WO2017154890A1 - アルゴンまたは水素を含む銅及び銅合金ターゲット - Google Patents
アルゴンまたは水素を含む銅及び銅合金ターゲット Download PDFInfo
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- WO2017154890A1 WO2017154890A1 PCT/JP2017/008965 JP2017008965W WO2017154890A1 WO 2017154890 A1 WO2017154890 A1 WO 2017154890A1 JP 2017008965 W JP2017008965 W JP 2017008965W WO 2017154890 A1 WO2017154890 A1 WO 2017154890A1
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- WIPO (PCT)
- Prior art keywords
- sputtering target
- raw material
- gas
- purity
- wtppm
- Prior art date
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- 239000010949 copper Substances 0.000 title claims abstract description 106
- 229910052786 argon Inorganic materials 0.000 title claims abstract description 62
- 229910052739 hydrogen Inorganic materials 0.000 title claims abstract description 58
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 229910000881 Cu alloy Inorganic materials 0.000 title claims abstract description 37
- 239000001257 hydrogen Substances 0.000 title claims abstract description 18
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 238000005477 sputtering target Methods 0.000 claims abstract description 113
- 229910052802 copper Inorganic materials 0.000 claims abstract description 27
- 239000002994 raw material Substances 0.000 claims description 89
- 239000011572 manganese Substances 0.000 claims description 17
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- 229910052748 manganese Inorganic materials 0.000 claims description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 4
- 238000012545 processing Methods 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims 1
- 239000007789 gas Substances 0.000 abstract description 82
- 238000004544 sputter deposition Methods 0.000 abstract description 22
- 238000002844 melting Methods 0.000 description 49
- 230000008018 melting Effects 0.000 description 49
- 229910052751 metal Inorganic materials 0.000 description 49
- 239000002184 metal Substances 0.000 description 49
- 238000007664 blowing Methods 0.000 description 42
- 238000000034 method Methods 0.000 description 39
- 238000005266 casting Methods 0.000 description 29
- 238000010438 heat treatment Methods 0.000 description 26
- 238000011156 evaluation Methods 0.000 description 23
- 239000010410 layer Substances 0.000 description 21
- 238000012360 testing method Methods 0.000 description 21
- 230000008569 process Effects 0.000 description 18
- 239000000463 material Substances 0.000 description 15
- 238000001514 detection method Methods 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 8
- 238000009792 diffusion process Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 230000002159 abnormal effect Effects 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 230000009471 action Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 238000010309 melting process Methods 0.000 description 2
- 239000012768 molten material Substances 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000001020 plasma etching Methods 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- MZLGASXMSKOWSE-UHFFFAOYSA-N tantalum nitride Chemical compound [Ta]#N MZLGASXMSKOWSE-UHFFFAOYSA-N 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/34—Sputtering
- C23C14/3407—Cathode assembly for sputtering apparatus, e.g. Target
- C23C14/3414—Metallurgical or chemical aspects of target preparation, e.g. casting, powder metallurgy
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/01—Alloys based on copper with aluminium as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/05—Alloys based on copper with manganese as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23C—COATING 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
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/14—Metallic material, boron or silicon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/34—Gas-filled discharge tubes operating with cathodic sputtering
- H01J37/3411—Constructional aspects of the reactor
- H01J37/3414—Targets
- H01J37/3426—Material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/34—Gas-filled discharge tubes operating with cathodic sputtering
- H01J37/3488—Constructional details of particle beam apparatus not otherwise provided for, e.g. arrangement, mounting, housing, environment; special provisions for cleaning or maintenance of the apparatus
- H01J37/3491—Manufacturing of targets
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D1/00—Treatment of fused masses in the ladle or the supply runners before casting
- B22D1/002—Treatment with gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D21/00—Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
- B22D21/02—Casting exceedingly oxidisable non-ferrous metals, e.g. in inert atmosphere
- B22D21/025—Casting heavy metals with high melting point, i.e. 1000 - 1600 degrees C, e.g. Co 1490 degrees C, Ni 1450 degrees C, Mn 1240 degrees C, Cu 1083 degrees C
Definitions
- the present invention relates to a copper or copper alloy sputtering target used for forming a wiring of a semiconductor device, etc., in particular, a copper or copper alloy sputtering target capable of sustaining stable discharge while responding to the demand for low pressure process, It relates to the manufacturing method.
- Al aluminum
- LSIs large scale integrated circuits
- MPU microprocessor
- the elements of the wiring in the circuit has also been made thinner, and the wiring resistance increases when the old Al wiring is used, which causes a new problem that the signal delay and power loss increase. Came to occur.
- the signal delay of the element prevents the operation speed of the MPU or the like from increasing, and the power loss increases to such an extent that the power consumption and heat generation of the semiconductor device cannot be ignored.
- the diffusion barrier layer made of a material such as tantalum (Ta) or tantalum nitride (TaN) having a function of preventing the diffusion of Cu is formed as a base of the Cu wiring, and the problem of diffusion is dealt with in advance.
- Grooves are formed in the wiring site by lithography, and after flowing Cu so as to fill the inside of the grooves, the surface is planarized by a chemical mechanical polishing (CMP) process, thereby removing excess Cu overflowing on the surface.
- CMP chemical mechanical polishing
- a diffusion barrier layer is formed by a process such as sputtering in the groove formed in the interlayer insulating film, and Cu is poured therein.
- a process such as sputtering in the groove formed in the interlayer insulating film
- Cu is poured therein.
- a thick Cu wiring layer is formed by sputtering under a higher film formation rate or a wet process such as a plating method.
- Patent Document 1 when a Cu seed layer is formed by sputtering, argon (Ar) used as a discharge gas during sputtering is taken into the Cu layer, and the Cu layer becomes a rough and non-uniform layer. It describes the problem.
- This document discloses a technique in which Ar is introduced to a pressure at which discharge is easily performed at the start of discharge in which sputtering is performed and then the plasma is ignited, and then the supply of Ar is shut off or sputtering is continued with a sufficiently low Ar supply amount. is doing.
- studies from the viewpoint of controlling the process conditions have been conventionally performed.
- this document does not fully study from the viewpoint of the characteristics of the sputtering target.
- Patent Document 2 in order to deal with such a problem, it is described that a Cu sputtering target is purified as much as possible to eliminate impurity elements as much as possible. Such a technique is effective for pure copper, but is not substantially applicable to a Cu alloy sputtering target containing a predetermined element such as Al.
- the technique can be applied simply and easily because, for example, a high-purity anode and an electrolytic solution are required for manufacturing a sputtering target, and a clean room of a specific class or higher is required.
- Patent Document 3 a predetermined amount of a metal element such as silver (Ag), gold (Au), or copper (Cu) is added to a tantalum (Ta) sputtering target, so that a stable discharge can be maintained for a long time.
- a metal element such as silver (Ag), gold (Au), or copper (Cu) is added to a tantalum (Ta) sputtering target, so that a stable discharge can be maintained for a long time.
- the technique regarding the sputtering target which can be performed is disclosed.
- this document relates to Ta, and there is no rationality that can be applied to Cu.
- the inclusion of impurity elements other than the desired alloy elements generally changes the resistance characteristics of the Cu layer. Is not preferred.
- Patent Documents 4 to 6 describe that when a copper alloy serving as a base material of a sputtering target was cast, melting was performed in an Ar atmosphere as an inert atmosphere.
- the atmosphere at the time of casting is simply Ar, and the disclosure of the technical idea that a predetermined amount of a gas component is positively introduced into the target for some reason is disclosed.
- a special technical operation such as spraying Ar gas at a specific flow rate on the surface of the raw material melt is performed.
- these documents have no description or suggestion about the amount of Ar contained in the copper alloy after casting nor the relationship between the amount of Ar and the discharge stabilization of sputtering, and technical problems and actions related to them. It is not even aware of the effects.
- an object of the present invention is to provide a copper or copper alloy sputtering target in which discharge is stable and sustainable even under conditions where it is difficult to continuously perform sputtering discharge such as low pressure and low gas flow rate.
- an object of the present invention is to provide a method by which such a sputtering target can be easily produced.
- Ar or H atoms contained in the base material of the sputtering target are intermittently released to the target surface during sputtering and contribute to stable continuation of the sputtering discharge. Even under such conditions where continuous discharge is difficult, sputtering film formation can be carried out stably and easily.
- the Ar or H content of the sputtering target of the present invention is low enough that the incorporation into the deposited Cu or Cu alloy layer does not cause a problem, the design of the wiring layer composition and the degree of freedom of process conditions are reduced. Can be expanded.
- the sputtering target can be manufactured by a relatively simple means, it is possible to improve the productivity of the above-described sputtering target, thereby suppressing an increase in manufacturing cost of the final product.
- the sputtering target of the present invention is made of pure Cu except for inevitable impurities, or in a base material made of a Cu alloy containing elements such as Al, Mn, Sn, Ti, and Zn in Cu at a predetermined composition ratio, Ar or H Either or both of them are contained in an amount of 1 wtppm or more and 10 wtppm or less for Ar or H, respectively. It is considered that Ar or H atoms contained in these target base materials are intermittently released from the target surface during sputtering, and cause a high density of discharge gas locally in the vicinity of the target surface.
- the content of Ar or H in the sputtering target needs to be 1 wtppm or more for each of Ar or H contained. If it is less than this, the amount for sustaining the discharge becomes insufficient, and there is a possibility that the plasma cannot be maintained stably.
- the content of Ar or H in the sputtering target is preferably 1.5 wtppm or more for each of Ar or H contained, and may be 2 wtppm or more.
- the upper limit of the content is 10 wtppm.
- the upper limit of the content is preferably 8 ppm or less, and more preferably 5 ppm or less.
- Ar having a large ionization cross section by electrons and a small ionization potential.
- Ar is a relatively inexpensive element among rare gases, and is an element that also has various characteristics that contribute to ionization as described above.
- the Ar once released from the target surface and ionized can reach the plasma sheath on the target surface again, and can contribute to sputtering of Cu or Cu alloy as the target material.
- H has a reducing action
- the alloy is preferably a Cu alloy containing either Al or Mn.
- a diffusion barrier layer for preventing the diffusion of Cu is necessary.
- Mn an interlayer insulating film or element isolation can be achieved.
- the action of oxygen and Mn in the oxide insulating layer such as a film reacting to self-form the diffusion barrier layer can be given to Cu.
- Al it is possible to obtain an effect of suppressing electromigration in the Cu wiring that has been manifested by miniaturization of the Cu wiring.
- Mn and Al are preferably contained in an amount of 0.1 at% or more, and more preferably 0.5 at% or more. Further, if the added amount is too large, the resistivity is lowered and the original technical advantage of Cu wiring is lost. Therefore, the upper limit of the content is preferably 5 at% in the case of Al, and 15 at% in the case of Mn. % Is preferable.
- the sputtering target of the present invention is not particularly limited in the production method, and any one of Ar or H or both can be contained in the range of 1 wtppm to 10 wtppm for Ar or H, respectively. It may be manufactured by any method.
- either Cu or Cu alloy ingot serving as a target base material may be Ar or H, or both of Ar and H may be 1 wtppm or more and 10 wtppm or less. It is effective to produce Cu or Cu alloy ingots contained in the range of.
- a method for producing this ingot a method for introducing Ar or H into the atmosphere when producing a Cu or Cu alloy ingot by melt casting can be mentioned.
- a Cu or Cu alloy ingot as a base material of a sputtering target can be manufactured by melting and casting a single element Cu metal as a raw material and adding a single element metal as an alloy element source other than Cu as necessary. It is common. Moreover, you may use the material which Cu and the other metal element alloyed at the time of a raw material.
- Argon gas or hydrogen (H 2 ) gas is blown into the molten metal at the time of melting and casting. It is preferable to use high-purity argon gas and high-purity hydrogen gas, respectively, as the gases to be used.
- the amount of Ar and H introduced into the casting ingot can be adjusted by controlling the atmospheric composition, pressure, flow rate, etc. during casting. These parameters are controlled and adjusted so that a target amount of Ar or H is contained in the ingot as a base material of the sputtering target.
- a method in which these gases are blown during the heating and melting of the raw material in a heating and melting furnace in which the atmosphere can be controlled, in a holding furnace for the molten raw material after heating and melting A method of spraying these gases, a method of circulating these gases in an atmosphere during an electrical melting process such as high-frequency induction heating or electron beam melting, or a method of spraying these gases on the surface of a molten metal, a plasma torch, etc. Examples include various methods that are put to practical use as a copper melting casting method, such as a method in which these gases are circulated in an atmosphere during a heating and melting process using, or a method of spraying these gases on the surface of a molten metal.
- a Cu or Cu alloy ingot containing a target amount of Ar or H is processed as necessary to obtain a sputtering target.
- processing such as forging and rolling for controlling the microstructure of the structure, heat treatment, etc. may be performed in addition to processing such as cutting and surface polishing for final shape adjustment.
- the content of Ar or H is 1 wtppm or more and 10 wtppm or less when the final process is completed and the sputtering target is obtained.
- the content of Ar in the Cu or Cu alloy base material is determined by an inert gas melting-thermal conductivity analyzer (TC-436 manufactured by LECO), and the content of H is non-dispersive infrared absorption.
- TC-436 manufactured by LECO
- H non-dispersive infrared absorption
- Example 1 A high purity Cu having a purity of 6N was used as a raw material, and this was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, the shortest distance between the leading edge of the blowing port and the molten metal surface is set to 100 mm from the circular gas blowing nozzle having a diameter of 5 mm toward the surface of the molten raw material. , H 2 gas was continuously sprayed at a flow rate of 0.7 scfm (19.81 slm), and Ar gas was 24 scfm (679.2 slm). After the melting step, the molten metal was cooled to obtain a cast ingot.
- the casting ingot After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- This sputtering target was analyzed for the contents of Ar and H. As a result, the H content was 2 wtppm, and the Ar content was 1.5 wtppm.
- the evaluation method in this test is that the target is mounted on the magnetron cathode of the sputtering apparatus, the chamber is evacuated to a base vacuum level (base pressure), Ar is introduced at 4 sccm, and 38 kW of power is applied to the target in this state. It measures the continuous duration of the generated plasma. The maximum evaluation time was 350 seconds. The results are also shown in Table 1. With the target of Example 1, it was possible to maintain the plasma continuously and stably over the maximum evaluation time of 350 seconds.
- Example 2 A high purity Cu having a purity of 6N was used as a raw material, and this was heated and melted to obtain a raw material melt. At that time, the shortest distance between the leading edge of the blowing port and the surface of the molten metal from the rectangular gas blowing nozzle having a long side of 8 mm and a short side of 3 mm to the surface of the molten material during the heating and melting of the raw material The distance was set to 120 mm, and H 2 gas was continuously sprayed at a flow rate of 0.4 scfm (11.32 slm) and Ar gas 14 scfm (396.2 slm). After the melting step, the molten metal was cooled to obtain a cast ingot.
- the casting ingot After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the sputtering target was analyzed for the contents of Ar and H. As a result, the H content was 1.2 wtppm, and the Ar content was 1 wtppm. Furthermore, when this discharge target was subjected to the same discharge stability evaluation test as in Example 1, the continuous plasma duration was 320 seconds.
- Example 3 A high purity Cu having a purity of 6N was used as a raw material, and this was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, from the elliptical gas blowing nozzle having a major axis of 10 mm and a minor axis of 4 mm to the surface of the molten material, the shortest distance between the leading edge of the blowing port and the molten metal surface The distance was set to 90 mm and sprayed continuously at a flow rate of H 2 gas 0 scfm (0 slm) and Ar gas 8 scfm (226.4 slm). After the melting step, the molten metal was cooled to obtain a cast ingot.
- the casting ingot After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the H content was less than 1 wtppm (less than the detection limit), and the Ar content was 1.2 wtppm.
- the continuous plasma duration was 314 seconds.
- Example 4 A high purity Cu having a purity of 6N was used as a raw material, and this was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, from the gas blowing nozzle of the isosceles triangle whose blowing port shape is 10 mm in height and 10 mm in the base, toward the surface of the raw material melt, between the leading edge of the blowing port and the molten metal surface. The shortest distance was 110 mm, and the H 2 gas was continuously sprayed at a flow rate of 0.5 scfm (14.15 slm) and Ar gas 0 scfm (0 slm).
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the H content was 1.2 wtppm
- the Ar content was less than 1 wtppm (less than the detection limit).
- this sputtering target was subjected to the same discharge stability evaluation test as in Example 1, the continuous duration of the plasma was 307 seconds.
- Example 5 0.1 wt% of high-purity Al having a purity of 5N or more was added to high-purity Cu having a purity of 6N as a raw material, and this was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, the shortest distance between the leading edge of the blowing port and the molten metal surface is set to 120 mm from the circular gas blowing nozzle having a diameter of 7 mm toward the surface of the molten metal. , H 2 gas was continuously sprayed at a flow rate of 0.3 scfm (8.49 slm) and Ar gas at 10 scfm (283 slm).
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the sputtering target was analyzed for the contents of Ar and H. The amount of H was 1.5 wtppm, and the amount of Ar was 1 wtppm. Furthermore, when the same discharge stability evaluation test as in Example 1 was performed on this sputtering target, the continuous duration of plasma was 299 seconds.
- Example 6 1.0 wt% of high purity Al having a purity of 5N or more was added to high purity Cu having a purity of 6N to obtain a raw material, which was heated and melted to obtain a raw material melt.
- the shortest distance between the tip of the blowing port and the molten metal surface is set to 130 mm from the circular gas blowing nozzle having a diameter of 10 mm toward the surface of the molten raw material.
- H 2 gas was continuously blown at a flow rate of 0.2 scfm (8.49 slm) and Ar gas 8 scfm (283 slm). After the melting step, the molten metal was cooled to obtain a cast ingot.
- the casting ingot After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the sputtering target was analyzed for the contents of Ar and H.
- the amount of H was 1.4 wtppm, and the amount of Ar was 1 wtppm.
- the continuous plasma duration was 304 seconds.
- Example 7 5.0 wt% of high purity Al having a purity of 5N or more was added to high purity Cu having a purity of 6N to obtain a raw material, which was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, from the elliptical gas blowing nozzle having a major diameter of 15 mm and a minor diameter of 10 mm from the elliptical gas blowing nozzle toward the surface of the raw material melt, between the most advanced of the blowing port and the surface of the molten metal.
- the shortest distance was set to 80 mm, and H 2 gas was continuously sprayed at a flow rate of 0.5 scfm (14.15 slm) and Ar gas 16 scfm (452.8 slm).
- the molten metal was cooled to obtain a cast ingot.
- the sputtering target was analyzed for the contents of Ar and H.
- the amount of H was 2.1 wtppm, and the amount of Ar was 2 wtppm.
- the plasma continuous duration was 311 seconds.
- Example 8 High purity Al having a purity of 5N or more was added to high purity Cu having a purity of 6N to obtain a raw material, and this was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, from the gas blowing nozzle with an isosceles triangle having a bottom of 15 mm mm and a height of 10 mm toward the surface of the raw material melt, between the leading edge of the blowing port and the surface of the molten metal The shortest distance was 110 mm, and H 2 gas was continuously sprayed at a flow rate of 0 scfm (0 slm) and Ar gas at 10 scfm (283 slm).
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the H content was less than 1 wtppm (less than the detection limit), and the Ar content was 1.3 wtppm.
- the continuous plasma duration was 305 seconds.
- Example 9 0.5 wt% of high-purity Al having a purity of 5N or more was added to high-purity Cu having a purity of 6N to obtain a raw material, which was heated and melted to obtain a raw material melt.
- the shape of the blowing port is from a square gas blowing nozzle having a long side of 15 mm and a short side of 10 mm toward the surface of the raw material melt, between the leading edge of the blowing port and the molten metal surface.
- the shortest distance was set to 130 mm, and the H 2 gas was continuously sprayed at a flow rate of 0.4 scfm (11.32 slm) and Ar gas 0 scfm (0 slm).
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the H content was 1.3 wtppm
- the Ar content was less than 1 wtppm (less than the detection limit).
- the plasma continuous duration was 296 seconds.
- Example 10 0.1 wt% of high-purity Mn having a purity of 4N or more was added to high-purity Cu having a purity of 6N to obtain a raw material, which was heated and melted to obtain a raw material melt.
- the shape of the blowing port is from a square gas blowing nozzle having a long side of 15 mm and a short side of 10 mm toward the surface of the raw material melt, between the leading edge of the blowing port and the molten metal surface.
- the shortest distance was 90 mm, and H 2 gas was continuously sprayed at a flow rate of 0.3 scfm (8.49 slm) and Ar gas at 10 scfm (283 slm).
- the molten metal was cooled to obtain a cast ingot.
- After taking out the casting ingot it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- This sputtering target was analyzed for the contents of Ar and H.
- the H content was 1.2 wtppm
- the Ar content was 1.4 wtppm.
- the plasma continuous duration was 334 seconds.
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- This sputtering target was analyzed for the contents of Ar and H. As a result, the H content was 1.8 wtppm, and the Ar content was 1.5 wtppm. Furthermore, when the same discharge stability evaluation test as that of Example 1 was performed on this sputtering target, the plasma continuous duration was 305 seconds.
- Example 12 15 wt% of high-purity Mn having a purity of 4N or more was added to high-purity Cu having a purity of 6N to obtain a raw material, which was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, from the gas injection nozzle having an elliptical shape with a 20 mm long change and a short side of 10 mm to the surface of the raw material melt, between the tip of the injection port and the molten metal surface. The shortest distance was 100 mm, and H 2 gas was continuously blown at a flow rate of 0.4 scfm (11.32 slm) and Ar gas 15 scfm (424.5 slm).
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the sputtering target was analyzed for the contents of Ar and H. The amount of H was 1.5 wtppm, and the amount of Ar was 1 wtppm. Furthermore, when this discharge target was subjected to the same discharge stability evaluation test as in Example 1, the plasma continuous duration was 289 seconds.
- Example 13 8.0 wt% of high purity Mn having a purity of 4N or more was added to high purity Cu having a purity of 6N to obtain a raw material, and this was heated and melted to obtain a raw material melt.
- the shortest distance between the leading edge of the blowing port and the molten metal surface is set to 80 mm from the square gas blowing nozzle having a side of 5 mm toward the surface of the molten raw material.
- H 2 gas 0 scfm (0 slm) and Ar gas 6 scfm (169.8 slm) were continuously blown.
- the molten metal was cooled to obtain a cast ingot.
- the casting ingot After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the H content was less than 1 wtppm (less than the detection limit), and the Ar content was 1.4 wtppm.
- the plasma continuous duration was 300 seconds.
- Example 14 1.0 wt% of high purity Mn having a purity of 4N or more was added to high purity Cu having a purity of 6N to obtain a raw material, which was heated and melted to obtain a raw material melt. At that time, during the heating and melting of the raw material, the shortest distance between the tip of the blowing port and the molten metal surface is set to 90 mm from the circular gas blowing nozzle having a diameter of 8 mm toward the surface of the molten raw material. , H 2 gas was continuously sprayed at a flow rate of 0.3 scfm (8.49 slm) and Ar gas at 0 scfm (0 slm).
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- the H content was 1.2 wtppm
- the Ar content was less than 1 wtppm (less than the detection limit).
- the plasma continuous duration was 280 seconds.
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- This sputtering target was analyzed for the contents of Ar and H. As a result, both the H content and the Ar content were less than 1 wtppm (less than the detection limit). Furthermore, when the same discharge stability evaluation test as in Example 1 was performed on this sputtering target, the plasma continuous duration was only 87 seconds, which was significantly shorter than in each example. .
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- This sputtering target was analyzed for the contents of Ar and H. As a result, both the H content and the Ar content were less than 1 wtppm (less than the detection limit). Further, when the same discharge stability evaluation test as in Example 1 was conducted on this sputtering target, the plasma continuous duration was 122 seconds, which was significantly shorter than in each Example.
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- This sputtering target was analyzed for the contents of Ar and H. As a result, both the H content and the Ar content were less than 1 wtppm (less than the detection limit). Further, when the same discharge stability evaluation test as in Example 1 was conducted on this sputtering target, the plasma continuous duration was 143 seconds, which was significantly shorter than in each Example.
- the molten metal was cooled to obtain a cast ingot. After taking out the casting ingot, it was processed into a shape having a diameter of 440 mm and a thickness of 12 mm to obtain a Cu sputtering target.
- This sputtering target was analyzed for the contents of Ar and H. As a result, both the H content and the Ar content were less than 1 wtppm (less than the detection limit). Furthermore, when the same discharge stability evaluation test as in Example 1 was performed on this sputtering target, the plasma continuous duration was only 75 seconds, which was significantly shorter than in each example. .
- the discharge is continuously maintained as compared with the conventional sputtering target even under conditions where it is difficult to maintain a continuous discharge as a discharge gas condition such as a low pressure condition and a low flow rate condition.
- a discharge gas condition such as a low pressure condition and a low flow rate condition.
- the sputtering target of the present invention can be effectively used for processes such as a Cu wiring type such as LIS, which has recently been required to have a low pressure sputtering process.
- the design of the wiring layer composition and the degree of freedom of process conditions can be expanded, so that it can be said that the applicability and technical contribution in industrial fields such as semiconductor device manufacturing are extremely high.
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Abstract
Description
1)銅または銅合金からなるスパッタリングターゲットであって、アルゴンまたは水素のいずれか、あるいは両者を、アルゴンまたは水素それぞれについて1wtppm以上10wtppm以下含有することを特徴とするスパッタリングターゲット、
2)前記アルゴンまたは水素のうち、アルゴンのみを含有することを特徴とする前記1)に記載のスパッタリングターゲット、
3)前記アルゴンまたは水素のうち、水素のみを含有することを特徴とする前記1)に記載のスパッタリングターゲット、
4)前記アルゴンと水素の両者を含有することを特徴とする前記1)に記載のスパッタリングターゲット、
5)前記スパッタリングターゲットが、アルミニウムまたはマンガンの何れかを含む銅合金からなることを特徴とする、前記1)~4)のいずれか一に記載のスパッタリングターゲット、
6)前記銅合金が、アルミニウムを0.1~5wt%、またはマンガンを0.1~15wt%含む銅合金であることを特徴とする、前記1)~5)のいずれか一に記載のスパッタリングターゲット、
7)前記1)~6)のいずれか一に記載のスパッタリングターゲットの製造方法であって、原料をアルゴン、または水素、あるいはそれら両者を原料に吹き込みながら溶解する工程、前記溶解した原料を冷却固化して銅または銅合金インゴットとする工程前記インゴットを加工処理してスパッタリングターゲットとする工程を含むことを特徴とする、スパッタリングターゲットの製造方法、
純度6Nの高純度Cuを原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径5mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を100mmとして、H2ガス0.7scfm(19.81slm)、Arガス24scfm(679.2slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は2wtppm、Ar量は1.5wtppmであった。
純度6Nの高純度Cuを原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が長辺8mm短辺3mmの長方形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を120mmとして、H2ガス0.4scfm(11.32slm)、Arガス14scfm(396.2slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.2wtppm、Ar量は1wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は320秒であった。
純度6Nの高純度Cuを原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が長径10mm短径4mmの楕円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を90mmとして、H2ガス0scfm(0slm)、Arガス8scfm(226.4slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1wtppm未満(検出限界未満)、Ar量は1.2wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は314秒であった。
純度6Nの高純度Cuを原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が底辺10mm高さ10mmの二等辺三角形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を110mmとして、H2ガス0.5scfm(14.15slm)、Arガス0scfm(0slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.2wtppm、Ar量は1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は307秒であった。
純度6Nの高純度Cuに純度5N以上の高純度Alを0.1wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径7mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を120mmとして、H2ガス0.3scfm(8.49slm)、Arガス10scfm(283slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.5wtppm、Ar量は1wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は299秒であった。
純度6Nの高純度Cuに純度5N以上の高純度Alを1.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径10mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を130mmとして、H2ガス0.2scfm(8.49slm)、Arガス8scfm(283slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.4wtppm、Ar量は1wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は304秒であった。
純度6Nの高純度Cuに純度5N以上の高純度Alを5.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が長径15mm、短径10mmの楕円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を80mmとして、H2ガス0.5scfm(14.15slm)、Arガス16scfm(452.8slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は2.1wtppm、Ar量は2wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は311秒であった。
純度6Nの高純度Cuに純度5N以上の高純度Alを3.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が底辺15mmm、高さ10mmの二等辺三角形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を110mmとして、H2ガス0scfm(0slm)、Arガス10scfm(283slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1wtppm未満(検出限界未満)、Ar量は1.3wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は305秒であった。
純度6Nの高純度Cuに純度5N以上の高純度Alを0.5wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が長辺15mmm、短辺10mmの四角形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を130mmとして、H2ガス0.4scfm(11.32slm)、Arガス0scfm(0slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.3wtppm、Ar量は1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間296秒であった。
純度6Nの高純度Cuに純度4N以上の高純度Mnを0.1wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が長辺15mmm、短辺10mmの四角形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を90mmとして、H2ガス0.3scfm(8.49slm)、Arガス10scfm(283slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.2wtppm、Ar量は1.4wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間334秒であった。
純度6Nの高純度Cuに純度4N以上の高純度Mnを2.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が底辺12mm、高さ8mmの二等辺三角形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を50mmとして、H2ガス0.5scfm(14.15slm)、Arガス17scfm(481.1slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.8wtppm、Ar量は1.5wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間305秒であった。
純度6Nの高純度Cuに純度4N以上の高純度Mnを15wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が長変20mm、短辺10mmの楕円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を100mmとして、H2ガス0.4scfm(11.32slm)、Arガス15scfm(424.5slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.5wtppm、Ar量は1wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間289秒であった。
純度6Nの高純度Cuに純度4N以上の高純度Mnを8.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が一辺5mmの正方形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を80mmとして、H2ガス0scfm(0slm)、Arガス6scfm(169.8slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1wtppm未満(検出限界未満)、Ar量は1.4wtppmであった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間300秒であった。
純度6Nの高純度Cuに純度4N以上の高純度Mnを1.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径8mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を90mmとして、H2ガス0.3scfm(8.49slm)、Arガス0scfm(0slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量は1.2wtppm、Ar量は1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間280秒であった。
純度6Nの高純度Cuを原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径5mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を500mmとして、H2ガス0scfm(0slm)、Arガス6scfm(169.8slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量、Ar量ともに1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は135秒であり、各実施例と比較して大幅に短いものであった。
純度6Nの高純度Cuを原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径50mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を200mmとして、H2ガス0.5scfm(14.15slm)、Arガス0scfm(0slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量、Ar量ともに1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は125秒であり、各実施例と比較して大幅に短いものであった。
純度6Nの高純度Cuに純度5N以上の高純度Alを2.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径50mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を200mmとして、H2ガス0.3scfm(8.49slm)、Arガス10scfm(283slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量、Ar量ともに1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間はわずか87秒であり、各実施例と比較して大幅に短いものであった。
純度6Nの高純度Cuに純度5N以上の高純度Alを0.5wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径5mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を500mmとして、H2ガス0scfm(0slm)、Arガス6scfm(169.8slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量、Ar量ともに1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は122秒であり、各実施例と比較して大幅に短いものであった。
純度6Nの高純度Cuに純度4N以上の高純度Mnを0.1wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径50mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を200mmとして、H2ガス0.4scfm(11.32slm)、Arガス14scfm(396.2slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量、Ar量ともに1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間は143秒であり、各実施例と比較して大幅に短いものであった。
純度6Nの高純度Cuに純度4N以上の高純度Mnを1.0wt%添加して原料とし、これを加熱溶解して原料溶湯とした。その際、原料の加熱溶解の間、吹き込み口形状が直径5mmの円形のガス吹込みノズルから、原料溶湯の表面へ向けて、吹き込み口の最先端と溶湯表面との間の最短距離を500mmとして、H2ガス0.1scfm(2.83slm)、Arガス4scfm(113.2slm)の流量で継続的に吹き掛けた。溶解工程の後、溶湯の冷却を行うことで鋳造インゴットを得た。鋳造インゴットを取り出した後、直径440mm、厚さ12mmの形状に加工してCuスパッタリングターゲットとした。このスパッタリングターゲットについて、ArおよびHそれぞれの含有量分析を行ったところ、H量、Ar量ともに1wtppm未満(検出限界未満)であった。さらに、このスパッタリングターゲットについて、実施例1と同様の放電安定性の評価試験を行ったところ、プラズマの連続持続時間はわずか75秒であり、各実施例と比較して大幅に短いものであった。
Claims (7)
- 銅または銅合金からなるスパッタリングターゲットであって、アルゴンまたは水素のいずれか、あるいは両者を、アルゴンまたは水素それぞれについて1wtppm以上10wtppm以下含有することを特徴とするスパッタリングターゲット。
- 前記アルゴンまたは水素のうち、アルゴンのみを含有することを特徴とする請求項1に記載のスパッタリングターゲット。
- 前記アルゴンまたは水素のうち、水素のみを含有することを特徴とする請求項1または2に記載のスパッタリングターゲット。
- 前記アルゴンと水素の両者を含有することを特徴とする請求項1に記載のスパッタリングターゲット
- 前記スパッタリングターゲットが、アルミニウムまたはマンガンの何れかを含む銅合金からなることを特徴とする、請求項1~4のいずれか一項に記載のスパッタリングターゲット。
- 前記銅合金が、アルミニウムを0.1~5wt%、またはマンガンを0.1~15wt%含む銅合金であることを特徴とする、請求項1~5のいずれか一項に記載のスパッタリングターゲット。
- 請求項1~6のいずれか一項に記載のスパッタリングターゲットの製造方法であって、
銅または銅合金原料を用意する工程、
前記用意した原料をアルゴン、または水素、あるいはそれら両者を導入した雰囲気中で溶解する工程、
前記溶解した原料を冷却固化して銅または銅合金インゴットとする工程
前記インゴットを加工処理してスパッタリングターゲットとする工程
を含むことを特徴とする、
スパッタリングターゲットの製造方法。
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2017
- 2017-03-07 EP EP17763230.4A patent/EP3428309A4/en not_active Withdrawn
- 2017-03-07 US US16/082,967 patent/US20190085442A1/en not_active Abandoned
- 2017-03-07 SG SG11201807093PA patent/SG11201807093PA/en unknown
- 2017-03-07 KR KR1020187026266A patent/KR102192280B1/ko active IP Right Grant
- 2017-03-07 JP JP2018504501A patent/JP6567762B2/ja active Active
- 2017-03-07 CN CN201780015432.1A patent/CN108699680A/zh active Pending
- 2017-03-07 WO PCT/JP2017/008965 patent/WO2017154890A1/ja active Application Filing
- 2017-03-09 TW TW106107674A patent/TW201804009A/zh unknown
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WO2003064722A1 (fr) * | 2002-01-30 | 2003-08-07 | Nikko Materials Company, Limited | Cible de pulverisation d'alliage de cuivre et procede de fabrication de cette cible |
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Also Published As
Publication number | Publication date |
---|---|
KR102192280B1 (ko) | 2020-12-17 |
EP3428309A1 (en) | 2019-01-16 |
JP6567762B2 (ja) | 2019-08-28 |
US20190085442A1 (en) | 2019-03-21 |
SG11201807093PA (en) | 2018-09-27 |
TW201804009A (zh) | 2018-02-01 |
CN108699680A (zh) | 2018-10-23 |
EP3428309A4 (en) | 2020-02-12 |
KR20180111994A (ko) | 2018-10-11 |
JPWO2017154890A1 (ja) | 2018-07-05 |
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