TWI671271B - Laminated body, semiconductor package and its manufacturing method, electronic machine - Google Patents
Laminated body, semiconductor package and its manufacturing method, electronic machine Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C4/00—Compositions for glass with special properties
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
- C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B17/00—Forming molten glass by flowing-out, pushing-out, extruding or drawing downwardly or laterally from forming slits or by overflowing over lips
- C03B17/06—Forming glass sheets
- C03B17/064—Forming glass sheets by the overflow downdraw fusion process; Isopipes therefor
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
- C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
- C03C3/087—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal containing calcium oxide, e.g. common sheet or container glass
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
- C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
- C03C3/091—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
- C03C3/093—Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/677—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere for conveying, e.g. between different workstations
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L24/00—Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
- H01L24/01—Means 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
- H01L24/10—Bump connectors ; Manufacturing methods related thereto
- H01L24/11—Manufacturing methods
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2224/00—Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
- H01L2224/01—Means 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
- H01L2224/10—Bump connectors; Manufacturing methods related thereto
- H01L2224/12—Structure, shape, material or disposition of the bump connectors prior to the connecting process
- H01L2224/12105—Bump connectors formed on an encapsulation of the semiconductor or solid-state body, e.g. bumps on chip-scale packages
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L24/00—Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
- H01L24/01—Means 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
- H01L24/18—High density interconnect [HDI] connectors; Manufacturing methods related thereto
- H01L24/19—Manufacturing methods of high density interconnect preforms
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L24/00—Arrangements for connecting or disconnecting semiconductor or solid-state bodies; Methods or apparatus related thereto
- H01L24/93—Batch processes
- H01L24/95—Batch processes at chip-level, i.e. with connecting carried out on a plurality of singulated devices, i.e. on diced chips
- H01L24/96—Batch processes at chip-level, i.e. with connecting carried out on a plurality of singulated devices, i.e. on diced chips the devices being encapsulated in a common layer, e.g. neo-wafer or pseudo-wafer, said common layer being separable into individual assemblies after connecting
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Abstract
本發明的技術課題創作出不易產生加工基板的尺寸變化的支持基板及使用其的積層體,藉此有助於半導體封裝的高密度安裝。本發明的支持玻璃基板的特徵在於20℃~200℃的溫度範圍的平均線熱膨脹係數超過81×10-7/℃且為110×10-7/℃以下。 The technical problem of the present invention is to create a supporting substrate and a laminated body using the supporting substrate that are less likely to cause dimensional changes in a processed substrate, thereby contributing to high-density mounting of a semiconductor package. The support glass substrate of the present invention is characterized in that an average linear thermal expansion coefficient in a temperature range of 20 ° C. to 200 ° C. exceeds 81 × 10 -7 / ° C. and is 110 × 10 -7 / ° C. or less.
Description
本發明是有關於一種支持玻璃基板及使用其的積層體,具體而言,是有關於一種在半導體封裝(package)的製造步驟中用於加工基板的支持的支持玻璃基板及使用其的積層體。 The present invention relates to a supporting glass substrate and a laminated body using the same, and more particularly, to a supporting glass substrate and a laminated body using the same in a manufacturing process of a semiconductor package for supporting the substrate. .
對行動電話、筆記型個人電腦、個人數位助理(Personal Data Assistance,PDA)等攜帶型電子機器要求小型化及輕量化。伴隨於此,該些電子機器中使用的半導體晶片(chip)的安裝空間亦受到嚴格限制,從而半導體晶片的高密度安裝成為問題。因此,近年來,藉由三維安裝技術,即,將半導體晶片彼此積層而將各半導體晶片間進行配線連接,來實現半導體封裝的高密度安裝。 Portable electronic devices such as mobile phones, notebook personal computers, and personal data assistants (PDAs) are required to be miniaturized and lightened. Along with this, the mounting space of semiconductor chips used in these electronic devices is also severely restricted, and high-density mounting of semiconductor chips has become a problem. Therefore, in recent years, high-density mounting of semiconductor packages has been achieved by three-dimensional mounting technology, that is, by stacking semiconductor wafers on each other and wiring connections between the semiconductor wafers.
而且,現有的晶圓級封裝(Wafer-level packaging,WLP)中,藉由將凸塊以晶圓的狀態形成後,利用切割進行單片化而製作。然而,現有的WLP除難以增加接腳(pin)數外,是在半導體晶片的背面露出的狀態下安裝,因而存在半導體晶片容易產生缺陷等問題。 In addition, in a conventional wafer-level packaging (WLP), bumps are formed in a wafer state and then singulated to form wafers. However, conventional WLPs are difficult to increase the number of pins, and are mounted in a state where the back surface of the semiconductor wafer is exposed. Therefore, there is a problem that semiconductor wafers are prone to defects.
因此,作為新的WLP,提出扇出(fan out)型的WLP。扇出型的WLP中,能夠增加接腳數,且藉由對半導體晶片的端部進行保護,而可防止半導體晶片的缺陷等。 Therefore, as a new WLP, a fan-out type WLP is proposed. In a fan-out type WLP, the number of pins can be increased, and by protecting the ends of the semiconductor wafer, defects such as the semiconductor wafer can be prevented.
扇出型的WLP中,具有利用樹脂的密封材對多個半導體晶片進行模製,而形成加工基板後,在加工基板的一表面進行配線的步驟,以及形成焊料凸塊的步驟等。 The fan-out type WLP includes a step of molding a plurality of semiconductor wafers with a resin sealing material to form a processed substrate, a step of wiring on one surface of the processed substrate, and a step of forming a solder bump.
該些步驟伴隨著約200℃的熱處理進行,因而有密封材變形而加工基板的尺寸發生變化之虞。若加工基板尺寸變化,則難以對加工基板的一表面高密度地進行配線,且亦難以準確地形成焊料凸塊。 These steps are accompanied by a heat treatment at about 200 ° C, so that the sealing material may be deformed and the size of the processed substrate may change. If the size of the processing substrate changes, it is difficult to perform high-density wiring on one surface of the processing substrate, and it is also difficult to accurately form solder bumps.
為了抑制加工基板的尺寸變化,有效的是使用用以對加工基板進行支持的支持基板。然而,即便在使用了支持基板的情況下,亦存在加工基板的尺寸發生變化的情況。 In order to suppress the dimensional change of the processing substrate, it is effective to use a support substrate for supporting the processing substrate. However, even when a support substrate is used, the size of a processing substrate may change.
本發明鑒於所述情況而完成,其技術課題在於創作出不易產生加工基板的尺寸變化的支持基板及使用其的積層體,由此有助於半導體封裝的高密度安裝。 The present invention has been made in view of the above circumstances, and a technical problem of the present invention is to create a support substrate and a laminated body using the support substrate that are unlikely to cause dimensional changes in a processed substrate, thereby contributing to high-density mounting of a semiconductor package.
本發明者反覆進行了各種實驗,結果發現,採用玻璃基板作為支持基板,並且嚴格規定該玻璃基板的熱膨脹係數,藉此可解決所述技術課題,從而提出本發明。即,本發明的支持玻璃基板的特徵在於:在20℃~200℃的溫度範圍的平均線熱膨脹係數超過81×10-7/℃且為110×10-7/℃以下。此處,「在20℃~200℃的溫度範圍的平均線熱膨脹係數」可利用膨脹計(dilatometer)進行 測定。 The present inventors conducted various experiments repeatedly, and as a result, found that a glass substrate is used as a support substrate, and the thermal expansion coefficient of the glass substrate is strictly specified, so that the technical problem can be solved, and the present invention is proposed. That is, the support glass substrate of the present invention is characterized in that an average linear thermal expansion coefficient in a temperature range of 20 ° C. to 200 ° C. exceeds 81 × 10 -7 / ° C and is 110 × 10 -7 / ° C or less. Here, the "average linear thermal expansion coefficient in a temperature range of 20 ° C to 200 ° C" can be measured using a dilatometer.
玻璃基板容易使表面平滑化且具有剛性。由此,若使用玻璃基板作為支持基板,則能夠牢固且準確地對加工基板進行支持。而且,玻璃基板容易透過紫外光、紅外光等光。由此,若使用玻璃基板作為支持基板,則可藉由利用紫外線硬化型黏著劑等設置黏著層等而容易固定加工基板與支持玻璃基板。而且,亦可藉由設置吸收紅外線的剝離層等而容易地將加工基板與支持玻璃基板分離。作為其他方式,可藉由利用紫外線硬化型膠帶等設置黏著層等而容易地將加工基板與支持玻璃基板分離。 The glass substrate is easy to smooth and rigid. Accordingly, if a glass substrate is used as the support substrate, the processing substrate can be firmly and accurately supported. In addition, the glass substrate easily transmits light such as ultraviolet light and infrared light. Therefore, if a glass substrate is used as the support substrate, the processing substrate and the support glass substrate can be easily fixed by providing an adhesive layer or the like using an ultraviolet curing adhesive or the like. Furthermore, the processing substrate and the supporting glass substrate can be easily separated by providing a release layer or the like that absorbs infrared rays. As another method, the processing substrate and the supporting glass substrate can be easily separated by providing an adhesive layer or the like with an ultraviolet curable tape or the like.
而且,本發明的支持玻璃基板中,將20℃~200℃的溫度範圍的平均線熱膨脹係數規定為超過81×10-7/℃且為110×10-7/℃以下。據此,在加工基板內半導體晶片的比例少而密封材的比例多的情況下,加工基板與支持玻璃基板的熱膨脹係數容易匹配。而且,若兩者的熱膨脹係數匹配,則在加工處理時容易抑制加工基板的尺寸變化(尤其是翹曲變形)。結果,能夠對加工基板的一表面高密度地進行配線,且亦能夠準確地形成焊料凸塊。 In the support glass substrate of the present invention, an average linear thermal expansion coefficient in a temperature range of 20 ° C. to 200 ° C. is specified to be more than 81 × 10 -7 / ° C. and 110 × 10 -7 / ° C. or less. Accordingly, when the proportion of the semiconductor wafer in the processed substrate is small and the proportion of the sealing material is large, the thermal expansion coefficients of the processed substrate and the supporting glass substrate are easily matched. In addition, if the thermal expansion coefficients of the two are matched, it is easy to suppress dimensional changes (especially warpage deformation) of the processed substrate during processing. As a result, high-density wiring can be performed on one surface of the processed substrate, and solder bumps can be accurately formed.
第二,本發明的支持玻璃基板的特徵在於:在30℃~380℃的溫度範圍的平均線熱膨脹係數超過85×10-7/℃且為115×10-7/℃以下。此處,「在30℃~380℃的溫度範圍的平均線熱膨脹係數」可利用膨脹計進行測定。 Second, the support glass substrate of the present invention is characterized in that an average linear thermal expansion coefficient in a temperature range of 30 ° C to 380 ° C exceeds 85 × 10 -7 / ° C and is 115 × 10 -7 / ° C or less. Here, the "average linear thermal expansion coefficient in a temperature range of 30 ° C to 380 ° C" can be measured using an expansion meter.
第三,本發明的支持玻璃基板較佳為在半導體封裝的製 造步驟中用於加工基板的支持。 Third, the supporting glass substrate of the present invention is preferably manufactured in a semiconductor package. Support for processing substrates in the manufacturing steps.
第四,本發明的支持玻璃基板較佳為利用溢流下拉法成形而成。 Fourth, the supporting glass substrate of the present invention is preferably formed by an overflow down-draw method.
第五,本發明的支持玻璃基板較佳為楊氏模量為65GPa以上。此處,「楊氏模量」是指藉由彎曲共振法測定的值。另外,1GPa相當於約101.9Kgf/mm2。 Fifth, the supporting glass substrate of the present invention preferably has a Young's modulus of 65 GPa or more. Here, the "Young's modulus" means a value measured by a bending resonance method. In addition, 1 GPa corresponds to about 101.9 Kgf / mm 2 .
第六,本發明的支持玻璃基板較佳為作為玻璃組成,以質量%計含有50%~80%的SiO2、1%~20%的Al2O3、0%~20%的B2O3、0%~10%的MgO、0%~10%的CaO、0%~7%的SrO、0%~7%的BaO、0%~7%的ZnO、0%~25%的Na2O、以及0%~25%的K2O。 Sixth, the supporting glass substrate of the present invention is preferably used as a glass composition, and contains 50% to 80% SiO 2 , 1% to 20% Al 2 O 3 , and 0% to 20% B 2 O in terms of mass%. 3 , 0% to 10% MgO, 0% to 10% CaO, 0% to 7% SrO, 0% to 7% BaO, 0% to 7% ZnO, 0% to 25% Na 2 O, and K 2 O of 0% to 25%.
第七,本發明的支持玻璃基板較佳為作為玻璃組成,以質量%計含有55%~70%的SiO2、3%~18%的Al2O3、0%~8%的B2O3、0%~5%的MgO、0%~10%的CaO、0%~5%的SrO、0%~5%的BaO、0%~5%的ZnO、2%~23%的Na2O、以及0%~20%的K2O。 Seventh, the supporting glass substrate of the present invention is preferably a glass composition, and contains 55% to 70% SiO 2 , 3% to 18% Al 2 O 3 , and 0% to 8% B 2 O in terms of mass%. 3 , 0% ~ 5% MgO, 0% ~ 10% CaO, 0% ~ 5% SrO, 0% ~ 5% BaO, 0% ~ 5% ZnO, 2% ~ 23% Na 2 O, and K 2 O of 0% to 20%.
第八,本發明的支持玻璃基板較佳為板厚小於2.0mm,板厚偏差為30μm以下,且翹曲量為60μm以下。此處,「翹曲量」是指支持玻璃基板整體中的最高位點與最小平方焦點面之間的最大距離的絕對值、和最低位點與最小平方焦點面之間的最大距離的絕對值的合計,例如可藉由神鋼(KOBELCO)科研公司製造的Bow/Warp測定裝置SBW-331ML/d進行測定。 Eighth, the supporting glass substrate of the present invention preferably has a plate thickness of less than 2.0 mm, a plate thickness deviation of 30 μm or less, and a warpage amount of 60 μm or less. Here, the "warpage amount" means the absolute value of the maximum distance between the highest position and the least square focal plane in the entire glass substrate, and the absolute value of the maximum distance between the lowest position and the least square focal plane. The total can be measured by, for example, a Bow / Warp measuring device SBW-331ML / d manufactured by Kobelco Scientific.
第九,本發明的積層體至少包括加工基板、及用以對加工基板進行支持的支持玻璃基板,其特徵在於支持玻璃基板為所述支持玻璃基板。 Ninth, the laminated body of the present invention includes at least a processing substrate and a supporting glass substrate for supporting the processing substrate, characterized in that the supporting glass substrate is the supporting glass substrate.
第十,本發明的積層體較佳為加工基板至少包括以密封材模製的半導體晶片。 Tenth, the laminated body of the present invention is preferably a processing substrate including at least a semiconductor wafer molded with a sealing material.
第十一,本發明的半導體封裝的製造方法的特徵在於包括下述步驟:準備至少包括加工基板及用以對加工基板進行支持的支持玻璃基板的積層體;搬送積層體;以及對加工基板進行加工處理,並且支持玻璃基板為所述支持玻璃基板。另外,「搬送積層體的步驟」與「對加工基板進行加工處理的步驟」無須分開進行,亦可同時進行。 Eleventh, the method for manufacturing a semiconductor package of the present invention is characterized by comprising the steps of: preparing a laminated body including at least a processed substrate and a glass substrate supporting the processed substrate; transporting the laminated body; and processing the processed substrate The processing and supporting glass substrate is the supporting glass substrate. In addition, "the step of conveying a laminated body" and "the step of processing a processed substrate" need not be performed separately, and may be performed simultaneously.
第十二,本發明的半導體封裝的製造方法較佳為加工處理包括在加工基板的一表面進行配線的步驟。 Twelfth, the method for manufacturing a semiconductor package according to the present invention is preferably a process including a step of wiring on one surface of a processed substrate.
第十三,本發明的半導體封裝的製造方法較佳為加工處理包括在加工基板的一表面形成焊料凸塊的步驟。 Thirteenth, the method for manufacturing a semiconductor package of the present invention preferably includes a step of forming a solder bump on one surface of the processed substrate.
第十四,本發明的半導體封裝的製造方法的特徵在於利用所述半導體封裝的製造方法製作。 Fourteenth, the method for manufacturing a semiconductor package according to the present invention is characterized by using the method for manufacturing a semiconductor package.
第十五,本發明的電子機器包括半導體封裝,其特徵在於半導體封裝為所述半導體封裝。 Fifteenth, the electronic device of the present invention includes a semiconductor package, which is characterized in that the semiconductor package is the semiconductor package.
1、27‧‧‧積層體 1.27‧‧‧layer
10、26‧‧‧支持玻璃基板 10, 26‧‧‧ Support glass substrate
11、24‧‧‧加工基板 11, 24‧‧‧ processing substrate
12‧‧‧剝離層 12‧‧‧ peeling layer
13、21、25‧‧‧黏著層 13, 21, 25‧‧‧ Adhesive layer
20‧‧‧支持構件 20‧‧‧ supporting components
22‧‧‧半導體晶片 22‧‧‧Semiconductor wafer
23‧‧‧密封材 23‧‧‧sealing material
28‧‧‧配線 28‧‧‧ Wiring
29‧‧‧焊料凸塊 29‧‧‧solder bump
圖1是表示本發明的積層體的一例的概念立體圖。 FIG. 1 is a conceptual perspective view showing an example of a laminated body of the present invention.
圖2(a)~圖2(g)是表示扇出型的WLP的製造步驟的概念剖面圖。 2 (a) to 2 (g) are conceptual cross-sectional views showing manufacturing steps of a fan-out type WLP.
本發明的支持玻璃基板中,20℃~200℃的溫度範圍的平均線熱膨脹係數超過81×10-7/℃且為110×10-7/℃以下,較佳為82×10-7/℃以上且95×10-7/℃以下,尤佳為83×10-7/℃以上且91×10-7/℃以下。若20℃~200℃的溫度範圍的平均線熱膨脹係數為所述範圍外,則加工基板與支持玻璃基板的熱膨脹係數難以匹配。而且,若兩者的熱膨脹係數不匹配,則加工處理時容易產生加工基板的尺寸變化(尤其是翹曲變形)。 In the support glass substrate of the present invention, the average linear thermal expansion coefficient in a temperature range of 20 ° C to 200 ° C exceeds 81 × 10 -7 / ° C and is 110 × 10 -7 / ° C or lower, preferably 82 × 10 -7 / ° C The above is 95 × 10 -7 / ° C or less, and particularly preferably 83 × 10 -7 / ° C or more and 91 × 10 -7 / ° C or less. If the average linear thermal expansion coefficient in the temperature range of 20 ° C to 200 ° C is outside the range, it is difficult to match the thermal expansion coefficients of the processed substrate and the support glass substrate. Moreover, if the thermal expansion coefficients of the two do not match, dimensional changes (especially warpage deformation) of the processed substrate are liable to occur during processing.
30℃~380℃的溫度範圍的平均線熱膨脹係數超過85×10-7/℃且為115×10-7/℃以下,較佳為86×10-7/℃以上且100×10-7/℃以下,尤佳為87×10-7/℃以上且95×10-7/℃以下。若30℃~380℃的溫度範圍的平均線熱膨脹係數為所述範圍外,則加工基板與支持玻璃基板的熱膨脹係數難以匹配。而且,若兩者的熱膨脹係數不匹配,則加工處理時容易產生加工基板的尺寸變化(尤其是翹曲變形)。 The average linear thermal expansion coefficient in a temperature range of 30 ° C to 380 ° C exceeds 85 × 10 -7 / ° C and is 115 × 10 -7 / ° C or lower, preferably 86 × 10 -7 / ° C or higher and 100 × 10 -7 / The temperature is not more than 87 ° C, more preferably not less than 87 × 10 -7 / ° C and not more than 95 × 10 -7 / ° C. If the average linear thermal expansion coefficient in the temperature range of 30 ° C to 380 ° C is outside the range, it is difficult to match the thermal expansion coefficients of the processed substrate and the support glass substrate. Moreover, if the thermal expansion coefficients of the two do not match, dimensional changes (especially warpage deformation) of the processed substrate are liable to occur during processing.
本發明的支持玻璃基板較佳為作為玻璃組成,以質量%計含有50%~80%的SiO2、1%~20%的Al2O3、0%~20%的B2O3、0%~10%的MgO、0%~10%的CaO、0%~7%的SrO、0%~7%的BaO、0%~7%的ZnO、0%~25%的Na2O以及0%~25%的K2O。以下表示如所述般限定各成分的含量的理由。另外,各成分的含 量的說明中,%表達除進行特別說明的情況外,是表示質量%。 The supporting glass substrate of the present invention is preferably a glass composition, and contains 50% to 80% SiO 2 , 1% to 20% Al 2 O 3 , 0% to 20% B 2 O 3 , and 0% by mass. % ~ 10% MgO, 0% ~ 10% CaO, 0% ~ 7% SrO, 0% ~ 7% BaO, 0% ~ 7% ZnO, 0% ~ 25% Na 2 O, and 0 % ~ 25% of K 2 O. The reason for limiting the content of each component as described above is shown below. In addition, in the description of the content of each component,% expression expresses% by mass unless otherwise specified.
SiO2是形成玻璃的骨架的主成分。SiO2的含量較佳為50%~80%,55%~75%,58%~70%,尤佳為60%~68%。若SiO2的含量過少,則楊氏模量、耐酸性容易降低。另一方面,若SiO2的含量過多,則高溫黏度增高,熔融性容易降低,除此之外白矽石(cristobalite)等的失透結晶容易析出,液相溫度容易上升。 SiO 2 is a main component that forms the skeleton of glass. The content of SiO 2 is preferably 50% to 80%, 55% to 75%, 58% to 70%, and particularly preferably 60% to 68%. When the content of SiO 2 is too small, the Young's modulus and acid resistance tend to decrease. On the other hand, if the content of SiO 2 is too large, the high-temperature viscosity increases and the meltability tends to decrease. In addition, devitrified crystals such as cristobalite tend to precipitate and the liquidus temperature tends to rise.
Al2O3為提高楊氏模量的成分,並且為抑制分相、失透的成分。Al2O3的含量較佳為1%~20%,3%~18%,4%~16%,5%~13%,6%~12%,尤佳為7%~10%。若Al2O3的含量過少,則楊氏模量容易降低,且玻璃容易分相、失透。另一方面,若Al2O3的含量過多,則高溫黏度增高,熔融性、成形性容易降低。 Al 2 O 3 is a component that increases the Young's modulus and is a component that suppresses phase separation and devitrification. The content of Al 2 O 3 is preferably 1% to 20%, 3% to 18%, 4% to 16%, 5% to 13%, 6% to 12%, and particularly preferably 7% to 10%. When the content of Al 2 O 3 is too small, the Young's modulus is liable to decrease, and the glass is liable to phase separation and devitrification. On the other hand, if the content of Al 2 O 3 is too large, the high-temperature viscosity increases, and the meltability and formability tend to decrease.
B2O3為提高熔融性、耐失透性的成分,且為改善容易劃傷性並提高強度的成分。B2O3的含量較佳為0%~20%,1%~12%,2%~10%,尤佳為3%~8%。若B2O3的含量過少,則熔融性、耐失透性容易降低,且對氫氟酸系藥液的耐受性容易降低。另一方面,若B2O3的含量過多,則楊氏模量、耐酸性容易降低。 B 2 O 3 is a component that improves the meltability and devitrification resistance, and is a component that improves the scratch resistance and the strength. The content of B 2 O 3 is preferably 0% to 20%, 1% to 12%, 2% to 10%, and particularly preferably 3% to 8%. When the content of B 2 O 3 is too small, meltability and devitrification resistance tend to decrease, and resistance to a hydrofluoric acid-based chemical solution tends to decrease. On the other hand, when the content of B 2 O 3 is too large, the Young's modulus and acid resistance tend to decrease.
自提高楊氏模量的觀點考慮,Al2O3-B2O3較佳為超過0%,1%以上,3%以上,5%以上,7%以上,尤佳為9%以上。另外,「Al2O3-B2O3」是指從Al2O3的含量減去B2O3的含量所得的值。 From the viewpoint of increasing the Young's modulus, Al 2 O 3 -B 2 O 3 is preferably more than 0%, more than 1%, more than 3%, more than 5%, more than 7%, and more preferably more than 9%. In addition, "Al 2 O 3 -B 2 O 3 " means a value obtained by subtracting the content of B 2 O 3 from the content of Al 2 O 3 .
MgO為降低高溫黏性而提高熔融性的成分,且為鹼土類金屬氧化物中顯著提高楊氏模量的成分。MgO的含量較佳為0%~10%,0%~8%,0%~5%,0%~3%,0%~2%,尤佳為0%~1%。 若MgO的含量過多,則耐失透性容易降低。 MgO is a component that lowers the viscosity at high temperatures and improves the meltability, and is a component that significantly increases the Young's modulus among alkaline earth metal oxides. The content of MgO is preferably 0% to 10%, 0% to 8%, 0% to 5%, 0% to 3%, 0% to 2%, and particularly preferably 0% to 1%. When the content of MgO is too large, devitrification resistance is liable to decrease.
CaO為降低高溫黏性而顯著提高熔融性的成分。而且為鹼土類金屬氧化物中因導入原料相對廉價故使原料成本低廉化的成分。CaO的含量較佳為0%~10%,0.5%~8%,1%~6%,尤佳為2%~5%。若CaO的含量過多,則玻璃容易失透。另外,若CaO的含量過少,則難以享有所述效果。 CaO is a component that lowers the viscosity at high temperatures and significantly improves the meltability. In addition, it is a component of the alkaline-earth metal oxides that reduces the cost of raw materials because the raw materials are relatively inexpensive to introduce. The content of CaO is preferably 0% to 10%, 0.5% to 8%, 1% to 6%, and particularly preferably 2% to 5%. When the content of CaO is too large, the glass is liable to be devitrified. When the content of CaO is too small, it is difficult to enjoy the effects.
SrO為抑制分相的成分,且為提高耐失透性的成分。SrO的含量較佳為0%~7%,0%~5%,0%~3%,尤佳為0%~小於1%。若SrO的含量過多,則玻璃容易失透。 SrO is a component that suppresses phase separation and is a component that improves devitrification resistance. The content of SrO is preferably 0% to 7%, 0% to 5%, 0% to 3%, and particularly preferably 0% to less than 1%. When the content of SrO is too large, the glass is liable to be devitrified.
BaO為提高耐失透性的成分。BaO的含量較佳為0%~7%,0%~5%,0~3%,0%~小於1%。若BaO的含量過多,則玻璃容易失透。 BaO is a component which improves devitrification resistance. The content of BaO is preferably 0% to 7%, 0% to 5%, 0 to 3%, and 0% to less than 1%. When the content of BaO is too large, the glass is liable to be devitrified.
質量比CaO/(MgO+CaO+SrO+BaO)較佳為0.5以上,0.6以上,0.7以上,0.8以上,尤佳為0.9以上。若質量比CaO/(MgO+CaO+SrO+BaO)過小,則原料成本容易高漲。另外,「CaO/(MgO+CaO+SrO+BaO)」是指將CaO的含量除以MgO、CaO、SrO及BaO的合計量所得的值。 The mass ratio CaO / (MgO + CaO + SrO + BaO) is preferably 0.5 or more, 0.6 or more, 0.7 or more, 0.8 or more, and particularly preferably 0.9 or more. If the mass is too small compared to CaO / (MgO + CaO + SrO + BaO), the cost of raw materials tends to increase. In addition, "CaO / (MgO + CaO + SrO + BaO)" is a value obtained by dividing the content of CaO by the total amount of MgO, CaO, SrO, and BaO.
ZnO為降低高溫黏性而顯著提高熔融性的成分。ZnO的含量較佳為0%~7%,0.1%~5%,尤佳為0.5%~3%。若ZnO的含量過少,則難以享有所述效果。另外,若ZnO的含量過多,則玻璃容易失透。 ZnO is a component that lowers the viscosity at high temperatures and significantly improves the meltability. The content of ZnO is preferably 0% to 7%, 0.1% to 5%, and particularly preferably 0.5% to 3%. When the content of ZnO is too small, it is difficult to enjoy the effects. When the content of ZnO is too large, the glass is liable to be devitrified.
Na2O為對於使熱膨脹係數適當化而言重要的成分,且 為降低高溫黏性並顯著提高熔融性,並且有助於玻璃原料的初期的熔融的成分。Na2O的含量較佳為0%~25%,5%~25%,8%~24%,11%~23%,13%~21%,尤佳為超過15%~19%。若Na2O的含量過少,則有熔融性容易降低,除此之外熱膨脹係數不合理地降低之虞。另一方面,若Na2O的含量過多,則有熱膨脹係數不合理地增高之虞。 Na 2 O is a component that is important for proper thermal expansion coefficient, is a component that lowers the high-temperature viscosity and significantly improves the meltability, and contributes to the initial melting of the glass raw material. The content of Na 2 O is preferably 0% to 25%, 5% to 25%, 8% to 24%, 11% to 23%, 13% to 21%, particularly preferably more than 15% to 19%. If the content of Na 2 O is too small, the meltability tends to decrease, and in addition, the thermal expansion coefficient may decrease unreasonably. On the other hand, if the content of Na 2 O is too large, the thermal expansion coefficient may increase unreasonably.
自使熱膨脹係數適當化的觀點考慮,質量比Al2O3/Na2O較佳為0.20~1.3,0.25~1.0,0.30~0.85,0.35~0.65,尤佳為0.40~0.55。 From the viewpoint of optimizing the thermal expansion coefficient, the mass ratio Al 2 O 3 / Na 2 O is preferably 0.20 to 1.3, 0.25 to 1.0, 0.30 to 0.85, 0.35 to 0.65, and particularly preferably 0.40 to 0.55.
K2O為用以調整熱膨脹係數的成分,且為降低高溫黏性並提高熔融性,並且有助於玻璃原料的初期的熔融的成分。K2O的含量較佳為0%~25%,0%~20%,0%~15%,0%~10%,0%~6%,尤佳為0%~1%。若K2O的含量過多,則有熱膨脹係數不合理地增高之虞。 K 2 O is a component for adjusting the thermal expansion coefficient, a component that lowers the high-temperature viscosity and improves the meltability, and contributes to the initial melting of the glass raw material. The content of K 2 O is preferably 0% to 25%, 0% to 20%, 0% to 15%, 0% to 10%, 0% to 6%, and particularly preferably 0% to 1%. If the content of K 2 O is too large, the thermal expansion coefficient may increase unreasonably.
Na2O+K2O的含量較佳為12%~35%,15%~25%,16%~23%,17%~22%,尤佳為18%~21%。據此,容易將20℃~200℃的溫度範圍的平均線熱膨脹係數規定為超過81×10-7/℃~110×10-7/℃。另外,「Na2O+K2O」為Na2O與K2O的合計量。 The content of Na 2 O + K 2 O is preferably 12% to 35%, 15% to 25%, 16% to 23%, 17% to 22%, and particularly preferably 18% to 21%. Accordingly, it is easy to specify an average linear thermal expansion coefficient in a temperature range of 20 ° C. to 200 ° C. to exceed 81 × 10 -7 / ° C to 110 × 10 -7 / ° C. In addition, "Na 2 O + K 2 O" is the total amount of Na 2 O and K 2 O.
在重視熔融性提高的情況下,質量比Na2O/(Na2O+K2O)較佳為超過0.5,0.6以上,0.7以上,0.8以上,0.9以上,尤佳為0.95以上,在重視化學耐久性的情況下,較佳為0.65以下,0.6以下,0.55以下,小於0.5,0.45以下,尤佳為0.4以下。另外, 「Na2O/(Na2O+K2O)」是指將Na2O的含量除以Na2O與K2O的合計量所得的值。 In the case of improving the meltability, the mass ratio Na 2 O / (Na 2 O + K 2 O) is preferably more than 0.5, 0.6 or more, 0.7 or more, 0.8 or more, 0.9 or more, particularly preferably 0.95 or more. In the case of chemical durability, it is preferably 0.65 or less, 0.6 or less, 0.55 or less, less than 0.5, 0.45 or less, and particularly preferably 0.4 or less. In addition, "Na 2 O / (Na 2 O + K 2 O) " refers to the content of Na 2 O Na 2 O divided by the total value of the resulting amount of K 2 O of.
除所述成分以外,亦可導入其他成分作為任意成分。另外,自的確享有本發明的效果的觀點考慮,所述成分以外的其他成分的含量較佳為以合計量計為10%以下,尤佳為5%以下。 In addition to the components described above, other components may be introduced as optional components. In addition, from the standpoint of enjoying the effects of the present invention, the content of the components other than the components is preferably 10% or less in total, and more preferably 5% or less.
Fe2O3為可作為雜質成分或澄清劑成分導入的成分。然而,若Fe2O3的含量過多,則有紫外線透過率降低之虞。即,若Fe2O3的含量過多,則難以經由黏著層、剝離層而適當進行加工基板與支持玻璃基板的黏著與脫落。由此,Fe2O3的含量較佳為0.05%以下,0.03%以下,尤佳為0.02%以下。另外,本發明中提及的「Fe2O3」包含2價氧化鐵與3價氧化鐵,2價氧化鐵換算為Fe2O3,而進行處理。關於其他氧化物,同樣地以表述的氧化物為基準而進行處理。 Fe 2 O 3 is a component that can be introduced as an impurity component or a clarifier component. However, if the content of Fe 2 O 3 is too large, the ultraviolet transmittance may be reduced. That is, if the content of Fe 2 O 3 is too large, it is difficult to appropriately adhere and peel off the processed substrate and the supporting glass substrate through the adhesive layer and the release layer. Therefore, the content of Fe 2 O 3 is preferably 0.05% or less, 0.03% or less, and particularly preferably 0.02% or less. In addition, the "Fe 2 O 3 " mentioned in the present invention includes divalent iron oxide and trivalent iron oxide, and the divalent iron oxide is converted into Fe 2 O 3 and processed. The other oxides are treated similarly based on the expressed oxides.
作為澄清劑,As2O3、Sb2O3有效地發揮作用,就環境的觀點而言,較佳為極力減少該些成分。As2O3的含量較佳為1%以下,0.5%以下,尤佳為0.1%以下,理想的是實質不含有。此處,「實質不含有As2O3」是指玻璃組成中的As2O3的含量小於0.05%的情況。而且,Sb2O3的含量較佳為1%以下,0.5%以下,尤佳為0.1%以下,理想的是實質不含有。此處,「實質不含有Sb2O3」是指玻璃組成中的Sb2O3的含量小於0.05%的情況。 As fining agents, As 2 O 3 and Sb 2 O 3 effectively function, and from the viewpoint of the environment, it is preferable to reduce these components as much as possible. The content of As 2 O 3 is preferably 1% or less, 0.5% or less, and particularly preferably 0.1% or less. It is desirable that it is substantially not contained. Here, "substantially not containing As 2 O 3 " means a case where the content of As 2 O 3 in the glass composition is less than 0.05%. In addition, the content of Sb 2 O 3 is preferably 1% or less, 0.5% or less, and particularly preferably 0.1% or less. It is desirable that it is substantially not contained. Here, "substantially does not contain Sb 2 O 3 " refers to a case where the content of Sb 2 O 3 in the glass composition is less than 0.05%.
SnO2為高溫區域具有良好的澄清作用的成分,且為使高溫黏性降低的成分。SnO2的含量較佳為0%~1%,0.001%~1%, 0.01%~0.9%,尤佳為0.05%~0.7%。若SnO2的含量過多,則SnO2的失透結晶容易析出。另外,若SnO2的含量過少,則難以享有所述效果。 SnO 2 is a component having a good clarifying effect in a high-temperature region and a component that lowers the viscosity at high temperatures. The content of SnO 2 is preferably 0% to 1%, 0.001% to 1%, 0.01% to 0.9%, and particularly preferably 0.05% to 0.7%. When the content of SnO 2 is too large, devitrified crystals of SnO 2 are liable to precipitate. If the content of SnO 2 is too small, it is difficult to enjoy the effects.
進而,只要不破壞玻璃特性,亦可分別導入F、Cl、SO3、C、或Al、Si等金屬粉末至3%左右作為澄清劑。而且,CeO2等亦可導入3%左右,但需要留意紫外線透過率的降低。 Furthermore, as long as the glass characteristics are not impaired, metal powders such as F, Cl, SO 3 , C, or Al, Si may be introduced to about 3% as a clarifying agent. In addition, CeO 2 and the like can be introduced at about 3%, but it is necessary to pay attention to the decrease in ultraviolet transmittance.
Cl為促進玻璃的熔融的成分。若向玻璃組成中導入Cl,則可實現熔融溫度的低溫化、澄清作用的促進,結果,容易達成熔融成本的低廉化、玻璃製造爐的長壽命化。然而,若Cl的含量過多,則有使玻璃製造爐周圍的金屬零件腐蝕之虞。由此,Cl的含量較佳為3%以下,1%以下,0.5%以下,尤佳為0.1%以下。 Cl is a component that promotes melting of glass. When Cl is introduced into the glass composition, the melting temperature can be lowered and clarification can be promoted. As a result, it is easy to reduce the melting cost and prolong the life of the glass manufacturing furnace. However, if the content of Cl is too large, there is a possibility that metal parts around the glass manufacturing furnace may be corroded. Therefore, the content of Cl is preferably 3% or less, 1% or less, 0.5% or less, and particularly preferably 0.1% or less.
P2O5為可抑制失透結晶的析出的成分。然而,若大量導入P2O5,則玻璃容易分相。由此,P2O5的含量較佳為0%~2.5%,0%~1.5%,0%~0.5%,尤佳為0%~0.3%。 P 2 O 5 is a component that can suppress the precipitation of devitrified crystals. However, when a large amount of P 2 O 5 is introduced, the glass is liable to phase separation. Therefore, the content of P 2 O 5 is preferably 0% to 2.5%, 0% to 1.5%, 0% to 0.5%, and particularly preferably 0% to 0.3%.
TiO2為降低高溫黏性並提高熔融性的成分,並且為抑制曝曬作用(solarization)的成分。然而,若大量導入TiO2,則玻璃著色,透過率容易降低。由此,TiO2的含量較佳為0%~5%,0%~3%,0%~1%,尤佳為0%~0.02%。 TiO 2 is a component that lowers the high-temperature viscosity and improves the meltability, and is a component that suppresses solarization. However, when TiO 2 is introduced in a large amount, the glass is colored and the transmittance tends to decrease. Therefore, the content of TiO 2 is preferably 0% to 5%, 0% to 3%, 0% to 1%, and particularly preferably 0% to 0.02%.
ZrO2為改善耐藥品性、楊氏模量的成分。然而,若大量導入ZrO2,則玻璃容易失透,而且導入原料為難熔解性,因而有未熔解的結晶性異物混入至製品基板之虞。由此,ZrO2的含量較佳為0%~5%,0%~3%,0%~1%,尤佳為0%~0.5%。 ZrO 2 is a component that improves chemical resistance and Young's modulus. However, if ZrO 2 is introduced in a large amount, the glass is liable to be devitrified, and the introduction raw material is difficult to dissolve. Therefore, unmelted crystalline foreign matter may be mixed into the product substrate. Therefore, the content of ZrO 2 is preferably 0% to 5%, 0% to 3%, 0% to 1%, and particularly preferably 0% to 0.5%.
Y2O3、Nb2O5、La2O3中具有提高應變點、楊氏模量等的作用。然而,當該些成分的含量分別為5%,尤其大於1%時,則有原料成本、製品成本高漲之虞。 Y 2 O 3 , Nb 2 O 5 , and La 2 O 3 have the effects of increasing the strain point and Young's modulus. However, when the content of these components is 5%, especially more than 1%, there is a risk that the cost of raw materials and products will increase.
本發明的支持玻璃基板較佳為具有以下的特性。 The support glass substrate of the present invention preferably has the following characteristics.
本發明的支持玻璃基板中,楊氏模量較佳為65GPa以上,67GPa以上,68GPa以上,69GPa以上,70GPa以上,71GPa以上,72GPa以上,尤佳為73GPa以上。若楊氏模量過低,則難以維持積層體的剛性,加工基板容易產生變形、翹曲、破損。 In the supporting glass substrate of the present invention, the Young's modulus is preferably 65 GPa or more, 67 GPa or more, 68 GPa or more, 69 GPa or more, 70 GPa or more, 71 GPa or more, 72 GPa or more, and particularly preferably 73 GPa or more. When the Young's modulus is too low, it is difficult to maintain the rigidity of the laminated body, and the processed substrate is liable to be deformed, warped, and damaged.
液相溫度較佳為小於1150℃,1120℃以下,1100℃以下,1080℃以下,1050℃以下,1010℃以下,980℃以下,960℃以下,950℃以下,尤佳為940℃以下。據此,容易利用下拉法、尤其溢流下拉法成形玻璃基板,因而容易製作板厚小的玻璃基板,並且即便不對表面進行研磨,亦可減小板厚偏差。或,藉由少量的研磨便可將整體板厚偏差減小至小於2.0μm,尤其減小至小於1.0μm。結果,亦可使玻璃基板的製造成本低廉化。進而,在玻璃基板的製造步驟時,容易防止產生失透結晶且玻璃基板的生產性降低的事態。此處,「液相溫度」可藉由如下而算出,即,將通過標準篩30目(500μm)而殘留於50目(300μm)的玻璃粉末放入至鉑舟後,在溫度梯度爐中保持24小時,測定結晶析出的溫度。 The liquidus temperature is preferably less than 1150 ° C, 1120 ° C or lower, 1100 ° C or lower, 1080 ° C or lower, 1050 ° C or lower, 1010 ° C or lower, 980 ° C or lower, 960 ° C or lower, or 950 ° C or lower, particularly preferably 940 ° C or lower. Accordingly, it is easy to form the glass substrate by the down-draw method, especially the overflow down-draw method, so that it is easy to produce a glass substrate having a small thickness, and the thickness variation can be reduced without polishing the surface. Or, by a small amount of grinding, the overall plate thickness deviation can be reduced to less than 2.0 μm, especially to less than 1.0 μm. As a result, the manufacturing cost of the glass substrate can also be reduced. Furthermore, in the manufacturing process of a glass substrate, it is easy to prevent the situation where devitrification crystal | crystallization arises and productivity of a glass substrate falls. Here, the "liquid phase temperature" can be calculated by putting glass powder that has passed through a standard sieve 30 mesh (500 μm) and remained at 50 mesh (300 μm) into a platinum boat, and then holds it in a temperature gradient furnace. At 24 hours, the temperature at which crystals were precipitated was measured.
液相溫度下的黏度較佳為104.6dPa.s以上,105.0dPa.s以上,105.2dPa.s以上,105.4dPa.s以上,105.6dPa.s以上,尤佳為 105.8dPa.s以上。據此,因利用下拉法、尤其溢流下拉法容易成形玻璃基板,故容易製作板厚小的玻璃基板,並且即便不對表面進行研磨,亦可提高板厚偏差。或,藉由少量的研磨便可將整體板厚偏差減小至小於2.0μm,尤其減小至小於1.0μm。結果,可使玻璃基板的製造成本低廉化。進而,在玻璃基板的製造步驟時,容易防止產生失透結晶而玻璃基板的生產性降低的事態。此處,「液相溫度下的黏度」可利用鉑球提拉法進行測定。另外,液相溫度下的黏度為成形性的指標,液相溫度下的黏度越高,成形性越高。 The viscosity at the liquidus temperature is preferably 10 4.6 dPa. Above s, 10 5.0 dPa. s above, 10 5.2 dPa. Above s, 10 5.4 dPa. above s, 10 5.6 dPa. Above s, especially preferred is 10 5.8 dPa. s or more. Accordingly, since the glass substrate is easily formed by the down-draw method, particularly the overflow down-draw method, it is easy to produce a glass substrate having a small thickness, and the thickness variation can be increased without polishing the surface. Or, by a small amount of grinding, the overall plate thickness deviation can be reduced to less than 2.0 μm, especially to less than 1.0 μm. As a result, the manufacturing cost of the glass substrate can be reduced. Furthermore, in the manufacturing process of a glass substrate, it is easy to prevent a situation where devitrification crystal | crystallization arises and productivity of a glass substrate falls. Here, the "viscosity at the liquidus temperature" can be measured by a platinum ball pulling method. In addition, the viscosity at the liquidus temperature is an index of moldability, and the higher the viscosity at the liquidus temperature, the higher the moldability.
102.5dPa.s下的溫度較佳為1580℃以下,1500℃以下,1450℃以下,1400℃以下,1350℃以下,尤佳為1200℃~1300℃。若102.5dPa.s下的溫度增高,則熔融性降低,玻璃基板的製造成本高漲。此處,「102.5dPa.s下的溫度」可利用鉑球提拉法進行測定。另外,102.5dPa.s下的溫度相當於熔融溫度,該溫度越低,熔融性越高。 10 2.5 dPa. The temperature at s is preferably 1580 ° C or lower, 1500 ° C or lower, 1450 ° C or lower, 1400 ° C or lower, or 1350 ° C or lower, and particularly preferably 1200 ° C to 1300 ° C. If 10 2.5 dPa. As the temperature at s increases, the meltability decreases, and the manufacturing cost of the glass substrate increases. Here, the "temperature at 10 2.5 dPa · s" can be measured by a platinum ball pulling method. In addition, 10 2.5 dPa. The temperature at s corresponds to the melting temperature, and the lower the temperature, the higher the melting property.
本發明的支持玻璃基板較佳為利用下拉法、尤佳為利用溢流下拉法成形而成。溢流下拉法為如下方法,即,使熔融玻璃從耐熱性的流槽狀構造物的兩側溢出,使溢出的熔融玻璃一邊在流槽狀構造物的下頂端合流,一邊向下方延伸成形而製造玻璃基板。溢流下拉法中,應成為玻璃基板的表面的面不與流槽狀耐火物接觸,而以自由表面的狀態成形。因此,容易製作板厚小的玻璃基板,並且即便不對表面進行研磨,亦可減小板厚偏差。或, 可利用少量的研磨,將整體板厚偏差減小至小於2.0μm,尤其可減小至小於1.0μm。結果,可使玻璃基板的製造成本低廉化。 The supporting glass substrate of the present invention is preferably formed by using a down-draw method, and particularly preferably by an overflow down-draw method. The overflow down-draw method is a method in which molten glass overflows from both sides of a heat-resistant trough-like structure, and the overflowing molten glass is formed while converging at the lower end of the trough-like structure while extending downward. Manufacture of glass substrate. In the overflow down-draw method, the surface that should be the surface of the glass substrate does not come into contact with the channel-shaped refractory, but is formed in a free surface state. Therefore, it is easy to produce a glass substrate with a small plate thickness, and the plate thickness variation can be reduced without polishing the surface. or, A small amount of grinding can be used to reduce the overall plate thickness deviation to less than 2.0 μm, especially to less than 1.0 μm. As a result, the manufacturing cost of the glass substrate can be reduced.
作為玻璃基板的成形方法,除溢流下拉法以外,例如可採用流孔下引法、再拉法、浮式法等。 As a method for forming the glass substrate, in addition to the overflow down-draw method, for example, a down-hole drawing method, a re-draw method, and a float method can be used.
本發明的玻璃基板較佳為大致圓板狀或晶圓狀,其直徑較佳為100mm以上且500mm以下,尤佳為150mm以上且450mm以下。據此,容易適用於半導體封裝的製造步驟。亦可視需要,加工成除此以外的形狀,例如矩形等形狀。 The glass substrate of the present invention is preferably substantially disc-shaped or wafer-shaped, and its diameter is preferably 100 mm or more and 500 mm or less, and particularly preferably 150 mm or more and 450 mm or less. This makes it easy to apply to the manufacturing steps of the semiconductor package. If necessary, it can be processed into other shapes, such as rectangular shapes.
本發明的玻璃基板中,正圓度較佳為1mm以下,0.1mm以下,0.05mm以下,尤佳為0.03mm以下。正圓度越小,越容易適用於半導體封裝的製造步驟。另外,正圓度的定義為從晶圓的外形的最大值減去最小值所得的值。 In the glass substrate of the present invention, the roundness is preferably 1 mm or less, 0.1 mm or less, 0.05 mm or less, and particularly preferably 0.03 mm or less. The smaller the roundness, the easier it is to apply to the manufacturing steps of a semiconductor package. The roundness is defined as a value obtained by subtracting the minimum value from the maximum value of the outer shape of the wafer.
本發明的支持玻璃基板中,板厚較佳為小於2.0mm,1.5mm以下,1.2mm以下,1.1mm以下,1.0mm以下,尤佳為0.9mm以下。板厚越薄,則積層體的質量越輕,因而操作性提高。另一方面,若板厚過薄,則支持玻璃基板自身的強度降低,難以發揮作為支持基板的功能。由此,板厚較佳為0.1mm以上,0.2mm以上,0.3mm以上,0.4mm以上,0.5mm以上,0.6mm以上,尤佳為超過0.7mm。 In the support glass substrate of the present invention, the plate thickness is preferably less than 2.0 mm, 1.5 mm or less, 1.2 mm or less, 1.1 mm or less, 1.0 mm or less, and particularly preferably 0.9 mm or less. The thinner the thickness of the plate, the lighter the weight of the laminated body, and thus the operability is improved. On the other hand, if the plate thickness is too thin, the strength of the supporting glass substrate itself decreases, and it becomes difficult to perform the function as a supporting substrate. Therefore, the plate thickness is preferably 0.1 mm or more, 0.2 mm or more, 0.3 mm or more, 0.4 mm or more, 0.5 mm or more, and 0.6 mm or more, and more preferably 0.7 mm or more.
本發明的支持玻璃基板中,板厚偏差較佳為30μm以下,20μm以下,10μm以下,5μm以下,4μm以下,3μm以下,2μm以下,1μm以下,尤佳為0.1μm~小於1μm。而且算術平 均粗糙度Ra較佳為100nm以下,50nm以下,20nm以下,10nm以下,5nm以下,2nm以下,1nm以下,尤佳為0.5nm以下。表面精度越高,越可容易提高加工處理的精度。因尤其可提高配線精度,故可進行高密度的配線。而且,支持玻璃基板的強度提高,支持玻璃基板及積層體不易破損。進而,可增加支持玻璃基板的再利用次數。另外,「算術平均粗糙度Ra」可藉由觸針式表面粗糙度計或原子力顯微鏡(atomic force microscope,AFM)進行測定。 In the support glass substrate of the present invention, the plate thickness deviation is preferably 30 μm or less, 20 μm or less, 10 μm or less, 5 μm or less, 4 μm or less, 3 μm or less, 2 μm or less, and 1 μm or less, particularly preferably 0.1 μm to less than 1 μm. And arithmetic flat The average roughness Ra is preferably 100 nm or less, 50 nm or less, 20 nm or less, 10 nm or less, 5 nm or less, 2 nm or less, and 1 nm or less, and more preferably 0.5 nm or less. The higher the surface accuracy, the easier it is to improve the accuracy of processing. Since wiring accuracy can be improved in particular, high-density wiring can be performed. In addition, the strength of the supporting glass substrate is improved, and the supporting glass substrate and the laminated body are not easily broken. Furthermore, the number of reuses of the supporting glass substrate can be increased. The "arithmetic average roughness Ra" can be measured by a stylus surface roughness meter or an atomic force microscope (AFM).
本發明的支持玻璃基板較佳為在利用溢流下拉法成形後,對表面進行研磨。據此,板厚偏差容易規定為2μm以下,1μm以下,尤其容易規定為小於1μm。 The support glass substrate of the present invention preferably has a surface polished after being formed by an overflow down-draw method. This makes it easy to specify a plate thickness variation of 2 μm or less, and 1 μm or less, and it is particularly easy to specify a thickness of less than 1 μm.
本發明的支持玻璃基板中,翹曲量較佳為60μm以下,55μm以下,50μm以下,1μm~45μm,尤佳為5μm~40μm。翹曲量越小,越容易提高加工處理的精度。因尤其可提高配線精度,故可進行高密度的配線。 In the support glass substrate of the present invention, the amount of warpage is preferably 60 μm or less, 55 μm or less, 50 μm or less, 1 μm to 45 μm, and particularly preferably 5 μm to 40 μm. The smaller the amount of warpage, the easier it is to improve the accuracy of processing. Since wiring accuracy can be improved in particular, high-density wiring can be performed.
本發明的支持玻璃基板中,板厚方向上、波長300nm下的紫外線透過率較佳為40%以上,50%以上,60%以上,70%以上,尤佳為80%以上。若紫外線透過率過低,則因紫外光的照射而難以利用黏著層將加工基板與支持基板黏著。而且,在利用紫外線硬化型膠帶等設置黏著層等的情況下,難以將加工基板與支持玻璃基板容易地分離。另外,「板厚方向上、波長300nm下的紫外線透過率」可藉由如下來評價,即,例如使用雙光束型分光 光度計,測定波長300nm的分光透過率。 In the supporting glass substrate of the present invention, the ultraviolet transmittance in the thickness direction and at a wavelength of 300 nm is preferably 40% or more, 50% or more, 60% or more, 70% or more, and particularly preferably 80% or more. If the ultraviolet transmittance is too low, it becomes difficult to adhere the processing substrate and the support substrate by the adhesive layer due to the irradiation of the ultraviolet light. In addition, when an adhesive layer or the like is provided using an ultraviolet curing tape or the like, it is difficult to easily separate the processing substrate from the supporting glass substrate. The "ultraviolet transmittance in the thickness direction and at a wavelength of 300 nm" can be evaluated by using, for example, a two-beam type beam splitting A photometer measures the spectral transmittance at a wavelength of 300 nm.
本發明的支持玻璃基板較佳為不進行離子交換處理,且較佳為表面不具有壓縮應力層。若進行離子交換處理,則支持玻璃基板的製造成本高漲。進而,若進行離子交換處理,則難以減小支持玻璃基板的整體板厚偏差。另外,本發明的支持玻璃基板不排除進行離子交換處理而在表面形成壓縮應力層的形態。若就提高機械強度的觀點而言,較佳為進行離子交換處理,而在表面形成壓縮應力層。 The support glass substrate of the present invention is preferably not subjected to ion exchange treatment, and preferably has no compressive stress layer on the surface. If an ion exchange process is performed, the manufacturing cost of a support glass substrate will increase. Furthermore, if an ion exchange process is performed, it will become difficult to reduce the variation in the overall thickness of the supporting glass substrate. The support glass substrate of the present invention does not exclude a form in which a compressive stress layer is formed on the surface by performing an ion exchange process. From the viewpoint of improving the mechanical strength, it is preferable to perform an ion exchange treatment and form a compressive stress layer on the surface.
本發明的積層體至少包括加工基板及用以對加工基板進行支持的支持玻璃基板,其特徵在於:支持玻璃基板為所述支持玻璃基板。此處,本發明的積層體的技術特徵(較佳的構成、效果)與本發明的支持玻璃基板的技術特徵重複。由此,本說明書中,關於該重複部分省略詳細的記載。另外,因容易將加工基板與支持玻璃基板固定,故亦可將紫外線硬化型膠帶用作黏著層。 The laminated body of the present invention includes at least a processing substrate and a supporting glass substrate for supporting the processing substrate, and is characterized in that the supporting glass substrate is the supporting glass substrate. Here, the technical features (preferred structure and effect) of the laminated body of the present invention are the same as those of the glass substrate support of the present invention. Therefore, in this specification, detailed descriptions of the overlapping portions are omitted. In addition, since the processing substrate and the supporting glass substrate can be easily fixed, an ultraviolet curing tape can also be used as an adhesive layer.
本發明的積層體較佳為在加工基板與支持玻璃基板之間具有黏著層。黏著層較佳為樹脂,例如,較佳為熱硬化性樹脂、光硬化性樹脂(尤佳為紫外線硬化樹脂)等。而且,較佳為具有耐受半導體封裝的製造步驟的熱處理的耐熱性者。由此,半導體封裝的製造步驟中黏著層不易熔解,可提高加工處理的精度。 The laminated body of the present invention preferably has an adhesive layer between the processing substrate and the supporting glass substrate. The adhesive layer is preferably a resin, and for example, a thermosetting resin, a photocurable resin (particularly, an ultraviolet curable resin), and the like are preferable. Moreover, it is preferable that it has heat resistance which can endure the heat processing of the manufacturing process of a semiconductor package. Therefore, the adhesive layer is not easily melted in the manufacturing steps of the semiconductor package, and the accuracy of processing can be improved.
本發明的積層體較佳為進而在加工基板與支持玻璃基板之間,更具體而言在加工基板與黏著層之間具有剝離層。據此,在對加工基板進行特定的加工處理後,使加工基板容易自支持玻 璃基板剝離。自生產性的觀點考慮,加工基板的剝離較佳為藉由雷射光等照射光而進行。作為雷射光源,可使用釔-鋁-石榴石(Yttrium Aluminium Garnet,YAG)雷射(波長1064nm)、半導體雷射(波長780nm~1300nm)等紅外光雷射光源。而且,剝離層中可使用藉由照射紅外線雷射而分解的樹脂。而且,亦可將效率優良地吸收紅外線並轉換為熱的物質添加到樹脂中。例如,亦可將碳黑、石墨粉、微粒子金屬粉末、染料、顏料等添加到樹脂中。 The laminated body of the present invention preferably further has a release layer between the processing substrate and the supporting glass substrate, and more specifically, between the processing substrate and the adhesive layer. According to this, after a specific processing process is performed on the processing substrate, the processing substrate is easily self-supported. The glass substrate was peeled. From the viewpoint of productivity, peeling of the processed substrate is preferably performed by irradiation with light such as laser light. As the laser light source, an infrared light laser source such as a Yttrium Aluminium Garnet (YAG) laser (wavelength 1064 nm) or a semiconductor laser (wavelength 780 nm to 1300 nm) can be used. Further, a resin that is decomposed by irradiating infrared laser can be used for the release layer. Furthermore, a substance that absorbs infrared rays with high efficiency and converts them into heat may be added to the resin. For example, carbon black, graphite powder, fine metal powder, dye, pigment, etc. may be added to the resin.
剝離層包含因雷射光等照射光而產生「層內剝離」或「界面剝離」的材料。即,包含下述材料,即,若照射固定強度的光,則原子或分子的原子間或分子間的結合力消失或減少,而產生剝蝕(ablation)等,從而產生剝離。另外,存在因照射光的照射而剝離層中所含的成分成為氣體並釋放而導致分離的情況,及剝離層吸收光而成為氣體,且其蒸汽釋放而導致分離的情況。 The release layer includes materials that cause "in-layer peeling" or "interface peeling" due to irradiation light such as laser light. That is, it includes a material that, when light of a fixed intensity is irradiated, the bonding force between atoms or molecules of atoms or molecules disappears or decreases, and ablation or the like occurs, thereby causing peeling. In addition, there is a case where a component contained in the peeling layer becomes a gas and is released due to irradiation with the irradiation light, and separation occurs, and a peeling layer absorbs light and becomes a gas, and the vapor is released to cause separation.
本發明的積層體中,支持玻璃基板較佳為大於加工基板。由此,在對加工基板與支持玻璃基板進行支持時,即便在兩者的中心位置稍微隔開的情況下,加工基板的緣部亦不易從支持玻璃基板突出。 In the laminated body of the present invention, the supporting glass substrate is preferably larger than the processing substrate. Therefore, when the processing substrate and the supporting glass substrate are supported, even when the center positions of the processing substrate and the supporting glass substrate are slightly spaced apart, the edges of the processing substrate do not easily protrude from the supporting glass substrate.
本發明的半導體封裝的製造方法的特徵在於包括下述步驟:準備至少包括加工基板及用以對加工基板進行支持的支持玻璃基板的積層體;搬送積層體;以及對加工基板進行加工處理,並且支持玻璃基板為所述支持玻璃基板。此處,本發明的半導體 封裝的製造方法的技術特徵(較佳的構成、效果)與本發明的支持玻璃基板及積層體的技術特徵重複。由此,本說明書中,關於該重複部分省略詳細記載。 The method for manufacturing a semiconductor package according to the present invention is characterized by comprising the steps of: preparing a laminated body including at least a processed substrate and a supporting glass substrate for supporting the processed substrate; transporting the laminated body; The supporting glass substrate is the supporting glass substrate. Here, the semiconductor of the present invention The technical characteristics (preferred structure and effect) of the manufacturing method of the package are the same as those of the supporting glass substrate and the laminated body of the present invention. Therefore, in this specification, detailed descriptions of the overlapping portions are omitted.
本發明的半導體封裝的製造方法中,加工處理較佳為在加工基板的一表面進行配線的處理或在加工基板的一表面形成焊料凸塊的處理。本發明的半導體封裝的製造方法中,在該些處理時加工基板尺寸不易變化,因而可適當地進行該些步驟。 In the method for manufacturing a semiconductor package of the present invention, the processing is preferably a process of performing wiring on one surface of the processed substrate or a process of forming solder bumps on one surface of the processed substrate. In the manufacturing method of the semiconductor package of the present invention, the dimensions of the processed substrate are not easily changed during these processes, and therefore these steps can be appropriately performed.
作為加工處理,除所述以外,亦可為對加工基板的一表面(通常為與支持玻璃基板為相反側的表面)進行機械研磨的處理,對加工基板的一表面(通常為與支持玻璃基板為相反側的表面)進行乾式蝕刻的處理,對加工基板的一表面(通常為與支持玻璃基板為相反側的表面)進行濕式蝕刻的處理中的任一者。另外,本發明的半導體封裝的製造方法中,在加工基板上不易產生翹曲,並且可維持積層體的剛性。結果,可適當進行所述加工處理。 As the processing treatment, in addition to the above, it is also possible to mechanically polish one surface of the processing substrate (usually the surface opposite to the supporting glass substrate), and one surface of the processing substrate (usually the supporting glass substrate). The surface on the opposite side) is subjected to dry etching, and one surface of the processing substrate (usually the surface on the opposite side to the supporting glass substrate) is subjected to wet etching. In addition, in the method for manufacturing a semiconductor package according to the present invention, warpage does not easily occur on the processed substrate, and the rigidity of the laminated body can be maintained. As a result, the processing can be appropriately performed.
本發明的半導體封裝的特徵在於藉由所述半導體封裝的製造方法製作。此處,本發明的半導體封裝的技術特徵(較佳的構成、效果)與本發明的支持玻璃基板,積層體及半導體封裝的製造方法的技術特徵重複。由此,本說明書中關於該重複部分省略詳細記載。 The semiconductor package of the present invention is characterized by being manufactured by the manufacturing method of the semiconductor package. Here, the technical features (preferred structure and effects) of the semiconductor package of the present invention overlap with those of the method for manufacturing a support glass substrate, a laminated body, and a semiconductor package of the present invention. Therefore, detailed descriptions of the overlapping portions are omitted in this specification.
本發明的電子機器包括半導體封裝,其特徵在於:半導體封裝為所述半導體封裝。此處,本發明的電子機器的技術特徵 (較佳的構成、效果)與本發明的支持玻璃基板、積層體、半導體封裝的製造方法、半導體封裝的技術特徵重複。由此,本說明書中關於該重複部分省略詳細記載。 An electronic device of the present invention includes a semiconductor package, which is characterized in that the semiconductor package is the semiconductor package. Here, the technical features of the electronic device of the present invention The (preferred structure and effect) overlaps the technical characteristics of the supporting glass substrate, the laminated body, the method for manufacturing a semiconductor package, and the semiconductor package of the present invention. Therefore, detailed descriptions of the overlapping portions are omitted in this specification.
一邊參考圖式一邊對本發明進行進一步說明。 The present invention will be further described with reference to the drawings.
圖1是表示本發明的積層體1的一例的概念立體圖。圖1中,積層體1包括支持玻璃基板10及加工基板11。支持玻璃基板10為了防止加工基板11的尺寸變化,而貼附於加工基板11。支持玻璃基板10與加工基板11之間配置著剝離層12與黏著層13。剝離層12與支持玻璃基板10接觸,黏著層13與加工基板11接觸。 FIG. 1 is a conceptual perspective view showing an example of a laminated body 1 according to the present invention. In FIG. 1, the laminated body 1 includes a support glass substrate 10 and a processing substrate 11. The support glass substrate 10 is attached to the processing substrate 11 in order to prevent the dimensional change of the processing substrate 11. A release layer 12 and an adhesive layer 13 are disposed between the supporting glass substrate 10 and the processing substrate 11. The peeling layer 12 is in contact with the supporting glass substrate 10, and the adhesive layer 13 is in contact with the processing substrate 11.
根據圖1可知,積層體1按照支持玻璃基板10、剝離層12、黏著層13、加工基板11的順序積層配置。支持玻璃基板10的形狀根據加工基板11而決定,圖1中,支持玻璃基板10及加工基板11的形狀均為大致圓板形狀。剝離層12例如可使用藉由照射雷射而分解的樹脂。而且,亦可將效率優良地吸收雷射光並轉換為熱的物質添加到樹脂中。例如,亦可將碳黑、石墨粉、微粒子金屬粉末、染料、顏料等添加到樹脂中。剝離層12藉由電漿化學氣相沈積(Chemical Vapor Deposition,CVD)、溶膠-凝膠法(sol-gel method)的旋塗等而形成。黏著層13包含樹脂,例如藉由各種印刷法、噴墨法、旋塗法、輥式塗佈法等塗佈形成。而且,亦可使用紫外線硬化型膠帶。黏著層13在藉由剝離層12從加工基板11剝離支持玻璃基板10後,藉由溶劑等加以溶解去除。紫 外線硬化型膠帶在照射紫外線後,可藉由剝離用膠帶而去除。 As can be seen from FIG. 1, the laminated body 1 is laminated in the order of the supporting glass substrate 10, the peeling layer 12, the adhesive layer 13, and the processing substrate 11. The shape of the supporting glass substrate 10 is determined according to the processing substrate 11. In FIG. 1, the shapes of the supporting glass substrate 10 and the processing substrate 11 are both approximately circular plate shapes. As the release layer 12, for example, a resin that is decomposed by irradiation with a laser can be used. Furthermore, a substance that absorbs laser light with high efficiency and converts it into heat may be added to the resin. For example, carbon black, graphite powder, fine metal powder, dye, pigment, etc. may be added to the resin. The release layer 12 is formed by plasma chemical vapor deposition (CVD), spin coating by a sol-gel method, or the like. The adhesive layer 13 includes a resin, and is formed by, for example, coating by various printing methods, inkjet methods, spin coating methods, and roll coating methods. Moreover, an ultraviolet curable tape can also be used. After the support layer 13 is peeled off the support glass substrate 10 from the processing substrate 11 by the release layer 12, it is dissolved and removed by a solvent or the like. purple The outer-curing tape can be removed with a peeling tape after irradiating ultraviolet rays.
圖2(a)~圖2(f)是表示fan out型的WLP的製造步驟的概念剖面圖。圖2(a)表示在支持構件20的一表面上形成黏著層21的狀態。亦可視需要在支持構件20與黏著層21之間形成剝離層。接下來,如圖2(b)所示,在黏著層21上貼附多個半導體晶片22。此時,使半導體晶片22的主動側的面與黏著層21接觸。接下來,圖2(c)所示,利用樹脂的密封材23對半導體晶片22進行模製。密封材23使用壓縮成形後的尺寸變化、成形配線時的尺寸變化少的材料。繼而,如圖2(d)、圖2(e)所示,在將半導體晶片22經模製的加工基板24從支持構件20分離後,經由黏著層25,而與支持玻璃基板26黏著固定。此時,加工基板24的表面內的與埋入半導體晶片22側的表面為相反側的表面配置於支持玻璃基板26側。如此,可獲得積層體27。另外,亦可視需要在黏著層25與支持玻璃基板26之間形成剝離層。進而,在搬送所獲得的積層體27後,如圖2(f)所示,在加工基板24的埋入半導體晶片22側的表面形成配線28後,形成多個焊料凸塊29。最後,在加工基板24從支持玻璃基板26分離後,將加工基板24切斷為每個半導體晶片22,並用於之後的封裝步驟(圖2(g))。 2 (a) to 2 (f) are conceptual cross-sectional views showing manufacturing steps of a fan out WLP. FIG. 2 (a) shows a state where the adhesive layer 21 is formed on one surface of the support member 20. Optionally, a release layer may be formed between the support member 20 and the adhesive layer 21. Next, as shown in FIG. 2 (b), a plurality of semiconductor wafers 22 are attached to the adhesive layer 21. At this time, the active-side surface of the semiconductor wafer 22 is brought into contact with the adhesive layer 21. Next, as shown in FIG. 2 (c), the semiconductor wafer 22 is molded using a resin sealing material 23. As the sealing material 23, a material having less dimensional change after compression molding and less dimensional change during wiring molding is used. Next, as shown in FIGS. 2 (d) and 2 (e), the semiconductor wafer 22 is separated from the support member 20 by the molded processing substrate 24, and then adhered and fixed to the support glass substrate 26 via the adhesive layer 25. At this time, a surface on the side of the surface of the processing substrate 24 opposite to the surface on the side of the embedded semiconductor wafer 22 is disposed on the side of the supporting glass substrate 26. In this way, a laminated body 27 can be obtained. In addition, if necessary, a release layer may be formed between the adhesive layer 25 and the supporting glass substrate 26. Further, after the obtained laminated body 27 is transferred, as shown in FIG. 2 (f), after wiring 28 is formed on the surface of the substrate 24 on the side where the semiconductor wafer 22 is embedded, a plurality of solder bumps 29 are formed. Finally, after the processing substrate 24 is separated from the supporting glass substrate 26, the processing substrate 24 is cut into each semiconductor wafer 22 and used for subsequent packaging steps (FIG. 2 (g)).
[實施例1] [Example 1]
以下,基於實施例對本發明進行說明。另外,以下的實施例僅為例示。本發明不受以下的實施例任何限定。 Hereinafter, the present invention will be described based on examples. The following examples are merely examples. The present invention is not limited in any way by the following examples.
表1、表2表示本發明的實施例(試樣No.1~試樣 No.34)。 Tables 1 and 2 show examples of the present invention (Sample No. 1 to Sample No. 34).
首先,將以成為表中的玻璃組成的方式調合玻璃原料所得的玻璃配料放入至鉑坩堝中,以1550℃熔融4小時。當玻璃配料熔解時,使用鉑攪拌器進行攪拌,而進行均質化。然後,使熔融玻璃向碳板上流出,而成形為板狀後,從比緩冷點高20℃左右 的溫度開始,以3℃/min緩冷至常溫為止。對所獲得的各試樣,評價20℃~200℃的溫度範圍的平均線熱膨脹係數α20~200,30℃~380℃的溫度範圍的平均線熱膨脹係數α30~380,密度ρ,應變點Ps,緩冷點Ta,軟化點Ts,高溫黏度104.0dPa.s下的溫度,高溫黏度103.0dPa.s下的溫度,高溫黏度102.5dPa.s下的溫度,高溫黏度102.0dPa.s下的溫度,液相溫度TL,液相溫度TL下的黏度η,楊氏模量E及波長300nm下的紫外線透過率T。 First, a glass ingredient obtained by blending glass raw materials so as to have a glass composition in a table was placed in a platinum crucible and melted at 1550 ° C. for 4 hours. When the glass batch is melted, it is homogenized by stirring using a platinum stirrer. Then, the molten glass was caused to flow out onto the carbon plate to be formed into a plate shape, and then gradually cooled from a temperature of about 20 ° C higher than the slow cooling point to normal temperature at 3 ° C / min. Each sample obtained, evaluation of a temperature range of 20 ℃ ~ 200 ℃ average linear thermal expansion coefficient α 20 ~ 200, average linear thermal expansion coefficient of the temperature range of 30 ℃ ~ 380 ℃ of α 30 ~ 380, the density [rho], the strain point Ps, slow cooling point Ta, softening point Ts, high temperature viscosity 10 4.0 dPa. Temperature at s, high temperature viscosity 10 3.0 dPa. Temperature at s, high temperature viscosity 10 2.5 dPa. Temperature at s, high temperature viscosity 10 2.0 dPa. Temperature at s, liquidus temperature TL, viscosity η at liquidus temperature TL, Young's modulus E, and ultraviolet transmittance T at a wavelength of 300nm.
20℃~200℃的溫度範圍的平均線熱膨脹係數α20~200、30℃~380℃的溫度範圍的平均線熱膨脹係數α30~380為利用膨脹計測定的值。 The average linear thermal expansion coefficient in the temperature range of 20 ℃ ~ 200 ℃ α 20 ~ 200, average linear thermal expansion coefficient in the temperature range of 30 ℃ ~ 380 ℃ α 30 ~ 380 is measured using the expanded values.
密度ρ為利用周知的阿基米德法測定的值。 The density ρ is a value measured by a well-known Archimedes method.
應變點Ps、緩冷點Ta、軟化點Ts為基於美國試驗材料協會(American Society for Testing and Materials,ASTM)C336的方法測定的值。 The strain point Ps, the slow cooling point Ta, and the softening point Ts are values measured based on the method of the American Society for Testing and Materials (ASTM) C336.
高溫黏度104.0dPa.s、103.0dPa.s、102.5dPa.s下的溫度為利用鉑球提拉法測定的值。 High temperature viscosity 10 4.0 dPa. s, 10 3.0 dPa. s, 10 2.5 dPa. The temperature at s is a value measured by a platinum ball pulling method.
液相溫度TL是如下的值,即,將通過標準篩30目(500μm)而殘留於50目(300μm)的玻璃粉末放入至鉑舟中,在溫度梯度爐中保持24小時後,藉由顯微鏡觀察測定結晶析出的溫度所得。液相溫度下的黏度η為利用鉑球提拉法測定液相溫度TL下的玻璃的黏度所得的值。 The liquid phase temperature TL is a value obtained by putting glass powder remaining in a 50 mesh (300 μm) through a standard sieve of 30 mesh (500 μm) into a platinum boat, and holding it in a temperature gradient furnace for 24 hours. Obtained by measuring the temperature at which crystals are precipitated with a microscope. The viscosity η at the liquidus temperature is a value obtained by measuring the viscosity of the glass at the liquidus temperature TL using a platinum ball pulling method.
楊氏模量E是指藉由共振法測定的值。 The Young's modulus E is a value measured by a resonance method.
如根據表1、表2可知,試樣No.1~試樣No.34中,20℃~200℃的溫度範圍的平均線熱膨脹係數α20~200為81.5×10-7/℃~107.8×10-7/℃,30℃~380℃的溫度範圍的平均線熱膨脹係數α30~380為85.4×10-7/℃~114.0×10-7/℃。由此,認為試樣No.1~試樣No.34適合作為半導體封裝的製造步驟中用於加工基板的支持的支持玻璃基板。 As can be seen from Tables 1 and 2, in Sample No. 1 to Sample No. 34, the average linear thermal expansion coefficient α 20 to 200 in a temperature range of 20 ° C to 200 ° C is 81.5 × 10 -7 / ° C to 107.8 × 10 -7 / ℃, average linear thermal expansion coefficient in the temperature range of 30 ℃ ~ 380 ℃ α 30 ~ 380 is 85.4 × 10 -7 /℃~114.0×10 -7 / ℃ . Therefore, it is considered that sample No. 1 to sample No. 34 are suitable as a supporting glass substrate for supporting a processed substrate in a manufacturing step of a semiconductor package.
[實施例2] [Example 2]
如以下般製作[實施例2]的各試樣。首先,以成為表1、表2中記載的試樣No.1~試樣No.34的玻璃組成的方式調合玻璃原料後,供給至玻璃熔融爐中以1500℃~1600℃熔融,然後將熔融玻璃供給至溢流下拉成形裝置,分別成形為板厚0.7mm。在將所獲得的玻璃基板(整體板厚偏差約4.0μm)加工為Φ300mm×0.7mm厚後,藉由研磨裝置將其兩表面進行研磨處理。具體而言,由外徑不同的一對研磨墊夾著玻璃基板的兩表面,一邊使玻璃基板與一對研磨墊一併旋轉,一邊對玻璃基板的兩表面進行研磨處理。在研磨處理時,有時進行控制,以使玻璃基板的一部分從研磨墊突出。另外,研磨墊為胺基甲酸酯(urethane)製,研磨處理時使用的研磨漿料的平均粒徑為2.5μm,研磨速度為15m/min。對所獲得的各研磨處理完畢的玻璃基板,藉由神鋼(KOBELCO)科研公司製造的Bow/Warp測定裝置SBW-331ML/d測定整體板厚偏差與翹曲量。結果,整體板厚偏差分別小於1.0μm,翹曲量分別為35μm以下。 Each sample of [Example 2] was prepared as follows. First, a glass raw material is prepared so that it may become the glass composition of the sample No.1-sample No.34 shown in Table 1, Table 2, and it is supplied to a glass melting furnace and melt | dissolves at 1500 degreeC-1600 degreeC, and it melts The glass was supplied to an overflow down-draw forming device, and each was formed into a plate thickness of 0.7 mm. After the obtained glass substrate (whole plate thickness deviation of about 4.0 μm) was processed to a thickness of Φ300 mm × 0.7 mm, both surfaces thereof were polished by a polishing apparatus. Specifically, both surfaces of the glass substrate are sandwiched between a pair of polishing pads having different outer diameters, and both surfaces of the glass substrate are polished while the glass substrate and the pair of polishing pads are rotated together. During the polishing process, control may be performed so that a part of the glass substrate protrudes from the polishing pad. The polishing pad was made of urethane. The average particle diameter of the polishing slurry used in the polishing process was 2.5 μm, and the polishing rate was 15 m / min. With respect to each of the obtained glass substrates subjected to the polishing treatment, a Bow / Warp measuring device SBW-331ML / d manufactured by Kobelco Scientific Co., Ltd. was used to measure the overall plate thickness deviation and warpage amount. As a result, the overall plate thickness deviations were less than 1.0 μm, and the warpage amounts were 35 μm or less.
Claims (13)
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
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JP2014178807 | 2014-09-03 | ||
JP2014-178807 | 2014-09-03 | ||
JP2014210437 | 2014-10-15 | ||
JP2014-210437 | 2014-10-15 | ||
JP2015031495 | 2015-02-20 | ||
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JP7011215B2 (en) * | 2016-12-14 | 2022-02-10 | 日本電気硝子株式会社 | Support glass substrate and laminate using it |
WO2018110163A1 (en) * | 2016-12-14 | 2018-06-21 | 日本電気硝子株式会社 | Glass support substrate and laminate using same |
CN110944953A (en) * | 2017-07-26 | 2020-03-31 | Agc株式会社 | Supporting glass for semiconductor package |
CN116462405A (en) * | 2017-07-26 | 2023-07-21 | 日本电气硝子株式会社 | Support glass substrate and laminated substrate using same |
JP7280546B2 (en) * | 2017-11-09 | 2023-05-24 | 日本電気硝子株式会社 | Glass plate and wavelength conversion package using the same |
CN111741933B (en) * | 2018-02-20 | 2023-05-16 | 日本电气硝子株式会社 | Glass |
JP7445186B2 (en) * | 2018-12-07 | 2024-03-07 | 日本電気硝子株式会社 | glass |
CN111056752B (en) * | 2019-12-18 | 2023-12-22 | 东旭集团有限公司 | Glass substrate assembly for display panel and method for manufacturing glass substrate assembly |
US20240228362A9 (en) * | 2021-02-05 | 2024-07-11 | Nippon Sheet Glass Company, Limited | Glass composition, glass filler, and method for manufacturing the same |
WO2023032163A1 (en) * | 2021-09-03 | 2023-03-09 | 株式会社レゾナック | Method for producing semiconductor device, provisional fixation material, and application of provisional fixation material for production of semiconductor device |
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JP2011138695A (en) * | 2009-12-28 | 2011-07-14 | Koito Mfg Co Ltd | Lamp for vehicle |
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JP4151161B2 (en) * | 1998-08-11 | 2008-09-17 | 旭硝子株式会社 | Substrate glass |
JP2002025040A (en) * | 2000-06-30 | 2002-01-25 | Hitachi Ltd | Glass substrate for magnetic disk and magnetic disk using the same |
JP4692915B2 (en) * | 2002-05-29 | 2011-06-01 | 日本電気硝子株式会社 | Front glass substrate for plasma display devices. |
JP2004067460A (en) * | 2002-08-07 | 2004-03-04 | Central Glass Co Ltd | Glass composition |
JP5140014B2 (en) * | 2009-02-03 | 2013-02-06 | 富士通株式会社 | Manufacturing method of semiconductor device |
JP5402184B2 (en) * | 2009-04-13 | 2014-01-29 | 日本電気硝子株式会社 | Glass film and method for producing the same |
JP5483262B2 (en) * | 2009-12-04 | 2014-05-07 | 日本電気硝子株式会社 | Laminated glass |
WO2013118897A1 (en) * | 2012-02-09 | 2013-08-15 | 旭硝子株式会社 | Glass substrate for transparent conductive film formation, and substrate with transparent conductive film |
JP5796905B2 (en) * | 2012-12-25 | 2015-10-21 | 日本電気硝子株式会社 | Tempered glass substrate, glass and method for producing tempered glass substrate |
JP6593669B2 (en) * | 2013-09-12 | 2019-10-23 | 日本電気硝子株式会社 | Support glass substrate and carrier using the same |
CN115636583A (en) * | 2014-04-07 | 2023-01-24 | 日本电气硝子株式会社 | Supporting glass substrate and laminate using same |
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