TWI290505B - Chemical mechanical polishing pad, manufacturing process thereof and chemical mechanical polishing method - Google Patents

Chemical mechanical polishing pad, manufacturing process thereof and chemical mechanical polishing method Download PDF

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Publication number
TWI290505B
TWI290505B TW094112745A TW94112745A TWI290505B TW I290505 B TWI290505 B TW I290505B TW 094112745 A TW094112745 A TW 094112745A TW 94112745 A TW94112745 A TW 94112745A TW I290505 B TWI290505 B TW I290505B
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Taiwan
Prior art keywords
chemical mechanical
mechanical polishing
water
polishing pad
grinding
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TW094112745A
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Chinese (zh)
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TW200600261A (en
Inventor
Yukio Hosaka
Yuuji Shimoyama
Hiroshi Shiho
Nobuo Kawahashi
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Jsr Corp
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D11/00Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
    • B24D11/001Manufacture of flexible abrasive materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24BMACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
    • B24B37/00Lapping machines or devices; Accessories
    • B24B37/04Lapping machines or devices; Accessories designed for working plane surfaces
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24BMACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
    • B24B37/00Lapping machines or devices; Accessories
    • B24B37/04Lapping machines or devices; Accessories designed for working plane surfaces
    • B24B37/042Lapping machines or devices; Accessories designed for working plane surfaces operating processes therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
    • B24D3/20Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic
    • B24D3/28Resins or natural or synthetic macromolecular compounds

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
  • Mechanical Treatment Of Semiconductor (AREA)

Abstract

A chemical mechanical polishing pad having a polishing surface with an arithmetic mean roughness (Ra) of 0.1 to 15 mum, a 10 point height (Rz) of 40 to 150 mum, a core roughness depth (Rk) of 12 to 50 mum and a reduced peak height (Rpk) of 7 to 40 mum, a manufacturing process thereof and a chemical mechanical polishing method. Even when the chemical mechanical polishing of a large-diameter wafer as an object to be polished is carried out by this pad, a polished surface having excellent in-plane uniformity and flatness can be formed.

Description

1290505 九、發明說明: 【發明所屬之技術領域】 本發明係關於一種化學機械研磨墊、其製造方法及化學 機械研磨方法。 « 更明確言之,其係關於一種化學機械研磨墊、其製造方 ’ 法及使用該化學機械研磨墊之化學機械研磨方法,該化學 機械研磨墊能夠在進行表面化學機械研磨時提供具有極佳 的平面内均勻度及平坦度之一經研磨的表面。 • 【先前技術】 在用以製造一半導體元件之方法中,採用CMP(化學機械 研磨)作為能夠將一極平坦的表面提供給一晶圓之一技 術。CMP技術係藉由讓作為研磨粒水性分散液之化學機械 研磨漿料在一化學機械研磨墊表面上流下來,同時對著該 化學機械研磨墊之表面按壓欲研磨之表面並讓該欲研磨之 表面滑動接觸到該化學機械研磨墊之表面,從而對一表面 進行化學機械研磨。已知在此CMP中該化學機械研磨墊之 _ 性能特徵及特性對研磨結果有很大的影響。1290505 IX. DESCRIPTION OF THE INVENTION: TECHNICAL FIELD The present invention relates to a chemical mechanical polishing pad, a method of manufacturing the same, and a chemical mechanical polishing method. « More specifically, it relates to a chemical mechanical polishing pad, its manufacturer's method and a chemical mechanical polishing method using the chemical mechanical polishing pad, which can provide excellent surface chemical mechanical polishing. One of the in-plane uniformity and flatness of the ground surface. • [Prior Art] In the method for manufacturing a semiconductor element, CMP (Chemical Mechanical Polishing) is employed as a technique capable of supplying a flat surface to a wafer. The CMP technique is performed by allowing a chemical mechanical polishing slurry as an aqueous dispersion of abrasive particles to flow down on the surface of a chemical mechanical polishing pad while pressing the surface to be ground against the surface of the chemical mechanical polishing pad and allowing the surface to be ground. Sliding contact with the surface of the chemical mechanical polishing pad to chemically grind a surface. It is known that the performance characteristics and characteristics of the chemical mechanical polishing pad in this CMP have a great influence on the polishing result.

已知的化學機械研磨墊包括,例如包含相當多孔的聚胺 基甲酸酯發泡樹脂墊以及包含相當多分散於一非發泡基質 中的水溶性精細粒子之一墊(前者係揭示於Jp_AKnown chemical mechanical polishing pads include, for example, a pad comprising a relatively porous polyurethane foaming resin and a pad comprising a relatively large amount of water-soluble fine particles dispersed in a non-foamed matrix (the former is disclosed in Jp_A).

及 JP_A 8-216029 中,而後者係揭示於 jp_A 2000_34416、JP_A 2000-33552及JP-A 2001-334455中)(本文所使用的術語 「JP·A」表示「未經審核而公佈的曰本專利申請案」)。 由於現在用以製造半導體之方法中需要提高生產力,因 101279.doc • 6 - 1290505 此需要化學機械研磨的晶圓之直徑變得越來越大。 在藉由傳統上已知的方法在一大直徑晶圓上進行化學 機械研磨時,化學機械研磨後經研磨表面之平面内均勻度 及平坦度可能變得不令人滿意。 【發明内容】 鑒於上述問題,本發明之一目的係提供一種化學機械研 磨墊、其製造方法及化學機械研磨方法,該墊即使在作為 一欲研磨物件之一大直徑晶圓上進行化學機械研磨時亦能 夠提供具有極佳的平面内均勻度及平坦度之一經研磨的表 面0 從以下說明中,將會明白本發明之其他目的及優點。 依據本發明,首先,本發明之上述目的及優點係藉由具 有一研磨表面與一非研磨表面之一化學機械研磨墊而實 現’該研磨表面之算術平均粗糙度(Ra)為0.1至15 μηι,10 點面度(Rz)為40至150 μηι,核心粗糙深度(Rk)為12至50 μηι ’以及減小之峰值高度(Rpk# 7至4〇叫。 其次,本發明之上述目的及優點係藉由製造上述化學機 械研磨墊之一方法而實現,其包含以下步驟: 模製一研磨層;以及 至少將欲成為該研磨層的研磨表面之該表面磨光。 第三’本發明之上述目的及優點係藉由化學機械研磨方 法而實現’該方法包含藉由上述化學機械研磨墊來對一欲 研磨物件進行化學機械研磨。 【實施方式】 101279.doc 1290505 本發明之化學機械研磨墊之研磨表面之算術平均粗糙度 (Ra)為〇· 1至15 μπι ’ 10點高度(Rz)為40至150 μιη,核心粗链 深度(Rk)為12至5 0 μηι,以及減小之峰值高度(Rpk)為7至40 μπι。 該些值係定義為依據藉由測量設定於該墊表面上的複數 個測量線而獲得之粗链度輪廓而計算出的下列數值之平均 數。例如,可藉由來自Mitani公司的LM手冊(模擬版)3.62 版所揭示之一方法來計算出該些數值。 若評估長度L之粗糙度輪廓的X軸係繪製為與該粗糙度輪 廓的平均線平行之方向,y轴係繪製為該粗糙度輪廓之縱向 放大方向,而測量出的粗糙度輪廓係以等式y=f(x)來表示, 則該算術平均粗糙度(Ra)係由以下等式(1)表示之一值。 (ο 若評估長度L之粗糙度輪廓的X轴係繪製為與該粗糙度輪 廓之平均線平行之方向,y軸係繪製為該粗糙度輪廓之縱向 放大方向時,分別以^至!^來表示在該縱向放大方向上從 該平均線起最高峰至第五高峰的頂部距離,而以¥1至¥5來 表示從該平均線起最低谷至第五低谷的底部距離(參見圖 則該10點高度(Rz)係由以下等式(2)來表示之一值。 (2) - i>·、 該核心粗糙深度(Rk)與減小之峰值高度(Rpk)係以由評 估長度為L的#縫度輪廓導出之一材料比率曲線來定義。 材料比率曲線表示藉由將一截切面⑽丨⑽丨)繪製為 101279.doc 1290505 縱向軸而將一材料比率繪製為水平轴而獲得之一曲線。本 文使用的術語「截切面」表示當以與上述算術平均粗糙度 (Ra)中相同的等式y==f(x)來表示該粗糙度輪廓時之一特定 的y值。術語「材料比率」係當該粗链度輪廓係切割於一特 定的截切面時,一切割部分的長度與該評估長度L之一百分 比。當該截切面處於該粗糙度輪廓中的最高峰之頂部時, 該材料比率為0%,而當該截切面處於該最低谷之底部時則 為100%(參見圖2)。 若在如上所述而定義之材料比率曲線上設定二點八與B 且該專二點之間的材料比率之差為4〇%,而該等二點之間 的截切面之差係最小,而點C係連接該等點A、B並在二方 向上延伸之一直線與表示0%的材料比率之一線之間的交 叉點’而點D係連接該荨點A、B之直線與表示1 〇 〇 %的材料 比率之一線之間的交叉點(參見圖3),則該核心粗糙深度 (Rk)係點C與D之間的截切面之差。 若穿過上述核心粗縫深度(Rk)定義中的點c之截切面與 該材料比率曲線之間的交叉點為一點Η,該材料比率曲線與 表示0%的材料比率之線之間的交叉點為點I,且在表示〇〇/〇 的材料比率之一直線上設定一點J以確保該線區段CH、線區 段CI及曲線HI所圍繞之區域變成等於該三角形CHJ之區域 (參見圖4。圖4中的A1係該線區段CH、線區段CI及該曲線 HI所圍繞之區域,即該三角形CHJ之區域),則減小之峰值 高度(Rpk)係該等點C與J之間的截切面之差。 如下所述,將用以測量上述算術平均粗糙度(Ra)、1 〇點 101279.doc 1290505 高度(Rz)、核心粗糙深度(Rk)及減小之峰值高度(Rpk)之複 數個測量線設定於該墊上。 首先,將該等複數個測量線之中心點設定如下。對於該 專測置線之中心點’從該塾的研磨表面之一端處的一任意 點至另一點緣製長度變成最長的虛擬直線(當該墊之研磨 表面為圓形時,上述虛擬直線變成形成該墊表面的一圓之 直径)’從而以大致相等的間隔在該虛擬直線上設定至5〇 個點’但該虛擬直線長度從該中心至二側之一 5 %區域與該 •虛擬直線長度從該等二端起之5%區域除外。該等測量線的 中心點之數目較佳的係25至50。 可在本發明之化學機械研磨墊之研磨表面中形成一(或 多個)溝槽,下面將對此進行說明。在此情況下,該等測量 線之中心點應設定成使得所有如下所述而設定的測量線皆 存在於該研磨表面内除該(等)溝槽以外之一部分中。1〇至5〇 個測量點不一定係依據形成於該研磨表面中的溝槽形狀而 φ 以大致相等的間隔設定於上述虛擬直線上。在此情況下, 可在以相等間隔設定的各點中,藉由排除該等測量線部分 地與該溝槽部分重疊之點來確定上述的點數目。將與該等 虛擬直線交又以設定該等複數個點並穿過「該等測量線的 中〜點」之直線假定並視為測量線。該等測量線之長度可 月b係1至15 mm ’並以上述測量線之中心點作為其中心。 可藉由使用一可購得之表面粗糙度計量器來測量上述粗 糙度輪廓。 、牙於本發明之化學機械研磨墊,由此測量出的該研磨表 101279.doc 1290505 面之一術平均粗糖度(Ra)為0 · 1至15 μιη。此值較佳的係〇 1 至12 μιη。該1〇點南度(Rz)係40至150 μιη。其較佳的係4〇至 130 μιη。該核心粗链深度(Rk)為12至50 μιη。其較佳的係12 至45 μπχ。該減小之峰值咼度(Rpk)為7至40 μιη。其較佳的 係 7 至 3 Ο μπι。 當使用具有該些值之化學機械研磨塾來實施該化學機械 研磨步驟時,可獲得具有極佳的平面内均勻度及平坦度之 一研磨表面。此效果在對一大直徑晶圓進行化學機械研磨 拋光時尤為明顯。 本發明之化學機械研磨墊之厚度分布較佳的係5〇 ^❿或 更小。藉由將該化學機械研磨墊之厚度分布設定為5〇 ^瓜或 更小’而呈現出本發明之有利效果。此值更佳的係4〇 或 更小,尤其較佳的係30 μιη或更小。藉由將該化學機械研磨 塾之厚度分布設定於此範圍,即使在對作為一欲研磨物件 之一大直徑晶圓進行化學機械研磨時,亦能獲得具有極佳 的平面内均勻度及平坦度之一經研磨的表面。 藉由在設定於該塾表面上的複數個測量點測量該厚度, 可依據以下等式而計算出該厚度分布。厚度分布=(厚度最 大測量值)一(厚度最小測量值)。 在從該塾的研磨表面之一端處的一任意點至另一點緣製 且其長度因此而變成最大之虛擬直線(當該墊之研磨表面 為圓形時,上述虛擬直線變成形成該墊表面的一圓之直徑) 上以相等的間隔設定10至5 0個測量點,但是該虛擬直線長 度從該中心至二側之一 5%區域以及該虛擬直線長度從二 101279.doc • 11 - 1290505 i^起之5%區域除外。測量點之數目較佳的係25至50。And JP_A 8-216029, the latter being disclosed in jp_A 2000_34416, JP_A 2000-33552, and JP-A 2001-334455) (The term "JP·A" as used herein means "unaudited and published patent" Application"). Because of the need to increase productivity in the methods used to fabricate semiconductors, the diameter of wafers requiring chemical mechanical polishing is becoming larger as 101279.doc • 6 - 1290505. When chemical mechanical polishing is performed on a large diameter wafer by a conventionally known method, the in-plane uniformity and flatness of the ground surface after chemical mechanical polishing may become unsatisfactory. SUMMARY OF THE INVENTION In view of the above problems, it is an object of the present invention to provide a chemical mechanical polishing pad, a method of manufacturing the same, and a chemical mechanical polishing method for chemical mechanical polishing on a large-diameter wafer as a workpiece to be polished. It is also possible to provide a surface 0 which has excellent in-plane uniformity and flatness. The other objects and advantages of the present invention will become apparent from the following description. According to the present invention, first of all, the above objects and advantages of the present invention are achieved by a chemical mechanical polishing pad having an abrasive surface and a non-abrasive surface. The arithmetic mean roughness (Ra) of the abrasive surface is 0.1 to 15 μm. The 10-point facet (Rz) is 40 to 150 μηι, the core roughness depth (Rk) is 12 to 50 μηι ' and the reduced peak height (Rpk# 7 to 4 〇. Second, the above objects and advantages of the present invention) By the method of manufacturing one of the above chemical mechanical polishing pads, comprising the steps of: molding an abrasive layer; and polishing at least the surface of the abrasive surface to be the abrasive layer. The object and the advantages are achieved by a chemical mechanical polishing method. The method comprises chemical mechanical polishing of a workpiece to be polished by the above chemical mechanical polishing pad. [Embodiment] 101279.doc 1290505 The chemical mechanical polishing pad of the present invention The arithmetic mean roughness (Ra) of the ground surface is 〇·1 to 15 μπι '10 points height (Rz) is 40 to 150 μηη, and the core thick chain depth (Rk) is 12 to 50 μm. The reduced peak height (Rpk) is 7 to 40 μπι. These values are defined as the average of the following values calculated from the thick chain profile obtained by measuring a plurality of measurement lines set on the surface of the pad. For example, the values can be calculated by one of the methods disclosed in the LM manual (analog version) version 3.62 from Mitani. If the X-axis system of the roughness profile of the evaluation length L is plotted as the roughness profile The average line is parallel to the direction, the y-axis is drawn as the longitudinal magnification direction of the roughness profile, and the measured roughness profile is expressed by the equation y=f(x), then the arithmetic mean roughness (Ra) A value is expressed by the following equation (1). (ο If the X-axis system of the roughness profile of the evaluation length L is drawn in a direction parallel to the average line of the roughness profile, the y-axis system is drawn as the roughness profile. When the longitudinal direction is enlarged, the top distance from the highest peak to the fifth peak in the longitudinal enlargement direction is represented by ^ to !^, and the lowest from the average line is represented by ¥1 to ¥5. The bottom distance from the valley to the fifth trough (see The 10 point height (Rz) is represented by the following equation (2): (2) - i>, the core roughness depth (Rk) and the decreasing peak height (Rpk) are Evaluate a material ratio curve derived from the #slit profile derived length L. The material ratio curve represents a material ratio drawn as a horizontal axis by plotting a section plane (10) 丨(10)丨 as 101279.doc 1290505 longitudinal axis A curve is obtained. The term "cut surface" as used herein means a specific y when the roughness profile is expressed by the same equation y==f(x) as in the arithmetic mean roughness (Ra) described above. value. The term "material ratio" is a percentage of the length of a cut portion to the estimated length L when the thick chain profile is cut at a particular cut surface. The material ratio is 0% when the cut surface is at the top of the highest peak in the roughness profile and 100% when the cut surface is at the bottom of the lowest valley (see Figure 2). If the difference between the material ratios between the two points and the special point is set to 4% on the material ratio curve defined as described above, and the difference between the cut surfaces between the two points is the smallest, And point C is a point connecting the points A, B and extending one line in two directions with a line representing a material ratio of 0%' and the point D is a line connecting the points A, B and the representation 1 The intersection between the lines of one of the material ratios of 〇〇% (see Figure 3), then the core roughness depth (Rk) is the difference between the tangent planes between points C and D. If the intersection between the cross-section of the point c in the definition of the core nick depth (Rk) and the material ratio curve is a point Η, the intersection between the material ratio curve and the line representing the material ratio of 0% The point is point I, and a point J is set on a straight line indicating the material ratio of 〇〇/〇 to ensure that the area surrounded by the line segment CH, the line segment CI, and the curve HI becomes equal to the area of the triangle CHJ (see the figure). 4. A1 in Fig. 4 is the line segment CH, the line segment CI and the region surrounded by the curve HI, that is, the region of the triangle CHJ), and the reduced peak height (Rpk) is the point C and The difference between the cut planes between J. As described below, a plurality of measurement lines for measuring the above arithmetic mean roughness (Ra), 1 〇 point 101279.doc 1290505 height (Rz), core roughness depth (Rk), and decreasing peak height (Rpk) are set. On the mat. First, the center points of the plurality of measurement lines are set as follows. For the center point of the dedicated line, the virtual line from the arbitrary point at one end of the grinding surface of the crucible to the other point becomes the longest virtual line (when the grinding surface of the mat is circular, the virtual line becomes a diameter of a circle forming the surface of the pad) so as to be set to 5 〇 dots on the virtual straight line at substantially equal intervals 'but the imaginary straight line length is from the center to a 5% region of the two sides and the virtual straight line length Except for the 5% area from these two ends. The number of center points of the measurement lines is preferably 25 to 50. One (or more) grooves may be formed in the abrasive surface of the CMP pad of the present invention, as will be explained below. In this case, the center points of the measurement lines should be set such that all of the measurement lines set as described below are present in the polishing surface in a portion other than the (equal) groove. The 1 〇 to 5 测量 measurement points are not necessarily set on the virtual straight line at substantially equal intervals depending on the shape of the grooves formed in the polishing surface. In this case, the number of dots described above can be determined by excluding the points at which the measurement lines partially overlap the groove portions at respective points set at equal intervals. A line that intersects the virtual lines and sets the plurality of points and passes through the "middle-point" of the measurement lines is assumed to be a measurement line. The length of the measuring lines can be 1 to 15 mm ′ for the month b and centered on the center point of the above measuring line. The above roughness profile can be measured by using a commercially available surface roughness meter. The tooth of the chemical mechanical polishing pad of the present invention, and the average roughness (Ra) of the surface of the grinding table 101279.doc 1290505 thus measured is from 0.1 to 15 μm. This value is preferably from 1 to 12 μιη. The 1 point south (Rz) is 40 to 150 μm. It is preferably from 4 to 130 μm. The core thick chain depth (Rk) is 12 to 50 μηη. It is preferably 12 to 45 μπχ. The reduced peak intensity (Rpk) is 7 to 40 μηη. It is preferably 7 to 3 Ο μπι. When the chemical mechanical polishing step is carried out using a chemical mechanical polishing crucible having such values, an abrasive surface having excellent in-plane uniformity and flatness can be obtained. This effect is especially noticeable for chemical mechanical polishing of large diameter wafers. The thickness distribution of the chemical mechanical polishing pad of the present invention is preferably 5 〇 ^ ❿ or less. The advantageous effects of the present invention are exhibited by setting the thickness distribution of the chemical mechanical polishing pad to 5 〇 melon or less. This value is preferably 4 或 or less, and particularly preferably 30 μm or less. By setting the thickness distribution of the chemical mechanical polishing crucible to this range, even in the case of chemical mechanical polishing of a large-diameter wafer as a workpiece to be polished, excellent in-plane uniformity and flatness can be obtained. One of the ground surfaces. By measuring the thickness at a plurality of measurement points set on the surface of the crucible, the thickness distribution can be calculated according to the following equation. Thickness distribution = (maximum thickness measurement) 1 (minimum thickness measurement). a virtual straight line which is formed from an arbitrary point at one end of the grinding surface of the crucible to another point and whose length thus becomes the largest (when the grinding surface of the mat is circular, the virtual straight line becomes the surface forming the mat 10 to 50 measuring points are set at equal intervals on the diameter of a circle, but the length of the virtual straight line is from the center to one of the two sides of the 5% area and the length of the virtual straight line is from two 101279.doc • 11 - 1290505 i^ Except for the 5% area. The number of measurement points is preferably from 25 to 50.

可在本發明之化學機械研磨墊之研磨表面中形成一(或 夕個)溝槽,下面將對此進行說明。在此情況下,應在該研 磨表面上除該(等)溝槽以外之一部分中設定該等測量點。在 某情況中,10至50個測量點不一定係依據形成於該研磨 表面中的溝槽形狀而以大致相等的間隔設定於上述虛擬直 線上。在此情況下,可在以大致相等的間隔設定之各點中, 藉由排除在該(等)溝槽中的點來確定上述測量點之數目。 可藉由將該化學機械研磨墊放置於一水平平面上並測量 該測量點與該水平平面之間的距離,而知道每一測量點處 之厚度。可使用-接觸型距離計量器來測量該測量點與該 水平平面之間的距離。-可購得之上述計量器產品係A (or evening) groove may be formed in the abrasive surface of the CMP pad of the present invention, as will be explained below. In this case, the measurement points should be set in the portion of the grinding surface other than the (etc.) groove. In some cases, 10 to 50 measurement points are not necessarily set on the virtual straight line at substantially equal intervals depending on the shape of the grooves formed in the polishing surface. In this case, the number of the above-mentioned measurement points can be determined by excluding the points in the (etc.) grooves at points set at substantially equal intervals. The thickness at each measurement point can be known by placing the chemical mechanical polishing pad on a horizontal plane and measuring the distance between the measurement point and the horizontal plane. A contact type distance gauge can be used to measure the distance between the measurement point and the horizontal plane. - The above-mentioned meter product series available for purchase

Manual 3-D計量器(Mitutoyo公司)。 本發明之化學機械研磨堅之形狀不受特定限制。其可魚 係碟片狀、腰帶狀或滾筒狀。較佳的係,依據一研磨則 適當地選擇該化學機械研磨墊之形狀。該化學機械研㈣ 在使用前之尺寸不受特定限制一碟片狀化學機械研磨鸯 之直徑為’例如〇.5至_⑽’較佳的係i .〇至250 em,更佳 的係撕脈m。其厚度為,例如,大於…職及小於ι〇( mm’尤其較佳的係1至1〇mm。 本發明之化學機械研磨塾可能 -/、有在該研磨表面中之 ::多個:任意形狀的溝槽或凹痕部分。該(等)溝槽或凹痕 刀係用來固持一用於化學機械研磨之八 π㈣__提供),並將此水性分散二== 101279.doc •12· 1290505 磨物件之研磨表面,保㈣如晶片及由化學機械研磨臨時 產生的研磨液體廢料之類的廢料並成為向外部排放廢料之 一路線。 上述溝槽之形狀並不受特定限制,而可能係圓形、方格 狀或放射狀。上述凹痕部分之形狀係圓形或多角形。該(等) 溝槽或凹痕部分之區段形式不受特定限制。其可能係,例 如’矩形、梯形、u形或v形。 ^ 該等溝槽或該等凹痕部分之數目可能係一或多個。 該(等)溝槽或凹痕部分之尺寸不受特定限制。該(等)溝槽 寬度或該(等)凹痕部分之最短直徑可能係,例如,〇.丨mm 或更大,明確言之係〇·1至〇·5 mm,更明確言之係〇 2至3 〇 mm。該(等)溝槽寬度或該(等)凹痕部分之深度可能係,例 如’ 〇·1 mm或更大,明確言之係⑴丨至]」,更明確言之 係 0.2至 2.0 mm。 上述溝槽或凹痕部分的内壁之表面粗糙度較佳的係2〇 μΠ1或更小’更佳的係15 μπι或更小。藉由將該(等)溝槽寬度 或該(等)凹痕部分的内壁之表面粗糙度設定於此範圍,當藉 由此墊來實施化學機械研磨時,可防止該物件之經研磨的 表面受刮擦並有利於提高研磨速度及該研磨墊之使用壽 命。藉由將該(等)溝槽或凹痕部分的内壁之表面粗糙度設定 於此範圍而使該研磨速度獲得提高,其原因係假定為,由 於更好地實施將一用於化學機械研磨的水性分散液分布於 經研磨表面之功能。藉由將該(等)溝槽或凹痕部分的内壁之 表面粗糙度設定於此範圍而使該研磨墊之使用壽命獲得提 101279.doc -13- l29〇5〇5 高’其原因係假定為,由於更好地實施排放由化學機械研 磨而產生的廢料之功能。 可藉由一表面粗糙度光學計量器或表面粗糙度接觸型計 量器來測量上述表面粗链度。上述表面粗糖度光學計量器 之範例包括一 3-D表面結構分析顯微鏡、掃描雷射顯微鏡及 電子束表面形式分析器。上述接觸型表面粗糙度計量器之 範例包括一示蹤器型表面粗糙度計量器。Manual 3-D meter (Mitutoyo). The shape of the chemical mechanical polishing of the present invention is not particularly limited. The fish can be in the form of a disc, a belt or a drum. Preferably, the shape of the chemical mechanical polishing pad is appropriately selected in accordance with a grinding. The chemical mechanical research (4) before use, the size is not subject to a specific limitation. The diameter of a disc-shaped chemical mechanical polishing crucible is 'for example, 〇.5 to _(10)', the preferred one is i.〇 to 250 em, and the better is torn. Pulse m. The thickness is, for example, greater than... and less than ι (mm' is particularly preferred from 1 to 1 mm. The chemical mechanical polishing of the present invention may be -/, in the abrasive surface:: multiple: Any groove or dent portion of any shape. The groove or dent is used to hold an eight π(tetra)__ for chemical mechanical polishing, and this aqueous dispersion is two == 101279.doc •12 · 1290505 Abrasive surface of abrasive articles, and (4) scraps such as wafers and grinding liquid waste temporarily produced by chemical mechanical grinding and become a route for discharging waste to the outside. The shape of the above grooves is not particularly limited, and may be circular, square or radial. The shape of the above-mentioned dimple portion is circular or polygonal. The segment form of the (or the like) groove or the indent portion is not particularly limited. It may be, for example, 'rectangular, trapezoidal, u-shaped or v-shaped. ^ The number of such grooves or such indented portions may be one or more. The size of the (or the like) groove or the dent portion is not particularly limited. The width of the groove or the shortest diameter of the (etc.) dimple portion may be, for example, 〇.丨mm or larger, specifically 〇·1 to 〇·5 mm, more specifically the system 2 to 3 〇mm. The width of the (or other) groove or the depth of the (etc.) dent portion may be, for example, < 〇·1 mm or more, specifically (1) 丨 to], and more specifically 0.2 to 2.0 mm. The surface roughness of the inner wall of the groove or the indented portion is preferably 2 〇 μΠ 1 or less, and more preferably 15 μm or less. By setting the width of the groove or the surface roughness of the inner wall of the indented portion to this range, when the chemical mechanical polishing is performed by the pad, the ground surface of the object can be prevented. It is scratched and helps to increase the grinding speed and the service life of the polishing pad. The polishing rate is improved by setting the surface roughness of the inner wall of the groove or the indented portion to this range, which is assumed to be due to better implementation of a chemical mechanical polishing. The aqueous dispersion functions as a distributed surface. By setting the surface roughness of the inner wall of the groove or the dent portion to this range, the service life of the polishing pad is increased by 101279.doc -13-l29〇5〇5 high'. In order to better implement the function of discharging waste generated by chemical mechanical grinding. The above surface roughness can be measured by a surface roughness optical meter or a surface roughness contact type meter. Examples of the above surface roughness optical meter include a 3-D surface structure analysis microscope, a scanning laser microscope, and an electron beam surface format analyzer. An example of the above contact type surface roughness meter includes a tracer type surface roughness meter.

本發明之化學機械研磨墊可進一步具有在該非研磨表面 (該墊之後側)上之一(或多個)溝槽或凹痕部分。 該(等)溝槽或凹痕部分有助於抑制在該化學機械研磨步 驟中在該研磨表面上產生—表面缺陷。假定即使在諸如粗 糙粒子之類的外來物質(該些外來物質可能係包含在用於 =學機械研磨之水性分散液中或在由該化學機械研磨製造 私序產生的切割晶片中)進入該研磨墊與該欲研磨物件之 間時’該(等)凹痕部分亦可用來緩解局部產生的過大壓力從 而減少經研磨表面上的表面缺陷數目。 上述溝槽或凹痕部分之形狀不受特定限制。該(等)溝槽 之形狀可能係螺旋形、環形或方格狀。該(等)㈣部分之形 狀可能係圓形或多角形。 該(等)溝槽或凹痕部分可妒從^立 丨刀了月匕係任意尺寸。當該(等)凹痕4 刀係圓形時,其直徑可能伤The CMP pad of the present invention may further have one (or more) grooves or dent portions on the non-abrasive surface (the back side of the pad). The (or the like) groove or indentation portion helps to suppress the occurrence of surface defects on the abrasive surface in the chemical mechanical polishing step. It is assumed that even if foreign substances such as coarse particles (which may be contained in an aqueous dispersion for mechanical polishing or in a dicing wafer produced by the chemical mechanical polishing manufacturing process) enter the polishing The portion of the indentation between the pad and the article to be abraded can also be used to relieve excessive pressure generated locally to reduce the number of surface defects on the surface being abraded. The shape of the above groove or dent portion is not particularly limited. The shape of the (etc.) groove may be spiral, circular or square. The shape of the (etc.) (4) portion may be circular or polygonal. The (or other) groove or dent portion can be arbitrarily smashed from the 丨 了. When the (etc.) dent 4 knife is round, its diameter may be injured.

月匕係1至300 mm,明確言之係5至2C mm,更明確言之係1〇 产15〇mm。當該(等)溝槽係螺旋狀 衣"方格狀時’其寬度可能為〇ι至2〇随,明確言之名 .1至1〇咖。該(等)溝槽或凹痕部分之深度可能係,例女 101279.doc -14- 1290505 0·01至2.0mm,明確言之係o.l至1.5mm,更明確言之係〇·ι 至1 ·0 mm ’而不論其形狀如何。 該專溝槽或凹痕部分之數目可能係一或多個。 本發明之化學機械研磨墊具有如上所述之一 50 μηχ或更 小之厚度分布,且視需要在該研磨表面及/或該非研磨表面 中具有一(或多個)溝槽或凹痕部分。儘管用以製造該墊之方 法不受特定限制,但亦可藉由(例如)包含以下步驟之一方法 來製造該墊。 (1) 製備一用於化學機械研磨墊的組成物之步驟; (2) 將用於化學機械研磨墊之上述組成物模製成一研磨層 之步驟;以及 (3) 將至少上述研磨層之研磨表面磨光之步驟。 隨後將對上面每一步驟進行詳細說明。 (1)製備一用於化學機械研磨墊的組成物之步驟 本發明之化學機械研磨墊可由任何材料製成,只要能實 現本發明之目的便可。較佳的係,在研磨開始之前應形成 多孔,該等孔具有以下二功能:在化學機械研磨期間固持 一用於化學機械研磨的水性分散液;以及,讓研磨晶片暫 時保持不受該化學機械研磨墊功能的影響。因此,該化學 機械研磨墊較佳的係由以下材料製成:由水溶性粒子與一 包含分散於其巾的水溶性粒子之非水溶性基質組成之一材 料;或者’由多個凹穴與一包含分散於其中的多個凹穴之 非水溶性基f材料組成之—材料,例如,—發泡塑料。 -中的刖材料中,該等水溶性粒子在研磨時接觸到 101279.doc -15- 1290505 一包含該水性媒介與一固體的水性漿料媒介,並溶解或膨 脹以致被消除’而該漿料可能係固持於藉消除而形成之多 孔内。在後一材料中,可將該漿料固持於形成為該等凹穴 之多孔内。 上述「非水洛性基質」之材料不受特定限制,但較佳的 係一有機材料,因為有機材料容易模製成具有一預定形狀 及預定特性且能提供合適的硬度及合適的彈性。該有機材 料之範例包括熱塑性樹脂、彈性體、橡膠(例如,交聯橡膠) 及可固化樹脂(例如,可熱固化或光固化的樹脂以及藉由熱 里或光而固化之樹脂)。其可能係單獨或組合使用。 在該些材料範例中,上述熱塑性樹脂包括丨,2_聚丁二稀樹 脂、聚烯烴樹脂(例如,聚乙烯、聚苯乙烯樹脂)、聚丙烯酸 樹脂(例如,以丙烯酸(甲)酯為主的樹脂)、乙烯基酯樹脂(除 丙烯酸樹酯外)、聚酯樹脂、聚酰胺樹脂、氟樹脂(例如,聚 偏二氟乙烯)、聚碳酸酯樹脂及聚甲醛樹脂。 上述彈性體包括:二烯烴彈性體(例如,12—聚丁二烯、 聚烯烴彈性體(TPO))、以苯乙烯為主的彈性體(例如,苯乙 晞-丁二稀-苯乙晞塊狀共聚物及其氫化塊狀共聚 物)(SEBS)、熱塑性聚胺基甲酸酯彈性體(TPU)、熱塑性彈 性體(例如,聚酯彈性體(TPEE)及聚酰胺彈性體(TPAE))、 聚矽氧樹脂彈性體及氟樹脂彈性體。該等橡膠包括:共軛 的二烯橡膠,例如,丁二烯橡膠(高順丁橡膠、低順丁橡膠 等)、異戊二烯橡膠、苯乙烯-丁二烯橡膠及苯乙烯-異戊二 烯橡膠、腈橡膠(例如丙浠腈-丁二烯橡膠)、丙烯酸橡膠、 101279.doc -16 - 1290505 乙烯基-α-烯烴橡膠(例如,乙烯-丙烯橡膠及乙烯-丙烯-二 烯橡膠),及其他橡膠(例如,丁基橡膠、聚矽氧橡膠及氟橡 膠)。 上述可固化樹脂包括氨基鉀酸酯樹脂、環氧樹脂、丙烯 酸樹脂、不飽和聚酯樹脂、聚胺基甲酸酯脲樹脂、脲樹脂、 矽樹脂、酚樹脂及乙烯基酯樹脂。 可藉由一酸酐基團、羧基團、羥氫氧基團、環氧基團或 氨基團來修改上述有機材料。可藉由修改來調整下面將要 說明的水溶性粒子及有機材料漿料之親合性。 該些有機材料可單獨使用或將其中的二或更多材料組合 起來使用。 進一步,該有機材料可能係一部分或整體交聯的聚合物 或非交聯聚合物。因此,該非水溶性基質可能係由一交聯 聚合物單獨組成,或由一交聯聚合物與一非交聯聚合物之 一混合物組成,或由一非交聯聚合物單獨組成。其較佳的 係由一交聯聚合物單獨組成或由一交聯聚合物與一非交聯 聚合物之一混合物組成。當獲得一交聯聚合物時,向該水 溶性基質提供彈性恢復力,並可減少因研磨期間施加給該 化學機械研磨墊之剪切應力而引起的位移。進一步,可有 效地防止該等多孔因該非水溶性基質在研磨及表面修整期 間的過度延伸而產生塑性變形,以及有效地防止該化學機 械研磨墊之表面過度起毛。因此,即使在表面修整期間亦 月巨有效地形成該等多孔,從而可抑制該漿料在研磨期間之 可保留性,且進一步使得該墊極少起毛,從而不會損壞研 101279.doc -17- 1290505 磨平坦度上述材料之交聯方法不受特定限制。例如,可 採用的交聯方法有n有機過氧化氫、硫續或硫確化 合物之化學交聯或者藉由施加—電子束之輻射交聯。 交聯的聚合物可能係一交聯橡膠、可固化樹脂、交聯的 熱固樹月曰或出自上述有機材料之交聯彈性體。其中,較佳 的係一交聯的熱塑性樹脂及/或交聯彈性體,因為此等二者 對於許多類漿料巾包含的㈣或強驗皆能保持穩定且極少The lunar system is 1 to 300 mm, which is clearly 5 to 2 cm, and more specifically 1 to 15 mm. When the (equal) grooved spiral coat "checkered shape, its width may be 〇ι to 2〇, clearly stated. 1 to 1 〇. The depth of the (or other) groove or dent portion may be, for example, female 101279.doc -14- 1290505 0·01 to 2.0 mm, specifically ol to 1.5 mm, more specifically 〇·ι to 1 · 0 mm ' regardless of its shape. The number of recessed or indented portions may be one or more. The CMP pad of the present invention has a thickness distribution of 50 μηχ or less as described above, and optionally has one (or more) grooves or dent portions in the abrasive surface and/or the non-abrasive surface. Although the method for manufacturing the mat is not particularly limited, the mat may be fabricated by, for example, one of the following steps. (1) a step of preparing a composition for a chemical mechanical polishing pad; (2) a step of molding the above composition for a chemical mechanical polishing pad into a polishing layer; and (3) at least the above-mentioned polishing layer The step of polishing the surface. Each of the above steps will be described in detail later. (1) Step of preparing a composition for a chemical mechanical polishing pad The chemical mechanical polishing pad of the present invention can be made of any material as long as the object of the present invention can be achieved. Preferably, the pores are formed before the start of the grinding, the pores having the following two functions: holding an aqueous dispersion for chemical mechanical polishing during chemical mechanical polishing; and allowing the abrasive wafer to be temporarily protected from the chemical mechanical The effect of the polishing pad function. Accordingly, the CMP pad is preferably made of a material consisting of water-soluble particles and a water-insoluble matrix comprising water-soluble particles dispersed in the towel; or 'by a plurality of pockets A material comprising a water-insoluble base material comprising a plurality of pockets dispersed therein, for example, a foamed plastic. In the bismuth material, the water-soluble particles are contacted with 101279.doc -15-12090505 during grinding, containing an aqueous medium and a solid aqueous slurry medium, and dissolved or expanded to be eliminated. It may be held in a porous body formed by elimination. In the latter material, the slurry can be held within the pores formed into the pockets. The material of the above "non-aqueous matrix" is not particularly limited, but is preferably an organic material because the organic material is easily molded to have a predetermined shape and predetermined characteristics and can provide a suitable hardness and a suitable elasticity. Examples of the organic material include thermoplastic resins, elastomers, rubbers (e.g., crosslinked rubber), and curable resins (e.g., heat curable or photocurable resins and resins which are cured by heat or light). They may be used singly or in combination. In the material examples, the above thermoplastic resin includes ruthenium, 2-polybutylene resin, polyolefin resin (for example, polyethylene, polystyrene resin), polyacrylic resin (for example, mainly acrylic acid). Resin), vinyl ester resin (except acrylic resin), polyester resin, polyamide resin, fluororesin (for example, polyvinylidene fluoride), polycarbonate resin, and polyacetal resin. The above elastomers include: diene elastomers (for example, 12-polybutadiene, polyolefin elastomer (TPO)), styrene-based elastomers (for example, styrene-butadiene-phenethyl hydrazine) Block copolymers and their hydrogenated block copolymers) (SEBS), thermoplastic polyurethane elastomers (TPU), thermoplastic elastomers (eg, polyester elastomers (TPEE) and polyamide elastomers (TPAE) ), a polyoxyxene elastomer and a fluororesin elastomer. The rubbers include: conjugated diene rubbers such as butadiene rubber (high butadiene rubber, low butadiene rubber, etc.), isoprene rubber, styrene-butadiene rubber, and styrene-isoprene. Rubber, nitrile rubber (eg acrylonitrile-butadiene rubber), acrylic rubber, 101279.doc -16 - 1290505 vinyl-α-olefin rubber (for example, ethylene-propylene rubber and ethylene-propylene-diene rubber), And other rubbers (for example, butyl rubber, polyoxyethylene rubber and fluororubber). The above curable resin includes a urethane resin, an epoxy resin, an acrylic resin, an unsaturated polyester resin, a polyurethane urea resin, a urea resin, an anthracene resin, a phenol resin, and a vinyl ester resin. The above organic material may be modified by an anhydride group, a carboxyl group, a hydroxyl group, an epoxy group or an amino group. The affinity of the water-soluble particles and the organic material slurry to be described below can be adjusted by modification. These organic materials may be used singly or in combination of two or more of them. Further, the organic material may be a partially or wholly crosslinked polymer or a non-crosslinked polymer. Therefore, the water-insoluble substrate may be composed of a cross-linked polymer alone, or a mixture of a cross-linked polymer and a non-cross-linked polymer, or a single non-cross-linked polymer. It preferably consists of a crosslinked polymer alone or a mixture of a crosslinked polymer and a non-crosslinked polymer. When a crosslinked polymer is obtained, an elastic restoring force is supplied to the water-soluble matrix, and displacement due to shear stress applied to the CMP pad during grinding can be reduced. Further, it is possible to effectively prevent the porous from being plastically deformed due to excessive elongation of the water-insoluble substrate during grinding and surface finishing, and to effectively prevent excessive surface fuzzing of the surface of the chemical mechanical polishing pad. Therefore, even when the surface is trimmed, the pores are formed efficiently, so that the retentivity of the slurry during the grinding can be suppressed, and the mat is further made to be less fluffy, so that the wafer is not damaged. 1290505 Grinding flatness The crosslinking method of the above materials is not particularly limited. For example, crosslinking methods which can be employed are chemical crosslinking of n organic hydrogen peroxide, sulfur or sulfur-reducing compounds or radiation crosslinking by application-electron beam. The crosslinked polymer may be a crosslinked rubber, a curable resin, a crosslinked thermosetting tree, or a crosslinked elastomer derived from the above organic materials. Among them, a crosslinked thermoplastic resin and/or a crosslinked elastomer are preferred because they are stable and rarely stable for many types of pulp towels.

因吸水而軟化。在該交聯熱塑樹脂及交聯彈性體中,更佳 的係與一有機過氧化氫交聯者,而尤其較佳的係交聯的L2— 聚丁二稀。 該交聯聚合物之含量不受特定限制,但較佳的係體積之 30%或更多,更佳的係體積之50%或更多,尤其較佳的係體 積之70%,並且可能係該非水溶性基質體積之1〇〇%。當該 非水溶性基質中的交聯聚合物之含量低於體積之3〇%時, 因包含該父聯聚合物而獲得之效果不一定能完全實現。 *上述包含一交聯聚合物的非水溶性基質之一樣本依據 JIS K 6251在80°C下斷裂時,上述非水溶性基質斷裂後的殘 餘伸長(簡稱為「斷裂後殘餘伸長」)可能為1〇〇%或更少。 即,該樣本在斷裂後各基準點之間的總距離變成斷裂前各 基準點之間距離的2倍或更小。此斷裂後殘餘伸長較佳的係 30%或更小,更佳的係1〇%或更小,尤其較佳的係5%或更 小而一般為0%或更大。當上述斷裂後殘餘伸長高於1〇〇% 時,從該化學機械研磨墊之表面刮掉或在研磨及表面更新 時拉伸的細片往往會不利地填充該等孔。該「斷裂後殘餘 101279.doc -18 - 1290505 伸長」作為一伸長,係藉由從每一 m攸母I率點與一拉力測試中 的斷裂且分割樣本之斷裂邱八 辦褽邛为之間的總距離中減去測試前Softened by water absorption. Among the crosslinked thermoplastic resins and crosslinked elastomers, it is more preferred to crosslink with an organic hydrogen peroxide, and particularly preferably a crosslinked L2-polybutadiene. The content of the crosslinked polymer is not particularly limited, but is preferably 30% or more by volume, more preferably 50% or more by volume, particularly preferably 70% by volume, and may be 1% by volume of the water-insoluble substrate. When the content of the crosslinked polymer in the water-insoluble matrix is less than 3 % by volume, the effect obtained by including the parent polymer may not be fully realized. * When one of the above samples of the water-insoluble matrix comprising a crosslinked polymer is broken at 80 ° C according to JIS K 6251, the residual elongation after the breakage of the water-insoluble matrix (abbreviated as "residual elongation after fracture") may be 1% or less. That is, the total distance between the reference points of the sample after the fracture becomes twice or less the distance between the reference points before the fracture. The residual elongation after the breaking is preferably 30% or less, more preferably 1% by weight or less, particularly preferably 5% or less and generally 0% or more. When the residual elongation after the above fracture is higher than 1%, the fines scraped off from the surface of the chemical mechanical polishing pad or stretched during polishing and surface renewal tend to disadvantageously fill the pores. The "residual residual 101279.doc -18 - 1290505 elongation" as an elongation is obtained by breaking from each m攸I rate point and a tensile test and dividing the sample. Before the total distance minus the test

各基準點之㈣距離而獲得,在該拉力測試中,依據JISK 6251中蚊的「硫化橡膠拉力測試方法」,—第3號讀形 樣本在50()mm/min之拉力速度與㈣之測試溫度下斷裂。 該測試係實施於因為在實際研磨時會因滑動接觸而 產生熱量。According to the (4) distance of each reference point, in the tensile test, according to the "Vulcanized Rubber Tensile Test Method" of the mosquito in JIS K 6251, the tensile test speed of the No. 3 reading sample at 50 () mm/min and the test temperature of (4) Break down. This test is carried out because heat is generated by sliding contact during actual grinding.

上述「水溶性粒子」係在其接觸到在該化學機械研磨塾 中作為水性分散液之襞料時從該非水溶性基f中消除的粒 子。當該等粒子一旦接觸水便溶解於該漿料所包含的水中 時或當該等粒子因吸收此水分而膨脹並膠化時,可發生此 消除情形。進一步,此溶解或膨脹之成因,不僅在於其與 水接觸,而且還在於其接觸包含一以乙醇為主的溶劑(例 如’甲醇)之一水性混合媒介。 該專水;谷性粒子除產生形成多孔之效果,還產生令化學 機械研磨墊之凹痕硬度增加之效果。例如,可藉由添加該 等水溶性粒子來設定本發明之化學機械研磨墊之蕭氏硬度 (ShorDhardness),較佳的係35或更大,更佳的係50至9〇, 尤其較佳的係60至85而一般為100或更小。當該蕭氏硬度為 35或更大時,向該欲研磨物件施加的壓力可能增加,而該 研磨速度可能因此而提高。此外,獲得較高的研磨平坦度。 因此’該等水溶性粒子尤其較佳的係由一固體物質製成, 該固體物質能確保該化學機械研磨墊具有足夠高的凹痕硬 度。 101279.doc -19- 1290505 該等水溶性粒子之材料不受特定限制。其係,例如,有 機水溶性粒子或無機水溶性粒子。用以形成該等有機水溶 f生粒子之範例包括··醣類(多醣,例如澱粉、糊精及環糊精、 礼糖、甘露醇等)、纖維素(例如,羥丙基纖維素、甲基纖維 素等)、蛋白質、聚乙烯乙醇、聚乙烯吡咯烷酮、聚丙烯酸、 聚乙烯氧化物、水溶性光敏樹脂、續化聚異戊:烯及石黃化 聚八戊一稀共聚物。用以形成該等無機水溶性粒子的材料 之範例包括:醋酸鉀、硝酸鉀、碳酸鉀、碳酸氫鉀'氣化 鉀、溴化鉀、磷酸鉀、硝酸鎂。該些水溶性粒子可單獨使 用或者一或更多類粒子組合起來使用。該等水溶性粒子可 月匕係由一預疋的單一材料製成或者由二或多個不同材料製 成。 " 該等水溶性粒子之平均粒徑較佳的係0 1至5〇〇 μπι,更佳 的係0.5至100 μιη。該等孔較大,其較佳的係〇1至5〇〇, 更佳的係0·5至1〇〇 μπι。當該等水溶性粒子之平均粒徑小於 〇· 1 μηι時,所幵> 成的多孔之尺寸變得小於所使用的研磨 粒,彳火而幾乎不能獲得能夠完全固持漿料之一化學機械研 磨墊。當該平均粒徑大於μιη時,所形成的多孔變得過大, 從而所獲得的化學機械研磨墊之機械強度及研磨速度可能 降低。 以該水溶性基質與該等水溶性粒子之總體積為1〇〇% 計,該等水溶性粒子之含量較佳的係體積的i至9〇%,更佳 的係體積的1至60%,尤其較佳的係體積的2至4〇%。當該等 水溶性粒子之含量低於體積的1%時,所獲得之化學機械研 101279.doc -20 - 1290505 磨墊中並不完全形成多孔,而且該研磨速度可能降低。當 該等水溶性粒子之含量高於體積的9〇%時,可能難以完全 防止存在於所獲得的化學機械研磨墊内部之水溶性粒子膨 脹或溶解,從而使得難以令所獲得的化學機械研磨墊之硬 度及機械強度保持於適當的值。 較佳的係,該等水溶性粒子應僅在其係曝露於該化學機 械研磨墊之表面層時才溶解於水中,而當其存在於該化學 機械研磨墊内部中時不應吸收水氣或膨脹。因此,該等水 ;谷性粒子可能具有一外殼以抑制其最外部分的至少部分上 之水氣吸收。此外殼可能係實體吸附於該水溶性粒子、化 學鍵接至該水溶性粒子,或藉由實體吸附及化學鍵接而與 該水溶性粒子接觸。該外殼係由環氧樹脂、聚醯亞胺、聚 酰胺或聚矽酸鹽製成。即使在其僅形成於該水溶性粒子之 部分上,亦能充分獲得上述效果。 上述非水溶性基質可包含一相容性試劑來控制其對於該 等水溶性粒子之親合性及該等水溶性粒子在該非水溶性基 質中的可分散性。該相容性試劑之範例包括··均聚物、塊 狀共聚物及經一酸酐基團修改的隨機共聚物、羧基團、氫 基團、%氧基團、唑啉基團或氨基團、非離子表面活性劑 及輕合劑。 該化學機械研磨墊包含上述後面的非水溶性基質材料 (發泡塑料等)(該材料包含分散於其中的凹穴),組成該化學 機械研磨墊之非水溶性基質材料係,例如,聚胺基甲酸酯、 二聚氰胺樹脂、聚酯、聚颯或聚乙烯乙酯。 101279.doc -21 - 1290505 分散於該非水溶性基質材料中的凹穴之平均尺寸較佳的 係0.1至500 pm,更佳的係 在某-情況下’例如’ 化學機械研磨塾包含一非水 溶|±基質材料(該材料包含分散於其中的凹穴),則發泡塑料 不-疋能滿足對該墊表面之算術平均粗糙度㈣、1〇點高 .度(RZ)、核心粗糙深度(Rk)及減小之峰值高度(Rpk)之要 求’而依據該等凹穴尺寸,本發明之化學機械研磨塾應達 到該些要求。因此,本發明之化學機械研磨塾較佳的係具 籲 #由水溶性粒子與-非水溶性基f (該基f包含分散於其 中的水溶性粒子)組成的材料製成之一研磨層。 從上述材料巾獲制於—化學機械研㈣的組成物之方 法不受特定限制。例如,可藉由一捏合機而將包括一預定 的有機材料在内之所需材料捏合,從而獲得該組成物。可 使用一傳統上已知的捏合機,例如滾筒、捏合機、萬馬力 機(Banbury mixer)或擠出機(單螺杆多螺杆)。 用於一包含水溶性粒子的化學機械研磨墊之組成物(從 而獲得一包含水溶性粒子的化學機械研磨墊)可藉由(例如) 將一非水溶性基質、水溶性粒子及其他添加劑捏合在一起 而獲得。一般地,其係在受熱條件下捏合在一起,從而使 得容易在捏合時對其進行處理❶該等水溶性粒子在該捏合 溫度下較佳的係固體。在其為固體時,其可以上述較佳的 平均粒徑而分散,而無關乎其與該非水溶性基質之相容 性。因此,在此情況下,較佳的係依據所使用的非水溶性 基貝之處理溫度來選擇該等水溶性粒子之類型。 101279.doc -22- 1290505 (2)由用於一化學機械研磨墊之組成物來模製一研磨層之 步驟 形成一能成為本發明之化學機械研磨墊的研磨層之方法 不受特別限制。例如,用於將成為一研磨層的化學機械研 磨墊之組成物係製備並模製成一所需的粗糖形式以製造該 研磨層。此刻,使用具有一圖案之一金屬模來模製用於一 化學機械研磨墊之組成物,該圖案應成為欲形成於該研磨 層的前表面及/後表面上之一(或多個)溝槽及/或凹痕部 分,從而使得可與該研磨層之粗糙形式一起同時形成該(等) 溝槽及/或凹痕部分。當藉由模製來形成該(等)溝槽及/或凹 痕。卩为時,可簡化此步驟,而且該(等)溝槽及/或凹痕部分 的内壁之表面粗糙度可容易地形成為2〇 μιη或更小。 在製成一不具有任何此等溝槽及/或凹痕部分的研磨層 之後’可藉由切割或沈孔而形成在該研磨層的前表面及/後 表面上之溝槽及/或凹痕部分。為藉由切割或沈孔來形成該 (等)溝槽及/或凹痕部分,可在(3)該磨光步驟(接下來將對此 進行說明)之前或之後實施形成該(等)溝槽及/或凹痕部分 之步驟。 (3)將至少上述研磨層之研磨表面磨光之步驟 隨後’將由此形成的研磨層之至少研磨表面磨光。 術語「磨光」表示用砂紙研磨。藉由用一黏合劑將研磨 粒黏合至一襯底物(例如,薄片狀或腰帶狀的紙或布)而獲得 該砂紙。該等研磨粒之材料係天然礦物之精細晶體或一人 造無機化合物之精細顆粒。該等天然礦物之範例包括金剛 101279.doc -23- 1290505 砂及石福石,而該等人造無機化合物之範例包括氧化鋁及 碳化矽。 用於上述磨光步驟的研磨粒之尺寸較佳的係20至200 ,更佳的係25至150 μπι。該砂紙之砂礫尺寸較佳的係8〇 至600 ’更佳的係120至400。 對於磨光,較佳的係使用寬度比上述研磨層的研磨表面 更寬之砂紙。 可藉由將上述研磨層固定於一水平平面上且該研磨表面 面朝上、讓整個研磨表面接觸到該砂紙並讓該砂紙相對於 該研磨表面以較佳的係〇]至1〇〇 m/min而更佳的係〇.5至5〇 m/min之相對速度移動,來實施磨光。此運動可能係旋轉運 動或線性運動,其以介於該研磨層的研磨表面與該砂紙之 間的接觸部分為標準。 磨掉(即藉由磨光而移除)的研磨層量較佳的係〇·〇5至3.0 mm ’更佳的係(^至〕』 mm ° 可僅藉由一單一類型的砂紙或藉由在多個階段中砂礫尺 寸各異之不同類型的砂紙來實施磨光。其中,較佳的係藉 由在多個階段砂礫尺寸各異之不同類型的砂紙來實施磨 光。階段之數目較佳的係2至10,更佳的係3至6。磨掉(即 藉由磨光而移除)的研磨層厚度較佳的係〇 〇1至15 mm,更 佳的係0· 1至1 ·〇 mm。當藉由在多個階段砂礫尺寸各異之不 同類型的砂紙來實施磨光時,較佳的係首先使用砂蝶尺寸 較大之一砂紙,接下來使用砂礫尺寸較小之一妙紙。 可使用一喷砂裝置、砂帶研磨機、滾筒研磨機、膨脹研 101279.doc -24- 1290505 磨機、砂環研磨機、電解研磨機或電解與顆粒研磨機。其 中,較佳的係使用一砂帶研磨機。可購得之砂帶研磨機產 品包括:Amitec有限公司的TS130D研磨機、Kikukawa Tekkosho有限公司的T-142DG寬帶砂光機及Meinan Machinery Works公司的寬帶砂光機。 藉由實施此磨光,可容易地獲得厚度分布為50 μιη或更小 並具有一研磨表面之化學機械研磨墊,其研磨表面之算術 平均粗糙度(Ra)為0.1至15 μιη、10點高度(rz)為4〇至15〇 μιη、核心粗糙深度(Rk)為12至50 μηχ,以及減小之峰值高度 (Rpk)為 7至 40 μιη。 隨後,將對本發明之化學機械研磨方法進行說明。 本發明之化學機械研磨方法與已知的化學機械研磨方法 基本相同,不同之處僅係在一可購得之研磨機中放置上述 的本發明之化學機械研磨墊。 欲研磨表面之類型不受特定限制,但可以使用導線材料 之一金屬膜、阻障金屬膜或絕緣膜。上述金屬膜的材料之 範例包括鎢、鋁、銅及包含該些金屬中的至少一金屬之合 金。上述阻障金屬膜的材料之範例包括鈕、鈦、氮化鈕及 氮化欽。該絕緣膜的材料之範例包括氧切。應依據欲研 磨表面之類型及化學機械研磨之目的來適當地選擇用於化 學機械研磨的水性分散液之類型。 欲藉由本發明之化學機械研磨方法來研磨的物件較佳的 係在欲研磨表面上具有上述材料中的至少一材料之一半導 體晶圓。儘管該半導體晶圓可能係任何尺寸,但對於大直 101279.doc -25- 1290505 徑的半導體晶圓之化學機械研磨而言,本發明之化學機械 研磨方法表現出明顯的優勢。該大直徑半導體晶圓表示直 徑大於8英寸而較佳的係1〇英寸或更大之一半導體晶圓。 如上所述,本發明之化學機械研磨墊有一優點係,藉由 將該墊之表面粗糙度設定於一特定範圍來增加研磨一晶圓 時的穩定性。即,對於一傳統上已知的研磨墊,在將一薪 新的墊放置於該研磨機中以研磨一晶圓之前需要對斷裂作 表面修整。藉由設定上述表面粗糙度,在將該墊放置於該 研磨機中後,不用實施斷裂之表面修整或者僅實施時間週 期比先前技術中更短之斷裂表面修整,便可從該第一晶圓 獲得穩定的研磨性能。 依據本發明,提供一種化學機械研磨墊、其製造方法及 化學機械研磨方法,該化學機械研磨墊即使在作為一欲研 磨物件之一大直徑晶圓上進行化學機械研磨時亦能提供一 具有極佳的平面内均勻度及平坦度之經研磨的表面。 範例 範例1 藉由一受熱於155°C之擠出機,將占體積聚丁 二烯(JSR公司的JSR RB830)與占體積2〇/〇的β-環糊精(橫濱 Bio研究公司的Dexy Pearl(p_i00捏合在一起作為一水溶性 物質。然後,以1,2-聚丁二烯之質量為1〇〇份計,添加依質 1計為1·0份數量(等於依質量計0·4份之純過氧化二異丙 苯)之Percumyl D40(商標名稱,其係由NOF公司製造,包含 依質量計為40%的過氧化二異丙苯),並將所添加的 101279.doc -26 - 1290505The above "water-soluble particles" are particles which are eliminated from the water-insoluble group f when they are brought into contact with the raw material in the chemical mechanical polishing crucible as an aqueous dispersion. This elimination can occur when the particles are dissolved in the water contained in the slurry upon contact with water or when the particles swell and gel due to absorption of the moisture. Further, this dissolution or expansion is caused not only by its contact with water, but also by its contact with an aqueous mixed medium containing an ethanol-based solvent such as 'methanol. The special water; in addition to the effect of forming a porous layer, the granulated particles also have an effect of increasing the hardness of the dent of the chemical mechanical polishing pad. For example, the Shore Dhardness of the CMP pad of the present invention can be set by adding the water-soluble particles, preferably 35 or more, more preferably 50 to 9 Torr, and particularly preferably It is 60 to 85 and is generally 100 or less. When the Shore hardness is 35 or more, the pressure applied to the article to be ground may increase, and the polishing speed may be increased accordingly. In addition, higher grinding flatness is obtained. Therefore, the water-soluble particles are particularly preferably made of a solid material which ensures that the chemical mechanical polishing pad has a sufficiently high dent hardness. 101279.doc -19- 1290505 The materials of the water-soluble particles are not particularly limited. The system is, for example, organic water-soluble particles or inorganic water-soluble particles. Examples of such organic water-soluble f-particles include: sugars (polysaccharides such as starch, dextrin and cyclodextrin, sugar, mannitol, etc.), cellulose (for example, hydroxypropylcellulose, A) Cellulose, etc.), protein, polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acid, polyethylene oxide, water-soluble photosensitive resin, polycondensed polyisoprene: alkene and feldsparic polyocta-dilute copolymer. Examples of the material for forming the inorganic water-soluble particles include potassium acetate, potassium nitrate, potassium carbonate, potassium hydrogencarbonate, potassium vapor, potassium bromide, potassium phosphate, and magnesium nitrate. These water-soluble particles may be used singly or in combination of one or more types of particles. The water-soluble particles may be made of a single material of a pre-twisted or made of two or more different materials. " The average particle size of the water-soluble particles is preferably from 0 1 to 5 μ μm, more preferably from 0.5 to 100 μηη. The holes are larger, and the preferred ones are 1 to 5 inches, more preferably 0.5 to 1 μm. When the average particle diameter of the water-soluble particles is less than 〇·1 μηι, the size of the porous layer becomes smaller than the abrasive grains used, and the smoldering hardly obtains one chemical mechanical machine capable of completely holding the slurry. Grinding pad. When the average particle diameter is larger than μηη, the formed porosity becomes excessively large, so that the mechanical strength and the polishing speed of the obtained chemical mechanical polishing pad may be lowered. The content of the water-soluble particles is preferably from 1 to 9% by volume, more preferably from 1 to 60% by volume of the system, based on the total volume of the water-soluble substrate and the water-soluble particles. Particularly preferred is 2 to 4% by volume of the system. When the content of the water-soluble particles is less than 1% by volume, the obtained chemical mechanical film 101279.doc -20 - 1290505 is not completely formed in the polishing pad, and the polishing speed may be lowered. When the content of the water-soluble particles is more than 9% by volume, it may be difficult to completely prevent the water-soluble particles present inside the obtained chemical mechanical polishing pad from swelling or dissolving, thereby making it difficult to obtain the obtained chemical mechanical polishing pad. The hardness and mechanical strength are maintained at appropriate values. Preferably, the water-soluble particles should be dissolved in water only when they are exposed to the surface layer of the chemical mechanical polishing pad, and should not absorb moisture when they are present in the interior of the chemical mechanical polishing pad or Swell. Thus, the water; gluten particles may have an outer shell to inhibit moisture absorption on at least a portion of its outermost portion. The shell may be physically adsorbed to the water soluble particles, chemically bonded to the water soluble particles, or contacted with the water soluble particles by physical adsorption and chemical bonding. The outer casing is made of epoxy resin, polyimide, polyamide or polysilicate. Even if it is formed only on the portion of the water-soluble particles, the above effects can be sufficiently obtained. The water-insoluble substrate may comprise a compatibilizing agent to control its affinity for the water-soluble particles and the dispersibility of the water-soluble particles in the water-insoluble substrate. Examples of the compatibilizing agent include: a homopolymer, a bulk copolymer, and a random copolymer modified with a monoanhydride group, a carboxyl group, a hydrogen group, a % oxygen group, an oxazoline group or an amino group, Nonionic surfactants and light combination agents. The chemical mechanical polishing pad comprises the above-mentioned non-water-soluble matrix material (foamed plastic or the like) (which contains a cavity dispersed therein), and a water-insoluble matrix material system constituting the chemical mechanical polishing pad, for example, a polyamine Carbamate, melamine resin, polyester, polyfluorene or polyethylene ethyl ester. 101279.doc -21 - 1290505 The average size of the cavities dispersed in the water-insoluble matrix material is preferably from 0.1 to 500 pm, more preferably in the case of - for example, the chemical mechanical polishing crucible comprises a non-water soluble solution. |±The matrix material (the material contains the recesses dispersed therein), the foamed plastic does not meet the arithmetic mean roughness (4), 1〇 point height (RZ), core roughness depth of the surface of the mat ( Rk) and reduced peak height (Rpk) requirements. Depending on the size of the pockets, the chemical mechanical polishing crucible of the present invention should meet these requirements. Accordingly, the preferred embodiment of the chemical mechanical polishing crucible of the present invention is an abrasive layer made of a material consisting of water-soluble particles and a water-insoluble group f (the base f contains water-soluble particles dispersed therein). The method of obtaining the composition of the chemical mechanical research (4) from the above-mentioned material towel is not particularly limited. For example, the composition can be obtained by kneading a desired material including a predetermined organic material by a kneading machine. A conventionally known kneading machine such as a drum, a kneader, a Banbury mixer or an extruder (single-screw multi-screw) can be used. A composition for a chemical mechanical polishing pad comprising water-soluble particles (and thereby obtaining a chemical mechanical polishing pad comprising water-soluble particles) can be kneaded by, for example, a water-insoluble substrate, water-soluble particles, and other additives. Get together. Generally, they are kneaded together under heat, so that they are easily handled at the time of kneading, and the water-soluble particles are preferably solid at the kneading temperature. When it is a solid, it can be dispersed in the above preferred average particle size irrespective of its compatibility with the water-insoluble substrate. Therefore, in this case, it is preferred to select the type of the water-soluble particles depending on the treatment temperature of the water-insoluble base used. 101279.doc -22- 1290505 (2) Step of molding an abrasive layer from a composition for a chemical mechanical polishing pad A method of forming an abrasive layer which can be a chemical mechanical polishing pad of the present invention is not particularly limited. For example, a composition for a chemical mechanical polishing pad to be an abrasive layer is prepared and molded into a desired form of raw sugar to produce the abrasive layer. At this point, a composition for a chemical mechanical polishing pad is molded using a metal mold having a pattern which should be one (or more) grooves to be formed on the front and/or back surfaces of the polishing layer. The grooves and/or indentations are such that the (and the like) grooves and/or indentations can be formed simultaneously with the roughened form of the abrasive layer. The grooves and/or indentations are formed by molding. In the meantime, this step can be simplified, and the surface roughness of the inner wall of the groove and/or the indented portion can be easily formed to be 2 μm or less. After forming an abrasive layer without any such grooves and/or indentations, grooves and/or depressions may be formed on the front and/or back surfaces of the abrasive layer by cutting or countersinking. Trace part. To form the (and other) grooves and/or indentations by cutting or countersinking, the formation of the (and other) grooves may be performed before or after (3) the buffing step (which will be described next) / or the step of the dent portion. (3) a step of polishing at least the abrasive surface of the above-mentioned abrasive layer. Subsequently, at least the polished surface of the thus formed abrasive layer is polished. The term "polish" means grinding with sandpaper. The sandpaper is obtained by bonding abrasive particles to a substrate (e.g., a sheet or belt-like paper or cloth) with a binder. The materials of the abrasive grains are fine crystals of natural minerals or fine particles of one-man inorganic compound. Examples of such natural minerals include King Kong 101279.doc -23- 1290505 sand and stone fossils, and examples of such artificial inorganic compounds include alumina and tantalum carbide. The size of the abrasive particles used in the above polishing step is preferably from 20 to 200, more preferably from 25 to 150 μm. The grit of the sandpaper preferably has a size of from 8 600 to 600 Å and more preferably from 120 to 400. For buffing, it is preferred to use a sandpaper having a width wider than that of the above-mentioned abrasive layer. By fixing the above-mentioned abrasive layer on a horizontal plane with the abrasive surface facing up, the entire abrasive surface is brought into contact with the sandpaper and the sandpaper is preferably 〇] to 1 μm relative to the abrasive surface. /min and a better system 〇. 5 to 5 〇 m / min relative speed movement to perform polishing. This movement may be a rotational motion or a linear motion, with a portion between the abrasive surface of the abrasive layer and the sandpaper as a standard. The amount of abrasive layer that is worn away (ie, removed by buffing) is preferably 〇·〇5 to 3.0 mm. The better system (^ to) mm ° can be borrowed from a single type of sandpaper or borrowed Polishing is carried out by different types of sandpaper having different grit sizes in a plurality of stages. Among them, it is preferred to perform buffing by different types of sandpaper having different grit sizes at various stages. Preferably, the system is from 2 to 10, more preferably from 3 to 6. The thickness of the abrasive layer which is ground off (i.e., removed by buffing) is preferably from 1 to 15 mm, more preferably from 0.1 to 1. 1 · 〇mm. When polishing is carried out by different types of sandpaper with different grit sizes in multiple stages, it is preferred to first use a sandpaper with a larger size of the sand butterfly, and then use a smaller grit size. A wonderful paper. You can use a sand blasting device, a belt grinding machine, a roller grinding machine, an expansion grinding machine 101279.doc -24-1290505 grinding machine, sand ring grinding machine, electrolytic grinding machine or electrolysis and particle grinding machine. A good belt grinding machine is used. The available belt grinding machine products include: TS13 of Amitec Co., Ltd. 0D grinder, T-142DG wide belt sander from Kikukawa Tekkosho Co., Ltd. and wide belt sander from Meinan Machinery Works. By performing this buffing, it is easy to obtain a thickness distribution of 50 μm or less and have a grind The chemical mechanical polishing pad of the surface has an arithmetic mean roughness (Ra) of 0.1 to 15 μm, a height of 10 points (rz) of 4 to 15 μm, and a core roughness depth (Rk) of 12 to 50 μηχ. And the reduced peak height (Rpk) is 7 to 40 μηη. Subsequently, the chemical mechanical polishing method of the present invention will be described. The chemical mechanical polishing method of the present invention is basically the same as the known chemical mechanical polishing method, and the difference is only The above-described chemical mechanical polishing pad of the present invention is placed in a commercially available grinding machine. The type of the surface to be ground is not particularly limited, but a metal film, a barrier metal film or an insulating film of the wire material may be used. Examples of the material of the metal film include tungsten, aluminum, copper, and an alloy containing at least one of the metals. Examples of the material of the barrier metal film include a button, titanium, Nitride button and nitride. Examples of the material of the insulating film include oxygen cutting. The type of aqueous dispersion for chemical mechanical polishing should be appropriately selected depending on the type of surface to be polished and the purpose of chemical mechanical polishing. The article polished by the chemical mechanical polishing method of the present invention is preferably a semiconductor wafer having at least one of the above materials on the surface to be polished. Although the semiconductor wafer may be of any size, it is for a large straight 101279. The chemical mechanical polishing method of the present invention exhibits significant advantages in the chemical mechanical polishing of semiconductor wafers of the diameter of doc - 25 - 1290505. The large diameter semiconductor wafer represents a semiconductor wafer having a diameter greater than 8 inches and preferably one inch or more. As described above, the chemical mechanical polishing pad of the present invention has an advantage in that the stability of the polishing of a wafer is increased by setting the surface roughness of the pad to a specific range. That is, for a conventionally known polishing pad, it is necessary to surface trim the fracture before placing a new pad in the grinder to grind a wafer. By setting the surface roughness described above, the first wafer can be removed from the first wafer after the pad is placed in the grinder without performing a surface modification of the fracture or only performing a fracture surface modification having a shorter time period than in the prior art. Achieve stable grinding performance. According to the present invention, there is provided a chemical mechanical polishing pad, a method of manufacturing the same, and a chemical mechanical polishing method, which can provide a pole even when chemical mechanical polishing is performed on a large-diameter wafer as a workpiece to be polished. Good surface roughness and flatness of the ground surface. EXAMPLES Example 1 A volume of polybutadiene (JSR RB830 of JSR) and a β-cyclodextrin of 2 〇/〇 (Dexy of Yokohama Bio Research Co., Ltd.) were heated by an extruder heated at 155 °C. Pearl (p_i00 is kneaded together as a water-soluble substance. Then, based on the mass of 1,2-polybutadiene, the amount of 1,0 parts is added according to the mass 1 (equal to the mass based on 0· 4 parts of pure dicumyl peroxide, Percumyl D40 (trade name, manufactured by NOF, containing 40% by weight of dicumyl peroxide), and added 101279.doc - 26 - 1290505

PercumylD40與上述捏合產物進一步捏合,並且在170CC下 於一壓模中讓所產生的產物交聯18分鐘以獲得直徑為810 cm而厚度為3·3 mm之一碟片狀產物。將此模製產物放置於 一寬帶砂光裝置(Meinan Machinery Works公司)之插入部分 中,並藉由以500 rpm之轉速旋轉一滾筒來讓該模製產物進 行0.1 m/sec速度之移動而以砂礫尺寸為120、150、220及320 之砂紙(Novatec有限公司)來磨光該模製產物之表面,從而 藉母一步驟而從該表面移除0·04 mm。結果,獲得一模製產 物,其平均厚度為2·5 mm、厚度分布為20 μηι、算術平均粗 輪度(Ra)為4·4 μπι、10點局度(Rz)為125 μηι、核心粗糙深度 (Rk)為16 μπι以及減小之峰值高度(Rpk)為14 μηι。 對於上述磨光,模製產物與砂紙(其在介於該模製產物與 該砂紙之間的接觸表面上)之間的相對速度為5 m/min。 從藉由Manual 3_D計量器(Mitutoyo公司)而在該直徑方 向上(但從該中心至該等二側之一 4〇 min區域與從該等二侧 起的40 mm區域除外)於彼此等距的33個點測量出的該模製 產物之研磨表面厚度,依據以下等式而計算出上述厚度分 布0 厚度分布=(厚度最大測量值)一(厚度最小測量值) 該算術平均粗糙度(Ra)、10點高度(Rz)、核心粗糙深度 (Rk)及減小之峰值高度(Rpk)皆係由該粗糙度輪廓計算得出 之平均值,該粗糙度輪廓係藉由採用Laser Tech公司的 1LM21P並在該模製產物的研磨表面之直徑方向上以彼此 等距之10個點來測量垂直於該墊直徑方向的丨〇個測量線 101279.doc -27- 1290505 (評估長度為10 mm)(但從作為中心的二端起之4〇 mm區域 除外)而獲得。 藉由一切割機(Kato機械有限公司)而在該模製產物的磨 光表面中形成寬度為〇.5 111111、間距為2111111而深度為1〇111111 之同中心溝槽,以製造一化學機械研磨墊。該等溝槽的内 壁之表面粗糙度為6 μιη。 將此化學機械研磨些放置於Applied Material有限公司生 產的Applied Reflexion化學機械研磨機中,以實施斷裂之表 面修整,同時在以下條件下提供去離子水。 平臺轉速:120 rpm 去離子水的提供速度:l〇〇ml/min 研磨時間:600秒 然後’在以下條件下,在具有一作為欲研磨物件的 PETEOS膜之一 12英寸晶圓上進行化學機械研磨。該 PETEOS膜係藉由一化學汽相沈積方法且將電漿用作一促 進條件而由四乙基矽酸鹽(TEOS)形成之一氧化矽膜。 平臺轉速:120 rpm 研磨頭轉速·· 36 rpm 研磨塵力: 定位環壓力=7.5 psi 區域1之塵力=6.0 psi 區域2之壓力=3.0 pSi 區域3之壓力=3.5 psi 水性分散液之提供速度·· 3〇〇 ml/min 101279.doc -28 - 1290505 研磨時間:60秒 用於化學機械研磨之水性分散液·· CMS1101(JSR Corporation) 在具有一作為欲研磨物件的PETEOS膜之12英寸晶圓之 直控方向上(但從該等二端起的5 mm區域除外),於彼此等 距的33個點測量在化學機械研磨之前或之後該PETE0S膜 之厚度。依據以下等式,由該等測量結果計算出該研磨速 度及該平面内均勻度。 研磨數量=研磨前的厚度_研磨後的厚度 研磨速度=Σ (研磨數量)/研磨時間 平面内均勻度=(研磨數量標準差+平均研磨數量)Χ 100 (%) 表1中顯示該等結果。可以說,當該平面内均勻度為3% 或更小時’該平面内均勻度令人滿意。 範例2 平均厚度為2.5 mm、厚度分布為20 μηι、算術平均粗糙度 (Ra)為3·4 μηι、10點高度(rz)為jog 、核心粗糖深度(处) 為18 μηι以及減小之峰值高度μιη之一模製產物 之獲得方式與範例1中基本相同,不同之處僅係使用了占體 積的80%之1,2_聚丁二烯、占體積的2〇%之卜環糊精以及按 1,2-聚丁二烯之質量為ι〇〇份而依質量計占〇.8份之 Percumyl D40(等於依質量計占〇32份之純過氧化二異丙 苯)。 以與範例1中相同的方式,在該模製產物的磨光表面中形 101279.doc -29- 1290505 成見度為0.5 mm、間距為2 mm、深度為1 .〇 mm而内壁之表 面粗糙度為5 μπι之同中心溝槽,以製造一化學機械研磨墊。 藉由以與範例1中相同的方式使用此化學機械研磨墊來 進行評估。表1中顯示該等結果。 範例3 平均厚度為2.5 mm、厚度分布為25 μηι、算術平均粗糙度 (Ra)為3.8 μπι、10點高度(rz)為115 μηι、核心粗糙深度(Rk) 為15 μπι以及減小之峰值高度㊉冲^為^ μπχ之一模製產物 之獲得方式與範例1中基本相同,不同之處僅係使用了占體 積的64%之1,2-聚丁二烯、占體積的16%之苯乙烯-丁二烯塊 狀共聚物(JSR公司的TR2827)及占體積的20%之環糊精。 以與範例1中相同的方式,在該模製產物的磨光表面中形 成寬度為0 · 5 mm、間距為2 mm、深度為1 · 〇 mm而内壁之表 面粗縫度為4·5 μπι之同中心溝槽,以製造一化學機械研磨 墊。 藉由以與範例1中相同的方式使用此化學機械研磨墊來 進行評估。表1中顯示該等結果。 比較性範例1 平均厚度為2.5 mm、厚度分布為70 μηι、算術平均粗糙度 (Ra)為1.5 μπι、10點高度(rz)為25 μπι、核心粗链深度(Rk) 為8 μπι以及減小之峰值高度(Rpk)為6 μιη之一模製產物之 獲得方式與範例1中基本相同,不同之處僅係使用了平均厚 度為2.5 mm之一模來獲得一模製產物且未磨光該模製產 物0 101279.doc -30- 1290505 以與範例1中相同的方式,在該模製產物的研磨表面中形 成寬度為0.5 mm、間距為2 mm、深度為ι·〇 mm而内壁之表 面粗糙度為5·5 μηι之同中心溝槽,以製造一化學機械研磨 墊。 藉由以與範例1中相同的方式使用此化學機械研磨墊來 進行評估。表1中顯示該等結果。 表1 研磨速度(A/min) 平面内均勻度(%) 範例1 2850 1.0 範例2 2700 2.0 範例3 2750 1.5 比較性範例1 2800 8.0 範例4Percumyl D40 was further kneaded with the above kneaded product, and the resulting product was crosslinked in a stamper at 170 cc for 18 minutes to obtain a disc-like product having a diameter of 810 cm and a thickness of 3·3 mm. The molded product was placed in an insertion portion of a wide belt sanding device (Meinan Machinery Works), and the molded product was moved at a speed of 0.1 m/sec by rotating a roller at 500 rpm. Sandpaper having a grit size of 120, 150, 220, and 320 (Novatec Co., Ltd.) was used to polish the surface of the molded product, thereby removing 0.04 mm from the surface in one step. As a result, a molded product having an average thickness of 2.5 mm, a thickness distribution of 20 μηι, an arithmetic mean coarse rotation (Ra) of 4·4 μπι, a 10-point degree (Rz) of 125 μηι, and a core roughness was obtained. The depth (Rk) is 16 μm and the reduced peak height (Rpk) is 14 μηι. For the above buffing, the relative speed between the molded product and the sandpaper, which is on the contact surface between the molded product and the sandpaper, was 5 m/min. Equidistant from each other in the diametrical direction by the Manual 3_D meter (Mitutoyo Corporation) (but from the center to the 4 〇 min area of the two sides and the 40 mm area from the two sides) The thickness of the polished surface of the molded product measured at 33 points is calculated according to the following equation: 0 thickness distribution = (maximum thickness measurement value) 1 (minimum thickness measurement value) The arithmetic mean roughness (Ra ), 10 point height (Rz), core roughness depth (Rk), and reduced peak height (Rpk) are average values calculated from the roughness profile by using Laser Tech 1LM21P and measuring 10 measuring points perpendicular to the diameter direction of the pad in the diameter direction of the grinding surface of the molded product 101279.doc -27- 1290505 (evaluation length 10 mm) (However, except for the 4〇mm area from the two ends of the center). A concentric groove having a width of 〇.5 111111, a pitch of 2111111 and a depth of 1〇111111 is formed in the polished surface of the molded product by a cutter (Kato Machinery Co., Ltd.) to manufacture a chemical machine Grinding pad. The inner wall of the grooves has a surface roughness of 6 μm. The chemical mechanical polishing was placed in an Applied Reflexion chemical mechanical mill manufactured by Applied Material Co., Ltd. to perform surface modification of the fracture while providing deionized water under the following conditions. Platform speed: 120 rpm Deionized water supply speed: l〇〇ml/min Grinding time: 600 seconds and then 'chemical mechanically on a 12-inch wafer with one PETEOS film as the object to be polished under the following conditions Grinding. The PETEOS film is a ruthenium oxide film formed from tetraethyl phthalate (TEOS) by a chemical vapor deposition method and using the plasma as a promoting condition. Platform speed: 120 rpm Grinding head speed · · 36 rpm Grinding dust force: Positioning ring pressure = 7.5 psi Zone 1 dust force = 6.0 psi Zone 2 pressure = 3.0 pSi Zone 3 pressure = 3.5 psi Aqueous dispersion supply speed ··3〇〇ml/min 101279.doc -28 - 1290505 Grinding time: 60 seconds for aqueous dispersion for chemical mechanical polishing · CMS1101 (JSR Corporation) 12-inch crystal with a PETEOS film as the object to be polished In the direction of direct control of the circle (except for the 5 mm region from the two ends), the thickness of the PETEOS film before or after chemical mechanical polishing was measured at 33 points equidistant from each other. The polishing speed and the in-plane uniformity are calculated from the measurements according to the following equation. Grinding quantity = thickness before grinding _ thickness after grinding = grinding speed (number of grinding) / grinding time in-plane uniformity = (standard deviation of grinding quantity + average grinding quantity) Χ 100 (%) These results are shown in Table 1. . It can be said that the uniformity in the in-plane is satisfactory when the in-plane uniformity is 3% or less. Example 2 The average thickness is 2.5 mm, the thickness distribution is 20 μηι, the arithmetic mean roughness (Ra) is 3·4 μηι, the 10-point height (rz) is jog, the core coarse sugar depth (at the surface) is 18 μηι, and the peak is reduced. The molded product of one of the heights μηη is obtained in substantially the same manner as in the first example, except that 80% of the volume, 1, 2-polybutadiene, and 2% by volume of the cyclodextrin are used. And 8 parts by mass of Percumyl D40 (equal to 32 parts by mass of pure dicumyl peroxide) by mass of 1,2-polybutadiene. In the same manner as in Example 1, in the polished surface of the molded product, 101279.doc -29-1290505 has a visibility of 0.5 mm, a pitch of 2 mm, a depth of 1. 〇mm and a rough surface of the inner wall. A central groove of 5 μm is used to make a chemical mechanical polishing pad. The evaluation was carried out by using this chemical mechanical polishing pad in the same manner as in Example 1. These results are shown in Table 1. Example 3 The average thickness is 2.5 mm, the thickness distribution is 25 μηι, the arithmetic mean roughness (Ra) is 3.8 μπι, the 10-point height (rz) is 115 μηι, the core roughness depth (Rk) is 15 μπι, and the peak height is reduced. The method of obtaining a molded product of ten puncturing ^μπχ is basically the same as that in the first example, except that 64% of the volume of 1,2-polybutadiene and 16% of the volume of benzene are used. Ethylene-butadiene block copolymer (TR2827 from JSR Corporation) and 20% by volume of cyclodextrin. In the same manner as in Example 1, a width of 0 · 5 mm, a pitch of 2 mm, a depth of 1 · 〇 mm and a rough surface of the inner wall of 4·5 μπι were formed in the polished surface of the molded product. The same central groove to make a chemical mechanical polishing pad. The evaluation was carried out by using this chemical mechanical polishing pad in the same manner as in Example 1. These results are shown in Table 1. Comparative Example 1 has an average thickness of 2.5 mm, a thickness distribution of 70 μηι, an arithmetic mean roughness (Ra) of 1.5 μπι, a 10-point height (rz) of 25 μπι, a core thick chain depth (Rk) of 8 μπι and a decrease. A molded product having a peak height (Rpk) of 6 μηη was obtained in substantially the same manner as in Example 1, except that a mold having an average thickness of 2.5 mm was used to obtain a molded product and was not polished. Molded product 0 101279.doc -30- 1290505 In the same manner as in Example 1, a surface having a width of 0.5 mm, a pitch of 2 mm, and a depth of ι·〇mm was formed in the ground surface of the molded product. The same center groove is used to make a chemical mechanical polishing pad with a roughness of 5·5 μηι. The evaluation was carried out by using this chemical mechanical polishing pad in the same manner as in Example 1. These results are shown in Table 1. Table 1 Grinding speed (A/min) In-plane uniformity (%) Example 1 2850 1.0 Example 2 2700 2.0 Example 3 2750 1.5 Comparative example 1 2800 8.0 Example 4

具有-PETEOS膜的12英寸晶圓之化學機械研磨之實施 方式與細中基本相同’不同之處僅在於不實施該斷裂表 面修整。隨後’在具有-PETE〇s膜的難12英寸晶圓上連 續進行化學機械研磨。表2顯示每一晶圓之研磨速度。 比較性範例2 ^ 在刚固晶圓上進行化學機械研磨之方式與範例4中基本相 同,不同之處僅係使用了採用與比較性範例ι中相同 製造出之化學機械研磨塾。表2顯示每一晶圓之研磨速度: 101279.doc -31- 1290505 表2 晶圓之研磨順序 研磨速度(Λ/min) 範例4 比較性範例2 1 2830 1830 2 2850 1850 3 2870 1910 4 2820 2100 5 2840 2510 6 2850 2840 7 2880 2860 8 2870 2870 9 2850 2840 10 2840 2830The chemical mechanical polishing of a 12-inch wafer having a -PETEOS film is carried out in substantially the same manner as in the elaboration' except that the fracture surface trimming is not performed. Chemical mechanical polishing was then continued on a difficult 12-inch wafer with a -PETE〇s film. Table 2 shows the grinding speed for each wafer. Comparative Example 2 ^ The method of chemical mechanical polishing on a rigid-solid wafer is basically the same as in Example 4 except that the chemical mechanical polishing crucible manufactured in the same manner as in Comparative Example 1 is used. Table 2 shows the grinding speed of each wafer: 101279.doc -31- 1290505 Table 2 Grinding sequence grinding speed of wafer (Λ/min) Example 4 Comparative example 2 1 2830 1830 2 2850 1850 3 2870 1910 4 2820 2100 5 2840 2510 6 2850 2840 7 2880 2860 8 2870 2870 9 2850 2840 10 2840 2830

【圖式簡單說明】 圖1係顯示10點高度(Rz)之定義之一圖式; 圖2係顯示一材料比率曲線之定義之一圖式; 圖3係顯示核心粗糙深度(Rk)之定義之一曲線;以及 圖4係顯示減小之峰值高度(Rpk)之定義之一圖式。 101279.doc 32-BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a diagram showing the definition of a 10-point height (Rz); Figure 2 is a diagram showing a definition of a material ratio curve; Figure 3 is a definition showing the core roughness depth (Rk) One of the curves; and Figure 4 shows one of the definitions of the reduced peak height (Rpk). 101279.doc 32-

Claims (1)

1290505 十、申請專利範圍: i 一種具有一研磨表面與一非研磨表面之化學機械研磨 塾’該研磨表面之算術平均粗糙度(Ra)為0.1至15 μηι,10 點高度(Rz)為40至150 μηι,核心粗糙度深度(Rk)為12至50 ’以及減小之峰值高度(Rpk)為7至40 μηι。 2·如睛求項1之化學機械研磨墊,其具有5〇 μηι或更小之厚 度分布。 3· 一種製造如請求項1或2之化學機械研磨墊之方法,其包 含以下步驟: 模製一研磨層;以及 磨光至少欲成為該研磨層的研磨表面之該表面。 4· 一種化學機械研磨方法,其包含化學機械研磨一欲藉由 如請求項1或2之化學機械研磨墊來研磨之物件。1290505 X. Patent Application Range: i A chemical mechanical polishing having an abrasive surface and a non-abrasive surface. The abrasive surface has an arithmetic mean roughness (Ra) of 0.1 to 15 μηι and a 10-point height (Rz) of 40 to 150 μηι, core roughness depth (Rk) of 12 to 50 ' and reduced peak height (Rpk) of 7 to 40 μηι. 2. A chemical mechanical polishing pad according to claim 1, which has a thickness distribution of 5 〇 μη or less. A method of manufacturing a chemical mechanical polishing pad according to claim 1 or 2, comprising the steps of: molding an abrasive layer; and polishing the surface of the abrasive surface to be at least the abrasive layer. A chemical mechanical polishing method comprising chemical mechanical polishing of an article to be ground by a chemical mechanical polishing pad according to claim 1 or 2. 101279.doc101279.doc
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Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070161720A1 (en) * 2005-11-30 2007-07-12 Applied Materials, Inc. Polishing Pad with Surface Roughness
JP2007255277A (en) * 2006-03-23 2007-10-04 Jtekt Corp Cam follower
JP5347524B2 (en) * 2008-01-24 2013-11-20 Jsr株式会社 Composition for forming polishing layer of chemical mechanical polishing pad, chemical mechanical polishing pad, and chemical mechanical polishing method
TWI568541B (en) * 2010-12-22 2017-02-01 Jsr Corp Chemical mechanical grinding method
US9108293B2 (en) * 2012-07-30 2015-08-18 Rohm And Haas Electronic Materials Cmp Holdings, Inc. Method for chemical mechanical polishing layer pretexturing
JP2014095392A (en) * 2012-11-07 2014-05-22 Toyota Motor Corp Gear and manufacturing method thereof
JP6010511B2 (en) 2013-08-22 2016-10-19 株式会社荏原製作所 Method for measuring surface roughness of polishing pad
KR102176900B1 (en) * 2016-10-31 2020-11-10 교세라 가부시키가이샤 Probe card substrate, probe card and inspection device
CN109997085B (en) * 2016-11-29 2021-12-24 京瓷株式会社 Watch case
JPWO2018181347A1 (en) * 2017-03-31 2020-03-05 古河電気工業株式会社 Polishing pad
JP7083256B2 (en) 2018-02-19 2022-06-10 富士電機株式会社 Semiconductor module and its manufacturing method
JP7118841B2 (en) * 2018-09-28 2022-08-16 富士紡ホールディングス株式会社 polishing pad
US11759909B2 (en) * 2020-06-19 2023-09-19 Sk Enpulse Co., Ltd. Polishing pad, preparation method thereof and method for preparing semiconductor device using same
CN112461265B (en) * 2020-11-20 2023-03-24 大连理工大学 Nano manufacturing method of quartz hemispherical harmonic oscillator
KR102512675B1 (en) * 2020-12-30 2023-03-21 에스케이엔펄스 주식회사 Polishing pad, manufacturing method thereof and preparing method of semiconductor device using the same

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08216029A (en) 1995-02-07 1996-08-27 Daiki:Kk Precision-polishing sheet
US6126532A (en) * 1997-04-18 2000-10-03 Cabot Corporation Polishing pads for a semiconductor substrate
US5921855A (en) 1997-05-15 1999-07-13 Applied Materials, Inc. Polishing pad having a grooved pattern for use in a chemical mechanical polishing system
JP3668046B2 (en) 1998-05-11 2005-07-06 株式会社東芝 Polishing cloth and method for manufacturing semiconductor device using the polishing cloth
JP3918359B2 (en) 1998-05-15 2007-05-23 Jsr株式会社 Polymer composition for polishing pad and polishing pad
JP2000296461A (en) * 1999-04-13 2000-10-24 Speedfam-Ipec Co Ltd Backing pad structure
US6679769B2 (en) * 2000-09-19 2004-01-20 Rodel Holdings, Inc Polishing pad having an advantageous micro-texture and methods relating thereto
US6641471B1 (en) * 2000-09-19 2003-11-04 Rodel Holdings, Inc Polishing pad having an advantageous micro-texture and methods relating thereto
JP2003039329A (en) * 2001-08-02 2003-02-13 Mitsubishi Materials Corp Single layer grinding wheel and manufacturing method therefor
US7374474B2 (en) * 2001-10-09 2008-05-20 Hitachi Chemical Co., Ltd. Polishing pad for CMP, method for polishing substrate using it and method for producing polishing pad for CMP
TW200305482A (en) * 2002-03-25 2003-11-01 Thomas West Inc Smooth pads for CMP and polishing substrates
US20030216111A1 (en) * 2002-05-20 2003-11-20 Nihon Microcoating Co., Ltd. Non-foamed polishing pad and polishing method therewith
JP4790973B2 (en) * 2003-03-28 2011-10-12 Hoya株式会社 Method for manufacturing glass substrate for information recording medium using polishing pad and glass substrate for information recording medium obtained by the method
JP2004303983A (en) * 2003-03-31 2004-10-28 Fuji Photo Film Co Ltd Polishing pad

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