JP2015048456A - Connection material, connection structure, and method for producing the connection structure - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a connection material capable of being swiftly hardened, increasing the heat resistance of a hardened matter, and also increasing connection reliability at high temperature under high moisture after connection.SOLUTION: There is provided a connection material including: a phenol novolak type epoxy resin; an epoxy monomer; and an acid generator, in which the weight average molecular weight of the phenol novolak type epoxy resin is 8,000 or higher, and the acid generator being a sulfonium borate complex or a sulfonium antimony complex.

Description

  The present invention relates to a connection material that can be suitably used for electrically connecting electrodes of various connection target members. The present invention also relates to a connection structure using the connection material and a method for manufacturing the connection structure.

  The epoxy resin composition has properties that the cured product has high adhesive strength and is excellent in water resistance and heat resistance of the cured product. For this reason, epoxy resin compositions are widely used in various applications such as electronics, architecture, and vehicles. Moreover, in order to electrically connect various connection object members, conductive particles may be blended in the epoxy resin composition. The epoxy resin composition containing conductive particles is called an anisotropic conductive material.

  In order to obtain various connection structures, the anisotropic conductive material is, for example, a connection between a flexible printed circuit board and a glass substrate (FOG (Film on Glass)) or a connection between a semiconductor chip and a flexible printed circuit board (COF ( Chip on Film)), connection between a semiconductor chip and a glass substrate (COG (Chip on Glass)), connection between a flexible printed circuit board and a glass epoxy substrate (FOB (Film on Board)), and the like.

  The following Patent Document 1 includes an alicyclic epoxy compound, a cation generator, a second cation polymerizable compound having a lower cation polymerizable property than the alicyclic epoxy compound, and an anisotropic material containing conductive particles. An electrically conductive material is disclosed. In Patent Document 1, as the second cationically polymerizable compound, bisphenol type epoxy resin derived from epichlorohydrin and bisphenol A, bisphenol F or the like, polyglycidyl ether, polyglycidyl ester, aromatic epoxy compound, cresol novolac type Epoxy resin, novolak epoxy compound such as phenol novolac epoxy resin, glycidylamine epoxy compound, glycidyl ester epoxy compound, biphenyl diglycidyl ether, triglycidyl isocyanurate, polyglycidyl methacrylate, and glycidyl methacrylate and glycidyl methacrylate copolymer Examples thereof include copolymers with possible vinyl monomers. Patent Document 1 describes that various polymers may be added as appropriate for the purpose of thickening or forming a film. Examples of the polymer include polyimide, polyamide, phenoxy resins, polymethacrylates, polyacrylates, polyimides, polyurethanes, polyesters, polyester urethanes, polyvinyl butyrals, SBS and its epoxy modified products, SEBS and its modified products. , NBR and hydrides thereof.

JP 2011-111557 A

  When the electrodes are connected using the anisotropic conductive material described in Patent Document 1, the anisotropic conductive material may not be cured rapidly at low temperatures. When the anisotropic conductive material does not cure quickly at low temperature, it is necessary to heat at high temperature for a long time, and as a result, thermal degradation of the connection target member tends to be a problem.

  Furthermore, when a conventional anisotropic conductive material is used, the heat resistance of the cured product is lowered, and the connection resistance value may be increased when the connection structure is exposed to high temperature and high humidity. is there.

  An object of the present invention is to provide a connection material that can be quickly cured at a low temperature, increase the heat resistance of the cured product, and increase connection reliability under high temperature and high humidity after connection. Moreover, the objective of this invention is providing the manufacturing method of the connection structure and connection structure using the said connection material.

  According to a wide aspect of the present invention, a phenol novolac epoxy resin, an epoxy monomer, and an acid generator are included, the phenol novolac epoxy resin has a weight average molecular weight of 8000 or more, and the acid generator is sulfonium. A connection material is provided that is a borate complex or a sulfonium antimony complex.

  In a specific aspect of the connection material according to the present invention, the epoxy monomer is a bisphenol A type epoxy monomer, a bisphenol E type epoxy monomer, or a bisphenol F type epoxy monomer.

  In a specific aspect of the connection material according to the present invention, a content of the phenol novolac epoxy resin is 40 wt% or more and 70 wt% or less in a total of 100 wt% of the phenol novolac epoxy resin and the epoxy monomer. And the content of the epoxy monomer is 30% by weight or more and 60% by weight or less.

  On the specific situation with the connection material which concerns on this invention, the said connection material contains electroconductive particle.

  According to a wide aspect of the present invention, a first connection target member having a first electrode on the surface, a second connection target member having a second electrode on the surface, the first connection target member, and the A connection portion connecting the second connection target member, the connection portion is formed of the connection material described above, and the first electrode and the second electrode are electrically connected. A connection structure is provided.

  On the specific situation with the connection structure which concerns on this invention, a said 1st connection object member is a board | substrate, a said 2nd connection object member is a semiconductor chip, and the said connection structure is a liquid crystal display element.

  According to a wide aspect of the present invention, a step of forming a connection material layer on the surface of the first connection target member having the first electrode on the surface using the connection material described above, On the surface opposite to the first connection target member side, the second connection target member having the second electrode on the surface is disposed and provisional pressure bonding is performed, whereby the first connection target member and A step of obtaining a laminate in which the connection material layer and the second connection target member are temporarily press-bonded, and a main press-bonding of the laminate, and the connection material layer is heated and cured to form a connection portion. Then, the first connection target member and the second connection target member are connected by the connection portion, and the first electrode and the second electrode are electrically connected. A method for manufacturing a connection structure is provided, comprising the step of obtaining the connection structure.

  On the specific situation with the manufacturing method of the connection structure which concerns on this invention, the heating temperature of the said connection material layer is made 30 degreeC or more lower than the glass transition temperature of the hardened | cured material of the said connection material layer after this crimping | compression-bonding.

  On the specific situation with the manufacturing method of the connection structure which concerns on this invention, the said connection material layer is not heated to the temperature exceeding 120 degreeC, but is heated and hardened to the temperature of 120 degrees C or less.

  In a specific aspect of the method for manufacturing a connection structure according to the present invention, a substrate is used as the first connection target member, a semiconductor chip is used as the second connection target member, and a liquid crystal display element is used as the connection structure. Get.

  The connection material according to the present invention includes a phenol novolac type epoxy resin, an epoxy monomer, and an acid generator. The phenol novolac type epoxy resin has a weight average molecular weight of 8000 or more, and the acid generator is a sulfonium borate. Since it is a complex or a sulfonium antimony complex, it can be rapidly cured at a low temperature. Furthermore, the heat resistance of the cured product of the connection material according to the present invention can be improved. Furthermore, after connecting a connection object member using the connection material which concerns on this invention, the connection reliability under high temperature, high humidity can be improved.

FIG. 1 is a cross-sectional view schematically showing a connection structure according to an embodiment of the present invention. FIG. 2 is a cross-sectional view schematically showing a connection structure according to another embodiment of the present invention. FIGS. 3A to 3C are schematic perspective views for explaining each step of an example of the method for manufacturing the connection structure according to the embodiment of the present invention. 4A to 4C are schematic perspective views for explaining each step of another example of the method for manufacturing the connection structure according to the embodiment of the present invention. FIG. 5 is a cross-sectional view showing an example of conductive particles.

  Details of the present invention will be described below.

(Connection material)
The connection material according to the present invention includes a phenol novolac type epoxy resin, an epoxy monomer, and an acid generator. In the connection material according to the present invention, the phenol novolac epoxy resin has a weight average molecular weight of 8000 or more. In the connection material according to the present invention, among the phenoxy resins, a phenol novolac type epoxy resin is selected and used, and a phenol novolac type epoxy resin having a weight average molecular weight of 8000 or more is further selected and used. In the connection material according to the present invention, the acid generator is a sulfonium borate complex or a sulfonium antimony complex. In the connection material according to the present invention, a sulfonium borate complex or a sulfonium antimony complex is selected and used among the acid generators.

  Since the connection material according to the present invention has the above-described configuration, it can be quickly cured at a low temperature. For example, the connection material according to the present invention can be cured rapidly even at 120 ° C. or lower, and can be cured rapidly even at 100 ° C. or lower. Furthermore, the heat resistance of the cured product of the connection material according to the present invention can be improved. The glass transition temperature of the cured product of the connection material according to the present invention can be increased, and the glass transition temperature of the cured product can be 130 ° C. or higher, and can be 150 ° C. or higher. Furthermore, after connecting a connection object member using the connection material which concerns on this invention, the connection reliability under high temperature, high humidity can be improved. For example, even if the obtained connection structure is exposed to high temperature and high humidity, it is possible to suppress an increase in connection resistance.

  In a liquid crystal display element, a semiconductor chip may be mounted on a glass substrate by a COG method. When obtaining this liquid crystal display element, generally, a connection material is disposed on a glass substrate. Next, the semiconductor chips are stacked and thermocompression bonded so that the electrodes of the glass substrate and the electrodes of the semiconductor chip face each other. Thereby, the connection material is cured and the electrodes are electrically connected to obtain a liquid crystal display element.

  In recent years, in a liquid crystal display element, a narrow frame of a liquid crystal panel and a thin glass substrate have progressed. For this reason, the liquid crystal display element obtained becomes easy to warp by the heating at the time of obtaining a liquid crystal display element. Further, when the liquid crystal display element is warped, display unevenness is likely to occur. Furthermore, in a liquid crystal display element, thermal degradation may be a big problem. Since the connection material according to the present invention can be quickly cured at a low temperature, it can be suitably used for the liquid crystal display element as described above. By using the connection material according to the present invention, thermal deterioration can be suppressed, warpage of the liquid crystal display element can be suppressed, and display unevenness of the liquid crystal display element can be suppressed.

  The connecting material is preferably curable by both light irradiation and heating. The connection material is preferably cured by light irradiation and heating.

  The viscosity of the connecting material at 30 ° C. is preferably 10 Pa · s or more, more preferably 50 Pa · s or more, preferably 3000 Pa · s or less, more preferably 2000 Pa · s or less. The viscosity is measured using an E-type viscometer at 30 ° C. and 2.5 rpm. Specific examples of the E-type viscometer include “TV-35” (rotor No. 7) manufactured by Toki Sangyo Co., Ltd.

The glass transition temperature of the cured product of the connection material is preferably 130 ° C. or higher, more preferably 150 ° C. or higher. When the glass transition temperature is equal to or higher than the lower limit, the heat resistance of the cured product is further increased. The cured product for measuring the glass transition temperature is obtained by irradiating a 30 μm-thick connection material with light so that the light irradiation intensity is 200 mW / cm ² and simultaneously heating and curing at 120 ° C. for 10 seconds. It is preferred that

  The connection material according to the present invention is suitably used for connection between electrodes. The connection material according to the present invention may be used to electrically connect electrodes such as bump electrodes so as to be in direct contact with each other. The connection material according to the present invention may contain conductive particles. The connection material according to the present invention does not contain or contain conductive particles, and preferably contains conductive particles. The connection material according to the present invention may be used for electrically connecting the electrodes with conductive particles.

  The connecting material can be used as a paste and a film. The connection material containing conductive particles can be used as a conductive paste and a conductive film. The conductive paste is preferably an anisotropic conductive paste. The conductive film is preferably an anisotropic conductive film.

  Hereinafter, each component contained in the connection material according to the present invention will be described.

[Phenol novolac type epoxy resin]
In the connection material according to the present invention, since the phenol novolac type epoxy resin is used, compared with the case where an epoxy resin other than the phenol novolac type epoxy resin is used, the heat resistance of the cured product is further improved, and the connection structure is further provided. The connection reliability under high temperature and high humidity can be improved. The phenol novolac type epoxy resin is a curable compound. As for the said phenol novolak-type epoxy resin, only 1 type may be used and 2 or more types may be used together.

  The phenol novolac type epoxy resin is a polymer. The phenol novolac epoxy resin has a weight average molecular weight of 8000 or more. When the weight average molecular weight is less than 8000, it is difficult to sufficiently increase the glass transition temperature of the cured product, and the connection reliability of the connection structure under high temperature and high humidity tends to be lowered. The weight average molecular weight of the phenol novolac epoxy resin is preferably 10,000 or more, and preferably 20000 or less.

  The weight average molecular weight is a weight average molecular weight in terms of polystyrene measured by gel permeation chromatography (GPC). Examples of the column for measuring the weight average molecular weight include Shodex LF-804 (manufactured by Showa Denko KK).

[Epoxy monomer]
By using the above epoxy monomer together with the above phenol novolac type epoxy resin, the curability of the connection material is further improved, and the heat resistance of the cured product and the connection reliability of the connection structure under high temperature and high humidity are further increased. Get higher. The epoxy monomer is a monomer having an epoxy group. The epoxy monomer is a curable compound. As for the said epoxy monomer, only 1 type may be used and 2 or more types may be used together.

  Examples of the epoxy monomer include bisphenol A type epoxy monomer, bisphenol E type epoxy monomer, bisphenol F type epoxy monomer, bisphenol S type epoxy monomer, biphenyl type epoxy monomer, dicyclopentadiene type epoxy monomer, naphthalene type epoxy monomer, aliphatic skeleton Examples thereof include an epoxy monomer containing, a phenol novolac type epoxy monomer, a biphenyl novolac type epoxy monomer, a naphthalene phenol novolac type epoxy monomer, a glycidylamine type epoxy monomer, and an alkyl polyol type epoxy monomer.

  From the viewpoint of further improving the heat resistance of the cured product and the connection reliability of the connection structure under high temperature and high humidity, the epoxy monomer is a bisphenol A type epoxy monomer, a bisphenol E type epoxy monomer or a bisphenol F type epoxy monomer. It is preferably a bisphenol E type epoxy monomer or a bisphenol A type epoxy monomer, more preferably a bisphenol E type epoxy monomer. As for these preferable epoxy monomers, only 1 type may be used and 2 or more types may be used together.

  When the connection material contains conductive particles, the total content of the phenol novolac epoxy resin and the epoxy monomer is preferably 50% in 100% by weight of all components excluding the conductive particles of the connection material. % Or more, more preferably 55% by weight or more, preferably 99% by weight or less, more preferably 95% by weight or less, still more preferably 90% by weight or less, and particularly preferably 85% by weight or less.

  When the connection material does not include conductive particles, the total content of the phenol novolac epoxy resin and the epoxy monomer in 100% by weight of the connection material is preferably 60% by weight or more, more preferably 65%. % By weight or more, preferably 99% by weight or less, more preferably 95% by weight or less.

  In a total of 100% by weight of the phenol novolac epoxy resin and the epoxy monomer, the content of the phenol novolac epoxy resin is 20% by weight or more and 70% by weight or less, and the content of the epoxy monomer is 30% by weight. Preferably, the content of the phenol novolac type epoxy resin is 40% by weight or more and 70% by weight or less, and the content of the epoxy monomer is 30% by weight or more and 60% by weight. % Or less is more preferable. When the content of the phenol novolac epoxy resin is relatively increased, the heat resistance of the cured product and the connection reliability of the connection structure under high temperature and high humidity tend to be further increased. When the content of the epoxy monomer is relatively increased, the fast curability of the connecting material tends to be further improved.

[Acid generator]
The acid generator is a sulfonium borate complex or a sulfonium antimony complex. As for the said acid generator, only 1 type may be used and 2 or more types may be used together. The connecting material may contain only one of a sulfonium borate complex and a sulfonium antimony complex as the acid generator, or may contain both a sulfonium borate complex and a sulfonium antimony complex.

  The acid generator is preferably a sulfonium borate complex from the viewpoint of achieving both the fast curability of the connecting material and the effect of suppressing metal corrosion at a higher level.

Examples of the anion of the acid generator include a borate anion, an antimony anion, and a phosphate anion. In the present invention, the anion is limited to a borate anion and an antimony anion. Examples of the anion in the acid generator include BF ₄ ⁻ , B (C ₆ F ₅ ) ₄ ^—, and SbF ₆ ^— . BF ₄ ⁻ , B (C ₆ F ₅ ) ₄ ⁻ , or SbF ₆ ⁻ is preferable, BF ₄ ⁻ or B (C ₆ F ₅ ) ₄ ⁻ is more preferable, and B (C ₆ F ₅ ) ₄ ⁻ is more preferable. preferable.

  Examples of the cation in the acid generator include a sulfonium cation and an iodonium cation. In the present invention, the cation is limited to a sulfonium cation. The sulfonium borate complex and the sulfonium antimony complex each have a sulfonium cation. The sulfonium cation preferably has an aromatic skeleton, and is preferably an aromatic sulfonium cation.

  Although the said sulfonium cation is not specifically limited, It is preferable that it is a sulfonium cation represented by following formula (11). If an acid generator containing a sulfonium cation represented by the following formula (11) is used, both the fast curability of the connecting material and the effect of inhibiting metal corrosion can be achieved at a higher level. In the following formula (11), the bonding site of R3 bonded to the benzene ring is not particularly limited. However, R3 is preferably bonded to the para-position of the benzene ring with respect to the sulfur atom.

  In said formula (11), R1 and R2 are respectively a C1-C10 alkyl group, an aryl group, or an aralkyl group, and R3 is a hydroxyl group or a C1-C10 organic group. The organic group in R3 may contain a sulfur atom. It is preferable that the organic group in R3 contains only a carbon atom and a hydrogen atom, or contains only a carbon atom, a hydrogen atom, and a sulfur atom.

  The content of the acid generator is preferably 0.1 parts by weight or more, more preferably 0.2 parts by weight or more, preferably 8 parts per 100 parts by weight in total of the phenol novolac type epoxy resin and the epoxy monomer. It is 6 parts by weight or less, more preferably 6 parts by weight or less. When the content of the acid generator is not less than the above lower limit and not more than the above upper limit, the connecting material can be appropriately cured. Moreover, the connection material can be photocured satisfactorily by irradiating the connection material with light.

[Conductive particles]
The connection material preferably includes conductive particles. The connection material containing conductive particles is preferably a conductive connection material. The said electroconductive particle should just have an electroconductive part on the electroconductive surface. The conductive part is preferably a conductive layer.

  FIG. 5 is a cross-sectional view showing an example of conductive particles. The conductive particles 31 may include base material particles 32 and a conductive layer 33 disposed on the surface of the base material particles 32. The conductive particles may be metal particles whose entirety is a conductive portion. Among these, from the viewpoint of reducing the cost and increasing the flexibility of the conductive particles to increase the conduction reliability between the electrodes, the base particles and the conductive material disposed on the surface of the base particles are used. Conductive particles having a layer are preferred.

  Examples of the substrate particles include resin particles, inorganic particles excluding metal particles, organic-inorganic hybrid particles, and metal particles. The substrate particles are preferably substrate particles excluding metal particles, and are preferably resin particles, inorganic particles excluding metal particles, or organic-inorganic hybrid particles.

  The substrate particles are preferably resin particles formed of a resin. When connecting between electrodes using electroconductive particle, after arrange | positioning electroconductive particle between electrodes, electroconductive particle is compressed by crimping | bonding. When the substrate particles are resin particles, the conductive particles are likely to be deformed during the pressure bonding, and the contact area between the conductive particles and the electrode is increased. For this reason, the conduction | electrical_connection reliability between electrodes becomes still higher.

  Examples of the resin for forming the resin particles include polyolefin resin, acrylic resin, phenol resin, melamine resin, benzoguanamine resin, urea resin, epoxy resin, unsaturated polyester resin, saturated polyester resin, polyethylene terephthalate, polysulfone, and polyphenylene. Examples thereof include oxide, polyacetal, polyimide, polyamideimide, polyetheretherketone, polyethersulfone, divinylbenzene polymer, and divinylbenzene copolymer. Examples of the divinylbenzene copolymer include divinylbenzene-styrene copolymer and divinylbenzene- (meth) acrylic acid ester copolymer. Since the hardness of the resin particles can be easily controlled within a suitable range, the resin for forming the resin particles is a polymer obtained by polymerizing one or more polymerizable monomers having an ethylenically unsaturated group. It is preferably a coalescence.

  Examples of the inorganic substance for forming the inorganic particles include silica and carbon black. Examples of the organic / inorganic hybrid particles include organic / inorganic hybrid particles formed of a crosslinked alkoxysilyl polymer and an acrylic resin.

  When the substrate particles are metal particles, examples of the metal for forming the metal particles include silver, copper, nickel, silicon, gold, and titanium.

  The metal for forming the conductive part is not particularly limited. Furthermore, in the case where the conductive particles are metal particles that are conductive parts as a whole, the metal for forming the metal particles is not particularly limited. Examples of the metal include gold, silver, palladium, copper, platinum, zinc, iron, tin, lead, aluminum, cobalt, indium, nickel, chromium, titanium, antimony, bismuth, thallium, germanium, cadmium, silicon, and these. And the like. Examples of the metal include tin-doped indium oxide (ITO) and solder. Especially, since the connection resistance between electrodes becomes still lower, an alloy containing tin, nickel, palladium, copper or gold is preferable, and nickel or palladium is preferable.

  The conductive layer may be formed of a single layer. The conductive layer may be formed of a plurality of layers. That is, the conductive layer may have a stacked structure of two or more layers. When the conductive layer is formed of a plurality of layers, the outermost layer is preferably a gold layer, a nickel layer, a palladium layer, a copper layer, or an alloy layer containing tin and silver, and is a gold layer. Is more preferable. When the outermost layer is these preferred conductive layers, the connection resistance between the electrodes is further reduced. Moreover, when the outermost layer is a gold layer, the corrosion resistance is further enhanced.

  The method for forming the conductive layer on the surface of the substrate particles is not particularly limited. As a method for forming the conductive layer, for example, a method by electroless plating, a method by electroplating, a method by physical vapor deposition, and a method of coating the surface of base particles with metal powder or a paste containing metal powder and a binder Etc. Especially, since formation of a conductive layer is simple, the method by electroless plating is preferable. Examples of the method by physical vapor deposition include methods such as vacuum vapor deposition, ion plating, and ion sputtering.

  The average particle diameter of the conductive particles is preferably 0.5 μm or more, more preferably 1 μm or more, preferably 500 μm or less, more preferably 100 μm or less, still more preferably 80 μm or less, and particularly preferably 70 μm or less. When the average particle diameter of the conductive particles is not less than the above lower limit and not more than the above upper limit, the contact area between the conductive particles and the electrode becomes sufficiently large when the electrodes are connected using the conductive particles, and the conductive Aggregated conductive particles are less likely to be formed when the layer is formed. Further, the distance between the electrodes connected via the conductive particles does not become too large, and the conductive layer is difficult to peel from the surface of the base material particles.

  The “average particle size” of the conductive particles indicates a number average particle size. The average particle diameter of the conductive particles can be obtained by observing 50 arbitrary conductive particles with an electron microscope or an optical microscope and calculating an average value.

  The thickness of the conductive layer is preferably 0.005 μm or more, more preferably 0.01 μm or more, preferably 10 μm or less, more preferably 1 μm or less, and still more preferably 0.3 μm or less. When the thickness of the conductive layer is not less than the above lower limit and not more than the above upper limit, sufficient conductivity is obtained, and the conductive particles do not become too hard, and the conductive particles are sufficiently deformed when connecting the electrodes. .

  When the conductive layer is formed of a plurality of layers, the thickness of the outermost conductive layer is preferably 0.001 μm or more, more preferably the thickness of the gold layer when the outermost layer is a gold layer. It is 0.01 μm or more, preferably 0.5 μm or less, more preferably 0.1 μm or less. When the thickness of the outermost conductive layer is not less than the above lower limit and not more than the above upper limit, the coating with the outermost conductive layer becomes uniform, corrosion resistance is sufficiently high, and the connection resistance between the electrodes is sufficiently high. Lower. Further, the thinner the gold layer when the outermost layer is a gold layer, the lower the cost.

  The thickness of the conductive layer can be measured, for example, by observing a cross section of the conductive particles or the conductive particles using a transmission electron microscope (TEM).

  From the viewpoint of increasing the contact area between the electrode and the conductive particle and further improving the conduction reliability between the electrodes, the conductive particle is composed of the base material and the conductive material disposed on the surface of the base material particle. It is preferable to have a layer (first conductive layer).

  The content of the conductive particles is not particularly limited. In 100% by weight of the connection material, the content of the conductive particles is preferably 0.1% by weight or more, more preferably 0.5% by weight or more, still more preferably 1% by weight or more, preferably 40% by weight or less. More preferably, it is 30 weight% or less, More preferably, it is 19 weight% or less. A conductive particle can be easily arrange | positioned between the upper and lower electrodes which should be connected as content of the said electroconductive particle is more than the said minimum and below the said upper limit. Furthermore, it becomes difficult to electrically connect adjacent electrodes that should not be connected via a plurality of conductive particles. That is, a short circuit between adjacent electrodes can be further prevented.

[Other ingredients]
In addition to the components described above, the connection material according to the present invention is a polymer other than a phenol novolac epoxy resin, a monomer other than an epoxy monomer, a filler, an extender, a softener, a plasticizer, a colorant, an antioxidant, Various additives such as a heat stabilizer, a light stabilizer, an ultraviolet absorber, a lubricant, an antistatic agent and a flame retardant may be contained.

  The connection material according to the present invention may contain a silane coupling agent. The silane coupling agent has a role of improving the adhesiveness of the connection material.

  Specific examples of the silane coupling agent include γ-aminopropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropyltriethoxysilane, And γ-isocyanatopropyltrimethoxysilane. As for these silane coupling agents, only 1 type may be used and 2 or more types may be used together.

  The silane coupling agent preferably does not have a nitrogen atom, preferably does not have a sulfur atom, and preferably does not have both a nitrogen atom and a sulfur atom. By using a silane coupling agent having no nitrogen atom and sulfur atom, the fast curability of the connecting material can be further enhanced.

  The content of the silane coupling agent is preferably 0.5 parts by weight or more and preferably 5 parts by weight or less based on 100 parts by weight of the total of the phenol novolac type epoxy resin and the epoxy monomer. When the content of the silane coupling agent is not less than the above lower limit, the adhesiveness of the connection portion is further increased. When the content of the silane coupling agent is not more than the above upper limit, the bleeding out of the excess silane coupling agent is suppressed, and the fast curability of the connecting material is further enhanced.

  The connection material according to the present invention may contain a curing retarder. By using the curing retarder, the storage stability of the connecting material can be improved.

  The said hardening retarder is not specifically limited, A polyether compound etc. are mentioned. The polyether compound is not particularly limited, and examples thereof include polyethylene glycol, polypropylene glycol, polytetramethylene glycol, and a crown ether compound. Of these, crown ether compounds are preferred.

  The crown ether compound is not particularly limited, and has, for example, 12-crown-4, 15-crown-5, 18-crown-6, 24-crown-8, and a structure represented by the following formula (31). Compounds and the like.

  In said formula (31), R1-R12 represents a hydrogen atom or a C1-C20 substituted or unsubstituted alkyl group, respectively. However, at least one of R1 to R12 represents an alkyl group having 1 to 20 carbon atoms. The substituted or unsubstituted alkyl group is one or more functional groups selected from the group consisting of an alkoxyl group having 1 to 20 carbon atoms, a halogen atom, a hydroxyl group, a carboxyl group, and a carboxylic acid alkyl ester group having 1 to 20 carbon atoms. It may be substituted with a group, and adjacent Rn and Rn + 1 (where n represents an even number of 1 to 12) may together form a cyclic alkyl skeleton. The C1-C20 alkoxyl group may be linear or branched.

  Among the compounds represented by the above formula (31), a compound having at least one cyclohexyl group is preferable. The presence of the cyclohexyl group stabilizes the skeleton of the crown ether and increases the delay effect.

  Specific examples of the compound having a cyclohexyl group and represented by the above formula (31) include a compound represented by the following formula (31A).

  The compound represented by the above formula (31A) has two cyclohexyl groups at positions symmetrical with respect to a line passing through the center of the 18-crown-6-ether molecule. For this reason, it is considered that the delay effect is enhanced without causing distortion or the like in the skeleton of the 18-crown-6-ether molecule.

  The content of the curing retardant is preferably 0.01 parts by weight or more, more preferably 0.05 parts by weight or more, preferably 5 parts by weight, based on 100 parts by weight of the total of the phenol novolac type epoxy resin and the epoxy monomer. It is 3 parts by weight or less, more preferably 3 parts by weight or less. When the content of the curing retarder is not less than the above lower limit and not more than the above upper limit, the storage stability of the connection material is further increased, and the curing rate of the connection material is further moderated.

(Connection structure and method of manufacturing connection structure)
The connection structure according to the present invention includes a first connection target member, a second connection target member, and a connection portion. The first connection object member has a first electrode on the surface. The second connection object member has a second electrode on the surface. The connection portion connects the first connection target member and the second connection target member. The connection part is formed of the connection material described above. In the connection structure, the first electrode and the second electrode are electrically connected.

  The method for manufacturing a connection structure according to the present invention includes a step of forming a connection material layer on the surface of the first connection target member using the connection material described above, and the first of the connection material layer. By placing the second connection target member on the surface opposite to the connection target member side and performing temporary pressure bonding, the first connection target member, the connection material layer, and the second connection target A step of obtaining a laminate in which a member is temporarily press-bonded, a main press-bonding of the laminate, the connection material layer is heated and cured to form a connection portion, and the first connection target member and the above And a step of obtaining a connection structure in which a second connection target member is connected by the connection part, and the first electrode and the second electrode are electrically connected.

  In the manufacturing method of the connection structure according to the present invention, before the temporary pressure bonding, at the time of the temporary pressure bonding, or before the main pressure bonding after the temporary pressure bonding, the connection material layer is irradiated with light, at the time of the main pressure bonding, or It is preferable that the connection material layer is irradiated with light before curing of the connection material layer after the pressure bonding is completed. You may irradiate the said connection material layer with light before temporary crimping | compression-bonding at the time of temporary crimping | compression-bonding, or before the final crimping after temporary crimping | compression-bonding. More preferably, the connection material layer is irradiated with light at the time of the main pressure bonding or before the curing of the connection material layer after the main pressure bonding is completed.

  In FIG. 1, the connection structure which concerns on one Embodiment of this invention is typically shown with sectional drawing.

The connection structure 1 shown in FIG. 1 is a connection that connects the first connection target member 2, the second connection target member 4, and the first connection target member 2 and the second connection target member 4. Part 3. The connection part 3 is formed with the connection material mentioned above. The connection structure 1 is a liquid crystal display element. The first connection target member 2 is a substrate. The second connection target member 4 is a semiconductor chip.

  The first connection target member 2 has a plurality of first electrodes 2a on the surface (upper surface). The second connection target member 4 has a plurality of second electrodes 4a on the surface (lower surface). The first electrode 2 a and the second electrode 4 a are electrically connected by one or a plurality of conductive particles 5.

  FIG. 2 is a cross-sectional view schematically showing a connection structure according to another embodiment of the present invention.

  The connection structure 11 shown in FIG. 2 is a connection that connects the first connection target member 12, the second connection target member 14, and the first connection target member 12 and the second connection target member 14. Unit 13. The connection part 13 is formed with the connection material mentioned above. The connection structure 11 is a liquid crystal display element. The first connection target member 12 is a substrate. The second connection target member 14 is a semiconductor chip.

  The first connection object member 12 has a plurality of first electrodes 12a on the surface (upper surface). The second connection target member 14 has a plurality of second electrodes 14a on the surface (lower surface). The first electrode 12a and the second electrode 14a are electrically connected by being in direct contact with each other.

  The electrode width (the first electrode width and the second electrode width) is preferably 5 μm or more, more preferably 10 μm or more, preferably 3000 μm or less, more preferably 2000 μm or less. The inter-electrode width (the first inter-electrode width and the second inter-electrode width) is preferably 3 μm or more, more preferably 10 μm or more, preferably 3000 μm or less, more preferably 2000 μm or less. Further, L / S (line / space) as electrode width / interelectrode width is preferably 5 μm / 5 μm or more, more preferably 10 μm / 10 μm or more, preferably 3000 μm / 3000 μm or less, more preferably 2000 μm / 2000 μm or less. is there.

  The connection structure 1 shown in FIG. 1 can be obtained through the steps shown in FIGS. 3A to 3C, for example, as follows.

  As shown to Fig.3 (a), the 1st connection object member 2 which has the 1st electrode 2a on the surface is prepared. Next, the connection material layer 3 </ b> A is disposed on the surface of the first connection target member 2 using a connection material including a plurality of conductive particles 5 (not shown) (first step). At this time, it is preferable that one or a plurality of conductive particles 5 be disposed on the first electrode 2a. Here, the connecting material is applied using the dispenser 21.

  In the first step, the connecting material is preferably applied using a dispenser. In application by a dispenser, the connection material can be arranged with high accuracy in a predetermined region.

  Next, the 2nd connection object member 4 which has the 2nd electrode 4a on the surface is arranged on the surface opposite to the 1st connection object member 2 side of 3A of connection materials, and temporary pressure bonding is performed. At this time, the first electrode 2a and the second electrode 4a are opposed to each other. As shown in FIG.3 (b), the laminated body 1X by which the 1st connection object member 2, the connection material layer 3A, and the 2nd connection object member 4 were temporarily press-bonded is obtained (2nd process). Here, in order to perform temporary pressure bonding, the temporary pressure bonding member 22 is lowered.

  In the second step, the pressure during temporary pressure bonding is preferably 0.1 MPa or more, more preferably 0.3 MPa or more, preferably 5 MPa or less, more preferably 3 MPa or less. When the pressure at the time of the temporary pressure bonding is not less than the above lower limit and not more than the above upper limit, a laminate that has been preliminarily pressure bonded can be obtained.

  In the second step, the temperature at the time of provisional pressure bonding is preferably 25 ° C. or higher, more preferably 30 ° C. or higher, preferably 150 ° C. or lower, more preferably 120 ° C. or lower. When the temperature at the time of the temporary pressure bonding is not less than the above lower limit and not more than the above upper limit, a laminate that has been preliminarily pressure bonded can be obtained.

  Next, by heating the laminated body 1X and performing the main pressure bonding, and before the curing of the connection material layer 3A after the main pressure bonding or after the main pressure bonding is completed, the connection material layer 3A is irradiated with light. Then, the connecting material layer 3A is cured to form the connecting portion 3. As shown in FIG.3 (c), the connection structure 1 to which the 1st connection object member 2, the connection part 3, and the 2nd connection object member 4 were finally press-bonded is obtained (3rd process). Here, in order to perform the main press bonding, the main press bonding member 23 is lowered. In addition, the connection portion 3 is formed by irradiating the connection material layer 3 </ b> A with light from the light irradiation device 24 toward the upper side from the lower side of the first connection target member 2. The first connection target member 2 is preferably a transparent substrate, and is preferably a glass substrate.

  In the third step, it is preferable that the laminate is heated so that the temperature of the connecting material layer is higher than that before pressure bonding. That is, in the third step, it is preferable that the laminate is always heated at the time of the final press bonding. It is preferable to heat the laminate so that the temperature of the connecting material layer is 5 ° C. or more higher than that before the main press bonding, and the lamination layer so that the temperature of the connecting material layer is 10 ° C. or higher than before the main press bonding. More preferably, the body is heated. As the heating temperature is higher, the connecting material is sufficiently cured, and the adhesion between the layers is further increased.

  In the third step, the heating temperature for heating the laminate is preferably 120 ° C. or lower, more preferably 100 ° C. or lower, still more preferably 90 ° C. or lower, still more preferably 80 ° C. or lower, particularly preferably. 70 ° C. or lower, most preferably 60 ° C. or lower. As the heating temperature is lower, warping and thermal deterioration of the connection structure are further suppressed. It is particularly preferable to cure the connecting material layer by heating it to a temperature of 120 ° C. or lower without heating it to a temperature exceeding 120 ° C. Most preferably, the connecting material layer is heated to a temperature of 100 ° C. or lower and not cured at a temperature exceeding 100 ° C.

  From the viewpoint of rapidly curing at a low temperature and further improving the heat resistance of the cured product, the heating temperature of the connection material layer is 30 ° C. or higher than the glass transition temperature of the cured product of the connection material layer after the main pressure bonding. It is preferable to make it low. In other words, it is preferable to select and use the connection material so that the heating temperature of the connection material layer is 30 ° C. or more lower than the glass transition temperature of the cured product of the connection material layer after the main pressure bonding.

  In the third step, the heating time is preferably 1 second or longer, more preferably 3 seconds or longer, preferably 20 seconds or shorter, more preferably 10 seconds or shorter. When the heating time is equal to or more than the lower limit, the connection material layer is sufficiently cured. When the heating time is less than or equal to the upper limit, warping and thermal deterioration of the connection structure can be further suppressed.

  In the third step, the pressure during the main pressure bonding is preferably 1 MPa or more, more preferably 5 MPa or more, preferably 180 MPa or less, more preferably 150 MPa or less per electrode area of the semiconductor chip. When the pressure at the time of the main press-bonding is not less than the above lower limit and not more than the above upper limit, a liquid crystal display element that is satisfactorily press-bonded can be obtained. Further, when the connection material contains conductive particles, the first and second electrodes are electrically connected to each other by compressing the conductive particles with the first electrode and the second electrode by pressurization during the main press bonding. The contact area with the conductive particles increases. For this reason, conduction reliability increases. By compressing the conductive particles, even if the distance between the first and second electrodes increases, the particle diameter of the conductive particles increases so as to follow the expansion.

  In the third step, the light irradiation may be performed at the time of the main pressure bonding, or may be performed before the curing of the connecting material layer 3A after the main pressure bonding is completed. For example, light transmitted through the substrate can be guided to the connection material layer by irradiating the connection material layer with light from the surface side opposite to the connection material layer of the substrate.

In order to effectively proceed photocuring of the connecting material layer, the integrated light quantity at the time of irradiating light is preferably 50 mJ / cm ² or more, more preferably 100 mJ / cm ² or more, preferably 100000mJ / cm ² or less, More preferably, it is 50000 J / cm ² or less. When the integrated light amount is not less than the above lower limit and not more than the above upper limit, the connecting material layer is cured more efficiently.

  The light source used when irradiating light is not specifically limited. Examples of the light source include a light source having a sufficient light emission distribution at a wavelength of 420 nm or less. Specific examples of the light source include, for example, a low pressure mercury lamp, a medium pressure mercury lamp, a high pressure mercury lamp, an ultrahigh pressure mercury lamp, a chemical lamp, a black light lamp, a microwave excitation mercury lamp, a metal halide lamp, and an LED lamp.

  The connection structure 1 shown in FIG. 1 can also be obtained through the steps shown in FIGS. 4A to 4C as follows, for example. In this case, the preferable range of the integrated light amount when irradiating light, the pressure at the time of temporary pressure bonding, the pressure at the time of main pressure bonding, the heating temperature, and the heating time is a range in each step shown in FIGS. Is the same.

  As shown in FIG. 4A, the connection material layer 3A is arranged on the surface of the first connection target member 2 using a connection material containing a plurality of conductive particles 5 (not shown) (first). Step 1). Here, the connecting material is applied using the dispenser 21.

  Next, the 2nd connection object member 4 which has the 2nd electrode 4a on the surface is arranged on the surface opposite to the 1st connection object member 2 side of 3A of connection materials, and temporary pressure bonding is performed. At this time, the first electrode 2a and the second electrode 4a are opposed to each other. In addition, the light is irradiated to the connection material layer 3A before the temporary pressure bonding, at the time of the temporary pressure bonding, or before the main pressure bonding after the temporary pressure bonding. As shown in FIG.4 (b), the laminated body 1X by which the 1st connection object member 2, the connection material layer 3A, and the 2nd connection object member 4 were temporarily press-bonded is obtained (2nd process). Here, in order to perform temporary pressure bonding, the temporary pressure bonding member 22 is lowered. Moreover, light is irradiated to the connection material layer 3 </ b> A from the light irradiation device 24 toward the upper side from the lower side of the second connection target member 2.

  In the second step, the light irradiation may be performed before temporary pressure bonding, may be performed at the time of temporary pressure bonding, or may be performed before the main pressure bonding after temporary pressure bonding. For example, the light transmitted through the first connection target member can be guided to the connection material layer by irradiating the connection material layer with light from the surface side opposite to the connection material layer of the first connection target member. .

  In order to effectively advance the photocuring of the connection material layer, it is preferable that the integrated light amount when irradiating light is not less than the above-described lower limit and not more than the above-described upper limit.

  The time from the irradiation of light to the final pressing is preferably 60 minutes or less, more preferably 10 minutes or less.

  In the second step, the pressure at the time of provisional pressure bonding is preferably not less than the above-described lower limit and not more than the above-described upper limit.

  Next, the connection body 3 </ b> A is cured to form the connection portion 3 by heating the laminated body 1 </ b> X and performing the main pressure bonding. As shown in FIG.4 (c), the connection structure 1 to which the 1st connection object member 2, the connection part 3, and the 2nd connection object member 4 were press-bonded is obtained (3rd process). Here, in order to perform the main press bonding, the main press bonding member 23 is lowered.

  In the third step, the heating temperature for heating the laminate is preferably not less than the above-described lower limit and not more than the above-described upper limit. In the third step, the heating time is preferably not less than the above-described lower limit and not more than the above-described upper limit.

  The said 1st, 2nd connection object member is not specifically limited. Specifically, the first and second connection target members include electronic components such as semiconductor chips, capacitors, and diodes, and circuit boards such as printed boards, flexible printed boards, glass epoxy boards, and glass boards. Examples include parts. The conductive material is preferably a conductive material used for connecting electronic components. The conductive material is preferably a conductive material used for electrical connection between electrodes. The conductive material is preferably a liquid and is a conductive material that is applied to the upper surface of the connection target member in a liquid state.

  Examples of the electrode provided on the connection target member include metal electrodes such as a gold electrode, a nickel electrode, a tin electrode, an aluminum electrode, a copper electrode, a molybdenum electrode, and a tungsten electrode. When the connection object member is a flexible printed board, the electrode is preferably a gold electrode, a nickel electrode, a tin electrode, or a copper electrode. When the connection target member is a glass substrate, the electrode is preferably an aluminum electrode, a copper electrode, a molybdenum electrode, or a tungsten electrode. In addition, when the said electrode is an aluminum electrode, the electrode formed only with aluminum may be sufficient and the electrode by which the metal oxide layer was laminated | stacked on the surface of the aluminum layer may be sufficient. Examples of the material for the metal oxide layer include indium oxide doped with a trivalent metal element and zinc oxide doped with a trivalent metal element. Examples of the trivalent metal element include Sn, Al, and Ga.

  Since the connection material can be rapidly cured at a low temperature, it is preferable that the first connection target member is a substrate, the second connection target member is a semiconductor chip, and the connection structure is a liquid crystal display. An element is preferred.

  Hereinafter, the present invention will be specifically described with reference to Examples and Comparative Examples. The present invention is not limited only to the following examples.

(polymer)
Phenol novolac type epoxy resin A (DIC Corporation "EPICLON N-730A", weight average molecular weight 1000)
Phenol novolac-type epoxy resin B (“EPICLON N-740” manufactured by DIC, weight average molecular weight 1530)
Phenol novolac epoxy resin C (“EPICLON N-770” manufactured by DIC, weight average molecular weight 14000)
Phenol novolac epoxy resin D (“EPICLON N-775” manufactured by DIC, weight average molecular weight 18000)

(monomer)
Epoxy monomer A (bisphenol F type epoxy monomer, “EXA-830CRP” manufactured by DIC)
Epoxy monomer B (bisphenol A type epoxy monomer, “EXA-850CRP” manufactured by DIC)
Epoxy monomer C (bisphenol E type epoxy monomer, “Epo X-R1710” manufactured by Printec Co., Ltd.)

(Acid generator)
Acid generator A (acid generator represented by the following formula (21X))

  Acid generator B (acid generator represented by the following formula (21Y))

  Acid generator C (acid generator represented by the following formula (a))

(Curing agent)
Curing agent A (imidazole compound, “2MZ-H” manufactured by Shikoku Chemicals)

(Conductive particles)
Conductive particles A (conductive particles having a surface of divinylbenzene resin particles coated with a nickel layer having a thickness of 0.08 μm and a surface of the nickel plating layer coated with a gold plating layer having a thickness of 0.03 μm, average particles (Diameter 3μm)

(Other ingredients)
Silane coupling agent A (3-glycidoxypropyltriethoxysilane, “KBM-403” manufactured by Shin-Etsu Chemical Co., Ltd.)

(Example 1)
Preparation of connecting material:
50 parts by weight of phenol novolac type epoxy resin C (“EPICLON N-770” manufactured by DIC, weight average molecular weight 14000) and 50 parts by weight of epoxy monomer A (bisphenol F type epoxy monomer, “EXA-830CRP” manufactured by DIC) 4 parts by weight of acid generator A (acid generator represented by the above formula (21X)) and silane coupling agent A (3-glycidoxypropyltriethoxysilane, "KBM-403" manufactured by Shin-Etsu Chemical Co., Ltd. ) 1 part by weight was added and a connecting material was obtained by stirring at 2000 rpm for 5 minutes using a planetary stirrer.

Fabrication of connection structure:
A glass substrate (thickness: 300 μm) having an L / S of 20 μm / 20 μm and a Mo / Al / Mo electrode pattern having 998 electrodes formed on the upper surface was prepared. Further, a semiconductor chip (18 mm × 1.1 mm) having a gold electrode pattern on the lower surface with L / S of 20 μm / 20 μm, 998 electrodes, and bump height of 15 μm was prepared.

  On the glass substrate, the connection material immediately after fabrication was applied using a dispenser so as to have a width of 2.3 mm and a thickness of 30 μm to form a connection material layer.

Next, the semiconductor chip was stacked on the connection material layer at 100 ° C. (temporary pressure bonding temperature) so that the electrodes face each other and are connected. Thereafter, the temperature of the heating head is adjusted so that the temperature of the connecting material layer becomes 120 ° C. (final pressure bonding temperature), the heating head is placed on the upper surface of the semiconductor chip, and 1 second after immediately after the heating head is placed on the semiconductor chip. A connection structure was obtained by irradiating ultraviolet rays of 365 nm for 10 seconds so that the light irradiation intensity was 200 mW / cm ² and curing the connection material at 120 ° C. for 10 seconds to form a connection portion.

(Examples 2-11 and Comparative Examples 1-5)
A connection material was obtained in the same manner as in Example 1 except that the types and blending amounts of the blending components were set as shown in Table 1 below. In addition, as shown in Table 2 below, the main pressure bonding temperature, the light irradiation intensity, and the time from when the heating head is placed on the semiconductor chip to the time of irradiation with ultraviolet rays (the time from immediately after the main pressure bonding to the start of UV irradiation). A connection structure was obtained in the same manner as in Example 1 except that the setting was made.

(Evaluation)
(1) Glass transition temperature of cured product Using a dynamic viscoelasticity device ("DVA-200" manufactured by IT Measurement & Control Co., Ltd.), the heating rate was 5 ° C / min from room temperature, the deformation rate was 0.1%, and 10Hz. Under the conditions, the glass transition temperature of the cured product was measured. In Examples, when the time from immediately after the main press-bonding to the start of UV irradiation is 1 second, the glass transition temperature of the cured product obtained by changing the time to 0 seconds is It was the same as the glass transition temperature of the cured product at 1 second.

(2) Warpage of Connection Structure The amount of warpage of the semiconductor chip of the obtained connection structure was measured using a shape measurement laser microscope (“VK-X200 series” manufactured by Keyence Corporation). The displacement from the end of the semiconductor chip to the maximum height at the center was taken as the value of warpage.

(3) Conduction reliability (connection resistance value)
The connection resistance between the upper and lower electrodes of the obtained connection structure was measured by a four-terminal method. The average value of the connection resistance at 30 locations was calculated. Note that the connection resistance can be obtained by measuring the voltage when a constant current is passed from the relationship of voltage = current × resistance. The conduction reliability between the electrodes in the obtained connection structure was determined according to the following criteria.

[Judgment criteria for conduction reliability]
○○: Connection resistance is less than 1.5Ω ○: Connection resistance is 1.5Ω or more and less than 3Ω Δ: Connection resistance is 3Ω or more and less than 5Ω ×: Connection resistance is 5Ω or more

(4) Connection reliability The obtained connection structure was allowed to stand for 500 hours at 60 ° C. and a relative humidity of 90%. The connection resistance after standing was measured in the same manner as in the above (3) evaluation of conduction reliability. Connection reliability was determined according to the following criteria.

[Connection reliability criteria]
○○: Connection resistance is less than 3Ω ○: Connection resistance is 3Ω or more and less than 5Ω Δ: Connection resistance is 5Ω or more and less than 10Ω ×: Connection resistance is 10Ω or more

(5) Storage stability Viscosity η1 at 25 ° C. of the obtained connection material was measured using an E-type viscosity measuring device (“VISCOMETER TV-22” manufactured by TOKI SANGYO CO. LTD, cone rotor: No. 7, temperature: 25 )) At 25 ° C. and 2.5 rpm. Next, the connecting material was left at 25 ° C. for 168 hours. The viscosity η2 at 25 ° C. of the connecting material after standing was measured in the same manner. Storage stability was determined according to the following criteria.

[Criteria for storage stability]
◯: Ratio of viscosity η2 to viscosity η1 is less than 1.2 ○: Ratio of viscosity η2 to viscosity η1 is 1.2 or more and less than 1.4 Δ: Ratio of viscosity η2 to viscosity η1 is 1.4 or more, 1 Less than 6 x: Ratio of viscosity η2 to viscosity η1 is 1.6 or more

  The composition of the connecting material, the manufacturing conditions of the connecting structure and the results are shown in Tables 1 and 2 below.

DESCRIPTION OF SYMBOLS 1,11 ... Connection structure 1X ... Laminated body 2,12 ... 1st connection object member 2a, 12a ... 1st electrode 3,13 ... Connection part 3A ... Connection material layer 4,14 ... 2nd connection object member 4a, 14a ... 2nd electrode 5 ... Conductive particle 21 ... Dispenser 22 ... Temporary pressure bonding member 23 ... Main pressure bonding member 24 ... Light irradiation device 31 ... Conductive particle 32 ... Base material particle 33 ... Conductive layer

Claims (10)

Including a phenol novolac type epoxy resin, an epoxy monomer, and an acid generator,
The phenol novolac type epoxy resin has a weight average molecular weight of 8000 or more,
A connection material, wherein the acid generator is a sulfonium borate complex or a sulfonium antimony complex.   The connection material according to claim 1, wherein the epoxy monomer is a bisphenol A type epoxy monomer, a bisphenol E type epoxy monomer, or a bisphenol F type epoxy monomer.   In a total of 100% by weight of the phenol novolac type epoxy resin and the epoxy monomer, the content of the phenol novolac type epoxy resin is 40% by weight or more and 70% by weight or less, and the content of the epoxy monomer is 30% by weight. The connection material according to claim 1, wherein the connection material is not less than 60% and not more than 60% by weight.   Connection material of any one of Claims 1-3 containing electroconductive particle. A first connection object member having a first electrode on its surface;
A second connection target member having a second electrode on its surface;
A connection portion connecting the first connection target member and the second connection target member;
The connection part is formed of the connection material according to any one of claims 1 to 4,
A connection structure in which the first electrode and the second electrode are electrically connected. The first connection target member is a substrate;
The second connection target member is a semiconductor chip;
The connection structure according to claim 5, which is a liquid crystal display element. Forming a connection material layer on the surface of the first connection target member having the first electrode on the surface, using the connection material according to any one of claims 1 to 4;
By placing a second connection target member having a second electrode on the surface thereof on the surface opposite to the first connection target member side of the connection material layer, and performing temporary pressure bonding, the first Obtaining a laminate in which the connection target member, the connection material layer, and the second connection target member are temporarily press-bonded;
The laminated body is subjected to final pressure bonding, the connection material layer is heated and cured to form a connection portion, and the first connection target member and the second connection target member are connected by the connection portion. And a step of obtaining a connection structure in which the first electrode and the second electrode are electrically connected to each other.   The manufacturing method of the connection structure of Claim 7 which makes heating temperature of the said connection material layer 30 degreeC or more lower than the glass transition temperature of the hardened | cured material of the said connection material layer after this crimping | compression-bonding.   The manufacturing method of the connection structure of Claim 7 or 8 which heats and cures the said connection material layer to the temperature of 120 degrees C or less, without heating to the temperature exceeding 120 degreeC. A substrate is used as the first connection target member,
A semiconductor chip is used as the second connection target member,
The manufacturing method of the connection structure of any one of Claims 7-9 which obtains a liquid crystal display element as the said connection structure.

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