JP5521036B2 - Cu-In-Ga-Se alloy powder manufacturing method, Cu-In-Ga-Se alloy sintered body manufacturing method, and Cu-In-Ga-Se alloy powder - Google Patents
Cu-In-Ga-Se alloy powder manufacturing method, Cu-In-Ga-Se alloy sintered body manufacturing method, and Cu-In-Ga-Se alloy powderInfo
- Publication number
- JP5521036B2 JP5521036B2 JP2012517125A JP2012517125A JP5521036B2 JP 5521036 B2 JP5521036 B2 JP 5521036B2 JP 2012517125 A JP2012517125 A JP 2012517125A JP 2012517125 A JP2012517125 A JP 2012517125A JP 5521036 B2 JP5521036 B2 JP 5521036B2
- Authority
- JP
- Japan
- Prior art keywords
- alloy
- powder
- mixed
- region
- alloy powder
- 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.)
- Expired - Fee Related
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C28/00—Alloys based on a metal not provided for in groups C22C5/00 - C22C27/00
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Powder Metallurgy (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Physical Vapour Deposition (AREA)
Description
本発明は、スパッタリングターゲットとして用いることが可能なCu−In−Ga−Se合金焼結体の製造方法に関し、さらにCu−In−Ga−Se合金焼結体の原料であるCu−In−Ga合金粉末及びCu−In−Ga−Se合金粉末並びにそれらの製造方法に関する。 The present invention relates to a method for producing a Cu—In—Ga—Se alloy sintered body that can be used as a sputtering target, and further, a Cu—In—Ga alloy that is a raw material for a Cu—In—Ga—Se alloy sintered body. The present invention relates to a powder, a Cu—In—Ga—Se alloy powder, and a production method thereof.
Cu−In−Ga−Se合金(以下、CIGS)からなるCIGS層を吸収層とするCu(In、Ga)Se2系太陽電池は、薄膜太陽電池の中では最も変換効率が高く長期信頼性も実証されているため、次世代太陽電池として有力視されている。このCIGS層の形成方法は、Cu−Ga膜及びIn膜を積層で成膜し、Se雰囲気中で熱処理する方法が広く知られている。A Cu (In, Ga) Se 2 solar cell having a CIGS layer made of a Cu—In—Ga—Se alloy (hereinafter, CIGS) as an absorption layer has the highest conversion efficiency and long-term reliability among thin film solar cells. Since it has been proven, it is considered to be a promising next-generation solar cell. As a method for forming this CIGS layer, a method in which a Cu—Ga film and an In film are stacked and heat-treated in an Se atmosphere is widely known.
例えば、特許文献1には、この方法によるCIGS層の形成方法が開示されている。Cu−Ga膜及びIn膜の形成には、Cu−Ga合金ターゲット及びInターゲットを用いたスパッタリング法が用いられている。SeをSeターゲットを用いたスパッタリング法により供給すると、Seイオンによるダメージにより形成されたCIGS層の変換効率が小さくなるため、Seは熱処理により供給するとされている。 For example, Patent Document 1 discloses a method for forming a CIGS layer by this method. For the formation of the Cu—Ga film and the In film, a sputtering method using a Cu—Ga alloy target and an In target is used. If Se is supplied by a sputtering method using a Se target, the conversion efficiency of the CIGS layer formed by damage caused by Se ions is reduced, and therefore Se is supplied by heat treatment.
しかしながら、特許文献1に記載の方法では、多層膜の積層やSe雰囲気処理を行うためにCIGS層の製造コストを削減することは困難である。ここで、CIGSからなるスパッタリングターゲットであるCIGSターゲットを用いてスパッタリング法によりCIGS層を形成することができれば、多層膜の積層やSe雰囲気処理の必要はなく、製造コストを低減させることが可能である。 However, with the method described in Patent Document 1, it is difficult to reduce the manufacturing cost of the CIGS layer in order to perform multilayer film stacking and Se atmosphere treatment. Here, if a CIGS layer can be formed by a sputtering method using a CIGS target that is a sputtering target made of CIGS, it is not necessary to stack a multilayer film or to perform an Se atmosphere treatment, and it is possible to reduce manufacturing costs. .
ところがCIGSターゲットの作製は困難であるとされてきた。その理由は、各元素の単金属を溶解、混合してCIGSを作製する際にInとSeが爆発的な発熱反応を示すためである。そこで本発明者らは、この点を考慮してCIGSターゲットとして用いることが可能な、CIGS焼結体を安全に製造する方法を検討した。 However, it has been difficult to produce a CIGS target. The reason is that In and Se exhibit an explosive exothermic reaction when a single metal of each element is dissolved and mixed to produce CIGS. In view of this point, the present inventors studied a method for safely manufacturing a CIGS sintered body that can be used as a CIGS target.
以上のような事情に鑑み、本発明の目的は、安全に製造することが可能なCu−In−Ga−Se合金焼結体、その材料及びそれらの製造方法を提供することにある。 In view of the circumstances as described above, an object of the present invention is to provide a Cu—In—Ga—Se alloy sintered body, a material thereof, and a method for producing them, which can be produced safely.
上記目的を達成するため、本発明の一実施形態に係るCu−In−Ga−Se合金を作製するためのCu−In−Ga合金粉末の製造方法は、Cu−In−Ga合金溶湯を作製する。Cu−In−Ga合金薄帯は、上記Cu−In−Ga合金溶湯をストリップキャスト法により凝固させて作製される。上記Cu−In−Ga合金薄帯は粉砕される。 In order to achieve the above object, a method for producing a Cu—In—Ga alloy powder for producing a Cu—In—Ga—Se alloy according to an embodiment of the present invention produces a molten Cu—In—Ga alloy. . The Cu—In—Ga alloy ribbon is produced by solidifying the above-described molten Cu—In—Ga alloy by a strip casting method. The Cu—In—Ga alloy ribbon is pulverized.
この製造方法によれば、Inを主成分とする第1の領域と、Cu−Ga合金を主成分とし上記第1の領域中に分散した粒径1μm以下の粒状である第2の領域とを有するCu−In−Ga合金粉末を製造することが可能である。このCu−In−Ga合金粉末をSe粉末と混合して溶融させると、Cu、In、Ga及びSeの各元素が合金化する。ここで、このCu−In−Ga合金粉末は、第1の領域と第2の領域とを有しているため、合金化の際に第1の領域で発生するSeとInの発熱反応が、第2の領域で発生するSeとCuの吸熱反応により減殺され、系全体の発熱が抑制される。これにより、爆発的反応による溶湯の飛散が防止され、安全にCu−In−Ga−Sn合金粉末を作製することが可能となる。 According to this manufacturing method, the first region containing In as a main component and the second region containing a Cu—Ga alloy as a main component and having a particle size of 1 μm or less dispersed in the first region are provided. Cu-In-Ga alloy powder can be produced. When this Cu-In-Ga alloy powder is mixed with Se powder and melted, Cu, In, Ga and Se elements are alloyed. Here, since this Cu—In—Ga alloy powder has the first region and the second region, the exothermic reaction of Se and In that occurs in the first region during alloying, It is diminished by the endothermic reaction of Se and Cu generated in the second region, and the heat generation of the entire system is suppressed. Thereby, scattering of the molten metal due to explosive reaction is prevented, and Cu—In—Ga—Sn alloy powder can be produced safely.
上記目的を達成するため、本発明の一実施形態に係るCu−In−Ga−Se合金粉末の製造方法は、Cu−In−Ga合金溶湯を作製する。Cu−In−Ga合金薄帯は、上記Cu−In−Ga合金溶湯をストリップキャスト法により凝固させて作製される。Cu−In−Ga合金粉末は、上記Cu−In−Ga合金薄帯を粉砕して作製される。Cu−In−Ga合金及びSe混合粉末は、上記Cu−In−Ga合金粉末とSe粉末とが混合されて作製される。上記Cu−In−Ga合金及びSe混合粉末は焼成される。 In order to achieve the above object, a Cu—In—Ga—Se alloy powder production method according to an embodiment of the present invention produces a Cu—In—Ga alloy melt. The Cu—In—Ga alloy ribbon is produced by solidifying the above-described molten Cu—In—Ga alloy by a strip casting method. The Cu—In—Ga alloy powder is produced by pulverizing the Cu—In—Ga alloy ribbon. The Cu—In—Ga alloy and the Se mixed powder are produced by mixing the Cu—In—Ga alloy powder and the Se powder. The Cu—In—Ga alloy and Se mixed powder are fired.
この製造方法によれば、Cu−In−Ga合金及びSe混合粉末の焼成の際に、溶融したSeとInの発熱反応に起因する爆発的反応による溶湯の飛散が防止され、Cu−In−Ga−Se合金粉末を製造することが可能である。 According to this manufacturing method, when the Cu—In—Ga alloy and the Se mixed powder are fired, the molten metal is prevented from being scattered due to an explosive reaction caused by the exothermic reaction between molten Se and In, and Cu—In—Ga. -It is possible to produce Se alloy powder.
上記目的を達成するため、本発明の一実施形態に係るCu−In−Ga−Se合金焼結体の製造方法は、Cu−In−Ga合金溶湯を作製する。Cu−In−Ga合金薄帯は、上記Cu−In−Ga合金溶湯をストリップキャスト法により凝固させて作製される。Cu−In−Ga合金粉末は、上記Cu−In−Ga合金薄帯を粉砕して作製される。Cu−In−Ga合金及びSe混合粉末は、上記Cu−In−Ga合金粉末とSe粉末とが混合されて作製される。Cu−In−Ga−Se合金粉末は、上記Cu−In−Ga合金及びSe混合粉末が焼成されて作製される。上記Cu−In−Ga−Se合金粉末は、焼結される。 In order to achieve the above object, a Cu—In—Ga—Se alloy sintered body manufacturing method according to an embodiment of the present invention produces a Cu—In—Ga alloy molten metal. The Cu—In—Ga alloy ribbon is produced by solidifying the above-described molten Cu—In—Ga alloy by a strip casting method. The Cu—In—Ga alloy powder is produced by pulverizing the Cu—In—Ga alloy ribbon. The Cu—In—Ga alloy and the Se mixed powder are produced by mixing the Cu—In—Ga alloy powder and the Se powder. The Cu—In—Ga—Se alloy powder is produced by firing the Cu—In—Ga alloy and Se mixed powder. The Cu—In—Ga—Se alloy powder is sintered.
この製造方法によれば、Cu−In−Ga合金及びSe混合粉末の焼成の際に、溶融したSeとInの発熱反応に起因する爆発的反応による溶湯の飛散が防止され、Cu−In−Ga−Se合金粉末が作製される。Cu−In−Ga−Se合金粉末を焼結する際には、既にSeとInの合金化は完了、もしくはほぼ完了しているため、SeとInの発熱反応に起因する爆発的反応は発生せず、Cu−In−Ga−Se合金焼結体を製造することが可能である。 According to this manufacturing method, when the Cu—In—Ga alloy and the Se mixed powder are fired, the molten metal is prevented from being scattered due to an explosive reaction caused by the exothermic reaction between molten Se and In, and Cu—In—Ga. -Se alloy powder is produced. When sintering Cu—In—Ga—Se alloy powder, since the alloying of Se and In is already completed or almost completed, no explosive reaction due to the exothermic reaction of Se and In occurs. First, it is possible to manufacture a Cu—In—Ga—Se alloy sintered body.
上記Cu−In−Ga−Se合金焼結体の製造方法は、上記Cu−In−Ga−Se合金粉末を焼結して作製された上記Cu−In−Ga−Se合金焼結体をターゲット形状に加工する工程をさらに有してもよい。 The Cu-In-Ga-Se alloy sintered body is manufactured by sintering the Cu-In-Ga-Se alloy powder, which is prepared by sintering the Cu-In-Ga-Se alloy powder. You may further have the process processed into.
この製造方法によれば、上記Cu−In−Ga−Se合金焼結体をCu−In−Ga−Se合金からなるスパッタリングターゲットとすることが可能である。 According to this manufacturing method, the Cu—In—Ga—Se alloy sintered body can be used as a sputtering target made of a Cu—In—Ga—Se alloy.
上記目的を達成するため、本発明の一実施形態に係るCu−In−Ga−Se合金を作製するためのCu−In−Ga合金粉末は、第1の領域と、第2の領域とを具備する。
上記第1の領域は、Inを主成分とする。
上記第2の領域は、Cu−Ga合金を主成分とし、上記第1の領域中に分散した粒径1μm以下の粒状である。In order to achieve the above object, a Cu—In—Ga alloy powder for producing a Cu—In—Ga—Se alloy according to an embodiment of the present invention includes a first region and a second region. To do.
The first region contains In as a main component.
The second region has a particle size of 1 μm or less dispersed mainly in the Cu—Ga alloy and dispersed in the first region.
このCu−In−Ga合金粉末をSe粉末と混合して溶融させると、Cu、In、Ga及びSeの各元素が合金化する。ここで、このCu−In−Ga合金粉末は、Inを主成分とする第1の領域と、第1の領域中に分散したCu−Ga合金を主成分とする第2の領域を有している。このため、合金化の際に第1の領域で発生するSeとInの発熱反応が、第2の領域で発生するSeとCuの吸熱反応により減殺され、系全体の発熱が抑制される。これにより、爆発的反応による溶湯の飛散が防止され、安全にCu−In−Ga−Sn合金を作製することが可能となる。 When this Cu-In-Ga alloy powder is mixed with Se powder and melted, Cu, In, Ga and Se elements are alloyed. Here, the Cu—In—Ga alloy powder has a first region mainly containing In and a second region mainly containing a Cu—Ga alloy dispersed in the first region. Yes. For this reason, the exothermic reaction of Se and In that occurs in the first region during alloying is reduced by the endothermic reaction of Se and Cu that occurs in the second region, so that the heat generation of the entire system is suppressed. Thereby, scattering of the molten metal due to an explosive reaction is prevented, and a Cu—In—Ga—Sn alloy can be produced safely.
上記目的を達成するため、本発明の一実施形態に係るCu−In−Ga−Se合金粉末は、Inを主成分とする第1の領域と、Cu−Ga合金を主成分とし上記第1の領域中に分散した粒径1μm以下の粒状である第2の領域とを有するCu−In−Ga合金粉末と、上記Cu−In−Ga合金粉末と混合されたSe粉末とが焼成されて形成される。 In order to achieve the above object, a Cu—In—Ga—Se alloy powder according to an embodiment of the present invention includes a first region containing In as a main component, and a first region containing a Cu—Ga alloy as a main component. A Cu—In—Ga alloy powder having a second region having a particle diameter of 1 μm or less dispersed in the region and a Se powder mixed with the Cu—In—Ga alloy powder are formed by firing. The
このCu−In−Ga−Se合金粉末は含有するSeとInの合金化が完了、もしくはほぼ完了しているため、焼結されることによりSeとInの発熱反応に起因する爆発的反応を発生することなくCu−In−Ga−Se合金焼結体となることが可能である。 This Cu-In-Ga-Se alloy powder is completely or almost completely alloyed with Se and contains, so it generates an explosive reaction due to the exothermic reaction of Se and In. It is possible to obtain a Cu—In—Ga—Se alloy sintered body without performing the above process.
本発明の実施形態に係る、Cu−In−Ga−Se合金ターゲットの製造方法について説明する。
図1は、Cu−In−Ga−Se合金ターゲットの製造方法を示すフローチャートである。同図に示す各ステップについて、順に説明する。The manufacturing method of the Cu-In-Ga-Se alloy target based on embodiment of this invention is demonstrated.
FIG. 1 is a flowchart showing a method for producing a Cu—In—Ga—Se alloy target. Each step shown in FIG.
[Cu−In−Ga混合粉末の製造方法]
Cu(銅)インゴット、In(インジウム)インゴット及びGa(ガリウム)インゴットを準備する。各インゴットは、後述するCu−In−Ga合金の物質量比となる量とする。例えば(Cu:In:Ga=1:0.8:0.2)とすることができる。[Method for producing Cu-In-Ga mixed powder]
A Cu (copper) ingot, an In (indium) ingot, and a Ga (gallium) ingot are prepared. Each ingot is set to an amount that is a material amount ratio of a Cu—In—Ga alloy described later. For example, (Cu: In: Ga = 1: 0.8: 0.2).
上記各インゴットを溶解させ、混合する(St101)。インゴットの溶解はトリアーク炉によってすることができる。また、各インゴットを溶解させることが可能な他の加熱手段を用いてもよい。溶解した各インゴットの混合は、Cu、In及びGaの混合による発熱反応は問題にならないため、通常の混合手段によってすることができる。これにより、「Cu−In−Ga合金溶湯」が形成される。 The above ingots are dissolved and mixed (St101). The ingot can be melted by a triarc furnace. Moreover, you may use the other heating means which can melt | dissolve each ingot. The melted ingots can be mixed by an ordinary mixing means because the exothermic reaction due to the mixing of Cu, In and Ga does not matter. Thereby, “Cu—In—Ga alloy molten metal” is formed.
図2(a)は、上記各インゴットの溶解及び混合によって形成されたCu−In−Ga合金インゴットの写真である。図2(b)は、図2(a)に示したCu−In−Ga合金インゴットの切断面の写真である。なお、これらの図に示すCu−In−Ga合金インゴットは説明のためであり、本実施形態ではCu−In−Ga合金溶湯の状態で、次のSt102に進む。 FIG. 2A is a photograph of a Cu—In—Ga alloy ingot formed by melting and mixing the above ingots. FIG. 2B is a photograph of the cut surface of the Cu—In—Ga alloy ingot shown in FIG. Note that the Cu—In—Ga alloy ingot shown in these drawings is for explanation, and in this embodiment, the process proceeds to the next St102 in the state of the molten Cu—In—Ga alloy.
次に、St101において形成されたCu−In−Ga合金溶湯を「ストリップキャスト(Strip Cast)法」によって凝固させる(St102)。ストリップキャスト法とは金属溶湯の急冷鋳造法のひとつであり、以下で概要を説明する。 Next, the Cu—In—Ga alloy melt formed in St101 is solidified by the “Strip Cast method” (St102). The strip cast method is one of the rapid casting methods of molten metal, and the outline will be described below.
図3は、ストリップキャスト法の態様を示す模式図である。図3に示すように、坩堝1から金属溶湯Yをロール2に近接するタンディッシュ3へ供給する。タンディッシュ3の底部にはスリット状のノズルが形成されており、このノズルから溶湯Yがロール2の周面へ供給される。ロール2は所定の速度で回転しており、供給された金属溶湯Yはロール2の表面で冷却されて凝固し、金属薄帯Hが形成される。なお、ロール2は、銅等の熱伝導性の高い金属材料で形成され、内部が冷却水等によって冷却されてもよい。ストリップキャスト法では、ロール2の回転速度、タンディッシュ3とロール2との間隔、タンディッシュ3のノズルの大きさ等によって金属薄帯Hの厚さを制御することができる。 FIG. 3 is a schematic view showing an aspect of the strip casting method. As shown in FIG. 3, the molten metal Y is supplied from the crucible 1 to the tundish 3 adjacent to the roll 2. A slit-like nozzle is formed at the bottom of the tundish 3, and the molten metal Y is supplied from this nozzle to the peripheral surface of the roll 2. The roll 2 is rotated at a predetermined speed, and the supplied molten metal Y is cooled and solidified on the surface of the roll 2, and a metal ribbon H is formed. The roll 2 may be formed of a metal material having high thermal conductivity such as copper, and the inside may be cooled by cooling water or the like. In the strip casting method, the thickness of the metal ribbon H can be controlled by the rotation speed of the roll 2, the distance between the tundish 3 and the roll 2, the size of the nozzle of the tundish 3, and the like.
本実施形態では、このストリップキャスト法を用いて、Cu−In−Ga合金溶湯を凝固させ、「Cu−In−Ga合金薄帯」を作製する。ロールの回転速度は1m/secとすることができる。なお、ロールの回転速度を0.5m/secとすると形成されたCu−In−Ga合金薄帯の厚さが厚く、手で割れない程度の強度となるため、1m/sec程度の回転速度が好適である。図4に、ロールの回転速度を1m/secとして形成されたCu−In−Ga合金薄帯の写真を示す。ストリップキャスト法を用いることにより、後述する、In中に粒状のCu−Ga合金が分散した構造を有するCu−In−Ga合金を作製することが可能となる。 In the present embodiment, this strip cast method is used to solidify the molten Cu—In—Ga alloy to produce a “Cu—In—Ga alloy ribbon”. The rotation speed of the roll can be 1 m / sec. In addition, when the rotational speed of the roll is 0.5 m / sec, the formed Cu—In—Ga alloy ribbon is thick and does not break by hand, so the rotational speed is about 1 m / sec. Is preferred. FIG. 4 shows a photograph of a Cu—In—Ga alloy ribbon formed with a roll rotation speed of 1 m / sec. By using the strip casting method, a Cu—In—Ga alloy having a structure in which granular Cu—Ga alloy is dispersed in In, which will be described later, can be manufactured.
このようにして、Cu、In及びGaの各インゴットから、Cu−In−Ga合金が形成される。このCu−In−Ga合金の構造について説明する。図5は、図4に示したCu−In−Ga合金薄帯の破断面をSEM(Scanning Electron Microscope:走査型電子顕微鏡)より撮像したSEM像である。図5(a)の拡大倍率は5000倍であり、図5(b)の拡大倍率は20000倍である。なお、図5において網状に表れた模様は、サンプルの切断面に生じた母相(In)の脆性破断線である。 In this way, a Cu—In—Ga alloy is formed from each of the Cu, In, and Ga ingots. The structure of this Cu—In—Ga alloy will be described. FIG. 5 is an SEM image obtained by imaging the fracture surface of the Cu—In—Ga alloy ribbon shown in FIG. 4 using a scanning electron microscope (SEM). The magnification of FIG. 5 (a) is 5000 times, and the magnification of FIG. 5 (b) is 20000 times. Note that the pattern appearing in a net shape in FIG. 5 is a brittle fracture line of the parent phase (In) generated on the cut surface of the sample.
これらの図に示すように、本実施形態の方法により形成されるCu−In−Ga合金は領域R1及びR2として示す2つの領域を含み、塊状の領域R1に、粒状の領域R2が分散している。塊状の領域を第1の領域R1とし、粒状の領域を第2の領域R2とする。第1の領域R1の主成分はInであり、第2の領域R2の主成分はCu−Ga合金である。 As shown in these drawings, the Cu—In—Ga alloy formed by the method of the present embodiment includes two regions indicated as regions R1 and R2, and the granular region R2 is dispersed in the massive region R1. Yes. A lump-like area is referred to as a first area R1, and a granular area is referred to as a second area R2. The main component of the first region R1 is In, and the main component of the second region R2 is a Cu—Ga alloy.
図6は第1の領域R1及び第2の領域R2のEDX(Energy Dispersive X-ray spectroscopy:エネルギー分散型X線分)定性分析の結果を示すグラフである。グラフの横軸は入射電子線の照射エネルギー(keV)であり、縦軸はX線のカウント数(cps:count per second)である。また、グラフに各元素の特性X線の文献値を示す。同図に示すように、第1の領域R1はInが主成分であり、第2の領域R2はCu−Ga合金が主成分であるといえる。即ち、このCu−In−Ga合金は、Inを主成分とする第1の領域R1中に、Cu−Ga合金を主成分とする粒状の第2の領域R2が分散している構造となっている。 FIG. 6 is a graph showing the results of EDX (Energy Dispersive X-ray spectroscopy) qualitative analysis of the first region R1 and the second region R2. The horizontal axis of the graph is the irradiation energy (keV) of the incident electron beam, and the vertical axis is the X-ray count (cps: count per second). Moreover, the literature value of the characteristic X-ray of each element is shown in the graph. As shown in the figure, it can be said that the first region R1 is mainly composed of In, and the second region R2 is mainly composed of a Cu—Ga alloy. That is, this Cu—In—Ga alloy has a structure in which granular second regions R2 mainly composed of Cu—Ga alloy are dispersed in the first regions R1 mainly composed of In. Yes.
図7は、本実施形態の方法により形成されるCu−In−Ga合金のXRD(X-Ray Diffractometer:X線回折法)の結果を示すグラフである。グラフの横軸はX線の入射角度(°)、縦軸は回折強度である。また、グラフに純Cu及び純Inの文献値を示す。同図に示すように、このグラフから純Inに同定されるピークが確認され、純Cuに同定されるピークが確認されない。したがって、このCu−In−Ga合金は純Inと、合金化したCuを含むものといえ、上記EDX分析の結果と一致する。 FIG. 7 is a graph showing the results of XRD (X-Ray Diffractometer) of a Cu—In—Ga alloy formed by the method of this embodiment. The horizontal axis of the graph is the X-ray incident angle (°), and the vertical axis is the diffraction intensity. Moreover, the literature value of pure Cu and pure In is shown on a graph. As shown in the figure, the peak identified in pure In is confirmed from this graph, and the peak identified in pure Cu is not confirmed. Therefore, it can be said that this Cu—In—Ga alloy contains pure In and alloyed Cu, which is consistent with the result of the above EDX analysis.
図1に戻り、以上のような構造を有するCu−In−Ga合金薄帯を粉砕する(St103)。Cu−In−Ga合金薄帯は、上記ストリップキャスト法により手で割ることが可能な程度の強度に形成されているため、任意の手段により粉砕することが可能である。粉砕後、粉粒の粒径が140μm以下となるように分級する。これにより、「Cu−In−Ga合金粉末」が作製される。 Returning to FIG. 1, the Cu—In—Ga alloy ribbon having the above structure is pulverized (St103). Since the Cu—In—Ga alloy ribbon is formed to such a strength that it can be broken by the above-mentioned strip casting method, it can be pulverized by any means. After pulverization, classification is performed so that the particle size of the powder particles is 140 μm or less. Thereby, “Cu—In—Ga alloy powder” is produced.
[Cu−In−Ga合金粉末の製造方法]
次に、Cu−In−Ga合金粉末をSe(セレン)粉末と混合する(St104)。Se粉末は、後述するCu−In−Ga−Se合金の物質量比となる量とする。例えば、(Cu:In:Ga:Se=1:0.8:0.2:2)となる量とすることができる。この混合により、「Cu−In−Ga合金及びSe混合粉末」が作製される。[Method for producing Cu-In-Ga alloy powder]
Next, the Cu—In—Ga alloy powder is mixed with Se (selenium) powder (St104). The Se powder is an amount that is a material amount ratio of a Cu—In—Ga—Se alloy described later. For example, the amount can be (Cu: In: Ga: Se = 1: 0.8: 0.2: 2). By this mixing, “Cu—In—Ga alloy and Se mixed powder” is produced.
続いて、Cu−In−Ga合金及びSe混合粉末を焼成する(St105)。焼成は各元素が空気中の酸素と反応しないように、Ar等の不活性ガス雰囲気下で行う。後述するが、焼成温度は500℃以上、特に620℃が好適である。焼成時間は焼成が十分に進行する時間、例えば12時間とすることができる。焼成によって、Cu−In−Ga合金及びSe混合粉末が合金化され、「Cu−In−Ga−Se合金粉末」が形成される。 Subsequently, the Cu—In—Ga alloy and Se mixed powder are fired (St105). Firing is performed in an inert gas atmosphere such as Ar so that each element does not react with oxygen in the air. As will be described later, the firing temperature is preferably 500 ° C. or higher, particularly 620 ° C. The firing time can be set to a time during which firing proceeds sufficiently, for example, 12 hours. By firing, the Cu—In—Ga alloy and the Se mixed powder are alloyed to form “Cu—In—Ga—Se alloy powder”.
合金化の過程において、Cu−In−Ga合金及びSe混合粉末中のIn及びSeが融点(In:156℃、Se:217℃)を越えるが、InとSeの爆発的反応は発生しない。図8は、Cu−In−Ga合金及びSe混合粉末を500℃で12時間焼成して形成したCu−In−Ga−Se合金粉末の写真である。同図に示すように、焼成中にSeが発熱反応により飛散した形跡はみられない。 In the alloying process, In and Se in the Cu—In—Ga alloy and the Se mixed powder exceed the melting points (In: 156 ° C., Se: 217 ° C.), but no explosive reaction between In and Se occurs. FIG. 8 is a photograph of a Cu—In—Ga—Se alloy powder formed by firing a Cu—In—Ga alloy and Se mixed powder at 500 ° C. for 12 hours. As shown in the figure, there is no evidence of Se scattering during the firing due to an exothermic reaction.
これは、図5に示したように、Inを主成分とする第1の領域R1中に、Cu−Ga合金を主成分とする粒状の第2の領域R2が分散しているためである。すなわち、第2の領域R2に含まれるCuとSeの合金化反応は吸熱反応を呈し、当該反応がInとSeの発熱反応で生じる熱が減殺されるためであると考えられる。本実施形態によって作製されたCu−In−Ga合金は第2の領域R2が第1の領域R1中に分散しているために特にこの熱の減殺が促進され、系全体の発熱が抑制される。 This is because, as shown in FIG. 5, the granular second region R2 containing Cu—Ga alloy as the main component is dispersed in the first region R1 containing In as the main component. That is, it is considered that the alloying reaction of Cu and Se contained in the second region R2 exhibits an endothermic reaction, and the heat generated by the exothermic reaction of In and Se is reduced. In the Cu—In—Ga alloy produced according to this embodiment, since the second region R2 is dispersed in the first region R1, this heat depletion is particularly promoted, and the heat generation of the entire system is suppressed. .
図9は、Cu−In−Ga合金及びSe混合粉末のTG(Thermogravimetric)/DTA(Differential Thermal Analysis)(熱重量示差熱分析)の結果を示すグラフである。また、図10は、比較として示すIn及びSe混合粉末のTG/DTAの結果を示すグラフである。両図においてグラフの横軸はサンプル温度(℃)であり、縦軸はTGについてサンプルの重量変化(%)(右目盛り)、DTAについてリファレンスとサンプルの温度差(熱電対の起電力(μV))(左目盛り)である。 FIG. 9 is a graph showing the results of TG (Thermogravimetric) / DTA (Differential Thermal Analysis) of the Cu—In—Ga alloy and Se mixed powder. FIG. 10 is a graph showing the TG / DTA results of the In and Se mixed powders shown as a comparison. In both figures, the horizontal axis of the graph is the sample temperature (° C.), the vertical axis is the change in weight of the sample (%) for TG (right scale), and the temperature difference between the reference and the sample for DTA (electromotive force (μV) of the thermocouple) ) (Left scale).
図10に示すIn及びSe混合粉末のDTAの結果では、220℃付近でInとSeの合金化に伴なう発熱反応が発生していることがわかる。これに対し、図9に示す本実施形態に係るCu−In−Ga合金及びSe混合粉末のDTAの結果では、明確な発熱は確認されない。即ち、InとSeの合金化に伴なう発熱が減殺されていることがわかる。また、図10に示すTGの結果から、400℃付近で重量変化が生じており、この温度付近でCu−In−Ga−Se合金(CIGS)相が生成されているとみられる。 From the DTA result of the In and Se mixed powder shown in FIG. 10, it can be seen that an exothermic reaction accompanying the alloying of In and Se occurs at around 220 ° C. On the other hand, no clear heat generation is confirmed in the DTA result of the Cu—In—Ga alloy and Se mixed powder according to the present embodiment shown in FIG. That is, it can be seen that the heat generated by the alloying of In and Se is reduced. Further, from the result of TG shown in FIG. 10, a change in weight occurs near 400 ° C., and it seems that a Cu—In—Ga—Se alloy (CIGS) phase is generated near this temperature.
作製されたCu−In−Ga−Se合金が実際に合金化されているかをXRDを用いて確認した。図11は、焼成前のCu−In−Ga合金及びSe混合粉末(以下、焼成前サンプル)と焼成後のCu−In−Ga−Se合金粉末(以下、焼成後サンプル)のXRDの結果を示すグラフである。グラフには、Cu−In−Ga−Se合金(CuIn0.8Ga0.2Se2)、Se及びInの文献値を示す。なお、焼成条件は温度620℃、12時間である。It was confirmed using XRD whether the produced Cu—In—Ga—Se alloy was actually alloyed. FIG. 11 shows the XRD results of the Cu—In—Ga alloy and Se mixed powder before firing (hereinafter referred to as a sample before firing) and the Cu—In—Ga—Se alloy powder after firing (hereinafter referred to as a sample after firing). It is a graph. The graph shows literature values of Cu—In—Ga—Se alloy (CuIn 0.8 Ga 0.2 Se 2 ), Se and In. The firing conditions are a temperature of 620 ° C. and 12 hours.
同図に示すように、焼成前サンプルでは、Se及びInに同定されるピークがみられる一方、当然にCu−In−Ga−Se合金に同定されるピークはみられない。これに対し焼成後のサンプルでは、Se及びInに同定されるピークが消失し、Cu−In−Ga−Se合金に同定されるピークが出現している。即ち、焼成によりCu−In−Ga−Se合金(CIGS)相が生成していることが確認された。 As shown in the figure, in the sample before firing, peaks identified in Se and In are observed, but naturally peaks identified in the Cu—In—Ga—Se alloy are not observed. On the other hand, in the sample after firing, the peaks identified in Se and In disappear, and the peaks identified in the Cu—In—Ga—Se alloy appear. That is, it was confirmed that a Cu—In—Ga—Se alloy (CIGS) phase was generated by firing.
次に、焼成温度について検討する。図12は、それぞれ焼成温度500℃と620℃で12時間焼成した焼成後サンプルのXRDの結果である。グラフには、Cu−In−Ga−Se合金(CuIn0.8Ga0.2Se2)の文献値を示す。同図に示すように、焼成温度を500℃とした焼成後サンプルに比べ、620℃とした焼成後サンプルの方が先鋭なピークである。即ち、焼成温度を620℃とした方がCIGS相がより単相化していることがわかる。Next, the firing temperature is examined. FIG. 12 shows XRD results of samples after firing that were fired at firing temperatures of 500 ° C. and 620 ° C. for 12 hours, respectively. The graph shows literature values of a Cu—In—Ga—Se alloy (CuIn 0.8 Ga 0.2 Se 2 ). As shown in the figure, the sample after firing at 620 ° C. has a sharper peak than the sample after firing at 500 ° C. That is, it can be seen that the CIGS phase becomes more single phase when the firing temperature is set to 620 ° C.
図13(a)は焼成前サンプル、図13(b)は500℃で12時間焼成した焼成後サンプル、図13(c)は620℃で12時間焼成した焼成後サンプルのSEM像(拡大倍率3000倍)である。図13(a)に示すSEM像は、粒径100μm程度のCu−In−Ga合金の粉粒に、より微細な粒径1μm程度のSeの粉粒が付着している状態である。図13(b)に示す500℃で焼成した焼成後サンプルのSEM像では、Cu−In−Ga−Se合金が多少溶融し、Seの粉粒がCu−In−Ga−Se合金の内部に取り込まれている状態である。図13(c)に示す620℃で焼成した焼成後サンプルのSEM像では、Cu−In−Ga−Se合金がより溶融し、Seの粉粒がCu−In−Ga−Se合金のさらに内部に取り込まれている状態である。以上のように、焼成温度を620℃とすることによりCIGS相が十分に単層化させることが可能である。 13A is a sample before baking, FIG. 13B is a sample after baking for 12 hours at 500 ° C., and FIG. 13C is an SEM image (magnification of 3000) of the sample after baking for 12 hours at 620 ° C. Times). The SEM image shown in FIG. 13A is a state in which finer Se particles having a particle size of about 1 μm are attached to Cu-In—Ga alloy particles having a particle size of about 100 μm. In the SEM image of the fired sample fired at 500 ° C. shown in FIG. 13B, the Cu—In—Ga—Se alloy is somewhat melted, and Se particles are taken into the Cu—In—Ga—Se alloy. It is in the state. In the SEM image of the sample after firing baked at 620 ° C. shown in FIG. 13C, the Cu—In—Ga—Se alloy is further melted, and Se particles are further contained in the Cu—In—Ga—Se alloy. It is in a state of being captured. As described above, by setting the firing temperature to 620 ° C., the CIGS phase can be sufficiently made into a single layer.
[Cu−In−Ga−Se合金焼結体の製造方法]
図1に戻り、焼成により作製されたCu−In−Ga−Se合金粉末を焼結してCu−In−Ga−Se合金焼結体を作製する(St106)。焼結は、放電プラズマ焼結法(SPS:Spark Plasma Sintering)やホットプレス法(HP:Hot press)等の方法によって行うことができる。焼結の際には、既にCu−In−Ga−Se合金粉末に含まれていたSeとInの合金化は完了、もしくはほぼ完了しているため、SeとInの発熱反応に起因する爆発的反応は発生せず、Cu−In−Ga−Se合金焼結体を製造することが可能である。[Method for producing sintered Cu-In-Ga-Se alloy]
Returning to FIG. 1, a Cu—In—Ga—Se alloy powder produced by firing is sintered to produce a Cu—In—Ga—Se alloy sintered body (St106). Sintering can be performed by a method such as a spark plasma sintering (SPS) method or a hot press (HP) method. At the time of sintering, the alloying of Se and In already contained in the Cu—In—Ga—Se alloy powder is completed or almost completed, so explosive due to the exothermic reaction of Se and In. Reaction does not occur, and it is possible to produce a Cu—In—Ga—Se alloy sintered body.
次に、Cu−In−Ga−Se合金焼結体を加工して、Cu−In−Ga−Se合金ターゲットを作製する(St107)。この加工は、切削、研削等の任意の手法によって行うことができる。以上のようにして、Cu、In、Ga及びSeの単金属を原料として、Cu−In−Ga−Se合金ターゲットを作製することが可能である。 Next, the Cu—In—Ga—Se alloy sintered body is processed to produce a Cu—In—Ga—Se alloy target (St107). This processing can be performed by any method such as cutting and grinding. As described above, a Cu—In—Ga—Se alloy target can be manufactured using a single metal of Cu, In, Ga, and Se as a raw material.
以上のように本実施形態の製造方法では、Inを主成分とする第1の領域R1と、Cu−Ga合金を主成分とし第1の領域中R1に分散した粒径1μm以下の粒状である第2の領域R2とを有するCu−In−Ga合金粉末を製造する。Cu−In−Ga合金粉末をSe粉末と混合して合金化する際に、第1の領域R1で発生するSeとInの発熱反応が、第2の領域R2で発生するSeとCuの吸熱反応により減殺され、系全体の発熱が抑制される。これにより、爆発的反応による溶湯の飛散が防止され、安全にCu−In−Ga−Sn合金焼結体を作製することが可能となる。 As described above, in the manufacturing method of the present embodiment, the first region R1 containing In as the main component and the particle size of 1 μm or less dispersed in R1 in the first region containing the Cu—Ga alloy as the main component. A Cu—In—Ga alloy powder having the second region R2 is manufactured. When Cu—In—Ga alloy powder is mixed with Se powder and alloyed, the exothermic reaction of Se and In generated in the first region R1 is the endothermic reaction of Se and Cu generated in the second region R2. To reduce the heat generated by the entire system. Thereby, scattering of the molten metal due to explosive reaction is prevented, and it becomes possible to produce a Cu—In—Ga—Sn alloy sintered body safely.
本発明は上述の実施形態にのみ限定されるものではなく、本発明の要旨を逸脱しない範囲内において変更され得る。 The present invention is not limited only to the above-described embodiment, and can be changed within a range not departing from the gist of the present invention.
上記実施形態では、Cu、In、Ga及びSeを合金化するものとしたが、他の元素をさらに追加してもよい。この場合であっても、SeとInの発熱反応がCuとInの吸熱反応によって減殺され、爆発的反応を抑制することが可能である。 In the above embodiment, Cu, In, Ga, and Se are alloyed, but other elements may be further added. Even in this case, the exothermic reaction of Se and In is attenuated by the endothermic reaction of Cu and In, and the explosive reaction can be suppressed.
上記実施形態では、Cu−In−Ga−Sn合金焼結体の例として、Cu−In−Ga−Sn合金ターゲットを示した。しかし、Cu−In−Ga−Sn合金焼結体はスパッタリングターゲットには限られず、他の用途に用いることも可能である。 In the said embodiment, the Cu-In-Ga-Sn alloy target was shown as an example of a Cu-In-Ga-Sn alloy sintered compact. However, the Cu—In—Ga—Sn alloy sintered body is not limited to the sputtering target, and can be used for other purposes.
R1…第1の領域
R2…第2の領域R1 ... first region R2 ... second region
Claims (5)
前記Cu−In−Ga合金溶湯をストリップキャスト法により凝固させてCu−In−Ga合金薄帯を作製し、
前記Cu−In−Ga合金薄帯を粉砕してCu−In−Ga合金粉末を作製し、
前記Cu−In−Ga合金粉末とSe粉末とを混合してCu−In−Ga合金及びSe混合粉末を作製し、
前記Cu−In−Ga合金及びSe混合粉末を焼成する
Cu−In−Ga−Se合金粉末の製造方法。 Create a Cu-In-Ga alloy melt,
Cu—In—Ga alloy melt is solidified by a strip cast method to produce a Cu—In—Ga alloy ribbon ,
Cu-In-Ga alloy powder is pulverized to produce Cu-In-Ga alloy powder,
Cu—In—Ga alloy powder and Se powder are mixed to produce a Cu—In—Ga alloy and Se mixed powder,
The manufacturing method of the Cu-In-Ga-Se alloy powder which bakes the said Cu-In-Ga alloy and Se mixed powder.
前記Cu−In−Ga合金溶湯をストリップキャスト法により凝固させてCu−In−Ga合金薄帯を作製し、
前記Cu−In−Ga合金薄帯を粉砕してCu−In−Ga合金粉末を作製し、
前記Cu−In−Ga合金粉末とSe粉末とを混合してCu−In−Ga合金及びSe混合粉末を作製し、
前記Cu−In−Ga合金及びSe混合粉末を焼成してCu−In−Ga−Se合金粉末を作製し、
前記Cu−In−Ga−Se合金粉末を焼結する
Cu−In−Ga−Se合金焼結体の製造方法。 Create a Cu-In-Ga alloy melt,
Cu—In—Ga alloy melt is solidified by a strip cast method to produce a Cu—In—Ga alloy ribbon ,
Cu-In-Ga alloy powder is pulverized to produce Cu-In-Ga alloy powder,
Cu—In—Ga alloy powder and Se powder are mixed to produce a Cu—In—Ga alloy and Se mixed powder,
The Cu—In—Ga alloy and Se mixed powder are fired to produce a Cu—In—Ga—Se alloy powder,
The manufacturing method of the Cu-In-Ga-Se alloy sintered compact which sinters the said Cu-In-Ga-Se alloy powder.
前記Cu−In−Ga−Se合金粉末を焼結して作製された前記Cu−In−Ga−Se合金焼結体をターゲット形状に加工する工程をさらに有する
Cu−In−Ga−Se合金焼結体の製造方法。 It is a manufacturing method of the Cu-In-Ga-Se alloy sintered compact according to claim 2,
Cu-In-Ga-Se alloy sintering further comprising a step of processing the Cu-In-Ga-Se alloy sintered body produced by sintering the Cu-In-Ga-Se alloy powder into a target shape. Body manufacturing method.
Cu−In−Ga−Se合金粉末。 A Cu-In-Ga alloy having a first region containing In as a main component and a second region containing a Cu-Ga alloy as a main component and dispersed in the first region and having a particle size of 1 µm or less. Cu-In-Ga-Se alloy powder formed by firing powder and Se powder mixed with the Cu-In-Ga alloy powder.
前記Cu−In−Ga合金溶湯を凝固させて、Inを主成分とする第1の領域とCu−Ga合金を主成分とし前記第1の領域中に分散した粒径1μm以下の粒状である第2の領域とを有するCu−In−Ga合金薄帯を作製し、
前記Cu−In−Ga合金薄帯を粉砕してCu−In−Ga合金粉末を作製し、
前記Cu−In−Ga合金粉末とSe粉末とを混合してCu−In−Ga合金及びSe混合粉末を作製し、
前記Cu−In−Ga合金及びSe混合粉末を焼成する
Cu−In−Ga−Se合金粉末の製造方法。 Create a Cu-In-Ga alloy melt,
The Cu—In—Ga alloy molten metal is solidified to form a first region having In as a main component and a particle having a particle size of 1 μm or less dispersed in the first region and having a Cu—Ga alloy as a main component. A Cu-In-Ga alloy ribbon having two regions,
Cu-In-Ga alloy powder is pulverized to produce Cu-In-Ga alloy powder,
Cu—In—Ga alloy powder and Se powder are mixed to produce a Cu—In—Ga alloy and Se mixed powder,
The manufacturing method of the Cu-In-Ga-Se alloy powder which bakes the said Cu-In-Ga alloy and Se mixed powder.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2012517125A JP5521036B2 (en) | 2010-05-24 | 2011-05-20 | Cu-In-Ga-Se alloy powder manufacturing method, Cu-In-Ga-Se alloy sintered body manufacturing method, and Cu-In-Ga-Se alloy powder |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010118679 | 2010-05-24 | ||
| JP2010118679 | 2010-05-24 | ||
| PCT/JP2011/002813 WO2011148600A1 (en) | 2010-05-24 | 2011-05-20 | Process for producing cu-in-ga alloy powder, process for producing cu-in-ga-se alloy powder, process for producing sintered cu-in-ga-se alloy, cu-in-ga alloy powder, and cu-in-ga-se alloy powder |
| JP2012517125A JP5521036B2 (en) | 2010-05-24 | 2011-05-20 | Cu-In-Ga-Se alloy powder manufacturing method, Cu-In-Ga-Se alloy sintered body manufacturing method, and Cu-In-Ga-Se alloy powder |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPWO2011148600A1 JPWO2011148600A1 (en) | 2013-07-25 |
| JP5521036B2 true JP5521036B2 (en) | 2014-06-11 |
Family
ID=45003600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012517125A Expired - Fee Related JP5521036B2 (en) | 2010-05-24 | 2011-05-20 | Cu-In-Ga-Se alloy powder manufacturing method, Cu-In-Ga-Se alloy sintered body manufacturing method, and Cu-In-Ga-Se alloy powder |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JP5521036B2 (en) |
| TW (1) | TW201200270A (en) |
| WO (1) | WO2011148600A1 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5588757B2 (en) * | 2010-06-21 | 2014-09-10 | 株式会社アルバック | In-Se alloy powder, In-Se alloy sintered body, Ga-Se alloy powder, Ga-Se alloy sintered body, In-Ga-Se alloy powder, In-Ga-Se alloy sintered body, Cu-In- Method for producing Ga-Se alloy powder and Cu-In-Ga-Se alloy sintered body |
| JP5767447B2 (en) * | 2010-06-29 | 2015-08-19 | 株式会社コベルコ科研 | Method for producing powder containing Cu, In, Ga and Se elements, and sputtering target containing Cu, In, Ga and Se elements |
| JP5533607B2 (en) * | 2010-11-30 | 2014-06-25 | 三菱マテリアル株式会社 | Sputtering target and manufacturing method thereof |
| EP2791054A4 (en) * | 2011-12-15 | 2016-03-09 | Midsummer Ab | RECYCLING OF COPPER, INDIUM AND GALLIUM DISELENIURE |
| WO2013129044A1 (en) * | 2012-02-27 | 2013-09-06 | 株式会社日本マイクロニクス | Method for fabricating alloy for cigs solar cell |
| JP5993945B2 (en) * | 2012-05-15 | 2016-09-21 | 株式会社日本マイクロニクス | Alloy for n-type light absorption layer, method for producing the same, and solar cell |
| WO2013172252A1 (en) * | 2012-05-15 | 2013-11-21 | 株式会社 日本マイクロニクス | ALLOY FOR Na-ADDED LIGHT-ABSORBING LAYER, METHOD FOR PRODUCING SAME, AND SOLAR CELL |
| JP2013253308A (en) * | 2012-06-08 | 2013-12-19 | Futek Furnace Inc | Method for manufacturing cigs sputtering target |
| KR101483254B1 (en) | 2013-07-15 | 2015-01-15 | 한국생산기술연구원 | The method of fabricating quarternary Se compounds sintered materials for use of sputtering targets |
| JP6769332B2 (en) * | 2017-02-16 | 2020-10-14 | 三菱マテリアル株式会社 | Sputtering target and its manufacturing method |
| CN107626929B (en) * | 2017-08-04 | 2021-04-30 | 领凡新能源科技(北京)有限公司 | Method for preparing alloy powder |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009120862A (en) * | 2007-11-12 | 2009-06-04 | Mitsubishi Materials Corp | Cu-In-Ga ternary sintered alloy sputtering target and method for producing the same |
| JP2009287092A (en) * | 2008-05-30 | 2009-12-10 | Mitsubishi Materials Corp | Method for producing sputtering target for use in forming chalcopyrite type semiconductor film |
-
2011
- 2011-05-20 JP JP2012517125A patent/JP5521036B2/en not_active Expired - Fee Related
- 2011-05-20 WO PCT/JP2011/002813 patent/WO2011148600A1/en not_active Ceased
- 2011-05-23 TW TW100117936A patent/TW201200270A/en unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009120862A (en) * | 2007-11-12 | 2009-06-04 | Mitsubishi Materials Corp | Cu-In-Ga ternary sintered alloy sputtering target and method for producing the same |
| JP2009287092A (en) * | 2008-05-30 | 2009-12-10 | Mitsubishi Materials Corp | Method for producing sputtering target for use in forming chalcopyrite type semiconductor film |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011148600A1 (en) | 2011-12-01 |
| TW201200270A (en) | 2012-01-01 |
| JPWO2011148600A1 (en) | 2013-07-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5521036B2 (en) | Cu-In-Ga-Se alloy powder manufacturing method, Cu-In-Ga-Se alloy sintered body manufacturing method, and Cu-In-Ga-Se alloy powder | |
| JP5767447B2 (en) | Method for producing powder containing Cu, In, Ga and Se elements, and sputtering target containing Cu, In, Ga and Se elements | |
| CN102630254B (en) | Low melting point sputter targets for chalcogenide photovoltaic applications and methods of manufacturing the same | |
| JP2012507631A (en) | Chalcogenide alloy sputter target for photovoltaic applications and method of manufacturing the same | |
| JP5182494B2 (en) | Manufacturing method of sputtering target for chalcopyrite type semiconductor film formation | |
| TWI424080B (en) | Sputtering target and its manufacturing method | |
| JP5594618B1 (en) | Sputtering target and manufacturing method thereof | |
| CN101906552A (en) | Cu-Ga alloy, sputtering target, method for producing Cu-Ga alloy, and method for producing sputtering target | |
| JP5919738B2 (en) | Sputtering target and manufacturing method thereof | |
| WO2011126092A1 (en) | Method for producing cu-ga alloy powder, cu-ga alloy powder, method for producing cu-ga alloy sputtering target, and cu-ga alloy sputtering target | |
| JP5973041B2 (en) | Cu-Ga sputtering target and method for producing Cu-Ga sputtering target | |
| TWI438296B (en) | Sputtering target and its manufacturing method | |
| JP6634750B2 (en) | Sputtering target and method for manufacturing the same | |
| JP6176535B2 (en) | Sputtering target and manufacturing method thereof | |
| JP2014098206A (en) | Cu-Ga BINARY SPUTTERING TARGET AND PRODUCTION METHOD THEREOF | |
| JP2006086512A (en) | Thermoelectric conversion system using filled skutterudite alloy. | |
| Wu et al. | Investigation on melt growth (Mg, Co, Ni, Cu, Zn) O oxide ceramics prepared by laser directed energy deposition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20131224 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140127 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140218 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140303 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20140325 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20140407 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5521036 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |