TW200814172A - Dicing/die bonding film - Google Patents
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- TW200814172A TW200814172A TW95133866A TW95133866A TW200814172A TW 200814172 A TW200814172 A TW 200814172A TW 95133866 A TW95133866 A TW 95133866A TW 95133866 A TW95133866 A TW 95133866A TW 200814172 A TW200814172 A TW 200814172A
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200814172200814172
Zl^OJpil 九、發明說明: 【發明所屬之技術領域】 本發明關於—種切晶(dicing)、黏晶 film)。切晶、黏晶片,太义 〇ncl (workU丰導俨曰η 於固定晶片狀工件 )(丰V収日日片(chip)等)與電極部件之黏接 设於工件(半導體晶圓(wafe〇等)的狀態下,可用 工件供於切晶。又’本發明關於—種使用該切晶、黏晶片Zl^OJpil IX. Description of the Invention: [Technical Field of the Invention] The present invention relates to a dicing film. Cleavage, sticky wafer, Taiyi 〇ncl (workU 俨曰 on fixed wafer-like workpiece) (Feng V receiving day (chip), etc.) and electrode parts are attached to the workpiece (semiconductor wafer (wafe In the state of 〇, etc., the workpiece can be used for dicing. Further, the present invention relates to the use of the diced, bonded wafer.
Cj 之晶片狀工件的固定方法及半導體裝置的製造方法。^ 關於-種藉㈣較方法或製造方法崎接固定有 工件的半導體裝置。 狀 【先前技術】 於先前半導體裝置之製造中,可使用銀漿料將半導體 晶片固定於引線框架(lead frame)或電極部件上。相關固 疋處理疋在於引線框架之晶片座(die pacJ )等之上進行將 料(paste)塗敷後,再於其上搭載半導體晶片,使漿料^ 硬化而實施。 形成電路圖案之半導體晶圓是根據需要於利用背面研 磨而調整厚度(背面研磨步驟(Backgrind step))後,切 曰曰成半導體晶片(切日日步驟(dicing step )),藉由黏接劑將 該半導體晶片固定於引線框架等被黏接體上(晶粒黏著步 驟( die attach step)),進而進行焊線接合步驟(wire bonding step)。於切晶步驟中,為了除去切割屑,通常以適度液壓 清洗半導體晶圓。 於該處理步驟中,另外塗布黏接劑於引線框架或形成 5 200814172 ziyojpu /左r '雖从便黏接劑屛 必須嶋置及長時間爾之於=化,且塗布黏接齊 5漏號公報(第】頁)令提出有—日本專曰利特開昭6〇、 不僅於切晶步驟令黏接保持半導:刀曰曰、黏晶片,其 步驟中亦賦予必要 、曰曰員,而且於晶粒黏著 該切晶、』 黏接劑層而成者,其為於其黏二式設置 c 離,將盆夂自□你、^才 成晶片與黏接劑層—倂制 挥隹將”各自回收,再經由其黏 ㈣ 4口 ZlEL J~ HTj 〇 於此,切晶、黏晶片針對切割半導體晶s 支持基材與黏接劑層不會剝離之強黏著力, 後’可容易地將半導體晶片與黏接劑層 剝離。 被黏接體上而成者。 ㈢U疋方、引線框架等 於此,切晶、黏晶片針對切割半導體晶圓古 :基材與黏接劑層不會剝離夕故办著力,、謀求二 攸支持基材上一倂A method of fixing a wafer-like workpiece of Cj and a method of manufacturing a semiconductor device. ^ About - (4) A semiconductor device in which a workpiece is fixed in comparison with a method or a manufacturing method. [Prior Art] In the manufacture of a conventional semiconductor device, a silver paste can be used to fix a semiconductor wafer on a lead frame or an electrode member. The related solid processing is carried out by applying a paste on a wafer holder (die pacJ) of a lead frame, and then mounting a semiconductor wafer thereon to harden the slurry. The semiconductor wafer forming the circuit pattern is cut into a semiconductor wafer (dicing step) by adjusting the thickness (backgrind step) by back grinding as needed, by means of an adhesive The semiconductor wafer is fixed to a bonded body such as a lead frame (die attach step), and a wire bonding step is further performed. In the dicing step, in order to remove the cutting chips, the semiconductor wafer is usually cleaned with moderate hydraulic pressure. In the processing step, the adhesive is additionally applied to the lead frame or formed 5 200814172 ziyojpu / left r ' Although it must be disposed from the adhesive, and it is long-term, and the coating is adhered to the 5 The bulletin (page) has been proposed to have a special Japanese-made 曰 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅 不仅Moreover, in the case where the crystal grain adheres to the crystal-cutting layer, the adhesive layer is formed by setting the c-type apart from the smear, and the sputum is formed into a wafer and an adhesive layer. Will be "recovered separately, and then through its sticky (four) 4-port ZlEL J~ HTj 〇 here, cleavage, sticky wafer for cutting semiconductor crystal s support substrate and adhesive layer will not peel off the strong adhesion, after 'easy The semiconductor wafer and the adhesive layer are peeled off. The bonded body is formed. (3) The U-square and the lead frame are equal to this, and the dicing and bonding wafers are used for cutting the semiconductor wafer: the substrate and the adhesive layer are not Peeling off the eve of the day, and seeking a second support for the substrate
但是,若為上述結構之切晶、黏晶片,則難 接劑層之黏著力。因此,揭示有—種藉由於支持基材^ 接劑層之間設置黏著劑層,以黏著性與剝離性之平衡良好 之方式而構成的切晶、黏晶片(參照日本專利特開平2 一 248064號公報(第1頁))。 另外,於切晶步驟中,在切斷形成電路圖案之半導體 晶圓時,存有自切晶、黏晶片中產生絲狀屑,並附著於半 導體晶片或切晶、黏晶片的情況。該絲狀屑進而於以下步 驟即晶粒黏著步驟、焊線接合步驟中,會附著於被黏接體 即有機基板或引線框架、或者半導體晶片上,不僅會使操 6 200814172 1 :性顯著降低,而且使半導體晶片之 為大問題。 」奍丨生F牛低,從而成 本發明是鑒於上述問題而成者, =狀屑的產生,防止半導體晶片 黏曰曰片;使用其之晶片狀工件 二::、 得到的半導體裝置及其製造方法。4猎由•法所 【發明内容】 Ο ο 本發明者等為達成上述目的而進行了研☆义 現,產生絲狀屑是由藉由切割刀片切斷 ^:果电 亚籍由採用下述結構而完成了本發明。支、土材引起的’ 即,本發明之切晶、黏晶片是為解決 ΐ劑層及晶片黏接用黏接劑層依次積層於支=== 晶、黏晶片,其特徵在於:上述黏著劑層=基2的刀0 pm,於23。〇的於彈性模料1χΐ〇4〜ΐχΐ(^又為1〇〜8〇 上述結構之發明,藉由將黏著劑層之厚二 Γιο 蚊於預著劑層的彈性成分(即,硬产) 。又疋於預德圍内。即,藉由 更度) 切晶時之切人深度止於❹泡 歧值耗圍内,使 割。其峨谢娜材被切 …則存有例如切割工件時=由:^模數未滿 但是,藉由設定於上賴值範_由^==形。 是可謀求’經晶片化的工件之一部分破以= 少。進而’若彈性模數超物。、,二 7 200814172 V03pir 日日片黏接用黏接劑 上述數值範圍内足的情況。但是,若設於 確實地將工件固定於切晶Ρ、工:度:低,其結果是可 飛片或不齊。 ♦曰曰片上,而抑制切晶時產生 =3 是放射線硬化型黏著劑層。 貼附之部分所對應::曰曰片黏接:黏接劑層上之工件 數值範圍。刀卜足上述黏著劑層的彈性模數的 較好的是,於上述黏著 界面上,上述工件貼所庫曰曰^接用黏接劑層的 其以外部分之_ Λ刀斤對c的界面上的制離性大於 上述界面的對上的剝離性。 晶片黏接用點接劑層所對應的黏著^ Φ方、上補者劑層之 附部分所對應的部分的中,形成上述工件貼 者全部所對應的部分的i著力彳!^分之一部分或 藉由形成上料槿,::、、,α構而仔到。 分或者全部所對應的部分中工:::::分以外部分的-部 分相比,成為黏接劑層與晶片勒=部分所對應的部 邮態。其結果是,例如於切晶=接制層適度地黏接 著劑層與晶片黏接用多 三申(expand)時,黏 4工件貼附部分所對應另一方面, =。因此,即使對於如例如超刀tb〇可更輕易地 日日片,亦不會招致切晶 mmxl〇 mm之大型 得到的晶片狀工件,彳/Λ义σ奋易地剝離於切晶後所 黏 晶 件处而可獲得拾取性優良的切晶 等時的保持力與拾取時 較好的无However, in the case of the dicing or sticky wafer of the above structure, the adhesion of the adhesive layer is difficult. Therefore, it is disclosed that a crystal-cutting or adhesive wafer is formed in such a manner that an adhesive layer is provided between the support substrate layers, and the balance between adhesion and peelability is good (refer to Japanese Patent Laid-Open No. Hei 2 248064). Bulletin (page 1)). Further, in the dicing step, when the semiconductor wafer on which the circuit pattern is formed is cut, there are cases where filamentous chips are generated from the diced wafer or the bonded wafer, and adhered to the semiconductor wafer or the diced or bonded wafer. The filamentous chips are further adhered to the organic substrate or the lead frame or the semiconductor wafer to be bonded, in the following steps, that is, the die bonding step and the bonding wire bonding step, which not only significantly reduces the performance of the device; And make semiconductor wafers a big problem. "The F-bull is low, so the cost invention is based on the above problems, the generation of the chip, the prevention of the semiconductor wafer adhesive sheet; the use of the wafer-like workpiece 2::, the obtained semiconductor device and its manufacture method. 4 猎 由 法 法 【 【 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本 本The present invention has been completed in structure. The dicing and viscous wafers of the present invention are used to solve the adhesion layer of the enamel layer and the wafer bonding layer, and are sequentially laminated on the y=== crystal and sticky wafer, which is characterized in that: Agent layer = base 2 knife 0 pm, at 23. 〇 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性 弹性It is also in the pre-department area. That is, by cutting the crystal, the cutting depth is stopped within the circumference of the bubble. The 峨 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜 娜It is possible to seek to "part of the wafer-formed part to be broken = less. Further, if the elastic modulus is super. , 2, 7 200814172 V03pir Adhesive for bonding adhesives in the above range of values. However, if it is set to securely fix the workpiece to the dicing die, the degree of work: low, the result is that the piece can be flying or not. ♦ On the enamel sheet, when the dicing is suppressed, =3 is a radiation-curable adhesive layer. Attached to the part:: 曰曰 bonded: the value range of the workpiece on the adhesive layer. Preferably, the elastic modulus of the adhesive layer is such that, at the adhesive interface, the workpiece is attached to the interface of the adhesive layer of the adhesive layer. The above-mentioned disproportionability is greater than the peeling property of the above interface. In the portion corresponding to the adhesive portion corresponding to the attached portion of the patch bonding layer for the wafer bonding, the portion corresponding to the entire portion of the workpiece sticker is formed. Or by forming a loading 槿, ::,,, α, and abbreviated. Part or all of the corresponding part of the work::::: part of the part other than the portion of the adhesive layer and the wafer part = the corresponding zip state. As a result, for example, when the dicing = bonding layer moderately adheres to the bonding of the layer to the wafer, the adhesion of the workpiece is corresponding to the other side, =. Therefore, even if it is easier to use a day-to-day film such as a super knife tb, it will not incur a wafer-shaped workpiece obtained by cutting a large size of mmxl〇mm, and the 彳/Λ义σ is easily peeled off after being diced. At the crystal part, the holding force at the time of picking and the like having excellent pick-up property and the like are better.
Ο 200814172 ziyojpn 片。即,上述結構可適度平衡切晶 的剝離性。 .,▼一 、处晶片黏接用黏接劑層之黏著力中, 對上述X件麗部分的I件的黏著力大於對上述工件貼附 部分所對應部分的黏著劑層的黏著力。 藉由形成上述結構,例如於拾取切割工件而得到的晶 片狀工件時,可容易地將該晶片狀工件在附設有晶片黏接 用黏接劑層的狀態下自黏著劑層剝離。 較好的是,上述工件貼附部分以外部分的一部分是切 晶環貼附部分。 較好的是’於上述晶片黏接用黏接劑層之黏著力中, 對上述切晶環貼附部分的切晶環的黏著力小於對上述切晶 環貼附部分所對應部分的黏著劑層的黏著力。 藉由形成上述結構,將切晶環製成可容易地自晶片黏 接用黏接劑層剝離,防止晶片黏接用黏接劑層貼著於該切 晶環上的狀態自黏著劑層剝離。 較好的是,上述晶片黏接用黏接劑層是作為工件貼附 部分而設置於上述黏著劑層上之一部分上’且於上述黏著 劑層中,工件貼附部分所對應部分的黏者力小於其以外部 分的黏著力。 藉此,即使於晶片黏接用黏接劑層是作為工件貼附部 分而設置於黏著劑層上的一部分上的結構之情形時,於拾 取晶片狀工件時,該晶片狀工件亦可於附設有晶片黏接用 黏接劑層的狀態下自黏著劑層容易地剝離。 200814172 i y\j^u\i ;处曰日月黏接用黏接劑層的黏著力中, 工件貼附部分的工件的黏著力大於對上述工件貼附 4刀所對應部分的黏著劑層的黏著力。 =此,與上述相同,於拾取晶片狀卫件時,該晶 容:::設有晶片黏接用黏接劑層的狀態下晴劑層 車乂好的疋’上述黏者劑層是藉由放射線硬化 oΟ 200814172 ziyojpn film. That is, the above structure can appropriately balance the peeling property of the crystal. In the adhesion of the adhesive layer for wafer bonding, the adhesion to the I member of the X-shaped portion is greater than the adhesion to the adhesive layer of the corresponding portion of the workpiece attachment portion. By forming the above-described structure, for example, when picking up a wafer-like workpiece obtained by cutting a workpiece, the wafer-like workpiece can be easily peeled off from the adhesive layer in a state in which the adhesive layer for wafer bonding is attached. Preferably, a part of the portion other than the attachment portion of the workpiece is a cleavage ring attachment portion. Preferably, in the adhesion of the adhesive layer for wafer bonding, the adhesion to the dicing ring of the dicing ring attachment portion is smaller than the adhesive portion of the corresponding portion of the dicing ring attachment portion. The adhesion of the layers. By forming the above structure, the dicing ring can be easily peeled off from the adhesive layer for bonding the wafer, and the adhesive layer for bonding the wafer is prevented from sticking to the dicing ring from the adhesive layer. . Preferably, the adhesive layer for bonding the wafer is provided on a portion of the adhesive layer as a workpiece attaching portion, and in the adhesive layer, the adhesive portion of the portion corresponding to the attached portion of the workpiece The force is less than the adhesion of the other part. Thereby, even when the adhesive layer for bonding the wafer is a structure which is provided on a part of the adhesive layer as the attachment portion of the workpiece, the wafer-shaped workpiece can be attached when the wafer-shaped workpiece is picked up. The adhesive layer is easily peeled off in the state of the adhesive layer for wafer bonding. 200814172 iy\j^u\i ; in the adhesion of the adhesive layer for the bonding of the sun and the moon, the adhesion of the workpiece in the attached part of the workpiece is greater than that of the adhesive layer of the corresponding portion of the workpiece attached to the workpiece. Adhesion. = In the same manner as above, in the case of picking up the wafer-shaped guard, the crystal contents are:: the state in which the adhesive layer of the wafer is bonded, the layer of the green layer is good, and the above-mentioned adhesive layer is borrowed. Hardened by radiation o
L 件貼附部分所對應部分是藉由卿 題而二料是為解決上述課 晶片黏接丄劑= =上述工件與上述晶 述晶片狀工件與上述晶片黏;刀晶咖 —併自上述黏著劑層上剝離的步驟·=的工,貼附部分 黏接劑層駐件貼附部分 =’广由上述晶片I占接用 體元件的步驟。 、曰犬工件黏接固定於半導 日日黏晶片,故而將工件至少愈 的黏著刮層的切 Π晶片狀時,切晶正於黏著二H =劑層^ 〜果是’可防止因切斷支縣材 o 〇 200814172 可減少晶片狀工件的碎屬。 動。其結果是, 於切晶、勒晶的不心故可將工件確實固定 又,本發士生之飛片或不齊。 二:::;=之晶片狀工件固定方法= 於半導體元件上^的黏接劑,將晶片狀工件黏接固定 題使用上述所纪載曰衣置之製造方法是為解決上述課 法,其特徵在置製造方 片黏接用黏接劑層的工件 ^接匕括.於上述晶 為將上述工件愈上述曰刀上昼接工件的步驟;作 狀的步驟的,:上;: 片狀工件金上述曰片勤^層—止切晶的步驟;將上述晶 述黏著劑層剝以:接: 件黏翻定於半導體元件的^賴接舰上述晶片狀工 的發明中使用具有厚度為10〜80 切晶曰=為1X104〜Ιχ, 可防止狀π防止支持基材細^ 屑的同時,二咸, 述課 200814172 21965pif 日日月黏接用黏接劑層 於半導體元件上。《黏接劑’將晶片狀卫件黏接固定 本發明藉由上逑戶斤…、 即,若根據本發法,而發揮如下述的效果。 10〜80 _、於23 =曰曰、黏晶片’則因具有厚度為 ΟThe part corresponding to the attachment part of the L piece is made by the second problem to solve the above-mentioned wafer bonding agent = = the above workpiece and the above-mentioned wafer wafer-like workpiece are adhered to the above wafer; the knife crystal coffee - and adhered from the above The step of peeling off the agent layer, the work of attaching a part of the adhesive layer, and the attaching part = 'the step of occupying the body element by the above wafer I. The 曰 dog workpiece is fixed and fixed on the semi-conductive day-day sticky wafer, so when the workpiece is at least more adhesively squeegee-cut, the dicing is positively adhered to the second H = agent layer ^ _ fruit is 'can prevent cut Broken branch material o 〇 200814172 can reduce the fragmentation of wafer-like workpieces. move. As a result, the workpiece can be surely fixed in the case of incision or crystallizing, and the flying piece of the hair is not uniform. The method of fixing the wafer-like workpiece of the second:::=== the bonding agent on the semiconductor component, and bonding the wafer-shaped workpiece to the fixed problem. The manufacturing method of using the above-mentioned device is to solve the above method. The method is characterized in that: the workpiece is formed by bonding the adhesive layer of the adhesive sheet; and the step of splicing the workpiece to the workpiece is performed on the workpiece; the step of forming: upper;: sheet The step of the above-mentioned wafer layer of the workpiece gold is removed; the layer of the above-mentioned wafer is peeled off: the material is bonded to the semiconductor device, and the thickness of the wafer is 10~80 dicing 曰 = 1X104~Ιχ, which prevents the shape π from supporting the fineness of the supporting substrate, while the salty, the class 200814172 21965pif adhesive bonding layer is applied to the semiconductor element. "Adhesive" adheres and fixes the wafer-shaped guard. The present invention exerts the following effects by the above-described method. 10~80 _, at 23 = 曰曰, sticky wafer ’ because of thickness Ο
著劑層,故可防止切二^數為1x104〜lxi0】〇Pa的黏 是可防iL產生絲狀4 °。',支持基材被蝴,其結果 片狀工件而被污染。〃、'、σ果是,可防止絲狀屬附著於晶 【實施方式】 一面參照圖式 其中,將無須說明 擴大或縮小等的圖 面就本發明之實施形態說明於下。 之。卩分省略,又,為便於說明,而存有 示的部分。 圖1是顯示實施例中本發明的切晶、黏晶片的一個例 子的2面杈式圖。如同一圖中所示,切晶、黏晶片10為, 將黏著劑層2、晶片黏接用黏接劑層3及可剝離的保護層4 依次積層於支持基材1上的結構。 上述支持基材1是切晶、黏晶片薄膜10的強度母體。 支持基材1,例如可列舉:低密度聚乙烯、直鏈狀聚乙烯、 中密度聚乙烯、高密度聚乙烯、超低密度聚乙烯、無規共 聚合聚丙烯、欲段共聚合聚丙烯、均聚丙烯、聚丁烯、聚 曱基戊烯等聚烯烴,乙烯-乙酸乙酯共聚物、乙烯_丙烯共 聚物、離子聚合物樹脂、乙烯_(曱基)丙烯酸共聚物、乙烯 -(曱基)丙烯酸酯(無規、交替)共聚物、乙烯-丁烯共聚物、 乙烯己烯共聚物、聚胺基曱酸酯、聚對苯二曱酸乙二酿、 200814172With the agent layer, it can prevent the cut of the number of 1x104~lxi0] 〇Pa's viscosity to prevent iL from producing a filamentous 4 °. ', the support substrate is smeared, and as a result, the sheet-like workpiece is contaminated. 〃, ', σ 是 是 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝 丝It. The points are omitted, and the parts are shown for convenience of explanation. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a two-faced plan view showing an example of a diced or bonded wafer of the present invention in an embodiment. As shown in the same figure, the dicing wafer 10 is a structure in which an adhesive layer 2, a die bonding adhesive layer 3, and a peelable protective layer 4 are sequentially laminated on a support substrate 1. The support substrate 1 is a strength precursor of the diced, bonded wafer film 10. The support substrate 1 may, for example, be a low density polyethylene, a linear polyethylene, a medium density polyethylene, a high density polyethylene, an ultra low density polyethylene, a random copolymerized polypropylene, or a copolymerized polypropylene. Polyolefins such as homopolypropylene, polybutene, polydecylpentene, ethylene-ethyl acetate copolymer, ethylene-propylene copolymer, ionic polymer resin, ethylene-(mercapto)acrylic acid copolymer, ethylene-(曱Acrylate (random, alternating) copolymer, ethylene-butene copolymer, ethylene hexene copolymer, polyamino phthalate, polyethylene terephthalate, brewing, 200814172
i VUJLMI ♦奈一甲酸乙二酯等聚酯、聚碳酸酯、聚醯亞胺、 _、聚醯亞胺、聚醚醯亞胺、聚醯胺、全芳香二二醚 希方 胺(ar咖de)(紙)、破璃、破璃 素糸樹脂、㈣氧聽、包含這些混合㈣_膠^、准 又,亦可列舉上述樹脂的交聯體等聚合才勿。 、 又,支持基材1亦可使用未延伸者。進而,i VUJLMI ♦ polyester such as ethylene glycol dicarboxylate, polycarbonate, polyimine, _, polyimine, polyether phthalimide, polyamine, full aromatic diethylene ether ercoamine De) (paper), broken glass, arginine resin, (4) oxygen listening, including these mixing (four) _ glue ^, quasi-, can also be mentioned as the cross-linking of the above resin, such as polymerization. Further, the support substrate 1 may also be used without extension. and then,
據需,,亦可使用實施過單軸或者二轴延伸處理者。乂 包含藉由延伸處理等賦予了熱收縮性的樹脂⑼其 則可藉由於切晶後使其支持基材丨熱收縮,而= β著劑層2與晶片黏接用黏接劑層3的黏接面積曰 片狀工件回收的簡便化。 ”曰曰 ^提高與鄰接層之密著性、保持性等,支持基材丄的 ^面亦可f行常絲面處理。其方法,例如可列舉:鉻酸 露、火炎曝露、高壓電擊曝露、_輻射處 的塗布理處理,使用底塗劑(例如,後述黏著物質) μ 持基材1可適宜選擇使用其構成材料為同種或 ",。又,亦可根據需要使用混合有多種者。進而, 電能力,支持基材1亦可使用於上述塑膠薄膜 ^ 3金屬、合金或此等的氧化物等的,厚度為30 5 0 0 左 士" 、、=的¥電性物質的蒸鍍層的薄膜。進而,亦可 等。再^述溥膜彼此或者與其它薄膜進行貼合的層壓體 、。 ,支持基材1亦可為將使用單層或者上述材料之 200814172 =等大於等於2層之複層化的積層和 劑i 2為放射線硬 &、。再者,於黏著 其導:二=;:^著或剝離等時之靜樹 版日日g帶電破壞雷 有抗靜電能力。料抗靜電 夢、下’亦可使其具 Ο 導電劑支持㈣至黏著劑層、J:添加抗靜電劑或 金屬膜等之導電Μ 、°又匕3兒掎轉移複合物或 是以難以產^適^式進行,較好的 式。 τ心致切體晶圓變質的雜質離子的方 支持基材1之厚度為例如5〜 由上述熱收縮而可承受3 ^左右,若具有藉 ΛΑ ^ . 又日日片黏接用黏接劑;3 #七 的厚度,則無特別限制。再者=層3產生的張力 紫外線者。 支持基材1亦可為透過 上述黏著劑層2具有厚度為1〇〜 性模數成為lxlO4〜lxl〇lGp μ於C的弓早 止於黏著劑層2的範圍内,=為/使切晶時的切入深度 使黏著劑層2的厚度及彈性模到達支持基材卜用於 發明之作用、效果的切的數值範圍可充分發揮本 _的範_。 片之㈣數在25_〜50_ 内,而防23(:的彈性模數設於上述數值範圍 内而防止產生碎屑 -,並且防止拾取晶片狀工件時產生飛 200814172 ^iy〇jpn 巧戏不齊 上述彈性模數 尤其好的是lx「〇V;;更好的是〜Pa, 則容易切割到支接其以,a。右弹性模數未滿〗xio7 Pa, 切晶步驟會使晶片;工件容而^加^狀屬的產生。進而, 晶粒黏著步驟中,於取驟容易產生飛片,又,於 〇 存有切割刀片的磨耗量增曰加:;⑵=:。進而, 進而,將黏著劑層2之厚度 述:範。 為了防止晶片剖面缺損或 =數值粑圍内,是 的兼具性等。至於节尸# ”、日日片站接用黏接劑層;3 ^20^6〇 亥尽度,較好的是20〜70 μιη,更#0 疋2〇 60 _,尤其好的是20〜50 _。 更好的 性,層2關於與晶片簡用黏接劑層3的剝離 :曰=;關係的方式而構成(參_)。即,: ”曰曰片越用黏接劑層3的工件 : =雜用黏,心 的界面Β ^ ^日读為晶片黏接用黏接劑層3b)所對應 性^ S ’子有界面A的剝離性大於界面B的剝離 、“、。為了滿足該關係’黏著劑層2是以例如如下方 ^而設計:工件貼附部分3a (下述)所對應的部分2a (以 :’㈣黏者劑層2a)的黏著力小於其以外部分的一部分 ^者全部所對應的部分2b (以下,有時稱為黏著劑層2b) 的黏著力。 ^上述黏著劑層2a的黏著力,基於常溫(23T:)下的黏 著力(90度剝離力(peel)的值,剝離速度為3〇〇 _/_), 200814172 就晶圓值固定保持力或所形成晶片的回收性 較好的是小於等於〇.5 N/2Gmm,更佳 、方面而言, mm,尤其好的是 0.01 〜0.35 N/20 mm。另—〇.42 N/20 是黏著劑層2b之黏著力為〇.5〜2〇N/2〇mn^面’較好的 使為較低的剝離黏著力’亦可抑制黏二 黏者力所⑽的飛片等的產生,且 Μ層2b的 分的保持力。 」万、日日®加工時發揮充 黏著劑層2之其面内使黏著力不 舉使用放射線硬化型黏著劑。若藉由使=例如可列 著劑,對黏著劑層2進行部分性放射線昭射^硬化型黏 f部分中構成其之高分子化合物的交聯度,发::?大照 低黏著力。因此,於本實施形態中 p果疋可降 身m而使之硬化,可顯著降低黏著力。'另照射放 著劑層2b照射放射線,可唯持充八 + 不對黏 f層2可以黏接及剝離平衡性良好刀的;二力持黏著 越劑層3。即,可將黏著劑 垃日日片黏接用 3充分黏接,並使黏著劑層與晶=2 =黏接劑層 剝離變得容易,而謀求拾取性的提高 越劍層3的 構成黏著劑層2之黏著劑並盔特 本發明之上述放射線硬化型 宜的是 著劑層2a與黏著劑層2b的點因為容易產生黏 著劑可藉由照射料線等放射 :;崎線硬化型Ιέ 地降低其_。因此3=^_大,而容易 的黏著劑層23照射放射線使-化, 200814172 著下降的區域進行。因晶片黏接用黏接劑声 部分3a位於被硬化且黏著力下降的黏著% 力, 劑層2a與工件貼附部分3 χ & ,*占著 的性質。 %之界面’具有拾取時易於剥離 y方面’因未照射放射線之黏著劑層⑪ 化之放射線硬化型黏著劑而構成,故 ^更 著,纽果m二片接用黏接劑層3可確實地黏 之放射線硬化型黏著劑而構成的 固定減4以土日f用於將日日片狀工件(半導體晶片等) 或者曰曰片狀工件等被黏接體(半導 的晶片黏接用黏接劑層3的平衡。 θ f成黏著劑層2的黏著劑並無特別限制,較適宜的 二本,咖線硬化型黏著劑。放射線硬化型黏著劑, 地使料有碳碳雙鍵#放射線硬化性^官 (J 此基,且顯示出黏著性者。 5射線硬化型黏著劑’例如可例示:於上述丙烯酸系 =、橡膠系黏著劑、聚石夕氧系黏著劑、聚乙烯咖 練壓力感應黏著劑中,添加有放射線硬化性單 =成刀或养聚物成分的添加型放射線硬化型黏著劑。上 =感應黏著·不適應半導體晶圓或者玻璃等污染的電 丄令件之超純水或料有機溶劑的潔淨清洗性等方面而 各,較好的是以丙烯酸系聚合物作為原料聚合物(_ 200814172 ζι^ο^ριτ polymer )的丙烯酸系黏著劑。 上述丙稀酸系聚合物’例如可列舉:以(曱基)丙稀酸 烷基醋(例如,曱酉旨、乙酿、丙醋、異丙g|、丁§旨、異丁 酉曰第—丁基酉曰、第二丁基醋、戊酿、異戍醋、己醋、庚 酯、辛s旨、2-乙基己基S旨、異辛g旨、壬§旨、癸醋、異癸醋、 + -絲S旨、十二垸基g旨、十三烧基§|、十四烧基醋、十 力烧基醋、十八燒基酿、二十烧基酿等烧基的碳數為卜 π 3G ’尤其是雜f7 4〜18的直鏈狀或者支鏈狀烧基醋等) 及(甲基)丙稀酸環垸基酉旨(例如,環戊醋、環己醋等)中 =1種或2種以上作為單體成分而使用的丙烯酸系聚合物 等。再者,(曱基)丙烯酸醋是指丙稀酸酷以及/或者甲基丙 烯酸酯,本發明的(甲基)的意思全部相同。 上述丙炸S义系XK合物以凝集力、耐敎性的改性箄為目 r亦可根據需要含有可與上述(甲細=;環 ^基酯進行共聚合的其他單體成分所對應的單位。如此之 單體成分例如可列舉:丙烯酸、曱基丙烯酸、(曱基)丙烯 〇 酸羧乙酯、(曱基)丙烯酸羧戊酯、甲叉丁二酸、順丁烯二 酸、反丁烯二酸、丁烯酸等含有羧基的單體;順丁烯二酸 I 酐、甲叉丁二酸酐等酸酐單體;(曱基)丙烯酸2_羥基乙酯、 (曱基)丙稀酸2-羥基丙酯、(甲基)丙烯酸4_羥基丁酯、(曱 基)丙烯酸6-羥基己酯、(曱基)丙烯酸8_羥基^、(曱基) 丙烯酸10-羥基癸酯、(曱基)丙烯酸12_羥基十二烷基酯、(曱 基)丙烯酸(4_羥基曱基環己基)曱酯等含有羥基的單體;苯 乙烯磺酸、丙烯磺酸、2-(曱基)丙烯醯胺_2_曱基丙磺酸、(曱 18 200814172If necessary, it is also possible to use a single-axis or two-axis extension processor. The resin (9) which is provided with heat shrinkability by elongation treatment or the like can be thermally contracted by the support substrate after dicing, and the adhesive layer 2 of the β-coating layer 2 and the wafer is bonded. The bonding area is simple and easy to recover from the sheet-like workpiece.曰曰^Improve the adhesion to the adjacent layer, maintainability, etc., and support the surface of the substrate to be treated with a regular surface. For example, chromic acid dew, fire exposure, high-voltage electric shock exposure _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ Further, the electric power, the supporting substrate 1 can also be used for the above-mentioned plastic film, metal, alloy or oxides thereof, and having a thickness of 30 5 0 0 士士" The film of the vapor-deposited layer may be, for example, a laminate in which the ruthenium film is bonded to another film or the other film, and the support substrate 1 may be a single layer or the above-mentioned material of 200814172 = equal to or greater than The layered layer 2 and the agent i 2 are radiated hard & Electrostatic ability. Antistatic dream, under 'can also make it with conductive agent Holding (4) to the adhesive layer, J: adding antistatic agent or metal film, etc., conductive Μ, ° 匕 3 掎 掎 transfer compound or difficult to produce ^ suitable ^ type, better formula. The thickness of the support substrate 1 of the impurity ion of the bulk wafer is, for example, 5~ can be withstand about 3^ by the above heat shrinkage, and if there is a binder, the adhesive for the bonding of the day; 3 #七The thickness is not particularly limited. In addition, the tension ultraviolet rays generated by the layer 3 may be such that the support substrate 1 may have a thickness of 1 〇 through the adhesive layer 2, and the modulus becomes lxlO4~lxl〇lGp μ in C The bow is as early as the range of the adhesive layer 2, and the thickness of the adhesive layer 2 and the elastic mode of the adhesive layer 2 reach the range of the cut value of the effect and effect of the invention for the invention. The model can be fully utilized. The number of the film is in the range of 25_~50_, and the modulus of the 23 (: is set to the above numerical range to prevent the generation of debris), and the fly is prevented from being picked up when the wafer-shaped workpiece is picked up. 200814172 ^iy〇jpn The above-mentioned elastic modulus is especially good for lx "〇V;; better is Pa, it is easy to cut to the support, a. The right elastic modulus is less than xio7 Pa, the dicing step will cause the wafer; the workpiece is filled and the genus is generated. Further, in the die attach step, It is easy to produce a flying piece, and the amount of wear of the cutting blade is increased by the following: (2) =: Further, the thickness of the adhesive layer 2 is described as follows: To prevent wafer profile defect or = value In the encirclement, it is both sexual and so on. As for the corpse #", the Japanese film station uses the adhesive layer; 3 ^ 20 ^ 6 〇 尽 , , ,, preferably 20~70 μιη, more #0疋2〇60 _, especially good is 20~50 _. More preferably, layer 2 is formed by means of a peeling of the adhesive layer 3 from the wafer: 曰 =; relationship (see _). That is,: "The more the piece of the workpiece is bonded with the adhesive layer 3: = miscellaneous adhesive, the interface of the core Β ^ ^ is read as the adhesive layer 3b for wafer bonding) The peelability of A is greater than the peeling of interface B, ",. In order to satisfy the relationship, the adhesive layer 2 is designed, for example, as follows: the portion 2a corresponding to the workpiece attaching portion 3a (described later) (with: '(four) adhesive layer 2a) has a smaller adhesive force than the outer portion The adhesion of the portion 2b (hereinafter sometimes referred to as the adhesive layer 2b) corresponding to all of the components is the same. ^The adhesion of the above adhesive layer 2a is based on the adhesion at normal temperature (23T:) (the value of 90 degree peeling force (peel), the peeling speed is 3 〇〇 _ / _), 200814172 fixed value of wafer value Or the recyclability of the formed wafer is preferably 小于.5 N/2 Gmm or less, more preferably, mm, particularly preferably 0.01 to 0.35 N/20 mm. Another - 〇.42 N / 20 is the adhesive layer 2b adhesion is 〇. 5~2 〇 N / 2 〇 ^ ^ surface 'better of the lower peel adhesion' can also inhibit sticky viscous The generation of the flying piece or the like of the force (10), and the holding force of the enthalpy layer 2b. In the in-plane of the adhesive layer 2 during the processing of 10,000 and DAY, the adhesion-free adhesive is not used. When the adhesive layer 2 is subjected to partial radiation, the degree of crosslinking of the polymer compound constituting the adhesive layer 2 is caused by, for example, an index of adhesion, and the like: Therefore, in the present embodiment, p can be hardened by lowering the body m, and the adhesion can be remarkably lowered. 'Another radiation agent layer 2b is irradiated with radiation, but it can only be filled with eight + not sticky. Layer 2 can be bonded and peeled off with a good balance of the knife; That is, the adhesive agent can be adhered to the adhesive sheet 3 sufficiently, and the adhesive layer and the crystal = 2 = adhesive layer can be easily peeled off, and the pickup property can be improved. Adhesive agent of the agent layer 2 and the above-mentioned radiation hardening type of the present invention is preferably a point of the agent layer 2a and the adhesive layer 2b because the adhesive agent is easily generated by irradiation of a material line or the like: Reduce its _. Therefore, 3 = ^ _ is large, and the easy adhesive layer 23 illuminates the radiation, and the region is lowered in 200814172. Since the adhesive portion 3a of the wafer bonding is located at a bonding force which is hardened and the adhesion is lowered, the agent layer 2a and the workpiece attaching portion 3 χ & The interface of % has a radiation-curable adhesive which is easy to peel off when picking up, and is formed by the adhesive layer 11 which is not irradiated with radiation. Therefore, the adhesive layer 3 of the two pieces of New Nut m can be confirmed. The fixing of the ground-cured radiation-curing adhesive is reduced by 4 times. It is used to bond the workpieces (semiconductor wafers, etc.) or the workpieces such as the slab-like workpieces (the semi-conductive wafer bonding adhesive) The balance of the adhesive layer 3. The adhesive of θ f into the adhesive layer 2 is not particularly limited, and is preferably a two-part, coffee-curable adhesive. The radiation-curable adhesive has a carbon-carbon double bond. Radiation-hardening property (J-based, and adhesiveness is shown. The 5-ray hardening type adhesive agent is exemplified by the above-mentioned acrylic type, rubber-based adhesive, poly-stone-based adhesive, polyethylene coffee) Adding a radiation-curable adhesive to a pressure-sensitive adhesive, a radiation-curable adhesive with a radiation-curable single = a knife or an agglomerate component. Upper = Inductive Adhesive - Not suitable for contaminated electrical parts such as semiconductor wafers or glass Ultrapure water or organic solvent Each of the cleansing and cleaning properties is preferably an acrylic adhesive having an acrylic polymer as a base polymer (_200814172 ζι^ο^ριτ polymer). Examples of the acrylic polymer are as follows: (Alkyl) acrylic acid alkyl vinegar (for example, 曱酉 、, 乙, 丙 、, isopropyl g |, 丁 司, Isobutyl butyl phthalate, second butyl vinegar, glutinous, Isocyanine, hexyl vinegar, heptyl ester, hexyl sulphate, 2-ethylhexyl S, isooctyl, 壬§, vinegar, isophthalic acid, + - silk S, 12 垸The carbon number of the burning base of the thirteen-burning base §|, the fourteen-burning vinegar, the ten-burning vinegar, the eighteen-burning base, and the twenty-burning base is π 3G 'especially miscellaneous f7 4~18 In the case of a linear or branched sulphuric acid vinegar or the like, and (meth)acrylic acid cyclic oxime (for example, cyclopentyl vinegar, cyclohexan vinegar, etc.), 1 or 2 or more monomers are used as a monomer component. The acrylic polymer to be used, etc. Further, the (meth) acrylate vinegar means acrylic acid and/or methacrylate, and the meaning of (meth) in the present invention is the same. The XK compound may be a unit corresponding to the other monomer component which is copolymerized with the above-mentioned (meth) = ring-based ester, as needed, for the purpose of modifying the enthalpy of the XK compound. Examples of the monomer component include acrylic acid, mercaptoacrylic acid, (mercapto)acrylic acid carboxyethyl ester, (mercapto)acrylic acid carboxypentyl ester, methylidene succinic acid, maleic acid, and fumaric acid. a monomer having a carboxyl group such as crotonic acid; an acid anhydride monomer such as maleic acid anhydride or methylene succinic anhydride; 2-hydroxyethyl (meth) acrylate, 2-hydroxyl (meth) acrylate Propyl ester, 4-hydroxybutyl (meth)acrylate, 6-hydroxyhexyl (meth)acrylate, 8-hydroxyl (meth)acrylate, 10-hydroxydecyl (meth)acrylate, (fluorenyl) a hydroxyl group-containing monomer such as 12-hydroxydodecyl acrylate or (4-hydroxydecylcyclohexyl) decyl acrylate; styrene sulfonic acid, propylene sulfonic acid, 2-(indenyl) propylene oxime Amine_2_mercaptopropanesulfonic acid, (曱18 200814172
Z J VODpiT 基)丙烯醯胺丙磺酸、(曱基)丙烯酸磺丙基酯 含有祕的單體;丙_氧二= 基的单體;丙烯_、丙烯腈等。這些 ^ χκ σ的早肢成分可使用丨種或2種以上。 取 合單體的使用量較好的是小於等於全單體成分的仙重= %。 要八::二丙烯酸聚合物為可被交聯’故可根據需 ^有夕“性早體等作為共聚合用單體成分。 =單體其例如可列舉:己二醇二叫^ ^ )丙烯酸醋、(聚)丙三醇二(甲基)丙烯酸醋、 L j —(f基㈣㈣、*細醇:(曱基)丙烯酸醋、 ^甲^丙烧三(甲基)丙稀酸酿、季戊四醇三(甲基)丙稀酸 o 取曰^季其t四醇六(曱基)丙稀酸隨、環氧(甲基)丙稀酸醋、 ^ (甲基)丙晞㈣、胺基甲酸醋(甲基)丙稀酸醋等。這些 體亦可使们種或2種以上。就黏著特性等觀 成分單㈣制量較好的是小於等於全單體 上的婦酸系聚合物的製備’例如可對1種或2種以 =聚合方式或懸濁聚合方式等適二方二進;方 晶圓等方面而言,較好的是抑制了低 刀子里物質含置的組成,就相關二 量平均分子量為大於等於3。 二好== 丙烯酸系聚合物作為主成分者,因而、,: 200814172 ^ 1 父聯方式或外部交聯方式等而製成適宜的交聯類型。Z J VODpiT base) acrylamide propyl sulfonic acid, sulfonyl (mercapto) acrylate propyl monomer containing a secret monomer; a monomer of propylene-oxygen bis group; propylene _, acrylonitrile, and the like. These early components of the χκ σ can be used in two or more species. The amount of the monomer to be used is preferably equal to or less than the weight of the all monomer component = %. It is required that the diacrylic acid polymer can be cross-linked, so that it can be used as a monomer component for copolymerization according to the need, such as the "pregnancy", etc. = monomer can be exemplified by: hexanediol dioxin ^ ^ ) Acrylic vinegar, (poly) glycerol di(meth)acrylic acid vinegar, L j — (f-based (tetra) (tetra), * fine alcohol: (mercapto) acrylic vinegar, ^ 甲 丙 烧 tri (methyl) acrylic acid , pentaerythritol tris(meth)acrylic acid o, 曰, 季, t, tetraol, hexamethyl acrylate, epoxy (meth) acrylate, ^ (methyl) propylene (tetra), amine Formic acid vinegar (meth) acrylic acid vinegar, etc. These bodies may also be seeded or more than two. In terms of adhesion characteristics, etc., the composition of the single (four) is preferably less than or equal to the polymerization of the total monomeric acid. For example, the preparation of the material can be carried out by one or two types, such as a polymerization method or a suspension polymerization method; in terms of a square wafer, etc., it is preferable to suppress the composition of the substance in the low knife. , the correlation average molecular weight is greater than or equal to 3. Two good == Acrylic polymer as a main component, and thus: 200814172 ^ 1 The parent-linked method or the external cross-linking method is suitable Crosslinking type.
o 又,為了控制黏著劑層2的交聯密度,例如可採用: 使用夕g月b兴氰酸酷系化合物、環氧系化合物、三聚氰胺 系化ΰ物、金屬鹽系化合物、金屬螯合物系化合物、胺基 樹脂系化合物或過氧化物等適宜的外部交聯劑而進行交聯 處理的方式;或將具有大於等於2個之碳-碳雙鍵的低分子 化合物進行混合,藉由能量線照射等進行交聯處理的方式 等適且方式。於使用外部交聯劑之情形時,其使用量可藉 由與應交聯的原料聚合物的平衡,進而根據黏著劑的使用 用途而適宜決定。一般而言,相對於1〇〇重量份的上述原 料聚合物,較好的是添加小於等於5重量份左右,更好的 疋添加0_1〜5重量份。再者,黏著劑中除上述成分以外, 亦可根據需要使用各種黏著賦予劑、防老化劑等添加劑。 所添加的放射線硬化性單體成分,例如可列舉:胺基 曱酸酯(曱基)丙烯酸酯、三經曱基丙烧三(曱基)丙稀酸醋、 四經曱基曱烧四(曱基)丙烯酸醋、季戊四醇三(曱基)丙烯酸 醋,季戊四醇四(曱基)丙烯酸酉旨、二季戊四醇單經基五(甲 基)丙烯酸酯、二季戊四醇六(曱基)丙烯酸酯、丨,4_丁二酽 二(曱基)丙烯酸酯等。 ’ 子 又,放射線硬化性寡聚物成分,可列舉:胺基甲酸醋 系、聚醚系、聚酯系、聚碳酸酯系、聚丁二烯系等夂種芙 ^ 100-30000 ^ 放射線硬化性單體成分或寡聚物成分的添加量,可根據上 述黏著劑層的種類,而適錢定黏著㈣黏著力料降低 20 200814172o In order to control the crosslinking density of the adhesive layer 2, for example, it is possible to use: a cyanocyanate compound, an epoxy compound, a melamine-based compound, a metal salt compound, or a metal chelate compound. a method of crosslinking treatment by a suitable external crosslinking agent such as a compound, an amine resin compound or a peroxide; or mixing a low molecular compound having two or more carbon-carbon double bonds by energy A method of performing cross-linking treatment such as line irradiation or the like is suitable. In the case of using an external crosslinking agent, the amount thereof can be appropriately determined by the balance with the raw material polymer to be crosslinked, and further depending on the use of the adhesive. In general, it is preferred to add about 5 parts by weight or less, more preferably 0 to 5 parts by weight, based on 1 part by weight of the above-mentioned raw material polymer. Further, in addition to the above components, additives such as various adhesion-imparting agents and anti-aging agents may be used as needed in the adhesive. Examples of the radiation curable monomer component to be added include, for example, an amino decanoate (mercapto) acrylate, a tri-sulfonic acid propyl sulfonate, and a ruthenium ruthenium sulphate. Acrylic acid vinegar, pentaerythritol tris(fluorenyl) acrylate vinegar, pentaerythritol tetrakis(mercapto) acrylate, dipentaerythritol mono-perylene penta(meth) acrylate, dipentaerythritol hexa(meth) acrylate, hydrazine, 4_butyl bis(indenyl) acrylate and the like. In addition, the radiation-curable oligomer component may, for example, be an amino acid vinegar-based, polyether-based, polyester-based, polycarbonate-based or polybutadiene-based compound. 100-30000 ^ Radiation hardening The amount of the monomer component or the oligomer component can be adjusted according to the type of the above-mentioned adhesive layer, and the adhesion is lowered. (4) The adhesive strength is lowered 20 200814172
Zi^ojpn 里。般而5,相對於100重量份的構成黏著劑之丙稀酸 系聚合物等原料聚合物,例如為5〜,重量份,較好的是 70〜150重量份左右。 Ο ο 又,放射線硬化型黏著劑,除上述添加型之放射線硬 =型黏著劑之外’亦可列舉使用於聚合物側鏈或主鏈中或 者主鏈末端具有碳%雙鍵的内在型之放射線硬化型黏著 =作為原《合物。_在型放射線硬化型黏著劑,無須 έ有低分子成分的絲物成分等,或者所含有Μ,且寡 分等!f隨著時間而於黏著劑中活動,可形成穩定 層結構的黏者劑層,故較好。 田& t:有:石反雙鍵的原料聚合物,可無特別限制地使 1、验* % Γ鍵且具有黏著性者。如此之原料聚合物較好 =::Γ’“聚ϊ物作為基本骨架者。丙烯酸系聚合物 '土月木’可列牛上述所例示的丙烯酸系聚合物。 於上述丙雜“合物中導人碳碳 =限制’可採用各種方法,就分子設計方面而言,碳、_ 石反雙鍵可容易地導人聚合物懷。例如 聚合物上;聚合具有官能基之單體後,Ξί有可 Μ““基反應的s能基以碳·碳雙_ =鍵之放射線硬化性的狀態下,進行縮合或= 羧基與環氧基、 即使於這些官能 輕基與異氰酸酯 运些g 3b基的組合的例子,可列舉 敌基與氮丙<基、雜料請g旨基等 基的組合中,就反應追蹤的容易度而言 21 200814172Zi^ojpn. In general, the raw material polymer such as an acrylic polymer constituting the adhesive is, for example, 5 to a part by weight, preferably about 70 to 150 parts by weight. Further, the radiation-curable adhesive may be an intrinsic type which is used in a polymer side chain or a main chain or has a carbon-% double bond at the end of the main chain, in addition to the above-mentioned added type of radiation hard type-type adhesive. Radiation hardening type adhesion = as the original compound. _In the type of radiation-curing adhesive, it is not necessary to have a low-molecular-weight silk component, or contain bismuth, and oligo! It is preferable that f is active in the adhesive over time to form an adhesive layer of a stable layer structure. Field & t: There is a raw material polymer of stone anti-double bond, which can be made without any limitation, and is characterized by an adhesive bond. Such a raw material polymer is preferably =:: Γ' "poly ruthenium as a basic skeleton. Acrylic polymer 'soil moon' can be listed as the acrylic polymer exemplified above. The introduction of carbon and carbon = limit 'can be used in various ways. In terms of molecular design, carbon, _ stone anti-double bond can easily lead the polymer. For example, on a polymer; after polymerizing a monomer having a functional group, Ξ 有 "" The s-energy group of the base reaction is condensed or = carboxyl and epoxy in a state in which the carbon-carbon double _= bond is radially hardenable. Examples of the combination of these functional light groups and isocyanate-supporting g 3b groups include a combination of an enemy group and an aza-propyl group, a base, and a heterogeneous group, and the ease of reaction tracking.言21 200814172
Z1 VODpiT 基的組合較為適宜。又,若為藉由這些官能美 人 土曰、J '、且己,而 生成具有上述碳-碳雙鍵的丙烯酸系聚合物的、组人 1 — & 基亦可為丙烯酸系聚合物與上述化合物之任—個^ ^ g 1 較好組合中,較適宜的是丙稀酸系聚合物具有声芙 ^ 化合物具有異氰酸酯基的情形。於該情妒日^山上述 y τΓ 具有碳·瑞等 - 鍵之異氰酸酯化合物,例如可列舉:甲其;^ μ , Τ基丙烯醯異氰酸酯 - (methacryloyl isocyanate)、異氰酸 2_甲其工 α ^ 土^3 /布酉监氧基^乙 酯、異氰酸間異丙烯基-α,α-二曱基苄妒楚 /、 Λ , 曰寺0又,丙烯酸系 ( “物,可使㈣上述所齡的含麵基的單體或2々其 乙基乙烯醚、4-羥基丁基乙烯醚、二? — π ’工土 ^ A 醇早乙烯基醚的 醚糸化合物等進行共聚合者。 上述内在型放射線硬化型黏著劑,可單獨使用且 舰·碳雙鍵的職聚合物(尤其輯㈣聚合物/,、作亦 可於不會損害特性的程度上添加上述放射線硬化性單體成 分或寡聚物成分。相對於⑽重量部的原料聚合物放 硬化性寡聚物成分等,通常於小於等於3〇重量份的範圍 Q 内’較好的是0〜1〇重量份的範圍。 述放射線硬化型黏著劑於藉由紫外線等進行硬化的 -’含有光聚合引發劑。光聚合弓丨發劑,例如可列舉: 經基乙氧基)苯基㈣基么丙基购、α_經基部甲基 曱基苯丙_、1老基己基苯基酮等^酉同 22 &,甲氧基苯乙酮、2,2·二甲氧基-2·苯基苯乙酉同、 Ζ〆-—乙氧基本乙酮、丨_翔其 土衣已基本基酮、2-曱基-[4-(曱 石瓜基)-本基]-2_嗎口林基丙院4耸贫 寺本乙酮糸化合物;安息香乙 22 200814172 Z1vojpn 醚、安息香異丙_、茴香甲_等安息香_系化合物;2-甲 基-2-經基苯丙銅等α_§同系化合物、节基二甲基縮酮等縮嗣 系化合物;2♦細氣等芳香族伽氣系化合物;1-苯紛 -1,1-丙院二終2-(間乙氣基幾基)肪等光活性肪系化合物; 一苯曱酮、苯曱醯苯甲酸、3_3,_二曱基_4_曱氧基二笨曱酮 等二苯甲酮系化合物;噻噸酮(thi〇xanth〇ne)、2_氣噻噸 酮、2-甲基噻噸酮,2,4-二曱基噻噸酮、異丙基噻噸酮、2,4_ 一氣嗔17頓酮’ 2,4-一乙基嗟°頓酮、2,4-二異丙基°塞°頓酮等σ塞 σ頓酮糸化合物,樟腦醒(camph〇r〇quinone);鹵化酮;酸 基膦氧化物(acylphosphinoxyde );醯基膦酸鹽 (acylphosphinate)等。相對於1〇〇重量份的構成黏著劑 的丙烯酸系聚合物等原料聚合物,光聚合引發劑的添加量 為例如0.05〜20重量份左右。 又,用於形成黏著劑層2的放射線硬化型黏著劑,例 如可列舉:於日本專利特開昭60 — 196956號公報中所揭示 的含有,具有大於等於2個不飽和鍵結之加成聚合性化合 物、具有環氧基之;):完氧基石夕;):完等聚合性化合物,及羰基化 合物、有機硫黃化合物、過氧化物、胺、鏽鹽系化合物等 光聚合引發劑的橡膠系黏著劑或丙稀酸系黏著劑等。上述 具有大於等於2個不飽和鍵結的加成聚合性化合物,例如 可列舉:丙烯酸或曱基丙浠酸多元醇系酯或者寡酯、環氧 系或胺基甲酸酯系化合物等。 一般而言,上述光聚合性化合物或光聚合引發劑的添 加量,每100重量份原料聚合物各自為10〜500重量份, 23 200814172 21965pif 較好的是0·05〜20重量份。除這些添加成分以外,/ 據需要另外添加於乙二醇二縮水甘油醚等分子中I亦可根 或2個以上的環氧基的環氧基官能性交聯劑,1個 劑的交聯效果。 k向勒著 於使用上述放射線硬化型黏著劑的黏著劑層2 可根據需要而含有藉由放射線照射著色的化合物。。丄亦 • 利用放射線照射使黏著劑層2含有經著色的化合可麵由 對經放射線照射的部分著色。藉此,例如亦可;工仕而僅 〇 部分3a所對應的黏著劑層2a著色。其結果是,可1貼附 視對直接判明黏著劑層2是否被放射線照射,從而,由目 別工件貼附部分3a,且容易貼合工件。又,於藉由識 态等檢測半導體元件時,提高檢測精度,拾取半舰士 ^ 時不會產生誤操作。 、&凡件 藉由放射線照射而著色的化合物於放射線照射前為益 色或淡色,其是藉由放射線照射而成為有色的化合物。相、 關化合物的較好的具體例可列舉:無色染料(leuc〇dye)。 〇 無色染料,可較好使用常用的三苯基曱烷系、螢光黃母體 (fluoran )系、g分嗟嗪(phenothiazine )系、金普胺 (Auramine)系、螺口比喃(Spir〇pyran)系者。具體而言, 可列舉3-[N-(對曱苯基胺基)]_7_笨胺螢光黃母體、3-肝(對 曱苯基)-N-甲基胺基]-7-苯胺螢光黃母體、3_[N_(對曱苯 基)乙基胺基]-7-苯胺螢光黃母體、3-二乙基胺基曱基 7本&C ^光頁母體、結晶紫内醋(CryStal vi〇let iact〇ne )、 ,4 _二(二曱基胺基)三苯基曱醇、4,4f,4n-三(二甲基胺基) 24 200814172 zivcopir 三苯基甲烧等。 與這些無色(leue。)染料共同較好地使用的 列舉自先前所使用的苯酚甲醛樹脂俨; 的产报日士#电于又脰進而,於使色調變化 的,亦可組合使用各種成色劑。 如此之藉由放射線照射的著色化合物,若機 溶媒等後,既可含於放射線硬化型黏著劑中,又,亦玎f Π ϋ 成微粉末狀而含於雜著· 2中。較理想的是,該化合 ,的使用比例於黏著劑層2中為〇〇〗〜1〇重量%,較好的 疋0.5 5重里/〇。若纟亥化合物的比例超過1 〇重量%,則因 方、钻著9彳層2中所^射的放射線會為該化合物所吸收,故 有日守上述黏著劑層2a的硬化會不充分,且黏著力未充分下 降。另一方面,若使用化合物比例未滿〇 〇1重量%的量, 則於放射線照射時,有時黏著薄片未充分著色,且於半導 體元件之拾取時,有時容易產生誤操作。 於藉由放射線硬化型黏著劑形成黏著劑層2之情形 時’可列舉:於支持基材1上形成放射線硬化型黏著劑層 2後,於工件貼附部分3a所對應的部分上,部分性照射放 射線而使之硬化形成黏著劑層2a的方法。部分性放射線照 射可經由形成工件貼附部分3a以外部分(3b等)所對應 的圖案的光罩而進行。又,可列舉光點性照射紫外線而使 之硬化的方法等。放射線硬化型的黏著劑層2的形成,可 藉由於分離體(seperator)上所設置者轉印至支持基材1 上而進行。部分性放射線硬化亦可於分離體上所設置的放 25 o o 200814172 z 1 vcopir 射線硬化型至黏著劑層2上進行。 又,於藉由放射線硬化型黏著劑形成黏著 形時,亦可使用支持基材!的至少單面的工伽\ = 3應的部分以外部分的全部或者—部分_光者 成放射線硬化型之骑㈣2後照射放射紗1上 7 對應的部分硬化,可形成黏著力'降低‘ 者_ 2a。遮光材料可使用可於支持薄膜上成為去, 可以印刷絲鍍等而形成。絲據該製造方法,則可 製造本發明的切晶、黏晶片。 、回夕 士 ^者’於照射放射線時由氧氣導致硬化抑制的情米 日守,父好的是以某些方法自放射線硬化型的 Μ 氣(空氣)。例如可列舉以分離體包覆蝴: ^法ί面的方法’或於氮氣環境中照射紫外線等放射線 2劑層2的厚度’並無特別限定,就防止晶片切剖 、、貝及固定保持黏接層的兼具性等方面而古, 是1〜5〇陣左右。較好的是2〜3〇_,更好的是t μηι 〇 晶片黏接用黏接劑層3具有如下機能:於將哼声 壓接的工件(半導體日日日圓等)切斷成晶片狀時,^於丁 件而對其m持;於安裝晶片狀卫件靖#(半邮曰 片等)時’作為該切斷片與基板或晶片狀工件片= ㈣層而發揮作用。晶片黏接用黏接劑層3,尤為重上 疋具有於:n件切斷時不使切斷片飛散的程度_接性。、 26 200814172 :具體而言可適宜使用 刼月曰。這些材料可單獨 、土蚵如、,4硬化性 黏接用黏接劑層3較好的是^^ 。又,晶片 體晶圓:,者切晶環者。更好的,可= 用作晶片黏接劑之熱可塑 、吊,皿下粘者者。 Ο u 劑)’例如可列舉:飽如曰(熱可塑性晶片黏接 系樹脂、酿胺系樹脂(尼龍系樹1熱^塑二生聚胺基甲酸醋 熱硬化性樹脂(熱硬 二:、亞胺系樹脂等。又, 步驟(B-Stage)化> 刼且的疋脱溶劑化、薄片化、B 脂與熱可紐樹脂的混合物者’ ;f熱硬化性樹 膠系、胺基甲酸酉旨系、邮交高的聚石夕氧系、橡 作晶片黏接劑。 系、丙烯酸系等樹脂亦可用 熱傳導性等目接3接刮層3中為了賦予導電性、提高 電性物質,可歹:舉ΓΓ,、導電填充料)。導 的球狀、針狀、2二、·呂、金、銅、鎳、導電性合金等 晶碳黑,石墨等 屬粉’氧化結等金屬氧化物,非結 同的接移溫度* …、更化/皿度不同的熱硬化性樹脂,而 200814172 具有2層以上的多層 的切割步驟中使用切削水,故而存因工曰件(半導體晶圓等) 3吸濕,達到常熊以 —…存有曰曰片黏接用黏接劑層 水率下直接與基i等^含2的情形。若於如此之高含 階段,於黏接界面上八] 、子有於後處理(afterCure) 因此,晶片黏接用蒸氣,從而產生氣泡的情形。 的薄膜而構成片黏接劑夾住透濕性較高 u 於後處理階段,水筮氣可透過舊 。因此,晶二= 構造依4層有婦、薄膜、黏接·的^ (半劑層3是兼有於切晶時保待黏接工件 亚無特別限定,例如為Η⑻ 力尸度 更好的是5〜50 _左右。 〜7〇_, 晶片黏接用黏接劑層3,其對工件貼A combination of Z1 VODpiT groups is suitable. Further, the group 1 - & base group which is an acrylic polymer having the above carbon-carbon double bond by these functional beauty soils, J' and its own may be an acrylic polymer and the above Any of the compounds - ^ ^ g 1 In a preferred combination, it is preferred that the acrylic acid polymer has a case where the compound has an isocyanate group. In the case of the above-mentioned y τ 上述 Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ Γ 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异^ ^ 土^3 / 酉 酉 氧基 氧基 ^ ^ ^ 氧基 、 、 、 氧基 氧基 氧基 氧基 氧基 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 异 氧基 氧基 氧基 氧基 氧基 氧基 氧基 氧基 氧基 氧基 α (4) copolymerization of a monomer having a surface group of the above-mentioned age or an ether oxime compound of ethylene vinyl ether, 4-hydroxybutyl vinyl ether, di-n-π 'situ The above-mentioned intrinsic radiation curable adhesive can be used alone and the carrier of the carbon double bond (especially the polymer) can be added to the extent that the properties are not impaired. The body component or the oligomer component is usually in a range of less than or equal to 3 parts by weight, preferably 0 to 1 part by weight, based on the weight of the (10) by weight of the raw material polymer-setting hardenable oligomer component. Scope. The radiation-curing adhesive is hardened by ultraviolet rays or the like - The initiator is a photopolymerization hair styling agent, for example, a ethoxylated phenyl (tetra) propyl propyl group, an α yl group, a methyl phenyl phenyl propyl group, a hexyl phenyl ketone ketone, etc. ^酉同22 &, methoxyacetophenone, 2,2. dimethoxy-2-phenylphenyl hydrazine, Ζ〆--ethoxybenthanone, 丨_xiang its basic clothes have been basic Ketone, 2-mercapto-[4-(曱石瓜基)-本基]-2_口口林基丙院4塔贫寺本乙酮糸 compound; benzoin B 22 200814172 Z1vojpn ether, benzoin isopropyl _, Anise _ _ benzoin _ series compounds; 2-methyl-2- phenyl phenyl propyl and other α § homologous compounds, thiol ketal and other condensate compounds; 2 ♦ fine gas and other aromatic galaxies a compound; 1-benzophenone-1, 1-propanol-terminated 2-(m-hexyl)-based photoactive aliphatic compound; benzophenone, benzoquinone benzoic acid, 3_3, dioxin a benzophenone-based compound such as _4_nonoxy dioxin; thioxanthone (thi〇xanth〇ne), 2_ thioxanthone, 2-methylthioxanthone, 2,4-di Thiophenone, isopropyl thioxanthone, 2,4_one gas 嗔 17 ketone ' 2,4-ethyl oxime ketone, 2,4- a isopropyl sigmazone oxime compound such as diisopropyl thiophene ketone, camph〇r〇quinone; a halogenated ketone; acylphosphinoxyde; acylphosphinate. The amount of the photopolymerization initiator added is, for example, about 0.05 to 20 parts by weight based on 1 part by weight of the raw material polymer such as the acrylic polymer constituting the pressure-sensitive adhesive, and the radiation curing type for forming the pressure-sensitive adhesive layer 2 The adhesive agent may, for example, be an addition polymerizable compound having two or more unsaturated bonds and having an epoxy group as disclosed in Japanese Laid-Open Patent Publication No. SHO 60-196956. (Ji Shi Xi;): a rubber-based adhesive or an acrylic-based adhesive which completes a polymerizable compound, and a photopolymerization initiator such as a carbonyl compound, an organic sulfur compound, a peroxide, an amine or a rust salt compound. The above-mentioned addition polymerizable compound having two or more unsaturated bonds may, for example, be acrylic acid or mercaptopropionic acid polyol ester or oligoester, epoxy or urethane compound. In general, the amount of the photopolymerizable compound or the photopolymerization initiator added is 10 to 500 parts by weight per 100 parts by weight of the base polymer, and 23 200814172 21965 pif is preferably 0. 05 to 20 parts by weight. In addition to these added components, / if necessary, an epoxy functional crosslinker which may be added to a molecule such as ethylene glycol diglycidyl ether, or may have two or more epoxy groups, and the crosslinking effect of one agent . The adhesive layer 2 which is used in the above-described radiation curable adhesive can contain a compound colored by radiation irradiation as needed. .丄 Also • Radiation irradiation is used to cause the adhesive layer 2 to contain a colored compound to be colored by the portion irradiated with radiation. Thereby, for example, it is also possible to color only the adhesive layer 2a corresponding to the portion 3a. As a result, it is possible to directly determine whether or not the adhesive layer 2 is irradiated with radiation by attaching the pair of eyes, thereby attaching the portion 3a to the workpiece and easily attaching the workpiece. Further, when the semiconductor element is detected by the identification state or the like, the detection accuracy is improved, and when the half warship is picked up, no erroneous operation occurs. , & Everything A compound colored by radiation is a colored or light color before irradiation with radiation, which is a colored compound by radiation irradiation. Preferable specific examples of the phase-closing compound include a leuco dye (leuc〇dye). 〇 leuco dye, preferably used triphenyl decane, fluoran, phenothiazine, Auramine, Spir〇 Pyran). Specifically, 3-[N-(p-phenylphenylamino)]-7-phenylamine fluorescent yellow mother, 3-hepatic (p-phenylene)-N-methylamino]-7-aniline Fluorescent yellow mother, 3_[N_(p-phenylene)ethylamino]-7-phenylamine fluorescent yellow mother, 3-diethylamino fluorenyl 7 & C ^ light page precursor, crystal violet Vinegar (CryStal vi〇let iact〇ne ), 4 _ bis (didecylamino) triphenyl decyl alcohol, 4, 4f, 4n-tris(dimethylamino) 24 200814172 zivcopir triphenyl ketone Wait. The phenol formaldehyde resin used in the above-mentioned colorless (leue.) dyes can be preferably used in combination with the phenol formaldehyde resin which has been used in the past, and the coloring agent can be used in combination with various color formers. . The coloring compound irradiated by the radiation may be contained in the radiation curable adhesive after the solvent or the like, and may be contained in the hybrid 2 in a fine powder form. Preferably, the compounding ratio is used in the adhesive layer 2 to be 〇〇 〜 1 〇 by weight, preferably 疋 0.5 5 mph. If the proportion of the compound is more than 1% by weight, the radiation emitted by the 9 layer 2 will be absorbed by the compound, so that the curing of the adhesive layer 2a may be insufficient. And the adhesion is not fully reduced. On the other hand, when the compound ratio is less than 〇1% by weight, the adhesive sheet may not be sufficiently colored during radiation irradiation, and erroneous operation may occur easily when the semiconductor element is picked up. In the case where the adhesive layer 2 is formed by the radiation-curable adhesive, a part of the portion corresponding to the workpiece attaching portion 3a is formed after the radiation-curable adhesive layer 2 is formed on the support substrate 1. A method of irradiating radiation to harden it to form the adhesive layer 2a. The partial radiation irradiation can be performed through a mask that forms a pattern corresponding to a portion (3b or the like) other than the workpiece attachment portion 3a. Further, a method of curing by ultraviolet light and curing it may be mentioned. The formation of the radiation-curable adhesive layer 2 can be carried out by transferring onto the support substrate 1 by a person provided on a seperator. Partial radiation hardening can also be carried out on the release layer of the 25 o o 200814172 z 1 vcopir ray hardening type to the adhesive layer 2. Further, when the adhesive shape is formed by the radiation-curable adhesive, a supporting substrate can also be used! At least one side of the work gamma \ = 3 part of the part other than the part or part of the light into the radiation hardening type riding (four) 2 after the irradiation of the radiation yarn 1 on the corresponding part of the hardening, can form the adhesion 'lower' _ 2a. The light-shielding material can be formed by using a support film, printing wire plating, or the like. According to this manufacturing method, the crystal cut and sticky wafer of the present invention can be produced. In the evening, when the radiation is irradiated, the oxygen is caused by the inhibition of the hardening of the rice. The father is good by some method of self-radiation hardening type of helium (air). For example, a method of coating a butterfly with a separator: a method of 'methods' or a thickness of the radiation agent 2 for irradiating ultraviolet rays or the like in a nitrogen atmosphere is not particularly limited, and the wafer is prevented from being cut, and the film is fixed and adhered. The combination of the layer and the other is ancient, and it is about 1 to 5 arrays. Preferably, the adhesive layer 3 for the wafer bonding has the following function: the workpiece (the semiconductor day, the Japanese yen, etc.) which is crimped by the click is cut into a wafer shape. When it is mounted on a wafer, it is used as a wafer or a wafer-shaped workpiece piece = (four) layer when the wafer-shaped guard member Jing # (half-mail film, etc.) is mounted. The adhesive layer 3 for wafer bonding, in particular, has a degree of adhesion to the extent that the cut piece does not scatter when the n pieces are cut. , 26 200814172 : Specifically, it is suitable to use 刼月曰. These materials may be individually, soiled, and the adhesive layer 3 of the hardenable adhesive layer is preferably ^^. Also, the wafer wafer: the person who cuts the ring. Better, it can be used as a thermoplastic adhesive for hanging wafer adhesives, hanging under the dish. Ο ' ' 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热 热Imine-based resin, etc. Further, step (B-Stage)> 疋 desolvation, flaking, mixture of B-fat and thermocohol resin'; thermosetting gum, urethane聚 酉 、 、 聚 聚 聚 、 、 、 、 、 、 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡 橡It can be 歹: ΓΓ,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,, Material, non-consistent transfer temperature*, refining/different thermosetting resin, and 200814172 using two or more layers of multi-layer cutting step using cutting water, so the work piece (semiconductor wafer) Etc.) 3 moisture absorption, to reach the often bear - ... there is a bond between the adhesive layer and the adhesive layer directly The case where i or the like contains 2. If it is in such a high-containing stage, the bonding is performed on the bonding interface, and the sub-processing is performed after the process (afterCure), so that the wafer is bonded with vapor, thereby generating bubbles. The sheet adhesive has a high moisture permeability. In the post-treatment stage, the water vapor can pass through the old. Therefore, the crystal 2 = structure has 4 layers of women, film, and bonding. There is no particular limitation on the adhesion of the workpiece during the dicing, for example, Η(8) is better than 5~50 _. 〇7〇_, the adhesion layer 3 for wafer bonding, which is attached to the workpiece
C 著劑層_著力較好的是,4= 勺#者力大於對黏著劑層2&的黏著力 可根據工件_而適賴整。 ㈣黏考力’ 離力T牛貝ί附部分3a的對黏著劑層2a的黏著力(9〇度剝 隹力(Ped)的值,剝離速度300 mm/mir〇,如 較好的是小於等於Q.5腦mm,更好的是〇.〇丨〜Q.42 = ’ mm,尤其好的是0.01〜0.35 N/20 mm。另一方而 貼附部分3a的工件的黏著力(與上述相同條件),就2 28 200814172C. The coating layer _ is better, the force of 4 = scoop # is greater than the adhesion to the adhesive layer 2 & (4) Adhesive strength 'Separation force T Niubei ί part 3a adhesion to the adhesive layer 2a (9 隹 peeling force (Ped) value, peeling speed 300 mm / mir 〇, if better is less than It is equal to Q.5 brain mm, and more preferably 〇.〇丨~Q.42 = 'mm, especially 0.01~0.35 N/20 mm. The adhesion of the workpiece attached to the other part 3a (with the above) The same conditions), just 2 28 200814172
^l^ODpiT 時:拾取時、黏晶片時的可靠性、拾取性方面而言,較好 的疋小於等於10〜50 N/20 mm,更好的是1〇〜3〇 N/2〇 mm 〇 主农切剎作為工件的半導體晶圓而使用切晶環(晶圓環) 丨月形日^,本發明之切晶、黏晶片可採用以下結構。圖3 疋顯示本發明之切晶、黏晶片的其他例子的剖面模式圖。 ,4疋顯不於切晶、黏晶片上貼附半導體晶圓及切晶環的 Ο c 情形的平面圖。如圖3所示,切晶、黏晶片u是於支持基 材1上具有黏著劑層2,、於該黏著劑I 2,上具有晶片黏接 用黏接劑層3的構成。晶片黏接用黏接劑層3,於上述部分 3b的部分上设置有切晶環貼附部分3b'。又,於黏著劑 層21上設置有與切晶環貼附部分3b,所對應的部分'沘八& 為黏著劑層2b,)。進而’黏著劑層2ι,其切晶環貼附部分 3b,與對應其而形成的黏著劑層2b,的界面b,的剝離力是設 計成界面A的剝離力大於界面b,的剝離力的關係。 圖2之黏著劑層2中,黏著劑層2a以外的全部成 層2b ’但如圖3所示,黏著劑層2a以外 二:月1 為黏著劑層2b、 卜的彳分亦可作 於切晶、黏晶片u巾,於將工件貼附部分 分作為切晶環貼附部分3b,之情形時,於晶 乂外邠 層3,之切晶環貼附部分3b,中,對切晶環::?用黏接劑 著劑層2b,的黏著力較好的是設計成對切曰t與對於點 於對黏著劑層2b1的|占著力。對切晶環 著力小 環種類進行適宜調整。 "考力可根據切晶 29^l^ODpiT: In terms of picking, reliability and pick-up when sticking the wafer, a better 疋 is less than or equal to 10 to 50 N/20 mm, more preferably 1 〇 to 3 〇 N/2 〇 mm. 〇The main agricultural cutting brake uses a dicing ring (wafer ring) as the semiconductor wafer of the workpiece. The dicing and bonding wafer of the present invention can adopt the following structure. Fig. 3 is a cross-sectional schematic view showing another example of the diced and bonded wafer of the present invention. 4疋 is not a plan view of the Ο c case where the semiconductor wafer and the dicing ring are attached to the diced wafer. As shown in Fig. 3, the dicing die, the adhesive wafer u has an adhesive layer 2 on the supporting substrate 1, and the adhesive I 2 has a structure for bonding the adhesive layer 3 for wafer bonding. The adhesive bonding layer 3 for wafer bonding is provided with a dicing ring attaching portion 3b' on a portion of the above portion 3b. Further, the adhesive layer 21 is provided with a dicing ring attaching portion 3b, and the corresponding portion '沘8 & is the adhesive layer 2b'). Further, the peeling force of the adhesive layer 2, the cleavage ring attaching portion 3b, and the adhesive layer 2b formed corresponding thereto is designed such that the peeling force of the interface A is larger than the peeling force of the interface b. relationship. In the adhesive layer 2 of Fig. 2, all of the layers 2b other than the adhesive layer 2a are formed. However, as shown in Fig. 3, the adhesive layer 2a is two: the month 1 is the adhesive layer 2b, and the bismuth can also be used for cutting. The crystal and the adhesive wafer u towel are used to divide the attached portion of the workpiece into the dicing ring attaching portion 3b, in the case of the outer layer 3 of the wafer, the cleavage ring attaching portion 3b, and the tangential ring ::? With the adhesive agent layer 2b, the adhesion is preferably designed to be a pair of tangent t and for the adhesion to the adhesive layer 2b1. Appropriate adjustments are made to the type of cleavage ring. "考力 can be based on cutting crystal 29
200814172 z I ^OJUII 上诚相η」Γ 劑層3,的黏著劑層2b,的黏著力(於 ί另=件)’如上所述較好的是Ο.5〜麵2—左 力(與上述:同::片)黏::f接劑層3,㈣ 議於等於…咖疆,更好的是0.5〜5 層2中,工件貼附部分3a所對應的黏著劑; 力是設計隸―的= 繼a的黏著;寸部分%的黏著 小於等於。增一 如上所述較好的是 其好的是咖,〜G.42膽咖,尤 2± 圖5是本發明之+ 日日黏接用黏接劑層的結構。 圓。如上;二、#= 黏著劑層2 ’於該黏著劑層2上I有!1上具有 3"的結構。 ,、有日日片黏接用黏接劑層 對^曰片黏接用毒占接齋丨厚 〇 & 上述同m件下),如上料較2,著力(於 ,更好〜⑽卿咖,==㈣Μ _ =::广方面,對晶物用^ 二:於上述同樣條件下),就切晶時的工件的 '、拾取性方面而言’較好的是小於“:5t 200814172 腦麵,更好的是1〇〜3〇則咖。 1G〜12的晶片黏接用黏接層3、3" 二二4進行保護。即’可任意設置保護層4。 保ΰ隻滑4具有保譜曰μ 4 示。又日日片黏接用黏接劑層3、3”到供於實際 七”、、' ^作為保護材料的功能。再者,保護層 4可進: 黏著劑層2上轉印晶片黏接用黏接劑層3、%時的 保4層4可於切晶、黏晶片11〜12之晶月黏接 劑層3,3”上貼著工件時進行剝离隹。保護層4,可列 t ·小⑽、聚丙烯或’表面包覆有氟系剝離劑、長键烧 基丙稀酸酯系剝離劑等剝離劑的塑膠薄膜或 本發明之切晶、黏晶片1G〜12可適當剝離任意設置於 曰曰片黏接用黏接劑層3、3”上的分離體,並以如下之方式 =°即’於切晶、黏晶片薄膜1〇〜12之晶片黏接用黏接 劑们a (3”)上壓接I件’將其黏接保持而使之固定。壓 接可措由通常方法進行。被黏接體卫件,例如可使用:半 2體晶圓、多層基板、整體密封模鱗。本發明中被黏接 月豆或工件可適宜使用半導體晶圓。 一繼而,如圖6所示,將工件切割成晶片狀。同圖是顯 樣子的剖面模朗。切晶至少可進行至完全切斷晶 =接=接劑層3(3’、3”)為止。對於黏著劑層2⑺, i達:持其Π副刀片13切入深度達到預定值為土且未 I 等。切晶藉由旋轉圓形刀“-d e)寺以適宜方法將亦包括晶片黏接用黏接劑層3在内 200814172 ziyo^pir 的工件製成晶片狀工件(半導體晶片等)。 〇 繼而,將晶片狀工件與晶片黏接用黏接劑層3的工件 貼附,分3a (或者晶片黏接用黏接劑層3”)自黏著劑層2 的黏著劑層2a上一併剝離。所拾取的晶片狀工件經由工件 貼附部分3a #,黏翻定於作為獅接體的半導體元件 上。半導體元件可列舉··引線框架、TAB薄膜、基板或者 另外衣作的晶片狀1件等。被黏接體,例如既可為容易變 形的變形型被黏接體,亦可為難以變形的非變形型被黏接 ,(半導體日日日圓等)。被黏接體較適宜的是半導體晶圓。於 晶片黏接用黏接劑層3、3’、3"為熱硬化型之情形時,可夢 ^加熱硬化將工_顧定㈣轉體上,而提高耐^ 又。再者,㈣晶片黏接用黏接劑層3 黏接固定於基板者,可餘畴一㈣=件 生,*或::引?曰曰片1〇〜12 ’於防止黏接或剝離等時產 起等)帶電㈣致電 方式賦予抗靜電能力:於支持基材下適, 片黏接用黏接劑層3、3’、3”上添加抗靜二2'或晶 的方法;於支持基材1上附設包含“^彳“电性物質 膜等導電層等。這些方式較好的是=~移複合物或金屬 體晶圓變質的雜質離子的方式。^產生可能使半導 導性等目的下所添加的導電性物質' =導電性、提高熱傳 狀金屬粉儒等金屬氧化 舉:銀、銘、金、鋼、錄、導電性人填充料可列 於,备儿M w ^ ^ 〇至等球狀、針狀、片 石墨等 32 200814172200814172 z I ^OJUII 上相相η"Γ Agent layer 3, the adhesive layer 2b, the adhesion (in ί other = piece) 'as mentioned above is better Ο.5~ face 2 - left force (with The above: the same:: piece) sticky::f the agent layer 3, (four) is equal to ... yam, better is 0.5~5 layer 2, the adhesive attached to the workpiece attached part 3a; force is the design ―== Following the adhesion of a; the adhesion of the inch part is less than or equal to. It is preferable that the above is a good coffee, a G.42 gallbladder, and a special one. Fig. 5 is a structure of the adhesive layer for the daily bonding of the present invention. circle. As above; #2, the adhesive layer 2' has a structure of 3" on the adhesive layer 2; , there is a bonding layer for the bonding of the day and the film to the bonding of the 曰 曰 占 占 占 占 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 〇 上述 上述 上述 上述 上述咖, == (4) Μ _ =:: broad aspect, for crystals ^ 2: under the same conditions as above), in terms of the workpiece when cutting, 'pickup aspect' is better than less than: "5t 200814172 The brain surface is better than 1〇~3〇. The 1G~12 wafer bonding is protected by the adhesive layer 3, 3" 22: 4. The protective layer can be arbitrarily set. It has a spectrum 曰μ 4 and a bonding layer 3, 3" for the bonding of the day to the actual seven", "^ as a protective material. Furthermore, the protective layer 4 can be: Adhesive On the layer 2, the adhesive layer 3 for the transfer of the wafer bonding adhesive layer 3 and the layer 4 of the protective layer 4 can be peeled off when the workpiece is attached to the crystal moon bonding layer 3, 3" of the dicing wafers 11 to 12 Leave. The protective layer 4 may be a plastic film of a stripper such as a t (small) (10), polypropylene or a surface coated with a fluorine-based release agent or a long-bonded acryl-based release agent, or a diced or bonded wafer of the present invention. 1G to 12 can appropriately peel off the separator which is arbitrarily disposed on the adhesive layer 3, 3" for the bonding of the ruthenium, and the wafer of the dicing wafer film 1 〇 12 can be obtained in the following manner. Adhesive adhesives a (3") are crimped onto the I piece to hold it in place and secure it. The crimping can be carried out by the usual method. For bonded body parts, for example, a half-body wafer, a multi-layer substrate, and an integral sealing die scale can be used. In the present invention, a semiconductor wafer can be suitably used for being bonded to a moon bean or a workpiece. Then, as shown in Fig. 6, the workpiece is cut into a wafer shape. The same figure shows the profile of the profile. The dicing can be carried out at least until the crystal layer 3 (3', 3") is completely cut. For the adhesive layer 2 (7), i reaches: the kerf sub-blade 13 has a depth of cut to a predetermined value and does not I. Etch. The wafer is formed into a wafer-like workpiece (semiconductor wafer, etc.) by a method of rotating the circular knife "-de" to a workpiece including the adhesion layer 3 for wafer bonding in 200814172 ziyo^pir. Then, the wafer-like workpiece is attached to the workpiece of the adhesive bonding layer 3 for bonding the wafer, and the bonding 3a (or the adhesive bonding layer 3 for wafer bonding) is applied from the adhesive layer 2a of the adhesive layer 2 together. The wafer-shaped workpiece picked up is attached to the semiconductor element as a lion body via the workpiece attaching portion 3a #. The semiconductor element can be exemplified by a lead frame, a TAB film, a substrate, or a wafer-like film 1 The bonded body may be, for example, a deformable bonded body that is easily deformed, or a non-deformable type that is difficult to deform, (semiconductor day, etc.). The bonded body is suitable. It is a semiconductor wafer. When the adhesive layer 3, 3', 3" for the wafer bonding is in the case of a heat-hardening type, it is possible to heat-harden the workmanship, and to improve the resistance. Furthermore, (4) the adhesive bonding layer 3 for bonding the wafer is fixed to the substrate, and the remaining domains may be one (four)=pieces, * or :: lead sheets 1〇~12' to prevent adhesion or peeling, etc. At the time of production, etc.) (4) Calling method to give anti-static ability: suitable for supporting substrates, bonding for sheet bonding Layers 3, 3 ', 3 "= 2 adding the antistatic' method or crystal; attached to the support 1 on a substrate comprising," left foot ^ "film electrically conductive material layer and the like. These methods are preferably a mode in which the impurity ions of the composite or the metal wafer are deteriorated. ^ Produces a conductive substance that may be added under the purpose of semi-conductivity, etc. = = conductivity, improved metal oxidation of heat-transfer metal powder, etc.: silver, Ming, gold, steel, recorded, conductive human filler Listed in, prepared for M w ^ ^ 〇 to equal spherical, needle-like, graphite, etc. 32 200814172
VODpiT 以下,對本發明的適宜實施例加以例示性詳細說 但,本實施例中所記載的材料及添加量等,只要無特別限 定的記載,則本發明的範圍並非僅限於此等者,而僅 獨的說明例。 ^ (實施例1) • 於包含厚度為60 之聚乙烯薄膜的支持基材上,塗 . 布可藉由紫外線硬化的丙烯酸系黏著劑的溶液,並乾燥、 形成厚度為20 的黏著劑層。其後,經由遮罩,僅:晶 5 圓所貼附的部分照射500 mJ/cm2的紫外線,獲得包含該支 持基材及於晶圓上所貼附之部分被紫外線所硬化的黏著劑VODpiT Hereinafter, the preferred embodiments of the present invention will be described in more detail. However, the materials, the amounts of addition, and the like described in the examples are not limited thereto, and the scope of the present invention is not limited thereto. A unique example. ^ (Example 1) • On a support substrate comprising a polyethylene film having a thickness of 60, the cloth was dried by a solution of an ultraviolet-curable acrylic adhesive and dried to form an adhesive layer having a thickness of 20. Thereafter, only a portion of the crystal 5 circle is irradiated with ultraviolet rays of 500 mJ/cm 2 through the mask, and an adhesive containing the support substrate and the portion adhered to the wafer which is cured by ultraviolet rays is obtained.
層的黏著薄膜A。黏著劑層厚度的測定方法及紫外線的照 射條件述如下所述。 I 可紫外線硬化的丙烯酸系黏著劑的溶液的製備如下所 述。即,將70重量份的丙烯酸丁酯、3〇重量份的丙烯酸 乙酯及5重量份的丙烯酸於乙酸乙酯中以通常方法進行共 聚合,獲得重量平均分子量為80萬的丙烯酸系聚合物。其 次,於1〇〇重量份的該丙烯酸系聚合物中,添加0·5重量 ~ 份的多官能環氧化合物作為交聯劑、20重量份的二季戊四 、 醇單羥基五丙烯酸酯作為光聚合性化合物、1重量份的α_ 赵基環己基苯基酮作為光聚合引發劑,將此等均勻溶解於 作為有機溶劑的曱苯中,獲得濃度為3 〇重量%的丙烯酸系 黏著劑溶液。 於此,測定黏著薄膜Α於23°C的彈性模數。其結果為 3xl〇8 Pa。測定方法詳述如下。 33 200814172 -1 其二欠,樂1作曰y乐 量份的以丙騎妾用黏接劑層。即,相對於100重 酸I系聚合物(根上=基丙烯酸甲醋作為主成分的内烯 將3重量份的多官能里^份)製,Paracr0n w_ 197CM), 樹脂(日本 ^认酿糸交聯劑、23重量份的環氧 份的笨吩樹脂(=上股份)製’阳⑽1難),6重量 溶解於甲‘芙㈣學(股份)製,驗XLC_LL), 土乙基酮中,並將濃度調整為2〇重量%。 ο ο 對苯二^接齡成物溶液塗布於包含厚度為5G_的聚 Α。再者成尽度為2〇 晶片黏接用黏接劑層 進行^氧^==枝雜料m薄膜 ^ 刹的钻者溥胺Α上的黏著劑層側上,而獲得本竇 知例的切晶、黏晶片。 4只 (貫施例2 ) 本κ施例中,除使用以丙烯酸丁酯作為主成分的聚合 ^ (根上工業(股份)製,Paracron SN— 710)代替以丙 烯@义乙酯-甲基丙烯酸曱酯作為主成分的丙烯酸酯系聚合 ,,且將黏著薄膜A的厚度變更為30 μηι以外,以與上述 實施例1同樣的方式製作本實施例的切晶、黏晶片。 (實施例3) 於含有厚度為80 μηι的聚乙烯薄膜的支持基材上,塗 布可务、外線硬化的丙烯酸系黏著劑的溶液,並進行乾燥, 34 200814172 ^1^ϋ!>ρΐΐ 而形成厚度為70 的黏著劑層。其後’經由遮罩,僅於 晶圓所貼附的部分照射500 mJ/cm2的紫外線,獲得包含該 支持基材及於晶圓所貼附部分被紫外線硬化的黏著劑層的 黏著薄膜B。紫外線照射條件如下所述。 η ο 可紫外線硬化的丙烯酸系黏著劑的溶液的製備如下所 述。即,將包含5 0重量份的丙細酸乙S旨、5 0重量份的丙 烯酸丁酯、16重量份的丙烯酸2-羥基乙酯的添加組成物於 曱本溶液中進行共聚合’獲知重I平均分子量為5 〇萬的丙 烯酸系聚合物。 其次’相對於100重量份的該丙稀酸系聚合物,使2〇 重量份的異氰酸2-甲基丙烯醯氧基乙酯進行加成反應,於 來s物分子内側鍵導入碳炭雙鍵。該側鍵長度為13個原 =。相對於100重量份的該聚合物,進而添加\重量份的 多官能異氰酸酯系交聯劑,3重量份的苯乙酮系光聚合引 $劑,將此等均勻溶解於作為有機溶劑的甲苯中,而獲得 濃度為20重量〇/〇的上述丙烯酸系黏著劑溶液。 又 其結果為 7 凋疋黏者薄膜B於231的彈性模數 4xl〇7 Pa。再者,測定方法詳述如下。 =’除將厚度變更為1G 外,以與上述實施例 :樣的方式製作晶片黏接用黏接劑層A。繼而, 薄膜轉寫至包含上述丙烯酸系黏著劑的:著 (比較i Γ) ’而㈣本實施例的切晶、黏晶片。 μπι以外,以與上述實 除將黏著劑層的厚度設為100 35 200814172 晶、_占晶片 施例1同樣的方式製作該比較例的切 (比較例2) 除將黏著劑層的厚度設為3 _以外,以與上述實施 例3同樣的方式製作該比較例的切晶、黏晶片。 (比較例3) 士曰曰 〇 〇 含厚度為60 ,的聚乙烯薄膜的支持基材上,塗 布可I外線硬化的丙稀酸系黏著劑的溶液,並進行乾燥, 而形成厚度為3G_的黏著劑層。其後,經由遮罩,僅於 ==附部分照射500 mJ/cm2的紫外線,_衫鼓 晶圓所貼附之部分被紫外線硬化的黏著劑層的 黏者溥C。紫外線照射條件述於下。 、可i外線硬化的丙烯酸系黏著劑的溶液的製備如下所 述。即,將包含⑽重量份的丙烯酸丁酯與2重量份的丙 烯酸的單體混合物,使用曱笨2⑻重量份及G1重量份的 偶=異丁腈’藉由通常方法進行共聚合,獲得重量平均分 子i為'力30萬的丙烯酸系聚合物。#次’於⑽重量份的 該丙稀酸系聚合物中,添加G.5重量份的多官能環氧化合 物作為父聯劑、5重量份的二季戊四醇單經基五丙稀酸醋 作為f聚合性化合物、丨重量份的α_Μ基環已基苯基銅作 為光承&引發劑,將此等均勻溶解於作為有機溶劑的曱苯 中’而猹得濃度為3G重量%的上述丙雜系黏著劑溶液。 ,此’測定黏著薄膜C於23°C的彈性模數。其結果為 7x10 Pa。再者,測定方法詳述如下。 除將黏著劑層的厚度設為i μΐΏ以外,以與上述實施 200814172 似 pit 例1同樣的方式製作該比較例的切晶、黏晶片。 (比較例4) 於包含厚度為60 μπι的聚乙烯薄膜的支持基材上,塗 布可紫外線硬化的丙烯酸系黏著劑的溶液,並進行乾燥, 而形成厚度為30 μιη的黏著劑層。其後,經由遮罩,僅於 • 晶圓所貼附部分照射500 mJ/cm2的紫外線,獲得包含該支 • 持基材及於晶圓所貼附部分被紫外線硬化的黏著劑層的黏 著薄膜D。紫外線照射條件述於下。 可各外線硬化的丙烯酸系黏著劑的溶液的製備如下所 述。即,使用200重量份的甲苯及〇」重量份的偶氮異丁 腈二藉由通常方法與包含1〇〇重量份之曱基丙烯酸曱酯、5 重夏份之丙烯酸的單體混合物進行共聚合,獲得重量平均 分子量為40萬的丙烯酸系聚合物。其次,於1〇〇重量份的 該丙烯酸系聚合物中,添加3重量份的多官能環氧化合物 作為交聯劑、30重量份的二季戊四醇單羥基五丙稀酸酿作 為光聚合性化合物、3重f份的心減環己基苯基_為 U 光聚合引發劑,將此等均句溶解於作為有機溶劑的甲醇 中,而獲得濃度30重量%的上述丙烯酸系黏著劑溶液。 , 於此,測定黏著薄膜D於231的彈性模數。其結果為 8xl0]GPa。再者,測定方法詳述如下。 . 繼而使用黏著薄膜D,以與上述實施例1同樣的方式 製作該比較例的切晶、黏晶片。 (實施例4) 於包含厚度為60 μηι的聚乙烯薄膜的支持基材上,塗 37 200814172 ^ j yujnu 布可紫外線硬化的丙烯酸系黏著劑的溶液,並進行乾燥, 而形成厚度為10 μιη的黏著劑層。其後,經由遮罩,僅於 晶圓所貼附部分照射500 mJ/cm2之紫外線,獲得包含j亥支 持基材及於晶圓所貼附部分被紫外線硬化的黏著劑層的黏 著薄膜a。黏著劑層厚度的測定方法及紫外線照射條 下所述。 oAdhesive film A of the layer. The method for measuring the thickness of the adhesive layer and the irradiation conditions for ultraviolet rays are as follows. The preparation of a solution of an ultraviolet curable acrylic adhesive is as follows. Namely, 70 parts by weight of butyl acrylate, 3 parts by weight of ethyl acrylate, and 5 parts by weight of acrylic acid were copolymerized in ethyl acetate by a usual method to obtain an acrylic polymer having a weight average molecular weight of 800,000. Next, in an amount of 1 part by weight of the acrylic polymer, 0.5 to 5 parts by weight of a polyfunctional epoxy compound is added as a crosslinking agent, and 20 parts by weight of dipentaerythritol or an alcohol monohydroxypentaacrylate is used as light. The polymerizable compound and 1 part by weight of α-radiocyclohexyl phenyl ketone were used as a photopolymerization initiator, and these were uniformly dissolved in toluene as an organic solvent to obtain an acrylic pressure-sensitive adhesive solution having a concentration of 3 〇% by weight. Here, the elastic modulus of the adhesive film enthalpy at 23 ° C was measured. The result is 3xl 〇 8 Pa. The measurement method is detailed below. 33 200814172 -1 The second is owed, and the music is used as a layer of adhesive for the C. That is, it is made of 100 parts by weight of the acid I-based polymer (3 parts by weight of the polyene in the internal olefin as the main component), Paracr0n w_ 197CM), and the resin (Japan) The joint agent, 23 parts by weight of the epoxy part of the phenophene resin (= the upper share) made 'yang (10) 1 difficult), 6 parts dissolved in the 'fu (four) school (share) system, test XLC_LL), earth ethyl ketone, The concentration was adjusted to 2% by weight. ο ο The solution of the benzoate compound is coated on a polycrystalline ruthenium having a thickness of 5G_. Furthermore, the adhesiveness layer of the 2 〇 wafer bonding adhesive layer is performed on the side of the adhesive layer on the driller's amidoxime, and the sinus is known. Cut crystal, sticky wafer. 4 (Centre Example 2) In the κ application, except for the polymerization using butyl acrylate as a main component (Paracron SN-710, manufactured by Gensei Industrial Co., Ltd.) instead of propylene@yiethyl-methacrylic acid The diced or bonded wafer of this example was produced in the same manner as in the above Example 1 except that the oxime ester was polymerized as the main component and the thickness of the adhesive film A was changed to 30 μm. (Example 3) A solution of a virgin-curable acrylic adhesive was applied to a support substrate containing a polyethylene film having a thickness of 80 μm, and dried, 34 200814172 ^1^ϋ!> An adhesive layer having a thickness of 70 is formed. Thereafter, ultraviolet rays of 500 mJ/cm 2 were irradiated only to the portion to which the wafer was attached via the mask, and the adhesive film B including the support substrate and the adhesive layer which was cured by ultraviolet rays on the portion to which the wafer was attached was obtained. The ultraviolet irradiation conditions are as follows. The preparation of a solution of η ο ultraviolet curable acrylic adhesive is as follows. That is, an additive composition containing 50 parts by weight of propionic acid B, 50 parts by weight of butyl acrylate, and 16 parts by weight of 2-hydroxyethyl acrylate was copolymerized in a sputum solution. An acrylic polymer having an average molecular weight of 50,000. Next, 'with respect to 100 parts by weight of the acrylic acid polymer, 2 parts by weight of 2-methylpropenyloxyethyl isocyanate is subjected to an addition reaction, and carbon carbon is introduced into the inner side of the s molecule. Double key. The side key length is 13 original =. Further, with respect to 100 parts by weight of the polymer, a part by weight of a polyfunctional isocyanate crosslinking agent and 3 parts by weight of an acetophenone-based photopolymerization agent are added, and these are uniformly dissolved in toluene as an organic solvent. The above acrylic adhesive solution having a concentration of 20% by weight of rhodium was obtained. The result is 7 elastic modulus of the film B at 231 4xl 〇 7 Pa. Furthermore, the measurement method is described in detail below. =' The adhesive layer A for wafer bonding was produced in the same manner as in the above embodiment except that the thickness was changed to 1 G. Then, the film is transferred to the above-mentioned acrylic adhesive: (Comparative i Γ)' and (4) the diced or bonded wafer of this embodiment. In the same manner as in the above, the thickness of the adhesive layer was set to 100 35 200814172 crystal, and the same as in the wafer application example 1 (Comparative Example 2) except that the thickness of the adhesive layer was set to be the same as μπι. A diced or bonded wafer of this comparative example was produced in the same manner as in the above Example 3 except for _. (Comparative Example 3) On a support substrate of a polyethylene film having a thickness of 60 Å, a solution of an externally-cured acrylic adhesive was applied and dried to form a thickness of 3 G_. Adhesive layer. Thereafter, ultraviolet rays of 500 mJ/cm2 were irradiated only through the mask at the portion of the mask, and the portion of the adhesive layer adhered to the ultraviolet ray was adhered to the adhesive layer. The ultraviolet irradiation conditions are described below. A solution of an acrylic adhesive which can be cured by an external wire is prepared as follows. That is, a monomer mixture containing (10) parts by weight of butyl acrylate and 2 parts by weight of acrylic acid is copolymerized by a usual method using a mixture of 2 (8) parts by weight and G1 parts by weight of 'iso-butyronitrile' to obtain a weight average. The molecule i is an acrylic polymer having a force of 300,000. #次的(10) parts by weight of the acrylic acid polymer, adding 5 parts by weight of a polyfunctional epoxy compound as a parent crosslinking agent, and 5 parts by weight of dipentaerythritol monopyridyl propylene vinegar as f The polymerizable compound, ruthenium by weight of α-fluorenylcyclohexylphenyl copper as a light-supporting & initiator, uniformly dissolved in toluene as an organic solvent, and obtained a concentration of 3 g% by weight of the above-mentioned acrylic Adhesive solution. This measured the elastic modulus of the adhesive film C at 23 °C. The result is 7x10 Pa. Furthermore, the measurement method is described in detail below. The dicing wafer or the adhesive wafer of this comparative example was produced in the same manner as in the above-described embodiment of 200814172, except that the thickness of the adhesive layer was i μΐΏ. (Comparative Example 4) A solution of an ultraviolet curable acrylic adhesive was applied to a support substrate comprising a polyethylene film having a thickness of 60 μm, and dried to form an adhesive layer having a thickness of 30 μm. Thereafter, an ultraviolet ray of 500 mJ/cm 2 is irradiated only to the portion to be attached to the wafer via the mask, and an adhesive film including the support substrate and the adhesive layer which is cured by ultraviolet rays on the attached portion of the wafer is obtained. D. The ultraviolet irradiation conditions are described below. The preparation of a solution of an externally hardened acrylic adhesive is as follows. That is, 200 parts by weight of toluene and hydrazine by weight of azoisobutyronitrile were used in common by a monomer mixture containing 1 part by weight of decyl methacrylate and 5 parts by weight of acrylic acid. Polymerization was carried out to obtain an acrylic polymer having a weight average molecular weight of 400,000. Next, 3 parts by weight of a polyfunctional epoxy compound is added as a crosslinking agent, and 30 parts by weight of dipentaerythritol monohydroxypentaacrylic acid is added as a photopolymerizable compound to 1 part by weight of the acrylic polymer. 3 parts by weight of heart-reduced cyclohexylphenyl group was a U-photopolymerization initiator, and these uniform terms were dissolved in methanol as an organic solvent to obtain a 30% by weight of the above acrylic-based pressure-sensitive adhesive solution. Here, the elastic modulus of the adhesive film D at 231 was measured. The result is 8xl0]GPa. Furthermore, the measurement method is described in detail below. Then, using the adhesive film D, the crystal-cut and sticky wafer of this comparative example was produced in the same manner as in the above Example 1. (Example 4) On a support substrate comprising a polyethylene film having a thickness of 60 μm, a solution of an ultraviolet-curable acrylic adhesive of 37 200814172 ^ j yujnu was applied and dried to form a thickness of 10 μm. Adhesive layer. Thereafter, ultraviolet rays of 500 mJ/cm2 were irradiated only to the portion to which the wafer was attached via the mask, and an adhesive film a containing the adhesive layer of the substrate supported on the wafer and the ultraviolet-cured portion adhered to the wafer was obtained. The method for measuring the thickness of the adhesive layer and the ultraviolet irradiation strip are as described below. o
、、」糸外踝硬化的丙烯酸系黏著劑的溶液的製備如下 ΐ西’將70重量份的丙稀酸丁酉旨、30錄份的丙稀酸 量份的丙騎於乙酸乙自旨中以通常方法進行共 =亍直里十均刀子里為80萬的丙稀 ^於_重量份之該丙烯酸系聚合物中 勿: 伤的多官能環氧化合物作為二· 醇單經基五_酸酉旨作為^2G重讀的二季戊四 黏著劑溶液。 X侍/辰度18重量。/。的丙烯酸系 於此,測定黏著薄膣 8xl〇6Pa。再者,測定方、於、23°C的彈性模數。其結果為 其次,製作晶片黏接1迷如下。 量份的以丙烯酸乙酯_曱站接劑層。即,相對於100重 酸酯系聚合物(根上工土丙烯酸曱酯作為主成分的丙烯 197C]V[),將3重量份的夕業(股份)製,Paracron W〜 量份的環氧樹脂(日;^環f 了能異氰酸酯系交聯劑、23重 6重量份的苯酚樹腊长孔樹脂(股份〕製,Epicoat 10〇4〕、 曰二井化學(股份)製,Milex 200814172 vo^pir irL),溶解於甲基乙_,並將濃度調整為2〇重 苯二=接=溶液r於包含厚度為的對The preparation of the solution of the externally hardened acrylic adhesive is as follows: 70 parts by weight of butyl acrylate, 30 parts of acrylic acid in the amount of C The method is carried out in a total of 80 里 里 十 为 为 为 为 为 于 于 于 于 于 于 于 于 于 于 于 于 于 于 于 于 于 于 于 : : : : : : : : : : : : : : : : : : A dipentaerythritol solution as a ^2G reread. X wait / Chen degree 18 weight. /. The acrylic was used here to measure the adhesion of the thin layer 8xl〇6Pa. Further, the modulus of elasticity at 23 ° C was measured. As a result, the fabrication of the wafer bonding 1 is as follows. The parts are in the form of ethyl acrylate. In other words, with respect to the 100-weight acid ester-based polymer (propylene 197C]V[) having a ruthenium acrylate as a main component, 3 parts by weight of the epoxy resin of Paracron W~ parts (Japanese; ^ ring f can be isocyanate cross-linking agent, 23 parts by weight of 6 parts by weight of phenol tree wax long hole resin (shares), Epicoat 10〇4], 曰二井化学(股份), Milex 200814172 vo^pir irL), dissolved in methyl ethyl _, and adjusted to a concentration of 2 〇 heavy benzene = = solution r in a pair containing thickness
夂自日溥胺的脫模處理 j3TDetachment treatment of nicotinamide j3T
下乾燥3分鐘,形成 、/、後,於12〇〇C v战y子度為2〇 pm的晶]m a。再者,脱握声:ί田# ^接用黏接劑屬 丹有蛛處理缚膜是使用於 μ 進行聚矽氧脫模處理者。 γ敲乙一知缚臈上 n o 繼而,將晶片黏接 η 酸系黏著劑之Λ伐s a和舄至包含上述丙烯 有刹之黏者溥腠A上的黏著劑層上, , 例的切晶、黏晶片。 而後件本貫施 (實施例5 ) 於本實施例中,除使用以丙稀酸 合物(根上工章(則制D "曰作為主成分的聚 丙烯酸乙,甲上九製 。n SN—71°)代替以 -物上Ϊ: 甲醋作為主成分的丙稀酸醋系聚 :及將黏者劑層厚度變更為3〇 μιη以外,以盥上述命 “列4,的方式製作本實施例的切晶、黏晶片。Λ (實施例6) 右^包含厚度為叫111的聚乙烯薄膜的支持基材上,塗 線硬化的丙烯酸系黏著劑的溶液,並進行乾燥了 :形成厚度為70 μηι的黏著劑層。其後,經由遮罩,僅於 曰㈡所貼附部分照射5〇〇 mJ/cm2的紫外線,獲得包含該支 ,^材及於晶圓所貼附部分被紫外線硬化的黏著劑層的黏 著薄膜b。紫外線照射條件如下所述。 】 可紫外線硬化的丙烯酸系黏著劑的溶液的製備如下所 39 200814172 厶 1 jpil 述。即,將包含 里置份的丙烯明、%舌旦八 烯酸丁醋、16重量份的丙雜2_經基乙 里^的兩 曱苯溶液中進行共聚合,而獲得重量平均分子 1失且成物於 丙烯酸系聚合物。 子里為5〇萬的 其次,相對於100重量份的該丙稀 重量份的異氰酸2-甲基丙_氧基乙使20 ηDry for 3 minutes, form, /, after, at 12 ° C v war y sub-degree of 2 〇 pm crystal] m a. In addition, the disengagement sound: 田田# ^ Use adhesive agent 丹 has a spider treatment of the binding film is used in μ for poly-oxygen release treatment. γ 乙 一 一 一 no no no no no no , , , , , , , , , , , , , , , , , , , , , , , 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片 晶片Sticky wafer. The latter part is applied (Example 5) in this example, except that the acrylic acid compound is used (the root of the work chapter (the D " 制 as the main component of the polyacrylic acid B, the ninth system. n SN -71°) In place of the 物 Ϊ Ϊ 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙 丙The dicing and sticky wafer of the example. 实施 (Example 6) A solution containing a line-hardened acrylic adhesive on a support substrate of a polyethylene film having a thickness of 111, and dried: forming a thickness It is a layer of adhesive of 70 μηι. Thereafter, only 5 〇〇mJ/cm 2 of ultraviolet light is irradiated through the mask to the portion to which the ruthenium (2) is attached, and the portion to be attached to the wafer is exposed to ultraviolet rays. Adhesive film b of the cured adhesive layer. The ultraviolet irradiation conditions are as follows. 】 The solution of the ultraviolet-curable acrylic adhesive is prepared as follows: 200814172 厶1 jpil, that is, the propylene containing the inner portion, % succinic acid butyl vinegar, 16 parts by weight of propylene 2 _ base Copolymerization is carried out in a solution of bismuth benzene, and a weight average molecule of 1 is obtained, and the product is obtained from an acrylic polymer. The amount of 5% in the sub-particle is the next, and the difference is 100 parts by weight relative to the weight of the propylene. 2-methylpropoxy-oxyl cyanate makes 20 η
聚合物分子内侧鏈導人碳·錢鍵。該側鏈於 子。相對於100 f量份的該聚合物,進、又「個原 多官能異氰酸料交聯劑、3重量份的笨 發劑,將此等均勾溶解於作為有機 J先:二弓丨 濃度為27 的上述丙烯酸系黏著劑溶液。中而後得 於此’測定黏著薄膜b於23。〇的彈 盆 3xl05Pa。再者’測定方法詳述如下。 …、、°果為 ,人’〜、上述實闕4同樣的方式製作晶片黏接用 減劑層a,繼而,將晶片黏接用黏接劑層&轉寫人The inner chain of the polymer molecule leads to the carbon and money bond. The side chain is in the sub. With respect to 100 f parts of the polymer, the "original polyfunctional isocyanate cross-linking agent, 3 parts by weight of the stupid agent" are dissolved in the organic J first: two bows The above-mentioned acrylic adhesive solution having a concentration of 27 is obtained from the above, and the adhesive film b is measured at 23 〇 of the bomb pot 3xl05Pa. Further, the measurement method is described in detail as follows: ..., °, fruit, human '~, In the same manner as in the above, the wafer bonding reducing layer a is produced in the same manner, and then the bonding layer for the bonding of the wafers &
亡述丙稀酸系黏著劑之黏著薄膜A上的黏著劑層側上,= 獲得本實施例的切晶、黏晶片。 O (比較例5) 除將黏著劑層厚度設為100 μηι以外,以與上述實施 例4同樣的方式製作該比較例的切晶、黏晶片。 、 (比較例6) 於包含厚度為60 μηι的聚乙烯薄膜的支持基材上,塗 布可紫外線硬化的丙烯酸系黏著劑的溶液,並進行乾燥, 而形成厚度為3〇 μ1Ώ的黏著劑層。其後,經由遮罩,僅於 40 200814172On the side of the adhesive layer on the adhesive film A of the acrylic acid adhesive, the dicing and sticking wafer of the present embodiment were obtained. O (Comparative Example 5) A diced or bonded wafer of the comparative example was produced in the same manner as in the above Example 4 except that the thickness of the adhesive layer was changed to 100 μm. (Comparative Example 6) A solution of an ultraviolet curable acrylic adhesive was applied onto a support substrate comprising a polyethylene film having a thickness of 60 μm, and dried to form an adhesive layer having a thickness of 3 μm. Thereafter, via the mask, only 40 200814172
I 晶圓所貼附部分照射500 mJ/cm2的紫外線,獲得包含該t 持基材及於晶圓所貼附部分被紫外線硬化的黏著劑層的點 著薄膜c。紫外線照射條件如下所述。 4 o u 可紫外線硬化的丙烯酸系黏著劑的溶液的製備如下戶斤 述。即’使用200重量份的曱苯及0.1重量份的偶氣異丁 腈以通常方法與包含1〇〇重量份的丙烯酸曱酯、2重量八 的丙酸的單體混合物進行共聚合,而獲得重量平均分子 量為30萬的丙烯酸系聚合物。其次,於1〇〇重量份的該 烯酸系聚合物中,添加〇·5重量份的多官能環氧化合物作 為父聯劑、5重量份的二季戊四醇單羥基五丙烯酸酯作為 光聚合性化合物、1重量份的.羥基環己基苯基酮作為光 聚合引發劑,將此等均勻溶解於作為有機溶劑的甲笨中, 而獲得〉辰度30重量%的上述丙烯酸系黏著劑溶液。 於此,測定黏著薄膜〇於23°C的彈性模數。其結果為 3xK)3 Pa。再者,測定方法詳述於下。 一 、其次,使用黏著薄膜c,以與上述實施例1同樣的方 式製作該比較例的切晶、黏晶片。 (比較^列7) 。方;包含厚度為6〇 μΐγι的聚乙烯薄膜的支持基材上,塗 可紫外線硬化的丙烯酸系黏著劑的溶液,並進行乾燥, 2形成厚度為30 μηι的黏著劑層。其後,經由遮罩,僅於 所貼附部分照射500 mJ/cm2的紫外線,獲得包含該支 * = ^及於晶圓所貼附部分被紫外線硬化的黏著劑層的黏 耆溽瞑d。紫外線照射條件如下所述。 41 200814172 21965pif 可紫外線硬化的丙稀酸系黏著劑的溶液的製備如下所 述。即,使用200重量份的甲苯及Ο·!重量份的偶氮異丁 腈以通常方法與包含1〇〇重量份的丙烯酸甲酯、5重量严 的丙細酸的單體混合物進行共聚合,而獲得重量平均分子 量為40萬的丙烯酸系聚合物。其次,於100重量份的該丙 烯酸系聚合物中,添加3重量份的多官能環氧化合物作為 ' 交聯劑、30重量份的二季戊四醇單羥基五丙烯酸酯作為光 、 聚合性化合物、3重量份的α-羥基環己基苯基酮作為光聚 f 合引發劑,將此等均勻溶解於作為有機溶劑的曱醇中,獲 得濃度27重量%的上述丙烯酸系黏著劑溶液。 於此’測定黏著薄膜d於23 C的彈性模數。其結果為 5 X1 〇1Q P a。再者’測定方法詳述於下。 其次,使用黏著薄膜d,以與上述實施例4同樣的方 式製作該比較例的切晶、黏晶片。 (切晶及拾取) 使用實施例1〜6以及比較例1〜7的各切晶、黏晶片, 〇 按以下要領,實際進行半導體晶圓的切晶、黏晶,並評價 各切晶、黏晶片的性能。 、 對形成電路圖案的半導體晶圓(直徑為8英吋,厚度 為0.6 mm)進行背面研磨處理,並使用厚度為〇· 15 mm的 鏡面晶圓(mirror wafer)作為工件。磨光裝置是使用DISCO 公司製造的DFG — 840 (商品名)。將該鏡片晶圓於各自之 切晶、黏晶片上,於40°C下進行輥壓接並貼合,進而進行 切晶。貼合是使用日東精機(股份)製造的晶圓貼合裝置 42 200814172 /ivtopir (DR—8500)。又,士曰 晶 的片尺寸的方式進行全日二以成為5 mm邊長的正方形 體晶圓及切晶、黏晶片刀:。針對切斷後的半導 察方法及切晶條件詳述於;了、有热絲狀屬。絲狀屑的觀 步驟。進而,自各:=:¾ ,並進行飛片及拾取針 调查所拾取的晶片有無碎屑。败方法 又, »著劑層厚度的測定方法] 所述。 黏著劑層厚度的測定是藉由· gauge)進行。 T泌里執(dial [紫外線照射條件] 紫外線(UV)照射裝置:Ν;ΕΧΜ-11〇 精機(股份)製) 同。口名,曰東 u 紫外線照射累計光量:500 mJ/cm2 [彈性模數的測定方法] 彈性模數是使用Rheometric公司製造的觀 _ 定儀(商品名:RSA- Π )進行測定。測定條::頻令剛 1 Hz、樣品厚度為2 mm、壓接加重為10〇 g,升π ^率為 5〇C/min,於⑼艺〜2〇〇。〇的範圍内,取於2 二卜度為 [切晶條件] 值。 切晶裝置:DFD —651 (商品名,DISCO公司勢) 切晶速度:8〇mm/sec 43 200814172 21965pif 公司製) 切割刀片:2050HECC (商 旋轉數:40,000 rpm 對切晶、黏晶片的切入深度:μη (參照圖6) 切割方式:全切割、A模式 晶片尺寸·· 5 mm邊長的正方形 [絲狀屑的觀察方法] 〇The portion to which the wafer is attached is irradiated with ultraviolet rays of 500 mJ/cm2 to obtain a film c containing the adhesive layer of the t-holding substrate and the portion adhered to the wafer by ultraviolet rays. The ultraviolet irradiation conditions are as follows. The preparation of a solution of 4 o u ultraviolet-curable acrylic adhesive is as follows. That is, '200 parts by weight of toluene and 0.1 parts by weight of azo isobutyronitrile are copolymerized in a usual manner with a monomer mixture containing 1 part by weight of decyl acrylate and 2 parts by weight of propionic acid. An acrylic polymer having a weight average molecular weight of 300,000. Next, 5 parts by weight of a polyfunctional epoxy compound as a parent binder and 5 parts by weight of dipentaerythritol monohydroxypentaacrylate are added as a photopolymerizable compound to 1 part by weight of the olefinic polymer. 1 part by weight of a hydroxycyclohexyl phenyl ketone was used as a photopolymerization initiator, and these were uniformly dissolved in a ruthenium as an organic solvent to obtain an acrylic pressure-sensitive adhesive solution having a density of 30% by weight. Here, the elastic modulus of the adhesive film enthalpy at 23 ° C was measured. The result is 3xK)3 Pa. Furthermore, the measurement method is described in detail below. First, using the adhesive film c, the crystal-cut and sticky wafer of this comparative example was produced in the same manner as in the above-described Example 1. (Compare ^ column 7). A solution of a UV-curable acrylic adhesive was applied to a support substrate comprising a polyethylene film having a thickness of 6 μ μ μm, and dried to form an adhesive layer having a thickness of 30 μm. Thereafter, ultraviolet rays of 500 mJ/cm2 were irradiated only to the attached portion via the mask, and a tack d including the adhesive layer of the portion * = ^ and the portion adhered to the wafer by the ultraviolet rays was obtained. The ultraviolet irradiation conditions are as follows. 41 200814172 21965 pif The preparation of a UV curable acrylic adhesive is as follows. That is, 200 parts by weight of toluene and hydrazine parts by weight of azoisobutyronitrile are copolymerized in a usual manner with a monomer mixture containing 1 part by weight of methyl acrylate and 5 parts by weight of propionic acid. An acrylic polymer having a weight average molecular weight of 400,000 was obtained. Next, in 100 parts by weight of the acrylic polymer, 3 parts by weight of a polyfunctional epoxy compound is added as a 'crosslinking agent, and 30 parts by weight of dipentaerythritol monohydroxypentaacrylate is used as a light, a polymerizable compound, and 3 parts by weight. The α-hydroxycyclohexyl phenyl ketone was used as a photopolymerization initiator, and these were uniformly dissolved in decyl alcohol as an organic solvent to obtain a 27% by weight of the above acrylic pressure-sensitive adhesive solution. Here, the elastic modulus of the adhesive film d at 23 C was measured. The result is 5 X1 〇1Q P a. Further, the measurement method is described in detail below. Next, using the adhesive film d, the diced and bonded wafer of this comparative example was produced in the same manner as in the above-mentioned Example 4. (Cut-graining and pick-up) Using each of the dicing crystals and the adhesive wafers of Examples 1 to 6 and Comparative Examples 1 to 7, dicing and die-molding of the semiconductor wafer were carried out in the following manner, and each of the crystal cutting and adhesion was evaluated. The performance of the wafer. A semiconductor wafer (with a diameter of 8 inches and a thickness of 0.6 mm) forming a circuit pattern was subjected to back grinding treatment, and a mirror wafer having a thickness of 〇·15 mm was used as a workpiece. The polishing device is DFG-840 (trade name) manufactured by DISCO. The lens wafers were placed on respective diced and bonded wafers, and rolled and bonded at 40 ° C to perform dicing. The bonding is a wafer bonding apparatus manufactured by Nitto Seiki Co., Ltd. 42 200814172 /ivtopir (DR-8500). In addition, the film size of the gem crystal is carried out on a full-day basis to form a square wafer with a length of 5 mm and a diced, bonded wafer cutter: The semi-descriptive method and the dicing conditions after the cutting are detailed, and there is a filamentous genus. The observation of filamentous debris. Further, from each: =: 3⁄4, and the wafer picked up by the flying piece and the pick-up needle was investigated for the presence or absence of debris. The method of defeating is also described in the method of measuring the thickness of the coating layer. The thickness of the adhesive layer was measured by a gauge. T secretion control (dial [ultraviolet irradiation conditions] ultraviolet (UV) irradiation device: Ν; ΕΧΜ-11〇 fine machine (share) system). The name of the mouth, 曰东 u The cumulative amount of ultraviolet light: 500 mJ/cm2 [Method for measuring the modulus of elasticity] The modulus of elasticity is measured using a calibrator (trade name: RSA- Π) manufactured by Rheometric. Measuring strip:: frequency is just 1 Hz, sample thickness is 2 mm, crimping weight is 10 〇 g, π φ is 5 〇 C / min, at (9) art ~ 2 〇〇. In the range of 〇, take 2 2 degrees as the [Cutting condition] value. Cleavage device: DFD — 651 (trade name, DISCO company potential) Crystal cutting speed: 8〇mm/sec 43 200814172 21965pif company) Cutting blade: 2050HECC (commercial rotation number: 40,000 rpm tangential depth of dicing and bonding wafer :μη (Refer to Fig. 6) Cutting method: full-cut, A-mode wafer size·· Square with 5 mm side length [Method of observing filamentous chips] 〇
U 將包括所切斷的半導體晶圓的中心線的左右3庐 (合計7條線)以光學顯微鏡⑼倍)進行觀察,叶^ 於等於10 _的長絲狀屬的個數(參照圖4) 察是於半導體晶片的表面及_,及m 斷的線近傍的表面上進行。 乃0所切 [延伸條件] cm 切晶環:2 —8_1 (商品名、DISCO公司製,内徑19 5 切除量:5 mm 黏晶機(die bonder) : SPA〜3〇〇 (商 新川製) [碎屑評價方法] ^曰曰曰後,,拾取(剝離)5〇個任意半導體晶片 月ΐ i’ f察半導體晶片侧面的碎屑。以三角形狀的晶片碎片 作為碎屑進行觀察,並計數大於等於2()叫尺寸者。T [拾取性評價] 石割的5mmx5mm正方形的半導體晶片時, 霍⑽+ V胜晶片底面是否附著有黏著劑。再者,於拾取時, 44 200814172 z 1 將於80 WW的高壓水銀燈下放置了〗◦秒鐘 放射線硬化後,進彳f拾取。其結果是,將無=,層 完成,可拾取的情形設為。,產生破損、缺損=員而 誤之情形設為X,而進行評價。 、次心取錯 (結果) ' 如自下述表1以及表2可知,於實施例1〜6中 :到絲狀屑’於比較例2中,任意處均觀“ o o 、關於碎屑,其雖於實施例3及4中產生了若干個 f於晶片性能上可使用的狀態。於實施例1、2、4及5二 几全未產生碎屑,較為良好。另一方面,於比較例丨、3、 4 5,6中可觀察到碎屑的產生,為晶片性能上無法使用 ,狀態。又,關於產生飛片,於各實施例中完全未觀察到, 可確認其具有用於固定半導體晶片的充分黏著力。另'一方 面,,比較例4中可觀察到多次飛片,可確認其黏著劑層 的黏著力不足。又,比較例7的切晶、黏晶片*可貼 晶環,因而無法進行切晶。 *由此等試驗結果亦可明暸,若黏著劑層較薄,則藉由 =刦刀片切斷支持基材,容易產生絲狀屑。另一方面,如 厚度過厚,則會產生碎屑,並可確認半導體品位顯著下降。 45 200814172U. The left and right 3庐 (total 7 lines) including the center line of the cut semiconductor wafer are observed by an optical microscope (9 times), and the number of filaments of the leaf is equal to 10 _ (refer to FIG. 4). The inspection is performed on the surface of the semiconductor wafer and on the surface of the _, and m-break line. It is cut by 0 [extension condition] cm dicing ring: 2 - 8_1 (trade name, manufactured by DISCO, inner diameter 19 5 removal amount: 5 mm die bonder: SPA~3〇〇 (Shangxinchuan system [Debris evaluation method] ^, after picking up (peeling) 5 任意 arbitrary semiconductor wafers ΐ ' 察 察 察 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体Counting is greater than or equal to 2 () called the size. T [Pickup evaluation] When cutting a 5mm x 5mm square semiconductor wafer, Huo (10) + V wins the bottom of the wafer with adhesive attached. Furthermore, at the time of picking, 44 200814172 z 1 Under the high-pressure mercury lamp of 80 WW, the radiation is hardened by the second, and then the 彳f is picked up. As a result, there will be no =, the layer is completed, and the pick-up situation is set. The damage is generated, and the defect is wrong. In the case where the case is X, the evaluation is performed. The second center error is taken (result). As can be seen from Tables 1 and 2 below, in Examples 1 to 6: the filamentous chips are in any of Comparative Example 2. Looking at "oo, about debris, which produced several f in Examples 3 and 4 The state in which the performance of the wafer can be used. It is good that no debris is generated in the first, second, fourth, and fifth embodiments. On the other hand, the crumb can be observed in the comparative examples 3, 3, 45, and 6. The generation is incapable of using the state of the wafer, and further, regarding the generation of the flying sheet, it is not observed at all in the examples, and it is confirmed that it has sufficient adhesion for fixing the semiconductor wafer. On the other hand, comparison In Example 4, a plurality of flyers were observed, and it was confirmed that the adhesiveness of the adhesive layer was insufficient. Further, the crystal cut and the adhesive wafer* of Comparative Example 7 could be attached to the crystal ring, and thus the crystal cutting could not be performed. As a result, it is also clear that if the adhesive layer is thin, the support substrate is cut by the robbing blade, and filamentous chips are easily generated. On the other hand, if the thickness is too thick, chipping occurs, and the semiconductor grade can be confirmed. Significant decline. 45 200814172
Vb!>pit [表l] 實施例1 貫施例2 實施例3 比較例1 比較例2 比較例3 比較例4 黏著劑層之厚度(μπι) 20 30 70 100 3 30 30 彈性模數(Pa) 3χ108 3xlQ8 4χ107 3χ108 3χ108 7χ105 8χ1〇10 晶片黏接用黏接劑之厚度 20 (m) 20 10 20 20 20 20 晶片表面的絲狀屑數(個) 0 0 0 0 30 0 0 晶片背面的絲狀屑數(個) 0 0 0 0 17 0 0 切晶、黏晶片表面的絲狀屑 數(個) 0 0 0 0 120 0 0 最大晶片缺損個數(個/50 0 個) 0 2 35 0 48 26 _產生飛片(個/50個) 0 0 0 0 0 0 35 拾取性(一) 〇 〇 〇 〇 〇 X 〇 [表2] 著劑層之厚唐 彈性模數(Pa) H翌接用黏接劑之厚度(um) ~ίΑ表面的絲狀屑數(個) 晶片缺損個數(個) 實施例4 10 8χ1〇6 20 實施例5 30 8χ106 20 實施例6 70 3χ105 比較例. 100 3χ106 20 35 比較例6 30 3χ103 20 48 比較例 30 5χ1010 20 無法切晶 【圖式簡單說明】 黏晶片的一個實施例的剖 晶 圖1疋顯示本發明的切 面模式圖。 雜驗朗·11述的黏著劑層*曰片 面模式圖,x明的切晶、黏晶片的其它實施例的剖 切二晶,—半導體晶圓及 46 200814172 vo^pir 圖5是顯示本發明的切晶、黏晶片的進而其他實施例 的剖面模式圖。 圖6是顯示將工件切晶成晶片狀時的情形的剖面模式 圖。 【主要元件符號說明】 1 :支持基材 • 2、2Π :黏著劑層 2a:工件貼附部分所對應的部分 〇 2b :工件貼附部分以外部分一部分或者全部所對應的 部分 2b’ :切晶環貼附部分所對應的部分 3、31、3” :晶片黏接用黏接劑層 3a :工件貼附部分 3b’ :切晶環貼附部分 3b :工件貼附部分以外的部分 4 :保護層 I: 10、Η、12 :黏晶片 13 :切割刀片 - A : 3a所對應的界面 B : 3b所對應的界面 B’ : 3b’所對應的界面 47Vb!>pit [Table 1] Example 1 Example 2 Example 3 Comparative Example 1 Comparative Example 2 Comparative Example 3 Comparative Example 4 Thickness of the adhesive layer (μπι) 20 30 70 100 3 30 30 Elastic modulus ( Pa) 3χ108 3xlQ8 4χ107 3χ108 3χ108 7χ105 8χ1〇10 Thickness of adhesive for wafer bonding 20 (m) 20 10 20 20 20 20 Number of filaments on the surface of the wafer (0) 0 0 0 0 30 0 0 On the back of the wafer Number of filaments (0) 0 0 0 0 17 0 0 Number of filaments on the surface of the diced and bonded wafers (0) 0 0 0 0 120 0 0 Maximum number of wafer defects (number / 50 0) 0 2 35 0 48 26 _Generating flying pieces (one/50 pieces) 0 0 0 0 0 0 35 Picking property (1) 〇〇〇〇〇X 〇[Table 2] Thickness of the coating layer Tang elastic modulus (Pa) H翌Thickness of adhesive used (um) ~ Number of filamentous chips on the surface (number) Number of wafer defects (number) Example 4 10 8χ1〇6 20 Example 5 30 8χ106 20 Example 6 70 3χ105 Comparative Example. 100 3χ106 20 35 Comparative Example 6 30 3χ103 20 48 Comparative Example 30 5χ1010 20 Cannot be crystallized [Simplified drawing] Cross-section crystal 1 of one embodiment of the adhesive wafer Display tangential plane schematic view of the present invention. Miscellaneous test layer 11 曰 面 面 模式 , , , , , , , , , 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 、 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体 半导体A cross-sectional schematic view of another embodiment of a diced, viscous wafer. Fig. 6 is a schematic cross-sectional view showing a state in which a workpiece is crystallized into a wafer shape. [Main component symbol description] 1 : Support substrate • 2, 2Π: Adhesive layer 2a: Part corresponding to the workpiece attachment part 〇2b: Part or all of the part 2b' other than the workpiece attachment part: Cleavage Portion 3, 31, 3" corresponding to the ring attachment portion: adhesive layer 3a for wafer bonding: workpiece attachment portion 3b': dicing ring attachment portion 3b: portion other than the attachment portion of the workpiece 4: protection Layer I: 10, Η, 12: adhesive wafer 13: cutting blade - A: interface corresponding to 3a B: interface corresponding to 3b interface B': 3b' corresponding to interface 47
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JP5367990B2 (en) * | 2008-01-25 | 2013-12-11 | リンテック株式会社 | Laser dicing sheet and chip body manufacturing method |
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JP2009260332A (en) * | 2008-03-26 | 2009-11-05 | Furukawa Electric Co Ltd:The | Adhesive tape with antistatic property for fixing semiconductor wafer |
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