TW201337021A - Sputtering target - Google Patents
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- TW201337021A TW201337021A TW102108011A TW102108011A TW201337021A TW 201337021 A TW201337021 A TW 201337021A TW 102108011 A TW102108011 A TW 102108011A TW 102108011 A TW102108011 A TW 102108011A TW 201337021 A TW201337021 A TW 201337021A
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- 238000005477 sputtering target Methods 0.000 title claims abstract description 87
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 79
- 229910052802 copper Inorganic materials 0.000 claims abstract description 61
- 239000010949 copper Substances 0.000 claims abstract description 61
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 39
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 39
- 239000011593 sulfur Substances 0.000 claims abstract description 39
- 238000004544 sputter deposition Methods 0.000 abstract description 70
- 239000002245 particle Substances 0.000 abstract description 14
- 239000010409 thin film Substances 0.000 abstract description 6
- -1 splashes Substances 0.000 abstract description 5
- 239000000428 dust Substances 0.000 abstract description 3
- 239000010408 film Substances 0.000 description 65
- 239000013078 crystal Substances 0.000 description 35
- 230000015572 biosynthetic process Effects 0.000 description 30
- 230000000052 comparative effect Effects 0.000 description 22
- 238000000034 method Methods 0.000 description 22
- 239000000758 substrate Substances 0.000 description 22
- 238000000137 annealing Methods 0.000 description 16
- 238000004519 manufacturing process Methods 0.000 description 16
- 238000012545 processing Methods 0.000 description 16
- 239000000463 material Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 11
- 210000001161 mammalian embryo Anatomy 0.000 description 11
- 238000001192 hot extrusion Methods 0.000 description 9
- 238000012790 confirmation Methods 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 8
- 238000005482 strain hardening Methods 0.000 description 8
- 239000004065 semiconductor Substances 0.000 description 7
- 235000012431 wafers Nutrition 0.000 description 7
- 239000012535 impurity Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000007670 refining Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000002441 X-ray diffraction Methods 0.000 description 4
- 230000002159 abnormal effect Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000004973 liquid crystal related substance Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000001953 recrystallisation Methods 0.000 description 4
- 239000011669 selenium Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 230000003746 surface roughness Effects 0.000 description 4
- 230000005856 abnormality Effects 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229910052797 bismuth Inorganic materials 0.000 description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
- 238000005097 cold rolling Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000005098 hot rolling Methods 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 101000582320 Homo sapiens Neurogenic differentiation factor 6 Proteins 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 102100030589 Neurogenic differentiation factor 6 Human genes 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 238000001755 magnetron sputter deposition Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000013077 target material Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000010622 cold drawing Methods 0.000 description 1
- 238000000641 cold extrusion Methods 0.000 description 1
- 238000010273 cold forging Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000013500 data storage Methods 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 230000010365 information processing Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000004857 zone melting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/08—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/34—Sputtering
- C23C14/3407—Cathode assembly for sputtering apparatus, e.g. Target
- C23C14/3414—Metallurgical or chemical aspects of target preparation, e.g. casting, powder metallurgy
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physical Vapour Deposition (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
Description
本發明係關於一種由高純度銅構成之濺鍍靶,該高純度銅係用以形成例如構成以液晶顯示器為代表之平面面板(flat panel)顯示元件的金屬薄膜、構成半導體元件製造用光罩之遮光膜、構成LSI等半導體元件之金屬配線及構成磁紀錄媒體之銅薄膜等。 The present invention relates to a sputtering target made of high-purity copper for forming, for example, a metal thin film constituting a flat panel display element typified by a liquid crystal display, and a photomask for manufacturing a semiconductor element. A light-shielding film, a metal wiring constituting a semiconductor element such as an LSI, and a copper thin film constituting a magnetic recording medium.
用以將上述銅薄膜等形成於被濺鍍物之方法使用有濺鍍法。 A sputtering method is used to form the copper thin film or the like on the object to be sputtered.
濺鍍法係藉由如下步驟而於濺鍍對象物上形成與靶相同組成之薄膜的成膜方法:將上述之濺鍍靶(以下稱為「靶」)以面對基板等濺鍍對象物之形式設置,於真空條件下流入Ar等氣體,於靶之被濺鍍面與濺鍍對象物之間藉由施加電壓而使其放電,使離子化之Ar撞擊靶而形成。 The sputtering method is a film formation method of forming a thin film having the same composition as that of a target on a sputtering target by the following steps: sputtering the target (hereinafter referred to as "target") to face a substrate or the like In a form, a gas such as Ar is introduced under a vacuum condition, and a voltage is applied between the sputtered surface of the target and the object to be sputtered by applying a voltage, and the ionized Ar is struck against the target.
如此之濺鍍法經過因應各個不同目的之程序而用於半導體元件、磁紀錄媒體、半導體元件製造用光罩、液晶顯示器等構成部等不同之領域。 Such a sputtering method is used in various fields such as a semiconductor element, a magnetic recording medium, a photomask for manufacturing a semiconductor element, and a liquid crystal display, etc., in accordance with a program for various purposes.
但是,來自靶之濺鍍物質本來係附著於面對該濺鍍靶之例如基板等濺鍍靶對象物,但並不一定侷限於垂直地濺鍍,會朝各種方向濺出。 However, the sputtering material from the target is originally adhered to a sputtering target object such as a substrate facing the sputtering target, but is not necessarily limited to vertical sputtering, and is splashed in various directions.
如此之飛濺物質稱為顆粒,有叢集化而直接附著於基板上之情形、或附著於基板以外之濺鍍裝置內機器的情況,有時亦有剝落且懸浮而再附著於基板之情形。 Such a spattery substance is referred to as a granule, and when it is clustered and directly adhered to a substrate, or when it is attached to a device in a sputtering apparatus other than the substrate, it may be peeled off and suspended to adhere to the substrate.
於濺鍍法中,如此之各種現象為發生顆粒、飛濺及粉塵等粗大叢集之主要原因,且有損及膜厚均一性之課題。 In the sputtering method, such various phenomena are the main cause of coarse clusters such as particles, splashes, and dust, and the problem of uniformity of film thickness is impaired.
為了解決如此課題,進而加強對以往於濺鍍程序中氣體壓力、投入電力、靶-基板間距離等濺鍍條件的檢討,而提出各種文獻。 In order to solve such a problem, various literatures have been proposed to review the sputtering conditions such as the gas pressure, the input power, and the distance between the target and the substrate in the sputtering process.
認為產生粗大叢集之發生等異常成膜之問題,其起因除了濺鍍處理條件以外,亦起因於靶本身之配向性、表面粗糙度等表面狀態。 It is considered that the problem of abnormal film formation such as occurrence of coarse clusters is caused by the surface state such as the orientation of the target itself and the surface roughness, in addition to the sputtering treatment conditions.
例如,若靶表面存在裂縫(瑕疵)則電荷會集中於裂縫部分之邊緣(端部),而發生異常放電(電弧)。如此一來則電弧造成之飛濺發生會變多,發生成膜異常,而成膜至配線圖案失敗情況會變多,因此產生良率下降之課題。 For example, if there is a crack (瑕疵) on the surface of the target, the electric charge will concentrate on the edge (end) of the crack portion, and an abnormal discharge (arc) will occur. As a result, the occurrence of spatter due to the arc increases, and film formation abnormality occurs, and the failure of the film formation to the wiring pattern increases, which causes a problem of a decrease in yield.
根據該背景來看,應將靶表面之裂縫數或大小減低,而近年有著眼於靶表面狀態之各種提案。 From this background, the number or size of cracks on the target surface should be reduced, and in recent years there have been various proposals for the state of the target surface.
例如,專利文獻1之「濺鍍靶及其製造方法」亦為其中之1者。 For example, "sputter target and its manufacturing method" of Patent Document 1 is also one of them.
專利文獻1中揭示有為了用作為濺鍍靶而藉由對濺鍍靶施以例如機械加工、研磨加工、化學蝕刻等,而調整為可減低結球(nodule)及顆粒之產生的特定表面粗糙度之濺鍍靶及其製造方法。 Patent Document 1 discloses that a specific surface roughness which can reduce the generation of nodules and particles can be adjusted by applying, for example, machining, polishing, chemical etching, or the like to the sputtering target as a sputtering target. Sputter target and its manufacturing method.
如上述之專利文獻1般,為了改善靶本身之表面狀態,而提出有著眼於靶本身之表面粗糙度或組織配向性者。但是,其幾乎不瞭解起因為組成靶本身之元素種類或其含量之影響,且幾乎無著眼於靶元素之組成以提高膜厚之均一性的文獻。 As in the above-described Patent Document 1, in order to improve the surface state of the target itself, it is proposed to have the surface roughness or the tissue alignment of the target itself. However, it hardly understands the literature on the composition of the target itself or its content, and has little focus on the composition of the target element to increase the uniformity of the film thickness.
具體而言,以往關於著眼於靶元素組成之技術僅不過為了解 決MOS特性之不穩定特性而提出如下技術:減低靶本身中所含被視為雜質之鈉或鉀等鹼金屬之含量的技術,或為了防止氧化而減低鐵、鎳等重金屬含量的技術;而現今狀態中則有無法充分地防止伴隨靶表面裂縫而發生成膜異常的課題。 Specifically, the previous technology for focusing on the composition of target elements is just to understand In order to reduce the unstable characteristics of the MOS characteristics, the following techniques are proposed: a technique for reducing the content of an alkali metal such as sodium or potassium as an impurity contained in the target itself, or a technique for reducing the content of heavy metals such as iron and nickel in order to prevent oxidation; In the present state, there is a problem that the film formation abnormality may not be sufficiently prevented from occurring along with the crack of the target surface.
[專利文獻1]日本特開平11-1766號公報 [Patent Document 1] Japanese Patent Laid-Open No. Hei 11-1766
因此,本發明提供一種濺鍍靶,其目的在於提供防止靶之濺鍍時發生飛濺,提高由濺鍍所形成的薄膜膜厚之均一性。 Accordingly, the present invention provides a sputtering target, which aims to prevent spatter from occurring during sputtering of a target and to improve uniformity of film thickness formed by sputtering.
本發明為以純度為99.9質量%以上之銅作為主成分之濺鍍靶,其特徵在於含有10ppm以下之硫(S)、及2ppm以下之鉛(Pb)。此處之ppm係指質量ppm。 The present invention is a sputtering target containing copper having a purity of 99.9% by mass or more as a main component, and is characterized by containing 10 ppm or less of sulfur (S) and 2 ppm or less of lead (Pb). The ppm here means the mass ppm.
本發明之一態樣係上述銅之純度為99.96質量%以上。 In one aspect of the invention, the purity of the copper is 99.96 mass% or more.
藉由上述構成,可構成使濺鍍表面及內部之特定尺寸以上寬度之裂縫(瑕疵)大幅減低的靶,故可防止濺鍍處理時之異常放電(電弧)發生。 According to the above configuration, it is possible to form a target in which the crack (瑕疵) having a width larger than the specific size of the sputtering surface and the inside is greatly reduced, so that abnormal discharge (arc) during the sputtering process can be prevented from occurring.
藉此,可提供防止靶之濺鍍時發生飛濺且提高由濺鍍所形成的薄膜膜厚之均一性的濺鍍靶。 Thereby, it is possible to provide a sputtering target which prevents spattering during sputtering of the target and improves the uniformity of the film thickness of the thin film formed by sputtering.
本實施形態中濺鍍靶較佳為銅純度99.96質量%以上,進而更佳為99.99質量%以上,但只要為99.9質量%以上則無特別限定。 In the present embodiment, the sputtering target is preferably 99.96 mass% or more, and more preferably 99.99 mass% or more. However, the sputtering target is not particularly limited as long as it is 99.9% by mass or more.
即,作為本發明濺鍍靶之主成分銅,不僅為無氧銅(99.96%以上之高純度銅)亦包含精銅。 That is, the main component copper of the sputtering target of the present invention contains not only oxygen-free copper (99.96% or more of high-purity copper) but also refined copper.
濺鍍靶雖然至少其濺鍍面之平均結晶粒徑較佳為例如200μm以下,但濺鍍面之平均結晶粒徑並無特別限定。 In the sputtering target, at least the average crystal grain size of the sputtering surface is preferably 200 μm or less, but the average crystal grain size of the sputtering surface is not particularly limited.
本發明之濺鍍靶的形狀並無限定,例如為圓筒狀、板狀、條狀等。 The shape of the sputtering target of the present invention is not limited, and examples thereof include a cylindrical shape, a plate shape, and a strip shape.
本發明之靶的製造方法亦無特別限定。即,使硫(S)之含量為10ppm以下且鉛(Pb)含量為2ppm以下的調節方法並無特別限定。 The method for producing the target of the present invention is also not particularly limited. In other words, the method of adjusting the content of sulfur (S) to 10 ppm or less and the content of lead (Pb) to 2 ppm or less is not particularly limited.
例如,於銅精煉時可先儘可能地去除硫(S)或鉛(Pb),之後可於進行鑄造錠時反而添加硫(S)與鉛(Pb),以使硫(S)與鉛(Pb)之含量分別滿足特定之重量%濃度以下之範圍的方式進行調節。 For example, in copper refining, sulfur (S) or lead (Pb) may be removed as much as possible, and then sulfur (S) and lead (Pb) may be added during casting of the ingot to make sulfur (S) and lead ( The content of Pb) is adjusted so as to satisfy a range of a specific weight% or less.
此處,關於銅精煉時去除硫(S)或鉛(Pb)之方法(銅精煉法)亦無限定,例如硫(S)可以在例如吹入氧、脫硫、之後進行脫氧而製造無氧銅時,進行去除。 Here, the method of removing sulfur (S) or lead (Pb) during copper refining (copper refining method) is also not limited. For example, sulfur (S) can be deoxygenated, for example, by blowing oxygen, desulfurization, and then producing oxygen-free. When copper is used, it is removed.
鉛(Pb)例如可藉由電精煉而去除,但期望銅更加高純度化之情形時,可藉由使用帶域溶化法(zone melting,帶溶融法)等而去除。 Lead (Pb) can be removed, for example, by electric refining. However, when copper is desired to be more highly purified, it can be removed by using a zone melting method or the like.
根據本發明,可提供防止靶之濺鍍時發生飛濺且提高由濺鍍所形成的薄膜膜厚之均一性之濺鍍靶。 According to the present invention, it is possible to provide a sputtering target which prevents spattering during sputtering of a target and improves uniformity of film thickness formed by sputtering.
圖1係表示對應於靶之硫與鉛含有率之裂縫個數的關係圖。 Fig. 1 is a graph showing the relationship between the number of cracks corresponding to the sulfur content of the target and the lead content.
圖2係表示對應於靶之硫與鉛含有率之裂縫個數的關係圖。 Fig. 2 is a graph showing the relationship between the number of cracks corresponding to the sulfur content of the target and the lead content.
圖3係表示裂縫個數與電弧次數之關係圖。 Fig. 3 is a graph showing the relationship between the number of cracks and the number of arcs.
圖4係表示符合靶表面之裂縫定義之裂縫部分的照片。 Fig. 4 is a photograph showing a crack portion conforming to the definition of the crack of the target surface.
圖5係表示不符合靶表面之裂縫定義之微小瑕疵的照片。 Figure 5 is a photograph showing a small flaw that does not conform to the definition of the crack of the target surface.
以下說明本發明之一實施形態。 An embodiment of the present invention will be described below.
本實施形態中濺鍍靶,係以純度為99.9(3N)質量%以上之銅為主成分,且含有10ppm以下之硫(S)及2ppm以下之鉛(Pb)。 In the present embodiment, the sputtering target contains copper having a purity of 99.9 (3N)% by mass or more as a main component, and contains 10 ppm or less of sulfur (S) and 2 ppm or less of lead (Pb).
其他,以適當之質量%濃度含有例如鉍(Bi)、硒(Se)及碲(Te)等化學成分。 Others include chemical components such as bismuth (Bi), selenium (Se), and tellurium (Te) at a suitable mass% concentration.
又,至少濺鍍靶的濺鍍面之平均結晶粒徑為200μm以下,例如構成外徑150mm以上,壁厚20mm以上之圓筒狀的大型圓筒狀靶材。 Further, at least the sputtering target surface of the sputtering target has an average crystal grain size of 200 μm or less, for example, a cylindrical large-sized cylindrical target having an outer diameter of 150 mm or more and a wall thickness of 20 mm or more.
以下說明上述之濺鍍靶的製造方法。 The method for producing the above-described sputtering target will be described below.
於作為銅原料之黃銅礦添加焦炭(cokes)等且在融煉爐中溶融,藉此獲得主要為除去鐵分之冰銅(copper matte)為銅精製之中間製品。其次將冰銅放入迴轉爐(revolving furnace),吹入氧氣而氧化去除硫等雜質,精煉粗銅(銅含有率約98%)。此時可藉由進行超過2000℃之高溫而將粗銅還原。 Cokes or the like as a copper raw material is added and cokeed in a melting furnace, whereby an intermediate product mainly obtained by removing copper from copper matte is obtained. Next, the matte is placed in a revolving furnace, oxygen is blown in, and impurities such as sulfur are oxidized to refine the blister copper (the copper content is about 98%). At this time, the crude copper can be reduced by performing a high temperature exceeding 2000 °C.
之後,粗銅可藉由於硝酸浴中或硫酸浴中電解精煉而精製成99.99%以上之純銅。 Thereafter, the blister copper can be refined into 99.99% or more of pure copper by electrolytic refining in a nitric acid bath or a sulfuric acid bath.
藉此,將除極力降低硫(S)、鉛(Pb)以外,亦極力降低鉍(Bi)、硒(Se)及碲(Te)等其他雜質含量之銅進行真空感應溶解(vacuum induction melting)。進而,添加硫(S)與鉛(Pb)並控制含量在硫(S)之含量為10ppm以下、且滿足鉛(Pb)之含量為2ppm以下之範囲,可藉此獲得以純度為99.9(3N)質量%以上之銅作為主成分、且含有10ppm以下之硫(S)及2ppm以下之鉛(Pb)的錠。 In this way, in addition to reducing sulfur (S) and lead (Pb) as much as possible, copper is also reduced in the amount of other impurities such as bismuth (Bi), selenium (Se), and strontium (Te), and vacuum induction melting is performed. . Further, sulfur (S) and lead (Pb) are added to control the content of sulfur (S) to be 10 ppm or less, and the content of lead (Pb) is 2 ppm or less, thereby obtaining a purity of 99.9 (3N). An ingot having a mass% or more of copper as a main component and containing 10 ppm or less of sulfur (S) and 2 ppm or less of lead (Pb).
其次,將錠切成特定之尺寸,製作熱加工用之胚(billet)。 Next, the ingot is cut into a specific size to prepare a billet for thermal processing.
特別是,例如製作直徑為300mm、質量為300kg~400kg之胚以製造大型之靶。 In particular, for example, an embryo having a diameter of 300 mm and a mass of 300 kg to 400 kg is produced to manufacture a large-sized target.
此外,作為熱加工用材料之胚可作成圓柱狀或板狀等合適於之後的加工作業之他種形狀,但為獲得圓柱狀之濺鍍靶而將胚形成為圓筒狀。 Further, the embryo which is a material for hot working may be formed into a cylindrical shape or a plate shape and the like which is suitable for the subsequent processing operation, but the embryo is formed into a cylindrical shape in order to obtain a cylindrical sputtering target.
濺鍍靶係使用上述之熱擠壓用胚,並依序經過熱加工步驟、冷加工及應變去除退火步驟而作成。 The sputtering target system is formed by using the above-described hot extrusion embryo and sequentially subjected to a thermal processing step, a cold working, and a strain removal annealing step.
詳細說明,熱加工係對由高純度銅構成之胚進行例如熱擠壓加工、熱加壓加工、熱鍛造或熱壓延等適當加工之步驟,藉由該熱加工以給予應變之方式來對胚以固定之加工量實施熱加工。 In detail, the hot working is a step of performing appropriate processing such as hot extrusion processing, hot press processing, hot forging or hot rolling on an embryo made of high-purity copper by means of the hot working to give strain. The embryo is subjected to thermal processing in a fixed amount of processing.
繼而,上述加工量係以厚度減少(壓下量)與初期厚度之比乘以100%的比率、或以剪切應變量而適當地定義。 Then, the above-described processing amount is appropriately defined by a ratio of the thickness reduction (depression amount) to the initial thickness multiplied by 100% or by a shear strain amount.
特別是,於進行熱擠壓步驟作為熱加工之情形時,預先進行熱加工之準備,亦即使熱加工用胚超過500℃之溫度,接著於600~900℃下熱擠壓。 In particular, when the hot extrusion step is performed as a hot working, the hot working is prepared in advance, and even if the hot working embryo exceeds a temperature of 500 ° C, it is then hot extruded at 600 to 900 ° C.
之後的冷加工係對經熱加工材料進行例如冷壓延、冷鍛造、冷擠壓等適當加工之步驟,冷加工例如以冷壓延來進行時,對經熱加工材料以80~120℃/秒之冷卻速度冷卻至室溫左右,以如下條件進行縮徑:在大氣條件下對圓筒狀之經熱加工材料於至少每1次之冷拉伸給予15%以上之應變的縮徑率;而加工成所需之最終厚度的靶材。 The subsequent cold working is a step of performing suitable processing such as cold rolling, cold forging, cold extrusion, etc. on the hot-worked material, and cooling processing at a temperature of 80 to 120 ° C / sec for the hot-worked material, for example, by cold rolling. Cooling to about room temperature, reducing the diameter under the following conditions: under atmospheric conditions, the cylindrical hot-worked material is subjected to a reduction ratio of strain of 15% or more at least once per cold drawing; The final thickness of the target is required.
繼而,上述縮徑率係以厚度減少量(壓下量)與初期厚度之比乘以100%所得的比率、或以剪切應變量所定義者。 Then, the above-mentioned reduction ratio is defined by a ratio obtained by multiplying the ratio of the thickness reduction amount (depression amount) to the initial thickness by 100%, or by a shear strain amount.
其次進行之應變去除退火步驟中,對冷加工後之經冷拉伸材料例如於300℃~600℃之溫度範圍施以退火以作為銅之再結化。 In the second strain annealing step, the cold drawn material after cold working is subjected to annealing, for example, at a temperature ranging from 300 ° C to 600 ° C to be re-synthesized as copper.
更佳為,可藉由於300℃~500℃之溫度範圍施以保持約1小時左右之間的退火而去除靶之殘留應力(應變)。 More preferably, the residual stress (strain) of the target can be removed by annealing at a temperature ranging from 300 ° C to 500 ° C for about 1 hour.
再者,應變去除退火步驟係於大氣條件下進行退火,亦或為了將靶之氧化抑制在最小限而於保護環境中對靶進行退火。 Furthermore, the strain relief annealing step is performed under atmospheric conditions, or the target is annealed in a protective environment in order to minimize oxidation of the target.
由於濺鍍靶內存在之應變對靶物質之濺出有影響,因此應變去除退火步驟在可去除造成應變之主因的內部應力此一方面為有效。但是若退火溫度過低則不進行再結晶化,若退火溫度過高則會產生粒之過大成長,故若考慮此點則必須設定在例如250℃以上的適當之退火溫度 Since the strain present in the sputter target has an effect on the splash of the target material, the strain-removal annealing step is effective in that it can remove the internal stress causing the main cause of the strain. However, if the annealing temperature is too low, recrystallization does not occur. If the annealing temperature is too high, excessive growth of the particles occurs. Therefore, if this point is considered, it is necessary to set an appropriate annealing temperature of, for example, 250 ° C or higher.
藉由上述之步驟,可製造以純度為99.9質量%以上之銅為主成分,含有10ppm以下之硫(S)及2ppm以下之鉛(Pb)的濺鍍靶。 By the above-described steps, a sputtering target containing copper (S) having a purity of 99.9% by mass or more and containing 10 ppm or less of sulfur (S) and 2 ppm or less of lead (Pb) can be produced.
如此以硫(S)及鉛(Pb)之含量分別成為10ppm以下及2ppm以下之方式製造濺鍍靶,藉此可圖求減低於濺鍍靶表面(被濺鍍面)及內部之特定尺寸以上之瑕疵。 When the content of sulfur (S) and lead (Pb) is 10 ppm or less and 2 ppm or less, the sputtering target can be produced, and the thickness can be reduced to less than the specific surface size (sputtered surface) and the internal size of the sputtering target. After that.
詳細說明,藉由對上述之胚進行熱加工步驟時之熱,而導致胚之結晶粒徑變大且產生裂縫等表面粗糙,但先前已知藉由添加硫(S)而可獲得防止如此現象等效果。另一方面,亦已知:若將硫(S)添加至例如18ppm以上,則於組織中發生細微裂縫等不良傷害會產生。 In detail, the heat of the hot working step of the embryo is caused to cause the crystal grain size of the embryo to become large and surface roughness such as cracks to be generated, but it has been previously known to prevent such a phenomenon by adding sulfur (S). And so on. On the other hand, it is also known that when sulfur (S) is added to, for example, 18 ppm or more, adverse damage such as fine cracks occurs in the tissue.
因此,將硫(S)之含量設定為特定質量%濃度以下為重要,且發現:本實施形態之靶不只僅限於硫(S)含量,亦將硫(S)之含量設定為10ppm以下、且鉛(Pb)之含量設定為2ppm以下,藉此可減低靶表面及內部之瑕疵。 Therefore, it is important to set the content of sulfur (S) to a specific mass% or less, and it has been found that the target of the present embodiment is not limited to the sulfur (S) content, and the sulfur (S) content is also set to 10 ppm or less. The content of lead (Pb) is set to 2 ppm or less, whereby the target surface and the inside can be reduced.
藉此,於濺鍍處理時可減低發生自靶之電弧的發生次數,防 止飛濺等粗大叢集之發生,且提高由濺鍍所形成的薄膜膜厚之均一性。 Thereby, the number of occurrences of the arc generated from the target can be reduced during the sputtering process, and the prevention The occurrence of coarse clusters such as splashing is prevented, and the uniformity of the film thickness formed by sputtering is improved.
特別是,近年由於用於大型電視用液晶顯示器等,因此朝向 例如成為超過2m基板尺寸等基板尺寸大型化演進,伴隨於此,於作成配線之濺鍍步驟中亦必須成膜至大型基板或晶圓。 In particular, in recent years, it has been used as a liquid crystal display for large televisions. For example, a substrate size such as a substrate size of more than 2 m is required to be enlarged, and accordingly, it is necessary to form a film onto a large substrate or wafer in the sputtering step of forming wiring.
因此,使用之濺鍍靶本身亦大型化,濺鍍靶材之每一部位的 組織容易不均一,且對膜厚精度及發生粗大叢集有影響變大之課題。 Therefore, the sputtering target itself is also enlarged, and each part of the target is sputtered. The organization is prone to non-uniformity, and has a problem that the film thickness accuracy and the occurrence of coarse clusters become large.
進而,為了成膜至大型基板或晶圓而對大型濺鍍靶進行濺鍍 處理之情況,濺鍍處理時賦予之施加電壓亦必須要提高。因此,隨之而來地,當其於濺鍍表面有特定尺寸以上之瑕疵(裂縫)之情形時,亦有電弧發生次數變多之課題。 Furthermore, large-scale sputtering targets are sputtered for film formation onto large substrates or wafers. In the case of treatment, the applied voltage applied during the sputtering process must also be increased. Therefore, in the case where there is a flaw (crack) of a specific size or more on the sputtering surface, there is a problem that the number of arc generations increases.
如此一來,則當使用大型被濺鍍對象之情形時會產生如下更 為顯著的課題:電弧造成之飛濺的發生會變多,發生成膜異常,而成膜至配線圖案失敗之情況會變多。 In this way, when using a large sputtered object, the following will occur. A significant problem is that the occurrence of spatter due to an arc increases, and film formation abnormality occurs, and the film formation to the wiring pattern fails.
相對於此,本實施形態之濺鍍靶使硫(S)之含量為10ppm以 下且將鉛(Pb)之含量設定於2ppm以下,藉此可減低靶表面及內部之瑕疵,於濺鍍處理時可減低發生來自靶之電弧的發生次數,因此,特別是可防止伴隨著基板或晶圓之大型化而變得明顯之電弧發生次數變多的問題,大型之基板或晶圓亦可提高成膜精度。 On the other hand, the sputtering target of the present embodiment has a sulfur (S) content of 10 ppm. By setting the content of lead (Pb) to 2 ppm or less, the target surface and the inside of the target can be reduced, and the number of occurrences of arcing from the target can be reduced during the sputtering process, so that the substrate can be prevented in particular. Or the problem that the number of arc occurrences becomes obvious when the wafer is enlarged, and a large substrate or wafer can also improve the film formation accuracy.
以下,說明效果確認實驗。 Hereinafter, an effect confirmation experiment will be described.
(效果確認實驗1) (Effect confirmation experiment 1)
效果確認實驗1中,依作為錠中所含之不可避免之雜質的硫 (S)及鉛(Pb)之含有率的不同來製造先前例之靶及本實施例之靶,藉由對每一分別製造之靶所進行之濺鍍處理而產生之靶表面之裂縫個數與電弧之發生次數進行檢測。 In the effect confirmation experiment 1, sulfur is used as an unavoidable impurity contained in the ingot. The difference between the content ratio of (S) and lead (Pb) to produce the target of the prior art and the target of the present embodiment, and the number of cracks on the target surface generated by the sputtering treatment of each separately manufactured target The number of occurrences of the arc is detected.
再者,濺鍍處理係使用DC磁控濺鍍裝置,並且以如下之設 定作為濺鍍條件來進行處理:使到達真空鍍為4×10-5Pa、氬壓力為0.3Pa、氧分壓為1×10-3Pa、投入電量為2W/cm2。 Further, the sputtering treatment was performed by using a DC magnetron sputtering apparatus, and was treated as a sputtering condition with the following settings: a vacuum plating of 4 × 10 -5 Pa was reached, an argon pressure was 0.3 Pa, and an oxygen partial pressure was 1 × 10 -3 Pa, and the input electric quantity is 2 W/cm 2 .
又,效果確認實驗1中使用有板厚為30mm之板狀濺鍍靶。 Further, in the effect confirmation experiment 1, a plate-shaped sputtering target having a thickness of 30 mm was used.
先前例之靶,該靶所含之化學成分及其含量係滿足JIS H3100-C1020之規格的電子管用無氧銅。 In the target of the prior art, the chemical component contained in the target and the content thereof are oxygen-free copper for an electron tube satisfying the specifications of JIS H3100-C1020.
詳細說明,先前例之靶係硫(S)為18ppm以下、鉛(Pb)為10ppm以下、鉍(Bi)為3ppm以下及確(Te)為5ppm以下,以銅純度為99.9質量%以上之銅為主成分。 In detail, the target system has a sulfur (S) of 18 ppm or less, a lead (Pb) of 10 ppm or less, a bismuth (Bi) of 3 ppm or less, and a true (Te) of 5 ppm or less, and a copper purity of 99.9% by mass or more. Main ingredient.
但是,先前之靶,係硫(S)之含量為10ppm以下、但鉛(Pb)之含量大於2ppm者,鉛(Pb)之含量為2ppm以下、但硫(S)之含量大於10ppm者,或硫(S)之含量大於10ppm且鉛(Pb)之含量大於2ppm者。 However, the previous target is a sulfur (S) content of 10 ppm or less, but a lead (Pb) content of more than 2 ppm, a lead (Pb) content of 2 ppm or less, but a sulfur (S) content of more than 10 ppm, or The content of sulfur (S) is greater than 10 ppm and the content of lead (Pb) is greater than 2 ppm.
具體而言,製作先前例1~5及比較例共計6種試樣來作為先前例之靶,關於硫(S)及鉛(Pb)之含有率,分別如表1所示,先前例1為15ppm、5ppm,先前例2為15ppm、2ppm,先前例3為15ppm、1ppm,先前例4為10ppm、5ppm,先前例5為5ppm、5ppm、比較例為8ppm、5ppm。 Specifically, six samples of the previous examples 1 to 5 and the comparative examples were prepared as targets of the prior examples, and the contents of sulfur (S) and lead (Pb) are shown in Table 1, respectively. 15 ppm and 5 ppm, the former example 2 was 15 ppm and 2 ppm, the former example 3 was 15 ppm and 1 ppm, the previous example 4 was 10 ppm and 5 ppm, the previous example 5 was 5 ppm, 5 ppm, and the comparative example was 8 ppm and 5 ppm.
再者,比較例之靶係使用與「專利第3975414號」所揭示之實施例的銅錠相同之化學組成。 Further, the target of the comparative example used the same chemical composition as the copper ingot of the example disclosed in "Patent No. 3975414".
【表1】
相對於此,實施例之靶係以純度為99.9質量%以上之銅為主成分,且含有10ppm以下之硫(S)及2ppm以下之鉛(Pb)。 On the other hand, the target of the example has copper having a purity of 99.9% by mass or more as a main component, and contains 10 ppm or less of sulfur (S) and 2 ppm or less of lead (Pb).
具體而言,製作實施例1~4之4種試樣作為本實施例之靶,且關於硫(S)及鉛(Pb)之含有率,分別如表1所示,實施例1為10ppm、2ppm,實施例2為10ppm、1ppm,實施例3為5ppm、2ppm,實施例4為5ppm、1ppm。 Specifically, four kinds of samples of Examples 1 to 4 were produced as targets of the present example, and the contents of sulfur (S) and lead (Pb) were as shown in Table 1, and Example 1 was 10 ppm. 2 ppm, Example 2 was 10 ppm and 1 ppm, Example 3 was 5 ppm and 2 ppm, and Example 4 was 5 ppm and 1 ppm.
再者,表1顯示有每一先前例、比較例及實施例之硫(S)及鉛(Pb)的含量,並且後述之實驗結果顯示每一先前例及實施例之靶表面所具有之裂縫個數與濺鍍處理時所發生之電弧次數。 Further, Table 1 shows the contents of sulfur (S) and lead (Pb) in each of the previous examples, comparative examples, and examples, and the experimental results described later show cracks in the target surfaces of each of the prior examples and examples. The number of arcs that occur during the sputtering process.
關於實驗結果,先前例1~5、比較例及實施例1~4之靶表面之裂縫個數〔個/100mm2〕、濺鍍處理中電弧發生次數係如表1、圖1、圖2及圖3所示。 Regarding the experimental results, the number of cracks on the target surface of the previous examples 1 to 5, the comparative examples, and the examples 1 to 4 [one/100 mm 2 ], and the number of arc occurrences in the sputtering process are as shown in Table 1, FIG. 1, FIG. 2, and Figure 3 shows.
此外,比較例之靶表面之裂縫個數〔個/100mm2〕、濺鍍處理中電弧發生次數僅示於表1中。 Further, the number of cracks on the target surface of the comparative example [one/100 mm 2 ] and the number of arc occurrences in the sputtering treatment are shown only in Table 1.
此處之裂縫個數〔個/100mm2〕係表示濺鍍靶表面(或剖面)之檢查面積100mm2內的裂縫數;電弧次數係表示具有30mm厚度之板狀靶材,其厚度達20mm為止、即對厚度方向(深度方向)經濺鍍處理使用10mm為止時所發生之電弧發生次數。 Here, the number of cracks (number / 100 mm 2 ) indicates the number of cracks in the inspection area of 100 mm 2 of the surface (or section) of the sputtering target; the number of arcs indicates a plate-shaped target having a thickness of 30 mm, and the thickness thereof is 20 mm. That is, the number of arc occurrences occurring when the thickness direction (depth direction) is 10 mm by sputtering.
又,濺鍍處理中發生之電弧次數係使用電弧計數器來計測。作為電弧計數器,使用LANDMARK TECHNOLOGY公司製之資料儲存器。此外,作為目視電弧次數,認為當電弧次數超過30次時,對於對向基板上之電極等異常成膜處之增加而導致之製品損失率增大會明顯表現。 Further, the number of arcs generated during the sputtering process is measured using an arc counter. As the arc counter, a data storage device manufactured by LANDMARK TECHNOLOGY is used. Further, as the number of visual arcs, it is considered that when the number of arcs exceeds 30 times, the increase in the product loss rate due to an increase in abnormal film formation on the counter substrate or the like is apparent.
再者,圖1係表示將硫(S)含有率〔ppm〕繪於橫軸之情況中每一實施例1~4、先前例1~5的硫(S)及鉛(Pb)之成分濃度與裂縫個數〔個/100mm2〕之關係圖。圖2係表示將鉛(Pb)含有率〔ppm〕繪於橫軸之情況中每一實施例1~4、先前例1~5的硫(S)及鉛(Pb)之成分濃度與裂縫個數〔個/100mm2〕之關係圖。圖3係表示每一實施例1~4、先前例1~5的裂縫個數與電弧發生次數之關係圖。 Further, Fig. 1 shows the concentration of sulfur (S) and lead (Pb) in each of Examples 1-4 and Previous Examples 1 to 5 in the case where the sulfur (S) content rate [ppm] is plotted on the horizontal axis. Diagram of the number of cracks [/100mm 2 ]. 2 is a graph showing the concentration and crack of sulfur (S) and lead (Pb) in each of Examples 1-4 and Previous Examples 1 to 5 in the case where the lead (Pb) content (ppm) is plotted on the horizontal axis. A graph of the number [/100mm 2 ]. Fig. 3 is a graph showing the relationship between the number of cracks and the number of arc occurrences in each of Examples 1 to 4 and Previous Examples 1 to 5.
又,若瑕疵之開裂大則電荷會集中於瑕疵之邊緣部分,濺鍍中電弧會發生,因此效果確認實驗1中,就對電弧之發生有影響之範圍的裂縫尺寸而言,如圖4(a)、(b)所示,定義為以瑕疵之寬度(瑕疵之開裂)為0.003mm以上尺寸者視為裂縫並進行計數。 In addition, if the cracking of the crucible is large, the electric charge will concentrate on the edge portion of the crucible, and an arc will occur during the sputtering. Therefore, in the effect confirmation experiment 1, the crack size in the range influencing the occurrence of the arc is as shown in Fig. 4 ( A) and (b) are defined as those in which the width of the crucible (cracking of crucible) is 0.003 mm or more, and the crack is counted.
此處,如圖4(a)所示之瑕疵為具有最大0.3mm之寬度,圖4(b)為具有最大0.004mm之寬度的瑕疵,由於該等寬度方向均為0.003mm以 上,故該等瑕疵符合本實施形態中裂縫之定義。 Here, as shown in FIG. 4(a), the crucible has a width of at most 0.3 mm, and FIG. 4(b) is a crucible having a width of at most 0.004 mm, since the width directions are both 0.003 mm. Therefore, the 瑕疵 corresponds to the definition of the crack in the embodiment.
再者,圖4(a)之瑕疵,其長邊方向之長度為3.34mm;圖4(b)之瑕疵,其長邊方向之長度為0.031mm。 Further, in Fig. 4(a), the length in the longitudinal direction is 3.34 mm; and in Fig. 4(b), the length in the longitudinal direction is 0.031 mm.
另一方面,圖5所示之瑕疵較0.003mm寬度小,並且為與晶界同等大小的寬度者,因此為不符合裂縫之定義者。 On the other hand, the crucible shown in Fig. 5 is smaller than the width of 0.003 mm and is the same size as the grain boundary, and therefore is not defined by the definition of the crack.
即,當瑕疵之寬度小於上述之0.003mm之情形時,瑕疵之長邊方向之長度即便為如圖5所示般例如超過4mm之長度,亦不影響電弧之發生,因此,如圖5所示之瑕疵並不符合本實施形態中裂縫之定義。 That is, when the width of the crucible is less than the above-mentioned 0.003 mm, the length of the long side direction of the crucible is not more than 4 mm as shown in FIG. 5, and does not affect the occurrence of the arc, and therefore, as shown in FIG. It is not in accordance with the definition of the crack in this embodiment.
如表1、圖1、圖2及圖3所示,於先前例1~5、比較例之情形時,濺鍍靶表面(被濺鍍表面)之裂縫個數均多於50〔個/100mm2〕。相對於此,可確認於實施例1~4之情形時均為50〔個/100mm2〕以下。 As shown in Table 1, Figure 1, Figure 2 and Figure 3, in the case of the previous examples 1 to 5 and the comparative example, the number of cracks on the surface of the sputtering target (sputtered surface) was more than 50 [/100 mm 2 ]. On the other hand, in the case of Examples 1 to 4, it was confirmed that it was 50 [pieces/100 mm 2 ] or less.
同時,於先前例1~5及比較例之情形時,電弧之發生次數多於30次,相對於此,可確認於實施例1~4之情形時少於30次。 Meanwhile, in the cases of the previous examples 1 to 5 and the comparative examples, the number of occurrences of the arc was more than 30 times, whereas it was confirmed that the number of occurrences of the examples 1 to 4 was less than 30 times.
因此可確認如表1及圖3所示,若使裂縫個數為50〔個/100mm2〕以下則電弧發生次數可抑制在30次以下。 Therefore, as shown in Table 1 and FIG. 3, when the number of cracks is 50 [/100 mm 2 ] or less, the number of arc generations can be suppressed to 30 or less.
由上可確認:如實施例1~4所示,使濺鍍靶以純度99.9質量%以上之銅作為主成分,使硫(S)為10ppm以下之含量且鉛(Pb)為2ppm以下之含量,藉此可使電弧之發生次數低於30次;而其與硫(S)及鉛(Pb)之含量分別未滿足如此條件的先前例1~5之靶相比,可明顯地抑制。 From the above, it can be confirmed that the sputtering target has a purity of 99.9% by mass or more of copper as a main component, and a content of sulfur (S) of 10 ppm or less and a content of lead (Pb) of 2 ppm or less. Thereby, the number of occurrences of the arc can be made less than 30 times, and it can be remarkably suppressed as compared with the targets of the previous examples 1 to 5 in which the contents of sulfur (S) and lead (Pb) do not satisfy the above conditions, respectively.
此外,實際對先前例1~5、比較例及實施例1~4,分別確認經靶之濺鍍處理之基板時,當使用先前例1~5及比較例的濺鍍靶之情況,基板發生了飛濺等粗大叢集,相對於此,當使用實施例1~4的濺鍍靶 之情況,並未發生飛濺等粗大叢集,可於基板形成均一膜厚之薄膜。 Further, in the case of the previous examples 1 to 5, the comparative examples, and the examples 1 to 4, when the substrate subjected to the sputtering treatment of the target was confirmed, when the sputtering targets of the previous examples 1 to 5 and the comparative examples were used, the substrate occurred. In contrast to the coarse clusters such as splashes, the sputtering targets of Examples 1 to 4 are used. In the case where a large cluster such as a splash does not occur, a film having a uniform film thickness can be formed on the substrate.
繼而,對可保持低電阻同時,亦圖求成膜速度提高的濺鍍靶及其製造方法進行說明。 Next, a sputtering target which can maintain a low resistance while improving the film formation speed and a method for manufacturing the same will be described.
詳細說明,濺鍍法係如上所述,於被濺鍍物上形成與濺鍍靶相同組成之薄膜的成膜方法,但如此之濺鍍法中,圖求最終製品之成本減低,因此生產力(throughput,產量)提升之要求變高,且至今反覆對濺鍍過程中之濺鍍條件進行進一步的檢討,且一直試著謀求提高濺鍍時成膜速度。 In detail, the sputtering method is a film forming method of forming a film having the same composition as that of the sputtering target on the sputtered material as described above, but in the sputtering method, the cost of the final product is reduced, and thus productivity is improved ( The demand for improvement in throughput has increased, and the sputtering conditions during the sputtering process have been further reviewed, and attempts have been made to increase the film formation speed during sputtering.
然而,濺鍍時之成膜速度取決於氣體壓力、投入電力及靶-基板間距離等濺鍍條件,該等濺鍍條件不僅對成膜速度,對膜厚之均一性等薄膜特性亦有影響之虞,僅根據成膜速度提高之觀點設定濺鍍條件,當膜厚均一性受到妨害時,亦會有例如電阻增大、或顆粒、飛濺、粉塵等粗大叢集發生。 However, the film formation rate at the time of sputtering depends on the sputtering conditions such as the gas pressure, the input power, and the distance between the target and the substrate, and the sputtering conditions affect not only the film formation speed but also the film characteristics such as the uniformity of the film thickness. Thereafter, the sputtering conditions are set only in view of the improvement of the film formation speed, and when the film thickness uniformity is impaired, for example, an increase in electrical resistance or coarse clusters such as particles, splashes, and dust may occur.
電阻之增大為處理訊號之延遲的主要原因,粗大叢集之產生亦有引起斷線之問題。 The increase in resistance is the main cause of the delay in processing the signal, and the generation of coarse clusters also causes problems with disconnection.
即,為了保持薄膜品質,同時圖求濺鍍時之成膜速度的提高,不僅止於濺鍍條件之研究中存在有限制。 That is, in order to maintain the film quality and at the same time to improve the film formation speed at the time of sputtering, there is a limit not only in the study of the sputtering conditions.
因此,近年為了保持薄膜之品質同時,亦圖求濺鍍時之成膜速度進一步提高,除濺鍍條件以外,亦進行著眼於濺鍍材本身之特性,即濺鍍之結晶方位或結晶粒徑、濺鍍材所含之雜質含量等各種提案。 Therefore, in recent years, in order to maintain the quality of the film, it is also required to further increase the film formation speed during sputtering. In addition to the sputtering conditions, attention is also paid to the characteristics of the sputtering material itself, that is, the crystal orientation or crystal grain size of the sputtering. Various proposals such as the content of impurities contained in the sputtered material.
例如,特開2002-220759號公報(以下稱為「引用技術文獻1」)之「銅濺鍍靶之加工方法」亦為其中之一。 For example, the "Processing Method of Copper Sputtering Target" of JP-A-2002-220759 (hereinafter referred to as "Citation of Technical Document 1") is also one of them.
先行技術文獻1中揭示一種銅濺鍍靶之加工方法,其至少由 99.999%高純度銅構成,平均粒度為10~30μm,含有結晶方位(111)、(200)、(220)及(311)配向,且為具有各配向的粒子之量少於50百分比之結晶方位;且揭示有如下要旨:可藉由使用如此之銅濺鍍靶、而將均一性優異之膜濺鍍至晶圓。 The prior art document 1 discloses a method for processing a copper sputtering target, which is at least 99.999% high-purity copper, with an average particle size of 10~30μm, containing crystal orientation (111), (200), (220) and (311) alignment, and having a crystal orientation with less than 50% of the particles in each alignment. Further, it is revealed that a film excellent in uniformity can be sputtered onto a wafer by using such a copper sputtering target.
如此,利用如此濺鍍之結晶方位、結晶粒徑或銅純度等而改變濺鍍特性,故而隨著著眼於該方面之各種研究及開發的進行,而達到一定程度之確保低於先前之電阻,同時亦圖求成膜速度之提高的效果。 In this way, the sputtering characteristics are changed by the crystal orientation, the crystal grain size, the copper purity, and the like of the sputtering. Therefore, with the progress of various research and development in this respect, it is ensured that the electrical resistance is lower than the previous resistance. At the same time, the effect of increasing the film formation speed is also sought.
然而,邁向大型電視用液晶顯示器等基板尺寸之大型化,例如成為超過2m之基板尺寸等,於作成配線之濺鍍步驟中亦必須要成膜至大型基板或晶圓,伴隨於此,使用之濺鍍靶本身亦大型化,而於濺鍍靶材之每一部位容易使銅組織不均一,且對膜厚精度及發生粗大叢集的影響變大。 However, the size of a substrate such as a liquid crystal display for a large-sized television is increased to a size of, for example, a substrate of more than 2 m, and it is necessary to form a film onto a large substrate or wafer in the sputtering step of forming a wiring. The sputtering target itself is also large in size, and the copper structure is easily uneven in each part of the sputtering target, and the influence on the film thickness precision and the occurrence of coarse clustering becomes large.
進而,隨著近年半導體裝置等資訊處理之高速化及高機能化,進行閘極(gate)或配線之微細化、複雜化。然而,若為高速化而將大電流流過微細化之配線,則電流密度增加,電流密度之增加會招致電阻增大,如此電阻值之增大會成為處理訊號之延遲或可靠度下降之原因,而成為對半導體裝置高速化的阻礙。 Further, with the increase in speed and high performance of information processing such as semiconductor devices in recent years, gates and wirings have been made finer and more complicated. However, if a large current flows through the miniaturized wiring for high speed, the current density increases, and an increase in current density causes an increase in resistance, and such an increase in the resistance value may cause a delay in processing signals or a decrease in reliability. This has become an obstacle to the speeding up of semiconductor devices.
因此,以下說明可保持低電阻,同時亦圖求成膜速度提高的濺鍍靶及其製造方法。 Therefore, the following description can maintain a low resistance, and at the same time, a sputtering target having an improved film formation speed and a method of manufacturing the same are also described.
如此之濺鍍靶係由純度為99.9%(3N)以上之高純度銅構成者,其特徵在於結晶方位滿足以下〔數學式1〕及〔數學式2〕;該結晶方位係於進行濺鍍之濺鍍面中結晶結構之米勒指數(miller indices)為以(111) 面、(200)面、(220)面及(311)面所示之各配向面的X射線繞射波峰強度I(111)、I(200)、I(220)、I(311);〔數學式1〕I(111)/〔I(111)+I(200)+I(220)+I(311)〕≧0.40;且〔數學式2〕I(111)>I(200);I(111)>I(220);I(111)>I(311)。 Such a sputtering target is composed of high-purity copper having a purity of 99.9% (3N) or more, and is characterized in that the crystal orientation satisfies the following [Formula 1] and [Math 2]; the crystal orientation is performed by sputtering. The Miller indices of the crystal structure in the sputtered surface are (111) X-ray diffraction peak intensities I(111), I(200), I(220), I(311) of the respective alignment planes shown on the surface, (200) plane, (220) plane, and (311) plane; Mathematical Formula 1] I(111)/[I(111)+I(200)+I(220)+I(311)]≧0.40; and [Math 2] I(111)>I(200); I (111)>I(220); I(111)>I(311).
又,濺鍍靶更佳為於〔數學式1〕中滿足以下〔數學式1’〕:〔數學式1’〕I(111)/〔I(111)+I(200)+I(220)+I(311)〕≧0.55。 Further, it is preferable that the sputtering target satisfies the following [Formula 1'] in [Formula 1]: [Math 1'] I(111)/[I(111)+I(200)+I(220) +I(311)〕≧0.55.
進而,濺鍍靶之特徵在於滿足以下〔數學式3a〕、〔數學式3b〕及〔數學式4〕之關係:〔數學式3a〕I(200)>I(220);〔數學式3b〕I(200)>I(311);及〔數學式4〕I(200)≧0.42×I(111)。 Further, the sputtering target is characterized by satisfying the following relationship of [Formula 3a], [Formula 3b], and [Formula 4]: [Math 3a] I(200)>I(220); [Math 3b] I(200)>I(311); and [Math 4] I(200)≧0.42×I(111).
此處,〔數學式1〕及〔數學式1’〕之左邊係表示對I(111)、I(200)、I(220)、I(311)全體I(111)所占之配向率(以下稱為「(111)面之配向率」),使該〔數學式1〕及〔數學式1’〕之左邊為〔數學式1L〕。 Here, the left side of [Formula 1] and [Formula 1'] indicates the alignment ratio of I (111), I (200), I (220), and I (311) all I (111) ( Hereinafter, the "alignment ratio of the (111) plane" is referred to as "the mathematical expression 1" and the left side of the mathematical expression 1'.
又,如上所述,可藉由滿足〔數學式2〕而使在(111)面、 (200)面、(220)面、(311)面之中(111)面為最多結晶配向率。銅等FCC金屬之原子密度於上述之4個配向面之中,也是在(111)面為最高,且(111)面為最密。於如此關係之下,如〔數學式1〕之關係所示、使(111)面之配向率(〔數學式1L))為40%以上,藉此,可使自濺鍍靶表面濺出之銅原子多於先前。 Further, as described above, the (111) plane can be made by satisfying [Equation 2]. Among the (200) plane, (220) plane, and (311) plane, the (111) plane is the most crystallographic alignment ratio. The atomic density of the FCC metal such as copper is among the above four alignment planes, and is also the highest on the (111) plane, and the (111) plane is the densest. Under such a relationship, as shown in the relationship of [Formula 1], the alignment ratio of the (111) plane ([Formula 1L)) is 40% or more, whereby the surface of the sputtering target can be splashed. Copper atoms are more than before.
本實施形態之濺鍍靶中〔數學式1L〕,即,使(111)面之配向率為40%以上,其可有效利用具有上述(111)面的銅原子放出密度高於其他配向面之特性。 In the sputtering target of the present embodiment, [Formula 1L], that is, the alignment ratio of the (111) plane is 40% or more, and the copper atom having the (111) plane can be effectively used with a higher emission density than the other alignment planes. characteristic.
其結果可使成膜速度提高。此外,使來自濺鍍靶表面大量之銅原子密集地濺出,藉此可進行成為均一膜厚之銅膜的成膜,且可確保低電阻。 As a result, the film formation speed can be improved. Further, a large amount of copper atoms from the surface of the sputtering target are densely splashed, whereby film formation of a copper film having a uniform film thickness can be performed, and low resistance can be secured.
因此,即便進行基板或晶圓等大型化,或半導體裝置之閘極或配線之微細化、複雜化,亦可圖求訊號處理高速化、實現高可靠度,同時圖求因產量提高而最終製品之成本減低。 Therefore, even if the size of the substrate or the wafer is increased, or the gate or wiring of the semiconductor device is made finer or more complicated, the signal processing can be speeded up and high reliability can be achieved, and the final product can be improved due to the increase in yield. The cost is reduced.
又,令〔數學式1L〕之分母為〔I(111)+I(200)+I(220)+I(311)〕,即4個配向面分別之X射線繞射之波峰強度的和,其理由如下。 Further, let the denominator of [Math 1L] be [I(111) + I(200) + I(220) + I(311)], that is, the sum of the peak intensities of the X-ray diffractions of the four alignment faces, The reason is as follows.
其原因在於,若由後述之退火步驟進行再結晶,則於純銅之情形時容易產生(111)面、(200)面、(220)面及(311)面,藉由使用此主要之4個配向面之波峰強度的和作為〔數學式1L〕之分母,可算出符合實際之銅結晶方位的正確配向率。 The reason for this is that when recrystallization is performed by an annealing step described later, the (111) plane, the (200) plane, the (220) plane, and the (311) plane are likely to be generated in the case of pure copper, and the main four are used. The sum of the peak intensities of the alignment faces is the denominator of [Math. 1L], and the correct alignment ratio in accordance with the actual copper crystal orientation can be calculated.
即,原因在於,〔數學式1〕中,以實際之銅結晶方位所含的主要之4個配向面之波峰強度的和作為分母而使用之〔數學式1L〕顯示了40%以上之關係,因此,相較於以主要之4個配向面中之一部分即例如2 個配向面之波峰強度的和作為〔數學式1L〕之分母使用之情況,可算出符合實際之銅結晶方位的正確配向率。 In other words, in [Equation 1], the relationship between the peak intensity of the four main alignment faces included in the actual copper crystal orientation is used as the denominator (Formula 1L), and the relationship is 40% or more. Therefore, compared to one of the four main alignment planes, for example, 2 The sum of the peak intensities of the alignment faces is used as the denominator of [Equation 1L], and the correct alignment ratio in accordance with the actual copper crystal orientation can be calculated.
又,藉由使濺鍍靶如上所述般滿足以下〔數學式3a〕及〔數學式3b〕的結晶方位,則在上述各配向面中亦可使(200)面僅次於(111)面為第二高之結晶配向率;〔數學式3a〕I(200)>I(220);〔數學式3b〕I(200)>I(311)。 Further, by satisfying the crystal orientations of the following [Formula 3a] and [Formula 3b] as described above, the (200) plane may be next to the (111) plane in each of the above-mentioned alignment surfaces. It is the second highest crystal orientation ratio; [Math 3a] I(200)>I(220); [Math 3b] I(200)>I(311).
繼而,於銅等FCC金屬之中,由於(111)面、(200)面、(220)面及(311)面各配向面中、(200)面之原子密度僅次於(111)面為第二高,故(220)面及(311)面相比,較能使銅原子密集地濺出。 Then, among the FCC metals such as copper, the atomic density of the (200) plane in the (111) plane, the (200) plane, the (220) plane, and the (311) plane is second only to the (111) plane. The second highest, so the (220) surface and the (311) surface are more likely to splash copper atoms densely.
因此,由於可與(111)面同時,使銅原子自濺鍍靶表面密集地濺出,故而可使成膜速度提高,且可電阻低地形成均一膜厚。 Therefore, since the copper atoms can be densely sputtered from the surface of the sputtering target simultaneously with the (111) plane, the film formation speed can be improved, and a uniform film thickness can be formed with low electrical resistance.
而且,如上所述,由於(200)面處於原子密度低於(111)面,而可以低能量使其自濺鍍靶表面飛濺,因此與僅提高(111)面之結晶配向率之情況相比,其可將銅原子之濺出能量整體抑制為較低,且可造成濺鍍時電壓(以下稱為「濺鍍電壓」)之降低。 Further, as described above, since the (200) plane is at an atomic density lower than the (111) plane, it can be splashed from the surface of the sputtering target with low energy, and thus compared with the case where only the crystal orientation ratio of the (111) plane is increased. It can suppress the sputtering energy of copper atoms as a whole and can cause a decrease in voltage (hereinafter referred to as "sputtering voltage") at the time of sputtering.
又,如上所述於濺鍍時,(111)面可使銅原子密集地飛散,另一方面,與(111)面相比,(200)面較無法密集地飛散,但具有可確保較低銅原子濺出能量的特性。 Further, as described above, at the time of sputtering, the (111) plane can densely scatter copper atoms, and on the other hand, the (200) plane is less likely to be densely scattered than the (111) plane, but it can ensure lower copper. The nature of the atom's splashing energy.
因此,如上所述,使濺鍍靶為滿足以下〔數學式4〕之關 係的結晶方位,藉此能有效利用分別與(111)面及(200)面之配向面特性,不僅結晶配向率提升為最高之(111)面,同時亦可使(200)面之結晶配向率高於其他之配向面;〔數學式4〕I(200)≧0.42×I(111)。 Therefore, as described above, the sputtering target is made to satisfy the following [Formula 4] The crystal orientation of the system, whereby the alignment characteristics of the (111) plane and the (200) plane can be effectively utilized, and the crystal orientation ratio is improved to the highest (111) plane, and the crystal orientation of the (200) plane can also be made. The rate is higher than the other alignment planes; [Math 4] I (200) ≧ 0.42 × I (111).
因此,可藉由使銅原子密集地飛散,而確保高成膜速度,並且與僅使(111)面之結晶配向率高於其他配向面的情況相比,可較低地抑制飛濺之能量(濺鍍電壓)。 Therefore, the high film formation speed can be ensured by causing the copper atoms to be densely scattered, and the energy of the splash can be suppressed lower than when only the crystal orientation ratio of the (111) plane is higher than that of the other alignment faces ( Sputtering voltage).
進而,可藉由滿足以下〔數學式4’〕之結晶方位,使I(200)之結晶配向率與其他配向面相比更高於〔數學式4〕之情況,因此,可確保高成膜速度,同時亦可更進一步將飛濺能量(濺鍍電壓)抑制為較低,故較佳; Further, by satisfying the crystal orientation of the following [Formula 4'], the crystal orientation ratio of I(200) can be made higher than that of the other alignment surface by [Formula 4], so that a high film formation speed can be ensured. At the same time, it is also preferable to further suppress the splash energy (sputtering voltage) to be lower;
〔數學式4’〕I(200)≧0.80×I(111)。 [Math 4'] I (200) ≧ 0.80 × I (111).
又,濺鍍靶之特徵在於結晶粒之粒徑為65~200μm。 Further, the sputtering target is characterized in that the crystal grain has a particle diameter of 65 to 200 μm.
濺鍍靶於結晶粒之粒徑大的情況時,為了使銅原子自靶表面飛出而必須有高能量。因此,藉由將結晶粒之粒徑設定於65~200μm的較小值之範圍,可將用以使銅原子自靶表面飛出的能量抑制為較低。 When the particle size of the sputtering target is large, the sputtering target must have high energy in order to fly copper atoms out of the target surface. Therefore, by setting the particle size of the crystal grains to a range of a small value of 65 to 200 μm, the energy for causing the copper atoms to fly out from the target surface can be suppressed to be low.
因此,本實施形態之濺鍍靶由於係以高配向率將需要高能量使銅原子自靶表面飛出之配向面即(111)面、(200)面加以配向,故將結晶粒之粒徑設定於較小值之範圍,特別有效於將用以使銅原子自靶表面飛出之能量抑制為最低。 Therefore, since the sputtering target of the present embodiment is aligned with the (111) plane and the (200) plane which require high energy to cause copper atoms to fly out from the target surface, the particle size of the crystal grain is set. Setting it to a smaller value is particularly effective in minimizing the energy used to fly copper atoms out of the target surface.
進而,較佳為以結晶粒之粒徑為65~160μm之較小值範 圍的方式形成濺鍍靶。 Further, it is preferable that the particle size of the crystal grain is a small value of 65 to 160 μm. The sputtering method forms a sputtering target.
藉此,於使結晶粒之粒徑範圍為65~200μm的情況相比,可將用以使銅原子自靶表面飛出之能量抑制為更低。 Thereby, the energy for causing the copper atoms to fly out from the target surface can be suppressed to be lower than when the particle size of the crystal grains is in the range of 65 to 200 μm.
以下說明上述之濺鍍靶之製造方法。 The method of manufacturing the above-described sputtering target will be described below.
首先,將普通之電解銅於硝酸浴或硫酸浴中電解精製,將極力減低雜質含量的銅進行真空感應溶解,而獲得由99.9%(3N)以上之高純度銅構成之錠。將錠切成特定之尺寸,製作熱加工用胚。 First, ordinary electrolytic copper is electrolytically refined in a nitric acid bath or a sulfuric acid bath, and copper which is extremely low in impurity content is subjected to vacuum induction dissolution to obtain an ingot composed of high purity copper of 99.9% (3N) or more. The ingot is cut into a specific size to prepare a preform for hot working.
濺鍍靶係使用上述之熱擠壓用胚,且依序經過熱擠壓步驟、冷加工及退火步驟而作成。 The sputtering target system is formed by using the above-described hot extrusion embryo and sequentially subjected to a hot extrusion step, a cold working, and an annealing step.
詳細說明,於熱擠壓步驟中,預先進行熱加工之準備,亦即使熱加工用胚超過500℃之溫度,接著於500~900℃利用熱擠壓,更佳為於660~800℃之下進行熱擠壓。 In detail, in the hot extrusion step, the hot working is prepared in advance, and even if the hot working embryo exceeds 500 ° C, the hot extrusion is performed at 500 to 900 ° C, preferably at 660 to 800 ° C. Hot extrusion.
之後,於冷加工中,以50℃/秒以上、更佳為80℃/秒~120℃/秒之冷卻速度冷卻至室溫左右。 Thereafter, in the cold working, the temperature is cooled to about room temperature at a cooling rate of 50 ° C /sec or more, more preferably 80 ° C / sec to 120 ° C / sec.
退火步驟中,銅之再結晶化例如以250℃~400℃、更佳為300℃~400℃之溫度進行。若溫度過低則不進行再結晶化,若溫度過高則產生粒之過大成長。存在於銅材料內之應變會影響靶物質之飛出,故進行退火步驟來先去除造成應變之主要因素之內部應力是有效的,並利用退火步驟可去除內部應力。 In the annealing step, the recrystallization of copper is carried out, for example, at a temperature of from 250 ° C to 400 ° C, more preferably from 300 ° C to 400 ° C. If the temperature is too low, recrystallization does not occur, and if the temperature is too high, excessive growth of the particles occurs. The strain existing in the copper material affects the flying of the target material, so it is effective to perform the annealing step to remove the internal stress which is the main factor causing the strain, and the internal stress can be removed by the annealing step.
可由上述之本實施形態之製造方法而製造,以I(111)之配向率成為40%以上之方式進行製造。 It can be produced by the above-described production method of the present embodiment, and is manufactured such that the alignment ratio of I(111) is 40% or more.
又,如上所述,由於使濺鍍靶成為滿足〔數學式1L〕≧0.55 的結晶方位者,則與〔數學式L〕≧0.40之情況相比,亦可提高於各配向面中面密度高之(111)面的配向率,並可使大量之銅原子自濺鍍靶表面飛出。 Further, as described above, since the sputtering target is satisfied [Math. 1L] ≧ 0.55 Compared with the case of [Formula L] ≧ 0.40, the orientation of the (111) plane having a high areal density in each alignment plane can be increased, and a large amount of copper atoms can be self-sputtered. The surface flies out.
藉此,可使成膜速度更加提高,同時藉由將銅原子自濺鍍靶表面密集地濺出,而可形成電阻低且均一之膜厚。 Thereby, the film formation speed can be further improved, and at the same time, a copper film can be densely sputtered from the surface of the sputtering target to form a film having a low electric resistance and a uniform film thickness.
以下說明效果確認實驗。 The effect confirmation experiment will be described below.
(效果確認實驗2) (Effect confirmation experiment 2)
效果確認實驗2中,製造實施例5到10之濺鍍靶作為上述之濺鍍靶的一實施例,並且製造作為本實施例之比較對照之比較例1A、2A之濺鍍靶,分別比較膜電阻率、成膜速度。 In the effect confirmation experiment 2, the sputtering targets of Examples 5 to 10 were fabricated as an example of the above-described sputtering target, and the sputtering targets of Comparative Examples 1A and 2A which are comparative controls of the present example were produced, and the films were respectively compared. Resistivity, film formation speed.
實施例5到10、及比較例1A、2A之濺鍍靶由分別具有表2所示純度之銅材料所構成。 The sputtering targets of Examples 5 to 10 and Comparative Examples 1A and 2A were composed of copper materials each having the purity shown in Table 2.
比較例1A、2A之濺鍍靶係藉由以往進行之普遍的製造方法來製造,更詳細而言,係對由高純度銅構成之錠,進行熱壓延、熱加壓等熱加工,繼而於施以冷壓延等冷加工後,進行最後之熱處理而製成,但熱壓延係例如加熱至930°溫度來進行等,且亦於與實施例5到10不同的以 往之製造條件下進行冷加工、熱處理步驟。 The sputtering targets of Comparative Examples 1A and 2A are produced by a conventional manufacturing method which has been conventionally performed. More specifically, the ingots made of high-purity copper are subjected to hot working such as hot rolling and hot pressing, and then After the cold working such as cold rolling is applied, the final heat treatment is performed, but the hot rolling is performed, for example, by heating to a temperature of 930 °, and is also different from Examples 5 to 10. The cold working and heat treatment steps are carried out under the manufacturing conditions.
另一方面,實施例5到10之靶材依如下方法製成:依熱擠壓步驟、冷加工步驟、退火步驟此順序來進行,且分別於製造上述之本實施形態的濺鍍靶之製造條件下進行。 On the other hand, the targets of Examples 5 to 10 were produced by the following steps: in the order of the hot extrusion step, the cold working step, and the annealing step, and in the manufacturing conditions of the sputtering target of the present embodiment described above, respectively. Go on.
實施例5到10及比較例1A、2A之濺鍍靶,其任一者均經由上述之步驟而製造,且藉由車床等任意機械加工等追加加工至所需之靶形狀之狀態,以利使用。 Each of the sputtering targets of Examples 5 to 10 and Comparative Examples 1A and 2A is produced by the above-described steps, and is additionally processed to a desired target shape by any machining or the like such as a lathe. use.
該等濺鍍靶之(111)面之配向比、平均結晶粒徑及膜電阻率如表2所示。 Table 2 shows the alignment ratio, average crystal grain size, and film resistivity of the (111) plane of the sputtering target.
此處,關於(111)面之配向率,相對於比較例1A、2A之濺鍍靶小於40%,實施例5到10之濺鍍靶係由上述之本實施形態之製造方法而製造,因此實施例5到8之濺鍍靶均為40%以上,再者,實施例9、10之濺鍍靶均為55%以上。 Here, the alignment ratio of the (111) plane is less than 40% with respect to the sputtering targets of Comparative Examples 1A and 2A, and the sputtering targets of Examples 5 to 10 are manufactured by the above-described manufacturing method of the present embodiment, The sputtering targets of Examples 5 to 8 were all 40% or more, and further, the sputtering targets of Examples 9 and 10 were both 55% or more.
再者,為算出〔數學式1〕所示之(111)面配向比所需之(111)面、(200)面、(220)面及(311)面之各配向面的X射線繞射之波峰強度,其藉由如下方法進行:自作為濺鍍靶使用之表面射入X射線,測定來自各繞射面之強度,算出其中顯示特別高波峰的(111)面、(200)面、(220)面及(311)面之X射線繞射的波峰強度。 Further, in order to calculate the X-ray diffraction of each of the (111) plane, the (200) plane, the (220) plane, and the (311) plane of the (111) plane alignment ratio shown in [Formula 1] The peak intensity is obtained by injecting X-rays from a surface used as a sputtering target, measuring the intensity from each diffraction surface, and calculating a (111) plane and a (200) plane in which a particularly high peak is displayed. The peak intensity of the X-ray diffraction of the (220) plane and the (311) plane.
此外,X射線照射條件,其X射線之種類為CuKα1、管電壓為40kV、管電流為20mA。 Further, under the X-ray irradiation conditions, the X-ray type was CuKα1, the tube voltage was 40 kV, and the tube current was 20 mA.
又,於銅材料板中之結晶粒徑係於上述之各部位,在作為濺鍍靶使用之表面進行顯微組織觀察,基於JIS H 0501(切斷法)測定結晶粒 徑,並根據其算出平均結晶粒徑。 In addition, the crystal grain size in the copper material sheet is in each of the above-mentioned portions, and the microstructure is observed on the surface used as the sputtering target, and the crystal grain is measured based on JIS H 0501 (cutting method). The diameter is calculated from the average crystal grain size.
於退火加工後進行之濺鍍的追加加工,為了排除所得之濺鍍靶靶面對粗糙度之影響,粗糙度係將最大粗糙度Ra皆統一研磨成0.5~0.8μm。 The additional processing of the sputtering after the annealing process is performed to eliminate the influence of the roughness of the obtained sputtering target, and the roughness is uniformly ground to 0.5 to 0.8 μm.
使用上述之實施例5到10之濺鍍靶及比較例1A、2A之濺鍍靶進行濺鍍,測定成膜至被濺鍍物之銅膜之膜電阻率及成膜速度,其結果如表2之結果。 The sputtering target of the above-described Examples 5 to 10 and the sputtering targets of Comparative Examples 1A and 2A were used for sputtering, and the film resistivity and film formation rate of the copper film formed into the object to be sputtered were measured, and the results are shown in the table. 2 results.
此外,濺鍍係使用作成上述般之濺鍍靶,利用DC磁控濺鍍裝置於膜厚0.7mm之日本電玻璃公司製OA-10玻璃基板實施濺鍍,而作成0.3μm膜厚之銅配線。濺鍍條件係使Ar氣體壓力為0.3Pa、放電電力為500W。 In addition, sputtering was carried out by using a sputtering target as described above, and sputtering was performed on a OA-10 glass substrate manufactured by Nippon Electric Glass Co., Ltd. having a thickness of 0.7 mm by a DC magnetron sputtering apparatus to form a copper wiring having a film thickness of 0.3 μm. . The sputtering conditions were such that the Ar gas pressure was 0.3 Pa and the discharge power was 500 W.
首先,著眼於膜電阻率之結果,則比較例1A、2A分別為2.1〔μΩcm〕、2.2〔μΩcm〕,相對於此,實施例5、6、8~10為與該等值大致相同即分別為2.2〔μΩcm〕、2.2〔μΩcm〕、2.1〔μΩcm〕、2.1〔μΩcm〕、2.0〔μΩcm〕。於實施例9之情形時為1.8〔μΩcm〕,與比較例1A、2A之情形相比為較低值。 First, focusing on the results of the film resistivity, Comparative Examples 1A and 2A were 2.1 [μΩcm] and 2.2 [μΩcm], respectively, and Examples 5, 6, and 8 to 10 were substantially the same as the respective values. It is 2.2 [μΩcm], 2.2 [μΩcm], 2.1 [μΩcm], 2.1 [μΩcm], and 2.0 [μΩcm]. In the case of Example 9, it was 1.8 [μΩcm], which was a lower value than the case of Comparative Examples 1A and 2A.
認為其主要原因在於,實施例7之濺鍍靶係由純度5N(99.999%)以上形成之高純度銅所構成,因此,其平均結晶粒徑亦小於其他之濺鍍靶。 The main reason is that the sputtering target of Example 7 is composed of high-purity copper having a purity of 5 N (99.999%) or more, and therefore, the average crystal grain size is also smaller than that of other sputtering targets.
又,著眼於成膜速度之結果,則比較例1A、2A均為8〔Å/s〕,相對於此,實施例5到10為12〔Å/s〕、11〔Å/s〕、12〔Å/s〕、10〔Å/s〕、14〔Å/s〕、15〔Å/s〕,其任一者均快於比較例1A、2A。特別是, 實施例9、10的確相對於比較例1A、2A較快,並且亦大幅地快於其他實施例5到8。 Further, in view of the film formation rate, Comparative Examples 1A and 2A were both 8 [Å/s], whereas Examples 5 to 10 were 12 [Å/s], 11 [Å/s], and 12 [Å/s], 10 [Å/s], 14 [Å/s], and 15 [Å/s], either of them were faster than Comparative Examples 1A and 2A. especially, Examples 9, 10 were indeed faster relative to Comparative Examples 1A, 2A, and also significantly faster than the other Examples 5 through 8.
由上可證明,藉由使(111)面之配向率為40%以上,可發揮使具有I(111)之銅原子密集地濺出的效果,故而確保優異之膜電阻率,同時亦能謀求提高成膜速度。 From the above, it can be proved that by setting the alignment ratio of the (111) plane to 40% or more, the copper atom having I(111) can be splashed intensively, and therefore, an excellent film resistivity can be secured, and at the same time, it is possible to achieve Increase the film formation speed.
特別是可證明,可藉由使(111)面之配向率為55%以上,而更顯著地發揮如具有I(111)般效果,確保優異之膜電阻率,同時亦更加提高成膜速度。 In particular, it has been confirmed that the ratio of the (111) plane is 55% or more, and the effect of I(111) is more remarkable, and the film resistivity is excellent, and the film formation speed is further improved.
本實施形態之濺鍍靶並不僅限於上述之實施形態,能以各種實施形態、製造方法進行製造。 The sputtering target of the present embodiment is not limited to the above embodiment, and can be manufactured by various embodiments and production methods.
例如,本實施形態之濺鍍靶較佳為I(111)、I(200)、I(220)、I(311)滿足例如〔數學式3〕之關係,即,滿足I(200)>I(220)、I(200)>I(311)之關係,但只要滿足〔數學式1〕、〔數學式2〕之關係,亦包含不一定滿足〔數學式3〕之關係的構成。 For example, in the sputtering target of the present embodiment, I (111), I (200), I (220), and I (311) satisfy the relationship of, for example, [Formula 3], that is, I(200)>I is satisfied. (220), I(200)>I(311), but if the relationship between [Mathematical Formula 1] and [Mathematical Formula 2] is satisfied, a configuration that does not necessarily satisfy the relationship of [Mathematical Formula 3] is also included.
同樣地,本實施形態之濺鍍靶較佳為I(111)、I(200)、I(220)、I(311)滿足例如〔數學式4〕之關係,即,滿足I(200)≧0.42×I(111)之關係,但只要滿足〔數學式1〕、〔數學式2〕之關係,亦包含不一定滿足〔數學式4〕之關係的構成。 Similarly, in the sputtering target of the present embodiment, I (111), I (200), I (220), and I (311) satisfy the relationship of, for example, [Formula 4], that is, I(200) is satisfied. In the relationship of 0.42 × I (111), as long as the relationship between [Mathematical Formula 1] and [Mathematical Formula 2] is satisfied, a configuration that does not necessarily satisfy the relationship of [Mathematical Formula 4] is also included.
再者,本發明並不限於上述之實施形態,亦能以其他各種之實施形態來形成。 Furthermore, the present invention is not limited to the above embodiments, and can be formed in other various embodiments.
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JP2012053266A JP6182296B2 (en) | 2012-03-09 | 2012-03-09 | Sputtering target and manufacturing method thereof |
JP2012053267A JP5950632B2 (en) | 2012-03-09 | 2012-03-09 | Manufacturing method of sputtering target |
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WO2018117717A1 (en) * | 2016-12-23 | 2018-06-28 | 희성금속 주식회사 | Method for predicting deposition speed of sputtering target, sputtering target having deposition speed controlled thereby and method for manufacturing same |
KR102560279B1 (en) * | 2020-11-10 | 2023-07-27 | 오리엔탈 카퍼 씨오., 엘티디. | Method for manufacturing copper cylindrical target from hot extrusion technique for thin film coating using sputtering method |
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