TW202202587A - Adhesive sheet for semiconductor device production and method for producing semiconductor device using same - Google Patents

Adhesive sheet for semiconductor device production and method for producing semiconductor device using same Download PDF

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TW202202587A
TW202202587A TW110118522A TW110118522A TW202202587A TW 202202587 A TW202202587 A TW 202202587A TW 110118522 A TW110118522 A TW 110118522A TW 110118522 A TW110118522 A TW 110118522A TW 202202587 A TW202202587 A TW 202202587A
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adhesive sheet
semiconductor device
adhesive
lead frame
adhesive layer
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水谷大祐
近藤恭史
付文峰
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日商巴川製紙所股份有限公司
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J109/00Adhesives based on homopolymers or copolymers of conjugated diene hydrocarbons
    • C09J109/02Copolymers with acrylonitrile
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/06Non-macromolecular additives organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J179/00Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09J161/00 - C09J177/00
    • C09J179/04Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/35Heat-activated
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/50Assembly of semiconductor devices using processes or apparatus not provided for in a single one of the subgroups H01L21/06 - H01L21/326, e.g. sealing of a cap to a base of a container
    • H01L21/56Encapsulations, e.g. encapsulation layers, coatings
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00Details of semiconductor or other solid state devices
    • H01L23/12Mountings, e.g. non-detachable insulating substrates
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00Details of semiconductor or other solid state devices
    • H01L23/48Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor
    • H01L23/50Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor for integrated circuit devices, e.g. power bus, number of leads
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/47Structure, shape, material or disposition of the wire connectors after the connecting process
    • H01L2224/48Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
    • H01L2224/4805Shape
    • H01L2224/4809Loop shape
    • H01L2224/48091Arched
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42Wire connectors; Manufacturing methods related thereto
    • H01L2224/47Structure, shape, material or disposition of the wire connectors after the connecting process
    • H01L2224/48Structure, shape, material or disposition of the wire connectors after the connecting process of an individual wire connector
    • H01L2224/481Disposition
    • H01L2224/48151Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive
    • H01L2224/48221Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked
    • H01L2224/48245Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic
    • H01L2224/48247Connecting between a semiconductor or solid-state body and an item not being a semiconductor or solid-state body, e.g. chip-to-substrate, chip-to-passive the body and the item being stacked the item being metallic connecting the wire to a bond pad of the item
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/93Batch processes
    • H01L2224/95Batch processes at chip-level, i.e. with connecting carried out on a plurality of singulated devices, i.e. on diced chips
    • H01L2224/97Batch processes at chip-level, i.e. with connecting carried out on a plurality of singulated devices, i.e. on diced chips the devices being connected to a common substrate, e.g. interposer, said common substrate being separable into individual assemblies after connecting
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/15Details of package parts other than the semiconductor or other solid state devices to be connected
    • H01L2924/181Encapsulation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
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  • Manufacturing & Machinery (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Adhesive Tapes (AREA)

Abstract

The present invention provides: an adhesive sheet which sufficiently and stably adheres to the back surface of a lead frame and the back surface of a sealing resin, and is not separated therefrom before a separation step even if subjected to a thermal history associated with QFN assembly, and which is free from leakage of the sealing resin, while being able to be easily separated in the separation step without the occurrence of adhesive residue, namely without leaving some adhesive behind, or without the occurrence of breakage; and a method for producing a semiconductor device, said method using this adhesive sheet. An adhesive sheet for semiconductor device production according to the present invention comprises a base material and a thermosetting adhesive layer that is provided on one surface of the base material; and this adhesive sheet for semiconductor device production is bonded to a lead frame or a wiring board of a semiconductor device in a removable manner. The adhesive layer of this adhesive sheet contains (a) a carboxyl group-containing acrylonitrile-butadiene copolymer, (b) an epoxy resin having a structural formula (1), (c) a compound containing two or more maleimide groups, and (d) a latent curing agent.

Description

半導體裝置製造用接著片材及使用有其之半導體裝置之製造方法Adhesive sheet for semiconductor device manufacturing and method for manufacturing semiconductor device using the same

本發明係有關一種以QFN(Quad Flat Non-lead,四方平面無引線)方式組裝半導體裝置時可適於用作遮罩膠帶之接著片材及使用有其之半導體裝置之製造方法。The present invention relates to a bonding sheet suitable for use as a masking tape when assembling a semiconductor device in a QFN (Quad Flat Non-lead) manner, and a manufacturing method of a semiconductor device using the same.

背景技術 近年,以行動電話為首之IT機器漸趨小型化、薄型化、多機能化,為了因應其需求,半導體裝置(半導體封裝體)之更高密度安裝技術之必要性正在提升當中。 就回應該需求之CSP(Chip Size Package,晶片尺寸封裝)技術而言,QFN方式受到矚目(參照專利文獻1及專利文獻2),尤其是廣泛採用在100接腳(pin)以下之少接腳類型半導體裝置的製造上。Background technique In recent years, IT equipments such as mobile phones are becoming smaller, thinner and more functional. In order to meet the needs, the need for higher density mounting technology of semiconductor devices (semiconductor packages) is increasing. In terms of CSP (Chip Size Package) technology that responds to this demand, the QFN method has attracted attention (refer to Patent Document 1 and Patent Document 2), and in particular, fewer pins below 100 pins are widely used. type in the manufacture of semiconductor devices.

於此,就運用QFN方式之一般QFN封裝體之組裝方法而言,概略來說已知有下述方法。首先於貼附步驟中,在引線框架一面上貼附接著片材,接著於黏晶(die attach)步驟中,在已形成在引線框架之多數半導體元件搭載部(晶座(die pad)部)上一一搭載IC晶片等半導體元件。接著,在銲線接合步驟中,以接合線將引線框架之沿著各個半導體元件搭載部外周配設的多數引線與半導體元件電性連接。接著,於密封步驟中以密封樹脂將搭載於引線框架之半導體元件予以密封。 之後,於剝離步驟中,將接著片材從引線框架剝離,可藉此形成排列有多數QFN封裝體之QFN單元。最後於切割步驟中,將該QFN單元沿各個QFN封裝體外周切割,可藉此製造多數QFN封裝體。Here, the following methods are generally known as an assembling method of a general QFN package using the QFN method. First, in the attaching step, an adhesive sheet is attached to one side of the lead frame, and then in the die attach step, most of the semiconductor element mounting parts (die pad parts) that have been formed on the lead frame are attached. The previous one mounts semiconductor elements such as IC chips. Next, in the wire bonding step, a plurality of leads arranged along the outer periphery of each semiconductor element mounting portion of the lead frame and the semiconductor elements are electrically connected with bonding wires. Next, in the sealing step, the semiconductor element mounted on the lead frame is sealed with a sealing resin. Then, in the peeling step, the adhesive sheet is peeled off from the lead frame, thereby forming a QFN cell in which a plurality of QFN packages are arranged. Finally, in the dicing step, the QFN unit is diced along the periphery of each QFN package, whereby most of the QFN packages can be fabricated.

用於此種用途之接著片材被要求具有下述特性:剝離步驟之前,不會從引線框架背面及密封樹脂背面剝離而可充分且安定地貼附,並且,在剝離步驟時可輕易剝離,引線框架背面及密封樹脂背面不會有接著劑殘留之殘膠現象或接著片材破裂等不良情況。 尤其,近年來為了減低半導體裝置之成本,已漸行使用由銅合金構成之引線框架。對此種由銅合金構成之引線框架使用接著片材時,肇因於構成引線框架之屬過渡金屬之銅對高分子材料有氧化劣化的催化作用,故於貼膠(taping)步驟後,因承受伴隨QFN封裝體組裝而來之熱歷程,高分子材料之接著劑容易氧化劣化,從引線框架剝離接著片材時便出現容易發生重剝離及殘膠之問題。The adhesive sheet used for this purpose is required to have the following characteristics: it can be attached sufficiently and stably without peeling from the back side of the lead frame and the back side of the sealing resin before the peeling step, and can be easily peeled off during the peeling step, The backside of the lead frame and the backside of the sealing resin will not have any problems such as residual adhesive residues of the adhesive residue or cracking of the adhesive sheet. In particular, in recent years, in order to reduce the cost of semiconductor devices, lead frames made of copper alloys have been increasingly used. When an adhesive sheet is used for such a lead frame composed of copper alloy, it is due to the catalytic effect of copper, which is a transition metal constituting the lead frame, on the oxidative degradation of the polymer material. Due to the thermal history accompanying the assembly of the QFN package, the adhesive of the polymer material is easy to be oxidized and deteriorated, and the problems of heavy peeling and adhesive residue are prone to occur when the adhesive sheet is peeled off from the lead frame.

因此,迄今使用之接著片材並未充分滿足可供用在由銅合金構成之引線框架的實用等級。 舉例來說,習知之接著片材有下述型態之物:在由耐熱性薄膜構成之基材上積層有接著劑層,且該接著劑層含有丙烯腈-丁二烯共聚物與雙順丁烯二醯亞胺樹脂(參照專利文獻3)。使用此種接著片材時,因貼膠步驟後之黏晶固化處理、銲線接合步驟及樹脂密封步驟所施加之熱能,接著劑層中之丙烯腈-丁二烯共聚物容易劣化,而發生在剝離步驟中變得難以剝離、接著片材破裂、發生殘膠等問題。 先行技術文獻 專利文獻Therefore, the adhesive sheets used hitherto have not sufficiently met the practical grades available for use in lead frames composed of copper alloys. For example, the conventional adhesive sheet has the following type: an adhesive layer is laminated on a base material composed of a heat-resistant film, and the adhesive layer contains acrylonitrile-butadiene copolymer and biscis Butenediimide resin (refer to Patent Document 3). When this adhesive sheet is used, the acrylonitrile-butadiene copolymer in the adhesive layer is easily deteriorated due to the heat energy applied in the die-bonding curing process, the wire bonding step and the resin sealing step after the adhesive bonding step. In the peeling step, it becomes difficult to peel off, and then the sheet is broken, and problems such as adhesive residue occur. prior art literature Patent Literature

[專利文獻1]日本特開2003-165961號公報 [專利文獻2]日本特開2005-142401號公報 [專利文獻3]日本特開2008-095014號公報[Patent Document 1] Japanese Patent Laid-Open No. 2003-165961 [Patent Document 2] Japanese Patent Laid-Open No. 2005-142401 [Patent Document 3] Japanese Patent Laid-Open No. 2008-095014

發明概要 發明欲解決之課題 本發明鑑於上述事由,而以提供具有下述特性之接著片材作為本發明之課題:在QFN封裝體之組裝方法中之剝離步驟之前,即使承受伴隨QFN組裝而來之熱歷程,也不會自引線框架背面及密封樹脂背面剝離,可充分且安定地貼附於其等之上,亦無密封樹脂溢漏,並且,可在剝離步驟輕易剝離,不會發生接著劑殘留之殘膠或破裂。更進一步來說,則以提供使用有該接著片材之半導體裝置製造方法作為本發明之課題。 用以課題之手段Summary of Invention The problem to be solved by the invention In view of the above-mentioned reasons, the present invention aims to provide an adhesive sheet having the following characteristics: Even if it is subjected to the thermal history accompanying QFN assembly before the peeling step in the assembly method of the QFN package, it will not It can be peeled off from the back side of the lead frame and the back side of the sealing resin, so that it can be fully and stably attached to them, and there is no leakage of the sealing resin, and it can be easily peeled off in the peeling step, and there will be no adhesive residue or cracking. . Furthermore, it is the subject of this invention to provide the manufacturing method of the semiconductor device using this adhesive sheet. means of teaching

本發明之半導體裝置製造用接著片材之特徵在於:其將會以可剝離方式貼附於半導體裝置之引線框架或配線基板上,且具備基材以及設在該基材之一面上之熱硬化型接著劑層,該熱硬化性接著劑層含有含羧基之丙烯腈-丁二烯共聚物(a)、具下述結構式(1)之環氧樹脂(b)、含2個以上順丁烯二醯亞胺基之化合物(c)及潛伏型硬化劑(d)。The adhesive sheet for manufacturing a semiconductor device of the present invention is characterized in that it will be releasably attached to a lead frame or a wiring board of a semiconductor device, and has a base material and a heat-hardening sheet provided on one surface of the base material. type adhesive layer, the thermosetting adhesive layer contains carboxyl-containing acrylonitrile-butadiene copolymer (a), epoxy resin (b) having the following structural formula (1), containing two or more cis-butadiene The enediimide-based compound (c) and the latent hardener (d).

[化學式1]

Figure 02_image003
[Chemical formula 1]
Figure 02_image003

此外,前述含羧基之丙烯腈-丁二烯共聚物(a)宜為:丙烯腈含量為5~50質量%且由數量平均分子量算出之羧基當量為100~20000之含羧基之丙烯腈-丁二烯共聚物。In addition, the aforementioned carboxyl-containing acrylonitrile-butadiene copolymer (a) is preferably a carboxyl-containing acrylonitrile-butadiene with an acrylonitrile content of 5 to 50% by mass and a carboxyl group equivalent calculated from the number average molecular weight of 100 to 20,000 Diene copolymer.

相對於前述含羧基之丙烯腈-丁二烯共聚物(a)100質量份,前述環氧樹脂(b)、前述含2個以上順丁烯二醯亞胺基之化合物(c)及前述潛伏型硬化劑(d)宜合計為30~300質量份。 進一步來說,前述潛伏型硬化劑(d)宜為與環氧樹脂之反應開始溫度為100℃以上之硬化劑。 此外,本發明之半導體裝置之製造方法特徵在於具備下列步驟: 貼附步驟,其係在引線框架或配線基板上貼附本發明之半導體裝置製造用接著片材; 黏晶步驟,其係在前述引線框架或配線基板上搭載半導體元件; 銲線接合步驟,其係使前述半導體元件與外部連接端子導通; 密封步驟,其係以密封樹脂來密封前述半導體元件;以及 剝離步驟,其係於前述密封步驟後,將半導體裝置製造用接著片材從引線框架或配線基板剝離。 發明效果With respect to 100 parts by mass of the carboxyl group-containing acrylonitrile-butadiene copolymer (a), the epoxy resin (b), the compound (c) containing two or more maleimide groups, and the latent The type hardener (d) is preferably 30 to 300 parts by mass in total. Furthermore, it is preferable that the said latent hardener (d) is a hardener whose reaction initiation temperature with an epoxy resin is 100 degreeC or more. In addition, the manufacturing method of the semiconductor device of the present invention is characterized by having the following steps: an attaching step of attaching the adhesive sheet for manufacturing a semiconductor device of the present invention on a lead frame or a wiring substrate; a die bonding step, which is to mount a semiconductor element on the aforementioned lead frame or wiring substrate; a wire bonding step, which is to make the aforementioned semiconductor element and external connection terminals conduct; a sealing step of sealing the aforementioned semiconductor element with a sealing resin; and A peeling process peels the adhesive sheet for semiconductor device manufacture from a lead frame or a wiring board after the said sealing process. Invention effect

若依本發明,可提供一種接著片材,其在剝離步驟前即使承受伴隨QFN組裝而來之熱歷程,也不會從引線框架背面及密封樹脂背面剝離,可充分且安定地貼附而無密封樹脂溢漏,且可在剝離步驟輕易剝離,不會發生接著劑殘留之殘膠或斷裂。若依本發明,可進一步提供一種使用有本發明之接著片材的半導體裝置製造方法。According to the present invention, it is possible to provide an adhesive sheet which can be sufficiently and stably attached without peeling off from the back surface of the lead frame and the back surface of the sealing resin even if it is subjected to the thermal history accompanying the QFN assembly before the peeling step. The sealing resin leaks and can be easily peeled off in the peeling step without adhesive residue or breakage. According to the present invention, a method for manufacturing a semiconductor device using the adhesive sheet of the present invention can be further provided.

用以實施發明之形態 茲就本發明詳細說明如下。 [半導體裝置製造用接著片材] 本發明之半導體裝置製造用接著片材(以下稱為接著片材)具備基材及設於該基材之一面上之熱硬化型接著劑層。本發明之接著片材將會以可剝離方式貼附在半導體裝置之引線框架或配線基板上,前述接著劑層含有:含羧基之丙烯腈-丁二烯共聚物(a)、具下列結構式(1)之環氧樹脂(b)、含2個以上順丁烯二醯亞胺基之化合物(c)及潛伏型硬化劑(d)。本發明之接著片材在以QFN方式組裝半導體裝置時係作為遮罩膠帶使用。Form for carrying out the invention The present invention is described in detail as follows. [Adhesive Sheet for Semiconductor Device Manufacturing] The adhesive sheet for semiconductor device manufacturing of the present invention (hereinafter referred to as an adhesive sheet) includes a base material and a thermosetting adhesive layer provided on one surface of the base material. The adhesive sheet of the present invention will be releasably attached to the lead frame or wiring substrate of a semiconductor device, and the adhesive layer contains: a carboxyl group-containing acrylonitrile-butadiene copolymer (a) having the following structural formula The epoxy resin (b) of (1), the compound (c) containing two or more maleimide groups, and the latent hardener (d). The adhesive sheet of the present invention is used as a mask tape when assembling a semiconductor device by a QFN method.

[化學式2]

Figure 02_image005
[Chemical formula 2]
Figure 02_image005

構成本發明接著片材之含羧基之丙烯腈-丁二烯共聚物(a)(以下有時稱為(a)成分)擔負使加熱初期之接著劑層熔融黏度維持適度的功能等,在此同時,對已硬化之接著劑層則賦予其良好之柔軟性及接著性。透過含有該共聚物,本案發明之接著片材可形成對耐熱性薄膜等所構成之基材具良好密著性且不會破裂之接著劑層。就含羧基之丙烯腈-丁二烯共聚物(a)而言,可無限制地使用習知物質,但以丙烯腈含量為5~50質量%者為宜,10~40質量%者更佳。丙烯腈含量若小於上述範圍,對溶劑之溶解性及與其他成分之相溶性降低,所得接著劑層之均勻性有降低之傾向。另一方面,若丙烯腈含量超過上述範圍,所得接著劑層對引線框架及密封樹脂之接著性將變得過度,將其用於接著片材時,有剝離步驟時難以剝離、接著片材破裂之可能性。The carboxyl group-containing acrylonitrile-butadiene copolymer (a) (hereinafter sometimes referred to as component (a)) constituting the adhesive sheet of the present invention has a function of maintaining an appropriate melt viscosity of the adhesive layer in the initial stage of heating, and the like here At the same time, the hardened adhesive layer is given good flexibility and adhesion. By containing the copolymer, the adhesive sheet of the present invention can form an adhesive layer that has good adhesion to a base material composed of a heat-resistant film or the like and is not cracked. For the carboxyl group-containing acrylonitrile-butadiene copolymer (a), known substances can be used without limitation, but the content of acrylonitrile is preferably 5 to 50 mass %, more preferably 10 to 40 mass % . If the content of acrylonitrile is less than the above range, the solubility to the solvent and the compatibility with other components will decrease, and the uniformity of the obtained adhesive layer tends to decrease. On the other hand, if the content of acrylonitrile exceeds the above-mentioned range, the adhesiveness of the obtained adhesive layer to the lead frame and the sealing resin becomes excessive, and when it is used for an adhesive sheet, it is difficult to peel off during a peeling step, and the adhesive sheet is broken the possibility.

含羧基之丙烯腈-丁二烯共聚物以從數量平均分子量算出之羧基當量以100~20000範圍者為宜,200~10000者更佳。羧基當量若小於上述範圍,與其他成分之反應性變得過高,所得接著劑層之保存安定性有降低之傾向。另一方面,羧基當量若超過上述範圍,因與其他成分之反應性不足,所得接著劑層容易成為低B階段。結果,將其使用在接著片材時,在加熱初期,即接著片材之貼附步驟及黏晶固化處理等時,接著片材在加熱之際,接著劑層低黏度化,而容易在接著劑層引起發泡或流出,熱安定性有降低之傾向。 另,由數量平均分子量算出之羧基當量意指數量平均分子量(Mn)除以每分子平均之羧基數(官能基數)所得數值,如下式所示。 羧基當量=Mn/官能基數For the carboxyl group-containing acrylonitrile-butadiene copolymer, the carboxyl group equivalent calculated from the number average molecular weight is preferably in the range of 100 to 20,000, more preferably 200 to 10,000. If the carboxyl group equivalent is less than the above range, the reactivity with other components becomes too high, and the storage stability of the obtained adhesive layer tends to decrease. On the other hand, when the carboxyl group equivalent exceeds the above-mentioned range, the resulting adhesive layer tends to become a low B stage due to insufficient reactivity with other components. As a result, when it is used in the bonding of sheets, at the initial stage of heating, that is, during the attaching step of the bonding sheet and the die-bonding curing process, etc., when the bonding sheet is heated, the viscosity of the adhesive layer is reduced, and it is easy to bond. The agent layer causes foaming or outflow, and the thermal stability tends to decrease. The carboxyl group equivalent calculated from the number-average molecular weight means a value obtained by dividing the number-average molecular weight (Mn) by the average number of carboxyl groups (functional groups) per molecule, as shown in the following formula. Carboxyl equivalent = Mn/number of functional groups

環氧樹脂(b)(以下有時也稱為(b)成分)與含有2個以上順丁烯二醯亞胺基之化合物(c)擔負接著劑層之熱硬化性,藉由併用其等,可形成熱安定性優異且易於剝離步驟中剝離、不發生殘膠及斷裂之接著劑層。尤其,環氧樹脂(b)可對接著劑層賦予韌性,可藉由使接著劑層含有該成分而在剝離步驟中抑制接著劑層破裂所引起之殘膠。The epoxy resin (b) (hereinafter sometimes referred to as the component (b)) and the compound (c) containing two or more maleimide groups are responsible for the thermosetting properties of the adhesive layer, and by using them together, etc. , it can form an adhesive layer with excellent thermal stability and easy to peel off in the peeling step, without adhesive residue and breakage. In particular, the epoxy resin (b) can impart toughness to the adhesive layer, and by making the adhesive layer contain this component, it is possible to suppress the adhesive residue caused by the rupture of the adhesive layer in the peeling step.

含有2個以上順丁烯二醯亞胺基之化合物(c)(以下有時也稱為(c)成分)在對接著劑層賦予熱安定性之同時,也發揮調整接著劑層接著性之作用,可藉由含有該成分來適度控制接著片材之接著性,而在基材表面形成可在剝離步驟容易剝離之接著劑層。 就含2個以上順丁烯二醯亞胺基之化合物(c)之具體例而言,可適於使用構成雙順丁烯二醯亞胺樹脂之化合物,可舉如下列式(2-1)~(2-3)所示之物等,其中尤以下列式(2-1)或(2-3)所示化合物在對溶劑之溶解性的觀點上甚有用。The compound (c) containing two or more maleimide groups (hereinafter also referred to as the component (c)) not only imparts thermal stability to the adhesive layer, but also adjusts the adhesiveness of the adhesive layer. By containing this component, the adhesiveness of the adhesive sheet can be appropriately controlled, and an adhesive layer that can be easily peeled off in the peeling step can be formed on the surface of the substrate. As a specific example of the compound (c) containing two or more maleimide groups, compounds constituting the bismaleimide resin can be suitably used, and examples of the following formula (2-1) ) to (2-3), among which compounds represented by the following formula (2-1) or (2-3) are particularly useful from the viewpoint of solubility in solvents.

[化學式3]

Figure 02_image007
[Chemical formula 3]
Figure 02_image007

潛伏型硬化劑(d)(以下有時也稱為(d)成分)可藉由含在接著劑層中而將接著劑層調整成更低B階段狀態,因此可在低溫下進行貼膠。此外,在黏晶固化步驟等中,接著劑藉由在所含潛伏型硬化劑(d)之反應開始溫度以上之溫度下加熱,可快速進行硬化反應而呈現高彈性模數之狀態。 潛伏型硬化劑(d)係指與環氧樹脂之反應開始溫度在100℃以上之硬化劑。就此種潛伏型硬化劑而言,可舉如2-苯基-4,5-二羥基甲基咪唑(四國化成工業社製,商品名:CUREZOL 2PHZ-PW,反應開始溫度:150℃)、2-苯基-4-甲基-5-羥基甲基咪唑(四國化成工業社製,商品名:CUREZOL 2P4MHZ-PW,反應開始溫度:130℃)等。於此,反應開始溫度係指與環氧樹脂混合、昇溫時觀察到硬化發熱之溫度。使用DSC(示差掃描熱量測定)來測定。 潛伏型硬化劑(d)之含量相對於含羧基之丙烯腈-丁二烯共聚物(a)100質量份以0.05~20質量份為宜,更宜為0.1~10質量份。潛伏型硬化劑(d)之含量若在上述範圍內,可將接著劑層調整成更低B階段狀態,因此可在低溫下進行貼膠,並且可在黏晶固化等步驟中使接著劑層快速硬化。The latent curing agent (d) (hereinafter sometimes referred to as the component (d)) can adjust the adhesive layer to a lower B-stage state by being contained in the adhesive layer, so that it can be pasted at a low temperature. In addition, in the die-bonding curing step or the like, the adhesive can be rapidly cured by heating at a temperature higher than the reaction start temperature of the latent curing agent (d) contained, thereby exhibiting a state of high elastic modulus. The latent hardener (d) refers to a hardener whose reaction initiation temperature with the epoxy resin is 100°C or higher. Examples of such latent curing agents include 2-phenyl-4,5-dihydroxymethylimidazole (manufactured by Shikoku Chemical Industry Co., Ltd., trade name: CUREZOL 2PHZ-PW, reaction initiation temperature: 150°C), 2-phenyl-4-methyl-5-hydroxymethylimidazole (manufactured by Shikoku Chemical Industry Co., Ltd., trade name: CUREZOL 2P4MHZ-PW, reaction initiation temperature: 130° C.) and the like. Here, the reaction start temperature refers to the temperature at which the heat generation of curing is observed when mixing with the epoxy resin and raising the temperature. Measured using DSC (Differential Scanning Calorimetry). The content of the latent hardener (d) is preferably 0.05 to 20 parts by mass, more preferably 0.1 to 10 parts by mass, relative to 100 parts by mass of the carboxyl group-containing acrylonitrile-butadiene copolymer (a). If the content of the latent hardener (d) is within the above range, the adhesive layer can be adjusted to a lower B-stage state, so the sticking can be performed at a low temperature, and the adhesive layer can be made in steps such as sticking and curing. Fast hardening.

另,就上述(a)~(d)之各成分而言,任一者皆可使用由1種化合物構成之物,也可使用2種以上化合物之混合物。In addition, about each component of said (a)-(d), what consists of 1 type of compound may be used for any one, and the mixture of 2 or more types of compounds may be used.

就各成分之比率而言,相對於(a)成分100質量份,(b)成分、(c)成分與(d)成分合計宜為30~300質量份,更宜30~200質量份。若(b)成分、(c)成分與(d)成分合計小於上述範圍,則接著劑層之反應性降低,即使透過加熱也不易進行不熔不融化,因熱安定性降低而有接著力增強之傾向。另一方面,若超過上述範圍,則加熱初期之接著劑層之熔融黏度不足,使用該接著劑層之接著片材在貼膠步驟後之黏晶固化處理等時,有接著劑層流出、發泡之虞。The ratio of each component is preferably 30 to 300 parts by mass, more preferably 30 to 200 parts by mass, based on 100 parts by mass of (a) component, (b) component, (c) component, and (d) component in total. If the total of the components (b), (c), and (d) is less than the above-mentioned range, the reactivity of the adhesive layer decreases, and the infusibility and infusibility of the adhesive layer are not easily performed even by heating, and the thermal stability decreases and the adhesive force increases. tendency. On the other hand, if it exceeds the above-mentioned range, the melt viscosity of the adhesive layer at the initial stage of heating is insufficient, and the adhesive layer may flow out and develop when the adhesive sheet using the adhesive layer is subjected to the sticking and curing treatment after the adhesive bonding step. Danger of bubbles.

進一步來說,相對於(b)成分之(c)成分質量比((c)/(b))以0.1~10之範圍為宜。若小於上述範圍,所得接著劑層容易在常溫下進行硬化反應,而有保存安定性變差、接著力變得過強而讓使用其之接著片材變得無法在剝離步驟中剝離或斷裂之虞。另一方面,若超過上述範圍,則在接著片材製造時會有該接著劑層與由耐熱性薄膜構成之基材之接著性降低的情況,且有接著劑層發泡、所得接著片材容易殘膠之傾向。Further, the mass ratio ((c)/(b)) of the (c) component with respect to the (b) component is preferably in the range of 0.1 to 10. If it is less than the above range, the obtained adhesive layer tends to undergo a hardening reaction at room temperature, and the storage stability is deteriorated, and the adhesive force becomes too strong, so that the adhesive sheet using the adhesive cannot be peeled off or broken in the peeling step. Yu. On the other hand, when the above-mentioned range is exceeded, the adhesiveness between the adhesive layer and the base material composed of the heat-resistant film may decrease during the production of the adhesive sheet, and the adhesive layer may foam, resulting in an adhesive sheet. Tendency to glue residue easily.

本發明之半導體裝置製造用接著片材中之接著劑層可進一步含有反應性矽氧烷化合物。反應性矽氧烷化合物可使構成接著劑層之各成分的相溶性提高,同時提高接著劑層從密封樹脂剝離之剝離性。藉由使該化合物含於接著劑層中,可形成接著劑層中各成分相溶良好且無成分分離、析出等不良情況之均勻接著劑層。結果,可使接著劑層之接著強度變得更均勻,而可抑制肇因於接著強度發生局部性高低所致之剝離性降低、殘膠等不良情況。The adhesive layer in the adhesive sheet for manufacturing a semiconductor device of the present invention may further contain a reactive siloxane compound. The reactive siloxane compound can improve the compatibility of the components constituting the adhesive layer, and at the same time improve the peelability of the adhesive layer from the sealing resin. By including this compound in the adhesive layer, a uniform adhesive layer can be formed in which each component in the adhesive layer is compatible with each other and has no problems such as component separation and precipitation. As a result, the adhesive strength of the adhesive layer can be made more uniform, and defects such as a decrease in peelability and adhesive residue caused by localized high and low adhesive strength can be suppressed.

就反應性矽氧烷化合物而言,可無限制地使用透過胺基改質、環氧基改質、羧基改質、巰基改質等反應基而賦予反應性之矽氧烷化合物。其等當中,尤以1,3-雙(3-胺基丙基)四甲基二矽氧烷、胺基丙基末端之二甲基矽氧烷4聚物或8聚物、雙(3-胺基苯氧基甲基)四甲基二矽氧烷在可與(b)成分及(c)成分快速進行反應之點上較為理想。反應性矽氧烷化合物係如前述般,以使用矽氧烷結構二末端上鍵結有反應基者在反應性觀點上較理想,但亦可使用僅有單側末端、或是末端中有一者具反應性另一者呈非反應性之矽烷偶合劑。As the reactive siloxane compound, siloxane compounds imparted with reactivity through reactive groups such as amino group modification, epoxy group modification, carboxyl group modification, and mercapto group modification can be used without limitation. Among them, especially 1,3-bis(3-aminopropyl)tetramethyldisiloxane, aminopropyl-terminated dimethylsiloxane 4- or 8-mer, bis(3 -Aminophenoxymethyl)tetramethyldisiloxane is preferable in that it can react rapidly with (b) component and (c) component. The reactive siloxane compound is as described above, and it is preferable to use a siloxane structure with reactive groups bonded to both ends, but it is also possible to use only one end or one of the ends. Reactive and non-reactive silane coupling agents.

本發明之半導體裝置製造用接著片材中,接著劑層之反應性矽氧烷化合物之反應基數相對於(b)成分之環氧基數與(c)成分之順丁烯二醯亞胺基數之合計的比以0.05~1.2為宜,更宜為0.1~0.8。若小於上述範圍,接著劑層整體之反應性降低,難以透過黏晶固化處理等進行硬化反應,結果有時接著力會變得過強。另一方面,若超過上述範圍,反應過剩進行過度,接著劑層調製時容易引發凝膠化等問題,接著力容易變弱。In the adhesive sheet for manufacturing a semiconductor device of the present invention, the number of reactive groups of the reactive siloxane compound in the adhesive layer is relative to the number of epoxy groups in the component (b) and the number of maleimide groups in the component (c). The total ratio is preferably 0.05 to 1.2, more preferably 0.1 to 0.8. If it is less than the above-mentioned range, the reactivity of the entire adhesive layer decreases, and it becomes difficult to carry out a hardening reaction through a die-bonding curing treatment or the like, and as a result, the adhesive force may become too strong. On the other hand, if it exceeds the above-mentioned range, the reaction is excessively advanced, problems such as gelation are likely to occur during preparation of the adhesive layer, and the adhesive force is likely to become weak.

接著劑層除了成分(a)~成分(d)等必要成分之外,亦可在不影響接著劑層之接著性的範圍內添加有機過氧化物、三苯基膦等反應促進劑。透過添加其等,也可能將接著劑層在常溫下之狀態控制在良好之B階段。 進一步來說,為了控制熔融黏度、提升導熱性及賦予阻燃性等目的,亦可將平均粒徑1μm以下之填料添加至接著劑層中。填料可舉如二氧化矽、氧化鋁、氧化鎂、氮化鋁、氮化硼、氧化鈦、碳酸鈣、氫氧化鋁等無機填料以及聚矽氧樹脂、氟樹脂等有機填料等。使用填料時,宜令其含量在接著劑層中佔1~40質量%。In addition to the necessary components such as components (a) to (d), the adhesive layer may also be added with reaction accelerators such as organic peroxides and triphenylphosphine within a range that does not affect the adhesiveness of the adhesive layer. By adding them, it is also possible to control the state of the adhesive layer at normal temperature to a good B-stage. Furthermore, for the purpose of controlling melt viscosity, improving thermal conductivity, and imparting flame retardancy, a filler having an average particle size of 1 μm or less can also be added to the adhesive layer. Examples of fillers include inorganic fillers such as silica, alumina, magnesia, aluminum nitride, boron nitride, titanium oxide, calcium carbonate, and aluminum hydroxide, and organic fillers such as polysiloxane and fluororesin. When a filler is used, the content of the filler is preferably 1 to 40% by mass in the adhesive layer.

本發明之接著片材係在基材之耐熱性薄膜之單面上形成有上述接著劑層者。 製造此種接著片材時,首先調製至少由下述成分構成之接著劑塗料:上述含羧基之丙烯腈-丁二烯共聚物(a)、具前述結構式(1)之環氧樹脂(b)、含2個以上順丁烯二醯亞胺基之化合物(c)、潛伏型硬化劑(d)及溶劑。接著,在耐熱性薄膜之單面上,以令乾燥後接著劑層厚度宜1~50μm更宜3~20μm之方式塗佈該塗料並予以乾燥即可。此外,為了保護接著劑層,宜在所形成之接著劑層上進一步設置剝離性保護薄膜,此時,亦可在保護薄膜上塗佈塗料並乾燥來形成接著劑層,並在其上設置耐熱性薄膜,藉此方法來製造接著片材。另,保護薄膜係於接著片材使用時剝離。The adhesive sheet of the present invention is one in which the above-mentioned adhesive layer is formed on one side of the heat-resistant film of the base material. When manufacturing such an adhesive sheet, firstly, an adhesive coating composed of at least the following components is prepared: the carboxyl group-containing acrylonitrile-butadiene copolymer (a), the epoxy resin (b) having the above-mentioned structural formula (1) ), a compound (c) containing two or more maleimide groups, a latent hardener (d) and a solvent. Next, on one side of the heat-resistant film, the coating is applied and dried so that the thickness of the adhesive layer after drying is preferably 1-50 μm, more preferably 3-20 μm. In addition, in order to protect the adhesive layer, it is advisable to further provide a peelable protective film on the formed adhesive layer. At this time, a coating can also be applied on the protective film and dried to form an adhesive layer, and a heat-resistant film can be provided on it. The adhesive film is produced by this method. In addition, the protective film is peeled off when the adhesive sheet is used.

耐熱性薄膜可舉如由聚醯亞胺、聚苯硫醚、聚醚碸、聚醚醚酮、液晶聚合物、聚對酞酸乙二酯及聚萘二甲酸乙二酯等構成之耐熱性塑膠薄膜以及環氧樹脂-玻璃布等複合耐熱薄膜等,尤以聚醯亞胺為宜。 聚醯亞胺薄膜之厚度以12.5~125μm為宜,更宜為25~50μm。若小於上述範圍,接著片材有韌性變得不足而難以處置之傾向,若超過上述範圍,則QFN組裝時貼膠步驟及剝離步驟之作業有變得困難之傾向。The heat-resistant film includes, for example, a heat-resistant film composed of polyimide, polyphenylene sulfide, polyether sulfide, polyether ether ketone, liquid crystal polymer, polyethylene terephthalate, polyethylene naphthalate, and the like. Plastic film and composite heat-resistant film such as epoxy resin-glass cloth, etc., especially polyimide is suitable. The thickness of the polyimide film is preferably 12.5-125 μm, more preferably 25-50 μm. If it is less than the above-mentioned range, the adhesive sheet tends to have insufficient toughness and is difficult to handle, and if it exceeds the above-mentioned range, the operations of the sticking step and the peeling step during QFN assembly tend to be difficult.

就接著劑塗料所使用之溶劑而言,可適於使用烴類、醇類、酮類、醚類(四氫呋喃等)等有機溶劑及水等中之1種以上,其使用量僅需適當調整至用作塗料之適切黏度即可。此外,塗料之性狀可為溶液、乳劑及懸浮液中之任一者,可因應所使用之塗佈裝置及環境條件等來適當選擇。As for the solvent used in the adhesive coating, one or more of organic solvents such as hydrocarbons, alcohols, ketones, ethers (tetrahydrofuran, etc.), and water, etc. can be suitably used, and the usage amount only needs to be appropriately adjusted to It can be used as the appropriate viscosity of the coating. In addition, the properties of the coating material can be any of solutions, emulsions and suspensions, and can be appropriately selected according to the coating equipment used and environmental conditions.

剝離性保護薄膜可舉如聚乙烯、聚丙烯、氯乙烯、氟系樹脂及聚矽氧等塑膠薄膜以及已透過被覆聚矽氧等而對聚對酞酸乙二酯、聚萘二甲酸乙二酯及紙等賦予剝離性而成之物。The peelable protective film includes plastic films such as polyethylene, polypropylene, vinyl chloride, fluorine-based resin, and polysiloxane, as well as polyethylene terephthalate, polyethylene naphthalate, etc., which have been coated with polysiloxane, etc. Ester, paper, etc., which impart releasability.

[半導體裝置之製造方法] 使用本發明之接著片材之半導體裝置之製造方法具備下列步驟:貼附步驟,其係於引線框架或配線基板上貼附接著片材;黏晶步驟,其係在引線框架或配線基板上搭載半導體元件;銲線接合步驟,其係使半導體元件與外部連接端子導通;密封步驟,其係以密封樹脂密封半導體元件;以及,剝離步驟,其係在密封步驟後從引線框架或配線基板剝離接著片材。[Manufacturing method of semiconductor device] The manufacturing method of a semiconductor device using the adhesive sheet of the present invention includes the following steps: an attaching step in which the adhesive sheet is attached to a lead frame or a wiring substrate; and a die bonding step in which it is mounted on the lead frame or the wiring substrate a semiconductor element; a wire bonding step of conducting the semiconductor element with an external connection terminal; a sealing step of sealing the semiconductor element with a sealing resin; and a peeling step of peeling off the lead frame or the wiring board after the sealing step Sheet.

以下,參照圖1~2,就使用本發明接著片材之半導體裝置製造方法之一例予以說明。圖1係一由搭載半導體元件之側觀看之引線框架俯視圖;圖2A~圖2F為步驟圖,顯示使用圖1所示引線框架來製造QFN封裝體之方法,為圖1之引線框架的A-A’截面圖。Hereinafter, with reference to FIGS. 1-2, an example of the manufacturing method of the semiconductor device using the adhesive sheet of this invention is demonstrated. 1 is a top view of the lead frame viewed from the side on which the semiconductor element is mounted; FIGS. 2A to 2F are step diagrams showing a method for manufacturing a QFN package using the lead frame shown in FIG. 1 , which are A- A' section view.

首先,準備圖1所示概略結構之引線框架20。引線框架20中,搭載IC晶片等半導體元件之多數半導體元件搭載部(晶座部)21係形成為矩陣狀,且沿著各半導體元件搭載部21外周,形成有多數引線22(外部連接端子)。 引線框架20之材質可舉如習知物,可舉例如:銅板及銅合金板、或對其等設有打底鍍層(strike plating)之物,以及在銅合金板表面依序設置鍍鎳層、鍍鈀層及鍍金層之物。First, a lead frame 20 having a schematic structure shown in FIG. 1 is prepared. In the lead frame 20 , a plurality of semiconductor element mounting portions (seat portions) 21 on which semiconductor elements such as IC chips are mounted are formed in a matrix, and a plurality of leads 22 (external connection terminals) are formed along the outer periphery of each semiconductor element mounting portion 21 . . The lead frame 20 can be made of conventional materials, such as copper plate and copper alloy plate, or those provided with strike plating, and nickel plating layers are sequentially arranged on the surface of the copper alloy plate. , Palladium-plated and gold-plated objects.

如圖2A所示,在引線框架20之一面(下面),以接著劑層(省略圖示)抵接引線框架20之方式貼附接著片材10(貼附步驟)。將接著片材10貼附於引線框架20之方法有積層法、加壓法等,在生產性觀點下,以可連續進行貼膠步驟之積層法為宜。本步驟之接著片材10之溫度可舉例如常溫(5~35℃)至150℃,且60~120℃更佳。若以較150℃更高之溫度進行貼附,引線框架容易發生翹曲。 若本步驟中引線框架20發生翹曲,黏晶步驟及銲線接合步驟之定位會變得困難,變得難以搬運至加熱爐,而有使QFN封裝體之生產性降低之虞。As shown in FIG. 2A , the adhesive sheet 10 is attached to one surface (lower surface) of the lead frame 20 so that an adhesive layer (not shown) abuts the lead frame 20 (attachment step). The method of attaching the adhesive sheet 10 to the lead frame 20 includes a lamination method, a pressing method, and the like, and from the viewpoint of productivity, a lamination method that can continuously perform the gluing process is preferable. The temperature of the adhesive sheet 10 in this step can be, for example, from normal temperature (5-35°C) to 150°C, and more preferably 60-120°C. If it is attached at a temperature higher than 150°C, the lead frame is likely to warp. If the lead frame 20 is warped in this step, the positioning of the die bonding step and the wire bonding step will be difficult, and it will be difficult to transport to the heating furnace, which may reduce the productivity of the QFN package.

如圖2B所示,於引線框架20之半導體元件搭載部21中之未貼附接著片材10之側,透過黏晶劑(省略圖示)載置IC晶片等半導體元件30。此時,引線框架20因翹曲受到抑制,可容易進行定位。接著,半導體元件30正確地載置於預定位置上。之後,加熱至100~200℃左右使黏晶劑硬化,將半導體元件30固定、搭載在半導體元件搭載部21(黏晶劑硬化處理。以上為黏晶步驟)。此時,接著片材10之接著劑層硬化而接著於引線框架上。As shown in FIG. 2B , a semiconductor element 30 such as an IC chip is mounted on the side of the semiconductor element mounting portion 21 of the lead frame 20 on which the sheet 10 is not attached through a die bonder (not shown). At this time, warpage of the lead frame 20 is suppressed, and positioning can be facilitated. Next, the semiconductor element 30 is accurately placed on a predetermined position. After that, it is heated to about 100 to 200° C. to harden the die bonder, and the semiconductor element 30 is fixed and mounted on the semiconductor element mounting portion 21 (the die bonder hardening process. The above is the die bond step). At this time, the adhesive layer of the adhesive sheet 10 is hardened and attached to the lead frame.

若自接著片材10及黏晶劑等產生之排氣成分附著於引線框架20及半導體元件30,銲線接合步驟中容易發生銲線接合不良所致之產率降低。因此,在黏晶步驟後、銲線接合步驟前,對引線框架20及半導體元件30施行電漿處理(電漿清洗步驟)。電漿處理可舉下述方法為例:在氬氣或氬氣與氫氣之混合氣體等氣體環境下,將貼附有接著片材10且搭載有半導體元件30之引線框架20(以下有時稱為半成品)照射電漿。電漿處理中之電漿照射輸出功率可設成諸如150~600W。此外,電漿處理時間可設成諸如0.1~15分鐘。If the outgas components generated from the bonding sheet 10 and the die attach agent adhere to the lead frame 20 and the semiconductor element 30 , the yield due to poor wire bonding is likely to occur in the wire bonding step. Therefore, after the die bonding step and before the wire bonding step, a plasma treatment (plasma cleaning step) is performed on the lead frame 20 and the semiconductor element 30 . Plasma treatment can be exemplified by the following method: in a gas atmosphere such as argon gas or a mixed gas of argon gas and hydrogen gas, the lead frame 20 (hereinafter sometimes referred to as the adhesive sheet 10 on which the semiconductor element 30 is mounted is attached) For semi-finished products) irradiate plasma. The plasma irradiation output power in the plasma treatment can be set to, for example, 150-600W. In addition, the plasma treatment time may be set to, for example, 0.1 to 15 minutes.

如圖2C所示,以金線、銅線、覆鈀銅線等接合線31,將半導體元件30與引線框架20之引線22(外部連接端子)電性導通(銲線接合步驟)。本步驟係一邊於加熱器組件(heater block)上將半成品加熱至150~250℃左右一邊進行。本步驟之加熱時間可設成諸如5~60分鐘。 於銲線接合步驟中,若半成品受到加熱,接著劑層中含有氟添加劑時,氟添加劑會轉移至接著劑層表面,因此後述剝離步驟中接著片材10會變得容易從引線框架20及密封樹脂40剝離。As shown in FIG. 2C , the semiconductor element 30 and the leads 22 (external connection terminals) of the lead frame 20 are electrically connected with bonding wires 31 such as gold wires, copper wires, and palladium-clad copper wires (wire bonding step). This step is performed while heating the semi-finished product to about 150-250° C. on a heater block. The heating time in this step can be set to, for example, 5 to 60 minutes. In the wire bonding step, if the semi-finished product is heated and the adhesive layer contains a fluorine additive, the fluorine additive will be transferred to the surface of the adhesive layer, so that the adhesive sheet 10 can be easily removed from the lead frame 20 and the sealant in the peeling step described later. The resin 40 is peeled off.

如圖2D所示,將圖2C所示半成品載置於模具內,使用密封樹脂(模材)射出至模具內部並予充填。將任意量充填至模具內部後,於任意壓力下維持模具內部,以密封樹脂40密封半導體元件30(密封步驟)。密封樹脂可使用習知物,可舉例如環氧樹脂與無機填料等之混合物。 如圖2E所示,將接著片材10從密封樹脂40及引線框架20剝離,藉此獲得排列有多數QFN封裝體50之QFN單元60(剝離步驟)。As shown in FIG. 2D , the semi-finished product shown in FIG. 2C is placed in a mold, and a sealing resin (mold) is used to inject and prefill the inside of the mold. After filling the inside of the mold with an arbitrary amount, the inside of the mold is maintained under an arbitrary pressure, and the semiconductor element 30 is sealed with the sealing resin 40 (sealing step). As a sealing resin, a conventional thing can be used, for example, the mixture of an epoxy resin, an inorganic filler, etc. is mentioned. As shown in FIG. 2E , the adhesive sheet 10 is peeled off from the sealing resin 40 and the lead frame 20 , thereby obtaining a QFN cell 60 in which a plurality of QFN packages 50 are arranged (peeling step).

如圖2F所示,將QFN單元60沿著各QFN封裝體50之外周切割,藉此獲得多數QFN封裝體50(切割步驟)。As shown in FIG. 2F, the QFN cells 60 are cut along the outer periphery of each QFN package 50, thereby obtaining a plurality of QFN packages 50 (cutting step).

另,於上述實施形態中,係以使用引線框架之QFN封裝體製造方法為例進行說明,但本發明不限於此,亦可適用於使用引線框架之QFN封裝體以外之半導體裝置製造方法及使用配線基板之半導體裝置製造方法。In addition, in the above-mentioned embodiments, the method for manufacturing a QFN package using a lead frame is described as an example, but the present invention is not limited to this, and can also be applied to a method for manufacturing a semiconductor device other than a QFN package using a lead frame and its use A method of manufacturing a semiconductor device of a wiring board.

本發明之接著片材中,接著劑層係使含羧基之丙烯腈-丁二烯共聚物(a)之羧基與環氧樹脂(b)之環氧丙基交聯來呈現B階段狀態(半硬化狀態),藉此而可製成低玻璃轉移溫度(10℃~50℃)。具有低玻璃轉移溫度之接著劑層的接著片材可在相對較低溫之加熱條件下,具體來說則是在60~150℃下利用輥壓層合機等連續進行貼膠步驟,生產性優異。In the adhesive sheet of the present invention, the adhesive layer exhibits a B-stage state (semi-semi hardened state), thereby enabling a low glass transition temperature (10°C to 50°C). The adhesive sheet with an adhesive layer with a low glass transition temperature can be continuously glued under a relatively low temperature heating condition, specifically, at 60~150°C using a roll laminator, etc., with excellent productivity. .

此外,本發明之接著片材中低玻璃轉移溫度(-30℃~50℃)之接著劑層在加熱時可獲得高彈性模數之特性。近年,以銲線接合步驟之降低成本為目的,取代習知之金線,利用低成本之銅線或覆鈀銅線進行接合之製品已開始普及。銅線或覆鈀銅線為彈性較金更高之金屬,為了製作安定之形狀,需要在較習知金線更高之負載下進行加工。 若將此種較大負載施加於引線框架,貼附於引線框架下部之接著片材之接著劑層若為低彈性模數,該接著劑層會變形而在接著劑層已變形狀態下進行樹脂密封。如此一來,會從已變形之接著劑層部分發生密封樹脂溢漏。此外,從引線框架剝離接著片材時,接著劑層會從該已變形之接著劑層部分開始斷裂,也會產生引線框架表面上殘留接著劑之問題。不僅如此,銲線接合時若接著劑呈低彈性模數,接著劑會變形而使銲線負載不易傳送,也容易發生銲線接合不良。本發明之接著片材中,接著劑層如上述般具有高彈性模數之特性,因此即便使用銅線或覆鈀銅線來進行銲線接合,也不易發生銲線接合不良、密封樹脂溢漏及接著劑層殘留等問題。In addition, the adhesive layer with low glass transition temperature (-30°C to 50°C) in the adhesive sheet of the present invention can obtain the characteristics of high elastic modulus when heated. In recent years, for the purpose of reducing the cost of the wire bonding step, products using low-cost copper wire or palladium-clad copper wire for bonding have become popular instead of the conventional gold wire. Copper wire or palladium-clad copper wire is a metal with higher elasticity than gold. In order to make a stable shape, it needs to be processed under a higher load than the conventional gold wire. If such a large load is applied to the lead frame, if the adhesive layer of the adhesive sheet attached to the lower part of the lead frame has a low elastic modulus, the adhesive layer will be deformed, and the resin will be processed in the deformed state of the adhesive layer. seal. As a result, leakage of the sealing resin occurs from the deformed adhesive layer portion. In addition, when the adhesive sheet is peeled off from the lead frame, the adhesive layer is broken from the deformed adhesive layer portion, and there is also a problem that the adhesive remains on the surface of the lead frame. In addition, if the adhesive has a low modulus of elasticity during wire bonding, the adhesive will be deformed, making it difficult to transmit the load on the wire, and wire bonding failure is likely to occur. In the adhesive sheet of the present invention, since the adhesive layer has the characteristics of high elastic modulus as described above, even if a copper wire or a palladium-clad copper wire is used for wire bonding, poor wire bonding and leakage of the sealing resin are unlikely to occur. And problems such as residual adhesive layer.

此外,本發明之接著片材中,接著劑層具有含2個以上順丁烯二醯亞胺基之化合物(c),因此製造接著片材時之乾燥過程中,可適切控制接著劑層之硬化而將接著劑層製成高B階段狀態,因而可抑止對引線框架之接著強度增高,結果,可抑制密封樹脂溢漏、接著劑殘留於引線框架及剝離時接著劑層發生斷裂。 實施例In addition, in the adhesive sheet of the present invention, the adhesive layer has the compound (c) containing two or more maleimide groups, so during the drying process when the adhesive sheet is produced, the amount of the adhesive layer can be appropriately controlled. By curing the adhesive layer to a high B-stage state, the increase in the bonding strength to the lead frame can be suppressed. As a result, leakage of the sealing resin, remaining of the adhesive on the lead frame, and rupture of the adhesive layer during peeling can be suppressed. Example

以下,顯示實施例以就本發明予以具體說明。 [實施例1~4及比較例1~3] (接著劑塗料之組成) 按表1所示質量比率,將(a)~(d)成分、其他成分及溶劑之四氫呋喃(THF)混合,調製出接著劑塗料。 接著,於厚度25μm之聚醯亞胺薄膜(DU PONT-TORAY CO., LTD.製,商品名Kapton 100EN)之單面上,以塗料乾燥後之接著劑層厚度為5μm之方式塗佈該接著劑後,於設定為80℃之熱風循環型烘箱中乾燥,獲得接著片材。 另,使用之各成分詳情如下。Hereinafter, examples are shown to specifically illustrate the present invention. [Examples 1 to 4 and Comparative Examples 1 to 3] (Composition of Adhesive Coating) The components (a) to (d), the other components, and tetrahydrofuran (THF) of the solvent were mixed at the mass ratios shown in Table 1 to prepare an adhesive paint. Next, on one side of a polyimide film with a thickness of 25 μm (manufactured by DU PONT-TORAY CO., LTD., trade name Kapton 100EN), the adhesive layer was applied so that the thickness of the adhesive layer after the coating was dried was 5 μm. After the preparation, it was dried in a hot air circulation type oven set at 80° C. to obtain an adhesive sheet. In addition, the details of each ingredient used are as follows.

・含羧基之丙烯腈-丁二烯共聚物:從數量平均分子量算出之羧基當量1500、丙烯腈含量27質量% ・具結構式(1)之環氧樹脂:分子量630、官能基當量210g/eq ・雙酚A二苯基醚雙順丁烯二醯亞胺:分子量570、官能基當量285g/eq ・2-苯基-4,5-二羥基甲基咪唑(四國化成工業社製,商品名:CUREZOL 2PHZ-PW,反應開始溫度:150℃) ・2-苯基-4-甲基-5-羥基甲基咪唑(四國化成工業社製,商品名:CUREZOL 2P4MHZ-PW,反應開始溫度:130℃) ・2-乙基-4-甲基咪唑(四國化成工業社製,商品名:CUREZOL 2E4MZ,反應開始溫度:90℃) ・2-十一烷基咪唑(四國化成工業社製,商品名:CUREZOL C11Z,反應開始溫度:90℃)・Carboxyl group-containing acrylonitrile-butadiene copolymer: Carboxyl group equivalent calculated from number average molecular weight 1500, acrylonitrile content 27% by mass ・Epoxy resin with structural formula (1): molecular weight 630, functional group equivalent 210g/eq ・Bisphenol A diphenyl ether bismaleimide: molecular weight 570, functional group equivalent 285g/eq ・2-Phenyl-4,5-dihydroxymethylimidazole (manufactured by Shikoku Chemical Industry Co., Ltd., trade name: CUREZOL 2PHZ-PW, reaction start temperature: 150°C) ・2-Phenyl-4-methyl-5-hydroxymethylimidazole (manufactured by Shikoku Chemical Industry Co., Ltd., trade name: CUREZOL 2P4MHZ-PW, reaction start temperature: 130°C) ・2-Ethyl-4-methylimidazole (manufactured by Shikoku Chemical Industry Co., Ltd., trade name: CUREZOL 2E4MZ, reaction start temperature: 90°C) ・2-Undecylimidazole (manufactured by Shikoku Chemical Industry Co., Ltd., trade name: CUREZOL C11Z, reaction start temperature: 90°C)

[表1]

Figure 02_image009
[Table 1]
Figure 02_image009

針對上述所得實施例及比較例之接著片材進行後續測定及評價,將其結果示於表2。Subsequent measurements and evaluations were performed on the adhesive sheets of the above-obtained Examples and Comparative Examples, and the results are shown in Table 2.

(1)對Cu板之剝離強度 被貼附體:銅板(古河製125μm64型) 接著片材尺寸:寬度10mm×長度50mm 加工:使用輥壓層合機,令已將各例所得接著片材貼附於被貼附體所得之物為試驗體。令此時之積層條件為溫度80℃、壓力4N/cm、壓附速度0.5m/分鐘。 保存:將經上述加工之接著片材按下列2個條件保存,對保存後各接著片材進行剝離強度之測定及評價。 <條件1> 將經上述加工之接著片材保存於設定為60℃之恒溫槽120小時。 <條件2> 將經上述加工之接著片材保存於設定為60℃之恒溫槽120小時後,進一步於設定為40℃之恒溫槽中保存1週。 測定:使用萬能拉伸試驗機,常溫下測定試驗體之90°剝離強度。固定銅板,將接著片材朝垂直方向拉伸來測定。令拉伸速度為50mm/分鐘。 評價:剝離強度若慮及以積層方式貼膠時之量產性,實用上15gf/cm以上為無問題之接著強度。令15gf/cm以上為A,小於15gf/cm為X。(1) Peel strength to Cu board Attached body: Copper plate (125μm64 type made by Furukawa) Next sheet size: width 10mm x length 50mm Processing: Using a roll laminator, the adhesive sheet obtained in each example was attached to a to-be-attached body as a test body. The lamination conditions at this time were set to a temperature of 80° C., a pressure of 4 N/cm, and a pressing speed of 0.5 m/min. Storage: The adhesive sheet processed as described above was preserved under the following two conditions, and the peel strength was measured and evaluated for each adhesive sheet after storage. <Condition 1> The adhesive sheet processed as described above was stored in a thermostatic bath set at 60° C. for 120 hours. <Condition 2> After the adhesive sheet processed as described above was stored in a thermostat set at 60°C for 120 hours, it was further stored in a thermostat set at 40°C for 1 week. Measurement: Using a universal tensile testing machine, measure the 90° peel strength of the test body at room temperature. The copper plate was fixed, and the adhesive sheet was stretched in the vertical direction to measure. The stretching speed was made 50 mm/min. Evaluation: Considering the mass productivity when the peeling strength is applied by lamination, practically 15 gf/cm or more is a non-problematic adhesive strength. Let A be 15 gf/cm or more, and X be less than 15 gf/cm.

(2)加熱後之彈性模數 加工:於厚度38μm且已施行脫模處理之聚對酞酸乙二酯薄膜(PET薄膜)的單面上,以乾燥後接著劑層厚度為5μm之方式塗佈前述所得各例之接著劑塗料後,乾燥而獲得接著片材。接著,預想黏晶固化處理,使用通風烘箱將該接著片材以175℃加熱60分鐘。 測定:將加熱後之接著片材中之接著劑層從PET薄膜剝離,使用DMA(動態機械分析儀,Dynamic Mechanical Analyzer)測定拉伸貯藏彈性模數。DMA使用VIBRON測定器(ORIENTEC CORPORATION製,RHEOVIBRONDDV-II-EP),於頻率11Hz、昇溫速度10℃/分鐘、荷重1.0gf下進行測定。 評價:預想銲線接合步驟時之施加溫度,令200℃下之拉伸貯藏彈性模數為6MPa以上者為A,200℃下之拉伸貯蔵彈性模數小於6MPa者為X。(2) Elastic modulus after heating Processing: On one side of a polyethylene terephthalate film (PET film) with a thickness of 38 μm and having been subjected to mold release treatment, the adhesive coating of each example obtained above was applied in a manner that the thickness of the adhesive layer after drying was 5 μm. Then, the adhesive sheet was obtained by drying. Next, in anticipation of a die-bonding curing process, the adhesive sheet was heated at 175° C. for 60 minutes using a ventilation oven. Measurement: The adhesive layer in the adhesive sheet after heating was peeled off from the PET film, and the tensile storage elastic modulus was measured using a DMA (Dynamic Mechanical Analyzer). DMA was measured using a VIBRON measuring device (manufactured by ORIENTEC CORPORATION, RHEOVIBRONDDV-II-EP) at a frequency of 11 Hz, a temperature increase rate of 10° C./min, and a load of 1.0 gf. Evaluation: The temperature applied during the wire bonding step is expected, and the tensile storage elastic modulus at 200°C is 6 MPa or more as A, and the tensile storage elastic modulus at 200°C is less than 6 MPa as X.

(4)對樹脂密封步驟後之試驗體的剝離強度、膠帶剝離後接著劑殘留物之有無 加工、測定方法: (i)試驗體之製作與熱處理 將各例所得在聚醯亞胺薄膜上具有接著劑層之接著片材裁切為寬度50mm×長度60mm後,預想實際上伴隨QFN組裝之熱歷程等,先依序實施下列(a)~(d)。 (a)將各例所得接著片材裁切為寬度50mm×長度60mm,使用輥壓層合機將其貼附在50mm×100mm之外尺寸57.5mm×53.5mm銅合金製試驗用引線框架(表面打底鍍層,8×8個陣列排列,封裝體尺寸5mm×5mm,32接腳)。此時,令積層條件為溫度80℃、壓力4N/cm、壓附速度0.5m/分鐘。 (b)將貼附有接著片材之銅合金製試驗用引線框架以通風烘箱加熱175℃/60分鐘。這是預想黏晶固化處理所做之處理。 (c)電漿照射處理:以Yield Engineering Systems, Inc.製1000P,氣體種類使用Ar,處理450W/60秒。 (d)200℃/30分鐘加熱:為預想銲線接合步驟而做之處理,使用熱板進行加熱。 接著對已完成(a)~(d)之熱處理之被貼附體,於其之與接著片材貼附面相反面之銅材露出面上,使用模壓機在175℃/3分鐘之條件下積層密封樹脂(樹脂密封步驟)。密封樹脂使用Sumitomo Bakelite Co., Ltd.製之環氧模具樹脂(EME-G631BQ)。(4) Peel strength to test body after resin sealing step, presence or absence of adhesive residue after tape peeling Processing and measurement methods: (i) Preparation and heat treatment of test body After cutting the adhesive sheet with an adhesive layer on the polyimide film obtained in each example into a width of 50mm × length of 60mm, it is expected that the thermal history of QFN assembly will actually be accompanied by the following (a)~( d). (a) The adhesive sheet obtained in each example was cut into a width of 50 mm × length of 60 mm, and was attached to a test lead frame (surface 50 mm × 100 mm, 57.5 mm × 53.5 mm) made of copper alloy using a roll laminator. Bottom plating, 8 × 8 arrays, package size 5mm × 5mm, 32 pins). At this time, the lamination conditions were set to a temperature of 80° C., a pressure of 4 N/cm, and a pressing speed of 0.5 m/min. (b) The lead frame for a test made of copper alloy to which the adhesive sheet was attached was heated at 175° C./60 minutes in a ventilation oven. This is what the sticky die curing process is supposed to do. (c) Plasma irradiation treatment: 1000P manufactured by Yield Engineering Systems, Inc., Ar gas was used, and treatment was performed at 450W/60 seconds. (d) Heating at 200° C./30 minutes: Heating with a hot plate was performed in anticipation of the wire bonding step. Next, on the adhered body that has completed the heat treatment of (a) to (d), on the exposed surface of the copper material opposite to the adhered surface of the adhesive sheet, use a molding machine under the conditions of 175°C/3 minutes. Laminate a sealing resin (resin sealing step). As the sealing resin, epoxy mold resin (EME-G631BQ) manufactured by Sumitomo Bakelite Co., Ltd. was used.

(ii)剝離強度之測定、膠帶剝離後接著劑殘留物之有無 針對上述樹脂密封步驟後之試驗體,使用萬能拉伸試驗機,常溫下測定90°剝離強度。另,固定試驗體,將接著片材之角落部分朝垂直方向拉伸來測定。令拉伸速度為300mm/分鐘。此外,膠帶剝離後有無接著劑殘留物係以光學顯微鏡(KEYENCE CORPORATION製數位顯微鏡VHX-500),以倍率100倍確認。 評價: A:剝離強度小於1000gf/50mm,剝離之接著片材未斷裂,引線框架材表面及密封樹脂表面未有接著劑殘留。 B:剝離強度為1000gf/50mm以上,剝離之接著片材未斷裂,引線框架材表面及密封樹脂表面未有接著劑殘留。 X:觀察到接著片材斷裂或觀察到引線框架材表面及密封樹脂表面有接著劑殘留,符合上述中至少任一者。(ii) Determination of peel strength, presence or absence of adhesive residue after tape peeling The 90° peel strength was measured at room temperature using a universal tensile tester with respect to the test body after the above-mentioned resin sealing step. In addition, the test body was fixed, and the corner portion of the adhesive sheet was stretched in the vertical direction for measurement. The stretching speed was set to 300 mm/min. In addition, the presence or absence of adhesive residue after the tape peeling was confirmed with an optical microscope (Digital Microscope VHX-500 manufactured by KEYENCE CORPORATION) at a magnification of 100 times. evaluate: A: The peel strength is less than 1000 gf/50 mm, the adhesive sheet after peeling is not broken, and no adhesive remains on the surface of the lead frame material and the surface of the sealing resin. B: The peeling strength is 1000 gf/50 mm or more, the adhesive sheet after peeling is not broken, and no adhesive remains on the surface of the lead frame material and the surface of the sealing resin. X: The adhesive sheet was observed to be broken, or the adhesive residue was observed on the surface of the lead frame material and the surface of the sealing resin, and at least one of the above was satisfied.

[表2]

Figure 02_image011
[Table 2]
Figure 02_image011

從上述表2明顯看出,實施例1~4之接著片材在對Cu板之剝離強度、加熱後之彈性模數、對樹脂密封步驟後之試驗體之剝離強度、及膠帶剝離後有無接著劑殘留物之全部評價上皆是實用上無問題之結果。 相對於此,比較例1及比較例2之接著片材係對Cu板之接著強度偏低且容易發生密封樹脂溢漏之接著膠帶。此外,比較例3之接著片材係加熱後彈性模數偏低且在銅線之銲線接合上容易發生銲線連接不良之接著膠帶,並且,在對樹脂密封步驟後之試驗體的剝離強度評價中,牢固接著在銅合金製試驗用引線框架上,而有接著片材破裂之問題。 產業上之可利用性As is apparent from Table 2 above, the adhesive sheets of Examples 1 to 4 exhibited peel strength to the Cu board, elastic modulus after heating, peel strength to the test body after the resin sealing step, and whether or not the adhesive tape was peeled off. All evaluations of agent residues were practically non-problematic results. On the other hand, the adhesive sheets of Comparative Example 1 and Comparative Example 2 are adhesive tapes whose adhesive strength to the Cu board is relatively low and leakage of the sealing resin is likely to occur. In addition, the adhesive sheet of Comparative Example 3 is an adhesive tape whose elastic modulus is low after heating and is prone to bond wire bonding failure in copper wire bonding, and the peel strength of the test body after the resin sealing step In the evaluation, it was firmly attached to the copper alloy test lead frame, but there was a problem that the adhesive sheet was broken. industrial availability

本發明之半導體裝置製造用接著片材可適於用在利用QFN方式之QFN封裝體組裝方法上。藉由將其利用在半導體裝置製造方法中,可在QFN組裝過程之剝離步驟中容易地剝離接著片材,並且,接著片材上不會發生接著劑殘膠,也不會使接著片材發生斷裂。The adhesive sheet for manufacturing a semiconductor device of the present invention can be suitably used in a QFN package assembling method using the QFN method. By using it in the semiconductor device manufacturing method, the adhesive sheet can be easily peeled off in the peeling step of the QFN assembly process, and the adhesive residue does not occur on the adhesive sheet, nor does the adhesive sheet occur. fracture.

10:半導體裝置製造用接著片材 20:引線框架 21:晶座部 22:引線 30:半導體元件 31:接合線 40:密封樹脂 50:QFN封裝體 60:QFN單元 A-A’:剖線10: Adhesive sheet for semiconductor device manufacturing 20: Lead frame 21: Crystal seat part 22: Leads 30: Semiconductor components 31: Bonding Wire 40: Sealing resin 50: QFN package 60: QFN unit A-A': section line

圖1為俯視圖,其顯示用於本發明之半導體裝置製造方法之引線框架之一例。 圖2A為步驟圖,其說明本發明之半導體裝置之製造方法。 圖2B為步驟圖,其說明本發明之半導體裝置之製造方法。 圖2C為步驟圖,其說明本發明之半導體裝置之製造方法。 圖2D為步驟圖,其說明本發明之半導體裝置之製造方法。 圖2E為步驟圖,其說明本發明之半導體裝置之製造方法。 圖2F為步驟圖,其說明本發明之半導體裝置之製造方法。FIG. 1 is a plan view showing an example of a lead frame used in a method of manufacturing a semiconductor device of the present invention. FIG. 2A is a step diagram illustrating a manufacturing method of the semiconductor device of the present invention. FIG. 2B is a step diagram illustrating a manufacturing method of the semiconductor device of the present invention. FIG. 2C is a step diagram illustrating a manufacturing method of the semiconductor device of the present invention. FIG. 2D is a step diagram illustrating a manufacturing method of the semiconductor device of the present invention. FIG. 2E is a step diagram illustrating a manufacturing method of the semiconductor device of the present invention. FIG. 2F is a step diagram illustrating a manufacturing method of the semiconductor device of the present invention.

(無)(without)

Claims (5)

一種半導體裝置製造用接著片材,將會以可剝離方式貼附於半導體裝置之引線框架或配線基板上,其特徵在於具備: 基材;及 熱硬化型接著劑層,其設在該基材之一面上,且含有含羧基之丙烯腈-丁二烯共聚物(a)、具有下述結構式(1)之環氧樹脂(b)、含2個以上順丁烯二醯亞胺基之化合物(c)及潛伏型硬化劑(d); [化學式1]
Figure 03_image003
An adhesive sheet for manufacturing a semiconductor device, which is to be releasably attached to a lead frame or a wiring board of a semiconductor device, characterized by comprising: a base material; and a thermosetting adhesive layer provided on the base material On one side, it contains a carboxyl-containing acrylonitrile-butadiene copolymer (a), an epoxy resin (b) having the following structural formula (1), and an epoxy resin containing two or more maleimide groups Compound (c) and latent hardener (d); [Chemical formula 1]
Figure 03_image003
.
如請求項1之半導體裝置製造用接著片材,其中前述含羧基之丙烯腈-丁二烯共聚物(a)係一丙烯腈含量為5~50質量%且由數量平均分子量算出之羧基當量為100~20000之含羧基之丙烯腈-丁二烯共聚物。The adhesive sheet for manufacturing a semiconductor device according to claim 1, wherein the carboxyl group-containing acrylonitrile-butadiene copolymer (a) is an acrylonitrile content of 5 to 50% by mass and the carboxyl group equivalent calculated from the number average molecular weight is 100~20000 carboxyl-containing acrylonitrile-butadiene copolymer. 如請求項1之半導體裝置製造用接著片材,其中相對於前述含羧基之丙烯腈-丁二烯共聚物(a)100質量份,前述環氧樹脂(b)、前述含2個以上順丁烯二醯亞胺基之化合物(c)與前述潛伏型硬化劑(d)合計為30~300質量份。The adhesive sheet for manufacturing a semiconductor device according to claim 1, wherein the epoxy resin (b), the epoxy resin (b), the cis-butadiene containing two or more cis-butadiene groups, relative to 100 parts by mass of the carboxyl group-containing acrylonitrile-butadiene copolymer (a) The total amount of the compound (c) of an enediimide group and the aforementioned latent curing agent (d) is 30 to 300 parts by mass. 如請求項1之半導體裝置製造用接著片材,其中前述潛伏型硬化劑(d)係一與環氧樹脂之反應開始溫度為100℃以上之硬化劑。The adhesive sheet for semiconductor device manufacturing according to claim 1, wherein the latent curing agent (d) is a curing agent whose reaction initiation temperature with the epoxy resin is 100° C. or higher. 一種半導體裝置之製造方法,其特徵在於具備以下步驟: 貼附步驟,其係於引線框架或配線基板上貼附如請求項1之半導體裝置製造用接著片材; 黏晶步驟,其係於前述引線框架或配線基板上搭載半導體元件; 銲線接合步驟,其係使前述半導體元件與外部連接端子導通; 密封步驟,其係以密封樹脂密封前述半導體元件;以及 剝離步驟,其係於前述密封步驟後,將半導體裝置製造用接著片材從引線框架或配線基板剝離。A method of manufacturing a semiconductor device, comprising the following steps: an attaching step of attaching the adhesive sheet for manufacturing a semiconductor device as claimed in claim 1 on a lead frame or a wiring substrate; a die bonding step, which is to mount a semiconductor element on the aforementioned lead frame or wiring substrate; a wire bonding step, which is to make the aforementioned semiconductor element and external connection terminals conduct; a sealing step of sealing the aforementioned semiconductor element with a sealing resin; and A peeling process peels the adhesive sheet for semiconductor device manufacture from a lead frame or a wiring board after the said sealing process.
TW110118522A 2020-05-26 2021-05-21 Adhesive sheet for semiconductor device production and method for producing semiconductor device using same TW202202587A (en)

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