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TW201523808A - Bottom filling material and method of manufacturing semiconductor device using same - Google Patents

Bottom filling material and method of manufacturing semiconductor device using same Download PDF

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TW201523808A
TW201523808A TW103131080A TW103131080A TW201523808A TW 201523808 A TW201523808 A TW 201523808A TW 103131080 A TW103131080 A TW 103131080A TW 103131080 A TW103131080 A TW 103131080A TW 201523808 A TW201523808 A TW 201523808A
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temperature
underfill material
semiconductor wafer
electrode
epoxy resin
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TW103131080A
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TWI649842B (en
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森山浩伸
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迪睿合股份有限公司
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • 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
    • C09J5/00Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
    • C09J5/06Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving heating of the applied adhesive
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22Di-epoxy compounds
    • C08G59/24Di-epoxy compounds carbocyclic
    • 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
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • H10W72/01325
    • H10W72/0198
    • H10W72/072
    • H10W72/07232
    • H10W72/073
    • H10W72/07338
    • H10W72/241
    • H10W72/252
    • H10W72/325
    • H10W72/353
    • H10W72/354
    • H10W74/15
    • H10W90/724
    • H10W90/734
    • H10W99/00

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  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Wire Bonding (AREA)
  • Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)

Abstract

提供一種可抑制空隙產生之底部填充材料及使用其之半導體裝置之製造方法。係將底部填充材料(20)預先貼合於形成有附焊料電極之半導體晶片(10),搭載於形成有與附焊料電極對向之對向電極的電路基板(30),並將半導體晶片(10)與電路基板(30)熱壓接,該底部填充材料(20)含有環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物,搭載時之儲存彈性模數為3000Pa以上,最低熔融黏度到達溫度為125℃以下。 Provided is an underfill material capable of suppressing generation of voids and a method of manufacturing a semiconductor device using the same. The underfill material (20) is bonded in advance to the semiconductor wafer (10) on which the solder electrode is formed, and is mounted on the circuit substrate (30) on which the counter electrode facing the solder electrode is formed, and the semiconductor wafer ( 10) thermocompression bonding with the circuit substrate (30), the underfill material (20) containing an epoxy resin, an acid anhydride, an acrylic resin, and an organic peroxide, and the storage elastic modulus at the time of mounting is 3,000 Pa or more, and the lowest melt viscosity is reached. The temperature is below 125 °C.

Description

底部填充材料及使用其之半導體裝置的製造方法 Underfill material and method of manufacturing semiconductor device using same

本發明係關於一種用於搭載半導體晶片之底部填充材料、及使用其之半導體裝置之製造方法。 The present invention relates to an underfill material for mounting a semiconductor wafer, and a method of fabricating a semiconductor device using the same.

近年來,於半導體晶片之構裝方法中,為了縮短步驟,業界正研究使用在半導體IC(Integrated Circuit,積體電路)電極上貼附底部填充膜之「預供給型底部填充膜(PUF:Pre-applied Underfill Film)」。 In recent years, in the semiconductor wafer mounting method, in order to shorten the steps, the industry is investigating the use of a pre-supply underfill film (PUF: Pre) on which an underfill film is attached to a semiconductor IC (Integrated Circuit) electrode. -applied Underfill Film)".

使用該預供給型底部填充膜之搭載方法例如藉由如下方式進行(例如參照專利文獻1)。 The mounting method using the pre-feed type underfill film is performed, for example, as follows (for example, refer to Patent Document 1).

步驟A:於晶圓上貼附底部填充膜,進行切割而獲得半導體晶片。 Step A: attaching an underfill film to the wafer and performing dicing to obtain a semiconductor wafer.

步驟B:於基板上進行半導體晶片之位置對準。 Step B: Performing alignment of the semiconductor wafer on the substrate.

步驟C:藉由高溫、高壓將半導體晶片與基板壓接,藉由焊點凸塊之金屬鍵而確保傳導,及藉由底部填充膜之硬化而進行半導體晶片與基板之接著。 Step C: The semiconductor wafer is bonded to the substrate by high temperature and high pressure, the conduction is ensured by the metal bond of the bump bump, and the semiconductor wafer and the substrate are bonded by hardening of the underfill film.

此種方法存在於搭載半導體晶片時容易夾帶空隙,於加熱壓接後空隙仍殘留之情況。又,即便於搭載時未產生空隙之情形,以短時間 升溫之壓接分佈中亦存在於升溫過程中產生空隙之情況。 In such a method, when a semiconductor wafer is mounted, it is easy to entrap a void, and the void remains after the thermocompression bonding. Moreover, even if there is no gap at the time of mounting, it takes a short time. In the pressure-bonding distribution of the temperature rise, there is also a case where a void is generated during the temperature rise.

[專利文獻1]日本特開2005-28734號公報 [Patent Document 1] Japanese Patent Laid-Open Publication No. 2005-28734

本發明係鑒於此種習知之實際情況而提出者,提供一種可抑制空隙產生之底部填充材料及使用其之半導體裝置之製造方法。 The present invention has been made in view of such conventional circumstances, and provides an underfill material capable of suppressing generation of voids and a method of manufacturing a semiconductor device using the same.

為了解決上述課題,本發明係一種於將形成有附焊料電極之半導體晶片搭載於形成有與上述附焊料電極對向之對向電極的電子零件時,被預先貼合於上述半導體晶片的底部填充材料,其特徵在於:含有環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物,上述搭載時之儲存彈性模數為3000Pa以上,最低熔融黏度到達溫度為125℃以下。 In order to solve the above problems, the present invention is a method in which a semiconductor wafer on which a solder electrode is formed is mounted on an electronic component in which a counter electrode opposed to the solder electrode is formed, and is bonded to an underfill of the semiconductor wafer in advance. The material is characterized in that it contains an epoxy resin, an acid anhydride, an acrylic resin, and an organic peroxide, and the storage elastic modulus at the time of mounting is 3,000 Pa or more, and the lowest melt viscosity reaches 125 ° C or lower.

又,本發明之半導體裝置之製造方法的特徵在於含有:搭載步驟:於第1溫度將形成有附焊料電極且於該電極面貼合有底部填充材料之半導體晶片搭載於形成有與上述附焊料電極對向之對向電極的電子零件;及熱壓接步驟:將上述半導體晶片與上述電子零件升溫至第2溫度進行熱壓接,其中上述底部填充材料含有環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物,第1溫度下之儲存彈性模數為3000Pa以上,最低熔融黏度到達溫度為125℃以下。 Moreover, the method of manufacturing a semiconductor device according to the present invention includes the step of mounting a semiconductor wafer having a solder electrode formed thereon and having an underfill material bonded to the electrode surface, and the solder is formed on the electrode. An electronic component opposite to the opposite electrode of the electrode; and a thermocompression bonding step: thermocompression bonding the semiconductor wafer and the electronic component to a second temperature, wherein the underfill material comprises an epoxy resin, an acid anhydride, an acrylic resin, And the organic peroxide has a storage elastic modulus of 3,000 Pa or more at the first temperature and a minimum melt viscosity of 125 ° C or less.

根據本發明,由於搭載時之底部填充材料之儲存彈性模數高,最低熔融黏度到達溫度低,故可排除搭載時之空隙,並且可抑制加熱壓接時之空隙之產生。 According to the present invention, since the storage elastic modulus of the underfill material at the time of mounting is high and the lowest melt viscosity reaches a low temperature, voids at the time of mounting can be eliminated, and generation of voids at the time of thermocompression bonding can be suppressed.

1‧‧‧晶圓 1‧‧‧ wafer

2‧‧‧底部填充膜 2‧‧‧ underfill film

3‧‧‧治具 3‧‧‧ fixture

4‧‧‧刀片 4‧‧‧blade

10‧‧‧半導體晶片 10‧‧‧Semiconductor wafer

11‧‧‧半導體 11‧‧‧ Semiconductor

12‧‧‧電極 12‧‧‧ electrodes

13‧‧‧焊料 13‧‧‧ solder

20‧‧‧底部填充材料 20‧‧‧ Underfill material

21‧‧‧接著劑層 21‧‧‧ adhesive layer

30‧‧‧電路基板 30‧‧‧ circuit board

31‧‧‧基材 31‧‧‧Substrate

32‧‧‧對向電極 32‧‧‧ opposite electrode

圖1係示意性地表示搭載前之半導體晶片與電路基板之剖面圖。 Fig. 1 is a cross-sectional view schematically showing a semiconductor wafer and a circuit board before mounting.

圖2係示意性地表示搭載時之半導體晶片與電路基板之剖面圖。 Fig. 2 is a cross-sectional view schematically showing a semiconductor wafer and a circuit board during mounting.

圖3係示意性地表示熱壓接後之半導體晶片與電路基板之剖面圖。 Fig. 3 is a cross-sectional view schematically showing a semiconductor wafer and a circuit board after thermocompression bonding.

圖4係表示本實施形態之半導體裝置的製造方法之流程圖。 Fig. 4 is a flow chart showing a method of manufacturing the semiconductor device of the embodiment.

圖5係示意性地表示在晶圓上貼附底部填充膜之步驟之立體圖。 Fig. 5 is a perspective view schematically showing a step of attaching an underfill film to a wafer.

圖6係示意性地表示切割晶圓之步驟之立體圖。 Fig. 6 is a perspective view schematically showing a step of cutting a wafer.

圖7係示意性地表示拾取半導體晶片之步驟之立體圖。 Fig. 7 is a perspective view schematically showing a step of picking up a semiconductor wafer.

圖8係表示實施例之壓接分佈之曲線圖。 Fig. 8 is a graph showing the crimp distribution of the embodiment.

以下,按照下述順序對本發明之實施形態進行詳細說明。 Hereinafter, embodiments of the present invention will be described in detail in the following order.

1.底部填充材料 Underfill material

2.半導體裝置之製造方法 2. Method of manufacturing a semiconductor device

3.實施例 3. Embodiment

<1.底部填充材料> <1. Underfill material>

本實施形態之底部填充材料係於將形成有附焊料電極之半導體晶片搭載於形成有與附焊料電極對向之對向電極的電子零件時,被預先貼合於半導體晶片者。 In the underfill material of the present embodiment, when a semiconductor wafer on which a solder electrode is formed is mounted on an electronic component on which a counter electrode facing the solder electrode is formed, the semiconductor wafer is bonded to the semiconductor wafer in advance.

圖1係模式性地表示搭載前之半導體晶片與電路基板之剖面圖,圖2係模式性地表示搭載時之半導體晶片與電路基板之剖面圖,及 圖3係模式性地表示熱壓接後之半導體晶片與電路基板之剖面圖。 1 is a cross-sectional view schematically showing a semiconductor wafer and a circuit board before mounting, and FIG. 2 is a cross-sectional view schematically showing a semiconductor wafer and a circuit board during mounting, and 3 is a cross-sectional view schematically showing a semiconductor wafer and a circuit board after thermocompression bonding.

如圖1~圖3所示,本實施形態之底部填充材料20係預先貼合於形成有附焊料電極之半導體晶片10的電極面而使用,利用底部填充材料20硬化而成之接著層21,將半導體晶片10與形成有與附焊料電極對向之對向電極之電路基板30進行接合。 As shown in FIG. 1 to FIG. 3, the underfill material 20 of the present embodiment is used in advance to be bonded to the electrode surface of the semiconductor wafer 10 on which the solder electrode is attached, and the underlayer 21 is cured by the underfill material 20, The semiconductor wafer 10 is bonded to the circuit substrate 30 on which the counter electrode facing the solder electrode is formed.

半導體晶片10於矽等半導體11表面形成有積體電路,並具有稱為凸塊之連接用附焊料電極。附焊料電極係於由銅等構成之電極12上接合有焊料13者,且具有將電極12厚度與焊料13厚度合計之厚度。 The semiconductor wafer 10 has an integrated circuit formed on the surface of the semiconductor 11 such as germanium, and has a solder electrode for connection called a bump. The solder electrode is bonded to the electrode 12 made of copper or the like and has a thickness in which the thickness of the electrode 12 and the thickness of the solder 13 are combined.

作為焊料,可使用Sn-37Pb共晶焊料(熔點183℃)、Sn-Bi焊料(熔點139℃)、Sn-3.5Ag(熔點221℃)、Sn-3.0Ag-0.5Cu(熔點217℃)、Sn-5.0Sb(熔點240℃)等。 As the solder, Sn-37Pb eutectic solder (melting point 183 ° C), Sn-Bi solder (melting point 139 ° C), Sn-3.5 Ag (melting point 221 ° C), Sn-3.0 Ag-0.5 Cu (melting point 217 ° C), Sn-5.0Sb (melting point 240 ° C) and the like.

電路基板30於例如硬質基板、可撓性基板等基材31上形成有電路。又,於搭載半導體晶片10之構裝部形成有對向電極32,該對向電極32在與半導體晶片10之附焊料電極對向之位置具有特定厚度。 The circuit board 30 is formed with a circuit on a base material 31 such as a rigid substrate or a flexible substrate. Further, a counter electrode 32 is formed on the mounting portion on which the semiconductor wafer 10 is mounted, and the counter electrode 32 has a specific thickness at a position facing the solder electrode of the semiconductor wafer 10.

底部填充材料20含有膜形成樹脂、環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物。 The underfill material 20 contains a film forming resin, an epoxy resin, an acid anhydride, an acrylic resin, and an organic peroxide.

膜形成樹脂相當於平均分子量為10000以上之高分子量樹脂,就膜形成性之觀點而言,較佳為10000~80000左右之平均分子量。作為膜形成樹脂,可使用苯氧基樹脂、環氧樹脂、改質環氧樹脂、胺基甲酸酯樹脂等各種樹脂。該等膜形成樹脂可單獨使用1種,亦可組合2種以上而使用。該等之中,就膜形成狀態、連接可靠性等觀點而言,本實施形態較佳使用苯氧基樹脂。 The film-forming resin corresponds to a high molecular weight resin having an average molecular weight of 10,000 or more, and is preferably an average molecular weight of about 10,000 to 80,000 from the viewpoint of film formability. As the film forming resin, various resins such as a phenoxy resin, an epoxy resin, a modified epoxy resin, and a urethane resin can be used. These film-forming resins may be used alone or in combination of two or more. Among these, a phenoxy resin is preferably used in the present embodiment from the viewpoint of film formation state, connection reliability, and the like.

作為環氧樹脂,例如可列舉:倍環戊二烯型環氧樹脂、縮水甘油醚型環氧樹脂、縮水甘油胺型環氧樹脂、雙酚A型環氧樹脂、雙酚F型環氧樹脂、雙酚S型環氧樹脂、螺環型環氧樹脂、萘型環氧樹脂、聯苯型環氧樹脂、萜烯型環氧樹脂、四溴雙酚A型環氧樹脂、甲酚酚醛清漆型環氧樹脂、苯酚酚醛清漆型環氧樹脂、α-萘酚酚醛清漆型環氧樹脂、溴化苯酚酚醛清漆型環氧樹脂等。該等環氧樹脂可單獨使用1種,亦可組合2種以上而使用。該等之中,就高接著性、耐熱性之方面而言,本實施形態較佳使用倍環戊二烯型環氧樹脂。 Examples of the epoxy resin include a pentacyclopentadiene type epoxy resin, a glycidyl ether type epoxy resin, a glycidylamine type epoxy resin, a bisphenol A type epoxy resin, and a bisphenol F type epoxy resin. , bisphenol S type epoxy resin, spiral ring type epoxy resin, naphthalene type epoxy resin, biphenyl type epoxy resin, terpene type epoxy resin, tetrabromobisphenol A type epoxy resin, cresol novolac Type epoxy resin, phenol novolac type epoxy resin, α-naphthol novolac type epoxy resin, brominated phenol novolak type epoxy resin, and the like. These epoxy resins may be used alone or in combination of two or more. Among these, a pentacyclopentadiene type epoxy resin is preferably used in the present embodiment in terms of high adhesion and heat resistance.

酸酐具有去除焊料表面之氧化膜之助熔功能,因此可獲得優異之連接可靠性。作為酸酐,例如可列舉:四丙烯基琥珀酸酐、十二烯基琥珀酸酐等脂肪族酸酐,六氫鄰苯二甲酸酐、甲基四氫鄰苯二甲酸酐等脂環式酸酐,鄰苯二甲酸酐、偏苯三甲酸酐、均苯四甲酸二酐等芳香族酸酐等。該等環氧硬化劑可單獨使用1種,亦可組合2種以上而使用。該等環氧硬化劑之中,就該等中之焊料連接性之方面而言,較佳使用脂肪族酸酐。 The acid anhydride has a fluxing function of removing an oxide film on the surface of the solder, so that excellent connection reliability can be obtained. Examples of the acid anhydride include aliphatic acid anhydrides such as tetrapropenyl succinic anhydride and dodecenyl succinic anhydride; alicyclic acid anhydrides such as hexahydrophthalic anhydride and methyltetrahydrophthalic anhydride; and phthalic acid. An aromatic acid anhydride such as formic anhydride, trimellitic anhydride or pyromellitic dianhydride. These epoxy curing agents may be used alone or in combination of two or more. Among these epoxy hardeners, aliphatic acid anhydrides are preferably used in terms of solder connectivity in these.

又,較佳添加硬化促進劑。作為硬化促進劑之具體例,可列舉:2-甲基咪唑、2-乙基咪唑、2-乙基-4-甲基咪唑等咪唑類、1,8-二氮雙環(5,4,0)十一烯-7鹽(DBU鹽)、2-(二甲基胺基甲基)苯酚等三級胺類、三苯基膦等膦類、辛酸錫等金屬化合物等。 Further, it is preferred to add a hardening accelerator. Specific examples of the curing accelerator include imidazoles such as 2-methylimidazole, 2-ethylimidazole, and 2-ethyl-4-methylimidazole, and 1,8-diazabicyclo (5,4,0). a tertiary amine such as undecene-7 salt (DBU salt) or 2-(dimethylaminomethyl)phenol; a phosphine such as triphenylphosphine; or a metal compound such as tin octylate.

作為丙烯酸樹脂,可使用單官能(甲基)丙烯酸酯、2官能以上之(甲基)丙烯酸酯。作為單官能(甲基)丙烯酸酯,可列舉:(甲基)丙烯酸甲酯、(甲基)丙烯酸乙酯、(甲基)丙烯酸正丙酯、(甲基)丙烯酸異丙酯、(甲基)丙烯酸正丁酯等。作為2官能以上之(甲基)丙烯酸酯,可列舉:雙酚F-EO 改質二(甲基)丙烯酸酯、雙酚A-EO改質二(甲基)丙烯酸酯、三羥甲基丙烷PO改質(甲基)丙烯酸酯、多官能(甲基)丙烯酸胺基甲酸酯等。該等丙烯酸樹脂可單獨使用,亦可組合2種以上而使用。該等之中,本實施形態較佳使用2官能(甲基)丙烯酸酯。 As the acrylic resin, a monofunctional (meth) acrylate or a bifunctional or higher (meth) acrylate can be used. Examples of the monofunctional (meth) acrylate include methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, and (methyl). ) n-butyl acrylate and the like. Examples of the bifunctional or higher (meth) acrylate include bisphenol F-EO. Modified di(meth)acrylate, bisphenol A-EO modified di(meth)acrylate, trimethylolpropane PO modified (meth)acrylate, polyfunctional (meth)acrylic acid amine Acid esters, etc. These acrylic resins may be used singly or in combination of two or more. Among these, in the present embodiment, a bifunctional (meth) acrylate is preferably used.

作為有機過氧化物,例如可列舉:過氧化酯、過氧縮酮、過氧化氫、過氧化二烷基、過氧化二醯基、過氧化二碳酸酯等。該等有機過氧化物可單獨使用,亦可組合2種以上而使用。該等之中,本實施形態較佳使用過氧化酯。 Examples of the organic peroxide include peroxyester, peroxyketal, hydrogen peroxide, dialkyl peroxide, dinonyl peroxide, and peroxydicarbonate. These organic peroxides may be used singly or in combination of two or more. Among these, in the present embodiment, a peroxyester is preferably used.

又,作為其他添加組成物,較佳含有無機填料。藉由含有無機填料,可調整壓接時之樹脂層的流動性。作為無機填料,可使用矽石、滑石、氧化鈦、碳酸鈣、氧化鎂等。 Moreover, as another additive composition, it is preferable to contain an inorganic filler. By containing an inorganic filler, the fluidity of the resin layer at the time of pressure bonding can be adjusted. As the inorganic filler, vermiculite, talc, titanium oxide, calcium carbonate, magnesium oxide, or the like can be used.

並且,亦可視需要添加環氧系、胺基系、巰基-硫醚系、脲基系等之矽烷偶合劑。 Further, a decane coupling agent such as an epoxy group, an amine group, a mercapto-thioether system or a urea group may be added as needed.

藉由如此併用硬化反應相對較慢之環氧系、與硬化反應相對較快之丙烯酸,即便於在10秒以內到達250℃之短時間升溫分佈下進行壓接之情形時,亦可防止空隙之產生。 By using the epoxy-based epoxy resin which is relatively slow in the hardening reaction and the acrylic acid which is relatively fast in the hardening reaction, even when the pressure is applied under a short-time temperature-increasing distribution of 250 ° C within 10 seconds, the void can be prevented. produce.

又,搭載底部填充材料時之儲存彈性模數為3000Pa以上。藉此,可排除搭載時之空隙。搭載時之溫度較佳為30℃以上且較底部填充材料之最低熔融黏度到達溫度高30℃以下,更具體而言,較佳為30℃以上155℃以下。 Further, the storage elastic modulus when the underfill material is mounted is 3,000 Pa or more. Thereby, the gap at the time of mounting can be eliminated. The temperature at the time of mounting is preferably 30 ° C or more and is 30 ° C or less higher than the lowest melt viscosity of the underfill material, and more specifically, 30 ° C or more and 155 ° C or less.

又,底部填充材料之最低熔融黏度到達溫度為125℃以下。藉此,可抑制加熱壓接時之空隙產生。最低熔融黏度到達溫度下之最低熔 融黏度較佳為1000Pa‧s以上2000Pa‧s以下。 Further, the minimum melt viscosity of the underfill material reaches a temperature of 125 ° C or less. Thereby, generation of voids at the time of thermocompression bonding can be suppressed. Minimum melting viscosity reaches the lowest melting temperature The melt viscosity is preferably 1000 Pa ‧ or more and 2000 Pa ‧ or less.

其次,對上述底部填充材料形成為膜狀之預供給型底部填充膜之製造方法進行說明。首先,使含有膜形成樹脂、環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物之接著劑組成物溶解於溶劑中。作為溶劑,可使用甲苯、乙酸乙酯等、或該等之混合溶劑。於製備樹脂組成物後,利用棒式塗佈機、塗佈裝置等塗佈於剝離基材上。 Next, a method of producing the pre-filled underfill film in which the underfill material is formed into a film shape will be described. First, an adhesive composition containing a film-forming resin, an epoxy resin, an acid anhydride, an acrylic resin, and an organic peroxide is dissolved in a solvent. As the solvent, toluene, ethyl acetate or the like, or a mixed solvent of these may be used. After the resin composition is prepared, it is applied onto a release substrate by a bar coater, a coating device, or the like.

剝離基材例如係由如下積層構造構成,而防止組成物之乾燥,並且維持組成物之形狀,上述積層構造係將聚矽氧等剝離劑塗佈於PET(Poly Ethylene Terephthalate,聚對苯二甲酸乙二酯)、OPP(Oriented Polypropylene,延伸聚丙烯)、PMP(Poly-4-methylpentene-1,聚-4-甲基戊烯-1)、PTFE(Polytetrafluoroethylene,聚四氟乙烯)等而成。 The release substrate is composed of, for example, a laminated structure that prevents drying of the composition and maintains the shape of the composition. The laminate structure is applied to a PET (Poly Ethylene Terephthalate, polyethylene terephthalate). Ethylene diester), OPP (Oriented Polypropylene), PMP (Poly-4-methylpentene-1, poly-4-methylpentene-1), PTFE (Polytetrafluoroethylene, polytetrafluoroethylene).

其次,藉由熱烘箱、加熱乾燥裝置等使塗佈於剝離基材上之樹脂組成物乾燥。藉此,可獲得特定厚度之預供給型底部填充膜。 Next, the resin composition applied to the release substrate is dried by a hot oven, a heating and drying device or the like. Thereby, a pre-feed type underfill film of a specific thickness can be obtained.

<2.半導體裝置之製造方法> <2. Method of Manufacturing Semiconductor Device>

其次,對使用上述預供給型底部填充膜之半導體裝置之製造方法進行說明。 Next, a method of manufacturing a semiconductor device using the above-described pre-supply underfill film will be described.

圖4係表示本實施形態之半導體裝置的製造方法之流程圖。如圖4所示,本實施形態之半導體裝置之製造方法含有:底部填充膜貼附步驟S1、切割步驟S2、半導體晶片搭載步驟S3、及熱壓接步驟S4。 Fig. 4 is a flow chart showing a method of manufacturing the semiconductor device of the embodiment. As shown in FIG. 4, the manufacturing method of the semiconductor device of this embodiment includes an underfill film attaching step S1, a dicing step S2, a semiconductor wafer mounting step S3, and a thermocompression bonding step S4.

圖5係模式性地表示在晶圓上貼附底部填充膜之步驟的立體圖。如圖5所示,底部填充膜貼附步驟S1係藉由具有大於晶圓1直徑之直徑且具有環狀或框狀框架的治具3以固定晶圓1,於晶圓1上貼附底部填 充膜2。底部填充膜2係於切割晶圓1時保護並固定晶圓1,於拾取時作為保持之切割膠帶發揮功能。再者,於晶圓1內嵌製作有大量IC(Integrated Circuit),於晶圓1之接著面對每個如圖1所示般藉由劃線劃分之半導體晶片10設置附焊料電極。 Fig. 5 is a perspective view schematically showing a step of attaching an underfill film to a wafer. As shown in FIG. 5, the underfill film attaching step S1 is to fix the wafer 1 by attaching the jig 3 having a diameter larger than the diameter of the wafer 1 and having a ring-shaped or frame-like frame, and attaching the bottom to the wafer 1. fill Fill the film 2. The underfill film 2 protects and fixes the wafer 1 when the wafer 1 is diced, and functions as a dicing tape to be held at the time of picking up. Further, a large number of ICs (Integrated Circuits) are embedded in the wafer 1, and a solder electrode is disposed on the wafer 1 to the semiconductor wafer 10 which is divided by the scribe lines as shown in FIG.

圖6係模式性地表示切割晶圓之步驟之立體圖。如圖6所示,切割步驟S2係沿劃線按壓刀片4來切削晶圓1,而分割成各個半導體晶片。 Fig. 6 is a perspective view schematically showing a step of cutting a wafer. As shown in FIG. 6, the cutting step S2 presses the blade 4 along the scribe line to cut the wafer 1 and divides it into individual semiconductor wafers.

圖7係模式性地表示拾取半導體晶片之步驟之立體圖。如圖7所示,各附底部填充膜之半導體晶片10係於保持底部填充膜之狀態下被拾取。 Fig. 7 is a perspective view schematically showing a step of picking up a semiconductor wafer. As shown in FIG. 7, each of the semiconductor wafers 10 with the underfill film is picked up while maintaining the underfill film.

如圖2所示,半導體晶片搭載步驟S3係將附底部填充膜之半導體晶片10與電路基板30經由底部填充膜進行配置。又,將附底部填充膜之半導體晶片10以附焊料電極與對向電極32對向之方式進行位置對準而配置。然後,藉由加熱接合機,於使底部填充膜產生流動性但未發生正式硬化之程度的特定溫度、壓力、時間之條件下進行加熱按壓而搭載。 As shown in FIG. 2, in the semiconductor wafer mounting step S3, the semiconductor wafer 10 with the underfill film and the circuit substrate 30 are placed via the underfill film. Further, the semiconductor wafer 10 with the underfill film is placed in such a manner that the solder electrodes are aligned with the counter electrode 32. Then, by heating the bonding machine, the underfill film is heated and pressed under the conditions of a specific temperature, pressure, and time to which fluidity is generated without causing the main hardening.

搭載時之溫度條件較佳為30℃以上且較底部填充膜之最低熔融黏度到達溫度高30℃以下,更具體而言,較佳為30℃以上155℃以下。又,壓力條件較佳為50N以下,更佳為40N以下。又,時間條件較佳為0.1秒以上10秒以下,更佳為0.1秒以上1.0秒以下。藉此,可成為不使附焊料電極熔融而與電路基板30側之電極接觸之狀態,可成為底部填充膜未完全硬化之狀態。又,由於在低溫下進行固定,故可抑制空隙之產生,減少對半導體晶片10之損壞。 The temperature condition at the time of mounting is preferably 30 ° C or higher and the lowest melting viscosity of the underfill film is 30 ° C or less higher than the temperature, and more specifically, preferably 30 ° C or more and 155 ° C or less. Further, the pressure condition is preferably 50 N or less, more preferably 40 N or less. Further, the time condition is preferably 0.1 second or longer and 10 seconds or shorter, more preferably 0.1 second or longer and 1.0 second or shorter. Thereby, the solder electrode can be melted and brought into contact with the electrode on the circuit board 30 side, and the underfill film can be in a state in which it is not completely cured. Moreover, since the fixing is performed at a low temperature, generation of voids can be suppressed, and damage to the semiconductor wafer 10 can be reduced.

以下之熱壓接步驟S4係於以特定升溫速度自第1溫度升溫至第2溫度之接合條件下,使附焊料電極之焊料熔融而形成金屬鍵,並且使底部填充膜完全硬化。 The following thermocompression bonding step S4 is performed by melting the solder of the solder electrode to form a metal bond under the bonding condition of raising the temperature from the first temperature to the second temperature at a specific temperature increase rate, and completely curing the underfill film.

又,升溫速度較佳為50℃/sec以上150℃/sec以下。又,第2溫度亦取決於焊料之種類,較佳為200℃以上280℃以下,更佳為220℃以上260℃以下。又,時間條件較佳為5秒以上500秒以下,更佳為5秒以上100秒以下。藉此,可使附焊料電極與基板電極進行金屬鍵結,並且使底部填充膜完全硬化,而將半導體晶片10之電極與電路基板30之電極電性地、機械性地連接。 Further, the temperature increase rate is preferably 50 ° C / sec or more and 150 ° C / sec or less. Further, the second temperature is also preferably 200 ° C or more and 280 ° C or less, more preferably 220 ° C or more and 260 ° C or less, depending on the type of the solder. Further, the time condition is preferably 5 seconds or longer and 500 seconds or shorter, more preferably 5 seconds or longer and 100 seconds or shorter. Thereby, the solder electrode and the substrate electrode can be metal-bonded, and the underfill film can be completely cured, and the electrode of the semiconductor wafer 10 and the electrode of the circuit substrate 30 can be electrically and mechanically connected.

又,於熱壓接步驟S4中,接合頭至搭載後之底部填充膜的開始熔融溫度為止係藉由樹脂之彈性模數而保持為一定高度,其後因升溫所伴隨之樹脂熔融而瞬間下降,到達頭之最低點。該最低點係根據頭之下降速度與樹脂之硬化速度的關係而決定。樹脂硬化進一步進行後,頭之高度隨著樹脂及頭之熱膨脹而緩慢地上升。如此,藉由在自第1溫度升溫至第2溫度之時間內使接合頭下降至最低點,可抑制隨著樹脂熔融之空隙產生。 Further, in the thermocompression bonding step S4, the bonding temperature of the bonding head to the underfill film after mounting is maintained at a constant height by the elastic modulus of the resin, and then the resin is melted and rapidly drops due to the temperature rise. , reaching the lowest point of the head. The lowest point is determined by the relationship between the rate of decrease of the head and the hardening speed of the resin. After the resin hardening is further carried out, the height of the head gradually rises as the resin and the head thermally expand. As described above, by lowering the bonding head to the lowest point in the time from the first temperature rise to the second temperature, generation of voids due to melting of the resin can be suppressed.

如此,本實施形態之半導體裝置之製造方法係藉由將底部填充材料20預先貼合於形成有附焊料電極之半導體晶片10,而可排除搭載時之空隙,並且可抑制加熱壓接時之空隙產生,上述底部填充材料20含有環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物,搭載時之儲存彈性模數為3000Pa以上,最低熔融黏度到達溫度為125℃以下。 As described above, in the method of manufacturing the semiconductor device of the present embodiment, the underfill material 20 is bonded to the semiconductor wafer 10 on which the solder electrode is formed in advance, thereby eliminating voids during mounting and suppressing voids during heating and pressure bonding. The underfill material 20 contains an epoxy resin, an acid anhydride, an acrylic resin, and an organic peroxide. The storage modulus at the time of mounting is 3,000 Pa or more, and the lowest melt viscosity reaches 125 ° C or lower.

再者,上述實施形態係使底部填充膜作為切割膠帶發揮功 能,但並不限定於此,亦可另外使用切割膠帶,於切割後使用底部填充膜進行覆晶構裝。 Furthermore, in the above embodiment, the underfill film is used as a dicing tape. However, the present invention is not limited thereto, and a dicing tape may be additionally used, and after the dicing, the underfill film is used for the flip chip mounting.

[其他實施形態] [Other Embodiments]

又,本技術亦可應用於藉由向設置於半導體晶片之小孔內填充金屬,而電連接堆積成夾層狀之多個晶片基板的TSV(Through Silicon Via,矽穿孔)技術。 Further, the present technology can also be applied to a TSV (Through Silicon Via) technique in which a plurality of wafer substrates stacked in a sandwich shape are electrically connected by filling a metal hole in a semiconductor wafer.

即,亦可應用於將具有形成有附焊料電極之第一面、及於第一面之相反側形成有與附焊料電極對向之對向電極的第二面之多個晶片基板積層的半導體裝置之製造方法。 That is, it is also applicable to a semiconductor in which a plurality of wafer substrates having a first surface on which a solder electrode is formed and a second surface on which a counter electrode facing the solder electrode is formed on the opposite side of the first surface are laminated. The manufacturing method of the device.

於此情形時,於第一晶片基板之第一面側貼附有底部填充膜之狀態下,搭載於第二晶片基板之第二面。其後,可藉由在附焊料電極之焊料的熔點以上之溫度將第一晶片基板之第一面與第二晶片基板之第二面熱壓接,而獲得積層有多個晶片基板之半導體裝置。 In this case, the second wafer substrate is mounted on the second surface of the second wafer substrate with the underfill film attached to the first surface of the first wafer substrate. Thereafter, the first surface of the first wafer substrate and the second surface of the second wafer substrate are thermocompression bonded at a temperature above the melting point of the solder with the solder electrode to obtain a semiconductor device in which a plurality of wafer substrates are laminated. .

[實施例] [Examples]

<3.實施例> <3. Example>

以下,對本發明之實施例進行說明。於本實施例中,製作預供給型底部填充膜,對最低熔融黏度到達溫度、及搭載溫度(60℃)之儲存彈性模數進行測量。然後,使用底部填充膜將具有附焊料電極之IC晶片、及具有與其對向之電極的IC基板連接而製作構裝體,對空隙進行評價。再者,本發明並不限定於該等實施例。 Hereinafter, embodiments of the invention will be described. In the present example, a pre-feed type underfill film was produced, and the storage modulus of the lowest melt viscosity reached and the mounting temperature (60 ° C) was measured. Then, an IC wafer having a solder electrode and an IC substrate having electrodes opposed thereto were connected using an underfill film to fabricate a package, and the voids were evaluated. Furthermore, the invention is not limited to the embodiments.

最低熔融黏度到達溫度及搭載溫度下之儲存彈性模數之測量、構裝體之製作、及空隙之評價係以如下方式進行。 The measurement of the storage elastic modulus at the lowest melt viscosity reaching temperature and the mounting temperature, the production of the structure, and the evaluation of the voids were carried out as follows.

[最低熔融黏度到達溫度、及搭載溫度下之儲存彈性模數之測量] [Measurement of the lowest melt viscosity to the temperature and the storage elastic modulus at the mounting temperature]

針對各底部填充膜,利用流變儀(TA公司製造之ARES)於5℃/min、1Hz之條件下測量樣品之最低熔融黏度到達溫度、及於搭載溫度(60℃)之儲存彈性模數。 For each underfill film, the lowest melt viscosity reaching temperature of the sample and the storage elastic modulus at the mounting temperature (60 ° C) were measured by a rheometer (ARES manufactured by TA Corporation) at 5 ° C/min and 1 Hz.

[構裝體之製作] [Production of the body]

於50℃、0.5MPa之條件下利用壓製機將底部填充膜貼合於晶圓上,進行切割而獲得具有附焊料電極之IC晶片。 The underfill film was bonded to the wafer by a press at 50 ° C and 0.5 MPa, and dicing was performed to obtain an IC wafer having a solder-attached electrode.

IC晶片係大小為7mm,厚度為200μm,且具有周邊配置之凸塊(30μm、85μm間距、280針)者,該周邊配置之凸塊於厚度20μm之由Cu構成的電極前端形成有厚度16μm之焊料(Sn-3.5Ag、熔點221℃)。 The IC chip has a size of 7 mm, a thickness of 200 μm, and has bumps in the peripheral configuration ( In the case of 30 μm, 85 μm pitch, and 280 stitches, the peripherally disposed bumps were formed with a solder having a thickness of 16 μm (Sn-3.5Ag, melting point 221 ° C) at the electrode tip end made of Cu having a thickness of 20 μm.

又,與其對向之IC基板同樣具有大小為7mm、厚度200μm且形成有由厚度20μm之Cu構成之電極的周邊配置之凸塊(30μm、85μm間距、280針)。 Further, similarly to the opposing IC substrate, there is a bump having a size of 7 mm and a thickness of 200 μm and formed with an electrode made of Cu having a thickness of 20 μm ( 30 μm, 85 μm pitch, 280 pins).

其次,於60℃、0.5秒、30N之條件下利用覆晶接合機將IC晶片搭載於IC基板上。 Next, the IC wafer was mounted on the IC substrate by a flip chip bonding machine under conditions of 60 ° C, 0.5 second, and 30 N.

其後,如圖8所示之壓接分佈般,於10秒內使溫度自60℃上升至250℃,利用覆晶接合機進行熱壓接。又,於自60℃升溫至250℃之時間內,使接合頭下降至最低點(30N)。進而,於150℃、2小時之條件下進行硬化(cure)而獲得構裝體。再者,使用覆晶接合機時之溫度係藉由熱電偶測量樣品之實際溫度而得者。 Thereafter, as in the pressure bonding distribution shown in Fig. 8, the temperature was raised from 60 ° C to 250 ° C in 10 seconds, and thermocompression bonding was performed by a flip chip bonding machine. Further, the bonding head was lowered to the lowest point (30 N) during the time from 60 ° C to 250 ° C. Further, it was cured at 150 ° C for 2 hours to obtain a package. Further, the temperature at which the flip chip bonding machine is used is obtained by measuring the actual temperature of the sample by a thermocouple.

[空隙之評價] [Evaluation of voids]

利用SAT(Scanning Acoustic Tomograph,超音波影像裝置)觀察各構裝體,將空隙為IC晶片面積之1%以下者設為○,將空隙超過IC晶片面積之1%者設為×。 Each of the structures was observed by a SAT (Scanning Acoustic Tomograph), and the void was 1% or less of the area of the IC wafer, and the void was more than 1% of the area of the IC wafer.

[實施例1] [Example 1]

調配苯氧基樹脂(品名:PKHH,聯合碳業公司製造)13.7質量份、環氧樹脂(品名:HP7200H,大日本油墨化學公司製造)23.3質量份、酸酐(品名:MH-700,新日本理化公司製造)13.7質量份、咪唑(品名:2MZ-A,四國化成工業公司製造)0.1質量份、丙烯酸樹脂(品名:DCP,新中村化學公司製造)8.7質量份、起始劑(品名:Perbutyl Z,日本油脂公司製造)0.5質量份、填料A(品名:SO-E5,Admatechs公司製造)35.0質量份、及填料B(品名:艾羅技RY200,日本艾羅技公司製造)5.0質量份,而製備底部填充膜之樹脂組成物。利用棒式塗佈機將其塗佈於經剝離處理之PET(Polyethylene terephthalate),利用80℃之烘箱乾燥3分鐘,製作厚度50μm之底部填充膜(保護剝離PET(25μm)/底部填充膜(50μm)/基底剝離PET(50μm))。 13.7 parts by mass of phenoxy resin (product name: PKHH, manufactured by Union Carbon Co., Ltd.), epoxy resin (product name: HP7200H, manufactured by Dainippon Ink Chemical Co., Ltd.) 23.3 parts by mass, acid anhydride (product name: MH-700, New Japan Physical and Chemical) Manufactured by the company, 13.7 parts by mass, imidazole (product name: 2MZ-A, manufactured by Shikoku Chemical Industry Co., Ltd.) 0.1 parts by mass, acrylic resin (product name: DCP, manufactured by Shin-Nakamura Chemical Co., Ltd.) 8.7 parts by mass, starting agent (product name: Perbutyl Z, manufactured by Nippon Oil & Fats Co., Ltd., 0.5 parts by mass, filler A (product name: SO-E5, manufactured by Admatechs Co., Ltd.), 35.0 parts by mass, and filler B (product name: Aerotech RY200, manufactured by Japan Aerotech Co., Ltd.), 5.0 parts by mass, and prepared The resin composition of the underfill film. It was applied to a peeled PET (Polyethylene terephthalate) by a bar coater, and dried in an oven at 80 ° C for 3 minutes to prepare an underfill film having a thickness of 50 μm (protective peeling PET (25 μm) / underfill film (50 μm). ) / substrate peeling PET (50 μm)).

於表1中表示實施例1之底部填充膜之評價結果。底部填充膜之最低熔融黏度到達溫度為125℃。又,搭載溫度下之儲存彈性模數為3300Pa。又,使用底部填充膜製作之構裝體的空隙之評價為○。 The evaluation results of the underfill film of Example 1 are shown in Table 1. The lowest melt viscosity of the underfill film reached a temperature of 125 °C. Moreover, the storage elastic modulus at the mounting temperature was 3,300 Pa. Moreover, the evaluation of the void of the structure produced using the underfill film was ○.

[實施例2] [Embodiment 2]

調配苯氧基樹脂(品名:PKHH,聯合碳業公司製造)13.7質量份、環氧樹脂(品名:HP7200H,大日本油墨化學公司製造)17.5質量份、酸酐(品 名:MH-700,新日本理化公司製造)10.3質量份、咪唑(品名:2MZ-A,四國化成工業公司製造)0.1質量份、丙烯酸樹脂(品名:DCP,新中村化學公司製造)17.5質量份、起始劑(品名:Perbutyl Z,日本油脂公司製造)0.9質量份、填料A(品名:SO-E5,Admatechs公司製造)35.0質量份、及填料B(品名:艾羅技RY200,日本艾羅技公司製造)5.0質量份,而製備底部填充膜之樹脂組成物。利用棒式塗佈機將其塗佈於經剝離處理之PET(Polyethylene terephthalate),利用80℃之烘箱乾燥3分鐘,製作厚度50μm之底部填充膜(保護剝離PET(25μm)/底部填充膜(50μm)/基底剝離PET(50μm))。 13.7 parts by mass of phenoxy resin (product name: PKHH, manufactured by Union Carbon Co., Ltd.), epoxy resin (product name: HP7200H, manufactured by Dainippon Ink Chemical Co., Ltd.), 17.5 parts by mass, anhydride (product) Name: MH-700, manufactured by Nippon Chemical and Chemical Co., Ltd.) 10.3 parts by mass, imidazole (product name: 2MZ-A, manufactured by Shikoku Chemical Industry Co., Ltd.) 0.1 parts by mass, acrylic resin (product name: DCP, manufactured by Shin-Nakamura Chemical Co., Ltd.) 17.5 Parts, starting agent (product name: Perbutyl Z, manufactured by Nippon Oil & Fats Co., Ltd.) 0.9 parts by mass, filler A (product name: SO-E5, manufactured by Admatechs Co., Ltd.) 35.0 parts by mass, and filler B (product name: Aerotech RY200, Japan Ai Luoji The resin composition of the underfill film was prepared by 5.0 parts by mass of the company. It was applied to a peeled PET (Polyethylene terephthalate) by a bar coater, and dried in an oven at 80 ° C for 3 minutes to prepare an underfill film having a thickness of 50 μm (protective peeling PET (25 μm) / underfill film (50 μm). ) / substrate peeling PET (50 μm)).

於表1中表示實施例2之底部填充膜之評價結果。底部填充膜之最低熔融黏度到達溫度為118℃。又,搭載溫度下之儲存彈性模數為3300Pa。又,使用底部填充膜製作之構裝體的空隙之評價為○。 The evaluation results of the underfill film of Example 2 are shown in Table 1. The lowest melt viscosity of the underfill film reached a temperature of 118 °C. Moreover, the storage elastic modulus at the mounting temperature was 3,300 Pa. Moreover, the evaluation of the void of the structure produced using the underfill film was ○.

[實施例3] [Example 3]

調配苯氧基樹脂(品名:PKHH,聯合碳業公司製造)13.7質量份、環氧樹脂(品名:HP7200H,大日本油墨化學公司製造)18.3質量份、酸酐(品名:MH-700,新日本理化公司製造)10.8質量份、咪唑(品名:2MZ-A,四國化成工業公司製造)0.1質量份、丙烯酸樹脂(品名:DCP,新中村化學公司製造)6.8質量份、起始劑(品名:Perbutyl Z,日本油脂公司製造)0.4質量份、填料A(品名:SO-E5,Admatechs公司製造)44.5質量份、及填料B(品名:艾羅技RY200,日本艾羅技公司製造)5.0質量份,而製備底部填充膜之樹脂組成物。利用棒式塗佈機將其塗佈於經剝離處理之PET(Polyethylene terephthalate),利用80℃之烘箱乾燥3分鐘,製作厚度50μm 之底部填充膜(保護剝離PET(25μm)/底部填充膜(50μm)/基底剝離PET(50μm))。 13.7 parts by mass of phenoxy resin (product name: PKHH, manufactured by Union Carbon Co., Ltd.), epoxy resin (product name: HP7200H, manufactured by Dainippon Ink Chemical Co., Ltd.), 18.3 parts by mass, acid anhydride (product name: MH-700, New Japan Physical and Chemical) Made by the company, 10.8 parts by mass, imidazole (product name: 2MZ-A, manufactured by Shikoku Chemical Industry Co., Ltd.) 0.1 parts by mass, acrylic resin (product name: DCP, manufactured by Shin-Nakamura Chemical Co., Ltd.) 6.8 parts by mass, starting agent (product name: Perbutyl Z, manufactured by Nippon Oil & Fats Co., Ltd., 0.4 parts by mass, filler A (product name: SO-E5, manufactured by Admatechs Co., Ltd.), 44.5 parts by mass, and filler B (product name: Ai Luoji RY200, manufactured by Japan Aerotech Co., Ltd.), 5.0 parts by mass, and prepared The resin composition of the underfill film. It was applied to a PET (Polyethylene terephthalate) by a bar coater, and dried in an oven at 80 ° C for 3 minutes to prepare a thickness of 50 μm. Underfill film (protective release PET (25 μm) / underfill film (50 μm) / substrate release PET (50 μm)).

於表1中表示實施例3之底部填充膜之評價結果。底部填充膜之最低熔融黏度到達溫度為125℃。又,搭載溫度下之儲存彈性模數為4000Pa。又,使用底部填充膜製作之構裝體的空隙之評價為○。 The evaluation results of the underfill film of Example 3 are shown in Table 1. The lowest melt viscosity of the underfill film reached a temperature of 125 °C. Further, the storage elastic modulus at the mounting temperature was 4000 Pa. Moreover, the evaluation of the void of the structure produced using the underfill film was ○.

[比較例1] [Comparative Example 1]

調配苯氧基樹脂(品名:PKHH,聯合碳業公司製造)13.7質量份、環氧樹脂(品名:HP7200H,大日本油墨化學公司製造)29.0質量份、酸酐(品名:MH-700,新日本理化公司製造)17.1質量份、咪唑(品名:2MZ-A,四國化成工業公司製造)0.1質量份、填料A(品名:SO-E5,Admatechs公司製造)35.0質量份、及填料B(品名:艾羅技RY200,日本艾羅技公司製造)5.0質量份,而製備底部填充膜之樹脂組成物。利用棒式塗佈機將其塗佈於經剝離處理之PET(Polyethylene terephthalate),利用80℃之烘箱乾燥3分鐘,製作厚度50μm之底部填充膜(保護剝離PET(25μm)/底部填充膜(50μm)/基底剝離PET(50μm))。 13.7 parts by mass of phenoxy resin (product name: PKHH, manufactured by Union Carbon Co., Ltd.), epoxy resin (product name: HP7200H, manufactured by Dainippon Ink Chemical Co., Ltd.) 29.0 parts by mass, acid anhydride (product name: MH-700, New Japan Physical and Chemical) The company manufactures 17.1 parts by mass, imidazole (product name: 2MZ-A, manufactured by Shikoku Chemical Industry Co., Ltd.) 0.1 parts by mass, filler A (product name: SO-E5, manufactured by Admatechs) 35.0 parts by mass, and filler B (name: Ai The resin composition of the underfill film was prepared by 5.0 parts by mass of Logitech RY200, manufactured by Aerotech of Japan. It was applied to a peeled PET (Polyethylene terephthalate) by a bar coater, and dried in an oven at 80 ° C for 3 minutes to prepare an underfill film having a thickness of 50 μm (protective peeling PET (25 μm) / underfill film (50 μm). ) / substrate peeling PET (50 μm)).

於表1中表示比較例1之底部填充膜之評價結果。底部填充膜之最低熔融黏度到達溫度為135℃。又,搭載溫度下之儲存彈性模數為3300Pa。又,使用底部填充膜製作之構裝體的空隙之評價為×。 Table 1 shows the evaluation results of the underfill film of Comparative Example 1. The lowest melt viscosity of the underfill film reached a temperature of 135 °C. Moreover, the storage elastic modulus at the mounting temperature was 3,300 Pa. Moreover, the evaluation of the void of the structure produced using the underfill film was ×.

[比較例2] [Comparative Example 2]

調配苯氧基樹脂(品名:PKHH,聯合碳業公司製造)13.7質量份、環氧樹脂(品名:HP7200H,大日本油墨化學公司製造)25.9質量份、酸酐(品名:MH-700,新日本理化公司製造)15.3質量份、咪唑(品名:2MZ-A, 四國化成工業公司製造)0.1質量份、丙烯酸樹脂(品名:DCP,新中村化學公司製造)9.6質量份、起始劑(品名:Perbutyl Z,日本油脂公司製造)0.6質量份、填料A(品名:SO-E5,Admatechs公司製造)30.0質量份、及填料B(品名:艾羅技RY200,日本艾羅技公司製造)5.0質量份,而製備底部填充膜之樹脂組成物。利用棒式塗佈機將其塗佈於經剝離處理之PET(Polyethylene terephthalate),利用80℃之烘箱乾燥3分鐘,製作厚度50μm之底部填充膜(保護剝離PET(25μm)/底部填充膜(50μm)/基底剝離PET(50μm))。 13.7 parts by mass of phenoxy resin (product name: PKHH, manufactured by Union Carbon Co., Ltd.), epoxy resin (product name: HP7200H, manufactured by Dainippon Ink Chemical Co., Ltd.) 25.9 parts by mass, acid anhydride (product name: MH-700, New Japan Physical and Chemical) Made by the company) 15.3 parts by mass, imidazole (product name: 2MZ-A, (manufactured by Shikoku Chemicals Co., Ltd.) 0.1 parts by mass, acrylic resin (product name: DCP, manufactured by Shin-Nakamura Chemical Co., Ltd.) 9.6 parts by mass, starting agent (product name: Perbutyl Z, manufactured by Nippon Oil Co., Ltd.) 0.6 parts by mass, filler A (product name) : SO-E5, manufactured by Admatechs Co., Ltd., 30.0 parts by mass, and a filler B (product name: Aerotech RY200, manufactured by Ai Luo Technology Co., Ltd.) in an amount of 5.0 parts by mass to prepare a resin composition of an underfill film. It was applied to a peeled PET (Polyethylene terephthalate) by a bar coater, and dried in an oven at 80 ° C for 3 minutes to prepare an underfill film having a thickness of 50 μm (protective peeling PET (25 μm) / underfill film (50 μm). ) / substrate peeling PET (50 μm)).

於表1中表示比較例2之底部填充膜之評價結果。底部填充膜之最低熔融黏度到達溫度為125℃。又,搭載溫度下之儲存彈性模數為2800Pa。又,使用底部填充膜製作之構裝體的空隙之評價為×。 The evaluation results of the underfill film of Comparative Example 2 are shown in Table 1. The lowest melt viscosity of the underfill film reached a temperature of 125 °C. Moreover, the storage elastic modulus at the mounting temperature was 2,800 Pa. Moreover, the evaluation of the void of the structure produced using the underfill film was ×.

比較例1於晶片搭載後未觀察到空隙,但於熱壓接後觀察到空隙。又,比較例2於晶片搭載後觀察到空隙,於熱壓接後亦觀察到空隙。 另一方面,實施例1~3可藉由使用底部填充膜而抑制空隙之產生,該底部填充膜含有環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物,搭載時之儲存彈性模數為3000Pa以上,最低熔融黏度到達溫度為125℃以下。 In Comparative Example 1, no void was observed after the wafer was mounted, but a void was observed after thermocompression bonding. Further, in Comparative Example 2, voids were observed after the wafer was mounted, and voids were also observed after thermocompression bonding. On the other hand, Examples 1 to 3 can suppress the generation of voids by using an underfill film containing an epoxy resin, an acid anhydride, an acrylic resin, and an organic peroxide, and the storage elastic modulus at the time of mounting is Above 3000Pa, the lowest melt viscosity reaches a temperature below 125 °C.

Claims (6)

一種底部填充材料,係於將形成有附焊料電極之半導體晶片搭載於形成有與該附焊料電極對向之對向電極的電子零件時,被預先貼合於該半導體晶片,該底部填充材料含有環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物,該搭載時之儲存彈性模數為3000Pa以上,最低熔融黏度到達溫度為125℃以下。 An underfill material is preliminarily bonded to a semiconductor wafer in which a semiconductor wafer on which a solder electrode is formed is mounted on an electronic component on which a counter electrode facing the solder electrode is formed, and the underfill material contains The epoxy resin, the acid anhydride, the acrylic resin, and the organic peroxide have a storage elastic modulus of 3,000 Pa or more and a minimum melt viscosity of 125 ° C or less. 如申請專利範圍第1項之底部填充材料,其中該搭載時之溫度為30℃以上155℃以下。 The underfill material according to the first aspect of the patent application, wherein the temperature at the time of mounting is 30 ° C or more and 155 ° C or less. 如申請專利範圍第1或2項之底部填充材料,其中該環氧樹脂為倍環戊二烯型環氧樹脂,該酸酐為脂肪族酸酐。 The underfill material of claim 1 or 2, wherein the epoxy resin is a cyclopentadiene type epoxy resin, and the acid anhydride is an aliphatic acid anhydride. 如申請專利範圍第1或2項之底部填充材料,其中該丙烯酸樹脂為2官能(甲基)丙烯酸酯,該有機過氧化物為過氧化酯。 The underfill material of claim 1 or 2, wherein the acrylic resin is a bifunctional (meth) acrylate, and the organic peroxide is a peroxyester. 如申請專利範圍第3項之底部填充材料,其中該丙烯酸樹脂為2官能(甲基)丙烯酸酯,該有機過氧化物為過氧化酯。 An underfill material according to claim 3, wherein the acrylic resin is a bifunctional (meth) acrylate, and the organic peroxide is a peroxyester. 一種半導體裝置之製造方法,其含有:搭載步驟:於第1溫度將形成有附焊料電極且於該電極面貼合有底部填充材料之半導體晶片搭載於形成有與該附焊料電極對向之對向電極的電子零件;及熱壓接步驟:將該半導體晶片與該電子零件升溫至第2溫度進行熱壓接, 該底部填充材料含有環氧樹脂、酸酐、丙烯酸樹脂、及有機過氧化物,第1溫度下之儲存彈性模數為3000Pa以上,最低熔融黏度到達溫度為125℃以下。 A method of manufacturing a semiconductor device, comprising: mounting a semiconductor wafer on which a solder electrode is formed at a first temperature and an underfill material is bonded to the electrode surface; and the pair is opposed to the solder electrode An electronic component to the electrode; and a thermocompression bonding step: the semiconductor wafer and the electronic component are heated to a second temperature for thermocompression bonding, The underfill material contains an epoxy resin, an acid anhydride, an acrylic resin, and an organic peroxide. The storage elastic modulus at the first temperature is 3,000 Pa or more, and the lowest melt viscosity reaches 125 ° C or lower.
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