproduce head |
| KR100439143B1 (en) * | 2000-09-26 | 2004-07-05 | 마쯔시다덴기산교 가부시키가이샤 | Magnetic resistance element and magnetic device using the same |
| KR20110013350A (en) | 2008-05-26 | 2011-02-09 | 테이진 카세이 가부시키가이샤 | Flame Retardant Polycarbonate Resin Composition |
| US8278377B2 (en) | 2008-05-26 | 2012-10-02 | Teijin Chemicals, Ltd. | Flame retardant polycarbonate resin composition |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2560482B2 (en) | 1996-12-04 |
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