JP7249725B2 - Surface treated cerium oxide powder and polishing composition - Google Patents

Surface treated cerium oxide powder and polishing composition Download PDF

Info

Publication number
JP7249725B2
JP7249725B2 JP2020511755A JP2020511755A JP7249725B2 JP 7249725 B2 JP7249725 B2 JP 7249725B2 JP 2020511755 A JP2020511755 A JP 2020511755A JP 2020511755 A JP2020511755 A JP 2020511755A JP 7249725 B2 JP7249725 B2 JP 7249725B2
Authority
JP
Japan
Prior art keywords
acid
cerium oxide
oxide powder
peak area
polishing composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
JP2020511755A
Other languages
Japanese (ja)
Other versions
JP2021508308A (en
Inventor
ホ ソン,セ
サン チョ,ムーン
Original Assignee
アドバンスト ナノ プロダクツ カンパニー リミテッド
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by アドバンスト ナノ プロダクツ カンパニー リミテッド filed Critical アドバンスト ナノ プロダクツ カンパニー リミテッド
Publication of JP2021508308A publication Critical patent/JP2021508308A/en
Application granted granted Critical
Publication of JP7249725B2 publication Critical patent/JP7249725B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F17/00Compounds of rare earth metals
    • C01F17/20Compounds containing only rare earth metals as the metal element
    • C01F17/206Compounds containing only rare earth metals as the metal element oxide or hydroxide being the only anion
    • C01F17/224Oxides or hydroxides of lanthanides
    • C01F17/235Cerium oxides or hydroxides
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09GPOLISHING COMPOSITIONS; SKI WAXES
    • C09G1/00Polishing compositions
    • C09G1/02Polishing compositions containing abrasives or grinding agents
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/14Anti-slip materials; Abrasives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Treatment Of Semiconductor (AREA)
  • Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Description

本発明は、表面処理された酸化セリウム粉末及び研磨組成物に関する。 The present invention relates to surface-treated cerium oxide powders and polishing compositions.

半導体素子の高集積化に伴い、フォトリソグラフィーマージンを確保し且つ配線の長さを最小化するために、下部膜の平坦化技術が要求される。下部膜を平坦化するための方法として、BPSG(BoroPhosphorus Silicate Glass)リフロー、SOG(Spin On Glass)エッチバック(etch back)、化学機械研磨(Chemical Mechanical Polishing、以下「CMP」という)工程などがある。CMP工程は、リフロー工程やエッチバック工程で達成できない広い空間領域の平坦化及び低温平坦化を達成することができるので、次世代の半導体素子で有力な平坦化技術として台頭している。 As semiconductor devices become more highly integrated, planarization techniques for lower layers are required in order to secure a photolithographic margin and minimize the length of interconnections. Methods for planarizing the lower layer include BPSG (BoroPhosphorus Silicate Glass) reflow, SOG (Spin On Glass) etch back, chemical mechanical polishing (CMP), and the like. . The CMP process is emerging as a promising planarization technique for next-generation semiconductor devices because it can achieve planarization of a wide spatial region and low-temperature planarization that cannot be achieved by the reflow process or the etch-back process.

しかし、配線抵抗を低減するために配線の厚さを増加させるにつれて、金属間の電気的絶縁のための金属間絶縁層(InterMetal Dielectric layer、以下「IMD」という)のデポ量も相対的に増加することにより、CMP段階で平坦化させるための絶対除去量が大幅に増加している。
ところが、従来のCMP用スラリーは、除去速度が遅いため、CMP時間が非常に長くなることにより、工程生産性に劣るという問題点がある。
However, as the thickness of the wiring increases to reduce the wiring resistance, the deposition amount of an intermetal dielectric layer (IMD) for electrical insulation between metals also increases. By doing so, the absolute removal amount for planarization in the CMP step is greatly increased.
However, since the conventional CMP slurry has a slow removal rate, the CMP time is very long, resulting in poor process productivity.

韓国公開特許第10-2002-0007607号明細書Korean Patent No. 10-2002-0007607

本発明は、研磨速度に非常に優れた、表面処理された酸化セリウム粉末及びこれを含む研磨組成物を提供することを目的とする。 SUMMARY OF THE INVENTION An object of the present invention is to provide a surface-treated cerium oxide powder and a polishing composition containing the same, which have excellent polishing speed.

上記の課題を解決するための手段として、
本発明は、有機物で表面処理された酸化セリウム粉末であって、X線光電子分光(XPS)測定時のO-Cピーク面積がO-Ceピーク面積よりもさらに大きい酸化セリウム粉末を提供する。特に、O-Cピーク面積がO-Ceピーク面積に対して1.1倍乃至4.0倍の範囲内である酸化セリウム粉末を提供する。
As a means to solve the above problems,
The present invention provides a cerium oxide powder surface-treated with an organic substance, which has an OC peak area larger than an O-Ce peak area when measured by X-ray photoelectron spectroscopy (XPS). In particular, a cerium oxide powder is provided in which the O--C peak area is in the range of 1.1 to 4.0 times the O--Ce peak area.

また、本発明は、有機物で表面処理された酸化セリウム粉末であって、アルゴンイオンで2KeV、300sの条件にて表面エッチングした後、XPS測定時のO-Ceピーク面積がO-Cピーク面積よりもさらに大きい酸化セリウム粉末を提供する。特に、OCのピーク面積がO-Ceピーク面積に対して0.10倍乃至0.40倍の範囲内である酸化セリウム粉末を提供する。 The present invention also provides a cerium oxide powder surface-treated with an organic substance, which is surface-etched with argon ions under conditions of 2 KeV and 300 s. also provide larger cerium oxide powders. In particular, a cerium oxide powder is provided in which the OC peak area is in the range of 0.10 to 0.40 times the O—Ce peak area.

また、本発明は、有機物で表面処理された酸化セリウム粉末において、次の数式を満足する酸化セリウム粉末を提供する。 In addition, the present invention provides a cerium oxide powder surface-treated with an organic substance that satisfies the following formula.

4.0≦A/B≦40
A:表面測定条件でのXPS測定時のO-Cピーク面積/O-Ceピーク面積
B:エッチング測定条件でのXPS測定時のO-Cピーク面積/O-Ceピーク面積
4.0≤A/B≤40
A: OC peak area/O—Ce peak area during XPS measurement under surface measurement conditions B: OC peak area/O—Ce peak area during XPS measurement under etching measurement conditions

特に、次の数式を満足する酸化セリウム粉末を提供する。 In particular, a cerium oxide powder that satisfies the following formula is provided.

10.0≦A/B≦35.0 10.0≤A/B≤35.0

前記有機物は、酢酸、ギ酸、ピバル酸、プロピオン酸、4-ヒドロキシフェニル酢酸を含むカルボン酸、パルミチン酸、ステアリン酸、オレイン酸、アラキドン酸、リノール酸、リノレン酸を含む炭素数8~20の飽和または不飽和脂肪酸の中から選択でき、前記酸化セリウム粉末は、研磨剤の用途に使用できる。 The organic substance is a carboxylic acid including acetic acid, formic acid, pivalic acid, propionic acid, 4-hydroxyphenylacetic acid, palmitic acid, stearic acid, oleic acid, arachidonic acid, linoleic acid, and linolenic acid. or unsaturated fatty acids, and the cerium oxide powder can be used as an abrasive.

また、本発明は、研磨剤及び溶剤を含む研磨組成物であって、前記研磨剤は、前記酸化セリウム粉末を含む研磨組成物を提供する。 The present invention also provides a polishing composition comprising an abrasive and a solvent, wherein the abrasive comprises the cerium oxide powder.

上述した構成的特徴を有する本発明は、研磨速度に非常に優れた、表面処理された酸化セリウム粉末及びこれを含む研磨組成物を提供することができる。 INDUSTRIAL APPLICABILITY The present invention having the above structural features can provide a surface-treated cerium oxide powder having a very high polishing rate and a polishing composition containing the same.

以下、実施例によって本発明をより詳細に説明する。下記の説明は、本発明の具体的な一例についてのものであるので、たとえ断定的、限定的な表現があっても、特許請求の範囲から定められる権利範囲を限定するものではない。 The present invention will be described in more detail below by way of examples. The following description is of a specific example of the present invention, and therefore any categorical, limiting statements should not limit the scope of rights defined by the claims.

本発明による一実施例は、有機物で表面処理された酸化セリウム粉末であって、X線光電子分光(XPS)測定時のO-Cピーク面積がO-Ceピーク面積よりもさらに大きい酸化セリウム粉末を提供する。特に、O-Cピーク面積がO-Ceピーク面積に対して1.1倍乃至4.0倍の範囲内である酸化セリウム粉末を提供する。 An embodiment according to the present invention is a cerium oxide powder surface-treated with an organic substance, wherein the OC peak area when measured by X-ray photoelectron spectroscopy (XPS) is larger than the O-Ce peak area. offer. In particular, a cerium oxide powder is provided in which the O--C peak area is in the range of 1.1 to 4.0 times the O--Ce peak area.

本発明に係る別の一実施例は、有機物で表面処理された酸化セリウム粉末であって、2KeV、300sの条件で表面エッチングした後、XPS測定時のO-Ceピーク面積がO-Cピーク面積よりもさらに大きい酸化セリウム粉末を提供する。特に、O-Cピーク面積がO-Ceピーク面積に対して0.10倍乃至0.40倍の範囲内である酸化セリウム粉末を提供する。 Another embodiment according to the present invention is a cerium oxide powder surface-treated with an organic substance, and after surface etching under conditions of 2 KeV and 300 s, the O—Ce peak area during XPS measurement is To provide a cerium oxide powder that is even larger than In particular, a cerium oxide powder is provided in which the O--C peak area is in the range of 0.10 to 0.40 times the O--Ce peak area.

本発明に係る別の一実施例は、有機物で表面処理された酸化セリウム粉末であって、次の数式を満足する酸化セリウム粉末を提供する。 Another embodiment of the present invention provides a cerium oxide powder surface-treated with an organic material, wherein the cerium oxide powder satisfies the following formula.

4.0≦A/B≦40
A:表面測定条件でのXPS測定時のO-Cピーク面積/O-Ceピーク面積
B:エッチング測定条件でのXPS測定時のO-Cピーク面積/O-Ceピーク面積
4.0≤A/B≤40
A: OC peak area/O—Ce peak area during XPS measurement under surface measurement conditions B: OC peak area/O—Ce peak area during XPS measurement under etching measurement conditions

特に、次の数式を満足する酸化セリウム粉末を提供する。 In particular, a cerium oxide powder that satisfies the following formula is provided.

10.0≦A/B≦35.0 10.0≤A/B≤35.0

本発明者は、酸化セリウム粉末の表面処理が研磨速度に関連することを確認した。特に、どのように表面処理が施されたかによって、研磨速度性能に大きな影響を及ぼし、XPS測定時に上記の範囲を満足すればこそ研磨速度が著しく向上することを見出し、後述する実施例から分かるように、上記の範囲内で研磨速度に非常に優れることを確認した。 The inventors have confirmed that the surface treatment of the cerium oxide powder is related to the polishing rate. In particular, it was found that the polishing rate performance is significantly affected by how the surface treatment is performed, and that the polishing rate is significantly improved only when the above range is satisfied during XPS measurement. As can be seen from the examples described later. In addition, it was confirmed that the polishing rate was very excellent within the above range.

上記の範囲を満足する酸化セリウム粉末と研磨組成物の製造方法は、制限されず、様々な方法で製造できる。酸化セリウム粉末は、湿式酸化法、ゾルゲル(Sol Gel)法、水熱合成法、か焼法などを使用することができ、後述する実施例で望ましい方法を提示する。つまり、セリウム前駆体と塩基性物質とを混合してセリウム前駆体を酸化させて酸化セリウムを得ることができる。その後、洗浄及び乾燥を行い、粉砕した後、熱処理して有機物で表面処理した後、水で希釈して酸化セリウム粉末を含む研磨組成物を得ることができる。本発明の一実施例に係る酸化セリウム粉末を得るために、有機物の種類や有機物の含有量などが重要な因子として作用できるが、実施例を介して具体的に例示している。セリウム前駆体としては、特に制限されず、好ましくは塩の形態であり得る。その非制限的な例としては硝酸セリウム(cerium nitrate)、酢酸セリウム(cerium acetate)、これらの水和物などがあり、これらは単独で或いは2種以上組み合わせて使用できる。 The method for producing the cerium oxide powder and the polishing composition satisfying the above range is not limited and can be produced by various methods. A wet oxidation method, a sol-gel method, a hydrothermal synthesis method, a calcination method, etc., can be used to prepare the cerium oxide powder, and preferred methods will be presented in Examples below. That is, cerium oxide can be obtained by mixing a cerium precursor and a basic substance and oxidizing the cerium precursor. Then, it is washed and dried, pulverized, heat-treated, surface-treated with an organic material, and diluted with water to obtain a polishing composition containing cerium oxide powder. In order to obtain the cerium oxide powder according to an embodiment of the present invention, the type of organic matter, the content of the organic matter, etc. may act as important factors, which are illustrated in detail through examples. The cerium precursor is not particularly limited, and may preferably be in the form of a salt. Non-limiting examples thereof include cerium nitrate, cerium acetate, hydrates thereof, and the like, which can be used alone or in combination of two or more.

酸化セリウム粉末を表面処理するために使用する有機物は、制限されないが、酢酸、ギ酸、ピバル酸、プロピオン酸、4-ヒドロキシフェニル酢酸などのカルボン酸、パルミチン酸、ステアリン酸、オレイン酸、アラキドン酸、リノール酸、リノレン酸などの炭素数8~20の飽和または不飽和脂肪酸などを挙げることができる。表面処理方法としては、粉末を別個の分散機を用いて表面処理剤でコーティングする方法があり、この他にも、表面処理は、水に酸化セリウム粉末と表面処理剤を仕込んで撹拌することにより研磨組成物を製造する過程において行われてもよいが、これに限定されない。 Organic substances used for surface treatment of cerium oxide powder include, but are not limited to, acetic acid, formic acid, pivalic acid, propionic acid, carboxylic acids such as 4-hydroxyphenylacetic acid, palmitic acid, stearic acid, oleic acid, arachidonic acid, Examples include saturated or unsaturated fatty acids having 8 to 20 carbon atoms such as linoleic acid and linolenic acid. As a surface treatment method, there is a method in which the powder is coated with a surface treatment agent using a separate disperser. In addition, the surface treatment is performed by adding cerium oxide powder and a surface treatment agent to water and stirring. It may be performed in the process of manufacturing the polishing composition, but is not limited to this.

酸化セリウム粉末を含む研磨組成物は、溶剤として、水を使用してもよく、有機溶剤を一部混合して使用してもよい。この他にも、多様な添加剤、例えば、分散剤、欠陥抑制剤、酸化剤、研磨促進剤、pH調整剤などが含まれ得る。
以下、実施例についてより詳細に説明する。
The polishing composition containing the cerium oxide powder may use water as a solvent, or may be partially mixed with an organic solvent. In addition, various additives such as dispersants, defect inhibitors, oxidizing agents, polishing accelerators, pH adjusters, etc. may be included.
Examples will be described in more detail below.

<実施例1>
硝酸セリウム水和物(Ce(NO・6HO)2.5kgを水3.5kgに溶解した後、1時間撹拌して前駆体溶液を製造した。アンモニア水3.2kgを0.4kg/minの流量で前駆体溶液に投入し、前駆体溶液は攪拌した。アンモニア水の投入が完了した後、80℃に昇温し、圧力を2barに昇圧して攪拌しながら12時間反応させた。得られた酸化セリウムをフィルタープレスで濾過、洗浄し、200℃で12時間乾燥させた後、粉砕し、ベルト炉にて900℃で90分間熱処理を行った。その後、酢酸を酸化セリウム粉末に対して重量%添加して分散機で分散させて表面処理し、0.3μmのノミナル(nominal)フィルターで濾過し、希釈して酸化セリウムスラリーを製造した。
粉末の表面処理特性を分析するために、次の条件でX線光電子分光(XPS)を行って粉末の表面を測定し、その結果を表2に示した。
<Example 1>
2.5 kg of cerium nitrate hydrate (Ce(NO 3 ) 3.6H 2 O) was dissolved in 3.5 kg of water and stirred for 1 hour to prepare a precursor solution. 3.2 kg of aqueous ammonia was added to the precursor solution at a flow rate of 0.4 kg/min, and the precursor solution was stirred. After the addition of aqueous ammonia was completed, the temperature was raised to 80° C., the pressure was raised to 2 bar, and the reaction was carried out for 12 hours while stirring. The obtained cerium oxide was filtered with a filter press, washed, dried at 200° C. for 12 hours, pulverized, and heat-treated at 900° C. for 90 minutes in a belt furnace. After that, 1 % by weight of acetic acid was added to the cerium oxide powder, dispersed in a disperser, surface-treated, filtered through a 0.3 μm nominal filter, and diluted to prepare a cerium oxide slurry.
In order to analyze the surface treatment properties of the powder, X-ray photoelectron spectroscopy (XPS) was performed under the following conditions to measure the surface of the powder, and the results are shown in Table 2.

<測定条件>
1.XPS装備名/メーカー:K-Alpha+/ThermoFisher Scientific製
<Measurement conditions>
1. XPS equipment name/manufacturer: K-Alpha+/ThermoFisher Scientific

2.測定条件
1)X線源:Monochromated Al X-Ray sources(Al Kα line:1486.6eV)
2)X線電源:12kV、10mA
3)サンプリングエリア:400μm(直径)
4)ナロースキャン:パスエネルギー(pass energy)40eV、ステップサイズ0.05eV
5)真空:3x10-9mbar
6)キャリブレーション:No
7)フラッドガンは電荷補償に使用される(Flood gun is used for charge compensation):ON
2. Measurement conditions 1) X-ray source: Monochromated Al X-Ray sources (Al Kα line: 1486.6 eV)
2) X-ray power supply: 12kV, 10mA
3) Sampling area: 400 μm (diameter)
4) Narrow scan: pass energy 40 eV, step size 0.05 eV
5) Vacuum: 3x10-9mbar
6) Calibration: No
7) Flood gun is used for charge compensation: ON

また、粉末表面の一部を下記の条件でエッチングし、上記の条件でXPSを行い、その結果を表2に示した。 Also, part of the powder surface was etched under the following conditions, and XPS was performed under the above conditions.

<エッチング条件>
Arイオンエッチング:2keV、600sec、ラスターサイズ2x2mm
また、酸化セリウムスラリーの研磨テストのために、下記の条件でテストし、その結果を表2に示した。
<Etching conditions>
Ar ion etching: 2 keV, 600 sec, raster size 2 x 2 mm
Also, for the polishing test of the cerium oxide slurry, tests were conducted under the following conditions, and the results are shown in Table 2.

研磨テスト:CMP装備(モデル名:斗山UNIPLA231)
パッド:IC1000TM A2 PAD 20‘*1.18’ ACAO:1Y10
時間:60秒
スピンドル速度:85rpm
ウエハー圧力:5psi
スラリーフローレート:200cc/min
ウエハー:8inch(PETEOS)
ウエハー厚さ:12000Å
Polishing test: CMP equipment (model name: Doosan UNIPLA231)
Pad: IC1000TM A2 PAD 20'*1.18' ACAO: 1Y10
Time: 60 seconds Spindle speed: 85 rpm
Wafer pressure: 5 psi
Slurry flow rate: 200cc/min
Wafer: 8 inch (PETEOS)
Wafer thickness: 12000 Å

<実施例2>乃至<実施例5>
実施例1において下記表1に提示した条件以外は実施例1と同様にして行った。
<Example 2> to <Example 5>
Example 1 was carried out in the same manner as in Example 1 except for the conditions shown in Table 1 below.

<比較例1>乃至<比較例3>
実施例1において下記表1に提示した条件以外は実施例1と同様にして行った。
<Comparative Example 1> to <Comparative Example 3>
Example 1 was carried out in the same manner as in Example 1 except for the conditions shown in Table 1 below.

Figure 0007249725000001
Figure 0007249725000001

Figure 0007249725000002
Figure 0007249725000002

表2より、A/Bの値が高い場合には、研磨速度(RR)値が高いが、比較例2のようにA/Bの値が過度に高い場合には、むしろRR値が低いことが分かった。このようにA/Bの値が研磨速度性能と深く関連していることを確認することができる。 From Table 2, when the A/B value is high, the polishing rate (RR) value is high, but when the A/B value is excessively high as in Comparative Example 2, the RR value is rather low. I found out. Thus, it can be confirmed that the value of A/B is closely related to the polishing speed performance.

また、Aの値は1よりも高く、Bの値は1よりも低い場合には、RR値が高いことが分かった。 It was also found that when the value of A is higher than 1 and the value of B is lower than 1, the RR value is high.

また、O-Cピーク面積がO-Ceピーク面積に対して1.1倍乃至4.0倍の範囲内である場合には研磨速度に優れており、O-Cピーク面積がO-Ceピーク面積に対して0.10倍乃至0.40倍の範囲内である場合には研磨速度に優れていることを確認することができる。 Further, when the OC peak area is in the range of 1.1 to 4.0 times the O—Ce peak area, the polishing rate is excellent, and the OC peak area is the O—Ce peak. It can be confirmed that the polishing rate is excellent when it is within the range of 0.10 to 0.40 times the area.

Claims (3)

酢酸、ギ酸、ピバル酸、プロピオン酸、パルミチン酸、ステアリン酸、オレイン酸、アラキドン酸、リノール酸、リノレン酸から選ばれた一種以上の飽和または不飽和カルボン酸から選択される有機物で表面処理された酸化セリウム粉末であって、
下記の測定値の比率が10.0≦A/B≦35.0
である粉末。
A:表面測定条件でのXPS測定時のO-Cピーク面積/O-Ceピーク面積
B:エッチング測定条件でのXPS測定時のO-Cピーク面積/O-Ceピーク面積
surface-treated with an organic material selected from one or more saturated or unsaturated carboxylic acids selected from acetic acid, formic acid, pivalic acid, propionic acid, palmitic acid, stearic acid, oleic acid, arachidonic acid, linoleic acid, and linolenic acid A cerium oxide powder,
The ratio of the following measured values is 10.0 ≤ A/B ≤ 35.0
A powder that is
A: OC peak area/O—Ce peak area during XPS measurement under surface measurement conditions B: OC peak area/O—Ce peak area during XPS measurement under etching measurement conditions
請求項1に記載の研摩剤用酸化セリウム粉末。 The cerium oxide powder for abrasives according to claim 1. 請求項1または2に記載の酸化セリウム粉末と溶剤からなる研磨剤組成物。An abrasive composition comprising the cerium oxide powder according to claim 1 or 2 and a solvent.
JP2020511755A 2017-08-31 2017-08-31 Surface treated cerium oxide powder and polishing composition Active JP7249725B2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/KR2017/009568 WO2019045151A1 (en) 2017-08-31 2017-08-31 Surface-treated cerium oxide powder and polishing composition

Publications (2)

Publication Number Publication Date
JP2021508308A JP2021508308A (en) 2021-03-04
JP7249725B2 true JP7249725B2 (en) 2023-03-31

Family

ID=65527670

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2020511755A Active JP7249725B2 (en) 2017-08-31 2017-08-31 Surface treated cerium oxide powder and polishing composition

Country Status (2)

Country Link
JP (1) JP7249725B2 (en)
WO (1) WO2019045151A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112538623A (en) * 2020-12-01 2021-03-23 上海易慧机电科技有限公司 Stainless steel surface passivation process

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007051057A (en) 2005-08-12 2007-03-01 Degussa Ag Cerium oxide powder and cerium oxide dispersion liquid
JP2012146974A (en) 2010-12-24 2012-08-02 Hitachi Chem Co Ltd Polishing solution and substrate polishing method using polishing solution
CN104178033A (en) 2013-05-27 2014-12-03 天津西美半导体材料有限公司 Nano cerium oxide polishing liquid composition

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09139368A (en) * 1995-11-14 1997-05-27 Sony Corp Chemically and mechanically polishing method
US6332835B1 (en) * 1997-11-20 2001-12-25 Canon Kabushiki Kaisha Polishing apparatus with transfer arm for moving polished object without drying it
US8877207B2 (en) * 2010-09-17 2014-11-04 University Of Central Florida Research Foundation, Inc. Nanoparticles of cerium oxide targeted to an amyloid-beta antigen of Alzheimer's disease and associated methods
US8859428B2 (en) * 2012-10-19 2014-10-14 Air Products And Chemicals, Inc. Chemical mechanical polishing (CMP) composition for shallow trench isolation (STI) applications and methods of making thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007051057A (en) 2005-08-12 2007-03-01 Degussa Ag Cerium oxide powder and cerium oxide dispersion liquid
JP2012146974A (en) 2010-12-24 2012-08-02 Hitachi Chem Co Ltd Polishing solution and substrate polishing method using polishing solution
CN104178033A (en) 2013-05-27 2014-12-03 天津西美半导体材料有限公司 Nano cerium oxide polishing liquid composition

Also Published As

Publication number Publication date
JP2021508308A (en) 2021-03-04
WO2019045151A1 (en) 2019-03-07

Similar Documents

Publication Publication Date Title
KR101623428B1 (en) Metal compound coated colloidal particles, process for making and use therefor
KR100928456B1 (en) Chemical mechanical polishing slurry composition including non-ionized, heat activated nano catalyst and polishing method using the same
CN106103637B (en) The manufacture method of abrasive composition and Ginding process and abrasive composition
TWI406815B (en) Method for preparing cerium oxide, cerium oxide prepared therefrom and cmp slurry comprising the same
JP2007266500A (en) Touch-up cmp slurry and manufacturing method of semiconductor device fabrication
JP2005286336A (en) Abrasives and compositions for chemical mechanical planarization of tungsten and titanium
JP2023539508A (en) Cerium oxide particles, slurry composition for chemical mechanical polishing containing the same, and method for manufacturing semiconductor devices
JP2015019058A (en) Aqueous dispersion for chemical mechanical polishing, and chemical mechanical polishing method
JP7249725B2 (en) Surface treated cerium oxide powder and polishing composition
TW201712098A (en) Chemical mechanical polishing composition and chemical mechanical polishing method capable of performing high speed polishing reducing the corrosion of tungsten film surface
DE10060343A1 (en) Polishing slurry for the chemical mechanical polishing of metal and dielectric structures
JP2011181884A (en) Cmp polishing liquid and polishing method using the cmp polishing liquid
TW201529770A (en) Manufacturing method of polishing agent, polishing method, and manufacturing method of semiconductor integrated circuit device
KR101915642B1 (en) Surface-treated cerium oxide powder and CMP composition
KR20150112849A (en) Polishing composition
TWI621673B (en) Cmp slurry composition for organic film ?????????????????????????????????????????????????????????????and polishing method using the same
JP7038022B2 (en) Abrasive grain dispersion for polishing containing ceria-based fine particle dispersion, its manufacturing method, and ceria-based fine particle dispersion.
Zhang et al. Synthesis of Al2O3@ MnO2 composite abrasives and their chemical mechanical polishing performance on silicon carbide (SiC)
JP7133414B2 (en) Polishing composition
TWI734803B (en) Manufacturing method of polishing composition and polishing method
TW202106849A (en) Abrasive grains and chemical mechanical polishing composition
KR20220060342A (en) Method for producing composite particles in which the core is coated with cerium oxide particles, and composite particles manufactured thereby
JPH10172934A (en) Composition for polishing
JP2009206148A (en) Polishing composition
TW201533184A (en) Polishing agent, polishing method, and manufacturing method of semiconductor integrated circuit device

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20200827

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20210113

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20210914

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20211214

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20220112

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20220214

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20220311

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20220531

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20220831

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20221031

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20221124

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20221215

RD01 Notification of change of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7421

Effective date: 20221219

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20221221

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20230221

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20230319

R150 Certificate of patent or registration of utility model

Ref document number: 7249725

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150