WO2011062021A1 - Bi-ge-o sintered body sputtering target, method for producing same, and optical recording medium - Google Patents

Bi-ge-o sintered body sputtering target, method for producing same, and optical recording medium Download PDF

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WO2011062021A1
WO2011062021A1 PCT/JP2010/068547 JP2010068547W WO2011062021A1 WO 2011062021 A1 WO2011062021 A1 WO 2011062021A1 JP 2010068547 W JP2010068547 W JP 2010068547W WO 2011062021 A1 WO2011062021 A1 WO 2011062021A1
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geo
sputtering target
target
powder
sintered body
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PCT/JP2010/068547
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French (fr)
Japanese (ja)
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淳史 奈良
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Jx日鉱日石金属株式会社
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Priority to CN201080050662.XA priority Critical patent/CN102597303B/en
Priority to JP2010548692A priority patent/JP5265710B2/en
Publication of WO2011062021A1 publication Critical patent/WO2011062021A1/en

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    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
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    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • C23C14/3407Cathode assembly for sputtering apparatus, e.g. Target
    • C23C14/3414Metallurgical or chemical aspects of target preparation, e.g. casting, powder metallurgy
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    • G11B7/243Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising inorganic materials only, e.g. ablative layers
    • GPHYSICS
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    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/26Apparatus or processes specially adapted for the manufacture of record carriers
    • G11B7/266Sputtering or spin-coating layers
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    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
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    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3298Bismuth oxides, bismuthates or oxide forming salts thereof, e.g. zinc bismuthate
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    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5445Particle size related information expressed by the size of the particles or aggregates thereof submicron sized, i.e. from 0,1 to 1 micron
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    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
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    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/242Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
    • G11B7/243Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising inorganic materials only, e.g. ablative layers
    • G11B2007/24302Metals or metalloids
    • G11B2007/24312Metals or metalloids group 14 elements (e.g. Si, Ge, Sn)
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
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    • G11B7/243Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising inorganic materials only, e.g. ablative layers
    • G11B2007/24302Metals or metalloids
    • G11B2007/24314Metals or metalloids group 15 elements (e.g. Sb, Bi)
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/242Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
    • G11B7/243Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising inorganic materials only, e.g. ablative layers
    • G11B2007/24318Non-metallic elements
    • G11B2007/2432Oxygen

Definitions

  • the present invention relates to a Bi—Ge—O-based sintered sputtering target, a method for producing the target, and an optical recording medium. Particularly, since it has excellent thermal shock resistance and can be sputtered at high power, production efficiency is greatly improved. To obtain an optical recording medium in which no target cracks occur during sputtering, particle generation is small, a high-quality thin film can be stably produced, and recording bit errors do not occur.
  • the present invention relates to a Bi—Ge—O-based sintered sputtering target that can be manufactured, a method for manufacturing the target, and an optical recording medium.
  • a write once read many (WORM) optical recording medium is an optical recording medium capable of high-density recording even with a laser beam in a blue wavelength region (350 to 500 nm), particularly a multilayer recording medium having high recording sensitivity.
  • An optical recording medium having a recording layer In order to meet the demand for higher density optical discs, higher density has been achieved by multilayering. Similarly, optical recording media for high-density recording are being developed for optical discs using blue LDs.
  • a film having a stable composition and structure as well as a film having excellent light transmission characteristics are required. Since it is often an oxide and generally has a high melting point, a sputtering method is often used as a film formation method.
  • a sputtering target suitable for obtaining such a film is required.
  • the form and structure of the compound constituting the target also affect the sputtering characteristics, stable sputtering is performed when the compound constituting the target is suitable for the required film characteristics. Whether it can be done is a problem.
  • the generation of particles may increase depending on the target material, which may reduce the quality.
  • the occurrence of a recording bit error due to particles or the like becomes a serious problem. This causes a problem that the product becomes defective and the yield decreases.
  • Patent Document 1 discloses an optical recording medium in which at least a recording layer is formed on a substrate, the main components of the constituent elements of the recording layer are Bi and O (oxygen), contain B, Ge, An optical recording medium containing at least one element X selected from Li, Sn, Cu, Fe, Pd, Zn, Mg, Nd, Mn, and Ni is described.
  • Patent Document 2 discloses that the recording layer has Bi, M (M is Mg, Al, Cr, Mn, Co, Fe, Cu, Zn, Li, Si, Ge, Zr, Ti, Hf, Sn, Mo, V, Nb, Y, Ta) and oxygen, and the recording mark portion on which the information is recorded is composed of crystals of the elements contained in the recording layer and / or oxides of these elements.
  • M Mg, Al, Cr, Mn, Co, Fe, Cu, Zn, Li, Si, Ge, Zr, Ti, Hf, Sn, Mo, V, Nb, Y, Ta
  • a write-once optical recording medium characterized by containing crystals is described.
  • Patent Documents 3 to 8 have been proposed. Under such circumstances, a combination of optical recording media composed of bismuth (Bi), germanium (Ge), and oxygen (O) is conceivable, and these optical recording media are described as being formed by sputtering of a sintered target. There is also.
  • this Bi-Ge-O-based sintered sputtering target is vulnerable to thermal shock, and often cracks and cracks occur during sputtering with high power, resulting in the generation of particles and improving the quality of the recording film and the like. There was a problem to lose.
  • JP 2008-210492 A JP 2006-116948 A JP 2003-48375 A JP 2005-161831 A JP 2005-108396 A JP 2007-169779 A JP 2008-273167 A Japanese Patent No. 4271063
  • the present invention relates to a Bi—Ge—O-based sintered sputtering target, a method for producing the target, and an optical recording medium. Particularly, since it has excellent thermal shock resistance and can be sputtered at high power, production efficiency is greatly improved. To obtain an optical recording medium in which no target cracks occur during sputtering, particle generation is small, a high-quality thin film can be stably produced, and recording bit errors do not occur. It is an object of the present invention to provide a Bi—Ge—O-based sintered sputtering target, a method for producing the target, and an optical recording medium.
  • the present inventors have conducted intensive research. As a result, the Bi 12 GeO 20 particles in the dispersion system are made fine particles, so that the thermal expansion / contraction of each particle during heating / cooling is reduced. It was found that the amount was reduced and the thermal shock resistance was improved.
  • the present invention is based on this finding, 1) A sintered compact target composed of bismuth (Bi), germanium (Ge), and oxygen (O), and the atomic ratio of Bi and Ge is 0.57 ⁇ (Bi / (Bi + Ge)) ⁇ 0.75.
  • Bi—Ge—O-based sintered sputtering target characterized by being composed of two phases of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 as crystal phases 2) Bi 12 GeO 20 and Bi 4 Ge
  • the present invention also provides: 6) Bi 12 GeO 20 powder obtained by mixing a GeO 2 powder 14.3 mol% and Bi 2 O 3 powder 85.7 mol%, followed by solid phase reaction, GeO 2 powder 60.0 mol%, and Bi 2 O 3 powder Bi-Ge-O is characterized in that a sintered body is produced by hot-pressing Bi 4 Ge 3 O 12 powder obtained by mixing solid phase reaction after mixing 40.0 mol%.
  • the Bi—Ge—O-based sintered sputtering target of the present invention is particularly excellent in thermal shock resistance and can be sputtered at high power, so that significant improvement in production efficiency can be expected. There is an excellent effect that an optical recording medium can be obtained, in which cracks do not occur, particle generation is small, a high-quality thin film can be stably produced, and no recording bit error occurs.
  • FIG. 2 is a photograph showing a scanning electron microscope observation result of the sintered body obtained in Example 1.
  • FIG. 6 is a photograph showing a scanning electron microscope observation result of a sintered body obtained in Comparative Example 1.
  • the Bi—Ge—O based sintered sputtering target of the present invention is a sintered target made of bismuth (Bi), germanium (Ge), and oxygen (O), and the atomic ratio of Bi and Ge is 0. .57 ⁇ (Bi / (Bi + Ge)) ⁇ 0.75, and the crystal phase is composed of two phases of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 .
  • a recording film using this composition is a suitable composition that can achieve high-density recording by multilayering, and can stably perform good sputtering film formation.
  • Bi 12 GeO 20 and Bi 4 Ge 3 O 12 In general, when a powder of bismuth oxide (Bi 2 O 3 ) and germanium oxide (GeO 2 ) is used as a starting material and sintered to produce the composition target, Bi 12 GeO 20 and Bi 4 Ge 3 O 12 The two-phase coexistence composition.
  • Bi 12 GeO 20 and Bi 4 Ge 3 O 12 have a large difference in thermal expansion coefficient, they are extremely vulnerable to thermal shock, and there arises a problem that cracking occurs during sputtering film formation at high power.
  • the thermal expansion coefficient of Bi 12 GeO 20 is 1.39 ⁇ 10 ⁇ 5
  • the thermal expansion coefficient of Bi 4 Ge 3 O 12 is 6.00 ⁇ 10 ⁇ 6 .
  • Bi 4 Ge 3 O 12 serves as a base material, and Bi 12 GeO 20 particles are dispersed.
  • the thermal expansion / shrinkage amount of each particle during heating / cooling is reduced and the thermal shock resistance is improved.
  • the Bi 2 O 3 and GeO 2 as starting materials when pulverized in a state of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 coexist, Bi 4 Ge 3 O 12 is selectively milled Therefore, it was found that the dispersion system Bi 12 GeO 20 was not easily pulverized. Therefore, Bi 12 GeO 20 and Bi 4 Ge 3 O 12 were used as starting materials, and Bi 12 GeO 20 was finely pulverized in advance to improve thermal shock resistance.
  • the thermal shock resistance of the target was improved, which enabled film formation with high power, and a great advantage that production efficiency could be increased was obtained.
  • the generation of particles caused by cracks and cracks is remarkably reduced, making it possible to produce stable high quality thin films, producing no recording bit errors, and producing optical recording media that can achieve high recording density.
  • the effect that it becomes possible was obtained. It is effective in improving the thermal shock resistance that the molar ratio of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 is (Bi 12 GeO 20 / Bi 4 Ge 3 O 12 ) ⁇ 0.56.
  • the particle size of Bi 12 GeO 20 in the target sintered body is made finer, it is more effective that the maximum particle size is 3 microns or less, preferably the average particle size is 1 ⁇ m or less.
  • the target was subjected to thermal shock by quenching in water after heating at 200 ° C. for 30 minutes, it was possible to achieve an average bending strength reduction rate of 50% or less before and after the thermal shock.
  • the present invention includes an optical recording medium formed by sputtering using the above target.
  • Bi 12 GeO 20 powder and Bi 4 Ge 3 O 12 powder are used as starting materials, and the atomic ratio of Bi and Ge is 0. .57 ⁇ (Bi / (Bi + Ge)) ⁇ 0.75, and then mixed by hot pressing at 600 to 840 ° C. and pressure of 0 to 400 kg / cm 2 to produce a sintered body. Is particularly effective. Also in this case, it is effective to use Bi 12 GeO 20 powder finely pulverized to an average particle size of 1 ⁇ m or less.
  • This sintering condition is a suitable condition for obtaining a target having a uniform composition.
  • the target can be manufactured under sintering conditions outside the above range, the reproducibility of the target quality is inferior, so that the above range is desirable.
  • the atomic ratio of Bi to Ge in the raw material stage, 0.57 ⁇ (Bi / (Bi + Ge)) ⁇ 0.75 is directly reflected on the target, and a target having the same composition ratio can be obtained.
  • Example 1 Bi 12 GeO 20 powder and Bi 4 Ge 3 O 12 powder were prepared in advance using powders of bismuth oxide and germanium oxide having a purity of 3N (99.9%) as a starting material. However, Bi 12 GeO 20 powder 16.67 mol% and Bi 4 Ge 3 O 12 powder 83.33 mol% were mixed and mixed, and the mixed powder was filled in a carbon die so as to be 0.67. Then, hot pressing was performed under the conditions of a temperature of 700 ° C. and a pressure of 250 kg / cm 2 .
  • the sintered body after hot pressing was finished to obtain a target.
  • the relative density of the target was 96% (7.15 g / cm 3 at 100% density).
  • the sintered body by X-ray diffraction measurement it was confirmed that a two-phase structure of Bi 12 GeO 20, Bi 4 Ge 3 O 12.
  • a scanning electron microscope photograph of this sintered body is shown in FIG. Thereby, it was confirmed that Bi 4 Ge 3 O 12 became a base material (gray portion in the photograph) and Bi 12 GeO 20 was a dispersion (white portion in the photograph). It was also confirmed that the maximum particle size of Bi 12 GeO 20 was 3 ⁇ m or less and the average particle size was 1 ⁇ m or less.
  • this target was heated at 200 ° C. for 30 minutes and then subjected to thermal shock by quenching in water. Thereafter, a bending test according to JIS standard 1601 (from 5 arbitrary points in the target, a test piece having a width of 4 ⁇ 0.1 mm, a height of 3 ⁇ 0.1 mm, and a length of 40 to 50 mm was sampled and measured. The average value of the measurement results of the points was determined), and the average bending strength ratio (strength reduction rate) before and after the thermal shock was measured. The measurement results are similarly shown in Table 1. Some variation occurred depending on the measurement location, but all were less than 50%, and the rate of decrease in strength was small.
  • Comparative Example 1 A powder of bismuth oxide and germanium oxide having a purity of 3N (99.9%) is used as a starting material, and GeO 2 powder is 50.0 mol% so that the atomic ratio of Bi and Ge is 0.67, respectively. After preparing 50.0 mol% of Bi 2 O 3 powder, it was mixed, and the powder after mixing was filled in a carbon die, and hot pressing was performed under conditions of a temperature of 730 ° C. and a pressure of 250 kg / cm 2 .
  • the sintered body after hot pressing was finished to obtain a target.
  • the relative density of the target was 103% (7.44 g / cm 3 at 100% density).
  • the crystal phase of the target was a two-phase structure of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 .
  • a scanning electron microscope photograph of this sintered body is shown in FIG. Thereby, it was confirmed that Bi 4 Ge 3 O 12 became a base material (gray portion in the photograph) and Bi 12 GeO 20 was a dispersion (white portion in the photograph). Further, it was confirmed that the maximum particle size of Bi 12 GeO 20 was 8 ⁇ m or less and the average particle size was 4 ⁇ m or less.
  • this target was heated at 200 ° C. for 30 minutes, and then subjected to thermal shock by quenching in water. Then, the bending strength test by JIS1601 was implemented.
  • the measurement results of the average bending strength ratio (strength reduction rate) before and after the thermal shock are also shown in Table 1. As a result, the reduction rate of the average bending strength was 82.1%.
  • this target it was pre-sputtered on a glass substrate at 1 kW for about 1 hour, then 10 s spatter at 2 kW and 5 s stop were repeated 10 times. After this sputtering cycle, the chamber was opened and visually observed. When the abnormality of the target was observed, the target was cracked. In addition, the generation of particles was remarkably increased compared to the examples. This is thought to be caused by cracks in the target during sputtering.
  • the Bi—Ge—O-based sintered sputtering target of the present invention and the method for producing the target since it is particularly excellent in thermal shock resistance and can be sputtered at high power, significant improvement in production efficiency can be expected.
  • the target is not cracked during sputtering, the generation of particles is small, a high-quality thin film can be stably produced, and an optical recording medium free from recording bit errors can be obtained. Has an excellent effect.
  • the production efficiency of film formation of the optical recording medium can be increased, and a suitable target for manufacturing the optical recording medium can be provided.

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Abstract

Disclosed are: a Bi-Ge-O sintered body sputtering target which is composed of bismuth (Bi), germanium (Ge) and oxygen (O) and characterized in that the atom number ratio of Bi and Ge satisfies 0.57 < (Bi/(Bi + Ge)) < 0.75 and the crystal phase is configured of two phases, namely Bi12GeO20 and Bi4Ge3O12; a method for producing the Bi-Ge-O sintered body sputtering target; and an optical recording medium. Specifically disclosed is a Bi-Ge-O sintered body sputtering target which has excellent thermal shock resistance and is capable of achieving greatly improved production efficiency since the Bi-Ge-O sintered body sputtering target enables high-power sputtering. The Bi-Ge-O sintered body sputtering target does not suffer from cracks and generates little particles during the sputtering, so that a thin film with high quality can be stably produced and an optical recording medium that is free from recording bit errors can be obtained. Also specifically disclosed are: a method for producing the Bi-Ge-O sintered body sputtering target; and an optical recording medium.

Description

Bi-Ge-O系焼結体スパッタリングターゲット及びその製造方法並びに光記録媒体Bi-Ge-O-based sintered sputtering target, manufacturing method thereof, and optical recording medium
 本発明は、Bi-Ge-O系焼結体スパッタリングターゲット及び同ターゲットの製造方法並びに光記録媒体に関し、特に耐熱衝撃性に優れ、高パワーでのスパッタリングが可能であるため生産効率の大幅な改善が期待できると共に、スパッタリングの際にターゲットの割れが発生せず、パーティクルの発生が少なく、安定して高品質の薄膜の作製が可能であり、記録ビットのエラー発生のない光記録媒体を得ることができるBi-Ge-O系焼結体スパッタリングターゲット及び同ターゲットの製造方法並びに光記録媒体に関する。 The present invention relates to a Bi—Ge—O-based sintered sputtering target, a method for producing the target, and an optical recording medium. Particularly, since it has excellent thermal shock resistance and can be sputtered at high power, production efficiency is greatly improved. To obtain an optical recording medium in which no target cracks occur during sputtering, particle generation is small, a high-quality thin film can be stably produced, and recording bit errors do not occur. The present invention relates to a Bi—Ge—O-based sintered sputtering target that can be manufactured, a method for manufacturing the target, and an optical recording medium.
 追記型(WORM:Write Once Read Many)光記録媒体は、青色波長領域(350~500nm)のレーザ光でも高密度の記録を行なうことが可能な光記録媒体、特に、高い記録感度を持つ多層の記録層を持つ光記録媒体である。
 光ディスクは高密度化への要求に対応する為、多層化による高密度化が行われている。青色LDを用いる光ディスクにおいても同様に、高密度記録用の光記録媒体の開発が行われている。
A write once read many (WORM) optical recording medium is an optical recording medium capable of high-density recording even with a laser beam in a blue wavelength region (350 to 500 nm), particularly a multilayer recording medium having high recording sensitivity. An optical recording medium having a recording layer.
In order to meet the demand for higher density optical discs, higher density has been achieved by multilayering. Similarly, optical recording media for high-density recording are being developed for optical discs using blue LDs.
 高密度多層記録が可能な追記型光記録媒体を実現するには、安定した組成、構造を持つ材料であることは勿論、光透過特性に優れた膜が必要であるが、そのような材料は酸化物であることが多く、一般的に融点が高い為、成膜法としてスパッタリング法が用いられることが多い。 In order to realize a write-once type optical recording medium capable of high-density multilayer recording, a film having a stable composition and structure as well as a film having excellent light transmission characteristics are required. Since it is often an oxide and generally has a high melting point, a sputtering method is often used as a film formation method.
 従って、そのような膜を得るのに適したスパッタリングターゲットが必要となる。しかし、ターゲットを構成する化合物の形態、構造などが、スパッタリング特性にも影響するため、ターゲットを構成する化合物を、必要な膜の特性に適したものとした時に、良好なスパッタリングを安定して行うことが出来るか否かが問題となる。 Therefore, a sputtering target suitable for obtaining such a film is required. However, since the form and structure of the compound constituting the target also affect the sputtering characteristics, stable sputtering is performed when the compound constituting the target is suitable for the required film characteristics. Whether it can be done is a problem.
 スパッタリング法を用いて基板への光記録媒体用薄膜を形成する場合、ターゲットの材料によってパーティクルの発生が多くなり、品質を低下させる場合がある。特に高記録密度媒体ではパーティクルなどによる記録ビットのエラー発生が深刻な問題となる。これが原因で、不良品となって歩留まりが低下するという問題が発生する。 When a thin film for an optical recording medium is formed on a substrate using a sputtering method, the generation of particles may increase depending on the target material, which may reduce the quality. Particularly in a high recording density medium, the occurrence of a recording bit error due to particles or the like becomes a serious problem. This causes a problem that the product becomes defective and the yield decreases.
 従来、提案されている光記録媒体として、多数の材料の提案がなされている。例えば、特許文献1には、基板上に少なくとも記録層を形成した光記録媒体であって、記録層の構成元素の主成分がBi及びO(酸素)であり、Bを含有し、さらにGe、Li、Sn、Cu、Fe、Pd、Zn、Mg、Nd、Mn、Niから選択される少なくとも一種の元素Xを含有する光記録媒体が記載されている。 Conventionally, many materials have been proposed as optical recording media that have been proposed. For example, Patent Document 1 discloses an optical recording medium in which at least a recording layer is formed on a substrate, the main components of the constituent elements of the recording layer are Bi and O (oxygen), contain B, Ge, An optical recording medium containing at least one element X selected from Li, Sn, Cu, Fe, Pd, Zn, Mg, Nd, Mn, and Ni is described.
 また、特許文献2には、記録層が、Bi、M(MはMg、Al、Cr、Mn、Co、Fe、Cu、Zn、Li、Si、Ge、Zr、Ti、Hf、Sn、Mo、V、Nb、Y、Taのうち少なくとも一つの元素)及び酸素を含有し、情報が記録された記録マーク部が、該記録層に含有される元素の結晶及び/又はそれらの元素の酸化物の結晶を含むことを特徴とする追記型光記録媒体が記載されている。 Patent Document 2 discloses that the recording layer has Bi, M (M is Mg, Al, Cr, Mn, Co, Fe, Cu, Zn, Li, Si, Ge, Zr, Ti, Hf, Sn, Mo, V, Nb, Y, Ta) and oxygen, and the recording mark portion on which the information is recorded is composed of crystals of the elements contained in the recording layer and / or oxides of these elements. A write-once optical recording medium characterized by containing crystals is described.
 この他にも、特許文献3-特許文献8が提案されている。このような中で、ビスマス(Bi)、ゲルマニウム(Ge)、酸素(O)からなる光記録媒体の組合せが考えられ、またこれらの光記録媒体を、焼結体ターゲットのスパッタリングにより成膜する記載もある。しかし、このBi-Ge-O系焼結体スパッタリングターゲットというのは、熱衝撃に弱く、高パワーによるスパッタリング時に割れ、亀裂が入ることが多く、これによるパーティクルが発生し、記録膜等の品質を損ねる問題があった。 In addition, Patent Documents 3 to 8 have been proposed. Under such circumstances, a combination of optical recording media composed of bismuth (Bi), germanium (Ge), and oxygen (O) is conceivable, and these optical recording media are described as being formed by sputtering of a sintered target. There is also. However, this Bi-Ge-O-based sintered sputtering target is vulnerable to thermal shock, and often cracks and cracks occur during sputtering with high power, resulting in the generation of particles and improving the quality of the recording film and the like. There was a problem to lose.
特開2008-210492号公報JP 2008-210492 A 特開2006-116948号公報JP 2006-116948 A 特開2003-48375号公報JP 2003-48375 A 特開2005-161831号公報JP 2005-161831 A 特開2005-108396号公報JP 2005-108396 A 特開2007-169779号公報JP 2007-169779 A 特開2008-273167号公報JP 2008-273167 A 特許第4271063号公報Japanese Patent No. 4271063
 本発明は、Bi-Ge-O系焼結体スパッタリングターゲット及び同ターゲットの製造方法並びに光記録媒体に関し、特に耐熱衝撃性に優れ、高パワーでのスパッタリングが可能であるため生産効率の大幅な改善が期待できると共に、スパッタリングの際にターゲットの割れが発生せず、パーティクルの発生が少なく、安定して高品質の薄膜の作製が可能であり、記録ビットのエラー発生のない光記録媒体を得ることができるBi-Ge-O系焼結体スパッタリングターゲット及び同ターゲットの製造方法並びに光記録媒体を提供することを課題とする。 The present invention relates to a Bi—Ge—O-based sintered sputtering target, a method for producing the target, and an optical recording medium. Particularly, since it has excellent thermal shock resistance and can be sputtered at high power, production efficiency is greatly improved. To obtain an optical recording medium in which no target cracks occur during sputtering, particle generation is small, a high-quality thin film can be stably produced, and recording bit errors do not occur. It is an object of the present invention to provide a Bi—Ge—O-based sintered sputtering target, a method for producing the target, and an optical recording medium.
 上記の課題を解決するために、本発明者らは鋭意研究を行った結果、分散系のBi12GeO20粒子を微粒子化することで、個々の粒子の加熱・冷却時の熱膨張・熱収縮量が減少し、耐熱衝撃性が向上するとの知見を得た。 In order to solve the above-mentioned problems, the present inventors have conducted intensive research. As a result, the Bi 12 GeO 20 particles in the dispersion system are made fine particles, so that the thermal expansion / contraction of each particle during heating / cooling is reduced. It was found that the amount was reduced and the thermal shock resistance was improved.
 本発明は、この知見に基づき、
 1)ビスマス(Bi)、ゲルマニウム(Ge)、酸素(O)からなる焼結体ターゲットであって、BiとGeの原子数比が、0.57<(Bi/(Bi+Ge))<0.75であり、結晶相としてBi12GeO20、BiGe12の2相から構成されることを特徴とするBi-Ge-O系焼結体スパッタリングターゲット
 2)Bi12GeO20とBiGe12のモル比が、(Bi12GeO20/BiGe12)<0.56であることを特徴とする上記1)記載のBi-Ge-O系焼結体スパッタリングターゲット
 3)ターゲット焼結体中のBi12GeO20の最大粒径が3μm以下であることを特徴とする上記1)又は2)記載のBi-Ge-O系焼結体スパッタリングターゲット
 4)ターゲットに200°C、30分の加熱後、水中急冷による熱衝撃を与えた場合の、該熱衝撃前後の平均曲げ強度低下率が50%以下であることを特徴とする上記1)~3)のいずれか一項に記載の焼結体スパッタリングターゲット
 5)上記1)~4)のいずれか一項に記載のターゲットを用いてスパッタリングすることにより成膜した光記録媒体、を提供する。
The present invention is based on this finding,
1) A sintered compact target composed of bismuth (Bi), germanium (Ge), and oxygen (O), and the atomic ratio of Bi and Ge is 0.57 <(Bi / (Bi + Ge)) <0.75. Bi—Ge—O-based sintered sputtering target characterized by being composed of two phases of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 as crystal phases 2) Bi 12 GeO 20 and Bi 4 Ge The Bi—Ge—O-based sintered sputtering target according to 1) above, wherein the molar ratio of 3 O 12 is (Bi 12 GeO 20 / Bi 4 Ge 3 O 12 ) <0.56 3) above 1) or 2) Bi-GeO oxide sintered sputtering target 4 according) data maximum particle size of the Bi 12 GeO 20 of the target sintered body in is equal to or is 3μm or less 1) to 3) above, wherein the average bending strength reduction rate before and after the thermal shock is 50% or less when the get is subjected to thermal shock by quenching in water after heating at 200 ° C. for 30 minutes. 5) A sintered sputtering target according to any one of 5) and 5) an optical recording medium formed by sputtering using the target according to any one of 1) to 4) above.
 また、本発明は、
 6)GeO粉14.3mol%及びBi粉85.7mol%を混合後、固相反応させて得たBi12GeO20粉と、GeO粉60.0mol%及びBi粉40.0mol%を混合後、固相反応させて得たBiGe12粉末とを出発原料とし、ホットプレスすることにより、焼結体を作製することを特徴とするBi-Ge-O系焼結体スパッタリングターゲットの製造方法
 7)Bi12GeO20粉とBiGe12粉末とを出発原料とし、BiとGeの原子数比が、0.57<(Bi/(Bi+Ge))<0.75となるように混合した後、600~840°C、加圧力0~400kg/cmでホットプレスすることにより、焼結体を作製することを特徴とする上記6)記載のBi-Ge-O系焼結体スパッタリングターゲットの製造方法
 8)平均粒径を1μm以下に微粉砕したBi12GeO20粉を使用することを特徴とする上記6)又は7)記載のBi-Ge-O系焼結体スパッタリングターゲットの製造方法、を提供する。
The present invention also provides:
6) Bi 12 GeO 20 powder obtained by mixing a GeO 2 powder 14.3 mol% and Bi 2 O 3 powder 85.7 mol%, followed by solid phase reaction, GeO 2 powder 60.0 mol%, and Bi 2 O 3 powder Bi-Ge-O is characterized in that a sintered body is produced by hot-pressing Bi 4 Ge 3 O 12 powder obtained by mixing solid phase reaction after mixing 40.0 mol%. 7) Manufacturing method of sintered body sputtering target 7) Bi 12 GeO 20 powder and Bi 4 Ge 3 O 12 powder are used as starting materials, and the atomic ratio of Bi and Ge is 0.57 <(Bi / (Bi + Ge)) <6> The Bi according to 6) above, wherein the sintered body is prepared by hot pressing at 600 to 840 ° C. and an applied pressure of 0 to 400 kg / cm 2 after mixing so as to satisfy <0.75. -Ge- Method for producing O-based sintered sputtering target 8) Bi-Ge-O-based firing as described in 6) or 7) above, wherein Bi 12 GeO 20 powder finely pulverized to an average particle size of 1 μm or less is used. A method for producing a combined sputtering target is provided.
 本発明のBi-Ge-O系焼結体スパッタリングターゲットは、特に耐熱衝撃性に優れ、高パワーでのスパッタリングが可能であるため生産効率の大幅な改善が期待できると共に、スパッタリングの際にターゲットの割れが発生せず、パーティクルの発生が少なく、安定して高品質の薄膜の作製が可能であり、記録ビットのエラー発生のない光記録媒体を得ることができるという優れた効果を有する。 The Bi—Ge—O-based sintered sputtering target of the present invention is particularly excellent in thermal shock resistance and can be sputtered at high power, so that significant improvement in production efficiency can be expected. There is an excellent effect that an optical recording medium can be obtained, in which cracks do not occur, particle generation is small, a high-quality thin film can be stably produced, and no recording bit error occurs.
実施例1で得られた焼結体の走査型電子顕微鏡観察結果を示す写真である。2 is a photograph showing a scanning electron microscope observation result of the sintered body obtained in Example 1. FIG. 比較例1で得られた焼結体の走査型電子顕微鏡観察結果を示す写真である。6 is a photograph showing a scanning electron microscope observation result of a sintered body obtained in Comparative Example 1.
 本発明のBi-Ge-O系焼結体スパッタリングターゲットは、ビスマス(Bi)、ゲルマニウム(Ge)、酸素(O)からなる焼結体ターゲットであって、BiとGeの原子数比が、0.57<(Bi/(Bi+Ge))<0.75であり、結晶相としてBi12GeO20、BiGe12の2相から構成されることを特徴とする。この組成を利用した記録膜は、多層化による高密度記録が達成できる好適な組成であり、良好なスパッタリング成膜を安定的に行うことが可能である。 The Bi—Ge—O based sintered sputtering target of the present invention is a sintered target made of bismuth (Bi), germanium (Ge), and oxygen (O), and the atomic ratio of Bi and Ge is 0. .57 <(Bi / (Bi + Ge)) <0.75, and the crystal phase is composed of two phases of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 . A recording film using this composition is a suitable composition that can achieve high-density recording by multilayering, and can stably perform good sputtering film formation.
 一般に、酸化ビスマス(Bi)と酸化ゲルマニウム(GeO)の粉末を出発原料とし、これを焼結して、当該組成ターゲットを作製した場合、Bi12GeO20とBiGe12の2相共存組成となる。
 ところが、Bi12GeO20とBiGe12は熱膨張係数差が大きいため、熱衝撃に極めて弱くなり、高パワーでのスパッタリング成膜時に割れが発生するという問題が発生する。因みに、Bi12GeO20の熱膨張係数は1.39×10-5で、BiGe12の熱膨張係数は6.00×10-6である。
In general, when a powder of bismuth oxide (Bi 2 O 3 ) and germanium oxide (GeO 2 ) is used as a starting material and sintered to produce the composition target, Bi 12 GeO 20 and Bi 4 Ge 3 O 12 The two-phase coexistence composition.
However, since Bi 12 GeO 20 and Bi 4 Ge 3 O 12 have a large difference in thermal expansion coefficient, they are extremely vulnerable to thermal shock, and there arises a problem that cracking occurs during sputtering film formation at high power. Incidentally, the thermal expansion coefficient of Bi 12 GeO 20 is 1.39 × 10 −5 , and the thermal expansion coefficient of Bi 4 Ge 3 O 12 is 6.00 × 10 −6 .
 一方、当該組成範囲内では、BiGe12が母材となり、Bi12GeO20粒子が分散する系となる。このとき、分散系のBi12GeO20粒子を微粒子化することで、個々の粒子の加熱・冷却時の熱膨張・熱収縮量が減少し、耐熱衝撃性が向上することが判明した。
 また、BiとGeOを出発原料とし、Bi12GeO20とBiGe12が共存する状態で微粉砕を行うと、BiGe12が選択的に微粉砕されてしまい、分散系のBi12GeO20が粉砕されにくいことが判明した。
 そこで、Bi12GeO20とBiGe12を出発原料とし、あらかじめBi12GeO20を微粉砕することで、耐熱衝撃性の向上を実現した。
On the other hand, within the composition range, Bi 4 Ge 3 O 12 serves as a base material, and Bi 12 GeO 20 particles are dispersed. At this time, it has been found that by making the Bi 12 GeO 20 particles in the dispersion system fine particles, the thermal expansion / shrinkage amount of each particle during heating / cooling is reduced and the thermal shock resistance is improved.
Also, the Bi 2 O 3 and GeO 2 as starting materials, when pulverized in a state of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 coexist, Bi 4 Ge 3 O 12 is selectively milled Therefore, it was found that the dispersion system Bi 12 GeO 20 was not easily pulverized.
Therefore, Bi 12 GeO 20 and Bi 4 Ge 3 O 12 were used as starting materials, and Bi 12 GeO 20 was finely pulverized in advance to improve thermal shock resistance.
 この結果、ターゲットの耐熱衝撃性が向上し、これによって高パワーでの成膜が可能となり、生産効率を上昇させることができる大きな利点が得られた。
 また、割れや亀裂が原因となるパーティクルの発生が著しく減少し、安定した高品質の薄膜の作製が可能となり、記録ビットのエラー発生のない、そして高記録密度が達成できる光記録媒体の製造が可能となるという効果が得られた。
 Bi12GeO20とBiGe12のモル比を(Bi12GeO20/BiGe12)<0.56とすることが、耐熱衝撃性を向上させる上で有効である。
 さらに、ターゲット焼結体中のBi12GeO20の粒径を微細化する場合に、最大粒径が3ミクロン以下、好ましくは平均粒径が1μm以下とすることがさらに有効である。上記のターゲットは、200°C、30分の加熱後、水中急冷による熱衝撃を与えた場合の、該熱衝撃前後の平均曲げ強度低下率が50%以下を達成することが可能となった。
As a result, the thermal shock resistance of the target was improved, which enabled film formation with high power, and a great advantage that production efficiency could be increased was obtained.
In addition, the generation of particles caused by cracks and cracks is remarkably reduced, making it possible to produce stable high quality thin films, producing no recording bit errors, and producing optical recording media that can achieve high recording density. The effect that it becomes possible was obtained.
It is effective in improving the thermal shock resistance that the molar ratio of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 is (Bi 12 GeO 20 / Bi 4 Ge 3 O 12 ) <0.56.
Further, when the particle size of Bi 12 GeO 20 in the target sintered body is made finer, it is more effective that the maximum particle size is 3 microns or less, preferably the average particle size is 1 μm or less. When the target was subjected to thermal shock by quenching in water after heating at 200 ° C. for 30 minutes, it was possible to achieve an average bending strength reduction rate of 50% or less before and after the thermal shock.
 従来品のBi12GeO20とBiGe12の2相共存組成のターゲットの場合には、前記熱衝撃前後の平均曲げ強度低下率が80%を超えているのに対して、大きな改善効果があった。これによって、ターゲットの熱衝撃による割れを抑制する上で、ターゲットの特性を直接的に評価できるものである。
 本発明は、上記のターゲットを用いてスパッタリングすることにより成膜した光記録媒体を包含するものである。
In the case of a target having a two-phase coexisting composition of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 as a conventional product, the average bending strength reduction rate before and after the thermal shock exceeds 80%, which is a significant improvement. There was an effect. This makes it possible to directly evaluate the characteristics of the target in order to suppress cracking of the target due to thermal shock.
The present invention includes an optical recording medium formed by sputtering using the above target.
 Bi-Ge-O系焼結体スパッタリングターゲットの製造に際しては、GeO粉14.3mol%及びBi粉85.7mol%を混合後、固相反応させて得たBi12GeO20粉と、GeO粉60.0mol%及びBi粉40.0mol%を混合後、固相反応させて得たBiGe12粉末とを出発原料とし、これらを混合してホットプレスすることにより、焼結体を作製することができる。 In the production of the Bi—Ge—O based sintered sputtering target, 14.3 mol% of GeO 2 powder and 85.7 mol% of Bi 2 O 3 powder were mixed, and then Bi 12 GeO 20 powder obtained by solid phase reaction was used. Then, 60.0 mol% of GeO 2 powder and 40.0 mol% of Bi 2 O 3 powder are mixed, and then Bi 4 Ge 3 O 12 powder obtained by solid phase reaction is used as a starting material, and these are mixed and hot pressed. Thus, a sintered body can be produced.
 さらに、本願発明のBi-Ge-O系焼結体スパッタリングターゲットの製造に際しては、Bi12GeO20粉とBiGe12粉末とを出発原料とし、BiとGeの原子数比が、0.57<(Bi/(Bi+Ge))<0.75となるように混合した後、600~840°C、加圧力0~400kg/cmでホットプレスすることにより、焼結体を作製することが特に有効である。
 この場合にも、平均粒径が1μm以下に微粉砕したBi12GeO20粉を使用することが有効である。
Furthermore, in the production of the Bi—Ge—O based sintered sputtering target of the present invention, Bi 12 GeO 20 powder and Bi 4 Ge 3 O 12 powder are used as starting materials, and the atomic ratio of Bi and Ge is 0. .57 <(Bi / (Bi + Ge)) <0.75, and then mixed by hot pressing at 600 to 840 ° C. and pressure of 0 to 400 kg / cm 2 to produce a sintered body. Is particularly effective.
Also in this case, it is effective to use Bi 12 GeO 20 powder finely pulverized to an average particle size of 1 μm or less.
 この焼結条件は、均一組成のターゲットを得ることができる好適な条件である。上記の範囲を外れる焼結条件でターゲットを製造することも可能であるが、ターゲット品質の再現性が劣るので、上記の範囲とするのが望ましい。また、前記原料段階のBiとGeの原子数比、0.57<(Bi/(Bi+Ge))<0.75は、ターゲットに直接反映され、同組成比のターゲットを得ることができる。 This sintering condition is a suitable condition for obtaining a target having a uniform composition. Although the target can be manufactured under sintering conditions outside the above range, the reproducibility of the target quality is inferior, so that the above range is desirable. Further, the atomic ratio of Bi to Ge in the raw material stage, 0.57 <(Bi / (Bi + Ge)) <0.75 is directly reflected on the target, and a target having the same composition ratio can be obtained.
 以下、実施例および比較例に基づいて説明する。なお、本実施例はあくまで一例であり、この例によって何ら制限されるものではない。すなわち、本発明は特許請求の範囲によってのみ制限されるものであり、本発明に含まれる実施例以外の種々の変形を包含するものである。 Hereinafter, description will be made based on examples and comparative examples. In addition, a present Example is an example to the last, and is not restrict | limited at all by this example. In other words, the present invention is limited only by the scope of the claims, and includes various modifications other than the examples included in the present invention.
(実施例1)
 純度3N(99.9%)の酸化ビスマスと酸化ゲルマニウムの粉末を出発原料とし、予めBi12GeO20粉とBiGe12粉末を準備し、これらをそれぞれ、BiとGeの原子数比が、0.67となるように、Bi12GeO20粉16.67mol%とBiGe12粉83.33mol%を調合した後、混合し、さらに混合後の粉末をカーボン製ダイスに充填し、温度700°C、圧力250kg/cmの条件でホットプレスを行った。
Example 1
Bi 12 GeO 20 powder and Bi 4 Ge 3 O 12 powder were prepared in advance using powders of bismuth oxide and germanium oxide having a purity of 3N (99.9%) as a starting material. However, Bi 12 GeO 20 powder 16.67 mol% and Bi 4 Ge 3 O 12 powder 83.33 mol% were mixed and mixed, and the mixed powder was filled in a carbon die so as to be 0.67. Then, hot pressing was performed under the conditions of a temperature of 700 ° C. and a pressure of 250 kg / cm 2 .
 ホットプレス後の焼結体を仕上げ加工してターゲットとした。ターゲットの相対密度は96%(100%密度で7.15g/cm)であった。
 この焼結体の、X線回折測定により、Bi12GeO20、BiGe12の2相構造であることを確認した。
 次に、この焼結体の走査型電子顕微鏡観察写真を図1に示す。これにより、BiGe12が母材(写真の灰色部分)となり、Bi12GeO20が分散系(写真の白色部分)であることを確認した。またBi12GeO20の最大粒径が3μm以下であり、平均粒径が1μm以下であることを確認した。
The sintered body after hot pressing was finished to obtain a target. The relative density of the target was 96% (7.15 g / cm 3 at 100% density).
The sintered body by X-ray diffraction measurement, it was confirmed that a two-phase structure of Bi 12 GeO 20, Bi 4 Ge 3 O 12.
Next, a scanning electron microscope photograph of this sintered body is shown in FIG. Thereby, it was confirmed that Bi 4 Ge 3 O 12 became a base material (gray portion in the photograph) and Bi 12 GeO 20 was a dispersion (white portion in the photograph). It was also confirmed that the maximum particle size of Bi 12 GeO 20 was 3 μm or less and the average particle size was 1 μm or less.
 次に、このターゲットを200°C、30分の加熱後、水中急冷による熱衝撃を与えた。その後、JIS規格1601による曲げ試験(ターゲット中の任意の箇所5点から、幅4±0.1mm、高さ3±0.1mm、長さ40~50mmの試験片を採取して測定し、5点の測定結果の平均値を求める)を実施し、該熱衝撃前後の平均曲げ強度比(強度の低下率)を測定した。この測定結果を同様に表1に示す。測定箇所により多少のばらつきが生じたが、いずれも50%未満となり、強度の低下率が少なかった。 Next, this target was heated at 200 ° C. for 30 minutes and then subjected to thermal shock by quenching in water. Thereafter, a bending test according to JIS standard 1601 (from 5 arbitrary points in the target, a test piece having a width of 4 ± 0.1 mm, a height of 3 ± 0.1 mm, and a length of 40 to 50 mm was sampled and measured. The average value of the measurement results of the points was determined), and the average bending strength ratio (strength reduction rate) before and after the thermal shock was measured. The measurement results are similarly shown in Table 1. Some variation occurred depending on the measurement location, but all were less than 50%, and the rate of decrease in strength was small.
 次に、このターゲットを用いて、ガラス基板上に1kWで約1時間プレスパッタした後、2kWで10sスパッタ、5s停止を10,000回繰り返し、このスパッタサイクルの作業後、チャンバーを開放して目視により、ターゲットの異常を観察したが、ターゲットに割れや亀裂の発生は全く認められなかった。また、スパッタリング中のパーティクルの発生も少なかった。
 この結果、本願発明の実施例は、ターゲットの割れの発生がなく、生産効率を上げることができ、かつ安定して高品質の薄膜の作製が可能であり、記録ビットのエラー発生のない光記録媒体を得ることができるという優れた効果を有する良好なターゲットであった。
Next, using this target, pre-sputtering was performed on a glass substrate at 1 kW for about 1 hour, and then 10 s sputtering at 2 kW and 5 s stop were repeated 10,000 times. After this sputtering cycle, the chamber was opened and visually observed. Thus, the abnormality of the target was observed, but no cracks or cracks were observed in the target. Also, the generation of particles during sputtering was small.
As a result, according to the embodiment of the present invention, there is no generation of cracks in the target, the production efficiency can be increased, and a high-quality thin film can be stably produced. It was a good target having an excellent effect of being able to obtain a medium.
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001
(比較例1)
 純度3N(99.9%)の酸化ビスマスと酸化ゲルマニウムの粉末を出発原料とし、これらをそれぞれ、BiとGeの原子数比が、0.67となるように、GeO粉50.0mol%、Bi粉50.0mol%を調合した後、混合し、さらに混合後の粉末をカーボン製ダイスに充填し、温度730°C、圧力250kg/cmの条件でホットプレスを行った。
(Comparative Example 1)
A powder of bismuth oxide and germanium oxide having a purity of 3N (99.9%) is used as a starting material, and GeO 2 powder is 50.0 mol% so that the atomic ratio of Bi and Ge is 0.67, respectively. After preparing 50.0 mol% of Bi 2 O 3 powder, it was mixed, and the powder after mixing was filled in a carbon die, and hot pressing was performed under conditions of a temperature of 730 ° C. and a pressure of 250 kg / cm 2 .
 ホットプレス後の焼結体を仕上げ加工してターゲットとした。ターゲットの相対密度は103%(100%密度で7.44g/cm)であった。
 この焼結体のX線回折測定により、ターゲットの結晶相がBi12GeO20、BiGe12の2相構造であることを確認した。
 次に、この焼結体の走査型電子顕微鏡観察写真を図2に示す。これにより、BiGe12が母材(写真の灰色部分)となり、Bi12GeO20が分散系(写真の白色部分)であることを確認した。またBi12GeO20の最大粒径が8μm以下、平均粒径が4μm以下であることを確認した。
The sintered body after hot pressing was finished to obtain a target. The relative density of the target was 103% (7.44 g / cm 3 at 100% density).
From the X-ray diffraction measurement of this sintered body, it was confirmed that the crystal phase of the target was a two-phase structure of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 .
Next, a scanning electron microscope photograph of this sintered body is shown in FIG. Thereby, it was confirmed that Bi 4 Ge 3 O 12 became a base material (gray portion in the photograph) and Bi 12 GeO 20 was a dispersion (white portion in the photograph). Further, it was confirmed that the maximum particle size of Bi 12 GeO 20 was 8 μm or less and the average particle size was 4 μm or less.
 次に、このターゲットを200°C、30分の加熱後、水中急冷による熱衝撃を加えた。その後、JIS1601による曲げ強度試験を実施した。該熱衝撃前後の平均曲げ強度比(強度の低下率)の測定結果を、同様に表1に示す。この結果、平均曲げ強度の低下率が82.1%となった。
 次に、このターゲットを用いて、ガラス基板上に1kWで約1時間プレスパッタした後、2kWで10sスパッタ、5s停止を10回繰り返し、このスパッタサイクルの作業後、チャンバーを開放して目視により、ターゲットの異常を観察したところ、ターゲットに割れが発生していた。また、実施例に較べて、パーティクルの発生が著しく増加した。これはスパッタリング中のターゲットの割れが原因と考えられる。
Next, this target was heated at 200 ° C. for 30 minutes, and then subjected to thermal shock by quenching in water. Then, the bending strength test by JIS1601 was implemented. The measurement results of the average bending strength ratio (strength reduction rate) before and after the thermal shock are also shown in Table 1. As a result, the reduction rate of the average bending strength was 82.1%.
Next, using this target, it was pre-sputtered on a glass substrate at 1 kW for about 1 hour, then 10 s spatter at 2 kW and 5 s stop were repeated 10 times. After this sputtering cycle, the chamber was opened and visually observed. When the abnormality of the target was observed, the target was cracked. In addition, the generation of particles was remarkably increased compared to the examples. This is thought to be caused by cracks in the target during sputtering.
 本発明のBi-Ge-O系焼結体スパッタリングターゲット及びこのターゲットの製造方法によれば、特に耐熱衝撃性に優れ、高パワーでのスパッタリングが可能であるため生産効率の大幅な改善が期待できると共に、スパッタリングの際にターゲットの割れが発生せず、パーティクルの発生が少なく、安定して高品質の薄膜の作製が可能であり、記録ビットのエラー発生のない光記録媒体を得ることができるという優れた効果を有する。光記録媒体の成膜の生産効率を上げることができ、光記録媒体の製造に好適なターゲットを提供できる。 According to the Bi—Ge—O-based sintered sputtering target of the present invention and the method for producing the target, since it is particularly excellent in thermal shock resistance and can be sputtered at high power, significant improvement in production efficiency can be expected. At the same time, the target is not cracked during sputtering, the generation of particles is small, a high-quality thin film can be stably produced, and an optical recording medium free from recording bit errors can be obtained. Has an excellent effect. The production efficiency of film formation of the optical recording medium can be increased, and a suitable target for manufacturing the optical recording medium can be provided.

Claims (8)

  1.  ビスマス(Bi)、ゲルマニウム(Ge)、酸素(O)からなる焼結体ターゲットであって、BiとGeの原子数比が、0.57<(Bi/(Bi+Ge))<0.75であり、結晶相としてBi12GeO20、BiGe12の2相から構成されることを特徴とするBi-Ge-O系焼結体スパッタリングターゲット。 A sintered compact target composed of bismuth (Bi), germanium (Ge), and oxygen (O), and the atomic ratio of Bi and Ge is 0.57 <(Bi / (Bi + Ge)) <0.75 A Bi—Ge—O-based sintered sputtering target comprising two phases of Bi 12 GeO 20 and Bi 4 Ge 3 O 12 as crystal phases.
  2.  Bi12GeO20とBiGe12のモル比が、(Bi12GeO20/BiGe12)<0.56であることを特徴とする請求項1記載のBi-Ge-O系焼結体スパッタリングターゲット。 The Bi-Ge-O according to claim 1, wherein the molar ratio of Bi 12 GeO 20 to Bi 4 Ge 3 O 12 is (Bi 12 GeO 20 / Bi 4 Ge 3 O 12 ) <0.56. -Based sintered sputtering target.
  3.  ターゲット焼結体中のBi12GeO20の最大粒径が3μm以下であることを特徴とする請求項1又は2記載のBi-Ge-O系焼結体スパッタリングターゲット。 3. The Bi—Ge—O based sintered sputtering target according to claim 1, wherein the maximum particle size of Bi 12 GeO 20 in the target sintered body is 3 μm or less.
  4.  ターゲットに200°C、30分の加熱後、水中急冷による熱衝撃を与えた場合の、該熱衝撃前後の平均曲げ強度低下率が50%以下であることを特徴とする請求項1~3のいずれか一項に記載の焼結体スパッタリングターゲット。 The average bending strength reduction rate before and after the thermal shock when the target is subjected to thermal shock by quenching in water after heating at 200 ° C for 30 minutes is 50% or less. The sintered compact sputtering target as described in any one of Claims.
  5.  請求項1~4のいずれか一項に記載のターゲットを用いてスパッタリングすることにより成膜した光記録媒体。 An optical recording medium formed by sputtering using the target according to any one of claims 1 to 4.
  6.  GeO粉14.3mol%及びBi粉85.7mol%を混合後、固相反応させて得たBi12GeO20粉と、GeO粉60.0mol%及びBi粉40.0mol%を混合後、固相反応させて得たBiGe12粉末とを出発原料とし、ホットプレスすることにより、焼結体を作製することを特徴とするBi-Ge-O系焼結体スパッタリングターゲットの製造方法。 After mixing the GeO 2 powder 14.3 mol% and Bi 2 O 3 powder 85.7mol%, and Bi 12 GeO 20 powder obtained by a solid phase reaction, GeO 2 powder 60.0 mol% and Bi 2 O 3 powder 40. Bi-Ge-O-based sintering is characterized in that a sintered body is produced by hot-pressing Bi 4 Ge 3 O 12 powder obtained by solid-phase reaction after mixing 0 mol% as a starting material. A method for producing a combined sputtering target.
  7.  Bi12GeO20粉とBiGe12粉末とを出発原料とし、BiとGeの原子数比が、0.57<(Bi/(Bi+Ge))<0.75となるように混合した後、600~840°C、加圧力0~400kg/cmでホットプレスすることにより、焼結体を作製することを特徴とする請求項6記載のBi-Ge-O系焼結体スパッタリングターゲットの製造方法。 After mixing Bi 12 GeO 20 powder and Bi 4 Ge 3 O 12 powder as starting materials, the atomic ratio of Bi and Ge is mixed so that 0.57 <(Bi / (Bi + Ge)) <0.75 The Bi-Ge-O-based sintered sputtering target according to claim 6, wherein the sintered body is produced by hot pressing at 600 to 840 ° C and a pressing force of 0 to 400 kg / cm 2 . Production method.
  8.  平均粒径が1μm以下に微粉砕したBi12GeO20粉を使用することを特徴とする請求項6又は7記載のBi-Ge-O系焼結体スパッタリングターゲットの製造方法。 The method for producing a Bi-Ge-O-based sintered sputtering target according to claim 6 or 7, wherein Bi 12 GeO 20 powder finely pulverized to an average particle size of 1 µm or less is used.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103000198A (en) * 2011-09-09 2013-03-27 铼德科技股份有限公司 Optical recording medium and recording material for the same
JP2014141375A (en) * 2013-01-24 2014-08-07 Ulvac Japan Ltd Method for producing sintered compact powder, sintered compact powder, sputtering target, method for producing sputtering target and apparatus for producing sintered compact powder

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103586015B (en) * 2013-11-22 2015-07-22 武汉理工大学 Method for preparing regular-triangular-pyramid-shaped bismuth germinate visible-light catalyst

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51109300A (en) * 1975-03-20 1976-09-28 Matsushita Electric Ind Co Ltd Gerumaniumusanbisumasuhakumakuno seizohoho
JPS5313200A (en) * 1976-07-21 1978-02-06 Matsushita Electric Ind Co Ltd Production method of piezo-electric thin film
JPS58167429A (en) * 1982-03-26 1983-10-03 Otsuka Chem Co Ltd Amorphous material of bismuth-germanium type oxide and preparation thereof
JP2003277923A (en) * 2002-03-27 2003-10-02 Sumitomo Metal Mining Co Ltd Ge-Bi ALLOY TARGET FOR SPUTTERING AND PRODUCTION METHOD THEREOF

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101328573B (en) * 2004-08-31 2010-11-10 株式会社理光 Once-writing-in multi-reading optical recording medium, sputtering target
JP2008097802A (en) * 2006-09-15 2008-04-24 Tdk Corp Multilayer optical recording medium and recording method on multilayer optical recording medium
JP4764858B2 (en) * 2007-01-30 2011-09-07 株式会社リコー Optical recording medium, sputtering target, and manufacturing method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51109300A (en) * 1975-03-20 1976-09-28 Matsushita Electric Ind Co Ltd Gerumaniumusanbisumasuhakumakuno seizohoho
JPS5313200A (en) * 1976-07-21 1978-02-06 Matsushita Electric Ind Co Ltd Production method of piezo-electric thin film
JPS58167429A (en) * 1982-03-26 1983-10-03 Otsuka Chem Co Ltd Amorphous material of bismuth-germanium type oxide and preparation thereof
JP2003277923A (en) * 2002-03-27 2003-10-02 Sumitomo Metal Mining Co Ltd Ge-Bi ALLOY TARGET FOR SPUTTERING AND PRODUCTION METHOD THEREOF

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103000198A (en) * 2011-09-09 2013-03-27 铼德科技股份有限公司 Optical recording medium and recording material for the same
JP2014141375A (en) * 2013-01-24 2014-08-07 Ulvac Japan Ltd Method for producing sintered compact powder, sintered compact powder, sputtering target, method for producing sputtering target and apparatus for producing sintered compact powder

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