JP4776388B2 - Cerium oxide abrasive and substrate polishing method - Google Patents

Cerium oxide abrasive and substrate polishing method Download PDF

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JP4776388B2
JP4776388B2 JP2006029041A JP2006029041A JP4776388B2 JP 4776388 B2 JP4776388 B2 JP 4776388B2 JP 2006029041 A JP2006029041 A JP 2006029041A JP 2006029041 A JP2006029041 A JP 2006029041A JP 4776388 B2 JP4776388 B2 JP 4776388B2
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cerium oxide
particles
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寅之助 芦沢
裕人 大槻
誠人 吉田
裕樹 寺崎
靖 倉田
純 松沢
清仁 丹野
剛史 桜田
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Showa Denko Materials Co Ltd
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Hitachi Chemical Co Ltd
Showa Denko Materials Co Ltd
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Description

本発明は、酸化セリウム研磨剤及び基板の研磨法に関する。   The present invention relates to a cerium oxide abrasive and a method for polishing a substrate.

従来、半導体装置の製造工程において、プラズマ−CVD、低圧−CVD等の方法で形成されるSiO絶縁膜等無機絶縁膜層を平坦化するための化学機械研磨剤として、コロイダルシリカ系の研磨剤が一般的に検討されている。コロイダルシリカ系の研磨剤は、シリカ粒子を四塩化珪酸を熱分解する等の方法で粒成長させ、アルカリ溶液でpH調整を行って製造している。しかしながら、この様な研磨剤は無機絶縁膜の研磨速度が充分な速度を持たず、実用化には低研磨速度という技術課題がある。 Conventionally, a colloidal silica-based polishing agent as a chemical mechanical polishing agent for planarizing an inorganic insulating film layer such as a SiO 2 insulating film formed by a method such as plasma-CVD or low-pressure CVD in a manufacturing process of a semiconductor device Is generally considered. Colloidal silica-based abrasives are produced by growing silica particles by a method such as thermal decomposition of tetrachlorosilicic acid and adjusting the pH with an alkaline solution. However, such an abrasive does not have a sufficient polishing rate for the inorganic insulating film, and there is a technical problem of a low polishing rate for practical use.

一方、フォトマスクやレンズ等のガラス表面研磨として、酸化セリウム研磨剤が用いられている。酸化セリウム粒子は、シリカ粒子やアルミナ粒子に比べ硬度が低く、したがって研磨表面に傷が入りにくいことから仕上げ鏡面研磨に有用である。また、酸化セリウムは強い酸化剤として知られるように、化学的活性な性質を有している。この利点を活かし、絶縁膜用化学機械研磨剤への適用が有用である。しかしながら、ガラス表面研磨用酸化セリウム研磨剤は、不純物を多く含有するためそのまま半導体用研磨剤として適用することはできない。さらに、ガラス表面研磨用酸化セリウム研磨剤をそのまま無機絶縁膜研磨に適用すると、酸化セリウム粒子径(一次粒子や凝集粒子)が大きく、そのため絶縁膜表面に目視で観察できる研磨傷が入ってしまう。   On the other hand, cerium oxide abrasives are used for polishing glass surfaces such as photomasks and lenses. Cerium oxide particles have a lower hardness than silica particles and alumina particles, and are therefore useful for finish mirror polishing because they are less likely to scratch the polished surface. Moreover, cerium oxide has a chemically active property as known as a strong oxidant. Taking advantage of this advantage, application to a chemical mechanical polishing agent for insulating films is useful. However, the cerium oxide abrasive for polishing glass surfaces cannot be applied as it is as an abrasive for semiconductors because it contains many impurities. Further, when the cerium oxide abrasive for polishing the glass surface is applied as it is to the inorganic insulating film polishing, the cerium oxide particle diameter (primary particles and aggregated particles) is large, so that the surface of the insulating film can be visually observed.

本発明は、SiO絶縁膜等の被研磨面を傷なく高速に研磨することが可能な酸化セリウム研磨剤および基板の研磨法を提供するものである。 The present invention provides a cerium oxide abrasive capable of polishing a surface to be polished such as a SiO 2 insulating film at a high speed without damage and a method for polishing a substrate.

本発明の酸化セリウム研磨剤は、酸化セリウム粒子、分散剤、及び水を含むものである。酸化セリウムは炭酸塩、硝酸塩、硫酸塩、しゅう酸塩等のセリウム化合物を焼成または溶解−酸化することによって得られる。本発明の酸化セリウム研磨剤を構成する酸化セリウム粒子は、500nm以上の粒子径の含有量が全酸化セリウム粒子の3〜40体積%のもので、高速研磨が可能で研磨傷を防止できる。粒子径の中央値が150〜450nmであることが好ましい。酸化セリウム粒子の粒子径は、レーザー回折法(例えば測定装置、Malvern Instruments社製 Mastersizer Microplus、光源He−Neレーザー、粒子の屈折率1.9285、吸収0で測定)で測定する。中央値は、体積粒子径分布の中央値であり、粒子径の細かいものからその粒子の体積割合を積算していき50%になったときの粒子径を意味する。すなわち、ある区間Δの粒子径の範囲に体積割合Vi%の量の粒子が存在するとき、区間Δの平均粒子径をdiとすると粒子径diの粒子がVi体積%存在するとする。粒子径diの小さい方から粒子の存在割合Vi(体積%)を積算していき、Vi=50%になったときのdiを中央値とする。酸化セリウム研磨剤中の酸化セリウム粒子は、99体積%以上が3000nm以下であることが好ましい。本発明の基板の研磨法は、上記の酸化セリウム研磨剤で所定の基板、例えばSiO絶縁膜が形成された基板で研磨することを特徴とするものである。本発明は、粒子径を制御した酸化セリウム粒子を含む酸化セリウム研磨剤が、SiO絶縁膜等の被研磨面を傷なく高速に研磨することを見い出したことによりなされたものである。 The cerium oxide abrasive | polishing agent of this invention contains a cerium oxide particle, a dispersing agent, and water. Cerium oxide is obtained by baking or dissolving-oxidizing cerium compounds such as carbonates, nitrates, sulfates, and oxalates. The cerium oxide particles constituting the cerium oxide abrasive of the present invention have a particle diameter of 500 nm or more and 3 to 40% by volume of the total cerium oxide particles, enabling high-speed polishing and preventing polishing scratches. The median particle diameter is preferably 150 to 450 nm. The particle diameter of the cerium oxide particles is measured by a laser diffraction method (for example, a measurement apparatus, Mastersizer Microplus manufactured by Malvern Instruments, light source He-Ne laser, particle refractive index 1.9285, and measurement with zero absorption). The median is the median of the volume particle size distribution, and means the particle size when the volume ratio of the particles is accumulated from the finer particle size to 50%. That is, when particles having an amount of volume ratio Vi% exist in a range of particle diameters in a certain section Δ, assuming that the average particle diameter in the section Δ is di, particles having a particle diameter di exist in Vi volume%. The particle abundance ratio Vi (volume%) is integrated from the smaller particle diameter di, and di when Vi = 50% is set as the median. 99% by volume or more of the cerium oxide particles in the cerium oxide abrasive is preferably 3000 nm or less. The substrate polishing method of the present invention is characterized by polishing with a predetermined substrate, for example, a substrate on which an SiO 2 insulating film is formed, with the above cerium oxide abrasive. The present invention has been made by finding that a cerium oxide abrasive containing cerium oxide particles having a controlled particle size can polish a surface to be polished such as a SiO 2 insulating film at a high speed without damage.

本発明の研磨剤により、SiO絶縁膜等の被研磨面を傷なく高速に研磨することが可能となる。 The polishing agent of the present invention makes it possible to polish the surface to be polished such as the SiO 2 insulating film at high speed without scratching.

本発明の酸化セリウム研磨剤を構成する酸化セリウム粒子は、粒子径500nm以上の含有量が5〜40体積%であり、粒子径の中央値が150〜450nmであることが好ましい。本発明の酸化セリウム研磨剤は、粒子径500nm以上の含有量が5〜40体積%とサブミクロンの粒子が多いために、自然沈降で測定すると測定時間が1か月以上となるため、沈降測定の場合は、遠心沈降法が好ましい。酸化セリウム研磨剤中の酸化セリウム粒子は、99体積%以上が3000nm以下であることが好ましい。また半導体チップ研磨に使用することから、アルカリ金属およびハロゲン類の含有率は、10ppm以下に抑えることが好ましい。   The cerium oxide particles constituting the cerium oxide abrasive of the present invention preferably have a particle size of 500 nm or more in a content of 5 to 40% by volume and a median particle size of 150 to 450 nm. Since the cerium oxide abrasive of the present invention has a particle diameter of 500 nm or more and 5 to 40% by volume and many submicron particles, the measurement time is one month or more when measured by natural sedimentation. In this case, the centrifugal sedimentation method is preferable. 99% by volume or more of the cerium oxide particles in the cerium oxide abrasive is preferably 3000 nm or less. Moreover, since it uses for semiconductor chip grinding | polishing, it is preferable to suppress the content rate of alkali metal and halogens to 10 ppm or less.

本発明において、酸化セリウム粉末を作製する方法として、焼成法またはセリウム化合物水溶液の酸化法が使用できる。焼成温度は、600℃以上900℃以下が好ましい。セリウム化合物水溶液中で酸化する方法としては、セリウム水溶液に硝酸等の酸及び過酸化水素水等の酸化剤を加える方法がある。上記の方法により製造された酸化セリウム粒子は凝集しているため、機械的に粉砕することが好ましい。粉砕方法として、ジェットミル等による乾式粉砕や遊星ビーズミル等による湿式粉砕方法が好ましい。ジェットミルは、例えば化学工学業論文集第6巻第5号(1980)527〜532頁に説明されている。   In the present invention, as a method for producing the cerium oxide powder, a firing method or an oxidation method of a cerium compound aqueous solution can be used. The firing temperature is preferably 600 ° C. or higher and 900 ° C. or lower. As a method of oxidizing in a cerium compound aqueous solution, there is a method of adding an acid such as nitric acid and an oxidizing agent such as hydrogen peroxide to the cerium aqueous solution. Since the cerium oxide particles produced by the above method are agglomerated, it is preferably mechanically pulverized. As the pulverization method, a dry pulverization method such as a jet mill or a wet pulverization method such as a planetary bead mill is preferable. The jet mill is described, for example, in Chemical Engineering Papers Vol. 6 No. 5 (1980) pp. 527-532.

本発明における酸化セリウムスラリーは、例えば上記の特徴を有する酸化セリウム粒子とポリアクリル酸アンモニウム塩を含む分散剤と水からなる組成物を分散させることによって得られる。ここで、酸化セリウム粒子の濃度に制限はないが、懸濁液の取り扱いやすさから0.5以上20重量%以下の範囲が好ましい。また、分散剤として、半導体チップ研磨に使用することからNa、K等のアルカリ金属および、ハロゲン、イオウを含まないものとしてポリアクリル酸アンモニウム塩が好ましい。また、ポリアクリル酸アンモニウム塩と水溶性有機高分子類(ポリグリセリン脂肪酸エステル等)、水溶性陰イオン性界面活性剤(アルキルエーテルカルボン酸塩)、水溶性非イオン性界面活性剤(ポリエチレングリコールモノステアレート等)、水溶性アミン類(モノエタノールアミン等)から選ばれた少なくとも1種類を含む2種類以上の分散剤を使用してもよい。これらの分散剤添加量は、スラリー中の粒子の分散性および沈降防止、さらに研磨傷と分散剤添加量との関係から、酸化セリウム粒子100重量部に対して0.01以上2.0重量部以下の範囲が好ましい。ポリアクリル酸アンモニウム塩の分子量(重量平均分子量)は、1000〜10000が好ましく、3000〜8000がより好ましい。これらの酸化セリウム粒子を水中に分散させる方法としては、通常の撹拌機による分散処理の他にホモジナイザ−、超音波分散機、ビーズミル、遊星ボールミル、振動ミル等を用いることができる。分散後のスラリー中の大きな凝集粒子を分級により除去する方法としては、沈降分離法、液体サイクロン、フィルターろ過等を用いることができる。   The cerium oxide slurry in the present invention can be obtained, for example, by dispersing a composition composed of cerium oxide particles having the above characteristics, a dispersant containing polyacrylic acid ammonium salt, and water. Here, although there is no restriction | limiting in the density | concentration of a cerium oxide particle, The range of 0.5-20 weight% is preferable from the ease of handling of suspension. Moreover, since it uses for semiconductor chip grinding | polishing as a dispersing agent, an alkali metal, such as Na and K, and a polyacrylic acid ammonium salt as a thing which does not contain a halogen and sulfur are preferable. In addition, polyacrylic acid ammonium salt and water-soluble organic polymers (polyglycerin fatty acid ester, etc.), water-soluble anionic surfactant (alkyl ether carboxylate), water-soluble nonionic surfactant (polyethylene glycol monoester) Two or more dispersants including at least one selected from stearates and the like and water-soluble amines (monoethanolamine and the like) may be used. These dispersants are added in an amount of 0.01 to 2.0 parts by weight with respect to 100 parts by weight of the cerium oxide particles in view of the dispersibility of the particles in the slurry and the prevention of sedimentation, and the relationship between the polishing scratches and the amount of the dispersant added. The following ranges are preferred. 1000-10000 are preferable and, as for the molecular weight (weight average molecular weight) of polyacrylic acid ammonium salt, 3000-8000 are more preferable. As a method for dispersing these cerium oxide particles in water, a homogenizer, an ultrasonic disperser, a bead mill, a planetary ball mill, a vibration mill and the like can be used in addition to a dispersion treatment using a normal stirrer. As a method for removing large agglomerated particles in the dispersed slurry by classification, a sedimentation separation method, a hydrocyclone, filter filtration, or the like can be used.

本発明の酸化セリウム研磨剤は、上記スラリ−をそのまま使用してもよいが、N,N−ジエチルエタノ−ルアミン、N,N−ジメチルエタノ−ルアミン、アミノエチルエタノ−ルアミン等の添加剤を添加して研磨剤とすることができる。   The cerium oxide abrasive of the present invention may use the above slurry as it is, but an additive such as N, N-diethylethanolamine, N, N-dimethylethanolamine, aminoethylethanolamine is added. Thus, an abrasive can be obtained.

本発明の酸化セリウム研磨剤が使用される無機絶縁膜の作製方法として、低圧CVD法、プラズマCVD法等が挙げられる。低圧CVD法によるSiO絶縁膜形成は、Si源としてモノシラン:SiH、酸素源として酸素:Oを用いる。このSiH−O系酸化反応を400℃程度以下の低温で行わせることにより得られる。場合によっては、CVD後1000℃またはそれ以下の温度で熱処理される。高温リフローによる表面平坦化を図るために、リン:Pをドープするときには、SiH−O−PH系反応ガスを用いることが好ましい。プラズマCVD法は、通常の熱平衡下では高温を必要とする化学反応が低温でできる利点を有する。プラズマ発生法には、容量結合型と誘導結合型の2つが挙げられる。反応ガスとしては、Si源としてSiH、酸素源としてNOを用いたSiH−NO系ガスとテトラエトキシシラン(TEOS)をSi源に用いたTEOS−O系ガス(TEOS−プラズマCVD法)が挙げられる。基板温度は250℃〜400℃、反応圧力は67〜400Paの範囲が好ましい。このように、本発明のSiO絶縁膜にはリン、ホウ素等の元素がド−プされていても良い。 Examples of a method for manufacturing an inorganic insulating film in which the cerium oxide abrasive of the present invention is used include a low pressure CVD method and a plasma CVD method. In the formation of the SiO 2 insulating film by the low pressure CVD method, monosilane: SiH 4 is used as the Si source, and oxygen: O 2 is used as the oxygen source. It can be obtained by performing this SiH 4 —O 2 -based oxidation reaction at a low temperature of about 400 ° C. or less. In some cases, heat treatment is performed at a temperature of 1000 ° C. or lower after CVD. In order to achieve surface flattening by high-temperature reflow, when doping with phosphorus: P, it is preferable to use a SiH 4 —O 2 —PH 3 -based reactive gas. The plasma CVD method has an advantage that a chemical reaction requiring a high temperature can be performed at a low temperature under normal thermal equilibrium. There are two plasma generation methods, capacitive coupling type and inductive coupling type. The reaction as a gas, SiH 4 as an Si source, an oxygen source as N 2 O was used was SiH 4 -N 2 O-based gas and TEOS-O 2 based gas using tetraethoxysilane (TEOS) in an Si source (TEOS- Plasma CVD method). The substrate temperature is preferably 250 to 400 ° C., and the reaction pressure is preferably 67 to 400 Pa. Thus, elements such as phosphorus and boron may be doped in the SiO 2 insulating film of the present invention.

所定の基板として、半導体基板すなわち回路素子と配線パターンが形成された段階の半導体基板、回路素子が形成された段階の半導体基板等の半導体基板上に、SiO絶縁膜層が形成された基板が使用できる。このような半導体基板上に形成されたSiO絶縁膜層を、上記酸化セリウム研磨剤で研磨することによって、SiO絶縁膜層表面の凹凸を解消し、半導体基板全面に渡って平滑な面とする。ここで、研磨する装置としては、半導体基板を保持するホルダーと研磨布(パッド)を貼り付けた(回転数が変更可能なモータ等を取り付けてある)定盤を有する一般的な研磨装置が使用できる。研磨布としては、一般的な不織布、発泡ポリウレタン、多孔質フッ素樹脂等が使用でき、特に制限がない。また、研磨布には、スラリーが溜まる様な溝加工を施すことが好ましい。研磨条件には制限はないが、定盤の回転速度は、半導体が飛び出さない様に100rpm以下の低回転が好ましく、半導体基板にかける圧力は、研磨後に傷が発生しない様に1kg/cm以下が好ましい。研磨している間、研磨布にはスラリーをポンプ等で連続的に供給する。この供給量には制限はないが、研磨布の表面が常にスラリーで覆われていることが好ましい。 As the predetermined substrate, there is a semiconductor substrate, that is, a semiconductor substrate in which a circuit element and a wiring pattern are formed, and a substrate in which a SiO 2 insulating film layer is formed on a semiconductor substrate such as a semiconductor substrate in which a circuit element is formed. Can be used. By polishing the SiO 2 insulating film layer formed on such a semiconductor substrate with the cerium oxide abrasive, unevenness on the surface of the SiO 2 insulating film layer is eliminated, and a smooth surface over the entire surface of the semiconductor substrate is obtained. To do. Here, as a polishing apparatus, a general polishing apparatus having a surface plate with a holder for holding a semiconductor substrate and a polishing cloth (pad) attached (a motor etc. capable of changing the number of rotations) is used. it can. As an abrasive cloth, a general nonwoven fabric, a polyurethane foam, a porous fluororesin, etc. can be used, and there is no restriction | limiting in particular. Further, the polishing cloth is preferably subjected to groove processing so that slurry is accumulated. The polishing conditions are not limited, but the rotation speed of the surface plate is preferably low rotation of 100 rpm or less so that the semiconductor does not jump out, and the pressure applied to the semiconductor substrate is 1 kg / cm 2 so that no scratches are generated after polishing. The following is preferred. During polishing, slurry is continuously supplied to the polishing cloth with a pump or the like. Although there is no restriction | limiting in this supply amount, it is preferable that the surface of polishing cloth is always covered with the slurry.

研磨終了後の半導体基板は、流水中で良く洗浄後、スピンドライヤ等を用いて半導体基板上に付着した水滴を払い落としてから乾燥させることが好ましい。このようにして平坦化されたSiO絶縁膜層の上に、第2層目のアルミニウム配線を形成し、その配線間および配線上に再度上記方法により、SiO絶縁膜を形成後、上記酸化セリウム研磨剤を用いて研磨することによって、絶縁膜表面の凹凸を解消し、半導体基板全面に渡って平滑な面とする。この工程を所定数繰り返すことにより、所望の層数の半導体を製造する。 The semiconductor substrate after the polishing is preferably washed in running water, and then dried after removing water droplets adhering to the semiconductor substrate using a spin dryer or the like. On this way, the SiO 2 insulating film layer which is flattened, forming an aluminum wiring of the second layer, again by the above method on the inter-wiring and the wiring, after forming the SiO 2 insulating film, the oxide By polishing with a cerium abrasive, unevenness on the surface of the insulating film is eliminated, and a smooth surface is formed over the entire surface of the semiconductor substrate. By repeating this process a predetermined number of times, a desired number of semiconductor layers are manufactured.

本発明の酸化セリウム研磨剤は、半導体基板に形成されたSiO絶縁膜だけでなく、所定の配線を有する配線板に形成されたSiO絶縁膜、ガラス、窒化ケイ素等の無機絶縁膜、フォトマスク・レンズ・プリズム等の光学ガラス、ITO等の無機導電膜、ガラス及び結晶質材料で構成される光集積回路・光スイッチング素子・光導波路、光ファイバ−の端面、シンチレ−タ等の光学用単結晶、固体レ−ザ単結晶、青色レ−ザLED用サファイア基板、SiC、GaP、GaAs等の半導体単結晶、磁気ディスク用ガラス基板、磁気ヘッド等を研磨するために使用される。このように本発明において所定の基板とは、SiO絶縁膜が形成された半導体基板、SiO絶縁膜が形成された配線板、ガラス、窒化ケイ素等の無機絶縁膜が形成された基板、フォトマスク・レンズ・プリズム等の光学ガラス、ITO等の無機導電膜、ガラス及び結晶質材料で構成される光集積回路・光スイッチング素子・光導波路、光ファイバ−の端面、シンチレ−タ等の光学用単結晶、固体レ−ザ単結晶、青色レ−ザLED用サファイア基板、SiC、GaP、GaAs等の半導体単結晶、磁気ディスク用ガラス基板、磁気ヘッド等を含む。 Cerium oxide abrasive of the present invention is not only SiO 2 insulating film formed on a semiconductor substrate, SiO 2 insulating film formed on the wiring board having a predetermined wiring, glass, inorganic insulating films such as silicon nitride, Photo Optical glass for masks, lenses, prisms, etc., optical conductive circuits such as ITO, inorganic conductive films such as ITO, glass and crystalline materials, optical switching elements, optical waveguides, end faces of optical fibers, scintillators, etc. It is used for polishing single crystals, solid laser single crystals, sapphire substrates for blue laser LEDs, semiconductor single crystals such as SiC, GaP, and GaAs, glass substrates for magnetic disks, magnetic heads, and the like. Thus the predetermined substrate in the present invention, SiO 2 semiconductor substrate on which an insulating film is formed, SiO 2 insulating film is formed wiring board, a glass substrate an inorganic insulating film such as silicon nitride is formed, the photo Optical glass for masks, lenses, prisms, etc., optical conductive circuits such as ITO, inorganic conductive films such as ITO, glass and crystalline materials, optical switching elements, optical waveguides, end faces of optical fibers, scintillators, etc. Including single crystals, solid laser single crystals, sapphire substrates for blue laser LEDs, semiconductor single crystals such as SiC, GaP, and GaAs, glass substrates for magnetic disks, magnetic heads, and the like.

実施例1
(酸化セリウム粒子の作製1)
炭酸セリウム水和物2kgを白金製容器に入れ、800℃で2時間空気中で焼成することにより、黄白色の粉末を約1kg得た。この粉末をX線回折法で相同定を行ったところ、酸化セリウムであることを確認した。焼成粉末粒子径は30〜100μmであった。焼成粉末粒子表面を走査型電子顕微鏡で観察したところ、酸化セリウムの粒界が観察された。粒界に囲まれた酸化セリウム一次粒子径を測定したところ、その分布の中央値が190nm、最大値が500nmであった。焼成粉末についてX線回折精密測定を行い、その結果についてリートベルト法(RIETAN−94)による解析で、一次粒子径を表わす構造パラメーター:Xの値が0.080、等方的微少歪みを表わす構造パラメーター:Yの値が0.223であった。酸化セリウム粉末1kgをジェットミルを用いて乾式粉砕を行った。粉砕粒子について走査型電子顕微鏡で観察したところ、一次粒子径と同等サイズの小さな粒子の他に、1μmから3μmの大きな粉砕粒子と0.5から1μmの粉砕粒子が混在していた。これらの粉砕粒子は、一次粒子の凝集体ではない。粉砕粒子についてX線回折精密測定を行い、その結果についてリートベルト法(RIETAN−94)による解析で、一次粒子径を表わす構造パラメーター:Xの値が0.085、等方的微少歪みを表わす構造パラメーター:Yの値が0.264であった。この結果、粉砕による一次粒子径変量は殆どなく、また粉砕により粒子に歪みが導入されていた。さらに、BET法による比表面積測定の結果、10m/gであることがわかった。
Example 1
(Preparation of cerium oxide particles 1)
By putting 2 kg of cerium carbonate hydrate in a platinum container and firing in air at 800 ° C. for 2 hours, about 1 kg of yellowish white powder was obtained. When this powder was subjected to phase identification by X-ray diffraction, it was confirmed to be cerium oxide. The fired powder particle size was 30 to 100 μm. When the surface of the fired powder particles was observed with a scanning electron microscope, grain boundaries of cerium oxide were observed. When the primary particle diameter of cerium oxide surrounded by the grain boundaries was measured, the median value of the distribution was 190 nm and the maximum value was 500 nm. The X-ray diffraction precision measurement is performed on the calcined powder, and the result is analyzed by the Rietveld method (RIETAN-94). The structural parameter indicating the primary particle diameter: the value of X is 0.080, and the structure indicates isotropic strain Parameter: Y value was 0.223. 1 kg of cerium oxide powder was dry pulverized using a jet mill. When the pulverized particles were observed with a scanning electron microscope, large pulverized particles of 1 to 3 μm and pulverized particles of 0.5 to 1 μm were mixed in addition to small particles having the same size as the primary particle diameter. These pulverized particles are not aggregates of primary particles. The X-ray diffraction precision measurement is performed on the pulverized particles, and the result is analyzed by Rietveld method (RIETAN-94). The structure parameter indicating the primary particle diameter: the value of X is 0.085, and the structure represents isotropic strain Parameter: Y value was 0.264. As a result, there was almost no change in the primary particle size due to pulverization, and distortion was introduced into the particles due to pulverization. Furthermore, as a result of measuring the specific surface area by the BET method, it was found to be 10 m 2 / g.

(酸化セリウム粒子の作製2)
酸化セリウム粒子の作製1で用いたのと同じ炭酸セリウム水和物2kgを白金製容器に入れ、750℃で2時間空気中で焼成することにより、黄白色の粉末を約1kg得た。この粉末をX線回折法で相同定を行ったところ、酸化セリウムであることを確認した。焼成粉末粒子径は30〜100μmであった。焼成粉末粒子表面を走査型電子顕微鏡で観察したところ、酸化セリウムの粒界が観察された。粒界に囲まれた酸化セリウム一次粒子径を測定したところ、その分布の中央値が141nm、最大値が400nmであった。焼成粉末についてX線回折精密測定を行い、その結果についてリートベルト法(RIRTAN−94)による解析で、一次粒子径を表わす構造パラメーター:Xの値が0.101、等方的微少歪みを表わす構造パラメーター:Yの値が0.223であった。酸化セリウム粉末1kgをジェットミルを用いて乾式粉砕を行った。粉砕粒子について走査型電子顕微鏡で観察したところ、一次粒子径と同等サイズの小さな粒子の他に、1μmから3μmの大きな粉砕粒子と0.5から1μmの粉砕粒子が混在していた。これらの粉砕粒子は、一次粒子の凝集体ではない。粉砕粒子についてX線回折精密測定を行い、その結果についてリートベルト法(RIETAN−94)による解析で、一次粒子径を表わす構造パラメーター:Xの値が0.104、等方的微少歪みを表わす構造パラメーター:Yの値が0.315であった。この結果、粉砕による一次粒子径変量は殆どなく、また粉砕により粒子に歪みが導入されていた。さらに、BET法による比表面積測定の結果、16m/gであることがわかった。
(Preparation of cerium oxide particles 2)
Preparation of Cerium Oxide Particles 2 kg of the same cerium carbonate hydrate used in Step 1 was placed in a platinum container and baked in air at 750 ° C. for 2 hours to obtain about 1 kg of yellowish white powder. When this powder was subjected to phase identification by X-ray diffraction, it was confirmed to be cerium oxide. The fired powder particle size was 30 to 100 μm. When the surface of the fired powder particles was observed with a scanning electron microscope, grain boundaries of cerium oxide were observed. When the primary particle diameter of cerium oxide surrounded by the grain boundaries was measured, the median value of the distribution was 141 nm and the maximum value was 400 nm. X-ray diffraction precision measurement is performed on the calcined powder, and the result is analyzed by the Rietveld method (RIRTAN-94). The structure parameter indicating the primary particle size: X is 0.101, and the structure represents isotropic strain Parameter: Y value was 0.223. 1 kg of cerium oxide powder was dry pulverized using a jet mill. When the pulverized particles were observed with a scanning electron microscope, large pulverized particles of 1 to 3 μm and pulverized particles of 0.5 to 1 μm were mixed in addition to small particles having the same size as the primary particle diameter. These pulverized particles are not aggregates of primary particles. The X-ray diffraction precision measurement is performed on the pulverized particles, and the result is analyzed by the Rietveld method (RIETAN-94). The structure parameter indicating the primary particle size: the value of X is 0.104, and the structure indicates isotropic strain. Parameter: Y value was 0.315. As a result, there was almost no change in the primary particle size due to pulverization, and distortion was introduced into the particles due to pulverization. Furthermore, as a result of measuring the specific surface area by the BET method, it was found to be 16 m 2 / g.

(酸化セリウムスラリーの作製)
上記作製1、2の酸化セリウム粒子1kgとポリアクリル酸アンモニウム塩水溶液(40重量%)23gと脱イオン水8977gを混合し、撹拌しながら超音波分散を10分間施した。得られたスラリーを5μmフィルターでろ過をし、さらに脱イオン水を加えることにより3wt%研磨剤を得た。スラリーpHは8.3であった。スラリー粒子の粒度分布をレーザー回折法(測定装置:Malvern Instruments社製 Mastersizer Microplus、光源He−Neレーザー、粒子の屈折率1.9285、吸収0で測定)を用いて調べたところ、中央値が酸化セリウム粒子の作製1によるスラリーは200nm、酸化セリウム粒子の作製2によるスラリーは280nmであった。500nm以上の粒子の含有量は、酸化セリウム粒子の作製1によるスラリーが13.4体積%、酸化セリウム粒子の作製2によるスラリーが37.8体積%、最大粒子径は共に1950nmであった。スラリーの分散性およびスラリー粒子の電荷を調べるため、スラリーのゼータ電位を調べた。両側に白金製電極を取り付けてある測定セルに酸化セリウムスラリーを入れ、両電極に10Vの電圧を印加した。電圧を印加することにより電荷を持ったスラリー粒子は、その電荷と反対の極を持つ電極側に移動する。この移動速度を求めることにより、粒子のゼータ電位を求めることができる。ゼータ電位測定の結果、それぞれマイナスに荷電し、−38mV、−55mVと絶対値が大きく分散性が良好であることを確認した。
(Preparation of cerium oxide slurry)
1 kg of the cerium oxide particles of Preparations 1 and 2 above, 23 g of ammonium polyacrylate aqueous solution (40% by weight) and 8977 g of deionized water were mixed and subjected to ultrasonic dispersion for 10 minutes while stirring. The obtained slurry was filtered with a 5 μm filter, and deionized water was further added to obtain a 3 wt% abrasive. The slurry pH was 8.3. When the particle size distribution of the slurry particles was measured using a laser diffraction method (measurement device: Mastersizer Microplus, light source He-Ne laser, manufactured by Malvern Instruments, measured with a refractive index of particles 1.9285, absorption 0), the median value was oxidized. The slurry obtained by preparation 1 of cerium particles was 200 nm, and the slurry obtained by preparation 2 of cerium oxide particles was 280 nm. The content of the particles of 500 nm or more was 13.4% by volume of the slurry by preparation 1 of cerium oxide particles, 37.8% by volume of slurry by preparation 2 of cerium oxide particles, and the maximum particle size was both 1950 nm. To examine the dispersibility of the slurry and the charge of the slurry particles, the zeta potential of the slurry was examined. A cerium oxide slurry was placed in a measurement cell having platinum electrodes on both sides, and a voltage of 10 V was applied to both electrodes. Slurry particles having a charge by applying a voltage move to the side of the electrode having a pole opposite to the charge. By obtaining this moving speed, the zeta potential of the particles can be obtained. As a result of the zeta potential measurement, it was confirmed that each was negatively charged and had a large absolute value of −38 mV and −55 mV and good dispersibility.

(絶縁膜層の研磨)
保持する基板取り付け用の吸着パッドを貼り付けたホルダーに、TEOS−プラズマCVD法で作製したSiO絶縁膜を形成させたSiウエハをセットし、多孔質ウレタン樹脂製の研磨パッドを貼り付けた定盤上に、絶縁膜面を下にしてホルダーを載せ、さらに加工荷重が300g/cmになるように重しを載せた。定盤上に、上記の酸化セリウムスラリー(固形分:3重量%)を50cc/minの速度で滴下しながら、定盤を30rpmで2分間回転させ、絶縁膜を研磨した。研磨後ウエハをホルダーから取り外して、流水で良く洗浄後、超音波洗浄機によりさらに20分間洗浄した。洗浄後、ウエハをスピンドライヤーで水滴を除去し、120℃の乾燥機で10分間乾燥させた。光干渉式膜厚測定装置を用いて、研磨前後の膜厚変化を測定した結果、この研磨によりそれぞれ620nm、640nm(研磨速度:310nm/min、320nm/min)の絶縁膜が削られ、ウエハ全面に渡って均一の厚みになっていることがわかった。また、光学顕微鏡を用いて絶縁膜表面を観察したところ、明確な傷は見られなかった。
(Polishing the insulating film layer)
A Si wafer on which a SiO 2 insulating film formed by TEOS-plasma CVD method is set in a holder to which a suction pad for mounting a substrate to be held is attached, and a polishing pad made of porous urethane resin is attached. A holder was placed on the board with the insulating film side down, and a weight was placed so that the processing load was 300 g / cm 2 . While the above cerium oxide slurry (solid content: 3% by weight) was dropped on the surface plate at a speed of 50 cc / min, the surface plate was rotated at 30 rpm for 2 minutes to polish the insulating film. After polishing, the wafer was removed from the holder, washed thoroughly with running water, and further washed with an ultrasonic cleaner for 20 minutes. After washing, water droplets were removed from the wafer with a spin dryer, and the wafer was dried with a 120 ° C. dryer for 10 minutes. As a result of measuring the film thickness change before and after polishing using an optical interference type film thickness measuring apparatus, the insulating films of 620 nm and 640 nm (polishing rates: 310 nm / min and 320 nm / min) were removed by this polishing, respectively, and the entire wafer surface It was found that the thickness was uniform over the entire area. Further, when the surface of the insulating film was observed using an optical microscope, no clear scratch was found.

実施例2
(酸化セリウム粒子の作製)
炭酸セリウム水和物2kgを白金製容器に入れ、800℃で2時間空気中で焼成することにより、黄白色の粉末を約1kg得た。この粉末をX線回折法で相同定を行ったところ、酸化セリウムであることを確認した。焼成粉末粒子径は30〜100μmであった。焼成粉末粒子表面を走査型電子顕微鏡で観察したところ、酸化セリウムの粒界が観察された。粒界に囲まれた酸化セリウム一次粒子径を測定したところ、その分布の中央値が190nm、最大値が500nmであった。焼成粉末についてX線回折精密測定を行い、その結果についてリートベルト法(RIETAN−94)による解析で、一次粒子径を表わす構造パラメーター:Xの値が0.080、等方的微少歪みを表わす構造パラメーター:Yの値が0.223であった。酸化セリウム粉末1kgをジェットミルを用いて乾式粉砕を行った。粉砕粒子について走査型電子顕微鏡で観察したところ、一次粒子径と同等サイズの小さな粒子の他に、1μmから3μmの大きな粉砕粒子と0.5から1μmの粉砕粒子が混在していた。これらの粉砕粒子は、一次粒子の凝集体ではない。粉砕粒子についてX線回折精密測定を行い、その結果についてリートベルト法(RIETAN−94)による解析で、一次粒子径を表わす構造パラメーター:Xの値が0.085、等方的微少歪みを表わす構造パラメーター:Yの値が0.264であった。この結果、粉砕による一次粒子径変量は殆どなく、また粉砕により粒子に歪みが導入されていた。さらに、BET法による比表面積測定の結果、10m/gであることがわかった。
Example 2
(Production of cerium oxide particles)
By putting 2 kg of cerium carbonate hydrate in a platinum container and firing in air at 800 ° C. for 2 hours, about 1 kg of yellowish white powder was obtained. When this powder was subjected to phase identification by X-ray diffraction, it was confirmed to be cerium oxide. The fired powder particle size was 30 to 100 μm. When the surface of the fired powder particles was observed with a scanning electron microscope, grain boundaries of cerium oxide were observed. When the primary particle diameter of cerium oxide surrounded by the grain boundaries was measured, the median value of the distribution was 190 nm and the maximum value was 500 nm. The X-ray diffraction precision measurement is performed on the calcined powder, and the result is analyzed by the Rietveld method (RIETAN-94). The structural parameter indicating the primary particle diameter: the value of X is 0.080, and the structure indicates isotropic strain Parameter: Y value was 0.223. 1 kg of cerium oxide powder was dry pulverized using a jet mill. When the pulverized particles were observed with a scanning electron microscope, large pulverized particles of 1 to 3 μm and pulverized particles of 0.5 to 1 μm were mixed in addition to small particles having the same size as the primary particle diameter. These pulverized particles are not aggregates of primary particles. The X-ray diffraction precision measurement is performed on the pulverized particles, and the result is analyzed by Rietveld method (RIETAN-94). The structure parameter indicating the primary particle diameter: the value of X is 0.085, and the structure represents isotropic strain Parameter: Y value was 0.264. As a result, there was almost no change in the primary particle size due to pulverization, and distortion was introduced into the particles due to pulverization. Furthermore, as a result of measuring the specific surface area by the BET method, it was found to be 10 m 2 / g.

(酸化セリウムスラリーの作製)
上記の酸化セリウム粒子1kgとポリアクリル酸アンモニウム塩水溶液(40重量%)23gと脱イオン水8977gを混合し、撹拌しながら超音波分散を10分間施した。得られたスラリーを1μmフィルターでろ過をし、さらに脱イオン水を加えることにより3wt%研磨剤を得た。スラリーpHは8.3であった。スラリー粒子の粒度分布をレーザー回折法を用いて調べたところ、中央値が200nm、500nm以上の含有量は5.1体積%、最大粒子径は780nmであった。スラリーの分散性およびスラリー粒子の電荷を調べるため、スラリーのゼータ電位を調べた。両側に白金製電極を取り付けてある測定セルに酸化セリウムスラリーを入れ、両電極に10Vの電圧を印加した。電圧を印加することにより電荷を持ったスラリー粒子は、その電荷と反対の極を持つ電極側に移動する。この移動速度を求めることにより、粒子のゼータ電位を求めることができる。ゼータ電位測定の結果、マイナスに荷電し、−50mVと絶対値が大きく分散性が良好であることを確認した。
(Preparation of cerium oxide slurry)
1 kg of the above cerium oxide particles, 23 g of an aqueous polyacrylic acid ammonium salt solution (40% by weight), and 8977 g of deionized water were mixed and subjected to ultrasonic dispersion for 10 minutes while stirring. The obtained slurry was filtered with a 1 μm filter, and deionized water was further added to obtain a 3 wt% abrasive. The slurry pH was 8.3. When the particle size distribution of the slurry particles was examined using a laser diffraction method, the median value was 200 nm, the content of 500 nm or more was 5.1% by volume, and the maximum particle size was 780 nm. To examine the dispersibility of the slurry and the charge of the slurry particles, the zeta potential of the slurry was examined. A cerium oxide slurry was placed in a measurement cell having platinum electrodes on both sides, and a voltage of 10 V was applied to both electrodes. Slurry particles having a charge by applying a voltage move to the side of the electrode having a pole opposite to the charge. By obtaining this moving speed, the zeta potential of the particles can be obtained. As a result of the zeta potential measurement, it was confirmed that it was negatively charged, had an absolute value of −50 mV and a large dispersibility.

(絶縁膜層の研磨)
保持する基板取り付け用の吸着パッドを貼り付けたホルダーに、TEOS−プラズマCVD法で作製したSiO絶縁膜を形成させたSiウエハをセットし、多孔質ウレタン樹脂製の研磨パッドを貼り付けた定盤上に、絶縁膜面を下にしてホルダーを載せ、さらに加工荷重が300g/cmになるように重しを載せた。定盤上に、上記の酸化セリウムスラリー(固形分:3重量%)を50cc/minの速度で滴下しながら、定盤を30rpmで2分間回転させ、絶縁膜を研磨した。研磨後ウエハをホルダーから取り外して、流水で良く洗浄後、超音波洗浄機によりさらに20分間洗浄した。洗浄後、ウエハをスピンドライヤーで水滴を除去し、120℃の乾燥機で10分間乾燥させた。光干渉式膜厚測定装置を用いて、研磨前後の膜厚変化を測定した結果、この研磨により600nm(研磨速度:300nm/min)の絶縁膜が削られ、ウエハ全面に渡って均一の厚みになっていることがわかった。また、光学顕微鏡を用いて絶縁膜表面を観察したところ、明確な傷は見られなかった。
(Polishing the insulating film layer)
A Si wafer on which a SiO 2 insulating film formed by TEOS-plasma CVD method is set in a holder to which a suction pad for mounting a substrate to be held is attached, and a polishing pad made of porous urethane resin is attached. A holder was placed on the board with the insulating film side down, and a weight was placed so that the processing load was 300 g / cm 2 . While the above cerium oxide slurry (solid content: 3% by weight) was dropped on the surface plate at a speed of 50 cc / min, the surface plate was rotated at 30 rpm for 2 minutes to polish the insulating film. After polishing, the wafer was removed from the holder, washed thoroughly with running water, and further washed with an ultrasonic cleaner for 20 minutes. After washing, water droplets were removed from the wafer with a spin dryer, and the wafer was dried with a dryer at 120 ° C. for 10 minutes. As a result of measuring the change in film thickness before and after polishing using an optical interference type film thickness measuring device, the insulating film having a thickness of 600 nm (polishing rate: 300 nm / min) was removed by this polishing, and the thickness was uniform over the entire wafer surface. I found out that Further, when the surface of the insulating film was observed using an optical microscope, no clear scratch was found.

比較例1
実施例2で用いたのと同じ酸化セリウム粒子1kgとポリアクリル酸アンモニウム塩水溶液(40重量%)23gと脱イオン水8977gを混合し、撹拌しながら超音波分散を10分間施し、さらに脱イオン水を加えることにより3wt%研磨剤を得た。スラリーpHは8.2であった。スラリー粒子の粒度分布をレーザー回折法を用いて調べたところ、中央値は600nm、500nm以上の含有量は56体積%、最大粒子径は3300nmであった。スラリーの分散性およびスラリー粒子の電荷を調べるため、スラリーのゼータ電位を調べた。両側に白金製電極を取り付けてある測定セルに酸化セリウムスラリーを入れ、両電極に10Vの電圧を印加した。電圧を印加することにより電荷を持ったスラリー粒子は、その電荷と反対の極を持つ電極側に移動する。この移動速度を求めることにより、粒子のゼータ電位を求めることができる。ゼータ電位測定の結果、マイナスに荷電し、−35mVと絶対値が大きく分散性が良好であることを確認した。
Comparative Example 1
The same 1 kg of cerium oxide particles as used in Example 2, 23 g of an aqueous solution of ammonium polyacrylate (40% by weight) and 8977 g of deionized water were mixed, subjected to ultrasonic dispersion for 10 minutes with stirring, and further deionized water. Was added to obtain a 3 wt% abrasive. The slurry pH was 8.2. When the particle size distribution of the slurry particles was examined using a laser diffraction method, the median value was 600 nm, the content of 500 nm or more was 56% by volume, and the maximum particle size was 3300 nm. To examine the dispersibility of the slurry and the charge of the slurry particles, the zeta potential of the slurry was examined. A cerium oxide slurry was placed in a measurement cell having platinum electrodes on both sides, and a voltage of 10 V was applied to both electrodes. Slurry particles having a charge by applying a voltage move to the side of the electrode having a pole opposite to the charge. By obtaining this moving speed, the zeta potential of the particles can be obtained. As a result of the zeta potential measurement, it was confirmed that it was negatively charged and had a large absolute value of -35 mV and good dispersibility.

(絶縁膜層の研磨)
保持する基板取り付け用の吸着パッドを貼り付けたホルダーに、TEOS−プラズマCVD法で作製したSiO絶縁膜を形成させたSiウエハをセットし、多孔質ウレタン樹脂製の研磨パッドを貼り付けた定盤上に、絶縁膜面を下にしてホルダーを載せ、さらに加工荷重が300g/cmになるように重しを載せた。定盤上に、上記の酸化セリウムスラリー(固形分:3重量%)を50cc/minの速度で滴下しながら、定盤を30rpmで2分間回転させ、絶縁膜を研磨した。研磨後ウエハをホルダーから取り外して、流水で良く洗浄後、超音波洗浄機によりさらに20分間洗浄した。洗浄後、ウエハをスピンドライヤーで水滴を除去し、120℃の乾燥機で10分間乾燥させた。光干渉式膜厚測定装置を用いて、研磨前後の膜厚変化を測定した結果、この研磨により780nm(研磨速度:340nm/min)の絶縁膜が削られ、ウエハ全面に渡って均一の厚みになっていることがわかった。光学顕微鏡を用いて絶縁膜表面を観察したところ、幅の狭い傷がウエハ前面にわたって無数に見られた。
(Polishing the insulating film layer)
A Si wafer on which a SiO 2 insulating film formed by TEOS-plasma CVD method is set in a holder to which a suction pad for mounting a substrate to be held is attached, and a polishing pad made of porous urethane resin is attached. A holder was placed on the board with the insulating film side down, and a weight was placed so that the processing load was 300 g / cm 2 . While the above cerium oxide slurry (solid content: 3% by weight) was dropped on the surface plate at a speed of 50 cc / min, the surface plate was rotated at 30 rpm for 2 minutes to polish the insulating film. After polishing, the wafer was removed from the holder, washed thoroughly with running water, and further washed with an ultrasonic cleaner for 20 minutes. After washing, water droplets were removed from the wafer with a spin dryer, and the wafer was dried with a 120 ° C. dryer for 10 minutes. As a result of measuring the change in film thickness before and after polishing using an optical interference type film thickness measuring device, the insulating film having a thickness of 780 nm (polishing rate: 340 nm / min) was removed by this polishing, and the thickness was uniform over the entire surface of the wafer. I found out that When the surface of the insulating film was observed using an optical microscope, countless narrow scratches were seen over the front surface of the wafer.

比較例2
実施例と同様にTEOS−CVD法で作製したSiO絶縁膜を形成させたSiウエハについて、市販シリカスラリー(キャボット社製、商品名SS225)を用いて研磨を行った。この市販スラリーのpHは10.3で、SiO粒子を12.5wt%含んでいるものである。研磨条件は実施例と同一である。その結果、研磨による傷は見られず、また均一に研磨がなされたが、2分間の研磨により150nm(研磨速度:75nm/min)の絶縁膜層しか削れなかった。
Comparative Example 2
The Si wafer on which the SiO 2 insulating film produced by the TEOS-CVD method was formed as in the example was polished using a commercially available silica slurry (trade name SS225, manufactured by Cabot Corporation). This commercially available slurry has a pH of 10.3 and contains 12.5 wt% of SiO 2 particles. The polishing conditions are the same as in the example. As a result, scratches due to polishing were not observed and polishing was performed uniformly, but only an insulating film layer having a thickness of 150 nm (polishing rate: 75 nm / min) was removed by polishing for 2 minutes.

Claims (5)

半導体基板を研磨するための酸化セリウムスラリーであって、
該酸化セリウムスラリーは、炭酸塩、硝酸塩、硫酸塩、しゅう酸塩から選択されるセリウム化合物を600℃以上900℃以下で焼成し、これを粉砕して得られた、粒界に囲まれた一次粒子を有する、一次粒子の凝集体ではない粒子径0.5〜3μmの粒子を含む酸化セリウム粒子、水、及び分散剤を含み、
該酸化セリウムスラリー中の前記酸化セリウム粒子は、500nm以上の粒子径の含有量が全酸化セリウム粒子の3〜40体積%で、粒子径が3000nm以下である粒子が99体積%以上であり、
該酸化セリウムスラリー中の前記酸化セリウム粒子の粒子径は、前記酸化セリウムスラリーを、レーザー回折法(光源He−Neレーザー、粒子の屈折率1.9285、吸収0で測定)で測定して求められるスラリー粒子の粒子径である、
酸化セリウム研磨剤。
A cerium oxide slurry for polishing a semiconductor substrate,
Oxide Cerium slurry, carbonates, nitrates, sulfates, cerium compounds selected from the oxalate and calcined at 600 ° C. or higher 900 ° C. or less, obtained by pulverizing this, primary surrounded by grain boundaries Cerium oxide particles comprising particles having a particle size of 0.5 to 3 μm, which are not aggregates of primary particles, having particles, water, and a dispersing agent,
The cerium oxide particles in the cerium oxide slurry have a particle size content of 500 nm or more of 3 to 40% by volume of all cerium oxide particles , and particles having a particle size of 3000 nm or less are 99% by volume or more,
The particle diameter of the cerium oxide particles in the cerium oxide slurry is determined by measuring the cerium oxide slurry by a laser diffraction method (measured with a light source He—Ne laser, a particle refractive index of 1.9285, and zero absorption). The particle size of the slurry particles,
Cerium oxide abrasive.
SiO絶縁膜を研磨するための酸化セリウムスラリーであって、
該酸化セリウムスラリーは、炭酸塩、硝酸塩、硫酸塩、しゅう酸塩から選択されるセリウム化合物を600℃以上900℃以下で焼成し、これを粉砕して得られた、粒界に囲まれた一次粒子を有する、一次粒子の凝集体ではない粒子径0.5〜3μmの粒子を含む酸化セリウム粒子、水、及び分散剤を含み、
該酸化セリウムスラリー中の前記酸化セリウム粒子は、500nm以上の粒子径の含有量が全酸化セリウム粒子の3〜40体積%で、粒子径が3000nm以下である粒子が99体積%以上であり、
該酸化セリウムスラリー中の前記酸化セリウム粒子の粒子径は、前記酸化セリウムスラリーを、レーザー回折法(光源He−Neレーザー、粒子の屈折率1.9285、吸収0で測定)で測定して求められるスラリー粒子の粒子径である、
酸化セリウム研磨剤。
A cerium oxide slurry for polishing a SiO 2 insulating film,
Oxide Cerium slurry, carbonates, nitrates, sulfates, cerium compounds selected from the oxalate and calcined at 600 ° C. or higher 900 ° C. or less, obtained by pulverizing this, primary surrounded by grain boundaries Cerium oxide particles comprising particles having a particle size of 0.5 to 3 μm, which are not aggregates of primary particles, having particles, water, and a dispersing agent,
The cerium oxide particles in the cerium oxide slurry have a particle size content of 500 nm or more of 3 to 40% by volume of all cerium oxide particles , and particles having a particle size of 3000 nm or less are 99% by volume or more,
The particle diameter of the cerium oxide particles in the cerium oxide slurry is determined by measuring the cerium oxide slurry by a laser diffraction method (measured with a light source He—Ne laser, a particle refractive index of 1.9285, and zero absorption). The particle size of the slurry particles,
Cerium oxide abrasive.
前記酸化セリウム粒子は、粒子径の中央値が150〜450nmである、請求項1または請求項2に記載の酸化セリウム研磨剤。   The cerium oxide abrasive according to claim 1 or 2, wherein the cerium oxide particles have a median particle diameter of 150 to 450 nm. 請求項1または請求項3に記載の酸化セリウム研磨剤で半導体基板を研磨することを特徴とする半導体基板の研磨法。   A method for polishing a semiconductor substrate, comprising polishing the semiconductor substrate with the cerium oxide abrasive according to claim 1. 請求項2または請求項3に記載の酸化セリウム研磨剤で、SiO絶縁膜を研磨することを特徴とするSiO絶縁膜の研磨法。 Cerium oxide abrasive according to claim 2 or claim 3, polishing of the SiO 2 insulating film, characterized in that polishing the SiO 2 insulating film.
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