WO2016158268A1 - 接着組成物シートおよびその製造方法ならびに半導体装置 - Google Patents
接着組成物シートおよびその製造方法ならびに半導体装置 Download PDFInfo
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- WO2016158268A1 WO2016158268A1 PCT/JP2016/057400 JP2016057400W WO2016158268A1 WO 2016158268 A1 WO2016158268 A1 WO 2016158268A1 JP 2016057400 W JP2016057400 W JP 2016057400W WO 2016158268 A1 WO2016158268 A1 WO 2016158268A1
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- adhesive composition
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- organic compound
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/04—Non-macromolecular additives inorganic
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J201/00—Adhesives based on unspecified macromolecular compounds
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/10—Adhesives in the form of films or foils without carriers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having at least one potential-jump barrier or surface barrier, e.g. PN junction, depletion layer or carrier concentration layer
- H01L21/50—Assembly of semiconductor devices using processes or apparatus not provided for in a single one of the subgroups H01L21/06 - H01L21/326, e.g. sealing of a cap to a base of a container
- H01L21/52—Mounting semiconductor bodies in containers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/34—Arrangements for cooling, heating, ventilating or temperature compensation ; Temperature sensing arrangements
- H01L23/36—Selection of materials, or shaping, to facilitate cooling or heating, e.g. heatsinks
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/326—Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/20—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive itself
- C09J2301/208—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive itself the adhesive layer being constituted by at least two or more adjacent or superposed adhesive layers, e.g. multilayer adhesive
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
- C09J2301/408—Additional features of adhesives in the form of films or foils characterized by the presence of essential components additives as essential feature of the adhesive layer
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2463/00—Presence of epoxy resin
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2479/00—Presence of polyamine or polyimide
- C09J2479/08—Presence of polyamine or polyimide polyimide
Definitions
- the present invention relates to an adhesive composition sheet that can be used for bonding an electronic component such as a semiconductor chip and a heat radiator such as a wiring board, a heat spreader, or a heat sink, or bonding electronic components.
- Power semiconductors are mainly used for power control of hybrid vehicles and electric vehicles, and home appliances such as air conditioners with large power consumption.
- power semiconductors used in hybrid vehicles and electric vehicles have a large current capacity and a large amount of heat during use. Therefore, in order to prevent malfunction due to temperature rise, a cooling system with high heat dissipation is required. Heat generated in the power semiconductor is transferred to the heat sink through the heat spreader and cooled. Therefore, high thermal conductivity is required for the adhesive composition for bonding the heat spreader and the heat sink.
- an adhesive having a high thermal conductivity by highly filling alumina particles which are two or more types of high thermal conductive inorganic particles in a thermosetting resin such as an epoxy resin As a material used in the high thermal conductive adhesive composition, an adhesive having a high thermal conductivity by highly filling alumina particles which are two or more types of high thermal conductive inorganic particles in a thermosetting resin such as an epoxy resin.
- a composition has been proposed (see, for example, Patent Document 1).
- an adhesive composition containing a polyimide resin which has improved thermal conductivity, insulation and heat resistance by the addition of inorganic particles with high heat dissipation (see, for example, Patent Document 2).
- the adhesive composition which improved heat dissipation is proposed by adding the aluminum nitride which is highly heat conductive inorganic particle to resin (for example, refer patent document 3).
- An object of this invention is to provide the adhesive composition sheet with favorable heat conductivity of the film thickness direction after hardening.
- the present invention is an adhesive composition sheet containing an organic compound and inorganic particles, and the adhesive composition sheet is formed by laminating at least an A layer containing an organic compound and a B layer containing an organic compound and inorganic particles.
- the organic compound content of layer A is greater than the organic compound content of layer B, and the layer A and / or layer B contains thermally conductive inorganic particles having an anisotropic shape. It is an adhesive composition sheet.
- the present invention includes an adhesive composition sheet having a layer configuration of three or more layers in which the A layer and the B layer are alternately stacked.
- the present invention includes a semiconductor device including a cured product of the above adhesive composition sheet.
- the present invention is a method for manufacturing a semiconductor device including a step of bonding an electronic component and a heat radiator, or electronic components to each other via an adhesive composition sheet, and a step of curing the adhesive composition sheet.
- the adhesive composition sheet includes at least an A layer containing an organic compound and a B layer containing an organic compound and inorganic particles, and the organic compound content of the A layer is greater than the organic compound content of the B layer.
- the adhesive composition sheet of the present invention is an adhesive composition sheet containing an organic compound and inorganic particles, and the adhesive composition sheet comprises at least an A layer containing an organic compound and B containing an organic compound and inorganic particles.
- the layer A includes a layered structure, the organic compound content of the A layer is greater than the organic compound content of the B layer, and the A layer and / or the B layer has an anisotropic shape. Contains inorganic particles.
- the adhesive composition sheet may be a two-layer sheet in which the A layer and the B layer are laminated one by one, or a sheet having a total of three or more layers in which the A layer and the B layer are alternately laminated.
- a structure in which one A layer is stacked on both sides of the B layer may be used, or a structure in which one B layer is stacked on both sides of the A layer may be used.
- a multilayer structure may be used.
- the adhesive composition sheet of the present invention When the adhesive composition sheet of the present invention becomes a cured product, it exhibits better thermal conductivity in the film thickness direction than a conventional adhesive composition sheet. The reason is not clear, but the following reasons are possible.
- the thermal conductivity In the cured product of the adhesive composition sheet, heat flows fast inside the inorganic particles but slowly inside the organic compound. Therefore, the greater the proportion of the path through which heat is transferred occupied in the inorganic particles, the better the thermal conductivity.
- the adhesive composition sheet of the present invention when adhering objects to be bonded using the adhesive composition sheet of the present invention, when the adhesive composition sheet is interposed between the objects to be bonded and heated and / or pressurized, in the adhesive composition sheet, The organic compound diffuses from the A layer having a high organic compound content to the B layer having a low organic compound content. At this time, the thermally conductive inorganic particles having an anisotropic shape in the A layer and / or the B layer move with the flow of the organic compound and are oriented in the film thickness direction of the sheet.
- the thermal conductivity in the film thickness direction of the cured product of the adhesive composition sheet is improved.
- the thermally conductive inorganic particles are inorganic particles made of a material having high thermal conductivity such as carbon nanotube, boron nitride, aluminum nitride, silicon carbide, aluminum oxide. These inorganic particles have a thermal conductivity of about 3000 W / m ⁇ K for carbon nanotubes, about 40 W / m ⁇ K for boron nitride, 170 W / m ⁇ K for aluminum nitride, and 50 W / m for silicon carbide at a temperature of 30 ° C. -About K and aluminum oxide are about 20 W / m.K. These are very large values compared with the thermal conductivity of 0.1 to 0.3 W / m ⁇ K of general organic compounds.
- anisotropic inorganic particles are those in which the size of one direction of the inorganic particles is larger than the size of any other direction.
- the anisotropically shaped inorganic particles have a lengthwise dimension that is at least twice as large as the dimension in a cross section perpendicular to the lengthwise direction, and preferably at least four times and at most 500 times.
- the length direction means a direction in which the diameter of the particle is maximized.
- the dimension in the cross section perpendicular to the length direction means that the cross section includes the smallest circular shape including all of the cross section, a part of the cross section, and does not include a part other than the cross section. The largest circle among the circles is obtained and set as the average value of the diameters of these two circles.
- the anisotropic shape may be any of an elliptical shape, a scale shape, a crushed shape, a fibrous shape, and the like. Fibrous inorganic particles are particularly preferable because they have a large dimensional ratio with the cross section perpendicular to the length direction.
- anisotropic inorganic particles include carbon nanotubes, boron nitride nanotubes, scaly boron nitride, aluminum nitride whiskers, silicon carbide whiskers, and aluminum oxide whiskers.
- inorganic particles selected from carbon nanotubes and aluminum nitride whiskers are more preferable because they have high thermal conductivity and a large dimensional ratio between the fiber and the cross section perpendicular to the length direction.
- the inorganic particles may be in the form of a tube having a hollow inside.
- the inorganic particles in the adhesive composition paste are pulled in the application direction.
- the direction in which the dimension is large (hereinafter referred to as the length direction) tends to be oriented in a direction parallel to the surface of the sheet.
- the inorganic particles having an anisotropic shape are contained, it is difficult to form a heat conduction path in the film thickness direction of the sheet.
- the inorganic particles move in the thickness direction of the sheet with the flow of the organic compound diffusing from the A layer to the B layer.
- the film is oriented in the thickness direction of the sheet. Therefore, in the present invention, by using inorganic particles having an anisotropic shape, many heat conduction paths are formed in the film thickness direction of the adhesive composition sheet, so the film thickness direction of the cured product of the adhesive composition sheet. It is thought that the thermal conductivity to
- the cured product of the adhesive composition sheet of the present invention exhibits good thermal conductivity in the film thickness direction as described above, even if the content of inorganic particles is reduced as compared with the conventional adhesive composition sheet. It becomes possible to design the thermal conductivity in the film thickness direction equally. If the content of the inorganic particles can be reduced, the adhesiveness of the adhesive composition sheet and the toughness, transparency and insulation of the cured product of the adhesive composition sheet will be good. It is preferable that the adhesive composition sheet has high transparency because, when used for three-dimensional mounting in which semiconductor chips are stacked, alignment marks formed on the semiconductor chip through the adhesive composition sheet can be easily recognized.
- the anisotropic shaped inorganic particles may be contained in either the A layer or the B layer, or may be contained in both. As described above, the anisotropic shaped inorganic particles move in the thickness direction of the sheet with the flow of the organic compound from the A layer to the B layer. At this time, since the anisotropic shaped inorganic particles present in the A layer move a longer distance than the anisotropic shaped inorganic particles present in the B layer, the degree of orientation in the film thickness direction of the sheet becomes higher. Therefore, when the layer A contains anisotropic shaped inorganic particles, many heat conduction paths are formed in the film thickness direction of the adhesive composition sheet, and the heat conductivity in the film thickness direction becomes good. It is particularly preferable that at least the A layer contains inorganic particles having an anisotropic shape.
- Examples of the organic compound used for the A layer and the B layer include an epoxy compound, an imide compound, a urethane compound, and an acrylic compound.
- the cured product of the adhesive composition sheet of the present invention forms a rigid internal structure.
- the naphthalene skeleton epoxy compound include Epicron (registered trademark) HP-4032 and HP-4700 (trade names, manufactured by DIC Corporation).
- the anthracene skeleton epoxy compound include jER (registered trademark) YX8800 (trade name, manufactured by Mitsubishi Chemical Corporation).
- imide compounds examples include polyimide. Moreover, a polyurethane is mentioned as a urethane compound.
- the acrylic compound include acrylonitrile-butadiene copolymer (NBR), acrylonitrile-butadiene-methacrylic acid copolymer, and acrylonitrile-butadiene-acrylic acid copolymer.
- thermoplastic resin examples include imide compounds, urethane compounds, acrylic compounds, phenoxy resins, polyesters, polyamides, polypropylenes, styrene-butadiene copolymers (SBR), and the like.
- the organic compound used for the A layer and the organic compound used for the B layer may be the same or different.
- the content rate of the organic compound in A layer is 60 volume% or more and 100 volume% or less.
- the lower limit of the content is more preferably 70% by volume or more.
- the upper limit of the content is more preferably 99.8% by volume or less, and further preferably 99% by volume or less.
- the organic compound easily diffuses from the A layer to the B layer when the adhesive composition sheet is used, so the anisotropic present in the A layer and / or the B layer.
- Inorganic particles having a characteristic shape are also preferable because they are easy to move along with the flow of the organic compound, easily oriented in the film thickness direction, and improve the thermal conductivity in the film thickness direction of the cured product of the adhesive composition sheet.
- the adhesiveness of an adhesive composition sheet and a bonding target object improves and the reliability of a semiconductor device increases, it is preferable.
- the content of the organic compound is 99.8% by volume or less, since the inorganic particles are sufficiently connected when the adhesive composition sheet is used, the thermal conductivity of the cured product of the adhesive composition sheet is low. Since it improves, it is more preferable.
- the method for obtaining the organic compound content is as follows. First, the weight fraction of each component constituting the A layer is determined. For example, when the A layer is composed of three components, component A, component B, and component C, the weight fractions are Aw, Bw, and Cw, respectively. Next, the specific gravity of each component is obtained. The specific gravities of component A, component B, and component C are a, b, and c, respectively. A value obtained by dividing the weight fraction of each component by the specific gravity of the component, Aw / a, Bw / b, and Cw / c is the volume ratio of each component.
- the organic compound content (volume%) is (Aw / a) / ((Aw / a) + (Bw / b) + (Cw / c)) ⁇ 100.
- the content rate of the organic compound in B layer is 1 volume% or more and 40 volume% or less.
- the lower limit of the content is more preferably 5% by volume or more, and further preferably 10% by volume or more.
- the upper limit of the content is more preferably 30% by volume or less. It is preferable that the content of the organic compound is 1% by volume or more because the strength of the B layer is sufficient and the occurrence of cracks is suppressed. Moreover, since the adhesiveness of an adhesive composition sheet and a bonding target object improves and the reliability of a semiconductor device increases, it is preferable.
- the organic compound content is 40% by volume or less
- the organic compound easily diffuses from the A layer to the B layer when the adhesive composition sheet is used, so the A layer and / or the B layer.
- the inorganic particles having an anisotropic shape existing in the film are easily moved along with the flow of the organic compound, easily oriented in the film thickness direction, and the thermal conductivity in the film thickness direction of the cured product of the adhesive composition sheet is improved. .
- the content of the organic compound in the entire adhesive composition sheet including the A layer and the B layer is preferably 20% by volume or more and 60% by volume or less.
- the lower limit of the content is more preferably 25% by volume or more.
- the upper limit of the content is more preferably 50% by volume or less.
- the content is 20% by volume or more, film thickness unevenness, pinholes, cracks and the like are reduced, which is preferable.
- seat and an adhesion target object improves, the reliability of the semiconductor device using this increases, and it is preferable.
- the content is 60% by volume or less, the thermal conductivity of the cured product of the adhesive composition sheet is improved, and the linear expansion coefficient is lowered. Therefore, the reliability of the semiconductor device manufactured using this is improved. Is preferable.
- it is more preferable that the content is 25% by volume or more and 50% by volume or less because these effects are further enhanced.
- the A layer and / or the B layer contain inorganic particles having an anisotropic shape, but spherical inorganic particles may be used in combination.
- one of the layers may include both anisotropic shaped inorganic particles and spherical inorganic particles.
- either one of the layers may include anisotropic shaped inorganic particles, and the other layer may include spherical inorganic particles.
- the anisotropic shaped inorganic particles present in the A layer are more easily oriented in the film thickness direction of the sheet. Therefore, in the A layer, the anisotropic shaped inorganic particles are preferable as the inorganic particles. Even when anisotropically shaped inorganic particles and spherical inorganic particles are used in combination, it is preferable that the proportion of anisotropically shaped inorganic particles is large. Specifically, it is preferable that the content of the inorganic particles having an anisotropic shape is 60% by volume or more with respect to the total amount of the inorganic particles. The content of the anisotropic shaped inorganic particles is more preferably 80% by volume or more, and further preferably 90% by volume or more.
- the content rate of a spherical inorganic particle is 40 volume% or less with respect to the whole quantity of an inorganic particle, It is more preferable that it is 20 volume% or less, It is further more preferable that it is 10 volume% or less.
- the content of inorganic particles is higher than that in the A layer, spherical inorganic particles having excellent dispersibility are preferable. Even when anisotropically shaped inorganic particles and spherical inorganic particles are used in combination, it is preferable that the proportion of spherical inorganic particles is large.
- the content of spherical inorganic particles is preferably 60% by volume or more with respect to the total amount of inorganic particles. More preferably, the content of the spherical inorganic particles is more preferably 70% by volume or more, and further preferably 80% by volume or more.
- the content of anisotropic shaped inorganic particles is preferably 40% by volume or less, more preferably 30% by volume or less, and 20% by volume or less based on the total amount of inorganic particles. Further preferred.
- inorganic particles such as silicon oxide, titanium oxide, magnesium oxide, barium sulfate, and glass, in addition to the above heat conductive inorganic particles, within a range that does not impair the effects of the present invention. It may contain. When a plurality of types of inorganic particles are used, each particle can be identified by elemental analysis using EPMA.
- the maximum particle size of the inorganic particles is preferably 5 to 100 ⁇ m. Further, the lower limit of the maximum particle diameter is more preferably 10 ⁇ m or more. The upper limit of the maximum particle diameter is more preferably 50 ⁇ m or less.
- the maximum particle size of the inorganic particles is 5 ⁇ m or more, a heat conduction path is formed in which the large particles are connected inside the adhesive composition sheet. Therefore, the interface between the particles in the heat conduction path is smaller than in the case of small particles. This is preferable because the thermal conductivity of the cured product of the adhesive composition sheet is improved.
- the maximum particle size of the inorganic particles is 100 ⁇ m or less, the film thickness unevenness of the adhesive composition sheet is reduced, and thus the adhesiveness between the adhesive composition sheet and the object to be bonded is improved, and the reliability of the semiconductor device is increased. preferable.
- the inorganic particles preferably have a maximum particle size of 5 to 100 ⁇ m.
- particles having a small particle size also contain particles having a small particle size in the gap formed on the side of contact with the large particles. Since the heat conduction path by the inorganic particles is increased by entering, the heat conductivity of the cured product of the adhesive composition sheet is improved, which is preferable.
- the method of observing an inorganic particle directly with an optical microscope is mentioned for the measurement of the particle diameter of an inorganic particle. Or it can carry out by the optical microscope or the scanning electron microscope observation with respect to the cross section of the hardened
- the cross section of the cured product is preferably cut out using a cross section preparation apparatus using an ion beam or the like.
- the surface of the inorganic particles is modified with a compound such as a silane coupling agent
- the dispersibility of the inorganic particles in the adhesive composition sheet is preferably increased.
- the surface being modified with a specific compound means that the compound is bonded to atoms on the particle surface by a covalent bond or an ionic bond in a part or all of the particle surface.
- the silane coupling agent described below a hydroxyl group on the particle surface and a silanol group of the silane coupling agent form a covalent bond by dehydration condensation.
- silane coupling agent examples include vinyltrimethoxysilane, vinyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-acryloxypropyltrimethoxysilane, 3-acrylicsilane.
- the content of inorganic particles in the A layer is preferably 0% by volume or more and 40% by volume or less. Moreover, as a minimum of a content rate, it is more preferable that it is 0.2 volume% or more, and it is further more preferable that it is 1 volume% or more. The upper limit of the content is more preferably 30% by volume or less. When the content is 0.2% by volume or more, the inorganic particles are sufficiently connected when the adhesive composition sheet is used, so that the thermal conductivity of the cured product of the adhesive composition sheet is improved, which is preferable. Further, when the content is 40% by volume or less, the organic compound easily diffuses from the A layer to the B layer when the adhesive composition sheet is used, and therefore exists in the A layer and / or the B layer.
- Anisotropic inorganic particles are also preferable because they are easy to move with the flow of the organic compound, easily oriented in the film thickness direction, and improve the thermal conductivity in the film thickness direction of the cured product of the adhesive composition sheet. Moreover, since the adhesiveness of an adhesive composition sheet and a bonding target object improves and the reliability of a semiconductor device increases, it is preferable.
- the content of inorganic particles is preferably 60% by volume or more and 99% by volume or less.
- content rate it is more preferred that it is 70 volume% or more.
- content rate it is more preferable that it is 95 volume% or less, and it is further more preferable that it is 90 volume% or less.
- the content is 60% by volume or more, the thermal conductivity of the cured product of the adhesive composition sheet is improved, which is preferable. Further, it is preferable that the content is 99% by volume or less because the strength of the B layer is sufficient and the occurrence of cracks is suppressed.
- the adhesiveness of an adhesive composition sheet and a bonding target object improves and the reliability of a semiconductor device increases, it is preferable.
- the content of inorganic particles in the entire adhesive composition sheet including the A layer and the B layer is preferably 40% by volume or more and 80% by volume or less. Moreover, as a minimum of a content rate, it is more preferable that it is 50 volume% or more. The upper limit of the content is more preferably 75% by volume or less.
- the content is 40% by volume or more, the thermal conductivity of the cured product of the adhesive composition sheet is improved, and the linear expansion coefficient is lowered, so that the reliability of a semiconductor device manufactured using the same is improved. This is preferable.
- the aggregation of inorganic particles in the adhesive composition sheet is reduced when the content is 80% by volume or less, film thickness unevenness, pinholes, cracks, and the like are reduced, which is preferable.
- seat and an adhesion target object improves, the reliability of the semiconductor device using this increases, and it is preferable. It is more preferable that the content is 50% by volume or more and 75% by volume or less because these effects are further enhanced.
- the thermal conductivity in the film thickness direction of the cured product of the adhesive composition sheet is improved.
- the adhesiveness of an adhesive composition sheet and a bonding target object improves that the thickness of A layer is 5 micrometers or more, it is preferable. As a result, the reliability of the semiconductor device using this increases.
- the thickness of the A layer is 80 ⁇ m or less, since the inorganic particles are sufficiently connected when the adhesive composition sheet is used, it is preferable because the thermal conductivity of the cured product of the adhesive composition sheet is improved.
- the thickness of the B layer is 300 ⁇ m or less, a sufficient amount of the organic compound diffuses from the A layer to the B layer when the adhesive composition sheet is used, so that the inorganic particles present in the B layer are organic compounds. Since it moves with flow and becomes easy to be arranged and oriented in the film thickness direction, it is preferable because the thermal conductivity in the film thickness direction of the cured product of the adhesive composition sheet is improved. Moreover, since the adhesiveness of an adhesive composition sheet and a bonding target object improves that the thickness of B layer is 300 micrometers or less, it is preferable. As a result, the reliability of the semiconductor device using this increases.
- the total thickness of the adhesive composition sheet including the A layer and the B layer of the present invention is preferably 30 ⁇ m or more and 500 ⁇ m or less.
- the lower limit of the thickness is more preferably 50 ⁇ m or more, and further preferably 80 ⁇ m or more.
- an upper limit of thickness it is more preferable that it is 350 micrometers or less, and it is further more preferable that it is 250 micrometers or less.
- the thickness is 30 ⁇ m or more, the film thickness unevenness and pinholes of the adhesive composition sheet are reduced, and the adhesion between the adhesive composition sheet and the object to be bonded is improved.
- the thickness is 30 ⁇ m or more because the insulating property of the adhesive composition sheet is increased, and the reliability of the semiconductor device is increased.
- the thickness is 500 ⁇ m or less, the thermal resistance due to the adhesive composition sheet is reduced, so that the temperature rise of the semiconductor device is suppressed, and the reliability of the semiconductor device is increased.
- the adhesive composition sheet of the present invention can be cured by heating or ultraviolet irradiation after being bonded to an object to be bonded.
- a hardening accelerator in A layer and / or B layer.
- a hardening accelerator may be contained in both A layer and B layer, and may be contained only in one side.
- the hardening accelerator of A layer and the hardening accelerator of B layer may be respectively the same, and may differ.
- the curing accelerator examples include a microcapsule type curing accelerator, an imidazole curing accelerator, an amine curing accelerator, a phosphine curing accelerator, a phosphonium curing accelerator, a sulfonium curing accelerator, and an iodonium curing accelerator. Can be mentioned.
- microcapsule type curing accelerator examples include NOVACURE (registered trademark) HX-3941HP, HX-3922HP, HX-3932HP, HX-3042HP (the above-mentioned product name, manufactured by Asahi Kasei E-Materials Co., Ltd.) and the like. .
- sulfonium-based curing accelerator examples include Sun-Aid (registered trademark) SI-100, SI-150, SI-180, SI-200, SI-B3, SI-B4 (trade names, Sanshin Chemical Industry Co., Ltd.) )).
- the adhesive composition sheet may contain other additives such as a surfactant and an ion scavenger as long as the effects of the present invention are not impaired.
- the material for forming the A layer will be described as layer forming paste A
- the material for forming the B layer will be described as layer forming paste B
- a sheet formed using the layer forming paste A will be described as a layer forming sheet A
- a sheet manufactured using the layer forming paste B will be described as a layer forming sheet B.
- a paste (layer forming paste A and layer forming paste B) for forming each of the A layer and the B layer is prepared by mixing a predetermined amount of an organic compound, inorganic particles, and a solvent.
- a surfactant, an ion scavenger and the like may be mixed as necessary.
- a planetary mixer, a homogenizer, a ball mill, a bead mill, or the like can be used.
- the inorganic particles may be powdery particles in which primary particles are aggregated, or a dispersion of inorganic particles may be used.
- the surface of the inorganic particles is modified with a compound such as a silane coupling agent
- a compound such as a silane coupling agent
- the following is performed. Powdered inorganic particles in which primary particles are aggregated and a solvent are mixed, and the aggregated inorganic particles are loosened or crushed by a dispersing device such as a planetary mixer, a homogenizer, a ball mill, or a bead mill and dispersed in the solvent.
- a compound such as a silane coupling agent for surface modification is mixed with the obtained dispersion of inorganic particles, and the surface of the inorganic particles is mixed with the compound by stirring at a temperature of 100 ° C. or less for several hours.
- a compound for surface modification may be mixed in a solvent in advance, and the dispersion treatment and the surface treatment of the inorganic particles may be performed simultaneously. It is also possible to mix other compounds such as a dispersant and an antifoaming agent.
- the surface-modified inorganic particle dispersion may be used as it is to produce a layer forming paste, or the solvent is removed from the dispersion using a rotary evaporator, and the resulting inorganic particle powder is obtained.
- the layer forming paste may be produced by using it.
- the layer forming sheet A and the layer forming sheet B are prepared from the layer forming pastes of the A layer and the B layer prepared as described above.
- Examples of the method for producing the layer forming sheet include a method of removing the volatile components such as a solvent after applying the above layer forming paste on a peelable substrate. Specifically, first, the layer forming paste is applied onto the peelable substrate using an apparatus such as a bar coater, screen printing, blade coater, die coater, or comma coater.
- an apparatus such as a bar coater, screen printing, blade coater, die coater, or comma coater.
- the peelable substrate polyethylene terephthalate film, polyethylene naphthalate film, polyester film, polyvinyl chloride film, polycarbonate film, polyimide film, polytetrafluoroethylene film and other fluororesin films, polyphenylene sulfide film, polypropylene film, polyethylene film
- Examples of methods for removing volatile components such as solvents include heating with an oven or hot plate, vacuum drying, heating with electromagnetic waves such as infrared rays and microwaves, and the like.
- heating with electromagnetic waves such as infrared rays and microwaves, and the like.
- bubbles are generated when the adhesive composition sheet is cured by further high-temperature heating after the semiconductor chip, the circuit board, the heat sink, etc. are adhered via the adhesive composition sheet. May occur and the adhesive strength may be reduced.
- the heating for removing the solvent is excessive, curing of the adhesive composition sheet proceeds and the adhesive strength may be reduced.
- the drying conditions are preferably a drying temperature of 50 to 150 ° C. and a drying time of 2 to 30 minutes.
- an adhesive composition sheet can be produced by bonding the obtained layer forming sheet A and layer forming sheet B together.
- a two-layer adhesive composition sheet is obtained by laminating each sheet one by one.
- seat of 3 or more layers can be produced by bonding each sheet
- the lamination of the layer forming sheet can be performed using a laminating apparatus such as a roll laminator or a vacuum laminator.
- a laminating apparatus such as a roll laminator or a vacuum laminator.
- an adhesive composition sheet in which a plurality of layer forming sheets are laminated may be prepared by performing a lump bonding in a state where the layer forming sheets of a plurality of A layers and B layers are alternately arranged. it can. Batch bonding can be performed using a hot press apparatus.
- the bonding conditions are preferably a temperature of 50 to 150 ° C. and a pressure of 0.1 to 10 MPa.
- the method of laminating layers by applying a layer forming paste to the surface of a layer that has already been formed the surface of the layer that has already been formed may be eroded by the solvent in the layer forming paste that is formed later. Therefore, the method of producing the adhesive composition sheet by bonding the layer forming sheet A and the layer forming sheet B is more preferable.
- the adhesive composition sheet of the present invention can be suitably used for manufacturing a semiconductor device.
- the semiconductor device referred to in the present invention refers to all devices that can function by utilizing the characteristics of semiconductor elements.
- An electro-optical device or a semiconductor circuit substrate in which a semiconductor element is connected to a substrate, a stack of a plurality of semiconductor elements, and an electronic device including these are all included in the semiconductor device.
- a semiconductor element refers to an electronic component such as a semiconductor chip, a diode, or a transistor using a semiconductor.
- the semiconductor device of the present invention includes a cured product of the adhesive composition sheet of the present invention. Specifically, a semiconductor device in which an electronic component and a heat radiating body or electronic components are bonded to each other through a cured product of an adhesive composition sheet can be given.
- the electronic component or heat radiator to be bonded is referred to as a bonding object.
- the adhesive composition sheet of the present invention formed on a peelable substrate is bonded to one adhesive object, and then the peelable substrate is removed, and then the other adhesive object is bonded to the adhesive composition sheet. Affix to the opposite side of.
- a method can be performed in which the adhesive composition sheet of the present invention is interposed between two objects to be bonded and bonded together.
- the bonding is preferably performed, for example, at a temperature of room temperature to 150 ° C. and a pressure of 0.01 MPa to 10 MPa using a heating press device or the like.
- the layer forming sheet A and the layer forming sheet B are sequentially bonded to the bonding surface of one bonding target object, or the layer forming paste A and the layer forming paste B are applied.
- the A layer and the B layer are sequentially laminated, and finally, the adhesive composition sheet of the present invention may be formed between the adhesion objects by a method of bonding the other adhesion object.
- the layer forming sheet A and the layer forming sheet B are arranged between the bonding objects, and then press bonding is performed in a lump including the bonding objects.
- the cured product of the adhesive composition sheet preferably has a thermal diffusivity in the thickness direction of 0.8 ⁇ 10 ⁇ 6 m 2 / s or more, and preferably 1.2 ⁇ 10 ⁇ 6 m 2 / s or more. More preferably, it is more preferably 1.5 ⁇ 10 ⁇ 6 m 2 / s or more.
- the thermal diffusivity in the thickness direction of the cured product of the adhesive composition sheet is 0.8 ⁇ 10 ⁇ 6 m 2 / s or more, the heat generated from the semiconductor chip can be efficiently conducted to the outside. Since the temperature rise of the chip is suppressed, a highly reliable semiconductor device without malfunction can be provided.
- the thermal diffusivity in the thickness direction of the cured product of the adhesive composition sheet was measured using a thermal diffusivity measuring device (for example, a laser flash method thermal diffusivity measuring device “LFA447”) using a test piece obtained by cutting the cured product into 1 cm ⁇ 1 cm. (Manufactured by Netch Co., Ltd.)).
- a thermal diffusivity measuring device for example, a laser flash method thermal diffusivity measuring device “LFA447”
- A Polyimide polyimide A Under a dry nitrogen stream, 4.82 g (0.0165 mol) of 1,3-bis (3-aminophenoxy) benzene (hereinafter referred to as APB-N), 3,3′-diamino-4,4′-dihydroxydiphenyl Sulfone (hereinafter referred to as ABPS) 3.08 g (0.011 mol), 1,3-bis (3-aminopropyl) tetramethyldisiloxane (hereinafter referred to as SiDA) 4.97 g (0.02 mol), Then, 0.47 g (0.005 mol) of aniline as a terminal blocking agent was dissolved in 130 g of N-methyl-2-pyrrolidone (hereinafter referred to as NMP).
- NMP N-methyl-2-pyrrolidone
- BSAA 2,2-bis ⁇ 4- (3,4-dicarboxyphenoxy) phenyl ⁇ propane dianhydride
- (D) Inorganic particle AlN whisker A Aluminum powder “TFG-A30P” (manufactured by Toyo Aluminum Co., Ltd.) was processed into a plate-like molded body having a thickness of 0.5 mm by press molding. Next, this molded body was heated to 600 ° C. under a vacuum atmosphere of 150 Pa, and then kept in a nitrogen atmosphere of 0.5 MPa for 30 minutes using high-purity nitrogen gas to be reacted. The obtained product was whisker-like and was confirmed to have an AlN crystal structure by measurement using an X-ray diffraction analyzer “D8 ADVANCE” (trade name, manufactured by Bruker).
- the dimension in the length direction (hereinafter referred to as dimension ratio) with respect to the dimension in the cross section perpendicular to the length direction of the AlN whisker was 100 times.
- the maximum particle size was 50 ⁇ m.
- Carbon nanotube A (Honjo Chemical Co., Ltd., abbreviated as CNT-A, dimensional ratio: 400 times, maximum particle size: 10 ⁇ m)
- MBN-010T (trade name, scaly boron nitride particles, manufactured by Mitsui Chemicals, dimensional ratio: 5 times, maximum particle size: 1 ⁇ m)
- XGP trade name, scaly boron nitride particles, manufactured by Denki Kagaku Kogyo Co., Ltd., dimensional ratio: 10 times, maximum particle size: 40 ⁇ m
- FAN-f05 (trade name, spherical aluminum nitride particles, manufactured by Furukawa Denshi Co., Ltd., dimensional ratio: 1 time, maximum particle size: 10 ⁇
- Example 1 Each of layer forming pastes A-1 and B-1 is peeled off on a 75 ⁇ m-thick release film “SR-1” (trade name, manufactured by Otsuki Kogyo Co., Ltd.) using a bar coater. And dried for 10 minutes at 100 ° C. in a drying oven to prepare a layer forming sheet A-1 and a layer forming sheet B-1.
- the coating thickness was adjusted so that the thickness of the adhesive composition sheet after drying was 30 ⁇ m for the layer forming sheet A-1 and 80 ⁇ m for the layer forming sheet B-1 as shown in Table 6.
- the layer forming sheet A-1 and the layer forming sheet B-1 are bonded together at a temperature of 80 ° C. using a vacuum laminator “VTM-200M” (manufactured by Takatori Co., Ltd.).
- VTM-200M vacuum laminator
- a product sheet was prepared.
- the adhesive composition sheet was cured by heating in an oven at 200 ° C. for 1 hour. The thermal diffusivity and withstand voltage of the cured product of the obtained adhesive composition sheet were evaluated. The results are shown in Table 6.
- Examples 2 to 57, Comparative Examples 1 and 2 Evaluation was performed in the same manner as in Example 1 except that the type of layer forming paste and the thickness of the layer forming sheet were as shown in Tables 6 to 14. The results are shown in Tables 6-14.
- Example 58 In the same manner as in Example 1, a layer forming sheet A-1 and a layer forming sheet B-1 were produced. The coating thickness was adjusted so that the thickness after drying was 15 ⁇ m for the layer forming sheet A-1 and 80 ⁇ m for the layer forming sheet B-1. Two sheets A-1 for forming a layer were produced.
- the layer forming sheet A-1 and the layer forming B-1 are bonded at a temperature of 80 ° C. using a vacuum laminator “VTM-200M” (manufactured by Takatori Co., Ltd.).
- VTM-200M vacuum laminator
- a sheet was produced.
- the release film on the side of the layer-forming sheet B-1 of the adhesive composition sheet having the two-layer structure is peeled off, and another layer-forming sheet A-1 is placed thereon using a vacuum laminator. Bonding was performed at a temperature of 0 ° C. to prepare an adhesive composition sheet having a three-layer structure.
- the release film was peeled off from both sides of the adhesive composition sheet, and then heated in an oven at 200 ° C. for 1 hour to cure the adhesive composition sheet.
- the cured adhesive sheet obtained had a thermal diffusivity of 2.3 ⁇ 10 ⁇ 3 m 2 / s and a withstand voltage of 5 kV.
- the adhesive composition sheet was cured by heating in an oven at 200 ° C. for 1 hour.
- the thermal diffusivity and withstand voltage of the cured product of the obtained adhesive composition sheet were evaluated. The results are shown in Table 14.
- the adhesive composition sheet of the present invention is a highly thermally conductive semiconductor that can be used for bonding electronic components such as semiconductor chips used in automobiles, personal computers, portable terminals, etc., and wiring boards, heat sinks, and electronic components. It can be suitably used as an adhesive composition sheet for devices.
Abstract
Description
各実施例、比較例で得られた樹脂組成物シートの硬化物を1cm×1cmに切り出したものを試験片として、厚み方向の熱拡散率(m2/s)をレーザーフラッシュ法熱拡散率測定装置“LFA447”(商品名、ネッチ社製)を用いて測定した。
各実施例、比較例で得られた樹脂組成物シートの硬化物の耐電圧を、耐電圧測定装置“TOS5101”(商品名、菊水電子工業(株)製)を用いて評価した。温度23℃、湿度50%RHにおいて、シートの膜厚方向に0.5kV/秒の昇圧速度で直流電圧を印加して、0.2mA以上の電流が流れたときの電圧を耐電圧とした。5kVまで昇圧しても電流値が0.2mA未満で保たれた場合、耐電圧を5kVとした。
ポリイミドA
乾燥窒素気流下、1,3-ビス(3-アミノフェノキシ)ベンゼン(以下、APB-Nとする)4.82g(0.0165モル)、3,3’-ジアミノ-4,4’-ジヒドロキシジフェニルスルホン(以下、ABPSとする)3.08g(0.011モル)、1,3-ビス(3-アミノプロピル)テトラメチルジシロキサン(以下、SiDAとする)4.97g(0.02モル)、および、末端封止剤としてアニリン0.47g(0.005モル)をN-メチル-2-ピロリドン(以下、NMPとする)130gに溶解させた。ここに2,2-ビス{4-(3,4-ジカルボキシフェノキシ)フェニル}プロパン二無水物(以下、BSAAとする)26.02g(0.05モル)をNMP20gとともに加えて、25℃で1時間反応させ、次いで50℃で4時間撹拌した。その後、180℃でさらに5時間撹拌した。撹拌終了後、溶液を水3Lに投入し、ろ過して沈殿物を回収した。沈殿物を、水で3回洗浄した後、真空乾燥機を用いて80℃で20時間乾燥した。得られたポリマー固体の赤外分光測定をしたところ、1780cm-1付近、1377cm-1付近にポリイミドに起因するイミド構造の吸収ピークが検出された。このようにしてエポキシ基と反応可能な官能基を有し、ポリイミドAを得た。4gのポリイミドAにテトラヒドロフラン6gを加え、23℃で撹拌したところ溶解した。
エピクロン(登録商標)HP-4700(商品名、基本骨格:ナフタレン、DIC(株)製)
jER(登録商標)YL980(商品名、基本骨格:ビスフェノールA、三菱化学(株)製)。
キュアゾール(登録商標)2MAOK(イミダゾール、商品名、四国化成工業(株)製)
キュアゾール(登録商標)2P4MHZ(イミダゾール、商品名、四国化成工業(株)製)
サンエイド(登録商標)SI-200(スルホニウム塩、商品名、三新化学工業(株)製)。
AlNウイスカーA
アルミニウム粉末“TFG-A30P”(東洋アルミニウム(株)製)をプレス成形により厚さ0.5mmの板状の成形体に加工した。次いで、この成形体を150Paの真空雰囲気下で600℃まで昇温し、続いて高純度窒素ガスを用いて0.5MPaの窒素雰囲気下で30分間保持し、反応させた。得られた生成物はウイスカー状であり、X線回折分析装置“D8 ADVANCE”(商品名、ブルカー社製)を用いた測定により、AlNの結晶構造を有することを確認した。AlNウイスカーの長さ方向に垂直な断面における寸法に対する長さ方向の寸法(以下、寸法比とよぶ)は、100倍であった。また、最大粒子径は50μmであった。
カーボンナノチューブA(本荘ケミカル(株)製、CNT-Aと略す、寸法比:400倍、最大粒子径:10μm)
MBN-010T(商品名、鱗片状窒化硼素粒子、三井化学(株)製、寸法比:5倍、最大粒子径:1μm)
XGP(商品名、鱗片状窒化硼素粒子、電気化学工業(株)製、寸法比:10倍、最大粒子径:40μm)
FAN-f05(商品名、球状窒化アルミニウム粒子、古河電子(株)製、寸法比:1倍、最大粒子径:10μm)
FAN-f30(商品名、球状窒化アルミニウム粒子、古河電子(株)製、寸法比:1倍、最大粒子径:40μm)
AE9104-SXE(商品名、球状酸化アルミニウム粒子(株)アドマテックス製、寸法比:1倍、最大粒子径:20μm)
DAW-03DC(商品名、球状酸化アルミニウム粒子、電気化学工業(株)製、寸法比:1倍、最大粒子径:30μm)
スミコランダム(登録商標)AA-1.5(商品名、球状酸化アルミニウム粒子、住友化学(株)製)、寸法比:1倍、最大粒子径:2μm)。
シクロヘキサノン(和光純薬工業(株)製、CHNと略す)。
上記(a)~(e)各成分を表1のA-1に示す組成比になるように調合し、ボールミルを用いて材料が均一に混合するよう10時間の処理を行った。ボールミルでは直径が5mmのジルコニアボール“YTZボール”(商品名、(株)ニッカトー製)を使用した。ボールミル処理後、篩でジルコニアボールを除去し、層形成用ペーストA-1を得た。同様に表1~5のA-2~A-15、B-1~21に示す組成比で上記作業を行い、層形成用ペーストA-2~A-15、B-1~21を作製した。
層形成用ペーストA-1、B-1それぞれを、バーコーターを用いて、剥離性基材である厚さ75μmの離型フィルム“SR-1”(商品名、大槻工業(株)製)上に塗布し、乾燥オーブンで100℃で10分間乾燥を行って、層形成用シートA-1および層形成用シートB-1をそれぞれ作製した。ここで、乾燥後の接着組成物シートの厚みが、表6に示すとおり、層形成用シートA-1は30μm、層形成用シートB-1は80μmとなるように塗布厚みを調節した。
層形成用ペーストの種類、層形成用シートの膜厚を表6~14に示すとおりにした以外は実施例1と同様にして評価を行った。結果を表6~14に示す。
実施例1と同様にして、層形成用シートA-1と層形成用シートB-1を作製した。乾燥後の厚みが、層形成用シートA-1は15μm、層形成用シートB-1は80μmとなるように塗布厚みを調節した。層形成用シートA-1は2枚作製した。
層形成用ペーストB-17を、バーコーターを用いて、剥離性基材である厚さ75μmの離型フィルム“SR-1”(商品名、大槻工業(株)製)上に塗布し、乾燥オーブンで100℃で10分間乾燥を行って層形成用シートB-17を作製した。ここで、乾燥後の接着組成物シートの厚みが、表14に示すとおり、層形成用シートB-17が100μmとなるように塗布厚みを調節した。これにより単層構造の接着組成物シートを作製した。
層形成用ペーストの種類、層形成用シートの膜厚を表14に示すとおりにした以外は比較例5と同様にして、評価を行った。結果を表14に示す。
Claims (11)
- 有機化合物および無機粒子を含有する接着組成物シートであって、該接着組成物シートは、少なくとも有機化合物を含有するA層と有機化合物および無機粒子を含有するB層とが積層された構造を含み、A層の有機化合物の含有率がB層の有機化合物の含有率よりも大きく、かつ、前記A層および/またはB層が異方性形状の熱伝導性無機粒子を含有する半導体装置用接着組成物シート。
- 異方性形状の熱伝導性無機粒子の長さ方向の寸法が、長さ方向に垂直な断面における寸法に対して、4倍以上500倍以下である請求項1に記載の接着組成物シート。
- 異方性形状の熱伝導性無機粒子がカーボンナノチューブ、窒化硼素ナノチューブ、鱗片状窒化硼素、窒化アルミニウムウイスカー、炭化珪素ウイスカーおよび酸化アルミニウムウイスカーから選ばれる少なくとも1種の無機粒子である請求項1または2に記載の接着組成物シート。
- 前記A層の有機化合物の含有率が60体積%以上100体積%以下、前記B層の有機化合物の含有率が1体積%以上40体積%以下である請求項1~3のいずれかに記載の接着組成物シート。
- 前記A層が異方性形状の熱伝導性無機粒子を含有する請求項1~4のいずれかに記載の接着組成物シート。
- 前記A層が異方性形状の熱伝導性無機粒子を含有し、無機粒子の含有率が0.2体積%以上40体積%以下、有機化合物の含有率が60体積%以上99.8体積%以下である請求項5に記載の接着組成物シート。
- 前記B層が球状の熱伝導性無機粒子を含有する請求項1~6のいずれかに記載の接着組成物シート。
- 前記B層が球状の熱伝導性無機粒子を含有し、無機粒子の含有率が60体積%以上99体積%以下、有機化合物の含有率が1体積%以上40体積%以下である請求項7に記載の接着組成物シート。
- 前記A層および前記B層が交互に積層された三層以上の層構成を有する請求項1~8のいずれかに記載の接着組成物シート。
- 請求項1~9のいずれかに記載の接着組成物シートの硬化物を含む半導体装置。
- 電子部品と放熱体、もしくは、電子部品同士を、接着組成物シートを介して貼り合せる工程、および、前記接着組成物シートを硬化させる工程を含む半導体装置の製造方法であって、該接着組成物シートが、少なくとも有機化合物を含有するA層と有機化合物および無機粒子を含有するB層とを含み、A層の有機化合物の含有率がB層の有機化合物の含有率よりも大きく、かつ、前記A層および/またはB層が異方性形状の熱伝導性無機粒子を含有するものである半導体装置の製造方法。
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
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EP16772152.1A EP3275956B1 (en) | 2015-03-27 | 2016-03-09 | Adhesive composition sheet, process for producing same, and semiconductor device |
CN201680016393.2A CN107406728B (zh) | 2015-03-27 | 2016-03-09 | 粘接组合物片材及其制造方法以及半导体器件 |
JP2016514768A JP6809220B2 (ja) | 2015-03-27 | 2016-03-09 | 接着組成物シートおよびその製造方法ならびに半導体装置 |
SG11201707365YA SG11201707365YA (en) | 2015-03-27 | 2016-03-09 | Adhesive composition sheet, process for producing same, and semiconductor device |
KR1020177027666A KR102454630B1 (ko) | 2015-03-27 | 2016-03-09 | 접착 조성물 시트 및 그의 제조 방법, 및 반도체 장치 |
US15/551,663 US10563095B2 (en) | 2015-03-27 | 2016-03-09 | Adhesive composition sheet, method of producing same, and semiconductor device |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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EP3275956B1 (en) | 2019-07-24 |
CN107406728B (zh) | 2020-12-01 |
JP6809220B2 (ja) | 2021-01-06 |
SG11201707365YA (en) | 2017-10-30 |
JPWO2016158268A1 (ja) | 2018-01-18 |
US20180016470A1 (en) | 2018-01-18 |
US10563095B2 (en) | 2020-02-18 |
EP3275956A1 (en) | 2018-01-31 |
CN107406728A (zh) | 2017-11-28 |
TWI683880B (zh) | 2020-02-01 |
KR102454630B1 (ko) | 2022-10-17 |
TW201704396A (zh) | 2017-02-01 |
KR20170131475A (ko) | 2017-11-29 |
EP3275956A4 (en) | 2018-08-22 |
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