TW201942088A - Oxide sintered body, sputtering target and transparent conductive film - Google Patents

Oxide sintered body, sputtering target and transparent conductive film Download PDF

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TW201942088A
TW201942088A TW107139172A TW107139172A TW201942088A TW 201942088 A TW201942088 A TW 201942088A TW 107139172 A TW107139172 A TW 107139172A TW 107139172 A TW107139172 A TW 107139172A TW 201942088 A TW201942088 A TW 201942088A
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mass
sintered body
oxide sintered
transparent conductive
conductive film
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TWI768149B (en
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松元謙士
矢野智泰
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日商三井金屬鑛業股份有限公司
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    • 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
    • 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
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/08Oxides
    • 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

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  • Compositions Of Oxide Ceramics (AREA)
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Abstract

An oxide sintered body according to one of the embodiments of the present invention is an oxide sintered body containing indium, niobium, tin and oxygen, which contains indium in an amount of 90.0 mass% or more in terms of In2O3, niobium in an amount of 3.5 to 6.5 mass% in terms of Nb2O5, and tin in an amount of 0.5 to 2 mass% in terms of SnO2.

Description

氧化物燒結體、濺鍍靶及透明導電膜 Oxide sintered body, sputtering target and transparent conductive film

本發明所揭示之實施形態係關於氧化物燒結體、濺鍍膜及透明導電膜。 Embodiments disclosed in the present invention relate to an oxide sintered body, a sputtered film, and a transparent conductive film.

以往,已知一種透明導電膜的濺鍍靶,係於ITO(Indium Tin Oxide,氧化銦錫)添加鈮等,且用以使在紫色區域(例如,波長400nm)之穿透率得到改善之透明導電膜成膜者(例如,參照專利文獻1)。 In the past, a sputtering target for a transparent conductive film is known, which is made of ITO (Indium Tin Oxide, indium tin oxide), added with niobium, etc., and is used to improve the transparency in the purple region (for example, the wavelength of 400 nm). A person who forms a conductive film (for example, refer to Patent Document 1).

[先前技術文獻] [Prior technical literature] [專利文獻] [Patent Literature]

專利文獻1:國際公開第2011/052375號公報 Patent Document 1: International Publication No. 2011/052375

然而,藉由以往之濺鍍靶所成膜之透明導電膜,於紫外光區域(例如,波長300nm)或紫色區域(例如,波長400nm)等短波長區域下的穿透率仍有改善的空間。 However, the transparent conductive film formed by the conventional sputtering target still has room for improvement in transmittance in a short wavelength region such as an ultraviolet region (for example, a wavelength of 300 nm) or a purple region (for example, a wavelength of 400 nm). .

本實施形態之一樣態,係有鑑於上述情事 所研創者,其目的在於提供一種氧化物燒結體,其係在使用濺鍍靶所成膜之透明導電膜中,可提升紫外光區域或紫色區域等短波長區域的穿透率。 The state of this embodiment is based on the above circumstances The inventor's goal is to provide an oxide sintered body, which can improve the transmittance of a short-wavelength region such as an ultraviolet region or a purple region in a transparent conductive film formed using a sputtering target.

本實施形態之一樣態的氧化物燒結體,係含有銦、鈮、錫及氧,且以In2O3換算的話含有90.0質量%以上之前述銦,以Nb2O5換算的話含有3.5至6.5質量%之前述鈮,以SnO2換算的話含有0.5至2質量%之前述錫。 The same oxide sintered body of this embodiment contains indium, niobium, tin, and oxygen, and contains 90.0% by mass or more of the above indium in terms of In 2 O 3 and 3.5 to 6.5 in terms of Nb 2 O 5 The aforementioned niobium by mass contains 0.5 to 2 mass% of the aforementioned tin in terms of SnO 2 .

藉由本實施形態之一樣態,可提升所成膜之透明導電膜之紫外光區域或紫色區域等短波長區域的穿透率。 According to the state of this embodiment, the transmittance of the short-wavelength region such as the ultraviolet region or the purple region of the formed transparent conductive film can be improved.

第1圖係顯示實施例2及比較例1、4之透明導電膜之熱處理前之穿透率的波長相依性之圖表。 FIG. 1 is a graph showing the wavelength dependence of the transmittance before heat treatment of the transparent conductive films of Example 2 and Comparative Examples 1 and 4.

第2圖係顯示實施例2及比較例1、4之透明導電膜之熱處理後之穿透率的波長相依性之圖表。 FIG. 2 is a graph showing the wavelength dependence of the transmittance of the transparent conductive films of Example 2 and Comparative Examples 1 and 4 after heat treatment.

以下,參照添附圖式,說明本發明所揭示之氧化物燒結體、濺鍍靶及透明導電膜的實施形態。又,本發明並不受限於以下所示之實施形態。 Hereinafter, embodiments of the oxide sintered body, the sputtering target, and the transparent conductive film disclosed in the present invention will be described with reference to the accompanying drawings. The present invention is not limited to the embodiments described below.

實施形態之氧化物燒結體係含有銦(In)、鈮(Nb)、錫(Sn)及氧(O),可作為濺鍍靶使用。而實施形態之 氧化物燒結體,以In2O3換算的話含有90.0質量%以上之銦,以Nb2O5換算的話含有3.5至6.5質量%之鈮,以SnO2換算的話含有0.5至2質量%之錫。亦即,實施形態之氧化物燒結體係含有作為主成分之銦、與作為其他成分之鈮、錫及氧。 The oxide sintering system of the embodiment contains indium (In), niobium (Nb), tin (Sn), and oxygen (O), and can be used as a sputtering target. The oxide sintered body of the embodiment contains 90.0% by mass or more of indium in terms of In 2 O 3 , 3.5 to 6.5% by mass of niobium in terms of Nb 2 O 5 , and 0.5 to 2 mass in terms of SnO 2 . % Of tin. That is, the oxide sintering system of the embodiment contains indium as a main component, and niobium, tin, and oxygen as other components.

藉此,可提升將該氧化物燒結體用作為濺鍍靶所成膜之透明導電膜之在紫外光區域或紫色區域等短波長區域的穿透率。 Thereby, the transmittance of the transparent conductive film formed by using the oxide sintered body as a sputtering target in a short wavelength region such as an ultraviolet region or a purple region can be improved.

又,實施形態之透明導電膜係含有銦、鈮、錫及氧,且以In2O3換算的話含有90.0質量%以上之銦,以Nb2O5換算的話含有3.5至6.5質量%之鈮,以SnO2換算的話含有0.5至2質量%之錫。亦即,實施形態之透明導電膜係含有作為主成分之銦、與作為其他成分之鈮、錫及氧。 The transparent conductive film of the embodiment contains indium, niobium, tin, and oxygen, and contains 90.0% by mass or more of indium in terms of In 2 O 3 and 3.5 to 6.5% by mass of niobium in terms of Nb 2 O 5 . In terms of SnO 2 , it contains 0.5 to 2% by mass of tin. That is, the transparent conductive film of the embodiment contains indium as a main component, and niobium, tin, and oxygen as other components.

藉此,可提升該透明導電膜之在紫外光區域或紫色區域等短波長區域的穿透率。因此,藉由實施形態,例如將該透明導電膜應用於太陽電池的透明電極時,射入於該太陽電池之紫外光區域的光(亦即,紫外線)亦能運用於發電,故能提升太陽電池的發光效率。 Thereby, the transmittance of the transparent conductive film in a short-wavelength region such as an ultraviolet region or a purple region can be improved. Therefore, according to the embodiment, for example, when the transparent conductive film is applied to a transparent electrode of a solar cell, the light (that is, ultraviolet rays) incident on the ultraviolet light region of the solar cell can also be used for power generation, so the sun can be improved. The luminous efficiency of the battery.

實施形態之氧化物燒結體,以In2O3換算的話含有90.0質量%以上之銦。藉此,將該氧化物燒結體用作為濺鍍靶所成膜之透明導電膜時,可良好地維持導電性、穿透率。 The oxide sintered body of the embodiment contains 90.0% by mass or more of indium in terms of In 2 O 3 . Accordingly, when the oxide sintered body is used as a transparent conductive film formed by a sputtering target, the conductivity and transmittance can be favorably maintained.

又,實施形態之氧化物燒結體,以In2O3換 算的話,以含有91.5至96.0質量%的銦為佳,更佳為含有92.5至95.0質量%,又更佳為含有93.6至94.4質量%。 In addition, the oxide sintered body according to the embodiment preferably contains 91.5 to 96.0% by mass of indium, more preferably 92.5 to 95.0% by mass, and even more preferably 93.6 to 94.4% by mass in terms of In 2 O 3 . .

又,實施形態之氧化物燒結體,較佳係以Nb2O5換算的話含有4.0至6.0質量%之鈮,以SnO2換算的話含有0.5至2質量%之錫。藉此,將該氧化物燒結體用作為濺鍍靶所成膜之透明導電膜時,可良好地維持導電性。 The oxide sintered body of the embodiment preferably contains 4.0 to 6.0 mass% of niobium when converted into Nb 2 O 5 and 0.5 to 2 mass% of tin when converted into SnO 2 . Thereby, when this oxide sintered body is used as a transparent conductive film formed by a sputtering target, electrical conductivity can be favorably maintained.

又,實施形態之氧化物燒結體,更佳係以Nb2O5換算的話含有4.5至5.5質量%之鈮,以SnO2換算的話含有0.5至2質量%之錫,又更佳為係以Nb2O5換算的話含有4.8至5.2質量%之鈮,以SnO2換算的話含有0.8至1.2質量%之錫。 The oxide sintered body of the embodiment more preferably contains 4.5 to 5.5% by mass of niobium when converted into Nb 2 O 5 and 0.5 to 2% by mass of tin when converted into SnO 2 , and more preferably Nb It contains 4.8 to 5.2% by mass of niobium in terms of 2 O 5 and 0.8 to 1.2% by mass of tin in terms of SnO 2 .

實施形態之透明導電膜,以In2O3換算的話含有90.0質量%以上之銦。藉此,可良好地維持透明導電膜的導電性、穿透率。 The transparent conductive film of the embodiment contains 90.0% by mass or more of indium in terms of In 2 O 3 . Thereby, the conductivity and transmittance of the transparent conductive film can be favorably maintained.

又,實施形態之透明導電膜,以In2O3換算的話,以含有91.5至96.0質量%的銦為佳,更佳為含有92.5至95.0質量%,又更佳為含有93.6至94.4質量%。 In addition, the transparent conductive film according to the embodiment preferably contains 91.5 to 96.0% by mass of indium, more preferably 92.5 to 95.0% by mass, and even more preferably 93.6 to 94.4% by mass in terms of In 2 O 3 .

又,實施形態之透明導電膜,較佳係以Nb2O5換算的話含有4.0至6.0質量%之鈮,以SnO2換算的話含有0.5至2質量%之錫。藉此,可良好地維持該透明導電膜的導電性。 The transparent conductive film of the embodiment preferably contains 4.0 to 6.0 mass% of niobium when converted into Nb 2 O 5 and 0.5 to 2 mass% of tin when converted into SnO 2 . Thereby, the conductivity of the transparent conductive film can be favorably maintained.

再者,實施形態之透明導電膜,更佳係以Nb2O5換算的話含有4.5至5.5質量%之鈮,以SnO2換算 的話含有0.5至2質量%之錫,又更佳係以Nb2O5換算的話含有4.8至5.2質量%之鈮,以SnO2換算的話含有0.8至1.2質量%之錫。 Furthermore, the transparent conductive film of the embodiment more preferably contains 4.5 to 5.5 mass% of niobium when converted into Nb 2 O 5 and 0.5 to 2 mass% of tin when converted into SnO 2 , and more preferably Nb 2 O 5 contains 4.8 to 5.2 mass% of niobium, and SnO 2 contains 0.8 to 1.2 mass% of tin.

又,實施形態之氧化物燒結體及透明導電膜,更佳係由作為主成分之之銦、與作為其他成分之鈮、錫及氧所構成。 The oxide sintered body and the transparent conductive film of the embodiment are more preferably composed of indium as a main component and niobium, tin, and oxygen as other components.

又,實施形態之氧化物燒結體及透明導電膜,可含有來自原料等之不可避免的雜質。實施形態之氧化物燒結體中之不可避免的雜質,可舉例如Fe、Cr、Ni、Si、W、Zr等,該等之含量通常各為100ppm以下。 The oxide sintered body and the transparent conductive film of the embodiment may contain inevitable impurities derived from raw materials and the like. Examples of the unavoidable impurities in the oxide sintered body according to the embodiment include Fe, Cr, Ni, Si, W, and Zr. The content of each of these is generally 100 ppm or less.

又,實施形態之氧化物燒結體之比電阻較佳為7.0×10-4Ω.cm以下。藉此,當使用該氧化物燒結體作為濺鍍靶時,可進行使用廉價之DC電源的濺鍍,而能提升成膜速度。 The specific resistance of the oxide sintered body of the embodiment is preferably 7.0 × 10 -4 Ω. cm or less. Accordingly, when the oxide sintered body is used as a sputtering target, sputtering using an inexpensive DC power source can be performed, and the film forming speed can be increased.

又,實施形態之氧化物燒結體之比電阻更佳為5.0×10-4Ω.cm以下,又更佳為4.0×10-4Ω.cm以下、再更佳為3.0×10-4Ω.cm以下。 The specific resistance of the oxide sintered body of the embodiment is more preferably 5.0 × 10 -4 Ω. cm or less, and more preferably 4.0 × 10 -4 Ω. cm or less, and more preferably 3.0 × 10 -4 Ω. cm or less.

又,實施形態之氧化物燒結體的相對密度為95%以上。藉此,當使用該氧化物燒結體作為濺鍍靶時,可使DC濺鍍的放電狀態安定。又,實施形態之氧化物燒結體,較佳係相對密度為97%以上,更佳係相對密度為99%以上。 The relative density of the oxide sintered body of the embodiment is 95% or more. Thereby, when this oxide sintered body is used as a sputtering target, the discharge state of DC sputtering can be stabilized. The oxide sintered body of the embodiment preferably has a relative density of 97% or more, and more preferably has a relative density of 99% or more.

相對密度若為95%以上,則當使用該氧化物燒結體作為濺鍍靶時,可減少濺鍍靶中的空隙,而容易 防止大氣中氣體成分的侵入。又,於濺鍍時,不易產生源自於該空隙之異常放電、及濺鍍靶的破裂。 When the relative density is 95% or more, when the oxide sintered body is used as a sputtering target, the voids in the sputtering target can be reduced and it becomes easy. Prevent the intrusion of gas components in the atmosphere. Also, during sputtering, abnormal discharges from the voids and cracking of the sputtering target are unlikely to occur.

又,實施形態之透明導電膜,於波長300nm的穿透率較佳為52%以上,更佳為55%以上,又更佳為58%以上,再更佳為60%以上。 In the transparent conductive film of the embodiment, the transmittance at a wavelength of 300 nm is preferably 52% or more, more preferably 55% or more, still more preferably 58% or more, and still more preferably 60% or more.

<氧化物濺鍍靶之各製造步驟> <Each manufacturing step of oxide sputtering target>

實施形態之氧化物濺鍍靶例如可藉由如下述所示之方法製造。首先,混合原料粉末。原料粉末通常為In2O3粉末、Nb2O5粉末及SnO2粉末。各原料粉末之平均粒徑較佳係皆為5μm以下,又,各原料粉末彼此之平均粒徑差較佳為2μm以下。又,原料粉末之平均粒徑,係藉由雷射繞射散射式粒度分布測定法所測得之在累積體積50容量%之體積累積直徑D50The oxide sputtering target according to the embodiment can be produced, for example, by the following method. First, the raw material powder is mixed. The raw material powder is usually In 2 O 3 powder, Nb 2 O 5 powder, and SnO 2 powder. The average particle diameter of each raw material powder is preferably 5 μm or less, and the average particle size difference of each raw material powder is preferably 2 μm or less. In addition, the average particle diameter of the raw material powder is a volume cumulative diameter D 50 at a cumulative volume of 50% by volume measured by a laser diffraction scattering particle size distribution measurement method.

各原料粉末之混合比率,可以使氧化物燒結體成為所期望之構成元素比的方式適當地決定。 The mixing ratio of each raw material powder can be appropriately determined so that the oxide sintered body becomes a desired constituent element ratio.

各原料粉末,由於一般粒子呈現凝聚,故較佳為事先粉碎後混合、或一邊混合一邊進行粉碎。 Since each raw material powder generally exhibits agglomeration, it is preferred to pulverize before mixing, or to pulverize while mixing.

原料之粉碎方法或混合方法並無特別限制,例如可將原料粉末置入瓶中,以球磨機進行粉碎或混合。 There is no particular limitation on the method of pulverizing or mixing the raw materials. For example, the raw material powder can be put into a bottle and pulverized or mixed with a ball mill.

所得之混合粉末可直接成形作為成形體,並對其進行燒結,但亦可視需要於混合粉末加入黏結劑進行成形而作為成形體。該黏結劑可使用周知之粉末冶金法中製得成形體時所使用的黏結劑,例如聚乙烯醇、丙烯酸乳膠黏結劑等。又,亦可於混合粉末加入分散介質調製成 漿料,並對該漿料進行噴霧乾燥製作成顆粒,再使該顆粒成形。 The obtained mixed powder can be directly shaped into a shaped body and sintered, but a binder can be added to the mixed powder to form the shaped body as needed. The binder can be a binder used when a shaped body is produced in a known powder metallurgy method, such as polyvinyl alcohol, an acrylic latex binder, and the like. In addition, it can also be prepared by adding a dispersion medium to the mixed powder. The slurry is spray-dried to produce particles, and the particles are formed.

成形方法可使用以往之粉末冶金法所採用的方法,例如冷壓或CIP(Cold Isostatic Pressing:冷均壓成形)等。 For the forming method, a method adopted in the conventional powder metallurgy method can be used, such as cold pressing or CIP (Cold Isostatic Pressing).

又,亦可將混合粉末先進行暫時加壓以製作成暫時成形體,再將其粉碎後所得之粉碎粉末進行正式加壓以製作成形體。 In addition, the mixed powder may be temporarily pressed to produce a temporarily formed body, and then the pulverized powder obtained after pulverizing may be formally pressed to produce a formed body.

又,亦可使用滑鑄法(slip casting)等濕式成形法來製作成形體。成形體之相對密度通常為50至75%。 In addition, a molded body may be produced using a wet molding method such as a slip casting method. The relative density of the formed body is usually 50 to 75%.

接著,將所得之成形體進行燒製,以製作成燒結體。製作該燒結體之燒結爐並無特別限制,可使用製造陶瓷燒結體時能使用的燒結爐。 Next, the obtained formed body is fired to produce a sintered body. The sintering furnace for producing the sintered body is not particularly limited, and a sintering furnace that can be used when producing a ceramic sintered body can be used.

燒製溫度係以1300℃至1600℃為佳,更佳為1400℃至1600℃。燒結溫度愈高,愈可得到高密度的燒結體,另一方面,由抑制燒結體組織巨大化以防止破裂的觀點,較佳為控制在上述溫度以下。 The firing temperature is preferably 1300 ° C to 1600 ° C, and more preferably 1400 ° C to 1600 ° C. The higher the sintering temperature, the higher the density of the sintered body can be obtained. On the other hand, from the viewpoint of suppressing the enlargement of the sintered body structure to prevent cracking, it is preferable to control the temperature below the above temperature.

在該燒製溫度之保持時間係以3至30小時為佳,更佳為5至20小時。當保持時間在上述範圍內時,可得到高密度的燒結體。由高密度化及防止破裂的觀點考量,升溫速度較佳為100至500℃/h。燒製環境以氧環境為佳。 The holding time at this firing temperature is preferably 3 to 30 hours, and more preferably 5 to 20 hours. When the holding time is within the above range, a high-density sintered body can be obtained. From the viewpoint of high density and prevention of cracking, the temperature rising rate is preferably 100 to 500 ° C / h. The firing environment is preferably an oxygen environment.

接著,對所得之燒結體進行切削加工。該切削加工係使用平面研磨機等進行。又,切削加工後之表 面粗度Ra,可藉由選定切削加工所使用之磨石之研磨粒的大小來適當地進行控制。 Next, the obtained sintered body is subjected to cutting processing. This cutting process is performed using a plane grinder or the like. The table after cutting The surface roughness Ra can be appropriately controlled by selecting the size of the abrasive grains of the grindstone used in the cutting process.

藉由使切削加工後之燒結體與基材接合而製作成濺鍍靶。基材之材質可適當選擇不銹鋼、銅、或鈦等。接合材可使用銦等低熔點焊料。 A sintered body after cutting is bonded to a base material to produce a sputtering target. The material of the substrate can be appropriately selected from stainless steel, copper, or titanium. As the bonding material, a low melting point solder such as indium can be used.

(實施例) (Example)

[實施例1] [Example 1]

將平均粒徑為0.7μm之In2O3粉末、平均粒徑為1.2μm之Nb2O5粉末、及平均粒徑為0.9μm之SnO2粉末,於瓶中藉由氧化鋯球進行球磨機乾式混合,調製成混合粉末。 An In 2 O 3 powder having an average particle diameter of 0.7 μm, an Nb 2 O 5 powder having an average particle diameter of 1.2 μm, and an SnO 2 powder having an average particle diameter of 0.9 μm were subjected to a ball mill dry process in a bottle by using zirconia balls. Mix to prepare a mixed powder.

又,原料粉末之平均粒徑係使用日機裝股份有限公司製的粒度分布測定裝置HRA進行測定。於該測定時,溶劑係使用水,以測定物質之折射率2.20進行測定。 The average particle diameter of the raw material powder was measured using a particle size distribution measuring device HRA manufactured by Nikkiso Co., Ltd. In this measurement, water was used as the solvent, and the refractive index of the measurement substance was 2.20.

又,於調製混合粉末時,係以使銦以In2O3換算的話成為94.5質量%、鈮以Nb2O5換算的話成為5.0質量%、錫以SnO2換算的話成為0.5質量%的方式調配各原料粉末。 In addition, when preparing the mixed powder, it was prepared such that indium was 94.5% by mass in terms of In 2 O 3 , niobium was 5.0% by mass in terms of Nb 2 O 5 , and tin was 0.5% by mass in terms of SnO 2 . Each raw material powder.

接著,對於混合粉末添加6質量%之已稀釋為4質量%的聚乙烯醇,使用研缽將聚乙烯醇充分塗抹於粉末,使其通過5網眼的篩網。接著,將所得之粉末以200kg/cm2的條件暫時加壓,將所得之暫時成形體以研缽粉碎。接著,將所得之粉碎粉填充於加壓用模具,以加壓壓力1t/cm2進行成形60秒鐘,製得成形體。 Next, 6% by mass of polyvinyl alcohol diluted to 4% by mass was added to the mixed powder, and the polyvinyl alcohol was sufficiently applied to the powder using a mortar, and passed through a 5-mesh screen. Next, the obtained powder was temporarily pressed under the condition of 200 kg / cm 2 , and the obtained temporarily formed body was pulverized in a mortar. Next, the obtained pulverized powder was filled in a mold for pressurization, and formed at a pressurization pressure of 1 t / cm 2 for 60 seconds to obtain a formed body.

接著,將該成形體進行燒製而作成燒結體。該燒製係在爐內以10L/min流通氧的氧氣流環境下進行,並以燒製溫度1550℃、燒製時間9小時、升溫速度350℃/h、降溫速度100℃/h進行。 Next, the formed body is fired to form a sintered body. The firing was performed in an oxygen flow environment in which oxygen was passed through the furnace at 10 L / min, and was performed at a firing temperature of 1550 ° C, a firing time of 9 hours, a heating rate of 350 ° C / h, and a cooling rate of 100 ° C / h.

接著,對所得之燒結體進行切削加工,製得表面粗度Ra為1.0μm之寬度210mm×長度710mm×厚度6mm的氧化物燒結體。又,於該切削加工係使用#170的磨石。 Next, the obtained sintered body was subjected to cutting processing to obtain an oxide sintered body having a surface roughness Ra of 1.0 μm and a width of 210 mm × a length of 710 mm × a thickness of 6 mm. In this cutting process, a # 170 grindstone was used.

[實施例2至7] [Examples 2 to 7]

使用與實施例1同樣的方法,製得氧化物燒結體。又,實施例2至7中,於調製混合粉末時,係以使銦、鈮及錫之含有率以In2O3、Nb2O5及SnO2換算的話成為表1所記載之含有率的方式調配各原料粉末。 By the same method as in Example 1, an oxide sintered body was obtained. In addition, in Examples 2 to 7, when preparing the mixed powder, the content ratios of In, O, Nb, and Sn were converted to the content ratios shown in Table 1 when In 2 O 3 , Nb 2 O 5, and SnO 2 were converted. Way to prepare each raw material powder.

[比較例1至6] [Comparative Examples 1 to 6]

使用與實施例1同樣的方法,製得氧化物燒結體。又,比較例1至6中,於調製混合粉末時,係以使銦、鈮及錫之含有率以In2O3、Nb2O5及SnO2換算的話成為表1所記載之含有率的方式調配各原料粉末。 By the same method as in Example 1, an oxide sintered body was obtained. In Comparative Examples 1 to 6, when preparing the mixed powder, the content ratios shown in Table 1 were converted to the content ratios of indium, niobium, and tin in terms of In 2 O 3 , Nb 2 O 5, and SnO 2 . Way to prepare each raw material powder.

又,於實施例1至7及比較例1至6中,於調製各原料粉末時所測量之各元素的含有率,已藉ICP-AES(Inductively Coupled Plasma Atomic Emission Spectroscopy:感應耦合電漿原子發射光譜法)確認與所得之氧化物燒結體中之各元素的含有率相等。 In addition, in Examples 1 to 7 and Comparative Examples 1 to 6, the content ratios of the elements measured during the preparation of each raw material powder have been borrowed by ICP-AES (Inductively Coupled Plasma Atomic Emission Spectroscopy: inductively coupled plasma atomic emission). Spectroscopy) was confirmed to be equal to the content of each element in the obtained oxide sintered body.

接著,對上述所得之實施例1至7及比較 例1至6的氧化物燒結體,進行相對密度的測定。該相對密度係根據阿基米德法進行測定。 Next, the obtained Examples 1 to 7 and comparison The oxide sintered bodies of Examples 1 to 6 were measured for relative density. This relative density was measured according to the Archimedes method.

具體而言,係將氧化物燒結體之空中質量除以體積(燒結體之水中質量/在測量溫度的水比重),並以相對於理論密度ρ(g/cm3)之百分率的值作為相對密度(單位:%)。 Specifically, the air mass of the oxide sintered body is divided by the volume (mass in water of the sintered body / water specific gravity at the measurement temperature), and the value relative to the theoretical density ρ (g / cm 3 ) is used as the relative value. Density (unit:%).

又,該理論密度ρ(g/cm3)係由製造氧化物燒結體時所使用之原料粉末的質量%及密度計算出。具體而言,係依下述之式所計算出。 The theoretical density ρ (g / cm 3 ) is calculated from the mass% and the density of the raw material powder used when producing the oxide sintered body. Specifically, it is calculated by the following formula.

ρ={(C1/100)/ρ1+(C2/100)/ρ2+(C3/100)/ρ3}-1 ρ = {(C 1/100 ) / ρ 1 + (C 2/100) / ρ 2 + (C 3/100) / ρ 3} -1

又,上述式中之C1至C3及ρ1至ρ3,分別表示以下之值。 In addition, C 1 to C 3 and ρ 1 to ρ 3 in the above formulas respectively represent the following values.

.C1:氧化物燒結體製造時所使用之In2O3粉末的質量% . C 1 : mass% of In 2 O 3 powder used in production of oxide sintered body

.ρ1:In2O3之密度(7.18g/cm3) . ρ 1 : Density of In 2 O 3 (7.18g / cm 3 )

.C2:氧化物燒結體製造時所使用之Nb2O5粉末的質量% . C 2 : mass% of Nb 2 O 5 powder used in production of oxide sintered body

.ρ2:Nb2O5之密度(4.47g/cm3) . ρ 2 : density of Nb 2 O 5 (4.47g / cm 3 )

.C3:氧化物燒結體製造時所使用之SnO2粉末的質量% . C 3 : mass% of SnO 2 powder used in manufacturing the oxide sintered body

.ρ3:SnO2之密度(6.95g/cm3) . ρ 3 : Density of SnO 2 (6.95g / cm 3 )

接著,對上述所得之實施例1至7及比較例1至6之濺鍍靶用氧化物燒結體,分別進行比電阻(體電阻)的測定。 Next, the oxide sintered bodies for sputtering targets of Examples 1 to 7 and Comparative Examples 1 to 6 obtained above were measured for specific resistance (bulk resistance), respectively.

具體而言,係使用三菱化學股份有限公司製Loresta(註冊商標)HP MCP-T410(串列四探針TYPE ESP),使探針接觸加工後之氧化物燒結體的表面,以AUTO RANGE模式進行測定。測定部位為氧化物燒結體之中央附近及四角落共計五處,以各測定值之平均值作為該燒結體之體積電阻值。 Specifically, Loresta (registered trademark) HP MCP-T410 (tandem four-probe TYPE ESP) manufactured by Mitsubishi Chemical Corporation was used, and the probe was brought into contact with the surface of the oxide sintered body after processing. Measurements were performed in RANGE mode. The measurement locations were five locations near the center and four corners of the oxide sintered body, and the average value of each measurement value was used as the volume resistance value of the sintered body.

此處,關於實施例1至7及比較例1至6,將混合粉末時所含之各元素的含有率、與相對密度及比電阻(體電阻)的測定結果顯示於表1。 Here, Tables 1 show the measurement results of the content ratios, relative densities, and specific resistances (volume resistances) of the respective elements contained in the powders in Examples 1 to 7 and Comparative Examples 1 to 6.

可知實施例1至7之氧化物燒結體的比電阻皆為7.0×10-4Ω.cm以下。因此,藉由實施形態,當使用氧化物燒結體作為濺鍍靶時,可進行使用廉價DC電源的濺鍍,而能提升成膜速度。 It can be seen that the specific resistances of the oxide sintered bodies of Examples 1 to 7 are all 7.0 × 10 -4 Ω. cm or less. Therefore, according to the embodiment, when an oxide sintered body is used as a sputtering target, sputtering using an inexpensive DC power source can be performed, and the film forming speed can be increased.

接著,由上述實施例1至7及比較例1至6 之氧化物燒結體,製作實施例1至7及比較例1至6的濺鍍靶。該濺鍍靶係使用屬於低熔點焊料之銦作為接合材,並將上述所得之氧化物燒結體接合於銅製的基材而製作。 Next, from Examples 1 to 7 and Comparative Examples 1 to 6 described above, For the oxide sintered body, sputtering targets of Examples 1 to 7 and Comparative Examples 1 to 6 were produced. This sputtering target is produced by using indium, which is a low melting point solder, as a bonding material, and bonding the obtained oxide sintered body to a copper base material.

接著,使用所製作之實施例1至7及比較例1至6的濺鍍靶,以下述之條件進行濺鍍成膜,成膜為厚度100nm的薄膜。 Next, using the produced sputtering targets of Examples 1 to 7 and Comparative Examples 1 to 6, sputtering was performed to form a film under the following conditions, and a film having a thickness of 100 nm was formed.

.成膜裝置:真空機器工業股份有限公司製EX-3013M(DC濺鍍裝置) . Film-forming device: EX-3013M (DC sputtering device) made by Vacuum Machinery Industry Co., Ltd.

.到達真空度:未達1×10-4Pa . Reaching vacuum degree: less than 1 × 10 -4 Pa

.濺鍍氣體:Ar/O2混合氣體 . Sputtering gas: Ar / O 2 mixed gas

.濺鍍氣壓:0.4Pa . Sputtering pressure: 0.4Pa

.O2氣體流量:0至2.0sccm . O 2 gas flow: 0 to 2.0 sccm

.基板:玻璃基板(Corning公司製EAGLE XG(註冊商標)) . Substrate: Glass substrate (EAGLE XG (registered trademark) by Corning)

.基板溫度:室溫 . Substrate temperature: room temperature

.濺鍍電力:3W/cm2 . Sputtering power: 3W / cm 2

又,於實施例1至7及比較例1至6,藉由ICP-AES,確認到濺鍍靶所使用之氧化物燒結體中之各元素的含有率,與所成膜之透明導電膜中之各元素的含有率相等。 In addition, in Examples 1 to 7 and Comparative Examples 1 to 6, the content rate of each element in the oxide sintered body used for the sputtering target was confirmed by ICP-AES with the transparent conductive film formed. The content of each element is equal.

接著,分別由各玻璃基板裁切出既定的大小,對該切出的玻璃基板,測定所濺鍍成膜之實施例1至7及比較例1至6之透明導電膜中之穿透率的波長相依性。 Next, a predetermined size was cut out from each glass substrate, and the cut glass substrates were measured for the transmittance of the transparent conductive films of Examples 1 to 7 and Comparative Examples 1 to 6 sputtered into a film. Wavelength dependence.

再者,將所切出之玻璃基板於大氣中以200℃熱處理1小時,亦測定熱處理後之透明導電膜中之穿透 率的波長相依性。上述之熱處理前後之穿透率的波長相依性之測定條件,係如以下所述。 Furthermore, the cut glass substrate was heat-treated at 200 ° C for 1 hour in the air, and the penetration in the transparent conductive film after the heat treatment was also measured. The wavelength dependence of the rate. The measurement conditions of the wavelength dependency of the transmittance before and after the heat treatment are as follows.

.測定裝置:日立先端科技公司製 紫外可見近紅外分光光度計UH4150 . Measuring device: UV-NIR infrared spectrophotometer UH4150 made by Hitachi Advanced Technologies

.掃描速度:600nm/min . Scanning speed: 600nm / min

.波長範圍:200至2600nm . Wavelength range: 200 to 2600nm

又,於透明導電膜的穿透率測定中,先將未進行成膜之素玻璃基板裝設於裝置以測定基線,然後測定各成膜樣品的穿透率。 In the measurement of the transmittance of the transparent conductive film, a plain glass substrate on which no film formation has been performed is set on the device to measure the baseline, and then the transmittance of each film-forming sample is measured.

第1圖係顯示實施例2及比較例1、4之透明導電膜之熱處理前之穿透率的波長相依性之圖表,第2圖係顯示相同透明導電膜之熱處理後之穿透率的波長相依性之圖表。如第1圖及第2圖所示,藉由對經濺鍍成膜之透明導電膜施以既定的熱處理,可整體提升透明導電膜的穿透率。 Figure 1 is a graph showing the wavelength dependence of the transmittance before heat treatment of the transparent conductive films of Example 2 and Comparative Examples 1 and 4, and Figure 2 is a chart showing the wavelength of the transmittance after heat treatment of the same transparent conductive film. Dependency chart. As shown in FIG. 1 and FIG. 2, by applying a predetermined heat treatment to the transparent conductive film formed by sputtering, the transmittance of the transparent conductive film can be improved as a whole.

接著,進行成膜後之經熱處理之各透明導電膜之比電阻的測定。該透明導電膜之比電阻測定係使用共和理研公司製的四探針計測器K-705RS進行測定。 Next, the specific resistance of each transparent conductive film subjected to heat treatment after film formation is measured. The specific resistance of this transparent conductive film was measured using a four-probe measuring instrument K-705RS made by Kyowa Riken.

此處,對於上述實施例1至7及比較例1至6之透明導電膜,將熱處理前後之波長300nm、400nm及550nm下之穿透率的測定結果、與熱處理後之比電阻測定的結果顯示於表2。又,表2所示之比電阻測定的評價基準,係如以下所述。 Here, for the transparent conductive films of Examples 1 to 7 and Comparative Examples 1 to 6, the measurement results of the transmittance at the wavelengths of 300 nm, 400 nm, and 550 nm before and after the heat treatment, and the results of the specific resistance measurements after the heat treatment are shown.于 表 2。 In Table 2. The evaluation criteria for the specific resistance measurement shown in Table 2 are as follows.

A:比電阻為4.5×10-4Ω.cm以下。 A: The specific resistance is 4.5 × 10 -4 Ω. cm or less.

B:比電阻超過4.5×10-4Ω.cm且為6.0×10-4Ω.cm以下。 B: The specific resistance exceeds 4.5 × 10 -4 Ω. cm and 6.0 × 10 -4 Ω. cm or less.

C:比電阻超過6.0×10-4Ω.cm。 C: Specific resistance exceeds 6.0 × 10 -4 Ω. cm.

於熱處理後的透明導電膜中,將以In2O3換 算的話含有90.0質量%以上之銦、以Nb2O5換算的話含有3.5至6.5質量%之鈮、以SnO2換算的話含有0.5至2質量%之錫的實施例1至7,與未以該含有率含有鈮及錫的比較例1至6進行比較,可知藉由以In2O3換算的話含有90.0質量%以上之銦、以Nb2O5換算的話含有3.5至6.5質量%之鈮、以SnO2換算的話含有0.5至2質量%之錫,使在紫外光區域(波長300nm)的穿透率提升至52%以上。 The transparent conductive film after the heat treatment, will be In 2 O 3 equivalent, then indium oxide containing 90.0% by mass of, to Nb 2 O 5 equivalent words containing 3.5 to 6.5 mass% of niobium in terms of SnO 2 then contains 0.5 to 2 As compared with Examples 1 to 7 having a mass% of tin and Comparative Examples 1 to 6 not containing niobium and tin at the content ratios, it is found that 90.0 mass% or more of indium and Nb are contained in terms of In 2 O 3 conversion. It contains 3.5 to 6.5% by mass of niobium in terms of 2 O 5 and 0.5 to 2% by mass of tin in terms of SnO 2 to increase the transmittance in the ultraviolet region (wavelength 300 nm) to 52% or more.

又,於熱處理後之透明導電膜,於實施例1至7中,如表2及第2圖所示,不僅紫外光區域,連可見光區域(例如波長400nm至800nm)亦具有與比較例1至6同等以上的穿透率。亦即,於實施形態,當將該透明導電膜應用於太陽電池的透明電極時,可將射入於該太陽電池之廣範圍波長區域的光運用於發電。 In addition, the transparent conductive film after the heat treatment, as shown in Tables 2 and 2 in Examples 1 to 7, has not only the ultraviolet light region but also the visible light region (for example, a wavelength of 400 nm to 800 nm). 6 Penetration of equal or more. That is, in the embodiment, when the transparent conductive film is applied to a transparent electrode of a solar cell, light that has entered a wide range of wavelength regions of the solar cell can be used for power generation.

因此,藉由實施形態,可更提升應用該透明導電膜之太陽電池的發電效率。 Therefore, according to the embodiment, the power generation efficiency of the solar cell using the transparent conductive film can be further improved.

又,將以In2O3換算的話含有90.0質量%以上之銦、以Nb2O5換算的話含有4.0至6.0質量%之鈮、以SnO2換算的話含有0.5至2質量%之錫的實施例1至3、5、6,與未以該含有率含有鈮的實施例4、7連行比較,可知藉由以In2O3換算的話含有90.0質量%以上之銦、以Nb2O5換算的話含有4.0至6.0質量%之鈮、以SnO2換算的話含有0.5至2質量%之錫,可良好地維持透明導電膜的導電性。 Examples in which In 2 O 3 is converted to contain 90.0% by mass or more of indium, Nb 2 O 5 is converted to contain 4.0 to 6.0% by mass of niobium, and SnO 2 is converted to contain 0.5 to 2% by mass of tin. Comparing 1 to 3, 5, and 6 with Examples 4 and 7 that do not contain niobium at the content ratio, it can be seen that when converted to In 2 O 3 , 90.0% by mass or more of indium is contained, and when converted to Nb 2 O 5 It contains 4.0 to 6.0% by mass of niobium and 0.5 to 2% by mass of tin in terms of SnO 2 , so that the conductivity of the transparent conductive film can be maintained well.

再者,將以In2O3換算的話含有90.0質量% 以上之銦、以Nb2O5換算的話含有4.5至5.5質量%之鈮、以SnO2換算的話含有0.5至2質量%之錫的實施例1至3,與未以該含有率含有鈮的實施例4至7進行比較,可知藉由以In2O3換算的話含有90.0質量%以上之銦、以Nb2O5換算的話含有4.5至5.5質量%之鈮、以SnO2換算的話含有0.5至2質量%之錫,可使在紫色區域(波長400nm)之穿透率提升至93.2%以上。 In addition, the implementation of In 2 O 3 conversion contains 90.0 mass% or more of indium, Nb 2 O 5 conversion contains 4.5 to 5.5 mass% of niobium, and SnO 2 conversion contains 0.5 to 2 mass% of tin. Comparing Examples 1 to 3 with Examples 4 to 7 that did not contain niobium at this content rate, it was found that 90.0% by mass or more of indium was contained in terms of In 2 O 3 and 4.5 to 4 in terms of Nb 2 O 5 5.5% by mass of niobium and 0.5 to 2% by mass of tin in terms of SnO 2 can increase the transmittance in the purple region (wavelength 400nm) to 93.2% or more.

再者,將以In2O3換算的話含有90.0質量%以上之銦、以Nb2O5換算的話含有4.8至5.2質量%之鈮、並且以SnO2換算的話含有0.8至1.2質量%之錫的實施例2,與未以該含有率含有鈮及錫的實施例1、3至7進行比較,可知藉由以Nb2O5換算的話含有4.8至5.2質量%之鈮、以SnO2換算的話含有0.8至1.2質量%之錫,使於紫外光區域(波長300nm)的穿透率提升至61.4%以上,並且使於紫色區域(波長400nm)之穿透率提升至94.6%以上。 Furthermore, those containing 90.0% by mass or more of indium in terms of In 2 O 3 , 4.8 to 5.2% by mass of niobium in terms of Nb 2 O 5 , and 0.8 to 1.2% by mass of tin in terms of SnO 2 Comparing Example 2 with Examples 1, 3, and 7 that did not contain niobium and tin at this content ratio, it was found that 4.8 to 5.2% by mass of niobium was contained in terms of Nb 2 O 5 conversion, and it was contained in terms of SnO 2 conversion. 0.8 to 1.2% by mass of tin increases the transmittance in the ultraviolet region (wavelength 300nm) to more than 61.4%, and increases the transmittance in the purple region (wavelength 400nm) to more than 94.6%.

以上,針對本發明之實施形態進行說明,但本發明並不限定於上述之實施形態,只要在不脫離其主旨之範圍內便可進行各種變更。例如,於實施形態,雖然揭示將透明導電膜應用於太陽電池之例,但可應用實施形態之透明導電膜的裝置,並不限於太陽電池。 As mentioned above, although embodiment of this invention was described, this invention is not limited to the said embodiment, Various changes can be made in the range which does not deviate from the meaning. For example, in the embodiment, an example in which a transparent conductive film is applied to a solar cell is disclosed, but a device to which the transparent conductive film of the embodiment can be applied is not limited to a solar cell.

例如,當將實施形態之透明導電膜應用於液晶或有機EL(electro-luminescence)等影像顯示裝置之透明電極時,由於紫外光區域或紫色區域等之短波長區域的穿透率高,故能改善短波長區域的發光效率。 For example, when the transparent conductive film of the embodiment is applied to a transparent electrode of an image display device such as a liquid crystal or an organic EL (electro-luminescence), the short-wavelength region such as an ultraviolet region or a purple region has high transmittance, so Improve luminous efficiency in the short wavelength region.

又,藉由將實施形態之透明導電膜應用於紫外線燈等紫外線光源之光學系的抗靜電膜,可提升紫外光區域的發光效率,並且可在不產生靜電的情況下安定地發出紫外光。 In addition, by applying the transparent conductive film of the embodiment to an optical antistatic film of an ultraviolet light source such as an ultraviolet lamp, the luminous efficiency in the ultraviolet region can be improved, and ultraviolet light can be stably emitted without generating static electricity.

又,於實施形態,雖然揭示使用板狀之氧化物燒結體製作濺鍍靶之例,但氧化物燒結體的形狀並不限於板狀,亦可為圓筒狀等各種形狀。 In the embodiment, an example in which a sputtering target is produced using a plate-shaped oxide sintered body is disclosed. However, the shape of the oxide sintered body is not limited to a plate shape, and various shapes such as a cylindrical shape may be used.

更多的效果及變形例,可容易地由業者導出。因此,本發明之更廣泛的樣態,並不限定於以上所表示且記述之特定的詳細狀況及代表的實施形態。因此,只要不脫離錄附之申請專利範圍及其均等物所定義之整體發明概念的精神或範圍,可進行各種變更。 More effects and modifications can be easily derived by the operator. Therefore, the broader aspects of the present invention are not limited to the specific details and representative embodiments shown and described above. Therefore, various changes can be made without departing from the spirit or scope of the overall invention concept as defined by the scope of the appended patent application and its equivalents.

Claims (7)

一種氧化物燒結體,係含有銦、鈮、錫及氧,且以In2O3換算的話含有90.0質量%以上之前述銦,以Nb2O5換算的話含有3.5至6.5質量%之前述鈮,以SnO2換算的話含有0.5至2質量%之前述錫。 An oxide sintered body containing indium, niobium, tin, and oxygen, and containing 90.0 mass% or more of the aforementioned indium in terms of In 2 O 3 and 3.5 to 6.5% by mass of the aforementioned niobium in terms of Nb 2 O 5 , The Sn content is 0.5 to 2% by mass in terms of SnO 2 . 如申請專利範圍第1項所述之氧化物燒結體,係以Nb2O5換算的話含有4.0至6.0質量%之前述鈮。 The oxide sintered body described in item 1 of the scope of patent application contains 4.0 to 6.0% by mass of the aforementioned niobium when converted into Nb 2 O 5 . 如申請專利範圍第1或2項所述之氧化物燒結體,其比電阻為7.0×10-4Ω.cm以下。 The oxide sintered body according to item 1 or 2 of the patent application scope has a specific resistance of 7.0 × 10 -4 Ω. cm or less. 如申請專利範圍第1或2項所述之氧化物燒結體,其相對密度為95%以上。 The relative density of the oxide sintered body as described in item 1 or 2 of the patent application range is 95% or more. 一種濺鍍靶,係使用申請專利範圍第1或2項所述之氧化物燒結體作為靶材者。 A sputtering target is an oxide sintered body described in item 1 or 2 of the scope of patent application as a target. 一種透明導電膜,係含有銦、鈮、錫及氧,且以In2O3換算的話含有90.0質量%以上之前述銦,以Nb2O5換算的話含有3.5至6.5質量%之前述鈮,以SnO2換算的話含有0.5至2質量%之前述錫。 A transparent conductive film containing indium, niobium, tin, and oxygen, and containing 90.0% by mass or more of the aforementioned indium in terms of In 2 O 3 and 3.5 to 6.5% by mass of the aforementioned niobium in terms of Nb 2 O 5 , based on In terms of SnO 2 , the foregoing tin is contained in an amount of 0.5 to 2% by mass. 如申請專利範圍第6項所述之透明導電膜,其於波長300nm的穿透率為52%以上。 The transparent conductive film according to item 6 of the scope of application for patent, has a transmittance of more than 52% at a wavelength of 300 nm.
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