Magnetic recording medium, non-magnetic alloy film and sputtering target

Information

  • Patent Grant
  • 6174598
  • Patent Number
    6,174,598
  • Date Filed
    Monday, May 11, 1998
    26 years ago
  • Date Issued
    Tuesday, January 16, 2001
    23 years ago
Abstract
A low noise magnetic recording medium having a high coercive force and adapted for use with a MR head. The magnetic recording medium comprises a non-magnetic substrate having thereon a first non-magnetic underlayer and a magnetic layer comprising a Co alloy provided on the non-magnetic underlayer. The non-magnetic underlayer comprises an alloy represented by the formula: (Ni50Al)100−XMX, wherein M is one of Cr (X=1-40 at %), Mo (X=1-50 at %), W (X=1-60 at %), V (X=1-35 at %), Zr (X=1-25 at %), Nb (X=1-35 at %) and Pd (X=1-25 at %), and when M includes two or more of Cr, Mo, W, V, Zr, Nb and Pd, X is from 1 to 60 at %.
Description




FIELD OF THE INVENTION




The present invention relates to a magnetic recording medium such as a magnetic drum, a magnetic tape and a magnetic disc, and more particularly, to a magnetic recording medium having reduced medium noise.




BACKGROUND OF THE INVENTION




In recent years, the density of magnetic disc devices or the like has increased. To accommodate such higher densities, there is a need for a magnetic recording medium (hereinafter sometimes referred to as a “medium”) suitable for a magnetic head (hereinafter referred to as a “MR head”) using a high magnetic resistance effect that is capable of high reproduction sensitivity.




The MR head has low head noise as compared with conventional magnetoelectric induction type heads. Therefore, the reduction of medium noise has become very important for improving the S/N of the device as a whole.




In a magnetic recording disc for a hard disc device (HDD) commonly used at present, a non-magnetic underlayer (e.g., Cr, Cr alloy), a magnetic layer (e.g., CoCrTa, CoCrPtTa alloy) and a protective layer (e.g., carbon) are provided in sequence on a non-magnetic substrate. Also, a lubricating layer comprising a liquid lubricant is formed thereon.




In order to optimize the recording/reproducing properties of the above-described magnetic recording medium, JP-B-5-23564 (the term “JP-B” as used herein means an “examined Japanese patent publication”) proposes a Cr underlayer having a thickness of from 50 to 200 Å in order to increase squareness.




Furthermore, JP-A-1-232522 (the term “JP-A” as used herein means an “unexamined published Japanese patent application”) proposes to add one or more metals selected from Cu, Nb, Ti, V, Zr, Mo, Zn, W and Ta to the Cr underlayer in order to enhance the magnetic properties, and particularly coercive force.




Furthermore, EP 0,704,839A1 proposes to use an alloy having a B2 ordered structure (e.g., AlNi, AlCo, AlFe) as the underlayer to reduce the crystal size of the magnetic layer and thereby provide improved noise characteristics.




When the Cr underlayer is formed having a thickness of from 50 to 200 Å as proposed in JP-B-5-23564, the Cr crystal structure is not fully oriented toward the (200) plane. As a result, sufficiently high coercivity cannot be obtained and the medium is not suitable for a MR head.




In JP-A-1-232522, the thickness of the Cr underlayer is from 500 to 3,000 Å so that the Cr grains can be oriented toward the (200) plane. Consequently, the noise can be reduced. Furthermore, although Cr or a Cr alloy is used as the non-magnetic underlayer of the smoothened substrate, problems arise in that the anisotropy controlling effect of the disc by texturing or the like is lowered to cause a reduction in coercivity and in turn a decrease in the reproduction output.




When an Al alloy having a B2 ordered structure (e.g., AlNi, AlCo, AlFe, etc.) is used as an underlayer, as proposed in EP 0,704,839A1, the crystal size of the magnetic layer is reduced due to the Al—Ni alloy or Al—Co alloy and the noise is improved. However, it is difficult to increase coercivity using the Al—Ni alloy or to increase coercive squareness using Al—Co alloy. Accordingly, the reproduction output is small. Thus, a problem still remains in performing high density recording.




SUMMARY OF THE INVENTION




It is therefore an object of the present invention to provide a magnetic recording medium suitable for a MR head, having both reduced noise and high coercivity.




The present inventors studied the characteristics of the Al—Ni alloy by adding thereto various elements and as a result, discovered that by adding a predetermined amount of Cr, Mo, W, V, Zr, Nb or Pd, a low noise magnetic recording medium having high coercivity (Hc) can be obtained. The present invention has been achieved based on these findings.




That is, the present invention solves the above problems of the prior art by providing a magnetic recording medium comprising a non-magnetic substrate having thereon a first non-magnetic underlayer and a magnetic layer comprising a Co alloy provided on the non-magnetic underlayer, wherein said non-magnetic underlayer comprises an alloy represented by the formula: (Ni


50


Al)


100−X


M


X


(wherein M is one or more of Cr (X=1-40 at %), Mo (X=1-50 at %), W (X=1-60 at %), V (X=1-35 at %), Zr (X=1-25 at %), Nb (X=1-35 at %) and Pd (X=1-25 at %), and when M comprises two or more of Cr, Mo, W, V, Zr, Nb and Pd, X is from 1 to 60 at %. As used herein, “at %” means “atom %”.




In a preferred embodiment, the magnetic recording medium further comprises a protective layer provided on the magnetic layer. Also, when M comprises two or more of Cr, Mo, W, V, Zr, Nb and Pd, X is preferably from 1 t 50 at %.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

is a graph showing S/N ratio as a function of Cr content (at %) for a magnetic recording medium having a (Ni


50


Al)


100−X


Cr


X


alloy underlayer.





FIG. 2

is a graph showing S/N ratio as a function of Mo content (at %) for a magnetic recording medium having a (Ni


50


Al)


100−X


Mo


X


alloy underlayer.





FIG. 3

is a graph showing S/N ratio as a function of V content (at %) for a magnetic recording medium having a (Ni


50


Al)


100−X


V


X


alloy underlayer.





FIG. 4

is a graph showing S/N ratio as a function of Zr content (at %) for a magnetic recording medium having a (Ni


50


Al)


100−X


Zr


X


alloy underlayer.





FIG. 5

is a graph showing S/N ratio as a function of Nb content (at %) for a magnetic recording medium having a (Ni


50


Al)


100−X


Nb


X


alloy underlayer.





FIG. 6

is a graph showing S/N ratio as a function of Pd content (at %) for a magnetic recording medium having a (Ni


50


Al)


100−X


Pd


X


alloy underlayer.





FIG. 7

is a graph showing S/N ratio as a function of W content (at %) for a magnetic recording medium having a (Ni


50


Al)


100−X


W


X


alloy underlayer.





FIG. 8

shows a schematic cross section of the magnetic recording medium according to one embodiment of the present invention.











DESCRIPTION OF THE PREFERRED EMBODIMENTS




The mechanism which provides the improved magnetic characteristics of the present invention is not clearly understood. However, it is considered that the lattice constant expands by adding to an NiAl underlayer a third element such as Cr to better match the magnetic layer. As a result, the magnetic characteristics are improved. The lattice constants of various compositions are shown in the following Examples. Furthermore, although the lattice constant of an Ni


50


Al alloy is 2.887 Å, it is 2.890 Å or more in alloys having added thereto a third element such as Cr. Thus, for better matching, the lattice constant is preferably from 2.91 to 3.03 Å.




In the present invention, on the underlayer comprising a (Ni


50


Al)


100−X


M


X


alloy (first underlayer), a second underlayer comprising Cr or a Cr alloy comprising Cr and one or more of Ti, Mo, Al, Ta, W, Ni, B, Si and V depending on the intended application is preferably laminated thereon in order to further improve the properties of the inventive magnetic recording medium. When the second underlayer comprises a Cr alloy, the Cr content is preferably at least 50 at %.




The non-magnetic substrate for use in the present invention includes an Al alloy having formed thereon a NiP plating film (hereinafter referred to as a “NiP plated Al substrate”) commonly used as a substrate for magnetic recording media, a glass substrate which can provide excellent surface smoothness and a silicon substrate. In a recording medium for a MR head, as the recording density increases, the flying height of the head must be lowered. Accordingly, a smooth substrate surface is preferred. More specifically, the non-magnetic substrate for use in the present invention preferably has an average surface roughness Ra of 20 Å or less.




The magnetic layer of the present invention may comprise conventionally known Co alloy films such as a Co—Cr—Ta alloy, a Co—Cr—Pt alloy, a Co—Cr—Pt—Ta alloy and a Co—Cr—Ni alloy. However, in order to best provide the effects of the non-magnetic underlayer of the present invention, the use of a Co—Cr—Pt—Ta alloy is preferred.




The Co—Cr—Pt—Ta alloy represented by the compositional formula Co


(100−X−Y−Z)


Cr


X


Pt


Y


Ta


Z


preferably has a composition of 13 at % ≦X≦24 at %, 1 at % ≦Y≦12 at % and 2 at % ≦Z≦7 at %. The Cr content is from 13 to 24 at % because if it is less than 13 at %, the dispersion of Co particles due to segregation of Cr is insufficient, whereas if the Co content exceeds 20 at %, the coercivity Hc is noticeably reduced and the medium tends to be unsuitable as a MR head medium. The Pt content is from 1 to 12 at % because if it is less than 1 at %, high coercivity Hc cannot be obtained, whereas if it exceeds 12 at %, noise tends to increase. The Ta content is from 2 to 7 at % because if it is less than 2 at %, noise tends to increase, whereas if it exceeds 7 at %, high coercivity Hc is difficult to obtain.




The first underlayer of the present invention preferably has a thickness of from 25 to 1,500 Å. The first underlayer may have any thickness as long as it falls within this range, however, the first underlayer more preferably has a thickness of from 400 to 1,000 Å.




The second underlayer of the present invention preferably has a thickness of from 1 to 1,000 Å. The second underlayer may have any thickness as long as it falls within this range, however, the second underlayer more preferably has a thickness of from 50 to 200 Å.




The thickness of the Co alloy magnetic layer is not particularly limited. However, in the case of a magnetic recording medium for a MR head, the thickness is preferably adjusted to have a remanent magnetization layer thickness product BrT of from 50 to 130 Gμm. If the remanent magnetization layer thickness product BrT is less than 50 Gμm, proper output is difficult to attain, whereas if it exceeds 130 Gμm, properties suitable for a MR head medium are difficult to obtain.




The magnetic recording medium of the present invention can be produced by a conventionally known method. However, the first underlayer comprising or consisting essentially of a (Ni


50


Al)


100−X


M


X


alloy may be obtained by sputtering an alloy target, and preferably a sintered alloy target having the composition (Ni


50


Al)


100−X


M


X


(where M is one or more of Cr (X=1-40 at %), Mo (X=1-50 at %), W (X=1-60 at %), V (X=1-35 at %), Zr (X=1-25 at %), Nb (X=1-35 at %) and Pd (X=1-25 at %)) prepared according to the ingot method. The sintered alloy target may be produced by a conventionally known sintering method such as a HIP (hot isostatic press) method or hot press method, using an alloy powder having the final target composition, or using a plurality of alloy powders or a single metal powder capable of yielding the final target composition. Alloy powders and metal powders can also be produced by a conventionally known method such as the gas atomizing method.




The present invention is described below by reference to the following Examples, however, the present invention should not be construed as being limited thereto.




EXAMPLES




A NiP plated Al substrate was textured to have a surface roughness Ra of 25 Å and set in a DC magnetron sputtering apparatus. After evacuating to 2×10


−7


Torr, an alloy film shown in Tables 1 and 2 as a first underlayer was formed on the substrate to a thickness of 700 Å, and then a Cr film as a second underlayer was formed on the first underlayer to a thickness of 200 Å. The first underlayer was formed using a sintered target produced by a HIP technique having the composition of the desired alloy film. Subsequently, a Co


75


Cr


16


Pt


6


Ta


3


(at %) alloy magnetic layer or a Co


73


Cr


18


Pt


6


Ta


3


(at %) alloy magnetic layer was formed thereon. Furthermore, a carbon film as a protective layer was formed on the magnetic layer to a thickness of 100 Å. The Ar pressure was 3 mTorr during each of the film forming steps. The layer thickness of the magnetic layer was 145 Gμm in terms of its remanent magnetization layer thickness product (BrT). The structure of the magnetic recording medium thus obtained is schematically shown in FIG.


8


. In

FIG. 8

,


1


is a non-magnetic substrate (NiP plated Al substrate),


2


is a non-magnetic underlayer comprising a first underlayer


21


and a second underlayer


22


,


3


is a magnetic layer and


4


is a protective layer.




The magnetic properties of the magnetic recording media thus prepared were measured using a vibrating sample magnetometry (VSM) technique. The recording/reproducing properties were evaluated by obtaining a ratio of the recording/reproducing output to noise (S/N) using a composite thin film magnetic head having a magnetic resistant (MR) element in reproduction, at a linear recording density of 206.8 kFCI. As shown in Tables 1 and 2, S*(%) is the measured coercive squareness. The lattice constants of some of the first underlayers were measured by X-ray crystal structure diffraction. The results are shown in Table 1 (Co


75


Cr


16


Pt


6


Ta


3


(at %) alloy magnetic layer) and in Table 2 (Co


73


Cr


18


Pt


6


Ta


3


(at %) alloy magnetic layer). The S/N ratio as a function of M (both content and type of element) in the (Ni


50


Al)


100−X


M


X


first underlayer is shown in

FIGS. 1

to


7


.

















TABLE 1














Lattice







Composition of




Hc




S*




S/N




Constant






No.




First Underlayer




(Oe)




(%)




(dB)




(Å)











Example 1




(Ni


50


Al)


15


Cr




2749




88.6




34.31




2.977






Example 2




(Ni


50


Al)


30


Cr




2693




92.3




34.67






Example 3




(Ni


50


Al)


5


Mo




3037




81.4




34.74






Example 4




(Ni


50


Al)


10


Mo




2908




85.9




34.65






Example 5




(Ni


50


Al)


20


Mo




2891




82.1




34.50




2.958






Example 6




(Ni


50


Al)


33


Mo




2783




72.6




34.20






Example 7




(Ni


50


Al)


25


W




2779




84.7




34.47






Example 8




(Ni


50


Al)


35


W




2731




83.8




35.01




3.006






Example 9




(Ni


50


Al)


45


W




2795




80.0




34.80






Example 10




(Ni


50


Al)


5


V




2734




90.2




34.55




2.894






Example 11




(Ni


50


Al)


10


V




2719




91.3




34.32






Example 12




(Ni


50


Al)


15


V




2697




91.7




34.26






Example 13




(Ni


50


Al)


5


Zr




2845




88.9




34.63






Example 14




(Ni


50


Al)


10


Zr




2758




90.9




34.72




2.914






Example 15




(Ni


50


Al)


5


Nb




2875




87.0




34.34






Example 16




(Ni


50


Al)


10


Nb




2882




86.6




34.55




2.919






Example 17




(Ni


50


Al)


15


Pd




2916




78.6




34.52




3.013






Comparative




(Ni


50


Al)




2669




89.9




33.08




2.887






Example 1






Comparative




Cr




2496




80.8




32.39






Example 2






Comparative




(Ni


50


Al)


50


Cr




1977




87.8




32.69






Example 3






Comparative




(Ni


50


Al)


70


Mo




1534




65.8




33.57






Example 4






Comparative




(Ni


50


Al)


70


W




2401




82.7




32.31






Example 5






Comparative




(Ni


50


Al)


50


V




1759




80.1




33.07






Example 6






Comparative




(Ni


50


Al)


40


Zr




2033




73.7




32.18






Example 7






Comparative




(Ni


50


Al)


50


Nb




1628




75.2




32.84






Example 8






Comparative




(Ni


50


Al)


35


Pd




1762




55.9




32.73






Example 9











*magnetic alloy layer: Co


75


Cr


16


Pt


6


Ta


3




























TABLE 2










Composition of




Hc




S*





Lattice






No.




First Underlayer




(Oe)




(%)




S/N (dB)




Constant (Å)











Example 18




(Ni


50


Al)


15


Cr




2597




73.1




35.22




2.977






Example 19




(Ni


50


Al)


30


Cr




2557




82.4




34.36






Example 20




(Ni


50


Al)


5


Mo




2546




88.0




34.74






Example 21




(Ni


50


Al)


10


Mo




2556




81.9




34.42






Example 22




(Ni


50


Al)


20


Mo




2571




82.1




34.33




2.958






Example 23




(Ni


50


Al)


33


Mo




2658




70.9




34.25






Example 24




(Ni


50


Al)


25


W




2588




77.4




34.99






Example 25




(Ni


50


Al)


35


W




2587




75.7




35.03




3.006






Example 26




(Ni


50


Al)


45


W




2579




73.1




34.89






Example 27




(Ni


50


Al)


5


V




2580




82.4




34.76




2.894






Example 28




(Ni


50


Al)


10


V




2551




82.2




34.98






Example 29




(Ni


50


Al)


15


V




2604




81.2




35.14






Example 30




(Ni


50


Al)


5


Zr




2982




76.4




35.11






Example 31




(Ni


50


Al)


10


Zr




2901




77.6




35.28




2.914






Example 32




(Ni


50


Al)


5


Nb




2793




77.7




35.23






Example 33




(Ni


50


Al)


10


Nb




2803




76.5




35.33




2.919






Example 34




(Ni


50


Al)


15


Pd




2602




75.2




34.97




3.013






Comparative




Ni


50


Al




2504




84.4




34.08




2.887






Example 10






Comparative




Cr




2326




81.7




32.57






Example 11






Comparative




(Ni


50


Al)


50


Cr




2016




86.9




33.07






Example 12






Comparative




(Ni


50


Al)


70


Mo




1642




63.8




33.72






Example 13






Comparative




(Ni


50


Al)


70


W




2126




71.9




33.47






Example 14






Comparative




(Ni


50


Al)


50


V




1970




72.1




33.15






Example 15






Comparative




(Ni


50


Al)


40


Zr




1849




78.8




32.96






Example 16






Comparative




(Ni


50


Al)


50


Nb




1783




68.5




33.47






Example 17






Comparative




(Ni


50


Al)


35


Pd




1457




51.5




33.15






Example 18











*magnetic alloy layer: Co


73


Cr


18


Pt


6


Ta


3















It is seen from Table 1 (where a Co


75


Cr


16


Pt


6


Ta


3


(at %) alloy magnetic layer was used) that in Comparative Example 1 using Ni


50


Al (at %) as the first underlayer, the coercive force (Hc) was 2669 Oe, whereas in Examples 1 to 17 of the present invention, the coercive force (Hc) was 2,690 Oe or more. The S/N ratio was 33.08 dB in Comparative Example 1, but was remarkably 34.20 dB or more in Examples 1 to 17 of the present invention. The lattice constant was 2.887 Å in Comparative Example 1, and in all of the measured Examples of the present invention the lattice constant was larger than the value of Comparative Example 1.




Furthermore, it is seen from Table 2 (where a Co


73


Cr


18


Pt


6


Ta


3


(at %) alloy magnetic layer was used) that in Comparative Example 10 using Ni


50


Al (at %) as the first layer, the coercive force (Hc) was 2,504 Oe, whereas in Examples 18 to 34 of the present invention, the coercive force (Hc) was 2,546 Oe or more. In Comparative Example 10, the S/N ratio was 34.08 dB, but was 34.25 dB or more in Examples 18 to 34 of the present invention. The comparison between Tables 1 and 2 shows that the effects of the invention are enchanced with the use of a Co


73


Cr


18


Pt


6


Ta3 (at %) alloy magnetic layer.





FIG. 1

is a graph showing S/N as a function of Cr content in a (Ni


50


Al)


100−X


Cr


X


alloy underlayer. From

FIG. 1

, when the Cr content exceeds 40 at %, the S/N ratio is lower than that of the Cr-free alloy. Furthermore, the Cr content is preferably from 10 to 35 at %, more preferably from 15 to 35 at %.





FIG. 2

is a graph showing S/N as a function of Mo content in a (Ni


50


Al)


100−X


Mo


X


alloy underlayer. From

FIG. 2

, when the Mo content exceeds 50 at %, the S/N ratio is lower than that of the Mo-free alloy. Furthermore, the Mo content is preferably from 3 to 40 at %, more preferably from 5 to 30 at %.





FIG. 3

is a graph showing S/N as a function of V content in a (Ni


50


Al)


100−X


V


X


alloy underlayer. From

FIG. 3

, when the V content exceeds 35 at %, the S/N ratio is lower than that of the V-free alloy. Furthermore, the V content is preferably from 3 to 30 at %, more preferably from 5 to 20 at %.





FIG. 4

is a graph showing S/N as a function of Zr content in a (Ni


50


Al)


100−X


Zr


X


alloy underlayer. From

FIG. 4

, when the Zr content exceeds 25 at %, the S/N ratio is lower than that of the Zr-free alloy. Furthermore, the Cr content is preferably from 5 to 20 at %, more preferably from 5 to 15 at %.





FIG. 5

is a graph showing S/N as a function of Nb content in a (Ni


50


Al)


100−X


Nb


X


alloy underlayer. From

FIG. 5

, when the Nb content exceeds 35 at %, the S/N ratio is lower than that of the Nb-free alloy. Furthermore, the Cr content is preferably from 5 to 20 at %, more preferably from 5 to 15 at %.





FIG. 6

is a graph showing S/N as a function of Pd content in a (Ni


50


Al)


100−X


Pd


X


alloy underlayer. From

FIG. 6

, when the Pd content exceeds 25 at %, the S/N ratio is lower than that of the Pd-free alloy. Furthermore, the Pd content is preferably from 5 to 20 at %, more preferably from 10 to 20 at %.





FIG. 7

is a graph showing S/N as a function of W content in a (Ni


50


Al)


100−X


W


X


alloy underlayer. From

FIG. 7

, when the W content exceeds 60 at %, the S/N ratio is lower than that of the W-free alloy. Furthermore, the W content is preferably from 20 to 50 at %, more preferably from 25 to 40 at %.




As described above, the magnetic recording medium of the present invention can achieve high output without increasing the medium noise, and is well adapted as a high-density magnetic recording medium for use with a MR head.




While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.



Claims
  • 1. A magnetic recording medium comprising a non-magnetic substrate having thereon a first non-magnetic underlayer and a magnetic layer comprising a Co alloy provided on the non-magnetic underlayer, wherein said non-magnetic underlayer comprises an alloy represented by the formula: (Ni50Al)100−XMX, wherein M is one of Cr (X=1-40 at %), Mo (X=1-50 at %), W (X=1-60 at %), V (X=1-35 at %), Zr (X=1-25 at %), Nb (X=1-35 at %) and Pd (X=1-25 at %), and wherein M also includes two or more of Cr, Mo, W, V, Zr, Nb and Pd, when X is from 1 to 60 at %.
  • 2. The magnetic recording medium as claimed in claim 1, further comprising a second underlayer comprising Cr or a Cr alloy comprising Cr and one or more of Ti, Mo, Al, Ta, W, Ni, B, Si and V provided between said first underlayer and said magnetic layer.
  • 3. The magnetic recording medium as claimed in claim 1, wherein the (Ni50Al)100−XMX alloy of said first underlayer has a lattice constant of 2.88 Å or more.
  • 4. The magnetic recording medium as claimed in claim 2, wherein the (Ni50Al)100−XMX alloy of said first underlayer has a lattice constant of 2.88 Å or more.
  • 5. The magnetic recording medium as claimed in claim 1, wherein the (Ni50Al)100−XMX alloy of said first underlayer has a lattice constant of from 2.91 to 3.03 Å.
  • 6. The magnetic recording medium as claimed in claim 2, wherein the (Ni50Al)100−XMX alloy of said first underlayer has a lattice constant of from 2.91 to 3.03 Å.
  • 7. The magnetic recording medium as claimed in claim 1, wherein said non-magnetic substrate is selected from the group consisting of an Al substrate plated with NiP, a glass substrate and a silicon substrate.
  • 8. The magnetic recording medium as claimed in claim 2, wherein said non-magnetic substrate is selected from the group consisting of an Al substrate plated with NiP, a glass substrate and a silicon substrate.
  • 9. The magnetic recording medium as claimed in claim 1, wherein said magnetic layer comprises a CoCrPtTa alloy.
  • 10. The magnetic recording medium as claimed in claim 2, wherein said magnetic layer comprises a CoCrPtTa alloy.
  • 11. The magnetic recording medium as claimed in claim 2, wherein said second underlayer is laminated on said first underlayer.
  • 12. The magnetic recording medium as claimed in claim 1, wherein X in the formula (Ni50Al)100−XMX is from 1 to 50 at % when M comprises two or more of Cr, Mo, W, V, Zr, Nb and Pd.
  • 13. The magnetic recording medium as claimed in claim 1, further comprising a protective layer provided on said magnetic layer.
  • 14. The magnetic recording medium as claimed in claim 1, wherein the magnetic layer comprises a Co(100−X−Y−Z)CrXPtYTaZ alloy wherein 13 at % ≦X≦24 at %, 1 at % ≦Y≦12 at % and 2 at % ≦Z≦7 at %.
  • 15. The magnetic recording medium as claimed in claim 1, wherein said first underlayer has a thickness of from 25 to 1,500 Å.
  • 16. A non-magnetic alloy film having a composition of (Ni50Al)100−XMX, wherein is one of Cr (X=1-40 at %), Mo (X=1-50 at %), W (X=1-60 at %), V (X=1-35 at %), Zr (X=1-25 at %), Nb (X=1-35 at %) and Pd (X=1-25 at %), and wherein M also comprises two or more of Cr, Mo, W, V, Zr, Nb and Pd, when X is from 1 to 60 at %.
  • 17. A sputtering target comprising a sintered alloy having a composition of (Ni50Al)100−XMX, wherein M is one of Cr (X=1-40 at %), Mo (X=1-50 at %), W (X=1-60 at %), V (X=1-35 at %), Zr (X=1-25 at %), Nb (X=1-35 at %) and Pd (X=1-25 at %), and wherein M also comprises two or more of Cr, Mo, W, V, Zr, Nb and Pd, when X is from 1 to 60 at %.
Priority Claims (2)
Number Date Country Kind
9-267469 Sep 1997 JP
9-307658 Nov 1997 JP
CROSS REFERENCE TO RELATED APPLICATIONS

This application is an application filed under 35 U.S.C. §111 (a) claiming benefit pursuant to 35 U.S.C. §119(e) (1) of the filing date of the Provisional Application No. 60/069,646 filed Dec. 9, 1997 pursuant to 35 U.S.C. §111(b).

US Referenced Citations (3)
Number Name Date Kind
5302434 Doerner Apr 1994
5900324 Moroishi May 1999
5939202 Atoke Aug 1999
Provisional Applications (1)
Number Date Country
60/069646 Dec 1997 US