TWI608111B - Oxide sintered body, oxide sputtering target, high refractive index conductive oxide film, and oxide sintered body manufacturing method - Google Patents
Oxide sintered body, oxide sputtering target, high refractive index conductive oxide film, and oxide sintered body manufacturing method Download PDFInfo
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- TWI608111B TWI608111B TW103101125A TW103101125A TWI608111B TW I608111 B TWI608111 B TW I608111B TW 103101125 A TW103101125 A TW 103101125A TW 103101125 A TW103101125 A TW 103101125A TW I608111 B TWI608111 B TW I608111B
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- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000005477 sputtering target Methods 0.000 title description 14
- 239000000843 powder Substances 0.000 claims description 55
- 239000011651 chromium Substances 0.000 claims description 39
- 239000010936 titanium Substances 0.000 claims description 32
- 229910052804 chromium Inorganic materials 0.000 claims description 22
- 229910052719 titanium Inorganic materials 0.000 claims description 22
- 238000005245 sintering Methods 0.000 claims description 18
- 229910052718 tin Inorganic materials 0.000 claims description 18
- 229910010413 TiO 2 Inorganic materials 0.000 claims description 17
- 230000008033 biological extinction Effects 0.000 claims description 15
- 239000011701 zinc Substances 0.000 claims description 11
- 229910052738 indium Inorganic materials 0.000 claims description 10
- 229910052725 zinc Inorganic materials 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 239000002994 raw material Substances 0.000 claims description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 6
- 239000012298 atmosphere Substances 0.000 claims description 6
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 6
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 claims description 6
- 239000011261 inert gas Substances 0.000 claims description 5
- 229910006404 SnO 2 Inorganic materials 0.000 claims description 3
- 239000010408 film Substances 0.000 description 75
- 238000004544 sputter deposition Methods 0.000 description 52
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 26
- 238000002834 transmittance Methods 0.000 description 20
- 230000003287 optical effect Effects 0.000 description 18
- 239000000463 material Substances 0.000 description 15
- 239000011787 zinc oxide Substances 0.000 description 14
- 238000002156 mixing Methods 0.000 description 13
- 239000012300 argon atmosphere Substances 0.000 description 12
- 239000011812 mixed powder Substances 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000758 substrate Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 230000031700 light absorption Effects 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- -1 0.5 Pa Substances 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 101000892301 Phomopsis amygdali Geranylgeranyl diphosphate synthase Proteins 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- AZWHFTKIBIQKCA-UHFFFAOYSA-N [Sn+2]=O.[O-2].[In+3] Chemical compound [Sn+2]=O.[O-2].[In+3] AZWHFTKIBIQKCA-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009616 inductively coupled plasma Methods 0.000 description 1
- 238000002354 inductively-coupled plasma atomic emission spectroscopy Methods 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000012788 optical film Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000001552 radio frequency sputter deposition Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- OYQCBJZGELKKPM-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O-2].[Zn+2].[O-2].[In+3] OYQCBJZGELKKPM-UHFFFAOYSA-N 0.000 description 1
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- C04B35/453—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates
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- C04B35/457—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zinc, tin, or bismuth oxides or solid solutions thereof with other oxides, e.g. zincates, stannates or bismuthates based on tin oxides or stannates
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- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
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- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
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- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/34—Sputtering
- C23C14/3407—Cathode assembly for sputtering apparatus, e.g. Target
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Description
本發明係關於一種氧化物燒結體、氧化物濺鍍靶及高折射率之導電性氧化物薄膜以及氧化物燒結體之製造方法,尤其有關體電阻較低並可進行DC濺鍍之燒結體濺鍍靶以及使用其而製作之高折射率膜。 The present invention relates to an oxide sintered body, an oxide sputtering target, a high refractive index conductive oxide film, and a method for producing an oxide sintered body, and more particularly to a sintered body having a low volume resistance and capable of DC sputtering. A plating target and a high refractive index film produced using the same.
於顯示器或觸控板等各種光裝置中利用可見光之情形,使用之材料必須為透明,並於可見光區域之全域中,尤其期望具有高穿透率。又,各種光裝置中,有於與構成之膜材料或基板之界面之因折射率差產生之光損失的情況,作為改善該等之光損失的方法,有導入用以調整折射率或光學膜厚之光學調整膜的方法。光學調整膜所要求之折射率係視各種裝置之構造而不同,因此必須要有廣泛範圍之折射率。又,根據所使用之場所亦有具導電性之必要。 In the case where visible light is used in various optical devices such as a display or a touch panel, the material used must be transparent, and in the entire region of the visible light region, it is particularly desirable to have high transmittance. Further, in various optical devices, there is a case where light loss due to a refractive index difference is formed at an interface with a film material or a substrate which is formed, and a method for improving the light loss is introduced to adjust a refractive index or an optical film. Thick optical adjustment film method. The refractive index required for the optical adjustment film varies depending on the configuration of the various devices, and therefore a wide range of refractive indices is required. Also, there is a need for electrical conductivity depending on the location in which it is used.
通常作為透明且具導電性之材料,已知有ITO(氧化銦-氧化錫)、IZO(氧化銦-氧化鋅)、GZO(氧化鎵-氧化鋅)、AZO(氧化鋁-氧化鋅)等(專利文獻1~3)。然而,該等之材料係於波長550nm之折射率位於1.95~2.05左右之範圍者,無法作為用於光學調整之高折射率材料(n>2.05)或低折射率材料(n<1.95)來使用。又,ITO係為了提高穿透率,必須於成膜時加熱基板,或者於成膜後進行退火,因此有難以使用至 無法加熱之塑膠基板或有機EL裝置等用途的問題。又,IZO係因於短波長側具吸收性,故有變成呈黃色之膜的問題。 Generally, as a transparent and electrically conductive material, ITO (indium oxide-tin oxide), IZO (indium oxide-zinc oxide), GZO (gallium oxide-zinc oxide), AZO (alumina-zinc oxide), and the like are known ( Patent Documents 1 to 3). However, these materials are used in a range of 1.95 to 2.05 with a refractive index at a wavelength of 550 nm, and cannot be used as a high refractive index material (n>2.05) or a low refractive index material (n<1.95) for optical adjustment. . Further, in order to increase the transmittance, the ITO must be heated at the time of film formation or annealed after film formation, so that it is difficult to use until Problems such as the use of plastic substrates or organic EL devices that cannot be heated. Moreover, since IZO has absorption on the short-wavelength side, there is a problem that it becomes a yellow film.
專利文獻1:日本特開2007-008780 Patent Document 1: Japanese Special Open 2007-008780
專利文獻2:日本特開2009-184876 Patent Document 2: Japanese Special Open 2009-184876
專利文獻3:日本特開2007-238375 Patent Document 3: Japanese Special Open 2007-238375
本發明之課題在於提供一種可獲得能實現可見光之高穿透 率與高折射率之導電性薄膜的燒結體。此薄膜穿透率較高、且折射率較高,因此作為顯示器或觸控板等光裝置用之薄膜、尤其作為光學調整用之薄膜有用。又,本發明之課題在於提供一種相對密度較高、體電阻較低、可進行DC濺鍍之濺鍍靶。本發明之目的在於提高光裝置之特性、設備成本之低減化、大幅改善成膜之特性。 The object of the present invention is to provide a high penetration of visible light. A sintered body of a conductive film having a high refractive index. Since this film has a high transmittance and a high refractive index, it is useful as a film for an optical device such as a display or a touch panel, particularly as a film for optical adjustment. Further, an object of the present invention is to provide a sputtering target which has a relatively high relative density and a low bulk resistance and can perform DC sputtering. It is an object of the present invention to improve the characteristics of an optical device, reduce the cost of equipment, and greatly improve the characteristics of film formation.
為了解決上述課題,本發明者等人潛心研究,結果發現以下 見解:藉由使用後述所揭示之材料系統,可獲得高穿透率且高折射率之導電性薄膜,並可確保良好之光學特性,進而,可利用DC濺鍍穩定地成膜,並可改善使用該薄膜之光裝置之特性、提高生產性。 In order to solve the above problems, the inventors of the present invention have diligently studied and found the following. Insight: By using the material system disclosed later, a conductive film having high transmittance and high refractive index can be obtained, and good optical characteristics can be ensured, and further, film formation can be stably performed by DC sputtering, and can be improved. The characteristics of the optical device using the film are improved and productivity is improved.
本發明基於以上見解,提供下述之發明: The present invention provides the following invention based on the above findings:
1)一種燒結體,由銦(In)、及鈦(Ti)或鉻(Cr)、及鋅(Zn)或錫(Sn)、及氧(O)構成,以In2O3換算計含有2~65mol%之In,分別以TiO2換算或Cr2O3換算計含有2~65mol%之Ti或Cr,令In之原子比為A(at%)、Ti或Cr之原子比為B(at%)、Zn或Sn之原子比為C(at%)時,0.5≦A/B≦5,並且0<C/(A+B)<10。 1) A sintered body comprising indium (In), titanium (Ti) or chromium (Cr), zinc (Zn), tin (Sn), and oxygen (O), and contains 2 in terms of In 2 O 3 ~65 mol% of In contains 2 to 65 mol% of Ti or Cr in terms of TiO 2 or Cr 2 O 3 , and the atomic ratio of In is A (at%), and the atomic ratio of Ti or Cr is B (at When the atomic ratio of %), Zn or Sn is C (at%), 0.5 ≦ A/B ≦ 5, and 0 < C / (A + B) < 10.
2)如上述1)記載之燒結體,其中,以In2O3換算計含有2~30mol%之In,分別以TiO2換算或Cr2O3換算計含有3~30mol%之Ti或Cr,分別以ZnO換算或SnO2換算計含有40mol%以上之Zn或Sn。 2) As described above 1) sintered body according to claim 28, wherein to In 2 O 3 in terms of containing 2 ~ 30mol% of In, respectively, calculated as TiO 2 or Cr 2 O 3 in terms of containing 3 ~ 30mol% of Ti or Cr, 40 mol% or more of Zn or Sn is contained in terms of ZnO or SnO 2 , respectively.
3)如上述1)或2)記載之燒結體,其中,0<C/(A+B)<5。 3) The sintered body according to the above 1) or 2), wherein 0 < C / (A + B) < 5.
4)如上述1)~3)中任一項記載之燒結體,其相對密度為90%以上。 The sintered body according to any one of the above 1) to 3, wherein the sintered body has a relative density of 90% or more.
5)如上述1)~4)中任一項記載之燒結體,其體電阻為10Ω.cm以下。 5) The sintered body according to any one of the above 1) to 4, wherein the sintered body has a volume resistance of 10 Ω. Below cm.
6)一種薄膜,由銦(In)、及鈦(Ti)或鉻(Cr)、及鋅(Zn)或錫(Sn)、及氧(O)構成,以In2O3換算計含有2~65mol%之In,分別以TiO2換算或Cr2O3換算計含有2~65mol%之Ti或Cr,令In之原子比為A(at%)、Ti或Cr之原子比為B(at%)、Zn或Sn之原子比為C(at%)時,0.5≦A/B≦5,並且0<C/(A+B)<10。 6) A film comprising indium (In), titanium (Ti) or chromium (Cr), zinc (Zn), tin (Sn), and oxygen (O), and contains 2~ in terms of In 2 O 3 65 mol% of In contains 2 to 65 mol% of Ti or Cr in terms of TiO 2 or Cr 2 O 3 , and the atomic ratio of In is A (at%), and the atomic ratio of Ti or Cr is B (at%). When the atomic ratio of Zn or Sn is C (at%), 0.5 ≦ A/B ≦ 5, and 0 < C / (A + B) < 10.
7)如上述6)記載之薄膜,其中,於波長550nm之折射率為2.05以上。 7) The film according to the above 6), wherein the refractive index at a wavelength of 550 nm is 2.05 or more.
8)如上述6)或7)記載之薄膜,其中,於波長450nm之消光係數為0.05以下。 8) The film according to the above 6) or 7), wherein the extinction coefficient at a wavelength of 450 nm is 0.05 or less.
9)如上述6)~8)中任一項記載之薄膜,其比電阻為1MΩcm以下。 9) The film according to any one of the above 6), wherein the specific resistance is 1 MΩcm or less.
10)一種燒結體之製造方法,其為上述1)~5)中任一項記載之燒結體之製造方法,其於不活性氣體或真空氣氛下,以900℃以上1500℃以下將原料粉末加壓燒結,或者將原料粉末壓製成形後,於不活性氣體或真空氣氛下以1000℃以上1500℃以下對該成形體進行常壓燒結。 (10) A method for producing a sintered body according to any one of the above items 1 to 5, wherein the raw material powder is added at 900 ° C or more and 1500 ° C or less in an inert gas or a vacuum atmosphere. After the pressure sintering or the raw material powder is press-formed, the formed body is subjected to normal pressure sintering at 1000 ° C or more and 1500 ° C or less in an inert gas or a vacuum atmosphere.
根據本發明,採用如上述所示之材料系統,藉此可獲得高穿 透率且高折射率之導電性膜,並可確保所欲之光學特性。又,本發明具有如下之優異效果:各種光裝置之特性之提高、設備成本之低減化、成膜速度之提高所致之生產性大幅改善。 According to the present invention, a material system as described above is employed, whereby high wear can be obtained A conductive film having a high transmittance and a high refractive index, and ensuring desired optical characteristics. Further, the present invention has an excellent effect of improving the characteristics of various optical devices, reducing the cost of equipment, and improving the productivity of the film forming speed.
本發明之特徵在於:由銦(In)、及鈦(Ti)或鉻(Cr)、及 鋅(Zn)或錫(Sn)、及氧(O)構成,以In2O3換算計含有2~65mol%之In,分別以TiO2換算或Cr2O3換算計含有2~65mol%之Ti或Cr,令In之原子比為A(at%)、Ti或Cr之原子比為B(at%)、Zn或Sn之原子比為C(at%)時,0.5≦A/B≦5,並且0<C/(A+B)<10。藉此,可獲得具有高穿透率且高折射率之導電性膜。 The present invention is characterized in that it consists of indium (In), titanium (Ti) or chromium (Cr), zinc (Zn), tin (Sn), and oxygen (O), and contains 2 in terms of In 2 O 3 . ~65 mol% of In contains 2 to 65 mol% of Ti or Cr in terms of TiO 2 or Cr 2 O 3 , and the atomic ratio of In is A (at%), and the atomic ratio of Ti or Cr is B (at When the atomic ratio of %), Zn or Sn is C (at%), 0.5 ≦ A/B ≦ 5, and 0 < C / (A + B) < 10. Thereby, a conductive film having a high transmittance and a high refractive index can be obtained.
再者,本發明係將銦(In)、及鈦(Ti)或鉻(Cr)、及鋅(Zn)或錫(Sn)、及氧(O)設為構成元素,但於該材料中亦包含不可避免之雜質。 Further, in the present invention, indium (In), titanium (Ti) or chromium (Cr), and zinc (Zn), tin (Sn), and oxygen (O) are used as constituent elements, but in the material, Contains unavoidable impurities.
本發明之材料系統係包含以式:M1M2O3(M3O)m(M1:第 一成分、M2:第二成分、M3:第三成分、m為1以上之自然數)所表示之同系(homologous)化合物,作為可成為同系構造之材料且為高折射率材料,可列舉第一成分為In或Fe,第二成分為Ti、Cr、In、Fe或Sn,第三成分為Zn、Sn、Cu、Mn、Fe或Co。然而,Fe、Cu、Mn、Co因帶隙較小,導致於可見光領域產生吸收,故而不佳。 The material system of the present invention comprises the formula: M 1 M 2 O 3 (M 3 O) m (M 1 : first component, M 2 : second component, M 3 : third component, m is 1 or more natural The homologous compound represented by the number of the homologous compound is a material having a homologous structure and is a high refractive index material, and the first component is In or Fe, and the second component is Ti, Cr, In, Fe or Sn. The three components are Zn, Sn, Cu, Mn, Fe or Co. However, Fe, Cu, Mn, and Co are less likely to cause absorption in the visible light region due to a smaller band gap.
因此,決定採用In作為第一成分。又,第三成分決定採用Zn或Sn。 進而,為了高折射率化而無法使用In或Sn作為第二成分,故決定採用Ti 或Cr作為第二成分。 Therefore, it was decided to use In as the first component. Further, the third component determines the use of Zn or Sn. Further, in order to increase the refractive index and to use In or Sn as the second component, it was decided to use Ti. Or Cr as the second component.
於本發明中,In之含量以In2O3換算係設為2~65mol%。進 而較佳為設為2~30mol%。又,Ti或Cr之含量分別以TiO2換算或Cr2O3換算係設為3~65mol%。進而較佳為設為3~30mol%。為第三成分之Zn或Sn之含量可自In與Ti或Cr之含量及上述中規定之C/(A+B)之原子比來導出,但較佳為以ZnO或SnO換算係設為40mol%以上。藉此,可實現具有所欲之高穿透率且高折射率之導電性膜。 In the present invention, the content of In is set to 2 to 65 mol% in terms of In 2 O 3 . Further, it is preferably 2 to 30 mol%. Further, the content of Ti or Cr is set to 3 to 65 mol% in terms of TiO 2 conversion or Cr 2 O 3 conversion. Further, it is preferably 3 to 30 mol%. The content of Zn or Sn which is the third component can be derived from the atomic ratio of In and Ti or Cr and the above-mentioned C/(A+B), but it is preferably set to 40 mol in terms of ZnO or SnO. %the above. Thereby, a conductive film having a desired high transmittance and a high refractive index can be realized.
於本發明中,A/B之原子比係設為0.5≦A/B≦5。若超過此 範圍,則無法獲得所欲之光學特性,故而不佳。尤其,若A/B成為5以上,則存在高折射率材料(Ti或Cr)之含量減少,折射率降低之問題。又,於本發明中,C/(A+B)之原子比係設為0<C/(A+B)<10,進而較佳為設為0<C/(A+B)<5。若超過此範圍,與上述相同地存在高折射率材料之含量減少,無法獲得所欲之高折射率之問題。 In the present invention, the atomic ratio of A/B is set to 0.5 ≦A/B ≦5. If this is exceeded The range is not good enough to obtain the desired optical properties. In particular, when A/B is 5 or more, there is a problem that the content of the high refractive index material (Ti or Cr) is decreased and the refractive index is lowered. Further, in the present invention, the atomic ratio of C/(A+B) is set to 0 < C / (A + B) < 10, and further preferably set to 0 < C / (A + B) < 5. If it exceeds this range, the content of the high refractive index material is reduced as described above, and the problem of the desired high refractive index cannot be obtained.
於本發明之燒結體用作濺鍍靶之情形時,較佳為設為相對密 度90%以上。密度之提高具有提高濺鍍膜之均勻性、又抑制濺鍍時之微粒之產生的效果。可藉由下述之本發明之燒結體之製造方法,實現相對密度90%以上。 When the sintered body of the present invention is used as a sputtering target, it is preferably set to be relatively dense. More than 90%. The increase in density has an effect of improving the uniformity of the sputtering film and suppressing the generation of particles at the time of sputtering. The relative density of 90% or more can be achieved by the method for producing a sintered body of the present invention described below.
又,於本發明之燒結體用作濺鍍靶之情形時,較佳為設為體電阻10Ω.cm以下。藉由體電阻之下降,可利用DC濺鍍進行成膜。與RF(radio frequency)濺鍍相比,DC濺鍍成膜速度較快,濺鍍效率優異,可提高產出量。再者,視製造條件亦有進行RF濺鍍之情形,於該情形亦可提高成膜速度。 Moreover, when the sintered body of the present invention is used as a sputtering target, it is preferably set to have a bulk resistance of 10 Ω. Below cm. By the drop in bulk resistance, film formation can be performed by DC sputtering. Compared with RF (radio frequency) sputtering, DC sputtering has a faster deposition rate and excellent sputtering efficiency, which can increase the output. Further, depending on the manufacturing conditions, there is also a case where RF sputtering is performed, and in this case, the film formation speed can also be increased.
藉由本發明之濺鍍所製作之薄膜可達到於波長550nm之折 射率為2.05以上。又,本發明之薄膜可達到於波長450nm之消光係數為0.05以下。進而,本發明之薄膜可達到比電阻為1MΩ.cm以下。作為光學調整用之薄膜,此種高折射率且穿透率較高之導電性薄膜係於顯示器或觸控板等光裝置有用。尤其,本發明可獲得於波長450nm之消光係數為0.01以下並且於短波長區域幾乎無吸收之高折射率的膜,因此可說是用以獲得所欲之光學特性之優異的材料系統。 The film produced by the sputtering of the present invention can be folded at a wavelength of 550 nm. The rate of incidence is 2.05 or more. Further, the film of the present invention can have an extinction coefficient of 0.05 or less at a wavelength of 450 nm. Further, the film of the present invention can achieve a specific resistance of 1 MΩ. Below cm. As a film for optical adjustment, such a conductive film having a high refractive index and a high transmittance is useful for an optical device such as a display or a touch panel. In particular, the present invention can be obtained as a film having an extinction coefficient of a wavelength of 450 nm of 0.01 or less and a high refractive index which is hardly absorbed in a short-wavelength region, and thus can be said to be an excellent material system for obtaining desired optical characteristics.
於上述組成範圍中,本發明之薄膜係存在成為結晶化膜者與 成為非晶膜者。進而,亦存在呈兩者共存之局部結晶化膜的狀態者。於本發明中,關於此種膜之結晶性並無特別限制,可依所欲之結晶性調整組成。 再者,可藉由X光繞射法之繞射峰值之有無來評價膜之結晶性(結晶化膜、非晶膜、或部分結晶化膜)。 In the above composition range, the film of the present invention exists as a crystallized film and Become an amorphous film. Further, there is also a state in which the partially crystallized film coexists in both. In the present invention, the crystallinity of such a film is not particularly limited, and the composition can be adjusted depending on the desired crystallinity. Further, the crystallinity (crystallized film, amorphous film, or partially crystallized film) of the film can be evaluated by the presence or absence of the diffraction peak of the X-ray diffraction method.
本發明之燒結體可藉由於不活性氣體氣氛或真空氣氛下對 由各構成金屬之氧化物粉末所構成之原料粉末進行加壓燒結(熱壓)、或藉由將原料粉末壓製成形後,將該成形體常壓燒結而製造。此時,燒結溫度較佳為設為900℃以上1500℃以下。若未達900℃,則無法獲得高密度之燒結體,另一方面,若超過1500℃,則產生因材料之蒸發所導致之組成偏差或密度下降,故而不佳。 The sintered body of the present invention can be obtained by an inert gas atmosphere or a vacuum atmosphere The raw material powder composed of the oxide powder of each constituent metal is subjected to pressure sintering (hot pressing) or by press molding the raw material powder, and then the molded body is produced by normal pressure sintering. At this time, the sintering temperature is preferably set to 900 ° C or more and 1500 ° C or less. If it is less than 900 ° C, a sintered body having a high density cannot be obtained. On the other hand, if it exceeds 1500 ° C, a composition variation or a decrease in density due to evaporation of the material may occur, which is not preferable.
實施例 Example
以下,基於實施例及比較例進行說明。再者,本實施例畢竟為一例,並非藉由該例所受限者。即,本發明係僅藉由申請專利之範圍所限定,並亦包含本發明所含之實施例以外之各種變形。 Hereinafter, description will be made based on examples and comparative examples. Furthermore, this embodiment is an example after all, and is not limited by this example. That is, the present invention is limited only by the scope of the patent application, and includes various modifications other than the embodiments included in the invention.
實施例、比較例中之評價方法等係如下所述。 The evaluation methods and the like in the examples and comparative examples are as follows.
裝置:SII社製造之SPS3500DD Device: SPS3500DD manufactured by SII
方法:ICP-OES(高頻波感應耦合電漿發光分析法) Method: ICP-OES (high-frequency wave inductively coupled plasma luminescence analysis method)
利用游標卡尺對燒結體之尺寸進行長度量測,自其體積與測定重量算出燒結體密度。 The size of the sintered body was measured by a vernier caliper, and the density of the sintered body was calculated from the volume and the measured weight.
如下所示般,分別對原料之氧化物之單體密度乘以混合質量比,合計所獲得之值而求出理論密度。又,氧化物燒結體之密度除以理論密度再乘以100而求出相對密度。 As shown below, the theoretical density was obtained by multiplying the monomer density of the oxide of the raw material by the mixing mass ratio and summing the obtained values. Further, the density of the oxide sintered body was divided by the theoretical density and multiplied by 100 to determine the relative density.
理論密度=Σ{(各氧化物之單體密度×混合質量比)+(各氧化物之單體密度×混合質量比+…)} Theoretical density = Σ { (cell density of each oxide × mixed mass ratio) + (monomer density of each oxide × mixed mass ratio +...)
相對密度={(燒結體之密度)/(理論密度)}×100 Relative density = {(density of sintered body) / (theoretical density)} × 100
裝置:NPS社製造 電阻率測定器 Σ-5+ Device: manufactured by NPS Co., Ltd. Resistivity meter Σ-5+
方法:直流4探針法 Method: DC 4 probe method
裝置:SHIMADZU社製造 分光光度計 UV-2450 Device: manufactured by SHIMADZU, spectrophotometer UV-2450
方法:自穿透率、表背面反射率來算出 Method: Calculate self-transmission rate and surface reflectance
裝置:ANELVA SPL-500 Device: ANELVA SPL-500
基板:φ 4inch Substrate: φ 4inch
基板溫度:室溫 Substrate temperature: room temperature
(實施例1) (Example 1)
準備In2O3粉、TiO2粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1150℃、壓力250kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。 In 2 O 3 powder, TiO 2 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, this mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,150 ° C and a pressure of 250 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape.
繼而,使用上述之經精加工之直徑6英吋之靶,進行濺鍍。濺鍍條件設為:DC濺鍍、濺鍍功率500W、含有0~2vol%之氧之Ar氣體壓力0.5Pa,成膜至膜厚5000Å。再者,不進行濺鍍時之基板加熱或濺鍍後之退火。 Then, sputtering was performed using the above-mentioned finished 6-inch diameter target. The sputtering conditions were as follows: DC sputtering, sputtering power of 500 W, and Ar gas pressure of 0 to 2 vol% of oxygen, 0.5 Pa, and film formation to a film thickness of 5000 Å. Further, the substrate is not heated or the annealing after sputtering is performed.
結果示於表1。如表1所示,濺鍍靶係達到相對密度98.9%,體電阻為2.9×10-3Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.10(波長550nm)、消光係數為0.01(波長450nm)、電阻值為2.3×10-2Ω.cm以上,獲得高折射率且高穿透率之導電性膜。再者,關於電阻值,視濺鍍時之氧量會些許變動,存在氧量提高則電阻值上升之傾向。因此,記載其下限值。 The results are shown in Table 1. As shown in Table 1, the sputtering target system has a relative density of 98.9% and a bulk resistance of 2.9×10 -3 Ω. Cm, achieving stable DC sputtering. Further, the film deposited by sputtering has a refractive index of 2.10 (wavelength 550 nm), an extinction coefficient of 0.01 (wavelength: 450 nm), and a resistance value of 2.3 × 10 -2 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained. Further, regarding the resistance value, the amount of oxygen at the time of sputtering may vary slightly, and the resistance value may increase as the amount of oxygen increases. Therefore, the lower limit value is described.
(實施例2) (Example 2)
準備In2O3粉、TiO2粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1150℃、壓力250kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍靶係達到相對密度100.3%,體電阻為8.7×10-3Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.15(波長550nm)、消光係數未達0.01(波長450nm)、電阻值為1.8×10+2Ω.cm以上,獲得高折射率且高穿透率之導電性膜。 In 2 O 3 powder, TiO 2 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, this mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,150 ° C and a pressure of 250 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. The result is that the sputtering target reaches a relative density of 100.3% and a bulk resistance of 8.7×10 -3 Ω. Cm, achieving stable DC sputtering. Moreover, the refractive index of the film formed by sputtering is 2.15 (wavelength 550 nm), the extinction coefficient is less than 0.01 (wavelength 450 nm), and the resistance value is 1.8×10 +2 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained.
(實施例3) (Example 3)
準備In2O3粉、TiO2粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1100℃、壓力250kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍靶係達到相對密度99.5%,體電阻為3.5×10-3Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.22(波長550nm)、消光係數未達0.01(波長450nm)、電阻值為1.2×10+2Ω.cm以上,獲得高折射率且高穿透率之導電性膜。 In 2 O 3 powder, TiO 2 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, this mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,100 ° C and a pressure of 250 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. The result is that the sputtering target reaches a relative density of 99.5% and a bulk resistance of 3.5×10 -3 Ω. Cm, achieving stable DC sputtering. Moreover, the refractive index of the film formed by sputtering is 2.22 (wavelength 550 nm), the extinction coefficient is less than 0.01 (wavelength 450 nm), and the resistance value is 1.2×10 +2 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained.
(實施例4) (Example 4)
準備In2O3粉、Cr2O3粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1100℃、壓力350kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而, 使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍靶係達到相對密度100.2%,體電阻為8.0×10-4Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.10(波長550nm)、消光係數為0.02(波長450nm)、電阻值為2.8×10-2Ω.cm以上,獲得高折射率且高穿透率之導電性膜。 In 2 O 3 powder, Cr 2 O 3 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, this mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,100 ° C and a pressure of 350 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. The result is that the sputtering target system reaches a relative density of 100.2% and a bulk resistance of 8.0×10 -4 Ω. Cm, achieving stable DC sputtering. Further, the film deposited by sputtering has a refractive index of 2.10 (wavelength 550 nm), an extinction coefficient of 0.02 (wavelength: 450 nm), and a resistance value of 2.8 × 10 -2 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained.
(實施例5) (Example 5)
準備In2O3粉、TiO2粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1150℃、壓力250kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍靶係達到相對密度100.1%,體電阻為9.6×10-4Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.12(波長550nm)、消光係數未達0.01(波長450nm)、電阻值為8.7×10-3Ω.cm以上,獲得高折射率且高穿透率之導電性膜。 In 2 O 3 powder, TiO 2 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, this mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,150 ° C and a pressure of 250 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. The result is that the sputtering target reaches a relative density of 100.1% and a bulk resistance of 9.6×10 -4 Ω. Cm, achieving stable DC sputtering. Moreover, the film deposited by sputtering has a refractive index of 2.12 (wavelength 550 nm), an extinction coefficient of less than 0.01 (wavelength of 450 nm), and a resistance value of 8.7×10 -3 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained.
(實施例6) (Example 6)
準備In2O3粉、TiO2粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1100℃、壓力250kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍靶係達到相對密度99.8%,體電阻為8.4×10-4Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.05(波長550nm)、消光係數未達0.01(波長450nm)、電阻值為9.3×10-3Ω.cm以上,獲得高折 射率且高穿透率之導電性膜。 In 2 O 3 powder, TiO 2 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, this mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,100 ° C and a pressure of 250 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. The result is that the sputtering target reaches a relative density of 99.8% and a bulk resistance of 8.4×10 -4 Ω. Cm, achieving stable DC sputtering. Moreover, the refractive index of the film formed by sputtering is 2.05 (wavelength 550 nm), the extinction coefficient is less than 0.01 (wavelength 450 nm), and the resistance value is 9.3×10 -3 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained.
(實施例7) (Example 7)
準備In2O3粉、Cr2O3粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1150℃、壓力350kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍靶係達到相對密度98.2%,體電阻為5.2×10-3Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.07(波長550nm)、消光係數為0.03(波長450nm)、電阻值為3.6×10-2Ω.cm以上,獲得高折射率且高穿透率之導電性膜。 In 2 O 3 powder, Cr 2 O 3 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, the mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,150 ° C and a pressure of 350 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. The result is that the sputtering target reaches a relative density of 98.2% and a bulk resistance of 5.2×10 -3 Ω. Cm, achieving stable DC sputtering. Further, the film formed by sputtering has a refractive index of 2.07 (wavelength 550 nm), an extinction coefficient of 0.03 (wavelength: 450 nm), and a resistance value of 3.6 × 10 -2 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained.
(實施例8) (Example 8)
準備In2O3粉、TiO2粉、SnO2粉,並以表1所記載之調配比調合並混合該等粉末。繼而,將該混合粉壓製成形後,以氬氣氣氛下、溫度1300℃之條件將成形體常溫燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍靶係達到相對密度97.8%,體電阻為8.7×10-2Ω.cm,達成穩定之DC濺鍍。而且,濺鍍成膜出之薄膜之折射率為2.08(波長550nm)、消光係數為0.01(波長450nm)、電阻值為3.1×101Ω.cm以上,獲得高折射率且高穿透率之導電性膜。 In 2 O 3 powder, TiO 2 powder, and SnO 2 powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, after the mixed powder was press-formed, the formed body was sintered at room temperature under an argon atmosphere at a temperature of 1300 °C. Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. The result is that the sputtering target reaches a relative density of 97.8% and a bulk resistance of 8.7×10 -2 Ω. Cm, achieving stable DC sputtering. Further, the film formed by sputtering has a refractive index of 2.08 (wavelength 550 nm), an extinction coefficient of 0.01 (wavelength: 450 nm), and a resistance value of 3.1 × 10 1 Ω. Above cm, a conductive film having a high refractive index and a high transmittance is obtained.
(比較例1) (Comparative Example 1)
準備In2O3粉、Fe2O3粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1050℃、壓力350kgf/cm2之條件將此 混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍成膜出之薄膜之消光係數為0.16(波長450nm),於低波長區域產生光之吸收,無法獲得所欲之高穿透率膜。 In 2 O 3 powder, Fe 2 O 3 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, the mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1050 ° C and a pressure of 350 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. As a result, the film having a sputtered film had an extinction coefficient of 0.16 (wavelength: 450 nm), and absorption of light was generated in a low-wavelength region, and a desired high transmittance film could not be obtained.
(比較例2) (Comparative Example 2)
準備In2O3粉、TiO2粉、CuO粉,並以表1所記載之調配比調合並混合該等粉末。繼而,以氬氣氣氛下、溫度1050℃、壓力350kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍成膜出之薄膜之消光係數為0.2以上(波長450nm),於低波長區域產生光之吸收,無法獲得所欲之高穿透率膜。 In 2 O 3 powder, TiO 2 powder, and CuO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. Then, the mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1050 ° C and a pressure of 350 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. As a result, the extinction coefficient of the film formed by sputtering is 0.2 or more (wavelength: 450 nm), and light absorption occurs in a low-wavelength region, and a desired high-transmittance film cannot be obtained.
(比較例3) (Comparative Example 3)
準備In2O3粉、TiO2粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。此時,將In/Ti之原子比提高至8.0。繼而,以氬氣氣氛下、溫度1150℃、壓力250kgf/cm2之條件將此混合粉進行熱壓燒結。其後,機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍成膜出之薄膜之折射率為2.01(波長550nm),折射率下降,無法獲得所欲之高折射率膜。 In 2 O 3 powder, TiO 2 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. At this time, the atomic ratio of In/Ti was increased to 8.0. Then, this mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1,150 ° C and a pressure of 250 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. As a result, the refractive index of the film formed by sputtering was 2.01 (wavelength: 550 nm), and the refractive index was lowered, and the desired high refractive index film could not be obtained.
(比較例4) (Comparative Example 4)
準備In2O3粉、TiO2粉、ZnO粉,並以表1所記載之調配比調合並混合該等粉末。此時,將Zn/(In+Ti)之原子比提高至15。繼而,以氬氣氣氛下、溫度1050℃、壓力250kgf/cm2之條件將此混合粉進行熱壓燒結。其後, 機械加工此燒結體並精加工成靶形狀。繼而,使用上述之經精加工之直徑6英吋之靶,以與實施例1同樣之條件進行濺鍍。其結果為:濺鍍成膜出之薄膜之折射率為2.02(波長550nm),折射率下降,無法獲得所欲之高穿透率膜。 In 2 O 3 powder, TiO 2 powder, and ZnO powder were prepared, and the powders were blended and mixed in the blending ratios shown in Table 1. At this time, the atomic ratio of Zn/(In+Ti) was increased to 15. Then, the mixed powder was subjected to hot press sintering under the conditions of an argon atmosphere at a temperature of 1050 ° C and a pressure of 250 kgf / cm 2 . Thereafter, the sintered body is machined and finished into a target shape. Then, sputtering was carried out under the same conditions as in Example 1 using the above-mentioned finished 6-inch diameter target. As a result, the refractive index of the film formed by sputtering was 2.02 (wavelength: 550 nm), and the refractive index was lowered, and the desired high transmittance film could not be obtained.
產業上之利用性 Industrial use
藉由本發明之濺鍍而形成之薄膜係形成顯示器或觸控板中之光學調整用之薄膜或光碟之構造的一部分,並有於穿透率、折射率、導電性中具有極為優異之特性的效果。 The film formed by the sputtering of the present invention forms part of the structure of the optical adjustment film or the optical disk in the display or the touch panel, and has extremely excellent characteristics in transmittance, refractive index, and electrical conductivity. effect.
又,由本發明之燒結體所構成之濺鍍靶係體電阻值較低,且為高密度,因此可進行穩定之DC濺鍍。而且,具有如下之顯著效果:為該DC濺鍍之特徵之濺鍍控制性變得容易、成膜速度上升、可使濺鍍效率提高。又,可降低於成膜之際在濺鍍時產生之微粒,提高膜之品質。 Further, since the sputtering target system composed of the sintered body of the present invention has a low resistance value and a high density, stable DC sputtering can be performed. Further, it has a remarkable effect that the sputtering control property of the DC sputtering is easy, the film formation speed is increased, and the sputtering efficiency can be improved. Moreover, the particles generated at the time of sputtering at the time of film formation can be reduced, and the quality of the film can be improved.
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