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WO2020090205A1 - Semiconductor device and method for producing same - Google Patents

Semiconductor device and method for producing same Download PDF

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Publication number
WO2020090205A1
WO2020090205A1 PCT/JP2019/033371 JP2019033371W WO2020090205A1 WO 2020090205 A1 WO2020090205 A1 WO 2020090205A1 JP 2019033371 W JP2019033371 W JP 2019033371W WO 2020090205 A1 WO2020090205 A1 WO 2020090205A1
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WO
WIPO (PCT)
Prior art keywords
semiconductor chip
semiconductor device
areas
adhesive layer
manufacturing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2019/033371
Other languages
French (fr)
Japanese (ja)
Inventor
恵子 上野
一尊 本田
小川 剛
裕貴 柳田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Resonac Corp
Original Assignee
Hitachi Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP2020554783A priority Critical patent/JP7342879B2/en
Priority to KR1020217008275A priority patent/KR102727223B1/en
Priority to CN201980058834.9A priority patent/CN112703583B/en
Publication of WO2020090205A1 publication Critical patent/WO2020090205A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • H10W72/0711
    • H10W72/072
    • H10W74/012
    • H10W74/15
    • H10W74/473
    • H10W90/00
    • H10W99/00
    • H10W42/121
    • H10W70/65
    • H10W72/01336
    • H10W72/07141
    • H10W72/07232
    • H10W72/07234
    • H10W72/07235
    • H10W72/073
    • H10W72/07331
    • H10W72/07332
    • H10W72/07334
    • H10W72/07335
    • H10W72/07338
    • H10W72/07341
    • H10W72/241
    • H10W72/242
    • H10W72/244
    • H10W72/248
    • H10W72/252
    • H10W72/29
    • H10W72/325
    • H10W72/353
    • H10W72/354
    • H10W72/9415
    • H10W72/942
    • H10W72/952
    • H10W90/291
    • H10W90/297
    • H10W90/722
    • H10W90/724
    • H10W90/732
    • H10W90/734

Definitions

  • the present disclosure relates to a semiconductor device and a manufacturing method thereof.
  • Wire bonding is a method of connecting a semiconductor chip and a substrate by using a metal thin wire such as a gold wire.
  • a method called flip-chip connection (FC connection) is becoming widespread in order to meet the demand for higher functionality, higher integration, higher speed, etc. of semiconductor devices.
  • the FC connection is a method in which conductive protrusions called bumps are formed on a semiconductor chip or a substrate to directly connect the semiconductor chip and the substrate.
  • Examples of modes of FC connection include a method of metal bonding using solder, tin, gold, silver, copper, etc., a method of metal bonding by applying ultrasonic vibration, a method of maintaining mechanical contact by the contracting force of resin, and the like.
  • a method of metal bonding using solder, tin, gold, silver, copper or the like is common.
  • COB Chip On Board
  • FC connection method is known as a method for connecting a semiconductor chip and a substrate.
  • COB is a type of FC connection.
  • CoC Chip On Chip
  • CoW Chip On Wefer
  • Patent Document 1 discloses a method for bonding semiconductor wafers.
  • semiconductor devices are highly required to have high functionality, and specifically, thinning, downsizing, increase in the number of pins (bumps and / or wirings), There is a demand for narrowing the pitch or gap.
  • chip stack type packages that have multiple connection methods described above, such as POP (Package On Package), TSV (Through Silicon Via), etc.
  • POP Package On Package
  • TSV Through Silicon Via
  • the semiconductor chip spacing tends to become narrower during package assembly.
  • the interval between the adjacent semiconductor chips By narrowing the interval between the adjacent semiconductor chips, many semiconductor chips can be mounted on the substrate or the wafer, and the cost can be reduced. Further, by narrowing the interval between the adjacent semiconductor chips, it is possible to assemble different kinds of semiconductor chips in a small area, and it is possible to perform high-density mounting.
  • the shape of the adhesive layer is often the same square or rectangle as the semiconductor chip.
  • a portion where the resin material forming the adhesive layer protrudes from the semiconductor chip after the pressure bonding step is called a fillet. Since the resin material flows in a circular shape at the time of pressure bonding, the fillet at the corner of the semiconductor chip becomes smaller than the fillet at the side of the semiconductor chip. The fillet at the corner of the semiconductor chip (end of the side of the semiconductor chip) is called coverage.
  • the reliability of the semiconductor device tends to decrease.
  • the fillet on the side of the semiconductor chip becomes large, which makes it difficult to reduce the cost and mount the device at high density. That is, it is difficult to make both the fillet on the side of the semiconductor chip small and the coverage secured.
  • the present disclosure aims to provide a semiconductor device having a small fillet on the side of a semiconductor chip and ensuring coverage, and a manufacturing method thereof.
  • the manufacturing method according to the present disclosure includes a first member having a first connecting portion and a linearly extending side, a second member having a second connecting portion, a first member and a second member. And an adhesive layer disposed between the first connection portion and the second connection portion, the semiconductor device having the adhesive layer disposed between the first connection portion and the second connection portion.
  • a manufacturing method includes a laminating step of preparing a laminated body in which a first member, an adhesive layer, and a second member are laminated in this order, and a thickness direction with respect to the laminated body. And a pressing step of irradiating a laser beam for heating the laminated body in a state where a pressing force is applied to the laminated body, in the pressing step, from the peripheral portion of one side of the first member to the peripheral portion of the other end.
  • a laser is irradiated to the laminated body so that the laser irradiation portion, the laser non-irradiation portion, and the laser irradiation portion are formed in this order.
  • the corners of the first member (for example, a square or rectangular semiconductor chip) having the linearly extending sides are the laser irradiation parts, and the spaces between them are the laser non-irradiation parts.
  • the corner can be locally heated by the laser, the coverage at the corner of the first member can be secured, and the fillet on the side of the first member can be suppressed.
  • a manufacturing method includes a laminating step of preparing a laminated body in which a first member, an adhesive layer and a second member are laminated in this order, and a thickness direction with respect to the laminated body.
  • the side of the semiconductor chip is divided into three equal parts and divided into nine areas, and the area including one corner of the semiconductor chip is defined as area 1 among the nine areas, and the area 1 extends along the peripheral edge of the semiconductor chip.
  • the average temperature Tc of the outer surface of the semiconductor chip in the central portions of the areas 1, 3, 5, and 7, and the semiconductor in the central portions of the areas 2, 4, 6, and 8 The difference (Tc ⁇ Ts) from the average temperature Ts of the outer surface of the chip is 15 ° C. or more.
  • the manufacturing method according to the second embodiment by locally increasing the temperature of the corners (areas 1, 3, 5, 7) of the semiconductor chip, it is possible to secure the coverage in the corners of the first member. In addition, fillets on the sides of the first member are suppressed.
  • the areas 2, 4, 6, 8 when the laminate is heated by laser irradiation, may or may not be the laser non-irradiated portion.
  • the areas 2, 4, 6, and 8 may be irradiated with laser irradiation having an energy amount smaller than that of the areas 1, 3, 5, and 7.
  • the second member examples include a wiring board, a semiconductor chip, and a semiconductor wafer.
  • the adhesive layer contains, for example, a thermosetting resin having a weight average molecular weight of less than 10,000 and a curing agent, and may further contain a polymer component having a weight average molecular weight of 10,000 or more. ..
  • the adhesive layer is preferably a film adhesive from the viewpoint of improving the efficiency of the pressure bonding step.
  • the present disclosure provides a semiconductor device manufactured by the above manufacturing method.
  • the fillet on the side of the semiconductor chip is short and the coverage is secured. Due to these characteristics, high-density mounting is possible and excellent reliability is achieved.
  • a semiconductor device in which the fillet on the side of the semiconductor chip is small and coverage is secured, and a manufacturing method thereof.
  • FIG. 1 is a sectional view schematically showing an embodiment of a semiconductor device according to the present disclosure.
  • FIG. 2A is a cross-sectional view schematically showing a state in which preparation for carrying out the pressure bonding step is completed, and
  • FIG. 2B schematically shows a laminated body in which a semiconductor chip, an adhesive layer and a substrate are laminated in this order.
  • FIG. 2C is a cross-sectional view schematically showing a state in which the pressure-bonding step is performed on the laminated body.
  • FIG. 3 is a top view schematically showing an example of a region for irradiating the laminated body with laser in the pressure bonding step.
  • FIG. 1 is a sectional view schematically showing an embodiment of a semiconductor device according to the present disclosure.
  • FIG. 2A is a cross-sectional view schematically showing a state in which preparation for carrying out the pressure bonding step is completed
  • FIG. 2B schematically shows a laminated body in which a semiconductor chip, an adhesive layer and
  • FIG. 4 is a top view schematically showing an example of a state in which the adhesive layer protrudes from the semiconductor chip after the pressure bonding step.
  • FIG. 5 is a sectional view schematically showing an example of a semiconductor device manufactured by the TSV technique.
  • FIG. 6A is a top view schematically showing laser irradiation patterns in Example 1 and Comparative Example 1
  • FIG. 6B schematically shows laser irradiation patterns in Example 2 and Comparative Example 2. It is a top view shown.
  • FIG. 7 is a top view schematically showing laser irradiation patterns in Examples 3 and 4.
  • a semiconductor device 50 shown in FIG. 1 includes a semiconductor chip 10 (first member) having a copper pillar 10a and a solder bump 10b (first connecting portion), and a substrate 20 (having a wiring 20a (second connecting portion)).
  • the second member) and the adhesive layer 30 arranged between the semiconductor chip 10 and the substrate 20, and the solder bumps 10b and the wirings 20a are electrically connected.
  • the solder bump 10b contains, for example, a tin-silver alloy.
  • the surface of the wiring 20a is plated with gold, for example. By heating to a temperature higher than the melting point of the solder, the solder bump 10b and the wiring 20a can be connected.
  • a method of manufacturing the semiconductor device 50 will be described with reference to FIGS. 2A to 2C.
  • the semiconductor device 50 is manufactured, for example, through the following steps.
  • An adhesive-attached chip manufacturing step of preparing a chip having an adhesive layer 30 formed on the surface of the semiconductor chip 10 on which the copper pillars 10a and the solder bumps 10b are formed (see FIG. 2A).
  • a laminating step of preparing a laminated body 40 in which the semiconductor chip 10, the adhesive layer 30, and the substrate 20 are laminated in this order see FIG. 2B.
  • a pressure bonding step of irradiating the laminated body 40 with a laser L for heating while applying a pressing force F to the laminated body 40 in the thickness direction (see FIG. 2C).
  • a curing process of heating the laminated body 40 after the pressure bonding process.
  • the step of producing a chip with an adhesive is a step of producing a chip (chip with an adhesive) having the semiconductor chip 10 and the adhesive layer 30 formed so as to cover the copper pillars 10a and the like of the semiconductor chip 10. From the standpoint of workability, it is preferable to prepare a film-like adhesive in advance and to produce the chip with the adhesive through a step of laminating the film-like adhesive on an object. Lamination can be performed by hot pressing, roll laminating, vacuum laminating and the like. The size and thickness of the adhesive layer 30 may be appropriately set according to the size of the semiconductor chip 10, the bump height, and the like.
  • a chip with an adhesive may be produced by pasting a film adhesive cut to the size of the semiconductor chip 10 onto the semiconductor chip, or a film adhesive may be applied to a semiconductor wafer on which wirings and the like are formed. After adhering, the chips with adhesive may be produced by dicing into individual pieces. When a chip with an adhesive is produced by dicing, the semiconductor chip 10 and the adhesive layer 30 have the same shape and size.
  • the laminating step is a step of preparing a laminated body 40 in which the semiconductor chip 10, the adhesive layer 30, and the substrate 20 are laminated in this order. After the chip with the adhesive and the substrate 20 are aligned with each other, the chip with the adhesive and the substrate 20 are temporarily pressure-bonded to each other to produce the laminated body 40.
  • a normal crimping device can be used for the temporary crimping.
  • FIG. 3 is a top view schematically showing a region where a laser is applied to the laminated body in the pressure bonding step.
  • a laser bonder that can independently irradiate heating lasers on a total of 36 regions is used.
  • An example of a laser bonder having such performance is FDB250 manufactured by Shibuya Industry Co., Ltd.
  • the area irradiated with the laser is represented by a hatched circle, and the area not irradiated with the laser is represented by a white circle.
  • laser irradiation is performed from the peripheral portion (one corner C) of one end Sa of the side S of the semiconductor chip 10 to the peripheral portion (the other corner C) of the other end Sb.
  • the layer 40 is irradiated with a laser so that the portion A1, the laser non-irradiation portion A2, and the laser irradiation portion A1 are formed in this order.
  • the remaining three sides S of the semiconductor chip 10 are also irradiated with laser so that the laser irradiation part A1, the laser non-irradiation part A2, and the laser irradiation part A1 are formed in this order from one end to the other end. As shown in FIG.
  • the side of the semiconductor chip 10 is divided into three equal parts and divided into nine areas, and an area including one corner of the semiconductor chip 10 is defined as an area 1 among the nine areas. Areas arranged from 1 to along the peripheral edge of the semiconductor chip 10 are referred to as areas 2 to 8.
  • the areas 1, 3, 5, 7 are selectively irradiated with the laser L, and the areas 2, 4, 6, 8 and the area 9 including the center of the semiconductor chip 10 are not irradiated with the laser. That is, areas 1, 3, 5, and 7 are laser irradiation portions A1, and areas 2, 4, 6, 8, and 9 are laser non-irradiation portions A2.
  • the outer surface of the semiconductor chip 10 may be directly irradiated with the laser, or the semiconductor chip 10 may be irradiated with the laser L.
  • a plate (not shown) for applying the pressing force F may be irradiated with a laser.
  • the difference (Tc ⁇ Ts) from the average temperature Ts is preferably 15 ° C. or more.
  • Tc-Ts is 15 ° C. or higher means that the area including the corner of the semiconductor chip 10 is locally heated to a temperature higher than the other areas. By performing such heating in the pressure bonding step, the fillet on the side S of the semiconductor chip 10 can be shortened and the coverage can be secured.
  • Tc-Ts may be 15-30 ° C.
  • the temperature difference between the average temperature Ts of the outer surface of the semiconductor chip 10 in the central portions of the areas 2, 4, 6, and 8 and the temperature T9 of the outer surface of the semiconductor chip 10 in the central portion of the area 9 may be 5 ° C or higher.
  • the fact that Ts-T9 is 5 ° C. or higher means that the areas 2, 4, 6, 8 of the semiconductor chip 10 are heated so as to have a higher temperature than the area 9. That is, in the pressure bonding step of this embodiment, heating is performed so that the condition of Tc> Ts> T9 is satisfied, the temperature difference (Tc-Ts) is 15 ° C. or more, and the temperature difference (Ts-T9) is 5 ° C. or more. You may.
  • the temperature difference (Ts-T9) may be in the range of 5-40 ° C.
  • the crimping tool surface is brought into contact with the surface of the laminated body 40, and a pressing force F is applied to the laminated body 40. In this state, the surface of the crimping tool is heated.
  • the crimping tool surface is usually designed so that its surface temperature is as uniform as possible. For example, when the size of the semiconductor chip is about 30 mm ⁇ 30 mm, the temperature variation on the surface of the semiconductor chip during pressure bonding is usually less than 15 ° C.
  • the fillet width in the central portion of the side of the semiconductor chip tends to be large and the coverage tends to be insufficient. It should be noted that if the heating temperature is increased or the pressing force is increased in order to secure the coverage, the fillet width on the side of the semiconductor chip is further increased.
  • the present embodiment it is possible to suppress the fillet width and ensure the coverage by intentionally providing the temperature distribution on the surface of the crimping tool.
  • the areas 1, 3, 5, 7 of the semiconductor chip to a high temperature, it is possible to enhance the flow of the adhesive layers 30 respectively located at the corners C of the semiconductor chip 10, and to improve the coverage. Can be secured.
  • the flow of the adhesive layer 30 near the center of the side S of the semiconductor chip 10 can be relatively suppressed. Therefore, the fillet on the side S can be reduced.
  • the temperature rising rate of the entire semiconductor chip tends to increase.
  • the temperature rising rate it becomes easier to locally heat a specific area of the semiconductor chip, and it becomes easier to secure coverage while suppressing fillets.
  • the temperature rising rate is increased, the time for melting the solder is lengthened, which facilitates connection. This makes it possible to manufacture a highly reliable semiconductor device in a short time.
  • FIG. 4 is a top view schematically showing a state where the adhesive layer 30 protrudes from the semiconductor chip 10.
  • the width W F shown in FIG. 4 is the maximum width of the fillet on the side S of the semiconductor chip 10.
  • the maximum width of the fillet is measured on the four sides S of the semiconductor chip 10, and the average value is defined as the fillet width on the side of the semiconductor chip 10.
  • the widths w1 and w2 shown in FIG. 4 are the width ( ⁇ m) of the fillet at a position 200 ⁇ m from the corner C of the semiconductor chip 10.
  • the widths w1 and w2 of the four corners C of the semiconductor chip 10 are measured, and the average of the eight values is defined as the coverage ( ⁇ m) of the semiconductor chip 10.
  • the fillet width depends on the size and thickness of the semiconductor chip 10 and the amount of underfill (including liquid and film) supplied.
  • the fillet width is preferably as small as possible so long as there is no problem in reliability.
  • the fillet width is preferably 50 to 200 ⁇ m, more preferably 50 to 150 ⁇ m.
  • the coverage of the semiconductor chip 10 is preferably 5 to 100 ⁇ m, more preferably 10 to 100 ⁇ m. If the coverage is 10 ⁇ m or more, the reliability of the semiconductor device 50 tends to be further improved.
  • the coverage index (dimensionless) is calculated by dividing the coverage by the fillet width.
  • the coverage index is, for example, 0.1 to 1, and may be 0.2 to 0.5. If the coverage index is 0.1 or more, the reliability of the semiconductor device 50 tends to be sufficiently high.
  • the curing process is a process of heating the laminated body 40 after the pressure bonding process. From the viewpoint of reducing voids, this step is preferably performed in a pressurized atmosphere using a pressure oven or pressure reflow device.
  • the heating temperature is, for example, 130 to 200 ° C.
  • the pressure is, for example, 0.1 to 1 MPa.
  • a laser bonder is used in the pressure bonding step and heating is performed so that Tc-Ts is 15 ° C. or higher.
  • a temperature other than the laser bonder is used.
  • a crimping device may be used.
  • a pressure bonding tool having a convex portion at a position corresponding to the corner C may be used so that the temperature is easily transmitted only to the corner C of the semiconductor chip 10.
  • a crimping tool in which a region corresponding to the corner C of the semiconductor chip 10 is locally made of a material having high thermal conductivity may be used, or a portion other than the region may be made of a material having low thermal conductivity. You may use the crimping tool comprised by.
  • the case where the areas 2, 4, 6, and 8 are not irradiated with the laser is exemplified, but the areas 2, 4, 6, and 8 are irradiated with the laser as long as Tc-Ts can be set to 15 ° C. or higher. Alternatively (see Examples 3 and 4).
  • the semiconductor device 50 having the connecting portion between the semiconductor chip 10 and the substrate 20 is exemplified, but a mode in which the semiconductor chip and another semiconductor chip are connected may be used, and the semiconductor chip and the semiconductor wafer may be connected. It may be a modified mode.
  • the connection portion is not limited to the metal connection by the bump and the wiring, but may be the metal connection by the bump and the bump.
  • FIG. 5 is a sectional view schematically showing an example of a semiconductor device manufactured by the TSV technique.
  • a semiconductor device 70 shown in this figure has three semiconductor chips 11, 12 and 13 which are flip-chip connected and laminated via an adhesive layer 30, and an interface which is connected to the semiconductor chip 13 via the adhesive layer 30. And a poser 60.
  • the semiconductor chips 11, 12, 13 have penetrating electrode portions 11a, 12a, 13a. According to the semiconductor device 70 having such a configuration, signals can be exchanged from the back surface of the semiconductor chip.
  • the wiring can be vertically passed in the semiconductor chip, the semiconductor chips or the chip and the interposer can be flexibly connected to each other in the shortest distance.
  • the crimping step according to the present embodiment may be applied to the manufacture of a laminated chip including the semiconductor chips 11, 12, and 13, or may be applied to the laminated chip, the interposer 60, and the pressure bonding.
  • the semiconductor chip has sides that extend linearly, and has, for example, a square or rectangular shape.
  • the length of one side of the semiconductor chip is, for example, 0.1 to 300 mm, and may be 5 to 150 mm.
  • the semiconductor constituting the semiconductor chip is not particularly limited, and elemental semiconductors such as silicon and germanium and compound semiconductors such as gallium arsenide and indium phosphide can be cited.
  • the semiconductor chip can have conductive protrusions called bumps.
  • the bump contains gold, silver, copper, solder, tin, nickel, etc. as main components. These metals may be used alone or in combination of two or more. Further, it may be formed to have a structure in which these metals are laminated.
  • the main component of solder is, for example, an alloy of tin-silver, tin-lead, tin-bismuth, tin-copper, tin-silver-copper, or the like.
  • the bumps may be formed on a wiring board or the like connected to the semiconductor chip. As the metal forming the bumps, copper and solder are preferable from the viewpoint of low cost, and solder is more preferable from the viewpoint of connection reliability and suppression of warpage.
  • the semiconductor chip and wiring board can have a conductive surface called a pad.
  • the pad contains gold, silver, copper, solder, tin, nickel, etc. as a main component. These metals may be used alone or in combination of two or more. Further, it may be formed to have a structure in which these metals are laminated.
  • the main component of solder is, for example, an alloy of tin-silver, tin-lead, tin-bismuth, tin-copper, tin-silver-copper, or the like. Further, as the metal forming the pad, gold and solder are preferable from the viewpoint of connection reliability.
  • the wiring board is not particularly limited as long as it is a normal circuit board, and one having a wiring pattern formed on the insulating substrate by etching, one having a wiring pattern formed by printing a conductive substance on the surface of the insulating substrate, etc. Can be mentioned.
  • the insulating substrate is made of a resin material such as glass epoxy, polyester, ceramic, epoxy, bismaleimide triazine, and polyimide.
  • the -A metal layer may be formed on the surface of the wiring pattern.
  • the metal layer contains gold, silver, copper, solder, tin, nickel, etc. as a main component. These metals may be used alone or in combination of two or more. Further, it may be formed to have a structure in which these metals are laminated.
  • copper and solder are preferable from the viewpoint of low cost, and solder is more preferable from the viewpoint of connection reliability and suppression of warpage.
  • the semiconductor device may have the above-mentioned bump-bump connecting portion, bump-pad connecting portion, or bump-wiring connecting portion.
  • the adhesive layer preferably has excellent heat resistance so that it can be subjected to pressure bonding at a temperature of 200 ° C. or higher.
  • a metal such as solder can be melted by performing a pressure bonding process under a temperature condition of 200 ° C. or higher.
  • the adhesive layer contains a resin component having a weight average molecular weight of less than 10,000 from the viewpoint of suppressing the generation of voids.
  • the adhesive layer may further contain a polymer component having a weight average molecular weight of 10,000 or more.
  • the adhesive layer is preferably a film adhesive from the viewpoint of improving the efficiency of the pressure bonding step.
  • the "weight average molecular weight" used herein means a value measured in terms of polystyrene by using high performance liquid chromatography (C-R4A manufactured by Shimadzu Corporation).
  • component (a) Resin component having a weight average molecular weight of less than 10,000
  • the resin component having a weight average molecular weight of less than 10,000 includes an epoxy resin and an acrylic resin.
  • the component (a) is preferably a thermosetting resin, and in this case, the adhesive layer preferably contains the curing agent (b). Since a resin component having a relatively small molecular weight decomposes upon heating and causes voids, it is preferable to react with a curing agent from the viewpoint of heat resistance.
  • the epoxy resin is not particularly limited as long as it has two or more epoxy groups in the molecule, and examples thereof include bisphenol A type, bisphenol F type, naphthalene type, phenol novolac type, cresol novolak type, phenol aralkyl type, biphenyl. Type, triphenylmethane type, dicyclopentadiene type, and various polyfunctional epoxy resins can be used. These can be used alone or in combination of two or more.
  • the content of the epoxy resin is, for example, 10 to 50 parts by mass with respect to 100 parts by mass of the total mass of the adhesive layer.
  • the content of the epoxy resin is 10 parts by mass or more, it is easy to control the flow of the resin after curing, and when it is 50 parts by mass or less, the warpage of the package can be suppressed.
  • the acrylic resin is not particularly limited as long as it has at least one acryloyl group in the molecule, and examples thereof include bisphenol A type, bisphenol F type, naphthalene type, phenol novolac type, cresol novolac type, phenol aralkyl type, biphenyl type. , Triphenylmethane type, dicyclopentadiene type, fluorene type, adamantane type, and various polyfunctional acrylics can be used. These can be used alone or in combination of two or more.
  • the content of the acrylic resin is preferably 10 to 50 parts by mass, more preferably 15 to 40 parts by mass with respect to 100 parts by mass of the total mass of the adhesive layer.
  • the content of the acrylic resin is 10 parts by mass or more, it is easy to control the flow of the resin after curing, and when it is 50 parts by mass or less, the warpage of the package can be suppressed.
  • the acrylic resin is preferably solid at room temperature (25 ° C). Voids are less likely to occur in the solid form than in the liquid form, and the viscosity (tack) of the adhesive layer before curing (B stage) is small and the handling is excellent.
  • the number of functional groups of the acryloyl group is preferably 3 or less. When the number of functional groups of the acryloyl group is 3 or less, curing sufficiently progresses in a short time and a sufficiently high curing reaction rate can be achieved.
  • (B) Curing agent examples include a phenol resin curing agent, an acid anhydride curing agent, an amine curing agent, an imidazole curing agent, a phosphine curing agent, an azo compound and an organic peroxide. ..
  • the phenol resin-based curing agent is not particularly limited as long as it has two or more phenolic hydroxyl groups in the molecule, for example, phenol novolac, cresol novolac, phenol aralkyl resin, cresol naphthol formaldehyde polycondensate, triphenyl.
  • Methane-type polyfunctional phenols and various polyfunctional phenol resins can be used. These can be used alone or as a mixture of two or more kinds.
  • the equivalent ratio of the phenol resin type curing agent to the epoxy resin is preferably 0.3 to 1.5, from the viewpoint of good curability, adhesiveness and storage stability, and 0 0.4 to 1.0 is more preferable, and 0.5 to 1.0 is further preferable.
  • the equivalent ratio is 0.3 or more, the curability and the adhesive strength tend to be improved, and when it is 1.5 or less, the unreacted phenolic hydroxyl group does not remain excessively and the water absorption is It tends to be kept low and the insulation reliability tends to be improved.
  • acid anhydride curing agent for example, use methylcyclohexanetetracarboxylic dianhydride, trimellitic anhydride, pyromellitic dianhydride, benzophenonetetracarboxylic dianhydride and ethylene glycol bisanhydrotrimellitate. You can These can be used alone or as a mixture of two or more kinds.
  • the equivalent ratio of the acid anhydride type curing agent to the epoxy resin is preferably 0.3 to 1.5 from the viewpoint of good curability, adhesiveness and storage stability. , 0.4 to 1.0 are more preferable, and 0.5 to 1.0 are still more preferable. If the equivalent ratio is 0.3 or more, the curability and the adhesive strength tend to be improved, and if it is 1.5 or less, the unreacted acid anhydride does not remain excessively and the water absorption is It tends to be kept low and the insulation reliability tends to be improved.
  • amine-based curing agent for example, dicyandiamide can be used.
  • the equivalent ratio (amine / epoxy group, molar ratio) of the amine-based curing agent to the epoxy resin is preferably 0.3 to 1.5, and 0.4 to 1 from the viewpoint of good curability, adhesiveness and storage stability. 0.0 is more preferable, and 0.5 to 1.0 is still more preferable.
  • the equivalent ratio is 0.3 or more, the curability and the adhesive strength tend to be improved, and when it is 1.5 or less, unreacted amine does not remain excessively and the insulation reliability is improved. Tend to do.
  • imidazole type curing agent examples include 2-phenylimidazole, 2-phenyl-4-methylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-phenylimidazole, 1-cyanoethyl-2-undecylimidazole.
  • 1-cyanoethyl-2-undecylimidazole, 1-cyano-2-phenylimidazole, 1-cyanoethyl-2-undecylimidazole trimellitic acid from the viewpoint of excellent curability, storage stability and connection reliability.
  • Tate 1-cyanoethyl-2-phenylimidazolium trimellitate, 2,4-diamino-6- [2'-methylimidazolyl- (1 ')]-ethyl-s-triazine, 2,4-diamino-6- [2′-Ethyl-4′-methylimidazolyl- (1 ′)]-ethyl-s-triazine, 2,4-diamino-6- [2′-methylimidazolyl- (1 ′)]-ethyl-s-triazine Isocyanuric acid adduct, 2-phenylimidazole Isocyanuric acid adduct, 2-phenyl-4,5-dihydroxymethylimidazole and 2-phenyl -4-Methyl-5-hydroxymethylimidazole is preferred. These can be used alone or in combination of two or more. Further, these may be microencapsulated latent curing agents.
  • the content of the imidazole-based curing agent is preferably 0.1 to 20 parts by mass, more preferably 0.1 to 10 parts by mass, based on 100 parts by mass of the epoxy resin.
  • the content of the imidazole-based curing agent is 0.1 parts by mass or more, the curability tends to be improved, and when it is 20 parts by mass or less, the adhesive composition may be cured before the metal bond is formed. No connection failure tends to occur.
  • phosphine curing agent examples include triphenylphosphine, tetraphenylphosphonium tetraphenylborate, tetraphenylphosphonium tetra (4-methylphenyl) borate and tetraphenylphosphonium (4-fluorophenyl) borate.
  • the content of the phosphine-based curing agent is preferably 0.1 to 10 parts by mass, more preferably 0.1 to 5 parts by mass with respect to 100 parts by mass of the epoxy resin.
  • the content of the phosphine-based curing agent is 0.1 part by mass or more, the curability tends to be improved, and when it is 10 parts by mass or less, the adhesive composition may be cured before the metal bond is formed. No connection failure tends to occur.
  • Each of the phenolic resin-based curing agent, the acid anhydride-based curing agent and the amine-based curing agent may be used alone or in combination of two or more kinds.
  • the imidazole-based curing agent and the phosphine-based curing agent may be used alone, or may be used together with a phenol resin-based curing agent, an acid anhydride-based curing agent or an amine-based curing agent.
  • organic peroxides examples include ketone peroxides, peroxyketals, hydroperoxides, dialkyl peroxides, diacyl peroxides, peroxydicarbonates, and peroxyesters. From the viewpoint of storage stability, hydroperoxide, dialkyl peroxide and peroxy ester are preferable. Further, from the viewpoint of heat resistance, hydroperoxide and dialkyl peroxide are preferable. These may be used alone or in combination of two or more.
  • the content of the peroxide is preferably 0.5 to 10% by mass, more preferably 1 to 5% by mass based on the mass of the acrylic resin.
  • the content of peroxide is 0.5% by mass or more, the curing reaction easily proceeds sufficiently, while when it is 10% by mass or less, the molecular chain is shortened or unreacted groups remain. However, it is possible to sufficiently suppress the decrease in reliability.
  • the combination of the epoxy resin, the acrylic resin and the curing agent is not particularly limited as long as the curing proceeds, but from the viewpoint of handleability, storage stability and curability, phenol and imidazole are used as the curing agent together with the epoxy resin. It is preferable to use acid anhydride and imidazole, amine and imidazole, or imidazole alone. It is more preferable to use imidazole, which is excellent in quick-curing property, alone because the productivity is improved when connecting in a short time. Curing in a short time can suppress volatile components such as low-molecular components, so that the generation of voids is further suppressed. From the viewpoint of handleability and storage stability, it is preferable to use an organic peroxide as a curing agent used together with the acrylic resin.
  • (C) Polymer component having a weight average molecular weight of 10,000 or more As the polymer component having a weight average molecular weight of 10,000 or more (hereinafter referred to as "(c) component"), epoxy resin, phenoxy resin, polyimide resin, polyamide resin, polycarbodiimide resin , Cyanate ester resin, acrylic resin, polyester resin, polyethylene resin, polyether sulfone resin, polyetherimide resin, polyvinyl acetal resin, urethane resin, acrylic rubber, bismaleimide resin, and the like. Of these, epoxy resins, phenoxy resins, polyimide resins, acrylic resins, acrylic rubbers, and bismaleimide resins, which have excellent heat resistance and film forming properties, are more preferable. These may be used alone or in combination of two or more, and may be used as a copolymer of two or more.
  • the mass ratio of the component (c) and the epoxy resin is not particularly limited, but when the amount of the component (c) in the adhesive layer is 100 parts by mass, the mass of the epoxy resin may be 1 to 500 parts by mass. It is preferably 5 to 400 parts by mass, more preferably 10 to 300 parts by mass. When the amount of the epoxy resin is 1 part by mass or more, it is easy to secure sufficient adhesive force, and when it is 500 parts by mass or less, it is easy to secure sufficient film formability and film formability.
  • the epoxy resin mentioned here is a curing component having a glycidyl group and a molecular weight of less than 10,000.
  • the mass ratio of the component (c) and the acrylic resin is not particularly limited, but when the amount of the component (c) in the adhesive layer is 100 parts by mass, the mass of the acrylic resin is 1 to 1000 parts by mass.
  • the amount is preferably 5 to 500 parts by mass, more preferably 10 to 500 parts by mass.
  • the amount of the acrylic resin is 1 part by mass or more, it is easy to secure sufficient adhesive force, and when it is 1000 parts by mass or less, it is easy to secure sufficient film formability.
  • the glass transition temperature (Tg) of the component (c) is preferably 50 to 200 ° C. from the viewpoint of excellent adhesion of the adhesive layer to the substrate and semiconductor chip.
  • Tg of the component (c) is 50 ° C. or higher, the tack (viscosity) force of the adhesive layer can be sufficiently increased and the handleability is excellent.
  • the Tg of the component (c) is 200 ° C. or less, bumps formed on the semiconductor chip or irregularities such as electrodes or wiring patterns formed on the substrate are easily embedded in the adhesive layer, and voids are generated. Can be suppressed.
  • the Tg of the adhesive layer means a value measured using a DSC (DSC-7 type manufactured by Perkin Elmer Co., Ltd.) under the conditions of a sample amount of 10 mg, a heating rate of 10 ° C./minute, and a measurement atmosphere of air. ..
  • the weight average molecular weight of the component (c) is 10,000 or more in terms of polystyrene, but it is preferably 30,000 or more from the standpoint of achieving good film-forming property by itself.
  • the weight average molecular weight of the component (c) is 10,000 or more, it is easy to achieve sufficient film forming property.
  • the adhesive layer may further contain a flux agent.
  • the flux agent is a compound exhibiting flux activity (activity for removing oxides or impurities).
  • the fluxing agent include nitrogen-containing compounds having a non-covalent electron pair such as imidazoles and amines, carboxylic acids, phenols and alcohols.
  • the organic acid more strongly develops the flux activity than the alcohol or the like, and the connectivity is improved.
  • organic acids it is preferable to use carboxylic acid. Since the carboxylic acid reacts with the epoxy resin, there is an advantage that the amount remaining in the adhesive layer is sufficiently small.
  • the carboxylic acid as the flux agent is preferably solid.
  • the melting point of the flux agent is preferably 70 to 150 ° C.
  • the adhesive layer may further contain a filler having an insulating property.
  • a filler having an insulating property include inorganic fillers, whiskers and resin fillers. From the viewpoint of insulation reliability, it is preferable that the adhesive layer does not contain a conductive metal filler (for example, silver particles and solder particles).
  • inorganic fillers examples include glass, silica, alumina, titanium oxide, carbon black, mica and boron nitride. Of these, silica, alumina, titanium oxide and boron nitride are preferable, and silica, alumina and boron nitride are more preferable.
  • whiskers include aluminum borate, aluminum titanate, zinc oxide, calcium silicate, magnesium sulfate, and boron nitride.
  • the resin filler examples include polyurethane, polyimide, methyl methacrylate resin, and methyl methacrylate-butadiene-styrene copolymer resin (MBS). These fillers may be used alone or in combination of two or more.
  • the resin filler can give flexibility to the adhesive layer under a high temperature environment (for example, 260 ° C.) as compared with the inorganic filler, it can contribute to the improvement of reflow resistance. By improving the flexibility, the film forming property can also be improved.
  • a surface-treated filler may be used. By subjecting the filler to a surface treatment, the physical properties of the filler can be adjusted appropriately.
  • the surface treatment include glycidyl (epoxy), amine, phenyl, phenylamino, acryl (methacryl) or vinyl treatment. From the viewpoint of dispersibility, fluidity and adhesive strength, glycidyl type, phenylamino type and acryl (methacryl) type are preferable. From the viewpoint of storage stability, phenyl type and acrylic (methacrylic) type are more preferable. From the viewpoint of ease of surface treatment, silane treatment such as epoxysilane-based, aminosilane-based, and acrylsilane-based is preferable.
  • the average particle size of the filler is preferably 1.5 ⁇ m or less from the viewpoint of preventing biting during flip chip connection, and more preferably 1.0 ⁇ m or less from the viewpoint of visibility (transparency).
  • the "average particle size” as used herein means a value obtained by analyzing with a laser diffraction particle size distribution analyzer using MEK (methyl ethyl ketone) as a solvent.
  • the content of the filler is preferably 30 to 90% by mass, and more preferably 40 to 80% by mass, based on the mass of the solid content of the adhesive layer.
  • the content of the filler is 30% by mass or more, sufficient heat dissipation can be easily achieved, and voids can be formed and the moisture absorption rate can be reduced.
  • the content of the filler is 90% by mass or less, it is possible to suppress the viscosity from becoming excessively high, to ensure sufficiently high fluidity, and to sufficiently trap (fill) the filler into the connection portion. Can be suppressed to.
  • the adhesive layer may further contain additives such as an ion trapper, an antioxidant, a silane coupling agent, a titanium coupling agent and a leveling agent. These may be used alone or in combination of two or more. The content of these additives may be appropriately adjusted so that the effect of each additive is exhibited.
  • additives such as an ion trapper, an antioxidant, a silane coupling agent, a titanium coupling agent and a leveling agent.
  • the film adhesive can be produced as follows. That is, the above components are added to an organic solvent, and the mixed solution is stirred or kneaded to prepare a varnish. After the varnish is applied on the base material film that has been subjected to the mold release treatment, the organic solvent is reduced by heating to form the film adhesive on the base material film.
  • the varnish can be applied using, for example, a knife coater, a roll coater, an applicator, a die coater or a comma coater.
  • the substrate film is not particularly limited as long as it has heat resistance that can withstand the heating conditions when volatilizing the organic solvent, polyester film, polypropylene film, polyethylene terephthalate film, polyimide film, polyetherimide film, poly Examples include an ether naphthalate film and a methylpentene film.
  • the base film is not limited to a single layer made of these films, but may be a multilayer film made of two or more kinds of materials.
  • the conditions for volatilizing the organic solvent from the varnish are preferably heating at 50 to 200 ° C. for 0.1 to 90 minutes.
  • the content of the organic solvent is preferably reduced to 1.5% by mass or less if there is no influence on generation of voids after mounting or adjustment of viscosity.
  • a varnish film is formed on the surface of the semiconductor wafer by spin coating, and then a solvent is added by heating. You can reduce it.
  • Example 1 (Preparation of varnish for forming adhesive layer) A varnish was prepared by mixing the following compounds in the proportions shown in Table 1 and degassing in vacuum. MEK was used as the solvent.
  • Thermosetting resin epoxy resin having a weight average molecular weight of less than 10,000 -Trifunctional methane skeleton-containing polyfunctional solid epoxy (Mitsubishi Chemical Corporation, EP1032H60 (hereinafter referred to as "EP1032”), weight average molecular weight: 800 to 2000)
  • -Bisphenol F type liquid epoxy manufactured by Mitsubishi Chemical Corporation, YL983U (hereinafter referred to as "YL983", molecular weight: about 336)
  • YL7175 (manufactured by Mitsubishi Chemical Corporation, YL7175-1000 (hereinafter referred to as "YL7175”), weight average molecular weight: 1000 to 5000)
  • Curing agent 2,4-diamino-6- [2'-
  • a semiconductor chip with a solder bump (WALTS-TEG CC80 (product name), manufactured by Waltz Co., Ltd.) was prepared as a first member.
  • the structure of this semiconductor chip was as follows. -Chip size: 7.3 mm x 7.3 mm x 0.05 mmt ⁇ Bump height: approx. 45 ⁇ m (total height of copper pillar and solder) ⁇ Number of bumps: 1048 pins ⁇ Bump pitch: 80 ⁇ m
  • An adhesive piece was obtained by cutting the produced film-like adhesive into the same size as the semiconductor chip (7.3 mm ⁇ 7.3 mm). This adhesive piece was laminated on the surface of the semiconductor chip (the surface on which the solder was formed). The lamination was performed using a vacuum laminator V130 (Nikko Materials Co., Ltd.) under the conditions of 80 ° C./0.5 MPa / 60 s.
  • a semiconductor chip (WALTS-TEG IP80, manufactured by Waltz Co., Ltd.) was prepared as a second member.
  • the structure of this semiconductor chip was as follows. ⁇ Chip size: 10mm ⁇ 10mm ⁇ 0.1mmt -Metal forming the connecting portion: Ni / Au
  • the semiconductor chip with solder bumps was placed on the surface of the semiconductor chip (second member) on the side where the connection portion was formed such that the adhesive piece was in contact with this surface. Then, after performing a temporary pressure bonding step using a pressure bonding device (FCB3, manufactured by Panasonic Corporation), a pressure bonding step was performed using a laser bonder (FDB250, manufactured by Shibuya Industry Co., Ltd.). The temporary pressure bonding step was carried out under the condition of 80 ° C./25 N / 1 s. The crimping process was performed under the following conditions. ⁇ Crimping pressure: 30N -Pressing time: 1 second-Laser irradiation pattern: Fig.
  • a pressure oven device (VSU28, manufactured by Shin Apex Co., Ltd.) was used to perform the curing process under the conditions of 175 ° C./10 min / 0.4 MPa and a heating rate of 20 ° C./min.
  • VSU28 manufactured by Shin Apex Co., Ltd.
  • a semiconductor device according to this example was obtained through this curing process.
  • Example 2 A semiconductor device was manufactured in the same manner as in Example 1 except that the pressure bonding step was performed under the following conditions.
  • Example 1 A semiconductor device was manufactured in the same manner as in Example 1 except that the pressure bonding step was performed under the following conditions. ⁇ Crimping pressure: 30N ⁇ Crimping time: 1 second ⁇ Laser irradiation pattern: Fig.
  • ⁇ Comparative example 2> A semiconductor device was manufactured in the same manner as in Example 2 except that the pressure bonding step was performed under the following conditions. ⁇ Crimping pressure: 30N -Pressing time: 3 seconds-Laser irradiation pattern: Fig. 6 (b) (irradiated with a laser having a weaker intensity than in Comparative Example 1).
  • Example 3 A semiconductor device was manufactured in the same manner as in Example 1 except that the pressure bonding step was performed under the following conditions. After the pressure-bonding step, a curing oven was used under the same conditions as in Example 1 using a pressure oven device (PCOA-01, manufactured by NTT Advance Technology Co., Ltd.). ⁇ Crimping pressure: 30N ⁇ Crimping time: 1 second ⁇ Laser irradiation pattern: Fig. 7 (Areas 1, 3, 5, 7 are irradiated with a laser output of 100% and areas 2, 4, 6, 8 are irradiated with a laser of 10%.
  • Example 4 A semiconductor device was manufactured in the same manner as in Example 3 except that the pressure bonding step was performed under the following conditions. ⁇ Crimping pressure: 30N -Pressing time: 3 seconds-Laser irradiation pattern: Fig.
  • the void occurrence rates of the semiconductor devices according to the examples and comparative examples were evaluated by the following method.
  • an ultrasonic image diagnostic apparatus (Insight-300, manufactured by Insight Co., Ltd.) was used to take external images of the semiconductor devices according to the examples and comparative examples.
  • An image of the adhesive layer on the semiconductor chip was captured with a scanner (GT-9300UF, manufactured by EPSON Corporation). This image was subjected to color tone correction and two-gradation conversion by image processing software (Adobe Photoshop (registered trademark), Adobe Systems Incorporated) to identify the void portion, and the ratio of the void portion to the histogram was calculated.
  • the evaluation criteria are as follows. The results are shown in Tables 2 and 3.
  • a semiconductor device in which the fillet on the side of the semiconductor chip is small and coverage is secured, and a manufacturing method thereof.

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Abstract

A production method according to the present disclosure is for the production of a semiconductor device that comprises: a first member which has a first connection part and a side that extends linearly; a second member which has a second connection part; and an adhesive layer which is arranged between the first and second members. The production method according to the present disclosure comprises: a stacking step for preparing a multilayer body in which the first member, the adhesive layer and the second member are sequentially stacked in this order; and a compression bonding step wherein the multilayer body is irradiated with laser for the purpose of heating, while being applied with a pressing force in the thickness direction. In the compression bonding step, the multilayer body is irradiated with laser so that a laser irradiated part, a laser non-irradiated part and a laser irradiated part are sequentially formed in this order from the periphery of one end of the side of the first member toward the periphery of the other end.

Description

半導体装置及びその製造方法Semiconductor device and manufacturing method thereof

 本開示は半導体装置及びその製造方法に関する。 The present disclosure relates to a semiconductor device and a manufacturing method thereof.

 従来、半導体チップと基板の接続にはワイヤーボンディングが広く適用されてきた。ワイヤーボンディングは、金ワイヤ等の金属細線を用いて半導体チップと基板を接続する方式である。半導体装置に対する高機能化、高集積化及び高速化等の要求に対応するため、フリップチップ接続(FC接続)と称される方式が広まりつつある。FC接続は、半導体チップ又は基板にバンプと呼ばれる導電性突起を形成して、半導体チップと基板間で直接接続する方式である。 Conventionally, wire bonding has been widely applied to connect semiconductor chips and substrates. Wire bonding is a method of connecting a semiconductor chip and a substrate by using a metal thin wire such as a gold wire. A method called flip-chip connection (FC connection) is becoming widespread in order to meet the demand for higher functionality, higher integration, higher speed, etc. of semiconductor devices. The FC connection is a method in which conductive protrusions called bumps are formed on a semiconductor chip or a substrate to directly connect the semiconductor chip and the substrate.

 FC接続の態様として、はんだ、スズ、金、銀及び銅等を用いて金属接合させる方法、超音波振動を印加して金属接合させる方法、樹脂の収縮力によって機械的接触を保持する方法などが知られている。これらの方法のうち、接続部の信頼性の観点から、はんだ、スズ、金、銀及び銅等を用いて金属接合させる方法が一般的である。 Examples of modes of FC connection include a method of metal bonding using solder, tin, gold, silver, copper, etc., a method of metal bonding by applying ultrasonic vibration, a method of maintaining mechanical contact by the contracting force of resin, and the like. Are known. Among these methods, from the viewpoint of the reliability of the connection portion, a method of metal bonding using solder, tin, gold, silver, copper or the like is common.

 半導体チップと基板とを接続する方式として、COB(Chip On Board)型の接続方式が知られている。COBはFC接続の一種である。また、半導体チップと半導体チップとを接続するCoC(Chip On Chip)、及び、半導体チップとバンプもしくは配線を有する半導体ウエハとを接続するCoW(Chip On Wefer)もFC接続に分類される。特許文献1は、半導体ウエハの接合方法を開示する。 A COB (Chip On Board) type connection method is known as a method for connecting a semiconductor chip and a substrate. COB is a type of FC connection. Further, CoC (Chip On Chip) that connects semiconductor chips to each other and CoW (Chip On Wefer) that connects a semiconductor chip to a semiconductor wafer having bumps or wiring are also classified as FC connections. Patent Document 1 discloses a method for bonding semiconductor wafers.

特開2008-294382号公報JP, 2008-294382, A

 上述のとおり、半導体装置(以下、場合により、「パッケージ」という。)は高機能化が強く要求され、具体的には、薄型化、小型化、ピン(バンプ及び/又は配線)数の増加、ピッチ又はギャップの狭小化が求められている。更なる小型化、薄型化及び高機能化が要求されるパッケージを作製する技術として、上述の接続方式を多段化したチップスタック型パッケージ、POP(Package On Package)、TSV(Through Silicon Via)等の技術も普及し始めている。これらの技術は、平面状でなく立体状に部材を配置するためにパッケージを小さくでき、また、半導体装置の性能向上及びノイズ低減、実装面積の削減、省電力化にも有効であり、次世代の配線技術として注目されている。 As described above, semiconductor devices (hereinafter, sometimes referred to as “packages”) are highly required to have high functionality, and specifically, thinning, downsizing, increase in the number of pins (bumps and / or wirings), There is a demand for narrowing the pitch or gap. As technologies for manufacturing packages that require further miniaturization, thinning, and high functionality, chip stack type packages that have multiple connection methods described above, such as POP (Package On Package), TSV (Through Silicon Via), etc. Technology is also becoming widespread. These technologies can reduce the size of the package because the members are arranged in a three-dimensional shape instead of a planar shape, and are also effective in improving the performance of semiconductor devices, reducing noise, reducing the mounting area, and saving power. Is attracting attention as a wiring technology.

 低コスト化及び高生産性化の観点から、パッケージ組立ての際の半導体チップ間隔が狭くなる傾向にある。隣接する半導体チップの間隔を狭くすることで基板上又はウエハ上に多くの半導体チップを搭載することができ、低コスト化が可能となる。また、隣接する半導体チップの間隔を狭くすることで、異種の半導体チップを小範囲に組立てることができ、高密度化実装も可能となる。 From the viewpoint of cost reduction and high productivity, the semiconductor chip spacing tends to become narrower during package assembly. By narrowing the interval between the adjacent semiconductor chips, many semiconductor chips can be mounted on the substrate or the wafer, and the cost can be reduced. Further, by narrowing the interval between the adjacent semiconductor chips, it is possible to assemble different kinds of semiconductor chips in a small area, and it is possible to perform high-density mounting.

 ところで、接着剤層を介して半導体チップを基板又は半導体ウエハに圧着して接続を確保する場合、接着剤層の形状は半導体チップと同じ正方形又は長方形であることが多い。圧着工程後、接着剤層を構成する樹脂材料が半導体チップからはみ出している部分はフィレットと称される。圧着時において、樹脂材料は円状に流動するため、半導体チップの辺部分のフィレットに比べて、半導体チップの隅部のフィレットは小さくなる。半導体チップの隅部(半導体チップの辺の端部)におけるフィレットはカバレッジと称される。 By the way, when a semiconductor chip is pressure-bonded to a substrate or a semiconductor wafer via an adhesive layer to secure the connection, the shape of the adhesive layer is often the same square or rectangle as the semiconductor chip. A portion where the resin material forming the adhesive layer protrudes from the semiconductor chip after the pressure bonding step is called a fillet. Since the resin material flows in a circular shape at the time of pressure bonding, the fillet at the corner of the semiconductor chip becomes smaller than the fillet at the side of the semiconductor chip. The fillet at the corner of the semiconductor chip (end of the side of the semiconductor chip) is called coverage.

 半導体チップの隅部にフィレット(接着剤)が存在しない場合、半導体装置の信頼性が低下する傾向にある。カバレッジを確保するために、接着剤の流動性を高くしたり、圧着時の条件を高荷重化又は高温化したりことが考えられる。しかし、これらの手段によってカバレッジを確保できても、その反面、半導体チップの辺におけるフィレットが大きくなり、低コスト化及び高密度実装が困難となる。つまり、半導体チップの辺におけるフィレットを小さくすることと、カバレッジを確保することの両立は困難である。 If there is no fillet (adhesive) in the corner of the semiconductor chip, the reliability of the semiconductor device tends to decrease. In order to secure the coverage, it is conceivable to increase the fluidity of the adhesive or increase the load at the time of pressure bonding or increase the temperature. However, even if the coverage can be secured by these means, on the other hand, the fillet on the side of the semiconductor chip becomes large, which makes it difficult to reduce the cost and mount the device at high density. That is, it is difficult to make both the fillet on the side of the semiconductor chip small and the coverage secured.

 本開示は、半導体チップの辺におけるフィレットが小さく且つカバレッジが確保された半導体装置及びその製造方法を提供することを目的とする。 The present disclosure aims to provide a semiconductor device having a small fillet on the side of a semiconductor chip and ensuring coverage, and a manufacturing method thereof.

 本開示に係る製造方法は、第一の接続部を有し且つ直線状に延びる辺を有する第一の部材と、第二の接続部を有する第二の部材と、第一の部材と第二の部材との間に配置された接着剤層とを備え、第一の接続部と第二の接続部が電気的に接続されている半導体装置を製造するためのものである。 The manufacturing method according to the present disclosure includes a first member having a first connecting portion and a linearly extending side, a second member having a second connecting portion, a first member and a second member. And an adhesive layer disposed between the first connection portion and the second connection portion, the semiconductor device having the adhesive layer disposed between the first connection portion and the second connection portion.

 本開示の第一の形態に係る製造方法は、第一の部材、接着剤層及び第二の部材がこの順序で積層された積層体を準備する積層工程と、積層体に対して厚さ方向に押圧力を加えた状態で、積層体に対して加熱のためのレーザーを照射する圧着工程とを含み、圧着工程において、第一の部材の辺の一端の周縁部から他端の周縁部に向けて、レーザー照射部、レーザー非照射部及びレーザー照射部がこの順序で形成されるように、積層体に対してレーザーを照射する。 A manufacturing method according to a first embodiment of the present disclosure includes a laminating step of preparing a laminated body in which a first member, an adhesive layer, and a second member are laminated in this order, and a thickness direction with respect to the laminated body. And a pressing step of irradiating a laser beam for heating the laminated body in a state where a pressing force is applied to the laminated body, in the pressing step, from the peripheral portion of one side of the first member to the peripheral portion of the other end. A laser is irradiated to the laminated body so that the laser irradiation portion, the laser non-irradiation portion, and the laser irradiation portion are formed in this order.

 第一の形態に係る製造方法によれば、直線状に延びる辺を有する第一の部材(例えば、正方形又は長方形の半導体チップ)の隅部をレーザー照射部とし、その間をレーザー非照射部とすることで、レーザーによって隅部を局所的に加熱することができ、第一の部材の隅部におけるカバレッジを確保でき且つ第一の部材の辺におけるフィレットを抑制できる。 According to the manufacturing method of the first aspect, the corners of the first member (for example, a square or rectangular semiconductor chip) having the linearly extending sides are the laser irradiation parts, and the spaces between them are the laser non-irradiation parts. Thus, the corner can be locally heated by the laser, the coverage at the corner of the first member can be secured, and the fillet on the side of the first member can be suppressed.

 本開示の第二の形態に係る製造方法は、第一の部材、接着剤層及び第二の部材がこの順序で積層された積層体を準備する積層工程と、積層体に対して厚さ方向に押圧力を加えた状態で、積層体に対して熱を加える圧着工程とを含み、第一の部材が正方形又は長方形の形状を有する半導体チップであり、圧着工程において、以下の条件1を満たすように、積層体に対して熱を加える。
<条件1>
 半導体チップの辺を三等分して計九つのエリアに分割し、当該九つのエリアのうち、半導体チップの一つの隅部を含むエリアをエリア1とし、エリア1から半導体チップの周縁部に沿って並ぶエリアをエリア2~8としたとき、エリア1,3,5,7の各中心部における半導体チップの外表面の平均温度Tcと、エリア2,4,6,8の各中心部における半導体チップの外表面の平均温度Tsとの差(Tc-Ts)が15℃以上である。
A manufacturing method according to a second embodiment of the present disclosure includes a laminating step of preparing a laminated body in which a first member, an adhesive layer and a second member are laminated in this order, and a thickness direction with respect to the laminated body. A semiconductor chip having a square or rectangular shape in which the first member has a square shape or a rectangular shape, and the following condition 1 is satisfied in the pressure bonding step. So that heat is applied to the laminate.
<Condition 1>
The side of the semiconductor chip is divided into three equal parts and divided into nine areas, and the area including one corner of the semiconductor chip is defined as area 1 among the nine areas, and the area 1 extends along the peripheral edge of the semiconductor chip. When the areas arranged side by side are areas 2 to 8, the average temperature Tc of the outer surface of the semiconductor chip in the central portions of the areas 1, 3, 5, and 7, and the semiconductor in the central portions of the areas 2, 4, 6, and 8 The difference (Tc−Ts) from the average temperature Ts of the outer surface of the chip is 15 ° C. or more.

 第二の形態に係る製造方法によれば、半導体チップの隅部(エリア1,3,5,7)の温度を局所的に高くすることで、第一の部材の隅部におけるカバレッジを確保でき且つ第一の部材の辺におけるフィレットが抑制される。なお、第二の形態に係る製造方法において、レーザー照射によって積層体を加熱する場合、エリア2,4,6,8はレーザー非照射部であってもそうでなくてもよい。例えば、エリア2,4,6,8に対し、エリア1,3,5,7よりも少ないエネルギー量のレーザー照射を照射してもよい。 According to the manufacturing method according to the second embodiment, by locally increasing the temperature of the corners (areas 1, 3, 5, 7) of the semiconductor chip, it is possible to secure the coverage in the corners of the first member. In addition, fillets on the sides of the first member are suppressed. In the manufacturing method according to the second embodiment, when the laminate is heated by laser irradiation, the areas 2, 4, 6, 8 may or may not be the laser non-irradiated portion. For example, the areas 2, 4, 6, and 8 may be irradiated with laser irradiation having an energy amount smaller than that of the areas 1, 3, 5, and 7.

 より一層高度にカバレッジを確保し且つフィレットを抑制する観点から、第二の形態に係る製造方法の圧着工程において、以下の条件2を更に満たすように、積層体に対して熱を加えることが好ましい。
<条件2>
 上記九つのエリアのうち、半導体チップの中心を含むエリアをエリア9とすると、エリア2,4,6,8の各中心部における半導体チップの外表面の平均温度Tsと、エリア9の中心部における半導体チップの外表面の温度T9との差(Ts-T9)が5℃以上である。
From the viewpoint of securing coverage to a higher degree and suppressing fillets, it is preferable to apply heat to the laminate so as to further satisfy the following Condition 2 in the pressure bonding step of the manufacturing method according to the second embodiment. ..
<Condition 2>
If the area including the center of the semiconductor chip among the nine areas is referred to as area 9, the average temperature Ts of the outer surface of the semiconductor chip at the central portions of areas 2, 4, 6, and 8 and the central portion of area 9 The difference (Ts-T9) from the temperature T9 of the outer surface of the semiconductor chip is 5 ° C. or more.

 本開示において、第二の部材の具体例として、配線基板、半導体チップ及び半導体ウエハが挙げられる。 In the present disclosure, specific examples of the second member include a wiring board, a semiconductor chip, and a semiconductor wafer.

 接着剤層は、ボイド発生を抑制する観点から、例えば、重量平均分子量10000未満の熱硬化性樹脂と、硬化剤とを含有し、重量平均分子量10000以上の高分子成分を更に含有してもよい。接着剤層は、圧着工程の効率化の観点から、フィルム状接着剤であることが好ましい。 From the viewpoint of suppressing the generation of voids, the adhesive layer contains, for example, a thermosetting resin having a weight average molecular weight of less than 10,000 and a curing agent, and may further contain a polymer component having a weight average molecular weight of 10,000 or more. .. The adhesive layer is preferably a film adhesive from the viewpoint of improving the efficiency of the pressure bonding step.

 本開示は、上記製造方法によって製造された半導体装置を提供する。本開示に係る半導体装置は、半導体チップの辺におけるフィレットが短く且つカバレッジが確保されている。これらの特性により、高密度実装が可能であり且つ優れた信頼性を有する。 The present disclosure provides a semiconductor device manufactured by the above manufacturing method. In the semiconductor device according to the present disclosure, the fillet on the side of the semiconductor chip is short and the coverage is secured. Due to these characteristics, high-density mounting is possible and excellent reliability is achieved.

 本開示によれば、半導体チップの辺におけるフィレットが小さく且つカバレッジが確保された半導体装置及びその製造方法が提供される。 According to the present disclosure, there is provided a semiconductor device in which the fillet on the side of the semiconductor chip is small and coverage is secured, and a manufacturing method thereof.

図1は本開示に係る半導体装置の一実施形態を模式的に示す断面図である。FIG. 1 is a sectional view schematically showing an embodiment of a semiconductor device according to the present disclosure. 図2(a)は圧着工程を実施する準備が整った状態を模式的に示す断面図あり、図2(b)は半導体チップ、接着剤層及び基板がこの順序で積層された積層体を模式的に示す断面図であり、図2(c)は積層体に圧着工程を実施している様子を模式的に示す断面図である。FIG. 2A is a cross-sectional view schematically showing a state in which preparation for carrying out the pressure bonding step is completed, and FIG. 2B schematically shows a laminated body in which a semiconductor chip, an adhesive layer and a substrate are laminated in this order. FIG. 2C is a cross-sectional view schematically showing a state in which the pressure-bonding step is performed on the laminated body. 図3は圧着工程において積層体に対してレーザーを照射する領域の一例を模式的に示す上面図である。FIG. 3 is a top view schematically showing an example of a region for irradiating the laminated body with laser in the pressure bonding step. 図4は圧着工程後において半導体チップから接着剤層がはみ出した状態の一例を模式的に示す上面図である。FIG. 4 is a top view schematically showing an example of a state in which the adhesive layer protrudes from the semiconductor chip after the pressure bonding step. 図5はTSV技術によって製造された半導体装置の一例を模式的に示す断面図である。FIG. 5 is a sectional view schematically showing an example of a semiconductor device manufactured by the TSV technique. 図6(a)は実施例1及び比較例1におけるレーザーの照射パターンを模式的に示す上面図であり、図6(b)は実施例2及び比較例2におけるレーザーの照射パターンを模式的に示す上面図である。FIG. 6A is a top view schematically showing laser irradiation patterns in Example 1 and Comparative Example 1, and FIG. 6B schematically shows laser irradiation patterns in Example 2 and Comparative Example 2. It is a top view shown. 図7は実施例3,4におけるレーザーの照射パターンを模式的に示す上面図である。FIG. 7 is a top view schematically showing laser irradiation patterns in Examples 3 and 4.

 以下、図面を適宜参照しながら、本開示の実施形態について説明する。なお、本発明は以下の実施形態に限定されるものではない。 Hereinafter, embodiments of the present disclosure will be described with reference to the drawings as appropriate. The present invention is not limited to the embodiments below.

<半導体装置及びその製造方法>
 図1に示す半導体装置50は、銅ピラー10a及びはんだバンプ10b(第一の接続部)を有する半導体チップ10(第一の部材)と、配線20a(第二の接続部)を有する基板20(第二の部材)と、半導体チップ10と基板20との間に配置された接着剤層30とを備え、はんだバンプ10bと配線20aが電気的に接続されている。はんだバンプ10bは、例えば、スズ-銀合金を含む。配線20aは、例えば、表面に金メッキが施されている。はんだの融点よりも高い温度に加熱することで、はんだバンプ10bと配線20aとを接続することができる。
<Semiconductor Device and Manufacturing Method Thereof>
A semiconductor device 50 shown in FIG. 1 includes a semiconductor chip 10 (first member) having a copper pillar 10a and a solder bump 10b (first connecting portion), and a substrate 20 (having a wiring 20a (second connecting portion)). The second member) and the adhesive layer 30 arranged between the semiconductor chip 10 and the substrate 20, and the solder bumps 10b and the wirings 20a are electrically connected. The solder bump 10b contains, for example, a tin-silver alloy. The surface of the wiring 20a is plated with gold, for example. By heating to a temperature higher than the melting point of the solder, the solder bump 10b and the wiring 20a can be connected.

 図2(a)~図2(c)を参照しながら、半導体装置50の製造方法について説明する。半導体装置50は、例えば、以下の工程を経て製造される。
・半導体チップ10の銅ピラー10a及びはんだバンプ10bが形成されている側の面に接着剤層30が形成されたチップを準備する接着剤付きチップ作製工程(図2(a)参照)。
・半導体チップ10、接着剤層30及び基板20がこの順序で積層された積層体40を準備する積層工程(図2(b)参照)。
・積層体40に対して厚さ方向に押圧力Fを加えた状態で、積層体40に対して加熱のためのレーザーLを照射する圧着工程(図2(c)参照)。
・圧着工程後の積層体40を加熱するキュア工程。
A method of manufacturing the semiconductor device 50 will be described with reference to FIGS. 2A to 2C. The semiconductor device 50 is manufactured, for example, through the following steps.
An adhesive-attached chip manufacturing step of preparing a chip having an adhesive layer 30 formed on the surface of the semiconductor chip 10 on which the copper pillars 10a and the solder bumps 10b are formed (see FIG. 2A).
A laminating step of preparing a laminated body 40 in which the semiconductor chip 10, the adhesive layer 30, and the substrate 20 are laminated in this order (see FIG. 2B).
A pressure bonding step of irradiating the laminated body 40 with a laser L for heating while applying a pressing force F to the laminated body 40 in the thickness direction (see FIG. 2C).
A curing process of heating the laminated body 40 after the pressure bonding process.

(接着剤付きチップ作製工程)
 接着剤付きチップ作製工程は、半導体チップ10と、半導体チップ10の銅ピラー10a等を覆うように形成された接着剤層30とを有するチップ(接着剤付きチップ)を作製する工程である。作業性の観点から、フィルム状接着剤を事前に準備し、これを対象物にラミネートする工程を経て接着剤付きチップを作製することが好ましい。ラミネートは加熱プレス、ロールラミネート及び真空ラミネート等によって行うことができる。接着剤層30のサイズ及び厚さは、半導体チップ10のサイズ及びバンプ高さ等に応じて適宜設定すればよい。なお、半導体チップ10のサイズに切断されたフィルム状接着剤を半導体チップに貼り付けることによって接着剤付きチップを作製してもよいし、あるいは、配線等が形成された半導体ウエハにフィルム状接着剤を貼り付けた後、ダイシングによって個片化することで、接着剤付きチップを作製してもよい。なお、ダイシングによって接着剤付きチップを作製する場合、半導体チップ10と接着剤層30は同じ形状及びサイズとなる。
(Chip making process with adhesive)
The step of producing a chip with an adhesive is a step of producing a chip (chip with an adhesive) having the semiconductor chip 10 and the adhesive layer 30 formed so as to cover the copper pillars 10a and the like of the semiconductor chip 10. From the standpoint of workability, it is preferable to prepare a film-like adhesive in advance and to produce the chip with the adhesive through a step of laminating the film-like adhesive on an object. Lamination can be performed by hot pressing, roll laminating, vacuum laminating and the like. The size and thickness of the adhesive layer 30 may be appropriately set according to the size of the semiconductor chip 10, the bump height, and the like. Note that a chip with an adhesive may be produced by pasting a film adhesive cut to the size of the semiconductor chip 10 onto the semiconductor chip, or a film adhesive may be applied to a semiconductor wafer on which wirings and the like are formed. After adhering, the chips with adhesive may be produced by dicing into individual pieces. When a chip with an adhesive is produced by dicing, the semiconductor chip 10 and the adhesive layer 30 have the same shape and size.

(積層工程)
 積層工程は、半導体チップ10、接着剤層30及び基板20がこの順序で積層された積層体40を準備する工程である。接着剤付きチップと基板20との位置合わせを行った後、接着剤付きチップと基板20とを仮圧着することによって積層体40を作製する。仮圧着には通常の圧着装置を使用することができる。
(Lamination process)
The laminating step is a step of preparing a laminated body 40 in which the semiconductor chip 10, the adhesive layer 30, and the substrate 20 are laminated in this order. After the chip with the adhesive and the substrate 20 are aligned with each other, the chip with the adhesive and the substrate 20 are temporarily pressure-bonded to each other to produce the laminated body 40. A normal crimping device can be used for the temporary crimping.

(圧着工程)
 図3は圧着工程において積層体に対してレーザーを照射する領域を模式的に示す上面図である。本実施形態においては、計36の領域に加熱用のレーザーをそれぞれ独立して照射可能なレーザーボンダを使用する。このような性能を有するレーザーボンダとして、例えば、澁谷工業株式会社製のFDB250が挙げられる。図3において、計36の領域のうち、レーザーが照射された領域をハッチングを付した丸で表し、レーザーが照射されない領域を白い丸で表している。
(Crimping process)
FIG. 3 is a top view schematically showing a region where a laser is applied to the laminated body in the pressure bonding step. In the present embodiment, a laser bonder that can independently irradiate heating lasers on a total of 36 regions is used. An example of a laser bonder having such performance is FDB250 manufactured by Shibuya Industry Co., Ltd. In FIG. 3, out of a total of 36 areas, the area irradiated with the laser is represented by a hatched circle, and the area not irradiated with the laser is represented by a white circle.

 図3に示すように、圧着工程において、半導体チップ10の辺Sの一端Saの周縁部(一方の隅部C)から他端Sbの周縁部(他方の隅部C)に向けて、レーザー照射部A1、レーザー非照射部A2及びレーザー照射部A1がこの順序で形成されるように、積層体40に対してレーザーを照射する。半導体チップ10の残りの三つの辺Sについても、一端から他端に向けてレーザー照射部A1、レーザー非照射部A2及びレーザー照射部A1がこの順序で形成されるように、レーザーを照射する。図3に示すように、半導体チップ10の辺を三等分して計九つのエリアに分割し、当該九つのエリアのうち、半導体チップ10の一つの隅部を含むエリアをエリア1とし、エリア1から半導体チップ10の周縁部に沿って並ぶエリアをエリア2~8とする。本実施形態においては、エリア1,3,5,7に選択的にレーザーLを照射し、エリア2,4,6,8及び半導体チップ10の中心を含むエリア9にはレーザーを照射しない。つまり、エリア1,3,5,7がレーザー照射部A1であり、エリア2,4,6,8,9がレーザー非照射部A2である。なお、積層体40に向けてレーザーLを照射することによって、接着剤層30を加熱できる限り、半導体チップ10の外表面に直接的にレーザーを照射してもよいし、半導体チップ10に対して押圧力Fを加えるためのプレート(不図示)にレーザーを照射してもよい。 As shown in FIG. 3, in the pressure-bonding step, laser irradiation is performed from the peripheral portion (one corner C) of one end Sa of the side S of the semiconductor chip 10 to the peripheral portion (the other corner C) of the other end Sb. The layer 40 is irradiated with a laser so that the portion A1, the laser non-irradiation portion A2, and the laser irradiation portion A1 are formed in this order. The remaining three sides S of the semiconductor chip 10 are also irradiated with laser so that the laser irradiation part A1, the laser non-irradiation part A2, and the laser irradiation part A1 are formed in this order from one end to the other end. As shown in FIG. 3, the side of the semiconductor chip 10 is divided into three equal parts and divided into nine areas, and an area including one corner of the semiconductor chip 10 is defined as an area 1 among the nine areas. Areas arranged from 1 to along the peripheral edge of the semiconductor chip 10 are referred to as areas 2 to 8. In this embodiment, the areas 1, 3, 5, 7 are selectively irradiated with the laser L, and the areas 2, 4, 6, 8 and the area 9 including the center of the semiconductor chip 10 are not irradiated with the laser. That is, areas 1, 3, 5, and 7 are laser irradiation portions A1, and areas 2, 4, 6, 8, and 9 are laser non-irradiation portions A2. As long as the adhesive layer 30 can be heated by irradiating the laser L toward the stacked body 40, the outer surface of the semiconductor chip 10 may be directly irradiated with the laser, or the semiconductor chip 10 may be irradiated with the laser L. A plate (not shown) for applying the pressing force F may be irradiated with a laser.

 本実施形態において、エリア1,3,5,7の各中心部における半導体チップ10の外表面の平均温度Tcと、エリア2,4,6,8の各中心部における半導体チップ10の外表面の平均温度Tsとの差(Tc-Ts)が15℃以上であることが好ましい。Tc-Tsが15℃以上であることは、半導体チップ10の隅部を含むエリアが他のエリアよりも局所的に高温となるように加熱したことを意味する。圧着工程において、このような加熱をすることで、半導体チップ10の辺Sにおけるフィレットを短くすることができ且つカバレッジを確保することができる。Tc-Tsは15~30℃であってもよい。 In the present embodiment, the average temperature Tc of the outer surface of the semiconductor chip 10 in each central portion of the areas 1, 3, 5, and 7 and the average temperature Tc of the outer surface of the semiconductor chip 10 in each central portion of the areas 2, 4, 6, 8. The difference (Tc−Ts) from the average temperature Ts is preferably 15 ° C. or more. The fact that Tc-Ts is 15 ° C. or higher means that the area including the corner of the semiconductor chip 10 is locally heated to a temperature higher than the other areas. By performing such heating in the pressure bonding step, the fillet on the side S of the semiconductor chip 10 can be shortened and the coverage can be secured. Tc-Ts may be 15-30 ° C.

 本実施形態において、エリア2,4,6,8の各中心部における半導体チップ10の外表面の平均温度Tsと、エリア9の中心部における半導体チップ10の外表面の温度T9との温度差(Ts-T9)は5℃以上であってもよい。Ts-T9が5℃以上であることは、半導体チップ10のエリア2,4,6,8がエリア9よりも高温となるように加熱したことを意味する。すなわち、本実施形態の圧着工程において、Tc>Ts>T9の条件を満たし且つ温度差(Tc-Ts)が15℃以上であり温度差(Ts-T9)が5℃以上となるように、加熱してもよい。なお、温度差(Ts-T9)の範囲は5~40℃であってよい。 In the present embodiment, the temperature difference between the average temperature Ts of the outer surface of the semiconductor chip 10 in the central portions of the areas 2, 4, 6, and 8 and the temperature T9 of the outer surface of the semiconductor chip 10 in the central portion of the area 9 ( Ts-T9) may be 5 ° C or higher. The fact that Ts-T9 is 5 ° C. or higher means that the areas 2, 4, 6, 8 of the semiconductor chip 10 are heated so as to have a higher temperature than the area 9. That is, in the pressure bonding step of this embodiment, heating is performed so that the condition of Tc> Ts> T9 is satisfied, the temperature difference (Tc-Ts) is 15 ° C. or more, and the temperature difference (Ts-T9) is 5 ° C. or more. You may. The temperature difference (Ts-T9) may be in the range of 5-40 ° C.

 昇温可能な圧着ツール面を有する一般的な圧着装置を使用して圧着工程を実施する場合、積層体40の表面に圧着ツール面を当接させ、積層体40に対して押圧力Fを加えた状態で、圧着ツール面を昇温する。圧着ツール面は、通常、その表面温度がなるべく均一になるように設計されている。例えば、半導体チップのサイズが30mm×30mm程度であれば、圧着時の半導体チップの表面の温度ばらつきは、通常、15℃未満である。積層体40を均一に加熱して圧着工程を実施すると、半導体チップの辺の中央部におけるフィレット幅が大きく且つカバレッジが不足する傾向にある。なお、カバレッジを確保するため、加熱温度を高くしたり押圧力を高くしたりすると半導体チップの辺におけるフィレット幅がより一層も大きくなる。 When the crimping process is performed by using a general crimping device having a crimping tool surface capable of raising the temperature, the crimping tool surface is brought into contact with the surface of the laminated body 40, and a pressing force F is applied to the laminated body 40. In this state, the surface of the crimping tool is heated. The crimping tool surface is usually designed so that its surface temperature is as uniform as possible. For example, when the size of the semiconductor chip is about 30 mm × 30 mm, the temperature variation on the surface of the semiconductor chip during pressure bonding is usually less than 15 ° C. If the laminated body 40 is uniformly heated and the pressure bonding step is performed, the fillet width in the central portion of the side of the semiconductor chip tends to be large and the coverage tends to be insufficient. It should be noted that if the heating temperature is increased or the pressing force is increased in order to secure the coverage, the fillet width on the side of the semiconductor chip is further increased.

 これに対し、本実施形態によれば、圧着ツール面に温度分布を故意につけることで、フィレット幅の抑制とカバレッジの確保が可能となる。上述のとおり、半導体チップのエリア1,3,5,7を局所的に高温に加熱することで、半導体チップ10の隅部Cにそれぞれ位置する接着剤層30の流動を高めることができ、カバレッジを確保できる。他方、半導体チップ10のエリア2,4,6,8の加熱温度を相対的に低くすることで、半導体チップ10の辺Sの中央近傍における接着剤層30の流動を相対的に抑制することができ、辺Sにおけるフィレットを小さくすることができる。エリア2,4,6,8の平均温度Tsとエリア9の温度T9との差(Ts-T9)を5℃以上にすることで半導体チップ全体の昇温速度が速くなる傾向がある。昇温速度が速くなることで、半導体チップの特定のエリアを局所的に加熱しやすくなるため、よりフィレットを抑えながらカバレッジを確保しやすくなる。また、昇温速度が速くなることで、はんだが溶融する時間が長くなるため、接続がとりやすくなる。これにより、優れた信頼性の半導体装置を短時間で製造することが可能となる。 On the other hand, according to the present embodiment, it is possible to suppress the fillet width and ensure the coverage by intentionally providing the temperature distribution on the surface of the crimping tool. As described above, by locally heating the areas 1, 3, 5, 7 of the semiconductor chip to a high temperature, it is possible to enhance the flow of the adhesive layers 30 respectively located at the corners C of the semiconductor chip 10, and to improve the coverage. Can be secured. On the other hand, by relatively lowering the heating temperature of the areas 2, 4, 6, 8 of the semiconductor chip 10, the flow of the adhesive layer 30 near the center of the side S of the semiconductor chip 10 can be relatively suppressed. Therefore, the fillet on the side S can be reduced. By setting the difference (Ts-T9) between the average temperature Ts of the areas 2, 4, 6, and 8 and the temperature T9 of the area 9 to be 5 ° C. or more, the temperature rising rate of the entire semiconductor chip tends to increase. By increasing the temperature rising rate, it becomes easier to locally heat a specific area of the semiconductor chip, and it becomes easier to secure coverage while suppressing fillets. Further, since the temperature rising rate is increased, the time for melting the solder is lengthened, which facilitates connection. This makes it possible to manufacture a highly reliable semiconductor device in a short time.

 図4は半導体チップ10から接着剤層30がはみ出した状態を模式的に示す上面図である。図4に示す幅Wは、半導体チップ10の辺Sにおけるフィレットの最大幅である。半導体チップ10の四つの辺Sについて、フィレットの最大幅を測定し、その平均値が半導体チップ10の辺におけるフィレット幅と定義される。図4に示す幅w1,w2は、半導体チップ10の隅部Cから200μmの位置におけるフィレットの幅(μm)である。半導体チップ10の四つの隅部Cについて、幅w1,w2をそれぞれ測定し、計8つの値の平均値が半導体チップ10のカバレッジ(μm)と定義される。 FIG. 4 is a top view schematically showing a state where the adhesive layer 30 protrudes from the semiconductor chip 10. The width W F shown in FIG. 4 is the maximum width of the fillet on the side S of the semiconductor chip 10. The maximum width of the fillet is measured on the four sides S of the semiconductor chip 10, and the average value is defined as the fillet width on the side of the semiconductor chip 10. The widths w1 and w2 shown in FIG. 4 are the width (μm) of the fillet at a position 200 μm from the corner C of the semiconductor chip 10. The widths w1 and w2 of the four corners C of the semiconductor chip 10 are measured, and the average of the eight values is defined as the coverage (μm) of the semiconductor chip 10.

 フィレット幅は、半導体チップ10のサイズ及び厚さ並びにアンダーフィル(液状及びフィルム状を含む)の供給量に依存する。フィレット幅は信頼性に問題なければ小さいほど好ましい。例えば、ウエハ上に半導体チップを圧着する場合及び基板上に半導体チップを圧着する場合、フィレットは半導体チップ間隔の距離の半分以下であることが好ましい。フィレット幅は50~200μmであることが好ましく、50~150μmであることがより好ましい。半導体チップ10のカバレッジは、5~100μmであることが好ましく、10~100μmであることがより好ましい。カバレッジが10μm以上であれば、半導体装置50の信頼性をより一層向上できる傾向にある。カバレッジをフィレット幅で除すことによってカバレッジ指数(無次元)が算出される。カバレッジ指数は、例えば、0.1~1であり、0.2~0.5であってもよい。カバレッジ指数が0.1以上であれば、半導体装置50の信頼性を十分に高くできる傾向にある。 The fillet width depends on the size and thickness of the semiconductor chip 10 and the amount of underfill (including liquid and film) supplied. The fillet width is preferably as small as possible so long as there is no problem in reliability. For example, when the semiconductor chip is pressure-bonded on the wafer and when the semiconductor chip is pressure-bonded on the substrate, the fillet is preferably half or less of the distance between the semiconductor chips. The fillet width is preferably 50 to 200 μm, more preferably 50 to 150 μm. The coverage of the semiconductor chip 10 is preferably 5 to 100 μm, more preferably 10 to 100 μm. If the coverage is 10 μm or more, the reliability of the semiconductor device 50 tends to be further improved. The coverage index (dimensionless) is calculated by dividing the coverage by the fillet width. The coverage index is, for example, 0.1 to 1, and may be 0.2 to 0.5. If the coverage index is 0.1 or more, the reliability of the semiconductor device 50 tends to be sufficiently high.

(キュア工程)
 キュア工程は、圧着工程後の積層体40を加熱する工程である。この工程は、ボイド低減の観点から、加圧オーブン又は加圧リフロ装置を使用し、加圧雰囲気下で実施することが好ましい。加熱温度は、例えば、130~200℃である。圧力は、例えば、0.1~1MPaである。
(Cure process)
The curing process is a process of heating the laminated body 40 after the pressure bonding process. From the viewpoint of reducing voids, this step is preferably performed in a pressurized atmosphere using a pressure oven or pressure reflow device. The heating temperature is, for example, 130 to 200 ° C. The pressure is, for example, 0.1 to 1 MPa.

 本実施形態においては、圧着工程において、レーザーボンダを使用し、Tc-Tsが15℃以上となるように加熱する場合を例示したが、Tc-Tsを15℃以上にできる限り、レーザーボンダ以外の圧着装置を使用してもよい。例えば、半導体チップ10の隅部Cのみ温度が伝わり易いように、隅部Cに対応する位置に凸部を有する圧着ツールを使用してよい。あるいは、半導体チップ10の隅部Cに対応する領域が局所的に熱伝導性の高い材質で構成された圧着ツールを使用してよいし、あるいは、当該領域以外の部分が熱伝導性の低い材質で構成された圧着ツールを使用してもよい。 In this embodiment, a laser bonder is used in the pressure bonding step and heating is performed so that Tc-Ts is 15 ° C. or higher. However, as long as Tc-Ts can be set to 15 ° C. or higher, a temperature other than the laser bonder is used. A crimping device may be used. For example, a pressure bonding tool having a convex portion at a position corresponding to the corner C may be used so that the temperature is easily transmitted only to the corner C of the semiconductor chip 10. Alternatively, a crimping tool in which a region corresponding to the corner C of the semiconductor chip 10 is locally made of a material having high thermal conductivity may be used, or a portion other than the region may be made of a material having low thermal conductivity. You may use the crimping tool comprised by.

 本実施形態において、エリア2,4,6,8をレーザー非照射部とする場合を例示したが、Tc-Tsを15℃以上にできる限り、エリア2,4,6,8にレーザーを照射してもよい(実施例3,4参照)。 In the present embodiment, the case where the areas 2, 4, 6, and 8 are not irradiated with the laser is exemplified, but the areas 2, 4, 6, and 8 are irradiated with the laser as long as Tc-Ts can be set to 15 ° C. or higher. Alternatively (see Examples 3 and 4).

 本実施形態においては、半導体チップ10と基板20の接続部を有する半導体装置50を例示したが、半導体チップと他の半導体チップが接続された態様であってもよく、半導体チップと半導体ウエハが接続された態様であってもよい。また、接続部は、バンプと配線による金属接合に限られず、バンプとバンプによる金属接合であってもよい。 In the present embodiment, the semiconductor device 50 having the connecting portion between the semiconductor chip 10 and the substrate 20 is exemplified, but a mode in which the semiconductor chip and another semiconductor chip are connected may be used, and the semiconductor chip and the semiconductor wafer may be connected. It may be a modified mode. Further, the connection portion is not limited to the metal connection by the bump and the wiring, but may be the metal connection by the bump and the bump.

 本実施形態に係る圧着工程は、例えば、TSV(Through-Silicon Via)技術によって製造される半導体装置に適用してもよい。図5は、TSV技術によって製造された半導体装置の一例を模式的に示す断面図である。この図に示す半導体装置70は、接着剤層30を介してフリップチップ接続され且つ積層された三つの半導体チップ11,12,13と、半導体チップ13と接着剤層30を介して接続されたインタポーザー60とを備える。なお、半導体チップ11,12,13は、貫通電極部分11a,12a,13aを有する。かかる構成の半導体装置70によれば、半導体チップの裏面からも信号のやり取りができる。半導体チップ内で配線を垂直に通すことができるため、半導体チップ間、あるいは、チップとインタポーザーの間を最短に且つ柔軟に接続できる。本実施形態に係る圧着工程は、半導体チップ11,12,13を含む積層チップの製造に適用してもよいし、積層チップとインタポーザー60と圧着に適用してもよい。 The crimping step according to the present embodiment may be applied to, for example, a semiconductor device manufactured by the TSV (Through-Silicon Via) technology. FIG. 5 is a sectional view schematically showing an example of a semiconductor device manufactured by the TSV technique. A semiconductor device 70 shown in this figure has three semiconductor chips 11, 12 and 13 which are flip-chip connected and laminated via an adhesive layer 30, and an interface which is connected to the semiconductor chip 13 via the adhesive layer 30. And a poser 60. The semiconductor chips 11, 12, 13 have penetrating electrode portions 11a, 12a, 13a. According to the semiconductor device 70 having such a configuration, signals can be exchanged from the back surface of the semiconductor chip. Since the wiring can be vertically passed in the semiconductor chip, the semiconductor chips or the chip and the interposer can be flexibly connected to each other in the shortest distance. The crimping step according to the present embodiment may be applied to the manufacture of a laminated chip including the semiconductor chips 11, 12, and 13, or may be applied to the laminated chip, the interposer 60, and the pressure bonding.

 以下、本実施形態に係る半導体装置の製造方法に用いられる半導体チップ、基板及び接着剤層等について説明する。 Hereinafter, a semiconductor chip, a substrate, an adhesive layer, and the like used in the method for manufacturing a semiconductor device according to this embodiment will be described.

 半導体チップは、直線状に延びる辺を有し、例えば、正方形又は長方形の形状を有する。半導体チップの一辺の長さは、例えば、0.1~300mmであり、5~150mmであってもよい。半導体チップを構成する半導体としては、特に限定はなく、シリコン、ゲルマニウム等の元素半導体、ガリウムヒ素、インジウムリン等の化合物半導体などが挙げられる。 The semiconductor chip has sides that extend linearly, and has, for example, a square or rectangular shape. The length of one side of the semiconductor chip is, for example, 0.1 to 300 mm, and may be 5 to 150 mm. The semiconductor constituting the semiconductor chip is not particularly limited, and elemental semiconductors such as silicon and germanium and compound semiconductors such as gallium arsenide and indium phosphide can be cited.

 半導体チップは、バンプと称される導電性突起を有することができる。バンプは、主な成分として、金、銀、銅、はんだ、スズ、ニッケル等を含む。これらの金属は、一種が単独で又は二種以上が併用されていてもよい。また、これらの金属が積層された構造をなすように形成されていてもよい。なお、はんだの主成分は、例えば、スズ-銀、スズ-鉛、スズ-ビスマス、スズ-銅、スズ-銀-銅等の合金である。また、バンプは半導体チップと接続される配線基板等に形成されていてもよい。バンプを構成する金属としては、低コストの点から、銅、はんだが好ましく、接続信頼性及び反り抑制の点から、はんだが更に好ましい。 The semiconductor chip can have conductive protrusions called bumps. The bump contains gold, silver, copper, solder, tin, nickel, etc. as main components. These metals may be used alone or in combination of two or more. Further, it may be formed to have a structure in which these metals are laminated. The main component of solder is, for example, an alloy of tin-silver, tin-lead, tin-bismuth, tin-copper, tin-silver-copper, or the like. The bumps may be formed on a wiring board or the like connected to the semiconductor chip. As the metal forming the bumps, copper and solder are preferable from the viewpoint of low cost, and solder is more preferable from the viewpoint of connection reliability and suppression of warpage.

 半導体チップ及び配線基板は、パッドと呼ばれる導電性面を有することができる。パッドは、主な成分として、金、銀、銅、はんだ、スズ、ニッケル等を含む。これらの金属は、一種が単独で又は二種以上が併用されていてもよい。また、これらの金属が積層された構造をなすように形成されていてもよい。なお、はんだの主成分は、例えば、スズ-銀、スズ-鉛、スズ-ビスマス、スズ-銅、スズ-銀-銅等の合金である。また、パッドを構成する金属としては、接続信頼性の点から、金、はんだが好ましい。 The semiconductor chip and wiring board can have a conductive surface called a pad. The pad contains gold, silver, copper, solder, tin, nickel, etc. as a main component. These metals may be used alone or in combination of two or more. Further, it may be formed to have a structure in which these metals are laminated. The main component of solder is, for example, an alloy of tin-silver, tin-lead, tin-bismuth, tin-copper, tin-silver-copper, or the like. Further, as the metal forming the pad, gold and solder are preferable from the viewpoint of connection reliability.

 配線基板としては、通常の回路基板であれば特に制限はなく、エッチング処理によって絶縁基板に配線パターンを形成したもの、絶縁基板の表面に導電性物質を印刷して配線パターンを形成したものなどが挙げられる。絶縁基板は、ガラスエポキシ、ポリエステル、セラミック、エポキシ、ビスマレイミドトリアジン、ポリイミド等の樹脂材料からなる。 The wiring board is not particularly limited as long as it is a normal circuit board, and one having a wiring pattern formed on the insulating substrate by etching, one having a wiring pattern formed by printing a conductive substance on the surface of the insulating substrate, etc. Can be mentioned. The insulating substrate is made of a resin material such as glass epoxy, polyester, ceramic, epoxy, bismaleimide triazine, and polyimide.

 配線パターンの表面には、金属層が形成されていてもよい。金属層は、主な成分として、金、銀、銅、はんだ、スズ、ニッケル等を含む。これらの金属は、一種が単独で又は二種以上が併用されていてもよい。また、これらの金属が積層された構造をなすように形成されていてもよい。金属層を構成する金属としては、低コストの点から、銅、はんだが好ましく、接続信頼性及び反り抑制の点から、はんだが更に好ましい。 -A metal layer may be formed on the surface of the wiring pattern. The metal layer contains gold, silver, copper, solder, tin, nickel, etc. as a main component. These metals may be used alone or in combination of two or more. Further, it may be formed to have a structure in which these metals are laminated. As the metal constituting the metal layer, copper and solder are preferable from the viewpoint of low cost, and solder is more preferable from the viewpoint of connection reliability and suppression of warpage.

 半導体装置は、上述のバンプ-バンプ間の接続部、バンプ-パッド間の接続部、又は、バンプ-配線間の接続部を有していてもよい。 The semiconductor device may have the above-mentioned bump-bump connecting portion, bump-pad connecting portion, or bump-wiring connecting portion.

 接着剤層は、200℃以上の温度条件で圧着処理ができるように、優れた耐熱性を有していることが好ましい。200℃以上の温度条件で圧着処理することで、はんだ等金属を溶融させることができる。接着剤層は、ボイド発生を抑制する観点から、重量平均分子量10000未満の樹脂成分を含有する。接着剤層は、重量平均分子量10000以上の高分子成分を更に含有してもよい。接着剤層は、圧着工程の効率化の観点から、フィルム状接着剤であることが好ましい。なお、ここでいう「重量平均分子量」は、高速液体クロマトグラフィー(株式会社島津製作所製C-R4A)を用いて、ポリスチレン換算で測定される値を意味する。 The adhesive layer preferably has excellent heat resistance so that it can be subjected to pressure bonding at a temperature of 200 ° C. or higher. A metal such as solder can be melted by performing a pressure bonding process under a temperature condition of 200 ° C. or higher. The adhesive layer contains a resin component having a weight average molecular weight of less than 10,000 from the viewpoint of suppressing the generation of voids. The adhesive layer may further contain a polymer component having a weight average molecular weight of 10,000 or more. The adhesive layer is preferably a film adhesive from the viewpoint of improving the efficiency of the pressure bonding step. The "weight average molecular weight" used herein means a value measured in terms of polystyrene by using high performance liquid chromatography (C-R4A manufactured by Shimadzu Corporation).

(a)重量平均分子量10000未満の樹脂成分
 重量平均分子量10000未満の樹脂成分(以下、(a)成分)としては、エポキシ樹脂及びアクリル樹脂が挙げられる。(a)成分は、熱硬化性樹脂であることが好ましく、この場合、接着剤層は(b)硬化剤を含むことが好ましい。分子量が比較的小さい樹脂成分は加熱時に分解等してボイドの原因となるため、硬化剤と反応する方が耐熱性の観点から好ましい。
(A) Resin component having a weight average molecular weight of less than 10,000 The resin component having a weight average molecular weight of less than 10,000 (hereinafter, component (a)) includes an epoxy resin and an acrylic resin. The component (a) is preferably a thermosetting resin, and in this case, the adhesive layer preferably contains the curing agent (b). Since a resin component having a relatively small molecular weight decomposes upon heating and causes voids, it is preferable to react with a curing agent from the viewpoint of heat resistance.

 エポキシ樹脂は、分子内に二個以上のエポキシ基を有するものであれば特に制限はなく、例えば、ビスフェノールA型、ビスフェノールF型、ナフタレン型、フェノールノボラック型、クレゾールノボラック型、フェノールアラルキル型、ビフェニル型、トリフェニルメタン型、ジシクロペンタジエン型、各種多官能エポキシ樹脂を使用することができる。これらは一種を単独又は二種以上を併用することができる。 The epoxy resin is not particularly limited as long as it has two or more epoxy groups in the molecule, and examples thereof include bisphenol A type, bisphenol F type, naphthalene type, phenol novolac type, cresol novolak type, phenol aralkyl type, biphenyl. Type, triphenylmethane type, dicyclopentadiene type, and various polyfunctional epoxy resins can be used. These can be used alone or in combination of two or more.

 エポキシ樹脂の含有量は、接着剤層の全質量100質量部に対して、例えば10~50質量部である。エポキシ樹脂の含有量が10質量部以上であることで、硬化後の樹脂の流動を制御しやすく、他方、50質量部以下であることで、パッケージの反りを抑制できる。 The content of the epoxy resin is, for example, 10 to 50 parts by mass with respect to 100 parts by mass of the total mass of the adhesive layer. When the content of the epoxy resin is 10 parts by mass or more, it is easy to control the flow of the resin after curing, and when it is 50 parts by mass or less, the warpage of the package can be suppressed.

 アクリル樹脂は、分子内に一個以上のアクリロイル基を有するものであれば特に制限はなく、例えば、ビスフェノールA型、ビスフェノールF型、ナフタレン型、フェノールノボラック型、クレゾールノボラック型、フェノールアラルキル型、ビフェニル型、トリフェニルメタン型、ジシクロペンタジエン型、フルオレン型、アダマンタン型、各種多官能アクリルを使用することができる。これらは一種を単独で又は二種以上を併用することができる。 The acrylic resin is not particularly limited as long as it has at least one acryloyl group in the molecule, and examples thereof include bisphenol A type, bisphenol F type, naphthalene type, phenol novolac type, cresol novolac type, phenol aralkyl type, biphenyl type. , Triphenylmethane type, dicyclopentadiene type, fluorene type, adamantane type, and various polyfunctional acrylics can be used. These can be used alone or in combination of two or more.

 アクリル樹脂の含有量は、接着剤層の全質量100質量部に対して、10~50質量部が好ましく、15~40質量部がより好ましい。アクリル樹脂の含有量が10質量部以上であることで、硬化後の樹脂の流動を制御しやすく、他方、50質量部以下であることで、パッケージの反りを抑制できる。 The content of the acrylic resin is preferably 10 to 50 parts by mass, more preferably 15 to 40 parts by mass with respect to 100 parts by mass of the total mass of the adhesive layer. When the content of the acrylic resin is 10 parts by mass or more, it is easy to control the flow of the resin after curing, and when it is 50 parts by mass or less, the warpage of the package can be suppressed.

 アクリル樹脂は室温(25℃)で固形であることが好ましい。液状に比べて固形の方が、ボイドが発生しにくく、また、硬化前(Bステージ)の接着剤層の粘性(タック)が小さく取り扱いに優れる。アクリロイル基の官能基数は3官能基以下が好ましい。アクリロイル基の官能基数は3官能基以下であることで、短時間で硬化が十分に進行し、十分に高い硬化反応率を達成できる。 The acrylic resin is preferably solid at room temperature (25 ° C). Voids are less likely to occur in the solid form than in the liquid form, and the viscosity (tack) of the adhesive layer before curing (B stage) is small and the handling is excellent. The number of functional groups of the acryloyl group is preferably 3 or less. When the number of functional groups of the acryloyl group is 3 or less, curing sufficiently progresses in a short time and a sufficiently high curing reaction rate can be achieved.

(b)硬化剤
 硬化剤としては、例えば、フェノール樹脂系硬化剤、酸無水物系硬化剤、アミン系硬化剤、イミダゾール系硬化剤、ホスフィン系硬化剤、アゾ化合物及び有機過酸化物が挙げられる。
(B) Curing agent Examples of the curing agent include a phenol resin curing agent, an acid anhydride curing agent, an amine curing agent, an imidazole curing agent, a phosphine curing agent, an azo compound and an organic peroxide. ..

(フェノール樹脂系硬化剤)
 フェノール樹脂系硬化剤としては、分子内に二個以上のフェノール性水酸基を有するものであれば特に制限はなく、例えば、フェノールノボラック、クレゾールノボラック、フェノールアラルキル樹脂、クレゾールナフトールホルムアルデヒド重縮合物、トリフェニルメタン型多官能フェノール及び各種多官能フェノール樹脂を使用することができる。これらは単独で又は二種以上の混合物として使用することができる。
(Phenolic resin hardener)
The phenol resin-based curing agent is not particularly limited as long as it has two or more phenolic hydroxyl groups in the molecule, for example, phenol novolac, cresol novolac, phenol aralkyl resin, cresol naphthol formaldehyde polycondensate, triphenyl. Methane-type polyfunctional phenols and various polyfunctional phenol resins can be used. These can be used alone or as a mixture of two or more kinds.

 エポキシ樹脂に対するフェノール樹脂系硬化剤の当量比(フェノール性水酸基/エポキシ基、モル比)は、良好な硬化性、接着性及び保存安定性の観点から、0.3~1.5が好ましく、0.4~1.0がより好ましく、0.5~1.0が更に好ましい。当量比が0.3以上であると、硬化性が向上し接着力が向上する傾向があり、1.5以下であると未反応のフェノール性水酸基が過剰に残存することがなく、吸水率が低く抑えられ、絶縁信頼性が向上する傾向がある。 The equivalent ratio of the phenol resin type curing agent to the epoxy resin (phenolic hydroxyl group / epoxy group, molar ratio) is preferably 0.3 to 1.5, from the viewpoint of good curability, adhesiveness and storage stability, and 0 0.4 to 1.0 is more preferable, and 0.5 to 1.0 is further preferable. When the equivalent ratio is 0.3 or more, the curability and the adhesive strength tend to be improved, and when it is 1.5 or less, the unreacted phenolic hydroxyl group does not remain excessively and the water absorption is It tends to be kept low and the insulation reliability tends to be improved.

(酸無水物系硬化剤)
 酸無水物系硬化剤としては、例えば、メチルシクロヘキサンテトラカルボン酸二無水物、無水トリメリット酸、無水ピロメリット酸、ベンゾフェノンテトラカルボン酸二無水物及びエチレングリコールビスアンヒドロトリメリテートを使用することができる。これらは単独で又は二種以上の混合物として使用することができる。
(Acid anhydride curing agent)
As the acid anhydride-based curing agent, for example, use methylcyclohexanetetracarboxylic dianhydride, trimellitic anhydride, pyromellitic dianhydride, benzophenonetetracarboxylic dianhydride and ethylene glycol bisanhydrotrimellitate. You can These can be used alone or as a mixture of two or more kinds.

 エポキシ樹脂に対する酸無水物系硬化剤の当量比(酸無水物基/エポキシ基、モル比)は、良好な硬化性、接着性及び保存安定性の観点から、0.3~1.5が好ましく、0.4~1.0がより好ましく、0.5~1.0が更に好ましい。当量比が0.3以上であると、硬化性が向上し接着力が向上する傾向があり、1.5以下であると未反応の酸無水物が過剰に残存することがなく、吸水率が低く抑えられ、絶縁信頼性が向上する傾向がある。 The equivalent ratio of the acid anhydride type curing agent to the epoxy resin (acid anhydride group / epoxy group, molar ratio) is preferably 0.3 to 1.5 from the viewpoint of good curability, adhesiveness and storage stability. , 0.4 to 1.0 are more preferable, and 0.5 to 1.0 are still more preferable. If the equivalent ratio is 0.3 or more, the curability and the adhesive strength tend to be improved, and if it is 1.5 or less, the unreacted acid anhydride does not remain excessively and the water absorption is It tends to be kept low and the insulation reliability tends to be improved.

(アミン系硬化剤)
 アミン系硬化剤としては、例えばジシアンジアミドを使用することができる。エポキシ樹脂に対するアミン系硬化剤の当量比(アミン/エポキシ基、モル比)は、良好な硬化性、接着性及び保存安定性の観点から0.3~1.5が好ましく、0.4~1.0がより好ましく、0.5~1.0が更に好ましい。当量比が0.3以上であると、硬化性が向上し接着力が向上する傾向があり、1.5以下であると未反応のアミンが過剰に残存することがなく、絶縁信頼性が向上する傾向がある。
(Amine curing agent)
As the amine-based curing agent, for example, dicyandiamide can be used. The equivalent ratio (amine / epoxy group, molar ratio) of the amine-based curing agent to the epoxy resin is preferably 0.3 to 1.5, and 0.4 to 1 from the viewpoint of good curability, adhesiveness and storage stability. 0.0 is more preferable, and 0.5 to 1.0 is still more preferable. When the equivalent ratio is 0.3 or more, the curability and the adhesive strength tend to be improved, and when it is 1.5 or less, unreacted amine does not remain excessively and the insulation reliability is improved. Tend to do.

(イミダゾール系硬化剤)
 イミダゾール系硬化剤としては、例えば、2-フェニルイミダゾール、2-フェニル-4-メチルイミダゾール、1-ベンジル-2-メチルイミダゾール、1-ベンジル-2-フェニルイミダゾール、1-シアノエチル-2-ウンデシルイミダゾール、1-シアノ-2-フェニルイミダゾール、1-シアノエチル-2-ウンデシルイミダゾールトリメリテイト、1-シアノエチル-2-フェニルイミダゾリウムトリメリテイト、2,4-ジアミノ-6-[2’-メチルイミダゾリル-(1’)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2’-ウンデシルイミダゾリル-(1’)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2’-エチル-4’-メチルイミダゾリル-(1’)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2’-メチルイミダゾリル-(1’)]-エチル-s-トリアジンイソシアヌル酸付加体、2-フェニルイミダゾールイソシアヌル酸付加体、2-フェニル-4,5-ジヒドロキシメチルイミダゾール、2-フェニル-4-メチル-5-ヒドロキシメチルイミダゾール、及び、エポキシ樹脂とイミダゾール類の付加体が挙げられる。これらの中でも、優れた硬化性、保存安定性及び接続信頼性の観点から、1-シアノエチル-2-ウンデシルイミダゾール、1-シアノ-2-フェニルイミダゾール、1-シアノエチル-2-ウンデシルイミダゾールトリメリテイト、1-シアノエチル-2-フェニルイミダゾリウムトリメリテイト、2,4-ジアミノ-6-[2’-メチルイミダゾリル-(1’)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2’-エチル-4’-メチルイミダゾリル-(1’)]-エチル-s-トリアジン、2,4-ジアミノ-6-[2’-メチルイミダゾリル-(1’)]-エチル-s-トリアジンイソシアヌル酸付加体、2-フェニルイミダゾールイソシアヌル酸付加体、2-フェニル-4,5-ジヒドロキシメチルイミダゾール及び2-フェニル-4-メチル-5-ヒドロキシメチルイミダゾールが好ましい。これらは単独で又は二種以上を併用して用いることができる。また、これらをマイクロカプセル化した潜在性硬化剤としてもよい。
(Imidazole type curing agent)
Examples of the imidazole-based curing agent include 2-phenylimidazole, 2-phenyl-4-methylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-phenylimidazole, 1-cyanoethyl-2-undecylimidazole. , 1-cyano-2-phenylimidazole, 1-cyanoethyl-2-undecylimidazole trimellitate, 1-cyanoethyl-2-phenylimidazolium trimellitate, 2,4-diamino-6- [2'-methylimidazolyl -(1 ')]-Ethyl-s-triazine, 2,4-diamino-6- [2'-undecylimidazolyl- (1')]-ethyl-s-triazine, 2,4-diamino-6- [ 2'-Ethyl-4'-methylimidazolyl- (1 ')]-ethyl-s-triazine, 2,4-diamino -6- [2'-Methylimidazolyl- (1 ')]-ethyl-s-triazine isocyanuric acid adduct, 2-phenylimidazole isocyanuric acid adduct, 2-phenyl-4,5-dihydroxymethylimidazole, 2-phenyl -4-Methyl-5-hydroxymethylimidazole, and an adduct of an epoxy resin and an imidazole may be mentioned. Among these, 1-cyanoethyl-2-undecylimidazole, 1-cyano-2-phenylimidazole, 1-cyanoethyl-2-undecylimidazole trimellitic acid, from the viewpoint of excellent curability, storage stability and connection reliability. Tate, 1-cyanoethyl-2-phenylimidazolium trimellitate, 2,4-diamino-6- [2'-methylimidazolyl- (1 ')]-ethyl-s-triazine, 2,4-diamino-6- [2′-Ethyl-4′-methylimidazolyl- (1 ′)]-ethyl-s-triazine, 2,4-diamino-6- [2′-methylimidazolyl- (1 ′)]-ethyl-s-triazine Isocyanuric acid adduct, 2-phenylimidazole Isocyanuric acid adduct, 2-phenyl-4,5-dihydroxymethylimidazole and 2-phenyl -4-Methyl-5-hydroxymethylimidazole is preferred. These can be used alone or in combination of two or more. Further, these may be microencapsulated latent curing agents.

 イミダゾール系硬化剤の含有量は、エポキシ樹脂100質量部に対して、0.1~20質量部が好ましく、0.1~10質量部がより好ましい。イミダゾール系硬化剤の含有量が0.1質量部以上であると硬化性が向上する傾向があり、20質量部以下であると金属接合が形成される前に接着剤組成物が硬化することがなく、接続不良が発生しにくい傾向がある。 The content of the imidazole-based curing agent is preferably 0.1 to 20 parts by mass, more preferably 0.1 to 10 parts by mass, based on 100 parts by mass of the epoxy resin. When the content of the imidazole-based curing agent is 0.1 parts by mass or more, the curability tends to be improved, and when it is 20 parts by mass or less, the adhesive composition may be cured before the metal bond is formed. No connection failure tends to occur.

(ホスフィン系硬化剤)
 ホスフィン系硬化剤としては、例えば、トリフェニルホスフィン、テトラフェニルホスホニウムテトラフェニルボレート、テトラフェニルホスホニウムテトラ(4-メチルフェニル)ボレート及びテトラフェニルホスホニウム(4-フルオロフェニル)ボレートが挙げられる。
(Phosphine curing agent)
Examples of the phosphine-based curing agent include triphenylphosphine, tetraphenylphosphonium tetraphenylborate, tetraphenylphosphonium tetra (4-methylphenyl) borate and tetraphenylphosphonium (4-fluorophenyl) borate.

 ホスフィン系硬化剤の含有量は、エポキシ樹脂100質量部に対して、0.1~10質量部が好ましく、0.1~5質量部がより好ましい。ホスフィン系硬化剤の含有量が0.1質量部以上であると硬化性が向上する傾向があり、10質量部以下であると金属接合が形成される前に接着剤組成物が硬化することがなく、接続不良が発生しにくい傾向がある。 The content of the phosphine-based curing agent is preferably 0.1 to 10 parts by mass, more preferably 0.1 to 5 parts by mass with respect to 100 parts by mass of the epoxy resin. When the content of the phosphine-based curing agent is 0.1 part by mass or more, the curability tends to be improved, and when it is 10 parts by mass or less, the adhesive composition may be cured before the metal bond is formed. No connection failure tends to occur.

 フェノール樹脂系硬化剤、酸無水物系硬化剤及びアミン系硬化剤は、それぞれ一種を単独で又は二種以上を併用してもよい。イミダゾール系硬化剤及びホスフィン系硬化剤はそれぞれ単独で用いてもよいが、フェノール樹脂系硬化剤、酸無水物系硬化剤又はアミン系硬化剤と共に用いてもよい。 Each of the phenolic resin-based curing agent, the acid anhydride-based curing agent and the amine-based curing agent may be used alone or in combination of two or more kinds. The imidazole-based curing agent and the phosphine-based curing agent may be used alone, or may be used together with a phenol resin-based curing agent, an acid anhydride-based curing agent or an amine-based curing agent.

(有機過酸化物)
 有機過酸化物としては、例えば、ケトンパーオキサイド、パーオキシケタール、ハイドロパーオキサイド、ジアルキルパーオキサイド、ジアシルパーオキサイド、パーオキシジカーボネイト、パーオキシエステルが挙げられる。保存安定性の観点から、ハイドロパーオキサイド、ジアルキルパーオキサイド、パーオキシエステルが好ましい。更に、耐熱性の観点から、ハイドロパーオキサイド、ジアルキルパーオキサイドが好ましい。これらは、一種を単独で又は二種以上を併用しもよい。
(Organic peroxide)
Examples of organic peroxides include ketone peroxides, peroxyketals, hydroperoxides, dialkyl peroxides, diacyl peroxides, peroxydicarbonates, and peroxyesters. From the viewpoint of storage stability, hydroperoxide, dialkyl peroxide and peroxy ester are preferable. Further, from the viewpoint of heat resistance, hydroperoxide and dialkyl peroxide are preferable. These may be used alone or in combination of two or more.

 過酸化物の含有量は、アクリル樹脂の質量に対して0.5~10質量%が好ましく、1~5質量%がより好ましい。過酸化物の含有量が0.5質量%以上であることで、硬化反応が十分に進行しやすく、他方、10質量%以下であることで、分子鎖が短くなったり、未反応基が残存し信頼性が低下ことを十分に抑制できる。 The content of the peroxide is preferably 0.5 to 10% by mass, more preferably 1 to 5% by mass based on the mass of the acrylic resin. When the content of peroxide is 0.5% by mass or more, the curing reaction easily proceeds sufficiently, while when it is 10% by mass or less, the molecular chain is shortened or unreacted groups remain. However, it is possible to sufficiently suppress the decrease in reliability.

 なお、エポキシ樹脂、アクリル樹脂及び硬化剤の組み合わせは、硬化が進行すれば特に制限はないが、取り扱い性、保存安定性及び硬化性の観点から、エポキシ樹脂とともに使用する硬化剤として、フェノールとイミダゾール、酸無水物とイミダゾール、アミンとイミダゾール、又は、イミダゾールを単独で使用することが好ましい。短時間で接続すると生産性が向上することから、速硬化性に優れたイミダゾールを単独で使用することがより好ましい。短時間で硬化すると低分子成分等の揮発分が抑制できることから、ボイドの発生がより一層抑制される。取り扱い性及び保存安定性の観点から、アクリル樹脂とともに使用する硬化剤として、有機過酸化物を使用することが好ましい。 The combination of the epoxy resin, the acrylic resin and the curing agent is not particularly limited as long as the curing proceeds, but from the viewpoint of handleability, storage stability and curability, phenol and imidazole are used as the curing agent together with the epoxy resin. It is preferable to use acid anhydride and imidazole, amine and imidazole, or imidazole alone. It is more preferable to use imidazole, which is excellent in quick-curing property, alone because the productivity is improved when connecting in a short time. Curing in a short time can suppress volatile components such as low-molecular components, so that the generation of voids is further suppressed. From the viewpoint of handleability and storage stability, it is preferable to use an organic peroxide as a curing agent used together with the acrylic resin.

(c)重量平均分子量10000以上の高分子成分
 重量平均分子量10000以上の高分子成分(以下「(c)成分」という。)としては、エポキシ樹脂、フェノキシ樹脂、ポリイミド樹脂、ポリアミド樹脂、ポリカルボジイミド樹脂、シアネートエステル樹脂、アクリル樹脂、ポリエステル樹脂、ポリエチレン樹脂、ポリエーテルスルホン樹脂、ポリエーテルイミド樹脂、ポリビニルアセタール樹脂、ウレタン樹脂、アクリルゴム、ビスマレイミド樹脂等が挙げられる。これらのうち、耐熱性及びフィルム形成性に優れるエポキシ樹脂、フェノキシ樹脂、ポリイミド樹脂、アクリル樹脂、アクリルゴム、ビスマレイミド樹脂がより好ましい。これらは一種を単独で又は二種以上を併用してもよく、二種以上の共重合体として使用してもよい。
(C) Polymer component having a weight average molecular weight of 10,000 or more As the polymer component having a weight average molecular weight of 10,000 or more (hereinafter referred to as "(c) component"), epoxy resin, phenoxy resin, polyimide resin, polyamide resin, polycarbodiimide resin , Cyanate ester resin, acrylic resin, polyester resin, polyethylene resin, polyether sulfone resin, polyetherimide resin, polyvinyl acetal resin, urethane resin, acrylic rubber, bismaleimide resin, and the like. Of these, epoxy resins, phenoxy resins, polyimide resins, acrylic resins, acrylic rubbers, and bismaleimide resins, which have excellent heat resistance and film forming properties, are more preferable. These may be used alone or in combination of two or more, and may be used as a copolymer of two or more.

 (c)成分と、エポキシ樹脂の質量比は、特に制限されないが、接着剤層における(c)成分の量を100質量部としたとき、エポキシ樹脂の質量が1~500質量部であることが好ましく、5~400質量部であることがより好ましく、10~300質量部であることが更に好ましい。エポキシ樹脂の量が1質量部以上であることで、十分な接着力を確保しやすく、500質量部以下であることで、十分なフィルム形成性及び膜形成性を確保しやすい。なお、ここでいうエポキシ樹脂は、グリシジル基を有する分子量が10000未満の硬化成分である。 The mass ratio of the component (c) and the epoxy resin is not particularly limited, but when the amount of the component (c) in the adhesive layer is 100 parts by mass, the mass of the epoxy resin may be 1 to 500 parts by mass. It is preferably 5 to 400 parts by mass, more preferably 10 to 300 parts by mass. When the amount of the epoxy resin is 1 part by mass or more, it is easy to secure sufficient adhesive force, and when it is 500 parts by mass or less, it is easy to secure sufficient film formability and film formability. The epoxy resin mentioned here is a curing component having a glycidyl group and a molecular weight of less than 10,000.

 (c)成分と、アクリル樹脂の質量比は、特に制限されないが、接着剤層における(c)成分の量を100質量部としたとき、アクリル樹脂の質量が1~1000質量部であることが好ましく、5~500質量部であることがより好ましく、10~500質量部であることが更に好ましい。アクリル樹脂の量が1質量部以上であることで、十分な接着力を確保しやすく、1000質量部以下であることで、十分なフィルム形成性を確保しやすい。 The mass ratio of the component (c) and the acrylic resin is not particularly limited, but when the amount of the component (c) in the adhesive layer is 100 parts by mass, the mass of the acrylic resin is 1 to 1000 parts by mass. The amount is preferably 5 to 500 parts by mass, more preferably 10 to 500 parts by mass. When the amount of the acrylic resin is 1 part by mass or more, it is easy to secure sufficient adhesive force, and when it is 1000 parts by mass or less, it is easy to secure sufficient film formability.

 (c)成分のガラス転位温度(Tg)は、接着剤層の基板及び半導体チップへの貼付性に優れる観点から、50~200℃であることが好ましい。(c)成分のTgが50℃以上であることで、接着剤層のタック(粘性)力を十分に高くでき、取り扱い性に優れる。他方、(c)成分のTgが200℃以下であることで、半導体チップに形成されたバンプ、あるいは、基板に形成された電極又は配線パターン等の凹凸を接着剤層に埋め込みやすく、ボイドの発生を抑制できる。なお、接着剤層のTgは、DSC(パーキンエルマー社製DSC-7型)を用いて、サンプル量10mg、昇温速度10℃/分、測定雰囲気:空気の条件で測定される値を意味する。 The glass transition temperature (Tg) of the component (c) is preferably 50 to 200 ° C. from the viewpoint of excellent adhesion of the adhesive layer to the substrate and semiconductor chip. When the Tg of the component (c) is 50 ° C. or higher, the tack (viscosity) force of the adhesive layer can be sufficiently increased and the handleability is excellent. On the other hand, when the Tg of the component (c) is 200 ° C. or less, bumps formed on the semiconductor chip or irregularities such as electrodes or wiring patterns formed on the substrate are easily embedded in the adhesive layer, and voids are generated. Can be suppressed. The Tg of the adhesive layer means a value measured using a DSC (DSC-7 type manufactured by Perkin Elmer Co., Ltd.) under the conditions of a sample amount of 10 mg, a heating rate of 10 ° C./minute, and a measurement atmosphere of air. ..

 上述のとおり、(c)成分の重量平均分子量は、ポリスチレン換算で10000以上であるが、単独で良好なフィルム形成性を達成する観点から、30000以上であることが好ましい。(c)成分の重量平均分子量が10000以上であることで、十分なフィルム形成性を達成しやすい。 As described above, the weight average molecular weight of the component (c) is 10,000 or more in terms of polystyrene, but it is preferably 30,000 or more from the standpoint of achieving good film-forming property by itself. When the weight average molecular weight of the component (c) is 10,000 or more, it is easy to achieve sufficient film forming property.

 接着剤層は、フラックス剤を更に含有してもよい。フラックス剤は、フラックス活性(酸化物又は不純物を除去する活性)を示す化合物である。フラックス剤としては、イミダゾール類及びアミン類のように非共有電子対を有する含窒素化合物、カルボン酸類、フェノール類及びアルコール類が挙げられる。なお、アルコール等に比べて有機酸の方がフラックス活性を強く発現し、接続性が向上する。有機酸のなかでもカルボン酸を使用することが好ましい。カルボン酸は、エポキシ樹脂と反応するため、接着剤層に残存する量が十分に少なくなるという利点がある。耐熱性の観点から、フラックス剤としてのカルボン酸は、固形が好ましい。フラックス剤の融点は、安定性及び取り扱い性の観点から、70~150℃であることが好ましい。 The adhesive layer may further contain a flux agent. The flux agent is a compound exhibiting flux activity (activity for removing oxides or impurities). Examples of the fluxing agent include nitrogen-containing compounds having a non-covalent electron pair such as imidazoles and amines, carboxylic acids, phenols and alcohols. It should be noted that the organic acid more strongly develops the flux activity than the alcohol or the like, and the connectivity is improved. Among organic acids, it is preferable to use carboxylic acid. Since the carboxylic acid reacts with the epoxy resin, there is an advantage that the amount remaining in the adhesive layer is sufficiently small. From the viewpoint of heat resistance, the carboxylic acid as the flux agent is preferably solid. From the viewpoint of stability and handleability, the melting point of the flux agent is preferably 70 to 150 ° C.

 接着剤層は絶縁性を有するフィラを更に含有してもよい。接着剤層にフィラを配合することで、粘度及び硬化物の物性を制御することができるとともに、半導体チップ同士又は半導体チップと基板とを接続した際のボイドの発生を抑制でき且つ吸湿率を抑制できる。絶縁性を有するフィラとしては、無機フィラ、ウィスカー及び樹脂フィラが挙げられる。なお、絶縁信頼性の観点から、接着剤層は、導電性を有する金属フィラ(例えば、銀粒子及びはんだ粒子)を含有しないことが好ましい。 The adhesive layer may further contain a filler having an insulating property. By adding a filler to the adhesive layer, it is possible to control the viscosity and the physical properties of the cured product, and it is possible to suppress the occurrence of voids when connecting the semiconductor chips to each other or to the semiconductor chip and the substrate and suppress the moisture absorption rate. it can. Examples of the filler having an insulating property include inorganic fillers, whiskers and resin fillers. From the viewpoint of insulation reliability, it is preferable that the adhesive layer does not contain a conductive metal filler (for example, silver particles and solder particles).

 無機フィラとしては、例えば、ガラス、シリカ、アルミナ、酸化チタン、カーボンブラック、マイカ及び窒化ホウ素が挙げられる。これらのうち、シリカ、アルミナ、酸化チタン及び窒化ホウ素が好ましく、シリカ、アルミナ及び窒化ホウ素がより好ましい。ウィスカーとしては、例えば、ホウ酸アルミニウム、チタン酸アルミニウム、酸化亜鉛、珪酸カルシウム、硫酸マグネシウム、窒化ホウ素が挙げられる。樹脂フィラとしては、例えば、ポリウレタン、ポリイミド、メタクリル酸メチル樹脂、メタクリル酸メチル-ブタジエン-スチレン共重合樹脂(MBS)が挙げられる。これらのフィラは一種を単独で又は二種以上を併用してもよい。樹脂フィラは、無機フィラに比べて、高温環境下(例えば、260℃)にける柔軟性を接着剤層に付与できるため、耐リフロ性向上に寄与し得る。柔軟性が向上することで、フィルム形成性も向上し得る。 Examples of inorganic fillers include glass, silica, alumina, titanium oxide, carbon black, mica and boron nitride. Of these, silica, alumina, titanium oxide and boron nitride are preferable, and silica, alumina and boron nitride are more preferable. Examples of the whiskers include aluminum borate, aluminum titanate, zinc oxide, calcium silicate, magnesium sulfate, and boron nitride. Examples of the resin filler include polyurethane, polyimide, methyl methacrylate resin, and methyl methacrylate-butadiene-styrene copolymer resin (MBS). These fillers may be used alone or in combination of two or more. Since the resin filler can give flexibility to the adhesive layer under a high temperature environment (for example, 260 ° C.) as compared with the inorganic filler, it can contribute to the improvement of reflow resistance. By improving the flexibility, the film forming property can also be improved.

 分散性又は接着力向上の観点から、表面処理が施されたフィラを使用してもよい。フィラに対して表面処理を施すことで、フィラの物性を適宜調整することができる。表面処理としては、グリシジル系(エポキシ系)、アミン系、フェニル系、フェニルアミノ系、アクリル(メタクリル)系又はビニル系の処理が挙げられる。分散性、流動性及び接着力の観点から、グリシジル系、フェニルアミノ系、アクリル(メタクリル)系が好ましい。保存安定性の観点から、フェニル系、アクリル(メタクリル)系が更に好ましい。表面処理のし易さから、エポキシシラン系、アミノシラン系、アクリルシラン系等のシラン処理が好ましい。 From the viewpoint of improving dispersibility or adhesive strength, a surface-treated filler may be used. By subjecting the filler to a surface treatment, the physical properties of the filler can be adjusted appropriately. Examples of the surface treatment include glycidyl (epoxy), amine, phenyl, phenylamino, acryl (methacryl) or vinyl treatment. From the viewpoint of dispersibility, fluidity and adhesive strength, glycidyl type, phenylamino type and acryl (methacryl) type are preferable. From the viewpoint of storage stability, phenyl type and acrylic (methacrylic) type are more preferable. From the viewpoint of ease of surface treatment, silane treatment such as epoxysilane-based, aminosilane-based, and acrylsilane-based is preferable.

 フィラの平均粒径は、フリップチップ接続時のかみ込み防止の観点から、1.5μm以下であることが好ましく、視認性(透明性)の観点から、1.0μm以下であることがより好ましい。ここでいう「平均粒径」はレーザー回折式粒度分布測定装置でMEK(メチルエチルケトン)を溶媒として分析して得られる値を意味する。 The average particle size of the filler is preferably 1.5 μm or less from the viewpoint of preventing biting during flip chip connection, and more preferably 1.0 μm or less from the viewpoint of visibility (transparency). The "average particle size" as used herein means a value obtained by analyzing with a laser diffraction particle size distribution analyzer using MEK (methyl ethyl ketone) as a solvent.

 フィラの含有量は、接着剤層の固形分の質量を基準として、30~90質量%であることが好ましく、40~80質量%であることがより好ましい。フィラの含有量が30質量%以上であることで、十分な放熱性を達成しやすく、また、ボイドをできるとともに吸湿率を小さくすることができる。他方、フィラの含有量が90質量%以下であることで、粘度が過度に高くなることを抑制でき、十分に高い流動性を確保できるとともに、接続部へのフィラの噛み込み(トラッピング)を十分に抑制できる。 The content of the filler is preferably 30 to 90% by mass, and more preferably 40 to 80% by mass, based on the mass of the solid content of the adhesive layer. When the content of the filler is 30% by mass or more, sufficient heat dissipation can be easily achieved, and voids can be formed and the moisture absorption rate can be reduced. On the other hand, when the content of the filler is 90% by mass or less, it is possible to suppress the viscosity from becoming excessively high, to ensure sufficiently high fluidity, and to sufficiently trap (fill) the filler into the connection portion. Can be suppressed to.

 接着剤層は、イオントラッパー、酸化防止剤、シランカップリング剤、チタンカップリング剤及びレベリング剤等の添加剤を更に含有してもよい。これらは一種を単独で又は二種以上を併用してもよい。これらの添加剤の含有量は、各添加剤の効果が発現するように適宜調整すればよい。 The adhesive layer may further contain additives such as an ion trapper, an antioxidant, a silane coupling agent, a titanium coupling agent and a leveling agent. These may be used alone or in combination of two or more. The content of these additives may be appropriately adjusted so that the effect of each additive is exhibited.

 上述のとおり、作業性の観点から、接着剤付きチップを作製するにあたり、事前にフィルム状接着剤を準備することが好ましい。フィルム状接着剤は以下のようにして作製することができる。すなわち、上述の各成分を有機溶媒に加え、混合液を攪拌又は混錬することによってワニスを調製する。離型処理を施した基材フィルム上にワニスを塗布した後、加熱により有機溶媒を減少させることで、基材フィルム上にフィルム状接着剤が形成される。ワニスの塗布は、例えば、ナイフコーター、ロールコーター、アプリケーター、ダイコーター又はコンマコーターを用いて実施することができる。 As mentioned above, from the viewpoint of workability, it is preferable to prepare a film adhesive in advance before manufacturing the chip with the adhesive. The film adhesive can be produced as follows. That is, the above components are added to an organic solvent, and the mixed solution is stirred or kneaded to prepare a varnish. After the varnish is applied on the base material film that has been subjected to the mold release treatment, the organic solvent is reduced by heating to form the film adhesive on the base material film. The varnish can be applied using, for example, a knife coater, a roll coater, an applicator, a die coater or a comma coater.

 基材フィルムとしては、有機溶媒を揮発させる際の加熱条件に耐え得る耐熱性を有するものであれば特に制限はなく、ポリエステルフィルム、ポリプロピレンフィルム、ポリエチレンテレフタレートフィルム、ポリイミドフィルム、ポリエーテルイミドフィルム、ポリエーテルナフタレートフィルム、メチルペンテンフィルムが例示できる。基材フィルムは、これらのフィルムからなる単層のものに限られず、二種以上の材料からなる多層フィルムであってもよい。 The substrate film is not particularly limited as long as it has heat resistance that can withstand the heating conditions when volatilizing the organic solvent, polyester film, polypropylene film, polyethylene terephthalate film, polyimide film, polyetherimide film, poly Examples include an ether naphthalate film and a methylpentene film. The base film is not limited to a single layer made of these films, but may be a multilayer film made of two or more kinds of materials.

 ワニスから有機溶媒を揮発させる際の条件は、具体的には、50~200℃、0.1~90分間の加熱を行うことが好ましい。実装後のボイドの発生又は粘度調整に影響がなければ、有機溶媒の含有量は1.5質量%以下にまで低減させることが好ましい。 Specifically, the conditions for volatilizing the organic solvent from the varnish are preferably heating at 50 to 200 ° C. for 0.1 to 90 minutes. The content of the organic solvent is preferably reduced to 1.5% by mass or less if there is no influence on generation of voids after mounting or adjustment of viscosity.

 なお、表面に接着剤層が形成された半導体ウエハをダイシングすることによって接着剤付きチップを作製する場合、例えば、スピンコートによって半導体ウエハの表面にワニスの膜を形成し、その後、加熱により溶媒を減少させればよい。 When a chip with an adhesive is produced by dicing a semiconductor wafer having an adhesive layer formed on the surface, for example, a varnish film is formed on the surface of the semiconductor wafer by spin coating, and then a solvent is added by heating. You can reduce it.

 以下、本開示について、実施例を基づいて説明する。本発明は以下の実施例に限定されるものではない。 Below, the present disclosure will be described based on examples. The present invention is not limited to the examples below.

<実施例1>
(接着剤層形成用ワニスの調製)
 以下の化合物を表1に示す割合で混合するとともに、真空脱気することによってワニスを調製した。なお、溶剤としてMEKを使用した。
(1)重量平均分子量10000未満の熱硬化性樹脂(エポキシ樹脂)
・トリフェノールメタン骨格含有多官能固形エポキシ(三菱ケミカル株式会社製、EP1032H60(以下「EP1032」と表記する。)、重量平均分子量:800~2000)
・ビスフェノールF型液状エポキシ(三菱ケミカル株式会社製、YL983U(以下「YL983」と表記する。)、分子量:約336)
・可とう性半固形状エポキシ(三菱ケミカル株式会社製、YL7175-1000(以下「YL7175」と表記する。)、重量平均分子量:1000~5000)
(2)硬化剤
・2,4-ジアミノ-6-[2’-メチルイミダゾリル-(1’)]-エチル-s-トリアジンイソシアヌル酸付加体(四国化成工業株式会社製、2MAOK-PW(以下「2MAOK」と表記する。))
(3)重量平均分子量10000以上の高分子成分
・フェノキシ樹脂(東都化成工業株式会社、ZX1356-2(以下「ZX1356」と表記する。)、Tg:約71℃、重量平均分子量:約63000)
(4)フラックス剤(カルボン酸)
・グルタル酸(アルドリッチ社製、融点:約98℃)
(5)樹脂フィラ
・有機フィラ(ロームアンドハースジャパン株式会社製、EXL-2655:コアシェルタイプ有機微粒子)
(6)無機フィラ
・シリカフィラ(株式会社アドマテックス、SE2050、平均粒径:0.5μm)
・メタクリル表面処理ナノシリカフィラ(株式会社アドマテックス、YA050C-SM(以下「SMナノシリカ」表記とする。)、平均粒径:約50nm)
<Example 1>
(Preparation of varnish for forming adhesive layer)
A varnish was prepared by mixing the following compounds in the proportions shown in Table 1 and degassing in vacuum. MEK was used as the solvent.
(1) Thermosetting resin (epoxy resin) having a weight average molecular weight of less than 10,000
-Trifunctional methane skeleton-containing polyfunctional solid epoxy (Mitsubishi Chemical Corporation, EP1032H60 (hereinafter referred to as "EP1032"), weight average molecular weight: 800 to 2000)
-Bisphenol F type liquid epoxy (manufactured by Mitsubishi Chemical Corporation, YL983U (hereinafter referred to as "YL983"), molecular weight: about 336)
-Flexible semi-solid epoxy (manufactured by Mitsubishi Chemical Corporation, YL7175-1000 (hereinafter referred to as "YL7175"), weight average molecular weight: 1000 to 5000)
(2) Curing agent, 2,4-diamino-6- [2'-methylimidazolyl- (1 ')]-ethyl-s-triazine isocyanuric acid adduct (manufactured by Shikoku Chemicals Co., Ltd., 2MAOK-PW (hereinafter referred to as " 2MAOK ".))
(3) Polymer component / phenoxy resin having a weight average molecular weight of 10,000 or more (Toto Kasei Co., Ltd., ZX1356-2 (hereinafter referred to as “ZX1356”), Tg: about 71 ° C., weight average molecular weight: about 63000)
(4) Flux agent (carboxylic acid)
-Glutaric acid (Made by Aldrich, melting point: about 98 ° C)
(5) Resin filler / organic filler (Rohm and Haas Japan Co., Ltd., EXL-2655: core-shell type organic fine particles)
(6) Inorganic filler / silica filler (Admatex Co., SE2050, average particle size: 0.5 μm)
-Methacrylic surface-treated nano silica filler (Admatex Co., Ltd., YA050C-SM (hereinafter referred to as "SM nano silica"), average particle size: about 50 nm)

Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001

(フィルム状接着剤の作製)
 厚さ50μmの表面離型処理ポリエチレンテレフタレートフィルム(帝人フィルムソリューション株式会社製、商品名:テイジンテトロンフィルムA-63)上にワニスを塗工した。乾燥工程を経て、厚さ45μmのフィルム状接着剤を得た。
(Preparation of film adhesive)
A varnish was applied on a surface release-treated polyethylene terephthalate film (manufactured by Teijin Film Solutions Co., Ltd., trade name: Teijin Tetron Film A-63) having a thickness of 50 μm. After the drying step, a film adhesive having a thickness of 45 μm was obtained.

(半導体装置の製造)
 第一の部材としてのはんだバンプ付き半導体チップ(WALTS-TEG CC80(製品名)、株式会社ウォルツ製)を準備した。この半導体チップの構成は以下のとおりであった。
・チップサイズ:7.3mm×7.3mm×0.05mmt
・バンプ高さ:約45μm(銅ピラー及びはんだの高さの合計)
・バンプ数:1048ピン
・バンプピッチ:80μm
(Manufacturing of semiconductor devices)
A semiconductor chip with a solder bump (WALTS-TEG CC80 (product name), manufactured by Waltz Co., Ltd.) was prepared as a first member. The structure of this semiconductor chip was as follows.
-Chip size: 7.3 mm x 7.3 mm x 0.05 mmt
・ Bump height: approx. 45 μm (total height of copper pillar and solder)
・ Number of bumps: 1048 pins ・ Bump pitch: 80 μm

 作製したフィルム状接着剤を上記半導体チップと同じサイズ(7.3mm×7.3mm)に切り抜くことによって接着剤片を得た。この接着剤片を半導体チップの表面(はんだが形成されている側の面)にラミネートした。ラミネートは、真空ラミネータV130(ニッコー・マテリアルズ株式会社)を使用し、80℃/0.5MPa/60sの条件で実施した。 An adhesive piece was obtained by cutting the produced film-like adhesive into the same size as the semiconductor chip (7.3 mm × 7.3 mm). This adhesive piece was laminated on the surface of the semiconductor chip (the surface on which the solder was formed). The lamination was performed using a vacuum laminator V130 (Nikko Materials Co., Ltd.) under the conditions of 80 ° C./0.5 MPa / 60 s.

 第二の部材としての半導体チップ(WALTS-TEG IP80、株式会社ウォルツ製)を準備した。この半導体チップの構成は以下のとおりであった。
・チップサイズ:10mm×10mm×0.1mmt
・接続部を構成する金属:Ni/Au
A semiconductor chip (WALTS-TEG IP80, manufactured by Waltz Co., Ltd.) was prepared as a second member. The structure of this semiconductor chip was as follows.
・ Chip size: 10mm × 10mm × 0.1mmt
-Metal forming the connecting portion: Ni / Au

 半導体チップ(第二の部材)の接続部が形成されている側の面上に、この面と接着剤片が接するように、はんだバンプ付き半導体チップを載せた。そして、圧着装置(FCB3、パナソニック株式会社製)を使用して仮圧着工程を実施した後、レーザーボンダ(FDB250、澁谷工業株式会社製)を使用して圧着工程を実施した。仮圧着工程は80℃/25N/1sの条件で実施した。圧着工程は以下の条件で実施した。
・圧着圧力:30N
・圧着時間:1秒
・レーザー照射パターン:図6(a)(エリア1,3,5,7にレーザーを照射した。)
・レーザー照射時間:1秒
・エリア1,3,5,7の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Tc:235℃
・エリア2,4,6,8の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Ts:205℃
・エリア9の中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の温度T9:204℃
・温度差(Tc-Ts):30℃
・温度差(Ts-T9):1℃
The semiconductor chip with solder bumps was placed on the surface of the semiconductor chip (second member) on the side where the connection portion was formed such that the adhesive piece was in contact with this surface. Then, after performing a temporary pressure bonding step using a pressure bonding device (FCB3, manufactured by Panasonic Corporation), a pressure bonding step was performed using a laser bonder (FDB250, manufactured by Shibuya Industry Co., Ltd.). The temporary pressure bonding step was carried out under the condition of 80 ° C./25 N / 1 s. The crimping process was performed under the following conditions.
・ Crimping pressure: 30N
-Pressing time: 1 second-Laser irradiation pattern: Fig. 6 (a) (areas 1, 3, 5, 7 were irradiated with laser)
・ Laser irradiation time: 1 second ・ Average temperature of bonding tool surface (outer surface of semiconductor chip with solder bumps) Tc: 235 ° C. at each center of areas 1, 3, 5, 7
-Average temperature Ts of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) Ts: 205 ° C at the center of each of the areas 2, 4, 6, 8
-Temperature of bonding tool surface (outer surface of semiconductor chip with solder bumps) T9: 204 ° C in the center of area 9
・ Temperature difference (Tc-Ts): 30 ℃
・ Temperature difference (Ts-T9): 1 ° C

 圧着工程後、加圧オーブン装置(VSU28、株式会社シンアペックス製)を使用し、175℃/10min/0.4MPa及び昇温速度20℃/minの条件でキュア工程を実施した。このキュア工程を経て本実施例に係る半導体装置を得た。 After the crimping process, a pressure oven device (VSU28, manufactured by Shin Apex Co., Ltd.) was used to perform the curing process under the conditions of 175 ° C./10 min / 0.4 MPa and a heating rate of 20 ° C./min. A semiconductor device according to this example was obtained through this curing process.

<実施例2>
 圧着工程を以下の条件で実施したことの他は、実施例1と同様にして半導体装置を作製した。
・圧着圧力:30N
・圧着時間:3秒
・レーザー照射パターン:図6(a)(実施例1よりも弱い強度のレーザーを照射した。)
・レーザー照射時間:3秒
・エリア1,3,5,7の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Tc:225℃
・エリア2,4,6,8の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Ts:200℃
・エリア9の中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の温度T9:200℃
・温度差(Tc-Ts):25℃
・温度差(Ts-T9):0℃
<Example 2>
A semiconductor device was manufactured in the same manner as in Example 1 except that the pressure bonding step was performed under the following conditions.
・ Crimping pressure: 30N
-Crimping time: 3 seconds-Laser irradiation pattern: Fig. 6 (a) (irradiated with a laser having a weaker intensity than in Example 1).
-Laser irradiation time: 3 seconds-Average temperature Tc of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at each center of areas 1, 3, 5, and 7: 225 ° C
-Average temperature Ts of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at the center of each of the areas 2, 4, 6 and 8: 200 ° C
-Temperature T9 of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) in the center of area 9: 200 ° C
・ Temperature difference (Tc-Ts): 25 ° C
・ Temperature difference (Ts-T9): 0 ° C

<比較例1>
 圧着工程を以下の条件で実施したことの他は、実施例1と同様にして半導体装置を作製した。
・圧着圧力:30N
・圧着時間:1秒
・レーザー照射パターン:図6(b)(エリア1,3,5,7にレーザーを照射するとともに、このレーザーよりも弱い強度のレーザーをエリア2,4,6,8に照射した。)
・レーザー照射時間:1秒
・エリア1,3,5,7の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Tc:225℃
・エリア2,4,6,8の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Ts:215℃
・温度差(Tc-Ts):10℃
<Comparative Example 1>
A semiconductor device was manufactured in the same manner as in Example 1 except that the pressure bonding step was performed under the following conditions.
・ Crimping pressure: 30N
・ Crimping time: 1 second ・ Laser irradiation pattern: Fig. 6 (b) (Areas 1, 3, 5, 7 are irradiated with a laser, and a laser having a weaker intensity than this laser is irradiated in areas 2, 4, 6, 8) It was irradiated.)
-Laser irradiation time: 1 second-Average temperature Tc of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at the center of each of areas 1, 3, 5, and 7: 225 ° C
-Average temperature Ts of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at the center of each of the areas 2, 4, 6 and 8: 215 ° C
・ Temperature difference (Tc-Ts): 10 ℃

<比較例2>
 圧着工程を以下の条件で実施したことの他は、実施例2と同様にして半導体装置を作製した。
・圧着圧力:30N
・圧着時間:3秒
・レーザー照射パターン:図6(b)(比較例1よりも弱い強度のレーザーを照射した。)
・レーザー照射時間:3秒
・エリア1,3,5,7の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Tc:210℃
・エリア2,4,6,8の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Ts:205℃
・温度差(Tc-Ts):5℃
<Comparative example 2>
A semiconductor device was manufactured in the same manner as in Example 2 except that the pressure bonding step was performed under the following conditions.
・ Crimping pressure: 30N
-Pressing time: 3 seconds-Laser irradiation pattern: Fig. 6 (b) (irradiated with a laser having a weaker intensity than in Comparative Example 1).
-Laser irradiation time: 3 seconds-Average temperature Tc of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at the center of each of areas 1, 3, 5, 7: 210 ° C
-Average temperature Ts of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) Ts: 205 ° C at the center of each of the areas 2, 4, 6, 8
・ Temperature difference (Tc-Ts): 5 ℃

<実施例3>
 圧着工程を以下の条件で実施したことの他は、実施例1と同様にして半導体装置を作製した。なお、圧着工程後、加圧オーブン装置(PCOA-01、NTTアドバンステクノロジ株式会社製)を使用し、実施例1と同じ条件でキュア工程を実施した。
・圧着圧力:30N
・圧着時間:1秒
・レーザー照射パターン:図7(エリア1,3,5,7にレーザーを出力100%で照射し、エリア2,4,6,8の外側部分にレーザーを出力10%で照射した。)
・レーザー照射時間:1秒
・エリア1,3,5,7の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Tc:240℃
・エリア2,4,6,8の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Ts:211℃
・エリア9の中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の温度T9:205℃
・温度差(Tc-Ts):29℃
・温度差(Ts-T9):6℃
<Example 3>
A semiconductor device was manufactured in the same manner as in Example 1 except that the pressure bonding step was performed under the following conditions. After the pressure-bonding step, a curing oven was used under the same conditions as in Example 1 using a pressure oven device (PCOA-01, manufactured by NTT Advance Technology Co., Ltd.).
・ Crimping pressure: 30N
・ Crimping time: 1 second ・ Laser irradiation pattern: Fig. 7 (Areas 1, 3, 5, 7 are irradiated with a laser output of 100% and areas 2, 4, 6, 8 are irradiated with a laser of 10%. It was irradiated.)
-Laser irradiation time: 1 second-Average temperature Tc of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at each center of areas 1, 3, 5, 7: 240 ° C
・ Average temperature Ts of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at the center of each of the areas 2, 4, 6 and 8: 211 ° C.
・ Temperature of bonding tool surface (outer surface of semiconductor chip with solder bumps) T9: 205 ° C in the center of area 9
・ Temperature difference (Tc-Ts): 29 ℃
・ Temperature difference (Ts-T9): 6 ℃

<実施例4>
 圧着工程を以下の条件で実施したことの他は、実施例3と同様にして半導体装置を作製した。
・圧着圧力:30N
・圧着時間:3秒
・レーザー照射パターン:図7(実施例3よりも弱い強度のレーザーを照射した。)
・レーザー照射時間:3秒
・エリア1,3,5,7の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Tc:230℃
・エリア2,4,6,8の各中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の平均温度Ts:205℃
・エリア9の中心部におけるボンディングツール表面(はんだバンプ付き半導体チップの外表面)の温度T9:200℃
・温度差(Tc-Ts):20℃
・温度差(Ts-T9):5℃
<Example 4>
A semiconductor device was manufactured in the same manner as in Example 3 except that the pressure bonding step was performed under the following conditions.
・ Crimping pressure: 30N
-Pressing time: 3 seconds-Laser irradiation pattern: Fig. 7 (irradiated with a laser having a weaker intensity than in Example 3)
-Laser irradiation time: 3 seconds-Average temperature Tc of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at the center of each of areas 1, 3, 5 and 7: 230 ° C
-Average temperature Ts of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) Ts: 205 ° C at the center of each of the areas 2, 4, 6, 8
-Temperature T9 of the bonding tool surface (outer surface of the semiconductor chip with solder bumps) at the center of area 9: 200 ° C
・ Temperature difference (Tc-Ts): 20 ℃
・ Temperature difference (Ts-T9): 5 ℃

<半導体装置の評価>
 実施例及び比較例に係る半導体装置について以下の評価を行った。
<Evaluation of semiconductor device>
The following evaluations were performed on the semiconductor devices according to the examples and comparative examples.

(1)初期導通性の評価
 マルチメータ(R6871E、株式会社アドバンテスト製)を使用し、実施例及び比較例に係る半導体装置の初期接続抵抗値を測定し、初期導通性について評価を行った。評価基準は以下のとおりとした。表2及び表3に結果を示す。
 A:ペリフェラル部分の初期接続抵抗値が30~35Ωである。
 B:ペリフェラル部分の初期接続抵抗値が35Ω超である。
(1) Evaluation of Initial Conductivity Using a multimeter (R6871E, manufactured by Advantest Co., Ltd.), the initial connection resistance values of the semiconductor devices according to the examples and comparative examples were measured, and the initial conductivity was evaluated. The evaluation criteria are as follows. The results are shown in Tables 2 and 3.
A: The initial connection resistance value of the peripheral part is 30 to 35Ω.
B: The initial connection resistance value of the peripheral portion exceeds 35Ω.

(2)ボイド発生率の評価
 以下の方法により、実施例及び比較例に係る半導体装置のボイド発生率を評価した。まず、超音波映像診断装置(Insight-300、インサイト株式会社製)を使用し、実施例及び比較例に係る半導体装置の外観画像を撮影した。スキャナ(GT-9300UF、EPSON株式会社製)で半導体チップ上の接着剤層の画像を取り込んだ。この画像を画像処理ソフト(Adobe Photoshop(登録商標)、アドビシステムズ株式会社)によって色調補正及び二階調化することによってボイド部分を識別し、ヒストグラムによりボイド部分の占める割合を算出した。評価基準は以下のとおりとした。表2及び表3に結果を示す。
 A:半導体チップ上の接着剤部分の面積を基準として、ボイド部分の占める割合が5%以下である。
 B:半導体チップ上の接着剤部分の面積を基準として、ボイド部分の占める割合が5%超である。
(2) Evaluation of void occurrence rate The void occurrence rates of the semiconductor devices according to the examples and comparative examples were evaluated by the following method. First, an ultrasonic image diagnostic apparatus (Insight-300, manufactured by Insight Co., Ltd.) was used to take external images of the semiconductor devices according to the examples and comparative examples. An image of the adhesive layer on the semiconductor chip was captured with a scanner (GT-9300UF, manufactured by EPSON Corporation). This image was subjected to color tone correction and two-gradation conversion by image processing software (Adobe Photoshop (registered trademark), Adobe Systems Incorporated) to identify the void portion, and the ratio of the void portion to the histogram was calculated. The evaluation criteria are as follows. The results are shown in Tables 2 and 3.
A: The ratio of the void portion is 5% or less based on the area of the adhesive portion on the semiconductor chip.
B: Based on the area of the adhesive portion on the semiconductor chip, the proportion of the void portion is more than 5%.

(3)フィレット幅の評価
 実施例及び比較例に係る半導体装置をデジタルマイクロスコープ(VHX-5000、株式会社キーエンス製)を用いて上面から観察した。そして、正方形の半導体チップからはみ出している部分(フィレット)の最大値を測定した。半導体チップの四つの辺についてフィレット幅の最大値をそれぞれ測定し、その平均値をフィレット幅とした。表2及び表3に結果を示す。
(3) Evaluation of Fillet Width The semiconductor devices according to the examples and the comparative examples were observed from above using a digital microscope (VHX-5000, manufactured by Keyence Corporation). Then, the maximum value of the portion (fillet) protruding from the square semiconductor chip was measured. The maximum value of the fillet width was measured for each of the four sides of the semiconductor chip, and the average value was used as the fillet width. The results are shown in Tables 2 and 3.

(4)カバレッジの評価
 実施例及び比較例に係る半導体装置をデジタルマイクロスコープ(VHX-5000、株式会社キーエンス製)を用いて上面から観察した。そして、正方形の半導体チップからはみ出している部分(フィレット)の幅であって、半導体チップの角から200μmの位置の二点における幅(カバレッジ)を測定した(図4参照)。半導体チップの四つの角について計八点のカバレッジを測定し、その平均値を算出した。表2及び表3に結果を示す。なお、表2,3に記載の「カバレッジ指数」はカバレッジ(平均値)をフィレット幅(平均値)で除すことによって算出された値である。表中の「-」は未測定であることを意味する。
(4) Evaluation of Coverage The semiconductor devices according to the examples and comparative examples were observed from above using a digital microscope (VHX-5000, manufactured by Keyence Corporation). Then, the width (coverage) of a portion (fillet) protruding from the square semiconductor chip at two points at a position of 200 μm from the corner of the semiconductor chip was measured (see FIG. 4). Eight points of coverage were measured for the four corners of the semiconductor chip, and the average value was calculated. The results are shown in Tables 2 and 3. The "coverage index" shown in Tables 2 and 3 is a value calculated by dividing the coverage (average value) by the fillet width (average value). "-" In the table means not measured.

Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002

Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000003

 本開示によれば、半導体チップの辺におけるフィレットが小さく且つカバレッジが確保された半導体装置及びその製造方法が提供される。 According to the present disclosure, there is provided a semiconductor device in which the fillet on the side of the semiconductor chip is small and coverage is secured, and a manufacturing method thereof.

1~9…エリア、10…半導体チップ(第一の部材)、10a…銅ピラー(第一の接続部)、10b…はんだバンプ(第一の接続部)、11~13…半導体チップ、20…基板(第二の部材)、20a…配線(第二の接続部)、30…接着剤層、40…積層体、50,70…半導体装置、60…インタポーザー(第二の部材)、A1…レーザー照射部、A2…レーザー非照射部、C…隅部、F…押圧力、L…レーザー、S…辺、Sa…一端、Sb…他端 1 to 9 ... Area, 10 ... Semiconductor chip (first member), 10a ... Copper pillar (first connection part), 10b ... Solder bump (first connection part), 11 to 13 ... Semiconductor chip, 20 ... Substrate (second member), 20a ... Wiring (second connecting portion), 30 ... Adhesive layer, 40 ... Laminated body, 50, 70 ... Semiconductor device, 60 ... Interposer (second member), A1 ... Laser irradiation part, A2 ... Laser non-irradiation part, C ... Corner part, F ... Pressing force, L ... Laser, S ... Side, Sa ... One end, Sb ... Other end

Claims (9)

 第一の接続部を有し且つ直線状に延びる辺を有する第一の部材と、
 第二の接続部を有する第二の部材と、
 前記第一の部材と前記第二の部材との間に配置された接着剤層とを備え、
 前記第一の接続部と前記第二の接続部が電気的に接続されている半導体装置の製造方法であって、
 前記第一の部材、前記接着剤層及び前記第二の部材がこの順序で積層された積層体を準備する積層工程と、
 前記積層体に対して厚さ方向に押圧力を加えた状態で、前記積層体に対して加熱のためのレーザーを照射する圧着工程と、
を含み、
 前記圧着工程において、前記第一の部材の前記辺の一端の周縁部から他端の周縁部に向けて、レーザー照射部、レーザー非照射部及びレーザー照射部がこの順序で形成されるように、前記積層体に対してレーザーを照射する、半導体装置の製造方法。
A first member having a first connecting portion and having a linearly extending side;
A second member having a second connecting portion,
An adhesive layer disposed between the first member and the second member,
A method of manufacturing a semiconductor device, wherein the first connecting portion and the second connecting portion are electrically connected,
A laminating step of preparing a laminated body in which the first member, the adhesive layer and the second member are laminated in this order;
A pressing step of irradiating the laminated body with a laser for heating while pressing force is applied to the laminated body in the thickness direction,
Including,
In the crimping step, the laser irradiation portion, the laser non-irradiation portion, and the laser irradiation portion are formed in this order from the peripheral edge portion of the one end of the first member toward the peripheral edge portion of the other end, A method of manufacturing a semiconductor device, which comprises irradiating a laser beam onto the stacked body.
 前記第一の部材が正方形又は長方形の形状を有する半導体チップである、請求項1に記載の半導体装置の製造方法。 The method for manufacturing a semiconductor device according to claim 1, wherein the first member is a semiconductor chip having a square or rectangular shape.  第一の接続部を有し且つ直線状に延びる辺を有する第一の部材と、
 第二の接続部を有する第二の部材と、
 前記第一の部材と前記第二の部材との間に配置された接着剤層とを備え、
 前記第一の接続部と前記第二の接続部が電気的に接続されている半導体装置の製造方法であって、
 前記第一の部材、前記接着剤層及び前記第二の部材がこの順序で積層された積層体を準備する積層工程と、
 前記積層体に対して厚さ方向に押圧力を加えた状態で、前記積層体に対して熱を加える圧着工程と、
を含み、
 前記第一の部材が正方形又は長方形の形状を有する半導体チップであり、
 前記圧着工程において、以下の条件1を満たすように、前記積層体に対して熱を加える、半導体装置の製造方法。
<条件1>
 前記半導体チップの辺を三等分して計九つのエリアに分割し、当該九つのエリアのうち、前記半導体チップの一つの隅部を含むエリアをエリア1とし、前記エリア1から前記半導体チップの周縁部に沿って並ぶエリアをエリア2~8とすると、
 エリア1,3,5,7の各中心部における前記半導体チップの外表面の平均温度Tcと、
 エリア2,4,6,8の各中心部における前記半導体チップの外表面の平均温度Tsとの差(Tc-Ts)が15℃以上である。
A first member having a first connecting portion and having a linearly extending side;
A second member having a second connecting portion,
An adhesive layer disposed between the first member and the second member,
A method of manufacturing a semiconductor device, wherein the first connecting portion and the second connecting portion are electrically connected,
A laminating step of preparing a laminated body in which the first member, the adhesive layer and the second member are laminated in this order;
A pressure-bonding step of applying heat to the laminated body in a state in which a pressing force is applied to the laminated body in the thickness direction,
Including,
The first member is a semiconductor chip having a square or rectangular shape,
A method of manufacturing a semiconductor device, wherein heat is applied to the stacked body so as to satisfy the following Condition 1 in the pressure bonding step.
<Condition 1>
The side of the semiconductor chip is divided into three equal parts and divided into nine areas in total, and an area including one corner of the semiconductor chip is defined as an area 1 among the nine areas. If the areas lined up along the periphery are areas 2-8,
An average temperature Tc of the outer surface of the semiconductor chip at the center of each of the areas 1, 3, 5, 7;
The difference (Tc-Ts) from the average temperature Ts of the outer surface of the semiconductor chip at the central portions of the areas 2, 4, 6, and 8 is 15 ° C. or more.
 前記圧着工程において、以下の条件2を更に満たすように、前記積層体に対して熱を加える、請求項3に記載の半導体装置の製造方法。
<条件2>
 前記九つのエリアのうち、前記半導体チップの中心を含むエリアをエリア9とすると、
 エリア2,4,6,8の各中心部における前記半導体チップの外表面の平均温度Tsと、
 エリア9の中心部における前記半導体チップの外表面の温度T9との差(Ts-T9)が5℃以上である。
The method for manufacturing a semiconductor device according to claim 3, wherein in the pressure-bonding step, heat is applied to the stacked body so as to further satisfy the following Condition 2.
<Condition 2>
Of the nine areas, an area including the center of the semiconductor chip is an area 9,
An average temperature Ts of the outer surface of the semiconductor chip at the central portions of the areas 2, 4, 6, and 8,
The difference (Ts-T9) from the temperature T9 of the outer surface of the semiconductor chip in the central portion of the area 9 is 5 ° C. or more.
 前記第二の部材が配線基板、半導体チップ及び半導体ウエハからなる群から選ばれる部材である、請求項1~4のいずれか一項に記載の半導体装置の製造方法。 The method for manufacturing a semiconductor device according to claim 1, wherein the second member is a member selected from the group consisting of a wiring board, a semiconductor chip and a semiconductor wafer.  前記接着剤層が、重量平均分子量10000未満の熱硬化性樹脂と、硬化剤とを含有する、請求項1~5のいずれか一項に記載の半導体装置の製造方法。 6. The method for manufacturing a semiconductor device according to claim 1, wherein the adhesive layer contains a thermosetting resin having a weight average molecular weight of less than 10,000 and a curing agent.  前記接着剤層が、重量平均分子量10000以上の高分子成分を更に含有する、請求項6に記載の半導体装置の製造方法。 The method for manufacturing a semiconductor device according to claim 6, wherein the adhesive layer further contains a polymer component having a weight average molecular weight of 10,000 or more.  前記接着剤層がフィルム状接着剤である、請求項1~7のいずれか一項に記載の半導体装置の製造方法。 The method for manufacturing a semiconductor device according to claim 1, wherein the adhesive layer is a film adhesive.  請求項1~8のいずれか一項に記載の半導体装置の製造方法によって製造された半導体装置。 A semiconductor device manufactured by the method for manufacturing a semiconductor device according to any one of claims 1 to 8.
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