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TW201938513A - Sputtering target material and sputtering target - Google Patents

Sputtering target material and sputtering target Download PDF

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Publication number
TW201938513A
TW201938513A TW108107376A TW108107376A TW201938513A TW 201938513 A TW201938513 A TW 201938513A TW 108107376 A TW108107376 A TW 108107376A TW 108107376 A TW108107376 A TW 108107376A TW 201938513 A TW201938513 A TW 201938513A
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sputtering target
less
content
oxide
sno
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TW108107376A
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TWI742348B (en
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田尾幸樹
畠英雄
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日商鋼臂功科研股份有限公司
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G25/00Compounds of zirconium
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/453Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates
    • C04B35/457Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates based on tin oxides or stannates
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • 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
    • G11B7/252Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
    • G11B7/257Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of layers having properties involved in recording or reproduction, e.g. optical interference layers or sensitising layers or dielectric layers, which are protecting the recording layers
    • G11B7/2578Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of layers having properties involved in recording or reproduction, e.g. optical interference layers or sensitising layers or dielectric layers, which are protecting the recording layers consisting essentially of inorganic materials
    • 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
    • G11B7/26Apparatus or processes specially adapted for the manufacture of record carriers

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Physical Vapour Deposition (AREA)
  • Manufacturing Optical Record Carriers (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Optical Record Carriers And Manufacture Thereof (AREA)

Abstract

One embodiment of the present invention is a sputtering target material which contains an oxide of zinc (Zn), an oxide of tin (Sn) and an oxide of zirconium (Zr), but does not contain indium (In), and wherein: relative to all elements other than oxygen (O), the zinc content AZn is more than 0 at% but 50 at% or less, the tin content ASn is from 20 at% to 80 at% (inclusive), and the zirconium content AZr is more than 0 at% but 40 at% or less; the Zn content AZn satisfies formula (1); the ratio of the maximum value to the minimum value among the plurality of measured specific resistances is 3 or less; and the specific resistances are 5 * 10<SP>-1</SP> ([Omega].cm) or less. (1): AZn/(AZn + ASn) ≤ 0.6.

Description

濺鍍靶材和濺鍍靶Sputtering target and sputtering target

本發明是有關於一種濺鍍靶材和濺鍍靶。The invention relates to a sputtering target and a sputtering target.

光記錄媒體是由CD、DVD等光碟所代表,被分類為再生專用型、追記型、及重複錄寫型這三種。另外,作為光記錄媒體的記錄方式,已知有記錄層的構成材料發生相變化的方式、經多層化的記錄層進行層間反應的方式、及記錄層的構成材料進行分解的方式等。作為追記型的光碟的記錄層材料,至今為止廣泛使用有機色素材料,但近年來記錄的高密度化不斷發展,亦可使用無機材料。Optical recording media are represented by optical discs such as CDs and DVDs, and are classified into three types of reproduction-only type, write-once type, and re-write type. In addition, as a recording method of an optical recording medium, a method in which a constituent material of a recording layer undergoes a phase change, a method in which a multilayered recording layer performs an interlayer reaction, and a method in which a constituent material of a recording layer is decomposed. As a recording layer material of a write-once optical disc, an organic pigment material has been widely used until now. However, in recent years, the recording density has been increasing, and an inorganic material can also be used.

已知有:於在記錄層中採用金屬氧化物作為無機材料的情況下,藉由該氧化物的分解而進行資訊的記錄,但為了抑制記錄層的經時變化所引起的劣化而使記錄層的訊號特性良好,利用濺鍍法於記錄層的表背形成介電體層。提出一種ZrO2 -In2 O3 系濺鍍靶,其為形成介電體層(保護層)的濺鍍靶,並使所含有的鋯(Zr)的90%以上以Zr與銦(In)的複合氧化物相的形式分散於濺鍍靶材中,藉此耐裂紋性優異(日本專利特開2009-62585號公報)。根據該濺鍍靶,即便以高輸出進行濺鍍亦不會產生裂紋,因此可高效地形成介電體層,光記錄媒體的生產效率得到提高。It is known that when a metal oxide is used as an inorganic material in a recording layer, information is recorded by decomposition of the oxide, but the recording layer is suppressed in order to suppress deterioration due to changes with time of the recording layer. The signal characteristics are good, and a dielectric layer is formed on the front and back of the recording layer by sputtering. A ZrO 2 -In 2 O 3 based sputtering target is proposed, which is a sputtering target that forms a dielectric layer (protective layer), and makes more than 90% of the zirconium (Zr) contained in Zr and indium (In). The form of the composite oxide phase is dispersed in the sputtering target, thereby having excellent crack resistance (Japanese Patent Laid-Open No. 2009-62585). According to this sputtering target, cracks do not occur even if sputtering is performed at a high output, so that the dielectric layer can be efficiently formed, and the production efficiency of the optical recording medium is improved.

然而,若以高輸出進行濺鍍,則發生異常放電,濺鍍靶的基體成為粒狀的塊而於記錄層中飛散,即產生所謂的粒子,但所述ZrO2 -In2 O3 系濺鍍靶中有無法有效地抑制異常放電的擔憂。另外,藉由包含In的氧化物而可確保濺鍍靶的導電性,因此可提高形成速度而縮短步驟作業時間,但In被指定為特定化學物質,因此需要謀求健康障礙防止對策。
[現有技術文獻]
[專利文獻]
However, if sputtering is performed at a high output, abnormal discharge occurs, and the matrix of the sputtering target becomes a granular mass and scatters in the recording layer, that is, so-called particles are generated. However, the ZrO 2 -In 2 O 3 system is sputtered. There is a concern that the plating target cannot effectively suppress abnormal discharge. In addition, since the conductivity of the sputtering target can be ensured by the oxide containing In, the formation speed can be increased, and the step operation time can be shortened. However, In is designated as a specific chemical substance, and it is necessary to take measures to prevent health disorders.
[Prior Art Literature]
[Patent Literature]

[專利文獻1]日本專利特開2009-62585號公報[Patent Document 1] Japanese Patent Laid-Open No. 2009-62585

[發明所欲解決之課題][Problems to be Solved by the Invention]

本發明是基於所述情況而成者,其目的在於提供一種於形成光記錄媒體的介電體層時可有效地抑制異常放電、且無需健康障礙防止對策的濺鍍靶材和濺鍍靶。
[解決課題之手段]
The present invention has been made based on the above circumstances, and an object thereof is to provide a sputtering target and a sputtering target which can effectively suppress abnormal discharge when a dielectric layer of an optical recording medium is formed, and does not require a health obstacle prevention measure.
[Means for solving problems]

用以解決所述課題而成的本發明的一實施方式為一種濺鍍靶材,其包含鋅(Zn)的氧化物、錫(Sn)的氧化物及鋯(Zr)的氧化物,其中相對於氧(O)以外的所有元素,鋅的含量AZn 為超過0 at%且50 at%以下,錫的含量ASn 為20 at%以上且80 at%以下,及鋯的含量AZr 為超過0 at%且40 at%以下,而且鋅的含量AZn 滿足下述式(1);經測定的多個比電阻值中最大值相對於最小值的比為3以下,及所述比電阻值為5×10-1 (Ω·cm)以下;而且所述濺鍍靶材不含有銦(In)。
AZn /(AZn +ASn )≦0.6・・・・・(1)
One embodiment of the present invention, which is made to solve the above-mentioned problems, is a sputtering target, which includes zinc (Zn) oxide, tin (Sn) oxide, and zirconium (Zr) oxide. All elements other than oxygen (O), and Zn content a Zn is more than 0 at% and 50 at% or less, the content of a Sn of tin is at least 20 at% and 80 at% or less, and the content a Zr zirconium is exceeded 0 at% and 40 at% or less, and the content of zinc A Zn satisfies the following formula (1); the ratio of the maximum value to the minimum value among a plurality of measured specific resistance values is 3 or less, and the specific resistance value It is 5 × 10 -1 (Ω · cm) or less; and the sputtering target does not contain indium (In).
A Zn / (A Zn + A Sn ) ≦ 0.6 ・ ・ ・ ・ ・ (1)

該濺鍍靶材是由Zn的氧化物、Sn的氧化物及Zr的氧化物而形成,且含量為所述範圍,因此可製造形成具有優異的特性的介電體層的濺鍍靶。另外,經測定的多個比電阻值的最大值相對於最小值的比為3以下,比電阻值為5×10-1 (Ω·cm)以下,因此於利用濺鍍法形成介電體層時可有效地抑制異常放電,減少粒子的產生。另外,該濺鍍靶材不含有In元素,因此無需健康障礙防止對策。因而,可提高光記錄媒體的生產效率。The sputtering target is formed of an oxide of Zn, an oxide of Sn, and an oxide of Zr, and the content is within the above range. Therefore, a sputtering target capable of forming a dielectric layer having excellent characteristics can be manufactured. In addition, the ratio of the maximum value to the minimum value of the measured specific resistance values is 3 or less, and the specific resistance value is 5 × 10 -1 (Ω · cm) or less. Therefore, when a dielectric layer is formed by a sputtering method Can effectively suppress abnormal discharge and reduce the generation of particles. In addition, since the sputtering target does not contain In element, it is not necessary to take measures to prevent health disorders. Therefore, the production efficiency of the optical recording medium can be improved.

該濺鍍靶材可具有SnO2 相及Zn2 SnO4 相,所述Zn2 SnO4 相中的Zr元素濃度相對於所述SnO2 相中的Zr元素濃度的比為0.1以上且5以下。藉此,可製造強度優異的濺鍍靶。The sputtering target may have a SnO 2 phase and a Zn 2 SnO 4 phase, and a ratio of a Zr element concentration in the Zn 2 SnO 4 phase to a Zr element concentration in the SnO 2 phase is 0.1 or more and 5 or less. Thereby, a sputtering target with excellent strength can be manufactured.

該濺鍍靶材可包含ZrO2 的結晶粒,所述ZrO2 的結晶粒的平均粒徑為5 μm以下。藉此,可製造強度更優異的濺鍍靶。The sputter target may comprise ZrO 2 crystal grains of the ZrO 2 crystal grains of an average particle diameter of 5 μm or less. This makes it possible to produce a sputtering target having more excellent strength.

用以解決所述課題而成的本發明的另一實施方式為濺鍍靶,其包含所述濺鍍靶材。該濺鍍靶於利用濺鍍法形成介電體層時可有效地抑制異常放電,因此可有效地形成介電體層。
[發明的效果]
Another embodiment of the present invention that was made to solve the above-mentioned problems is a sputtering target including the sputtering target. This sputtering target can effectively suppress an abnormal discharge when a dielectric layer is formed by a sputtering method, and thus can effectively form a dielectric layer.
[Effect of the invention]

如以上般,本發明的濺鍍靶材和濺鍍靶於形成光記錄媒體的介電體層時可有效地抑制異常放電,且無需健康障礙防止對策。As described above, when the sputtering target and the sputtering target of the present invention are used to form a dielectric layer of an optical recording medium, abnormal discharge can be effectively suppressed, and no health obstacle prevention measures are required.

以下,對本發明的濺鍍靶材和濺鍍靶的實施形態進行詳細說明。Hereinafter, embodiments of the sputtering target and the sputtering target of the present invention will be described in detail.

[濺鍍靶]
作為本發明的一實施形態的濺鍍靶用於在光記錄媒體的記錄層的表背形成介電體層。該濺鍍靶是利用濺鍍靶材來製造,所述濺鍍靶材包含鋅(Zn)的氧化物、錫(Sn)的氧化物及鋯(Zr)的氧化物,其中相對於氧(O)以外的所有元素,鋅的含量AZn 為超過0 at%且50 at%以下,錫的含量ASn 為20 at%以上且80 at%以下,及鋯的含量為AZr 超過0 at%且40 at%以下,而且鋅的含量AZn 滿足下述式(1);經測定的多個比電阻值中最大值相對於最小值的比為3以下,及所述比電阻值為5×10-1 (Ω·cm)以下;而且所述濺鍍靶材不含有銦(In)。該濺鍍靶材為本發明的另一實施方式。
AZn /(AZn +ASn )≦0.6・・・・・(1)
[Sputter target]
A sputtering target as one embodiment of the present invention is used to form a dielectric layer on the front and back of a recording layer of an optical recording medium. The sputtering target is manufactured by using a sputtering target material, the sputtering target material including zinc (Zn) oxide, tin (Sn) oxide, and zirconium (Zr) oxide, with respect to oxygen (O All elements) other than the zinc content a Zn more than 0 at% and 50 at% or less, the content of a Sn of tin is at least 20 at% and 80 at% or less, and the content of zirconium is a Zr exceeds 0 at% and 40 at% or less, and the content of zinc A Zn satisfies the following formula (1); the ratio of the maximum value to the minimum value of the plurality of specific resistance values measured is 3 or less, and the specific resistance value is 5 × 10 -1 (Ω · cm) or less; and the sputtering target does not contain indium (In). The sputtering target is another embodiment of the present invention.
A Zn / (A Zn + A Sn ) ≦ 0.6 ・ ・ ・ ・ ・ (1)

<濺鍍靶材>
該濺鍍靶材包含Zn、Sn及Zr的各自的氧化物。藉由該濺鍍靶材包含Zn、Sn及Zr的各自的氧化物,可於介電體層包含同一氧化物。介電體層具有防止於記錄層的氧化物進行分解時所放出的氧自記錄層脫離的功能、保持記錄層的耐久性的功能、及調整透過光的量的功能。
< Sputtering target >
This sputtering target contains respective oxides of Zn, Sn, and Zr. Since the sputtering target contains respective oxides of Zn, Sn, and Zr, the same oxide can be contained in the dielectric layer. The dielectric layer has a function of preventing the oxygen released from the recording layer from decomposing from the recording layer, a function of maintaining the durability of the recording layer, and a function of adjusting the amount of transmitted light.

Zn是用以藉由與Sn同時添加至介電體層中來抑制形成於記錄層中的記錄標記的形狀或尺寸的偏差而使抖動降低的元素。Zn is an element for suppressing variations in the shape or size of a recording mark formed in the recording layer by adding it to the dielectric layer at the same time as Sn, thereby reducing jitter.

Sn是用以使介電體層具有防止記錄層的分解的氧氣阻擋功能的元素。Sn is an element for providing a dielectric layer with an oxygen barrier function to prevent decomposition of the recording layer.

Zr是用以提高介電體層的氧氣阻擋功能而抑制記錄層的記錄訊號的劣化的元素。Zr is an element for improving the oxygen barrier function of the dielectric layer and suppressing the deterioration of the recording signal of the recording layer.

該濺鍍靶材的Zn相對於氧以外的所有元素的含量AZn 的下限超過0 at%,較佳為20 at%,更佳為30 at%。另一方面,Zn的含量AZn 的上限為50 at%,較佳為47 at%,更佳為45 at%。於該濺鍍靶材的Zn的含量AZn 未滿所述下限的情況下,有於介電體層中Zn氧化物不足,介電體層無法充分地抑制形成於記錄層的記錄標記的形狀或尺寸的偏差的擔憂。另一方面,於Zn的含量AZn 超過所述上限的情況下,有使其他元素的氧化物的含量不足的擔憂。The lower limit of the content Zn of the sputtering target with respect to all elements other than oxygen, A Zn , exceeds 0 at%, preferably 20 at%, and more preferably 30 at%. On the other hand, the upper limit of the Zn content A Zn is 50 at%, preferably 47 at%, and more preferably 45 at%. In the case where the sputtering target A Zn content of Zn is less than the above lower limit, the dielectric layer has insufficient Zn oxide, the dielectric layer can not be sufficiently suppressed is formed in the shape or size of the recording mark of the recording layer Worries about deviations. On the other hand, when the Zn content A Zn exceeds the above-mentioned upper limit, there is a concern that the content of oxides of other elements may be insufficient.

該濺鍍靶材的Sn相對於氧以外的所有元素的含量ASn 的下限為20 at%,較佳為30 at%,更佳為40 at%。另一方面,Sn的含量ASn 的上限為80 at%,較佳為75 at%,更佳為70 at%。於該濺鍍靶材的Sn的含量ASn 未滿所述下限的情況下,有於介電體層中Sn氧化物不足,難以使介電體層具備防止記錄層的分解的氧氣阻擋功能的擔憂。另一方面,於Sn的含量ASn 超過所述上限的情況下,有使其他元素的氧化物的含量不足的擔憂。The lower limit of the content Sn of the sputtering target with respect to all elements other than oxygen, A Sn , is 20 at%, preferably 30 at%, and more preferably 40 at%. On the other hand, the upper limit of the Sn content A Sn is 80 at%, preferably 75 at%, and more preferably 70 at%. When the content A Sn of the sputtering target is less than the lower limit, there is a concern that Sn oxide is insufficient in the dielectric layer and it is difficult to provide the dielectric layer with an oxygen barrier function to prevent decomposition of the recording layer. On the other hand, when the content A of Sn exceeds the above-mentioned upper limit, the content of oxides of other elements may be insufficient.

該濺鍍靶材的Zr相對於氧以外的所有元素的含量AZr 的下限超過0 at%,較佳為5 at%,更佳為10 at%。另一方面,Zr的含量AZr 的上限為40 at%,較佳為35 at%,更佳為30 at%。於該濺鍍靶材的Zr的含量AZ r 未滿所述下限的情況下,有於介電體層中Zr氧化物不足,氧氣阻擋功能降低,難以抑制記錄層的記錄訊號的劣化的擔憂。另一方面,於Zr的含量AZr 超過所述上限的情況下,有使其他元素的氧化物的含量不足的擔憂。The lower limit of the content of Zr of this sputtering target with respect to all elements except oxygen, A Zr , exceeds 0 at%, preferably 5 at%, and more preferably 10 at%. On the other hand, the upper limit of the Zr content A Zr is 40 at%, preferably 35 at%, and more preferably 30 at%. When the Zr content A Z r of the sputtering target is less than the lower limit, there is a concern that Zr oxide is insufficient in the dielectric layer, the oxygen blocking function is reduced, and it is difficult to suppress deterioration of the recording signal of the recording layer. On the other hand, when the content A of Zr exceeds the upper limit, there is a concern that the content of oxides of other elements may be insufficient.

另外,Zn的含量AZn 滿足下述式(1)。下述式(1)的值的下限為0,更佳為0.1,進而佳為0.2。另一方面,下述式(1)的值的上限較佳為0.5,更佳為0.4。於下述式(1)的值超過所述上限的情況下,有介電體層中的Zn氧化物不必要地增大,介電體層的氧氣阻擋功能降低的擔憂。
AZn /(AZn +ASn )≦0.6・・・・・(1)
The Zn content A Zn satisfies the following formula (1). The lower limit of the value of the following formula (1) is 0, more preferably 0.1, and even more preferably 0.2. On the other hand, the upper limit of the value of the following formula (1) is preferably 0.5, and more preferably 0.4. When the value of the following formula (1) exceeds the upper limit, there is a concern that the Zn oxide in the dielectric layer is increased unnecessarily, and the oxygen barrier function of the dielectric layer is reduced.
A Zn / (A Zn + A Sn ) ≦ 0.6 ・ ・ ・ ・ ・ (1)

該濺鍍靶材不含有In。具體而言,In的含量未滿作為檢測極限的100 ppm。該濺鍍靶材由於不包含被指定為特定化學物質的In元素,故無需健康障礙防止對策。This sputtering target does not contain In. Specifically, the content of In is less than 100 ppm, which is the detection limit. Since this sputtering target does not contain the In element designated as a specific chemical substance, it is not necessary to take measures to prevent health disorders.

於該濺鍍靶材中所測定的多個比電阻值中,最大值相對於最小值的比的上限為3,更佳為2.4,進而佳為1.7。於所述比電阻的最大值相對於最小值的比超過所述上限的情況下,有於藉由使用該濺鍍靶材的濺鍍靶形成介電體層時無法充分地抑制異常放電的擔憂。Of the multiple specific resistance values measured in this sputtering target, the upper limit of the ratio of the maximum value to the minimum value is 3, more preferably 2.4, and even more preferably 1.7. When the ratio of the maximum value to the minimum value of the specific resistance exceeds the upper limit, there is a concern that an abnormal discharge cannot be sufficiently suppressed when a dielectric layer is formed by a sputtering target using the sputtering target.

該濺鍍靶材的比電阻值的上限為5×10-1 (Ω·cm),較佳為3×10-1 (Ω·cm),進而佳為1×10-1 (Ω·cm)。於所述比電阻值超過所述上限的情況下,有於藉由使用該濺鍍靶材的濺鍍靶形成介電體層時無法充分地抑制異常放電的擔憂。The upper limit of the specific resistance value of the sputtering target is 5 × 10 -1 (Ω · cm), preferably 3 × 10 -1 (Ω · cm), and further preferably 1 × 10 -1 (Ω · cm). . When the specific resistance value exceeds the upper limit, there is a concern that an abnormal discharge cannot be sufficiently suppressed when a dielectric layer is formed by a sputtering target using the sputtering target.

該濺鍍靶材具有SnO2 相及Zn2 SnO4 相。Zn2 SnO4 相中的Zr元素濃度相對於該SnO2 相中的Zr元素濃度的比的下限較佳為0.1,更佳為0.15,進而佳為0.2。另一方面,Zr元素濃度的比的上限較佳為5,更佳為4,進而佳為3。於Zr元素濃度的比未處於所述下限及上限的範圍的情況下,作為絕緣體的ZrO2 大量殘存,因此有產生以ZrO2 為起點的異常放電的擔憂。This sputtering target has a SnO 2 phase and a Zn 2 SnO 4 phase. The lower limit of the ratio of the Zr element concentration in the Zn 2 SnO 4 phase to the Zr element concentration in the SnO 2 phase is preferably 0.1, more preferably 0.15, and even more preferably 0.2. On the other hand, the upper limit of the ratio of the Zr element concentration is preferably 5, more preferably 4, and even more preferably 3. When the ratio of the Zr element concentration is not in the range of the lower limit and the upper limit, a large amount of ZrO 2 remains as an insulator, so there is a concern that an abnormal discharge starting from ZrO 2 may occur.

另外,於該濺鍍靶材中具有ZrO2 的結晶粒。該ZrO2 的結晶粒的平均粒徑的上限較佳為5 μm,更佳為4 μm,進而佳為3 μm。於ZrO2 的結晶粒的平均粒超過所述上限的情況下,有產生以作為絕緣體的ZrO2 為起點的異常放電的擔憂。In addition, the sputtering target has crystal grains of ZrO 2 . The upper limit of the average particle diameter of the ZrO 2 crystal particles is preferably 5 μm, more preferably 4 μm, and even more preferably 3 μm. When the average grain size of the crystal grains of ZrO 2 exceeds the above-mentioned upper limit, there is a concern that an abnormal discharge may occur from ZrO 2 as an insulator.

[濺鍍靶的製造方法]
該濺鍍靶可使用對將Zn、Sn及Zr的氧化物混合及燒結而成的氧化物燒結體即濺鍍靶材進行成形加工而得者來獲得。以下說明的濺鍍靶的製造方法示出其一例,並不限定於該製造方法。
[Manufacturing method of sputtering target]
The sputtering target can be obtained by forming a sputtering target that is an oxide sintered body obtained by mixing and sintering oxides of Zn, Sn, and Zr. The manufacturing method of the sputtering target demonstrated below shows an example, and it is not limited to this manufacturing method.

具體而言,該濺鍍靶的製造方法具有:將Zn、Sn及Zr混合的步驟(S01)、對所獲得的混合物進行乾燥的步驟(S02)、將經乾燥的混合物燒結而製成氧化物燒結體的步驟(S03)、對氧化物燒結體進行成形加工的步驟(S04)、以及將成形物接合於底板(backing plate)的步驟(S05)。Specifically, the method for producing a sputtering target includes a step (S01) of mixing Zn, Sn, and Zr, a step of drying the obtained mixture (S02), and sintering the dried mixture to form an oxide. A step (S03) of the sintered body, a step (S04) of forming the oxide sintered body, and a step (S05) of joining the formed article to a backing plate.

<混合步驟>
於將Zn、Sn及Zr混合的步驟(S01)中,分別以規定的比例調配粉末狀的Zn、Sn及Zr並加以混合。所使用的各原料粉末的純度較佳為分別為99.99%以上。若各原料粉末的純度未滿所述下限,則有損及使用該濺鍍靶而形成的介電體層的特性的擔憂。相對於氧化物燒結體中所含的除氧以外的所有金屬元素,各原料粉末的調配比例是以Zn為超過0 at%且50 at%以下、Sn為20 at%以上且80 at%以下、Zr為超過0 at%且40 at%以下、且Zn的含量相對於Zn及Sn的含量的和的比為0.6以下的方式進行調整。
< Mixing step >
In the step (S01) of mixing Zn, Sn, and Zr, powdery Zn, Sn, and Zr are prepared and mixed at predetermined ratios, respectively. The purity of each raw material powder used is preferably 99.99% or more. If the purity of each raw material powder is less than the said lower limit, there exists a possibility that the characteristic of the dielectric layer formed using this sputtering target may be impaired. With respect to all metal elements other than oxygen contained in the oxide sintered body, the blending ratio of each raw material powder is such that Zn is more than 0 at% and 50 at% or less, Sn is 20 at% and 80 at% or less, Zr is adjusted so that it exceeds 0 at% and 40 at% or less, and the ratio of the content of Zn to the sum of the contents of Zn and Sn is 0.6 or less.

混合的手段並無特別限定,例如可使用球磨機並將各原料粉末與水投入至球磨機中來加以混合。出於均勻混合的目的,亦可與水一同使用分散劑,為了於後述的預成形步驟中使成形容易,亦可使用黏合劑。球磨機的球或珠的材質並無特別限定,例如可列舉:尼龍、氧化鋁、氧化鋯等。The means for mixing is not particularly limited. For example, a ball mill can be used to mix each raw material powder and water into the ball mill. For the purpose of uniform mixing, a dispersant may be used together with water, and in order to facilitate molding in a preforming step described later, a binder may also be used. The material of the balls or beads of the ball mill is not particularly limited, and examples thereof include nylon, alumina, and zirconia.

<乾燥步驟>
於乾燥步驟(S02)中,例如使用噴霧乾燥機等,對混合步驟(S01)中所獲得的混合物進行乾燥。較佳為於乾燥後對混合物進行預成形。另外,於使用分散劑或黏合劑的情況下,較佳為對混合物進行脫脂。
< Drying step >
In the drying step (S02), for example, a spray dryer or the like is used to dry the mixture obtained in the mixing step (S01). Preferably, the mixture is pre-formed after drying. When a dispersant or a binder is used, the mixture is preferably degreased.

(預成形步驟)
對於經乾燥的混合物而言,為了提高設置於燒結爐時的操作性,較佳為進行預成形。預成形的方法並無特別限定,可列舉將乾燥後的混合物填充至規定尺寸的模具中,藉由模具壓製進行預成形。藉由模具壓製的加壓力例如可設為0.5 tonf/cm2 以上且1.0 tonf/cm2 以下。
(Preforming step)
In order to improve the workability when installed in a sintering furnace, the dried mixture is preferably preformed. The method of the preforming is not particularly limited, and examples thereof include filling a dried mixture into a mold having a predetermined size, and performing preforming by die pressing. The pressing force by the die pressing can be set to, for example, 0.5 tonf / cm 2 or more and 1.0 tonf / cm 2 or less.

(脫脂步驟)
於在混合步驟(S01)中添加分散劑或黏合劑的情況下,為了去除分散劑或黏合劑,較佳為對經乾燥的混合物或預成形物進行加熱並進行脫脂。加熱的條件並無特別限定,例如只要於大氣中,則可藉由將加熱溫度設為500℃並將保持時間設為5小時等來去除分散劑或黏合劑。
(Degreasing step)
In the case where a dispersant or a binder is added in the mixing step (S01), in order to remove the dispersant or the binder, the dried mixture or the preform is preferably heated and degreased. The heating conditions are not particularly limited. For example, as long as it is in the air, the dispersant or the binder can be removed by setting the heating temperature to 500 ° C. and the holding time to 5 hours.

<燒結步驟>
於燒結步驟(S03)中,對乾燥步驟(S02)中經乾燥的混合物進行燒結而製成氧化物燒結體。該氧化物燒結體為該濺鍍靶材。另外,藉由燒結而於該濺鍍靶材中形成SnO2 相及Zn2 SnO4 相,從而形成ZrO2 的結晶粒。燒結的加熱溫度的下限較佳為900℃,更佳為920℃,進而佳為940℃。另一方面,加熱溫度的上限較佳為1100℃,更佳為1050℃。於加熱溫度未滿所述下限的情況下,有無法使氧化物燒結體充分地縝密而材料強度降低的擔憂。另一方面,於加熱溫度超過所述上限的情況下,有結晶粒變粗大而材料強度降低的擔憂。
<Sintering step>
In the sintering step (S03), the dried mixture in the drying step (S02) is sintered to prepare an oxide sintered body. The oxide sintered body is the sputtering target. In addition, a SnO 2 phase and a Zn 2 SnO 4 phase are formed in the sputtering target by sintering, thereby forming ZrO 2 crystal grains. The lower limit of the sintering heating temperature is preferably 900 ° C, more preferably 920 ° C, and even more preferably 940 ° C. On the other hand, the upper limit of the heating temperature is preferably 1100 ° C, and more preferably 1050 ° C. When the heating temperature is less than the lower limit, there is a concern that the oxide sintered body cannot be sufficiently densified and the material strength is reduced. On the other hand, when the heating temperature exceeds the upper limit, there is a concern that crystal grains become coarse and the strength of the material decreases.

至所述加熱溫度為止的平均昇溫速度的上限較佳為600℃/hr,更佳為500℃/hr,進而佳為400℃/hr。於平均昇溫速度超過所述上限的情況下,有容易發生結晶粒的異常成長且無法充分地提高氧化物燒結體的相對密度的擔憂。The upper limit of the average heating rate to the heating temperature is preferably 600 ° C / hr, more preferably 500 ° C / hr, and even more preferably 400 ° C / hr. When the average temperature rise rate exceeds the upper limit, there is a concern that abnormal growth of crystal grains is likely to occur and the relative density of the oxide sintered body may not be sufficiently increased.

所述加熱溫度的保持時間的下限較佳為0.5小時,更佳為2小時,進而佳為3.5小時。另一方面,所述保持時間的上限較佳為24小時,更佳為12小時,進而佳為8小時。藉由將所述保持時間設為所述範圍,可獲得所期望的化合物相。The lower limit of the holding time of the heating temperature is preferably 0.5 hours, more preferably 2 hours, and even more preferably 3.5 hours. On the other hand, the upper limit of the holding time is preferably 24 hours, more preferably 12 hours, and even more preferably 8 hours. By setting the holding time to the range, a desired compound phase can be obtained.

較佳為於所述加熱後,進而於加熱溫度為400℃以上且700℃以下、保持時間為1小時以上且10小時以下的條件下進行加熱。藉此,可進一步提高氧化物燒結體的相對密度。After the heating, the heating is preferably performed under conditions of a heating temperature of 400 ° C. to 700 ° C. and a holding time of 1 hour to 10 hours. This can further increase the relative density of the oxide sintered body.

所述燒結較佳為於還原環境下進行。藉由於一氧化碳(CO)環境、真空環境等還原環境下進行所述燒結,可減少比電阻。關於其詳細機構,存在未明確的部分,但考察到藉由於產生氧缺損的還原環境下進行處理,載子增加,導電性得到提高。The sintering is preferably performed under a reducing environment. By performing the sintering under a reducing environment such as a carbon monoxide (CO) environment, a vacuum environment, and the like, the specific resistance can be reduced. Regarding the detailed mechanism, there are undetermined parts. However, it is considered that the carrier is increased and the conductivity is improved by processing in a reducing environment where an oxygen deficiency occurs.

或者,亦可於混合步驟(S01)中向材料粉末及水中投入碳(C),對該混合物進行乾燥(S02),從而對該經乾燥的混合物進行燒結。由於經乾燥的混合物內存在C,藉由加熱而發生還原反應,可獲得與在還原環境下進行燒結相同的效果。Alternatively, carbon (C) may be added to the material powder and water in the mixing step (S01), and the mixture may be dried (S02) to sinter the dried mixture. Since C exists in the dried mixture, a reduction reaction occurs by heating, and the same effect as that of sintering in a reducing environment can be obtained.

<成形步驟>
於成形步驟(S04)中,對所述氧化物燒結體(濺鍍靶材)進行成形加工,製成對應於各種用途的形狀。成形的手段並無特別限定,例如可採用冷等靜壓法(Cold Isostatic Pressing,CIP)。利用CIP的加壓力的下限較佳為800 kgf/cm2 ,更佳為900 kgf/cm2 ,進而佳為1000 kgf/cm2 。於利用CIP的加壓力未滿所述下限的情況下,有無法充分地提高氧化物燒結體的相對密度的擔憂。
< Forming step >
In the forming step (S04), the oxide sintered body (sputter target) is formed into a shape corresponding to various uses. The forming method is not particularly limited, and for example, Cold Isostatic Pressing (CIP) can be used. The lower limit of the pressing force by CIP is preferably 800 kgf / cm 2 , more preferably 900 kgf / cm 2 , and even more preferably 1000 kgf / cm 2 . When the pressing force by the CIP is less than the lower limit, there is a concern that the relative density of the oxide sintered body cannot be sufficiently increased.

<接合步驟>
於接合步驟(S05)中,將所述成形物接合於底板而獲得濺鍍靶。底板的原材料並無特別限定,較佳為導熱性優異的純銅或銅合金。接合的手段並無特別限定,例如可藉由接合劑來進行接合。接合劑的種類並無特別限定,可採用具有導電性的各種公知的接合劑,例如可列舉Sn系焊料材。接合方法並無特別限定,例如可將成形物及底板加熱至接合劑熔解的溫度,例如140℃以上且240℃以下,將熔解的接合劑塗佈於底板的接合面,並貼合成形物的接合面加以壓接後,進行冷卻。
< Joining procedure >
In the bonding step (S05), the formed article is bonded to the base plate to obtain a sputtering target. The raw material of the base plate is not particularly limited, and pure copper or a copper alloy having excellent thermal conductivity is preferred. The means for joining is not particularly limited, and for example, joining can be performed by a joining agent. The type of the bonding agent is not particularly limited, and various known bonding agents having conductivity can be used, and examples thereof include Sn-based solder materials. The bonding method is not particularly limited. For example, the molded article and the base plate can be heated to a temperature at which the bonding agent melts, for example, 140 ° C or higher and 240 ° C or lower. After the bonding surface is crimped, it is cooled.

[優點]
該濺鍍靶材和濺鍍靶包含Zn、Sn及Zr的各自的氧化物,該些元素的相對於氧以外的所有元素的含量為規定範圍,因此可形成具有優異的特性的介電體層。另外,比電阻值的最大值相對於最小值的比及比電阻值處於規定的範圍,因此可抑制濺鍍中的異常放電,從而可減少粒子的產生。進而,由於不含有In,故無需健康障礙防止對策。由此,藉由使用該濺鍍靶材和濺鍍靶,可安全且有效地生產光記錄媒體。
[advantage]
The sputtering target and the sputtering target contain respective oxides of Zn, Sn, and Zr, and the content of these elements with respect to all elements other than oxygen is within a predetermined range, so that a dielectric layer having excellent characteristics can be formed. In addition, since the ratio of the maximum value to the minimum value of the specific resistance value and the specific resistance value are in a predetermined range, abnormal discharge during sputtering can be suppressed, and generation of particles can be reduced. Furthermore, since it does not contain In, it is not necessary to take measures to prevent health disorders. Accordingly, by using the sputtering target and the sputtering target, an optical recording medium can be safely and efficiently produced.

根據該濺鍍靶的製造方法,可獲得強度優異的濺鍍靶。因而,可抑制接合步驟(S05)中的作業時的衝擊或藉由濺鍍的熱歷程中所產生的應力等造成的裂紋。另外,根據該濺鍍靶的製造方法,可容易地將比電阻、Zn2 SnO4 相中的Zr元素濃度相對於SnO2 相中的Zr元素濃度的比、及ZrO2 的結晶粒的平均粒徑設為所期望的值。由此,可比較容易地製造可安全且有效地形成介電體層的濺鍍靶。
[實施例]
According to this method for manufacturing a sputtering target, a sputtering target having excellent strength can be obtained. Therefore, it is possible to suppress cracks caused by an impact during the work in the joining step (S05) or a stress generated during a thermal history of sputtering. In addition, according to the method for manufacturing the sputtering target, specific resistance, the ratio of the concentration of the Zr element in the Zn 2 SnO 4 phase to the concentration of the Zr element in the SnO 2 phase, and the average grain size of the ZrO 2 crystal grains can be easily changed. The diameter is set to a desired value. This makes it relatively easy to manufacture a sputtering target that can safely and effectively form a dielectric layer.
[Example]

以下,藉由實施例來對本發明進行更詳細的說明,但本發明並不限定於該些實施例。Hereinafter, the present invention will be described in more detail through examples, but the present invention is not limited to these examples.

使用將Zn、Sn及Zr的調配條件設為表1的試樣1〜試樣3,於表2的製造條件下獲得實施例1〜實施例4、及比較例1〜比較例3的成形物。成形物的厚度分別設為6 mm。於混合步驟中,向試樣1〜試樣3中分別混合水與多羧酸銨。於燒結步驟中,於還原環境下進行熱壓。再者,表2中「N2 」表示氮氣。Samples 1 to 3 with the preparation conditions of Zn, Sn, and Zr set to Table 1 were used, and the molded articles of Examples 1 to 4 and Comparative Examples 1 to 3 were obtained under the manufacturing conditions of Table 2. . The thickness of the molded product was set to 6 mm. In the mixing step, water and ammonium polycarboxylate are mixed into samples 1 to 3, respectively. In the sintering step, hot pressing is performed under a reducing environment. In addition, "N 2 " in Table 2 means nitrogen.

[表1]
[Table 1]

[表2]
[Table 2]

<相的鑒定>
實施例1〜實施例4、及比較例1〜比較例3的相的鑒定是藉由X射線繞射於以下的條件下進行測定。再者,表記方法是基於國際繞射資料中心(International Centre for Diffraction Data,ICDD)的卡編號的化學式。
74-2184:Zn2 SnO4
77-0447:SnO2
74-1200:ZrO2
86-2265:Sn
750576:ZnO
分析條件:
靶:Cu
單色化:使用單色器(Kα
靶輸出:40 kV-200 mA
(連續燒測定)θ/2θ掃描
狹縫:發散角:1/2°、散射角:1/2°、光接收寬度:0.15 mm
單色器光接收狹縫寬度:0.6 mm
掃描速度:2°/min
取樣間隔:0.02°
測定角度(2θ):5°〜90°
分析裝置:理學電機製造的「X射線繞射裝置RINT-1500」
< Identification of phases >
The phases of Examples 1 to 4 and Comparative Examples 1 to 3 were identified by X-ray diffraction under the following conditions. Furthermore, the notation method is based on the chemical formula of the card number of the International Centre for Diffraction Data (ICDD).
74-2184: Zn 2 SnO 4
77-0447: SnO 2
74-1200: ZrO 2
86-2265: Sn
750576: ZnO
Analysis conditions:
Target: Cu
Monochrome: use a monochromator (K α )
Target output: 40 kV-200 mA
(Continuous firing measurement) θ / 2θ scanning slit: divergence angle: 1/2 °, scattering angle: 1/2 °, light receiving width: 0.15 mm
Monochromator light receiving slit width: 0.6 mm
Scanning speed: 2 ° / min
Sampling interval: 0.02 °
Measurement angle (2θ): 5 ° ~ 90 °
Analysis device: "X-ray diffraction device RINT-1500" manufactured by Rigaku

<Zr量的評價與平均粒徑>
成形物中的Zr量(Zr元素濃度)的評價、及ZrO2 的結晶粒的平均粒徑的測定是利用以下順序進行。
(1)於任意位置在厚度方向切斷成形物,並對其切斷面的任意位置進行鏡面研磨。
(2)使用掃描式電子顯微鏡(SEM)以倍率10000倍對經鏡面研磨的切斷面的組織進行照片拍攝,使用能量色散X射線光譜(EDS)來對相進行鑒定。將藉由SEM及EDS而檢測出的Zr的固溶量設為Zr元素濃度。另外,測量藉由SEM及EDS而檢測出的ZrO2 的結晶粒的平均粒徑。
(3)算出SnO2 相及Zn2 SnO4 相的所述Zr元素濃度的比率。
分析裝置:
SEM:日本電子股份有限公司製造的「JSM-7800F」
EDS:日本電子股份有限公司製造的「JED-2300」
<Evaluation of Zr content and average particle size>
The evaluation of the amount of Zr (the concentration of the Zr element) in the molded product and the measurement of the average particle diameter of the crystal grains of ZrO 2 were performed by the following procedures.
(1) The molded article is cut at an arbitrary position in the thickness direction, and the cut surface is mirror-polished at an arbitrary position.
(2) Using a scanning electron microscope (SEM) to take a photograph of the structure of the mirror-polished cut surface at a magnification of 10,000 times, and use energy dispersive X-ray spectroscopy (EDS) to identify the phase. The solid solution amount of Zr detected by SEM and EDS was set as the Zr element concentration. Moreover, the average particle diameter of the crystal grains of ZrO 2 detected by SEM and EDS was measured.
(3) A ratio of the Zr element concentration of the SnO 2 phase and the Zn 2 SnO 4 phase is calculated.
Analysis device:
SEM: "JSM-7800F" manufactured by Japan Electronics Co., Ltd.
EDS: "JED-2300" manufactured by Japan Electronics Co., Ltd.

<比電阻的測定方法>
比電阻是藉由4探針法來測定。具體而言,對成形物的表面進行鏡面研磨而使其平滑化。自所述成形物的中心以10 mm間隔接觸端子間的距離為1.5 mm的探針來測定。比電阻值是設為於10處測定的值的平均值,算出於10處測定的比電阻值的最大值相對於最小值的比、即後述的「比電阻偏差」。
測定裝置:三菱化學分析技術(Mitsubishi Chemical Analytech)公司製造的「Loresta GP測定器」
<Method for measuring specific resistance>
The specific resistance was measured by the 4-probe method. Specifically, the surface of the molded article is mirror-polished to smooth it. From the center of the molded article, a probe having a distance of 1.5 mm between the contact terminals was measured at 10 mm intervals. The specific resistance value is an average value of the values measured at 10 places, and the ratio of the maximum value to the minimum value of the specific resistance value measured at 10 places is calculated, that is, the "specific resistance deviation" described later.
Measuring device: "Loresta GP measuring device" manufactured by Mitsubishi Chemical Analytech

<相對密度>
相對密度是藉由如以下般測定的氣孔率來求出。首先,於任意位置在厚度方向切斷成形物,並對其切斷面的任意位置進行鏡面研磨。其次,使用SEM以1000倍對研磨面進行照片拍攝,測定於50 μm見方的區域佔據的氣孔的面積率(%)來設為氣孔率。對20個部位進行相同的操作,將其平均值設為該試樣的平均氣孔率(%)。相對密度是藉由〔100-平均氣孔率〕(%)來算出。
< Relative density >
The relative density is obtained from the porosity measured as follows. First, a molded article is cut at an arbitrary position in the thickness direction, and the cut surface is mirror-polished at an arbitrary position. Next, the polished surface was photographed at 1000 times using an SEM, and the area ratio (%) of the pores occupied by the area of 50 μm square was measured as the porosity. The same operation was performed on 20 locations, and the average value was set to the average porosity (%) of the sample. The relative density is calculated from [100-average porosity] (%).

<異常放電的有無>
異常放電的有無是如以下般來確認。將實施例1〜實施例4、及比較例1〜比較例3的成形物設為濺鍍靶。使用該濺鍍靶,於DC濺鍍功率200 W、Ar/0.1體積%O2 環境、壓力0.3 Pa的條件下利用濺鍍法而在記錄層上形成介電體層,計算每100 min.的電弧放電的產生次數來確認形成中的異常放電。
< Presence or absence of abnormal discharge >
The presence or absence of abnormal discharge was confirmed as follows. The formed articles of Examples 1 to 4 and Comparative Examples 1 to 3 were set as sputtering targets. Using this sputtering target, a dielectric layer was formed on the recording layer by a sputtering method under conditions of a DC sputtering power of 200 W, an Ar / 0.1 vol% O 2 environment, and a pressure of 0.3 Pa, and an arc per 100 minutes was calculated. The number of times of discharge was generated to confirm abnormal discharge during formation.

將測定結果示於表3中。再者,表3中所謂「比電阻偏差」,表示比電阻的最大值相對於最小值的比。所謂「Zr量比率」,表示Zn2 SnO4 相中的Zr元素濃度相對於SnO2 相中的Zr元素濃度的比。「-」表示未獲取資料。The measurement results are shown in Table 3. The "specific resistance deviation" in Table 3 indicates the ratio of the maximum value to the minimum value of the specific resistance. The "Zr amount ratio" means the ratio of the Zr element concentration in the Zn 2 SnO 4 phase to the Zr element concentration in the SnO 2 phase. "-" Means no data were obtained.

[表3]
[table 3]

比較例1中難以引起氧化物的還原,因此比電阻變大,發生異常放電。比較例2中Sn的含量超過80 at%,Zr的含量為0 at%,因此比電阻變大,發生異常放電。比較例3中於N2 環境下燒結時的還原變得不穩定,最外周部產生影響,因此比電阻的偏差變大,發生異常放電。
[產業上之可利用性]
In Comparative Example 1, it was difficult to cause reduction of the oxide, so the specific resistance became large, and abnormal discharge occurred. In Comparative Example 2, since the content of Sn exceeds 80 at% and the content of Zr is 0 at%, the specific resistance becomes large and abnormal discharge occurs. In Comparative Example 3, the reduction during sintering in an N 2 environment became unstable, and the outermost part affected, so the variation in the specific resistance became large, and abnormal discharge occurred.
[Industrial availability]

本發明的濺鍍靶材和濺鍍靶無需健康障礙防止對策,可抑制異常放電,因此可較佳地用於光記錄媒體的生產。The sputtering target and the sputtering target of the present invention do not require a health obstacle prevention measure and can suppress abnormal discharge, and therefore can be preferably used for the production of an optical recording medium.

no

no

Claims (5)

一種濺鍍靶材,其包含鋅(Zn)的氧化物、錫(Sn)的氧化物及鋯(Zr)的氧化物,其中 相對於氧(O)以外的所有元素, 鋅的含量AZn 為超過0 at%且50 at%以下, 錫的含量ASn 為20 at%以上且80 at%以下,及 鋯的含量AZr 為超過0 at%且40 at%以下,而且 所述鋅的含量AZn 滿足下述式(1); 經測定的多個比電阻值中最大值相對於最小值的比為3以下,及 所述比電阻值為5×10-1 (Ω·cm)以下;而且 所述濺鍍靶材不含有銦(In), AZn /(AZn +ASn )≦0.6・・・・・(1)。A sputtering target includes an oxide of zinc (Zn), an oxide of tin (Sn), and an oxide of zirconium (Zr), and the content of zinc A with respect to all elements other than oxygen (O) is Zn. exceeds 0 at% and 50 at% or less and Sn content of Sn a 20 at% or more and 80 at% or less, and the content of zirconium Zr a more than 0 at% and 40 at% or less, and the content a Zn Zn satisfies the following formula (1); the ratio of the maximum value to the minimum value among a plurality of specific resistance values measured is 3 or less, and the specific resistance value is 5 × 10 -1 (Ω · cm) or less; The sputtering target does not contain indium (In), and A Zn / (A Zn + A Sn ) ≦ 0.6 ・ ・ ・ ・ ・ (1). 如申請專利範圍第1項所述的濺鍍靶材,其具有SnO2 相及Zn2 SnO4 相,所述Zn2 SnO4 相中的Zr元素濃度相對於所述SnO2 相中的Zr元素濃度的比為0.1以上且5以下。The sputtering target according to item 1 of the patent application scope, which has a SnO 2 phase and a Zn 2 SnO 4 phase, and the Zr element concentration in the Zn 2 SnO 4 phase is relative to the Zr element in the SnO 2 phase. The ratio of the concentrations is 0.1 or more and 5 or less. 如申請專利範圍第1項所述的濺鍍靶材,其包含ZrO2 的結晶粒,所述ZrO2 的結晶粒的平均粒徑為5 μm以下。The patentable scope of the application of paragraph 1 sputtering target, comprising a crystalline ZrO 2 grains of the ZrO 2 crystal grains of an average particle diameter of 5 μm or less. 如申請專利範圍第2項所述的濺鍍靶材,其包含ZrO2 的結晶粒,所述ZrO2 的結晶粒的平均粒徑為5 μm以下。The patentable scope of the application of paragraph 2 sputtering target, comprising a crystalline ZrO 2 grains of the ZrO 2 crystal grains of an average particle diameter of 5 μm or less. 一種濺鍍靶,其包含如申請專利範圍第1項至第4項中任一項所述的濺鍍靶材。A sputtering target includes the sputtering target according to any one of claims 1 to 4 of the scope of patent application.
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