US20180251889A1 - Sintered compact magnesium oxide target for sputtering, and method for producing same - Google Patents

Sintered compact magnesium oxide target for sputtering, and method for producing same Download PDF

Info

Publication number
US20180251889A1
US20180251889A1 US15/969,958 US201815969958A US2018251889A1 US 20180251889 A1 US20180251889 A1 US 20180251889A1 US 201815969958 A US201815969958 A US 201815969958A US 2018251889 A1 US2018251889 A1 US 2018251889A1
Authority
US
United States
Prior art keywords
magnesium oxide
target
sintered compact
mgco
density
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
US15/969,958
Other versions
US10066290B1 (en
Inventor
Akira Hisano
Yuichiro Nakamura
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.)
JX Nippon Mining and Metals Corp
Original Assignee
JX Nippon Mining and Metals 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 JX Nippon Mining and Metals Corp filed Critical JX Nippon Mining and Metals Corp
Priority to US15/969,958 priority Critical patent/US10066290B1/en
Assigned to JX NIPPON MINING & METALS CORPORATION reassignment JX NIPPON MINING & METALS CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HISANO, AKIRA, NAKAMURA, YUICHIRO
Application granted granted Critical
Publication of US10066290B1 publication Critical patent/US10066290B1/en
Publication of US20180251889A1 publication Critical patent/US20180251889A1/en
Assigned to JX NIPPON MINING & METALS CORPORATION reassignment JX NIPPON MINING & METALS CORPORATION CHANGE OF ADDRESS Assignors: JX NIPPON MINING & METALS CORPORATION
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • C23C14/3407Cathode assembly for sputtering apparatus, e.g. Target
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/03Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on magnesium oxide, calcium oxide or oxide mixtures derived from dolomite
    • C04B35/04Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on magnesium oxide, calcium oxide or oxide mixtures derived from dolomite based on magnesium oxide
    • C04B35/053Fine ceramics
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes
    • C04B35/645Pressure sintering
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/08Oxides
    • C23C14/081Oxides of aluminium, magnesium or beryllium
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • C23C14/3407Cathode assembly for sputtering apparatus, e.g. Target
    • C23C14/3414Metallurgical or chemical aspects of target preparation, e.g. casting, powder metallurgy
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/44Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
    • C04B2235/442Carbonates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5445Particle size related information expressed by the size of the particles or aggregates thereof submicron sized, i.e. from 0,1 to 1 micron
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/72Products characterised by the absence or the low content of specific components, e.g. alkali metal free alumina ceramics
    • C04B2235/721Carbon content
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/74Physical characteristics
    • C04B2235/77Density
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/80Phases present in the sintered or melt-cast ceramic products other than the main phase
    • C04B2235/81Materials characterised by the absence of phases other than the main phase, i.e. single phase materials
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9646Optical properties
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9646Optical properties
    • C04B2235/9661Colour

Definitions

  • the present invention relates to a magnesium oxide target for use in forming a magnesium oxide layer for magnetic recording mediums of magnetic disk devices or tunneling magnetoresistance (TMR) elements and other electronic devices, and to the method of producing such a magnesium oxide target; and particularly relates to a sintered compact magnesium oxide target for sputtering of high purity and high density and which is free of color shading that occurs at the center of the target, and to the method of producing such a sintered compact magnesium oxide target for sputtering.
  • TMR tunneling magnetoresistance
  • the currently used magnetic recording medium structure such as a structure with increased magnetic crystalline anisotropy obtained by adding Pt to a Co—Cr-based alloy will become insufficient. This is because magnetic particles that behave with stable ferromagnetism at a size of 10 nm or less require even greater magnetic crystalline anisotropy.
  • a Fe—Pt phase having an L1 0 structure is attracting attention as a structure for use in an ultra-high density recording medium. Since the Fe—Pt phase having an L1 0 structure possesses high magnetic crystalline anisotropy in addition to yielding superior corrosion resistance and oxidation resistance, it is expected to be a structure that can be suitably applied to a magnetic recording medium.
  • a magnesium oxide film can be suitably used as the insulating layer, i.e., tunnel barrier of a TMR element that is used in a magnetic head (for hard disks) or an MRAM. While the foregoing magnesium oxide film has been conventionally formed via the vacuum deposition method, in recent years the sputtering method is being used to produce magnesium oxide films from the perspective of simplification of the production process and facilitation of the production of large screens.
  • JP-A-H10-130827 describes a magnesium oxide target made from a magnesium oxide sintered compact having a magnesium oxide purity of 99.9% or higher than a relative density of 99% or higher, wherein the magnesium oxide target has a fine structure in which the average grain size is 60 ⁇ m or less and round pores having an average grain size of 2 ⁇ m or less exist in the crystal grains, and is compatible up to a sputter deposition rate of 1000 ⁇ /min or more.
  • This technique is based on a method of adding fine magnesium oxide powder having an average grain size of 100 nm or less to high purity magnesium oxide powder and mixing and compacting the powders and subjecting the obtained compact to primary sintering and secondary sintering.
  • JP-A-H10-130828 relates to a magnesium oxide target made from a magnesium oxide sintered compact having a relative density of 99% or higher and capable of achieving a deposition rate of 500 ⁇ /min or higher in sputter deposition performed in an Ar atmosphere or Ar-O 2 mixed atmosphere, and proposes compacting high purity magnesium oxide powder having an average grain size of 0.1 to 2 ⁇ m based on CIP at a pressure of 3 t/cm 2 or higher, and sintering the obtained compact.
  • JP-A-H10-158826 describes a magnesium oxide target made from a magnesium oxide sintered compact having a magnesium oxide purity of 99.9% or higher and a relative density of 99.0% or higher, and compatible up to a sputter deposition rate of 600 ⁇ /min or more. This technique is based on a method of adding electromelted magnesium oxide powder and fine magnesium oxide powder having an average grain size of 100 nm or less to high purity magnesium oxide powder and mixing and compacting the powders and subjecting the obtained compact to primary sintering and secondary sintering.
  • JP-A-H10-158826 describes that a magnesium oxide film having favorable orientation, crystallinity and film properties can be deposited via the sputtering method at a high deposition rate.
  • JP-A-H10-237636 describes a target having MgO as its main component, as well as a method for producing such a target, and proposes dispersing La particles, Y particles and Sc particles in a target having MgO as its main component for use as a protective film of a dielectric layer of an Ac-type PDP in order to achieve a low discharge voltage, sputtering resistance during discharge, quick responsiveness to discharge, and insulation properties.
  • JP-A-H11-6058 proposes, in a target having MgO as its main component, dispersing LaB 6 particles in the MgO matrix, performing reduction treatment in a reduced gas atmosphere prior to sintering, and perfoiiiiing primary sintering and secondary sintering at a predetermined temperature in order to improve the strength, fracture toughness value, and resistance to thermal shock.
  • JP-A-H11-335824 prescribes the relative density and the average crystal grain size to be 0.5 to 100 ⁇ m in a target having MgO as its main component, and dispersing the rare earth elements of Sc, Y, La, Ce, Gd, Yb, and Nd in the MgO matrix.
  • JP-A-H11-139862 proposes sintering a MgO green compact based on the spark plasma sintering method in order to produce a high density sintered compact.
  • JP-A-2009-173502 and WO2009/096384 describe methods of obtaining a MgO sintered compact with numerous (111) planes aligned based on uniaxial pressure sintering and having an ultimate density of 3.568 g/cm 3 so as to achieve favorable mechanical property and theinial conductivity, and reduction in contamination of the atmosphere caused by the generation of gas, and propose subjecting MgO raw material powder having a grain size of 1 ⁇ m or less to uniaxial pressure sintering, and subsequently performing heat treatment in an oxygen atmosphere at a temperature of 1273 K or higher.
  • MgO is used as the raw material powder, and the method of increasing the density is limited to the sintering conditions.
  • JP-A-2000-169956 proposes a target for depositing a MgO film in a large size and uniform manner.
  • JP-A-2000-169956 proposes causing the grain size of the raw material powder to be 1 ⁇ m or less, subjecting the raw material powder to granulation, sintering the granulated raw material powder at a predetermined load and temperature, and finishing the surface of the target to achieve a center line average roughness Ra of 1 ⁇ m or less.
  • JP-A-H10-130827, JP-A-H10-130828, JP-A-H10-158826, JP-A-H10-237636, JP-A-H11-6058, JP-A-H11-335824, JP-A-2009-173502 , and WO2009/096384 describe the evaluation of the “bending strength” of a target
  • JP-A-2000-169956 describes the evaluation of the “deflective strength” of a target.
  • an object of this invention is to provide a target capable of realizing the above, and a method for producing such a target.
  • the present inventors discovered that a magnesium oxide target having a higher purity and a higher density can be obtained with inexpensive processing conditions in comparison to conventional methods based on the selection of raw material powders and the optimal setting of sintering conditions.
  • the present inventors additionally discovered that it is possible to produce a uniformly gray magnesium oxide target that is free of color shading, and which comprises a moderate oxygen defect.
  • the following invention is provided, namely, a sintered compact magnesium oxide target for sputtering having a purity of 99.99 wt % or higher excluding C, a density of 3.57 g/cm 3 or higher, and a whiteness of 60% or less.
  • the sintered compact magnesium oxide target may be produced by using a raw material obtained by adding MgCO 3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO).
  • MgO magnesium oxide
  • the sintered compact magnesium oxide target may have a whiteness of 55% or higher and 60% or less and/or a variation in the whiteness may be within 5%.
  • the invention also provides a method for producing a sintered compact magnesium oxide target.
  • the method uses a raw material obtained by adding MgCO 3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO), wherein raw material powders made of magnesium oxide (MgO) and MgCO 3 having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less are mixed, and the mixed powders are hot pressed at a temperature of 1500° C.
  • a sintered compact magnesium oxide target for sputtering having a purity of 99.99 wt % or higher excluding C, and a density of 3.57 g/cm 3 or higher.
  • the invention also provides a method for producing any of the sintered compact magnesium oxide targets described above which uses a raw material obtained by adding MgCO 3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO), wherein raw material powders made of magnesium oxide (MgO) and MgCO 3 having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less are mixed, and the mixed powders are hot pressed at a temperature of 1500° C.
  • a sintered compact magnesium oxide target for sputtering having a purity of 99.99 wt % or higher excluding C, and a density of 3.57 g/cm 3 or higher.
  • the present invention is effective in unifoimly depositing a magnesium oxide film, and specifically provides a high purity, high density sintered compact magnesium oxide target that is free of color shading and can be produced at a low cost by selecting the appropriate raw material powders. It is also possible to obtain a high- density target having a uniform composition. Moreover, the generation of particles during sputtering can be consequently inhibited. In addition, since it is possible to produce a sintered compact magnesium oxide target comprising a moderate oxygen defect, excessive oxygen is not generated during sputtering, and an effect of inhibiting oxidation of the adjacent deposition layer (metal layer) is exhibited.
  • FIG. 1 is a diagram showing the correlation of the additive amount of magnesium carbonate (MgCO 3 ) and the relative density of the sintered compact magnesium oxide target.
  • FIG. 2 is a diagram showing the correlation of the additive amount of magnesium carbonate (MgCO 3 ) and the whiteness of the sintered compact magnesium oxide target.
  • the sintered compact magnesium oxide target for sputtering of the present invention has a purity of 99.99 wt % or higher excluding C, a density of 3.57 g/cm 3 or higher, and a whiteness of 60% or less, and a major feature of the present invention is that the sintered compact magnesium oxide target for sputtering has a whiteness of 55% or higher and 60% or less.
  • This target can be realized by producing the target using a raw material obtained by adding MgCO 3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO).
  • MgCO 3 magnesium oxide
  • magnesium oxide (MgO) was sintered, but sufficient density could not be obtained unless the sintering temperature was set high.
  • the present invention can achieve a density of 3.57 g/cm 3 or more with a sintering temperature of 1500° C. or less as described below. This is a low temperature compared to conventional methods, and thus it is possible to reduce the production cost.
  • the present invention can obtain a sintered compact magnesium oxide target for sputtering having a purity of 99.99% or higher excluding C.
  • the variation in whiteness is preferably adjusted to be within 5%.
  • a MgCO 3 raw material in an amount of 5 wt % or more and less than 30 wt % is used.
  • This raw material has a purity of 99.99 wt % or higher excluding C, and, after mixing the MgCO 3 raw material powders having an average grain size of 0.5 ⁇ m or less, the mixed powders are hot pressed at a temperature of 1500° C. or less and an applied pressure of 300 kgf/cm 2 or more to obtain a target having a purity of 99.99 wt % or higher excluding C, and a density of 3.57 g/cm 3 or higher.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 ).
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing MgCO 3 in an amount of 6.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed. Note that the C content in this raw material powder was 0.86 wt %.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.576 g/cm 3 (relative density 99.74%) was obtained.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was gray, and the target possessed optical transparency.
  • the whiteness was 58.6%.
  • the variation in whiteness was 3.9%.
  • the whiteness by Hunter (Lab) was obtained by using the “micro surface spectral color difference meter VSS400” manufactured by Nippon Denshoku Industries.
  • the measuring range diameter in the foregoing case was 0.2 mm ⁇ . Three points were randomly measured to obtain the average value and variation ( ⁇ ) thereof.
  • the whiteness was measured, and the variation thereof was measured in a similar manner.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing MgCO 3 in an amount of 9.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed. Note that the C content in this raw material powder was 1.28 wt %.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.576 g/cm 3 (relative density 99.75%) was obtained.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was gray, and the target possessed optical transparency.
  • the whiteness was 57.6%.
  • the variation in whiteness was 0.6%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing MgCO 3 in an amount of 12.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed. Note that the C content in this raw material powder was 1.71 wt %.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.572 g/cm 3 (relative density 99.64%) was obtained.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was gray, and the target possessed optical transparency.
  • the whiteness was 55.6%.
  • the variation in whiteness was 3.2%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing MgCO 3 in an amount of 15.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed. Note that the C content in this raw material powder was 2.14 wt %.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.577 g/cm 3 (relative density 99.79%) was obtained.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was gray, and the target possessed optical transparency.
  • the whiteness was 56.6%.
  • the variation in whiteness was 1.1%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing MgCO 3 in an amount of 18.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed. Note that the C content in this raw material powder was 2.57 wt %.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.571 g/cm 3 (relative density 99.62%) was obtained.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was gray, and the target possessed optical transparency.
  • the whiteness was 56.1%.
  • the variation in whiteness was 3.4%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing magnesium oxide (MgO) having a purity of 99.99 wt % or higher and an average grain size of 0.5 ⁇ m or less was used. Note that magnesium carbonate (MgCO 3 ) was not added to this raw material powder. C content was ⁇ 10 ppm.
  • this raw material powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.280 g/cm 3 (relative density 91.49%) was obtained. In comparison to the Examples, the density decreased significantly.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was white, and the target did not possess optical transparency.
  • the whiteness was 91.3%.
  • the variation in whiteness was 1.4%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO 3 ) in an amount of 0.18 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed.
  • C content was 0.26 wt %.
  • the amount of magnesium carbonate (MgCO 3 ) did not satisfy the amount of the present invention.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.482 g/cm 3 (relative density 97.11%) was obtained. In comparison to the Examples, the density decreased significantly.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was white, and the target did not possess optical transparency.
  • the whiteness was 81.5%.
  • the variation in whiteness was 1.6%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO 3 ) in an amount of 3.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed.
  • C content was 0.43 wt %.
  • the amount of magnesium carbonate (MgCO 3 ) did not satisfy the amount of the present invention.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.540 g/cm 3 (relative density 98.74%) was obtained. In comparison to the Examples, the density decreased.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was light gray but “spots” appeared on the surface. The target possessed optical transparency.
  • the whiteness was 72.2%.
  • the variation in whiteness was 10.5%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO 3 ) in an amount of 4.2 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed.
  • C content was 0.60 wt %.
  • the amount of magnesium carbonate (MgCO 3 ) did not satisfy the amount of the present invention.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.568 g/cm 3 (relative density 99.53%) was obtained. In comparison to the Examples, the density decreased.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was light gray, and the target possessed optical transparency.
  • the whiteness was 63.5%.
  • the variation in whiteness was 0.3%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO 3 ) in an amount of 30.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed.
  • C content was 4.3 wt %.
  • the amount of magnesium carbonate (MgCO 3 ) exceeds the amount of the present invention.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.572 g/cm 3 (relative density 99.62%) was obtained, and the density was equivalent to the Examples.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was gray but “spots” appeared on the surface. This is considered to be a result of an increase in the amount of magnesium carbonate (MgCO 3 ).
  • the whiteness was 56.5%.
  • the variation in whiteness was 5.2%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO 3 ) in an amount of 48.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed.
  • C content was 6.8 wt %.
  • the amount of magnesium carbonate (MgCO 3 ) exceeds the amount of the present invention.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.577 g/cm 3 (relative density 99.78%) was obtained, and the density was equivalent to the Examples.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering.
  • the color was gray but “spots” appeared on the surface. This is considered to be a result of an increase in the amount of magnesium carbonate (MgCO 3 ).
  • the whiteness was 56.4%.
  • the variation in whiteness was 6.8%.
  • the sintered compact magnesium oxide target for sputtering was produced according to the following method.
  • a raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO 3 ) in an amount of 60.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 ⁇ m or less was mixed.
  • C content was 8.55 wt %.
  • the amount of magnesium carbonate (MgCO 3 ) considerably exceeds the amount of the present invention.
  • this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm 2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C.
  • magnesium carbonate (MgCO 3 ) is decomposed during sintering (MgCO 3 ⁇ MgO+CO 2 )
  • magnesium carbonate (MgCO 3 ) does not exist in the sintered target.
  • the density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.573 g/cm 3 (relative density 99.65%) was obtained, and the density was equivalent to the Examples.
  • the sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray but “spots” appeared on the surface. Moreover, cracks were generated in addition to the “spots”. This is considered to be a result of an increase in the amount of magnesium carbonate (MgCO 3 ).
  • the whiteness was 56.6%.
  • the variation in whiteness was 8.1%.
  • the relative density of the sintered compact magnesium oxide target of the present invention is affected by the additive amount of the magnesium carbonate (MgCO 3 ).
  • MgCO 3 magnesium carbonate
  • a density of 3.57 g/cm 3 (relative density of 99.5%) can be achieved by adding MgCO 3 in an amount of 5 wt % or more and less than 30 wt %. This is shown in FIG. 1 .
  • the whiteness of the sintered compact magnesium oxide target of the present invention is affected by the additive amount of the magnesium carbonate (MgCO 3 ).
  • the whiteness becomes 60% or less by adding MgCO 3 in an amount of 5 wt % or more and less than 30 wt %. This is shown in FIG. 2 .
  • a target produced by using a raw material obtained by adding MgCO 3 in an amount of 5 wt % or more and less than 30 wt % to the magnesium oxide (MgO) has a high density, and is effective as a sintered compact magnesium oxide target for sputtering.
  • the present invention yields a superior effect of being able to obtain a high purity, high density sintered compact magnesium oxide target that is free of color shading and can be produced at a low cost by selecting the appropriate raw material powder. It is also possible to improve the characteristics of the deposition of magnesium oxide. Further, the generation of particles during sputtering can be consequently inhibited. In addition, since it is possible to produce a sintered compact magnesium oxide target comprising a moderate oxygen defect, excessive oxygen is not generated during sputtering, and an effect of inhibiting oxidation of the adjacent deposition layer (metal layer) is exhibited.
  • the magnesium oxide sintered compact sputtering target of the present invention is useful as a magnesium oxide sputtering target for use in forming a magnesium oxide layer for magnetic recording mediums of magnetic disk devices or tunneling magnetoresistance (TMR) elements and other electronic devices.
  • TMR tunneling magnetoresistance

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Structural Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Physical Vapour Deposition (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

A sintered compact magnesium oxide target for sputtering has a purity of 99.99 wt % or higher excluding C, a density of 3.57 g/cm3 or higher, and a whiteness of 60% or less. To uniformly deposit a magnesium oxide film, a magnesium oxide target having a higher purity and a higher density is demanded. An object is to provide a target capable of realizing the above and a method for producing such a target. While a magnesium oxide sintered compact sputtering target is produced by hot-pressing a raw material powder, there is a problem in that color shading occurs in roughly φ60 (within a circle having a diameter of 60 mm) at the center part of the target. Conventionally, no particularly attention was given to this problem. However, in recent years, it has become necessary to investigate and resolve this problem in order to improve the deposition quality.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a divisional of co-pending U.S. application Ser. No. 14/356,395 which is a 371 National Stage of International Application No. PCT/JP2012/083391, filed Dec. 25, 2012, which claims the benefit under 35 USC 119 of Japanese Application No. 2011-285757, filed Dec. 27, 2011.
  • BACKGROUND
  • The present invention relates to a magnesium oxide target for use in forming a magnesium oxide layer for magnetic recording mediums of magnetic disk devices or tunneling magnetoresistance (TMR) elements and other electronic devices, and to the method of producing such a magnesium oxide target; and particularly relates to a sintered compact magnesium oxide target for sputtering of high purity and high density and which is free of color shading that occurs at the center of the target, and to the method of producing such a sintered compact magnesium oxide target for sputtering.
  • In recent years, pursuant to the downsizing and higher recording density of magnetic disks, research and development of magnetic recording mediums are being conducted, and in particular Co-based magnetic layers and under-layers have been improved variously. Meanwhile, the recording density of hard disks has been increasing rapidly year by year, and it is considered that current surface density of 600 Gbit/in2 will reach 1 Tbit/in2 in the future. When the recording density reaches 1 Tbit/in2, the recording bit size will be less than 10 nm and, in such a case, it is anticipated that the superparamagnetism caused by thermal fluctuation will become a problem. The currently used magnetic recording medium structure such as a structure with increased magnetic crystalline anisotropy obtained by adding Pt to a Co—Cr-based alloy will become insufficient. This is because magnetic particles that behave with stable ferromagnetism at a size of 10 nm or less require even greater magnetic crystalline anisotropy.
  • Due to the foregoing reason, a Fe—Pt phase having an L10 structure is attracting attention as a structure for use in an ultra-high density recording medium. Since the Fe—Pt phase having an L10 structure possesses high magnetic crystalline anisotropy in addition to yielding superior corrosion resistance and oxidation resistance, it is expected to be a structure that can be suitably applied to a magnetic recording medium.
  • When using a Fe—Pt layer as a structure for use in an ultra-high density recording medium, it is demanded to develop a technology of dispersing ordered Fe—Pt magnetic particles regulated in the same direction with a density as high as possible in a magnetically isolated state. While it is necessary to control the crystal orientation to provide magnetic anisotropy to the Fe—Pt thin film, this can be easily performed by selecting a single crystal substrate. In order to vertically align an easy axis, it has been reported that a magnesium oxide film is suitable as the under-layer of the Fe—Pt layer.
  • In addition, it is also known that a magnesium oxide film can be suitably used as the insulating layer, i.e., tunnel barrier of a TMR element that is used in a magnetic head (for hard disks) or an MRAM. While the foregoing magnesium oxide film has been conventionally formed via the vacuum deposition method, in recent years the sputtering method is being used to produce magnesium oxide films from the perspective of simplification of the production process and facilitation of the production of large screens.
  • There are the following publications as conventional technology.
  • JP-A-H10-130827 describes a magnesium oxide target made from a magnesium oxide sintered compact having a magnesium oxide purity of 99.9% or higher than a relative density of 99% or higher, wherein the magnesium oxide target has a fine structure in which the average grain size is 60 μm or less and round pores having an average grain size of 2 μm or less exist in the crystal grains, and is compatible up to a sputter deposition rate of 1000 Å/min or more. This technique is based on a method of adding fine magnesium oxide powder having an average grain size of 100 nm or less to high purity magnesium oxide powder and mixing and compacting the powders and subjecting the obtained compact to primary sintering and secondary sintering.
  • JP-A-H10-130828 relates to a magnesium oxide target made from a magnesium oxide sintered compact having a relative density of 99% or higher and capable of achieving a deposition rate of 500 Å/min or higher in sputter deposition performed in an Ar atmosphere or Ar-O2 mixed atmosphere, and proposes compacting high purity magnesium oxide powder having an average grain size of 0.1 to 2 μm based on CIP at a pressure of 3 t/cm2 or higher, and sintering the obtained compact.
  • JP-A-H10-158826 describes a magnesium oxide target made from a magnesium oxide sintered compact having a magnesium oxide purity of 99.9% or higher and a relative density of 99.0% or higher, and compatible up to a sputter deposition rate of 600 Å/min or more. This technique is based on a method of adding electromelted magnesium oxide powder and fine magnesium oxide powder having an average grain size of 100 nm or less to high purity magnesium oxide powder and mixing and compacting the powders and subjecting the obtained compact to primary sintering and secondary sintering. JP-A-H10-158826 describes that a magnesium oxide film having favorable orientation, crystallinity and film properties can be deposited via the sputtering method at a high deposition rate.
  • JP-A-H10-237636 describes a target having MgO as its main component, as well as a method for producing such a target, and proposes dispersing La particles, Y particles and Sc particles in a target having MgO as its main component for use as a protective film of a dielectric layer of an Ac-type PDP in order to achieve a low discharge voltage, sputtering resistance during discharge, quick responsiveness to discharge, and insulation properties.
  • JP-A-H11-6058 proposes, in a target having MgO as its main component, dispersing LaB6 particles in the MgO matrix, performing reduction treatment in a reduced gas atmosphere prior to sintering, and perfoiiiiing primary sintering and secondary sintering at a predetermined temperature in order to improve the strength, fracture toughness value, and resistance to thermal shock.
  • JP-A-H11-335824 prescribes the relative density and the average crystal grain size to be 0.5 to 100 μm in a target having MgO as its main component, and dispersing the rare earth elements of Sc, Y, La, Ce, Gd, Yb, and Nd in the MgO matrix.
  • JP-A-H11-139862 proposes sintering a MgO green compact based on the spark plasma sintering method in order to produce a high density sintered compact.
  • JP-A-2009-173502 and WO2009/096384 describe methods of obtaining a MgO sintered compact with numerous (111) planes aligned based on uniaxial pressure sintering and having an ultimate density of 3.568 g/cm3 so as to achieve favorable mechanical property and theinial conductivity, and reduction in contamination of the atmosphere caused by the generation of gas, and propose subjecting MgO raw material powder having a grain size of 1 μm or less to uniaxial pressure sintering, and subsequently performing heat treatment in an oxygen atmosphere at a temperature of 1273 K or higher. In the foregoing case, MgO is used as the raw material powder, and the method of increasing the density is limited to the sintering conditions.
  • JP-A-2000-169956 proposes a target for depositing a MgO film in a large size and uniform manner. In addition to prescribing the average crystal grain size, the density, the deflective strength, and the center line average roughness of the target surface, JP-A-2000-169956 proposes causing the grain size of the raw material powder to be 1 μm or less, subjecting the raw material powder to granulation, sintering the granulated raw material powder at a predetermined load and temperature, and finishing the surface of the target to achieve a center line average roughness Ra of 1 μm or less. Incidentally, while not directly related to the present invention, aforementioned JP-A-H10-130827, JP-A-H10-130828, JP-A-H10-158826, JP-A-H10-237636, JP-A-H11-6058, JP-A-H11-335824, JP-A-2009-173502 , and WO2009/096384 describe the evaluation of the “bending strength” of a target, and JP-A-2000-169956 describes the evaluation of the “deflective strength” of a target.
  • SUMMARY
  • In recent years, the use of a magnesium oxide film in recording mediums of magnetic disk devices (hard disks) or tunneling magnetoresistance (TMR) elements and other electronic devices is being considered, but a magnesium oxide target having a higher purity and a higher density is being demanded in order to uniformly deposit a magnesium oxide film. Nevertheless, since expectations for higher purification and densification are extremely high, it was conventionally difficult to produce a magnesium oxide target capable of meeting the foregoing demands. Thus, an object of this invention is to provide a target capable of realizing the above, and a method for producing such a target.
  • Moreover, while a magnesium oxide sintered compact sputtering target is produced by hot-pressing a raw material powder, there is a problem in that color shading occurs in roughly φ60 (within a circle having a diameter of 60 mm) at the center part of the target. Conventionally, no particularly attention was given to this problem. However, in recent years, it has become necessary to investigate and resolve this problem to improve the deposition quality.
  • In order to achieve the foregoing object, as a result of intense study, the present inventors discovered that a magnesium oxide target having a higher purity and a higher density can be obtained with inexpensive processing conditions in comparison to conventional methods based on the selection of raw material powders and the optimal setting of sintering conditions. In addition, with respect to the occurrence of color shading, the present inventors additionally discovered that it is possible to produce a uniformly gray magnesium oxide target that is free of color shading, and which comprises a moderate oxygen defect.
  • Based on the foregoing discovery, the following invention is provided, namely, a sintered compact magnesium oxide target for sputtering having a purity of 99.99 wt % or higher excluding C, a density of 3.57 g/cm3 or higher, and a whiteness of 60% or less. The sintered compact magnesium oxide target may be produced by using a raw material obtained by adding MgCO3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO). The sintered compact magnesium oxide target may have a whiteness of 55% or higher and 60% or less and/or a variation in the whiteness may be within 5%.
  • The invention also provides a method for producing a sintered compact magnesium oxide target. The method uses a raw material obtained by adding MgCO3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO), wherein raw material powders made of magnesium oxide (MgO) and MgCO3 having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less are mixed, and the mixed powders are hot pressed at a temperature of 1500° C. or less and an applied pressure of 300 kgf/cm2 or more to obtain a sintered compact magnesium oxide target for sputtering having a purity of 99.99 wt % or higher excluding C, and a density of 3.57 g/cm3 or higher.
  • The invention also provides a method for producing any of the sintered compact magnesium oxide targets described above which uses a raw material obtained by adding MgCO3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO), wherein raw material powders made of magnesium oxide (MgO) and MgCO3 having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less are mixed, and the mixed powders are hot pressed at a temperature of 1500° C. or less and an applied pressure of 300 kgf/cm2 or more to obtain a sintered compact magnesium oxide target for sputtering having a purity of 99.99 wt % or higher excluding C, and a density of 3.57 g/cm3 or higher.
  • The present invention is effective in unifoimly depositing a magnesium oxide film, and specifically provides a high purity, high density sintered compact magnesium oxide target that is free of color shading and can be produced at a low cost by selecting the appropriate raw material powders. It is also possible to obtain a high- density target having a uniform composition. Moreover, the generation of particles during sputtering can be consequently inhibited. In addition, since it is possible to produce a sintered compact magnesium oxide target comprising a moderate oxygen defect, excessive oxygen is not generated during sputtering, and an effect of inhibiting oxidation of the adjacent deposition layer (metal layer) is exhibited.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a diagram showing the correlation of the additive amount of magnesium carbonate (MgCO3) and the relative density of the sintered compact magnesium oxide target.
  • FIG. 2 is a diagram showing the correlation of the additive amount of magnesium carbonate (MgCO3) and the whiteness of the sintered compact magnesium oxide target.
  • DETAILED DESCRIPTION
  • The sintered compact magnesium oxide target for sputtering of the present invention has a purity of 99.99 wt % or higher excluding C, a density of 3.57 g/cm3 or higher, and a whiteness of 60% or less, and a major feature of the present invention is that the sintered compact magnesium oxide target for sputtering has a whiteness of 55% or higher and 60% or less.
  • This target can be realized by producing the target using a raw material obtained by adding MgCO3 in an amount of 5 wt % or more and less than 30 wt % to magnesium oxide (MgO). Note that the whiteness was measured using the micro surface spectral color difference meter VSS400 (JIS Z 8722, ASTM E 308) manufactured by Nippon Denshoku Industries. This Hunter-type color difference meter was used to measure L: luminosity and a·b (hue·chroma), and the whiteness was obtained from the following formula: W (whiteness)=100−((100−L)2+(a2+b2))1/2.
  • Conventionally, magnesium oxide (MgO) was sintered, but sufficient density could not be obtained unless the sintering temperature was set high. The present invention can achieve a density of 3.57 g/cm3 or more with a sintering temperature of 1500° C. or less as described below. This is a low temperature compared to conventional methods, and thus it is possible to reduce the production cost. In addition, the present invention can obtain a sintered compact magnesium oxide target for sputtering having a purity of 99.99% or higher excluding C.
  • As described above, it is even more advantageous to have an effect of reducing the nodules and particles because reduction of the variation in whiteness causes improvement in the uniformity of the sintered compact. Here, the variation in whiteness is preferably adjusted to be within 5%.
  • Upon producing the sintered compact magnesium oxide target for sputtering of the present invention, a MgCO3 raw material in an amount of 5 wt % or more and less than 30 wt % is used. This raw material has a purity of 99.99 wt % or higher excluding C, and, after mixing the MgCO3 raw material powders having an average grain size of 0.5 μm or less, the mixed powders are hot pressed at a temperature of 1500° C. or less and an applied pressure of 300 kgf/cm2 or more to obtain a target having a purity of 99.99 wt % or higher excluding C, and a density of 3.57 g/cm3 or higher. Note that magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2).
  • EXAMPLES
  • The Examples are now explained. Note that these Examples merely illustrate preferred representative examples, and it should be easy to understand that the present invention should not be limited to these Examples. The technical concept of the present invention shall be interpreted based on the overall descriptions of this specification and particularly based on the scope of claims.
  • Example 1
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing MgCO3 in an amount of 6.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. Note that the C content in this raw material powder was 0.86 wt %.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.576 g/cm3 (relative density 99.74%) was obtained.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray, and the target possessed optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 58.6%. In addition, the variation in whiteness was 3.9%. For this whiteness, the whiteness by Hunter (Lab) was obtained by using the “micro surface spectral color difference meter VSS400” manufactured by Nippon Denshoku Industries. The measuring range diameter in the foregoing case was 0.2 mmφ. Three points were randomly measured to obtain the average value and variation (σ) thereof. In the following Examples and Comparative Examples, the whiteness was measured, and the variation thereof was measured in a similar manner.
  • TABLE 1
    Additive Sinter- Variation C
    Amount of ing Sintered in Content
    MgCO3 Temper- Hold Pressing Compact Relative Optical White- White- in Raw
    Raw Material ature Time Pressure Density Density Trans- ness ness Material
    (wt. %) (° C.) (Hours) (kgf/cm2) (g/cm3) (%) Color parency (%) (%) (wt. %)
    Comparative 0.0 1500 2 300 3.280 91.49 White No 91.3 1.4 0.00
    Example 1
    Comparative 1.8 1500 2 300 3.482 97.11 White No 81.5 1.6 0.26
    Example 2
    Comparative 3.0 1500 2 300 3.540 98.74 Light Yes 72.2 10.5 0.43
    Example 3 gray,
    spots
    Comparative 4.2 1500 2 300 3.568 99.53 Light Yes 63.5 0.3 0.60
    Example 4 gray
    Example 1 6.0 1500 2 300 3.576 99.74 Gray Yes 58.6 3.9 0.86
    Example 2 9.0 1500 2 300 3.576 99.75 Gray Yes 57.6 0.6 1.28
    Example 3 12.0 1500 2 300 3.572 99.64 Gray Yes 55.6 3.2 1.71
    Example 4 15.0 1500 2 300 3.577 99.79 Gray Yes 56.6 1.1 2.14
    Example 5 18.0 1500 2 300 3.571 99.62 Gray Yes 56.1 3.4 2.57
    Comparative 30.0 1500 2 300 3.572 99.62 Gray, Yes 56.5 5.2 4.28
    Example 5 spots
    Comparative 48.0 1500 2 300 3.577 99.78 Gray, Yes 56.4 6.8 6.84
    Example 6 spots
    Comparative 60.0 1500 2 300 3.573 99.65 Gray, Yes 56.6 8.1 8.55
    Example 7 spots,
    cracks
  • Example 2
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing MgCO3 in an amount of 9.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. Note that the C content in this raw material powder was 1.28 wt %.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.576 g/cm3 (relative density 99.75%) was obtained.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray, and the target possessed optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 57.6%. In addition, the variation in whiteness was 0.6%.
  • Example 3
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing MgCO3 in an amount of 12.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. Note that the C content in this raw material powder was 1.71 wt %.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.572 g/cm3 (relative density 99.64%) was obtained.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray, and the target possessed optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 55.6%. In addition, the variation in whiteness was 3.2%.
  • Example 4
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing MgCO3 in an amount of 15.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. Note that the C content in this raw material powder was 2.14 wt %.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.577 g/cm3 (relative density 99.79%) was obtained.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray, and the target possessed optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 56.6%. In addition, the variation in whiteness was 1.1%.
  • Example 5
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing MgCO3 in an amount of 18.0 wt % and remainder being magnesium oxide (MgO) having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. Note that the C content in this raw material powder was 2.57 wt %.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.571 g/cm3 (relative density 99.62%) was obtained.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray, and the target possessed optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 56.1%. In addition, the variation in whiteness was 3.4%.
  • Comparative Example 1
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing magnesium oxide (MgO) having a purity of 99.99 wt % or higher and an average grain size of 0.5 μm or less was used. Note that magnesium carbonate (MgCO3) was not added to this raw material powder. C content was <10 ppm.
  • Subsequently, this raw material powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.280 g/cm3 (relative density 91.49%) was obtained. In comparison to the Examples, the density decreased significantly.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was white, and the target did not possess optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 91.3%. In addition, the variation in whiteness was 1.4%.
  • Comparative Example 2
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO3) in an amount of 0.18 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. C content was 0.26 wt %. In the foregoing case, the amount of magnesium carbonate (MgCO3) did not satisfy the amount of the present invention.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.482 g/cm3 (relative density 97.11%) was obtained. In comparison to the Examples, the density decreased significantly.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was white, and the target did not possess optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 81.5%. In addition, the variation in whiteness was 1.6%.
  • Comparative Example 3
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO3) in an amount of 3.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. C content was 0.43 wt %. In the foregoing case, the amount of magnesium carbonate (MgCO3) did not satisfy the amount of the present invention.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.540 g/cm3 (relative density 98.74%) was obtained. In comparison to the Examples, the density decreased.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was light gray but “spots” appeared on the surface. The target possessed optical transparency.
  • Moreover, upon examining the whiteness of the target, the whiteness was 72.2%. In addition, the variation in whiteness was 10.5%.
  • Comparative Example 4
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO3) in an amount of 4.2 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. C content was 0.60 wt %. In the foregoing case, the amount of magnesium carbonate (MgCO3) did not satisfy the amount of the present invention.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.568 g/cm3 (relative density 99.53%) was obtained. In comparison to the Examples, the density decreased.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was light gray, and the target possessed optical transparency. Moreover, upon examining the whiteness of the target, the whiteness was 63.5%. In addition, the variation in whiteness was 0.3%.
  • Comparative Example 5
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO3) in an amount of 30.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. C content was 4.3 wt %. In the foregoing case, the amount of magnesium carbonate (MgCO3) exceeds the amount of the present invention.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.572 g/cm3 (relative density 99.62%) was obtained, and the density was equivalent to the Examples.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray but “spots” appeared on the surface. This is considered to be a result of an increase in the amount of magnesium carbonate (MgCO3). Moreover, upon examining the whiteness of the target, the whiteness was 56.5%. In addition, the variation in whiteness was 5.2%.
  • Comparative Example 6
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO3) in an amount of 48.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. C content was 6.8 wt %. In the foregoing case, the amount of magnesium carbonate (MgCO3) exceeds the amount of the present invention.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.577 g/cm3 (relative density 99.78%) was obtained, and the density was equivalent to the Examples.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray but “spots” appeared on the surface. This is considered to be a result of an increase in the amount of magnesium carbonate (MgCO3). Moreover, upon examining the whiteness of the target, the whiteness was 56.4%. In addition, the variation in whiteness was 6.8%.
  • Comparative Example 7
  • The sintered compact magnesium oxide target for sputtering was produced according to the following method. A raw material powder containing magnesium oxide (MgO) and magnesium carbonate (MgCO3) in an amount of 60.0 wt % having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less was mixed. C content was 8.55 wt %. In the foregoing case, the amount of magnesium carbonate (MgCO3) considerably exceeds the amount of the present invention.
  • Subsequently, this mixed powder was hot pressed for 2 hours at a temperature of 1500° C. and an applied pressure of 300 kgf/cm2 to produce a magnesium oxide target having a purity of 99.99 wt % or higher excluding C. Note that, since magnesium carbonate (MgCO3) is decomposed during sintering (MgCO3→MgO+CO2), magnesium carbonate (MgCO3) does not exist in the sintered target. The density of the obtained MgO sintered compact was measured with the Archimedes method. Consequently, a density of 3.573 g/cm3 (relative density 99.65%) was obtained, and the density was equivalent to the Examples.
  • The sintered compact produced as described above was subject to grinding and polishing to obtain a sintered compact magnesium oxide target for sputtering. Upon visually observing the target, the color was gray but “spots” appeared on the surface. Moreover, cracks were generated in addition to the “spots”. This is considered to be a result of an increase in the amount of magnesium carbonate (MgCO3).
  • Moreover, upon examining the whiteness of the target, the whiteness was 56.6%. In addition, the variation in whiteness was 8.1%.
  • As evident from the foregoing Examples and Comparative Examples, the relative density of the sintered compact magnesium oxide target of the present invention is affected by the additive amount of the magnesium carbonate (MgCO3). A density of 3.57 g/cm3 (relative density of 99.5%) can be achieved by adding MgCO3 in an amount of 5 wt % or more and less than 30 wt %. This is shown in FIG. 1.
  • Moreover, the whiteness of the sintered compact magnesium oxide target of the present invention is affected by the additive amount of the magnesium carbonate (MgCO3). The whiteness becomes 60% or less by adding MgCO3 in an amount of 5 wt % or more and less than 30 wt %. This is shown in FIG. 2.
  • Accordingly, a target produced by using a raw material obtained by adding MgCO3 in an amount of 5 wt % or more and less than 30 wt % to the magnesium oxide (MgO) has a high density, and is effective as a sintered compact magnesium oxide target for sputtering.
  • Moreover, as evident from the foregoing Examples and Comparative Examples, it is more effective to adjust the variation in whiteness to be within 5% since an effect of decreasing the cracks and nodules of the sintered compact can be obtained.
  • The present invention yields a superior effect of being able to obtain a high purity, high density sintered compact magnesium oxide target that is free of color shading and can be produced at a low cost by selecting the appropriate raw material powder. It is also possible to improve the characteristics of the deposition of magnesium oxide. Further, the generation of particles during sputtering can be consequently inhibited. In addition, since it is possible to produce a sintered compact magnesium oxide target comprising a moderate oxygen defect, excessive oxygen is not generated during sputtering, and an effect of inhibiting oxidation of the adjacent deposition layer (metal layer) is exhibited.
  • Accordingly, the magnesium oxide sintered compact sputtering target of the present invention is useful as a magnesium oxide sputtering target for use in forming a magnesium oxide layer for magnetic recording mediums of magnetic disk devices or tunneling magnetoresistance (TMR) elements and other electronic devices.

Claims (1)

We claim:
1. A method for producing a sputtering target comprising a sintered compact of magnesium oxide, comprising the steps of:
adding raw material powder of MgCO3 in an amount of 5 wt % or more and less than 30 wt % to raw material powder of magnesium oxide (MgO), the raw material powders of magnesium oxide (MgO) and MgCO3 having a purity of 99.99 wt % or higher excluding C and an average grain size of 0.5 μm or less;
mixing the raw material powder of MgCO3 with the raw material powder of magnesium oxide (MgO) to produce a mixture; and
hot pressing the mixture at a temperature of 1500° C. or less and an applied pressure of 300 kgf/cm2 or more to obtain a sintered compact of magnesium oxide having a purity of 99.99 wt % or higher excluding C, a density of 3.57 g/cm3 or higher, and a whiteness of 60% or less.
US15/969,958 2011-12-27 2018-05-03 Sintered compact magnesium oxide target for sputtering, and method for producing same Active US10066290B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US15/969,958 US10066290B1 (en) 2011-12-27 2018-05-03 Sintered compact magnesium oxide target for sputtering, and method for producing same

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2011-285757 2011-12-27
JP2011285757 2011-12-27
PCT/JP2012/083391 WO2013099832A1 (en) 2011-12-27 2012-12-25 Sintered magnesium oxide target for sputtering, and method for producing same
US14/356,395 US9988709B2 (en) 2011-12-27 2012-12-25 Sintered compact magnesium oxide target for sputtering, and method for producing same
US15/969,958 US10066290B1 (en) 2011-12-27 2018-05-03 Sintered compact magnesium oxide target for sputtering, and method for producing same

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
PCT/JP2012/083391 Division WO2013099832A1 (en) 2011-12-27 2012-12-25 Sintered magnesium oxide target for sputtering, and method for producing same
US14/356,395 Division US9988709B2 (en) 2011-12-27 2012-12-25 Sintered compact magnesium oxide target for sputtering, and method for producing same

Publications (2)

Publication Number Publication Date
US10066290B1 US10066290B1 (en) 2018-09-04
US20180251889A1 true US20180251889A1 (en) 2018-09-06

Family

ID=48697317

Family Applications (2)

Application Number Title Priority Date Filing Date
US14/356,395 Active 2033-09-20 US9988709B2 (en) 2011-12-27 2012-12-25 Sintered compact magnesium oxide target for sputtering, and method for producing same
US15/969,958 Active US10066290B1 (en) 2011-12-27 2018-05-03 Sintered compact magnesium oxide target for sputtering, and method for producing same

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US14/356,395 Active 2033-09-20 US9988709B2 (en) 2011-12-27 2012-12-25 Sintered compact magnesium oxide target for sputtering, and method for producing same

Country Status (7)

Country Link
US (2) US9988709B2 (en)
JP (1) JP5654119B2 (en)
CN (1) CN103814152A (en)
MY (1) MY166187A (en)
SG (1) SG11201401078QA (en)
TW (1) TW201341561A (en)
WO (1) WO2013099832A1 (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102100850B1 (en) * 2012-11-07 2020-04-14 엔지케이 인슐레이터 엘티디 Ceramic material and sputtering-target member
KR102142037B1 (en) * 2012-11-07 2020-08-06 엔지케이 인슐레이터 엘티디 Ceramic material and sputtering-target member
WO2018013387A1 (en) * 2016-07-13 2018-01-18 Tosoh Smd, Inc. Magnesium oxide sputtering target and method of making same
CN106587940B (en) * 2016-12-02 2020-03-27 有研亿金新材料有限公司 High-purity compact magnesium oxide target material and preparation method thereof
US10704139B2 (en) * 2017-04-07 2020-07-07 Applied Materials, Inc. Plasma chamber target for reducing defects in workpiece during dielectric sputtering
JP6925165B2 (en) * 2017-05-19 2021-08-25 Jx金属株式会社 Sputtering target
WO2020054104A1 (en) * 2018-09-13 2020-03-19 Jx金属株式会社 Mgo sintered body sputtering target
KR20210047358A (en) 2018-10-10 2021-04-29 제이엑스금속주식회사 Magnesium oxide sputtering target
US11676632B2 (en) * 2019-12-26 2023-06-13 Resonac Corporation Magnetic recording medium, method of manufacturing magnetic recording medium and magnetic storage device
US11227751B1 (en) 2020-07-01 2022-01-18 Applied Materials, Inc. Plasma chamber target for reducing defects in workpiece during dielectric sputtering

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10130827A (en) * 1996-10-28 1998-05-19 Mitsubishi Materials Corp Mgo target and its production
JPH10130828A (en) * 1996-10-31 1998-05-19 Mitsubishi Materials Corp Mgo target and its production
JPH10158826A (en) 1996-12-04 1998-06-16 Mitsubishi Materials Corp Mgo target and its production
JPH10237636A (en) 1997-02-21 1998-09-08 Mitsubishi Materials Corp Target essentially consisting of mgo and its production
JP3417457B2 (en) 1997-06-13 2003-06-16 三菱マテリアル株式会社 Target containing MgO as main component and method for producing the same
US6056857A (en) * 1997-08-13 2000-05-02 Praxair S.T. Technology, Inc. Cryogenic annealing of sputtering targets
JPH11139862A (en) 1997-11-04 1999-05-25 Sumitomo Metal Mining Co Ltd High density magnesium oxide sintered compact and its production
JP3494205B2 (en) 1998-05-28 2004-02-09 三菱マテリアル株式会社 Target material containing MgO as a main component and method for producing the same
JP2000169956A (en) 1998-12-03 2000-06-20 Japan Energy Corp Magnesium oxide target for sputtering and its production
US6500321B1 (en) * 1999-05-26 2002-12-31 Novellus Systems, Inc. Control of erosion profile and process characteristics in magnetron sputtering by geometrical shaping of the sputtering target
CN1326909A (en) 2000-12-28 2001-12-19 蒋政 High density indium-tin oxide target material and its producing method
JP4904645B2 (en) 2001-08-10 2012-03-28 東ソー株式会社 Method for producing Mg-containing ITO sputtering target
TW200300455A (en) * 2001-11-30 2003-06-01 Mitsubishi Materials Corp MgO deposition material and production method of the same
US6652668B1 (en) * 2002-05-31 2003-11-25 Praxair S.T. Technology, Inc. High-purity ferromagnetic sputter targets and method of manufacture
KR100734460B1 (en) * 2003-09-26 2007-07-03 가부시끼가이샤 도시바 Sputtering target and process for producing si oxide film therewith
JP2008189493A (en) * 2007-02-02 2008-08-21 Sumitomo Electric Ind Ltd POLYCRYSTALLINE MgO SINTERED BODY
JP5231823B2 (en) * 2008-01-28 2013-07-10 日本タングステン株式会社 Polycrystalline MgO sintered body, method for producing the same, and MgO target for sputtering
JP4715859B2 (en) * 2008-04-15 2011-07-06 パナソニック株式会社 Plasma display device
WO2010029702A1 (en) 2008-09-09 2010-03-18 キヤノンアネルバ株式会社 Method for manufacturing magnetoresistive element, and storage medium used in the manufacturing method
FR2937320B1 (en) * 2008-10-17 2011-07-29 Saint Gobain Ct Recherches PROCESS FOR PRODUCING A MOLTEN CERAMIC PRODUCT, PRODUCT OBTAINED, AND USES THEREOF
CN101575203B (en) * 2009-06-19 2013-01-16 西北稀有金属材料研究院 Preparation method of ITO sputtering target material
US20120286219A1 (en) * 2010-01-07 2012-11-15 Jx Nippon Mining & Metals Corporation Sputtering target, semiconducting compound film, solar cell comprising semiconducting compound film, and method of producing semiconducting compound film
CN102198954A (en) * 2011-04-22 2011-09-28 辽宁中大超导材料有限公司 Impurity control method for sintered body magnesium oxide target
CN102212781B (en) * 2011-05-10 2013-09-11 孔伟华 Method for manufacturing high-density and low-cost zinc oxide aluminum sputtering target
US20160340255A1 (en) * 2014-01-29 2016-11-24 Hewlett-Packard Development Company, L.P. Oxygen conducting bismuth perovskite material
US10267761B2 (en) * 2016-06-14 2019-04-23 Delphi Technologies Ip Limited Material for sensing electrode of NOX gas sensor

Also Published As

Publication number Publication date
CN103814152A (en) 2014-05-21
JPWO2013099832A1 (en) 2015-05-07
TW201341561A (en) 2013-10-16
US9988709B2 (en) 2018-06-05
MY166187A (en) 2018-06-07
WO2013099832A1 (en) 2013-07-04
JP5654119B2 (en) 2015-01-14
US10066290B1 (en) 2018-09-04
US20140284212A1 (en) 2014-09-25
SG11201401078QA (en) 2014-09-26

Similar Documents

Publication Publication Date Title
US10066290B1 (en) Sintered compact magnesium oxide target for sputtering, and method for producing same
US10325762B2 (en) Sputtering target for forming magnetic recording film and process for producing same
US20180044779A1 (en) Fe-Pt-BASED SPUTTERING TARGET WITH DISPERSED C GRAINS
TWI583814B (en) Fe-Pt magnetic material sintered body
US10600440B2 (en) Sputtering target for forming magnetic recording film and method for producing same
WO2012017659A1 (en) Method for producing sputtering target, and sputtering target
TWI616425B (en) MgO-TiO sintered body target and manufacturing method thereof
US10090012B2 (en) Fe-bases magnetic material sintered compact
US20140360871A1 (en) Fe-Pt-Ag-C-Based Sputtering Target Having C Grains Dispersed Therein, and Method for Producing Same
TW201428119A (en) Fe-Pt SINTERED COMPACT SPUTTERING TARGET AND MANUFACTURING METHOD THEREFOR
WO2018043680A1 (en) NON-MAGNETIC MATERIAL-DISPERSED Fe-Pt SPUTTERING TARGET
CN114959599A (en) Sputtering target for forming magnetic recording film and method for producing same
WO2014141737A1 (en) Sputtering target
TWI589718B (en) Ceramic materials and sputtering target components
US9773653B2 (en) Ferromagnetic material sputtering target containing chromium oxide
TW201829811A (en) Physical vapor-deposition target member and sputtering target member, and physical vapor-deposition film and layer structure manufacturing method
JP2005097657A (en) Sputtering target for forming magnetic layer having reduced production of particle
JP7165023B2 (en) magnesium oxide sputtering target
TWI680198B (en) Ferromagnetic material sputtering target, manufacturing method thereof, and magnetic recording film manufacturing method
TW202325873A (en) Sputtering target member, sputtering target assembly, and film forming method

Legal Events

Date Code Title Description
FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STCF Information on status: patent grant

Free format text: PATENTED CASE

AS Assignment

Owner name: JX NIPPON MINING & METALS CORPORATION, JAPAN

Free format text: CHANGE OF ADDRESS;ASSIGNOR:JX NIPPON MINING & METALS CORPORATION;REEL/FRAME:057160/0114

Effective date: 20200629

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1551); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 4