TWI494226B - Adhesive tape for semiconductor wafer protection - Google Patents

Adhesive tape for semiconductor wafer protection Download PDF

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Publication number
TWI494226B
TWI494226B TW103114978A TW103114978A TWI494226B TW I494226 B TWI494226 B TW I494226B TW 103114978 A TW103114978 A TW 103114978A TW 103114978 A TW103114978 A TW 103114978A TW I494226 B TWI494226 B TW I494226B
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semiconductor wafer
adhesive tape
wafer
adhesive
film layer
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TW103114978A
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TW201500218A (en
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Masato Okura
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Furukawa Electric Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/29Laminated material

Description

半導體晶圓保護用黏著膠帶Adhesive tape for semiconductor wafer protection 技術領域Technical field

本發明有關於一種使用於氣體蝕刻程序及電漿切割程序之半導體晶圓保護用黏著膠帶。The present invention relates to an adhesive tape for semiconductor wafer protection used in a gas etching process and a plasma cutting process.

背景技術Background technique

半導體晶圓於表面上形成電路後,將對晶圓背面側施予研削加工,並進行用於調整晶圓厚度之背面研削程序及依預定之晶片尺寸將晶圓切片之切割程序。After the semiconductor wafer is formed on the surface of the wafer, the back side of the wafer is subjected to a grinding process, and a back grinding process for adjusting the thickness of the wafer and a cutting process for slicing the wafer according to a predetermined wafer size are performed.

近年,IC卡已普及且USB記憶體容量急速提昇,伴隨所重疊晶片之片數增加,而有進而薄型化之需求。因此,迄今厚度為200μ m~350μ m左右之半導體晶片需要減薄至厚度50~100μ m或以下。In recent years, IC cards have become widespread and the capacity of USB memory has rapidly increased, and the number of wafers to be overlapped has increased, and there has been a demand for further thinning. Therefore, semiconductor wafers having a thickness of about 200 μm to 350 μm have to be thinned to a thickness of 50 to 100 μm or less.

另,雖為提高功能而增加積層晶片之必要性,因而發展了晶片之薄膜化,但隨之亦增加了晶片之使用量,故需要增加單次加工所可製造之晶片數。對應於此,晶圓已大直徑化,目前則以12吋(300mm)晶圓之加工為主流。然而,為進而提昇晶片之加工效率,亦已進行18吋(450mm)晶圓加工之檢討。Further, although the necessity of increasing the number of laminated wafers for the purpose of improving the function, the thin film formation of the wafer has been developed, but the amount of wafer used has also increased, so that it is necessary to increase the number of wafers that can be manufactured in a single process. Corresponding to this, the wafer has been enlarged in diameter, and currently processing with 12 吋 (300 mm) wafers is the mainstream. However, in order to further improve the processing efficiency of the wafer, a review of 18 吋 (450 mm) wafer processing has also been conducted.

圖3(a)、(b)為顯示小直徑之半導體晶圓21及大徑之半導體晶圓31上之晶片之配置圖。如圖3(a)所示,呈棋盤格狀排列晶片23之晶片配置下,可藉以往之切割刀進行切割。然而,300mm以上之晶圓直徑下,對記憶體類裝置等尺寸較大之晶片形成配線時,愈朝晶圓表面進行圖案形成,無法使用之領域將增加,而造成無法作為產品使用之晶片之增加。因此,為提昇晶片之良率,如圖3(b)所示,刻正朝於半導體晶圓31之外周部密集配置晶片33之方式進行改變。由迄今依等間隔配置晶片之方式(圖3(a))改為朝各種不同方向而非等方向配置晶片之方式(圖3(b)),故切割道(切割線)並非直線,而難以藉刀片進行直線切割。3(a) and 3(b) are layout diagrams showing wafers on a small-diameter semiconductor wafer 21 and a large-diameter semiconductor wafer 31. As shown in Fig. 3(a), in the wafer arrangement in which the wafers 23 are arranged in a checkerboard pattern, the cutting can be performed by a conventional cutting blade. However, when a wafer having a larger size such as a memory device is formed at a wafer diameter of 300 mm or more, the pattern is formed on the surface of the wafer, and the field of unusable use is increased, resulting in a wafer that cannot be used as a product. increase. Therefore, in order to increase the yield of the wafer, as shown in FIG. 3(b), the wafer 33 is densely arranged toward the outer periphery of the semiconductor wafer 31. Since the wafers are arranged at equal intervals so far (Fig. 3(a)), the wafers are arranged in various directions instead of the equal directions (Fig. 3(b)), so the cutting lanes (cutting lines) are not straight lines, and it is difficult Straight cut with a blade.

對於上述問題,已提案一種使用雷射等而亦可就直線以外之狀況進行切割,朝半導體晶圓內部照射雷射光而選擇性地形成改質部,並形成切割線而以改質部為起點而分割半導體晶圓之所謂隱形切割法(專利文獻1)。然而,藉雷射切分晶片將使晶片受損,故尚存晶片之抗彎強度並未提高之問題。In order to solve the above problems, it has been proposed to use a laser or the like to cut a condition other than a straight line, irradiate laser light into the inside of the semiconductor wafer, selectively form a modified portion, and form a cutting line with the modified portion as a starting point. A so-called stealth dicing method for dividing a semiconductor wafer (Patent Document 1). However, by laser cutting the wafer, the wafer will be damaged, so that the bending strength of the remaining wafer is not improved.

對於上述問題,已提案一種電漿切割之方法(專利文獻2)。電漿切割乃以電漿選擇性地蝕刻未為遮罩所覆蓋之部位,而分割半導體晶圓之方法。採用上述切割方法,即可選擇性地切分晶片,乃即便切割道彎曲亦可正常進行切分之方法。且,蝕刻率極高,故近年已為最適用於晶片之切分之製程之一。然而,電漿切割時,係使用六氟化硫(SF6)或四氟化碳(CF4)等與晶圓之反應性極高之氟系氣體 作為電漿產生用氣體,並因其較高之蝕刻率而須對不進行蝕刻之面藉遮罩加以保護,且事前須以抗蝕劑或膠帶進行遮蔽。且,電漿蝕刻後將形成殘留其膜之狀態,故為去除抗蝕劑將使用大量溶劑,或無法去除抗蝕劑時將發生殘留而造成瑕疵晶片等各種問題尚未獲解決,故現下尚未普及。For the above problem, a method of plasma cutting has been proposed (Patent Document 2). Plasma cutting is a method of selectively etching a portion of a semiconductor wafer that is not covered by a mask by plasma. By the above cutting method, the wafer can be selectively sliced, and the cutting can be performed normally even if the cutting track is bent. Moreover, the etching rate is extremely high, so in recent years, it has become one of the processes most suitable for wafer segmentation. However, when plasma cutting, a fluorine-based gas that is highly reactive with a wafer such as sulfur hexafluoride (SF6) or carbon tetrafluoride (CF4) is used. As a gas for plasma generation, it is necessary to protect the surface which is not etched by a mask due to its high etching rate, and it is shielded by a resist or tape beforehand. Further, after the plasma is etched, a state in which the film remains is formed. Therefore, various problems such as the use of a large amount of solvent to remove the resist or the residue cannot be removed, resulting in defects such as a germanium wafer, have not yet been solved, so that it has not yet been popularized. .

又,電漿切割法將使晶圓曝置於電漿中而發熱形成高溫狀態,並發生半導體晶圓保護用黏著膠帶之加熱劣化之問題。加熱劣化後之半導體晶圓保護用黏著膠帶將於黏附體上殘留黏著劑,而喪失剝離功能,並失去半導體晶圓保護用黏著膠帶之效用。Further, the plasma cutting method exposes the wafer to the plasma to generate a high temperature state by heat generation, and causes a problem of heating deterioration of the adhesive tape for semiconductor wafer protection. The adhesive tape for semiconductor wafer protection after heat deterioration deteriorates the adhesive on the adhesive body, loses the peeling function, and loses the effect of the adhesive tape for semiconductor wafer protection.

另,近年,已新提案一種在藉前述隱形切割法而加工後,配合運用抑制對晶圓施加之能量,並控制蝕刻率之氣體群集式蝕刻法而成之加工方法。氣體群集式蝕刻法乃朝真空環境中吹入氣體而形成氣體分子之群集,並使其碰撞晶圓而進行晶圓之處理之方法(專利文獻3)。碰撞晶圓之群集對晶圓施加運動能量後,將分解成氣體分子而飛散。藉此,而可進行晶圓表面之蝕刻。在隱形切割法之加工後施予上述蝕刻處理,即可去除藉雷射而形成之改質部,並期待抗彎強度之提昇。且,氣體群集式蝕刻法使用三氟化氯(ClF3 )作為反應氣體,Cl-F之結合極少,故無須如四氟化碳(CF4 )等電漿產生用氣體般事前預先離子化,故對基板之損傷極少,無須藉遮罩加以保護,而可簡便地進行晶片之切分加工。In addition, in recent years, a new method of processing by a gas cluster etching method which suppresses the energy applied to a wafer and controls the etching rate after processing by the above-described stealth cutting method has been newly proposed. The gas cluster etching method is a method in which a gas is blown into a vacuum environment to form a cluster of gas molecules, and the wafer is processed to collide with the wafer (Patent Document 3). After the cluster of collision wafers applies kinetic energy to the wafer, it will decompose into gas molecules and scatter. Thereby, etching of the wafer surface can be performed. By applying the above etching treatment after the processing of the stealth cutting method, the modified portion formed by the laser can be removed, and the bending strength is expected to be improved. Further, in the gas cluster etching method, chlorine trifluoride (ClF 3 ) is used as the reaction gas, and the combination of Cl-F is extremely small, so that it is not required to be pre-ionized beforehand, such as a plasma generating gas such as carbon tetrafluoride (CF 4 ). Therefore, the damage to the substrate is extremely small, and it is not necessary to protect by the mask, and the wafer can be easily cut and processed.

採用氣體群集式蝕刻法等之氣體蝕刻程序與電 漿切割程序相同,在進行晶圓加工時,將因晶圓與氣體分子之化學反應而伴隨發熱現象。上述發熱亦可能超過200℃,伴隨上述發熱之加工方法則須防止基材薄膜因熱而熔附於保持半導體晶圓保護用膠帶之夾盤上,或基材薄膜收縮而導致半導體晶圓受損。Gas etching process and electricity using gas cluster etching The slurry cutting process is the same, and when wafer processing is performed, the phenomenon of heat generation is caused by the chemical reaction between the wafer and the gas molecules. The above-mentioned heat generation may also exceed 200 ° C. The processing method with the above-mentioned heat generation must prevent the base film from being thermally fused to the chuck holding the semiconductor wafer protective tape, or the substrate film shrinks and the semiconductor wafer is damaged. .

先行技術文獻Advanced technical literature 專利文獻Patent literature

專利文獻1:日本專利特開2003-33887號公報Patent Document 1: Japanese Patent Laid-Open Publication No. 2003-33887

專利文獻2:日本專利特開2007-19386號公報Patent Document 2: Japanese Patent Laid-Open Publication No. 2007-19386

專利文獻3:日本專利特開2011-171584號公報Patent Document 3: Japanese Patent Laid-Open Publication No. 2011-171584

發明概要Summary of invention

本發明目的即在提供一種即便在氣體蝕刻程序及電漿切割程序曝置於高溫中,亦不致熔附於夾盤上或過度收縮之具備耐熱性及耐熱收縮性之半導體晶圓保護用黏著膠帶。SUMMARY OF THE INVENTION The object of the present invention is to provide an adhesive tape for semiconductor wafer protection having heat resistance and heat shrink resistance which is not adhered to a chuck or excessively shrinkage even when exposed to a high temperature in a gas etching process and a plasma cutting process. .

為達成上述目的,而提供如下之發明。In order to achieve the above object, the following invention is provided.

(1)一種半導體晶圓保護用黏著膠帶,其特徵在於包含基材薄膜及基材薄膜之單面上形成之黏著劑層,且前述基材薄膜於未形成有前述黏著劑層之側的最外層具有含已硬化之樹脂之鑄膜層,令在使直徑3.0mm之SUS304製之探針接觸測定試樣時之速度為30mm/min,接觸載重為100gf,接 觸時間為1秒之條件下,依600mm/min之剝離速度朝上方剝除探針時之藉探針試驗所測得之前述鑄膜層之黏著力的峰值在200℃下為100kPa以下。(1) An adhesive tape for protecting a semiconductor wafer, comprising: an adhesive layer formed on one surface of a base film and a base film, wherein the base film is the most side on which the adhesive layer is not formed The outer layer has a cast film layer containing a hardened resin, so that the probe made of SUS304 having a diameter of 3.0 mm is brought into contact with the measurement sample at a speed of 30 mm/min, and the contact load is 100 gf. When the contact time was 1 second, the peak of the adhesion of the cast film layer measured by the probe test when the probe was peeled upward at a peeling speed of 600 mm/min was 100 kPa or less at 200 °C.

(2)如(1)記載之半導體晶圓保護用黏著膠帶,其特徵在於前述基材薄膜僅由鑄膜層所構成。(2) The adhesive tape for protecting a semiconductor wafer according to (1), wherein the base film is composed only of a cast film layer.

(3)如(1)或(2)記載之半導體晶圓保護用黏著膠帶,其特徵在於前述鑄膜層含有已硬化之丙烯酸系共聚物或聚酯樹脂。(3) The adhesive tape for protecting a semiconductor wafer according to (1) or (2), wherein the cast film layer contains a cured acrylic copolymer or a polyester resin.

(4)如(1)~(3)中任一記載之半導體晶圓保護用黏著膠帶,其特徵在於前述鑄膜層由已藉硬化劑或放射線而硬化之丙烯酸系共聚物所構成。(4) The adhesive tape for protecting a semiconductor wafer according to any one of (1) to (3), wherein the cast film layer is composed of an acrylic copolymer which has been cured by a curing agent or radiation.

(5)如(1)~(4)中任一記載之半導體晶圓保護用黏著膠帶,其特徵在於斷裂強度為0.5N/mm以上,斷裂延伸率為200%以上。(5) The adhesive tape for protecting a semiconductor wafer according to any one of (1) to (4), wherein the breaking strength is 0.5 N/mm or more, and the elongation at break is 200% or more.

(6)如(1)~(5)中任一記載之半導體晶圓保護用黏著膠帶,其特徵在於令在使直徑3.0mm之SUS304製之探針接觸測定試樣時之速度為30mm/min,接觸載重為100gf,接觸時間為1秒之條件下,依600mm/min之剝離速度朝上方剝除探針時之藉探針試驗所測得之前述黏著劑層之黏著力的峰值在25℃下為50~400kPa。(6) The adhesive tape for protecting a semiconductor wafer according to any one of (1) to (5), wherein the speed of the probe made of SUS304 having a diameter of 3.0 mm is 30 mm/min when it is brought into contact with the measurement sample. When the contact load is 100 gf and the contact time is 1 second, the adhesion of the adhesive layer measured by the probe test when the probe is peeled upward at a peeling speed of 600 mm/min is 25 ° C. The next is 50~400kPa.

依據本發明,可提供即便在氣體蝕刻程序及電漿切割程序中曝置於高溫下,亦不致熔附於夾盤上或過度收縮之具備耐熱性與耐熱收縮性之半導體晶圓保護用黏著膠 帶。According to the present invention, it is possible to provide a semiconductor wafer protective adhesive having heat resistance and heat shrink resistance which is not adhered to a chuck or excessively shrinkage even when exposed to a high temperature in a gas etching process or a plasma cutting process. band.

1、1a‧‧‧半導體晶圓保護 用黏著膠帶1, 1a‧‧‧Semiconductor wafer protection Adhesive tape

3‧‧‧基材薄膜3‧‧‧Substrate film

5‧‧‧黏著劑層5‧‧‧Adhesive layer

7‧‧‧鑄膜層7‧‧‧ cast film layer

9‧‧‧樹脂薄膜層9‧‧‧ resin film layer

11‧‧‧晶片11‧‧‧ wafer

13‧‧‧蝕刻氣體13‧‧‧etching gas

15‧‧‧環狀框架15‧‧‧Ring frame

17‧‧‧夾盤17‧‧‧ chuck

21‧‧‧半導體晶圓21‧‧‧Semiconductor wafer

23‧‧‧晶片23‧‧‧ wafer

31‧‧‧半導體晶圓31‧‧‧Semiconductor wafer

33‧‧‧晶片33‧‧‧ wafer

圖1(a)為顯示本實施形態之半導體晶圓保護用黏著膠帶1之截面圖,(b)為顯示本實施形態之半導體晶圓保護用黏著膠帶1a之截面圖。Fig. 1(a) is a cross-sectional view showing the adhesive tape 1 for semiconductor wafer protection of the embodiment, and Fig. 1(b) is a cross-sectional view showing the adhesive tape 1a for semiconductor wafer protection of the embodiment.

圖2說明使用本實施形態之半導體晶圓保護用黏著膠帶1之氣體蝕刻程序。Fig. 2 illustrates a gas etching process using the adhesive tape 1 for semiconductor wafer protection of the present embodiment.

圖3(a)為小直徑之半導體晶圓上之晶片之配置圖。(b)為大直徑之半導體晶圓上之晶片之配置圖。Figure 3 (a) is a configuration diagram of a wafer on a small-diameter semiconductor wafer. (b) is a configuration diagram of a wafer on a large-diameter semiconductor wafer.

用以實施發明之形態Form for implementing the invention

以下,基於附圖詳細說明本發明之實施形態。Hereinafter, embodiments of the present invention will be described in detail based on the drawings.

圖1(a)為顯示本實施形態之半導體晶圓保護用黏著膠帶1之截面圖,圖1(b)為顯示本實施形態之半導體晶圓保護用黏著膠帶1a之截面圖。Fig. 1(a) is a cross-sectional view showing the adhesive tape 1 for semiconductor wafer protection of the embodiment, and Fig. 1(b) is a cross-sectional view showing the adhesive tape 1a for semiconductor wafer protection of the embodiment.

半導體晶圓保護用黏著膠帶1包含基材薄膜3及設於基材薄膜3上之黏著劑層5。另,各層亦可配合使用程序及裝置而預先分割(預切)成預定形狀。進而,本實施形態之半導體晶圓保護用黏著膠帶1亦可為已分別分割成晶圓一片大小之形態,或將長形之薄片捲束成筒狀之形態。以下,即說明各層之構造。The adhesive tape 1 for semiconductor wafer protection includes a base film 3 and an adhesive layer 5 provided on the base film 3. Further, each layer may be pre-divided (precut) into a predetermined shape in accordance with a program and a device. Further, the adhesive tape 1 for semiconductor wafer protection of the present embodiment may be in a form in which the wafer is divided into a single wafer or a long sheet is wound into a tubular shape. Hereinafter, the structure of each layer will be described.

<基材薄膜><Substrate film>

基材薄膜3於未形成有黏著劑層5之側之最外層設有含有已硬化之樹脂之鑄膜層7。且,圖1(a)中,雖顯示積層有 鑄膜層7與樹脂薄膜層9之基材薄膜3,但僅限最外層為鑄膜層7,則亦可對基材薄膜3積層樹脂薄膜層9以外之樹脂層。The base film 3 is provided with a cast film layer 7 containing a hardened resin on the outermost layer on the side where the adhesive layer 5 is not formed. Moreover, in Fig. 1(a), although the laminate is shown In the base film 3 of the cast film layer 7 and the resin film layer 9, the resin film other than the resin film layer 9 may be laminated on the base film 3 only if the outermost layer is the cast film layer 7.

鑄膜層乃塗刷樹脂組成物而成之層。鑄膜層7使用可藉交聯而具有三次元網格構造之樹脂,故曝置於高溫下亦不易軟化,而不易熔附於夾盤上。且,鑄膜層7藉塗刷而形成,故殘餘應力較少,曝置於高溫下亦少發生熱收縮,且不易發生氣體蝕刻程序中之晶片位置偏移。The cast film layer is a layer formed by coating a resin composition. The cast film layer 7 uses a resin which can be crosslinked and has a three-dimensional mesh structure, so that it is not easily softened when exposed to a high temperature, and is not easily fused to the chuck. Further, since the cast film layer 7 is formed by brushing, the residual stress is small, heat shrinkage is less likely to occur at a high temperature, and wafer position shift in the gas etching process is less likely to occur.

另,如圖1(b)所示,亦可使用基材薄膜3僅由鑄膜層7所構成,並於鑄膜層7之單面側設有黏著劑層5之半導體晶圓保護用黏著膠帶1a。基材薄膜3僅由鑄膜層7所構成時,基材薄膜3之整體均由鑄膜層所構成,故半導體晶圓保護用黏著膠帶1a與使用積層有樹脂薄膜層9與鑄膜層7之基材薄膜3之半導體晶圓保護用黏著膠帶1相較,可構成熱收縮率較低之黏著膠帶。半導體晶圓保護用黏著膠帶1a之熱收縮率較低,故在曝置於高溫下之氣體蝕刻程序中,亦不易發生黏附體之晶片位置之偏移,且不易發生彎曲收縮。Further, as shown in FIG. 1(b), the base film 3 may be formed of only the cast film layer 7, and the adhesive layer 5 may be provided on the one side of the cast film layer 7 to protect the semiconductor wafer. Tape 1a. When the base film 3 is composed only of the cast film layer 7, the entire base film 3 is composed of a cast film layer, so that the adhesive tape 1a for semiconductor wafer protection and the resin film layer 9 and the cast film layer 7 are laminated. The adhesive tape 1 for semiconductor wafer protection of the base film 3 can constitute an adhesive tape having a low heat shrinkage ratio. Since the heat shrinkage rate of the adhesive tape 1a for semiconductor wafer protection is low, in the gas etching process exposed to a high temperature, the position of the wafer of the adherend is less likely to occur, and bending and shrinkage are less likely to occur.

又,鑄膜層7之黏著力在200℃時為100kPa以下,50kPa較佳,30kPa以下則更佳。此之黏著力乃藉探針試驗而測得之黏著力之峰值。鑄膜層7之黏著力在200℃時若超過100kPa,則在氣體蝕刻程序等中加熱時,容易附著於夾盤上。Further, the adhesion of the cast film layer 7 is 100 kPa or less at 200 ° C, preferably 50 kPa, and more preferably 30 kPa or less. This adhesion is the peak of the adhesion measured by the probe test. When the adhesive force of the cast film layer 7 exceeds 100 kPa at 200 ° C, it tends to adhere to the chuck when heated in a gas etching process or the like.

又,鑄膜層7之黏著力在25℃時宜為20kPa以下。鑄膜層7之黏著力在25℃時若超過20kPa,將不易在常溫下自夾盤剝除。且,將黏著膠帶捲筒化時可能發生沾黏。Further, the adhesion of the cast film layer 7 is preferably 20 kPa or less at 25 °C. If the adhesion of the cast film layer 7 exceeds 20 kPa at 25 ° C, it will not be easily peeled off from the chuck at normal temperature. Also, sticking may occur when the adhesive tape is rolled up.

樹脂薄膜層9雖無特別之限制,但使用之樹脂可列舉聚乙烯、聚丙烯、乙烯-丙烯共聚物、聚丁烯-1、聚-4-甲基戊烯-1、乙烯醋酸乙烯酯共聚物、乙烯-丙烯酸共聚物、離子聚合物等之α-烯之均聚物或共聚物或者其等之混合物、聚對苯二甲酸乙二酯、聚碳酸酯、聚甲基丙烯酸甲酯等之工程塑膠、聚胺甲酸酯、苯乙烯-乙烯-丁烯或戊烯系共聚物等之熱塑性彈性體等。The resin film layer 9 is not particularly limited, but examples of the resin used include polyethylene, polypropylene, ethylene-propylene copolymer, polybutene-1, poly-4-methylpentene-1, and ethylene vinyl acetate copolymerization. a homopolymer or copolymer of an α-olefin such as an ethylene-acrylic acid copolymer or an ionic polymer or a mixture thereof, polyethylene terephthalate, polycarbonate, polymethyl methacrylate or the like A thermoplastic elastomer such as an engineering plastic, a polyurethane, a styrene-ethylene-butylene or a pentene copolymer.

基材薄膜3之厚度宜為50~200μ m。The thickness of the base film 3 is preferably 50 to 200 μm .

又,基材薄膜3為樹脂薄膜層9與鑄膜層7之積層時,鑄膜層7之厚度宜為5~100μ m,5~50μ m則更佳。Further, when the base film 3 is a laminate of the resin film layer 9 and the cast film layer 7, the thickness of the cast film layer 7 is preferably 5 to 100 μm , more preferably 5 to 50 μm .

僅以鑄膜層7構成基材薄膜時,鑄膜層7之厚度宜為50~200μ m,50~100μ m則更佳。When the base film is formed only by the cast film layer 7, the thickness of the cast film layer 7 is preferably 50 to 200 μm , more preferably 50 to 100 μm .

樹脂薄膜層9之厚度雖無特別之限制,但一般通常在50~150μ m之範圍內。Although the thickness of the resin film layer 9 is not particularly limited, it is usually in the range of 50 to 150 μm .

鑄膜層7宜由塗刷丙烯酸系共聚物或聚酯樹脂組成物,進而藉硬化劑或放射線而硬化者所構成。與藉擠製法而形成,進而藉伸展程序而薄膜化之伸展薄膜相較,藉塗刷而形成之鑄膜層7之殘餘應力較少,曝置於高溫下亦較少熱收縮。且,本實施形態之鑄膜層7因交聯而具有三次元網格構造,200℃下之黏著力較小,故曝置於高溫下亦不致熔附於夾盤上。The cast film layer 7 is preferably composed of a composition coated with an acrylic copolymer or a polyester resin, and further cured by a hardener or radiation. Compared with the stretch film which is formed by the borrowing method and which is thinned by the stretching process, the cast film layer 7 formed by brushing has less residual stress, and is less heat-shrinked when exposed to high temperature. Further, the cast film layer 7 of the present embodiment has a three-dimensional mesh structure due to cross-linking, and the adhesive force at 200 ° C is small, so that it is not fused to the chuck when exposed to a high temperature.

又,半導體晶圓保護用黏著膠帶1及1a之斷裂強度宜為0.5N/mm以上,斷裂延伸率宜為200%以上。具備上述特性,即不致在對半導體晶圓進行貼附及剝離時引起破 裂等問題。Further, the breaking strength of the adhesive tapes 1 and 1a for semiconductor wafer protection is preferably 0.5 N/mm or more, and the elongation at break is preferably 200% or more. Having the above characteristics, that is, not causing damage when attaching and peeling off the semiconductor wafer Cracking and other issues.

(構成鑄膜層之樹脂)(resin constituting the cast film layer)

鑄膜層7由已硬化之樹脂所形成,尤其乃由丙烯酸系共聚物或聚酯樹脂硬化而成之樹脂所形成。丙烯酸系共聚物或聚酯樹脂並無特別之限制,可使用能量線硬化型樹脂、硬化劑硬化型樹脂或熱固性樹脂等,宜使用能量線硬化型樹脂或硬化劑硬化型之樹脂。使用能量線硬化型樹脂時,則於塗布後照射能量線而使樹脂硬化。使用硬化劑硬化型樹脂時,則對樹脂添加交聯劑,並於塗布、乾燥後予以熟化而使其硬化。使用熱固性樹脂時,則於塗布後予以加熱而使樹脂硬化。The cast film layer 7 is formed of a hardened resin, in particular, a resin obtained by hardening an acrylic copolymer or a polyester resin. The acrylic copolymer or the polyester resin is not particularly limited, and an energy ray-curable resin, a hardener-curable resin, a thermosetting resin, or the like can be used, and an energy ray-curable resin or a hardener-curable resin is preferably used. When an energy ray-curable resin is used, the resin is cured by irradiating an energy ray after application. When a hardener hardening type resin is used, a crosslinking agent is added to the resin, and after being applied and dried, it is aged and cured. When a thermosetting resin is used, it is heated after coating to harden the resin.

積層鑄膜層7與樹脂薄膜層9時,可列舉對樹脂薄膜層9塗布硬化型樹脂,並使其硬化之方法,以及藉接著劑等而接著已硬化之鑄膜之方法等。形成未積層之鑄膜層7時,則於剝離性之薄膜上塗布硬化型樹脂後,使其硬化,再自薄膜加以剝離,即製得鑄膜層7。In the case of laminating the cast film layer 7 and the resin film layer 9, a method of applying a curing resin to the resin film layer 9 and curing the film, and a method of adhering the cured film by an adhesive or the like may be mentioned. When the unlaminated cast film layer 7 is formed, the curable resin is applied onto the peelable film, and then cured, and then peeled off from the film to obtain a cast film layer 7.

(丙烯酸系共聚物)(acrylic copolymer)

用於形成鑄膜層7之丙烯酸系共聚物並無特別之限制,諸如使用能量線硬化型樹脂時,可為以丙烯酸系黏著劑與能量線聚合性化合物為主成分而組成者。該等丙烯酸系黏著劑及能量線聚合性化合物則可具體應用以下所列舉者。The acrylic copolymer for forming the cast film layer 7 is not particularly limited. For example, when an energy ray-curable resin is used, it may be composed of an acrylic adhesive and an energy ray polymerizable compound as a main component. The acrylic adhesive and the energy ray polymerizable compound can be specifically used as described below.

丙烯酸系黏著劑之成分為(甲基)丙烯酸系共聚物及硬化劑。(甲基)丙烯酸系共聚物可列舉諸如以(甲基)丙 烯酸酯為共聚物構成單位之共聚物,(甲基)丙烯酸酯與官能單體之共聚物及該等共聚物之混合物等。該等共聚物之分子量則就基材薄膜之延展性而言,適用重量平均分子量為1萬~20萬左右之低分子量者。The component of the acrylic adhesive is a (meth)acrylic copolymer and a curing agent. (meth)acrylic copolymers may be exemplified by (meth) propyl The enoate is a copolymer of a copolymer constituent unit, a copolymer of a (meth) acrylate and a functional monomer, a mixture of the copolymers, and the like. The molecular weight of the copolymers is preferably a low molecular weight having a weight average molecular weight of about 10,000 to 200,000 in terms of ductility of the base film.

又,硬化劑乃用於與(甲基)丙烯酸系共聚物所包含之官能基反應以調整黏著力及內聚力者。舉例言之,可列舉1,3-雙(N,N-二縮水甘油氨甲基)環己烷、1,3-雙(N,N-二縮水甘油氨甲基)甲苯、1,3-雙(N,N-二縮水甘油氨甲基)苯、N,N,N,N'-四縮水甘油基間二甲苯二胺等之分子中含有2個以上之環氧基之環氧化合物、2,4-二異氰酸甲伸苯酯、2,6-二異氰酸甲伸苯酯、1,3二異氰酸二甲苯酯、1,4二異氰酸二甲苯酯、二苯甲基-4,4-二異氰酸酯等之分子中含有2個以上之異氰酸基之異氰酸系化合物、四羥甲基-三-β-氮丙啶基丙酸酯、三羥甲基-三-β-氮丙啶基丙酸酯、三羥甲基丙烷-三-β-氮丙啶基丙酸酯、三羥甲基丙烷-三-β-(2-甲基氮丙啶)丙酸酯等之分子中含有2個以上之氮丙啶基之氮丙啶系化合物等。硬化劑之添加量可對應所需之黏著力而調整,對(甲基)丙烯酸系共聚物100質量份添加0.1~5.0質量份即屬適當。Further, the curing agent is used for reacting with a functional group contained in the (meth)acrylic copolymer to adjust the adhesion and cohesion. For example, 1,3-bis(N,N-diglycidylaminomethyl)cyclohexane, 1,3-bis(N,N-diglycidylaminomethyl)toluene, 1,3- An epoxy compound containing two or more epoxy groups in a molecule such as bis(N,N-diglycidylaminomethyl)benzene, N,N,N,N'-tetraglycidyl-m-xylylenediamine or the like 2,4-diisocyanate, phenyl 2,6-diisocyanate, 1,3 diisocyanate, 1,4 diisocyanate, diphenyl An isocyanate compound having two or more isocyanate groups in a molecule such as methyl-4,4-diisocyanate, tetramethylol-tris-β-aziridine propionate, or trimethylol -Tri-β-aziridine propionate, trimethylolpropane-tri-β-aziridine propionate, trimethylolpropane-tri-β-(2-methylaziridine) An aziridine-based compound containing two or more aziridine groups in a molecule such as a propionate. The amount of the curing agent to be added can be adjusted in accordance with the desired adhesive strength, and it is appropriate to add 0.1 to 5.0 parts by mass to 100 parts by mass of the (meth)acrylic copolymer.

另,使用硬化劑硬化型樹脂時,為抑制黏著力及確保作為薄膜之強度及延伸度,宜相對於可與(甲基)丙烯酸系共聚物中之硬化劑反應之官能基添加等量程度之硬化劑,諸如對(甲基)丙烯酸系共聚物100質量份添加2.0~30質量份即屬適當。Further, when a hardener-curable resin is used, it is preferable to add an equivalent amount to a functional group reactive with a hardener in a (meth)acrylic copolymer in order to suppress adhesion and ensure strength and elongation as a film. It is appropriate to add a hardener such as 2.0 to 30 parts by mass to 100 parts by mass of the (meth)acrylic copolymer.

能量線硬化型樹脂一般乃以前述丙烯酸系黏著 劑與能量線聚合性化合物為主成分而組成。能量線聚合性化合物則廣泛使用諸如於可藉紫外線之照射而立體網狀化之分子內至少含有2個以上之光聚合性碳-碳雙鍵之低分子量化合物。具體而言,可廣泛應用三羥甲基丙烷三丙烯酸酯、四羥甲基甲烷四丙烯酸酯、新戊四醇三丙烯酸酯、新戊四醇四丙烯酸酯、二新戊四醇單羥基五丙烯酸酯、二新戊四醇六丙烯酸酯、1,4-丁二醇二丙烯酸酯、1,6己二醇二丙烯酸酯、聚乙二醇二丙烯酸酯及寡酯丙烯酸酯等。The energy ray-curable resin is generally adhered to the aforementioned acrylic The agent and the energy ray polymerizable compound are mainly composed of a component. As the energy ray-polymerizable compound, a low molecular weight compound containing at least two photopolymerizable carbon-carbon double bonds in a molecule which can be three-dimensionally networked by irradiation with ultraviolet rays is widely used. Specifically, trimethylolpropane triacrylate, tetramethylol methane tetraacrylate, neopentyl alcohol triacrylate, neopentyl alcohol tetraacrylate, dipentaerythritol monohydroxypentaacrylic acid can be widely used. Ester, dipentaerythritol hexaacrylate, 1,4-butanediol diacrylate, 1,6 hexanediol diacrylate, polyethylene glycol diacrylate, and oligoester acrylate.

又,丙烯酸系黏著劑除上述之丙烯酸酯系化合物以外,亦可使用丙烯酸胺酯系低聚物。丙烯酸胺酯系低聚物乃對由聚酯型或聚醚型等之聚醇化合物與多價異氰酸酯化合物(諸如2,4-甲苯二異氰酸酯、2,6-甲苯二異氰酸酯、1,3-二甲苯二異氰酸酯、1,4-二甲苯二異氰酸酯、二苯甲基4,4-二異氰酸酯等)反應而得之末端異氰酸酯胺甲酸乙酯預聚物,使含有羥基之丙烯酸酯或甲基丙烯酸酯(諸如2-丙烯酸羥乙酯、2-甲基丙烯酸羥乙酯、2-丙烯酸羥丙酯、2-甲基丙烯酸羥丙酯、聚乙二醇丙烯酸酯、聚乙二醇甲基丙烯酸酯等)與其反應而製得。Further, the acrylic adhesive may be an urethane acrylate oligomer in addition to the above acrylate compound. The urethane acrylate oligomer is a polyvalent alcohol compound such as a polyester type or a polyether type and a polyvalent isocyanate compound (such as 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 1,3-two). a terminal isocyanate urethane prepolymer obtained by reacting toluene diisocyanate, 1,4-dimethylbenzene diisocyanate, diphenylmethyl 4,4-diisocyanate or the like to obtain a hydroxyl group-containing acrylate or methacrylate (such as 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, polyethylene glycol acrylate, polyethylene glycol methacrylate, etc. ) It is made by reacting with it.

能量線硬化型樹脂中之丙烯酸系黏著劑與能量線聚合性化合物之調配比例為對丙烯酸系黏著劑100質量份添加能量線聚合性化合物50~200質量份,而以在50~150質量份之範圍內調配為佳。上述調配比例之範圍內,可在能量線照射後大幅降低能量線硬化型樹脂之黏著力。The blending ratio of the acrylic adhesive to the energy ray-polymerizable compound in the energy ray-curable resin is 50 to 200 parts by mass, and 50 to 150 parts by mass, based on 100 parts by mass of the acrylic adhesive. The range is better. Within the range of the above-mentioned blending ratio, the adhesion of the energy ray-curable resin can be greatly reduced after the energy ray irradiation.

進而,能量線硬化型樹脂亦可以丙烯酸系黏著劑本身 作為能量線聚合性丙烯酸酯共聚物,而非如上般對丙烯酸系黏著劑調配能量線聚合性化合物。Further, the energy ray-curable resin may also be an acrylic adhesive itself. As the energy ray-polymerizable acrylate copolymer, the energy ray-polymerizable compound is blended with the acrylic adhesive as above.

又,藉能量線使能量線硬化型樹脂聚合時,可併用光聚合起始劑,諸如安息香異丙醚、安息香異丁醚、二苯基酮、米其勒酮、氯噻噸酮、苄基甲基縮酮、α-羥基環己基苯基酮、2-羥甲基苯丙烷等。於能量線硬化型樹脂中添加其等中至少1種,即可有效率地進行聚合反應。另,此之所謂能量線意指紫外線等光線或電子束等游離能量射線。Further, when the energy ray-curable resin is polymerized by an energy ray, a photopolymerization initiator such as benzoin isopropyl ether, benzoin isobutyl ether, diphenyl ketone, mischidone, chlorothioxanthone, benzyl group may be used in combination. Methyl ketal, α-hydroxycyclohexyl phenyl ketone, 2-hydroxymethyl phenylpropane, and the like. By adding at least one of these to the energy ray-curable resin, the polymerization reaction can be carried out efficiently. In addition, the so-called energy line means free energy rays such as ultraviolet rays or electron beams.

(聚酯樹脂)(polyester resin)

用於形成鑄膜層7之聚酯樹脂並無特別之限制,舉例言之,使用硬化劑硬化型樹脂時,則以硬化劑硬化型之聚酯樹脂組成物與硬化劑為主成分而組成之。The polyester resin for forming the cast film layer 7 is not particularly limited. For example, when a hardener-hardening resin is used, the hardener-curable polyester resin composition and the hardener are mainly composed. .

硬化劑硬化型聚酯樹脂組成物乃含有包含可與硬化劑反應之官能基之聚酯樹脂之組成物,可適當使用含有羥基之聚酯多元醇。The hardener-curable polyester resin composition is a composition containing a polyester resin containing a functional group reactive with a hardener, and a hydroxyl group-containing polyester polyol can be suitably used.

又,硬化劑乃用於與硬化劑硬化型聚酯樹脂組成物中含有之官能基反應以調整黏著力及內聚力者。可適當使用於前述分子中含有2個以上之異氰酸基之異氰酸酯系化合物。Further, the hardener is used for reacting with a functional group contained in the hardener-curable polyester resin composition to adjust the adhesion and cohesion. An isocyanate compound containing two or more isocyanate groups in the above molecule can be suitably used.

<黏著劑層><Adhesive layer>

黏著劑層5可藉對基材薄膜3塗刷黏著劑而形成。構成本實施形態之半導體晶圓保護用黏著膠帶1之黏著劑層5具有在氣體蝕刻程序時不致與晶片發生剝離程度之保持性即 可。且,宜為釋氣較少者以避免加熱時汙染晶圓及裝置。The adhesive layer 5 can be formed by applying an adhesive to the base film 3. The adhesive layer 5 constituting the adhesive tape 1 for semiconductor wafer protection of the present embodiment has a retentive property of not being peeled off from the wafer during the gas etching process. can. Also, it is desirable to have less outgassing to avoid contamination of the wafer and device during heating.

尤其,照射能量線等前之黏著劑層5之黏著力在25℃時宜為50~400kPa。上述之黏著力則可避免黏著物之半導體晶圓及晶片之間發生剝離。In particular, the adhesion of the adhesive layer 5 before the irradiation of the energy ray or the like is preferably 50 to 400 kPa at 25 °C. The adhesion described above avoids peeling between the semiconductor wafer and the wafer of the adhesive.

本實施形態中,構成黏著劑層5之黏著劑之組成雖無特別之限制,但為提昇剝離性,宜具備能量線硬化性,並宜為硬化後可輕易與晶片21剝離之材料。具有能量線硬化性之黏著劑諸如可使用形成鑄膜層7時所使用之以丙烯酸系黏著劑與能量線聚合性化合物為主成分而組成者。使用能量線硬化性之黏著劑時,為提昇耐熱性,亦可在氣體蝕刻程序前施予能量線硬化。In the present embodiment, the composition of the adhesive constituting the adhesive layer 5 is not particularly limited. However, in order to improve the peeling property, it is preferable to have energy ray curability, and it is preferable to be a material which can be easily peeled off from the wafer 21 after curing. The energy ray-curable adhesive may be composed of, for example, an acrylic adhesive and an energy ray polymerizable compound used as the main component of the cast film layer 7 . When an energy ray-curable adhesive is used, energy ray hardening may be applied before the gas etching process in order to improve heat resistance.

(用途)(use)

本實施形態之半導體晶圓保護用黏著膠帶1可適用於對藉隱形切割程序而切片後之晶片藉氣體而進行之蝕刻處理程序。The adhesive tape 1 for semiconductor wafer protection of the present embodiment can be applied to an etching process for performing gas on a wafer sliced by a stealth dicing process.

(氣體蝕刻程序)(gas etching procedure)

本實施形態之半導體晶圓保護用黏著膠帶1應用於氣體蝕刻程序時之膠帶之使用方法則參照圖2加以說明。The method of using the adhesive tape 1 for protecting a semiconductor wafer according to the present embodiment when applied to a gas etching process will be described with reference to FIG. 2 .

圖2為顯示藉隱形切割程序而對半導體晶圓已切片而成之晶片11藉蝕刻氣體13而進行蝕刻之氣體蝕刻程序之截面圖。如圖2所示,環狀框架15上固定之半導體晶圓保護用黏著膠帶上固定有半導體晶圓已藉隱形切割程序而切片後之多數晶片11。且,晶片11已為夾盤17所保持。然後,照射蝕刻氣體13,並蝕刻晶片11之露出面。2 is a cross-sectional view showing a gas etching process for etching a wafer 11 in which a semiconductor wafer has been sliced by an etching gas 13 by a stealth dicing process. As shown in FIG. 2, a plurality of wafers 11 on which a semiconductor wafer has been sliced by a stealth dicing process are fixed to an adhesive tape for protecting a semiconductor wafer fixed to the ring frame 15. Moreover, the wafer 11 has been held by the chuck 17. Then, the etching gas 13 is irradiated, and the exposed face of the wafer 11 is etched.

藉氣體蝕刻程序,可去除晶片切分面上殘留之因雷射光而形成之改質領域。改質領域已易於破碎,故若改質領域殘留於晶片11上,晶片11將自改質領域開始破裂。去除晶片11表面之改質領域及凹凸部分,即可提高晶片11之抗彎強度。氣體蝕刻則例舉於已減壓至1kPa左右之處理室內,依0.3~2.0MPa之壓力吹送已加熱至200℃之三氟化氯(ClF3 )氣體之方法。The gas etching process can remove the modified field formed by the laser light remaining on the wafer dicing surface. The field of modification has been easily broken, so if the field of modification remains on the wafer 11, the wafer 11 will begin to rupture from the field of modification. The bending strength of the wafer 11 can be improved by removing the modified region and the uneven portion of the surface of the wafer 11. The gas etching is exemplified by a method of blowing a chlorine trifluoride (ClF 3 ) gas heated to 200 ° C at a pressure of 0.3 to 2.0 MPa in a treatment chamber which has been depressurized to about 1 kPa.

此時,將藉照射已加熱之蝕刻氣體13,或於蝕刻氣體13與晶片11之間發生化學反應,而加熱半導體晶圓保護用黏著膠帶1。接觸夾盤17之部位雖藉朝夾盤17中循環冷卻水而冷卻,但未接觸夾盤17之部位及發熱大於冷卻能力時,半導體晶圓保護用黏著膠帶1亦可能被加熱至200℃左右。At this time, the semiconductor wafer protective adhesive tape 1 is heated by irradiating the heated etching gas 13 or chemical reaction between the etching gas 13 and the wafer 11. Although the portion contacting the chuck 17 is cooled by circulating cooling water into the chuck 17, but the portion where the chuck 17 is not contacted and the heat generation is greater than the cooling capacity, the adhesive tape 1 for semiconductor wafer protection may be heated to about 200 ° C. .

(本實施形態之效果)(Effect of this embodiment)

本實施形態中,接觸夾盤17之鑄膜層7即便加熱至200℃,黏著力依然在預定值以下,故本實施形態之半導體晶圓保護用黏著膠帶1可進行氣體蝕刻而不致熔附於夾盤17上。In the present embodiment, even if the casting layer 7 of the contact chuck 17 is heated to 200 ° C and the adhesive force is still below a predetermined value, the adhesive tape 1 for semiconductor wafer protection of the present embodiment can be gas-etched without being fused to On the chuck 17.

又,本實施形態中,基材薄膜3設有鑄膜層7,故半導體晶圓保護用黏著膠帶之熱收縮率較小,而可於氣體蝕刻程序中,避免晶片位置偏移及晶片彼此接觸。Further, in the present embodiment, since the base film 3 is provided with the cast film layer 7, the heat shrinkage rate of the adhesive tape for semiconductor wafer protection is small, and the wafer positional deviation and wafer contact can be avoided in the gas etching process. .

尤其,本實施形態中,僅以鑄膜層形成基材薄膜時,半導體晶圓保護用黏著膠帶之熱收縮率更小。In particular, in the present embodiment, when the base film is formed of only the cast film layer, the heat shrinkage rate of the adhesive tape for semiconductor wafer protection is smaller.

【實施例】[Examples]

其次,為進而闡明本實施形態之效果,將就實施例及比較例加以詳細說明,但本發明不受限於該等實施例。Next, in order to clarify the effects of the present embodiment, the examples and comparative examples will be described in detail, but the present invention is not limited to the examples.

[半導體晶圓保護用黏著膠帶之製作][Production of Adhesive Tape for Semiconductor Wafer Protection]

(1)基材薄膜之製作(1) Fabrication of substrate film

(鑄膜A與樹脂薄膜A之積層薄膜)(Laminated film of cast film A and resin film A)

使用住友化學出品之乙烯甲基丙烯酸甲酯(EMMA)樹脂「ACRYFT WD201(商品名)」,並藉T字模法而成形厚100μ m之樹脂薄膜A。A vinyl methacrylate (EMMA) resin "ACRYFT WD201 (trade name)" produced by Sumitomo Chemical Co., Ltd. was used, and a resin film A having a thickness of 100 μm was formed by a T-die method.

將紫外線硬化型丙烯酸系共聚物A塗刷於剝離薄膜上並使其乾燥後之厚度為30μ m,再予以貼合樹脂薄膜A,並照射紫外線而使其硬化,即製得總厚度130μ m之樹脂薄膜A與鑄膜A之積層薄膜。The ultraviolet curable acrylic copolymer A is applied onto a release film and dried to a thickness of 30 μm , and then the resin film A is bonded thereto and cured by irradiation with ultraviolet rays to obtain a total thickness of 130 μ. A laminated film of resin film A and cast film A of m.

紫外線硬化型丙烯酸系共聚物組成物A之組成如下。The composition of the ultraviolet curable acrylic copolymer composition A is as follows.

前述之丙烯酸酯共聚物及放射線聚合性化合物則如以下所述。The above acrylate copolymer and radiation polymerizable compound are as follows.

丙烯酸酯共聚物:共聚2-丙烯酸乙基己酯、甲基丙烯酸酯、2-丙烯酸羥乙 酯而得,重量平均分子量為10萬,玻璃轉化溫度為-10℃之共聚物。Acrylate copolymer: copolymerized 2-ethylhexyl acrylate, methacrylate, 2-hydroxy acrylate A copolymer having a weight average molecular weight of 100,000 and a glass transition temperature of -10 ° C.

放射線聚合性化合物:重量平均分子量為1100之環氧丙烯酸酯低聚物。Radiation-polymerizable compound: an epoxy acrylate oligomer having a weight average molecular weight of 1,100.

(鑄膜B)(cast film B)

將硬化劑硬化型聚酯樹脂組成物塗刷於剝離薄膜上並使其乾燥,再與其它剝離薄膜貼合後,予以熟化一周,並於硬化後自剝離薄膜加以剝除,而製得薄膜狀之鑄膜B。鑄膜B之乾燥後之厚度為70μ m。The hardener-curable polyester resin composition is applied onto the release film and dried, and after bonding with other release film, it is aged for one week, and after hardening, it is peeled off from the release film to obtain a film shape. Cast film B. The thickness of the cast film B after drying was 70 μm .

硬化劑硬化型聚酯樹脂組成物之組成如下。The composition of the hardener-curable polyester resin composition is as follows.

(樹脂薄膜B)(Resin film B)

使用100μ m之聚對苯二甲酸乙二酯薄膜(Teijin DuPont Films公司出品,G2:商品名)作為樹脂薄膜B。A 100 μm polyethylene terephthalate film (produced by Teijin DuPont Films, G2: trade name) was used as the resin film B.

(2)黏著劑組成物A之製備(2) Preparation of Adhesive Composition A

朝溶媒之甲苯400g中,在2小時內滴下2-丙烯酸乙基己酯446.5g、甲基丙烯酸甲酯45g、甲基丙烯酸3.4g、作為聚合反應起始劑之過氧化苯甲醯0.5g之混合液,同時在100℃之溫度下進行反應4小時而製得含有官能基之聚合物(2)之溶液。接著,對該聚合物(2)添加2-甲基丙烯酸羥乙酯5.1g及作為聚合抑制劑之氫醌0.1g以作為含有光聚合性碳-碳雙 鍵及官能基之化合物(1),並於120℃之溫度下反應6小時後,以醋酸加以中和,而製得化合物(A)之溶液。相對於該化合物(A)溶液中之化合物(A)100質量份,將聚異氰酸酯(Nippon Polyurethane公司出品:CORONATEL)(B)1質量份、光聚合起始劑(Nihon Ciba-Geigy公司出品Irgacure 184)0.5質量份加入化合物(A)溶液中加以混合,即製備成丙烯酸系能量線硬化性黏著劑組成物A。To 400 g of toluene in a solvent, 446.5 g of 2-ethylhexyl acrylate, 45 g of methyl methacrylate, 3.4 g of methacrylic acid, and 0.5 g of benzoyl peroxide as a polymerization initiator were dropped in 2 hours. The mixed solution was simultaneously subjected to a reaction at a temperature of 100 ° C for 4 hours to obtain a solution of the functional group-containing polymer (2). Next, 5.1 g of 2-hydroxyethyl methacrylate and 0.1 g of hydroquinone as a polymerization inhibitor were added to the polymer (2) as a photopolymerizable carbon-carbon double The compound (1) having a bond and a functional group is reacted at 120 ° C for 6 hours, and then neutralized with acetic acid to prepare a solution of the compound (A). 1 part by mass of a polyisocyanate (Nippon Polyurethane Co., Ltd.: CORONATEL) (B) and a photopolymerization initiator (Irgacure 184 manufactured by Nihon Ciba-Geigy Co., Ltd.), based on 100 parts by mass of the compound (A) in the solution of the compound (A). 0.5 parts by mass of the compound (A) was added and mixed to prepare an acrylic energy ray-curable adhesive composition A.

<第1實施例><First Embodiment>

朝鑄膜A與樹脂薄膜A積層而成之薄膜之樹脂薄膜A側塗布已製備之黏著劑組成物A並予以乾燥,即製成半導體晶圓保護用黏著膠帶。The prepared adhesive composition A is applied to the resin film A side of the film formed by laminating the cast film A and the resin film A, and dried to form an adhesive tape for protecting a semiconductor wafer.

<第2實施例><Second embodiment>

朝鑄膜B塗布黏著劑組成物A並予以乾燥,即製成半導體晶圓保護用黏著膠帶。The adhesive composition A is applied to the cast film B and dried to form an adhesive tape for protecting a semiconductor wafer.

<第1比較例><First Comparative Example>

朝樹脂薄膜A塗布黏著劑組成物A並予以乾燥,而製成半導體晶圓保護用黏著膠帶。The adhesive composition A is applied to the resin film A and dried to form an adhesive tape for protecting a semiconductor wafer.

<第2比較例><Second Comparative Example>

朝樹脂薄膜B塗布黏著劑組成物A並予以乾燥,而製成半導體晶圓保護用黏著膠帶。The adhesive composition A is applied to the resin film B and dried to form an adhesive tape for protecting a semiconductor wafer.

[半導體晶圓保護用黏著膠帶之物性與評價][Physical properties and evaluation of adhesive tape for semiconductor wafer protection]

(1)黏著力之測定(1) Determination of adhesion

使用RHESCA Corporation之黏性試驗機TAC-II進行測定。測定模式則採用加壓探針至設定之加壓值,並保持加 壓值至設定之時間經過為止,而持續進行控制之Constant Load。剝離隔片後,以未形成黏著劑層之側朝上而將基材薄膜置於載板上,並自上側以直徑3.0mm之SUS304製之探針接觸之。使探針接觸測定試樣時之速度為30mm/min,接觸載重為100gf,接觸時間為1秒。然後,以600mm/min之剝離速度朝上方剝除探針,並測定剝除所需之力,而以其峰值為黏著力。使黏著力對應所欲測定之溫度,而諸如將200℃時之黏著力之探針及板溫設為200℃。The measurement was carried out using a viscosity tester TAC-II of RHESCA Corporation. In the measurement mode, the pressure probe is used to set the pressure value, and the pressure is maintained. Constant Load that continues to control until the set time elapses. After peeling off the separator, the substrate film was placed on the carrier with the side on which the adhesive layer was not formed facing upward, and was contacted with a probe made of SUS304 having a diameter of 3.0 mm from the upper side. The probe was brought into contact with the measurement sample at a speed of 30 mm/min, a contact load of 100 gf, and a contact time of 1 second. Then, the probe was peeled upward at a peeling speed of 600 mm/min, and the force required for the peeling was measured, and the peak was used as the adhesive force. The adhesion is made to correspond to the temperature to be measured, and the probe and the sheet temperature such as the adhesion at 200 ° C are set to 200 ° C.

(2)氣體蝕刻程序之評價(2) Evaluation of gas etching procedures

對直徑6吋而厚100μ m之鏡面晶圓貼合半導體晶圓保護用黏著膠帶,並自晶圓面依10mm見方而加以切割(對基材之切口深度20μ m)成6吋晶圓後,再於真空處理室內,將半導體晶圓保護用黏著膠帶吸附於夾盤上,並進行ClF3 之氣體蝕刻30秒。另,此時朝夾盤內流入70℃之溫水,而進行半導體晶圓保護用黏著膠帶及晶圓之冷卻。本程序後則進行是否可自夾盤輕易剝離黏著膠帶之評價。A mirror wafer with a diameter of 6 inches and a thickness of 100 μm is bonded to the adhesive tape for semiconductor wafer protection, and is cut from the wafer surface by 10 mm square (the depth of the substrate is 20 μm ) into 6 wafers. Thereafter, in the vacuum processing chamber, the adhesive tape for protecting the semiconductor wafer was adsorbed on the chuck, and gas etching of ClF 3 was performed for 30 seconds. At this time, warm water of 70 ° C was poured into the chuck to cool the adhesive tape for the semiconductor wafer and the wafer. After the procedure, it is evaluated whether the adhesive tape can be easily peeled off from the chuck.

表中之○、×意義如下。The meanings of ○ and × in the table are as follows.

「○」:氣體蝕刻程序後,可自夾盤輕易剝離黏著膠帶。"○": After the gas etching process, the adhesive tape can be easily peeled off from the chuck.

「×」:氣體蝕刻程序後,無法自夾盤輕易剝離黏著膠帶,或黏著膠帶已斷裂、熔融。"X": After the gas etching process, the adhesive tape cannot be easily peeled off from the chuck, or the adhesive tape is broken and melted.

(3)晶片之位移評價(3) Displacement evaluation of the wafer

氣體蝕刻評價已評為可進行加工並自夾盤剝離膠帶者,藉光學顯微鏡各就5部位進行切割所致之晶片間隔是否 於氣體蝕刻程序中偏移之確認。舉例言之,相對於切割所致之切口寬度25μ m,氣體蝕刻程序後之晶片間之間隔為22μ m時,偏移為3μ m。所有部位之偏移均在±1μm以內者評為◎,且,所有部位之偏移均在±2.5μm以內者評為○,5部位中即便僅發生1部位之偏移為±2.5μm以上者亦將評為×。Gas etching evaluation has been evaluated as a process that can be processed and stripped from the chuck, and the wafer spacing caused by the cutting of the five parts by the optical microscope is confirmed by the offset in the gas etching process. For example, the offset is 3 μm with respect to the slit width of 25 μm due to the cutting, and the interval between wafers after the gas etching process is 22 μm . The deviation of all the parts within ±1μm was rated as ◎, and the deviation of all parts within ±2.5μm was rated as ○, and even if only one part of the 5 parts was shifted by ±2.5μm or more Will also be rated as ×.

(4)斷裂強度、斷裂延伸率(4) Breaking strength, elongation at break

依1號啞鈴形狀(JIS K 6301)衝穿黏著膠帶而製成試驗片,再使用拉伸試驗裝置(JIS B 7721)加以測定。對試驗片劃記40mm之標線後,再使用拉伸試驗機測定標線間分割時之載重(拉伸強度)與伸長度。但,拉伸速度為300mm/min。A test piece was prepared by punching through an adhesive tape in accordance with the No. 1 dumbbell shape (JIS K 6301), and then measured using a tensile tester (JIS B 7721). After the test piece was recorded with a 40 mm mark, the tensile tester was used to measure the load (tensile strength) and elongation at the time of dividing between the lines. However, the stretching speed was 300 mm/min.

如表1所示,第1~2實施例之半導體晶圓保護用黏著膠帶中,未形成黏著劑層之側為鑄膜層A~B,最外層之黏著力即便在200℃時亦為100kPa以下,故氣體蝕刻程序中未發生黏著膠帶之基材薄膜對夾盤之熔附。As shown in Table 1, in the adhesive tape for protecting a semiconductor wafer of the first to second embodiments, the side where the adhesive layer is not formed is the cast film layer A to B, and the adhesive force of the outermost layer is 100 kPa even at 200 ° C. Hereinafter, the base film of the adhesive tape does not adhere to the chuck in the gas etching process.

尤其,第2實施例之基材薄膜僅為鑄膜,故加熱亦較少收縮,氣體蝕刻程序中之晶片位移更少。In particular, the substrate film of the second embodiment is only a cast film, so that the heat is less contracted, and the wafer displacement in the gas etching process is less.

第1比較例則因基材薄膜之未形成黏著劑之側之最外層為樹脂薄膜A,故氣體蝕刻程序中,黏著膠帶之基材薄膜熔附於夾盤上。氣體蝕刻程序後,即難以自夾盤剝除基材薄膜。In the first comparative example, since the outermost layer on the side of the base film on which the adhesive is not formed is the resin film A, the base film of the adhesive tape is fused to the chuck in the gas etching process. After the gas etching process, it is difficult to strip the substrate film from the chuck.

第2比較例中,基材薄膜之未形成黏著劑之側之最外層之黏著力即便在200℃時亦為100kPa以下,但在蝕刻程序中之加熱之影響下,其則因薄膜成型時之殘餘應力而收縮,並導致黏著膠帶自夾盤懸浮,而未經夾盤進行冷卻,故已發現晶圓之變色及黏著劑之劣化。In the second comparative example, the adhesion of the outermost layer on the side where the adhesive film is not formed on the base film is 100 kPa or less even at 200 ° C. However, under the influence of the heating in the etching process, the film is formed by the film. Residual stress shrinks and causes the adhesive tape to float from the chuck without being cooled by the chuck, so the discoloration of the wafer and the deterioration of the adhesive have been found.

以上,已參照附圖而說明本發明之較佳實施形態,但本發明不受限於該等例示。本技術範疇之從業人士自可在本案所揭露之技術思想範疇內構思各種變更例或修正例,其等亦當然應理解為從屬於本發明之技術範圍。The preferred embodiments of the present invention have been described above with reference to the drawings, but the invention is not limited thereto. Those skilled in the art can devise various modifications and alterations within the scope of the technical idea disclosed in the present disclosure, and of course, should be construed as falling within the technical scope of the present invention.

1、1a‧‧‧半導體晶圓保護用黏著膠帶1, 1a‧‧‧Adhesive tape for semiconductor wafer protection

3‧‧‧基材薄膜3‧‧‧Substrate film

5‧‧‧黏著劑層5‧‧‧Adhesive layer

7‧‧‧鑄膜層7‧‧‧ cast film layer

9‧‧‧樹脂薄膜層9‧‧‧ resin film layer

Claims (6)

一種半導體晶圓保護用黏著膠帶,其特徵在於包含基材薄膜及前述基材薄膜之單面上形成之黏著劑層,且前述基材薄膜於未形成有前述黏著劑層之側的最外層具有含已硬化之樹脂之鑄膜層,令在使直徑3.0mm之SUS304製之探針接觸測定試樣時之速度為30mm/min,接觸載重為980mN(100gf),接觸時間為1秒之條件下,依600mm/min之剝離速度朝上方剝除探針時之藉探針試驗所測得之前述鑄膜層之黏著力的峰值在200℃時為100kPa以下。 An adhesive tape for protecting a semiconductor wafer, comprising: a base film and an adhesive layer formed on one surface of the base film, wherein the base film has an outermost layer on a side where the adhesive layer is not formed The cast film layer containing the hardened resin is set to have a speed of 30 mm/min when the probe made of SUS304 having a diameter of 3.0 mm is brought into contact with the measurement sample, a contact load of 980 mN (100 gf), and a contact time of 1 second. The peak of the adhesion of the cast film layer measured by the probe test when the probe was peeled upward at a peeling speed of 600 mm/min was 100 kPa or less at 200 °C. 如請求項1之半導體晶圓保護用黏著膠帶,其中前述基材薄膜僅由鑄膜層所構成。 The adhesive tape for protecting a semiconductor wafer according to claim 1, wherein the substrate film is composed only of a cast film layer. 如請求項1之半導體晶圓保護用黏著膠帶,其中前述鑄膜層含有已硬化之丙烯酸系共聚物或聚酯樹脂。 The adhesive tape for protecting a semiconductor wafer according to claim 1, wherein the cast film layer contains a hardened acrylic copolymer or a polyester resin. 如請求項1之半導體晶圓保護用黏著膠帶,其中前述鑄膜層由已藉硬化劑或放射線而硬化之丙烯酸系共聚物所構成。 The adhesive tape for protecting a semiconductor wafer according to claim 1, wherein the cast film layer is composed of an acrylic copolymer which has been hardened by a curing agent or radiation. 如請求項1之半導體晶圓保護用黏著膠帶,其中斷裂強度為0.5N/mm以上,斷裂延伸率為200%以上。 The adhesive tape for protecting a semiconductor wafer according to claim 1, wherein the breaking strength is 0.5 N/mm or more and the elongation at break is 200% or more. 如請求項1之半導體晶圓保護用黏著膠帶,其中令在使直徑3.0mm之SUS304製之探針接觸測定試樣時之速度為30mm/min,接觸載重為980mN(100gf),接觸時間為1秒之條件下,依600mm/min之剝離速度朝上方剝除探針 時之藉探針試驗所測得之前述黏著劑層之黏著力的峰值在25℃時為50~400kPa。 The adhesive tape for protecting a semiconductor wafer according to claim 1, wherein a probe made of SUS304 having a diameter of 3.0 mm is brought into contact with the measurement sample at a speed of 30 mm/min, a contact load of 980 mN (100 gf), and a contact time of 1 In the second condition, the probe is stripped upward at a peeling speed of 600 mm/min. The peak of the adhesion of the aforementioned adhesive layer measured by the probe test was 50 to 400 kPa at 25 °C.
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