WO2019082884A1 - Tin or tin alloy plating solution - Google Patents

Tin or tin alloy plating solution

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Publication number
WO2019082884A1
WO2019082884A1 PCT/JP2018/039332 JP2018039332W WO2019082884A1 WO 2019082884 A1 WO2019082884 A1 WO 2019082884A1 JP 2018039332 W JP2018039332 W JP 2018039332W WO 2019082884 A1 WO2019082884 A1 WO 2019082884A1
Authority
WO
WIPO (PCT)
Prior art keywords
tin
acid
plating solution
surfactant
alloy plating
Prior art date
Application number
PCT/JP2018/039332
Other languages
French (fr)
Japanese (ja)
Inventor
眞美 渡邉
京佳 薄
中矢 清隆
Original Assignee
三菱マテリアル株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2018197082A external-priority patent/JP6620859B2/en
Application filed by 三菱マテリアル株式会社 filed Critical 三菱マテリアル株式会社
Priority to US16/757,855 priority Critical patent/US11162182B2/en
Priority to KR1020207011532A priority patent/KR102221566B1/en
Priority to CN201880068798.XA priority patent/CN111279020B/en
Priority to EP18871709.4A priority patent/EP3702493A4/en
Publication of WO2019082884A1 publication Critical patent/WO2019082884A1/en

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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D7/00Electroplating characterised by the article coated
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/30Electroplating: Baths therefor from solutions of tin
    • C25D3/32Electroplating: Baths therefor from solutions of tin characterised by the organic bath constituents used
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/56Electroplating: Baths therefor from solutions of alloys
    • C25D3/60Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of tin
    • 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
    • C25D5/48After-treatment of electroplated surfaces
    • C25D5/50After-treatment of electroplated surfaces by heat-treatment
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05KPRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00Apparatus or processes for manufacturing printed circuits
    • H05K3/30Assembling printed circuits with electric components, e.g. with resistor
    • H05K3/32Assembling printed circuits with electric components, e.g. with resistor electrically connecting electric components or wires to printed circuits
    • H05K3/34Assembling printed circuits with electric components, e.g. with resistor electrically connecting electric components or wires to printed circuits by soldering
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/10Bump connectors; Manufacturing methods related thereto
    • H01L2224/11Manufacturing methods
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2224/00Indexing scheme for arrangements for connecting or disconnecting semiconductor or solid-state bodies and methods related thereto as covered by H01L24/00
    • H01L2224/01Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/10Bump connectors; Manufacturing methods related thereto
    • H01L2224/12Structure, shape, material or disposition of the bump connectors prior to the connecting process
    • H01L2224/14Structure, shape, material or disposition of the bump connectors prior to the connecting process of a plurality of bump connectors
    • H01L2224/1401Structure
    • H01L2224/1403Bump connectors having different sizes, e.g. different diameters, heights or widths

Definitions

  • the present invention relates to a tin or tin alloy plating solution for producing a bump serving as a bump electrode of tin or tin alloy on a substrate when the semiconductor integrated circuit chip is mounted on a circuit board. More specifically, the present invention relates to a tin or tin alloy plating solution which is excellent in via filling property to vias on a substrate and in which the height of the formed bumps is uniform, even for patterns having different bump diameters.
  • Priority is claimed on Japanese Patent Application No. 2017-205203 filed on Oct. 24, 2017, and Japanese Patent Application No. 2018-197082 filed on Oct. 19, 2018, the contents of which are incorporated herein by reference. Is incorporated herein by reference.
  • CSP Chip Size / CSP
  • the via opening which is a via body on the substrate side is filled with tin or tin alloy to form a bump which is a protruding electrode of a protruding metal terminal, and this bump Is loaded with semiconductor chips.
  • a conductive paste such as tin-based solder paste or a tin-based solder ball is filled in a via body portion, or a tin or tin alloy plating solution is used.
  • heat treatment is performed to melt the conductive paste, the solder ball or the tin plating deposition layer.
  • FIG. 1A A general method of forming bumps by electroplating will be described with reference to FIG.
  • a solder resist pattern having an opening is formed on the surface of the substrate 1 to which wiring and the like have been applied.
  • electroless plating is performed on the surface of the solder resist layer 2 to form a copper seed layer 3 for feeding.
  • a dry film resist layer 4 is formed on the surface of the copper seed layer 3, and a dry film resist pattern having an opening is formed so as to be connected to the opening of the solder resist layer 2.
  • electric tin plating is performed inside the via 6 of the dry film resist pattern by feeding power through the copper seed layer 3, and a tin plating deposition layer 7 (tin plating film is formed in the via 6 on the copper seed layer 3. Form).
  • the remaining tin plating deposition layer is melted by a reflow process to form tin bumps 8 as shown in FIG. 1 (b).
  • Patent Document 1 discloses a tin or tin alloy plating solution containing a specific ⁇ , ⁇ -unsaturated aldehyde or a specific ⁇ , ⁇ -unsaturated ketone compound. According to this patent document 1, this plating solution has a high via fill effect, and if this plating solution is used, tin plating is selectively deposited in the recess, so that a tin plating deposit substantially free of voids can be obtained. It is described that since there is no burnt or abnormal deposition on the surface of the formed tin-plated film, a tin-plated film having a practical and good appearance excellent in solderability, discoloration resistance and the like can be obtained.
  • Patent Document 2 contains (a) a carboxyl group-containing compound and (b) a carbonyl group-containing compound, and the component (a) is 1.3 g / L or more and the component (b) is 0.3 g / L.
  • the tin or tin alloy plating solution which is the above is disclosed.
  • this plating solution can be filled with blind vias or through holes with high reliability and in a short time by electroplating on an object to be plated having blind vias or through holes, and three-dimensional mounting of semiconductors. It is described that it can be used in the process of filling blind vias or through holes in printed wiring boards and in the formation of silicon through electrodes.
  • Patent Document 3 discloses a tin or tin alloy plating solution containing an inorganic acid and an organic acid, and a water-soluble salt thereof, a surfactant, and a leveling agent.
  • the surfactant is at least one nonionic surfactant selected from the group consisting of polyoxyalkylene phenyl ether or a salt thereof, and polyoxyalkylene polycyclic phenyl ether or a salt thereof, and polyoxyalkylene phenyl
  • the phenyl constituting the ether and the polycyclic phenyl constituting the polyoxyalkylene polycyclic phenyl ether may be substituted with an alkyl group having 1 to 24 carbon atoms or a hydroxy group, and the leveling agent is an aliphatic aldehyde, And at least one member selected from the group consisting of aromatic aldehydes, aliphatic ketones, and aromatic ketones; ⁇ , ⁇ -unsaturated carboxylic acids or their amides,
  • this patent document 3 contains a specific nonionic surfactant and two specific types of leveling agents, it is excellent in recess fillability and can suppress the generation of voids, which makes it possible It is described that if a plating solution is used, it is possible to provide a good bump which has no recess, is smooth, and does not generate a void after reflow.
  • Patent Document 4 discloses a soluble salt comprising either (A) a stannous salt and a mixture of a stannous salt and a salt of a metal selected from silver, copper, bismuth, nickel, indium, and gold. (B) an acid or a salt thereof, and (C) a filling organic compound selected from the group consisting of aromatic and aliphatic aldehydes, aromatic and aliphatic ketones, unsaturated carboxylic acids, and aromatic carboxylic acids; D) A galvanic tin or tin alloy plating solution for forming a bump electrode containing a nonionic surfactant is disclosed.
  • this plating solution is used by combining the component (D) with the specific compound (C) which suppresses the precipitation of the tin-based material, the precipitation of the upper portion of the via is effectively suppressed.
  • the deposition of the base material can be advanced from the bottom of the via preferentially toward the upper side of the via, and the via can be filled smoothly while preventing the generation of the void, and as a result, the reflow or reflow is not performed. It is described that the protruding electrodes can be formed well and the bonding strength and the electrical characteristics are excellent.
  • JP-A-2014-125662 (claim 2, paragraph [0020]) JP, 2015-007276, A (claim 1, paragraphs [0011] and [0012]) JP, 2015-193916, A (claim 1, paragraph [0019]) JP, 2016-074963, A (claim 1, paragraph [0019])
  • plating using a conventional tin or tin alloy plating solution improves the via filling property of either the small diameter or the large diameter. Is possible, but the via filling of the other is reduced. That is, in a substrate in which both small diameter and large diameter vias are present, it is difficult to plate both vias with good via filling when plating both vias simultaneously.
  • FIG. 2B when there are vias with different via filling properties (FIG. 2B), the height variation of the bumps after reflow becomes large, and the height uniformity of the bumps can not be achieved (FIG. 2). (D)). Therefore, in order to achieve bump height uniformity (FIG. 2C), as shown in FIG. 2A, it is necessary to improve the via filling property to both the small diameter and large diameter vias.
  • An object of the present invention is to provide a tin or tin alloy plating solution which is excellent in via filling property to vias on a substrate and in which the height of the formed bumps is uniform, even in the case of patterns having different bump diameters.
  • a soluble salt containing at least a stannous salt (B) an acid selected from organic and inorganic acids or a salt thereof, (C) a surfactant, D) A tin or tin alloy plating solution containing a leveling agent, wherein the surfactant comprises a phenyl surfactant and the phenyl surfactant is represented by the following general formula (1): It is characterized by being an ether.
  • a second aspect of the present invention is the invention based on the first aspect, further comprising two of a surfactant other than a phenyl surfactant, an antioxidant and an alcohol having 1 to 3 carbon atoms. It is characterized by further including the above.
  • a reflow process is performed to form bumps. Is a method of forming
  • a fourth aspect of the present invention is a method of manufacturing a circuit board using bumps formed by the method described in the third aspect.
  • the phenyl surfactant has a specific phenyl structure in which a of X in the general formula (1) and m of a polyoxyethylene group are each in a predetermined range.
  • the tin or tin alloy plating solution according to the second aspect of the present invention further comprises two or more of a surfactant other than a phenyl surfactant, an antioxidant, and an alcohol having 1 to 3 carbon atoms.
  • a surfactant other than a phenyl surfactant exhibit effects such as stabilization of the plating solution and improvement of solubility.
  • Antioxidants also prevent the oxidation of soluble stannous salts to stannic salts.
  • the alcohol is effective in improving the solubility of the surfactant.
  • a tin or tin plating deposition layer is formed on a substrate using the above-mentioned tin or tin alloy plating solution, and then reflow treatment is performed to form bumps. Even if the patterns have different bump diameters, bumps having a uniform height can be formed.
  • a highly reliable semiconductor device free of electrical connection defects is manufactured by manufacturing a circuit board using the bumps formed according to the method according to the third aspect. Can be made.
  • (A) is a cross-sectional block diagram in which the plating deposition layer was formed in the via
  • (b) is a cross-section block diagram after peeling a dry film and a copper seed layer and heating a plating deposition layer.
  • (A) is a cross-sectional view showing an example in which the plating deposition layer is uniformly formed in patterns different in bump diameter (via diameter)
  • (b) is a plating deposition layer in a pattern different in bump diameter (via diameter)
  • (D) is an example in which the height of the bumps formed varies after peeling the dry film and copper seed layer in (b) and heating the plating deposition layer. It is a cross-sectional block diagram which shows.
  • the tin or tin alloy plating solution of the present invention comprises (A) a soluble salt containing at least a stannous salt, (B) an acid selected from organic acids and inorganic acids, or a salt thereof, and (C) a surfactant. And (D) a leveling agent.
  • This surfactant contains a phenyl surfactant, and the phenyl surfactant is a polyoxyethylene bisphenol ether represented by the above general formula (1).
  • the soluble salt comprises any of a stannous salt and a mixture of a stannous salt and a salt of a metal selected from the group consisting of silver, copper, bismuth, nickel, antimony, indium and zinc.
  • the tin alloy of the present invention is an alloy of tin and a predetermined metal selected from silver, copper, bismuth, nickel, antimony, indium and zinc, and for example, tin-silver alloy, tin-copper alloy, tin-bismuth Alloys, tin-nickel alloys, tin-antimony alloys, tin-indium alloys, binary alloys of tin-zinc alloys, ternary alloys of tin-copper-bismuth, tin-copper-silver alloys and the like can be mentioned.
  • the soluble salt (A) of the present invention can form any metal ion such as Sn 2+ , Ag + , Cu + , Cu 2+ , Bi 3+ , Ni 2+ , Sb 3+ , In 3+ , Zn 2+ in the plating solution.
  • soluble salts of the metal such as oxides, halides of the metal, metal salts of the inorganic acid or the organic acid, and the like.
  • metal oxides include stannous oxide, copper oxide, nickel oxide, bismuth oxide, antimony oxide, indium oxide, zinc oxide and the like
  • metal halides include stannous chloride, bismuth chloride, bromide Bismuth, cuprous chloride, cupric chloride, nickel chloride, antimony chloride, indium chloride, zinc chloride and the like can be mentioned.
  • metal salts of inorganic acids or organic acids copper sulfate, stannous sulfate, bismuth sulfate, nickel sulfate, antimony sulfate, bismuth nitrate, silver nitrate, copper nitrate, antimony sulfate, indium nitrate, nickel nitrate, zinc nitrate, copper acetate Nickel acetate, nickel carbonate, sodium stannate, stannous borofluoride, stannous methanesulfonate, silver methanesulfonate, copper methanesulfonate, bismuth methanesulfonate, nickel methanesulfonate, indium metasulfonate, bismethane And zinc sulfonate, stannous ethane sulfonate, bismuth 2-hydroxypropane sulfonate and the like.
  • the acid or salt (B) of the present invention is selected from organic and inorganic acids or salts thereof.
  • the organic acids include organic sulfonic acids such as alkanesulfonic acids, alkanolsulfonic acids and aromatic sulfonic acids, and aliphatic carboxylic acids.
  • inorganic acids include borohydrofluoric acid, silicofluoric acid and sulfamine. Acid, hydrochloric acid, sulfuric acid, nitric acid, perchloric acid and the like can be mentioned.
  • the salts are salts of alkali metals, salts of alkaline earth metals, ammonium salts, amine salts, sulfonates and the like.
  • the component (B) is preferably an organic sulfonic acid from the viewpoint of the solubility of the metal salt and the ease of waste water treatment.
  • methanesulfonic acid and ethanesulfonic acid Other than 1-propanesulfonic acid, 2-propanesulfonic acid, 1-butanesulfonic acid, 2-butanesulfonic acid, pentanesulfonic acid and the like, hexanesulfonic acid, decanesulfonic acid, dodecanesulfonic acid and the like can be mentioned.
  • the aromatic sulfonic acid is basically benzenesulfonic acid, alkylbenzenesulfonic acid, phenolsulfonic acid, naphthalenesulfonic acid, alkylnaphthalenesulfonic acid, etc. Specifically, 1-naphthalenesulfonic acid, 2-naphthalene And sulfonic acid, toluene sulfonic acid, xylene sulfonic acid, p-phenol sulfonic acid, cresol sulfonic acid, sulfosalicylic acid, nitrobenzene sulfonic acid, sulfobenzoic acid, diphenylamine-4-sulfonic acid and the like.
  • aliphatic carboxylic acids examples include acetic acid, propionic acid, butyric acid, citric acid, tartaric acid, gluconic acid, sulfosuccinic acid, trifluoroacetic acid and the like.
  • the phenyl surfactant contained in the surfactant of the present invention is a polyoxyethylene bisphenol ether represented by the following general formula (1).
  • M is preferably 5 to 10.
  • the polyoxyethylene bisphenol ether represented by the above general formula (1) may contain ortho, meta and para isomers, and mixed isomers thereof.
  • the leveling agent (D) of the present invention is a first leveling agent in order to form a plating film uniformly and densely and to make the plating film smooth, in addition to enhance the via filling property and to suppress the generation of voids.
  • Two types of (D-1) and a second leveling agent (D-2) are used.
  • the first leveling agent (D-1) one or more selected from the group consisting of aliphatic aldehydes, aromatic aldehydes, aliphatic ketones and aromatic ketones may be mentioned, and the second leveling agent (D As -2), ⁇ , ⁇ -unsaturated carboxylic acids or their amides, or salts thereof can be mentioned.
  • the first leveling agent (D-1) is a carbonyl compound containing an aldehyde and a ketone, and does not contain the ⁇ , ⁇ -unsaturated carboxylic acid of the second leveling agent (D-2).
  • the following are exemplified.
  • Examples of aliphatic aldehydes include formaldehyde, acetaldehyde and allyl aldehyde.
  • aromatic aldehyde benzaldehyde, 2-chlorobenzaldehyde, 3-chlorobenzaldehyde, 4-chlorobenzaldehyde, 2,4-dichlorobenzaldehyde, 2,6-dichlorobenzaldehyde, 2,4,6-trichlorobenzaldehyde, 1- Naphthaldehyde, 2-naphthaldehyde, 2-hydroxy benzaldehyde, 3-hydroxy benzaldehyde, 4-hydroxy benzaldehyde, 2-methyl benzaldehyde, 3-methyl benzaldehyde, 4-methyl benzaldehyde, m-anisaldehyde, o-anisaldehyde, p- Anisaldehyde etc.
  • the preferred content of the first leveling agent (D-1) in the electroplating bath is 0.001 g / L It is ⁇ 0.3 g / L, more preferably 0.01 g / L ⁇ 0.25 g / L. If the content of the above component is small, the effect of the addition is not sufficient. On the other hand, if the content of the above component is too large, there is a possibility that the smoothing of the plating film is inhibited.
  • an amide of ⁇ , ⁇ -unsaturated carboxylic acid eg, acrylamide etc.
  • a salt of ⁇ , ⁇ -unsaturated carboxylic acid eg, potassium, sodium, ammonium
  • the preferred content of the second leveling agent (D-2) in the electroplating bath is 0.01 g / L It is ⁇ 50 g / L, more preferably 0.05 g / L to 30 g / L, still more preferably 0.05 g / L to 10 g / L. If the content of the above component is small, the effect of the addition is not sufficient. On the other hand, if the content of the above component is too large, there is a possibility that the smoothing of the plating film is inhibited.
  • a surfactant (E) other than a phenyl surfactant an antioxidant (F) and an alcohol having 1 to 3 carbon atoms (G) It is preferable to further include the above.
  • surfactants (E) in this case include usual anionic surfactants, cationic surfactants, nonionic surfactants and amphoteric surfactants.
  • anionic surfactants include polyoxyalkylene alkyl ether sulfates such as polyoxyethylene (ethylene oxide: 12 mol content) nonyl ether sodium sulfate, polyoxyethylene (ethylene oxide: 12 mol content) sodium dodecyl phenyl ether sulfate, etc.
  • alkylbenzene sulfonates such as polyoxyalkylene alkyl phenyl ether sulfates and sodium dodecylbenzene sulfonate
  • naphthol sulfonates such as sodium 1-naphthol-4-sulfonate and disodium 2-naphthol-3,6-disulfonate
  • (Poly) alkyl naphthalene sulfonates such as sodium diisopropyl naphthalene sulfonate, sodium dibutyl naphthalene sulfonate, sodium dodecyl sulfate, oleyl sulfate nato Alkyl sulfates such as Um like.
  • nonionic surfactants include sugar esters, fatty acid esters, C 1 -C 25 alkoxyl phosphate (salts), sorbitan esters, C 1 -C 22 fatty amides, etc. ethylene oxide (EO) and / or propylene oxide (PO 4) 2) to 300 mol of addition-condensed silicone), silicon-based polyoxyethylene ether, silicon-based polyoxyethylene ester, fluorine-based polyoxyethylene ether, fluorine-based polyoxyethylene ester, ethylene oxide and / or propylene oxide and alkyl oxide with alkylamine Or sulfated or sulfonated adducts of condensation products with diamines.
  • EO ethylene oxide
  • PO 4 propylene oxide
  • Amphoteric surfactants include betaine, carboxybetaine, imidazolinium betaine, sulfobetaine, aminocarboxylic acid and the like.
  • the antioxidant (F) is used to prevent the oxidation of soluble stannous salts to stannic salts.
  • hypophosphorous acids and the like ascorbic acid or a salt thereof, phenolsulfonic acid (Na), cresol sulfonic acid (Na), hydroquinone sulfonic acid (Na), hydroquinone, ⁇ or ⁇ -naphthol, catechol, Examples include resorcin, phloroglucin, hydrazine, phenolsulfonic acid, catecholsulfonic acid, hydroxybenzenesulfonic acid, naphtholsulfonic acid, and salts thereof.
  • the alcohol (G) having 1 to 3 carbon atoms is used to improve the solubility of the surfactant.
  • examples of the alcohol include methanol, ethanol, 1-propanol, 2-propanol and the like.
  • the alcohol can be used singly or in combination of two or more.
  • the content of the phenyl surfactant (C) in the plating solution is 0.5 g / L to 50 g / L, preferably 1 g / L to 5 g / L. If the content is less than the lower limit value, plating defects such as dendrite occur due to excessive supply of Sn ions. If the upper limit value is exceeded, it is difficult for Sn ions to reach the surface to be plated and the via filling property is inferior (deteriorated).
  • the predetermined soluble metal salt (A) can be used singly or in combination, and the content in the plating solution is 30 g / L to 100 g / L, preferably 40 g / L to 60 g / L. If the content is less than the appropriate range, the productivity is lowered, and if the content is increased, the cost of the plating solution is increased.
  • the inorganic acid, the organic acid or the salt thereof (B) can be used singly or in combination, and the content in the plating solution is 80 g / L to 300 g / L, preferably 100 g / L to 200 g / L. If the content is less than the appropriate range, the conductivity is low and the voltage is increased, and if the content is large, the viscosity of the plating solution is increased and the stirring speed of the plating solution is decreased.
  • the temperature of the electroplating solution of the present invention is generally 70 ° C. or less, preferably 10 to 40 ° C.
  • the current density at the time of plating film formation by electroplating is in the range of 0.1 A / dm 2 to 100 A / dm 2 , preferably in the range of 0.5 A / dm 2 to 20 A / dm 2 . If the current density is too low, productivity will deteriorate, and if it is too high, the height uniformity of the bumps will deteriorate.
  • the plating solution of tin or tin alloy containing the phenyl surfactant (C) of the present invention can be applied to a circuit board which is an object to be plated to form a predetermined metal film on the circuit board.
  • a circuit board a printed circuit board, a flexible printed circuit board, a semiconductor integrated circuit board and the like can be mentioned.
  • Tables 1 and 2 show structural formulas of polyoxyethylene bisphenol ether which is a phenyl surfactant (C) used in Examples 1 to 7 and Comparative Examples 1 and 2.
  • Example 1 (Building bath of Sn plating solution) A homogeneous solution is prepared by mixing an aqueous solution of methanesulfonic acid, methanesulfonic acid as a free acid, hydroquinone as an antioxidant, 1-naphthaldehyde as a first leveling agent, and methacrylic acid as a second leveling agent. After reaching the above, the polyoxyethylene bisphenol ether (weight average molecular weight: about 600 g / mol) of the above (C-1) was further added as a surfactant. Finally, ion exchange water was added, and a Sn plating solution of the following composition was prepared. In addition, the methanesulfonic acid Sn aqueous solution was prepared by electrolyzing a metal Sn plate in the methanesulfonic acid aqueous solution.
  • methanesulfonic acid Sn aqueous solution was prepared by electrolyzing a metal Sn plate in the methanesulfonic acid aqueous solution
  • Methanesulfonic acid Sn (as Sn 2+ ): 50 g / L Potassium methanesulfonate (as free acid): 100 g / L Phenyl surfactant (C-1): 2 g / L Hydroquinone (as antioxidant (F)): 1 g / L 1-naphthaldehyde (as a first leveling agent (D-1)): 0.1 g / L Methacrylic acid (as a second leveling agent (D-2)): 2 g / L Ion exchange water: balance
  • Examples 2 to 8 and Comparative Examples 1 to 2 In Examples 2 to 8 and Comparative Examples 1 to 2, polyoxyethylene bisphenol ethers ((C-2) to (C-10) having the structural formulas shown in Tables 1 to 2 as phenyl surfactants (C). was used. The Sn plating solutions of Examples 2 to 8 and Comparative Examples 1 and 2 were assembled in the same manner as Example 1 except for the above.
  • Ag is contained as a metal other than Sn (1.0 g / L as Ag + )
  • Cu is contained as a metal other than Sn (0 2 as Cu 2+. .5 g / L).
  • the via filling property of the tin or tin alloy plating deposition layer in the via and the “appearance of the tin or tin alloy plating deposition layer in the via” described later are measured for the plating deposition layer before reflow.
  • the height variation "and” voiding potential are measured for the bumps formed after reflow of the plated deposit. The results are shown in Table 3.
  • Examples 9 to 18 the weight average molecular weight of any of the first leveling agent (D-1), the second leveling agent (D-2) or a metal other than Sn and the phenyl surfactant is shown in Table 4.
  • the Sn plating solution was built up in the same manner as in Example 1 except that it was changed to
  • D1A is benzaldehyde
  • D1B is 4-chlorobenzaldehyde
  • D1C 1-naphthoaldehyde.
  • D2A is methacrylic acid
  • D2B acrylic acid
  • D2C is acrylamide.
  • the first leveling agent (D-1) is changed to either benzaldehyde, 4-chlorobenzaldehyde or 1-naphthaldehyde
  • the second leveling agent (D-2) is methacrylic acid, acrylic
  • examples 9 to 12 in which either acid or acrylamide was changed, both the via filling property and the appearance of the plating deposited layer were good, the variation in bump height was uniform, and voids were observed in the bumps.
  • the void generation tendency was OK.
  • Examples 17 to 18 which are respectively changed to 05 g / L and 30 g / L both the via filling property and the appearance of the plating deposited layer are good, the bump height variation is also uniform, and voids are formed in the bumps. It was not seen and the possibility of void generation was OK.
  • the tin or tin alloy plating solution of the present invention can be used for circuit boards such as printed circuit boards, flexible printed circuit boards, and semiconductor integrated circuits.

Abstract

A tin or tin alloy plating solution containing (A) a soluble salt including at least a first tin salt, (B) an acid selected from an organic acid and an inorganic acid or a salt thereof, (C) a phenyl-type surfactant comprising a polyoxyethylene bisphenol ether represented by general formula (1) and (D) a leveling agent. In formula (1), X represents CaH2a (a = 1 or 3) and m represents 2 to 12.

Description

錫又は錫合金めっき液Tin or tin alloy plating solution
 本発明は、半導体集積回路チップを回路基板に搭載する際に基板上に錫又は錫合金の突起電極となるバンプを製造するための錫又は錫合金のめっき液に関する。更に詳しくは、バンプ径が異なるパターンでも、基板上のビアへのビアフィリング性に優れ、かつ形成されたバンプの高さが均一になる錫又は錫合金めっき液に関するものである。
 本願は、2017年10月24日に日本に出願された特願2017-205203号及び2018年10月19日に日本に出願された特願2018-197082号に基づき優先権を主張し、その内容をここに援用する。
The present invention relates to a tin or tin alloy plating solution for producing a bump serving as a bump electrode of tin or tin alloy on a substrate when the semiconductor integrated circuit chip is mounted on a circuit board. More specifically, the present invention relates to a tin or tin alloy plating solution which is excellent in via filling property to vias on a substrate and in which the height of the formed bumps is uniform, even for patterns having different bump diameters.
Priority is claimed on Japanese Patent Application No. 2017-205203 filed on Oct. 24, 2017, and Japanese Patent Application No. 2018-197082 filed on Oct. 19, 2018, the contents of which are incorporated herein by reference. Is incorporated herein by reference.
 半導体集積回路チップ(以下、半導体チップという。)を搭載する回路基板では、軽薄短小に対応するため、パッケージ基板面積を、基板に搭載する半導体チップとほぼ等しい程度に小型化したCSP(Chip Size/scale Package)型の半導体装置が現在主として製造されている。この回路基板と半導体チップを接続するためには、基板側のビア胴体部であるビア開口部を錫又は錫合金で充填して突起状の金属端子の突起電極であるバンプを形成し、このバンプに半導体チップを装填している。 In a circuit board on which a semiconductor integrated circuit chip (hereinafter referred to as a semiconductor chip) is mounted, CSP (Chip Size / CSP) in which the package substrate area is reduced to approximately the same size as the semiconductor chip mounted on the substrate. At present, semiconductor devices of the scale package type are mainly manufactured. In order to connect the circuit board and the semiconductor chip, the via opening which is a via body on the substrate side is filled with tin or tin alloy to form a bump which is a protruding electrode of a protruding metal terminal, and this bump Is loaded with semiconductor chips.
 従来、この錫又は錫合金材料の充填によりバンプを形成するには、錫系はんだペーストなどの導電性ペーストや錫系はんだボールをビア胴体部に充填するか、或いは錫又は錫合金のめっき液を用いて電気めっき法でビア内に錫めっき堆積層を形成した後、熱処理によって導電性ペースト、はんだボール又は錫めっき堆積層を溶融させている。 Conventionally, in order to form a bump by filling the tin or tin alloy material, a conductive paste such as tin-based solder paste or a tin-based solder ball is filled in a via body portion, or a tin or tin alloy plating solution is used. After using the electroplating method to form a tin plating deposition layer in the via, heat treatment is performed to melt the conductive paste, the solder ball or the tin plating deposition layer.
 電気めっき法でバンプを形成する一般的な方法を図1を参照して説明する。図1(a)に示すように、配線などが施された基板1の表面に開口部を有するソルダーレジストパターンを形成する。次いで、ソルダーレジスト層2の表面に無電解めっきを行い、給電のための銅シード層3を形成する。次に、銅シード層3の表面にドライフィルムレジスト層4を形成し、ソルダーレジスト層2の開口部と接続するように、開口部を有するドライフィルムレジストパターンを形成する。次に、上記銅シード層3を通じて給電することにより、ドライフィルムレジストパターンのビア6の内部に電気錫めっきを行い、銅シード層3の上のビア6内に錫めっき堆積層7(錫めっき皮膜)を形成する。次に、ドライフィルムレジスト層と銅シード層を順次除去した後、残った錫めっき堆積層をリフロー処理により溶融し、図1(b)に示すように、錫バンプ8を形成する。 A general method of forming bumps by electroplating will be described with reference to FIG. As shown in FIG. 1A, a solder resist pattern having an opening is formed on the surface of the substrate 1 to which wiring and the like have been applied. Next, electroless plating is performed on the surface of the solder resist layer 2 to form a copper seed layer 3 for feeding. Next, a dry film resist layer 4 is formed on the surface of the copper seed layer 3, and a dry film resist pattern having an opening is formed so as to be connected to the opening of the solder resist layer 2. Next, electric tin plating is performed inside the via 6 of the dry film resist pattern by feeding power through the copper seed layer 3, and a tin plating deposition layer 7 (tin plating film is formed in the via 6 on the copper seed layer 3. Form). Next, after the dry film resist layer and the copper seed layer are sequentially removed, the remaining tin plating deposition layer is melted by a reflow process to form tin bumps 8 as shown in FIG. 1 (b).
 これまで、電気めっき法を用いて錫又は錫合金バンプを形成するに際しては、錫又は錫合金めっき液の含有成分を変えることにより、基板上のビアへのビアフィリング性やバンプ内のボイドの抑制に関する改善がなされてきた(例えば、特許文献1、2、3、4参照。)。 Until now, when forming a tin or tin alloy bump using electroplating, the composition of the tin or tin alloy plating solution is changed to suppress the via filling property to the via on the substrate or the void in the bump. Improvements have been made (see, for example, Patent Documents 1, 2, 3, 4).
 特許文献1には、特定のα,β-不飽和アルデヒド又は特定のα,β-不飽和ケトンの化合物を含む錫又は錫合金めっき液が開示されている。この特許文献1には、このめっき液はビアフィル効果が高く、このめっき液を用いると、凹部に選択的に錫めっきが堆積するため、実質的に空隙を有しない錫めっき堆積物が得られること、形成された錫めっき皮膜表面にヤケや異常析出が生じないため、はんだ付け性や耐変色性等にすぐれた実用的で良好な外観を有する錫めっき皮膜が得られることが記載されている。 Patent Document 1 discloses a tin or tin alloy plating solution containing a specific α, β-unsaturated aldehyde or a specific α, β-unsaturated ketone compound. According to this patent document 1, this plating solution has a high via fill effect, and if this plating solution is used, tin plating is selectively deposited in the recess, so that a tin plating deposit substantially free of voids can be obtained. It is described that since there is no burnt or abnormal deposition on the surface of the formed tin-plated film, a tin-plated film having a practical and good appearance excellent in solderability, discoloration resistance and the like can be obtained.
 また特許文献2には、(a)カルボキシル基含有化合物と、(b)カルボニル基含有化合物とを含有し、成分(a)が1.3g/L以上及び成分(b)が0.3g/L以上である錫又は錫合金めっき液が開示されている。この特許文献2には、このめっき液は、ブラインドビア又はスルーホールを有する被めっき物に電気めっきすることにより、ブラインドビア又はスルーホールを信頼性高く短時間で充填できること、及び半導体の3次元実装やプリント配線板におけるブラインドビア又はスルーホールの充填工程やシリコン貫通電極の形成に利用できることが記載されている。 Patent Document 2 contains (a) a carboxyl group-containing compound and (b) a carbonyl group-containing compound, and the component (a) is 1.3 g / L or more and the component (b) is 0.3 g / L. The tin or tin alloy plating solution which is the above is disclosed. In this patent document 2, this plating solution can be filled with blind vias or through holes with high reliability and in a short time by electroplating on an object to be plated having blind vias or through holes, and three-dimensional mounting of semiconductors. It is described that it can be used in the process of filling blind vias or through holes in printed wiring boards and in the formation of silicon through electrodes.
 また特許文献3には、無機酸及び有機酸、並びにその水溶性塩と、界面活性剤と、レベリング剤と、を含む錫又は錫合金めっき液が開示されている。ここで、界面活性剤は、ポリオキシアルキレンフェニルエーテル又はその塩、及びポリオキシアルキレン多環フェニルエーテル又はその塩よりなる群から選択される少なくとも一種の非イオン界面活性剤であり、ポリオキシアルキレンフェニルエーテルを構成するフェニル、及びポリオキシアルキレン多環フェニルエーテルを構成する多環フェニルは、炭素数1~24のアルキル基、又はヒドロキシ基で置換されていてもよく、レベリング剤は、脂肪族アルデヒド、芳香族アルデヒド、脂肪族ケトン、及び芳香族ケトンよりなる群から選択される少なくとも一種と;α,β-不飽和カルボン酸若しくはそのアミド、又はこれらの塩である。この特許文献3には、特定の非イオン界面活性剤と特定の二種類のレベリング剤を含むため、リセス埋め性に優れており、かつ、ボイドの発生を抑制することができ、これにより、このめっき液を用いれば、リセスが無く平滑で、しかもリフロー後のボイドも発生しない良好なバンプを提供できることが記載されている。 Patent Document 3 discloses a tin or tin alloy plating solution containing an inorganic acid and an organic acid, and a water-soluble salt thereof, a surfactant, and a leveling agent. Here, the surfactant is at least one nonionic surfactant selected from the group consisting of polyoxyalkylene phenyl ether or a salt thereof, and polyoxyalkylene polycyclic phenyl ether or a salt thereof, and polyoxyalkylene phenyl The phenyl constituting the ether and the polycyclic phenyl constituting the polyoxyalkylene polycyclic phenyl ether may be substituted with an alkyl group having 1 to 24 carbon atoms or a hydroxy group, and the leveling agent is an aliphatic aldehyde, And at least one member selected from the group consisting of aromatic aldehydes, aliphatic ketones, and aromatic ketones; α, β-unsaturated carboxylic acids or their amides, or salts thereof. Since this patent document 3 contains a specific nonionic surfactant and two specific types of leveling agents, it is excellent in recess fillability and can suppress the generation of voids, which makes it possible It is described that if a plating solution is used, it is possible to provide a good bump which has no recess, is smooth, and does not generate a void after reflow.
 更に特許文献4には、(A)第一錫塩と、第一錫塩及び銀、銅、ビスマス、ニッケル、インジウム、金から選ばれた金属の塩の混合物とのいずれかよりなる可溶性塩と、(B)酸又はその塩と、(C)芳香族及び脂肪族アルデヒド、芳香族及び脂肪族ケトン、不飽和カルボン酸類、芳香族カルボン酸類よりなる群から選ばれた充填用有機化合物と、(D)ノニオン系界面活性剤とを含有する突起電極形成用の電気錫又は錫合金めっき液が開示されている。この特許文献4には、このめっき液は、錫系材料の析出を抑制する特定の化合物(C)に成分(D)を組み合わせて使用するため、ビア上部の析出を効果的に抑制し、錫系材料の析出をビア底部から優先的にビア上方に向けて進行させることができ、もってボイドの発生を防止しながら円滑にビア充填することができ、結果として、リフローし、或いはリフローせずに突起電極を良好に形成することができ、接合強度や電気特性に優れることが記載されている。 Further, Patent Document 4 discloses a soluble salt comprising either (A) a stannous salt and a mixture of a stannous salt and a salt of a metal selected from silver, copper, bismuth, nickel, indium, and gold. (B) an acid or a salt thereof, and (C) a filling organic compound selected from the group consisting of aromatic and aliphatic aldehydes, aromatic and aliphatic ketones, unsaturated carboxylic acids, and aromatic carboxylic acids; D) A galvanic tin or tin alloy plating solution for forming a bump electrode containing a nonionic surfactant is disclosed. In this patent document 4, since this plating solution is used by combining the component (D) with the specific compound (C) which suppresses the precipitation of the tin-based material, the precipitation of the upper portion of the via is effectively suppressed. The deposition of the base material can be advanced from the bottom of the via preferentially toward the upper side of the via, and the via can be filled smoothly while preventing the generation of the void, and as a result, the reflow or reflow is not performed. It is described that the protruding electrodes can be formed well and the bonding strength and the electrical characteristics are excellent.
特開2014-125662号公報(請求項2、段落[0020])JP-A-2014-125662 (claim 2, paragraph [0020]) 特開2015-007276号公報(請求項1、段落[0011]、[0012])JP, 2015-007276, A (claim 1, paragraphs [0011] and [0012]) 特開2015-193916号公報(請求項1、段落[0019])JP, 2015-193916, A (claim 1, paragraph [0019]) 特開2016-074963号公報(請求項1、段落[0019])JP, 2016-074963, A (claim 1, paragraph [0019])
 近年では、一つの回路基板上に、バンプ径やバンプピッチが異なる配線パターンが混在するようになってきている。そのような複雑な配線パターンにおいて、バンプ径やバンプピッチが異なる場合も全てのバンプを均一な高さで形成することが求められている。上記特許文献1~4の錫又は錫合金めっき液によれば、バンプ内のボイドの発生が抑制され、基板上のビアに信頼性高く短時間で充填でき、ビアフィリング性や外観に優れる特長がある。しかしながら、これらの文献における基板用めっき液は、バンプの高さ均一性を図ることをその課題としていない。 In recent years, wiring patterns having different bump diameters and bump pitches are mixed on one circuit board. In such a complicated wiring pattern, it is required to form all the bumps with uniform height even when the bump diameter and the bump pitch are different. According to the tin or tin alloy plating solution of Patent Documents 1 to 4, the generation of voids in the bumps is suppressed, and the vias on the substrate can be reliably filled in a short time, and the features are excellent in via filling property and appearance. is there. However, the substrate plating solution in these documents does not have the problem of achieving height uniformity of the bumps.
 具体的には、図2に示すように、バンプ径が異なるパターンの場合、従来の錫又は錫合金めっき液を用いめっきを行うと、小径若しくは大径のどちらかのビアフィリング性を良くすることは可能であるが、もう一方のビアフィリング性が低下する。即ち、小径及び大径のビアが両方存在する基板において、両方のビアに対して同時にめっきする場合、ビアフィリング性良く両方のビアにめっきすることが困難であった。このように、ビアフィリング性の異なるビアが存在している場合(図2(b))、リフロー後のバンプの高さばらつきが大きくなり、バンプの高さ均一性を図ることができない(図2(d))。よって、バンプの高さ均一性(図2(c))を図るには、図2(a)に示すように、小径及び大径の両方のビアへのビアフィリング性を良くする必要がある。 Specifically, as shown in FIG. 2, in the case of patterns having different bump diameters, plating using a conventional tin or tin alloy plating solution improves the via filling property of either the small diameter or the large diameter. Is possible, but the via filling of the other is reduced. That is, in a substrate in which both small diameter and large diameter vias are present, it is difficult to plate both vias with good via filling when plating both vias simultaneously. As described above, when there are vias with different via filling properties (FIG. 2B), the height variation of the bumps after reflow becomes large, and the height uniformity of the bumps can not be achieved (FIG. 2). (D)). Therefore, in order to achieve bump height uniformity (FIG. 2C), as shown in FIG. 2A, it is necessary to improve the via filling property to both the small diameter and large diameter vias.
 本発明の目的は、バンプ径が異なるパターンでも、基板上のビアへのビアフィリング性に優れ、かつ形成されたバンプの高さが均一になる錫又は錫合金めっき液を提供することにある。 An object of the present invention is to provide a tin or tin alloy plating solution which is excellent in via filling property to vias on a substrate and in which the height of the formed bumps is uniform, even in the case of patterns having different bump diameters.
 本発明の第1の観点は、(A)少なくとも第一錫塩を含む可溶性塩と、(B)有機酸及び無機酸から選ばれた酸又はその塩と、(C)界面活性剤と、(D)レベリング剤とを含む錫又は錫合金めっき液であって、界面活性剤がフェニル系界面活性剤を含み、フェニル系界面活性剤が次の一般式(1)で表されるポリオキシエチレンビスフェノールエーテルであることを特徴とする。 According to a first aspect of the present invention, there is provided (A) a soluble salt containing at least a stannous salt, (B) an acid selected from organic and inorganic acids or a salt thereof, (C) a surfactant, D) A tin or tin alloy plating solution containing a leveling agent, wherein the surfactant comprises a phenyl surfactant and the phenyl surfactant is represented by the following general formula (1): It is characterized by being an ether.
Figure JPOXMLDOC01-appb-C000002
 但し、式(1)中、XはC2a(a=1又は3)であり、mは2~12である。
Figure JPOXMLDOC01-appb-C000002
However, in the formula (1), X is C a H 2a (a = 1 or 3), and m is 2 to 12.
 本発明の第2の観点は、第1の観点に基づく発明であって、更にフェニル系界面活性剤とは別の界面活性剤、酸化防止剤及び炭素数1~3のアルコールのうち、2つ以上を更に含むことを特徴とする。 A second aspect of the present invention is the invention based on the first aspect, further comprising two of a surfactant other than a phenyl surfactant, an antioxidant and an alcohol having 1 to 3 carbon atoms. It is characterized by further including the above.
 本発明の第3の観点は、第1又は第2の観点に記載の錫又は錫合金めっき液を用いて、基板上に錫又は錫合金めっき堆積層を形成した後、リフロー処理をしてバンプを形成する方法である。 According to a third aspect of the present invention, after a tin or tin alloy plating deposition layer is formed on a substrate using the tin or tin alloy plating solution described in the first or second aspect, a reflow process is performed to form bumps. Is a method of forming
 本発明の第4の観点は、第3の観点に記載の方法により形成されたバンプを用いて回路基板を製造する方法である。 A fourth aspect of the present invention is a method of manufacturing a circuit board using bumps formed by the method described in the third aspect.
 本発明の第1の観点の錫又は錫合金めっき液では、フェニル系界面活性剤が、一般式(1)におけるXのa及びポリオキシエチレン基のmをそれぞれ所定の範囲にした特定のフェニル構造を持つことにより、めっき時に、Snイオンの析出を抑制し、めっき対象表面に良好にめっきすることを可能にする。特にこのめっき液によれば、バンプ径が異なるパターンの場合、バンプ径が大きくても或いは小さくても、分極抵抗が大きいため、基板上のビアへのビアフィリング性に優れ、かつ形成されたバンプの高さが均一になる。 In the tin or tin alloy plating solution according to the first aspect of the present invention, the phenyl surfactant has a specific phenyl structure in which a of X in the general formula (1) and m of a polyoxyethylene group are each in a predetermined range. By suppressing the deposition of Sn ions during plating, it becomes possible to well plate the surface to be plated. In particular, according to this plating solution, in the case of a pattern having different bump diameters, the polarization resistance is large regardless of whether the bump diameter is large or small, so that the via filling property to the via on the substrate is excellent and the formed bumps The height of the
 本発明の第2の観点の錫又は錫合金めっき液では、フェニル系界面活性剤とは別の界面活性剤、酸化防止剤及び炭素数1~3のアルコールのうち、2つ以上を更に含むことにより、次の効果を奏する。フェニル系界面活性剤とは別の界面活性剤はめっき液の安定化、溶解性の向上等の効果を奏する。また酸化防止剤は可溶性第一錫塩の第二錫塩への酸化を防止する。更にアルコールは、界面活性剤の溶解性の向上に効果を奏する。 The tin or tin alloy plating solution according to the second aspect of the present invention further comprises two or more of a surfactant other than a phenyl surfactant, an antioxidant, and an alcohol having 1 to 3 carbon atoms. The following effects are achieved. Surfactants other than phenyl surfactants exhibit effects such as stabilization of the plating solution and improvement of solubility. Antioxidants also prevent the oxidation of soluble stannous salts to stannic salts. Furthermore, the alcohol is effective in improving the solubility of the surfactant.
 本発明の第3の観点のバンプの形成方法では、上記錫又は錫合金めっき液を用いて、基板上に錫又は錫めっき堆積層を形成した後、リフロー処理をしてバンプを形成することにより、バンプ径が異なるパターンでも、高さが均一なバンプを形成することができる。 In the bump forming method according to the third aspect of the present invention, a tin or tin plating deposition layer is formed on a substrate using the above-mentioned tin or tin alloy plating solution, and then reflow treatment is performed to form bumps. Even if the patterns have different bump diameters, bumps having a uniform height can be formed.
 本発明の第4の観点の回路基板の製造方法では、第3の観点の方法により形成されたバンプを用いて回路基板を製造することにより、電気的な接続不良のない信頼性の高い半導体装置を作製することができる。 In the method of manufacturing a circuit board according to the fourth aspect of the present invention, a highly reliable semiconductor device free of electrical connection defects is manufactured by manufacturing a circuit board using the bumps formed according to the method according to the third aspect. Can be made.
(a)は本発明のビア内にめっき堆積層が形成された断面構成図であり、(b)はドライフィルム及び銅シード層を剥離し、めっき堆積層を加熱した後の断面構成図である。(A) is a cross-sectional block diagram in which the plating deposition layer was formed in the via | veer of this invention, (b) is a cross-section block diagram after peeling a dry film and a copper seed layer and heating a plating deposition layer. . (a)はバンプ径(ビア径)が異なるパターンでめっき堆積層が均一に形成された例を示す断面構成図であり、(b)はバンプ径(ビア径)が異なるパターンでめっき堆積層が不均一に形成された例を示す断面構成図であり、(c)は(a)においてドライフィルム及び銅シード層を剥離し、めっき堆積層を加熱した後、形成されたバンプの高さが均一になった例を示す断面構成図であり、(d)は(b)においてドライフィルム及び銅シード層を剥離し、めっき堆積層を加熱した後、形成されたバンプの高さがばらついた例を示す断面構成図である。(A) is a cross-sectional view showing an example in which the plating deposition layer is uniformly formed in patterns different in bump diameter (via diameter), (b) is a plating deposition layer in a pattern different in bump diameter (via diameter) It is a cross-sectional block diagram which shows the example formed unevenly, (c) peels a dry film and a copper seed layer in (a), and after heating a plating deposition layer, the height of the formed bump is uniform. (D) is an example in which the height of the bumps formed varies after peeling the dry film and copper seed layer in (b) and heating the plating deposition layer. It is a cross-sectional block diagram which shows.
 次に本発明を実施するための形態を説明する。 Next, an embodiment of the present invention will be described.
 本発明の錫又は錫合金めっき液は、(A)少なくとも第一錫塩を含む可溶性塩と、(B)有機酸及び無機酸から選ばれた酸又はその塩と、(C)界面活性剤と、(D)レベリング剤とを含む。この界面活性剤はフェニル系界面活性剤を含み、フェニル系界面活性剤が上記一般式(1)で表されるポリオキシエチレンビスフェノールエーテルである。 The tin or tin alloy plating solution of the present invention comprises (A) a soluble salt containing at least a stannous salt, (B) an acid selected from organic acids and inorganic acids, or a salt thereof, and (C) a surfactant. And (D) a leveling agent. This surfactant contains a phenyl surfactant, and the phenyl surfactant is a polyoxyethylene bisphenol ether represented by the above general formula (1).
 上記可溶性塩は、第一錫塩と、この第一錫塩及び銀、銅、ビスマス、ニッケル、アンチモン、インジウム、亜鉛からなる群から選ばれた金属の塩の混合物とのいずれかよりなる。 The soluble salt comprises any of a stannous salt and a mixture of a stannous salt and a salt of a metal selected from the group consisting of silver, copper, bismuth, nickel, antimony, indium and zinc.
 本発明の錫合金は、錫と、銀、銅、ビスマス、ニッケル、アンチモン、インジウム、亜鉛より選ばれた所定金属との合金であり、例えば、錫-銀合金、錫-銅合金、錫-ビスマス合金、錫-ニッケル合金、錫-アンチモン合金、錫-インジウム合金、錫-亜鉛合金の2元合金、錫-銅-ビスマス、錫-銅-銀合金などの3元合金が挙げられる。 The tin alloy of the present invention is an alloy of tin and a predetermined metal selected from silver, copper, bismuth, nickel, antimony, indium and zinc, and for example, tin-silver alloy, tin-copper alloy, tin-bismuth Alloys, tin-nickel alloys, tin-antimony alloys, tin-indium alloys, binary alloys of tin-zinc alloys, ternary alloys of tin-copper-bismuth, tin-copper-silver alloys and the like can be mentioned.
 従って、本発明の可溶性塩(A)はめっき液中でSn2+、Ag、Cu、Cu2+、Bi3+、Ni2+、Sb3+、In3+、Zn2+などの各種金属イオンを生成する任意の可溶性塩を意味し、例えば、当該金属の酸化物、ハロゲン化物、無機酸又は有機酸の当該金属塩などが挙げられる。 Therefore, the soluble salt (A) of the present invention can form any metal ion such as Sn 2+ , Ag + , Cu + , Cu 2+ , Bi 3+ , Ni 2+ , Sb 3+ , In 3+ , Zn 2+ in the plating solution. And soluble salts of the metal, such as oxides, halides of the metal, metal salts of the inorganic acid or the organic acid, and the like.
 金属酸化物としては、酸化第一錫、酸化銅、酸化ニッケル、酸化ビスマス、酸化アンチモン、酸化インジウム、酸化亜鉛などが挙げられ、金属のハロゲン化物としては、塩化第一錫、塩化ビスマス、臭化ビスマス、塩化第一銅、塩化第二銅、塩化ニッケル、塩化アンチモン、塩化インジウム、塩化亜鉛などが挙げられる。 Examples of metal oxides include stannous oxide, copper oxide, nickel oxide, bismuth oxide, antimony oxide, indium oxide, zinc oxide and the like, and metal halides include stannous chloride, bismuth chloride, bromide Bismuth, cuprous chloride, cupric chloride, nickel chloride, antimony chloride, indium chloride, zinc chloride and the like can be mentioned.
 無機酸又は有機酸の金属塩としては、硫酸銅、硫酸第一錫、硫酸ビスマス、硫酸ニッケル、硫酸アンチモン、硝酸ビスマス、硝酸銀、硝酸銅、硝酸アンチモン、硝酸インジウム、硝酸ニッケル、硝酸亜鉛、酢酸銅、酢酸ニッケル、炭酸ニッケル、錫酸ナトリウム、ホウフッ化第一錫、メタンスルホン酸第一錫、メタンスルホン酸銀、メタンスルホン酸銅、メタンスルホン酸ビスマス、メタンスルホン酸ニッケル、メタスルホン酸インジウム、ビスメタンスルホン酸亜鉛、エタンスルホン酸第一錫、2-ヒドロキシプロパンスルホン酸ビスマスなどが挙げられる。 As metal salts of inorganic acids or organic acids, copper sulfate, stannous sulfate, bismuth sulfate, nickel sulfate, antimony sulfate, bismuth nitrate, silver nitrate, copper nitrate, antimony nitrate, indium nitrate, nickel nitrate, zinc nitrate, copper acetate Nickel acetate, nickel carbonate, sodium stannate, stannous borofluoride, stannous methanesulfonate, silver methanesulfonate, copper methanesulfonate, bismuth methanesulfonate, nickel methanesulfonate, indium metasulfonate, bismethane And zinc sulfonate, stannous ethane sulfonate, bismuth 2-hydroxypropane sulfonate and the like.
 本発明の酸又はその塩(B)は、有機酸及び無機酸、或いはその塩から選択される。上記有機酸には、アルカンスルホン酸、アルカノールスルホン酸、芳香族スルホン酸等の有機スルホン酸、或いは脂肪族カルボン酸などが挙げられ、無機酸には、ホウフッ化水素酸、ケイフッ化水素酸、スルファミン酸、塩酸、硫酸、硝酸、過塩素酸などが挙げられる。その塩は、アルカリ金属の塩、アルカリ土類金属の塩、アンモニウム塩、アミン塩、スルホン酸塩などである。当該成分(B)は、金属塩の溶解性や排水処理の容易性の観点から有機スルホン酸が好ましい。 The acid or salt (B) of the present invention is selected from organic and inorganic acids or salts thereof. Examples of the organic acids include organic sulfonic acids such as alkanesulfonic acids, alkanolsulfonic acids and aromatic sulfonic acids, and aliphatic carboxylic acids. Examples of inorganic acids include borohydrofluoric acid, silicofluoric acid and sulfamine. Acid, hydrochloric acid, sulfuric acid, nitric acid, perchloric acid and the like can be mentioned. The salts are salts of alkali metals, salts of alkaline earth metals, ammonium salts, amine salts, sulfonates and the like. The component (B) is preferably an organic sulfonic acid from the viewpoint of the solubility of the metal salt and the ease of waste water treatment.
 上記アルカンスルホン酸としては、化学式C2n+1SOH(例えば、n=1~5、好ましくは1~3)で示されるものが使用でき、具体的には、メタンスルホン酸、エタンスルホン酸、1―プロパンスルホン酸、2―プロパンスルホン酸、1―ブタンスルホン酸、2―ブタンスルホン酸、ペンタンスルホン酸などの他、ヘキサンスルホン酸、デカンスルホン酸、ドデカンスルホン酸などが挙げられる。 As the alkanesulfonic acid, those represented by a chemical formula C n H 2n + 1 SO 3 H (for example, n = 1 to 5, preferably 1 to 3) can be used. Specifically, methanesulfonic acid and ethanesulfonic acid Other than 1-propanesulfonic acid, 2-propanesulfonic acid, 1-butanesulfonic acid, 2-butanesulfonic acid, pentanesulfonic acid and the like, hexanesulfonic acid, decanesulfonic acid, dodecanesulfonic acid and the like can be mentioned.
 上記アルカノールスルホン酸としては、化学式C2p+1-CH(OH)-C2q-SOH(例えば、p=0~6、q=1~5)で示されるものが使用でき、具体的には、2―ヒドロキシエタン―1―スルホン酸、2―ヒドロキシプロパン―1―スルホン酸、2―ヒドロキシブタン―1―スルホン酸、2―ヒドロキシペンタン―1―スルホン酸などの外、1―ヒドロキシプロパン―2―スルホン酸、3―ヒドロキシプロパン―1―スルホン酸、4―ヒドロキシブタン―1―スルホン酸、2―ヒドロキシヘキサン―1―スルホン酸、2―ヒドロキシデカン―1―スルホン酸、2―ヒドロキシドデカン―1―スルホン酸などが挙げられる。 As the alkanol sulfonic acid, the formula C p H 2p + 1 -CH ( OH) -C q H 2q -SO 3 H ( e.g., p = 0 ~ 6, q = 1 ~ 5) shown are those can be used in, particularly In particular, 2-hydroxyethane-1-sulfonic acid, 2-hydroxypropane-1-sulfonic acid, 2-hydroxybutane-1-sulfonic acid, 2-hydroxypentane-1-sulfonic acid, etc., 1-hydroxy Propane-2-sulfonic acid, 3-hydroxypropane-1-sulfonic acid, 4-hydroxybutane-1-sulfonic acid, 2-hydroxyhexane-1-sulfonic acid, 2-hydroxydecane-1-sulfonic acid, 2-hydroxy And dodecane-1-sulfonic acid.
 上記芳香族スルホン酸は、基本的にはベンゼンスルホン酸、アルキルベンゼンスルホン酸、フェノールスルホン酸、ナフタレンスルホン酸、アルキルナフタレンスルホン酸などであって、具体的には、1-ナフタレンスルホン酸、2―ナフタレンスルホン酸、トルエンスルホン酸、キシレンスルホン酸、p―フェノールスルホン酸、クレゾールスルホン酸、スルホサリチル酸、ニトロベンゼンスルホン酸、スルホ安息香酸、ジフェニルアミン―4―スルホン酸などが挙げられる。 The aromatic sulfonic acid is basically benzenesulfonic acid, alkylbenzenesulfonic acid, phenolsulfonic acid, naphthalenesulfonic acid, alkylnaphthalenesulfonic acid, etc. Specifically, 1-naphthalenesulfonic acid, 2-naphthalene And sulfonic acid, toluene sulfonic acid, xylene sulfonic acid, p-phenol sulfonic acid, cresol sulfonic acid, sulfosalicylic acid, nitrobenzene sulfonic acid, sulfobenzoic acid, diphenylamine-4-sulfonic acid and the like.
 上記脂肪族カルボン酸としては、例えば、酢酸、プロピオン酸、酪酸、クエン酸、酒石酸、グルコン酸、スルホコハク酸、トリフルオロ酢酸などが挙げられる。 Examples of the aliphatic carboxylic acids include acetic acid, propionic acid, butyric acid, citric acid, tartaric acid, gluconic acid, sulfosuccinic acid, trifluoroacetic acid and the like.
 本発明の界面活性剤に含まれるフェニル系界面活性剤は、次の一般式(1)で表されるポリオキシエチレンビスフェノールエーテルである。 The phenyl surfactant contained in the surfactant of the present invention is a polyoxyethylene bisphenol ether represented by the following general formula (1).
Figure JPOXMLDOC01-appb-C000003
Figure JPOXMLDOC01-appb-C000003
 但し、式(1)中、XはC2a(a=1又は3)であり、mは2~12である。ここで、mが2未満では、めっき液中への溶解が困難であったり、めっきの外観異常が生じたりする不具合があり、12を超えると、ビアフィリング性が劣ったり、めっきの外観異常が生じたりする不具合がある。なお、mは5~10であることが好ましい。なお、上記一般式(1)で表されるポリオキシエチレンビスフェノールエーテルは、オルト、メタ及びパラの各異性体、並びにこれらの混合異性体を含有する場合もある。 However, in the formula (1), X is C a H 2a (a = 1 or 3), and m is 2 to 12. Here, if m is less than 2, there is a problem that dissolution in the plating solution is difficult or abnormal appearance of plating occurs, and if it exceeds 12, the via filling property is inferior or abnormal appearance of plating is There is a problem that occurs. M is preferably 5 to 10. The polyoxyethylene bisphenol ether represented by the above general formula (1) may contain ortho, meta and para isomers, and mixed isomers thereof.
 本発明のレベリング剤(D)は、めっき皮膜を均一かつ緻密に形成するとともにめっき皮膜を平滑にするために加えて、ビアフィリング性を高め、ボイドの発生を抑制するために、第1レベリング剤(D-1)及び第2レベリング剤(D-2)の2種類が用いられる。第1レベリング剤(D-1)としては、脂肪族アルデヒド、芳香族アルデヒド、脂肪族ケトン及び芳香族ケトンよりなる群より選ばれた1種又は2種以上が挙げられ、第2レベリング剤(D-2)としては、α,β-不飽和カルボン酸又はそのアミド、或いはこれらの塩が挙げられる。 The leveling agent (D) of the present invention is a first leveling agent in order to form a plating film uniformly and densely and to make the plating film smooth, in addition to enhance the via filling property and to suppress the generation of voids. Two types of (D-1) and a second leveling agent (D-2) are used. As the first leveling agent (D-1), one or more selected from the group consisting of aliphatic aldehydes, aromatic aldehydes, aliphatic ketones and aromatic ketones may be mentioned, and the second leveling agent (D As -2), α, β-unsaturated carboxylic acids or their amides, or salts thereof can be mentioned.
 第1レベリング剤(D-1)は、アルデヒドやケトンを含むカルボニル化合物であり、第2レベリング剤(D-2)のα,β-不飽和カルボン酸は含まない。具体的には、次のものが例示される。脂肪族アルデヒドとしては、ホルムアルデヒド、アセトアルデヒド、アリルアルデヒドなどが挙げられる。また、芳香族アルデヒドとしては、ベンズアルデヒド、2-クロロベンズアルデヒド、3-クロロベンズアルデヒド、4-クロロベンズアルデヒド、2,4-ジクロロベンズアルデヒド、2,6-ジクロロベンズアルデヒド、2,4,6-トリクロロベンズアルデヒド、1-ナフトアルデヒド、2-ナフトアルデヒド、2-ヒドロキシベンズアルデヒド、3-ヒドロキシベンズアルデヒド、4-ヒドロキシベンズアルデヒド、2-メチルベンズアルデヒド、3-メチルベンズアルデヒド、4-メチルベンズアルデヒド、m-アニスアルデヒド、o-アニスアルデヒド、p-アニスアルデヒドなどが挙げられる。また、脂肪族ケトンとしては、アセチルアセトンなどが挙げられる。更に、芳香族ケトンとしては、ベンジリデンアセトン(ベンザルアセトンと同義)、2-クロロアセトフェノン、3-クロロアセトフェノン、4-クロロアセトフェノン、2,4-ジクロロアセトフェノン、2,4,6-トリクロロアセトフェノンなどが挙げられる。これらは、単独で用いてもよいし、2種以上を用いてもよい。電気めっき浴中に占める第1レベリング剤(D-1)の好ましい含有量(単独で含むときは単独の量であり、2種以上を含むときはこれらの合計量)は、0.001g/L~0.3g/Lであり、より好ましくは0.01g/L~0.25g/Lである。上記成分の含有量が少ないとその添加効果が十分でなく、一方、上記成分の含有量が多すぎると、めっき皮膜の平滑化を阻害するおそれがある。 The first leveling agent (D-1) is a carbonyl compound containing an aldehyde and a ketone, and does not contain the α, β-unsaturated carboxylic acid of the second leveling agent (D-2). Specifically, the following are exemplified. Examples of aliphatic aldehydes include formaldehyde, acetaldehyde and allyl aldehyde. Also, as the aromatic aldehyde, benzaldehyde, 2-chlorobenzaldehyde, 3-chlorobenzaldehyde, 4-chlorobenzaldehyde, 2,4-dichlorobenzaldehyde, 2,6-dichlorobenzaldehyde, 2,4,6-trichlorobenzaldehyde, 1- Naphthaldehyde, 2-naphthaldehyde, 2-hydroxy benzaldehyde, 3-hydroxy benzaldehyde, 4-hydroxy benzaldehyde, 2-methyl benzaldehyde, 3-methyl benzaldehyde, 4-methyl benzaldehyde, m-anisaldehyde, o-anisaldehyde, p- Anisaldehyde etc. are mentioned. Moreover, as aliphatic ketone, acetylacetone etc. are mentioned. Further, as the aromatic ketone, benzylideneacetone (equivalent to benzalacetone), 2-chloroacetophenone, 3-chloroacetophenone, 4-chloroacetophenone, 2,4-dichloroacetophenone, 2,4,6-trichloroacetophenone, etc. It can be mentioned. These may be used alone or in combination of two or more. The preferred content of the first leveling agent (D-1) in the electroplating bath (it is a single amount when it is contained alone, and the total amount of these when it contains 2 or more types) is 0.001 g / L It is ̃0.3 g / L, more preferably 0.01 g / L ̃0.25 g / L. If the content of the above component is small, the effect of the addition is not sufficient. On the other hand, if the content of the above component is too large, there is a possibility that the smoothing of the plating film is inhibited.
 第2レベリング剤(D-2)としては、アクリル酸、メタクリル酸、ピコリン酸、クロトン酸、3-クロロアクリル酸、3,3-ジメチルアクリル酸、2,3-ジメチルアクリル酸、アクリル酸メチル、アクリル酸エチル、n-ブチルアクリラート、イソブチルアクリラート、2-エチルヘキシルアクリラート、エチルメタクリラート、n-ブチルメタクリラート、イソブチルメタクリラート、2-ヒドロキシエチルメタクリラート、2-ヒドロキシプロピルメタクリラート、2-ジメチルアミノエチルメタクリラート、メタクリル酸無水物、メチルメタクリル酸などが挙げられる。また、第2レベリング剤(D-2)には、α,β-不飽和カルボン酸のアミド(例えば、アクリルアミドなど)や、α,β-不飽和カルボン酸の塩(例えば、カリウム、ナトリウム、アンモニウムなどの塩)も含まれる。電気めっき浴中に占める第2レベリング剤(D-2)の好ましい含有量(単独で含むときは単独の量であり、2種以上を含むときはこれらの合計量)は、0.01g/L~50g/Lであり、より好ましくは0.05g/L~30g/L、更に好ましくは0.05g/L~10g/Lである。上記成分の含有量が少ないとその添加効果が十分でなく、一方、上記成分の含有量が多すぎると、めっき皮膜の平滑化を阻害するおそれがある。 As the second leveling agent (D-2), acrylic acid, methacrylic acid, picolinic acid, crotonic acid, 3-chloroacrylic acid, 3,3-dimethylacrylic acid, 2,3-dimethylacrylic acid, methyl acrylate, Ethyl acrylate, n-butyl acrylate, isobutyl acrylate, 2-ethylhexyl acrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2-hydroxy methacrylate Dimethylaminoethyl methacrylate, methacrylic anhydride, methyl methacrylic acid and the like can be mentioned. Further, as the second leveling agent (D-2), an amide of α, β-unsaturated carboxylic acid (eg, acrylamide etc.) or a salt of α, β-unsaturated carboxylic acid (eg, potassium, sodium, ammonium) Etc.) are also included. The preferred content of the second leveling agent (D-2) in the electroplating bath (it is a single amount when it is contained alone, and the total amount of these when it contains 2 or more types) is 0.01 g / L It is ̃50 g / L, more preferably 0.05 g / L to 30 g / L, still more preferably 0.05 g / L to 10 g / L. If the content of the above component is small, the effect of the addition is not sufficient. On the other hand, if the content of the above component is too large, there is a possibility that the smoothing of the plating film is inhibited.
 本発明の錫又は錫合金めっき液には、フェニル系界面活性剤とは別の界面活性剤(E)、酸化防止剤(F)及び炭素数1~3のアルコール(G)のうち、2つ以上を更に含むことが好ましい。 In the tin or tin alloy plating solution of the present invention, two of a surfactant (E) other than a phenyl surfactant, an antioxidant (F) and an alcohol having 1 to 3 carbon atoms (G) It is preferable to further include the above.
 この場合の他の界面活性剤(E)としては、通常のアニオン系界面活性剤、カチオン系界面活性剤、ノニオン系界面活性剤及び両性界面活性剤が挙げられる。 Examples of other surfactants (E) in this case include usual anionic surfactants, cationic surfactants, nonionic surfactants and amphoteric surfactants.
 アニオン系界面活性剤としては、ポリオキシエチレン(エチレンオキサイド:12モル含有)ノニルエーテル硫酸ナトリウム等のポリオキシアルキレンアルキルエーテル硫酸塩、ポリオキシエチレン(エチレンオキサイド:12モル含有)ドデシルフェニルエーテル硫酸ナトリウム等のポリオキシアルキレンアルキルフェニルエーテル硫酸塩、ドデシルベンゼンスルホン酸ナトリウム等のアルキルベンゼンスルホン酸塩、1-ナフトール-4-スルホン酸ナトリウム、2-ナフトール-3,6-ジスルホン酸ジナトリウム等のナフトールスルホン酸塩、ジイソプロピルナフタレンスルホン酸ナトリウム、ジブチルナフタレンスルホン酸ナトリウム等の(ポリ)アルキルナフタレンスルホン酸塩、ドデシル硫酸ナトリウム、オレイル硫酸ナトリウム等のアルキル硫酸塩等が挙げられる。 Examples of anionic surfactants include polyoxyalkylene alkyl ether sulfates such as polyoxyethylene (ethylene oxide: 12 mol content) nonyl ether sodium sulfate, polyoxyethylene (ethylene oxide: 12 mol content) sodium dodecyl phenyl ether sulfate, etc. Of alkylbenzene sulfonates such as polyoxyalkylene alkyl phenyl ether sulfates and sodium dodecylbenzene sulfonate, naphthol sulfonates such as sodium 1-naphthol-4-sulfonate and disodium 2-naphthol-3,6-disulfonate , (Poly) alkyl naphthalene sulfonates such as sodium diisopropyl naphthalene sulfonate, sodium dibutyl naphthalene sulfonate, sodium dodecyl sulfate, oleyl sulfate nato Alkyl sulfates such as Um like.
 カチオン系界面活性剤としては、モノ~トリアルキルアミン塩、ジメチルジアルキルアンモニウム塩、トリメチルアルキルアンモニウム塩、ドデシルトリメチルアンモニウム塩、ヘキサデシルトリメチルアンモニウム塩、オクタデシルトリメチルアンモニウム塩、ドデシルジメチルアンモニウム塩、オクタデセニルジメチルエチルアンモニウム塩、ドデシルジメチルベンジルアンモニウム塩、ヘキサデシルジメチルベンジルアンモニウム塩、オクタデシルジメチルベンジルアンモニウム塩、トリメチルベンジルアンモニウム塩、トリエチルベンジルアンモニウム塩、ヘキサデシルピリジニウム塩、ドデシルピリジニウム塩、ドデシルピコリニウム塩、ドデシルイミダゾリニウム塩、オレイルイミダゾリニウム塩、オクタデシルアミンアセテート、ドデシルアミンアセテートなどが挙げられる。 As a cationic surfactant, mono- to trialkylamine salts, dimethyldialkylammonium salts, trimethylalkylammonium salts, dodecyltrimethylammonium salts, hexadecyltrimethylammonium salts, octadecyltrimethylammonium salts, dodecyldimethylammonium salts, octadecenyl Dimethylethyl ammonium salt, dodecyl dimethyl benzyl ammonium salt, hexadecyl dimethyl benzyl ammonium salt, octadecyl dimethyl benzyl ammonium salt, trimethyl benzyl ammonium salt, triethyl benzyl ammonium salt, hexadecyl pyridinium salt, dodecyl pyridinium salt, dodecyl picolinium salt, dodecyl imidazo Rhinium salt, oleylimidazolinium salt, octadecylamine acetate DOO, and the like dodecylamine acetate.
 ノニオン系界面活性剤としては、糖エステル、脂肪酸エステル、C~C25アルコキシルリン酸(塩)、ソルビタンエステル、C~C22脂肪族アミドなどにエチレンオキシド(EO)及び/又はプロピレンオキシド(PO)を2~300モル付加縮合させたもの、シリコン系ポリオキシエチレンエーテル、シリコン系ポリオキシエチレンエステル、フッ素系ポリオキシエチレンエーテル、フッ素系ポリオキシエチレンエステル、エチレンオキサイド及び/又はプロピレンオキサイドとアルキルアミン又はジアミンとの縮合生成物の硫酸化あるいはスルホン化付加物などが挙げられる。 Examples of nonionic surfactants include sugar esters, fatty acid esters, C 1 -C 25 alkoxyl phosphate (salts), sorbitan esters, C 1 -C 22 fatty amides, etc. ethylene oxide (EO) and / or propylene oxide (PO 4) 2) to 300 mol of addition-condensed silicone), silicon-based polyoxyethylene ether, silicon-based polyoxyethylene ester, fluorine-based polyoxyethylene ether, fluorine-based polyoxyethylene ester, ethylene oxide and / or propylene oxide and alkyl oxide with alkylamine Or sulfated or sulfonated adducts of condensation products with diamines.
 両性界面活性剤としては、ベタイン、カルボキシベタイン、イミダゾリニウムベタイン、スルホベタイン、アミノカルボン酸などが挙げられる。 Amphoteric surfactants include betaine, carboxybetaine, imidazolinium betaine, sulfobetaine, aminocarboxylic acid and the like.
 上記酸化防止剤(F)は、可溶性第一錫塩の第二錫塩への酸化を防止するために用いられる。酸化防止剤としては、次亜リン酸類を初め、アスコルビン酸又はその塩、フェノールスルホン酸(Na)、クレゾールスルホン酸(Na)、ハイドロキノンスルホン酸(Na)、ヒドロキノン、α又はβ-ナフトール、カテコール、レゾルシン、フロログルシン、ヒドラジン、フェノールスルホン酸、カテコールスルホン酸、ヒドロキシベンゼンスルホン酸、ナフトールスルホン酸、或いはこれらの塩などが挙げられる。 The antioxidant (F) is used to prevent the oxidation of soluble stannous salts to stannic salts. As the antioxidant, hypophosphorous acids and the like, ascorbic acid or a salt thereof, phenolsulfonic acid (Na), cresol sulfonic acid (Na), hydroquinone sulfonic acid (Na), hydroquinone, α or β-naphthol, catechol, Examples include resorcin, phloroglucin, hydrazine, phenolsulfonic acid, catecholsulfonic acid, hydroxybenzenesulfonic acid, naphtholsulfonic acid, and salts thereof.
 上記炭素数が1~3のアルコール(G)は、上記界面活性剤の溶解性を向上させるために用いられる。アルコールとしては、メタノール、エタノール、1-プロパノール、2-プロパノール等が挙げられる。アルコールは、1種単独で、又は2種以上を組合せて用いることができる。 The alcohol (G) having 1 to 3 carbon atoms is used to improve the solubility of the surfactant. Examples of the alcohol include methanol, ethanol, 1-propanol, 2-propanol and the like. The alcohol can be used singly or in combination of two or more.
 フェニル系界面活性剤(C)のめっき液中における含有量は0.5g/L~50g/L、好ましくは1g/L~5g/Lである。含有量が下限値未満では、Snイオンの供給過多により、デンドライトなどのめっき不良が発生する。また上限値を超えると、めっき対象表面にSnイオンが到達し難くなりビアフィリング性が劣る(低下する)不具合がある。 The content of the phenyl surfactant (C) in the plating solution is 0.5 g / L to 50 g / L, preferably 1 g / L to 5 g / L. If the content is less than the lower limit value, plating defects such as dendrite occur due to excessive supply of Sn ions. If the upper limit value is exceeded, it is difficult for Sn ions to reach the surface to be plated and the via filling property is inferior (deteriorated).
 また、上記所定の可溶性金属塩(A)は単用又は併用でき、めっき液中での含有量は30g/L~100g/L、好ましくは40g/L~60g/Lである。含有量が適正範囲より少ないと生産性が落ち、含有量が多くなるとめっき液のコストが上昇してしまう。 The predetermined soluble metal salt (A) can be used singly or in combination, and the content in the plating solution is 30 g / L to 100 g / L, preferably 40 g / L to 60 g / L. If the content is less than the appropriate range, the productivity is lowered, and if the content is increased, the cost of the plating solution is increased.
 無機酸、有機酸又はその塩(B)は単用又は併用でき、めっき液中での含有量は80g/L~300g/L、好ましくは100g/L~200g/Lである。含有量が適正範囲より少ないと導電率が低く電圧が上昇し、含有量が多くなるとめっき液の粘度が上昇しめっき液の撹拌速度が低下してしまう。 The inorganic acid, the organic acid or the salt thereof (B) can be used singly or in combination, and the content in the plating solution is 80 g / L to 300 g / L, preferably 100 g / L to 200 g / L. If the content is less than the appropriate range, the conductivity is low and the voltage is increased, and if the content is large, the viscosity of the plating solution is increased and the stirring speed of the plating solution is decreased.
 一方、本発明の電気めっき液の液温は一般に70℃以下、好ましくは10~40℃である。電気めっきによるめっき膜形成時の電流密度は、0.1A/dm以上100A/dm以下の範囲、好ましくは0.5A/dm以上20A/dm以下の範囲である。電流密度が低すぎると生産性が悪化し、高すぎるとバンプの高さ均一性が悪化してしまう。 On the other hand, the temperature of the electroplating solution of the present invention is generally 70 ° C. or less, preferably 10 to 40 ° C. The current density at the time of plating film formation by electroplating is in the range of 0.1 A / dm 2 to 100 A / dm 2 , preferably in the range of 0.5 A / dm 2 to 20 A / dm 2 . If the current density is too low, productivity will deteriorate, and if it is too high, the height uniformity of the bumps will deteriorate.
 本発明のフェニル系界面活性剤(C)を含む錫又は錫合金のめっき液を被めっき物である回路基板に適用して、この回路基板に所定の金属皮膜を形成することができる。回路基板としては、プリント回路基板、フレキシブルプリント回路基板、半導体集積回路基板などが挙げられる。 The plating solution of tin or tin alloy containing the phenyl surfactant (C) of the present invention can be applied to a circuit board which is an object to be plated to form a predetermined metal film on the circuit board. As the circuit board, a printed circuit board, a flexible printed circuit board, a semiconductor integrated circuit board and the like can be mentioned.
 次に本発明の実施例を比較例とともに詳しく説明する。 Next, an example of the present invention will be described in detail along with a comparative example.
(実施例及び比較例で用いるフェニル系界面活性剤(C))
 実施例1~7及び比較例1~2において使用されるフェニル系界面活性剤(C)であるポリオキシエチレンビスフェノールエーテルの各構造式を表1~表2に示す。
(Phenyl-based surfactant (C) used in Examples and Comparative Examples)
Tables 1 and 2 show structural formulas of polyoxyethylene bisphenol ether which is a phenyl surfactant (C) used in Examples 1 to 7 and Comparative Examples 1 and 2.
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000005
Figure JPOXMLDOC01-appb-T000005
 <実施例1>
(Snめっき液の建浴)
 メタンスルホン酸Sn水溶液に、遊離酸としてのメタンスルホン酸と、酸化防止剤としてヒドロキノンと、第1レベリング剤として1-ナフトアルデヒドと、第2レベリング剤としてメタクリル酸を混合して、均一な溶液となった後、更に界面活性剤として上記(C-1)のポリオキシエチレンビスフェノールエーテル(質量平均分子量:約600g/mol)を加えた。そして最後にイオン交換水を加えて、下記組成のSnめっき液を建浴した。なお、メタンスルホン酸Sn水溶液は、金属Sn板をメタンスルホン酸水溶液中で電解させることにより調製した。
Example 1
(Building bath of Sn plating solution)
A homogeneous solution is prepared by mixing an aqueous solution of methanesulfonic acid, methanesulfonic acid as a free acid, hydroquinone as an antioxidant, 1-naphthaldehyde as a first leveling agent, and methacrylic acid as a second leveling agent. After reaching the above, the polyoxyethylene bisphenol ether (weight average molecular weight: about 600 g / mol) of the above (C-1) was further added as a surfactant. Finally, ion exchange water was added, and a Sn plating solution of the following composition was prepared. In addition, the methanesulfonic acid Sn aqueous solution was prepared by electrolyzing a metal Sn plate in the methanesulfonic acid aqueous solution.
(Snめっき液の組成)
 メタンスルホン酸Sn(Sn2+として):50g/L
 メタンスルホン酸カリウム(遊離酸として):100g/L
 フェニル系界面活性剤(C-1):2g/L
 ヒドロキノン(酸化防止剤(F)として):1g/L
 1-ナフトアルデヒド(第1レベリング剤(D-1)として):0.1g/L
 メタクリル酸(第2レベリング剤(D-2)として):2g/L
 イオン交換水:残部
(Composition of Sn plating solution)
Methanesulfonic acid Sn (as Sn 2+ ): 50 g / L
Potassium methanesulfonate (as free acid): 100 g / L
Phenyl surfactant (C-1): 2 g / L
Hydroquinone (as antioxidant (F)): 1 g / L
1-naphthaldehyde (as a first leveling agent (D-1)): 0.1 g / L
Methacrylic acid (as a second leveling agent (D-2)): 2 g / L
Ion exchange water: balance
 <実施例2~8、比較例1~2>
 実施例2~8及び比較例1~2では、フェニル系界面活性剤(C)として、表1~表2に示す構造式のポリオキシエチレンビスフェノールエーテル((C-2)~(C-10))を用いた。それ以外は、実施例1と同様にして、実施例2~8及び比較例1~2のSnめっき液を建浴した。なお、実施例3及び比較例2では、Sn以外の金属としてAgを含み(Agとして1.0g/L)、実施例5では、Sn以外の金属としてCuを含んでいる(Cu2+として0.5g/L)。
Examples 2 to 8 and Comparative Examples 1 to 2
In Examples 2 to 8 and Comparative Examples 1 to 2, polyoxyethylene bisphenol ethers ((C-2) to (C-10) having the structural formulas shown in Tables 1 to 2 as phenyl surfactants (C). Was used. The Sn plating solutions of Examples 2 to 8 and Comparative Examples 1 and 2 were assembled in the same manner as Example 1 except for the above. In Example 3 and Comparative Example 2, Ag is contained as a metal other than Sn (1.0 g / L as Ag + ), and in Example 5, Cu is contained as a metal other than Sn (0 2 as Cu 2+. .5 g / L).
 <比較試験及び評価>
 実施例1~8及び比較例1~2の10種類の建浴しためっき液を用いて、バンプ径の異なるパターンを有する基板に、電流密度2ASDの条件でめっきを行い、ビア内に錫又は錫合金めっき堆積層を形成した。そして、リフロー装置を用いて280℃まで加熱し、めっき堆積層を溶融させてバンプを形成した。これらのめっき堆積層及びバンプについて評価した。
 なお、後述する「ビア内の錫又は錫合金めっき堆積層のビアフィリング性」及び「ビア内の錫又は錫合金めっき堆積層の外観」はリフロー前のめっき堆積層について測定しており、「バンプ高さのばらつき」及び「ボイドの発生し易さ」は、めっき堆積層のリフロー後に形成されたバンプについて測定している。その結果を表3に示す。
<Comparison test and evaluation>
Using the plating solutions prepared in 10 types of baths of Examples 1 to 8 and Comparative Examples 1 to 2, a substrate having patterns with different bump diameters is plated at a current density of 2 ASD, and tin or tin in a via is formed. An alloy plating deposited layer was formed. And it heated to 280 degreeC using the reflow apparatus, the plating deposition layer was fuse | melted, and the bump was formed. These plating deposited layers and bumps were evaluated.
In addition, “the via filling property of the tin or tin alloy plating deposition layer in the via” and the “appearance of the tin or tin alloy plating deposition layer in the via” described later are measured for the plating deposition layer before reflow. The height variation "and" voiding potential "are measured for the bumps formed after reflow of the plated deposit. The results are shown in Table 3.
(1)ビア内の錫又は錫合金めっき堆積層のビアフィリング性
 レーザー顕微鏡を用い、ビア内の錫又は錫合金めっき堆積層を観察し、めっき堆積層の最も高い点から最も低い点までの高さの差を測定した。高さの差が5μmを超えた場合を「不良」とし、高さの差が5μm以下の場合を「良好」と判断し、表3の「ビアフィリング性」の欄に示した。
(1) Via Filling Property of Tin or Tin Alloy Plating Deposited Layer in Via Using a laser microscope, observing the tin or tin alloy plated deposition in the via, the height from the highest point to the lowest point of the plated deposited layer Difference was measured. The case where the difference in height exceeds 5 μm is regarded as “defective”, and the case where the difference in height is 5 μm or less is judged as “good”, and is shown in the “via filling property” column of Table 3.
(2)めっき堆積層の外観
 レーザー顕微鏡を用いて、ビア内の錫又は錫合金めっき堆積層を観察し、表面粗さRaを測定した。めっき堆積層の表面粗さRaが2μmを超えた場合を「不良」とし、2μm以下の場合を「良好」と判断し、表3の「めっき堆積層の外観」の欄に示した。
(2) Appearance of Plating Deposit Layer The tin or tin alloy plating deposition layer in the via was observed using a laser microscope to measure the surface roughness Ra. The case where the surface roughness Ra of the plating deposition layer exceeded 2 μm was regarded as “defective”, and the case of 2 μm or less was considered “good”, and it is shown in the “appearance of plating deposition layer” column of Table 3.
(3)バンプ高さのばらつき
 基板のバンプの高さを、自動外観検査装置を用いて測定した。測定したバンプ高さから、高さばらつきσ(標準偏差)を算出した。高さばらつきσが3以下である場合を「均一」とし、高さばらつきσが3を超える場合を「不均一」と判断し、その結果を表3の「バンプの高さばらつきσ」の欄に示した。
(3) Variation of Bump Height The height of the bumps on the substrate was measured using an automatic visual inspection apparatus. Height variation σ (standard deviation) was calculated from the measured bump height. The case where height variation σ is 3 or less is considered as “uniform”, and the case where height variation σ exceeds 3 is determined as “non-uniform”, and the result is the column of “bump height variation σ” in Table 3. It was shown to.
(4)ボイドの発生し易さ
 180μm、250μm、360μmの各ピッチ間隔で配列されかつ直径が70μm、90μm、120μmであるバンプ(計2000個)について、透過X線像を撮影した。撮影した画像を目視で観察し、バンプの大きさに対して1%以上の大きさのボイドが1つ以上見られた場合を「NG」とし、ボイドが見られない場合を「OK」とした。その結果を表3の「ボイド」の欄に示す。
(4) Ease of Void Generation Transmission X-ray images were taken of bumps (2000 in total) arranged at pitches of 180 μm, 250 μm and 360 μm and having a diameter of 70 μm, 90 μm and 120 μm. The photographed image was visually observed, and when one or more voids having a size of 1% or more were observed with respect to the size of the bumps, "NG" was determined, and when no voids were observed, "OK" . The results are shown in the "void" column of Table 3.
Figure JPOXMLDOC01-appb-T000006
Figure JPOXMLDOC01-appb-T000006
 表3から明らかなように、フェニル系界面活性剤として化合物No.C-9を用いた比較例1では、一般式(1)におけるmが1と小さすぎたため、ビアフィリング性は良好であり、バンプ中にボイドが見られずボイドの発生し易さもOKであったけれども、めっき堆積層の外観が不良であり、バンプの高さばらつきも不均一であった。また、フェニル系界面活性剤として化合物No.C-10を用いた比較例2では、一般式(1)におけるmが15と大きすぎたため、バンプ中にボイドが見られずボイドの発生し易さはOKであったけれども、ビアフィリング性及びめっき堆積層の外観がいずれも不良であり、バンプの高さばらつきも不均一であった。 As apparent from Table 3, compound nos. In Comparative Example 1 using C-9, since m in the general formula (1) was too small at 1, the via filling property is good, no void is observed in the bump, and the ease of occurrence of the void is also OK. However, the appearance of the plating deposition layer was poor, and the bump height variation was also uneven. Moreover, as a phenyl surfactant, the compound No. 1 is used. In Comparative Example 2 using C-10, m in the general formula (1) was too large to be 15, and no void was observed in the bump, and the void generation probability was OK, but via filling property and The appearances of the plated deposition layers were all poor, and the height variations of the bumps were also uneven.
 これらに対し、フェニル系界面活性剤として化合物No.C-1~C-8を用いた実施例1~8では、一般式(1)におけるmが2~12と適切な範囲内(2~12)であったため、ビアフィリング性及びめっき堆積層の外観がいずれも良好であり、バンプの高さばらつきも全て均一であり、かつバンプ中にボイドが見られずボイドの発生し易さもOKであった。 On the other hand, compound nos. In Examples 1 to 8 in which C-1 to C-8 were used, m in the general formula (1) was in the appropriate range (2 to 12), so that the via filling property and the plating deposited layer The appearance was all good, the height variations of the bumps were all uniform, and no voids were observed in the bumps, and the tendency to generate voids was also OK.
 <実施例9~18>
 実施例9~18では、第1レベリング剤(D-1)、第2レベリング剤(D-2)又はSn以外の金属のいずれかと、フェニル系界面活性剤の質量平均分子量を表4に示すように変更したこと以外は、実施例1と同様にして、Snめっき液を建浴した。なお、表4の第1レベリング剤(D-1)において、D1Aはベンズアルデヒドであり、D1Bは4-クロロベンズアルデヒドであり、D1Cは1-ナフトアルデヒドである。また、表4の第2レベリング剤(D-2)において、D2Aはメタクリル酸であり、D2Bはアクリル酸であり、D2Cはアクリルアミドである。
Examples 9 to 18
In Examples 9 to 18, the weight average molecular weight of any of the first leveling agent (D-1), the second leveling agent (D-2) or a metal other than Sn and the phenyl surfactant is shown in Table 4. The Sn plating solution was built up in the same manner as in Example 1 except that it was changed to In the first leveling agent (D-1) in Table 4, D1A is benzaldehyde, D1B is 4-chlorobenzaldehyde, and D1C is 1-naphthoaldehyde. Further, in the second leveling agent (D-2) in Table 4, D2A is methacrylic acid, D2B is acrylic acid, and D2C is acrylamide.
 <比較試験2及び評価>
 実施例9~18の10種類の建浴しためっき液を用いて、比較試験1と同様に、バンプ径の異なるパターンを有する基板に、電流密度2ASDの条件でめっきを行い、ビア内に錫又は錫合金めっき堆積層を形成した。そして、リフロー装置を用いて280℃まで加熱し、めっき堆積層を溶融させてバンプを形成して、「ビア内の錫又は錫合金めっき堆積層のビアフィリング性」、「ビア内の錫又は錫合金めっき堆積層の外観」、「バンプ高さのばらつき」及び「ボイドの発生し易さ」を評価した。その結果を表4に示す。
<Comparative test 2 and evaluation>
In the same manner as in Comparative Test 1, a substrate having patterns with different bump diameters is plated under the conditions of current density 2ASD using the 10 kinds of plating solutions prepared in Examples 9 to 18 and tin or in the vias A tin alloy plating deposited layer was formed. Then, it is heated to 280 ° C. using a reflow apparatus, and the plating deposition layer is melted to form a bump, “via filling property of tin or tin alloy plating deposition layer in via”, “tin or tin in via The appearance of the alloy plating deposited layer, the "variation in bump height" and the "probability of void generation" were evaluated. The results are shown in Table 4.
Figure JPOXMLDOC01-appb-T000007
Figure JPOXMLDOC01-appb-T000007
 表4から明らかなように、第1レベリング剤(D-1)をベンズアルデヒド、4-クロロベンズアルデヒド又は1-ナフトアルデヒドのいずれかに変更し、第2レベリング剤(D-2)をメタクリル酸、アクリル酸又はアクリルアミドのいずれかに変更した実施例9~12では、ビアフィリング性及びめっき堆積層の外観がいずれも良好であり、バンプの高さばらつきも均一であり、かつバンプ中にボイドが見られずボイドの発生し易さはOKであった。 As apparent from Table 4, the first leveling agent (D-1) is changed to either benzaldehyde, 4-chlorobenzaldehyde or 1-naphthaldehyde, and the second leveling agent (D-2) is methacrylic acid, acrylic In Examples 9 to 12 in which either acid or acrylamide was changed, both the via filling property and the appearance of the plating deposited layer were good, the variation in bump height was uniform, and voids were observed in the bumps. The void generation tendency was OK.
 また、第1レベリング剤(D-1)をベンズアルデヒド又は1-ナフトアルデヒドに変更し、第2レベリング剤(D-2)をメタクリル酸又はアクリルアミドに変更し、更にSn以外の金属としてCu又はAgを添加した実施例13~14では、ビアフィリング性及びめっき堆積層の外観がいずれも良好であり、バンプの高さばらつきも均一であり、かつバンプ中にボイドが見られずボイドの発生し易さはOKであった。 Also, change the first leveling agent (D-1) to benzaldehyde or 1-naphthaldehyde, change the second leveling agent (D-2) to methacrylic acid or acrylamide, and further add Cu or Ag as a metal other than Sn. In Examples 13 to 14 in which the additive was added, both of the via filling property and the appearance of the plating deposition layer were good, the variation in the height of the bumps was uniform, and no voids were observed in the bumps and the voids were easily generated. Was ok.
 更に、第1レベリング剤(D-1)の濃度を0.001g/L及び0.3g/Lにそれぞれ変更した実施例15~16と、第2レベリング剤(D-2)の濃度を0.05g/L及び30g/Lにそれぞれ変更した実施例17~18では、ビアフィリング性及びめっき堆積層の外観がいずれも良好であり、バンプの高さばらつきも均一であり、かつバンプ中にボイドが見られずボイドの発生し易さはOKであった。 Furthermore, Examples 15 to 16 in which the concentration of the first leveling agent (D-1) was changed to 0.001 g / L and 0.3 g / L, respectively, and the concentration of the second leveling agent (D-2) were adjusted to 0. In Examples 17 to 18 which are respectively changed to 05 g / L and 30 g / L, both the via filling property and the appearance of the plating deposited layer are good, the bump height variation is also uniform, and voids are formed in the bumps. It was not seen and the possibility of void generation was OK.
 本発明の錫又は錫合金めっき液は、プリント回路基板、フレキシブルプリント回路基板、半導体集積回路などの回路基板に利用することができる。 The tin or tin alloy plating solution of the present invention can be used for circuit boards such as printed circuit boards, flexible printed circuit boards, and semiconductor integrated circuits.
 1  基板
 2  ソルダーレジスト層
 3  銅シード層
 4  ドライフィルムレジスト層
 6  ビア
 7  錫めっき堆積層(錫めっき皮膜)
 8  錫バンプ
1 substrate 2 solder resist layer 3 copper seed layer 4 dry film resist layer 6 via 7 tin plating deposition layer (tin plating film)
8 tin bumps

Claims (4)

  1.  (A)少なくとも第一錫塩を含む可溶性塩と、
     (B)有機酸及び無機酸から選ばれた酸又はその塩と、
     (C)界面活性剤と、
     (D)レベリング剤と
     を含む錫又は錫合金めっき液であって、
     前記界面活性剤がフェニル系界面活性剤を含み、
     前記フェニル系界面活性剤が次の一般式(1)で表されるポリオキシエチレンビスフェノールエーテルであることを特徴とする錫又は錫合金めっき液。
    Figure JPOXMLDOC01-appb-C000001
     但し、式(1)中、XはC2a(a=1又は3)であり、mは2~12である。
    (A) a soluble salt containing at least a stannous salt,
    (B) An acid selected from organic acids and inorganic acids or salts thereof
    (C) a surfactant,
    (D) A tin or tin alloy plating solution comprising: a leveling agent;
    The surfactant comprises a phenyl surfactant,
    The tin or tin alloy plating solution, wherein the phenyl surfactant is a polyoxyethylene bisphenol ether represented by the following general formula (1).
    Figure JPOXMLDOC01-appb-C000001
    However, in the formula (1), X is C a H 2a (a = 1 or 3), and m is 2 to 12.
  2.  前記フェニル系界面活性剤とは別の界面活性剤、酸化防止剤及び炭素数1~3のアルコールのうち、2つ以上を更に含む請求項1記載の錫又は錫合金めっき液。 The tin or tin alloy plating solution according to claim 1, further comprising two or more of a surfactant other than the phenyl surfactant, an antioxidant, and an alcohol having 1 to 3 carbon atoms.
  3.  請求項1又は2記載の錫又は錫合金めっき液を用いて、基板上に錫又は錫合金めっき堆積層を形成した後、リフロー処理をしてバンプを形成する方法。 A method for forming a bump by reflow processing after forming a tin or tin alloy plating deposition layer on a substrate using the tin or tin alloy plating solution according to claim 1 or 2.
  4.  請求項3記載の方法により形成されたバンプを用いて回路基板を製造する方法。 A method of manufacturing a circuit board using bumps formed by the method according to claim 3.
PCT/JP2018/039332 2017-10-24 2018-10-23 Tin or tin alloy plating solution WO2019082884A1 (en)

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Publication number Priority date Publication date Assignee Title
JP2003082493A (en) * 2001-05-24 2003-03-19 Shipley Co Llc Tin plating
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JP2015193916A (en) 2014-03-18 2015-11-05 上村工業株式会社 Tin or tin alloy electroplating bath and method for producing bump
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