TWI220767B - Ionized physical vapor deposition process and apparatus thereof - Google Patents
Ionized physical vapor deposition process and apparatus thereof Download PDFInfo
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- TWI220767B TWI220767B TW092118826A TW92118826A TWI220767B TW I220767 B TWI220767 B TW I220767B TW 092118826 A TW092118826 A TW 092118826A TW 92118826 A TW92118826 A TW 92118826A TW I220767 B TWI220767 B TW I220767B
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- 238000005240 physical vapour deposition Methods 0.000 title claims abstract description 35
- 238000000034 method Methods 0.000 title claims abstract description 21
- 229910052751 metal Inorganic materials 0.000 claims abstract description 61
- 239000002184 metal Substances 0.000 claims abstract description 61
- 239000010409 thin film Substances 0.000 claims abstract description 21
- 238000006243 chemical reaction Methods 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 15
- 239000010408 film Substances 0.000 claims description 14
- 238000000151 deposition Methods 0.000 claims description 11
- 230000001133 acceleration Effects 0.000 claims description 8
- 239000010985 leather Substances 0.000 claims description 7
- 239000012495 reaction gas Substances 0.000 claims description 5
- 150000002500 ions Chemical class 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims 1
- 239000000758 substrate Substances 0.000 abstract description 9
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 abstract 4
- 239000013078 crystal Substances 0.000 description 10
- 239000013077 target material Substances 0.000 description 10
- 239000007789 gas Substances 0.000 description 7
- 230000008021 deposition Effects 0.000 description 5
- 238000005137 deposition process Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 150000002736 metal compounds Chemical class 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 230000005674 electromagnetic induction Effects 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- -1 group Chemical compound 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000427 thin-film deposition Methods 0.000 description 1
Classifications
-
- 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
- C23C14/3435—Applying energy to the substrate during sputtering
- C23C14/345—Applying energy to the substrate during sputtering using substrate bias
-
- 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
- C23C14/04—Coating on selected surface areas, e.g. using masks
- C23C14/046—Coating cavities or hollow spaces, e.g. interior of tubes; Infiltration of porous substrates
-
- 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
- C23C14/3471—Introduction of auxiliary energy into the plasma
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32009—Arrangements for generation of plasma specially adapted for examination or treatment of objects, e.g. plasma sources
- H01J37/32082—Radio frequency generated discharge
- H01J37/321—Radio frequency generated discharge the radio frequency energy being inductively coupled to the plasma
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/32431—Constructional details of the reactor
- H01J37/32697—Electrostatic control
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/34—Gas-filled discharge tubes operating with cathodic sputtering
- H01J37/3402—Gas-filled discharge tubes operating with cathodic sputtering using supplementary magnetic fields
- H01J37/3405—Magnetron sputtering
- H01J37/3408—Planar magnetron sputtering
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
- H01J37/34—Gas-filled discharge tubes operating with cathodic sputtering
- H01J37/3411—Constructional aspects of the reactor
- H01J37/3438—Electrodes other than cathode
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physical Vapour Deposition (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
Description
1220767 五、發明說明(1) 【發明所屬之技術領域】 本發明是有關於一種半導體製程及其設備,且特別是 有關於一種離子化物理氣相沈積(i ο n i z e d p h y s i c a 1 vapor deposition,I-PVD)製程及其設備。 【先前技術】 在半導體製程中,對於金屬薄膜之沈積可以使用物理 氣相沈積製程或是化學氣相沈積製程,而一般較常使用的 是物理氣相沈積製程。相較於化學氣相沈積製程,物理氣 相沈積製程之階梯覆蓋度(s t e p c 〇 v e r a g e )是較差的。 習知為了改善物理氣相沈積製程之階梯覆蓋度,有提 出一種離子化物理氣相沈積製程,其係藉由電磁感應線圈 或是磁極等離子化單元的設計,使得部分的中性金屬被離 子化(ionized),而離子化金屬(ionized metal)在電場 (靶材與晶圓之間的電場)之作用下,會往晶圓的方向力α 速,如此一來,離子化金屬便會垂直的射向晶圓,而提高 沈積之薄膜之階梯覆蓋度。 在上述習知技術中,通常會在革巴材施予一負偏壓,在 晶圓施予另一較小射頻負偏壓(R F n e g a t i ν e b i a s ),以使 帶正電的離子化金屬因受到施予負偏壓之晶圓的吸引而往 晶圓方向加速,但是也因如此,往往會在晶圓表面發現撞 擊損害,特別是發生在接觸窗處,導致接觸電阻(c ο n t a c t resistance)異常升高,損害的情形更是嚴重。 【發明内容】 因此本發明的目的就是提供一種離子化物理氣相沈積1220767 V. Description of the invention (1) [Technical field to which the invention belongs] The present invention relates to a semiconductor process and its equipment, and in particular, to an ionized physical vapor deposition (i ο nizedphysica 1 vapor deposition, I-PVD). ) Process and equipment. [Previous technology] In the semiconductor manufacturing process, a physical vapor deposition process or a chemical vapor deposition process can be used for metal thin film deposition, and a physical vapor deposition process is generally used. Compared with the chemical vapor deposition process, the step coverage of the physical gas deposition process (s t e p c 0 v e r a g e) is poor. It is known that in order to improve the step coverage of the physical vapor deposition process, an ionized physical vapor deposition process has been proposed, which uses the design of an ionization unit such as an electromagnetic induction coil or a magnetic pole to make part of the neutral metal ionized (Ionized), and the ionized metal (field between the target and the wafer) under the action of the force, the direction of the wafer force α speed, so that the ionized metal will be vertical It is directed at the wafer to increase the step coverage of the deposited film. In the above-mentioned conventional techniques, a negative bias voltage is usually applied to the leather material and another smaller radio frequency negative bias voltage (RF negati ν ebias) is applied to the wafer to make the positively charged ionized metal cause The wafer is accelerated toward the wafer by being attracted by the negatively biased wafer, but because of this, impact damage is often found on the wafer surface, especially at the contact window, resulting in contact resistance (c ntact resistance). It is abnormally high, and the damage is even more serious. [Summary of the Invention] Therefore, the object of the present invention is to provide an ionized physical vapor deposition
11439twf.ptd 第5頁 1220767 五、發明說明(2) 製程以及其 度,又同時 設備’ 不會對 以改善 晶圓表 本發明提出一種離子 其包括一反 及一 部, 表面 之用 代反 材以 之金 座之 距離 圚基 導電篩 其係用 ,並朝 。當然 應室之 及晶圓 屬。另 間,並 遠小於 座之距 本發明 應室、 網。其 以放置 向晶圚 ,亦可 頂蓋作 基座之 外,導 作為一 其距離 離係介 提出一 中 晶圓 ,晶 提供 屬靶 係g己 配置有一導 啟離子化單 施予 電漿反應室 材以及 置有離 另 一晶圓 子化單 電篩網 元,並 小負偏 發明在 且在 導電 由於本 導電篩網上施 篩網,如使一 一晶圓 基座, 以在反 為電極 間,其 電篩網 電極之 靶材之 於1至2 種離子 ,其中 基座, 元,在 。接著 對金屬 壓,以 接近晶 予負偏 來,離 物理氣 面造成 4匕物理 基座、 圓基座 。靶材 其中反 應室内 。另外 係用以 係S己置 用,且 距離, 公分。 化物理 電漿反 且在金 離子化 ,將晶 革巴材施 在晶圓 圓之上 壓,因 子4匕金 相沈積製程之階梯覆蓋 損害。 氣相沈積(I - P V D )設備 一離子 係S己置 係S己置 應室之 另外設 ,離子 離子化 在離子 導電篩 其例如 化單 在反 在反 頂蓋 置一 化單 由靶 化單 網距 是導 元、 應室 應室 係作 電極 元係 材上 元以 離晶 電篩 一革巴 内之 内之 為一 板, 配置 被撞 及晶 圓基 網距 材以 底 頂蓋 電極 以取 在靶 擊出 圓基 座之 離晶 沈積製程,其係首先 中係包括配置有一金 材以及晶圓基座之間 以及晶圓基座之間係 置在晶圓基座上,開 負偏壓,對導電篩網 氣相 應室 屬靶 單元 圓放 予一 上沈積一層薄膜 方處 此離 屬會 設置一導電篩網,並 子化金屬會加速射向 較為垂直的射在晶11439twf.ptd Page 5 1220767 V. Description of the invention (2) Process and its degree, and at the same time the equipment 'will not be used to improve the wafer table. The distance from the golden seat to the base-based conductive sieve is used, and facing. Of course, the room and wafer belong to. In addition, it is much smaller than the distance between the seats. It can be placed on the surface of the crystal core, or it can be used as a base, and a wafer is provided as a distance from the system. The crystal is provided as a target system. It has been configured with a guide ionization unit for plasma reaction. The room material and a single electric sieve element that is separated from another wafer, and a small negative bias, is used to apply a sieve on and on the conductive sieve, such as a one-by-one wafer base to use as the electrode on the opposite side. In the meantime, the target of the electric sieve electrode is between 1 and 2 ions, among which the base, the element, and the. Then press the metal to make a negative bias close to the crystal, resulting in a physical base of 4 daggers and a round base from the physical surface. The target is a reaction chamber. In addition, it is used for S, and distance, cm. Chemical physics Plasma and ionization of gold applied crystal leather material to the wafer circle, which was damaged by the step coverage of the 4D metallographic deposition process. Vapor deposition (I-PVD) equipment-an ion system, an S system, and an S system are separately installed in the chamber. Ionization is carried out on an ion conductive screen. For example, a conversion unit is placed on the reverse top cover. The grid distance is the guide element, and the chamber should be used as the electrode element. The upper element is a plate within one bar of the crystal electric sieve, and the impacted wafer-based grid distance material is arranged on the bottom to cover the electrode. Take the ionic deposition process where the target hits the round base. First, it consists of a gold material and a wafer base, and a wafer base is placed on the wafer base to open the negative bias. Pressure, the corresponding target unit of the conductive screen gas is rounded to a layer where a thin film is deposited. A conductive screen will be set in this area, and the metal will be accelerated to shoot more vertically on the crystal.
11439t.wf. pt.d 第6頁 1220767 五、發明說明(3) , 圓,進而提高薄膜之階梯覆蓋度。而當離子化金屬通過導 電篩網之後,因帶正電的離子化金屬受到施予負偏壓的導 電篩網吸引,而會減速的往晶圓方向沈積,如以一來,晶 圓表面就不會受到加速的離子化金屬的撞擊而造成損害。 為讓本發明之上述和其他目的、特徵、和優點能更明 顯易懂,下文特舉一較佳實施例,並配合所附圖式,作詳 細說明如下: 【實施方式】 請參照第1圖,其繪示依照本發明一較佳實施例之離 子化物理氣相沈積設備之示意圖。本發明之離子化物理氣 相沈積設備包括一反應室1 0 0、一晶圓基座1 0 4、一靶材 1 0 6、一離子化單元1 0 8以及一導電篩網1 1 0。 Μ 其中,晶圓基座1 0 4係設置在反應室1 0 0之底部,其係 用以放置一晶圓1 1 2 。 靶材1 0 6係固定在反應室1 0 0内之頂部處。在一較佳實 施例中,反應室1 0 0之頂蓋1 0 2係為一導電板,而能作為一 電極之用,且頂蓋1 0 2係連接至一電源供應器1 2 0 ,其例如 是直流電(D C )電源供應器。因此靶材1 0 6係固定在頂蓋1 0 2 之表面上,且乾材1 0 6係朝向晶圓基座1 0 4。在另一較佳實 施例中,反應室1 0 0内之頂部處係額外裝設一電極板1 0 2 , 且電極板1 0 2係連接至直流電(D C )電源供應器1 2 0。而靶材 靶材1 0 6係固定在電極板1 0 2之表面上,且靶材1 0 6係朝向 晶圓基座1 0 4。另外,靶材1 0 6例如是一金屬靶材,舉例如 鈦、鈷、鎳、组、鐫、紹、銅等金屬材質。11439t.wf. Pt.d Page 6 1220767 V. Description of the invention (3), round, and further improve the step coverage of the film. After the ionized metal passes through the conductive screen, the positively charged ionized metal is attracted by the negatively biased conductive screen, and it will be deposited in the direction of the wafer at a reduced speed. Will not be damaged by the impact of accelerated ionized metal. In order to make the above and other objects, features, and advantages of the present invention more comprehensible, a preferred embodiment is described below in detail with the accompanying drawings, as follows: [Embodiment] Please refer to FIG. 1 It shows a schematic diagram of an ionized physical vapor deposition apparatus according to a preferred embodiment of the present invention. The ionized physical gas phase deposition equipment of the present invention includes a reaction chamber 100, a wafer base 104, a target 106, an ionization unit 108, and a conductive screen 1110. Μ Among them, the wafer base 104 is disposed at the bottom of the reaction chamber 100, and is used to place a wafer 1 12. The target 106 is fixed at the top of the reaction chamber 100. In a preferred embodiment, the top cover 102 of the reaction chamber 100 is a conductive plate and can be used as an electrode, and the top cover 102 is connected to a power supply 1220. It is, for example, a direct current (DC) power supply. Therefore, the target material 106 is fixed on the surface of the top cover 102, and the dry material 106 is oriented toward the wafer base 104. In another preferred embodiment, an electrode plate 102 is additionally installed at the top of the reaction chamber 100, and the electrode plate 102 is connected to a direct current (DC) power supply 120. The target material 106 is fixed on the surface of the electrode plate 102, and the target material 106 faces the wafer base 104. In addition, the target material 106 is, for example, a metal target material, such as a metal material such as titanium, cobalt, nickel, group, hafnium, shaw, or copper.
1 1439twf.ptd 第7頁 1220767 五、發明說明(4) ^ 離子化單元1 0 8係配置在反應室1 0 0内,且設置在靶材 1 0 6以及晶圓基座1 0 4之間,其係用以離子化由靶材1 〇 6被 撞擊出的金屬。離子化單元1 0 8例如是電磁感應線圈、磁 極等單元,因此本發明離子化物理氣相沈積設備視其離子 化單元而可以是離子化金屬電製(ionized metal p 1 a s in a,I Μ P )物理氣相沈積設備、自行離子化電漿 (sel f-ionized plasma ,S I P )物理氣相沈積設備、凹狀陰 極磁控 ί賤鍵(hallow cathode magnetron sputtering , HCM sputtering)設備。倘若是應用在凹狀陰極磁控藏錢 設備,圖中電極板1 0 2將會配合磁極的設計而設計成凹狀 結構。 導電篩網1 1 0係配置在晶圓基座1 0 4以及離子化單元 ” 1 0 8之間,且導電篩網1 1 0與晶圓基座1 0 4之間的距離遠小 於導電篩網1 1 0與靶材1 0 6之間的距離。在一較佳實施例 中,導電篩網1 1 0與晶圓基座1 0 4之間的距離例如是介於1 公分至2公分之間。另外,導電篩網1 1 0之材質較佳的是與 靶材1 0 6之材質相同,以避免於沈積製程中造成污染。 導電篩網1 1 0係為具有網狀結構的金屬材料,其上視 圖如第2圖所示,因此導電篩網1 1 0本身具有導電性,以作 為一電極,且導電篩網1 1 0係連接至一電源供應器1 1 8 ,其 例如是射頻(R F )電源供應器。 除此之外,本發明之離子化物理氣相沈積設備更包括 一氣體供應裝置1 1 6 ,其係用於通入墮性氣體,如氬氣, 以進行物理氣相沈積製程形成金屬薄膜。另亦可選擇額外1 1439twf.ptd Page 7 1220767 V. Description of the Invention (4) ^ The ionization unit 1 0 8 is arranged in the reaction chamber 1 0 0 and is located between the target 10 6 and the wafer base 1 0 4 It is used to ionize the metal impacted by the target 106. The ionization unit 108 is, for example, an electromagnetic induction coil, a magnetic pole, or the like. Therefore, the ionized physical vapor deposition device of the present invention may be an ionized metal p 1 as in a, I M depending on its ionization unit. P) a physical vapor deposition device, a self-ionized plasma (SIP) physical vapor deposition device, and a concave cathode magnetron sputtering (HCM sputtering) device. If it is applied to a concave cathode magnetron hidden money device, the electrode plate 102 in the figure will be designed into a concave structure in accordance with the design of the magnetic pole. The conductive screen 1 10 is arranged between the wafer base 104 and the ionization unit "108, and the distance between the conductive screen 1 10 and the wafer base 104 is much smaller than the conductive screen The distance between the mesh 1 10 and the target material 106. In a preferred embodiment, the distance between the conductive screen 1 10 and the wafer base 104 is, for example, between 1 cm and 2 cm. In addition, the material of the conductive screen 1 10 is preferably the same as that of the target material 106 to avoid contamination during the deposition process. The conductive screen 1 10 is a metal having a mesh structure. The top view of the material is shown in Figure 2. Therefore, the conductive screen 1 1 0 itself has conductivity to serve as an electrode, and the conductive screen 1 10 is connected to a power supply 1 1 8. For example, it is Radio frequency (RF) power supply. In addition, the ionized physical vapor deposition device of the present invention further includes a gas supply device 1 1 6 which is used to pass a degrading gas such as argon for physical Vapor deposition process to form metal thin film.
114'39twf. pt.d 第8頁 1220767 五、發明說明(5) ^ 通入一反應氣體至反應室100中,使反應氣體參與沈積, 而形成金屬化合物薄膜。例如,當使用鈦為靶材1 0 6時, 利用氣體供應裝置1 1 6通入氬氣及氮氣於反應室1 0 0中,則 能沈積一氮化鈦薄膜於晶圓1 1 2表面上。 利用上述之離子化物理氣相沈積設備進行離子化物理 氣相沈積製程之詳細說明如下。 請參照第1圖,首先將晶圓1 1 2放置在反應室1 0 0内的 晶圓基座1 0 4上,準備於晶圓1 1 2表面上沈積一層薄膜。而 晶圓1 1 2之剖面示意圖如第3圖所示,其包括矽基底2 0 0 , 以及形成在基底200上之介電層202,且介電層202中具有 一開口 2 0 4 。 之後,開始電源供應器1 1 8、1 2 0,以對靶材1 0 6施予胃_ 一負偏壓,對導電篩網1 1 0施予另一較小負偏壓,以使電 漿撞擊靶材1 0 6 ,而轟擊出金屬1 1 3。在此同時,更開啟離 子化單元1 0 8 ,以使被轟擊出的金屬1 1 3被離子化成帶正電 的離子化金屬1 1 4 。 此時,因離子化金屬1 1 4與導電篩網1 1 0之間所產生的 電場會迫使離子化金屬1 1 4以加速度射向導電篩網1 1 0 ,如 此一來,離子化金屬1 1 4會垂直的射往晶圓1 1 2 ,而提高沈 積薄膜之階梯覆蓋度。而當離子化金屬1 1 4通過導電篩網 1 1 0之後,因帶正電的離子化金屬1 1 4受到施予負偏壓的導 電篩網1 1 0的吸引,因此會減速的往晶圓1 1 0方向沈積,而# 減低了離子化金屬1 1 4撞擊晶圓1 1 2的力量。請參照第3 圖,在介電層202以及基底200表面所沈積之薄膜206 ,其114'39twf. Pt.d Page 8 1220767 V. Description of the invention (5) ^ A reaction gas is introduced into the reaction chamber 100 so that the reaction gas participates in deposition to form a metal compound film. For example, when titanium is used as the target material 106, argon and nitrogen are passed into the reaction chamber 100 using the gas supply device 116, and a titanium nitride film can be deposited on the surface of the wafer 1 12 . The detailed description of the ionized physical vapor deposition process using the above-mentioned ionized physical vapor deposition equipment is as follows. Referring to FIG. 1, the wafer 1 12 is first placed on the wafer base 104 in the reaction chamber 100, and a thin film is prepared to be deposited on the surface of the wafer 1 12. A schematic cross-sectional view of the wafer 1 12 is shown in FIG. 3, which includes a silicon substrate 200, and a dielectric layer 202 formed on the substrate 200. The dielectric layer 202 has an opening 204. After that, the power supply devices 1 1 8 and 1 2 0 were started to apply a negative bias to the target 10 6 and another small negative bias to the conductive screen 1 1 0 to make the electricity The slurry hits the target 10 6 while bombarding the metal 1 1 3. At the same time, the ionization unit 1 0 8 is turned on so that the bombarded metal 1 1 3 is ionized into a positively charged ionized metal 1 1 4. At this time, the electric field generated between the ionized metal 1 1 4 and the conductive screen 1 1 0 will force the ionized metal 1 1 4 to shoot toward the conductive screen 1 1 0 with acceleration. As a result, the ionized metal 1 14 will shoot vertically to the wafer 1 1 2 to increase the step coverage of the deposited film. After the ionized metal 1 1 4 passes through the conductive screen 1 1 0, the positively charged ionized metal 1 1 4 is attracted by the conductive screen 1 1 0 that is applied with a negative bias, and therefore will decelerate toward the crystal. The circle 1 1 0 is deposited, and # reduces the force of the ionized metal 1 1 4 to hit the wafer 1 1 2. Referring to FIG. 3, a thin film 206 deposited on the surface of the dielectric layer 202 and the substrate 200 is shown in FIG.
1 1439 twf. pr.d 第9頁 1220767 五、發明說明(6) 階梯覆蓋度甚佳,而且介電層202以及基底200表面也不會 受到加速的離子化金屬1 1 4的撞擊而造成損害。 上述離子化物理氣相沈積設備進行離子化物理氣相沈 積製程中,以離子化金屬電漿(I Μ P )物理氣相沈積設備沈 積欽為例,對鈦革巴材施予之負偏壓例如是直流電(D C )電源 1 0 0 0 - 3 0 0 0瓦(W ),而對導電篩網施予之負偏壓例如是射頻 (R F )電源 5 0 - 2 0 0 瓦(W )。 在本發明另一較佳實施例中,於沈積薄膜2 0 6之前, 更包括先在介電層202以及基底200表面沈積一薄層,其詳 細說明如下。 請參照第1圖與第4 Α圖,同樣的,將晶圓1 1 2放置在反 應室1 0 0内的晶圚基座1 0 4上之後,首先開啟電源供應器 1 2 0 ,以對靶材1 0 6施予一負偏壓,而不對導電篩網1 1 0施 予偏壓。在此同時,更開啟離子化單元1 0 8 ,以使被轟擊 出的金屬1 1 3被離子化成帶正電的離子化金屬1 1 4。此時, 因導電篩網1 1 0並未施予偏壓,因此離子化金屬1 1 4會以較 低的加速度通過導電篩網1 1 0而射向晶圓1 1 2。請參照第4 A 圖,此時,便會在介電層202以及基底200表面沈積一層薄 層2 1 0 ,且薄層2 1 0之厚度約為薄膜最終厚度的2 0 %至3 0 %,其例如是4 0埃至5 0埃。由於上述步驟並未於導電篩網 施予偏壓,因此所沈積之薄層2 1 0之階梯覆蓋度並不佳。 但*於此薄層2 1 0相當薄,因此並不會影響最終薄膜之階 梯覆蓋度。 之後,請參照第1圖與第4 B圖,對靶材1 0 6施予一負偏1 1439 twf. Pr.d Page 9 1220767 V. Description of the invention (6) The step coverage is very good, and the surface of the dielectric layer 202 and the substrate 200 will not be damaged by the impact of the accelerated ionized metal 1 1 4 . In the above-mentioned ionized physical vapor deposition equipment for the ionized physical vapor deposition process, taking the ionized metal plasma (IMP) physical vapor deposition equipment deposition as an example, the negative bias applied to the titanium leather material For example, a direct current (DC) power source of 100-300 watts (W), and a negative bias applied to the conductive screen is, for example, a radio-frequency (RF) power source of 50-200 watts (W). In another preferred embodiment of the present invention, before depositing the thin film 206, it further includes depositing a thin layer on the surface of the dielectric layer 202 and the substrate 200, which is described in detail below. Please refer to FIG. 1 and FIG. 4A. Similarly, after placing the wafer 1 12 on the crystal base 1 104 in the reaction chamber 100, first turn on the power supply 1 2 0 to The target 10 6 is given a negative bias, and the conductive screen 1 10 is not biased. At the same time, the ionization unit 108 is turned on so that the bombarded metal 1 1 3 is ionized into a positively charged ionized metal 1 1 4. At this time, since the conductive screen 1 10 is not biased, the ionized metal 1 1 4 passes through the conductive screen 1 10 and shoots toward the wafer 1 12 with a low acceleration. Please refer to FIG. 4A. At this time, a thin layer 2 1 0 is deposited on the surface of the dielectric layer 202 and the substrate 200, and the thickness of the thin layer 2 1 0 is about 20% to 30% of the final thickness of the film. , Which is, for example, 40 angstroms to 50 angstroms. Since the above steps are not biased on the conductive screen, the step coverage of the deposited thin layer 210 is not good. But * here the thin layer 2 10 is quite thin, so it will not affect the step coverage of the final film. After that, please refer to Fig. 1 and Fig. 4 B to apply a negative bias to the target material 10 6
1 1 439 t.wf .ptd 第10頁 1220767 五、發明說明(7) 壓,對導電篩網1 1 0施予另一較小負偏壓,並且開啟離子 化單元1 0 8 ,以使被轟擊出的金屬1 1 3被離子化成帶正電的 離子化金屬114。 此時,因靶材1 0 6與導電篩網1 1 0之間所產生的電場會 迫使離子化金屬1 1 4以加速度射向晶圓1 1 2 ,如此一來,離 子化金屬1 1 4會垂直的射往晶圓11 2,而提高沈積薄膜之階 梯覆蓋度。而當離子化金屬1 1 4通過導電篩網1 1 0之後,因 帶正電的離子化金屬1 1 4受到施予負偏壓的導電篩網1 1 0的 吸引,因此會減速的往晶圓1 1 0方向沈積,而減低了離子 化金屬1 1 4撞擊晶圓1 1 2的力量。因此,會在薄層2 1 0之表 面上沈積薄膜2 0 6 (如第4 B圖所示),薄膜2 0 6之厚度例如是 2 0 0埃以上。所形成之薄膜2 0 6其階梯覆蓋度甚佳,而且因 介電層202以及基底200表面覆蓋有薄層210 ,因此可以避 免離子化金屬1 1 4直接撞擊晶圓而造成損害。 值得一提的是,在上述實施例中,若是欲沈積之薄膜 為金屬化合物薄膜,則進行沈積製程過程中,同時通入一 反應氣體至反應室1 0 0中,即可以沈積一層金屬化合物薄 膜。 由於本發明在接近晶圓之上方處設置一導電篩網,並 且在導電篩網上施予負偏壓,因此離子化金屬會加速射向 導電篩網,而提高了薄膜之階梯覆蓋度。而當離子化金屬 通過導電篩網之後,因離子化金屬受到施予負偏壓的導電 篩網吸引,而會減速的往晶圓方向沈積,如以一來,晶圓 表面就不會受到加速的離子化金屬的撞擊而造成損害。1 1 439 t.wf .ptd Page 10 1220767 V. Description of the invention (7) Apply another small negative bias to the conductive screen 1 1 0 and turn on the ionization unit 1 0 8 so that The bombarded metal 1 1 3 is ionized into a positively charged ionized metal 114. At this time, the electric field generated between the target material 106 and the conductive screen 1 1 0 will force the ionized metal 1 1 4 to shoot toward the wafer 1 1 2 at an acceleration. As a result, the ionized metal 1 1 4 It will be shot perpendicularly to the wafer 11 2 to improve the step coverage of the deposited film. After the ionized metal 1 1 4 passes through the conductive screen 1 1 0, the positively charged ionized metal 1 1 4 is attracted by the conductive screen 1 1 0 that is applied with a negative bias, and therefore will decelerate toward the crystal. Deposition in the circle 1 10 direction reduces the force of the ionized metal 1 1 4 to hit the wafer 1 12. Therefore, a thin film 2 06 (as shown in FIG. 4B) is deposited on the surface of the thin layer 2 10, and the thickness of the thin film 2 06 is, for example, more than 200 angstroms. The formed thin film 206 has excellent step coverage, and the surface of the dielectric layer 202 and the substrate 200 is covered with a thin layer 210, so that the ionized metal 1 4 can be prevented from directly hitting the wafer and causing damage. It is worth mentioning that, in the above embodiment, if the film to be deposited is a metal compound film, during the deposition process, a reaction gas is simultaneously introduced into the reaction chamber 100, and a metal compound film can be deposited. . Since a conductive screen is provided near the wafer and a negative bias is applied to the conductive screen, the ionized metal will be accelerated toward the conductive screen and the step coverage of the film is improved. After the ionized metal passes through the conductive screen, the ionized metal is attracted to the conductive screen applied with a negative bias, and will be deposited in the direction of the wafer at a reduced speed. For example, the wafer surface will not be accelerated. Damage caused by the impact of ionized metal.
11439twf.ptd 第11頁 1220767 五、發明說明(8) 本發明在沈積薄膜之前,可先在導電辦網上不施予偏 壓,以在晶圚表面上沈積一層薄層,其係可以保護晶圓表 面免於遭到後續薄膜沈積時,離子化金屬會直接撞擊而造 成的損害。 雖然本發明已以較佳實施例揭露如上,然其並非用以 限定本發明,任何熟習此技藝者,在不脫離本發明之精神 和範圍内’當可作些許之更動與〉閏飾’因此本發明之保護 範圍當視後附之申請專利範圍所界定者為準。11439twf.ptd Page 11 1220767 V. Description of the invention (8) The invention can deposit a thin layer on the surface of the crystallite without applying a bias voltage on the conductive grid before depositing the thin film, which can protect the crystal The round surface is protected from damage caused by the direct impact of the ionized metal during subsequent film deposition. Although the present invention has been disclosed in the preferred embodiment as above, it is not intended to limit the present invention. Anyone skilled in the art can make some changes and "decorations" without departing from the spirit and scope of the present invention. The protection scope of the present invention shall be determined by the scope of the attached patent application.
114'39twf . ptd 第12頁 1220767 圖式簡單說明 第1圖是依照本發明一較佳實施例之離子化物理氣相 沈積設備之不意圖; 第2圖是苐1圖中導電篩網之上視示意圖; 第3圖是依照本發明一較佳實施例於晶圓上沈積具有 ,甚佳階低覆蓋度之薄膜的剖面示意圖;以及 第4 A圖至第4 B圖是依照本發明另一較佳實施例於晶圓 上沈積具有甚佳階低覆蓋度之薄膜的剖面示意圖。 【圖式標示說明】 1 0 0 :反應室 1 0 2 :頂蓋(電極板) 1 0 4 ·晶圓基座 1 0 6 :靶材 1 0 8 :離子化單元 1 1 0 :導電篩網 1 1 2 :晶圓 1 1 3 :金屬 1 1 4 :離子化金屬 1 1 6 :氣體供應裝置 1 1 8、1 2 0 :電源供應器 200 :基底 2 0 2 :介電層 204 :開口 2 0 6 :薄膜 2 1 0 :薄層114'39twf. Ptd Page 12 1220767 Brief description of the drawing Figure 1 is the intention of the ionized physical vapor deposition equipment according to a preferred embodiment of the present invention; Figure 2 is above the conductive screen in Figure 1 FIG. 3 is a schematic cross-sectional view of a thin film having a very good step and low coverage deposited on a wafer according to a preferred embodiment of the present invention; and FIGS. 4A to 4B are another views according to the present invention. A schematic cross-sectional view of a preferred embodiment for depositing a thin film with excellent low-level coverage on a wafer. [Illustration of Graphical Indications] 1 0 0: reaction chamber 1 0 2: top cover (electrode plate) 1 0 4 · wafer base 1 0 6: target 1 0 8: ionization unit 1 1 0: conductive screen 1 1 2: wafer 1 1 3: metal 1 1 4: ionized metal 1 1 6: gas supply device 1 1 8, 1 2 0: power supply 200: substrate 2 0 2: dielectric layer 204: opening 2 0 6: thin film 2 1 0: thin layer
1 1 439t.wf.ptd 第13頁1 1 439t.wf.ptd Page 13
Claims (1)
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| TW092118826A TWI220767B (en) | 2003-07-10 | 2003-07-10 | Ionized physical vapor deposition process and apparatus thereof |
| US10/605,160 US20050006232A1 (en) | 2003-07-10 | 2003-09-12 | [ionized physical vapor deposition process and apparatus thereof] |
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| TW092118826A TWI220767B (en) | 2003-07-10 | 2003-07-10 | Ionized physical vapor deposition process and apparatus thereof |
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| WO2011141035A1 (en) * | 2010-05-10 | 2011-11-17 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Device and method for gas flow sputtering |
| US8753724B2 (en) * | 2012-09-26 | 2014-06-17 | Front Edge Technology Inc. | Plasma deposition on a partially formed battery through a mesh screen |
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| JPH0860355A (en) * | 1994-08-23 | 1996-03-05 | Tel Varian Ltd | Treating device |
| US5840167A (en) * | 1995-08-14 | 1998-11-24 | Lg Semicon Co., Ltd | Sputtering deposition apparatus and method utilizing charged particles |
| US5807467A (en) * | 1996-01-22 | 1998-09-15 | Micron Technology, Inc. | In situ preclean in a PVD chamber with a biased substrate configuration |
| US6827824B1 (en) * | 1996-04-12 | 2004-12-07 | Micron Technology, Inc. | Enhanced collimated deposition |
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