US20090008786A1 - Sputtering Target - Google Patents

Sputtering Target Download PDF

Info

Publication number
US20090008786A1
US20090008786A1 US12/223,499 US22349907A US2009008786A1 US 20090008786 A1 US20090008786 A1 US 20090008786A1 US 22349907 A US22349907 A US 22349907A US 2009008786 A1 US2009008786 A1 US 2009008786A1
Authority
US
United States
Prior art keywords
aluminum
ppm
alloy
purity
providing
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
US12/223,499
Inventor
Eugene Y. Ivanov
Yongwen Yuan
David B. Smathers
Ronald G. Jordan
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.)
Tosoh SMD Inc
Original Assignee
Tosoh SMD 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 Tosoh SMD Inc filed Critical Tosoh SMD Inc
Priority to US12/223,499 priority Critical patent/US20090008786A1/en
Assigned to TOSOH SMD, INC. reassignment TOSOH SMD, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: IVANOV, EUGENE Y., JORDAN, RONALD G., SMATHERS, DAVID B., YUAN, YONGWEN
Publication of US20090008786A1 publication Critical patent/US20090008786A1/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
    • 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
    • C23C14/0617AIII BV compounds, where A is Al, Ga, In or Tl and B is N, P, As, Sb or Bi
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/32Gas-filled discharge tubes
    • H01J37/32431Constructional details of the reactor
    • H01J37/32532Electrodes
    • H01J37/3255Material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/32Gas-filled discharge tubes
    • H01J37/34Gas-filled discharge tubes operating with cathodic sputtering
    • H01J37/3411Constructional aspects of the reactor
    • H01J37/3414Targets
    • H01J37/3426Material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001Technical content checked by a classifier
    • H01L2924/0002Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Definitions

  • the invention relates to a sputtering target suitable for forming wiring films of improved uniformity, thermal stability, and electromigration resistance for semiconductor integrated circuit devices and flat panel displays. It particularly relates to pure aluminum and aluminum alloy sputtering targets containing a small amount of alloying elements.
  • Aluminum wiring film formed by a sputtering method has been widely used in semiconductor integrated circuits and flat panel displays due to its low resistivity, good etchability, and low manufacturing cost.
  • Low resistivity and high thermal conductivity lead to low resistance-capacitance (R-C) delay associated with the interconnection network.
  • R-C delay is a critical factor in determining the signal propagation speed or the time constant in the devices and circuits. For example, it is necessary to maintain a low time constant and keep an electrical resistivity below 5 ⁇ cm and even below 3 ⁇ cm for the wiring films connecting the sources and drains of the amorphous thin film transistors (TFT) of liquid crystal displays (LCD) to sustain desirable display quality and power consumption when the size of the display panel becomes large.
  • TFT amorphous thin film transistors
  • LCD liquid crystal displays
  • the wiring film is of uniform thickness over the entire deposited substrate. This is especially true for large-scale integrated circuits consisting of multiple layers of multilevel structure having feature size of 1 micrometer or less.
  • the production of a single multilevel structure involves several sputtering and patterning process including depositing and patterning dielectric material, depositing a diffusion barrier layer, and depositing and patterning a conductive wiring film.
  • the variation in wiring film thickness not only causes inconsistent signal propagation speed and power consumption due to the varied film sheet resistance (Rs), which is inversely proportional to the film thickness, but also adversely affects the performance of the layers built on the wiring film or even causes short circuits between the conductive wire films as a result of the formation of large film bumps-hillocks.
  • the thickness uniformity of wiring films is believed to be directly influenced by the structural characteristics of the sputtering target including grain size, orientation, and the uniformity of their distribution.
  • the target grain structure is typically controlled through controlling its fabrication process consisting of mechanical deformation and thermal anneals.
  • a key step to form desirable target grain structure is to accumulate sufficient and uniformly distributed internal energy in the deformation process (roll, press, forge, extrusion or their combination).
  • the internal energy is the driving force for the grain refinement in the recrystallization anneal process.
  • high purity aluminum (5N or higher purity) can undergo a dynamic recrystallization during a hot deformation.
  • One of the consequences of the dynamic recrystallization is that the internal energy is partially lost.
  • the grain refinement process in the subsequent static recrystallization process can be incomplete or never happen due to insufficient internal energy.
  • the other consequence of the dynamic recrystallization is the formation of non strain-free recrystallization grains dispersed in the deformed matrix of high dislocation density.
  • This kind of nonuniform partial recrystallization structure results in considerable variations in the thickness or flatness characteristics of the deposited films because the recrystallization grains and deformed matrix have different sputtering behaviors.
  • An issue associated with the applications of pure aluminum film is its low electromigration resistance and thermal stability. Many aluminum wiring film failures are caused by the electromigration which occurs and leads to a directional mass transport associated with atomic flux divergence when the wiring film is subjected to high current densities. Voids or hillocks form in the films of low thermal stability subjected to a thermal treatment or a joule heat generated by a high current density. In general, the electromigration resistance increases with increasing thermal stability.
  • a common solution to enhance the thermal stability and electromigration is to alloy the aluminum. Adding up to 0.1 wt % Cu, Fe, Ti, and B alloying elements to the pure aluminum target has been reported to improve the thermal stability of the deposited films.
  • alloying aluminum with impurity elements can increase the electrical resistivity of aluminum.
  • adding alloying impurities to aluminum degrades the etchability of aluminum.
  • the commonly used Al alloying element Cu can deteriorate the patternability of Al because the Cu and Al can form very stable intermetallic precipitates which are difficult to be removed by Al etching reactant, and the etching reactant suitable for Al will react with Cu to form compounds that are insoluble in the commonly used cleaning solvents.
  • the present inventors have discovered an aluminum or aluminum alloy sputtering target containing 0.01 to 100 ppm one or more of other elements or secondary alloying elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM), and provided a manufacturing method for such a sputtering target.
  • elements or secondary alloying elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM)
  • the present invention provides a method to improve the performance of the films formed from the aluminum and aluminum alloy sputtering targets.
  • alloying elements including but not limited to Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM), to aluminum or aluminum alloy target improves the uniformity of the deposited films.
  • Adding alloying elements particularly Ni and Nd raises the recrystallization temperature of pure aluminum or aluminum alloys, effectively suppresses the dynamic recrystallization in hot deformed aluminum or aluminum alloys, and accumulates the internal energy driving the nucleation of new grains in the static recrystallization for cold worked aluminum or aluminum alloys.
  • FIG. 1 plots the film nonuniformity as a function of Ni content.
  • the dot-dashed line is an eye guideline.
  • FIG. 2 is the photographs of the sputtered surface of (a) an Al-30 ppm Si ConMag target and (b) an Al-30 ppm Si ConMag target with 4 ppm Ni addition.
  • the target without Ni addition consists of finer grains size compared to the target with Ni addition, which maintains coarse ingot grains containing deformed bands. The photos were taken after the targets had been sputtered for the first 50 wafers.
  • FIG. 3 is the metallographs of the targets (a) without Ni addition and (b) with 4 ppm Ni.
  • the target without Ni addition contains dynamic recrystallization (DRX) grains having serrated grain boundaries and subgrain boundaries.
  • DRX dynamic recrystallization
  • FIG. 4 is (a) SEM, (b) OIM inverse pole figure (IPF) map, and (c) OIM misorientation map of an Al-30 ppm Si ConMag target.
  • DRX dynamic recrystallization
  • FIG. 5 is (a) SEM, (b) OIM inverse pole figure (IPF) map, and (c) OIM misorientation map for a grain triple junction of a Ni alloyed Al-30 ppm Si ConMag target. These images show the Ni microalloyed target is free of dynamic recrystallization grains.
  • the IPF and OIM maps indicate that low angle subgrain boundaries consisting of dislocations exist within the deformed original grains consisting of large angle grain boundaries.
  • FIG. 6 plots the hardness as a function of anneal temperature for Al-30 ppm Si targets with and without Ni addition. Hardness is measured using 15 kg load and 1 ⁇ 8′′ ball. The Ni addition increases the hardness and recrystallization temperature of aluminum-30 ppm Si alloy.
  • FIG. 7 is resistivity of aluminum-30 ppm Si as a function of Ni content.
  • the aluminum and its alloy sputtering target encompassed by this invention can have any suitable geometry.
  • the present invention includes a method of manufacturing the aluminum and its alloy target containing one or more of alloying elements Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM).
  • the aluminum raw material will preferably have a purity of 99.999 wt %.
  • the Ni raw material will preferably have a purity of at least 99.95 wt %.
  • the Co raw material will preferably have a purity of 99.95 wt %.
  • the Ti raw material will preferably have a purity of 99.995 wt %.
  • the V raw material will preferably have a purity of 99.5 wt %.
  • the Cr will preferably have a purity of at least 99.9 wt %.
  • the Mn will preferably have a purity of at least 99.9 wt %.
  • the Mo will preferably have a purity of at least 99.95 wt %.
  • the Ta will preferably have a purity of at least 99.95 wt %.
  • the W will preferably have a purity of at least 99.95 wt %.
  • the aluminum, or aluminum and its primary alloying elements including Si and Cu, and one or more of other alloying elements Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM) are melted to form a molten alloy preferably through a vacuum induction melting or continuous casting process.
  • the molten alloy is subsequently cooled and cast to form ingot of aluminum or aluminum alloy containing one or more of alloying elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM).
  • alloying elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM).
  • REM rare earth metals
  • the secondary alloying elements in the aluminum or its alloy of the present invention can range from 0.01 to 100 ppm weight.
  • the resulting ingot can have any size and any suitable shapes including round, square, and rectangular.
  • the ingot of aluminum alloying with a small amount of one or more of alloying elements undergoes a thermomechanical process to form desirable grain structure.
  • the thermomechanical process includes but is not limited to hot or cold roll, hot or cold press, hot or cold forge, and anneals to form plate or blank.
  • the plate or blank of aluminum alloy is machined into a target with different geometry.
  • An exemplary aluminum-30 ppm Si ConMag target alloyed with less than 10 ppm Ni has been produced according to the process described above.
  • the Al of 99.999% purity is melted with a prescribed amount of Si of 99.999% or higher purity and Ni of 99.5% purity to produce an ingot with a preferable diameter from 75 mm to 200 mm by use of the vacuum induction melting method.
  • the composition of the resulting ingot measured by the GDMS method is listed in the Table 1. (The weight concentration unit is ppm for all elements).
  • the ingot is sawn into ingot slices of desirable heights.
  • the ingot slice is subjected to anneal in a temperature range of 250° C. to 600° C. for a time period up to 6 hours.
  • the ingot slice subsequently goes through a hot deformation of 40% ⁇ 80% reduction at a temperature range of 200° C. to 600° C. to make a blank.
  • the blank is machined to a ConMag target of conical shape with or without an anneal.
  • an aluminum-30 ppm Si ConMag target without Ni addition has been produced by the same fabrication process.
  • Table 1 compares the compositions of these two targets. The only difference between them is their Ni content, i.e., one is essentially a pure aluminum-30 ppm Si alloy. The other one is aluminum-30 ppm Si alloyed with ⁇ 4 ppm Ni.
  • the film nonuniformity is characterized using 9-point approach. The measurement indicates the nonuniformity is 14% for the films deposited from the target without Ni addition. The nonuniformity is 4% for the films deposited from the Ni alloyed target. It clearly shows a small amount of Ni addition significantly improves the film uniformity performance.
  • FIG. 1 plots the film nonuniformity as a function of Ni contents in aluminum-30 ppm Si alloy. It indicates the film nonuniformity decreases with increasing Ni contents. The film nonuniformity is dramatically improved with Ni addition as low as 0.2 ppm.
  • FIG. 2 exemplifies the macrostructure of the target with ⁇ 4 ppm Ni and the target without Ni addition.
  • the Ni alloyed target consists of well-defined non-recrystallization coarse grains containing deformation bands.
  • the target without Ni addition consists of fine and partial recrystallization grains.
  • the difference in structure for the targets with and without Ni additions is further confirmed by microstructure and texture examinations.
  • the target with Ni addition displays a highly deformed grain structure of high dislocation density and internal energy, a typical recovery structure of metallic materials after mechanical deformation while prior to the recrystallization stage.
  • grains with serrated grain boundaries and subgrains apparently reformed from the deformed grain matrix.
  • the formation of non-strain-free grains with subgrains is the characteristic microstructure feature of dynamic recrystallization.
  • the head to head metallograph comparison between pure aluminum-30 ppm Si and Ni microalloyed Al-30 ppm Si targets indicates that the Ni addition suppresses the dynamic recrystallization in the aluminum-30 ppm Si target ( FIG. 3 ).
  • the orientation imaging microscope (OIM) images further confirm there are numerous low angle subgrain boundaries existing within the deformed grains of Ni microalloyed target ( FIG. 4 ).
  • a low angle grain boundary usually consists of dislocations.
  • the presence of low angle subgrain boundaries of the grains in Ni microalloyed target suggests that the dislocations are piled up and pined at the subgrain boundaries during the hot deformation process.
  • the dynamic recrystallization is suppressed due to the immobile subgrain boundaries.
  • the internal energy stored in the subgrain boundaries of high density dislocation would drive the static recrystallization process to form uniform and fine grain structure.
  • new grains form to reduce the internal energy stored in the high dislocation density areas within the deformed grains.
  • the grain orientation and atom mobility should be different between the reformed dynamic recrystallization grains and the deformed matrix of high dislocation density and internal energy.
  • local sputtering rates are different between recrystallization grains and deformed matrix for a target subjected to a dynamic recrystallization process.
  • the films deposited from such a target will have considerable variations in film thickness or poor film uniformity.
  • the Ni microalloyed target is free of dynamic recrystallization structure. The whole target has consistent sputtering performance due to its uniform and consistent grain structure so the films deposited from the Ni microalloyed target have good film uniformity.
  • aluminum has face centered cubic (FCC) crystallographic structure and multiple ⁇ 111 ⁇ 110> dislocation slip systems.
  • FCC face centered cubic
  • a perfect dislocation moving along one slip system can glide to another equivalent slip system.
  • the consequence of the cross-slip of dislocation is that a perfect dislocation a/2 ⁇ 110> decomposes into two partial dislocations a/6 ⁇ 112>, where a is the lattice parameter of aluminum, and a region of stacking fault is created between the partial dislocations.
  • aluminum has much higher stacking fault energy (166 mJ/mm 2 ) than other FCC materials like copper (78 mJ/mm 2 ) and gold (45 mJ/mm 2 ).
  • the deformed aluminum or Al-30 ppm Si material will not be able to accumulate enough internal energy for the material as a whole to conduct the recrystallization after the deformation process because the dislocations are difficult to be pinned and piled up due to their cross-slip movement.
  • local grain nucleation can take place when a critical internal energy has been reached at high temperature (hot deformation).
  • the grain boundaries consisting of dislocations have high mobility. High grain boundary migration results in the growth of newly formed grains in local regions during hot deformation.
  • a process involving both grain nucleation and growth is the characteristic of the dynamic recrystallization.
  • the difference in microstructure nature between dynamically recrystallized grains and deformed matrix present in the target without Ni addition results in the high nonuniformity of thickness and electrical resistance for the deposited films.
  • This invention has discovered that adding secondary alloying elements including Ni to pure aluminum or its alloy effectively suppresses the dynamic recrystallization for hot worked aluminum or its alloy and enhances the static recrystallization for cold worked aluminum or its alloy.
  • FIG. 6 plots the hardness as a function of anneal temperature for aluminum-30 ppm Si targets with and without Ni addition. These targets were produced by the fabrication process described above. They were subjected to a hot deformation of 60% thickness reduction followed by a recrystallization anneal for 1 hour at a temperature ranging from 200° C. to 450° C.
  • FIG. 6 indicates the Ni addition increases the hardness of the aluminum-30 ppm Si material. Furthermore, the hardness decreases with increasing anneal temperature for the targets with or without Ni addition. The materials are softened and the hardness decreases when the work-hardening stress is released by forming new strain-free grains in the recrystallization process. With reference to FIG. 6 , the hardness declines suggest the recrystallization starting temperatures are about 260° C. and 200° C. for aluminum-30 ppm Si alloy with and without Ni addition, respectively. The recrystallization temperature of Ni microalloyed aluminum-30 ppm Si is 60° higher than that of non-Ni microalloyed aluminum-30 ppm Si.
  • Ni addition increases the recrystallization temperature and improves the thermal stability and electromigration resistance of aluminum and its alloys. Similar improvement in thermal stability and electromigration resistance can be attained in the aluminum by adding one or more of other elements including Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM). Alloying aluminum or its alloy targets with other secondary elements provides an approach to effectively enhance thermal stability and electromigration resistance. This enables the deposited films to have improved thermal stability, electromigration resistance, and hillock resistance.
  • other elements including Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM). Alloying aluminum or its alloy targets with other secondary elements provides an approach to effectively enhance thermal stability and electromigration resistance. This enables the deposited films to have improved thermal stability, electromigration resistance, and hillock resistance.
  • FIG. 7 plots the resistivity of aluminum-30 ppm Si as a function of the content of Ni addition. It shows the resistivity of Ni alloyed aluminum-30 ppm Si essentially does not change by adding a small amount of Ni.
  • the resistivity of aluminum-30 ppm Si with 4 ppm Ni is 2.71 micro-Ohm ⁇ cm, essentially the same as that of pure aluminum.
  • the Ni addition does not react with the Al etching reactant.
  • the films deposited from Ni microalloyed target sustain the etchability comparable to pure aluminum.

Abstract

The present invention provides a sputtering target comprising aluminum and one or more alloying elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM). The addition of very small amounts of alloying element to pure aluminum and aluminum alloy target improves the uniformity of the deposited wiring films through affecting the target's recrystallization process. The range of alloying element content is 0.01 to 100 ppm and preferably in the range of 0.1 to 50 ppm and more preferably from 0.1 to 10 ppm weight which is sufficient to prevent dynamic recrystallization of pure aluminum and aluminum alloys, such as 30 ppm Si alloy. The addition of small amount of alloying elements increases the thermal stability and electromigration resistance of pure aluminum and aluminum alloys thin films while sustaining their low electrical resistivity and good etchability. This invention also provides a method of manufacturing microalloyed aluminum and aluminum alloy sputtering target.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims the priority benefit of U.S. Provisional Patent Application Ser. No. 60/779,500 filed Mar. 6, 2006 and U.S. Provisional Patent Application Ser. No. 60/815,635 filed Jun. 22, 2006.
  • FIELD OF THE INVENTION
  • The invention relates to a sputtering target suitable for forming wiring films of improved uniformity, thermal stability, and electromigration resistance for semiconductor integrated circuit devices and flat panel displays. It particularly relates to pure aluminum and aluminum alloy sputtering targets containing a small amount of alloying elements.
  • BACKGROUND OF THE INVENTION
  • Aluminum wiring film formed by a sputtering method has been widely used in semiconductor integrated circuits and flat panel displays due to its low resistivity, good etchability, and low manufacturing cost. Low resistivity and high thermal conductivity lead to low resistance-capacitance (R-C) delay associated with the interconnection network. R-C delay is a critical factor in determining the signal propagation speed or the time constant in the devices and circuits. For example, it is necessary to maintain a low time constant and keep an electrical resistivity below 5 μΩ·cm and even below 3 μΩ·cm for the wiring films connecting the sources and drains of the amorphous thin film transistors (TFT) of liquid crystal displays (LCD) to sustain desirable display quality and power consumption when the size of the display panel becomes large.
  • For many applications it is critical that the wiring film is of uniform thickness over the entire deposited substrate. This is especially true for large-scale integrated circuits consisting of multiple layers of multilevel structure having feature size of 1 micrometer or less. The production of a single multilevel structure involves several sputtering and patterning process including depositing and patterning dielectric material, depositing a diffusion barrier layer, and depositing and patterning a conductive wiring film. The variation in wiring film thickness not only causes inconsistent signal propagation speed and power consumption due to the varied film sheet resistance (Rs), which is inversely proportional to the film thickness, but also adversely affects the performance of the layers built on the wiring film or even causes short circuits between the conductive wire films as a result of the formation of large film bumps-hillocks.
  • The thickness uniformity of wiring films is believed to be directly influenced by the structural characteristics of the sputtering target including grain size, orientation, and the uniformity of their distribution. The target grain structure is typically controlled through controlling its fabrication process consisting of mechanical deformation and thermal anneals. A key step to form desirable target grain structure is to accumulate sufficient and uniformly distributed internal energy in the deformation process (roll, press, forge, extrusion or their combination). The internal energy is the driving force for the grain refinement in the recrystallization anneal process. However, it has been observed that high purity aluminum (5N or higher purity) can undergo a dynamic recrystallization during a hot deformation. One of the consequences of the dynamic recrystallization is that the internal energy is partially lost. The grain refinement process in the subsequent static recrystallization process can be incomplete or never happen due to insufficient internal energy. The other consequence of the dynamic recrystallization is the formation of non strain-free recrystallization grains dispersed in the deformed matrix of high dislocation density. This kind of nonuniform partial recrystallization structure results in considerable variations in the thickness or flatness characteristics of the deposited films because the recrystallization grains and deformed matrix have different sputtering behaviors.
  • An issue associated with the applications of pure aluminum film is its low electromigration resistance and thermal stability. Many aluminum wiring film failures are caused by the electromigration which occurs and leads to a directional mass transport associated with atomic flux divergence when the wiring film is subjected to high current densities. Voids or hillocks form in the films of low thermal stability subjected to a thermal treatment or a joule heat generated by a high current density. In general, the electromigration resistance increases with increasing thermal stability. A common solution to enhance the thermal stability and electromigration is to alloy the aluminum. Adding up to 0.1 wt % Cu, Fe, Ti, and B alloying elements to the pure aluminum target has been reported to improve the thermal stability of the deposited films. However, alloying aluminum with impurity elements can increase the electrical resistivity of aluminum. On the other hand, adding alloying impurities to aluminum degrades the etchability of aluminum. The commonly used Al alloying element Cu can deteriorate the patternability of Al because the Cu and Al can form very stable intermetallic precipitates which are difficult to be removed by Al etching reactant, and the etching reactant suitable for Al will react with Cu to form compounds that are insoluble in the commonly used cleaning solvents.
  • Accordingly, there is an ever-increasing demand to develop an aluminum or aluminum alloy target resulting in wiring films with improved uniformity, electromigration resistance, and thermal stability while maintaining low resistivity and good etchability to meet the needs of current and future in semiconductor electronic devices and flat panel display applications.
  • SUMMARY OF THE INVENTION
  • The present inventors have discovered an aluminum or aluminum alloy sputtering target containing 0.01 to 100 ppm one or more of other elements or secondary alloying elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM), and provided a manufacturing method for such a sputtering target.
  • The present invention provides a method to improve the performance of the films formed from the aluminum and aluminum alloy sputtering targets. The addition of alloying elements including but not limited to Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM), to aluminum or aluminum alloy target improves the uniformity of the deposited films. Adding alloying elements particularly Ni and Nd raises the recrystallization temperature of pure aluminum or aluminum alloys, effectively suppresses the dynamic recrystallization in hot deformed aluminum or aluminum alloys, and accumulates the internal energy driving the nucleation of new grains in the static recrystallization for cold worked aluminum or aluminum alloys. Our data showed that even several ppm of Cu or Fe did not prevent the dynamic recrystallization in pure aluminum and aluminum-30 ppm Si alloy but as low as 0.1˜0.3 ppm Ni addition effectively restricts the dynamic recrystallization during the hot deformation of aluminum or aluminum-30 ppm Si alloy. We have discovered that the dynamic recrystallization is a source causing nonuniform grain structure and thus poor uniformity for the deposited films.
  • Small additions of secondary elements with surface-active properties to aluminum or aluminum alloys result in crystalline grain refinement of the deposited film and improvement in its thermal stability, electromigration resistance, and hillock resistance. A small amount of alloying element addition to aluminum or aluminum alloys does not change the resistivity and etchability of the deposited films.
  • BRIEF DESCRIPTION OF THE FIGURES
  • The below detailed description makes reference to the accompanying figures, in which:
  • FIG. 1 plots the film nonuniformity as a function of Ni content. The dot-dashed line is an eye guideline.
  • FIG. 2 is the photographs of the sputtered surface of (a) an Al-30 ppm Si ConMag target and (b) an Al-30 ppm Si ConMag target with 4 ppm Ni addition. The target without Ni addition consists of finer grains size compared to the target with Ni addition, which maintains coarse ingot grains containing deformed bands. The photos were taken after the targets had been sputtered for the first 50 wafers.
  • FIG. 3 is the metallographs of the targets (a) without Ni addition and (b) with 4 ppm Ni. The target without Ni addition contains dynamic recrystallization (DRX) grains having serrated grain boundaries and subgrain boundaries.
  • FIG. 4 is (a) SEM, (b) OIM inverse pole figure (IPF) map, and (c) OIM misorientation map of an Al-30 ppm Si ConMag target. These images indicate dynamic recrystallization (DRX) grains with serrated grain boundaries and subgrain boundaries form within the deformed original grains. The DRX grains have a much lower density of low angle subgrain boundaries than the deformed matrix.
  • FIG. 5 is (a) SEM, (b) OIM inverse pole figure (IPF) map, and (c) OIM misorientation map for a grain triple junction of a Ni alloyed Al-30 ppm Si ConMag target. These images show the Ni microalloyed target is free of dynamic recrystallization grains. The IPF and OIM maps indicate that low angle subgrain boundaries consisting of dislocations exist within the deformed original grains consisting of large angle grain boundaries.
  • FIG. 6 plots the hardness as a function of anneal temperature for Al-30 ppm Si targets with and without Ni addition. Hardness is measured using 15 kg load and ⅛″ ball. The Ni addition increases the hardness and recrystallization temperature of aluminum-30 ppm Si alloy.
  • FIG. 7 is resistivity of aluminum-30 ppm Si as a function of Ni content.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The aluminum and its alloy sputtering target encompassed by this invention can have any suitable geometry. The present invention includes a method of manufacturing the aluminum and its alloy target containing one or more of alloying elements Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM). The aluminum raw material will preferably have a purity of 99.999 wt %. The Ni raw material will preferably have a purity of at least 99.95 wt %. The Co raw material will preferably have a purity of 99.95 wt %. The Ti raw material will preferably have a purity of 99.995 wt %. The V raw material will preferably have a purity of 99.5 wt %. The Cr will preferably have a purity of at least 99.9 wt %. The Mn will preferably have a purity of at least 99.9 wt %. The Mo will preferably have a purity of at least 99.95 wt %. The Ta will preferably have a purity of at least 99.95 wt %. The W will preferably have a purity of at least 99.95 wt %. The aluminum, or aluminum and its primary alloying elements including Si and Cu, and one or more of other alloying elements Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM) are melted to form a molten alloy preferably through a vacuum induction melting or continuous casting process. The molten alloy is subsequently cooled and cast to form ingot of aluminum or aluminum alloy containing one or more of alloying elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM). It should be understood that the secondary alloying elements in the aluminum or its alloy of the present invention can range from 0.01 to 100 ppm weight. The resulting ingot can have any size and any suitable shapes including round, square, and rectangular. The ingot of aluminum alloying with a small amount of one or more of alloying elements undergoes a thermomechanical process to form desirable grain structure. The thermomechanical process includes but is not limited to hot or cold roll, hot or cold press, hot or cold forge, and anneals to form plate or blank. The plate or blank of aluminum alloy is machined into a target with different geometry.
  • An exemplary aluminum-30 ppm Si ConMag target alloyed with less than 10 ppm Ni has been produced according to the process described above. The Al of 99.999% purity is melted with a prescribed amount of Si of 99.999% or higher purity and Ni of 99.5% purity to produce an ingot with a preferable diameter from 75 mm to 200 mm by use of the vacuum induction melting method. The composition of the resulting ingot measured by the GDMS method is listed in the Table 1. (The weight concentration unit is ppm for all elements). The ingot is sawn into ingot slices of desirable heights. The ingot slice is subjected to anneal in a temperature range of 250° C. to 600° C. for a time period up to 6 hours. The ingot slice subsequently goes through a hot deformation of 40%˜80% reduction at a temperature range of 200° C. to 600° C. to make a blank. The blank is machined to a ConMag target of conical shape with or without an anneal. For comparison, an aluminum-30 ppm Si ConMag target without Ni addition has been produced by the same fabrication process. Table 1 compares the compositions of these two targets. The only difference between them is their Ni content, i.e., one is essentially a pure aluminum-30 ppm Si alloy. The other one is aluminum-30 ppm Si alloyed with ˜4 ppm Ni.
  • Sputtering has been performed on these two targets. The major sputtering conditions are listed in Table 2. The film nonuniformity is characterized using 9-point approach. The measurement indicates the nonuniformity is 14% for the films deposited from the target without Ni addition. The nonuniformity is 4% for the films deposited from the Ni alloyed target. It clearly shows a small amount of Ni addition significantly improves the film uniformity performance. A series of targets with varied Ni contents have been produced and sputtered using the above process and conditions. FIG. 1 plots the film nonuniformity as a function of Ni contents in aluminum-30 ppm Si alloy. It indicates the film nonuniformity decreases with increasing Ni contents. The film nonuniformity is dramatically improved with Ni addition as low as 0.2 ppm.
  • The structure examination reveals that the film nonuniformity is correlated to the target structure. After a short time period of sputtering (the first 50 wafers), we discovered the targets with Ni addition appeared to have nonrecrystallization structure while the targets without Ni addition appeared to have partial recrystallization structure. FIG. 2 exemplifies the macrostructure of the target with ˜4 ppm Ni and the target without Ni addition. The Ni alloyed target consists of well-defined non-recrystallization coarse grains containing deformation bands. In contrast, the target without Ni addition consists of fine and partial recrystallization grains.
  • The difference in structure for the targets with and without Ni additions is further confirmed by microstructure and texture examinations. As shown in FIG. 3, the target with Ni addition displays a highly deformed grain structure of high dislocation density and internal energy, a typical recovery structure of metallic materials after mechanical deformation while prior to the recrystallization stage. In contrast, for the target without Ni addition, grains with serrated grain boundaries and subgrains apparently reformed from the deformed grain matrix. The formation of non-strain-free grains with subgrains is the characteristic microstructure feature of dynamic recrystallization. These dynamic recrystallization grains distinguish from those strain-free static recrystallization grains of equalaxed shapes normally forming in the metallic materials after deformation, i.e., the target without Ni addition undergoes a dynamic recrystallization process involving in both grain nucleation and growth rather than the common static recrystallization.
  • The head to head metallograph comparison between pure aluminum-30 ppm Si and Ni microalloyed Al-30 ppm Si targets indicates that the Ni addition suppresses the dynamic recrystallization in the aluminum-30 ppm Si target (FIG. 3). The orientation imaging microscope (OIM) images further confirm there are numerous low angle subgrain boundaries existing within the deformed grains of Ni microalloyed target (FIG. 4). A low angle grain boundary usually consists of dislocations. The presence of low angle subgrain boundaries of the grains in Ni microalloyed target suggests that the dislocations are piled up and pined at the subgrain boundaries during the hot deformation process. The dynamic recrystallization is suppressed due to the immobile subgrain boundaries. If the cold deformation were applied on the Ni-microalloyed materials, the internal energy stored in the subgrain boundaries of high density dislocation would drive the static recrystallization process to form uniform and fine grain structure. During the dynamic recrystallization process, new grains form to reduce the internal energy stored in the high dislocation density areas within the deformed grains. As shown in FIG. 5, there is much lower density of low angle subgrain boundaries consisting of dislocations in the newly formed dynamic recrystallization grains than the deformed matrix. This confirms that dynamic recrystallization grains and deformed matrix have different dislocation density or internal energy. In other words, the dynamic recrystallization process consumes the internal energy stored in the deformed domains of dislocation density areas. The grain orientation and atom mobility should be different between the reformed dynamic recrystallization grains and the deformed matrix of high dislocation density and internal energy. Thus, it is not surprising that local sputtering rates are different between recrystallization grains and deformed matrix for a target subjected to a dynamic recrystallization process. As a result, the films deposited from such a target will have considerable variations in film thickness or poor film uniformity. On the other hand, the Ni microalloyed target is free of dynamic recrystallization structure. The whole target has consistent sputtering performance due to its uniform and consistent grain structure so the films deposited from the Ni microalloyed target have good film uniformity.
  • Through-process examinations have revealed that the dynamic recrystallization takes place during hot deformation. The metallic materials subjected to a mechanical deformation will experience a plastic deformation produced by the motion of dislocations. Dislocations can be piled up when they encounter obstacles such as grain boundaries, subgrain boundaries, and precipitates during the deformation process. This enables the deformed material to convert the mechanic work to its internal energy stored at the areas of high dislocation density. The stored internal energy is the driving force for the recrystallization process. The atoms in the areas of high dislocation density are in a high energy state and unstable. They tend to be easily removed by high-energy incident ions during sputtering. Therefore the target with this kind of highly deformed and not recrystallized structure is suitable for sputtering. However, aluminum has face centered cubic (FCC) crystallographic structure and multiple {111}<110> dislocation slip systems. A perfect dislocation moving along one slip system can glide to another equivalent slip system. The consequence of the cross-slip of dislocation is that a perfect dislocation a/2<110> decomposes into two partial dislocations a/6<112>, where a is the lattice parameter of aluminum, and a region of stacking fault is created between the partial dislocations. In fact, aluminum has much higher stacking fault energy (166 mJ/mm2) than other FCC materials like copper (78 mJ/mm2) and gold (45 mJ/mm2). If the stacking fault energy of pure aluminum or aluminum-30 ppm silicon materials can not be lowered during the target metallurgical and thermomechanical process, the deformed aluminum or Al-30 ppm Si material will not be able to accumulate enough internal energy for the material as a whole to conduct the recrystallization after the deformation process because the dislocations are difficult to be pinned and piled up due to their cross-slip movement. However, local grain nucleation can take place when a critical internal energy has been reached at high temperature (hot deformation). In addition, the grain boundaries consisting of dislocations have high mobility. High grain boundary migration results in the growth of newly formed grains in local regions during hot deformation.
  • A process involving both grain nucleation and growth is the characteristic of the dynamic recrystallization. The difference in microstructure nature between dynamically recrystallized grains and deformed matrix present in the target without Ni addition results in the high nonuniformity of thickness and electrical resistance for the deposited films. This invention has discovered that adding secondary alloying elements including Ni to pure aluminum or its alloy effectively suppresses the dynamic recrystallization for hot worked aluminum or its alloy and enhances the static recrystallization for cold worked aluminum or its alloy.
  • Lower thermal stability or abnormal growth in the deposited film is one of the major concerns associated with the utilization of pure aluminum sputtering target in forming wiring films. Low thermal stability or abnormal growth is characterized by a tendency of the individual crystal grains to grow when exposed to certain temperature. The higher the recrystallization or grain growth temperature, the higher the thermal stability. High thermal stability or low abnormal growth enhances the electromigration resistance and hillock resistance of the deposited films. FIG. 6 plots the hardness as a function of anneal temperature for aluminum-30 ppm Si targets with and without Ni addition. These targets were produced by the fabrication process described above. They were subjected to a hot deformation of 60% thickness reduction followed by a recrystallization anneal for 1 hour at a temperature ranging from 200° C. to 450° C. FIG. 6 indicates the Ni addition increases the hardness of the aluminum-30 ppm Si material. Furthermore, the hardness decreases with increasing anneal temperature for the targets with or without Ni addition. The materials are softened and the hardness decreases when the work-hardening stress is released by forming new strain-free grains in the recrystallization process. With reference to FIG. 6, the hardness declines suggest the recrystallization starting temperatures are about 260° C. and 200° C. for aluminum-30 ppm Si alloy with and without Ni addition, respectively. The recrystallization temperature of Ni microalloyed aluminum-30 ppm Si is 60° higher than that of non-Ni microalloyed aluminum-30 ppm Si. This indicates the Ni addition increases the recrystallization temperature and improves the thermal stability and electromigration resistance of aluminum and its alloys. Similar improvement in thermal stability and electromigration resistance can be attained in the aluminum by adding one or more of other elements including Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM). Alloying aluminum or its alloy targets with other secondary elements provides an approach to effectively enhance thermal stability and electromigration resistance. This enables the deposited films to have improved thermal stability, electromigration resistance, and hillock resistance.
  • Low resistivity and good etchability are desirable for wiring film applications. Our data also shows alloying aluminum or its alloys with a small amount of secondary elements does not significantly change the resistivity and patternability of the microalloyed aluminum and its alloys. FIG. 7 plots the resistivity of aluminum-30 ppm Si as a function of the content of Ni addition. It shows the resistivity of Ni alloyed aluminum-30 ppm Si essentially does not change by adding a small amount of Ni. For example, the resistivity of aluminum-30 ppm Si with 4 ppm Ni is 2.71 micro-Ohm·cm, essentially the same as that of pure aluminum. In addition, the Ni addition does not react with the Al etching reactant. The films deposited from Ni microalloyed target sustain the etchability comparable to pure aluminum.
  • The present invention has been disclosed in connection with the preferred embodiments thereof, it should be understood that the invention is not limited to the specific embodiments described since the means herein comprise preferred forms of putting the invention into effect, and other embodiments may be within the scope of the invention as defined by the following claims.
  • TABLE 1
    Al-30 ppm Si with
    Element Al-30 ppm Si Ni addition
    Si 30.3 30.5
    C 0.072 0.12
    O 0.58 0.48
    S 0.007 0.007
    B 0.13 0.13
    Na 0.01 0.009
    Mg 0.3 0.26
    P 0.19 0.17
    Cl 0.072 0.13
    Ca <0.05 0.11
    Ti 0.069 0.058
    V 0.029 0.024
    Cr 0.063 0.044
    Mn 0.044 0.04
    Fe 0.18 0.15
    Co <0.002 0.005
    Ni 0.02 3.76
    Zn 0.035 0.038
    Ga <0.01 <0.01
    Ge <0.02 <0.02
    As <0.005 <0.005
    Se <0.02 <0.03
    Rb <0.005 <0.005
    Zr 0.01 <0.005
    Nb 0.004 <0.002
    Mo <0.005 0.22
    Pd <0.005 <0.005
    Cd <0.01 <0.01
    In <0.005 <0.005
    Sn <0.05 <0.05
    Sb <0.005 <0.005
    Te <0.04 <0.04
    Cs <0.003 <0.003
    Ba <0.003 <0.003
    La 0.019 0.021
    Ce 0.009 0.005
    W <0.005 0.033
    Pt <0.005 0.1
    Au <0.02 <0.02
    Hg <0.005 <0.005
    Ti <0.005 <0.005
    Pb 0.009 <0.005
    Bi <0.002 <0.002
    Th 0.0012 0.001
    U <0.001 <0.001
  • TABLE 2
    Sputter Conditions
    Power 8.4 KW
    Target/substrate distance 7.05 cm
    Chamber argon pressure 6 Mt
    Starting chamber pressure 0.0002 mT
    Deposition time
    55 seconds
    Substrate temperature 250 degree Celsius
    Shutter delay 2.5 second
    Ramp time 2.5 second
    Film uniformity measurement 9-point approach

Claims (13)

1. A sputtering target for use in semiconductor integrated circuit devices, flat panel displays, and other applications made of aluminum and one or more of other elements or aluminum alloy and one or more of secondary elements.
2. The sputtering target of claim 1 wherein the one or more other elements or secondary elements including but not limited to Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM).
3. The sputtering target of claim 1 wherein the one or more of other elements or secondary elements being present in the aluminum or its alloy at a total concentration ranging from 0.01 ppm˜100 ppm weight and preferably in the range of 0.1 ppm to 10 ppm.
4. The sputtering target of claim 1 wherein adding one or more of other elements or secondary elements including Ni or Nd to aluminum or its alloy improves the thickness uniformity of the deposited films.
5. The sputtering target of claim 1 comprising aluminum or aluminum alloy and 0.01 ppm˜10 ppm Ni wherein the thickness nonuniformity of the deposited films decreases with increasing the content of Ni alloyed in the target.
6. The sputtering target of claim 1 wherein the addition of one or more other elements or secondary elements including Ni suppresses the dynamic recrystallization of hot worked aluminum or its alloy and improves the static recrystallization of cold worked aluminum or its alloy.
7. The sputtering target of claim 1 wherein the addition of a small amount of other elements or secondary elements including Ni does not increase the resistivity of the aluminum or its alloy.
8. The sputtering target of claim 1 wherein the deposited films attain good etchability.
9. The sputtering target of claim 1 wherein the addition of one or more of other elements or secondary elements including Ni increases the thermal stability, electromigration resistance, and hillock resistance of the deposited films.
10. A method of manufacturing an aluminum or its alloy sputtering target comprising:
providing an Al material with a purity of at least 99.999 wt %;
providing a Ni material with a purity of at least 99.95 wt %;
providing a Co material with a purity of at least 99.95 wt %;
providing a Ti material with a purity of at least 99.995 wt %;
providing a V material with a purity of at least 99.5 wt %;
providing a Cr material with a purity of at least 99.95 wt %;
providing a Mn material with a purity of at least 99.9 wt %;
providing a Mo material with a purity of at least 99.95 wt %;
providing a Nb material with a purity of at least 99.95 wt %;
providing a Ta material with a purity of at least 99.95 wt %;
providing a W material with a purity of at least 99.95 wt %;
providing a Nd material with a purity of at least 99 wt %;
The aluminum, or aluminum and its primary alloying elements including Si and Cu, and one or more of other elements melting together to form a molten aluminum alloy; and cooling and casting the molten alloy to form an aluminum alloy ingot.
11. The method of claim 10 wherein the aluminum or its alloy comprising from 0.01 ppm to 100 ppm one or more of other elements or secondary elements including Ni, Co, Ti, V, Cr, Mn, Mo, Nb, Ta, W, and rare earth metals (REM).
12. The method of claim 10 further comprising the aluminum alloy ingot materials subjected to a thermomechanical process to attain desirable grain structure.
13. The thermomechanical process of claim 12 comprising hot or cold press, hot roll, cold roll, hot or cold forge, extrusion and anneals.
US12/223,499 2006-03-06 2007-02-26 Sputtering Target Abandoned US20090008786A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/223,499 US20090008786A1 (en) 2006-03-06 2007-02-26 Sputtering Target

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US77950006P 2006-03-06 2006-03-06
US81563506P 2006-06-22 2006-06-22
PCT/US2007/004879 WO2007103014A2 (en) 2006-03-06 2007-02-26 Sputtering target
US12/223,499 US20090008786A1 (en) 2006-03-06 2007-02-26 Sputtering Target

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2007/004879 A-371-Of-International WO2007103014A2 (en) 2006-03-06 2007-02-26 Sputtering target

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/525,988 Continuation US8992748B2 (en) 2006-03-06 2012-06-18 Sputtering target

Publications (1)

Publication Number Publication Date
US20090008786A1 true US20090008786A1 (en) 2009-01-08

Family

ID=38335666

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/223,499 Abandoned US20090008786A1 (en) 2006-03-06 2007-02-26 Sputtering Target
US13/525,988 Active 2027-10-26 US8992748B2 (en) 2006-03-06 2012-06-18 Sputtering target

Family Applications After (1)

Application Number Title Priority Date Filing Date
US13/525,988 Active 2027-10-26 US8992748B2 (en) 2006-03-06 2012-06-18 Sputtering target

Country Status (5)

Country Link
US (2) US20090008786A1 (en)
KR (1) KR101376502B1 (en)
CN (1) CN101395296B (en)
TW (1) TWI398534B (en)
WO (1) WO2007103014A2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080223718A1 (en) * 2006-11-20 2008-09-18 Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) Ai-based alloy sputtering target and process for producing the same
US20130264093A1 (en) * 2011-01-24 2013-10-10 La Farga Lacambra, S.A.U. Electrical Conductor for Transporting Electrical Energy and Corresponding Production Method
JP2018523754A (en) * 2015-08-03 2018-08-23 ハネウェル・インターナショナル・インコーポレーテッドHoneywell International Inc. Frictionless forged aluminum alloy sputtering target with improved properties
CN109778126A (en) * 2019-03-13 2019-05-21 安泰天龙(天津)钨钼科技有限公司 A kind of preparation method of high-densit Ultra-fine Grained large scale molybdenum target material

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5379010B2 (en) * 2008-02-08 2013-12-25 Jx日鉱日石金属株式会社 Ytterbium sputtering target and method for producing the same.
CN101665909B (en) * 2009-10-23 2012-08-22 宁波江丰电子材料有限公司 Method for preparing target material
JP5457794B2 (en) * 2009-10-30 2014-04-02 株式会社神戸製鋼所 Al-based alloy sputtering target
WO2013001943A1 (en) * 2011-06-30 2013-01-03 Jx日鉱日石金属株式会社 Co-Cr-Pt-B ALLOY SPUTTERING TARGET AND METHOD FOR PRODUCING SAME
US10276356B2 (en) 2013-03-07 2019-04-30 Jx Nippon Mining & Metals Corporation Copper alloy sputtering target
CN106756830B (en) * 2016-12-21 2019-03-15 包头稀土研究院 The manufacturing method of alumal target
AT15596U1 (en) * 2017-02-28 2018-03-15 Plansee Composite Mat Gmbh Sputtering target and method for producing a sputtering target
KR20230095654A (en) * 2021-12-22 2023-06-29 주식회사 나이스엘엠에스 manufacturing method of Al sputtering target
KR20230095655A (en) * 2021-12-22 2023-06-29 주식회사 나이스엘엠에스 manufacturing method of Al sputtering target

Citations (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3926691A (en) * 1972-11-01 1975-12-16 Sherritt Gordon Mines Ltd Dispersion strengthened metals and alloys
US4033794A (en) * 1973-01-19 1977-07-05 The British Aluminum Company, Limited Aluminium base alloys
US4477793A (en) * 1982-06-30 1984-10-16 Fuji Electric Co., Ltd. Zinc oxide non-linear resistor
US4775814A (en) * 1986-05-21 1988-10-04 Hitachi, Ltd. Saw device
US4814053A (en) * 1986-04-04 1989-03-21 Seiko Epson Corporation Sputtering target and method of preparing same
US4874440A (en) * 1986-03-20 1989-10-17 Aluminum Company Of America Superplastic aluminum products and alloys
US4941032A (en) * 1986-03-03 1990-07-10 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Semiconductor device
US4960163A (en) * 1988-11-21 1990-10-02 Aluminum Company Of America Fine grain casting by mechanical stirring
US5229626A (en) * 1992-03-27 1993-07-20 Nichia Kagaku Kogyo K.K. Solid-state image converting device with dot-like layer
US5273910A (en) * 1990-08-08 1993-12-28 Minnesota Mining And Manufacturing Company Method of making a solid state electromagnetic radiation detector
US5284532A (en) * 1992-02-18 1994-02-08 Allied Signal Inc. Elevated temperature strength of aluminum based alloys by the addition of rare earth elements
US5296653A (en) * 1991-12-09 1994-03-22 Kabushiki Kaisha Toshiba Device having a multi-layered conductor structure
US5497255A (en) * 1993-10-30 1996-03-05 Victor Company Of Japan, Ltd. Spacial light modulation device including a pixel electode layer and a method for manufacturing the same
US5514909A (en) * 1993-07-27 1996-05-07 Kabushiki Kaisha Kobe Seiko Sho Aluminum alloy electrode for semiconductor devices
US5541007A (en) * 1991-01-17 1996-07-30 Mitsubishi Chemical Corporation Aluminum alloy wiring layer and aluminum alloy sputtering target
US5906717A (en) * 1994-04-28 1999-05-25 Sumitomo Chemical Company, Limited Sputtering target of single crystal aluminum alloy
US5982715A (en) * 1997-07-15 1999-11-09 Sharp Kabushiki Kaisha Magneto-optical recording medium having a signal reproducing region of the reproducing layer larger than the record bit in the recording layer
US6218206B1 (en) * 1998-03-31 2001-04-17 Mitsubishi Denki Kabushiki Kaisha Method for producing thin film transistor and thin film transistor using the same
US6252247B1 (en) * 1998-03-31 2001-06-26 Mitsubishi Denki Kabushiki Kaisha Thin film transistor, a method for producing the thin film transistor, and a liquid crystal display using a TFT array substrate
US6264813B1 (en) * 1996-12-04 2001-07-24 Aluminum Pechiney Cathodic sputtering targets made of aluminum alloy
US6329275B1 (en) * 1995-10-12 2001-12-11 Kabushiki Kaisha Toshiba Interconnector line of thin film, sputter target for forming the wiring film and electronic component using the same
US6423161B1 (en) * 1999-10-15 2002-07-23 Honeywell International Inc. High purity aluminum materials
US20030047812A1 (en) * 2001-08-31 2003-03-13 Vacuum Metallurgical Co., Ltd. (Shinkuu Yakin Kabushiki Kaisha) Thin film aluminum alloy and sputtering target to form the same
US20040126608A1 (en) * 2002-12-19 2004-07-01 Kabushiki Kaisha Kobe Seiko Sho(Kobe Steel, Ltd.) Electronic device, method of manufacture of the same, and sputtering target
US6929726B2 (en) * 1997-12-24 2005-08-16 Kabushiki Kaisha Toshiba Sputtering target, Al interconnection film, and electronic component
US6997995B2 (en) * 2000-12-15 2006-02-14 Leistrits Turbinenkomponenten Remscheid GmbH Method for producing components with a high load capacity from TiAl alloys
US7017382B2 (en) * 2000-03-28 2006-03-28 Honeywell International Inc. Methods of forming aluminum-comprising physical vapor deposition targets; sputtered films; and target constructions

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55157238A (en) 1979-05-28 1980-12-06 Hitachi Ltd Semiconductor device
US4248715A (en) * 1979-11-23 1981-02-03 Olivier Paul D Electrolytic chlorine generator
SU1160896A1 (en) 1983-04-08 1991-10-07 Институт электроники АН БССР Material for manufacturing thim-film interconnecting of integrated circuits
FR2555611B1 (en) 1983-11-25 1986-04-18 Rhone Poulenc Spec Chim PROCESS FOR THE PREPARATION OF ALUMINUM AND RARE EARTH ALLOYS
JPS6161257A (en) 1984-08-31 1986-03-29 Mitsubishi Electric Corp Moving body guide mechanism
JPS62235451A (en) 1986-04-03 1987-10-15 Nippon Mining Co Ltd Al alloy for semiconductor wiring material
JPH01233737A (en) 1988-03-15 1989-09-19 Hitachi Ltd Integrated circuit device and its manufacture; target for manufacturing wiring film in said device
JP2714606B2 (en) 1988-05-16 1998-02-16 日本電信電話株式会社 Wiring layer and its manufacturing method
JPH02159064A (en) 1988-12-13 1990-06-19 Matsushita Electric Ind Co Ltd Manufacture of semiconductor device
JPH02188922A (en) 1989-01-17 1990-07-25 Hitachi Ltd Electronic device and manufacture thereof
JPH0456136A (en) 1990-06-22 1992-02-24 Nippon Telegr & Teleph Corp <Ntt> Forming method of thin film for wiring
JPH04192332A (en) 1990-11-22 1992-07-10 Hitachi Ltd Manufacture of thin film wiring and thin film wiring and semiconductor device
EP0531808B1 (en) 1991-09-09 1997-02-05 Shin-Etsu Chemical Co., Ltd. Magneto-optical recording medium
JPH05335271A (en) 1992-06-03 1993-12-17 Mitsubishi Kasei Corp Sputtering target and manufacture thereof as well as wiring of electronic device
EP0573002A1 (en) 1992-06-03 1993-12-08 Ryoka Matthey Corporation Sputtering target, wiring method for electronic devices and electronic device
US5428249A (en) 1992-07-15 1995-06-27 Canon Kabushiki Kaisha Photovoltaic device with improved collector electrode
JPH06333926A (en) 1993-05-20 1994-12-02 Kojundo Chem Lab Co Ltd Aluminum alloy wiring material
JPH10330927A (en) 1997-06-05 1998-12-15 Riyouka Massey Kk Sputtering target material made of aluminum alloy
JPH10330928A (en) 1997-06-05 1998-12-15 Riyouka Massey Kk Sputtering target material and its production
JPH1134426A (en) 1997-07-24 1999-02-09 Fuji Xerox Co Ltd Printing control apparatus, printing control system, and printing control method
JPH11337976A (en) 1998-03-26 1999-12-10 Toshiba Corp Array substrate for display device and flat display device equipped with that array substrate
JP4192332B2 (en) 1999-04-19 2008-12-10 Jfeスチール株式会社 Manufacturing method of unidirectional electrical steel sheet
JP3634208B2 (en) 1999-09-21 2005-03-30 真空冶金株式会社 Electrode / wiring material for liquid crystal display and sputtering target
JP2001316803A (en) 2000-04-28 2001-11-16 Honeywell Electronics Japan Kk Method of manufacturing sputtering target material
JP4429520B2 (en) * 2000-12-04 2010-03-10 住友軽金属工業株式会社 Aluminum foil for anode electrolytic capacitors
US20040256218A1 (en) * 2002-05-31 2004-12-23 Glass Howard L. Thin films and methods of forming thin films utilizing ECAE-targets
JP4044383B2 (en) 2002-07-19 2008-02-06 株式会社神戸製鋼所 Manufacturing method of semiconductor device electrode / wiring
WO2006041989A2 (en) 2004-10-05 2006-04-20 Tosoh Smd, Inc. Sputtering target and method of its fabrication
JP5335271B2 (en) 2008-04-09 2013-11-06 キヤノン株式会社 Photoelectric conversion device and imaging system using the same

Patent Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3926691A (en) * 1972-11-01 1975-12-16 Sherritt Gordon Mines Ltd Dispersion strengthened metals and alloys
US4033794A (en) * 1973-01-19 1977-07-05 The British Aluminum Company, Limited Aluminium base alloys
US4477793A (en) * 1982-06-30 1984-10-16 Fuji Electric Co., Ltd. Zinc oxide non-linear resistor
US4941032A (en) * 1986-03-03 1990-07-10 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Semiconductor device
US4874440A (en) * 1986-03-20 1989-10-17 Aluminum Company Of America Superplastic aluminum products and alloys
US4814053A (en) * 1986-04-04 1989-03-21 Seiko Epson Corporation Sputtering target and method of preparing same
US4775814A (en) * 1986-05-21 1988-10-04 Hitachi, Ltd. Saw device
US4960163A (en) * 1988-11-21 1990-10-02 Aluminum Company Of America Fine grain casting by mechanical stirring
US5273910A (en) * 1990-08-08 1993-12-28 Minnesota Mining And Manufacturing Company Method of making a solid state electromagnetic radiation detector
US5541007A (en) * 1991-01-17 1996-07-30 Mitsubishi Chemical Corporation Aluminum alloy wiring layer and aluminum alloy sputtering target
US5296653A (en) * 1991-12-09 1994-03-22 Kabushiki Kaisha Toshiba Device having a multi-layered conductor structure
US5284532A (en) * 1992-02-18 1994-02-08 Allied Signal Inc. Elevated temperature strength of aluminum based alloys by the addition of rare earth elements
US5229626A (en) * 1992-03-27 1993-07-20 Nichia Kagaku Kogyo K.K. Solid-state image converting device with dot-like layer
US5514909A (en) * 1993-07-27 1996-05-07 Kabushiki Kaisha Kobe Seiko Sho Aluminum alloy electrode for semiconductor devices
US6033542A (en) * 1993-07-27 2000-03-07 Kabushiki Kaisha Kobe Seiko Sho Electrode and its fabrication method for semiconductor devices, and sputtering target for forming electrode film for semiconductor devices
US5497255A (en) * 1993-10-30 1996-03-05 Victor Company Of Japan, Ltd. Spacial light modulation device including a pixel electode layer and a method for manufacturing the same
US5906717A (en) * 1994-04-28 1999-05-25 Sumitomo Chemical Company, Limited Sputtering target of single crystal aluminum alloy
US6329275B1 (en) * 1995-10-12 2001-12-11 Kabushiki Kaisha Toshiba Interconnector line of thin film, sputter target for forming the wiring film and electronic component using the same
US6264813B1 (en) * 1996-12-04 2001-07-24 Aluminum Pechiney Cathodic sputtering targets made of aluminum alloy
US5982715A (en) * 1997-07-15 1999-11-09 Sharp Kabushiki Kaisha Magneto-optical recording medium having a signal reproducing region of the reproducing layer larger than the record bit in the recording layer
US6929726B2 (en) * 1997-12-24 2005-08-16 Kabushiki Kaisha Toshiba Sputtering target, Al interconnection film, and electronic component
US6218206B1 (en) * 1998-03-31 2001-04-17 Mitsubishi Denki Kabushiki Kaisha Method for producing thin film transistor and thin film transistor using the same
US6252247B1 (en) * 1998-03-31 2001-06-26 Mitsubishi Denki Kabushiki Kaisha Thin film transistor, a method for producing the thin film transistor, and a liquid crystal display using a TFT array substrate
US6423161B1 (en) * 1999-10-15 2002-07-23 Honeywell International Inc. High purity aluminum materials
US7017382B2 (en) * 2000-03-28 2006-03-28 Honeywell International Inc. Methods of forming aluminum-comprising physical vapor deposition targets; sputtered films; and target constructions
US6997995B2 (en) * 2000-12-15 2006-02-14 Leistrits Turbinenkomponenten Remscheid GmbH Method for producing components with a high load capacity from TiAl alloys
US20030047812A1 (en) * 2001-08-31 2003-03-13 Vacuum Metallurgical Co., Ltd. (Shinkuu Yakin Kabushiki Kaisha) Thin film aluminum alloy and sputtering target to form the same
US20040126608A1 (en) * 2002-12-19 2004-07-01 Kabushiki Kaisha Kobe Seiko Sho(Kobe Steel, Ltd.) Electronic device, method of manufacture of the same, and sputtering target
US20050184395A1 (en) * 2002-12-19 2005-08-25 Kabushiki Kaisha Kobe Seiko Sho(Kobe Steel, Ltd.) Electronic device, method of manufacture of the same, and sputtering target

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080223718A1 (en) * 2006-11-20 2008-09-18 Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) Ai-based alloy sputtering target and process for producing the same
US20130264093A1 (en) * 2011-01-24 2013-10-10 La Farga Lacambra, S.A.U. Electrical Conductor for Transporting Electrical Energy and Corresponding Production Method
JP2018523754A (en) * 2015-08-03 2018-08-23 ハネウェル・インターナショナル・インコーポレーテッドHoneywell International Inc. Frictionless forged aluminum alloy sputtering target with improved properties
JP7021069B2 (en) 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 Friction-free forged aluminum alloy sputtering target with improved properties
CN109778126A (en) * 2019-03-13 2019-05-21 安泰天龙(天津)钨钼科技有限公司 A kind of preparation method of high-densit Ultra-fine Grained large scale molybdenum target material

Also Published As

Publication number Publication date
WO2007103014A2 (en) 2007-09-13
US8992748B2 (en) 2015-03-31
CN101395296A (en) 2009-03-25
CN101395296B (en) 2012-03-28
KR20080100445A (en) 2008-11-18
WO2007103014A3 (en) 2007-11-01
KR101376502B1 (en) 2014-03-21
TWI398534B (en) 2013-06-11
US20120298506A1 (en) 2012-11-29
TW200734473A (en) 2007-09-16

Similar Documents

Publication Publication Date Title
US8992748B2 (en) Sputtering target
US6451135B1 (en) High-purity copper sputtering targets and thin films
US6791188B2 (en) Thin film aluminum alloy and sputtering target to form the same
JP5044509B2 (en) Method for manufacturing Al wiring film
JP4237742B2 (en) Manufacturing method of sputtering target
US20100000860A1 (en) Copper Sputtering Target With Fine Grain Size And High Electromigration Resistance And Methods Of Making the Same
JPH06299342A (en) Sputtering target made of high purity aluminum or its alloy
JP5520746B2 (en) Copper material for sputtering target and method for producing the same
US10297429B2 (en) High-purity copper-chromium alloy sputtering target
US20060037680A1 (en) Nickel alloy sputtering target
US20200181762A1 (en) Aluminum alloy sputtering target
JP4237743B2 (en) Method for producing ingot for sputtering target
US8097100B2 (en) Ternary aluminum alloy films and targets for manufacturing flat panel displays
TW202000941A (en) Aluminum alloy film, manufacturing method for the same, and thin film transistor
JP2003243325A (en) Sputtering target for forming copper alloy wiring film and copper alloy wiring film little affected by heat and formed by using the same
JP4213699B2 (en) Manufacturing method of liquid crystal display device
JP6589569B2 (en) Cu alloy sputtering target and Cu alloy film
JPH0681141A (en) Sputtering target

Legal Events

Date Code Title Description
AS Assignment

Owner name: TOSOH SMD, INC., OHIO

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:IVANOV, EUGENE Y.;YUAN, YONGWEN;SMATHERS, DAVID B.;AND OTHERS;REEL/FRAME:022065/0334

Effective date: 20080627

STCB Information on status: application discontinuation

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