US20070189916A1 - Sputtering targets and methods for fabricating sputtering targets having multiple materials - Google Patents

Sputtering targets and methods for fabricating sputtering targets having multiple materials Download PDF

Info

Publication number
US20070189916A1
US20070189916A1 US11/650,515 US65051507A US2007189916A1 US 20070189916 A1 US20070189916 A1 US 20070189916A1 US 65051507 A US65051507 A US 65051507A US 2007189916 A1 US2007189916 A1 US 2007189916A1
Authority
US
United States
Prior art keywords
sputter target
comprised
oxide
master alloy
phase
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.)
Abandoned
Application number
US11/650,515
Inventor
Wenjun Zhang
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.)
Heraeus Inc
Original Assignee
Heraeus Inc
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
Priority claimed from US10/200,590 external-priority patent/US6759005B2/en
Priority to US11/650,515 priority Critical patent/US20070189916A1/en
Application filed by Heraeus Inc filed Critical Heraeus Inc
Assigned to HERAEUS INCORPORATED reassignment HERAEUS INCORPORATED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ZHANG, WENJUN
Priority to TW096115669A priority patent/TW200829709A/en
Priority to KR1020070045176A priority patent/KR20080065211A/en
Priority to EP07108160A priority patent/EP1942205A3/en
Priority to CNA2007101085628A priority patent/CN101220457A/en
Priority to JP2007175131A priority patent/JP2008169464A/en
Publication of US20070189916A1 publication Critical patent/US20070189916A1/en
Priority to SG2012007357A priority patent/SG178742A1/en
Priority to SG2012007258A priority patent/SG178737A1/en
Priority to SG200716736-4A priority patent/SG144792A1/en
Abandoned legal-status Critical Current

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
    • C23C14/3414Metallurgical or chemical aspects of target preparation, e.g. casting, powder metallurgy
    • 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
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/007Alloys based on nickel or cobalt with a light metal (alkali metal Li, Na, K, Rb, Cs; earth alkali metal Be, Mg, Ca, Sr, Ba, Al Ga, Ge, Ti) or B, Si, Zr, Hf, Sc, Y, lanthanides, actinides, as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/03Alloys based on nickel or cobalt based on nickel
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C19/00Alloys based on nickel or cobalt
    • C22C19/07Alloys based on nickel or cobalt based on cobalt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C27/00Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
    • C22C27/06Alloys based on chromium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/001Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides
    • C22C32/0015Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides with only single oxides as main non-metallic constituents
    • C22C32/0026Matrix based on Ni, Co, Cr or alloys thereof
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/002Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/10Ferrous alloys, e.g. steel alloys containing cobalt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C5/00Alloys based on noble metals
    • C22C5/04Alloys based on a platinum group metal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • B22F2998/10Processes characterised by the sequence of their steps

Definitions

  • the present invention generally relates to sputtering targets and methods for fabricating sputtering targets and, in particular, relates to sputter targets comprising a plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe) and the second material comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, silicon (Si), a silicon (Si)-containing material, a silicide, an oxygen (O)-containing material, an oxide, boron (B), a boron (B)-containing material, or a boride, and further relates to methods for fabricating such sputter targets, and products produced thereby.
  • the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni
  • a typical sputtering system includes a plasma source for generating an electron or ion beam, a target that comprises a material to be atomized and a substrate onto which the sputtered material is deposited.
  • the process involves bombarding the target material with an electron or ion beam at an angle that causes the target material to be sputtered or eroded.
  • the sputtered target material is deposited as a thin film or layer on the substrate.
  • the present invention relates to a novel method of fabricating sputtering targets that include non-metals such as boron, carbon, nitrogen, oxygen, silicon, a boride, a carbide, a nitride, an oxide, a silicide, a boron (B)-containing material, a carbon (C)-containing material, a nitrogen (N)-containing material, an oxygen (O)-containing material, or a silicon (Si)-containing material, including mixtures of non-metals, compounds of non-metals, master alloys containing boron, carbon or silicon and products produced by these processes.
  • non-metals such as boron, carbon, nitrogen, oxygen, silicon, a boride, a carbide, a nitride, an oxide, a silicide, a boron (B)-containing material, a carbon (C)-containing material, a nitrogen (N)-containing material, an oxygen (O)-containing material, or a silicon (Si)-containing
  • a process comprises preparation of pre-alloyed powder(s) or master alloy powder(s) or selection of ultra fine compound powder(s) of about 0.01 to 50 microns, preferably 0.1 to 10 microns, more preferably 1.0 to 5.0 microns average particle size and most preferably less than 2 microns. It has been discovered that spitting will not occur when the above phases are in form of ultra fine particles of less than 50 microns, preferably less than 10 microns in size. After the ultra fine powders are blended together, the powder blend is canned, followed by a hot isostatic press (HIP) consolidation. Powder processing as above is employed to make the target materials because of unique advantages over the prior art's melting process, both technically and economically.
  • HIP hot isostatic press
  • a sputter target comprises a plurality of materials.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, or a silicide.
  • the second material constitutes a phase.
  • the phase of the second material has an average size between greater than 0 micron and 50 microns.
  • the first material comprises at least 15 atomic percent or greater.
  • a sputter target comprises a plurality of materials.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of an oxygen (O)-containing material or an oxide.
  • the second material constitutes a phase.
  • the phase of the second material has an average size between greater than 0 micron and 50 microns.
  • a sputter target comprises a plurality of materials.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of an oxygen (O)-containing material or an oxide.
  • the second material constitutes a phase.
  • the phase of the second material has an average size between greater than 0 micron and 50 microns. If the sputter target consists of chromium (Cr) and the oxygen (O)-containing material only, the oxygen (O)-containing material is an oxygen (O)-containing material other than simply chromium oxide. If the sputter target consists of chromium (Cr) and the oxide only, the oxide is an oxide other than simply chromium oxide.
  • a sputter target comprises a plurality of materials.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of boron (B), a boron (B)-containing material or a boride.
  • the second material constitutes a phase.
  • the phase of the second material has an average size between greater than 0 micron and less than 10 microns.
  • a sputter target comprises a plurality of materials.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of boron (B), a boron (B)-containing material or a boride.
  • the second material constitutes a phase.
  • the phase of the second material has an average size between greater than 0 micron and 50 microns.
  • a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, or a silicide.
  • the second material has an average particle size between greater than 0 micron and 50 microns.
  • the first material comprises at least 15 atomic percent or greater.
  • the plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of an oxygen (O)-containing material or an oxide.
  • the second material has an average particle size between greater than 0 micron and 50 microns.
  • the plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of an oxygen (O)-containing material or an oxide.
  • the second material has an average particle size between greater than 0 micron and 50 microns.
  • the plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • the oxygen (O)-containing material is an oxygen (O)-containing material other than simply chromium oxide. If the plurality of materials consists of chromium (Cr) and the oxide only, the oxide is an oxide other than simply chromium oxide.
  • a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of boron (B), a boron (B)-containing material or a boride.
  • the second material has an average particle size between greater than 0 micron and less than 10 microns.
  • the plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the second material is comprised of boron (B), a boron (B)-containing material or a boride.
  • the second material has an average particle size between greater than 0 micron and less than 50 microns.
  • the plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • FIG. 1 shows the process flow chart of the invention described herein according to one aspect of the present invention.
  • FIG. 2 illustrates a representative microstructure of a consolidated (CO 74 Cr 10 Pt 16 ) 92 —(SiO 2 ) 8 alloy according to one aspect of the present invention.
  • FIG. 3 illustrates a representative microstructure of a consolidated (CO 74 Cr 10 Pt 16 ) 92 —(SiO 2 ) 8 alloy according to one aspect of the present invention.
  • Appendix 1 shows a Periodic Table of elements.
  • Sputtering target materials for sputtering process range from pure metals to ever more complicated alloys. Complex 3 to 6 element alloys may be utilized for sputtering targets. Alloying additions such as boron, carbon, nitrogen, oxygen, silicon and so on are added to Cr—, Co—, Fe-based alloys to modify characteristics such as deposited film grain-size, surface energy and magnetic properties.
  • the presence of non-metal additions like boron, carbon, nitrogen, oxygen and silicon to target materials is either in the form of pure elements, e.g. boron and carbon, or in the form of compounds like boride, carbide, nitride and oxide.
  • the pure element phases such as boron and carbon and the compound phases like boride, carbide, nitride, oxide, and silicide, however cause spitting problems during sputtering.
  • the present invention provides a solution to this problem.
  • the powders of the present invention include elemental powders, pre-alloyed powders, powders of master alloys and/or intermetallic compound powders composed of 2 to 6 elements, including but not limited to Cr—, Co—, Ru—, Ni—, and/or Fe-based alloys.
  • master alloys include pre-alloyed powders, and pre-alloyed powders may be atomized master alloys.
  • the powders of the present invention contain pure Cr, Co, Ru, Ni, Fe, Pt and/or Ta and/or (optionally) pre-alloyed or master alloy powders of said pure elements, and include at least a boride, a boron (B)-containing material (e.g., boron based inorganic compound or master alloy), a carbide, a carbon (C)-containing material (e.g., carbon based inorganic compound or master alloy), a nitride, a nitrogen (N)-containing material, a silicide, a silicon (Si)-containing material (e.g., silicon based master alloy), an oxide, or an oxygen (O)-containing material of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB (see Appendix 1). These Roman numeral column numbers correspond to column numbers 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12,
  • Examples of a boron (B)-containing material include a boride; examples of a carbon (C)-containing material include a carbide; examples of a nitrogen (N)-containing material include a nitride; examples of a silicon (Si)-containing material include a silicide; and examples of an oxygen (O)-containing material includes an oxide.
  • the non-metallic additive is in combined form such as an inorganic compound or a master alloy of a non-metal although elemental additions may be used if desired.
  • Preferred doping non-metals are compounds of boron, carbon and nitrogen. In still other embodiments compounds of oxygen or silica are included as dopants.
  • Preferred doping compounds are borides or boron (B)-containing materials, carbides, or carbon (C)-containing materials and nitrides, as well as oxides and suicides or silicon (Si)-containing master alloys.
  • Especially preferred compounds are MoB, AlN (Aluminum Nitride), and B 4 C, as well as Al 2 O 3 , Cr 2 O 3 , SiO 2 , and mixtures thereof.
  • the amount of dopant may range from about 1 to 15 atomic percent (at. %), and preferably from 1 to 12 at. %.
  • the step of forming the doped elemental powders or alloys is carried out by mechanical mixing to achieve substantially uniform blending of the materials.
  • the canning step is carried out so as to avoid segregation of the doped element or alloy.
  • FIG. 1 shows the process flow for making the targets.
  • the first step is the preparation of raw material powders like atomized alloy powders of Ni—Al—B, Fe—B, Fe—C, Fe—Si and so on or the selection of commercially available ultra fine compound powders such as Al 2 O 3 , AlN, MoB and Cr 2 O 3 of 10 microns or less.
  • Atomized powders have very fine microstructure because of extremely quick cooling and rapid solidification; therefore it is the first choice as raw materials.
  • powders of fine microstructures can also be made by melting and mechanically crushing ingots much more economically than by atomization, especially for small quantities of powder.
  • Some ultra fine compound powders like Al 2 O 3 , AlN, MoB, Cr 2 O 3 , B 4 C and so on are also commercially available, and therefore save both time and money for new product development.
  • Special blending methods of various powders together are required because segregation occurs quite often, especially when powders of differing particle size and gravity are combined.
  • Those special blending and homogenizing methods include ball milling, v-blending, tubular blending, and attritor milling and/or wet blending. Therefore, it is preferred that the alloy powders and/or mixture be substantially homogeneous for best results.
  • Hot pressing in a graphite die could be used as well to consolidate the powder.
  • the powders are canned in preparation for consolidation.
  • a container is filled with the powder, evacuated under heat to ensure the removal of any moisture or trapped gasses present, and then sealed.
  • vacuum hot pressing the chamber is continuously evacuated prior to and during load application.
  • the geometry of the container is not limited in any manner, the container can possess a near-net shape geometry with respect to the final material configuration.
  • HIP Hot-Isostatic-Pressing
  • a HIP unit is typically a cylindrical pressure vessel large enough to house one or more containers.
  • the inner walls of the vessel can be lined with resistance heating elements, and the pressure can be controlled by the introduction of inert gas within the container.
  • HIP parameters including temperature, pressure and hold time will be minimized to prevent the growth of compound phases and grain size, as well as to save energy and to protect the environment.
  • Pressures of about 5 to about 60 ksi (preferably 10-20 ksi) at temperatures between about 500° C. to about 1500° C., are typically employed to achieve appropriate densities.
  • total hold times during isostatic pressing typically vary from about 0.5 to about 12 hours.
  • Pressure during vacuum hot pressing is varied from 0.5 to 5 ksi (preferably 1.5 to 2.5 ksi) at temperatures ranging from about 500° C. to 1500° C. (preferably 800-1000° C.).
  • other powder consolidation techniques such as hot pressing and cold pressing can also be employed independently or in conjunction with HIP processing.
  • the solid material form (billet) is removed from the encapsulation can, and a slice of the billet can then be sent to be tested as to various properties of the billet.
  • the billet can be subjected to optional thermo-mechanical processing to further manipulate the microstructural and macro-magnetic properties of the target.
  • the final shape and size of the sputter targets can be formed, for example, by processes such as wire EDM, saw, waterjet, lathe, grinder, mill, etc. In these steps, the target can be cleaned and subjected to a final inspection.
  • Table 1 shows examples of sputter target materials and their exemplary chemistry in accordance with one aspect of the present invention. TABLE 1 alloys manufactured using the method described herein. Materials Exemplary Chemistry Co—Cr—Pt—B Co61at %-Cr15at %-Pt12at %-B12at % Co—Cr—Pt—O—Si Co56at %-Cr18at %-Pt16at %-SiO 2 (0.5-10) mol % Co—Pt—B—C Co60at %-Pt20at %-B16at %-C4at % Co—Ta—N Co50at %-Ta50at % doped with nitrogen of 1-4 at.
  • Table 2 shows examples of sputter target materials and their exemplary phases in accordance with one aspect of the present invention.
  • the sputter target materials set forth in each row may include some or all of the exemplary phases described in the row, and they may include other additional phases.
  • Table 3 shows examples of sputter target materials and their exemplary powders that may be used to fabricate the sputter targets.
  • the sputter target materials set forth in each row may be fabricated using some of all of the powders set forth in the row and optionally using other additional powders.
  • the above alloy is made with the following powder blends: (1) Cr powder, Mo powder and ultra fine MoB compound powder, or (2) Cr powder, Mo powder and pre-alloyed Cr-3.1 wt % B powder (i.e., Cr-3.1 wt % B master alloy powder) that is made with a vacuum induction melter at 1730° C. and mechanically crushing cast ingots into powder at room temperature.
  • the pre-alloyed Cr-3.1 wt. % B powder can also be made by gas atomization. Special attention must be paid to mixing all powders together when ultra fine compound powder like MoB is used, otherwise segregation may occur. Herewith an attritor mill or a ball mill must be used for blending from 2 to 24 hours.
  • the HIP parameters for this kind of alloy include the temperature ranging from about 1000-1400° C., at a pressure from about 5-40 ksi and a hold time from about 1-12 hours.
  • the cooling rate must be controlled too, otherwise the HIPed billet may crack during cooling down.
  • a cooling rate of 3° C./min and a hold plateau at 800° C. for 6 hours is introduced to cooling phase.
  • a first alternative is the combination of Co powder, Cr powder, Pt powder and ultra fine Sio 2 compound powder.
  • a second alternative is the combination of Co powder, Cr powder, Pt powder, atomized Co—Si pre-alloy powder (i.e., Co—Si master alloy powder) and ultra fine Cr 2 O 3 compound powder.
  • the silicides are ultra fine and well dispersed in Co matrix of original gas-atomized Co—Si particles. Special mixing methods using an attritor mill or a ball mill for 2 to 24 hours must be employed here to mix all powders together homogeneously when ultra fine compound powders like SiO 2 and Cr 2 O 3 are used, otherwise segregation may occur.
  • the HIP parameters for this kind of alloy include the temperature ranging from about 600-1400° C., at a pressure from about 5-40 ksi and a hold time from about 1-12 hours.
  • Cr—Mo—X Cr80 at %-Mo20 at % doped with oxygen of 1-4 atomic % (at. %).
  • Regular Cr powder, Mo powder and partly oxidized Cr compound powder of oxygen level 15000 ppm are used to make the targets.
  • the Cr powder of high oxygen is produced by oxidizing Cr flakes at high temperature and then subjected to mechanical crushing. In this case, only a part of the surface area of Cr powder is covered with oxides. Special attention must be paid to Cr powder of high oxygen level and mixing all powders together in this case, otherwise segregation may occur.
  • an attritor mill or a ball mill may be used for blending from 2 to 24 hours.
  • the HIP parameters for this kind of alloy include the temperature ranging from about 800-1400° C., at a pressure from about 5-40 ksi and a hold time from about 1-12 hours.
  • the cooling rate must be controlled too, otherwise the HIPed billet may crack during cooling down. A cooling rate of 3° C./min and a hold plateau at 800° C. for 6 hours is introduced to cooling phase.
  • NiAl Sputtering Target Doped with Boron, Oxygen or Nitrogen—Ni50at %-Al50at % Doped with Boron of 1-4 at. %.
  • Gas-atomized NiAl intermetallic compound powder and ultra fine Al 2 O 3 compound powder and AlN compound powder of less than 5 microns in average particle diameter size were taken for making NiAl sputtering targets doped with oxygen or nitrogen.
  • gas-atomized NiAl powder boron-doped gas-atomized NiAl powder was also taken for making NiAl sputtering targets doped with boron and borides are ultra fine and well dispersed in the matrix.
  • Conventional gas atomization methods are used to manufacture the powders. Special attention must be paid to mixing all powders together when ultra fine compound powders like Al 2 O 3 and AlN are used, otherwise segregation may occur.
  • an attritor mill or a ball mill may be used for blending from 2 to 24 hours.
  • the HIP parameters for this kind of alloy include the temperature ranging from about 900-1400° C., at a pressure from about 5-40 ksi, and a hold time from about 1-12 hours.
  • the cooling rate must be controlled too, otherwise the HIPed billet may crack during cooling down.
  • a power-off furnace cooling and a hold plateau at 700° C. for 4 hours is introduced to cooling phase.
  • FIG. 2 illustrates a representative microstructure of a Co—Cr—Pt—O—Si sputter target according to one aspect.
  • the sputter target is manufactured using 100-mesh cobalt (Co) powder at 29.53 wt. %, 100-mesh Co-24.22Cr powder at 27.73 wt. %, >0 ⁇ m and ⁇ 5 ⁇ m SiO 2 powder at 6.13 wt. %, and platinum (Pt) powder at 36.61 wt. %.
  • the manufactured sputter target includes, for example, a first material, a second material and a third material.
  • the first material is comprised of Co (e.g., Co—Cr master alloy or Co).
  • the second material is comprised of an oxide, or more specifically SiO 2 compound in this example.
  • the third material is comprised of Pt.
  • the first material may constitute a first phase
  • the second material may constitute a second phase
  • the third material may constitute a third phase.
  • the second phase of the second material has an average size between greater than 0 and 50 microns.
  • the sputter target includes dark Co phases, dark Co—Cr master alloy phases, light Pt phases, and dark SiO 2 compound phases.
  • the SiO 2 compound phases have an average size between greater than 0 and 10 microns (e.g., between greater than 0 and 5 microns).
  • FIG. 3 illustrates a representative microstructure of a Co—Cr—Pt—O—Si sputter target according to one aspect.
  • the sputter target is manufactured using 16.97 wt. % cobalt (Co) powder, 5.49 wt. % CoSi 2 powder, 14.52 wt. % CoO powder, 26.4 wt. % Co-24.22Cr powder, and 36.62 wt. % platinum (Pt) powder.
  • the manufactured sputter target includes, for example, a first material, a second material and a third material.
  • the first material is comprised of Co (e.g., Co—Cr master alloy or Co).
  • the second material is comprised of a silicide, or more specifically CoSi 2 compound.
  • the third material is comprised of Pt.
  • the first material may constitute a first phase
  • the second material may constitute a second phase
  • the third material may constitute a third phase.
  • the second phase of the second material
  • the sputter target includes dark Co phases, dark Co—Cr master alloy phases, light Pt phases, and dark CoSi 2 compound phases.
  • the CoSi 2 compound phases have an average size between greater than 0 and 5 microns.
  • the Co phases have an average size between greater than 0 and 150 microns.
  • a sputter target comprises a plurality of materials.
  • the plurality of materials includes at least a first material and a second material.
  • the first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe).
  • the first material is comprised of one or more of the following according to one aspect: a cobalt (Co) element, a chromium (Cr) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a chromium (Cr) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a chromium (Cr) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, and an iron (Fe) based compound.
  • a cobalt (Co) element a chromium (Cr) element, a ruthenium (Ru) element, a nickel (Ni) based compound, and an iron (Fe) based compound.
  • the first material comprises at least 15 atomic percent or greater.
  • the first material constitutes a first phase, and the first phase has an average size between greater than 0 micron and 50 microns (i.e., 0 ⁇ phase size ⁇ 50 microns).
  • the present invention is not limited to these ranges, and in another embodiment, the first phase has an average size greater than 50 microns.
  • the second material is comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, a silicide, an oxygen (O)-containing material, an oxide, boron (B), a boron (B)-containing material, or a boride.
  • the second material is comprised of one or more of the following according to one aspect: MoB compound, Co—Cr—B master alloy, Co—B master alloy, Co—B compound, Cr—B master alloy, Cr—B compound (e.g., Cr 2 B), Ti—B compound (e.g., TiB 2 ), Ti—O compound, Ni—B master alloy, Ni—B compound, Al—B compound (e.g., AlB 2 ), Co—Si master alloy, Fe—Si master alloy, Cr—Si compound, silicon oxide compound (e.g., SiO 2 ), Co—Si compound (e.g., CoSi 2 , CO 2 Si), titanium oxide (e.g., TiO 2 ), chromium oxide (e.g., Cr 2 O 3 ), molybdenum oxide, aluminum oxide (e.g., Al 2 O 3 ), ruthenium oxide, C (e.g., graphite), Ta—C compound, Fe—C master alloy, Fe—C compound, aluminum nitride.
  • the second material constitutes a second phase
  • the second phase of the second material has an average size between greater than 0 micron and 50 microns (e.g., between greater than 0 micron and 20 microns, between greater than 0 micron and 10 microns, between 0.1 microns and 10 microns, between greater than 0 micron and 5 microns, between 1 micron and 5 microns, between greater than 0 micron and 2 microns, or less than 2 microns, etc.).
  • the plurality of materials further includes a third material.
  • the third material is comprised of one or more of the following: a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, and a refractory element based compound.
  • the third material is comprised of platinum (Pt) or tantalum (Ta).
  • the third material constitutes a third phase, and the third phase has an average size between greater than 0 micron and 50 microns (i.e., 0 ⁇ phase size ⁇ 50 microns). The present invention is not limited to these ranges, and in another embodiment, the third phase has an average size greater than 50 microns.
  • a sputter target is fabricated by blending a plurality of materials, canning and pressing.
  • the plurality of materials includes at least the first material and the second material described above.
  • the plurality of materials may also include the third material described above.
  • the plurality of materials may further include other materials.
  • each of the plurality of materials e.g., each of the first, second and third materials
  • Each of the first material, second material and third materials described above is in powder form for blending.
  • the particle size of the first material, the particle size of the second material, and particle size of the third material are the same as the size of the first phase, the size of the second phase, and the size of the third phase described above, respectively.
  • transition element examples include elements from the Periodic Table of elements shown in Roman numeral column number IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB according to one aspect of the present invention.
  • refractory element examples include elements from the Periodic Table of elements shown in Roman numeral column number IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB that have a melting point greater than or about equal to the melting point of iron (Fe) according to one aspect of the present invention.
  • cobalt-transition element based master alloy examples include a Co—Cr master alloy, a Co—Mn master alloy, a Co—Fe master alloy, a Co—Cr—B master alloy, and a Co—Ni master alloy according to one aspect of the present invention.
  • cobalt-refractory element based master alloy examples include a Co—Ta master alloy, a Co—Pt master alloy and a Co—Zr master alloy according to one aspect of the present invention.
  • transition element based compound examples include CoSi 2 , CrSi 2 , Fe 3 C, and Ni 3 Al according to one aspect of the present invention.
  • a refractory element based compound examples include TaC, Ta 2 C, TaB 2 , TaB, Mo 2 C, MoSi 2 , Mo 2 B and Mo 2 C according to one aspect of the present invention.
  • a master alloy is a combination of two or more elements consisting of a single or a multi-phase material, either as a simple solid solution (single-phase) of a minor element in a matrix of the major element or a combination of a solid solution and one or more secondary phases (multi-phase) having at least two constituents among the alloying elements.
  • Compounds of two or three different elements are substances containing a defined number of each atom species and having specific physical and chemical properties, on the whole, different from those which their constituents had as elementary substances.
  • a sputter target includes chromium and an oxide that is not a simple chromium oxide or Cr 2 O 3 .
  • such sputter target includes: chromium; chromium oxide or Cr 2 O 3 ; and other element(s), alloy(s) and/or compound(s).
  • such sputter target includes: chromium; and a compound(s) based on a chromium oxide (as opposed to a particular chromium oxide such as Cr 2 O 3 ).
  • a sputter target includes chromium and an oxide that is not a simple silicon dioxide (SiO 2 ).
  • such sputter target includes: chromium; silicon dioxide; and other element(s), alloy(s) and/or compound(s).
  • such sputter target includes: chromium; and a compound(s) based on a silicon oxide (as opposed to a particular silicon oxide such as siO 2 ).

Abstract

A sputter target comprises a plurality of materials. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, a silicide, an oxygen (O)-containing material, an oxide, boron (B), a boron (B)-containing material or a boride. The second material constitutes a phase where the phase of the second material has an average size between greater than 0 micron and 50 microns. According to one aspect, the first material comprises at least 15 atomic percent or greater. Methods of fabricating sputter targets by blending a plurality of materials are also disclosed.

Description

    CROSS-REFERENCES TO RELATED APPLICATIONS
  • This application is a continuation-in-part of U.S. patent application Ser. No. 10/739,401, filed Dec. 19, 2003, which is a continuation-in-part of U.S. patent application Ser. No. 10/200,590, filed Jul. 23, 2002, all of which are hereby incorporated by reference in their entirety for all purposes.
  • FIELD OF THE INVENTION
  • The present invention generally relates to sputtering targets and methods for fabricating sputtering targets and, in particular, relates to sputter targets comprising a plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe) and the second material comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, silicon (Si), a silicon (Si)-containing material, a silicide, an oxygen (O)-containing material, an oxide, boron (B), a boron (B)-containing material, or a boride, and further relates to methods for fabricating such sputter targets, and products produced thereby.
  • BACKGROUND OF THE INVENTION
  • Cathodic sputtering processes are widely used for the deposition of thin films of material onto desired substrates. A typical sputtering system includes a plasma source for generating an electron or ion beam, a target that comprises a material to be atomized and a substrate onto which the sputtered material is deposited. The process involves bombarding the target material with an electron or ion beam at an angle that causes the target material to be sputtered or eroded. The sputtered target material is deposited as a thin film or layer on the substrate.
  • SUMMARY OF THE INVENTION
  • According to one embodiment, the present invention relates to a novel method of fabricating sputtering targets that include non-metals such as boron, carbon, nitrogen, oxygen, silicon, a boride, a carbide, a nitride, an oxide, a silicide, a boron (B)-containing material, a carbon (C)-containing material, a nitrogen (N)-containing material, an oxygen (O)-containing material, or a silicon (Si)-containing material, including mixtures of non-metals, compounds of non-metals, master alloys containing boron, carbon or silicon and products produced by these processes. According to one embodiment, a process comprises preparation of pre-alloyed powder(s) or master alloy powder(s) or selection of ultra fine compound powder(s) of about 0.01 to 50 microns, preferably 0.1 to 10 microns, more preferably 1.0 to 5.0 microns average particle size and most preferably less than 2 microns. It has been discovered that spitting will not occur when the above phases are in form of ultra fine particles of less than 50 microns, preferably less than 10 microns in size. After the ultra fine powders are blended together, the powder blend is canned, followed by a hot isostatic press (HIP) consolidation. Powder processing as above is employed to make the target materials because of unique advantages over the prior art's melting process, both technically and economically.
  • According to one embodiment of the present invention, a sputter target comprises a plurality of materials. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, or a silicide. The second material constitutes a phase. The phase of the second material has an average size between greater than 0 micron and 50 microns. The first material comprises at least 15 atomic percent or greater.
  • According to one embodiment of the present invention, a sputter target comprises a plurality of materials. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of an oxygen (O)-containing material or an oxide. The second material constitutes a phase. The phase of the second material has an average size between greater than 0 micron and 50 microns.
  • According to one embodiment of the present invention, a sputter target comprises a plurality of materials. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of an oxygen (O)-containing material or an oxide. The second material constitutes a phase. The phase of the second material has an average size between greater than 0 micron and 50 microns. If the sputter target consists of chromium (Cr) and the oxygen (O)-containing material only, the oxygen (O)-containing material is an oxygen (O)-containing material other than simply chromium oxide. If the sputter target consists of chromium (Cr) and the oxide only, the oxide is an oxide other than simply chromium oxide.
  • According to one embodiment of the present invention, a sputter target comprises a plurality of materials. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of boron (B), a boron (B)-containing material or a boride. The second material constitutes a phase. The phase of the second material has an average size between greater than 0 micron and less than 10 microns.
  • According to one embodiment of the present invention, a sputter target comprises a plurality of materials. The plurality of materials includes at least a first material and a second material. The first material is comprised of ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of boron (B), a boron (B)-containing material or a boride. The second material constitutes a phase. The phase of the second material has an average size between greater than 0 micron and 50 microns.
  • According to one aspect of the present invention, a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, or a silicide. The second material has an average particle size between greater than 0 micron and 50 microns. The first material comprises at least 15 atomic percent or greater. The plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • According to one aspect of the present invention, a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of an oxygen (O)-containing material or an oxide. The second material has an average particle size between greater than 0 micron and 50 microns. The plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • According to one aspect of the present invention, a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of an oxygen (O)-containing material or an oxide. The second material has an average particle size between greater than 0 micron and 50 microns. The plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders. If the plurality of materials consists of chromium (Cr) and the oxygen (O)-containing material only, the oxygen (O)-containing material is an oxygen (O)-containing material other than simply chromium oxide. If the plurality of materials consists of chromium (Cr) and the oxide only, the oxide is an oxide other than simply chromium oxide.
  • According to one aspect of the present invention, a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of boron (B), a boron (B)-containing material or a boride. The second material has an average particle size between greater than 0 micron and less than 10 microns. The plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • According to one aspect of the present invention, a method of fabricating a sputter target comprises the steps of: blending a plurality of materials; canning; and pressing. The plurality of materials includes at least a first material and a second material. The first material is comprised of ruthenium (Ru), nickel (Ni), or iron (Fe). The second material is comprised of boron (B), a boron (B)-containing material or a boride. The second material has an average particle size between greater than 0 micron and less than 50 microns. The plurality of materials is comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • Reference is now made to the accompanying drawing wherein:
  • FIG. 1 shows the process flow chart of the invention described herein according to one aspect of the present invention.
  • FIG. 2 illustrates a representative microstructure of a consolidated (CO74Cr10Pt16)92—(SiO2)8 alloy according to one aspect of the present invention.
  • FIG. 3 illustrates a representative microstructure of a consolidated (CO74Cr10Pt16)92—(SiO2)8 alloy according to one aspect of the present invention.
  • Appendix 1 shows a Periodic Table of elements.
  • DETAILED DESCRIPTION OF THE INVENTION
  • Sputtering target materials for sputtering process range from pure metals to ever more complicated alloys. Complex 3 to 6 element alloys may be utilized for sputtering targets. Alloying additions such as boron, carbon, nitrogen, oxygen, silicon and so on are added to Cr—, Co—, Fe-based alloys to modify characteristics such as deposited film grain-size, surface energy and magnetic properties.
  • According to one embodiment, the presence of non-metal additions like boron, carbon, nitrogen, oxygen and silicon to target materials is either in the form of pure elements, e.g. boron and carbon, or in the form of compounds like boride, carbide, nitride and oxide. The pure element phases such as boron and carbon and the compound phases like boride, carbide, nitride, oxide, and silicide, however cause spitting problems during sputtering. The present invention provides a solution to this problem.
  • The powders of the present invention include elemental powders, pre-alloyed powders, powders of master alloys and/or intermetallic compound powders composed of 2 to 6 elements, including but not limited to Cr—, Co—, Ru—, Ni—, and/or Fe-based alloys. According to one aspect of the present invention, examples of master alloys include pre-alloyed powders, and pre-alloyed powders may be atomized master alloys.
  • The powders of the present invention contain pure Cr, Co, Ru, Ni, Fe, Pt and/or Ta and/or (optionally) pre-alloyed or master alloy powders of said pure elements, and include at least a boride, a boron (B)-containing material (e.g., boron based inorganic compound or master alloy), a carbide, a carbon (C)-containing material (e.g., carbon based inorganic compound or master alloy), a nitride, a nitrogen (N)-containing material, a silicide, a silicon (Si)-containing material (e.g., silicon based master alloy), an oxide, or an oxygen (O)-containing material of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB (see Appendix 1). These Roman numeral column numbers correspond to column numbers 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 and 14.
  • Examples of a boron (B)-containing material include a boride; examples of a carbon (C)-containing material include a carbide; examples of a nitrogen (N)-containing material include a nitride; examples of a silicon (Si)-containing material include a silicide; and examples of an oxygen (O)-containing material includes an oxide.
  • In preferred embodiments, the non-metallic additive is in combined form such as an inorganic compound or a master alloy of a non-metal although elemental additions may be used if desired. Preferred doping non-metals are compounds of boron, carbon and nitrogen. In still other embodiments compounds of oxygen or silica are included as dopants. Preferred doping compounds are borides or boron (B)-containing materials, carbides, or carbon (C)-containing materials and nitrides, as well as oxides and suicides or silicon (Si)-containing master alloys. Especially preferred compounds are MoB, AlN (Aluminum Nitride), and B4C, as well as Al2O3, Cr2O3, SiO2, and mixtures thereof. The amount of dopant may range from about 1 to 15 atomic percent (at. %), and preferably from 1 to 12 at. %.
  • In further embodiments, the step of forming the doped elemental powders or alloys is carried out by mechanical mixing to achieve substantially uniform blending of the materials. In further embodiments, the canning step is carried out so as to avoid segregation of the doped element or alloy.
  • FIG. 1 shows the process flow for making the targets. The first step is the preparation of raw material powders like atomized alloy powders of Ni—Al—B, Fe—B, Fe—C, Fe—Si and so on or the selection of commercially available ultra fine compound powders such as Al2O3, AlN, MoB and Cr2O3 of 10 microns or less. Atomized powders have very fine microstructure because of extremely quick cooling and rapid solidification; therefore it is the first choice as raw materials. In some cases powders of fine microstructures can also be made by melting and mechanically crushing ingots much more economically than by atomization, especially for small quantities of powder. Some ultra fine compound powders like Al2O3, AlN, MoB, Cr2O3, B4C and so on are also commercially available, and therefore save both time and money for new product development. Special blending methods of various powders together are required because segregation occurs quite often, especially when powders of differing particle size and gravity are combined. Those special blending and homogenizing methods include ball milling, v-blending, tubular blending, and attritor milling and/or wet blending. Therefore, it is preferred that the alloy powders and/or mixture be substantially homogeneous for best results.
  • Proper canning techniques are needed to avoid segregation during canning. Hot pressing in a graphite die could be used as well to consolidate the powder. The powders are canned in preparation for consolidation. In canning for example, a container is filled with the powder, evacuated under heat to ensure the removal of any moisture or trapped gasses present, and then sealed. In vacuum hot pressing, the chamber is continuously evacuated prior to and during load application. Although the geometry of the container is not limited in any manner, the container can possess a near-net shape geometry with respect to the final material configuration.
  • The encapsulate material from the canning step is then consolidated preferably via Hot-Isostatic-Pressing (HIP), a procedure known in the art. A HIP unit is typically a cylindrical pressure vessel large enough to house one or more containers. The inner walls of the vessel can be lined with resistance heating elements, and the pressure can be controlled by the introduction of inert gas within the container. HIP parameters including temperature, pressure and hold time will be minimized to prevent the growth of compound phases and grain size, as well as to save energy and to protect the environment. Pressures of about 5 to about 60 ksi (preferably 10-20 ksi) at temperatures between about 500° C. to about 1500° C., are typically employed to achieve appropriate densities. Depending upon the complexity of the cycle, total hold times during isostatic pressing typically vary from about 0.5 to about 12 hours. Pressure during vacuum hot pressing is varied from 0.5 to 5 ksi (preferably 1.5 to 2.5 ksi) at temperatures ranging from about 500° C. to 1500° C. (preferably 800-1000° C.). It is noteworthy that other powder consolidation techniques such as hot pressing and cold pressing can also be employed independently or in conjunction with HIP processing.
  • After consolidation, the solid material form (billet) is removed from the encapsulation can, and a slice of the billet can then be sent to be tested as to various properties of the billet. If desired, the billet can be subjected to optional thermo-mechanical processing to further manipulate the microstructural and macro-magnetic properties of the target. Also, the final shape and size of the sputter targets can be formed, for example, by processes such as wire EDM, saw, waterjet, lathe, grinder, mill, etc. In these steps, the target can be cleaned and subjected to a final inspection.
  • Table 1 shows examples of sputter target materials and their exemplary chemistry in accordance with one aspect of the present invention.
    TABLE 1
    alloys manufactured using the method described herein.
    Materials Exemplary Chemistry
    Co—Cr—Pt—B Co61at %-Cr15at %-Pt12at %-B12at %
    Co—Cr—Pt—O—Si Co56at %-Cr18at %-Pt16at %-SiO2
    (0.5-10) mol %
    Co—Pt—B—C Co60at %-Pt20at %-B16at %-C4at %
    Co—Ta—N Co50at %-Ta50at % doped with
    nitrogen of 1-4 at. %
    Co—Ta—Zr—O—Si Co85at %-Ta5at %-Zr5at %-SiO2
    (0.5-10) mol %
    Co—Ti—Pt—B Co62at %-Ti6at %-Pt12at %-B20at %
    Cr—B Cr97at %-B3at %
    Cr—Mo—B Cr80at %-Mo15at %-B5at %
    Cr—Mo—O Cr80at %-Mo20at % doped with oxygen
    of 1-4 at. %
    Cr—O Cr doped with oxygen of 1-4 at. %
    Cr—Ti—B Cr80at %-Ti16at %-B4at %
    Cr—V—O Cr80at %-V20at % doped with oxygen
    of 1-4 at. %
    Cr—V—Zr—O Cr79at %-V20at %-Zr1at % doped with
    oxygen of 1-4 at. %
    Cr—W—O Cr90at %-W10at % doped with oxygen
    of 1-4 at. %
    Cr—Zr—O Cr99at %-Zr1at % doped with oxygen
    of 1-4 at. %
    Fe—Co—B Fe56at %-Co31at %-B11at %
    Fe—Si—Al Fe73at %-Si17at %-Al10at %
    Fe—Ta—C Fe80at %-Ta8at %-C12at %
    Ni—Al—B Ni50at %-Al50at % doped with boron
    of 1-4 at. %
    Ni—Al—N Ni48at %-Al48at % doped with nitrogen
    of 4 at %
    Ni—Al—O Ni50at %-Al50at % doped with oxygen
    of 1-4 at. %
    Ru—Al—O Ru50at %-Al50at % doped with oxygen
    of 1-4 at. %
    Ru—Al—N Ru50at %-Al50at % doped with nitrogen
    of 1-4 at. %
  • Table 2 shows examples of sputter target materials and their exemplary phases in accordance with one aspect of the present invention. The sputter target materials set forth in each row may include some or all of the exemplary phases described in the row, and they may include other additional phases.
    TABLE 2
    alloys manufactured using the method described herein.
    Materials Exemplary Phases
    Co—Cr—Pt—B Co—Cr master alloy; Co—Cr—B master
    alloy; Pt; Co; Cr; Co—B master alloy;
    Co—B compound; Cr—B master alloy;
    Cr—B compound; Co—Pt master alloy
    Co—Cr—Pt—O—Si Co; Co—Cr master alloy; Pt; SiO2;
    Co—Cr—Pt master alloy
    Co—Ta—Zr—O—Si Co—Zr master alloy; Co—Ta master
    alloy; ZrO2; SiO2; Co; CoSi2; Co—Ta—Zr
    master alloy
    Co—Ti—Pt—B Co—B master alloy; Co—Ti master alloy;
    Co—Pt master alloy; Ti—B compound
    Cr—Ti—B Cr; Ti; Cr—B master alloy; Cr2B compound;
    TiB2 compound
    Fe—Ta—C Fe; C; Ta—C compound
    Fe—Ta—C Fe; Fe—C master alloy; Ta—C compound
    Ni—Al—B Ni; Ni—Al compound (e.g., NiAl, NiAl3);
    Ni—Al master alloy; Ni—B master alloy;
    Ni—B compound (e.g., Ni3B); AlB2 compound
    Ru—Al—O Ru; Al; aluminum oxide; ruthenium oxide;
    Ru—Al compound (e.g., Al6Ru, Al13Ru4,
    Al2Ru, AlRu)
  • Table 3 shows examples of sputter target materials and their exemplary powders that may be used to fabricate the sputter targets. The sputter target materials set forth in each row may be fabricated using some of all of the powders set forth in the row and optionally using other additional powders.
    TABLE 3
    alloys manufactured using the method described herein.
    Materials Exemplary Powders
    Co—Cr—Pt—O—Si Cr powder, Co—Cr master alloy powder,
    Pt powder; SiO2 compound powder
    Cr—Mo—B Cr powder; Mo powder; B powder
    Cr—Ti—B Cr powder; Ti powder; B powder
    Fe—Si—Al Fe—Si master alloy powder; Fe—Al
    master alloy powder; Fe—Si silicide
  • EXAMPLES
  • The following examples demonstrate the present invention further, but should not be construed as a limitation of the present invention. The processes for all materials are similar with each other as shown in FIG. 1, and the main differences are various combinations of raw materials (powders).
  • Example 1 Production Of Cr—Mo Based Sputtering Target with Boron Content—Cr80at %-Mo 15 at %-B5 at %
  • The above alloy is made with the following powder blends: (1) Cr powder, Mo powder and ultra fine MoB compound powder, or (2) Cr powder, Mo powder and pre-alloyed Cr-3.1 wt % B powder (i.e., Cr-3.1 wt % B master alloy powder) that is made with a vacuum induction melter at 1730° C. and mechanically crushing cast ingots into powder at room temperature. The pre-alloyed Cr-3.1 wt. % B powder can also be made by gas atomization. Special attention must be paid to mixing all powders together when ultra fine compound powder like MoB is used, otherwise segregation may occur. Herewith an attritor mill or a ball mill must be used for blending from 2 to 24 hours. The HIP parameters for this kind of alloy include the temperature ranging from about 1000-1400° C., at a pressure from about 5-40 ksi and a hold time from about 1-12 hours. The cooling rate must be controlled too, otherwise the HIPed billet may crack during cooling down. A cooling rate of 3° C./min and a hold plateau at 800° C. for 6 hours is introduced to cooling phase.
  • Example 2 Production Of Co—Cr—Pt Based Sputtering Target with SiO2 Content—Co56 at %-Cr18 at %-Pt16 at %-03.33 at %-Si 1.67 at %
  • Two different combinations of starting powders are employed herein. A first alternative is the combination of Co powder, Cr powder, Pt powder and ultra fine Sio2 compound powder. A second alternative is the combination of Co powder, Cr powder, Pt powder, atomized Co—Si pre-alloy powder (i.e., Co—Si master alloy powder) and ultra fine Cr2O3 compound powder. The silicides are ultra fine and well dispersed in Co matrix of original gas-atomized Co—Si particles. Special mixing methods using an attritor mill or a ball mill for 2 to 24 hours must be employed here to mix all powders together homogeneously when ultra fine compound powders like SiO2 and Cr2O3 are used, otherwise segregation may occur. The HIP parameters for this kind of alloy include the temperature ranging from about 600-1400° C., at a pressure from about 5-40 ksi and a hold time from about 1-12 hours.
  • Example 3 Production Of Cr—Mo—X (wherein X is Boride, Carbide, Nitride or Oxide, or Mixtures Thereof) Sputtering Target. To produce Cr—Mo—X, Cr Powder, Mo Powder, and One or Both of Cr Oxide Powder and Mo Oxide Powder are Utilized according to one Aspect of the Present Invention.
  • One example of Cr—Mo—X: Cr80 at %-Mo20 at % doped with oxygen of 1-4 atomic % (at. %).
  • Regular Cr powder, Mo powder and partly oxidized Cr compound powder of oxygen level 15000 ppm are used to make the targets. The Cr powder of high oxygen is produced by oxidizing Cr flakes at high temperature and then subjected to mechanical crushing. In this case, only a part of the surface area of Cr powder is covered with oxides. Special attention must be paid to Cr powder of high oxygen level and mixing all powders together in this case, otherwise segregation may occur. Herewith an attritor mill or a ball mill may be used for blending from 2 to 24 hours. The HIP parameters for this kind of alloy include the temperature ranging from about 800-1400° C., at a pressure from about 5-40 ksi and a hold time from about 1-12 hours. The cooling rate must be controlled too, otherwise the HIPed billet may crack during cooling down. A cooling rate of 3° C./min and a hold plateau at 800° C. for 6 hours is introduced to cooling phase.
  • Example 4 Production of NiAl Sputtering Target Doped with Boron, Oxygen or Nitrogen—Ni50at %-Al50at % Doped with Boron of 1-4 at. %.
  • Gas-atomized NiAl intermetallic compound powder and ultra fine Al2O3 compound powder and AlN compound powder of less than 5 microns in average particle diameter size were taken for making NiAl sputtering targets doped with oxygen or nitrogen. Besides gas-atomized NiAl powder, boron-doped gas-atomized NiAl powder was also taken for making NiAl sputtering targets doped with boron and borides are ultra fine and well dispersed in the matrix. Conventional gas atomization methods are used to manufacture the powders. Special attention must be paid to mixing all powders together when ultra fine compound powders like Al2O3 and AlN are used, otherwise segregation may occur. Herewith an attritor mill or a ball mill may be used for blending from 2 to 24 hours. The HIP parameters for this kind of alloy include the temperature ranging from about 900-1400° C., at a pressure from about 5-40 ksi, and a hold time from about 1-12 hours. The cooling rate must be controlled too, otherwise the HIPed billet may crack during cooling down. A power-off furnace cooling and a hold plateau at 700° C. for 4 hours is introduced to cooling phase.
  • FIG. 2 illustrates a representative microstructure of a Co—Cr—Pt—O—Si sputter target according to one aspect. The sputter target is manufactured using 100-mesh cobalt (Co) powder at 29.53 wt. %, 100-mesh Co-24.22Cr powder at 27.73 wt. %, >0 μm and <5 μm SiO2 powder at 6.13 wt. %, and platinum (Pt) powder at 36.61 wt. %. The manufactured sputter target includes, for example, a first material, a second material and a third material. The first material is comprised of Co (e.g., Co—Cr master alloy or Co). The second material is comprised of an oxide, or more specifically SiO2 compound in this example. The third material is comprised of Pt. The first material may constitute a first phase, the second material may constitute a second phase, and the third material may constitute a third phase. The second phase of the second material has an average size between greater than 0 and 50 microns.
  • The sputter target includes dark Co phases, dark Co—Cr master alloy phases, light Pt phases, and dark SiO2 compound phases. In this example, the SiO2 compound phases have an average size between greater than 0 and 10 microns (e.g., between greater than 0 and 5 microns).
  • FIG. 3 illustrates a representative microstructure of a Co—Cr—Pt—O—Si sputter target according to one aspect. The sputter target is manufactured using 16.97 wt. % cobalt (Co) powder, 5.49 wt. % CoSi2 powder, 14.52 wt. % CoO powder, 26.4 wt. % Co-24.22Cr powder, and 36.62 wt. % platinum (Pt) powder. The manufactured sputter target includes, for example, a first material, a second material and a third material. The first material is comprised of Co (e.g., Co—Cr master alloy or Co). The second material is comprised of a silicide, or more specifically CoSi2 compound. The third material is comprised of Pt. The first material may constitute a first phase, the second material may constitute a second phase, and the third material may constitute a third phase. The second phase of the second material has an average size between greater than 0 and 50 microns.
  • The sputter target includes dark Co phases, dark Co—Cr master alloy phases, light Pt phases, and dark CoSi2 compound phases. In this example, the CoSi2 compound phases have an average size between greater than 0 and 5 microns. The Co phases have an average size between greater than 0 and 150 microns.
  • According to one embodiment of the present invention, a sputter target comprises a plurality of materials. The plurality of materials includes at least a first material and a second material. The first material is comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe). For example, the first material is comprised of one or more of the following according to one aspect: a cobalt (Co) element, a chromium (Cr) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a chromium (Cr) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a chromium (Cr) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, and an iron (Fe) based compound. According to one aspect, the first material comprises at least 15 atomic percent or greater. According to one aspect, the first material constitutes a first phase, and the first phase has an average size between greater than 0 micron and 50 microns (i.e., 0<phase size≦50 microns). The present invention is not limited to these ranges, and in another embodiment, the first phase has an average size greater than 50 microns.
  • The second material is comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, a silicide, an oxygen (O)-containing material, an oxide, boron (B), a boron (B)-containing material, or a boride. For example, the second material is comprised of one or more of the following according to one aspect: MoB compound, Co—Cr—B master alloy, Co—B master alloy, Co—B compound, Cr—B master alloy, Cr—B compound (e.g., Cr2B), Ti—B compound (e.g., TiB2), Ti—O compound, Ni—B master alloy, Ni—B compound, Al—B compound (e.g., AlB2), Co—Si master alloy, Fe—Si master alloy, Cr—Si compound, silicon oxide compound (e.g., SiO2), Co—Si compound (e.g., CoSi2, CO2Si), titanium oxide (e.g., TiO2), chromium oxide (e.g., Cr2O3), molybdenum oxide, aluminum oxide (e.g., Al2O3), ruthenium oxide, C (e.g., graphite), Ta—C compound, Fe—C master alloy, Fe—C compound, aluminum nitride, cobalt nitride, chromium nitride, and iron nitride.
  • According to one aspect, the second material constitutes a second phase, and the second phase of the second material has an average size between greater than 0 micron and 50 microns (e.g., between greater than 0 micron and 20 microns, between greater than 0 micron and 10 microns, between 0.1 microns and 10 microns, between greater than 0 micron and 5 microns, between 1 micron and 5 microns, between greater than 0 micron and 2 microns, or less than 2 microns, etc.).
  • According to one aspect, the plurality of materials further includes a third material. According to one aspect, the third material is comprised of one or more of the following: a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, and a refractory element based compound. In another aspect, the third material is comprised of platinum (Pt) or tantalum (Ta). According to one aspect, the third material constitutes a third phase, and the third phase has an average size between greater than 0 micron and 50 microns (i.e., 0<phase size≦50 microns). The present invention is not limited to these ranges, and in another embodiment, the third phase has an average size greater than 50 microns.
  • According to one aspect of the present invention, a sputter target is fabricated by blending a plurality of materials, canning and pressing. The plurality of materials includes at least the first material and the second material described above. The plurality of materials may also include the third material described above. The plurality of materials may further include other materials. When the plurality of materials are blended, each of the plurality of materials (e.g., each of the first, second and third materials) is in powder form, for example, elemental powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders. Each of the first material, second material and third materials described above is in powder form for blending. According to one aspect, the particle size of the first material, the particle size of the second material, and particle size of the third material are the same as the size of the first phase, the size of the second phase, and the size of the third phase described above, respectively.
  • Some examples of a transition element include elements from the Periodic Table of elements shown in Roman numeral column number IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB according to one aspect of the present invention. Some examples of a refractory element include elements from the Periodic Table of elements shown in Roman numeral column number IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB that have a melting point greater than or about equal to the melting point of iron (Fe) according to one aspect of the present invention.
  • Some examples of a cobalt-transition element based master alloy include a Co—Cr master alloy, a Co—Mn master alloy, a Co—Fe master alloy, a Co—Cr—B master alloy, and a Co—Ni master alloy according to one aspect of the present invention. Some examples of a cobalt-refractory element based master alloy include a Co—Ta master alloy, a Co—Pt master alloy and a Co—Zr master alloy according to one aspect of the present invention.
  • Some examples of a transition element based compound include CoSi2, CrSi2, Fe3C, and Ni3Al according to one aspect of the present invention. Some examples of a refractory element based compound include TaC, Ta2C, TaB2, TaB, Mo2C, MoSi2, Mo2B and Mo2C according to one aspect of the present invention.
  • According to one aspect of the present invention, a master alloy is a combination of two or more elements consisting of a single or a multi-phase material, either as a simple solid solution (single-phase) of a minor element in a matrix of the major element or a combination of a solid solution and one or more secondary phases (multi-phase) having at least two constituents among the alloying elements. Compounds of two or three different elements are substances containing a defined number of each atom species and having specific physical and chemical properties, on the whole, different from those which their constituents had as elementary substances.
  • According to one aspect of the present invention, a sputter target includes chromium and an oxide that is not a simple chromium oxide or Cr2O3. For example, such sputter target includes: chromium; chromium oxide or Cr2O3; and other element(s), alloy(s) and/or compound(s). In another example, such sputter target includes: chromium; and a compound(s) based on a chromium oxide (as opposed to a particular chromium oxide such as Cr2O3).
  • According to one aspect of the present invention, a sputter target includes chromium and an oxide that is not a simple silicon dioxide (SiO2). For example, such sputter target includes: chromium; silicon dioxide; and other element(s), alloy(s) and/or compound(s). In another example, such sputter target includes: chromium; and a compound(s) based on a silicon oxide (as opposed to a particular silicon oxide such as siO2).
  • While this invention has been described with reference to several preferred embodiments, it is contemplated that various alterations and modifications thereof will become apparent to those skilled in the art upon a reading of the detailed description contained herein. It is therefore intended that the following claims are interpreted as including all such alterations and modifications as fall within the true spirit and scope of this invention.
    Figure US20070189916A1-20070816-P00001

Claims (85)

1. A sputter target comprising a plurality of materials, the plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, or a silicide, the second material constituting a phase, the phase of the second material having an average size between greater than 0 micron and 50 microns, the first material comprising at least 15 atomic percent or greater.
2. The sputter target of claim 1, wherein the carbide is a carbide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the nitride is a nitride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
3. The sputter target of claim 1, wherein the nitrogen (N)-containing material is a nitrogen (N)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB,
wherein the carbon (C)-containing material is a carbon (C)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB,
wherein the silicon (Si)-containing material is a silicon (Si)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the silicide is a silicide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
4. The sputter target of claim 1, wherein the second material is comprised of the carbide or the nitride,
wherein the carbide is a carbide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the nitride is a nitride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
5. The sputter target of claim 1, wherein the second material is comprised of the silicide,
wherein the silicide is a silicide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
6. The sputter target of claim 1, wherein the second material is comprised of the nitride, wherein the nitride is a nitride of aluminum (Al).
7. The sputter target of claim 1, wherein the phase of the second material has an average size between 0.1 microns and 10 microns.
8. The sputter target of claim 1, wherein the phase of the second material has an average size between 1 micron and 5 microns.
9. The sputter target of claim 1, wherein the phase of the second material has an average size less than 2 microns.
10. The sputter target of claim 1, wherein the first material is comprised of a cobalt (Co) element, a chromium (Cr) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a chromium (Cr) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a chromium (Cr) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, or an iron (Fe) based compound.
11. The sputter target of claim 1, wherein the first material constitutes a first phase, and the first phase of the first material has an average size between greater than 0 micron and 50 microns.
12. The sputter target of claim 1, wherein the plurality of materials includes a third material, the third material comprised of platinum (Pt) or tantalum (Ta).
13. The sputter target of claim 1, wherein the plurality of materials further includes a third material comprised of a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, or a refractory element based compound.
14. The sputter target of claim 13, wherein the third material constitutes a phase, and the phase of the third material has an average size between greater than 0 micron and 50 microns.
15. The sputter target of claim 1, wherein the sputter target comprises an alloy, the alloy including a plurality of phases, the plurality of phases including at least a first phase and a second phase, the first material constituting the first phase, the second phase being the phase of the second material, the first material comprised of a cobalt (Co) element, a chromium (Cr) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a chromium (Cr) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a chromium (Cr) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, or an iron (Fe) based compound.
16. A sputter target comprising a plurality of materials, the plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of an oxygen (O)-containing material or an oxide, the second material constituting a phase, the phase of the second material having an average size between greater than 0 micron and 50 microns.
17. The sputter target of claim 16, wherein the oxide is an oxide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
18. The sputter target of claim 16, wherein the oxygen (O)-containing material is an oxygen (O)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
19. The sputter target of claim 16, wherein the oxide is an oxide of one or more of transition or refractory elements.
20. The sputter target of claim 16, wherein the oxygen (O)-containing material is an oxygen (O)-containing material including one or more of transition or refractory elements.
21. The sputter target of claim 16, wherein the second material is comprised of the oxide, wherein the oxide is an oxide of silicon (Si), aluminum (Al) or titanium (Ti).
22. The sputter target of claim 16, wherein the second material is comprised of the oxide, wherein the oxide is silicon dioxide (SiO2).
23. The sputter target of claim 16, wherein the second material is comprised of the oxide, wherein the oxide is titanium oxide (TiO2).
24. The sputter target of claim 16, wherein the phase of the second material has an average size between 0.1 microns and 10 microns.
25. The sputter target of claim 16, wherein the phase of the second material has an average size between 1 micron and 5 microns.
26. The sputter target of claim 16, wherein the phase of the second material has an average size less than 2 microns.
27. The sputter target of claim 16, wherein the first material is comprised of a cobalt (Co) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, or an iron (Fe) based compound.
28. The sputter target of claim 16, wherein the first material constitutes a first phase, and the first phase of the first material has an average size between greater than 0 micron and 50 microns.
29. The sputter target of claim 16, wherein the plurality of materials includes a third material, the third material comprised of platinum (Pt) or tantalum (Ta).
30. The sputter target of claim 16, wherein the plurality of materials further includes a third material comprised of a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, or a refractory element based compound.
31. The sputter target of claim 30, wherein the third material constitutes a phase, and the phase of the third material has an average size between greater than 0 micron and 50 microns.
32. The sputter target of claim 16, wherein the sputter target comprises an alloy, the alloy including a plurality of phases, the plurality of phases including at least a first phase and a second phase, the first material constituting the first phase, the second phase being the phase of the second material, the first material comprised of a cobalt (Co) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, or an iron (Fe) based compound.
33. The sputter target of claim 16, wherein the sputter target is comprised of Co, Cr, Pt and SiO2.
34. The sputter target of claim 16, wherein the first material comprises at least 15 atomic percent or greater.
35. A sputter target comprising a plurality of materials, the plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of an oxygen (O)-containing material or an oxide, the second material constituting a phase, the phase of the second material having an average size between greater than 0 micron and 50 microns,
wherein if the sputter target consists of chromium (Cr) and the oxygen (O)-containing material only, the oxygen (O)-containing material is an oxygen (O)-containing material other than simply chromium oxide, and
wherein if the sputter target consists of chromium (Cr) and the oxide only, the oxide is an oxide other than simply chromium oxide.
36. The sputter target of claim 35, wherein the oxygen (O)-containing material is an oxygen (O)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the oxide is an oxide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
37. The sputter target of claim 35, wherein the oxide is an oxide of one or more of transition or refractory elements, and wherein the oxygen (O)-containing material is an oxygen (O)-containing material including one or more of transition or refractory elements.
38. The sputter target of claim 35, wherein the second material is comprised of the oxide, wherein the oxide is an oxide of silicon (Si), aluminum (Al) or titanium (Ti).
39. The sputter target of claim 35, wherein the second material is comprised of the oxide, wherein the oxide is silicon dioxide (SiO2).
40. The sputter target of claim 35, wherein the second material is comprised of the oxide, wherein the oxide is titanium oxide (TiO2).
41. The sputter target of claim 35, wherein the phase of the second material has an average size between 0.1 microns and 10 microns.
42. The sputter target of claim 35, wherein the phase of the second material has an average size between 1 micron and 5 microns.
43. The sputter target of claim 35, wherein the phase of the second material has an average size less than 2 microns.
44. The sputter target of claim 35, wherein the first material is comprised of a cobalt (Co) element, a chromium (Cr) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a chromium (Cr) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a chromium (Cr) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, or an iron (Fe) based compound,
wherein the first material constitutes a first phase, and the first phase of the first material has an average size between greater than 0 micron and 50 microns.
45. The sputter target of claim 35, wherein the plurality of materials includes a third material, the third material comprised of platinum (Pt) or tantalum (Ta).
46. The sputter target of claim 35, wherein the plurality of materials further includes a third material comprised of a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, or a refractory element based compound.
47. The sputter target of claim 46, wherein the third material constitutes a phase, and the phase of the third material has an average size between greater than 0 micron and 50 microns.
48. The sputter target of claim 35, wherein the sputter target comprises an alloy, the alloy including a plurality of phases, the plurality of phases including at least a first phase and a second phase, the first material constituting the first phase, the second phase being the phase of the second material, the first material comprised of a cobalt (Co) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, or an iron (Fe) based compound.
49. The sputter target of claim 35, wherein the sputter target is comprised of Co, Cr, Pt and SiO2.
50. The sputter target of claim 35, wherein the first material comprises at least 15 atomic percent or greater.
51. The sputter target of claim 35, wherein if the sputter target consists of chromium (Cr) and the oxygen (O)-containing material only, the oxygen (O)-containing material is an oxygen (O)-containing material other than simply chromium oxide or simply silicon dioxide (SiO2), and
wherein if the sputter target consists of chromium (Cr) and the oxide only, the oxide is an oxide other than simply chromium oxide or simply silicon dioxide (SiO2).
52. A sputter target comprising a plurality of materials, the plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of boron (B), a boron (B)-containing material or a boride, the second material constituting a phase, the phase of the second material having an average size between greater than 0 micron and less than 10 microns.
53. The sputter target of claim 52, wherein the boron (B)-containing material is a boron (B)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the boride is a boride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
54. The sputter target of claim 52, wherein the second material is comprised of boron (B).
55. The sputter target of claim 52, wherein the phase of the second material has an average size less than 2 microns.
56. The sputter target of claim 52, wherein the plurality of materials further includes a third material comprised of a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, or a refractory element based compound.
57. A sputter target comprising a plurality of materials, the plurality of materials including at least a first material and a second material, the first material comprised of ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of boron (B), a boron (B)-containing material or a boride, the second material constituting a phase, the phase of the second material having an average size between greater than 0 micron and 50 microns.
58. The sputter target of claim 57, wherein the boron (B)-containing material is a boron (B)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the boride is a boride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
59. The sputter target of claim 57, wherein the plurality of materials further includes a third material comprised of a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, or a refractory element based compound.
60. A method of fabricating a sputter target, the method comprising the steps of:
blending a plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of carbon (C), a carbon (C)-containing material, a carbide, a nitrogen (N)-containing material, a nitride, a silicon (Si)-containing material, or a silicide, the second material having an average particle size between greater than 0 micron and 50 microns, the first material comprising at least 15 atomic percent or greater, the plurality of materials comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders;
canning; and
pressing.
61. The method of claim 60, wherein the carbon (C)-containing material is a carbon (C)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB,
wherein the carbide is a carbide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB,
wherein the nitrogen (N)-containing material is a nitrogen (N)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB,
wherein the nitride is a nitride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB,
wherein the silicon (Si)-containing material is a silicon (Si)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the silicide is a silicide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
62. The method of claim 60, wherein the second material is comprised of the carbide, the nitride, or the silicide,
wherein the carbide is a carbide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB,
wherein the nitride is a nitride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the silicide is a silicide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
63. The method of claim 60, wherein the second material has an average particle size between 1 micron and 5 microns.
64. The method of claim 60, wherein the plurality of materials includes a third material, the third material comprised of platinum (Pt) or tantalum (Ta).
65. The method of claim 60, wherein the plurality of materials further includes a third material comprised of a transition element powder, a refractory element powder, a cobalt-transition element based master alloy powder, a cobalt-refractory element based master alloy powder, a transition element based compound powder, or a refractory element based compound powder.
66. A method of fabricating a sputter target, the method comprising the steps of:
blending a plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of an oxygen (O)-containing material or an oxide, the second material having an average particle size between greater than 0 micron and 50 microns, the plurality of materials comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders;
canning; and
pressing.
67. The method of claim 66, wherein the oxygen (O)-containing material is an oxygen (O)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the oxide is an oxide of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
68. The method of claim 66, wherein the second material has an average particle size between 1 micron and 5 microns.
69. The method of claim 66, wherein the plurality of materials further includes a third material comprised of a transition element, a refractory element, a cobalt-transition element based master alloy, a cobalt-refractory element based master alloy, a transition element based compound, or a refractory element based compound.
70. The method of claim 66, wherein the second material is comprised of the oxide, wherein the oxide is silicon dioxide (SiO2).
71. The method of claim 66, wherein the second material is comprised of the oxide, wherein the oxide is titanium oxide (TiO2).
72. A method of fabricating a sputter target, the method comprising the steps of:
blending a plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of an oxygen (O)-containing material or an oxide, the second material having an average particle size between greater than 0 micron and 50 microns, the plurality of materials comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders,
wherein if the plurality of materials consists of chromium (Cr) and the oxygen (O)-containing material only, the oxygen (O)-containing material is an oxygen (O)-containing material other than simply chromium oxide, and
wherein if the plurality of materials consists of chromium (Cr) and the oxide only, the oxide is an oxide other than simply chromium oxide;
canning; and
pressing.
73. The method of claim 72, wherein the second material is comprised of the oxide, wherein the oxide is an oxide of silicon (Si), aluminum (Al) or titanium (Ti).
74. The method of claim 72, wherein the second material has an average particle size less than 2 microns.
75. The method of claim 72, wherein the first material is comprised of a cobalt (Co) element, a chromium (Cr) element, a ruthenium (Ru) element, a nickel (Ni) element, an iron (Fe) element, a cobalt (Co) based master alloy, a chromium (Cr) based master alloy, a ruthenium (Ru) based master alloy, a nickel (Ni) based master alloy, an iron (Fe) based master alloy, a cobalt (Co) based compound, a chromium (Cr) based compound, a ruthenium (Ru) based compound, a nickel (Ni) based compound, or an iron (Fe) based compound.
76. The method of claim 72, wherein the plurality of materials includes a third material, the third material comprised of platinum (Pt) or tantalum (Ta).
77. The method of claim 72, wherein the sputter target is comprised of Co, Cr, Pt and SiO2.
78. The method of claim 72, wherein the second material is comprised of the oxide, wherein the oxide is silicon dioxide (SiO2).
79. The method of claim 72, wherein the second material is comprised of the oxide, wherein the oxide is titanium oxide (TiO2).
80. A method of fabricating a sputter target, the method comprising the steps of:
blending a plurality of materials including at least a first material and a second material, the first material comprised of cobalt (Co), chromium (Cr), ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of boron (B), a boron (B)-containing material or a boride, the second material having an average particle size between greater than 0 micron and less than 10 microns, the plurality of materials comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders;
canning; and
pressing.
81. The method of claim 80, the boron (B)-containing material is a boron (B)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the boride is a boride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
82. The method of claim 80, wherein the second material is comprised of boron (B).
83. A method of fabricating a sputter target, the method comprising the steps of:
blending a plurality of materials including at least a first material and a second material, the first material comprised of ruthenium (Ru), nickel (Ni), or iron (Fe), the second material comprised of boron (B), a boron (B)-containing material or a boride, the second material having an average particle size between greater than 0 micron and less than 50 microns, the plurality of materials comprised of multiple powders, one or more master alloy or compound powders, or a mixture of one or more powders with one or more master alloy or compound powders;
canning; and
pressing.
84. The method of claim 83, wherein the boron (B)-containing material is a boron (B)-containing material including one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB, and
wherein the boride is a boride of one or more elements from the Periodic Table of elements shown in Roman numeral column number IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB or IVB.
85. The method of claim 83, wherein the plurality of materials further includes a third material comprised of a transition element powder, a refractory element powder, a cobalt-transition element based master alloy powder, a cobalt-refractory element based master alloy powder, a transition element based compound powder, or a refractory element based compound powder.
US11/650,515 2002-07-23 2007-01-08 Sputtering targets and methods for fabricating sputtering targets having multiple materials Abandoned US20070189916A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
US11/650,515 US20070189916A1 (en) 2002-07-23 2007-01-08 Sputtering targets and methods for fabricating sputtering targets having multiple materials
TW096115669A TW200829709A (en) 2007-01-08 2007-05-03 Sputtering targets and methods for fabricating sputtering targets having multiple materials
KR1020070045176A KR20080065211A (en) 2007-01-08 2007-05-09 Sputtering targets and methods for fabricating sputtering targets having multiple materials
EP07108160A EP1942205A3 (en) 2007-01-08 2007-05-14 Sputtering targets and methods for fabricating sputtering targets having multiple materials
CNA2007101085628A CN101220457A (en) 2007-01-08 2007-06-05 Sputtering targets and methods for fabricating sputtering targets having multiple materials
JP2007175131A JP2008169464A (en) 2007-01-08 2007-07-03 Sputtering target and method for fabricating the same
SG200716736-4A SG144792A1 (en) 2007-01-08 2007-10-09 Sputtering targets and methods for fabricating sputtering targets having multiple materials
SG2012007258A SG178737A1 (en) 2007-01-08 2007-10-09 Sputtering targets and methods for fabricating sputtering targets having multiple materials
SG2012007357A SG178742A1 (en) 2007-01-08 2007-10-09 Sputtering targets and methods for fabricating sputtering targets having multiple materials

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US10/200,590 US6759005B2 (en) 2002-07-23 2002-07-23 Fabrication of B/C/N/O/Si doped sputtering targets
US10/739,401 US7311874B2 (en) 2002-07-23 2003-12-19 Sputter target and method for fabricating sputter target including a plurality of materials
US11/650,515 US20070189916A1 (en) 2002-07-23 2007-01-08 Sputtering targets and methods for fabricating sputtering targets having multiple materials

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US10/739,401 Continuation-In-Part US7311874B2 (en) 2002-07-23 2003-12-19 Sputter target and method for fabricating sputter target including a plurality of materials

Publications (1)

Publication Number Publication Date
US20070189916A1 true US20070189916A1 (en) 2007-08-16

Family

ID=39301096

Family Applications (1)

Application Number Title Priority Date Filing Date
US11/650,515 Abandoned US20070189916A1 (en) 2002-07-23 2007-01-08 Sputtering targets and methods for fabricating sputtering targets having multiple materials

Country Status (7)

Country Link
US (1) US20070189916A1 (en)
EP (1) EP1942205A3 (en)
JP (1) JP2008169464A (en)
KR (1) KR20080065211A (en)
CN (1) CN101220457A (en)
SG (3) SG144792A1 (en)
TW (1) TW200829709A (en)

Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060274236A1 (en) * 2005-06-03 2006-12-07 Samsung Electronics Co., Ltd. Display device, method of manufacturing the same and mask for manufacturing the same
US20080105542A1 (en) * 2006-11-08 2008-05-08 Purdy Clifford C System and method of manufacturing sputtering targets
WO2009012278A1 (en) * 2007-07-17 2009-01-22 Williams Advanced Materials, Inc. Process for the refurbishing of a sputtering target
US20100320084A1 (en) * 2008-03-28 2010-12-23 Nippon Mining And Metals Co., Ltd. Sputtering Target of Nonmagnetic-Particle-Dispersed Ferromagnetic Material
US20110003177A1 (en) * 2009-07-06 2011-01-06 Solar Applied Materials Technology Corp. Method for producing sputtering target containing boron, thin film and magnetic recording media
US20110241253A1 (en) * 2010-03-30 2011-10-06 China Steel Corporation Method for manufacturing cobalt alloy-based ceramic composite sputtering target
US20110247930A1 (en) * 2009-03-27 2011-10-13 Jx Nippon Mining & Metals Corporation Nonmagnetic Material Particle-Dispersed Ferromagnetic Material Sputtering Target
US8394243B1 (en) 2008-07-24 2013-03-12 Wd Media, Inc. Sputtered cobalt oxide for perpendicular magnetic recording medium with low media noise
CN103168328A (en) * 2010-12-17 2013-06-19 吉坤日矿日石金属株式会社 Sputtering target for magnetic recording film and method for producing same
US8488276B1 (en) 2008-09-30 2013-07-16 WD Media, LLC Perpendicular magnetic recording medium with grain isolation magnetic anistropy layer
CN103261469A (en) * 2010-12-17 2013-08-21 吉坤日矿日石金属株式会社 Ferromagnetic material sputtering target
CN103459656A (en) * 2011-03-30 2013-12-18 吉坤日矿日石金属株式会社 Sputtering target for magnetic recording film
TWI454588B (en) * 2011-03-30 2014-10-01 Tanaka Precious Metal Ind FePt-C sputtering target and its manufacturing method
US20140306144A1 (en) * 2010-08-06 2014-10-16 Tanaka Kikinzoku Kogyo K.K. Magnetron sputtering target and process for producing the same
US20140311901A1 (en) * 2011-11-17 2014-10-23 Tanaka Kikinzoku Kogyo K.K Magnetron sputtering target and method for manufacturing the same
US8993133B1 (en) 2010-12-23 2015-03-31 WD Media, LLC Intermediate layer for perpendicular magnetic recording medium with high permeability grain boundaries
US9011653B2 (en) 2010-11-29 2015-04-21 Mitsui Mining & Smelting Co., Ltd. Sputtering target
US9034155B2 (en) 2009-08-06 2015-05-19 Jx Nippon Mining & Metals Corporation Inorganic-particle-dispersed sputtering target
US9181617B2 (en) 2010-07-20 2015-11-10 Jx Nippon Mining & Metals Corporation Sputtering target of ferromagnetic material with low generation of particles
US9228251B2 (en) 2010-01-21 2016-01-05 Jx Nippon Mining & Metals Corporation Ferromagnetic material sputtering target
US20160053364A1 (en) * 2013-04-18 2016-02-25 Oerlikon Surface Solutions Ag, Trubbach ARC VAPORIZATION OF METALLIC, INTERMETALLIC, AND CERAMIC TARGET MATERIALS IN ORDER TO PRODUCE Al-Cr-N COATINGS
US9314846B2 (en) 2012-01-13 2016-04-19 Tanaka Kikinzoku Kogyo K.K. Process for producing FePt-based sputtering target
US9328412B2 (en) 2010-08-31 2016-05-03 Jx Nippon Mining & Metals Corporation Fe—Pt-based ferromagnetic material sputtering target
US9416439B2 (en) 2013-07-29 2016-08-16 Samsung Display Co., Ltd. Sputtering target, method of fabricating the same, and method of fabricating an organic light emitting display apparatus
US9540724B2 (en) 2012-06-18 2017-01-10 Jx Nippon Mining & Metals Corporation Sputtering target for magnetic recording film
US9567665B2 (en) 2010-07-29 2017-02-14 Jx Nippon Mining & Metals Corporation Sputtering target for magnetic recording film, and process for producing same
US9685184B1 (en) 2014-09-25 2017-06-20 WD Media, LLC NiFeX-based seed layer for magnetic recording media
US9761422B2 (en) 2012-02-22 2017-09-12 Jx Nippon Mining & Metals Corporation Magnetic material sputtering target and manufacturing method for same
US9793099B2 (en) 2012-03-15 2017-10-17 Jx Nippon Mining & Metals Corporation Magnetic material sputtering target and manufacturing method thereof
US9945026B2 (en) 2010-12-20 2018-04-17 Jx Nippon Mining & Metals Corporation Fe-Pt-based sputtering target with dispersed C grains
CN109112326A (en) * 2018-10-15 2019-01-01 河北四通新型金属材料股份有限公司 A kind of nickel carbon intermediate alloy and preparation method thereof
US20190010080A1 (en) * 2016-01-08 2019-01-10 Yej Glass Co., Ltd. Fluorinated Tin-Based Glass Frit And Method For Manufacturing Same
US10325762B2 (en) 2012-07-20 2019-06-18 Jx Nippon Mining & Metals Corporation Sputtering target for forming magnetic recording film and process for producing same
EP3587605A1 (en) * 2018-06-21 2020-01-01 INTEL Corporation Cobalt and nickel alloys for interconnects
US10755737B2 (en) * 2012-09-21 2020-08-25 Jx Nippon Mining & Metals Corporation Fe-Pt based magnetic material sintered compact

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080145688A1 (en) 2006-12-13 2008-06-19 H.C. Starck Inc. Method of joining tantalum clade steel structures
US8197894B2 (en) 2007-05-04 2012-06-12 H.C. Starck Gmbh Methods of forming sputtering targets
JP2009001862A (en) * 2007-06-21 2009-01-08 Mitsubishi Materials Corp Sputtering target for use in forming film of perpendicular magnetic recording medium having low relative magnetic permeability
JP2009215617A (en) * 2008-03-11 2009-09-24 Mitsui Mining & Smelting Co Ltd Sputtering target material containing cobalt, chromium, and platinum matrix phase and oxide phase and method for producing the same
JP5250838B2 (en) * 2009-01-27 2013-07-31 昭和電工株式会社 Magnetic recording medium manufacturing method, magnetic recording medium, and magnetic recording / reproducing apparatus
CN101880858B (en) * 2009-05-06 2015-07-29 光洋应用材料科技股份有限公司 The ferro-cobalt based alloy magnetic sputtering target material of high magnetic flux and manufacture method thereof
TWI393783B (en) * 2009-06-04 2013-04-21 Boron - containing target and its production method, film, magnetic recording media
TWI385264B (en) * 2009-07-01 2013-02-11 Univ Nat Chunghsing Method for preparing nitrogen-doped titania
JP2011021254A (en) * 2009-07-16 2011-02-03 Solar Applied Materials Technology Corp Method for producing boron-containing sputtering target, thin film and magnetic recording medium
JP5428995B2 (en) * 2010-03-28 2014-02-26 三菱マテリアル株式会社 Sputtering target for forming a magnetic recording medium film and method for producing the same
MY150826A (en) * 2010-07-20 2014-02-28 Jx Nippon Mining & Metals Corp Sputtering target of perromagnetic material with low generation of particles
WO2012029331A1 (en) * 2010-09-03 2012-03-08 Jx日鉱日石金属株式会社 Ferromagnetic material sputtering target
WO2012073879A1 (en) * 2010-11-29 2012-06-07 三井金属鉱業株式会社 Sputtering target
US8703233B2 (en) 2011-09-29 2014-04-22 H.C. Starck Inc. Methods of manufacturing large-area sputtering targets by cold spray
US20140231250A1 (en) * 2011-12-22 2014-08-21 Jx Nippon Mining & Metals Corporation C particle dispersed fe-pt-based sputtering target
JP5974327B2 (en) * 2012-10-25 2016-08-23 Jx金属株式会社 Nonmagnetic substance-dispersed Fe-Pt sputtering target
MY172839A (en) 2013-03-01 2019-12-12 Tanaka Precious Metal Ind Fept-c-based sputtering target and method for manufacturing same
MY175409A (en) * 2013-04-26 2020-06-24 Jx Nippon Mining & Metals Corp Sputtering target for magnetic recording film, and raw carbon material for use in producing same
MY177997A (en) * 2013-11-22 2020-09-29 Jx Nippon Mining & Metals Corp Sputtering target for forming magnetic recording film and method for producing same
CN105331939B (en) * 2014-08-15 2018-05-11 安泰科技股份有限公司 A kind of silicon-containing alloy target and preparation method thereof
CN104930735A (en) * 2015-03-24 2015-09-23 江苏奥蓝工程玻璃有限公司 Solar absorbing film and preparation method thereof
CN111136265B (en) * 2020-03-07 2022-02-18 北京安泰六九新材料科技有限公司 Titanium-silicon alloy target and manufacturing method thereof

Citations (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4820A (en) * 1846-10-21 Improvement in steam-engines
US589553A (en) * 1897-09-07 Half to francis j
US4609528A (en) * 1985-10-03 1986-09-02 General Electric Company Tri-nickel aluminide compositions ductile at hot-short temperatures
US4612165A (en) * 1983-12-21 1986-09-16 The United States Of America As Represented By The United States Department Of Energy Ductile aluminide alloys for high temperature applications
US4613368A (en) * 1985-10-03 1986-09-23 General Electric Company Tri-nickel aluminide compositions alloyed to overcome hot-short phenomena
US4675091A (en) * 1986-04-16 1987-06-23 United States Of America As Represented By The Secretary Of The Navy Co-sputtered thermionic cathodes and fabrication thereof
US4731116A (en) * 1985-12-23 1988-03-15 Schwarzkopf Development Corporation Sputter target and process for producing sputter target
US4917722A (en) * 1988-05-18 1990-04-17 Tosoh Corporation Single crystals of chromium and method for producing the same
US5320729A (en) * 1991-07-19 1994-06-14 Hitachi, Ltd. Sputtering target
US5415829A (en) * 1992-12-28 1995-05-16 Nikko Kyodo Co., Ltd. Sputtering target
US5470527A (en) * 1992-04-21 1995-11-28 Kabushiki Kaisha Toshiba Ti-W sputtering target and method for manufacturing same
US5530467A (en) * 1990-02-01 1996-06-25 Kabushiki Kaisha Toshiba Sputtering target, film resistor and thermal printer head
US5561833A (en) * 1993-03-11 1996-10-01 Japan Metals & Chemicals Co., Ltd. Method of making high oxygen chromium target
US5618397A (en) * 1993-05-07 1997-04-08 Japan Energy Corporation Silicide targets for sputtering
US5652877A (en) * 1991-01-18 1997-07-29 Centre National De La Recherche Aluminum alloys, substrates coated with these alloys and their applications
US5778302A (en) * 1995-09-14 1998-07-07 Tosoh Smd, Inc. Methods of making Cr-Me sputter targets and targets produced thereby
US5863398A (en) * 1996-10-11 1999-01-26 Johnson Matthey Electonics, Inc. Hot pressed and sintered sputtering target assemblies and method for making same
US5976326A (en) * 1994-04-06 1999-11-02 Komag, Incorporated Method of sputtering selected oxides and nitrides for forming magnetic media
US5989673A (en) * 1997-06-30 1999-11-23 Sony Corporation Caromium-tantalum oxides (Cr-TaOx), sputtering targets and thin film seedlayer/sublayers for thin film magnetic recording media
US6174597B1 (en) * 1996-07-26 2001-01-16 Kabushiki Kaisha Toshiba Magnetic recording apparatus
US6261984B1 (en) * 1998-10-08 2001-07-17 Tosoh Corporation Sputtering target and process for the preparation thereof
US20010008157A1 (en) * 1999-10-25 2001-07-19 Bishop David John Article comprising improved noble metal-based alloys and method for making the same
US6264813B1 (en) * 1996-12-04 2001-07-24 Aluminum Pechiney Cathodic sputtering targets made of aluminum alloy
US6309593B1 (en) * 1993-07-27 2001-10-30 Kabushiki Kaisha Toshiba Refractory metal silicide target, method of manufacturing the target, refractory metal silicide thin film, and semiconductor device
US20010044018A1 (en) * 2000-02-23 2001-11-22 Hiroyuki Uwazumi Sputtering target for production of magnetic recording medium, method for producing magnetic recording medium using same, and magnetic recording medium
US6328927B1 (en) * 1998-12-24 2001-12-11 Praxair Technology, Inc. Method of making high-density, high-purity tungsten sputter targets
US6406600B1 (en) * 1999-03-29 2002-06-18 Hitachi Metals, Ltd. CoPt-base sputtering target, method of making same, magnetic recording film and Co-Pt-base magnetic recording medium
US6417105B1 (en) * 1997-07-11 2002-07-09 Honeywell International Inc. Sputtering targets comprising aluminides or silicides
US20020102849A1 (en) * 1997-07-11 2002-08-01 Wuwen Yi Physical vapor deposition targets
US20020170821A1 (en) * 2001-04-11 2002-11-21 Michael Sandlin Mechanically alloyed precious metal magnetic sputtering targets fabricated using rapidly solidified alloy powders and elemental Pt metal
US6589311B1 (en) * 1999-07-07 2003-07-08 Hitachi Metals Ltd. Sputtering target, method of making same, and high-melting metal powder material
US6669830B1 (en) * 1999-11-25 2003-12-30 Idemitsu Kosan Co., Ltd. Sputtering target, transparent conductive oxide, and process for producing the sputtering target
US20040018110A1 (en) * 2002-07-23 2004-01-29 Wenjun Zhang Fabrication of b/c/n/o/si doped sputtering targets
US20040062675A1 (en) * 2002-06-07 2004-04-01 Wenjun Zhang Fabrication of ductile intermetallic sputtering targets
US20060233658A1 (en) * 2005-04-18 2006-10-19 Heraeus, Inc., A Corporation Of The State Of Arizona Enhanced formulation of cobalt alloy matrix compositions

Patent Citations (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4820A (en) * 1846-10-21 Improvement in steam-engines
US589553A (en) * 1897-09-07 Half to francis j
US4612165B1 (en) * 1983-12-21 1991-07-23 Us Energy
US4612165A (en) * 1983-12-21 1986-09-16 The United States Of America As Represented By The United States Department Of Energy Ductile aluminide alloys for high temperature applications
US4613368A (en) * 1985-10-03 1986-09-23 General Electric Company Tri-nickel aluminide compositions alloyed to overcome hot-short phenomena
US4609528A (en) * 1985-10-03 1986-09-02 General Electric Company Tri-nickel aluminide compositions ductile at hot-short temperatures
US4731116A (en) * 1985-12-23 1988-03-15 Schwarzkopf Development Corporation Sputter target and process for producing sputter target
US4675091A (en) * 1986-04-16 1987-06-23 United States Of America As Represented By The Secretary Of The Navy Co-sputtered thermionic cathodes and fabrication thereof
US4917722A (en) * 1988-05-18 1990-04-17 Tosoh Corporation Single crystals of chromium and method for producing the same
US5530467A (en) * 1990-02-01 1996-06-25 Kabushiki Kaisha Toshiba Sputtering target, film resistor and thermal printer head
US5652877A (en) * 1991-01-18 1997-07-29 Centre National De La Recherche Aluminum alloys, substrates coated with these alloys and their applications
US5320729A (en) * 1991-07-19 1994-06-14 Hitachi, Ltd. Sputtering target
US5470527A (en) * 1992-04-21 1995-11-28 Kabushiki Kaisha Toshiba Ti-W sputtering target and method for manufacturing same
US5415829A (en) * 1992-12-28 1995-05-16 Nikko Kyodo Co., Ltd. Sputtering target
US5561833A (en) * 1993-03-11 1996-10-01 Japan Metals & Chemicals Co., Ltd. Method of making high oxygen chromium target
US5618397A (en) * 1993-05-07 1997-04-08 Japan Energy Corporation Silicide targets for sputtering
US6309593B1 (en) * 1993-07-27 2001-10-30 Kabushiki Kaisha Toshiba Refractory metal silicide target, method of manufacturing the target, refractory metal silicide thin film, and semiconductor device
US5976326A (en) * 1994-04-06 1999-11-02 Komag, Incorporated Method of sputtering selected oxides and nitrides for forming magnetic media
US5778302A (en) * 1995-09-14 1998-07-07 Tosoh Smd, Inc. Methods of making Cr-Me sputter targets and targets produced thereby
US6174597B1 (en) * 1996-07-26 2001-01-16 Kabushiki Kaisha Toshiba Magnetic recording apparatus
US5863398A (en) * 1996-10-11 1999-01-26 Johnson Matthey Electonics, Inc. Hot pressed and sintered sputtering target assemblies and method for making same
US6264813B1 (en) * 1996-12-04 2001-07-24 Aluminum Pechiney Cathodic sputtering targets made of aluminum alloy
US5989673A (en) * 1997-06-30 1999-11-23 Sony Corporation Caromium-tantalum oxides (Cr-TaOx), sputtering targets and thin film seedlayer/sublayers for thin film magnetic recording media
US6417105B1 (en) * 1997-07-11 2002-07-09 Honeywell International Inc. Sputtering targets comprising aluminides or silicides
US20020102849A1 (en) * 1997-07-11 2002-08-01 Wuwen Yi Physical vapor deposition targets
US6261984B1 (en) * 1998-10-08 2001-07-17 Tosoh Corporation Sputtering target and process for the preparation thereof
US6328927B1 (en) * 1998-12-24 2001-12-11 Praxair Technology, Inc. Method of making high-density, high-purity tungsten sputter targets
US6406600B1 (en) * 1999-03-29 2002-06-18 Hitachi Metals, Ltd. CoPt-base sputtering target, method of making same, magnetic recording film and Co-Pt-base magnetic recording medium
US6676728B2 (en) * 1999-07-07 2004-01-13 Hitachi Metals, Ltd. Sputtering target, method of making same, and high-melting metal powder material
US6589311B1 (en) * 1999-07-07 2003-07-08 Hitachi Metals Ltd. Sputtering target, method of making same, and high-melting metal powder material
US20010008157A1 (en) * 1999-10-25 2001-07-19 Bishop David John Article comprising improved noble metal-based alloys and method for making the same
US6669830B1 (en) * 1999-11-25 2003-12-30 Idemitsu Kosan Co., Ltd. Sputtering target, transparent conductive oxide, and process for producing the sputtering target
US20010044018A1 (en) * 2000-02-23 2001-11-22 Hiroyuki Uwazumi Sputtering target for production of magnetic recording medium, method for producing magnetic recording medium using same, and magnetic recording medium
US20020170821A1 (en) * 2001-04-11 2002-11-21 Michael Sandlin Mechanically alloyed precious metal magnetic sputtering targets fabricated using rapidly solidified alloy powders and elemental Pt metal
US6797137B2 (en) * 2001-04-11 2004-09-28 Heraeus, Inc. Mechanically alloyed precious metal magnetic sputtering targets fabricated using rapidly solidfied alloy powders and elemental Pt metal
US20040062675A1 (en) * 2002-06-07 2004-04-01 Wenjun Zhang Fabrication of ductile intermetallic sputtering targets
US20040018110A1 (en) * 2002-07-23 2004-01-29 Wenjun Zhang Fabrication of b/c/n/o/si doped sputtering targets
US20040208774A1 (en) * 2002-07-23 2004-10-21 Wenjun Zhang Fabrication of B/C/N/O/Si doped sputtering targets
US20060233658A1 (en) * 2005-04-18 2006-10-19 Heraeus, Inc., A Corporation Of The State Of Arizona Enhanced formulation of cobalt alloy matrix compositions

Cited By (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060274236A1 (en) * 2005-06-03 2006-12-07 Samsung Electronics Co., Ltd. Display device, method of manufacturing the same and mask for manufacturing the same
US20080105542A1 (en) * 2006-11-08 2008-05-08 Purdy Clifford C System and method of manufacturing sputtering targets
WO2009012278A1 (en) * 2007-07-17 2009-01-22 Williams Advanced Materials, Inc. Process for the refurbishing of a sputtering target
US20090022616A1 (en) * 2007-07-17 2009-01-22 Robert Acker Process for the refurbishing of a sputtering target
US7871563B2 (en) 2007-07-17 2011-01-18 Williams Advanced Materials, Inc. Process for the refurbishing of a sputtering target
US20100320084A1 (en) * 2008-03-28 2010-12-23 Nippon Mining And Metals Co., Ltd. Sputtering Target of Nonmagnetic-Particle-Dispersed Ferromagnetic Material
US8936707B2 (en) 2008-03-28 2015-01-20 Jx Nippon Mining & Metals Corporation Sputtering target of nonmagnetic-particle-dispersed ferromagnetic material
US8932444B2 (en) 2008-03-28 2015-01-13 Jx Nippon Mining & Metals Corporation Sputtering target of nonmagnetic-particle-dispersed ferromagnetic material
US8568576B2 (en) 2008-03-28 2013-10-29 Jx Nippon Mining & Metals Corporation Sputtering target of nonmagnetic-particle-dispersed ferromagnetic material
US8394243B1 (en) 2008-07-24 2013-03-12 Wd Media, Inc. Sputtered cobalt oxide for perpendicular magnetic recording medium with low media noise
US8488276B1 (en) 2008-09-30 2013-07-16 WD Media, LLC Perpendicular magnetic recording medium with grain isolation magnetic anistropy layer
US20110247930A1 (en) * 2009-03-27 2011-10-13 Jx Nippon Mining & Metals Corporation Nonmagnetic Material Particle-Dispersed Ferromagnetic Material Sputtering Target
US9103023B2 (en) * 2009-03-27 2015-08-11 Jx Nippon Mining & Metals Corporation Nonmagnetic material particle-dispersed ferromagnetic material sputtering target
US20110003177A1 (en) * 2009-07-06 2011-01-06 Solar Applied Materials Technology Corp. Method for producing sputtering target containing boron, thin film and magnetic recording media
US9034155B2 (en) 2009-08-06 2015-05-19 Jx Nippon Mining & Metals Corporation Inorganic-particle-dispersed sputtering target
US9228251B2 (en) 2010-01-21 2016-01-05 Jx Nippon Mining & Metals Corporation Ferromagnetic material sputtering target
US20110241253A1 (en) * 2010-03-30 2011-10-06 China Steel Corporation Method for manufacturing cobalt alloy-based ceramic composite sputtering target
US8366994B2 (en) * 2010-03-30 2013-02-05 China Steel Corporation Method for manufacturing cobalt alloy-based ceramic composite sputtering target
US9181617B2 (en) 2010-07-20 2015-11-10 Jx Nippon Mining & Metals Corporation Sputtering target of ferromagnetic material with low generation of particles
US9567665B2 (en) 2010-07-29 2017-02-14 Jx Nippon Mining & Metals Corporation Sputtering target for magnetic recording film, and process for producing same
US9928996B2 (en) * 2010-08-06 2018-03-27 Tanaka Kikinzoku Kogyo K.K. Magnetron sputtering target and process for producing the same
US20140306144A1 (en) * 2010-08-06 2014-10-16 Tanaka Kikinzoku Kogyo K.K. Magnetron sputtering target and process for producing the same
US9328412B2 (en) 2010-08-31 2016-05-03 Jx Nippon Mining & Metals Corporation Fe—Pt-based ferromagnetic material sputtering target
US9011653B2 (en) 2010-11-29 2015-04-21 Mitsui Mining & Smelting Co., Ltd. Sputtering target
US20130206591A1 (en) * 2010-12-17 2013-08-15 Jx Nippon Mining & Metals Corporation Sputtering Target for Magnetic Recording Film and Method for Producing Same
CN103168328A (en) * 2010-12-17 2013-06-19 吉坤日矿日石金属株式会社 Sputtering target for magnetic recording film and method for producing same
CN103261469A (en) * 2010-12-17 2013-08-21 吉坤日矿日石金属株式会社 Ferromagnetic material sputtering target
US9945026B2 (en) 2010-12-20 2018-04-17 Jx Nippon Mining & Metals Corporation Fe-Pt-based sputtering target with dispersed C grains
US8993133B1 (en) 2010-12-23 2015-03-31 WD Media, LLC Intermediate layer for perpendicular magnetic recording medium with high permeability grain boundaries
US8858674B2 (en) 2011-03-30 2014-10-14 Tanaka Kikinzoku Kogyo K.K. FePt—C-based sputtering target and process for producing the same
US9228255B2 (en) 2011-03-30 2016-01-05 Tanaka Kikinzoku Kogyo K.K. FePt-C-based sputtering target and process for producing the same
TWI454588B (en) * 2011-03-30 2014-10-01 Tanaka Precious Metal Ind FePt-C sputtering target and its manufacturing method
CN103459656A (en) * 2011-03-30 2013-12-18 吉坤日矿日石金属株式会社 Sputtering target for magnetic recording film
US9683284B2 (en) 2011-03-30 2017-06-20 Jx Nippon Mining & Metals Corporation Sputtering target for magnetic recording film
US9502224B2 (en) * 2011-11-17 2016-11-22 Tanaka Kikinzoku Kogyo K.K. Magnetron sputtering target and method for manufacturing the same
US20140311901A1 (en) * 2011-11-17 2014-10-23 Tanaka Kikinzoku Kogyo K.K Magnetron sputtering target and method for manufacturing the same
US9314845B2 (en) 2012-01-13 2016-04-19 Tanaka Kikinzoku Kogyo K.K. Process for producing FePt-based sputtering target
US9358612B2 (en) 2012-01-13 2016-06-07 Tanaka Kikinzoku Kogyo K.K. FePt-based sputtering target
US9314846B2 (en) 2012-01-13 2016-04-19 Tanaka Kikinzoku Kogyo K.K. Process for producing FePt-based sputtering target
US9761422B2 (en) 2012-02-22 2017-09-12 Jx Nippon Mining & Metals Corporation Magnetic material sputtering target and manufacturing method for same
US9793099B2 (en) 2012-03-15 2017-10-17 Jx Nippon Mining & Metals Corporation Magnetic material sputtering target and manufacturing method thereof
US10325761B2 (en) 2012-03-15 2019-06-18 Jx Nippon Mining & Metals Corporation Magnetic material sputtering target and manufacturing method thereof
US9540724B2 (en) 2012-06-18 2017-01-10 Jx Nippon Mining & Metals Corporation Sputtering target for magnetic recording film
US10325762B2 (en) 2012-07-20 2019-06-18 Jx Nippon Mining & Metals Corporation Sputtering target for forming magnetic recording film and process for producing same
US10755737B2 (en) * 2012-09-21 2020-08-25 Jx Nippon Mining & Metals Corporation Fe-Pt based magnetic material sintered compact
US10937455B2 (en) * 2012-09-21 2021-03-02 Jx Nippon Mining & Metals Corporation Fe—Pt based magnetic material sintered compact
US20160053364A1 (en) * 2013-04-18 2016-02-25 Oerlikon Surface Solutions Ag, Trubbach ARC VAPORIZATION OF METALLIC, INTERMETALLIC, AND CERAMIC TARGET MATERIALS IN ORDER TO PRODUCE Al-Cr-N COATINGS
US9416439B2 (en) 2013-07-29 2016-08-16 Samsung Display Co., Ltd. Sputtering target, method of fabricating the same, and method of fabricating an organic light emitting display apparatus
US9685184B1 (en) 2014-09-25 2017-06-20 WD Media, LLC NiFeX-based seed layer for magnetic recording media
US20190010080A1 (en) * 2016-01-08 2019-01-10 Yej Glass Co., Ltd. Fluorinated Tin-Based Glass Frit And Method For Manufacturing Same
US10647608B2 (en) * 2016-01-08 2020-05-12 Yej Glass Co., Ltd. Fluorinated tin-based glass frit and method for manufacturing same
EP3587605A1 (en) * 2018-06-21 2020-01-01 INTEL Corporation Cobalt and nickel alloys for interconnects
US11769729B2 (en) 2018-06-21 2023-09-26 Intel Corporation Metal structures, devices, and methods
CN109112326A (en) * 2018-10-15 2019-01-01 河北四通新型金属材料股份有限公司 A kind of nickel carbon intermediate alloy and preparation method thereof

Also Published As

Publication number Publication date
TW200829709A (en) 2008-07-16
SG178742A1 (en) 2012-03-29
EP1942205A3 (en) 2009-09-09
KR20080065211A (en) 2008-07-11
SG144792A1 (en) 2008-08-28
JP2008169464A (en) 2008-07-24
SG178737A1 (en) 2012-03-29
CN101220457A (en) 2008-07-16
EP1942205A2 (en) 2008-07-09

Similar Documents

Publication Publication Date Title
US20070189916A1 (en) Sputtering targets and methods for fabricating sputtering targets having multiple materials
US7311874B2 (en) Sputter target and method for fabricating sputter target including a plurality of materials
US7229588B2 (en) Mechanically alloyed precious metal magnetic sputtering targets fabricated using rapidly solidified alloy powders and elemental Pt metal
US6042777A (en) Manufacturing of high density intermetallic sputter targets
US20080014109A1 (en) Enhanced sputter target manufacturing method
EP3124647B1 (en) Sputtering target comprising al-te-cu-zr alloy, and method for producing same
EP1511879A1 (en) Fabrication of ductile intermetallic sputtering targets
TWI675116B (en) Ti-Al alloy sputtering target
EP3170916B1 (en) Sputterring target comprising al-te-cu-zr-based alloy and method of manufacturing the same
EP1923481A2 (en) Enhanced sputter target manufacturing method

Legal Events

Date Code Title Description
AS Assignment

Owner name: HERAEUS INCORPORATED, ARIZONA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ZHANG, WENJUN;REEL/FRAME:019164/0030

Effective date: 20070328

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION