WO2014133124A1 - 導電性微粒子、異方性導電材料、及び、導電接続構造体 - Google Patents

導電性微粒子、異方性導電材料、及び、導電接続構造体 Download PDF

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WO2014133124A1
WO2014133124A1 PCT/JP2014/055035 JP2014055035W WO2014133124A1 WO 2014133124 A1 WO2014133124 A1 WO 2014133124A1 JP 2014055035 W JP2014055035 W JP 2014055035W WO 2014133124 A1 WO2014133124 A1 WO 2014133124A1
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Prior art keywords
layer
copper
fine particles
solder layer
conductive
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PCT/JP2014/055035
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English (en)
French (fr)
Inventor
浩也 石田
松下 清人
Original Assignee
積水化学工業株式会社
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Application filed by 積水化学工業株式会社 filed Critical 積水化学工業株式会社
Priority to US14/768,837 priority Critical patent/US9478326B2/en
Priority to JP2014511674A priority patent/JP5580954B1/ja
Priority to EP14756789.5A priority patent/EP2963655B1/en
Priority to CN201480005809.1A priority patent/CN104937675B/zh
Priority to KR1020157016027A priority patent/KR101561418B1/ko
Publication of WO2014133124A1 publication Critical patent/WO2014133124A1/ja

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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/60Electroplating characterised by the structure or texture of the layers
    • C25D5/615Microstructure of the layers, e.g. mixed structure
    • C25D5/619Amorphous layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/17Metallic particles coated with metal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/18Non-metallic particles coated with metal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/02Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape
    • B23K35/0222Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by mechanical features, e.g. shape for use in soldering, brazing
    • B23K35/0244Powders, particles or spheres; Preforms made therefrom
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/24Selection of soldering or welding materials proper
    • B23K35/26Selection of soldering or welding materials proper with the principal constituent melting at less than 400 degrees C
    • B23K35/262Sn as the principal constituent
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    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
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    • C23C18/00Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
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    • H05K2201/00Indexing scheme relating to printed circuits covered by H05K1/00
    • H05K2201/02Fillers; Particles; Fibers; Reinforcement materials
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    • H05K2203/04Soldering or other types of metallurgic bonding
    • H05K2203/0425Solder powder or solder coated metal powder

Definitions

  • the present invention relates to a conductive fine particle that is less likely to be disconnected due to breakage of a connection interface between an electrode and the conductive fine particle even when an impact due to dropping or the like is applied, and that is not easily fatigued even when subjected to repeated heating and cooling. Further, the present invention relates to an anisotropic conductive material using the conductive fine particles and a conductive connection structure.
  • soldering electrodes In an electronic circuit board, ICs and LSIs are connected by soldering electrodes to a printed circuit board.
  • soldering cannot efficiently connect the printed circuit board to the IC or LSI.
  • a BGA ball grid array
  • solder balls If the BGA is used, the solder ball mounted on the chip or the substrate can be melted at a high temperature to connect the substrate and the chip. Therefore, the production efficiency of the electronic circuit board is improved, and an electronic circuit board with an improved chip mounting density can be manufactured.
  • Patent Document 1 discloses a conductive material in which a conductive metal layer containing a highly conductive metal is formed on the surface of resin fine particles, and a solder layer is formed on the surface of the conductive metal layer. Fine particles have been disclosed. By using such conductive fine particles, the stress applied by the flexible resin fine particles to the conductive fine particles can be relaxed. Since the solder layer is formed on the outermost surface of the conductive fine particles, the electrodes can be easily conductively connected.
  • the conductive fine particles on which the solder layer is formed on the electrode of the substrate When mounting the conductive fine particles on which the solder layer is formed on the electrode of the substrate, the conductive fine particles are placed on the electrode formed on one substrate and reflowed to melt the solder layer, and the conductive fine particles Secure to the electrode. Thereafter, the electrodes formed on the other substrate and the electrodes formed on the one substrate are arranged so as to face each other, and the electrodes on the substrate are conductively connected by reflowing.
  • conductive fine particles having a solder layer formed on the surface of the core particle as disclosed in Patent Document 1 are used for conductive connection of an electronic circuit board having an electrode made of copper, which has become the mainstream in recent years, There has been a problem that disconnection due to destruction of the connection interface is likely to occur when an impact due to dropping or the like is applied.
  • the temperature inside the electronic device rises due to the heat generated by the electronic component. After the electronic device is used, the temperature inside the electronic device returns to room temperature. Cycle "is in progress. Even when this heat cycle was repeated, the connection interface between the electrode and the conductive fine particles was broken and sometimes disconnected.
  • Another object of the present invention is to provide an anisotropic conductive material using the conductive fine particles and a conductive connection structure.
  • the present invention provides conductive fine particles in which at least a conductive metal layer, a barrier layer, a copper layer, and a solder layer containing tin are laminated in this order on the surface of a core particle made of resin or metal, the copper layer And the solder layer are in direct contact with each other, and the conductive fine particles in which the ratio of copper in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 0.5 to 5% by weight.
  • the present invention is described in detail below.
  • the inventors have found that when conductive fine particles having a solder layer formed on the surface of core particles are used for conductive connection of an electronic circuit board having an electrode made of copper, impact due to dropping or the like may be applied.
  • the cause of the disconnection due to the destruction of the connection interface when the heat cycle is repeated is that a tin-copper intermetallic compound (hereinafter also simply referred to as “intermetallic compound”) is formed at the connection interface.
  • intermetallic compound tin-copper intermetallic compound
  • Intermetallic compounds are hard and brittle compared to copper and solder, so when impacts such as dropping are applied, or when the heat cycle is repeated, there are sites made of intermetallic compounds formed at the connection interface. It is thought that it is destroyed and disconnection occurs.
  • the present inventor by bringing the copper layer directly into contact with the solder layer so that the ratio to the tin contained in the solder layer is within a certain range, an impact due to dropping or the like is applied, The inventors have found that conductive fine particles that are less likely to be broken due to destruction of the connection interface can be obtained even when the heat cycle is repeated, and the present invention has been completed. This is because, when the copper layer is brought into direct contact with the solder layer of conductive fine particles in advance, when it is heated and melted during reflow, copper is first diffused from the copper layer into the solder layer and the copper in the solder layer is melted. This is thought to be because the momentum of “copper erosion” that attempts to take in more copper is suppressed, leaving pure copper in the electrode and preventing the formation of a large amount of intermetallic compounds at the connection interface.
  • the conductive fine particles of the present invention have a structure in which at least a conductive metal layer, a barrier layer, a copper layer, and a solder layer containing tin are laminated in this order on the surface of a core particle made of resin or metal.
  • the resin that forms the core particles include polyethylene resins, polypropylene resins, polystyrene resins, polyisobutylene resins, polybutadiene resins, polyvinyl chloride resins, polyvinylidene chloride resins, and polytetrafluoroethylene resins.
  • Examples thereof include acrylic resins such as methyl methacrylate resin and polymethyl acrylate resin, polyalkylene terephthalate resin, polysulfone resin, polycarbonate resin, polyamide resin, phenol formaldehyde resin, melamine formaldehyde resin, benzoguanamine formaldehyde resin, urea formaldehyde resin and the like.
  • the metal that forms the core particles include copper, nickel, silver, and the like.
  • core particles made of resin even if distortion or expansion / contraction due to changes in the external environment occurs on the substrate to which the conductive fine particles of the present invention are conductively connected, flexible resin becomes conductive fine particles. The applied stress can be relaxed.
  • core particles made of metal even if the chip generates heat, it can be expected that heat dissipation is improved by transmitting to the substrate through the particles.
  • the preferred lower limit of the 10% K value of the core particle is 1000 MPa and the preferred upper limit is 15000 MPa from the viewpoint of the shape when the conductive fine particles are compressed and deformed and the damage to the electrode.
  • the more preferable lower limit of the 10% K value is 2000 MPa, and the more preferable upper limit is 10,000 MPa.
  • the 10% K value is obtained by using a micro compression tester (for example, “PCT-200” manufactured by Shimadzu Corporation), and using a smooth indenter end face of a diamond cylinder having a diameter of 50 ⁇ m as a core particle made of resin.
  • Compressive displacement (mm) when compressed under conditions of 6 mN / sec and a maximum test load of 10 g can be obtained by the following equation.
  • K value (N / mm 2) ( 3 / ⁇ 2) ⁇ F ⁇ S -3/2 ⁇ R -1/2
  • F Load value (N) at 10% compression deformation of core particles made of resin
  • S Compression displacement (mm) in 10% compression deformation of core particles made of resin
  • R Radius of core particle made of resin (mm)
  • the core particle has a preferable lower limit of the average particle diameter of 10 ⁇ m and a preferable upper limit of 2000 ⁇ m.
  • a more preferable lower limit of the average particle diameter is 30 ⁇ m, and a more preferable upper limit is 1500 ⁇ m.
  • the more preferable lower limit of the average particle diameter is 50 ⁇ m, and the more preferable upper limit is 1000 ⁇ m.
  • the average particle diameter of the said core particle means the average value of the diameter obtained by observing 50 core particles selected at random using an optical microscope or an electron microscope.
  • the upper limit of the CV value of the particle diameter is preferably 15%.
  • a more preferable upper limit of the CV value is 10%.
  • the CV value is a numerical value indicated by a percentage (%) of a value obtained by dividing the standard deviation by the average particle diameter.
  • the method for producing the core particles made of the resin is not particularly limited, and examples thereof include a polymerization method, a method using a polymer protective agent, and a method using a surfactant.
  • the method by the said polymerization method is not specifically limited,
  • the method by polymerization methods such as emulsion polymerization, suspension polymerization, seed polymerization, dispersion polymerization, and dispersion seed polymerization, is mentioned.
  • the conductive metal layer has a role of improving the reliability of electrical connection between the conductive fine particles and the electrode.
  • the conductive metal layer may be directly formed on the core particle, and a base metal layer such as a nickel layer may be formed between the conductive metal layer and the core particle.
  • the metal forming the conductive metal layer examples include gold, silver, copper, platinum, palladium, cobalt, nickel, and the like. Especially, since it is excellent in the effect which improves the electrical connection reliability of electroconductive fine particles and an electrode, it is preferable that the said conductive metal layer contains copper.
  • the thickness of the said conductive metal layer is not specifically limited, From a viewpoint of electroconductivity and the softness
  • the thickness of the conductive metal layer is a thickness obtained by observing and measuring a section of 10 randomly selected conductive fine particles with a scanning electron microscope (SEM) and arithmetically averaging the measured values.
  • the barrier layer is located between the conductive metal layer and the copper layer, and has a role of preventing the metal constituting the conductive metal layer from diffusing into the solder layer during reflow.
  • pure copper is reduced due to copper erosion during reflow, a large amount of intermetallic compounds are formed and become brittle, causing disconnection.
  • electrical characteristics may be impaired due to a decrease in pure copper.
  • the material for forming the barrier layer examples include nickel, titanium, tantalum, titanium nitride, zirconia, and zirconia nitride. Especially, since the formation of the said barrier layer is easy, it is preferable that the said barrier layer contains nickel.
  • the barrier layer preferably has an amorphous structure, and specific examples include a nickel-phosphorus layer and a nickel-boron layer. When the barrier layer has an amorphous structure, the crystal grain boundary is reduced, so that copper hardly diffuses into the solder layer.
  • the thickness of the barrier layer is not particularly limited, from the viewpoint of preventing the diffusion of a metal such as copper into the solder layer and the formation of a hard and brittle intermetallic compound at the interface between the solder layer and the conductive metal layer.
  • a preferred lower limit is 0.2 ⁇ m and a preferred upper limit is 5 ⁇ m.
  • a more preferable lower limit of the thickness of the barrier layer is 0.5 ⁇ m, and a more preferable upper limit is 3 ⁇ m.
  • the thickness of the barrier layer is a thickness obtained by observing and measuring a section of 10 randomly selected conductive fine particles with a scanning electron microscope (SEM) and arithmetically averaging the measured values.
  • SEM scanning electron microscope
  • the conductive fine particles of the present invention are formed so that the copper layer and the solder layer are in direct contact with the outside of the barrier layer.
  • the solder layer has a role of being electrically connected between the electrodes of the substrate by melting by heating during reflow.
  • the solder layer is preferably formed on the outermost surface of the conductive fine particles.
  • the solder layer contains tin.
  • the solder layer preferably further contains silver.
  • a solder layer having a relatively low melting point and high strength can be obtained.
  • the silver content in the solder layer is not particularly limited, but the preferred lower limit of the ratio of silver to tin is 0.5% by weight, and the preferred upper limit is 10% by weight. Within this range, both a relatively low melting point and high strength can be achieved.
  • the solder layer may further contain a metal such as antimony, bismuth, indium, germanium, aluminum, zinc, nickel, and cobalt. Further, as will be described later, the solder layer may contain copper at a certain ratio.
  • the thickness of the solder layer is not particularly limited, the preferable lower limit is 1 ⁇ m and the preferable upper limit is 50 ⁇ m from the viewpoints of bondability with the electrode and dispersibility of the conductive fine particles when forming the solder layer.
  • the more preferable lower limit of the thickness of the solder layer is 3 ⁇ m, and the more preferable upper limit is 40 ⁇ m.
  • the thickness of the solder layer is a thickness obtained by observing and measuring a section of 10 randomly selected conductive fine particles with a scanning electron microscope (SEM) and arithmetically averaging the measured values.
  • the copper layer is formed so as to be in direct contact with the solder layer.
  • copper is first diffused from the copper layer into the solder layer at the time of heating and melting, and the copper concentration in the solder layer falls within a certain range.
  • the pure copper of the electrode is left, and a large amount of intermetallic compounds can be prevented from being formed at the connection interface.
  • the lower limit of the ratio of copper in the copper layer in direct contact with the solder layer with respect to tin contained in the solder layer is 0.5% by weight, and the upper limit is 5% by weight. If the copper ratio is less than 0.5% by weight, even if copper diffuses into the solder layer during reflow, the copper concentration will not be sufficient, and “copper erosion” cannot be sufficiently suppressed, and the purity of the electrode Therefore, it is impossible to prevent the formation of an intermetallic compound at the connection interface. If the copper ratio exceeds 5% by weight, the concentration of copper diffusing into the solder layer at the time of reflow becomes too high, the melting point of the solder rises, and the mountability is affected.
  • the upper limit with the preferable ratio of the copper in the copper layer which touches the said solder layer directly with respect to the tin contained in the said solder layer is 3 weight%.
  • the copper concentration diffused into the solder layer when the solder layer is heated and melted during reflow is in a certain range. It is important to make it. That is, when heated at 150 ° C. for 12 hours, the preferred lower limit of the copper concentration at any position of the solder layer is 0.5% by weight, the preferred upper limit is 40% by weight, and the more preferred lower limit is 0.7% by weight. A more preferred upper limit is 30% by weight.
  • the ratio of copper in the copper layer in direct contact with the solder layer corresponds to the concentration of copper diffused in the solder layer within this range when the solder layer is heated and melted during reflow.
  • the conductive fine particles of the present invention may further have nickel and / or cobalt attached to the surface of the solder layer. Since nickel, nickel and / or cobalt is attached to the surface of the solder layer, the crystal structure of the intermetallic compound formed at the connection interface between the conductive fine particles and the electrode after reflow is refined. Even when an impact due to the above is applied or the heat cycle is repeated, it is possible to obtain conductive fine particles that are less prone to disconnection due to destruction of the connection interface.
  • adhesion means that nickel and / or cobalt metal is present on the surface of the solder layer, and that the nickel and / or cobalt metal layer completely covers the surface of the solder layer. It means a state where it is not formed.
  • FIG. 1 is a schematic diagram showing an example of a preferred embodiment of the conductive fine particles of the present invention.
  • a base metal layer 2 a conductive metal layer 3, a barrier layer 4, a copper layer 5, and a solder layer 6 are formed in this order on the surface of a core particle 1 made of resin. . Further, nickel and / or cobalt 7 is attached to the surface of the solder layer 6.
  • the manufacturing method of the electroconductive fine particles of this invention is not specifically limited, A conventionally well-known method can be used.
  • the conductive fine particles of the present invention having the structure shown in FIG. 1 can be produced by the following method.
  • a nickel layer (hereinafter also referred to as a base nickel plating layer) is formed as a base plating layer on the surface of the core particles by an electroless plating method.
  • a conductive metal layer is formed on the surface of the base nickel plating layer.
  • the method for forming the conductive metal layer is not particularly limited, and examples thereof include a method using an electrolytic plating method, an electroless plating method, or the like.
  • a nickel layer is formed as a barrier layer on the surface of the conductive metal layer.
  • the method for forming the nickel layer is not particularly limited, and examples thereof include a method using an electrolytic plating method, an electroless plating method, or the like.
  • a copper layer is formed on the surface of the barrier layer.
  • the method for forming the copper layer is not particularly limited, and examples thereof include a method using an electrolytic plating method, an electroless plating method, or the like.
  • solder layer containing tin is formed on the surface of the copper layer.
  • the method for forming the solder layer is not particularly limited, and examples thereof include a method using an electrolytic plating method.
  • a method for attaching nickel and / or cobalt to the surface of the solder layer is not particularly limited, and examples thereof include a sputtering method and an electroless plating method.
  • An anisotropic conductive material can be produced by dispersing the conductive fine particles of the present invention in a binder resin. Such an anisotropic conductive material is also one aspect of the present invention.
  • anisotropic conductive material of the present invention examples include anisotropic conductive paste, anisotropic conductive ink, anisotropic conductive adhesive, anisotropic conductive film, and anisotropic conductive sheet.
  • the said binder resin is not specifically limited, A vinyl resin, a thermoplastic resin, curable resin, a thermoplastic block copolymer, an elastomer, etc. are mentioned.
  • the said vinyl resin is not specifically limited, Vinyl acetate resin, an acrylic resin, a styrene resin etc. are mentioned.
  • the thermoplastic resin is not particularly limited, and examples thereof include polyolefin resins, ethylene-vinyl acetate copolymers, polyamide resins and the like.
  • the said curable resin is not specifically limited, An epoxy resin, a urethane resin, a polyimide resin, an unsaturated polyester resin etc. are mentioned.
  • thermoplastic block copolymer is not particularly limited, but a styrene-butadiene-styrene block copolymer, a styrene-isoprene-styrene block copolymer, a hydrogenated product of a styrene-butadiene-styrene block copolymer, a styrene-isoprene. -Hydrogenated products of styrene block copolymers.
  • these resins may be used alone or in combination of two or more.
  • the curable resin may be any one of a room temperature curable resin, a thermosetting resin, a photocurable resin, and a moisture curable resin.
  • the anisotropic conductive material of the present invention can be used, for example, as a bulking agent, a plasticizer, an adhesive improver, an antioxidant, a heat stabilizer, a light stabilizer, an ultraviolet absorber, a colorant, You may contain various additives, such as a flame retardant and an organic solvent.
  • the method for producing the anisotropic conductive material of the present invention is not particularly limited.
  • the conductive fine particles of the present invention are added to the binder resin, and the mixture is uniformly mixed and dispersed. And a method for producing a conductive conductive ink, an anisotropic conductive adhesive, and the like.
  • the conductive fine particles of the present invention are added to the binder resin and dispersed uniformly, or dissolved by heating, release paper, release film, etc.
  • a method for producing an anisotropic conductive film, an anisotropic conductive sheet, etc. by coating the mold release treatment surface of the mold release material so as to have a predetermined thickness and drying or cooling as necessary. It is done.
  • An appropriate manufacturing method can be selected in accordance with the type of anisotropic conductive material.
  • a conductive connection structure using the conductive fine particles of the present invention or the anisotropic conductive material of the present invention is also one aspect of the present invention.
  • the conductive connection structure of the present invention is a conductive connection structure in which a pair of circuit boards are connected by filling the pair of circuit boards with the conductive fine particles of the present invention or the anisotropic conductive material of the present invention. It is.
  • conductive fine particles which are less likely to be disconnected due to the destruction of the connection interface between the electrode and the conductive fine particles even when an impact due to dropping or the like is applied, and which are not easily fatigued even when subjected to repeated heating and cooling. be able to.
  • an anisotropic conductive material using the conductive fine particles and a conductive connection structure can be provided.
  • Example 1 Preparation of core particles made of resin 50 parts by weight of divinylbenzene and 50 parts by weight of tetramethylolmethanetetraacrylate were copolymerized to form core particles made of resin (average particle diameter 180 ⁇ m, CV value 0.42%). Produced.
  • the obtained core particles were electroless nickel-plated to form a base nickel plating layer having a thickness of 0.3 ⁇ m on the surface of the core particles. Then, a copper layer (conductive metal layer) having a thickness of 7 ⁇ m was formed by performing electrolytic copper plating. Next, a nickel layer (barrier layer) having a thickness of 0.6 ⁇ m was formed by performing electrolytic nickel plating. Next, a copper layer having a thickness of 1 ⁇ m was formed by performing electrolytic copper plating. Subsequently, a solder layer containing tin having a thickness of 34 ⁇ m was formed by electrolytic plating.
  • the electrolytic plating solution is filtered, and the obtained particles are washed with water and then dried with a vacuum dryer at 50 ° C., and the surface of the core particles is coated with a base metal layer, a conductive metal layer, a barrier layer, copper Conductive fine particles in which a layer and a solder layer were sequentially formed were obtained.
  • the ratio of the copper contained in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 2.6% by weight.
  • Example 2 A base metal layer, a conductive metal layer, a barrier layer, a copper layer, and a solder layer were sequentially formed on the surface of the core particle in the same manner as in Example 1 except that the thickness of the copper layer in direct contact with the solder layer was 0.4 ⁇ m.
  • the formed conductive fine particles were obtained.
  • the ratio of copper contained in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 1.0% by weight.
  • Example 3 A base metal layer, a conductive metal layer, a barrier layer, a copper layer, and a solder layer are sequentially formed on the surface of the core particle in the same manner as in Example 1 except that the thickness of the copper layer in direct contact with the solder layer is 2 ⁇ m. Conductive fine particles were obtained. In the obtained conductive fine particles, the ratio of the copper contained in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 5.0% by weight.
  • Example 4 A base metal layer, a conductive metal layer, a barrier layer, a copper layer, and a solder layer are sequentially formed on the surface of the core particle in the same manner as in Example 1 except that the thickness of the copper layer in direct contact with the solder layer is 0.2 ⁇ m.
  • the formed conductive fine particles were obtained.
  • the ratio of copper contained in the copper layer in direct contact with the solder layer to tin contained in the solder layer is 0.5% by weight.
  • Example 5 A base metal layer, a conductive metal layer, a barrier layer, a copper layer, a solder layer, and solder are formed on the surface of the core particle in the same manner as in Example 1 except that nickel is attached to the surface of the solder layer by sputtering. Conductive fine particles in which nickel adhered to the layer were sequentially formed were obtained.
  • Example 6 In the same manner as in Example 1 except that nickel is attached to the surface of the solder layer by electroless plating, the base metal layer, the conductive metal layer, the barrier layer, the copper layer, the solder layer, Then, conductive fine particles were obtained in which nickel adhered to the solder layer was sequentially formed.
  • Example 7 In the same manner as in Example 1 except that cobalt was attached to the surface of the solder layer by electroless plating, the base metal layer, the conductive metal layer, the barrier layer, the copper layer, the solder layer, and As a result, conductive fine particles in which cobalt adhered to the solder layer was sequentially formed were obtained.
  • Example 8 Preparation of core particles made of resin 50 parts by weight of divinylbenzene and 50 parts by weight of tetramethylolmethanetetraacrylate were copolymerized to form core particles made of resin (average particle diameter 150 ⁇ m, CV value 0.38%). Produced.
  • the obtained core particles were electroless nickel-plated to form a base nickel plating layer having a thickness of 0.3 ⁇ m on the surface of the core particles.
  • a copper layer (conductive metal layer) having a thickness of 10 ⁇ m was formed by performing electrolytic copper plating.
  • a nickel layer (barrier layer) having a thickness of 0.6 ⁇ m was formed by performing electrolytic nickel plating.
  • a copper layer having a thickness of 0.5 ⁇ m was formed by performing electrolytic copper plating.
  • a solder layer containing tin having a thickness of 40 ⁇ m was formed by electrolytic plating.
  • the electrolytic plating solution is filtered, and the obtained particles are washed with water and then dried with a vacuum dryer at 50 ° C., and the surface of the core particles is coated with a base metal layer, a conductive metal layer, a barrier layer, copper Conductive fine particles in which a layer and a solder layer were sequentially formed were obtained.
  • the ratio of copper contained in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 1.0% by weight.
  • Example 9 In the same manner as in Example 8 except that nickel was adhered to the surface of the solder layer by electroless plating, the surface of the core particle was coated with a base metal layer, a conductive metal layer, a barrier layer, a copper layer, a solder layer, and Then, conductive fine particles were obtained in which nickel adhered to the solder layer was sequentially formed.
  • Example 10 In the same manner as in Example 1 except that cobalt was attached to the surface of the solder layer by electroless plating, the base metal layer, the conductive metal layer, the barrier layer, the copper layer, the solder layer, and As a result, conductive fine particles in which cobalt adhered to the solder layer was sequentially formed were obtained.
  • Example 1 Conductive fine particles in which a base metal layer, a conductive metal layer, a barrier layer, and a solder layer are sequentially formed on the surface of the core particle are the same as in Example 1 except that the copper layer that is in direct contact with the solder layer is not formed. Obtained.
  • Example 2 A base metal layer, a conductive metal layer, and a barrier layer are formed on the surface of the core particle in the same manner as in Example 1 except that a copper layer that is in direct contact with the solder layer is formed by electroless plating and the thickness is 0.05 ⁇ m.
  • a copper layer that is in direct contact with the solder layer is formed by electroless plating and the thickness is 0.05 ⁇ m.
  • conductive fine particles in which a copper layer and a solder layer were sequentially formed were obtained.
  • the ratio of copper contained in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 0.1% by weight.
  • Example 3 A base metal layer, a conductive metal layer, a barrier layer, a copper layer, and a solder layer were sequentially formed on the surface of the core particle in the same manner as in Example 1 except that the thickness of the copper layer in direct contact with the solder layer was 4 ⁇ m. Conductive fine particles were obtained. In the obtained conductive fine particles, the ratio of the copper contained in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 10% by weight.
  • Comparative Example 4 In the same manner as in Comparative Example 2 except that nickel was adhered to the surface of the solder layer by electroless plating, the surface of the core particle was coated with a base metal layer, a conductive metal layer, a barrier layer, a copper layer, a solder layer, and Then, conductive fine particles were obtained in which nickel adhered to the solder layer was sequentially formed.
  • Comparative Example 5 In the same manner as in Comparative Example 2 except that cobalt was attached to the surface of the solder layer by electroless plating, the surface of the core particle was coated with a base metal layer, a conductive metal layer, a barrier layer, a copper layer, a solder layer, and As a result, conductive fine particles in which cobalt adhered to the solder layer was sequentially formed were obtained.
  • Example 7 A base metal layer, a conductive metal layer, and a barrier layer are formed on the surface of the core particles in the same manner as in Example 8 except that a copper layer directly contacting the solder layer is formed by electroless plating and the thickness is 0.1 ⁇ m.
  • a copper layer directly contacting the solder layer is formed by electroless plating and the thickness is 0.1 ⁇ m.
  • conductive fine particles in which a copper layer and a solder layer were sequentially formed were obtained.
  • the ratio of the copper contained in the copper layer in direct contact with the solder layer to the tin contained in the solder layer is 0.2% by weight.
  • Comparative Example 8 In the same manner as in Comparative Example 7, except that nickel was adhered to the surface of the solder layer by electroless plating, the surface of the core particle was coated with a base metal layer, a conductive metal layer, a barrier layer, a copper layer, a solder layer, and Then, conductive fine particles were obtained in which nickel adhered to the solder layer was sequentially formed.
  • Comparative Example 9 In the same manner as in Comparative Example 2 except that cobalt was attached to the surface of the solder layer by electroless plating, the surface of the core particle was coated with a base metal layer, a conductive metal layer, a barrier layer, a copper layer, a solder layer, and As a result, conductive fine particles in which cobalt adhered to the solder layer was sequentially formed were obtained.
  • Temperature cycle test Flux (“WS-9160-M7” manufactured by Cookson Electronics Co., Ltd.) was applied to 121 electrode lands (diameter: 230 ⁇ m) provided at a pitch of 0.4 mm on a silicon chip (length 5 mm ⁇ width 5 mm). Applied. The obtained conductive fine particles were placed on all the electrode lands, reflowed (heating temperature 250 ° C., 30 seconds), and the conductive fine particles were mounted on the electrode lands. Next, a solder paste (“M705-GRN360-K2-V” manufactured by Senju Metal Industry Co., Ltd.) was applied to the printed circuit board on which the copper electrode (diameter 250 ⁇ m) was formed.
  • One silicon chip on which conductive fine particles were mounted was placed on a printed circuit board, reflowed (heating temperature 250 ° C., 30 seconds), and one silicon chip was mounted on the printed circuit board to obtain a conductive connection structure. Since the obtained conductive connection structure is formed with a daisy chain circuit, it can be detected even if one electrode land is disconnected.
  • a temperature cycle test in which one cycle was ⁇ 40 ° C. to 125 ° C. was performed. The heat profile for the temperature cycle test was held at ⁇ 40 ° C. for 10 minutes, raised from ⁇ 40 ° C. to 125 ° C. for 2 minutes, held at 125 ° C. for 10 minutes, and then from 125 ° C.
  • the temperature cycle test was evaluated according to the following criteria. A: The number of cycles in which the disconnection of the conductive connection structure was confirmed was 1000 cycles or more. X: The number of cycles in which disconnection of the conductive connection structure was confirmed was less than 1000 cycles.
  • Example 11 As a result of dispersing the particles of Example 1 in a binder resin and performing circuit connection, it was confirmed that electrical conduction was achieved.
  • conductive fine particles which are less likely to be disconnected due to the destruction of the connection interface between the electrode and the conductive fine particles even when an impact due to dropping or the like is applied, and which are not easily fatigued even when subjected to repeated heating and cooling. be able to.
  • an anisotropic conductive material using the conductive fine particles and a conductive connection structure can be provided.

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Abstract

本発明は、落下等による衝撃が加わっても電極と該導電性微粒子との接続界面の破壊による断線が生じにくく、加熱と冷却とを繰返し受けても疲労しにくい導電性微粒子、該導電性微粒子を用いてなる異方性導電材料、及び、導電接続構造体を提供することを目的とする。 本発明は、樹脂又は金属からなるコア粒子の表面に、少なくとも導電金属層、バリア層、銅層、及び、錫を含有するハンダ層がこの順に積層された導電性微粒子であって、前記銅層とハンダ層とが直接接しており、前記ハンダ層中に含まれる錫に対する前記ハンダ層に直接接する銅層における銅の比率が0.5~5重量%である導電性微粒子である。

Description

導電性微粒子、異方性導電材料、及び、導電接続構造体
本発明は、落下等による衝撃が加わっても電極と該導電性微粒子との接続界面の破壊による断線が生じにくく、加熱と冷却とを繰返し受けても疲労しにくい導電性微粒子に関する。また、該導電性微粒子を用いてなる異方性導電材料、及び、導電接続構造体に関する。
従来、電子回路基板において、ICやLSIは、電極をプリント基板にハンダ付けすることによって接続されていた。しかし、ハンダ付けでは、プリント基板と、ICやLSIとを効率的に接続することはできなかった。また、ハンダ付けでは、ICやLSIの実装密度を向上させることが困難であった。
これを解決するためにハンダを球状にした、いわゆる「ハンダボール」でICやLSIを基板に接続するBGA(ボールグリッドアレイ)が開発された。BGAを用いれば、チップ又は基板に実装されたハンダボールを高温で溶融させ、基板とチップとを接続することができる。したがって、電子回路基板の生産効率が改善され、チップの実装密度が向上した電子回路基板を製造することができる。
しかし、近年、基板の多層化が進み、多層基板は使用環境の影響を受けやすいことから、基板に歪みや伸縮が発生し、基板間の接続部に断線が発生するという問題があった。
例えば、ハンダボールを用いて、半導体が基板に接続されると、半導体と基板との線膨張係数が違うため、ハンダボールに応力が加わる。その結果、ハンダボールに亀裂が入り、断線することがあった。
このような問題に対し、特許文献1には、樹脂微粒子の表面に、導電性の高い金属が含まれる導電金属層が形成され、更に、導電金属層の表面に、ハンダ層が形成された導電性微粒子が開示されている。このような導電性微粒子を用いれば、柔軟な樹脂微粒子が導電性微粒子に加わる応力を緩和することができる。導電性微粒子の最表面にハンダ層が形成されているため、電極間を容易に導電接続することができる。
ハンダ層が形成された導電性微粒子を基板の電極に実装する場合、一方の基板に形成された電極上に、導電性微粒子を配置し、リフローすることでハンダ層を溶融させ、導電性微粒子を電極に固定する。その後、他方の基板に形成された電極と、一方の基板に形成された電極とが対向するように配置し、リフローすることで基板の電極間が導電接続される。
しかしながら、近年主流となっている銅からなる電極を有する電子回路基板の導電接続に特許文献1に開示されているようなコア粒子の表面にハンダ層が形成された導電性微粒子を用いた場合、落下等による衝撃が加わったときに接続界面の破壊による断線が生じやすいという問題があった。また、電子機器は使用されると、電子部品の発熱によって、電子機器内部の温度が上がり、電子機器の使用後は、電子機器内部の温度が室温に戻るという加熱-冷却の繰返し、いわゆる「ヒートサイクル」が進行している。このヒートサイクルが繰返されたときも、電極と導電性微粒子との接続界面が破壊され、断線することがあった。
特開2001-220691号公報
本発明は、落下等による衝撃が加わっても電極と該導電性微粒子との接続界面の破壊による断線が生じにくく、加熱と冷却とを繰返し受けても疲労しにくい導電性微粒子を提供することを目的とする。また、本発明は、該導電性微粒子を用いてなる異方性導電材料、及び、導電接続構造体を提供することを目的とする。
本発明は、樹脂又は金属からなるコア粒子の表面に、少なくとも導電金属層、バリア層、銅層、及び、錫を含有するハンダ層がこの順に積層された導電性微粒子であって、前記銅層とハンダ層とが直接接しており、前記ハンダ層中に含まれる錫に対する前記ハンダ層に直接接する銅層における銅の比率が0.5~5重量%である導電性微粒子である。
以下に本発明を詳述する。
本発明者は、鋭意検討の結果、銅からなる電極を有する電子回路基板の導電接続にコア粒子の表面にハンダ層が形成された導電性微粒子を用いた場合に、落下等による衝撃が加わったり、ヒートサイクルが繰返されたりしたときに接続界面の破壊による断線が生じる原因が、接続界面に錫-銅の金属間化合物(以下、単に「金属間化合物」ともいう。)が生成することであることを見出した。即ち、ハンダ層には錫が含まれるが、リフロー時に加熱してハンダ層を溶融させたときに、電極を構成する銅の一部を取り込んで、電極の純粋な銅を減少させ、接続界面に多量の金属間化合物が形成されると考えられる(以下、この現象を「銅食い」ともいう。)。金属間化合物は、銅やハンダに比べて硬く脆い性質であることから、落下等による衝撃が加わったり、ヒートサイクルが繰返されたりしたときに、接続界面に形成された金属間化合物からなる部位が破壊され、断線が生じるものと考えられる。
本発明者は、更に鋭意検討の結果、ハンダ層中に含まれる錫に対する比率が一定の範囲内になるように、ハンダ層に直接銅層を接触させることにより、落下等による衝撃が加わったり、ヒートサイクルが繰返されたりしたときにでも、接続界面の破壊による断線が生じにくい導電性微粒子が得られることを見出し、本発明を完成した。
これは、予め導電性微粒子のハンダ層に直接銅層を接触させることにより、リフロー時に加熱溶融したときに、まず銅層からハンダ層中に銅が拡散してハンダ層中の銅が溶け込むことから、それ以上の銅を取り込もうとする「銅食い」の勢いを抑制し、電極の純粋な銅を残し、接続界面に多量の金属間化合物が形成されるのを防止できるためと考えられる。
本発明の導電性微粒子は、樹脂又は金属からなるコア粒子の表面に、少なくとも導電金属層、バリア層、銅層、及び、錫を含有するハンダ層がこの順に積層された構造を有する。
上記コア粒子を形成する樹脂としては、例えば、ポリエチレン樹脂、ポリプロピレン樹脂、ポリスチレン樹脂、ポリイソブチレン樹脂、ポリブタジエン樹脂、ポリ塩化ビニル樹脂、ポリ塩化ビニリデン樹脂、ポリテトラフルオロエチレン樹脂等のポリオレフィン樹脂や、ポリメチルメタクリレート樹脂、ポリメチルアクリレート樹脂等のアクリル樹脂や、ポリアルキレンテレフタレート樹脂、ポリスルホン樹脂、ポリカーボネート樹脂、ポリアミド樹脂、フェノールホルムアルデヒド樹脂、メラミンホルムアルデヒド樹脂、ベンゾグアナミンホルムアルデヒド樹脂、尿素ホルムアルデヒド樹脂等が挙げられる。
上記コア粒子を形成する金属としては、例えば、銅、ニッケル、銀等が挙げられる。
なかでも、樹脂からなるコア粒子を用いた場合には、本発明の導電性微粒子を導電接続させた基板に、外環境変化による歪みや伸縮が発生しても、柔軟な樹脂が導電性微粒子に加わる応力を緩和できる。一方、金属からなるコア粒子を用いた場合には、チップが発熱しても、粒子を介して基板に伝達することで放熱性を向上させることが期待できる。
上記コア粒子が樹脂からなる場合には、導電性微粒子を圧縮変形させた場合の形状や、電極へのダメージの観点から、上記コア粒子の10%K値の好ましい下限は1000MPa、好ましい上限は15000MPaであり、上記10%K値のより好ましい下限は2000MPa、より好ましい上限は10000MPaである。
なお、上記10%K値は、微小圧縮試験器(例えば、島津製作所社製「PCT-200」)を用い、樹脂からなるコア粒子を直径50μmのダイアモンド製円柱の平滑圧子端面で、圧縮速度2.6mN/秒、最大試験荷重10gの条件下で圧縮した場合の圧縮変位(mm)を測定し、下記式により求めることができる。
  K値(N/mm)=(3/√2)・F・S-3/2・R-1/2
  F:樹脂からなるコア粒子の10%圧縮変形における荷重値(N)
  S:樹脂からなるコア粒子の10%圧縮変形における圧縮変位(mm)
  R:樹脂からなるコア粒子の半径(mm)
上記コア粒子は、コア粒子や導電性微粒子の分散性、異方性導電材料としての適正の観点から、平均粒子径の好ましい下限が10μm、好ましい上限が2000μmである。上記平均粒子径のより好ましい下限は30μm、より好ましい上限は1500μmである。上記平均粒子径の更に好ましい下限は50μm、更に好ましい上限は1000μmである。
なお、上記コア粒子の平均粒子径は、光学顕微鏡、又は、電子顕微鏡を用いて無作為に選んだ50個のコア粒子を観察して得られた直径の平均値を意味する。
上記コア粒子は、導電性微粒子の接続信頼性の観点から、粒子径のCV値の好ましい上限が15%である。CV値のより好ましい上限は10%である。なお、CV値は、標準偏差を平均粒子径で割った値の百分率(%)で示される数値である。
上記樹脂からなるコア粒子を作製する方法は特に限定されず、例えば、重合法による方法、高分子保護剤を用いる方法、界面活性剤を用いる方法等が挙げられる。
上記重合法による方法は特に限定されず、乳化重合、懸濁重合、シード重合、分散重合、分散シード重合等の重合法による方法が挙げられる。
上記導電金属層は、導電性微粒子と電極との電気的接続信頼性を高める役割を有する。
上記導電金属層は、上記コア粒子に直接形成されていてもよく、上記導電金属層と上記コア粒子との間に、ニッケル層等の下地金属層が形成されていてもよい。
上記導電金属層を形成する金属としては、例えば、金、銀、銅、白金、パラジウム、コバルト、ニッケル等が挙げられる。なかでも、導電性微粒子と電極との電気的接続信頼性を高める効果に優れることから、上記導電金属層は、銅を含有することが好ましい。
上記導電金属層の厚さは特に限定されないが、導電性や、導電性微粒子の柔軟性の観点から好ましい下限は1μm、好ましい上限は70μmである。上記導電金属層の厚さのより好ましい下限は3μm、より好ましい上限は50μmである。
なお、上記導電金属層の厚さは、無作為に選んだ10個の導電性微粒子の断面を走査型電子顕微鏡(SEM)により観察して測定し、測定値を算術平均した厚さである。
上記バリア層は、上記導電金属層と銅層との間にあって、リフロー時に上記導電金属層を構成する金属がハンダ層中に拡散してしまうのを防止する役割を有する。とりわけ、上記導電金属層に銅が含まれる場合、リフロー時にその銅が銅食いによって純粋な銅が減少し、多量の金属間化合物が形成され脆化して断線の原因となる。また純粋な銅が減少することにより、電気特性(導電性)が損なわれる可能性が生じる。
上記バリア層を形成する材料としては、例えば、ニッケル、チタン、タンタル、窒化チタン、ジルコニア、窒化ジルコニア等が挙げられる。なかでも、上記バリア層の形成が容易であることから、上記バリア層はニッケルを含有することが好ましい。また、上記バリア層は、アモルファス構造であることが好ましく、具体的には、ニッケル-リン層、ニッケル-ホウ素層等が挙げられる。上記バリア層がアモルファス構造であると、結晶粒界が少なくなるため、銅はハンダ層に拡散しにくくなる。
上記バリア層の厚さは特に限定されないが、ハンダ層中への銅等の金属の拡散や、ハンダ層と導電金属層との界面に、硬くて脆い金属間化合物の形成を防止する観点から、好ましい下限は0.2μm、好ましい上限は5μmである。上記バリア層の厚さのより好ましい下限は0.5μm、より好ましい上限は3μmである。
なお、上記バリア層の厚さは、無作為に選んだ10個の導電性微粒子の断面を走査型電子顕微鏡(SEM)により観察して測定し、測定値を算術平均した厚さである。
本発明の導電性微粒子では、上記バリア層の外側に、銅層とハンダ層とが直接接するように形成されている。
上記ハンダ層は、リフロー時の加熱により溶融して、基板の電極間を導電接続する役割を有する。上記ハンダ層は、導電性微粒子の最表面に形成されていることが好ましい。
上記ハンダ層は、錫を含有する。
上記ハンダ層は、更に、銀を含有することが好ましい。銀を含有することにより、比較的低融点で高強度のハンダ層とすることができる。
上記ハンダ層における銀の含有量は特に限定されないが、錫に対する銀の比率の好ましい下限は0.5重量%、好ましい上限は10重量%である。この範囲内であると、比較的低融点と高強度とを両立させることができる。
上記ハンダ層は、錫及び銀に加えて、更に、アンチモン、ビスマス、インジウム、ゲルマニウム、アルミニウム、亜鉛、ニッケル、コバルト等の金属を含有してもよい。また、後述するように上記ハンダ層は、一定の比率で銅を含有してもよい。
上記ハンダ層の厚さは特に限定されないが、電極との接合性や、ハンダ層形成時の導電性微粒子の分散性の観点から、好ましい下限は1μm、好ましい上限は50μmである。上記ハンダ層の厚さのより好ましい下限は3μm、より好ましい上限は40μmである。
なお、上記ハンダ層の厚さは、無作為に選んだ10個の導電性微粒子の断面を走査型電子顕微鏡(SEM)により観察して測定し、測定値を算術平均した厚さである。
上記銅層は、上記ハンダ層に直接接するように形成される。上記ハンダ層に銅層が直接接することにより、加熱溶融時にはまず銅層からハンダ層中に銅が拡散して、ハンダ層中の銅濃度が一定範囲になることから、「銅食い」を抑制し、電極の純粋な銅を残し、接続界面に多量の金属間化合物が形成されるのを防止できる。
上記ハンダ層中に含まれる錫に対する、上記ハンダ層に直接接する銅層における銅の比率の下限は0.5重量%、上限は5重量%である。銅の比率が0.5重量%未満であると、リフロー時にハンダ層中に銅が拡散しても充分な銅濃度とはならず、「銅食い」を充分には抑制できず、電極の純粋な銅を残し、接続界面に金属間化合物が形成されるのを防止できない。銅の比率が5重量%を超えると、リフロー時にハンダ層中に拡散する銅の濃度が高くなりすぎ、ハンダの融点が上昇し、実装性に影響が出る。上記ハンダ層中に含まれる錫に対する、上記ハンダ層に直接接する銅層における銅の比率の好ましい上限は3重量%である。
なお、「銅食い」を充分に抑制し、かつ、ハンダの融点の上昇を防止するためには、リフロー時にハンダ層を加熱溶融させたときにハンダ層中に拡散される銅濃度を一定の範囲にすることが重要である。即ち、150℃、12時間加熱したときに、ハンダ層の任意の位置における銅の濃度の好ましい下限が0.5重量%、好ましい上限が40重量%であり、より好ましい下限が0.7重量%、より好ましい上限が30重量%である。上記ハンダ層に直接接する銅層における銅の比率は、リフロー時にハンダ層を加熱溶融させたときにハンダ層中に拡散される銅濃度をこの範囲内にすることに対応したものである。
本発明の導電性微粒子は、更に、上記ハンダ層の表面にニッケル及び/又はコバルトが付着されていてもよい。ハンダ層の表面にニッケル、ニッケル及び/又はコバルトが付着されていることにより、リフロー後に導電性微粒子と電極との接続界面に形成される金属間化合物の結晶組織が微細化されることから、落下等による衝撃が加わったり、ヒートサイクルが繰返されたりしたときにでも、接続界面の破壊による断線がよりいっそう生じにくい導電性微粒子とすることができる。
なお、本願明細書において付着とは、上記ハンダ層の表面にニッケル及び/又はコバルトの金属が存在しており、かつ、上記ハンダ層の表面を完全に被覆するニッケル及び/又はコバルトの金属層が形成されていない状態を意味する。
図1に本発明の導電性微粒子の好ましい態様の一例を示す模式図を示した。
図1に示した導電性微粒子は、樹脂からなるコア粒子1の表面に、下地金属層2、導電金属層3、バリア層4、銅層5、及び、ハンダ層6がこの順に形成されている。また、ハンダ層6の表面には、ニッケル及び/又はコバルト7が付着されている。
本発明の導電性微粒子の製造方法は特に限定されず、従来公知の方法を用いることができる。例えば、図1に示した構造の本発明の導電性微粒子は、以下の方法により製造することができる。
まず、樹脂からなるコア粒子の表面に導電金属層を形成させる場合、コア粒子の表面に無電解メッキ法により下地メッキ層としてニッケル層(以下、下地ニッケルメッキ層ともいう)を形成させる。
次に、下地ニッケルメッキ層の表面に導電金属層を形成させる。
上記導電金属層を形成させる方法は特に限定されず、例えば、電解メッキ法、無電解メッキ法等による方法が挙げられる。
次に、上記導電金属層の表面にバリア層として例えばニッケル層を形成させる。
上記ニッケル層を形成させる方法は特に限定されず、例えば、電解メッキ法、無電解メッキ法等による方法が挙げられる。
次に、上記バリア層の表面に銅層を形成させる。
上記銅層を形成させる方法は特に限定されず、例えば、電解メッキ法、無電解メッキ法等による方法が挙げられる。
次に、上記銅層の表面に錫を含有するハンダ層を形成させる。
上記ハンダ層を形成させる方法は特に限定されず、例えば、電解メッキ法による方法が挙げられる。
次に、ハンダ層の表面にニッケル及び/又はコバルトを付着させる。
上記ハンダ層の表面にニッケル及び/又はコバルトを付着させる方法は特に限定されず、スパッタリング法や無電解メッキ法等が挙げられる。
本発明の導電性微粒子をバインダー樹脂に分散させることにより異方性導電材料を製造することができる。このような異方性導電材料もまた、本発明の1つである。
本発明の異方性導電材料は、例えば、異方性導電ペースト、異方性導電インク、異方性導電粘着剤、異方性導電フィルム、異方性導電シート等が挙げられる。
上記バインダー樹脂は特に限定されないが、ビニル樹脂、熱可塑性樹脂、硬化性樹脂、熱可塑性ブロック共重合体、エラストマー等が挙げられる。
上記ビニル樹脂は特に限定されないが、酢酸ビニル樹脂、アクリル樹脂、スチレン樹脂等が挙げられる。上記熱可塑性樹脂は特に限定されないが、ポリオレフィン樹脂、エチレン-酢酸ビニル共重合体、ポリアミド樹脂等が挙げられる。上記硬化性樹脂は特に限定されないが、エポキシ樹脂、ウレタン樹脂、ポリイミド樹脂、不飽和ポリエステル樹脂等が挙げられる。上記熱可塑性ブロック共重合体は特に限定されないが、スチレン-ブタジエン-スチレンブロック共重合体、スチレン-イソプレン-スチレンブロック共重合体、スチレン-ブタジエン-スチレンブロック共重合体の水素添加物、スチレン-イソプレン-スチレンブロック共重合体の水素添加物等が挙げられる。これらの樹脂は、単独で用いられてもよいし、2種以上が併用されてもよい。
また、上記硬化性樹脂は、常温硬化型樹脂、熱硬化型樹脂、光硬化型樹脂、湿気硬化型樹脂のいずれの硬化型樹脂であってもよい。
本発明の異方性導電材料は、必要に応じて、例えば、増量剤、可塑剤、粘接着性向上剤、酸化防止剤、熱安定剤、光安定剤、紫外線吸収剤、着色剤、難燃剤、有機溶媒等の各種添加剤を含有してもよい。
本発明の異方性導電材料の製造方法は特に限定されず、例えば、上記バインダー樹脂中に本発明の導電性微粒子を添加し、均一に混合して分散させ、異方性導電ペースト、異方性導電インク、異方性導電粘着剤等を製造する方法が挙げられる。また、本発明の異方性導電材料の製造方法として、上記バインダー樹脂中に本発明の導電性微粒子を添加し、均一に分散させるか、又は、加熱溶解させて、離型紙や離型フィルム等の離型材の離型処理面に所定の厚さとなるように塗工し、必要に応じて乾燥や冷却等を行って、異方性導電フィルム、異方性導電シート等を製造する方法も挙げられる。なお、異方性導電材料の種類に対応して、適宜の製造方法を選択することができる。
また、上記バインダー樹脂と、本発明の導電性微粒子とを混合することなく、別々に用いて異方性導電材料としてもよい。
本発明の導電性微粒子又は本発明の異方性導電材料を用いてなる導電接続構造体もまた、本発明の1つである。
本発明の導電接続構造体は、一対の回路基板間に、本発明の導電性微粒子又は本発明の異方性導電材料を充填することにより、一対の回路基板間を接続させた導電接続構造体である。
本発明によれば、落下等による衝撃が加わっても電極と該導電性微粒子との接続界面の破壊による断線が生じにくく、加熱と冷却とを繰返し受けても疲労しにくい導電性微粒子を提供することができる。また、該導電性微粒子を用いてなる異方性導電材料、及び、導電接続構造体を提供することができる。
本発明の導電性微粒子の好ましい態様の一例を示す模式図である。
以下に実施例を挙げて本発明の態様を更に詳しく説明するが、本発明はこれら実施例にのみ限定されるものではない。
(実施例1)
(1)樹脂からなるコア粒子の作製
ジビニルベンゼン50重量部と、テトラメチロールメタンテトラアクリレート50重量部とを共重合させ、樹脂からなるコア粒子(平均粒子径180μm、CV値0.42%)を作製した。
(2)導電性微粒子の作製
得られたコア粒子を無電解ニッケルメッキし、コア粒子の表面に厚さ0.3μmの下地ニッケルメッキ層を形成させた。次いで、電解銅メッキをすることにより、厚さ7μmの銅層(導電金属層)を形成させた。次いで、電解ニッケルメッキをすることにより、厚さ0.6μmのニッケル層(バリア層)を形成させた。次いで、電解銅メッキをすることにより、厚さ1μmの銅層を形成させた。次いで、電解メッキをすることにより、厚さ34μmの錫を含有するハンダ層を形成させた。最後に、電解メッキ液を濾過し、得られた粒子を水で洗浄した後、50℃の真空乾燥機で乾燥させて、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、2.6重量%である。
(実施例2)
ハンダ層に直接接する銅層の厚さを0.4μmとした以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、1.0重量%である。
(実施例3)
ハンダ層に直接接する銅層の厚さを2μmとした以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、5.0重量%である。
(実施例4)
ハンダ層に直接接する銅層の厚さを0.2μmとした以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、0.5重量%である。
(実施例5)
スパッタリング法により、ハンダ層の表面にニッケルを付着させた以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたニッケルが順次形成された導電性微粒子を得た。
(実施例6)
無電解メッキ法により、ハンダ層の表面にニッケルを付着させた以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたニッケルが順次形成された導電性微粒子を得た。
(実施例7)
無電解メッキ法により、ハンダ層の表面にコバルトを付着させた以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたコバルトが順次形成された導電性微粒子を得た。
(実施例8)
(1)樹脂からなるコア粒子の作製
ジビニルベンゼン50重量部と、テトラメチロールメタンテトラアクリレート50重量部とを共重合させ、樹脂からなるコア粒子(平均粒子径150μm、CV値0.38%)を作製した。
(2)導電性微粒子の作製
得られたコア粒子を無電解ニッケルメッキし、コア粒子の表面に厚さ0.3μmの下地ニッケルメッキ層を形成させた。次いで、電解銅メッキをすることにより、厚さ10μmの銅層(導電金属層)を形成させた。次いで、電解ニッケルメッキをすることにより、厚さ0.6μmのニッケル層(バリア層)を形成させた。次いで、電解銅メッキをすることにより、厚さ0.5μmの銅層を形成させた。次いで、電解メッキをすることにより、厚さ40μmの錫を含有するハンダ層を形成させた。最後に、電解メッキ液を濾過し、得られた粒子を水で洗浄した後、50℃の真空乾燥機で乾燥させて、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、1.0重量%である。
(実施例9)
無電解メッキ法により、ハンダ層の表面にニッケルを付着させた以外は実施例8と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたニッケルが順次形成された導電性微粒子を得た。
(実施例10)
無電解メッキ法により、ハンダ層の表面にコバルトを付着させた以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたコバルトが順次形成された導電性微粒子を得た。
(比較例1)
ハンダ層に直接接する銅層を形成しなかった以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層及びハンダ層が順次形成された導電性微粒子を得た。
(比較例2)
ハンダ層に直接接する銅層を無電解メッキで形成し、その厚さを0.05μmとした以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、0.1重量%である。
(比較例3)
ハンダ層に直接接する銅層の厚さを4μmとした以外は実施例1と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、10重量%である。
(比較例4)
無電解メッキ法により、ハンダ層の表面にニッケルを付着させた以外は比較例2と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたニッケルが順次形成された導電性微粒子を得た。
(比較例5)
無電解メッキ法により、ハンダ層の表面にコバルトを付着させた以外は比較例2と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたコバルトが順次形成された導電性微粒子を得た。
(比較例6)
ハンダ層に直接接する銅層を形成しなかった以外は実施例8と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層及びハンダ層が順次形成された導電性微粒子を得た。
(比較例7)
ハンダ層に直接接する銅層を無電解メッキで形成し、その厚さを0.1μmとした以外は実施例8と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層及びハンダ層が順次形成された導電性微粒子を得た。
なお、得られた導電性微粒子において、ハンダ層中に含まれる錫に対する、ハンダ層に直接接する銅層中に含有される銅の比率は、0.2重量%である。
(比較例8)
無電解メッキ法により、ハンダ層の表面にニッケルを付着させた以外は比較例7と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたニッケルが順次形成された導電性微粒子を得た。
(比較例9)
無電解メッキ法により、ハンダ層の表面にコバルトを付着させた以外は比較例2と同様にして、コア粒子の表面に、下地金属層、導電金属層、バリア層、銅層、ハンダ層、及び、ハンダ層に付着されたコバルトが順次形成された導電性微粒子を得た。
(評価)
実施例及び比較例で得られた導電性微粒子について以下の評価を行った。結果を表1に示した。
(1)150℃、12時間加熱後のハンダ層中の銅濃度の測定
得られた導電性微粒子を150℃、12時間加熱後、断面を取り、各粒子5個、2点の計10点について、SEM-EDXにてハンダ層中の銅濃度(重量%)を測定し、その最小値、最大値及び算術平均値を求めた。
(2)落下強度試験
シリコンチップ(縦5mm×横5mm)上に0.4mmピッチで121個設けられた電極ランド(直径230μm)にフラックス(クックソンエレクトロニクス社製「WS-9160-M7」)を塗布した。すべての電極ランドに、得られた導電性微粒子を配置し、リフロー(加熱温度250℃、30秒間)し、導電性微粒子を電極ランドに実装した。
次いで、銅電極(直径250μm)が形成されたプリント基板にハンダペースト(千住金属工業社製「M705-GRN360-K2-V」)を塗布した。導電性微粒子が実装されたシリコンチップ15個を、プリント基板に配置し、リフロー(加熱温度250℃、30秒間)し、シリコンチップ15個をプリント基板に実装し、導電接続構造体を得た。
JEDEC規格JESD22-B111に従い、得られた導電接続構造体の落下強度試験を行った。得られた導電接続構造体は、デイジーチェーン回路が形成されているため、1箇所の電極ランドの断線でも検出することができる。
15個のシリコンチップのすべてが断線する落下回数を測定した。
なお、電極ランドは、銅層で形成されていた。以下、同様である。
(3)温度サイクル試験
シリコンチップ(縦5mm×横5mm)上に0.4mmピッチで121個設けられた電極ランド(直径230μm)にフラックス(クックソンエレクトロニクス社製「WS-9160-M7」)を塗布した。すべての電極ランドに、得られた導電性微粒子を配置し、リフロー(加熱温度250℃、30秒間)し、導電性微粒子を電極ランドに実装した。
次いで、銅電極(直径250μm)が形成されたプリント基板にハンダペースト(千住金属工業社製「M705-GRN360-K2-V」)を塗布した。導電性微粒子が実装されたシリコンチップ1個を、プリント基板に配置し、リフロー(加熱温度250℃、30秒間)し、シリコンチップ1個をプリント基板に実装し、導電接続構造体を得た。
得られた導電接続構造体は、デイジーチェーン回路が形成されているため、1箇所の電極ランドの断線でも検出することができる。
得られた導電接続構造体を用いて、-40℃~125℃を1サイクルとする温度サイクル試験を行った。なお、温度サイクル試験のヒートプロファイルは、-40℃で10分間保持し、-40℃から125℃まで2分間で昇温させ、125℃で10分間保持し、125℃から-40℃まで2分間で降温させるヒートプロファイルであった。
温度サイクル試験は以下の基準で評価した。
○:導電接続構造体の断線が確認されるサイクル数が1000サイクル以上であった。
×:導電接続構造体の断線が確認されるサイクル数が1000サイクル未満であった。
Figure JPOXMLDOC01-appb-T000001
(実施例11)
実施例1の粒子をバインダー樹脂に分散させ、回路接続を実施した結果、電気導通することを確認した。
本発明によれば、落下等による衝撃が加わっても電極と該導電性微粒子との接続界面の破壊による断線が生じにくく、加熱と冷却とを繰返し受けても疲労しにくい導電性微粒子を提供することができる。また、該導電性微粒子を用いてなる異方性導電材料、及び、導電接続構造体を提供することができる。
1 コア粒子
2 下地金属層
3 導電金属層
4 バリア層
5 銅層
6 ハンダ層
7 ハンダ層に付着されたニッケル及び/又はコバルト
 

Claims (5)

  1. 樹脂又は金属からなるコア粒子の表面に、少なくとも導電金属層、バリア層、銅層、及び、錫を含有するハンダ層がこの順に積層された導電性微粒子であって、
    前記銅層とハンダ層とが直接接しており、前記ハンダ層中に含まれる錫に対する前記ハンダ層に直接接する銅層における銅の比率が0.5~5重量%である
    ことを特徴とする導電性微粒子。
  2. 150℃、12時間加熱したときに、ハンダ層の任意の位置における銅の濃度が0.5~40重量%であることを特徴とする請求項1記載の導電性微粒子。
  3. ハンダ層の表面にニッケル及び/又はコバルトが付着されていることを特徴とする請求項1又は2記載の導電性微粒子。
  4. 請求項1、2又は3記載の導電性微粒子がバインダー樹脂に分散されてなることを特徴とする異方性導電材料。
  5. 請求項1、2若しくは3記載の導電性微粒子、又は、請求項4記載の異方性導電材料を用いてなることを特徴とする導電接続構造体。
     
PCT/JP2014/055035 2013-02-28 2014-02-28 導電性微粒子、異方性導電材料、及び、導電接続構造体 WO2014133124A1 (ja)

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CN201480005809.1A CN104937675B (zh) 2013-02-28 2014-02-28 导电性微粒、各向异性导电材料和导电连接结构体
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