WO2012108506A1 - 酸化物焼結体およびスパッタリングターゲット - Google Patents
酸化物焼結体およびスパッタリングターゲット Download PDFInfo
- Publication number
- WO2012108506A1 WO2012108506A1 PCT/JP2012/052980 JP2012052980W WO2012108506A1 WO 2012108506 A1 WO2012108506 A1 WO 2012108506A1 JP 2012052980 W JP2012052980 W JP 2012052980W WO 2012108506 A1 WO2012108506 A1 WO 2012108506A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sintered body
- oxide sintered
- oxide
- sputtering target
- sputtering
- 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.)
- Ceased
Links
Images
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
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/453—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/453—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates
- C04B35/457—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates based on tin oxides or stannates
-
- 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
- C23C14/08—Oxides
-
- 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
- C23C14/08—Oxides
- C23C14/086—Oxides of zinc, germanium, cadmium, indium, tin, thallium or bismuth
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3284—Zinc oxides, zincates, cadmium oxides, cadmiates, mercury oxides, mercurates or oxide forming salts thereof
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3286—Gallium oxides, gallates, indium oxides, indates, thallium oxides, thallates or oxide forming salts thereof, e.g. zinc gallate
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3293—Tin oxides, stannates or oxide forming salts thereof, e.g. indium tin oxide [ITO]
Definitions
- the present invention relates to an oxide sintered body and a sputtering target used when an oxide semiconductor thin film of a thin film transistor (TFT) used in a display device such as a liquid crystal display or an organic EL display is formed by a sputtering method.
- TFT thin film transistor
- Amorphous (amorphous) oxide semiconductors used for TFTs have higher carrier mobility than general-purpose amorphous silicon (a-Si), a large optical band gap, and can be deposited at low temperatures. It is expected to be applied to next-generation displays that require high resolution and high-speed driving, and resin substrates with low heat resistance.
- a sputtering method is preferably used in which a sputtering target made of the same material as the film is sputtered. In-plane uniformity of component composition and film thickness in the film surface direction (in the film surface) is smaller in the thin film formed by sputtering compared to thin films formed by ion plating, vacuum evaporation, and electron beam evaporation. This is because it has the advantage that a thin film having the same composition as the sputtering target can be formed.
- the sputtering target is usually formed by mixing and sintering oxide powder and machining.
- an In-containing amorphous oxide semiconductor [In—Ga—Zn—O, In—Zn—O, In—Sn—O (ITO), etc.]
- In is used as a rare metal, there is a concern about an increase in material cost in a mass production process. Therefore, a ZTO-based oxide semiconductor that has been made amorphous by adding Sn to Zn has been proposed as an oxide semiconductor that does not contain expensive In and can reduce material costs and is suitable for mass production.
- No. 4 discloses a sputtering target useful for producing the ZTO-based oxide semiconductor film.
- Patent Document 1 proposes a method of suppressing the occurrence of abnormal discharge and cracking during sputtering by performing long-time baking and controlling the structure so as not to contain a tin oxide phase.
- Patent Document 2 also suppresses abnormal discharge during sputtering by increasing the density of the ZTO-based sintered body by performing a two-step process of a low-temperature calcined powder manufacturing process at 900 to 1300 ° C. and a main baking process.
- a method has been proposed.
- Patent Document 3 proposes a method of improving the conductivity and increasing the density by including a spinel-type AB 2 O 4 compound.
- Patent Document 4 proposes a method of obtaining a dense ZTO-based sintered body by performing two steps of a low-temperature calcined powder manufacturing process at 900 to 1100 ° C. and a main baking process.
- Patent Document 5 proposes a low In content ZTO-based sputtering target as a sputtering target for forming a transparent conductive film having a low specific resistance and a high relative density even if the amount of In in ITO is reduced.
- the bixbite structure compound represented by In 2 O 3 and Zn 2 SnO 4 are used.
- a sputtering target used for manufacturing an oxide semiconductor film for a display device and an oxide sintered body that is a material thereof have excellent conductivity and high relative density.
- An oxide semiconductor film obtained using the above sputtering target is desired to have high carrier mobility and very excellent in-plane uniformity.
- DC direct current
- RF high frequency
- the present invention has been made in view of the above circumstances, and an object thereof is suitably used for manufacturing an oxide semiconductor film for a display device, and an oxide sintered body having high conductivity (low electrical resistivity) and It is to provide a sputtering target. Another object of the present invention is to provide a sputtering target that is further excellent in discharge stability. Another object of the present invention is to form an oxide semiconductor film having high carrier mobility and extremely excellent in-plane uniformity at low cost and stably by a direct current sputtering method capable of high-speed film formation. An object is to provide an oxide sintered body and a sputtering target that can be formed into a film.
- the oxide sintered body of the present invention that has solved the above problems is an oxide sintered body obtained by mixing and sintering zinc oxide, tin oxide, and indium oxide powders,
- the oxide sintered body has a relative density of 90% or more and a specific resistance of 1 ⁇ ⁇ cm or less.
- the sputtering target of the present invention that has solved the above problems is a sputtering target obtained using the oxide sintered body according to any one of the above, and has a relative density of 90% or more and a specific resistance. Has a gist where it is 1 ⁇ ⁇ cm or less.
- the discharge stability is extremely high.
- An excellent sputtering target can be obtained.
- the sputtering target of the present invention uniformly includes a crystalline phase having excellent discharge stability as described above, an oxide semiconductor film having extremely excellent in-plane uniformity and high carrier mobility can be easily formed at high speed. Since the direct current sputtering method can form a film at a low cost and stably, the productivity of the thin film is improved.
- FIG. 1 is a diagram showing a basic process for producing an oxide sintered body and a sputtering target of the present invention.
- FIG. 2 is a diagram showing the X-ray diffraction result of the oxide sintered body of the present invention in FIG.
- the inventors of the present invention are oxide sintered bodies obtained by mixing and sintering zinc oxide, tin oxide, and indium oxide powders, and have high conductivity (low specific resistance) and high relative strength. It has a high density, can be applied with a direct current sputtering method, has excellent discharge stability when used as a sputtering target, and also has excellent in-plane uniformity and carrier movement. In order to provide an oxide sintered body for a sputtering target suitable for forming an oxide semiconductor thin film having a high degree of degree, studies have been repeated.
- the intensity is expressed as C
- the controlled object that satisfies the relationship of the above formula (1) achieves the intended purpose. I found it.
- extremely excellent in discharge stability means that abnormal discharge such as arcing is extremely small during sputtering. Specifically, when the number of arcing is measured by the method shown in the examples described later, the case where the number of arcing is 3 or less is evaluated as “very excellent in discharge stability”.
- excellent in in-plane uniformity means that when an oxide thin film is formed, the sheet resistance is uniform in the same film plane. That is, it means that the film thickness distribution is uniform in the film plane and the component composition is uniform. Specifically, when the sheet resistance was measured at nine locations in the same film plane by the method shown in the examples to be described later, all of the sheet resistance values at each location were all (average value of sheet resistance values at 9 locations). A case where it is controlled within a range of ⁇ 3% or less is evaluated as “excellent in-plane uniformity”.
- the composition of the oxide sintered body sputtering target
- a predetermined amount of In 2 O 3 is added to the ZTO-based oxide semiconductor oxide sintered body using ZnO and SnO 2 as raw materials.
- the relative density of the oxide sintered body is improved and the specific resistance is lowered, and as a result, stable DC discharge can be continuously obtained.
- a TFT having an oxide semiconductor thin film formed using the above sputtering target has very high characteristics such as a carrier density of 15 cm 2 / Vs or more.
- the [In] ratio is set higher than the above range, and the [Zn] ratio is set lower than the above range.
- the preferred composition ratio is different from the present invention that provides an oxide sintered body and a sputtering target suitable for forming an oxide semiconductor thin film.
- 2 ⁇ 34 ° “neighboring” generally means that the range includes 34 ° ⁇ 0.5 °. It is presumed that a crystal phase corresponding to Zn 4 Sn 2 InO 9.5 probably exists at the peak position.
- the vicinity” of 2 ⁇ 31 ° generally includes a range of 31 ° ⁇ 1 °. It is presumed that a crystal phase corresponding to ZnSnIn x O 3 + 1.5X exists at the peak position.
- 2 ⁇ 35 ° “neighboring” means that it generally includes a range of 35 ° ⁇ 0.4 °. It is presumed that a crystal phase corresponding to Zn Y In 2 O Y + 3 probably exists at the peak position.
- “2 ⁇ 26.5 °“ near ”” generally includes a range of 26.5 ° ⁇ 1 °. It is presumed that a crystal phase corresponding to SnO 2 probably exists at the peak position.
- the X-ray diffraction conditions in the present invention are as follows. Analysis device: “X-ray diffractometer RINT-1500” manufactured by Rigaku Corporation Analysis conditions Target: Cu Monochromatic: Uses a monochrome mate (K ⁇ ) Target output: 40kV-200mA (Continuous measurement) ⁇ / 2 ⁇ scanning Slit: Divergence 1/2 °, Scattering 1/2 °, Received light 0.15 mm Monochromator light receiving slit: 0.6mm Scanning speed: 2 ° / min Sampling width: 0.02 ° Measurement angle (2 ⁇ ): 5 to 90 °
- the characteristic part of the present invention is the above formula (1) from the viewpoint of remarkably improving the discharge stability during sputtering and the in-plane uniformity when an oxide semiconductor film is used.
- the relationship is set.
- satisfying the relationship of the above formula (1) [A / (A + B + C + D)] ⁇ 100 ⁇ 70) probably means that a crystal phase corresponding to Zn 4 Sn 2 InO 9.5 is mainly present. It is presumed that
- the ratio of [A / (A + B + C + D)] ⁇ 100 is less than 70, the discharge stability during sputtering and the in-plane uniformity when an oxide semiconductor film is formed are lowered.
- the ratio of [A / (A + B + C + D)] ⁇ 100 is preferably as large as possible, and 100 is most preferable.
- the ratio of [In] to [Zn] + [Sn] + [In] is referred to as the [In] ratio
- the ratio of [Zn] to [Zn] + [Sn] is referred to as the [Zn] ratio.
- the [In] ratio is preferably in the range of 0.01 to 0.35.
- the [In] ratio is less than 0.01, the relative density of the oxide sintered body cannot be improved and the specific resistance cannot be reduced, and the carrier mobility of the thin film after film formation becomes low.
- a more preferable [In] ratio is 0.10 or more.
- the [In] ratio exceeds 0.35, the TFT switching characteristics when a thin film is formed deteriorate.
- a more preferable [In] ratio is 0.30 or less, and further preferably 0.25 or less.
- [Zn] ratio is preferably 0.60 to 0.82.
- the [Zn] ratio is less than 0.60, the fine workability of the thin film formed by the sputtering method is lowered, and etching residues are likely to occur.
- the [Zn] ratio exceeds 0.82, the chemical resistance of the thin film after film formation is inferior, and the elution rate due to the acid is increased during fine processing, so that high-precision processing cannot be performed.
- a more preferable [Zn] ratio is 0.60 to 0.80.
- the oxide sintered body of the present invention satisfies a relative density of 90% or more and a specific resistance of 1 ⁇ ⁇ cm or less.
- the oxide sintered body of the present invention has a very high relative density, preferably 90% or more, and more preferably 95% or more.
- a high relative density not only can prevent the generation of cracks and nodules during sputtering, but also provides advantages such as maintaining a stable discharge continuously to the target life.
- the oxide sintered body of the present invention has a small specific resistance, preferably 1 ⁇ ⁇ cm or less, more preferably 0.1 ⁇ ⁇ cm or less. Accordingly, film formation by a direct current sputtering method using plasma discharge using a direct current power source is possible, and physical vapor deposition (sputtering method) using a sputtering target can be efficiently performed on the production line of the display device.
- the oxide sintered body of the present invention is obtained by mixing and sintering zinc oxide, tin oxide, and indium oxide powders, and the basic process from the raw material powder to the sputtering target is shown in FIG. .
- oxide powder is mixed, pulverized, dried, granulated, molded (molded (not shown)), sintered oxide sintered body, processed, bonded, and sputtering target formed. It shows the basic process to get.
- heat treatment may be performed as necessary after sintering.
- the present invention is characterized in that the sintering conditions are appropriately controlled as will be described in detail below, and the other steps are not particularly limited, and usually used steps can be appropriately selected. .
- this invention is not the meaning limited to this.
- zinc oxide powder, tin oxide powder, and indium oxide powder are mixed in a predetermined ratio, mixed and pulverized.
- the purity of each raw material powder used is preferably about 99.99% or more. This is because the presence of a trace amount of impurity elements may impair the semiconductor characteristics of the oxide semiconductor film.
- the blending ratio of each raw material powder is preferably controlled so that the ratio of Zn, Sn, and In is within the above-described range.
- Mixing and pulverization are preferably performed by using a pot mill and adding the raw material powder together with water.
- the balls and beads used in these steps are preferably made of materials such as nylon, alumina, zirconia, and the like.
- the mixed powder obtained in the above step is dried and granulated, and then molded.
- the crystal phase after sintering is controlled in the region defined by [A / (A + B + C + D)] ⁇ 100 ⁇ 70 as in the above formula (1), the crystal phase having a high melting point corresponding to the above A increases. It becomes difficult to secure. Therefore, in order to increase the density of the oxide sintered body, it is necessary to perform pressure sintering to form the oxide sintered body.
- the powder after drying and granulation is filled in, for example, a graphite mold of a predetermined size and fired at about 1000 ° C. to 1100 ° C. while being pressed with a graphite push rod or the like. It is done.
- the oxide sintered body of the present invention can be obtained by performing pressure sintering in a graphite mold.
- the sputtering target of the present invention can be obtained by processing and bonding according to a conventional method.
- the relative density and specific resistance of the sputtering target thus obtained are also very good, like the oxide sintered body, the preferred relative density is approximately 90% or more, and the preferred specific resistance is approximately 1 ⁇ ⁇ cm or less.
- Zinc oxide powder having a purity of 99.99%, tin oxide powder having a purity of 99.99%, and indium oxide powder having a purity of 99.99% are blended in various ratios as shown in Table 1, and mixed in a nylon ball mill for 20 hours. did.
- the mixed powder obtained in the above step was dried, granulated, filled into a graphite mold, and then sintered at a temperature shown in Table 1 while being pressurized at 30 MPa using a graphite rod.
- the various oxide sintered bodies thus obtained are subjected to X-ray diffraction under the above-mentioned conditions, and the XRD peak intensities A to D are measured to construct the formula (1) [A / (A + B + C + D) ] ⁇ 100 ratio was calculated. Further, the relative density of the oxide sintered body was measured by the Archimedes method, and the specific resistance was measured by the four-terminal method.
- the oxide sintered body was processed into a shape of ⁇ 4 inch ⁇ 5 mmt and bonded to a backing plate to obtain a sputtering target.
- the sputtering target thus obtained was attached to a sputtering apparatus, and an oxide semiconductor film was formed on a glass substrate (size: 100 mm ⁇ 100 mm ⁇ 0.50 mm) by a DC (direct current) magnetron sputtering method.
- the sputtering conditions were a DC sputtering power of 150 W, an Ar / 0.1 volume% O 2 atmosphere, and a pressure of 0.8 mTorr.
- a thin film transistor having a channel length of 10 ⁇ m and a channel width of 100 ⁇ m was manufactured, and carrier mobility was measured.
- Defect scatter failure state: When the number of occurrences of arcing is 10 times or more Possible (Slightly good state of spatter): 4-9 times of occurrence of arcing Good (good state of sputtering): When the number of occurrences of arcing is 3 times or less
- No. in Table 1 2, 3, 6, and 7 are examples of the present invention in which the ratio of [A / (A + B + C + D)] ⁇ 100 described above is 70 or more and satisfies the relationship of the formula (1) defined in the present invention.
- the relative density of the sputtering target was 90% or more, the specific resistance was 0.1 ⁇ ⁇ cm or less, and the sputtering stability was also very good. Further, the carrier mobility of the thin films formed using these sputtering targets was as high as 15 cm 2 / Vs or more, and the in-plane uniformity was extremely good.
- No. 1 in Table 1 No. 1 in Table 1.
- 4, 5, and 8 to 11 are comparative examples in which the ratio of [A / (A + B + C + D)] ⁇ 100 described above is less than 70 and does not satisfy the relationship of the formula (1) defined in the present invention.
- these characteristics are reduced as compared with the above-described examples of the present invention.
- some of these comparative examples have a carrier mobility of less than 15 cm 2 / Vs (Nos. 4 and 8).
- the sputtering target obtained by using the oxide sintered body that satisfies the requirements specified in the present invention and the composition ratio of the metal constituting the oxide sintered body also satisfies the preferable requirements of the present invention is In addition to having a high relative density and a low specific resistance, it was found that the stability during sputtering was also excellent. In addition, it was found that a thin film obtained using the above sputtering target is very useful as an oxide semiconductor thin film because it has high carrier mobility and extremely excellent in-plane uniformity.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Physical Vapour Deposition (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)
- Conductive Materials (AREA)
- Manufacturing Of Electric Cables (AREA)
Abstract
Description
[A/(A+B+C+D)]×100≧70 ・・・ (1)
[In]/([Zn]+[Sn]+[In])=0.01~0.35
[Zn]/([Zn]+[Sn])=0.60~0.82
[A/(A+B+C+D)]×100≧70 ・・・ (1)
分析装置:理学電機製「X線回折装置RINT-1500」
分析条件
ターゲット:Cu
単色化:モノクロメートを使用(Kα)
ターゲット出力:40kV-200mA
(連続測定)θ/2θ走査
スリット:発散1/2°、散乱1/2°、受光0.15mm
モノクロメータ受光スリット:0.6mm
走査速度:2°/min
サンプリング幅:0.02°
測定角度(2θ):5~90°
本発明の酸化物焼結体は、相対密度が非常に高く、好ましくは90%以上であり、より好ましくは95%以上である。高い相対密度は、スパッタリング中での割れやノジュールの発生を防止し得るだけでなく、安定した放電をターゲットライフまで連続して維持するなどの利点をもたらす。
本発明の酸化物焼結体は、比抵抗が小さく、1Ω・cm以下であることが好ましく、より好ましくは0.1Ω・cm以下である。これにより、直流電源を用いたプラズマ放電などによる直流スパッタリング法による成膜が可能となり、スパッタリングターゲットを用いた物理蒸着(スパッタリング法)を表示装置の生産ラインで効率よく行うことができる。
また、上記酸化物半導体膜が形成された試料を用いて、ガラス基板上の同一膜面内(サイズ:100mm×100mm×0.50mm)における任意の9箇所のシート抵抗を測定した。シート抵抗は、四端針法で測定し、下記基準で評価した。
良(膜均一性が良好):9箇所それぞれのシート抵抗の値が全て、(9箇所でのシート抵抗の平均値)に対して±3%以下の範囲内に制御されている場合
可(膜均一性がやや良好):9箇所のうち1~3箇所が、(9箇所でのシート抵抗の平均値)に対して±3%超の場合
不良(膜均一性が不良):9箇所のうち4箇所以上8箇所以下が、(9箇所でのシート抵抗の平均値)に対して±3%超の場合
上述したDCマグネトロンスパッタリングの際に発生するアーキングの発生数を、スパッタリング装置の電気回路に接続したアークモニターによりカウントした。詳細には、10分間のプリスパッタ(前述したスパッタリング条件と同じであり、DCスパッタリングパワー150W、Ar/0.1体積%O2雰囲気、圧力0.8mTorr)→前述したDCマグネトロンスパッタリングを10分間行なったときの、アーキングの発生回数を測定し、下記基準で放電安定性(スパッタ安定性)を評価した。
不良(スパッタ不良状態) :アーキング発生数が10回以上の場合
可 (スパッタやや良好状態):アーキング発生数が4~9回
良 (スパッタ良好状態) :アーキング発生数が3回以下の場合
Claims (4)
- 酸化亜鉛と、酸化スズと、酸化インジウムの各粉末と、を混合および焼結して得られる酸化物焼結体であって、
前記酸化物焼結体をX線回折し、
2θ=34°近傍のXRDピークの強度をA、
2θ=31°近傍のXRDピークの強度をB、
2θ=35°近傍のXRDピークの強度をC、
2θ=26.5°近傍のXRDピークの強度をD
で表したとき、下記式(1)を満足することを特徴とする酸化物焼結体。
[A/(A+B+C+D)]×100≧70 ・・・ (1) - 前記酸化物焼結体に含まれる金属元素の含有量(原子%)をそれぞれ、[Zn]、[Sn]、[In]としたとき、[Zn]+[Sn]+[In]に対する[In]の比、および[Zn]+[Sn]に対する[Zn]の比は、それぞれ下式を満足するものである請求項1に記載の酸化物焼結体。
[In]/([Zn]+[Sn]+[In])=0.01~0.35
[Zn]/([Zn]+[Sn])=0.60~0.82 - 相対密度90%以上、比抵抗1Ω・cm以下である請求項1または2に記載の酸化物焼結体。
- 請求項1~3のいずれかに記載の酸化物焼結体を用いて得られるスパッタリングターゲットであって、相対密度90%以上、比抵抗1Ω・cm以下であることを特徴とするスパッタリングターゲット。
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/981,729 US9175380B2 (en) | 2011-02-10 | 2012-02-09 | Oxide sintered body and sputtering target |
| CN201280005106.XA CN103298767B (zh) | 2011-02-10 | 2012-02-09 | 氧化物烧结体以及溅射标靶 |
| KR1020137021124A KR20130105735A (ko) | 2011-02-10 | 2012-02-09 | 산화물 소결체 및 스퍼터링 타깃 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011-027795 | 2011-02-10 | ||
| JP2011027795 | 2011-02-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2012108506A1 true WO2012108506A1 (ja) | 2012-08-16 |
Family
ID=46638718
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2012/052980 Ceased WO2012108506A1 (ja) | 2011-02-10 | 2012-02-09 | 酸化物焼結体およびスパッタリングターゲット |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9175380B2 (ja) |
| JP (1) | JP5750065B2 (ja) |
| KR (1) | KR20130105735A (ja) |
| CN (1) | CN103298767B (ja) |
| TW (1) | TWI519501B (ja) |
| WO (1) | WO2012108506A1 (ja) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013168748A1 (ja) | 2012-05-09 | 2013-11-14 | 株式会社神戸製鋼所 | 薄膜トランジスタおよび表示装置 |
| JP6068232B2 (ja) | 2012-05-30 | 2017-01-25 | 株式会社神戸製鋼所 | 薄膜トランジスタの半導体層用酸化物、薄膜トランジスタ、表示装置およびスパッタリングターゲット |
| KR101568631B1 (ko) | 2012-06-06 | 2015-11-11 | 가부시키가이샤 고베 세이코쇼 | 박막 트랜지스터 |
| JP6002088B2 (ja) | 2012-06-06 | 2016-10-05 | 株式会社神戸製鋼所 | 薄膜トランジスタ |
| JP2014225626A (ja) | 2012-08-31 | 2014-12-04 | 株式会社神戸製鋼所 | 薄膜トランジスタおよび表示装置 |
| JP6134230B2 (ja) | 2012-08-31 | 2017-05-24 | 株式会社神戸製鋼所 | 薄膜トランジスタおよび表示装置 |
| JP6284710B2 (ja) * | 2012-10-18 | 2018-02-28 | 出光興産株式会社 | スパッタリングターゲット、酸化物半導体薄膜及びそれらの製造方法 |
| KR101512819B1 (ko) * | 2013-02-27 | 2015-04-16 | 삼성코닝어드밴스드글라스 유한회사 | 산화아연계 스퍼터링 타겟, 그 제조방법 및 이를 통해 증착된 차단막을 갖는 박막트랜지스터 |
| WO2015068535A1 (ja) * | 2013-11-06 | 2015-05-14 | 三井金属鉱業株式会社 | スパッタリングターゲットおよびその製造方法 |
| JP6042520B1 (ja) * | 2015-11-05 | 2016-12-14 | デクセリアルズ株式会社 | Mn−Zn−O系スパッタリングターゲット及びその製造方法 |
| JP6724057B2 (ja) * | 2018-03-30 | 2020-07-15 | Jx金属株式会社 | スパッタリングターゲット部材 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007037191A1 (ja) * | 2005-09-27 | 2007-04-05 | Idemitsu Kosan Co., Ltd. | スパッタリングターゲット、透明導電膜及びタッチパネル用透明電極 |
| WO2008117810A1 (ja) * | 2007-03-26 | 2008-10-02 | Idemitsu Kosan Co., Ltd. | 非晶質酸化物半導体薄膜、その製造方法、薄膜トランジスタの製造方法、電界効果型トランジスタ、発光装置、表示装置及びスパッタリングターゲット |
| WO2010067571A1 (ja) * | 2008-12-12 | 2010-06-17 | 出光興産株式会社 | 複合酸化物焼結体及びそれからなるスパッタリングターゲット |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4560149B2 (ja) * | 1999-03-05 | 2010-10-13 | 出光興産株式会社 | 透明導電材料、透明導電ガラス及び透明導電フィルム |
| JP4933756B2 (ja) * | 2005-09-01 | 2012-05-16 | 出光興産株式会社 | スパッタリングターゲット |
| CN103469167A (zh) | 2005-09-01 | 2013-12-25 | 出光兴产株式会社 | 溅射靶、透明导电膜、透明电极和电极基板及其制造方法 |
| JP4552950B2 (ja) | 2006-03-15 | 2010-09-29 | 住友金属鉱山株式会社 | ターゲット用酸化物焼結体、その製造方法、それを用いた透明導電膜の製造方法、及び得られる透明導電膜 |
| JP4994068B2 (ja) * | 2006-08-09 | 2012-08-08 | 出光興産株式会社 | 酸化物導電性材料及びその製造方法 |
| JP5358891B2 (ja) | 2006-08-11 | 2013-12-04 | 日立金属株式会社 | 酸化亜鉛焼結体の製造方法 |
| JP5269501B2 (ja) | 2008-07-08 | 2013-08-21 | 出光興産株式会社 | 酸化物焼結体及びそれからなるスパッタリングターゲット |
| JP5024226B2 (ja) | 2008-08-06 | 2012-09-12 | 日立金属株式会社 | 酸化物焼結体およびその製造方法、スパッタリングターゲット、半導体薄膜 |
| JP5307144B2 (ja) | 2008-08-27 | 2013-10-02 | 出光興産株式会社 | 電界効果型トランジスタ、その製造方法及びスパッタリングターゲット |
| JP2010070410A (ja) * | 2008-09-17 | 2010-04-02 | Idemitsu Kosan Co Ltd | 酸化物焼結体の製造方法 |
-
2012
- 2012-02-08 JP JP2012025477A patent/JP5750065B2/ja active Active
- 2012-02-09 CN CN201280005106.XA patent/CN103298767B/zh active Active
- 2012-02-09 US US13/981,729 patent/US9175380B2/en active Active
- 2012-02-09 WO PCT/JP2012/052980 patent/WO2012108506A1/ja not_active Ceased
- 2012-02-09 KR KR1020137021124A patent/KR20130105735A/ko not_active Ceased
- 2012-02-10 TW TW101104383A patent/TWI519501B/zh active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007037191A1 (ja) * | 2005-09-27 | 2007-04-05 | Idemitsu Kosan Co., Ltd. | スパッタリングターゲット、透明導電膜及びタッチパネル用透明電極 |
| WO2008117810A1 (ja) * | 2007-03-26 | 2008-10-02 | Idemitsu Kosan Co., Ltd. | 非晶質酸化物半導体薄膜、その製造方法、薄膜トランジスタの製造方法、電界効果型トランジスタ、発光装置、表示装置及びスパッタリングターゲット |
| WO2010067571A1 (ja) * | 2008-12-12 | 2010-06-17 | 出光興産株式会社 | 複合酸化物焼結体及びそれからなるスパッタリングターゲット |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103298767A (zh) | 2013-09-11 |
| TW201249775A (en) | 2012-12-16 |
| JP5750065B2 (ja) | 2015-07-15 |
| JP2012180265A (ja) | 2012-09-20 |
| US9175380B2 (en) | 2015-11-03 |
| TWI519501B (zh) | 2016-02-01 |
| US20130306469A1 (en) | 2013-11-21 |
| KR20130105735A (ko) | 2013-09-25 |
| CN103298767B (zh) | 2014-09-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5750065B2 (ja) | 酸化物焼結体およびスパッタリングターゲット | |
| JP5651095B2 (ja) | 酸化物焼結体およびスパッタリングターゲット | |
| TWI476287B (zh) | Oxide sintered body and sputtering target | |
| JP5750063B2 (ja) | 酸化物焼結体およびスパッタリングターゲット | |
| WO2012118156A1 (ja) | 酸化物焼結体およびスパッタリングターゲット | |
| JP2012066968A (ja) | 酸化物焼結体およびスパッタリングターゲット | |
| CN104619674A (zh) | 氧化物烧结体及溅射靶、以及其制造方法 | |
| TW201538431A (zh) | 氧化物燒結體及濺鍍靶、與該氧化物燒結體之製造方法 | |
| WO2012096267A1 (ja) | 酸化物焼結体およびスパッタリングターゲット | |
| WO2012096343A1 (ja) | 酸化物焼結体およびスパッタリングターゲット | |
| TW201542464A (zh) | 氧化物燒結體、濺鍍用靶、及使用其而獲得之氧化物半導體薄膜 | |
| JP5750064B2 (ja) | 酸化物焼結体およびスパッタリングターゲット |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12745233 Country of ref document: EP Kind code of ref document: A1 |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 13981729 Country of ref document: US |
|
| ENP | Entry into the national phase |
Ref document number: 20137021124 Country of ref document: KR Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 12745233 Country of ref document: EP Kind code of ref document: A1 |