TW514661B - Chemical-mechanical abrasive composition for use in semiconductor processing - Google Patents

Chemical-mechanical abrasive composition for use in semiconductor processing Download PDF

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TW514661B
TW514661B TW87106624A TW87106624A TW514661B TW 514661 B TW514661 B TW 514661B TW 87106624 A TW87106624 A TW 87106624A TW 87106624 A TW87106624 A TW 87106624A TW 514661 B TW514661 B TW 514661B
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acid
group
weight
grinding
patent application
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TW87106624A
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Chinese (zh)
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Tzung-He Li
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Eternal Chemical Co Ltd
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  • Mechanical Treatment Of Semiconductor (AREA)
  • Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)

Abstract

A chemical-mechanical abrasive composition for use in polishing metal films in a semiconductor processing, which composition comprises 1-25% by weight of an abrasive particle, 1-10% by weight of an oxidant, and 0.1-20% by weight of a buffer agent for use as an abrasion enhancer, wherein the buffer agent comprises a persulfate group-containing compound or an iron (III) salt and a carboxy group- or an amido group-containing compound.

Description

514661 A7 B7 五、發明説明(1 ) 發明領域 本發明係關一種化學機械研磨組合物。本發明研磨組合 物具高度穩定性,可有效地應用於半導體晶圓表面之研磨。 發明背景 於半導體工業中,半導體晶圓表面之研磨係爲廣泛應用 之技術,以提高半導體晶圓及介電層之平坦性,以利於製 造金屬線路。一般而言,用於製造金屬線路之研磨方法, 係將半導體晶圓置於配有研磨頭之旋轉研磨平台上,於晶 圓表面施用包含研磨粒子與氧化劑之研磨漿液,以增進研 磨功效。 美國專利第5,225,034號揭示一種化學機械研磨漿液,其包 含AgN03、固體研磨物質、與選自H202、H0C1、K0C1、KMg〇4 或CH3COOOH之氧化劑。此研磨漿液係用於研磨半導體晶圓 上之銅層,以製造晶圓上之銅線。 美國專利第5,209,816號揭示一種使用化學機械研磨漿液以 將含A1或Ti金屬層磨光之方法,其研磨漿液除包含固體研 磨物質外,尚包含約0.1-20體積%之H3P04與約1-30體積%之 H2o2 〇 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 美國專利第4,959,113號係關一種使用水性研磨組合物以磨 光金屬表面之方法。此水性研磨組合物包含水、研磨劑(例 如 Ce02、Al2〇3、Zr02、Ti02、Si02、SiC、Sn02 及 TiC)、與 一種鹽類,此鹽類包含元素週期表IIA、ΠΙΑ、IVA或IVB 族之金屬陽離子與氯離子、溴離子、破離子、硝酸根、硫 酸根、磷酸根或過氯酸根之陰離子。此美國專利亦敎示使 -4- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) 514661 A7 B7 五、發明説明(2 ) 用鹽酸、硝酸、磷酸或硫酸以將其水性研磨組合物調配成 pH=l-6 〇 美國專利第5,391,258號揭示一種用於磨光含矽、矽石或矽 酸鹽之複合物之研磨組合物,其除包含研磨顆粒外,尚包 含過氧化氫與S太酸氫钾(potassium hydrogen phthalate)。 美國專利第5,114,437號係關一種用於磨光鋁基材之磨光組 合物,其包含平均顆粒尺寸介於0.2至5μπι之氧化鋁磨光劑 及選自硝酸鉻(III)、硝酸鑭、硝酸鋅(III)銨或硝酸钕之磨光促 進劑。 美國專利第5,084,071號係關一種使用化學機械磨光漿液以 將電子元件基材磨光之方法,其所使用之磨光漿液包含小 於1重量%之氧化鋁、研磨顆粒(例如,Si02、Ce02、SiC、 Si3N4或Fe203)、作爲研磨效率促進劑之過渡金屬螯合鹽(例 如,EDTA鐵銨)、及供該鹽使用之溶劑。 美國專利第5,480,476號係探討Ce4+與Zr4+陽離子對Si02類型 研磨劑拋光速率之影響。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 美國專利第5,366,542號揭示一種磨光組合物,其包括氧化 鋁研磨顆粒,及一選自多胺基羧酸(例如EDTA)或其鈉或鉀 鹽之螯合劑。此磨光組合物可進一步包含勃姆石(boehmite)或 鋁鹽。 美國專利第5,340,370號揭示一種用於例如鎢或氮化鎢薄膜 之化學機械磨光之漿液,其包含供薄膜使用之氰鐵酸鉀氧 化劑、研磨劑與水,其中該漿液具有2至4之pH値。 美國專利第5,516,346號揭示一種用於化學機械磨光鈦薄膜 -5- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) )丄4661 經濟部中央標準局員工消費合作社印製 Α7 Β7 五、發明説明(3 ) 之裝液’其包含濃度足以與該欽薄膜錯合之氟化钟與研磨 劑(例如氧化矽),其中該漿液具有低於8之pH値。 W0 96/16436揭示一種化學機械磨光漿液,其包含具有小於 〇·400微米中値顆徑之研磨顆粒、鐵鹽氧化劑、及丙二醇與 對羥基苯甲酸甲酯之水性界面活性劑懸浮液。 美國專利第5,476,606號揭示一種用於化學機械磨光金屬層 之漿液,其包含氧化金屬錯合物(例如硝酸鐵)之氧化劑、含 至少50% γ-相之熔融氧化鋁顆粒、與例如聚烷基矽氧烷或聚 氧化伸纟见基酸之非離子性界面活性劑添加劑。 上述先前技藝所敎示之研磨漿液均無法避免造成_離子 或過渡金屬之/亏染’或因採用南分子型界面活性劑,除容 易於研磨時起泡造成晶圓表面局部研磨不平均、粗度提高 之外’更因爲高分子型化合物之水溶性不佳,極易導致較 鬲》'亏染的可能性。 此外,美國專利第5,476,606號雖敎示使用低分子量超基幾 酸以抑制氧化物之研磨速率,因而提高金屬/氧化物之研磨 選擇率,然而由於羥基羧酸無法提高研磨顆粒之電位 (即,電動電位),因此,其於添加後往往造成漿液的不穩定 性。 ~ 综上所述,半導體製程之技藝中,仍企尋求具有較高品 質之化學機械研磨組合物,以克服上述先前技藝研磨組合 物所面臨之缺點。 發明簡述 本發明係提供一種用於研磨半導體製程中金屬薄膜之 (請先閱讀背面之注意事項再填寫本頁}514661 A7 B7 V. Description of the Invention (1) Field of the Invention The present invention relates to a chemical mechanical polishing composition. The polishing composition of the present invention has high stability and can be effectively applied to the polishing of the surface of a semiconductor wafer. BACKGROUND OF THE INVENTION In the semiconductor industry, the polishing of the surface of semiconductor wafers is a widely used technique to improve the flatness of semiconductor wafers and dielectric layers, and to facilitate the manufacture of metal circuits. Generally speaking, the polishing method for manufacturing metal circuits is to place a semiconductor wafer on a rotating polishing platform equipped with a polishing head, and apply a polishing slurry containing abrasive particles and an oxidizing agent on the surface of the wafer to improve the grinding efficiency. U.S. Patent No. 5,225,034 discloses a chemical mechanical polishing slurry comprising AgN03, a solid abrasive substance, and an oxidant selected from the group consisting of H202, H0C1, K0C1, KMg04, or CH3COOOH. This polishing slurry is used to polish copper layers on semiconductor wafers to make copper wires on wafers. U.S. Patent No. 5,209,816 discloses a method for polishing a metal layer containing A1 or Ti using a chemical mechanical polishing slurry. The polishing slurry contains about 0.1-20% by volume of H3P04 and about 1-30 in addition to solid abrasives. H2o2 by volume 〇 Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs (please read the precautions on the back before filling out this page) US Patent No. 4,959,113 relates to a method for polishing metal surfaces by using aqueous abrasive compositions . The aqueous abrasive composition includes water, abrasives (such as Ce02, Al2O3, Zr02, Ti02, Si02, SiC, Sn02, and TiC), and a salt containing the periodic table IIA, IIIA, IVA, or IVB. Group of metal cations and anions of chloride, bromide, ion, nitrate, sulfate, phosphate or perchlorate. This U.S. patent also states that the paper size is applicable to the Chinese National Standard (CNS) A4 specification (210X297 mm) 514661 A7 B7 V. Description of the invention (2) Use hydrochloric acid, nitric acid, phosphoric acid or sulfuric acid to grind it in water The composition is formulated to pH = 1-6. U.S. Patent No. 5,391,258 discloses a polishing composition for polishing a composite containing silicon, silica or silicate, which contains abrasive particles in addition to abrasive particles. Hydrogen oxide and S potassium hydrogen phthalate. U.S. Patent No. 5,114,437 relates to a polishing composition for polishing an aluminum substrate, which comprises an alumina polishing agent having an average particle size of 0.2 to 5 μm, and is selected from chromium (III) nitrate and lanthanum nitrate. Polishing accelerator for zinc (III) ammonium nitrate or neodymium nitrate. U.S. Patent No. 5,084,071 relates to a method for polishing electronic component substrates using a chemical mechanical polishing slurry. The polishing slurry used contains less than 1% by weight of alumina and abrasive particles (for example, Si02, Ce02, SiC, Si3N4 or Fe203), a transition metal chelate salt (for example, EDTA ammonium iron) as a grinding efficiency promoter, and a solvent for the salt. US Patent No. 5,480,476 discusses the effect of Ce4 + and Zr4 + cations on the polishing rate of SiO2 type abrasives. Printed by the Consumer Standards Cooperative of the Central Bureau of Standards of the Ministry of Economic Affairs (please read the notes on the back before filling this page) US Patent No. 5,366,542 discloses a polishing composition comprising alumina abrasive particles and a polyamine Chelating agents for acids (such as EDTA) or their sodium or potassium salts. This polishing composition may further comprise boehmite or an aluminum salt. U.S. Patent No. 5,340,370 discloses a slurry for chemical mechanical polishing of, for example, tungsten or tungsten nitride films, comprising a potassium cyanoferrate oxidant, an abrasive, and water for use in the film, wherein the slurry has a pH of 2 to 4 value. U.S. Patent No. 5,516,346 discloses a titanium film for chemical mechanical polishing. This paper size is applicable to the Chinese National Standard (CNS) A4 (210X297 mm). 丄 4661 Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs. Α7 Β7 5. Description of the invention (3) The filling liquid 'comprises a fluorinated bell and an abrasive (such as silicon oxide) at a concentration sufficient to be incompatible with the thin film, wherein the slurry has a pH of less than 8. WO 96/16436 discloses a chemical mechanical polishing slurry comprising abrasive particles having a median diameter of less than 400 microns, an iron salt oxidant, and an aqueous surfactant suspension of propylene glycol and methyl paraben. U.S. Patent No. 5,476,606 discloses a slurry for chemical mechanical polishing of a metal layer comprising an oxidizing agent that oxidizes a metal complex (such as iron nitrate), molten alumina particles containing at least 50% γ-phase, and, for example, a polyalkane Siloxane or polyoxyalkylene are nonionic surfactant additives based on acid. The polishing slurry shown by the above-mentioned previous techniques cannot avoid _ ion or transition metal / defective staining or the use of South molecular type surfactants, except for the local polishing unevenness and coarseness of the wafer surface which is easy to blister during polishing. In addition to the increase in degree, it is also because of the poor water solubility of polymer compounds, which can easily lead to the possibility of "defective staining". In addition, although U.S. Patent No. 5,476,606 shows that the use of a low molecular weight super quinic acid to suppress the polishing rate of the oxides, thereby improving the polishing selectivity of the metal / oxides, the potential of the abrasive particles cannot be increased by the hydroxycarboxylic acid (i.e., Electrokinetic potential), so it often causes slurry instability after addition. ~ In summary, in the technology of semiconductor manufacturing, companies are still looking for chemical mechanical polishing compositions of higher quality to overcome the disadvantages faced by the aforementioned prior art polishing compositions. Brief Description of the Invention The present invention provides a method for polishing metal thin films in semiconductor manufacturing processes (please read the precautions on the back before filling this page)

-6 - 經濟部中央標準局員工消費合作社印製 A7 -----_____ B7 __ 五、發明説明(4 ) 學機械研磨組合物,其包含卜25重量%之研磨顆粒;及〇1_2〇 重量%之同時作爲研磨促進劑之緩衝劑,其中該緩衝劑包括 含過硫酸基之化合物或含鐵(III)之鹽類及含羧基或醯胺基之 化合物。 發明詳細説明 本發明係提供一種用於研磨半導體製程中,研磨金屬薄 膜之化學機械研磨組合物,其包含卜25重量%,較佳爲3_10 重量°/°之研磨顆粒;及0.1_20重量%,較佳爲6-15重量%之 同時作爲研磨促進劑之緩衝劑,其中該緩衝劑包括含過硫 酸基之化合物或含鐵(m)之鹽類及含羧基或含醯胺基之化合 物。本發明化學機械研磨組合物可進一步包含丨_ 1〇重量%, 車父佳爲4-6重量%之氧化劑。 根據本發明,研磨組合物所使用之研磨顆粒可爲一般市 售者,例如 s1〇2、Al2〇3、Zrt)2、CeC>2、SlC、Fe2〇3、TiQ2、-6-Printed A7 by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs -----_____ B7 __ V. Description of the Invention (4) A mechanical grinding composition containing 25% by weight of abrasive particles; and 〇1_2〇 weight % As a buffering agent for grinding accelerator, wherein the buffering agent includes compounds containing persulfate group or salts containing iron (III) and compounds containing carboxyl group or amido group. Detailed description of the invention The present invention provides a chemical mechanical polishing composition for polishing a metal film in a semiconductor manufacturing process, which comprises 25% by weight of abrasive particles, preferably 3-10 weight ° / °; and 0.1-20% by weight, It is preferably 6-15% by weight of a buffering agent which is also used as a grinding accelerator, wherein the buffering agent includes a compound containing a persulfate group or a salt containing iron (m) and a compound containing a carboxyl group or a sulfonium group. The chemical-mechanical polishing composition of the present invention may further include 10-10% by weight, and Chevron is 4-6% by weight of an oxidizing agent. According to the present invention, the abrasive particles used in the abrasive composition may be general marketers, such as s102, Al203, Zrt) 2, CeC > 2, SlC, Fe203, TiQ2,

SisN4、或其混合物。此等研磨顆粒具有較高純度、高比表面 牙貝、及狹笮粒徑分佈等優點,因此適用於化學機械研磨組 合物中作爲研磨顆粒。 可用於本發明中之氧化劑係一般市售者,例如H202、 KI〇3、KBr〇3、K2Cr207、K2Mn207、KMn04、H0C1、 CH3CO〇〇H,或其混合物。 根據本發明,作爲緩衝劑成份之含過硫酸基化合物之實 例包括,ΗΑ2〇8、砂〇8、邮4)成〇8、邮2〇8、或其混合物, 而=爲缓衝劑成份之含鐵(111)之鹽類實例包括,氰鐵酸鉀、 硫酸銨鐵(III)、硝酸鐵(111)、或其混合物。 --_____ -7- 本紙張尺度適财關家縣(―CNS ) Α4規格(270^297^¾^----- (請先閱讀背面之注意事項再填寫本頁) k衣- 訂 五、 發明説明(5 A7 B7 可用於本發明緩衝劑中之含羧基化合物係選自: (1) 如下式之單羧基化合物: 0SisN4, or a mixture thereof. These abrasive particles have the advantages of high purity, high specific surface dentistry, and narrow particle size distribution, so they are suitable for use as abrasive particles in chemical mechanical polishing compositions. The oxidizing agents that can be used in the present invention are generally commercially available, such as H202, KI〇3, KBro3, K2Cr207, K2Mn207, KMn04, HOC1, CH3COOOH, or a mixture thereof. Examples of persulfate-containing compounds according to the present invention as a buffering agent component include ΗΑ208, 8〇8, 44) 至 0, 〇2, or a mixture thereof, and == Examples of the salts containing iron (111) include potassium ferricyanide, iron (III) ammonium sulfate, iron (111) nitrate, or a mixture thereof. --_____ -7- This paper is suitable for Guancai County (―CNS) Α4 size (270 ^ 297 ^ ¾ ^ ----- (Please read the precautions on the back before filling in this page) k-shirt-order five Description of the invention (5 A7 B7 The carboxyl-containing compound that can be used in the buffer of the present invention is selected from: (1) a monocarboxyl compound of the following formula: 0

Ri - C - 〇r2 其中,~爲氫、Cl-c6燒基或Ci_c6#f垸基;及心爲氯、 銨離子或鹼金屬離子(較佳爲鉀離子)。 此種單I基化合物之實例包括:甲酸、乙酸、丙酸、丁 酸、戊酸、己酸、羥基醋酸、乳酸 (2) 如下式之二羧基化合物: 揽4 〇 〇 R3〇-c-R4-c.〇r2 其中,〜爲-單鍵、Cl_C6垸基或Ci_Q㈣基;且心 及R3為氫、銨離子或鹼金屬離子(較佳爲卸離子)。 此種:竣基化合物之實例包括:乙二酸(草酸)、丙二酸' γ-1'琥珀酸)、戊二酸、羥基丁二酸(蘋果酸)、酒石 酸、半乳糖二酸及其鹽類。 (3) 二叛基化合物,例如檸檬酸及其鹽類。 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) ⑷基鉍化合物’例如甘胺酸、肌胺酸、二甲基 丙胺酸及其鹽類。 可用t作A本發明緩衝劑成份之含醯胺基化合物之實例 包括·甲醯胺、乙醯胺、丙醯胺、Ν·甲基甲醯胺、N_甲基 乙酸胺、尿素、甲基脲、乙基脲、二甲基脲及二乙基脲。 本發明研H合物所使用之作爲研磨促進劑之緩衝劑添 加劑可提供以下優點: 本紙張尺度顏悄 -8 514661 經濟部中央標準局員工消費合作社印製 A7 B7 五、發明説明(6 ) ⑴由於研磨漿液pH値之變化會影響研磨顆粒之ξ_電位,因 此’維持穩定之pH値對研磨漿液而言極爲重要。本發 明所使用緩衝劑可提供研磨漿液介於1 5至8 5間之pH 値,因此具有穩定研磨漿液pH値之功用。 (2) 本發明所使用之緩衝劑水溶性極佳,因此易於清除而不 會殘留在晶圓上。 (3) 本發明所使用之緩衝劑具有較大之分子,其不致滲入晶 圓中造成晶圓之污染。 ⑷本發明所使用之緩衝劑爲一般常見之化學品,其較不具 危險性,因此可顯著降低對半導體製程工作者之危險性 及不致對環境造成污染。 (5)本發明緩衝劑之各別成份係腐蝕性較低之化合物,然 而,根據本發明將此等腐蚀性較低之化合物組合使用 時,將產生非可預期之極強腐蝕性,因此,可有效提高 金屬薄膜之刮去速率。 本發明研磨組合物可包含’例如,水作爲媒質。在製備 過程中,可使用水以使研磨組合物呈衆液狀,較佳係使用 習知之去離子水。 本發明研磨組合物可藉由一般習知方 成備。例如,可 先將研磨顆粒加入水中,以具有高剪切 4丄士 〇刀切力心攪拌器持續攪 拌,直至研磨顆粒完全懸浮於水中形, 7纨永欣。之後,繼婧 加入水,以使漿液中之研磨顆粒達到 /、 〈固體含量。根 據本發明,漿液之固體含量爲1 -25重| 0/ , 、 里/〇,較佳爲3_10重 量%。然後將如上文所述之添加劑導入、 八所件 &lt; 高純度漿液 -9 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) (請先閱讀背面之注意事項再填寫本頁)Ri-C-〇r2 where ~ is hydrogen, Cl-c6 alkyl or Ci_c6 # f 垸 group; and the heart is chlorine, ammonium ion or alkali metal ion (preferably potassium ion). Examples of such mono-I-based compounds include: formic acid, acetic acid, propionic acid, butyric acid, valeric acid, hexanoic acid, glycolic acid, and lactic acid (2) a dicarboxylic compound of the formula: 4 〇R3〇-c-R4 -c.〇r2 wherein ~ is -single bond, Cl_C6fluorenyl or Ci_Qfluorenyl; and R3 is hydrogen, ammonium ion or alkali metal ion (preferably deionized ion). Examples of this type: Endyl compounds include: oxalic acid (oxalic acid), malonic acid 'γ-1' succinic acid), glutaric acid, hydroxysuccinic acid (malic acid), tartaric acid, galactic acid, and the like Salt. (3) Dialkyl compounds, such as citric acid and its salts. Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs (please read the notes on the back before filling this page) ⑷Bismuth compounds such as glycine, sarcosine, dimethylalanine and their salts. Examples of the amino group-containing compounds that can be used as the buffering agent component of the present invention include formamide, acetamide, propylamine, N-methylformamide, N-methylacetamide, urea, methyl Urea, ethylurea, dimethylurea and diethylurea. The buffer additive used as a grinding accelerator for the H-composite of the present invention can provide the following advantages: The paper size Yan quiet-8 514661 Printed by the Consumers' Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs A7 B7 V. Description of the invention (6) ⑴ Since the change of pH 値 of the grinding slurry will affect the ξ_ potential of the grinding particles, 'maintaining a stable pH 値 is extremely important for the grinding slurry. The buffer used in the present invention can provide a pH 研磨 of the grinding slurry between 15 and 85, and therefore has the function of stabilizing the pH 値 of the grinding slurry. (2) The buffer used in the present invention has excellent water solubility, so it can be easily removed without remaining on the wafer. (3) The buffering agent used in the present invention has larger molecules, which will not penetrate into the wafer and cause contamination of the wafer.缓冲 The buffering agent used in the present invention is a common chemical, which is less dangerous, so it can significantly reduce the danger to semiconductor process workers and not cause pollution to the environment. (5) The respective components of the buffering agent of the present invention are relatively less corrosive compounds. However, when these less corrosive compounds are used in combination according to the present invention, unexpectedly strong corrosiveness will be generated. Therefore, Can effectively improve the scraping rate of metal thin films. The abrasive composition of the present invention may include 'for example, water as a medium. In the preparation process, water may be used to make the grinding composition liquid, and it is preferable to use conventional deionized water. The abrasive composition of the present invention can be prepared by a conventional method. For example, you can first add the abrasive particles to water and continue to stir them with a high-shear 4 × 0 blade shear mixer until the abrasive particles are completely suspended in the water. After that, Jing added water to make the abrasive particles in the slurry reach /, <solid content. According to the present invention, the solids content of the slurry is 1 to 25 weight | 0 /,, lining / 0, preferably 3 to 10 weight%. Then import the additives as described above, Basuo Pieces &lt; High-Purity Slurry-9 This paper size applies to China National Standard (CNS) A4 specifications (210X 297 mm) (Please read the precautions on the back before filling this page )

A7 B7 五、發明説明(7 ) 中’再加入例如氨水,以_漿液之PH値在所需範圍之間。 例如’ #欲研磨之金屬薄膜冑W薄膜時’丨將pH値控制在 一 馬1·8-2.3 i間;备欲研磨之金屬薄膜 爲Ai薄膜時’ ♦ pn値控制在3 〇-4 5之間,較佳爲之 間;及當欲研磨之金屬薄膜爲Cu薄膜時,將⑻値控制在 5.5-9.0^.1 ? 6.〇.τ〇^Γ, 〇 本發明(研磨組合物。本發明研磨組合物之製備過程,可 於任何適當之溫度下進行,較佳係於2〇_4〇t之溫度下進 行。 以下實例將對本發明作進一步之説明,唯非用以限制本 發明之範圍,任何熟習此項技藝之人士可輕易達成之修飾 及改變’均涵蓋於本發明之範圍内。 實例1 本實例中係使用Degussa所生產之二氧化矽,其且有如 性質: 八a (1) 4%水性懸浮液之pH値係界於3 6_4 3之間; (2) 比表面積爲40-130平方公尺/克;及 (3) 比重爲S0.7克/毫升。 經濟部中央標準局員工消費合作社印製 ------:---II (請先閱讀背面之注意事項再填寫本頁} 訂A7 B7 5. In the description of the invention (7), for example, ammonia water is added, so that the pH of the slurry is between the required range. For example, '#When the metal film to be polished 胄 W film' 丨 Control pH 在 一 between 1 · 8-2.3 i; when the metal film to be polished is Ai film '♦ pn 値 is controlled to 3 〇-4 5 Between, preferably between; and when the metal thin film to be polished is a Cu thin film, ⑻ 値 is controlled to 5.5-9.0 ^ .1? 6.〇.τ〇 ^ Γ, 〇 the present invention (grinding composition. The preparation process of the grinding composition of the present invention can be carried out at any suitable temperature, preferably at a temperature of 20-40 t. The following examples will further illustrate the present invention, but are not intended to limit the present invention. The scope, modifications and changes that can be easily achieved by anyone skilled in the art are all included in the scope of the present invention. Example 1 In this example, the silicon dioxide produced by Degussa is used, and has the same properties: 八 a ( 1) The pH range of the 4% aqueous suspension is between 36 and 43; (2) the specific surface area is 40-130 m2 / g; and (3) the specific gravity is S0.7 g / ml. Central Ministry of Economic Affairs Printed by the Consumer Bureau of Standards Bureau ------: --- II (Please read the notes on the back before filling this page} Order

於室溫下,將5公斤上述二氧化矽加入2〇公斤之去離子 水中,以高剪切力攪拌器持續攪拌,直至二氧化矽完全縣 浮於水中而呈漿液狀。然後再加入20公斤之去離子水稀釋' 漿液,以使漿液之固體含量爲略大於11%。然後將丨5公斤 之乙二酸(草酸)及3公斤之硫酸銨鐵(111)加入漿液中,其迅速 落於聚液中。持續攪摔3小時後,再以NH4〇H調整槳液之pH -10- A7 A7 經濟部中央標準局員工消費合作社印製 __ ________ B7 一 五、發明説明(8 ) 一 I爲約2.0。過濾漿液以製得本發明之化學機械研磨組合 物’其固體含量爲約10%。所得研磨組合物之研磨測試結果, 知列於下文表1中。 重覆實例1相同之製備步驟,惟以1 5公斤之甲酸取代乙 —酸。所得研磨組合物之研磨測試牡果,茲列於下文表1 中。At room temperature, 5 kg of the above-mentioned silicon dioxide was added to 20 kg of deionized water, and stirring was continued with a high-shear mixer until the silicon dioxide completely floated in the water and became a slurry. Then, 20 kg of deionized water was added to dilute the slurry so that the solid content of the slurry was slightly greater than 11%. Then 5 kg of oxalic acid (oxalic acid) and 3 kg of ammonium iron sulfate (111) were added to the slurry, which quickly fell into the polymer solution. After continuing to stir for 3 hours, adjust the pH of the paddle fluid with NH4OH. -10- A7 A7 Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs __ ________ B7 V. Description of the invention (8) A I is about 2.0. The slurry was filtered to prepare a chemical mechanical polishing composition ' of the present invention having a solids content of about 10%. The grinding test results of the obtained grinding compositions are shown in Table 1 below. The same preparation procedure as in Example 1 was repeated, except that the acetic acid was replaced with 15 kg of formic acid. The grinding test results of the obtained grinding composition are listed in Table 1 below.

重覆實例1相同之製備步驟,惟以5公斤氧化鋁(Sumitomo 化學公司所生產,型號AKj^GOOg)取代二氧化矽,並以i 5 公斤檸檬酸取代乙二酸。所得研磨組合物之研磨測試結果, 公么列於下文表1中。 重覆實例3相同之製備步驟,惟以15公斤之羥基醋酸取 代檸檬酸。所得研磨組合物之研磨測試結果,茲列於下文 表1中。 重覆實例1相同之製備步驟,惟不添加硫酸銨鐵(III)。所 得研磨組合物之研磨測試結果,茲列於下文表1中。 比較例2 重覆實例3相同之製備步驟,惟不添加硫酸銨鐵(III)。所 得研磨組合物之研磨測試結果,茲列於下文表1中。 研磨測談 A.儀器:IPEC / Westech 472 ___- 11 - ___ 本紙張尺度適用中國國家標準(CNS ) A4規格(210X297公釐) (讀先閱讀背面之注意事項再填寫本頁)The same preparation steps as in Example 1 were repeated, except that 5 kg of alumina (manufactured by Sumitomo Chemical Co., model AKj ^ GOOg) was used to replace silicon dioxide, and i 5 kg of citric acid was used to replace oxalic acid. The grinding test results of the obtained grinding compositions are shown in Table 1 below. The same preparation procedure as in Example 3 was repeated, except that citric acid was replaced with 15 kg of glycolic acid. The grinding test results of the obtained grinding compositions are shown in Table 1 below. The same preparation steps as in Example 1 were repeated, except that ammonium iron (III) sulfate was not added. The grinding test results of the obtained grinding compositions are shown in Table 1 below. Comparative Example 2 The same preparation steps as in Example 3 were repeated, except that ammonium iron (III) sulfate was not added. The grinding test results of the obtained grinding compositions are shown in Table 1 below. Grinding test A. Apparatus: IPEC / Westech 472 ___- 11-___ This paper size is applicable to China National Standard (CNS) A4 specification (210X297 mm) (Read the precautions on the back before filling this page)

A7 B7 五、發明説明(9 ) ---^--:---φ^! (請先閱讀背面之注意事項再填寫本頁 β•條件:壓力:5psi 溫度·· 25°C 主軸轉速:45rpm 台板轉速·· 42 rpm 墊座型式:Rodel 1C 1400 漿液流速:150亳升/分鐘 C ·曰g 片·(1) W 薄膜:講自 silicon Valley Microelectronics,Inc.,係 以CVD技術於6吋矽晶圓上澱積0.8微米±5%之 薄膜 (2) Ti 薄膜:購自 silicon Valley Microelectronics,Inc.,係 訂 以CVD技術於6吋矽晶圓上澱積0.5微米±5%之 薄膜 (3) TiN 薄膜:購自 silicon Valley Microelectronics,Inc·,係 以CVD技術於6吋矽晶圓上澱積〇·5微米±5%之 薄膜 經濟部中央標準局員工消費合作社印製 ⑷氧化物薄膜:係委託國家毫微米元件實驗室, 於矽基材上熱生成之二氧化矽 D·漿液:取上述實例i_4及比較例^所得漿液,配以相同 體積、含2重量%氏〇2之水溶液,均勻攪拌15分鐘 後進行測試 研磨測試流程: 在研磨哥後,均需以膜厚測定儀測定膜之厚度。金屬膜 以四點探針量測薄膜之片電阻,再經以下公式換算得膜之 厚度: —________- 12 - 本紙張尺度適用中國國家標準(CNS ) A4規格(2i〇;^^v髮1 -*------- 514661 Α7 Β7 五、發明説明(1〇) T X R =電阻係數 (請先閱讀背面之注意事項再填寫本頁) 其中,T爲薄膜厚度(A),及R爲片電阻(Q/cm2),對各種金 屬薄膜而言,電阻係數(Ω/cm)係一常數。 本發明係採用KLA-Tericor公司之RS 75型機器測定金屬層 之膜厚。 氧化物之膜厚可直接藉由光學原理測得。本發明係使用 KLA-Tencor公司之SM300型機器測定熱氧化物之膜厚。 磨光速率之測定方式如下: 先以上述RS 75型機器測得金屬層之膜厚乃,分別以上述 實例漿液,依上述操作條件研磨丨分鐘後,以固態儀器公司 (Solid State Equipment Corporation)之 Evergreen Model 10X 型機器清洗 機台清洗晶圓,之後,將晶圓吹乾。再以Rg 75型機器測定 金屬層之膜厚T2。將Ti-T2即爲金屬層之磨光速率。 另外,以SM 300型機器測得熱氧化物之膜厚τ3,以相同 之漿液,相同之操作條件研磨丨分鐘後,經過清洗,測得膜 厚爲I。將T3 - A即爲熱氧化物之磨光速率。 所得測試數據茲列於下表1中: 經濟部中央標準局員工消費合作社印製 ___________~13- 本紙張尺度適用中國國家標準(CNS ) 五、發明説明(11) Α7 Β7 表1 移除速率 實例號 w(A/分鐘) Ti(A/分鐘) TiN(A/分鐘) Si02(A/分鐘) 實例1 4145 2976 983 237 實例2 4315 2921 950 201 實例3 5008 2337 3523 102 實例4 5273 1368 3899 210 比較例1 572 247 687 167 比較例2 1161 1198 1695 233 (請先閱讀背面之注意事項再填寫本頁) 费 經滴部中央標準局員工消費合作社印製 貫例5 重覆實例3相同之製備步驟,惟以3公斤之甲酸取代檸檬 阪’及以2公斤(NH4)2S2〇8取代硫酸铵鐵(πΐ),以氨水將pH値 碉整至4.0。所得研磨組合物之研磨測試結果,茲列於下文 表2中。實例6 重覆實例5相同之製備步驟,惟以3公斤之甘胺酸取代甲 酸,並以氨水將pH値調整至4.0。所得研磨組合物之研磨、、則 試結果,茲列於下文表2中。實例7 重覆實例5相同之製備步驟,惟以3公斤之甲醯胺取代 酸,並以氨水將pH値調整至4.0。所得研磨組合物之胡: τ磨蜊 試結果,茲列於下文表2中。 -14- 本紙張尺度適用中國國家標準(CNS ) A4規格(210X 公釐) mi -i·-·—— mi mi 1.、 mu mi ^ϋ·ϋ 、-口A7 B7 V. Description of the invention (9) --- ^-: --- φ ^! (Please read the precautions on the back before filling in this page. Β Conditions: Pressure: 5psi Temperature · 25 ° C Spindle speed: 45rpm platen rotation speed · 42 rpm Pedestal type: Rodel 1C 1400 Slurry flow rate: 150 liters / minute C · g pieces · (1) W film: from Silicon Valley Microelectronics, Inc., using CVD technology at 6 0.8 micron ± 5% thin film deposited on a 2-inch silicon wafer (2) Ti film: purchased from silicon Valley Microelectronics, Inc., is designed to deposit a 0.5 micron ± 5% thin film on a 6-inch silicon wafer by CVD technology (3) TiN thin film: purchased from silicon Valley Microelectronics, Inc., which uses CVD technology to deposit 0.5 micron ± 5% on 6-inch silicon wafers. Printed rubidium oxide by the Central Consumers Bureau of the Ministry of Economic Affairs. Thin film: The silicon dioxide D · slurry thermally generated on a silicon substrate was commissioned to the National Nanometer Component Laboratory: the slurry obtained in the above example i_4 and comparative example ^ was mixed with the same volume containing 2% by weight Aqueous solution, stir evenly for 15 minutes and then test the grinding process: After that, the thickness of the film needs to be measured with a film thickness tester. The metal film is measured with a four-point probe to measure the sheet resistance of the film, and the film thickness is converted by the following formula: —________- 12-This paper size applies to Chinese national standards (CNS) A4 specifications (2i〇; ^^ v issued 1-* ------- 514661 Α7 Β7 V. Description of the invention (1〇) TXR = resistivity (Please read the precautions on the back before filling this page ) Among them, T is the film thickness (A), and R is the sheet resistance (Q / cm2). For various metal films, the resistivity (Ω / cm) is a constant. The present invention uses RS from KLA-Tericor The 75 type machine measures the film thickness of the metal layer. The oxide film thickness can be directly measured by the optical principle. The present invention uses the SM300 model of KLA-Tencor company to measure the film thickness of the thermal oxide. The measuring method of the polishing rate As follows: First measure the film thickness of the metal layer with the above RS 75 machine, grind the slurry according to the above example, and grind it under the above operating conditions for 丨 minutes, and then clean it with the Evergreen Model 10X machine from Solid State Equipment Corporation. Machine cleaning wafer, after Blow the wafer dry. Then measure the film thickness T2 of the metal layer with an Rg 75 type machine. The Ti-T2 is the polishing rate of the metal layer. In addition, the film thickness τ3 of the thermal oxide was measured with a SM 300 machine. After grinding for 丨 minutes with the same slurry and the same operating conditions, the film thickness was measured to be I. T3-A is the polishing rate of thermal oxide. The test data obtained are listed in Table 1 below: Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs ___________ ~ 13- This paper size applies to the Chinese National Standard (CNS) V. Description of the invention (11) Α7 Β7 Table 1 Removal rate Example number w (A / minute) Ti (A / minute) TiN (A / minute) Si02 (A / minute) Example 1 4145 2976 983 237 Example 2 4315 2921 950 201 Example 3 5008 2337 3523 102 Example 4 5273 1368 3899 210 Comparative Example 1 572 247 687 167 Comparative Example 2 1161 1198 1695 233 (Please read the precautions on the back before filling out this page) Fei Jingdi Department Central Standard Bureau Staff Consumer Cooperative Co., Ltd. Printing Example 5 Repeat the same preparation steps as in Example 3 However, 3 kg of formic acid was used to replace Lemon Han 'and 2 kg (NH4) 2S2 08 was used to replace ammonium iron sulfate (πΐ), and the pH was adjusted to 4.0 with ammonia. The grinding test results of the obtained grinding compositions are shown in Table 2 below. Example 6 The same preparation procedure as in Example 5 was repeated, except that formic acid was replaced with 3 kg of glycine, and the pH was adjusted to 4.0 with ammonia water. The grinding and test results of the obtained grinding composition are shown in Table 2 below. Example 7 The same preparation procedure as in Example 5 was repeated, except that the acid was replaced with 3 kg of formamidine, and the pH was adjusted to 4.0 with ammonia water. Hu of the obtained grinding composition: τ grinding clam The test results are shown in Table 2 below. -14- This paper size is in accordance with Chinese National Standard (CNS) A4 (210X mm) mi -i ·-· —— mi mi 1., mu mi ^ ϋ · ϋ,-口

•I• I

LI 1 - -1 — — — — — —— — I 經濟部中央標準局員工消費合作社印製 ο 丄 4()61 Α7 -----------Β7_____ 五、發明説明(12) ~〜 达輕例3 重覆實例5相同之製備步驟,惟不添加(ΝΗ4)2§2〇8。所得研 磨組合物之研磨測試結果,茲列於下文表2中。 1磨測試 A·儀器:IPEC/Westech472 B ·條件:壓力:5 psi 溫度:25X: 主軸轉速:45 rpm 台板轉速:42 rpm 墊座型式:Rodel Politex 漿液流速:150毫升/分鐘 C·晶片:⑴ A1 薄膜:購自 silicon Valley Microelectronics,Inc.,係 以CVD技術於6吋矽晶圓上澱積0.85微米±5% 之薄膜,純度爲 A1 : 98.5%,Si : 1%,Cu : 0.5% (2) Ti 薄膜·講自 Silicon Valley Microelectronics,Inc.,係 以CVD技術於6吋矽晶圓上澱積0 5微米±5。/〇之 薄膜 (3) TiN 薄膜·講自 Silicon Valley Microelectronics,Inc.,係 以CVD技術於6忖石夕晶圓上澱積〇 5微米土5〇/0之 薄膜 ⑷氧化物薄膜··係委託國家毫微米元件實驗室, 於矽基材上熱生成之二氧化石夕 D·漿液:取上述實例5-7及比較例3所得漿液,配以相同體 -15- 本紙張尺度適用中國國家標準(CNS ) A4規格(210'/297公^ ~ -------- —衣-- (請先閱讀背面之注意事項再填寫本頁) -訂 W4661 A7 發明説明(13) 中 積、含5重量%氏〇2之水溶液, 進行測試 研磨測試流程如上文所述,所得測試數 均勻攪拌15分鐘後 據茲列於下表2 表2 ---------- 移除速率 實例號 Α1(Α/分鐘) Ti(A/分鐘) TiN(A/分鐘) Si〇2(&quot;分鐘) 實例5 3944 1704 3318 129 實例6 4682 1223 3380 117 實例7 3552 2279 4454 112 比較例3 1705 673 3237 192 * 衣 — I (請先閲讀背面之注意事項再填寫本頁) 訂 經濟部中央標準局員工消費合作社印製 ά-··、 |本 實例8LI 1--1 — — — — — — —— — I Printed by the Consumer Cooperatives of the Central Bureau of Standards of the Ministry of Economic Affairs (4 () 61 Α7 ----------- Β7 _____ V. Description of the Invention (12) ~~ Daqing Example 3 Repeat the same preparation steps as in Example 5 except that (NΗ4) 2§2108 is not added. The grinding test results of the obtained grinding compositions are shown in Table 2 below. 1 Mill test A · Instrument: IPEC / Westech472 B · Condition: Pressure: 5 psi Temperature: 25X: Spindle speed: 45 rpm Platen speed: 42 rpm Pedestal type: Rodel Politex Slurry flow rate: 150 ml / min C · Wafer: ⑴ A1 thin film: purchased from silicon Valley Microelectronics, Inc., is deposited by CVD technology on a 6-inch silicon wafer with a thickness of 0.85 micron ± 5%, the purity is A1: 98.5%, Si: 1%, Cu: 0.5% (2) Ti thin film · Speaking from Silicon Valley Microelectronics, Inc., it uses CVD technology to deposit 0.5 micron ± 5 on 6-inch silicon wafer. / 〇 的 膜 (3) TiN thin film · Speaking from Silicon Valley Microelectronics, Inc., it is based on the CVD technology to deposit a thin film of 0.5 micron soil 5 0/0 on a 6 忖 Shi Xi wafer. Entrusted to the National Nanometer Component Laboratory to thermally generate the silica dioxide D · slurry on a silicon substrate: Take the slurry obtained in the above Examples 5-7 and Comparative Example 3, with the same body-15. This paper size is applicable to China Standard (CNS) A4 specification (210 '/ 297cm ^ ~ -------- —Clothing-(Please read the precautions on the back before filling out this page)-Order W4661 A7 Invention Description (13) 5. The test solution containing 5% by weight of aqueous solution of 0% is tested as described above. The test number obtained is evenly stirred for 15 minutes and is listed in Table 2 below. Table 2 ---------- Remove Rate instance number A1 (A / minute) Ti (A / minute) TiN (A / minute) Si〇2 (&quot; minute) Example 5 3944 1704 3318 129 Example 6 4682 1223 3380 117 Example 7 3552 2279 4454 112 Comparative Example 3 1705 673 3237 192 * Clothing — I (Please read the precautions on the back before filling out this page) Order the staff of the Central Bureau of Standards of the Ministry of Economic Affairs Printed by the cooperative ά- ··, | Example 8

重覆實例5相同之製備步驟,惟以氨水將pH値調整J 6.5。 所得研磨組合物之研磨測試結果,茲列於下文表3中 實例9 重覆實例6相同之製備步驟,惟以氨水將pH値調整3 6.5。 所得研磨組合物之研磨測試結果,茲列於下文表3中 實例10 重覆實例7相同之製備步驟,惟以1.5公斤之乙醯胺取+ 甲酸。所得研磨組合物之研磨測試結果,茲列於下文表 中〇 -16 I度適用中國國家標準(CNS ) A4規格(210X297公釐) ^14661 A7 B7 五、發明説明(14) 生蓋例4 重覆比較例3相同之製備步驟,惟以氨水將pH値調整至 6·5。所得研磨組合物之研磨測試結果,茲列於下文表3中。 研磨测Μ Α·儀器:IPEC/Westech472 Β·條件:壓力:5psi 溫度:25°C 主軸轉速:45 rpm 台板轉速:42 rpm 墊座型式:Rodel 1C 1400 漿液流速:150毫升/分鐘 C .晶片:⑴ Cu 薄膜:購自 Silicon Valley Microelectronics,Inc.,係 以PVD技術於6吋矽晶圓上澱積0.85微米±5% 之薄膜 (2) Ti 薄膜:講自 Silicon Valley Microelectronics,Inc.,係 以CVD技術於6吋矽晶圓上澱積0.5微米±5%之 薄膜 經濟部中央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) (3) TiN 薄膜:講自 Silicon Valley Microelectronics,Inc.,係 以CVD技術於6吋矽晶圓上澱積0.5微米±5〇/〇之 薄膜 ⑷氧化物薄膜:係委託國家毫微米元件實驗室, 於石夕基材上熱生成之二氧化石夕 D ·漿液·取上述實例$ _ 1〇及比較例4所得漿液,配以相同體 積、含5重量%H2〇2之水溶液,均勾攪;拌15分鐘後 _ - 17-尽紙張尺度適用中國國家標準(CNS ) A4規格(210X 297公釐) ^&gt;14661 A7 B7 五、發明説明(15) 進行測試 研磨測試流程如上文所述,所得測試數據兹列於下表3中: 表3 ”號 (3ιι(Λ/分鐘) Ti( Α/分鐘) 實例8 7430 -----_. 1804 實例9 7217 1665 實例1 0 4001 1471 比較例4 7337 598 移除速率 4340 3677 203 211 ---,_ :__ 1#衣 II (請先閱讀背面之注意事項再填寫本頁)The same preparation steps as in Example 5 were repeated, except that the pH was adjusted to 6.5 with ammonia. The grinding test results of the obtained grinding composition are listed in Table 3 below. Example 9 The same preparation steps as in Example 6 were repeated, except that the pH was adjusted to 3 6.5 with ammonia water. The grinding test results of the obtained grinding composition are shown in Table 3 below. Example 10 was repeated with the same preparation steps as in Example 7, except that 1.5 kg of acetamide was used to obtain + formic acid. The grinding test results of the obtained grinding composition are listed in the following table. 0-16 I degree is applicable to China National Standard (CNS) A4 specification (210X297 mm) ^ 14661 A7 B7 V. Description of the invention (14) Cover example 4 The same preparation steps as in Comparative Example 3 were covered, except that the pH was adjusted to 6.5 with ammonia water. The grinding test results of the obtained grinding compositions are shown in Table 3 below. Grinding measurement Α · Instrument: IPEC / Westech472 Β · Conditions: Pressure: 5psi Temperature: 25 ° C Spindle speed: 45 rpm Platen speed: 42 rpm Pedestal type: Rodel 1C 1400 Slurry flow rate: 150 ml / min C. Wafer : ⑴ Cu thin film: purchased from Silicon Valley Microelectronics, Inc., which is based on PVD technology to deposit a 0.85 micron ± 5% thin film on a 6-inch silicon wafer. (2) Ti thin film: from Silicon Valley Microelectronics, Inc. Deposition of 0.5 micron ± 5% thin film on 6-inch silicon wafer by CVD technology. Printed by the Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs (please read the precautions on the back before filling this page). (3) TiN thin film: speak from Silicon Valley Microelectronics, Inc., uses CVD technology to deposit a 0.5 micron ± 50/0 thin film of rhenium oxide film on a 6-inch silicon wafer: it was commissioned to the National Nanometer Component Laboratory to heat on Shixi substrate Resulting Dioxide of the Oxygen D · Slurry · Take the slurry obtained from the above example $ _10 and Comparative Example 4 and mix it with the same volume of aqueous solution containing 5% by weight of H2O2; stir for 15 minutes _-17 -Applicable to Chinese national standards as far as possible CNS) A4 specification (210X 297 mm) ^ &gt; 14661 A7 B7 V. Description of the invention (15) The test grinding test process is as described above, and the test data obtained is listed in Table 3 below: Table 3 "No. (3ιι (Λ / minute) Ti (Α / minute) Example 8 7430 -----_. 1804 Example 9 7217 1665 Example 1 0 4001 1471 Comparative Example 4 7337 598 Removal rate 4340 3677 203 211 ---, _: __ 1 # 衣 II (Please read the precautions on the back before filling in this page)

、1T 由以上實例可知,本發明研廢相人札__ 令贫竹心、、且口物可有效提高金屬薄 膜,尤其Ti及TiN薄膜之研磨效率,#浐合, 1T From the above examples, it can be seen that the waste phase of the present invention can make people feel poor, and the mouthpiece can effectively improve the grinding efficiency of metal films, especially Ti and TiN films, # 浐 合

午亚知馬對Cu/Ti及Cu/TiN 之研磨選擇性。 經濟部中央標準局員工消費合作社印製 -18-Wu Yazhi's grinding selectivity for Cu / Ti and Cu / TiN. Printed by the Consumer Cooperatives of the Central Standards Bureau of the Ministry of Economic Affairs -18-

Claims (1)

514661 第〇871〇6624號專利申請案 B8 C8 中文申請專利範圍修正本(91年10月)D8 六、申請專利範圍 1. 一種用於半導體製程中研磨金屬薄膜之化學機械研磨 組合物,其包含1-25重量%之研磨顆粒;0.1-20重量% 之作為研磨促進劑之緩衝劑,其中該緩衝劑包括含過 硫酸基之化合物或含鐵(III)之鹽類及含羧基或醯胺基之 化合物;及1-10重量%之氧化劑, 其中該含過硫酸基化合物係選自由H2S208、K2S208、 (NH4)2S208、Na2S208及其混合物所組成之群,該含鐵(III) 之鹽類係選自由氰鐵酸鉀、硫酸銨鐵(III)、硝酸鐵(III) 及其混合物所組成之群,該含羧基化合物係選自由甲 酸、乙酸、丙酸、丁酸、戊酸、己酸、羥基醋酸、乳 酸、乙二酸、丙二酸、丁二酸、戊二酸、羥基丁二酸、 酒石酸、半乳糖二酸及檸檬酸、及其鹽類、及此等酸 及/或其鹽類之混合物所組成之群,而該含醯胺基化合 物係選自由甲醯胺、乙醯胺、丙醯胺、N-甲基甲醯胺、 N-甲基乙醯胺、尿素、甲基脲、乙基脲、二甲基脲及 二乙基脲所組成之群,及 其中該研磨劑係選自由Si02、Al2〇3、Zr02、Ce02、SiC、 Fe203、Ti02、Si3N4、或其混合物所組成之群,而該氧化 劑係選自由 H202、KI03、KBr〇3、K2Cr207、Κ2Μη207、KMn〇4、 HOC1、CH3COOOH、及其混合物所組成之群。 2. 根據申請專利範圍第1項之組合物,其係包含3-10重 量%之該研磨顆粒;及6-15重量%之該作為研磨促進劑 之緩衝劑。 O:\52\52484-911004.DOC\ 5 · 1 · 本紙張尺度適用中國國家標準(CNS) Α4規格(210X 297公釐) 裝 訂514661 Patent Application No. 0871〇6624 B8 C8 Chinese Patent Application Scope Amendment (October 91) D8 6. Patent Application Scope 1. A chemical mechanical polishing composition for polishing metal thin films in a semiconductor process, comprising 1-25% by weight of abrasive particles; 0.1-20% by weight of a buffering agent as a grinding accelerator, wherein the buffering agent includes a compound containing a persulfate group or a salt containing iron (III) and a carboxyl group or amidino group Compounds; and 1-10% by weight of an oxidizing agent, wherein the persulfate group-containing compound is selected from the group consisting of H2S208, K2S208, (NH4) 2S208, Na2S208, and mixtures thereof, and the iron (III) -containing salts are Selected from the group consisting of potassium ferricyanide, iron (III) ammonium sulfate, iron (III) nitrate and mixtures thereof, the carboxyl-containing compound is selected from the group consisting of formic acid, acetic acid, propionic acid, butyric acid, valeric acid, hexanoic acid, Glycolic acid, lactic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, hydroxysuccinic acid, tartaric acid, galactonic acid and citric acid, and their salts, and these acids and / or their salts A group of mixtures of The amido-containing compound is selected from the group consisting of formamide, acetamide, propylamine, N-methylformamide, N-methylacetamide, urea, methylurea, ethylurea, and dimethylurea. And diethylurea, and the abrasive is selected from the group consisting of Si02, Al2O3, Zr02, Ce02, SiC, Fe203, Ti02, Si3N4, or a mixture thereof, and the oxidant is selected from the group consisting of A group consisting of H202, KI03, KBr03, K2Cr207, K2Mη207, KMn04, HOC1, CH3COOOH, and mixtures thereof. 2. The composition according to item 1 of the scope of patent application, which comprises 3 to 10% by weight of the abrasive particles; and 6 to 15% by weight of the buffering agent as a grinding accelerator. O: \ 52 \ 52484-911004.DOC \ 5 · 1 · This paper size applies to China National Standard (CNS) Α4 size (210X 297 mm) binding 線 514661 8 8 8 8 A B c D 、申請專利範圍 3 ·根據申請專利範圍第1項之組合物,其係包含4-6重量 %之該氧化劑。 -2- O:\52\52484-911004.DOC\ 本紙張尺度適用中國國家標準(CNS) A4規格(210 χ 297公釐)Line 514661 8 8 8 8 A B c D, scope of patent application 3 · The composition according to item 1 of the scope of patent application, which contains 4-6% by weight of the oxidant. -2- O: \ 52 \ 52484-911004.DOC \ This paper size applies to China National Standard (CNS) A4 specification (210 x 297 mm)
TW87106624A 1998-04-29 1998-04-29 Chemical-mechanical abrasive composition for use in semiconductor processing TW514661B (en)

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