EP1552032A1 - Kupfer-sputtertargets und verfahren zur herstellung von kupfer-sputtertargets - Google Patents

Kupfer-sputtertargets und verfahren zur herstellung von kupfer-sputtertargets

Info

Publication number
EP1552032A1
EP1552032A1 EP03771624A EP03771624A EP1552032A1 EP 1552032 A1 EP1552032 A1 EP 1552032A1 EP 03771624 A EP03771624 A EP 03771624A EP 03771624 A EP03771624 A EP 03771624A EP 1552032 A1 EP1552032 A1 EP 1552032A1
Authority
EP
European Patent Office
Prior art keywords
target
less
copper
grain size
microns
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.)
Withdrawn
Application number
EP03771624A
Other languages
English (en)
French (fr)
Other versions
EP1552032A4 (de
Inventor
Vladimir Segal
Yi Wuwen
Stephane Ferrasse
Chi Tse Wu
Susan D. Strothers
Frank A. Alford
William B. Willett
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.)
Honeywell International Inc
Original Assignee
Honeywell International 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
Application filed by Honeywell International Inc filed Critical Honeywell International Inc
Publication of EP1552032A1 publication Critical patent/EP1552032A1/de
Publication of EP1552032A4 publication Critical patent/EP1552032A4/de
Withdrawn legal-status Critical Current

Links

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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21CMANUFACTURE OF METAL SHEETS, WIRE, RODS, TUBES OR PROFILES, OTHERWISE THAN BY ROLLING; AUXILIARY OPERATIONS USED IN CONNECTION WITH METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL
    • B21C23/00Extruding metal; Impact extrusion
    • B21C23/001Extruding metal; Impact extrusion to improve the material properties, e.g. lateral extrusion
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21CMANUFACTURE OF METAL SHEETS, WIRE, RODS, TUBES OR PROFILES, OTHERWISE THAN BY ROLLING; AUXILIARY OPERATIONS USED IN CONNECTION WITH METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL
    • B21C23/00Extruding metal; Impact extrusion
    • B21C23/01Extruding metal; Impact extrusion starting from material of particular form or shape, e.g. mechanically pre-treated
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/08Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/14Metallic material, boron or silicon
    • 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
    • C23C14/54Controlling or regulating the coating process
    • C23C14/548Controlling the composition
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12028Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
    • Y10T428/12063Nonparticulate metal component
    • Y10T428/12104Particles discontinuous
    • Y10T428/12111Separated by nonmetal matrix or binder [e.g., welding electrode, etc.]
    • Y10T428/12118Nonparticulate component has Ni-, Cu-, or Zn-base

Definitions

  • the invention pertains to copper-comprising monolithic sputtering targets and copper-comprising bonded sputtering targets.
  • the invention additionally pertains to methods of forming copper-comprising monolithic and bonded sputtering targets.
  • High-purity copper sputtering targets and copper alloy sputtering targets are currently used in a variety of applications including, for example, fabrication of integrated circuits.
  • the quality of copper-comprising structures such as interconnects and thin films can depend upon sputtering performance of the target.
  • Various factors of a sputtering target can influence the target's sputtering performance including: average grain size and grain size uniformity of the target material; crystallographic orientation/texture of the target material; structural and compositional homogeneity within the target; and the strength of the target material.
  • a smaller average grain size is associated with an increased strength of material.
  • the amount of alloying can affect strength and hardness of target materials, with increased alloying typically resulting in increased target strength.
  • a bonded copper sputtering target can have a high-purity copper target bonded to a backing plate comprising a relatively high strength material such as, for example, aluminum.
  • a relatively high strength material such as, for example, aluminum.
  • Conventional high-purity copper targets typically have an average grain size greater than 50 microns which can result in relatively low yield strength. The resulting grain size and structural non-uniformity of conventionally formed high-purity copper sputtering targets can detrimentally affect the quality of sputter-deposited high-purity copper films and interconnects.
  • One approach to increasing grain size uniformity and enhancing strength of copper materials for sputtering target purposes is to alloy the copper with one or more "alloying" elements.
  • alloying elements affects the resistivity of copper, it can be desirable to limit the total amount of alloying elements within a target material to no greater than 10 percent by weight.
  • the amount of alloying should be limited to less than or equal to 3% by weight.
  • Another draw back to alloying can be potential defects such as formation of second phase precipitates or segregation.
  • the invention encompasses a copper-comprising sputtering target.
  • the target contains at least 99.99% copper by weight and has an average grain size of from 1 micron to 50 microns.
  • the copper-comprising target has a yield strength of greater than or equal to about 15 ksi and a Brinell hardness (HB) of greater than about 40.
  • the invention encompasses a copper alloy sputtering target consisting essentially of less than or equal to about 99.99% copper by weight and at least one alloying element selected from the group consisting of Cd, Ca, Au, Ag, Be, Li, Mg, Al, Pd, Hg, Ni, In, Zn, B, Ga, Mn, Sn, Ge, W, Cr, O, Sb, Ir, P, As, Co, Te, Fe, S, Ti, Zr, Sc, Si, Mo, Pt, Nb, Re and Hf.
  • the target has a total amount of alloying elements of at least 100 ppm and less than 10% by weight.
  • the target also has an average grain size of from 1. micron to 50 microns and a grain size uniformity having a standard deviation throughout the target of less than about 15% of 1-sigma.
  • the invention encompasses a method of forming a monolithic sputtering target.
  • a copper billet consisting essentially of copper and less than or equal to 10% by weight of a total amount of one or more alloying elements is heated to a temperature of at least about 900° F and maintained at that temperature for at least about 45 minutes.
  • the billet is hot forged with a reduction in height of at least about 50% to form a forged block and the block is cold rolled to a reduction of at least about 60% to form a blank.
  • the blank is heated to induce recrystallization and to form a fine grain distribution having an average grain size less than about 100 microns.
  • the blank is subsequently formed into a monolithic target shape.
  • the invention encompasses a method of forming a copper- comprising sputtering target from a copper-billet having a purity of at least 99.99% copper.
  • the billet is hot forged at a temperature of greater than 300°C with a reduction in height of at least 40% to form a forged block.
  • the forged block is water quenched and subjected to an extrusion process comprising at least 4 passes of the forged block through equal channel angular extrusion (ECAE).
  • An optional solutionizing process can be conducted after the forging, followed by water quenching and the ECAE.
  • FIG. 1 is a flowchart diagram depicting a general overview of processing methods according to one aspect of the present invention.
  • Fig. 2 illustrates a square billet at an initial processing step according to the invention.
  • FIG. 3 is a diagrammatic cross-sectional view of a material being treated with an equal channel angular extrusion apparatus.
  • Fig. 4 shows a comparison of yield strength and ultimate tensile strength of various copper and copper alloys processed utilizing equal channel angular extrusion relative to standard 6N copper having a grain size of 40 microns and relative to various backing plates.
  • Fig. 5 is an image EBSD/SEM map of grain size distribution and texture for a 99.9999%) copper material (6N) after equal channel angular extrusion and subsequent annealing at 250°C for 5 hours according to one aspect of the invention.
  • Fig. 6 shows the grain area distribution for the material imaged in Fig. 5.
  • the average grain size of the material is about 6 microns.
  • Fig. 7 shows the resulting average grain size as a function of annealing treatment as measured by EBSD and optical microscopy.
  • the annealing treatments were performed on a copper material containing copper alloyed with 0.53 weight % Mg which had been subjected to 6 passes of equal channel angular extrusion through route D.
  • Fig. 8 shows the EBSD/SEM map of the Cu 0.53 wt% Mg ECAE material of Fig. 7 after annealing at 300°C for 2 hours.
  • Fig. 9 is an EBSD/SEM map of the grain structure of the Cu 0.53 wt% Mg material of Fig. 7 after annealing at 450°C for 1.5 hours.
  • Fig. 10 shows an image of the Fig. 9 material obtained utilizing optical microscopy.
  • Fig. 11 is a diagram depicting sampling of a target for grain size and texture measurement according to one aspect of the invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • the invention encompasses monolithic high-purity copper sputtering targets, bonded high-purity copper sputtering targets, monolithic copper alloy sputtering targets, bonded copper alloy sputtering targets, and methods of producing such targets.
  • high-purity copper can refer to copper or a copper material having at least 99.99% copper by weight.
  • the invention encompasses high-purity targets having from at least 99.99% to 99.99995% copper by weight.
  • the use of the term "monolithic" refers to a target that is utilized for sputtering without being bonded to a backing plate.
  • Bonded or monolithic high-purity targets according to the invention can have an average grain sizes of from less than 1 micron to less than or equal to about 100 microns, preferably less than 50 microns. In some instances, methods of the invention can be utilized to produce monolithic or bonded targets having an average grain size of from 1 to about 30 microns. Monolithic and bonded targets of high-purity copper according to the invention can, in particular instances, preferably have an average grain size of from 1 micron to about 20 microns, such as for example, from about 5 microns to about 10 microns.
  • High-purity targets of the invention can have a grain size uniformity across a sputtering surface of the target and/or throughout the entire target, the uniformity of grain size being such that a standard deviation (1-sigma) less than or equal to about 15% (also referred to as less than 15% non-uniformity). In particular instances the uniformity can reflect a standard deviation of less than or equal to 10% (1-sigma).
  • High-purity copper sputtering targets of the invention can have a yield strength that is at least about 10% greater than a target having a substantially identical elemental composition with an average grain size of 50 microns, and in some instances at least 10% greater than a target having a substantially identical elemental composition with an average grain size of 30 microns.
  • substantially identical elemental composition can refer to a material having no detectable composition differences.
  • the yield strength imparted to targets by the methods described below can typically be greater than or equal to about 15 ksi.
  • the high-purity copper targets of the invention can have an ultimate tensile strength of at least 15% greater than a target having a substantially identical elemental composition with an average grain size of 50 microns, and in some instances the ultimate tensile strength can be at least 15% greater than a target having a substantially identical elemental composition with an average grain size of 30 microns. Additionally, the hardness of the high-purity copper targets can be at least 15% greater than a target having a substantially identical elemental composition with an average grain size of 30 microns. In particular instances, high-purity targets of the invention can have a Brinell hardness of greater than about 40 HB, and in particular instances greater than about 60 HB.
  • the high-purity copper sputtering targets of the invention can have a purity of 99.99% (4N) or greater.
  • 4N purity of 99.99%
  • all percentages and included amounts are by weight unless • specifically indicated otherwise.
  • the high-purity target can preferably comprise 99.999% (5N) copper, can preferably comprise 99.9999% (6N) copper, or can preferably comprise 99.99995% (6N5) copper.
  • Bonded high-purity copper targets of the present invention can comprise the high-purity copper target diffusion bonded to a backing plate.
  • the bonded target can have a diffusion bond yield strength of greater than 10 ksi, preferably greater than or equal to about 15 ksi, and in particular instances can have a bond yield strength greater than or equal to about 30 ksi.
  • the target can be bonded to a backing plate utilizing an alternative bonding method comprising, for example, one or more of hipping, roll cladding, soldering, explosive bonding, and frictionless forging.
  • the alternative bonding method can preferably bond the high-purity copper target to the backing plate to produce a bond having a yield strength of greater than or equal to about 10 ksi.
  • a backing plate for utilization in bonded targets of the present invention can preferably be an aluminum or CuCr backing plate. As will be understood by those skilled in the art, alternative backing plate materials may also be utilized as appropriate.
  • the invention encompasses copper alloy sputtering targets that comprise less than or equal to about 99.99% copper by weight.
  • the copper alloy sputtering targets of the invention can consist essentially of less than or equal to about 99.99% copper by weight and at least one alloying element selected from the group consisting of Cd, Ca, Au, Ag, Be, Li, Mg, Al, Pd, Hg, Ni, In, Zn, B, Ga, Mn, Sn, Ge, W, Cr, O, Sb, Ir, P, As, Co, Te, Fe, S, Ti, Zr, Sc, Si, Pt, Nb, Re, Mo, and Hf.
  • the at least one alloying element can preferably be selected from Ag, Al, In, Zn, B, Ga, Mg, Sn, Ge, Ti and Zr.
  • a total amount of the at least one alloying element present in the target can preferably be from at least about 100 ppm by weight to less than about 10% by weight. In , some instances, the at least one alloying element can preferably be present at from at least 1000 ppm to less than about 3%, more less than about 2%, by weight.
  • Copper alloy sputtering targets according to the invention can, in particular aspects, have an average grain size of less than 1 micron.
  • the copper alloy sputtering target can comprise an average grain size of from 1 micron to about 100 microns, preferably less than 50 microns.
  • the copper alloy target can preferably have a grain size of from 1 to 30 microns.
  • Applications of the methods of the invention can, in some instances produce the target to have an average grain size of less than or equal to 20 microns, and in particular aspects from about 5 microns to about 10 microns.
  • copper alloy targets of the invention can have a grain size uniformity throughout the target and or across the sputtering surface of the target.
  • the average grain size throughout the target can have a grain size non-uniformity of less than 15% (referring to a standard deviation (1- sigma) in grain size of less than or equal to about 15%, and in particular instances can have a standard deviation (1-sigma) of less than or equal to about 10% (non-uniformity of less than or equal to 10%).
  • Copper alloy sputtering targets according to the invention can have a
  • targets of the invention can have a hardness of greater than or equal to about 60 HB.
  • the copper alloy targets can have a hardness uniformity across a sputtering surface and/or throughout the target.
  • the hardness throughout a copper alloy target can have a standard deviation (1-sigma) of less than about 5% (in other words, the target can have a non-uniformity of less than 5%).
  • the hardness uniformity can have a standard deviation of less than about 3.5% (1-sigma).
  • Copper alloy targets of the invention can be monolithic or in alternative embodiments can be bonded. Bonded copper alloy targets of the invention can be bonded to a backing plate by diffusion bonding or alternatively by a method utilizing one or more of hipping, roll cladding, soldering, explosive bonding, frictionless forging and other appropriate bonding techniques. Where the copper alloy target is bonded, the bond can have a bond yield strength of greater than about 10 ksi and preferably greater than about 15 ksi. [0036] Processing of copper materials in accordance with methods of the invention can produce copper targets having a texture ranging from extremely weak (close to random) to extremely strong, depending upon the processing routes utilized (discussed below).
  • the term “copper” (as used in the terms “copper target”, “copper material”, “copper billet”, etc.), can generally refer to either a high-purity copper or a copper alloy.
  • An exemplary copper target having a weak texture in accordance with the invention can have a crystal grain orientation distribution function (ODF) of less than or equal to about fifteen times random.
  • ODF crystal grain orientation distribution function
  • the target can have an extremely weak texture, characterized by an ODF less than about five times random.
  • the copper target can comprise a primary grain orientation wherein the term "primary” refers to a grain orientation that is present in the target in greater abundance than any single alternative grain orientation. It is noted that the term “primary” does not necessarily mean that a majority of the grains are present in this orientation. Rather, the term “primary” means that there is no single alternative orientation present in greater abundance within the target. In particular aspects, the methodology of the invention can be utilized to produce targets having a primary grain orientation other than (220).
  • Alternative processing in accordance with the invention can produce copper targets having a less random texture.
  • the invention encompasses processing which can induce strong textures in the copper articles produced, where the term "strong texture" can refer to a material having an ODF above about 15 times random.
  • Targets of the invention can additionally be produced to have an extremely strong texture characterized by an ODF above 20 times random.
  • the targets of the invention can preferably have a predominant grain orientation other than (220).
  • the size of copper targets produced utilizing methods in accordance with the invention is not limited to particular values. Additionally, the targets can be produced in a variety of shapes such as for example, circular or rectangular. Due to the increased strength of the materials produced by the methods described relative to conventional methods, larger copper target sizes can be produced relative to those produced by conventional methodologies. As discussed above, conventional copper targets are bonded to a backing plate to provide sufficient strength. The high strength of the materials of the invention can be especially advantageous since the increased strength can reduce or prevent warping of the target during fabrication and or sputtering processes. The methodology allows monolithic (non-bonded) copper targets to be utilized and allows larger target sizes for both bonded and monolithic targets. Bonded or monolithic targets of the invention can be produced for a variety of sputtering applications, including but not limited to 200 mm wafer processing and 300 mm wafer processing.
  • the targets and methods of the invention are described with specific reference to copper and copper alloys, it is to be understood that the invention encompasses alternative materials, including high-purity metals and alloy materials.
  • Exemplary alternative materials to which application of the described methodology can be particularly advantageous include aluminum, aluminum alloys, titanium, titanium alloys, tantalum, tantalum alloys, nickel, nickel alloys, molybdenum, molybdenum alloys, gold, gold alloys, silver, silver alloys, platinum and platinum alloys.
  • the listed alloys can preferably comprise less than or equal to 10% alloying element(s), by weight.
  • the temperatures and other values indicated for methodology described below with respect to copper materials can be adjusted based upon particular composition to which the methodology will be applied.
  • a material to be processed to form a sputtering target is provided in an initial processing step 100.
  • the initial material can be provided in the form of a billet such as the exemplary billet 12 depicted in Fig. 2.
  • billet 12 can comprise a lower face 14, an upper face 16 and can comprise a thickness of material between lower face 14 and upper face 16 indicated as T ⁇
  • Billet 12 can be a square or rectangular shape as indicated in Fig. 2 or alternatively can comprise a cylindrical or other shape (not shown).
  • Billet 12 can preferably comprise a cast material, although alternative billet materials are contemplated.
  • billet 12 be a cast material since cast materials can be provided in very pure form.
  • the targets produced by methodology of the invention typically have a composition that is substantially identical to the composition of the billet; where substantially identical refer to materials having no detectable composition differences.
  • the texture of the material of billet 12 can influence the texture and/or the difficulty in achieving a desired final texture of the article produced in accordance with the invention. Accordingly, billet 12 can be provided to have an initial texture that can favor production of the texture desired in the copper target. It can be advantageous to provide billet 12 having a strong texture where a strong texture is desired in the final article. It is to be noted however, that alternative methodology of the invention can be utilized to produce a weak or extremely weak texture from a billet having a strong texture. Additionally, a billet having a weak texture can be processed in accordance with methodology of the invention to produce a target having a strong or extremely strong texture. A billet having a particular primary or predominant grain orientation can be processed to produce a target having the same or a differing primary of predominant grain orientation, or to having no single predominant grain orientation.
  • billet 12 can comprise a high-purity copper material having at least 99.99% copper by weight.
  • billet 12 can consist essentially of copper having a 99.99% purity (4N), having a 99.999% purity (5N), having a 99.9999% purity (6N), or having a purity which exceeds 6N, for example 99.99995% copper by weight.
  • the invention also encompasses processes where billet 12 comprises an alternative high-purity metal such as aluminum, gold, silver, titanium tantalum, nickel, platinum or molybdenum.
  • Billet 12 can alternatively comprise less than 99.99% copper or less than
  • billet 12 will henceforth be referred to as a copper billet although it is to be understood that the invention encompasses alternative metals and their alloys.
  • copper billet 12 can preferably consist essentially of less than 99.99% copper and at least one alloying element selected from the group consisting of Cd, Ca, Au, Ag, Be, Li, Mg, Al, Pd, Hg, Ni, In, Zn, B, Ga, Mn, Sn, Ge, W, Cr, O, Sb, Ir, P, As, Co, Te, Fe, S, Ti, Zr, Sc, Si, Pt, Nb, Re, Mo, and Hf.
  • alloying element selected from the group consisting of Cd, Ca, Au, Ag, Be, Li, Mg, Al, Pd, Hg, Ni, In, Zn, B, Ga, Mn, Sn, Ge, W, Cr, O, Sb, Ir, P, As, Co, Te, Fe, S, Ti, Zr, Sc, Si, Pt, Nb, Re, Mo
  • a total amount of alloying element(s) in the copper billet can preferably be from at least 100 ppm by weight to less than or equal to about 10% by weight.
  • the copper billet can preferably comprise from at least 1000 ppm to less than or equal to about 3% alloying element(s), or more preferably less than or equal to about 2% total alloying element(s), by weight.
  • the alloying elements can preferably comprise one or more of Ag, Al, In, Zn, B, Ga, Mg, Sn, Ge, Ti and Zr.
  • the copper billet provided in step 100 can be subjected to a preliminary treatment 200.
  • Preliminary treatment 200 can comprise at least one of homogenizing, solutionizing and hot forging.
  • appropriate temperatures for conducting solutionizing, homogenizing or hot forging can depend upon the specific composition of billet 12.
  • the invention preferably comprises hot forging during preliminary treatment 200 to form a forged block.
  • Hot forging of copper billet 12 can be conducted a temperature of at least about 300°C, and can preferably be conducted at a temperature of at least about 500°C.
  • the hot forging can preferably reduce the initial thickness of billet 12 (Ti of Fig. 2) at least about 40% and in particular instances preferably at least about 50%.
  • hot forging can optionally be preceded by or followed by additional heat treatment which can comprise solutionizing and/or homogenizing of the copper material.
  • Heat treatment can be conducted at a temperature sufficient to induce solutionization and/or homogenization to occur in the particular composition being treated. This solutionizing/homogenizing temperature can preferably be maintained for a time sufficient to maximize the solutionization and/or homogenization of the composition. It is to be noted that temperatures sufficient for solutionizing or homogenizing can result in grain growth producing a grain size above the desired range of less than about 100 microns. Accordingly, conventional methods which attempt to achieve smaller grain sizes tend to minimize solutionizing or homogenizing treatments.
  • methodology according to the present invention allows post homogenizing/solutionizing reduction in grain size thereby achieving the benefits of both the solutionizing/homogenizing treatment and small grain size. It can be advantageous to solutionize and or homogenize during preliminary treatment step 200 to dissolve any precipitates and/or particles present in the copper billet. Homogenizing can additionally decrease or eliminate chemical segregation within billet 12.
  • Preliminary treatment processes of the present invention are not limited to particular ordering of homogenizing, solutionizing and/or hot forging treatments.
  • preliminary treatment 200 can comprise homogenizing of the copper billet followed by hot forging and subsequent solutionizing.
  • solutionizing is conducted followed by hot forging.
  • Exemplary preferred preliminary treatments are set forth below in descriptions of exemplary preferred embodiments of the invention.
  • the preliminary treatment can additionally include quenching following, and preferably immediately following hot forging.
  • quenching techniques can be utilized it can be preferable to utilize water quenching.
  • hot forging can comprise an initial heating and one or more subsequent re-heating events may be conducted.
  • the height reduction produced during each forging event between the initial heating and each subsequent reheating can vary depending on factors such as the particular composition and forging temperature utilized. Any quenching that is conducted can preferably occur only after the final reheating.
  • Exemplary reheating can comprise one or more reheating of the forged block to a temperature of 1400°F for at least about ten minutes subsequent to the initial hot forging.
  • preliminary treatment 200 can optionally comprise aging treatment.
  • the preliminary treatment comprises aging
  • billet 12 is preferably processed into a forged block prior to aging.
  • aging can be conducted as the final processing in the pretreatment stage.
  • aging can be utilized to induce formation of fine precipitates within the copper material.
  • Such induced precipitates can have an average diameter of less than about 0.5 microns.
  • it can be advantageous to induce precipitates by aging since such precipitates can promote development of fine and uniform grains during subsequent processing and can stabilize the grain structures so produced.
  • the hot forged and/or solutionized block formed during preliminary treatment 200 can subsequently undergo alternative processing as shown in Fig. 1.
  • the processed block can be subjected to equal channel angular extrusion (ECAE) processing 310 to form a target blank.
  • ECAE equal channel angular extrusion
  • FIG. 3 such illustrates an exemplary ECAE device 20.
  • Device 20 comprises a mold assembly 22 that defines a pair of intersecting channels 24 and 26. Intersecting channels 24 and 26 are identical or at least substantially identical in cross section, with the term "substantially identical" indicating that the channels are identical within acceptable tolerances of an ECAE apparatus.
  • a billet 28 (which can be the forged block described above) is extruded through channels 24 and 26.
  • Such extrusion results in plastic deformation of the billet by simple shear, layer after layer, in a thin zone located at the crossing plane of the channels.
  • channels 24 and 26 intersect at an angle of about 90°, it is to be understood that an alternative tool angle can be utilized (not shown).
  • a tool angle (channel intersect angle) of about 90° can be preferable since an optimal deformation (true shear strain) can be attained.
  • ECAE can introduce severe plastic deformation in the forged block material while leaving the dimension of the block unchanged.
  • ECAE can be a preferred method for inducing severe strain in a metallic material in that ECAE can be utilized at low loads and pressures to induce strictly uniform and homogenous straining.
  • ECAE is conducted at a strain rate and processing temperature sufficient to obtain desired microstructures (for example a weak texture and small grain size) within a copper billet or forged block, and to generate a uniform stress-strain state throughout the billet.
  • the copper material can be passed through an ECAE apparatus several times, and with numerous routes and at a temperature which can correspond to cold or hot processing of the material.
  • a preferred route to utilize with multiple passes through ECAE apparatus 20 can be the "route D", which corresponds to a constant 90° billet rotation before each successive pass. Since the ECAE route can affect structural orientation produced during dynamic recrystallization, one or more particular routes can be chosen for deformation passes to induce a desired orientation in the processed material.
  • the forged block processed in step 200 is subjected to at least four ECAE passes in process 310.
  • ECAE processing 310 comprises from four to eight passes, and can preferably comprise from four to six passes.
  • Such exemplary number is generally found sufficient to promote grain refinement to sub-micron size by mechanically induced dynamic recrystallization (where sub-micron refers to an average grain size of less than 1 micron).
  • ECAE passes one through three each successively creates defects (micro-bands; shear bands, arrays of dislocations, etc.). During these initial passes, thermodynamic rearrangement can occur creating cells and sub-grains and initiating mis-orientation of grain boundaries.
  • the texture strength of the material prior to ECAE can affect the strength that is produced during the initial three passes, with strong initial textures typically becoming randomized after a greater number of passes relative to materials having a weak initial texture.
  • Subsequent passes i.e. the fourth pass and any additional passes); create a dynamically recrystallized sub-micron grain size by inducing an increase in the number of high angle boundaries. During the dynamic recrystallization, the newly created grains gradually acquire a weaker texture and become increasingly equiaxed.
  • heating of ECAE apparatus die can be utilized to heat billet 28 during the ECAE passes.
  • the die can preferably be heated to less than the lowest temperature which can produce static recrystallization of the copper material being processed (alternatively referred to as the minimum recrystallization temperature), and can more preferably be heated to a temperature of from about 125°C to about 350°C.
  • intermediate annealing can optionally be performed between some or all of the ECAE passes. Intermediate annealing can be performed below the beginning temperature of static recrystallization, at or near the beginning temperature of static recrystallization (defined as the lowest temperature which begins to induce recrystallization of the material being processed) or within the range of temperature for full static recrystallization of the composition.
  • the temperature at which the intermediate anneal is conducted can influence the size and orientation of crystal grains and can therefore be utilized to promote a desired texture in a given instance.
  • any intermediate annealing at a temperature and for a time less than those which can result in static recrystallization of the material being processed. It can be advantageous to conduct intermediate annealing at temperatures lower than those which can induce static recrystallization to minimize surface cracking and enhanced microstructural uniformity.
  • intermediate annealing can preferably be conducted at temperatures of from about 125°C to about 225°C, and for a time of longer than about 1 hour. This can allow ECAE processing 310 to produce a high-purity copper material having extremely uniform and small grain sizes, for example, averaging from submicron grain sizes to about 20 microns.
  • sub-crystallization temperature intermediate annealing performed during ECAE processing 310 can preferably comprise temperatures from about 150°C to about 325°C, such temperature preferably being maintained for at least 1 hour.
  • This sub- recrystallization temperature annealing treatment can produce copper alloy material having an average grain size of less than 1 micron.
  • the high-purity copper and copper alloy materials produced by the ECAE methods described above can have an improved hardness relative to materials produced by conventional processing techniques.
  • the resulting hardness for 6N copper and various copper alloys processed in accordance with the methodology of the invention relative to the corresponding materials prior to ECAE are indicated in Table 1.
  • Fig. 4 compares the yield strengths and ultimate tensile strengths for high-purity copper and various copper alloys processed in accordance with methodology of the invention, relative to 6N copper having a grain size of 40 microns and relative to various baking plate materials.
  • Rolling treatment 330 preferably comprises subjecting the forged block produced by preliminary treatment 220 to cold rolling with a total reduction of at least 60% and preferably from 60% to 85%.
  • the cold rolling can comprise greater than four passes, preferably greater than eight passes and more preferably from eight to sixteen passes.
  • each of an initial four passes is preferably conducted to reduce the thickness of the block by from about 5% to about 6% for each pass.
  • a final four of the rolling passes each produce reduction of thickness of from about 10% to about 20%.
  • the relatively small reductions during the initial four passes can alleviate or prevent cracking during the rolling process.
  • the rolling can produce a small grain size in the resulting cold rolled high-purity copper or copper alloy material.
  • processing route 320 can be conducted as shown in Fig. 1.
  • Route 320 utilizes a combination of cold rolling and equal channel angular extrusion techniques.
  • it can be preferable to subject the hot forged block produced by preliminary treatment 200 to ECAE and a subsequent cold rolling treatment. It is to be understood however, that the invention contemplates performing cold rolling prior to ECAE, or both prior to and subsequent to ECAE.
  • the ECAE portion of process 320 can comprise the ECAE processing methods described above.
  • the ECAE extruded material can subsequently be cold rolled to a reduction of less than about 90% to form a blank.
  • the cold rolling portion of route 320 can preferably produce a reduction of at least about 60%.
  • the cold rolling processing of ECAE extruded material can comprise the rolling process described above with respect to rolling processing 330.
  • route 320 can combine the rolling with forging to produce the total reduction of at least 60% and less than 90%. Alternatively, a forging process can be utilized in an absence of rolling to produce the desired reduction of from 60% to 90%.
  • the induced orientation can comprise a primary grain orientation or can comprise a predominant grain orientation.
  • Rolling and/or forging can be used to create strong or extremely strong textures within the copper articles of the invention.
  • the strong textures created by the post-ECAE rolling/forging will be other than (220) texture.
  • the resulting blank comprising copper or copper alloy material can undergo a final target formation processing 500 and can optionally undergo an additional heat treatment 400 prior to the final target formation 500 as shown in Fig. 1.
  • Optional heat treatment process 400 can comprise conducting an annealing treatment at a temperature and time less than those that can induce onset of static recrystallization.
  • the low temperature anneal also referred to as recovery anneal, is conducted below the minimum temperature of static recrystallization.
  • Recovery annealing or optional absence of anneal can be advantageous for maintaining extremely small grain size.
  • Such low temperature or absence of anneal can result in a blank having an average grain size of less than about 1 micron.
  • the blank can be subjected to a temperature equal to or exceeding the minimum temperature to induce recrystallization for a time sufficient to form a final grain distribution within the blank.
  • static recrystallization can increase the grain size, the increase can be minimized by conducting the anneal close to the minimum temperature for recrystallization for a minimum time to produce the desired amount of recrystallization (partial or full recrystallization).
  • the recrystallization annealing can preferably conducted at a temperature of from about 350°C to about 500°C for a time period of from about 1 hour to about 8 hours.
  • the recrystallization annealing is preferably conducted at a temperature of from about 225°C to about 300°C for a time period of from about 1 hour to about 4 hours.
  • Figs. 5 and 6 show the grain size and distribution for 6N copper having an average grain size of about 6 microns produced using ECAE and subsequent annealing at 250°C for 5 hours in accordance with methodology of the invention.
  • Fig. 7 shows the evolution of grain size as a function of anneal treatment for copper alloyed with 0.53% Mg which has been subjected to six passes of ECAE through route D prior to the anneal.
  • Fig. 8 shows the grain size and distribution for the copper/0.53% Mg alloy of Fig. 7 after annealing at 300°C for 2 hours.
  • Figs 9 and 10 show the grain size and distribution for the copper/0.53% Mg alloy of Fig. 7 after annealing at 450°C for 1.5 hours, analyzed using EBSD/SEM (Fig. 9) and by optical microscopy (Fig. 10).
  • 330 can be subjected to an aging treatment (not shown) either in an absence of heat treatment step 400, or after heat treatment 400. Where aging is utilized, the aging can preferably be performed at a temperature less than about 500°C. As indicated above it can be advantageous to perform an aging step to increase the strength of the copper or copper alloy blank by inducing fine precipitates having an average precipitate size of less than about 0.5 microns.
  • the high-purity copper or copper alloy blank produced by methods of the present invention can be subjected to final target formation 500 to produce a monolithic target or alternatively to produce a bonded target (where "bonded target” refers to a sputtering target bonded to a support such as a backing plate).
  • final target formation can comprise, for example, machining of the blank to produce the desired target shape.
  • final formation step 500 can comprise production of a target which has a size appropriate for processing of 200 mm wafers or for processing of 300 mm wafers.
  • An exemplary monolithic copper or copper or copper alloy target in accordance with the invention which can be utilized for example, for processing of a 200 mm semiconductive wafer can have a 13.7 inch sputtering surface diameter, a 16.6 inch opposing surface (backside) diameter, and a thickness of about 0.89 inches.
  • a corresponding target which can be utilized for processing of 300 mm wafers can have a 17.5 inch sputtering surface diameter, a 20.7 inch backside diameter, and a thickness of about 1.0 inch.
  • the monolithic targets formed by methodology of the present invention can preferably be planar targets although other target shapes are contemplated as well as alternative sizes.
  • Monolithic targets produce in accordance with methodology of the invention can preferably have grain sizes of less than or equal to about 50 microns in order to maximize target strength.
  • Monolithic targets of the invention having submicron grain size can have a yield strength, ultimate tensile strength (UTS) and hardness at least about 50% greater than targets having a substantially identical composition with an average grain size of 30 microns.
  • Monolithic copper targets produced according to the invention which have an average grain size of from 1 to less than about 20 microns can have a strength enhancement of at least 10% over conventional copper targets.
  • a monolithic target can preferably be produced in an absence of heat treatment step 400.
  • the resulting monolithic target can retain the small grain size produced in the preceding processing.
  • the submicron grain size can be maintained in the final monolithic target to maximize the target strength.
  • heat treatment step 400 can be utilized during processing to produce the monolithic target which can produce a final grain distribution resulting in an average grain size of from about 1 micron to about 20 microns in the resulting monolithic target.
  • the target formation can comprise a bonding step in addition to any machining that is performed to form the desired target shape.
  • the bonding process can involve bonding the blank formed by the previous processing methods to a support such as a backing plate.
  • Exemplary backing plates can comprise, for example, aluminum and/or copper.
  • Exemplary backing plate materials are CuCr, Al 2024 and Al 6061 T4.
  • the bonding process can comprise one or more of hipping, rolling, cladding, soldering, explosive bonding, frictionless forging, diffusion bonding, or alternative methods known to those skilled in the art.
  • the bonding can produce a bond having a yield strength of at least about 10 ksi. In particular instances, the bonding produces a bond strength greater than or equal to about 15 ksi and in specific applications, produces a bond strength equal to or exceeding 30 ksi.
  • the various processing methods described above can be utilized to produce copper articles having extremely uniform and small grain sizes. Often, the grain sizes produced can average from submicron grains to about. This small grain size allows very high bonding strength to be obtained since high temperature bonding methods can be utilized. Where a bonded target will be produced, heating (heat treatment 400) can be combined with the bonding in the target formation process.
  • Bonding of high-purity copper targets according to methods of the invention can preferably be conducted at a temperature of less than or equal to about 325° C for a time of less than or equal to about 4 hours to minimize grain growth in the target. Although some grain growth may occur during high temperature bonding processes, the initial extremely fine grain size allows some grain growth to occur without resulting in the larger grain sizes observed in targets formed utilizing conventional processing methods. A resulting grain size of from 1 to about 20 microns in the final bonded targets of the invention allow strength enhancement of at least 10% over conventional copper targets. [0076] Formation of bonded copper alloy targets can preferably be conducted at a temperature and time less than those that produce full static recrystallization. Such bonding can preferably comprise conducting bonding at temperature of less than about 400°C for 4 hours and more preferably less than 350°C for 1-4 hours. Utilizing these bonding conditions, the copper alloy target can be formed to have an average grain size of less than 1 micron.
  • bonding can comprise a temperature which can result in recrystallization of the copper alloy.
  • a temperature which can result in recrystallization of the copper alloy.
  • it can be desirable to minimize the temperature and time of bonding to thereby minimize grain growth.
  • Recrystallization that occurs during bonding can preferably be such that the resulting average grain size produced in the copper alloy is from 1 to about 20 microns.
  • Such heat treatment for full recrystallization can preferably be conducted at a temperature of from about 200°C for at least about 1 hour and preferably between 350°C and 500°C for a time of greater than 1 hour.
  • a heat treating can be conducted either prior to the bonding step (i.e. heat treatment 400) or subsequent to the bonding step. It can be advantageous to combine bonding and heat treatment to enhance bond strength and recrystallize the copper or copper alloy material.
  • the bonded copper and bonded copper alloy targets formed in accordance with the methodology of the invention can have increased bond strength relative to bonded targets formed utilizing conventional methods. Diffusion bonding can be preferred for bonding targets to backing plates in some aspects of the invention. Where the grain size of the target blank is submicron, a very high strength diffusion bond can be produced due to enhanced diffusivity of the ultrafine grains. The resulting diffusion bond can have a yield strength of 15 ksi or above, which in some instances can equal or exceed 30 ksi. Additional advantages of bonded copper and copper alloy targets of the invention relative to conventional targets include improved resistance to target warping, reduced arcing.
  • Utilization of the targets of the invention for sputtering applications can provide an improved quality of film having fewer particles incorporated therein and can provide better uniformity of film thickness and therefore an improved resistance uniformity. Additionally, utilization of targets formed in accordance with methodology of the invention for semiconductor processing provides improved wafer to wafer uniformity of film thickness and resistance.
  • Monolithic high-purity copper and copper alloy targets formed in accordance with methodology of the invention can have a lifetime which is at least 30% longer and typically 40% longer relative to conventional bonded copper and copper alloy targets formed utilizing alternative methodologies.
  • the ability to achieve monolithic copper targets allows avoidance of debonding (separation from the backing plate) that can occur with conventional bonded targets.
  • the monolithic targets according to the invention additionally have increased resistance to target warping, reduction of arcing, reduced particle generation in thin films sputtered from such targets, enhanced uniformity of film thickness and resistivity. Additionally, monolithic targets in accordance with the invention have improved wafer to wafer consistency of film thickness and uniformity of resistivity.
  • Example 1 Production of High-purity Copper Monolithic Sputtering Targets
  • the billet is then hot forged, utilizing silica or graphite foil during forging, to a final height reduction of from 55-75% and is immediately water quenched.
  • the forged block is then cold-rolled using 16 passes, quenching after an initial 8 passes, with a total reduction of from about 60% to about 80%. Cracking is prevented during the cold-rolling by conducting each of the initial four passes to produce a reduction of from about 5% to about 6% per pass. Passes 13-16 are conducted to produce from about 10% to about 11% reduction per pass to achieve a small grain size.
  • the blank After cold-rolling, the blank is recrystallized by heating to about 480°F for about 120 minutes. The blank is machined to produce the final target.
  • the resulting high-purity copper monolithic target has an average grain size of less than 50 microns with a uniform grain distribution throughout the target.
  • Fig. 11 illustrates sampling locations utilized for analysis of the resulting monolithic target.
  • the target has a thickness of 0.89 inches.
  • the grain size measured at each point indicated at the sputtering surface, and the average thereof is given in Table 2.
  • An additional example of a high-purity target is formed as indicated in the preceding example with the exception that ECAE is included in the processing.
  • the ECAE is performed prior to the cold-rolling to reduce the grain size from that present in the as-cast billet.
  • the resulting target is analyzed as indicated above for the previous example.
  • the target had an average grain size of less than 15 microns throughout the target.
  • Copper alloy billets having less than 10% of Ag, Sn, Al, or Ti are heated and maintained at a temperature of about 900°F to about 1500°F for about 45 minutes. The billets are then hot forged to produce a final reduction of at least about 50%. Some of forged billets (depending on the alloy) are reheated for at least 10 minutes during the forging. After the final forging, the forged billets are immediately water quenched. The forged blocks are cold-rolled to a reduction of at least about 60% to form a blank which is recrystallized by heating to a temperature of from about 750°F to about 1200°F for 120 minutes. The recrystallized blanks are machined to form monolithic targets. Each of the targets has an average grain size of from about 15 microns to about 50 microns.
  • a specific target having copper alloyed with 0.3 atomic % Al was formed from a billet having a six inch diameter and a length of 11 inches.
  • the billet was initially heated for 1 hour at 1400°F and was initially forged to a height of 6 inches. After the initial forging, the billet was reheated for 15 minutes at 1400°F and was subsequently forged to a height of 3 inches. After final forging, the forged block was immediately water quenched. Cold rolling consisting of 17 passes was then conducted according to the rolling plan shown in Table 5 to form a rolled blank.
  • Example 3 Production of Copper Alloy Diffusion Bonded Sputtering Targets [0088] Copper alloy billets are provided and processed as described in example
  • the cold-rolled blanks are bonded to CuCr backing plates at a bonding temperature of about 450°C for about 120 minutes. Recrystallization of the alloy occurs during the bonding.
  • the bonded targets have a grain size of less than about 30 microns and a bond strength of up to about 30 ksi.
  • Copper billets of cast copper having a purity of at least 99.9999% are provided.
  • the high-purity copper billets are hot-forged at a temperature of least about 500°C with a reduction in height of at least about 40% to form forged blocks.
  • the forged blocks are solutionized by heating the blocks to a temperature of at least about 500°C which is maintained for at least about 1 hour.
  • the solutionized blocks are water quenched immediately after the heat treatment and are extruded utilizing from four to six passes of equal channel angular extrusion (ECAE) in accordance with route D (90 degree rotation of the blocks between successive passes) to produce a sub-micron microstructure.
  • ECAE channel angular extrusion
  • the blanks for monolithic targets are machined to produce the final target. Direct machining of the blanks produces targets having submicron grain size. Recrystallization is performed to produce monolithic targets having an average grain size of from 1 micron to about 20 microns.
  • the blanks for bonded targets are diffusion bonded to a backing plate.
  • Diffusion bonding is conducted at a temperature below 350°C for less than 4 hours.
  • the bond yield strength is greater than about 15 ksi.
  • the bonded targets have grain sizes of from submicron to about 20 microns.
  • the submicron targets have a strength enhancement of about 50% relative to conventional targets.
  • the bonded targets having a grain size of from 1 to about 20 microns have a strength enhancement of at least 10% relative to conventional copper targets.
  • Table 7 gives the three-point hardness measurements obtained from the top surface and bottom surface of the target of Table 6.
  • the average hardness is 53.3 HB with a standard deviation of 2.18 % (1-sigma).
  • Example 5 Production of Copper Alloy Sputtering Targets Utilizing ECAE
  • Copper billets containing copper alloyed with from 1000 ppm to less than or equal to about 10% of Ag, Al, In, Zn, B, Ga, Mg, Sn, Ge, Ti or Zr are provided.
  • the billets are hot forged at a temperature of at least about 500°C with a reduction of height of at least about 40% to form a forged blocks.
  • the forged blocks are solutionized by heating the forged blocks to a temperature of at least about 500°C and maintaining the temperature for at least about 1 hour to form a solutionized block.
  • the solutionized blocks are water quenched immediately after solutionizing.
  • the solutionized blocks are extruded by performing from four to six passes of ECAE.
  • the solutionized blocks are rotated 90 degrees between each of the passes in accordance with route D.
  • Intermediate annealing is conducted for at least one hour at a temperature of from about 150°C to about 325°C between some passes through ECAE.
  • the ECAE extruded blocks are cold-rolled to a reduction of at least about 60% to form a copper alloy blank.
  • a first monolithic copper alloy target is produced by machining a copper alloy blank produced as described to form a monolithic target.
  • the first monolithic target has an average grain size of less than 1 micron. Additionally, the first monolithic copper alloy target has a yield strength, ultimate tensile strength (UTS) and hardness at least about 50% greater than a target having a substantially identical elemental composition with an average grain size of 30 micron.
  • UTS ultimate tensile strength
  • a second monolithic copper alloy target is produced by heat-treating a copper alloy blank produced as described above. The heat treatment is conducted at a temperature of 350°C for about 1 hour.
  • the second target has an average grain size of from 1 micron to about 20 microns, has a substantial absence of precipitates (where substantial absence of precipitates refers to an absence of detectible precipitates), and has an absence of detectable segregation and a maximum void size of less than 1 micron.
  • a first bonded copper alloy target is produced by diffusion bonding a copper alloy blank produced as described, to a backing plate. The diffusion bonding is conducted at a temperature of less than 350°C for from one to four hours.
  • the first bonded alloy target has an average grain size of less than 1 micron.
  • a second bonded copper alloy target is produced by diffusion bonding a copper alloy blank produced as described above to a backing plate at a bonding temperature of from about 350°C to about 500°C for at least one hour.
  • the second bonded copper alloy target is fully recrystallized and has an average grain size of from about 1 micron to about 20 microns.

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EP03771624A 2002-07-16 2003-07-14 Kupfer-sputtertargets und verfahren zur herstellung von kupfer-sputtertargets Withdrawn EP1552032A4 (de)

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US10/614,807 US20040072009A1 (en) 1999-12-16 2003-07-09 Copper sputtering targets and methods of forming copper sputtering targets
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Families Citing this family (90)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6659331B2 (en) * 2002-02-26 2003-12-09 Applied Materials, Inc Plasma-resistant, welded aluminum structures for use in semiconductor apparatus
US7740721B2 (en) * 2003-03-17 2010-06-22 Nippon Mining & Metals Co., Ltd Copper alloy sputtering target process for producing the same and semiconductor element wiring
EP1656467A2 (de) * 2003-08-21 2006-05-17 Honeywell International Inc. Kupferhaltige pvd-targets und herstellungsverfahren dafür
WO2005064037A2 (en) * 2003-12-22 2005-07-14 Cabot Corporation High integrity sputtering target material and method for producing bulk quantities of same
JP4829476B2 (ja) * 2004-03-09 2011-12-07 オンセミコンダクター・トレーディング・リミテッド ショットキーバリアダイオードおよびその製造方法
WO2005094280A2 (en) * 2004-03-31 2005-10-13 Honeywell International Inc. High-strength backing plates, target assemblies, and methods of forming high-strength backing plates and target assemblies
JP4330517B2 (ja) * 2004-11-02 2009-09-16 株式会社神戸製鋼所 Cu合金薄膜およびCu合金スパッタリングターゲット並びにフラットパネルディスプレイ
EP2123791B1 (de) * 2005-03-28 2014-08-13 JX Nippon Mining & Metals Corporation Topfgeformtes Kupfersputtertarget
JP4756458B2 (ja) * 2005-08-19 2011-08-24 三菱マテリアル株式会社 パーティクル発生の少ないMn含有銅合金スパッタリングターゲット
CN100398682C (zh) * 2005-12-22 2008-07-02 上海交通大学 微米晶锰青铜合金的制备方法
KR100787883B1 (ko) * 2006-02-17 2007-12-27 데프트 가부시키가이샤 전자부품용 금속재료 및 금속재료의 가공방법
US8188599B2 (en) * 2006-02-28 2012-05-29 Advanced Interconnect Materials, Llc Semiconductor device, its manufacturing method, and sputtering target material for use in the method
CN101374611B (zh) * 2006-03-07 2015-04-08 卡伯特公司 制备变形金属制品的方法
US20070251819A1 (en) * 2006-05-01 2007-11-01 Kardokus Janine K Hollow cathode magnetron sputtering targets and methods of forming hollow cathode magnetron sputtering targets
US20070251818A1 (en) * 2006-05-01 2007-11-01 Wuwen Yi Copper physical vapor deposition targets and methods of making copper physical vapor deposition targets
KR20090051267A (ko) * 2006-09-08 2009-05-21 토소우 에스엠디, 인크 미세 그레인 사이즈 및 높은 전자 이동 저항성을 구비한 구리 스퍼터링 타겟 및 이를 제조하는 방법
JP5234306B2 (ja) * 2006-10-18 2013-07-10 三菱マテリアル株式会社 熱欠陥発生が少なくかつ表面状態の良好なtftトランジスターを用いたフラットパネルディスプレイ用配線および電極並びにそれらを形成するためのスパッタリングターゲット
JP4985083B2 (ja) * 2007-05-08 2012-07-25 三菱マテリアル株式会社 酸素含有銅ターゲットの製造方法
JP5263665B2 (ja) * 2007-09-25 2013-08-14 日立金属株式会社 配線膜用Cu合金膜および配線膜形成用スパッタリングターゲット材
JP4709238B2 (ja) * 2008-02-08 2011-06-22 株式会社日立製作所 Cu系配線用材料およびそれを用いた電子部品
JP4936560B2 (ja) * 2008-03-11 2012-05-23 三菱マテリアル株式会社 密着性に優れた銅合金複合膜の成膜方法およびこの成膜方法で使用するCa含有銅合金ターゲット
JP5233486B2 (ja) * 2008-08-01 2013-07-10 日立電線株式会社 無酸素銅スパッタリングターゲット材及び無酸素銅スパッタリングターゲット材の製造方法
TWI397597B (zh) * 2008-09-16 2013-06-01 Copper alloy target and its manufacturing method and application
EP2182083B1 (de) * 2008-11-04 2013-09-11 Solar Applied Materials Technology Corp. Sputter-Target aus Kupfer-Gallium-Legierung und Verfahren zu seiner Herstellung
CN101736289B (zh) * 2008-11-04 2012-06-27 光洋应用材料科技股份有限公司 铜合金靶材、其制造方法、及其制成的薄膜及太阳能电池
JP5192990B2 (ja) * 2008-11-11 2013-05-08 光洋應用材料科技股▲分▼有限公司 銅−ガリウム合金スパッタリングターゲット及びそのスパッタリングターゲットの製造方法並びに関連用途
CN101509125B (zh) * 2009-03-19 2011-01-05 金川集团有限公司 一种制备铜溅射靶材的方法
JP5622079B2 (ja) * 2009-03-27 2014-11-12 日立金属株式会社 スパッタリングターゲット
JP5643524B2 (ja) * 2009-04-14 2014-12-17 株式会社コベルコ科研 Cu−Ga合金スパッタリングターゲットおよびその製造方法
KR20120062802A (ko) * 2009-08-28 2012-06-14 후루카와 덴키 고교 가부시키가이샤 스퍼터링 타겟용 구리재료 및 그 제조방법
KR101515341B1 (ko) * 2009-09-18 2015-04-24 후루카와 덴키 고교 가부시키가이샤 스퍼터링 타겟에 사용되는 구리재료의 제조방법
CN101665909B (zh) * 2009-10-23 2012-08-22 宁波江丰电子材料有限公司 靶材的制备方法
JP5491845B2 (ja) * 2009-12-16 2014-05-14 株式会社Shカッパープロダクツ スパッタリングターゲット材
JP4869398B2 (ja) * 2009-12-22 2012-02-08 三菱伸銅株式会社 純銅板の製造方法及び純銅板
WO2011078188A1 (ja) * 2009-12-22 2011-06-30 三菱伸銅株式会社 純銅板の製造方法及び純銅板
JP4792115B2 (ja) * 2010-02-09 2011-10-12 三菱伸銅株式会社 純銅板の製造方法及び純銅板
JP4869415B2 (ja) * 2010-02-09 2012-02-08 三菱伸銅株式会社 純銅板の製造方法及び純銅板
JP4792116B2 (ja) * 2010-02-09 2011-10-12 三菱伸銅株式会社 純銅板の製造方法及び純銅板
JP5464352B2 (ja) * 2010-03-05 2014-04-09 三菱マテリアル株式会社 均一かつ微細結晶組織を有する高純度銅加工材の製造方法
JP5718896B2 (ja) 2010-03-11 2015-05-13 株式会社東芝 スパッタリングターゲットとその製造方法、および半導体素子の製造方法
JP5520746B2 (ja) * 2010-08-24 2014-06-11 古河電気工業株式会社 スパッタリングターゲット用銅材料及びその製造方法
KR20130122968A (ko) * 2011-03-01 2013-11-11 제이엑스 닛코 닛세키 킨조쿠 가부시키가이샤 구리 티탄 합금제 스퍼터링 타깃, 동 스퍼터링 타깃을 사용하여 형성한 반도체 배선 그리고 동 반도체 배선을 구비한 반도체 소자 및 디바이스
CN103620083A (zh) * 2011-06-30 2014-03-05 吉坤日矿日石金属株式会社 Co-Cr-Pt-B型合金溅射靶及其制造方法
JP6046422B2 (ja) 2011-09-07 2016-12-14 シア フォーム、インクShear Form, Inc. 剪断押出システム
JP5723247B2 (ja) * 2011-09-09 2015-05-27 株式会社Shカッパープロダクツ 円筒型スパッタリングターゲット材、それを用いた配線基板及び薄膜トランジスタの製造方法
KR20140091734A (ko) * 2011-09-14 2014-07-22 제이엑스 닛코 닛세키 킨조쿠 가부시키가이샤 고순도 구리망간 합금 스퍼터링 타깃
US9704695B2 (en) 2011-09-30 2017-07-11 Jx Nippon Mining & Metals Corporation Sputtering target and manufacturing method therefor
KR101645834B1 (ko) 2012-01-12 2016-08-04 제이엑스금속주식회사 고순도 구리 스퍼터링 타깃
JP5567042B2 (ja) * 2012-02-10 2014-08-06 株式会社Shカッパープロダクツ Tft用銅スパッタリングターゲット材
JP2014043643A (ja) * 2012-08-03 2014-03-13 Kobelco Kaken:Kk Cu合金薄膜形成用スパッタリングターゲットおよびその製造方法
JP6175248B2 (ja) * 2013-02-19 2017-08-02 株式会社フジクラ 導電材及びその製造方法
JP5594618B1 (ja) * 2013-02-25 2014-09-24 三菱マテリアル株式会社 スパッタリングターゲット及びその製造方法
WO2014136673A1 (ja) * 2013-03-07 2014-09-12 Jx日鉱日石金属株式会社 銅合金スパッタリングターゲット
CN103194722B (zh) * 2013-03-28 2016-04-27 深圳首创新能源股份有限公司 制造太阳能电池的方法
CN104128740A (zh) * 2013-05-02 2014-11-05 宁波江丰电子材料股份有限公司 一种铜靶材的制备方法
JP6274026B2 (ja) * 2013-07-31 2018-02-07 三菱マテリアル株式会社 銅合金スパッタリングターゲット及び銅合金スパッタリングターゲットの製造方法
TWI653349B (zh) * 2013-08-13 2019-03-11 日商大同特殊鋼股份有限公司 Cu合金靶用材料、Cu合金靶、Cu合金膜及觸控面板
CN103805927A (zh) * 2013-11-28 2014-05-21 青岛蓝图文化传播有限公司市南分公司 一种铜棒材的生产工艺方法
CN104694888B (zh) * 2013-12-09 2017-05-10 有研亿金新材料股份有限公司 一种高纯铜靶材的制备方法
US9761420B2 (en) * 2013-12-13 2017-09-12 Praxair S.T. Technology, Inc. Diffusion bonded high purity copper sputtering target assemblies
KR101645587B1 (ko) * 2014-04-18 2016-08-09 한국생산기술연구원 반도체 배선용 Cu-Mg 스퍼터링 타겟의 제조방법
JP6398594B2 (ja) * 2014-10-20 2018-10-03 三菱マテリアル株式会社 スパッタリングターゲット
JP6481473B2 (ja) * 2015-03-31 2019-03-13 三菱マテリアル株式会社 Ag合金スパッタリングターゲット
US10494712B2 (en) * 2015-05-21 2019-12-03 Jx Nippon Mining & Metals Corporation Copper alloy sputtering target and method for manufacturing same
CN106702120B (zh) * 2015-07-13 2018-08-28 宁波江丰电子材料股份有限公司 靶材热处理方法
WO2017014990A1 (en) * 2015-07-17 2017-01-26 Honeywell International Inc. Heat treatment methods for metal and metal alloy preparation
JP7021069B2 (ja) 2015-08-03 2022-02-16 ハネウェル・インターナショナル・インコーポレーテッド 向上した特性を有する無摩擦鍛造アルミニウム合金スパッタリングターゲット
WO2017033694A1 (ja) 2015-08-24 2017-03-02 三菱マテリアル株式会社 高純度銅スパッタリングターゲット材
TWI612025B (zh) * 2015-09-23 2018-01-21 住華科技股份有限公司 製作濺鍍靶材的銲料及其應用方法
CN105463246A (zh) * 2015-12-02 2016-04-06 苏州龙腾万里化工科技有限公司 一种磨削机仪器零件用耐用合金
CN105887028A (zh) * 2016-05-13 2016-08-24 洛阳高新四丰电子材料有限公司 一种大尺寸高纯铜平面靶材的制备方法
US10900102B2 (en) 2016-09-30 2021-01-26 Honeywell International Inc. High strength aluminum alloy backing plate and methods of making
JP6308278B2 (ja) * 2016-10-07 2018-04-11 三菱マテリアル株式会社 円筒型スパッタリングターゲット用熱間押出素材、及び、円筒型スパッタリングターゲットの製造方法
CN107012357B (zh) * 2017-03-22 2018-11-06 合肥达户电线电缆科技有限公司 一种铜合金线材及其制备方法
TWI663274B (zh) 2017-03-30 2019-06-21 日商Jx金屬股份有限公司 Sputtering target and manufacturing method thereof
JP7454329B2 (ja) * 2017-06-01 2024-03-22 三菱マテリアル株式会社 高純度電気銅板
WO2018221734A1 (ja) * 2017-06-01 2018-12-06 三菱マテリアル株式会社 高純度電気銅の製造方法
US11753733B2 (en) 2017-06-01 2023-09-12 Mitsubishi Materials Corporation Method for producing high-purity electrolytic copper
US10760156B2 (en) * 2017-10-13 2020-09-01 Honeywell International Inc. Copper manganese sputtering target
US11035036B2 (en) * 2018-02-01 2021-06-15 Honeywell International Inc. Method of forming copper alloy sputtering targets with refined shape and microstructure
BE1026683B1 (nl) * 2018-10-05 2020-05-07 Soleras Advanced Coatings Bvba Sputterdoel
US11450516B2 (en) * 2019-08-14 2022-09-20 Honeywell International Inc. Large-grain tin sputtering target
CN111876629B (zh) * 2020-08-04 2021-03-23 天水华洋电子科技股份有限公司 一种引线框架用高性能铜基合金材料及其制备方法
JP2022042859A (ja) * 2020-09-03 2022-03-15 オリエンタル コッパー シーオー.エルティーディー. 熱間押出プロセスからのスパッタリング法による薄膜コーティング技術のための銅ターゲットの製造
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JP7211558B2 (ja) * 2021-01-08 2023-01-24 国立大学法人九州大学 銅合金接合体及びその製造方法
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CN114196925A (zh) * 2021-12-13 2022-03-18 广东省科学院新材料研究所 一种含稀土金属的铜镍合金靶材、其制备方法及应用
CN114381631A (zh) * 2022-01-12 2022-04-22 深圳市众诚达应用材料科技有限公司 一种镀膜用靶材及其制备方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6113761A (en) * 1999-06-02 2000-09-05 Johnson Matthey Electronics, Inc. Copper sputtering target assembly and method of making same
EP1036859A1 (de) * 1999-03-18 2000-09-20 Applied Materials, Inc. Verbessertes Sputtertarget aus Kupfer zum Abscheiden
US20010023726A1 (en) * 1999-07-08 2001-09-27 Holger Koenigsmann Fabrication and bonding of copper sputter targets
US20010035238A1 (en) * 1999-11-24 2001-11-01 Shozo Nagano Physical vapor deposition target
WO2002036847A2 (en) * 2000-11-02 2002-05-10 Honeywell International Inc. Sputtering target

Family Cites Families (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3497402A (en) * 1966-02-03 1970-02-24 Nat Res Corp Stabilized grain-size tantalum alloy
US3653981A (en) * 1968-10-24 1972-04-04 Nippon Steel Corp Method for making ferritic stainless steel sheet having excellent workability
US3616282A (en) * 1968-11-14 1971-10-26 Hewlett Packard Co Method of producing thin-film circuit elements
US4000055A (en) * 1972-01-14 1976-12-28 Western Electric Company, Inc. Method of depositing nitrogen-doped beta tantalum
BE795763A (fr) * 1972-02-22 1973-08-22 Westinghouse Electric Corp Alliages ferreux et procedes pour fabriquer de tels alliages
DE2429434B2 (de) * 1974-06-19 1979-10-04 Siemens Ag, 1000 Berlin Und 8000 Muenchen Verfahren zur Herstellung von Widerständen und Kondensatoren in Dunnschichtschaltungen
DE3142541C2 (de) * 1981-10-27 1986-07-31 Demetron Gesellschaft für Elektronik-Werkstoffe mbH, 6540 Hanau Mehrstofflegierung für Targets von Katodenzerstäubungsanlagen
US4374717A (en) * 1981-11-05 1983-02-22 General Motors Corporation Plasma polymerized interfacial coatings for improved adhesion of sputtered bright metal on plastic
DE3246361A1 (de) * 1982-02-27 1983-09-08 Philips Patentverwaltung Gmbh, 2000 Hamburg Kohlenstoff enthaltende gleitschicht
JPS58157917A (ja) * 1982-03-15 1983-09-20 Kawasaki Steel Corp 磁気特性の優れた一方向性珪素鋼板の製造方法
JPS6066425A (ja) * 1983-09-22 1985-04-16 Nippon Telegr & Teleph Corp <Ntt> Lsi電極用の高純度モリブデンタ−ゲツトならびに高純度モリブデンシリサイドタ−ゲツトおよびその製造方法
US4663120A (en) * 1985-04-15 1987-05-05 Gte Products Corporation Refractory metal silicide sputtering target
US4889745A (en) * 1986-11-28 1989-12-26 Japan As Represented By Director General Of Agency Of Industrial Science And Technology Method for reactive preparation of a shaped body of inorganic compound of metal
JPS63216966A (ja) * 1987-03-06 1988-09-09 Toshiba Corp スパツタタ−ゲツト
DE3712281A1 (de) * 1987-04-10 1988-10-27 Heraeus Gmbh W C Verfahren zur herstellung von hochduktilem tantal-halbzeug
US4762558A (en) * 1987-05-15 1988-08-09 Rensselaer Polytechnic Institute Production of reactive sintered nickel aluminide material
US4883721A (en) * 1987-07-24 1989-11-28 Guardian Industries Corporation Multi-layer low emissivity thin film coating
US4960163A (en) * 1988-11-21 1990-10-02 Aluminum Company Of America Fine grain casting by mechanical stirring
US5468401A (en) * 1989-06-16 1995-11-21 Chem-Trend, Incorporated Carrier-free metalworking lubricant and method of making and using same
US5074907A (en) * 1989-08-16 1991-12-24 General Electric Company Method for developing enhanced texture in titanium alloys, and articles made thereby
US5194101A (en) * 1990-03-16 1993-03-16 Westinghouse Electric Corp. Zircaloy-4 processing for uniform and nodular corrosion resistance
US5409517A (en) * 1990-05-15 1995-04-25 Kabushiki Kaisha Toshiba Sputtering target and method of manufacturing the same
GB9016694D0 (en) * 1990-07-30 1990-09-12 Alcan Int Ltd Ductile ultra-high strength aluminium alloy extrusions
US5087297A (en) * 1991-01-17 1992-02-11 Johnson Matthey Inc. Aluminum target for magnetron sputtering and method of making same
US5171379A (en) * 1991-05-15 1992-12-15 Cabot Corporation Tantalum base alloys
EP0535314A1 (de) * 1991-08-30 1993-04-07 Mitsubishi Materials Corporation Zerstäubungstarget aus einer Platin-Kobalt-Legierung und Verfahren zu dessen Herstellung
US5231306A (en) * 1992-01-31 1993-07-27 Micron Technology, Inc. Titanium/aluminum/nitrogen material for semiconductor devices
JPH05214523A (ja) * 1992-02-05 1993-08-24 Toshiba Corp スパッタリングターゲットおよびその製造方法
US5330701A (en) * 1992-02-28 1994-07-19 Xform, Inc. Process for making finely divided intermetallic
US5693203A (en) * 1992-09-29 1997-12-02 Japan Energy Corporation Sputtering target assembly having solid-phase bonded interface
US5415829A (en) * 1992-12-28 1995-05-16 Nikko Kyodo Co., Ltd. Sputtering target
JP2857015B2 (ja) * 1993-04-08 1999-02-10 株式会社ジャパンエナジー 高純度アルミニウムまたはその合金からなるスパッタリングターゲット
US5400633A (en) * 1993-09-03 1995-03-28 The Texas A&M University System Apparatus and method for deformation processing of metals, ceramics, plastics and other materials
US5772860A (en) * 1993-09-27 1998-06-30 Japan Energy Corporation High purity titanium sputtering targets
US5677015A (en) * 1994-03-17 1997-10-14 Sony Corporation High dielectric constant material containing tantalum, process for forming high dielectric constant film containing tantalum, and semiconductor device using the same
US5513512A (en) * 1994-06-17 1996-05-07 Segal; Vladimir Plastic deformation of crystalline materials
FI100422B (fi) * 1994-07-11 1997-11-28 Metso Paper Inc Telan valmistus
US5590389A (en) * 1994-12-23 1996-12-31 Johnson Matthey Electronics, Inc. Sputtering target with ultra-fine, oriented grains and method of making same
US5850755A (en) * 1995-02-08 1998-12-22 Segal; Vladimir M. Method and apparatus for intensive plastic deformation of flat billets
JP3413782B2 (ja) * 1995-03-31 2003-06-09 日立金属株式会社 スパッタリング用チタンタ−ゲットおよびその製造方法
US5600989A (en) * 1995-06-14 1997-02-11 Segal; Vladimir Method of and apparatus for processing tungsten heavy alloys for kinetic energy penetrators
JP3654466B2 (ja) * 1995-09-14 2005-06-02 健司 東 アルミニウム合金の押出加工法及びそれにより得られる高強度、高靭性のアルミニウム合金材料
US5673581A (en) * 1995-10-03 1997-10-07 Segal; Vladimir Method and apparatus for forming thin parts of large length and width
JP3343774B2 (ja) * 1995-10-27 2002-11-11 トピー工業株式会社 鋳造アルミホイールの製造方法
JP3970323B2 (ja) * 1996-06-05 2007-09-05 デュラセル、インコーポレーテッド リチウム化リチウム酸化マンガンスピネルの改良された製造法
US5766380A (en) * 1996-11-05 1998-06-16 Sony Corporation Method for fabricating randomly oriented aluminum alloy sputtering targets with fine grains and fine precipitates
JPH10158829A (ja) * 1996-12-04 1998-06-16 Sony Corp スパッタリングターゲット組立体の製造方法
JP3867328B2 (ja) * 1996-12-04 2007-01-10 ソニー株式会社 スパッタリングターゲット及びその製造方法
US5994181A (en) * 1997-05-19 1999-11-30 United Microelectronics Corp. Method for forming a DRAM cell electrode
JP3403918B2 (ja) * 1997-06-02 2003-05-06 株式会社ジャパンエナジー 高純度銅スパッタリングタ−ゲットおよび薄膜
US6569270B2 (en) * 1997-07-11 2003-05-27 Honeywell International Inc. Process for producing a metal article
US5993621A (en) * 1997-07-11 1999-11-30 Johnson Matthey Electronics, Inc. Titanium sputtering target
TW580519B (en) * 1997-09-22 2004-03-21 Nat Res Inst Metals Super fine structure steel and manufacturing method thereof
US6348139B1 (en) * 1998-06-17 2002-02-19 Honeywell International Inc. Tantalum-comprising articles
US6193821B1 (en) * 1998-08-19 2001-02-27 Tosoh Smd, Inc. Fine grain tantalum sputtering target and fabrication process
US6351446B1 (en) * 1998-10-02 2002-02-26 Unaxis Balzers Aktiengesellschaft Optical data storage disk
US6348113B1 (en) * 1998-11-25 2002-02-19 Cabot Corporation High purity tantalum, products containing the same, and methods of making the same
US6123896A (en) * 1999-01-29 2000-09-26 Ceracon, Inc. Texture free ballistic grade tantalum product and production method
US6755796B2 (en) * 1999-02-07 2004-06-29 Medispec Ltd. Pressure-pulse therapy apparatus
US6192969B1 (en) * 1999-03-22 2001-02-27 Asarco Incorporated Casting of high purity oxygen free copper
JP2001049426A (ja) * 1999-07-08 2001-02-20 Praxair St Technol Inc 銅スパッタ・ターゲットの製造方法および銅スパッタ・ターゲットと裏当て板の組立体
US6521173B2 (en) * 1999-08-19 2003-02-18 H.C. Starck, Inc. Low oxygen refractory metal powder for powder metallurgy
US6391163B1 (en) * 1999-09-27 2002-05-21 Applied Materials, Inc. Method of enhancing hardness of sputter deposited copper films
US6454994B1 (en) * 2000-08-28 2002-09-24 Honeywell International Inc. Solids comprising tantalum, strontium and silicon
JP3971171B2 (ja) * 2000-12-05 2007-09-05 プラクスエアー エス ティー テクノロジー インコーポレーテッド 銅スパッターターゲットの加工方法
US6917999B2 (en) * 2001-06-29 2005-07-12 Intel Corporation Platform and method for initializing components within hot-plugged nodes
US6896748B2 (en) * 2002-07-18 2005-05-24 Praxair S.T. Technology, Inc. Ultrafine-grain-copper-base sputter targets
KR100583713B1 (ko) * 2003-01-22 2006-05-25 간사이 페인트 가부시키가이샤 광파이버용 피복조성물 및 피복 광파이버

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1036859A1 (de) * 1999-03-18 2000-09-20 Applied Materials, Inc. Verbessertes Sputtertarget aus Kupfer zum Abscheiden
US6113761A (en) * 1999-06-02 2000-09-05 Johnson Matthey Electronics, Inc. Copper sputtering target assembly and method of making same
US6331234B1 (en) * 1999-06-02 2001-12-18 Honeywell International Inc. Copper sputtering target assembly and method of making same
US20010023726A1 (en) * 1999-07-08 2001-09-27 Holger Koenigsmann Fabrication and bonding of copper sputter targets
US20010035238A1 (en) * 1999-11-24 2001-11-01 Shozo Nagano Physical vapor deposition target
WO2002036847A2 (en) * 2000-11-02 2002-05-10 Honeywell International Inc. Sputtering target

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2004011691A1 *

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