EP3693495A1 - Electroless palladium plating solution, and electroless palladium plated coating - Google Patents

Electroless palladium plating solution, and electroless palladium plated coating Download PDF

Info

Publication number
EP3693495A1
EP3693495A1 EP18864662.4A EP18864662A EP3693495A1 EP 3693495 A1 EP3693495 A1 EP 3693495A1 EP 18864662 A EP18864662 A EP 18864662A EP 3693495 A1 EP3693495 A1 EP 3693495A1
Authority
EP
European Patent Office
Prior art keywords
electroless
compound
plating
plating film
plating solution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP18864662.4A
Other languages
German (de)
French (fr)
Other versions
EP3693495A4 (en
Inventor
Tsuyoshi Maeda
Katsuhisa Tanabe
Shinsuke Wada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Uemera Kogyo Co Ltd
C Uyemura and Co Ltd
Original Assignee
Uemera Kogyo Co Ltd
C Uyemura and Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Uemera Kogyo Co Ltd, C Uyemura and Co Ltd filed Critical Uemera Kogyo Co Ltd
Publication of EP3693495A1 publication Critical patent/EP3693495A1/en
Publication of EP3693495A4 publication Critical patent/EP3693495A4/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • 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
    • C23C18/16Chemical 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 by reduction or substitution, e.g. electroless plating
    • C23C18/1601Process or apparatus
    • C23C18/1633Process of electroless plating
    • C23C18/1646Characteristics of the product obtained
    • C23C18/165Multilayered product
    • C23C18/1651Two or more layers only obtained by electroless plating
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • 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
    • C23C18/16Chemical 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 by reduction or substitution, e.g. electroless plating
    • C23C18/31Coating with metals
    • C23C18/42Coating with noble metals
    • C23C18/44Coating with noble metals using reducing agents

Definitions

  • the present invention relates to an electroless palladium plating solution and an electroless palladium plating film.
  • electroless nickel electroless palladium immersion gold which can add an effect of being excellent in plating film properties such as solder bondability and wire bondability, is commonly used as a method for treating a surface of a circuit of a printed board, or a mounting portion or a terminal portion of an IC package.
  • Ni plating film an electroless nickel plating film
  • Pd plating film electroless palladium plating film
  • Ad plating film an immersion gold plating film
  • plating film properties are improved by, for example, modifying an electroless palladium plating solution (hereinafter, sometimes referred to as an "electroless Pd plating solution") in order to secure plating film properties required with miniaturization and enhanced density of electronic components.
  • electroless Pd plating solution an electroless palladium plating solution
  • Patent Document 1 discloses an electroless Pd plating solution in which as a stabilizer, bismuth or a bismuth compound is used instead of a sulfur compound, resulting in formation of an electroless Pd plating film which has bath stability as high as that achieved with a sulfur compound, and is excellent in corrosion resistance, solder bondability and wire bondability.
  • Patent Document 1 JP4596553B1
  • Electroless Ni/Pd/Au plating films which are commonly used exhibit excellent wire bondability before being exposed to a high-temperature thermal history in reflow treatment or the like, but has the problem that wire bondability is significantly deteriorated after the high-temperature thermal history.
  • the present invention has been made in view of the circumstances as described above, and an object of the present invention is to provide an electroless Pd plating solution which enables formation of a Pd plating film forming a plating film having excellent wire bondability even after a high-temperature thermal history; and a Pd plating film.
  • Preferable embodiment of the present inventive electroless Pd plating solution includes any combination of the following options (i) to (iii).
  • the present invention includes an electroless Pd plating film containing phosphorus; and boron.
  • Preferable embodiment of the present invention includes a laminated film including the electroless Pd plating film and a gold plating film formed on a surface of the electroless Pd plating film.
  • the present invention includes an electronic equipment component including the electroless Pd plating film of the present invention.
  • a Pd plating film forming a plating film having excellent wire bondability even after a high-temperature thermal history in reflow treatment or the like can be obtained.
  • the present inventors have extensively conducted studies on a cause of a phenomenon in which when a layered plating film with a Au plating film formed on a Pd plating film (hereinafter, sometimes referred to as a "Pd/Au layered plating film”) is exposed to a high-temperature thermal history in reflow or the like, the connection success rate in subsequent wire bonding is significantly reduced. Resultantly, it has been considered that exposure to a high-temperature thermal history causes Pd to diffuse to a Au plating film surface, so that a Pd-Au solid solution is formed on the Au plating film surface, resulting in reduction of the connection success rate in wire bonding.
  • One solution for such a problem may be formation of a Au plating film with a large thickness, but this solution leads to a significant increase in cost.
  • the present inventors have further conducted studies, and resultantly found that when a Pd plating film containing both P and B (hereinafter, sometimes referred to as a "P-B-Pd ternary alloy film") is formed as an under-layer of the Au plating film, wire bondability after a high-temperature thermal history can be improved. That is, when the Pd plating film contains both P and B, formation of a Pd-Au solid solution on the Au plating film surface can be suppressed even when the film is exposed to a high-temperature thermal history, and as a result, wire bondability more excellent than ever before can be obtained even when the thickness of the film is equivalent to or less than that of a conventional Au plating film.
  • the electroless Pd plating solution of the present invention is an electroless Pd plating solution containing a palladium compound; at least one selected from the group consisting of a hypophosphorous acid compound and a phosphorus acid compound; at least one selected from the group consisting of an amine borane compound and a hydroboron compound; and a complexing agent.
  • a plurality of reducing agents used in the electroless Pd plating solution is known, and these reducing agents include hypophosphorous acid compounds, phosphorous acid compounds, amine borane compounds and hydroboron compounds used for the electroless Pd plating solution of the present invention.
  • reducing agents have not used in combination heretofore because when a plurality of reducing agents having different reducing capacities is used, the plating solution has poor stability, so that abnormal precipitation or the like occurs, leading to deterioration of plating film properties.
  • a hypophosphorous acid compound or a phosphorous acid compound has a sufficient reducing capacity on its own, and does not need to be combined with other reducing agents.
  • the palladium compound is a source of palladium ions for obtaining palladium plating.
  • the palladium compound is not limited as long as it is soluble in water, and examples of the palladium compound that can be used include inorganic water-soluble palladium salts such as palladium chloride, palladium sulfate and palladium acetate; and organic water-soluble palladium salts such as tetraaminepalladium hydrochloride, tetraaminepalladium sulfate, tetraaminepalladium acetate, tetraaminepalladium nitrate and dichlorodiethylene diaminepalladium. These palladium compounds may be used alone, or in combination of two or more thereof.
  • the Pd ion concentration in the electroless Pd plating solution is not limited, and when the Pd ion concentration is excessively low, the deposition rate of the plating film may be significantly reduced. On the other hand, when the Pd ion concentration is excessively high, the physical properties of the film may be deteriorated due to abnormal deposition or the like.
  • the content of the palladium compound in the plating solution is preferably 0.01 g/L or more, more preferably 0.1 g/L or more, still more preferably 0.3 g/L or more, and even more preferably 0.5 g/L or more, and preferably 10 g/L or less, more preferably 5 g/L or less, still more preferably 3 g/L or less in Pd ion concentration.
  • Pd ions are measured by atomic absorption spectrometry (AAS) using an atomic absorption spectrophotometer.
  • the electroless Pd plating solution of the present invention in order to exhibit an inhibitory effect on solid-dissolution of Pd, it is necessary that (1) at least one selected from the group consisting of a hypophosphorous acid compound and a phosphorus acid compound (hereinafter, sometimes referred to as a "phosphoric acid compound) be used in combination with (2) at least one selected from the group consisting of an amine borane compound and a hydroboron compound (hereinafter, sometimes referred to as a "boron compound").
  • a hypophosphorous acid compound and a phosphorus acid compound hereinafter, sometimes referred to as a "phosphoric acid compound
  • boron compound a hydroboron compound
  • hypophosphorous acid compound examples include hypophosphorous acid and hypophosphites such as sodium hypophosphite, and examples of the phosphite compound include phosphorous acid and phosphites such as sodium phosphite.
  • the hypophosphorous acid compounds and the phosphorous acid compounds may be used alone, or in combination of two or more thereof.
  • the content of the hypophosphorous acid compound and/or the phosphorous acid compound in the electroless Pd plating solution is excessively low, the deposition rate during the plating process is reduced, and it may be impossible to obtain a sufficient inhibitory effect on solid-dissolution of Pd in the Au plating film due to a high-temperature thermal history, leading to deterioration of wire bondability.
  • the inhibitory effect on solid-dissolution is improved, but the stability of the electroless Pd plating solution may be deteriorated.
  • the content of the hypophosphorous acid compound and the phosphorous acid compound in the electroless Pd plating solution is preferably 0.1 g/L or more, more preferably 0.5 g/L or more, still more preferably 1 g/L or more, even more preferably 2 g/L or more, and preferably 100 g/L or less, more preferably 50 g/L or less, still more preferably 20 g/L or less, even more preferably 15 g/L or less.
  • amine borane compounds serve as a source of boron to the Pd plating film, and act as a reducing agent for depositing palladium in the electroless Pd plating solution.
  • amine borane compound examples include dimethylamine borane (DMAB) and trimethylamine borane (TMAB)
  • hydroboron compound include alkali metal borohydrides such as sodium borohydride (SBH) and potassium borohydride (KBH).
  • SBH sodium borohydride
  • KH potassium borohydride
  • the content of the boron compound in the electroless Pd plating solution is excessively low, the deposition rate during the plating process is reduced, and it may be impossible to obtain a sufficient inhibitory effect on solid-dissolution of Pd in the Au plating film due to a high-temperature thermal history, leading to deterioration of wire bondability.
  • the inhibitory effect on solid-dissolution is improved, but the stability of the electroless Pd plating solution may be deteriorated.
  • the content of the boron compound in the electroless Pd plating solution is preferably 0.01 g/L or more, more preferably 0.1 g/L or more, still more preferably 0.5 g/L or more, even more preferably 1 g/L or more, and preferably 100 g/L or less, more preferably 50 g/L or less, still more preferably 30 g/L or less, even more preferably 20 g/L or less.
  • the complexing agent has mainly a stabilizing action on the solubility of Pd in the electroless Pd plating solution.
  • the complexing agent may be any of various known complexing agents, and is preferably at least one selected from the group consisting of ammonia and an amine compound, more preferably an amine compound.
  • the amine compound methylamine, dimethylamine, trimethylamine, benzylamine, methylenediamine, ethylenediamine, ethylenediamine derivative, tetramethylenediamine, diethylenetriamine, ethylenediaminetetraacetic acid (EDTA), alkali metal salts thereof, EDTA derivatives and glycine.
  • the complexing agents can be used alone, or in combination of two or more thereof.
  • the content of the complexing agent in the electroless Pd plating solution may be approximately adjusted so as to obtain the above-described action, and is preferably 0.5 g/L or more, more preferably 1 g/L or more, still more preferably 3 g/L or more, even more preferably 5 g/L or more, and preferably 50 g/L or less, more preferably 30 g/L or less.
  • the electroless Pd plating solution of the present invention exhibits the above-described effects as long as it has the above-described component composition
  • the electroless Pd plating solution may have only the component composition.
  • the electroless Pd plating solution may contain various additives such as a pH adjuster and a stabilizer may be added.
  • the pH of the electroless Pd plating solution of the present invention is excessively low, the deposition rate of Pd easily decreases, and when the pH is excessively high, the stability of the electroless Pd plating solution may be deteriorated.
  • the pH is preferably 4 to 10, more preferably 6 to 8.
  • the pH of the electroless Pd plating solution can be adjusted by adding a known pH adjuster.
  • the pH adjuster include acids such as hydrochloric acid, sulfuric acid, nitric acid, citric acid, malonic acid, malic acid, tartaric acid and phosphoric acid, and alkalis such as sodium hydroxide, potassium hydroxide and ammonia water. These pH adjusters can be used alone, or in combination of two or more thereof.
  • the stabilizer is optionally added for the purpose of, for example, securing plating stability, improving the appearance after plating, and adjusting the plating film formation rate.
  • the electroless Pd plating solution of the present invention may further contain a known sulfur-containing compound.
  • the sulfur-containing compound is preferably one or more selected from, for example, a thioether compound, a thiocyan compound, a thiocarbonyl compound, a thiol compound, thiosulfuric acid and a thiosulfate.
  • thioether compounds such as methionine, dimethylsulfoxide, thiodiglycolic acid and benzothiazole
  • thiocyan compounds such as thiocyanic acid, potassium thiocyanate, sodium thiocyanate and ammonium thiocyanate
  • thiocarbonyl compounds such as thiourea and derivatives thereof
  • thiol compounds such as cysteine, thiolactic acid, thioglycolic acid, mercaptoethanol and butanethiol
  • thiosulfates such as sodium thiosulfate.
  • the content of the stabilizer in the electroless Pd plating solution may be approximately adjusted so as to obtain an effect such as plating stability, and is preferably 0.1 mg/L or more, more preferably 0.5 mg/L or more, and preferably 500 mg/L or less, more preferably 100 mg/L or less.
  • the electroless Pd plating solution of the present invention does not contain a surfactant.
  • a surfactant is added to the electroless Pd plating solution of the present invention, the surfactant is adsorbed to a surface of the resulting Pd plating film, so that formability of the Au plating film is deteriorated. As a result, wire bondability is deteriorated.
  • the surfactant is any of various known nonionic, cationic, anionic and amphoteric surfactants.
  • the present invention includes a Pd plating film which is obtained using the electroless Pd plating solution, and contains P and B. Since the inhibitory effect on solid-dissolution of Pd is obtained as long as the Pd plating film contains both P and B, the content of each of P and B is not limited, and when the content of P or B contained in the Pd plating film increases, the inhibitory effect on solid-dissolution of Pd is further improved.
  • the content of P in the Pd plating film is preferably 0.1% by mass or more, more preferably 0.3% by mass or more, and preferably 10% by mass or less, more preferably 5% by mass or less.
  • the content of B in the Pd plating film is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and preferably 15% by mass or less, more preferably 10% by mass or less.
  • the mass ratio (P : B) of the content of P and B in the electroless Pd plating film is preferably 10 : 1 to 1 : 10, and more preferably 5 : 1 to 1 : 5.
  • the Pd plating film of the present invention may contain P and B, and further contain components derived from the above-described various additives. The balance consists of Pd and unavoidable impurities.
  • the electroless Pd plating solution of the present invention is also suitable for a Pd/Au layered plating film with an Au plating film stacked on a Pd plating film, which is preferably used for plating for bonding of electronic components, etc. Therefore, a layered plating film having the Pd plating film of the present invention and the Au plating film is also a preferred embodiment.
  • the Pd plating film of the present invention can be confirmed to have an inhibitory effect on solid-dissolution of Pd in a Pd/Au layered plating film in which at least a Au plating film is stacked.
  • the base that forms the Pd plating film is not limited, and examples thereof include various known base materials such as Al, Al-based alloys, Cu and Cu-based alloys, and plating films in which a base material is covered with a metal catalytic for reduction and deposition of the Pd plating film, such as Fe, Co, Ni, Cu, Zn, Ag, Au, Pt and alloys thereof. Even a noncatalytic metal can be used as an object to be plated in various methods.
  • the electroless Pd plating solution of the present invention can be applied to the ENEPIG process.
  • an electroless Ni/Pd/Au plating film including the Pd plating film of the present invention can be obtained by forming a Ni plating film, then a Pd plating film, and then a Au plating film on, for example, Al, anAl-based alloy, Cu or a Cu-based alloy that forms an electrode.
  • a common method may be employed for the formation of each plating film.
  • the plating conditions and plating apparatus at the time of performing electroless Ni plating using an electroless Ni plating solution are not particularly limited, and any of various known methods can be appropriately selected.
  • an object to be plated may be brought into contact with the electroless Ni plating solution at a temperature of 50 to 95°C for about 15 to 60 minutes.
  • the thickness of the Ni plating film may be appropriately set according to the required properties, and is typically about 3 to 7 ⁇ m. Any of various known compositions such as Ni-P alloys and Ni-B alloys can be used for the electroless Ni plating solution.
  • the plating conditions and plating apparatus at the time of performing electroless Pd plating using the electroless Pd plating solution of the present invention are not particularly limited, and any of various known methods can be appropriately selected.
  • an object to be plated, on which a Ni plating film is formed may be brought into contact with the electroless Pd plating solution at a temperature of 50 to 95°C for about 15 to 60 minutes.
  • the thickness of the Pd plating film may be appropriately set according to the required properties, and is typically about 0.001 to 0.5 ⁇ m.
  • the plating conditions and plating apparatus at the time of performing electroless gold plating using an electroless gold plating solution are not particularly limited, and any of various known methods can be appropriately selected.
  • an object to be plated, on which a Pd plating film is formed may be brought into contact with the electroless gold plating solution at a temperature of 40 to 90°C for about 3 to 20 minutes.
  • the thickness of the gold plating film may be appropriately set according to the required properties, and is typically about 0.01 to 2 ⁇ m.
  • the Pd plating film of the present invention When the Pd plating film of the present invention is used, palladium can be inhibited from being diffused to and solid-dissolved in the Au plating film from the Pd plating film due to a thermal history in a mounting process after formation of the film, such as reflow treatment, and therefore excellent wire bondability can be achieved even after the thermal history.
  • the temperature in the thermal history is a temperature at which the mounting process is carried out, and the temperature is not particularly limited.
  • excellent wire bondability can be achieved even after a thermal history at a high temperature of, for example, 50°C or higher, more preferably 100°C or higher.
  • the present invention also includes an electronic equipment component having the plating film.
  • the electronic equipment component include components that form electronic equipment, such as chip components, crystal oscillators, bumps, connectors, lead frames, hoop materials, semiconductor packages and printed circuit boards.
  • the plating film is suitably used for a technique for forming UBM (Under Barrier Metal) for solder bonding and wire bonding (W/B) to an A1 electrode or a Cu electrode on a wafer.
  • UBM Under Barrier Metal
  • a BGA substrate (Ball Grid Array: Uyemura & Co., Ltd., 5 cm x 5 cm) was sequentially subjected to the pretreatment and plating treatment shown in Table 1, thereby producing test pieces 1 to 20 in which a Ni plating film, a Pd plating film and a Au plating film are formed in this order from the substrate side. The wire bondability of each of the obtained test pieces was examined.
  • Wire bonding was performed using a test apparatus (SemiAutomatic Wire Bonder HB16 manufactured by TPT K.K.), and wire bondability was evaluated at each of 20 points under the following measurement conditions using Bond Tester SERIES 4000 manufactured by Dage Ltd. The measurement was performed before and after the heat treatment (in which the test piece was held at 175°C for 16 hours).
  • a test piece having an average wire bonding strength of 9.0 g or more after heat treatment was rated "Excellent”
  • a test piece having an average wire bonding strength of 8.5 g or more and less than 9.0 g after heat treatment was rated "Good”
  • a test piece having an average wire bonding strength of 7.5 g or more and less than 8.5 g after heat treatment was rated "Acceptable”
  • a test piece having an average wire bonding strength of less than 7.5 g after heat treatment was rated "Poor”.
  • Capillary B1014-51-18-12 (manufactured by PECO Ltd.) Wire: 1mil-Au wire (SPM Ltd.) Stage temperature: 150°C Ultrasonic wave (mW): 250 (1st), 250 (2nd) Bonding time (ms): 200 (1st), 50 (2nd) Tensile force (gf):25 (1st), 50 (2nd) Step (1st to 2nd length): 0.7mm Measurement method: Wire pull test Equipment: Universal Bond Tester #4000 (manufactured by Nordson Advanced Technology K.K.) Test speed: 170 ⁇ m/sec [Table 1] Steps Name of chemicals Treatment temperature Treatment time (min.) Target film thickness Pretreatment Cleaner ACL- 50°C 5 - Soft etching SP 25°C 1 - Pickling 10% H 2 SO 4 room temperature 1 - Predip 3% H 2 SO 4 room temperature 1 - activator MNK- 30°C 2 - plating treatment electroless Ni plating NPR- 80°C 30 6um electroless Pd plating see
  • test pieces Nos. 1 to 9 obtained using the electroless Pd plating solution containing a complexing agent, a hypophosphorous acid compound and/or a phosphorous acid compound, and an amine borane compound and/or a hydroboron compound as defined in the present invention were each rated “Good” or "Excellent” in evaluation of wire bondability after heat treatment.
  • test pieces Nos. 10 to 18 obtained using a Pd plating solution that did not satisfy the requirements of the present invention were each rated "Poor” in evaluation of wire bondability after heat treatment.
  • Test pieces Nos. 19 and 20 were each rated "Poor” in evaluation of wire bondability after heat treatment because they contained a surfactant.

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemically Coating (AREA)

Abstract

An object of the present invention is to provide an electroless Pd plating solution which enables formation of a Pd plating film forming a plating film having excellent wire bondability even after a high-temperature thermal history. An electroless Pd plating solution of the present invention solved above problems, the solution includes a Palladium compound, at least one selected from a group consisting of a hypophosphorous acid compound and a phosphorous acid compound, at least one selected from the group consisting of an amine borane compound and a hydroboron compound, and a complexing agent.

Description

    TECHNICAL FIELD
  • The present invention relates to an electroless palladium plating solution and an electroless palladium plating film.
  • BACKGROUND ART
  • In the electronics industry, electroless nickel electroless palladium immersion gold (ENEPIG), which can add an effect of being excellent in plating film properties such as solder bondability and wire bondability, is commonly used as a method for treating a surface of a circuit of a printed board, or a mounting portion or a terminal portion of an IC package. A plating film obtained by sequentially applying an electroless nickel plating film (hereinafter, sometimes referred to as a "Ni plating film"), an electroless palladium plating film (hereinafter, sometimes referred to as a "Pd plating film") and an immersion gold plating film (hereinafter, sometimes referred to as an "Au plating film") through the ENEPIG process (hereinafter, sometimes referred to as an "electroless Ni/Pd/Au plating film") is commonly used.
  • In recent years, a technique has been proposed in which plating film properties are improved by, for example, modifying an electroless palladium plating solution (hereinafter, sometimes referred to as an "electroless Pd plating solution") in order to secure plating film properties required with miniaturization and enhanced density of electronic components.
  • For example, Patent Document 1 discloses an electroless Pd plating solution in which as a stabilizer, bismuth or a bismuth compound is used instead of a sulfur compound, resulting in formation of an electroless Pd plating film which has bath stability as high as that achieved with a sulfur compound, and is excellent in corrosion resistance, solder bondability and wire bondability.
  • PRIOR ART DOCUMENT PATENT DOCUMENTS
  • Patent Document 1: JP4596553B1
  • SUMMARY OF THE INVENTION PROBLEMS TO BE SOLVED BY THE INVENTION
  • Electroless Ni/Pd/Au plating films which are commonly used exhibit excellent wire bondability before being exposed to a high-temperature thermal history in reflow treatment or the like, but has the problem that wire bondability is significantly deteriorated after the high-temperature thermal history.
  • The present invention has been made in view of the circumstances as described above, and an object of the present invention is to provide an electroless Pd plating solution which enables formation of a Pd plating film forming a plating film having excellent wire bondability even after a high-temperature thermal history; and a Pd plating film.
  • SOLUTION TO PROBLEM
  • An electroless Pd plating solution of the present invention solved above problems, the solution includes:
    • a Palladium compound;
    • at least one selected from a group consisting of a hypophosphorous acid compound and a phosphorous acid compound;
    • at least one selected from the group consisting of an amine borane compound and a hydroboron compound; and
    • a complexing agent.
  • Preferable embodiment of the the present inventive electroless Pd plating solution includes any combination of the following options (i) to (iii).
    1. (i) the amine borane compound is at least one selected from a group consisting of dimethylamine borane and trimethylamine borane;
    2. (ii) the hydroboron compound is borohydride salt;
    3. (iii) the complexing agent is at least one selected from a group consisting of ammonia and an amine compound;
  • The present invention includes an electroless Pd plating film containing phosphorus; and boron. Preferable embodiment of the present invention includes a laminated film including the electroless Pd plating film and a gold plating film formed on a surface of the electroless Pd plating film.
  • The present invention includes an electronic equipment component including the electroless Pd plating film of the present invention.
  • ADVANTAGEOUS EFFECTS OF INVENTION
  • By using the electroless Pd plating solution of the present invention, a Pd plating film forming a plating film having excellent wire bondability even after a high-temperature thermal history in reflow treatment or the like can be obtained.
  • DESCRIPTION OF EMBODIMENTS
  • The present inventors have extensively conducted studies on a cause of a phenomenon in which when a layered plating film with a Au plating film formed on a Pd plating film (hereinafter, sometimes referred to as a "Pd/Au layered plating film") is exposed to a high-temperature thermal history in reflow or the like, the connection success rate in subsequent wire bonding is significantly reduced. Resultantly, it has been considered that exposure to a high-temperature thermal history causes Pd to diffuse to a Au plating film surface, so that a Pd-Au solid solution is formed on the Au plating film surface, resulting in reduction of the connection success rate in wire bonding. One solution for such a problem may be formation of a Au plating film with a large thickness, but this solution leads to a significant increase in cost.
  • The present inventors have further conducted studies, and resultantly found that when a Pd plating film containing both P and B (hereinafter, sometimes referred to as a "P-B-Pd ternary alloy film") is formed as an under-layer of the Au plating film, wire bondability after a high-temperature thermal history can be improved. That is, when the Pd plating film contains both P and B, formation of a Pd-Au solid solution on the Au plating film surface can be suppressed even when the film is exposed to a high-temperature thermal history, and as a result, wire bondability more excellent than ever before can be obtained even when the thickness of the film is equivalent to or less than that of a conventional Au plating film.
  • AP-B-Pd ternary alloy film having such an effect can be easily formed by using the electroless Pd plating solution of the present invention. Specifically, the electroless Pd plating solution of the present invention is an electroless Pd plating solution containing a palladium compound; at least one selected from the group consisting of a hypophosphorous acid compound and a phosphorus acid compound; at least one selected from the group consisting of an amine borane compound and a hydroboron compound; and a complexing agent.
  • A plurality of reducing agents used in the electroless Pd plating solution is known, and these reducing agents include hypophosphorous acid compounds, phosphorous acid compounds, amine borane compounds and hydroboron compounds used for the electroless Pd plating solution of the present invention. However, reducing agents have not used in combination heretofore because when a plurality of reducing agents having different reducing capacities is used, the plating solution has poor stability, so that abnormal precipitation or the like occurs, leading to deterioration of plating film properties. In particular, a hypophosphorous acid compound or a phosphorous acid compound has a sufficient reducing capacity on its own, and does not need to be combined with other reducing agents. However, it has become evident that an inhibitory effect on solid-dissolution of Pd in the Au plating film due to a thermal history cannot be obtained by addition of a single reducing agent or combined use of reducing agents other than those described above, and only the above-described specific combination according to the present invention enables formation of a Pd plating film at a practical level without causing the above-described problems. Such an inhibitory effect on solid-dissolution is a unique effect which can be obtained only by the above-described combination.
  • Palladium compound
  • The palladium compound is a source of palladium ions for obtaining palladium plating. The palladium compound is not limited as long as it is soluble in water, and examples of the palladium compound that can be used include inorganic water-soluble palladium salts such as palladium chloride, palladium sulfate and palladium acetate; and organic water-soluble palladium salts such as tetraaminepalladium hydrochloride, tetraaminepalladium sulfate, tetraaminepalladium acetate, tetraaminepalladium nitrate and dichlorodiethylene diaminepalladium. These palladium compounds may be used alone, or in combination of two or more thereof. The Pd ion concentration in the electroless Pd plating solution is not limited, and when the Pd ion concentration is excessively low, the deposition rate of the plating film may be significantly reduced. On the other hand, when the Pd ion concentration is excessively high, the physical properties of the film may be deteriorated due to abnormal deposition or the like. Therefore, the content of the palladium compound in the plating solution is preferably 0.01 g/L or more, more preferably 0.1 g/L or more, still more preferably 0.3 g/L or more, and even more preferably 0.5 g/L or more, and preferably 10 g/L or less, more preferably 5 g/L or less, still more preferably 3 g/L or less in Pd ion concentration. Pd ions are measured by atomic absorption spectrometry (AAS) using an atomic absorption spectrophotometer.
  • In the electroless Pd plating solution of the present invention, in order to exhibit an inhibitory effect on solid-dissolution of Pd, it is necessary that (1) at least one selected from the group consisting of a hypophosphorous acid compound and a phosphorus acid compound (hereinafter, sometimes referred to as a "phosphoric acid compound) be used in combination with (2) at least one selected from the group consisting of an amine borane compound and a hydroboron compound (hereinafter, sometimes referred to as a "boron compound").
  • (1) At least one selected from the group consisting of a hypophosphorous acid compound and a phosphorous acid compound
  • These compounds serve as a source of P to the Pd plating film, and act as a reducing agent for depositing Pd in the electroless Pd plating solution. Examples of the hypophosphorous acid compound include hypophosphorous acid and hypophosphites such as sodium hypophosphite, and examples of the phosphite compound include phosphorous acid and phosphites such as sodium phosphite. The hypophosphorous acid compounds and the phosphorous acid compounds may be used alone, or in combination of two or more thereof. When the content of the hypophosphorous acid compound and/or the phosphorous acid compound in the electroless Pd plating solution is excessively low, the deposition rate during the plating process is reduced, and it may be impossible to obtain a sufficient inhibitory effect on solid-dissolution of Pd in the Au plating film due to a high-temperature thermal history, leading to deterioration of wire bondability. As the content of the hypophosphorous acid compound and the phosphorous acid compound in the electroless Pd plating solution increases, the inhibitory effect on solid-dissolution is improved, but the stability of the electroless Pd plating solution may be deteriorated. The content of the hypophosphorous acid compound and the phosphorous acid compound in the electroless Pd plating solution (a single-compound amount when one compound is contained, and the total amount when two or more compounds are contained) is preferably 0.1 g/L or more, more preferably 0.5 g/L or more, still more preferably 1 g/L or more, even more preferably 2 g/L or more, and preferably 100 g/L or less, more preferably 50 g/L or less, still more preferably 20 g/L or less, even more preferably 15 g/L or less.
  • (2) At least one selected from the group consisting of an amine borane compound and a hydroboron compound
  • These compounds serve as a source of boron to the Pd plating film, and act as a reducing agent for depositing palladium in the electroless Pd plating solution. Examples of the amine borane compound include dimethylamine borane (DMAB) and trimethylamine borane (TMAB), and examples of the hydroboron compound include alkali metal borohydrides such as sodium borohydride (SBH) and potassium borohydride (KBH). In the present invention, it is preferable to use at least one selected from the group consisting of dimethylamine borane, trimethylamine borane, sodium borohydride and potassium borohydride. When the content of the boron compound in the electroless Pd plating solution is excessively low, the deposition rate during the plating process is reduced, and it may be impossible to obtain a sufficient inhibitory effect on solid-dissolution of Pd in the Au plating film due to a high-temperature thermal history, leading to deterioration of wire bondability. As the content of the boron compound in the electroless Pd plating solution increases, the inhibitory effect on solid-dissolution is improved, but the stability of the electroless Pd plating solution may be deteriorated. The content of the boron compound in the electroless Pd plating solution (a single-compound amount when one compound is contained, and the total amount when two or more compounds are contained) is preferably 0.01 g/L or more, more preferably 0.1 g/L or more, still more preferably 0.5 g/L or more, even more preferably 1 g/L or more, and preferably 100 g/L or less, more preferably 50 g/L or less, still more preferably 30 g/L or less, even more preferably 20 g/L or less.
  • Complexing agent
  • The complexing agent has mainly a stabilizing action on the solubility of Pd in the electroless Pd plating solution. The complexing agent may be any of various known complexing agents, and is preferably at least one selected from the group consisting of ammonia and an amine compound, more preferably an amine compound. As the amine compound, methylamine, dimethylamine, trimethylamine, benzylamine, methylenediamine, ethylenediamine, ethylenediamine derivative, tetramethylenediamine, diethylenetriamine, ethylenediaminetetraacetic acid (EDTA), alkali metal salts thereof, EDTA derivatives and glycine. The complexing agents can be used alone, or in combination of two or more thereof. The content of the complexing agent in the electroless Pd plating solution (a single-compound amount when one compound is contained, and the total amount when two or more compounds are contained) may be approximately adjusted so as to obtain the above-described action, and is preferably 0.5 g/L or more, more preferably 1 g/L or more, still more preferably 3 g/L or more, even more preferably 5 g/L or more, and preferably 50 g/L or less, more preferably 30 g/L or less.
  • Since the electroless Pd plating solution of the present invention exhibits the above-described effects as long as it has the above-described component composition, the electroless Pd plating solution may have only the component composition. If necessary, the electroless Pd plating solution may contain various additives such as a pH adjuster and a stabilizer may be added.
  • pH adjuster
  • When the pH of the electroless Pd plating solution of the present invention is excessively low, the deposition rate of Pd easily decreases, and when the pH is excessively high, the stability of the electroless Pd plating solution may be deteriorated. The pH is preferably 4 to 10, more preferably 6 to 8. The pH of the electroless Pd plating solution can be adjusted by adding a known pH adjuster. Examples of the pH adjuster include acids such as hydrochloric acid, sulfuric acid, nitric acid, citric acid, malonic acid, malic acid, tartaric acid and phosphoric acid, and alkalis such as sodium hydroxide, potassium hydroxide and ammonia water. These pH adjusters can be used alone, or in combination of two or more thereof.
  • Stabilizer
  • The stabilizer is optionally added for the purpose of, for example, securing plating stability, improving the appearance after plating, and adjusting the plating film formation rate. The electroless Pd plating solution of the present invention may further contain a known sulfur-containing compound. The sulfur-containing compound is preferably one or more selected from, for example, a thioether compound, a thiocyan compound, a thiocarbonyl compound, a thiol compound, thiosulfuric acid and a thiosulfate. Specific examples thereof include thioether compounds such as methionine, dimethylsulfoxide, thiodiglycolic acid and benzothiazole; thiocyan compounds such as thiocyanic acid, potassium thiocyanate, sodium thiocyanate and ammonium thiocyanate; thiocarbonyl compounds such as thiourea and derivatives thereof; thiol compounds such as cysteine, thiolactic acid, thioglycolic acid, mercaptoethanol and butanethiol; and thiosulfates such as sodium thiosulfate. These sulfur-containing compounds can be used alone, or in combination of two or more thereof. The content of the stabilizer in the electroless Pd plating solution (a single-compound amount when one compound is contained, and the total amount when two or more compounds are contained) may be approximately adjusted so as to obtain an effect such as plating stability, and is preferably 0.1 mg/L or more, more preferably 0.5 mg/L or more, and preferably 500 mg/L or less, more preferably 100 mg/L or less.
  • The electroless Pd plating solution of the present invention does not contain a surfactant. When a surfactant is added to the electroless Pd plating solution of the present invention, the surfactant is adsorbed to a surface of the resulting Pd plating film, so that formability of the Au plating film is deteriorated. As a result, wire bondability is deteriorated. The surfactant is any of various known nonionic, cationic, anionic and amphoteric surfactants.
  • The present invention includes a Pd plating film which is obtained using the electroless Pd plating solution, and contains P and B. Since the inhibitory effect on solid-dissolution of Pd is obtained as long as the Pd plating film contains both P and B, the content of each of P and B is not limited, and when the content of P or B contained in the Pd plating film increases, the inhibitory effect on solid-dissolution of Pd is further improved. The content of P in the Pd plating film is preferably 0.1% by mass or more, more preferably 0.3% by mass or more, and preferably 10% by mass or less, more preferably 5% by mass or less. The content of B in the Pd plating film is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and preferably 15% by mass or less, more preferably 10% by mass or less. By appropriately controlling the ratio of P to B, the inhibitory effect on solid-dissolution of Pd is further improved. The mass ratio (P : B) of the content of P and B in the electroless Pd plating film is preferably 10 : 1 to 1 : 10, and more preferably 5 : 1 to 1 : 5. The Pd plating film of the present invention may contain P and B, and further contain components derived from the above-described various additives. The balance consists of Pd and unavoidable impurities.
  • The electroless Pd plating solution of the present invention is also suitable for a Pd/Au layered plating film with an Au plating film stacked on a Pd plating film, which is preferably used for plating for bonding of electronic components, etc. Therefore, a layered plating film having the Pd plating film of the present invention and the Au plating film is also a preferred embodiment. The Pd plating film of the present invention can be confirmed to have an inhibitory effect on solid-dissolution of Pd in a Pd/Au layered plating film in which at least a Au plating film is stacked. Therefore, the base that forms the Pd plating film is not limited, and examples thereof include various known base materials such as Al, Al-based alloys, Cu and Cu-based alloys, and plating films in which a base material is covered with a metal catalytic for reduction and deposition of the Pd plating film, such as Fe, Co, Ni, Cu, Zn, Ag, Au, Pt and alloys thereof. Even a noncatalytic metal can be used as an object to be plated in various methods.
  • In another preferred embodiment, the electroless Pd plating solution of the present invention can be applied to the ENEPIG process. In the ENEPIG process, an electroless Ni/Pd/Au plating film including the Pd plating film of the present invention can be obtained by forming a Ni plating film, then a Pd plating film, and then a Au plating film on, for example, Al, anAl-based alloy, Cu or a Cu-based alloy that forms an electrode. For the formation of each plating film, a common method may be employed. Hereinafter, a method for producing an electroless Ni/Pd/Au plating film having the Pd plating film of the present invention on the basis of the ENEPIG process will be described, but the conditions for formation of the Pd plating film of the present invention are not limited thereto, and can be appropriately changed on the basis of a known technique.
  • The plating conditions and plating apparatus at the time of performing electroless Ni plating using an electroless Ni plating solution are not particularly limited, and any of various known methods can be appropriately selected. For example, an object to be plated may be brought into contact with the electroless Ni plating solution at a temperature of 50 to 95°C for about 15 to 60 minutes. The thickness of the Ni plating film may be appropriately set according to the required properties, and is typically about 3 to 7 µm. Any of various known compositions such as Ni-P alloys and Ni-B alloys can be used for the electroless Ni plating solution.
  • The plating conditions and plating apparatus at the time of performing electroless Pd plating using the electroless Pd plating solution of the present invention are not particularly limited, and any of various known methods can be appropriately selected. For example, an object to be plated, on which a Ni plating film is formed, may be brought into contact with the electroless Pd plating solution at a temperature of 50 to 95°C for about 15 to 60 minutes. The thickness of the Pd plating film may be appropriately set according to the required properties, and is typically about 0.001 to 0.5 µm.
  • The plating conditions and plating apparatus at the time of performing electroless gold plating using an electroless gold plating solution are not particularly limited, and any of various known methods can be appropriately selected. For example, an object to be plated, on which a Pd plating film is formed, may be brought into contact with the electroless gold plating solution at a temperature of 40 to 90°C for about 3 to 20 minutes. The thickness of the gold plating film may be appropriately set according to the required properties, and is typically about 0.01 to 2 µm.
  • When the Pd plating film of the present invention is used, palladium can be inhibited from being diffused to and solid-dissolved in the Au plating film from the Pd plating film due to a thermal history in a mounting process after formation of the film, such as reflow treatment, and therefore excellent wire bondability can be achieved even after the thermal history. The temperature in the thermal history is a temperature at which the mounting process is carried out, and the temperature is not particularly limited. When the Pd plating film of the present invention is used, excellent wire bondability can be achieved even after a thermal history at a high temperature of, for example, 50°C or higher, more preferably 100°C or higher.
  • Electronic equipment components
  • The present invention also includes an electronic equipment component having the plating film. Examples of the electronic equipment component include components that form electronic equipment, such as chip components, crystal oscillators, bumps, connectors, lead frames, hoop materials, semiconductor packages and printed circuit boards. In particular, the plating film is suitably used for a technique for forming UBM (Under Barrier Metal) for solder bonding and wire bonding (W/B) to an A1 electrode or a Cu electrode on a wafer. By stacking an Au plating film on a Pd plating film obtained using the electroless Pd plating solution of the present invention, excellent wire bondability can be achieved even after a thermal history.
  • This application claims the benefit of the priority date of Japanese patent application No. 2017-195651 filed on October 6, 2017 . All of the contents of the Japanese patent application No. 2017-195651 filed on October 6, 2017 are incorporated by reference herein.
  • EXAMPLES
  • Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is in no way limited to the following examples, and of course, changes can be appropriately made as long as the above-described and later-described purposes are met. All of these changes are encompassed in the technical scope of the present invention.
  • A BGA substrate (Ball Grid Array: Uyemura & Co., Ltd., 5 cm x 5 cm) was sequentially subjected to the pretreatment and plating treatment shown in Table 1, thereby producing test pieces 1 to 20 in which a Ni plating film, a Pd plating film and a Au plating film are formed in this order from the substrate side. The wire bondability of each of the obtained test pieces was examined.
  • Wire bondability
  • Wire bonding was performed using a test apparatus (SemiAutomatic Wire Bonder HB16 manufactured by TPT K.K.), and wire bondability was evaluated at each of 20 points under the following measurement conditions using Bond Tester SERIES 4000 manufactured by Dage Ltd. The measurement was performed before and after the heat treatment (in which the test piece was held at 175°C for 16 hours). In evaluation of wire bondability, a test piece having an average wire bonding strength of 9.0 g or more after heat treatment was rated "Excellent", a test piece having an average wire bonding strength of 8.5 g or more and less than 9.0 g after heat treatment was rated "Good", a test piece having an average wire bonding strength of 7.5 g or more and less than 8.5 g after heat treatment was rated "Acceptable", and a test piece having an average wire bonding strength of less than 7.5 g after heat treatment was rated "Poor".
  • [Measurement conditions]
  • Capillary: B1014-51-18-12 (manufactured by PECO Ltd.)
    Wire: 1mil-Au wire (SPM Ltd.)
    Stage temperature: 150°C
    Ultrasonic wave (mW): 250 (1st), 250 (2nd)
    Bonding time (ms): 200 (1st), 50 (2nd)
    Tensile force (gf):25 (1st), 50 (2nd)
    Step (1st to 2nd length): 0.7mm
    Measurement method: Wire pull test
    Equipment: Universal Bond Tester #4000 (manufactured by Nordson Advanced Technology K.K.)
    Test speed: 170µm/sec [Table 1]
    Steps Name of chemicals Treatment temperature Treatment time (min.) Target film thickness
    Pretreatment Cleaner ACL-
    Figure imgb0001
    50°C 5 -
    Soft etching SP
    Figure imgb0002
    25°C 1 -
    Pickling 10% H2SO4 room temperature 1 -
    Predip 3% H2SO4 room temperature 1 -
    activator MNK-
    Figure imgb0003
    30°C 2 -
    plating treatment electroless Ni plating NPR-
    Figure imgb0004
    80°C 30 6um
    electroless Pd plating see Table 2 0.1um
    electroless Au plating TWX-
    Figure imgb0005
    80°C 13 0.1um
    Figure imgb0006
    1 available from C. Uyemura & Co., Ltd.
    Figure imgb0007
    Figure imgb0008
  • As shown in Table 2, test pieces Nos. 1 to 9 obtained using the electroless Pd plating solution containing a complexing agent, a hypophosphorous acid compound and/or a phosphorous acid compound, and an amine borane compound and/or a hydroboron compound as defined in the present invention were each rated "Good" or "Excellent" in evaluation of wire bondability after heat treatment.
  • On the other hand, test pieces Nos. 10 to 18 obtained using a Pd plating solution that did not satisfy the requirements of the present invention were each rated "Poor" in evaluation of wire bondability after heat treatment. Test pieces Nos. 19 and 20 were each rated "Poor" in evaluation of wire bondability after heat treatment because they contained a surfactant.

Claims (6)

  1. An electroless Pd plating solution comprising:
    a Palladium compound;
    at least one selected from a group consisting of a hypophosphorous acid compound and a phosphorous acid compound;
    at least one selected from the group consisting of an amine borane compound and a hydroboron compound; and
    a complexing agent.
  2. The electroless Pd plating solution according to claim 1 wherein,
    the amine borane compound is at least one selected from a group consisting of dimethylamine borane and trimethylamine borane; and
    the hydroboron compound is borohydride salt
  3. The electroless Pd plating solution according to claim 1 or 2 wherein,
    the complexing agent is at least one selected from a group consisting of ammonia and an amine compound.
  4. An electroless Pd plating film including phosphorus and boron.
  5. A laminated film comprising:
    the electroless Pd plating film according to claim 4;
    a gold plating film formed on a surface of the electroless Pd plating film.
  6. An electronic equipment component comprising:
    the electroless Pd plating film according to claim 4; or
    the laminated film according to claim 5.
EP18864662.4A 2017-10-06 2018-10-03 Electroless palladium plating solution, and electroless palladium plated coating Pending EP3693495A4 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017195651A JP7149061B2 (en) 2017-10-06 2017-10-06 Electroless palladium plating solution
PCT/JP2018/036970 WO2019069964A1 (en) 2017-10-06 2018-10-03 Electroless palladium plating solution, and electroless palladium plated coating

Publications (2)

Publication Number Publication Date
EP3693495A1 true EP3693495A1 (en) 2020-08-12
EP3693495A4 EP3693495A4 (en) 2021-09-29

Family

ID=65994683

Family Applications (1)

Application Number Title Priority Date Filing Date
EP18864662.4A Pending EP3693495A4 (en) 2017-10-06 2018-10-03 Electroless palladium plating solution, and electroless palladium plated coating

Country Status (7)

Country Link
US (1) US20200248312A1 (en)
EP (1) EP3693495A4 (en)
JP (1) JP7149061B2 (en)
KR (1) KR20200062265A (en)
CN (1) CN111164236A (en)
TW (1) TWI829653B (en)
WO (1) WO2019069964A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6572376B1 (en) * 2018-11-30 2019-09-11 上村工業株式会社 Electroless plating bath
CN117966140B (en) * 2024-01-31 2024-07-05 珠海斯美特电子材料有限公司 Chemical palladium plating solution and application thereof

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3418143A (en) * 1967-08-15 1968-12-24 Burroughs Corp Bath for the electroless deposition of palladium
WO1987005338A1 (en) * 1986-03-04 1987-09-11 Ishihara Chemical Co., Ltd. Palladium-base electroless plating solution
JP3204035B2 (en) * 1995-03-30 2001-09-04 上村工業株式会社 Electroless palladium plating solution and plating method
JP2000256866A (en) * 1999-03-10 2000-09-19 Hideo Honma Electroless nickel plating bath
JP2007009305A (en) * 2005-07-04 2007-01-18 Japan Pure Chemical Co Ltd Electroless palladium plating liquid, and three layer-plated film terminal formed using the same
US7704307B2 (en) 2005-07-20 2010-04-27 Nippon Mining & Metals Co., Ltd. Electroless palladium plating liquid
JP4974332B2 (en) * 2005-09-07 2012-07-11 一般財団法人電力中央研究所 Nanostructure and manufacturing method thereof
JP4511623B1 (en) * 2009-05-08 2010-07-28 小島化学薬品株式会社 Electroless palladium plating solution
JP5843249B2 (en) * 2010-04-19 2016-01-13 奥野製薬工業株式会社 Activation liquid for pretreatment of electroless palladium plating or electroless palladium alloy plating
EP2581470B1 (en) * 2011-10-12 2016-09-28 ATOTECH Deutschland GmbH Electroless palladium plating bath composition
TWI479048B (en) * 2011-10-24 2015-04-01 Kojima Chemicals Co Ltd Eletoroless palladium plating solution
US20140072706A1 (en) * 2012-09-11 2014-03-13 Ernest Long Direct Electroless Palladium Plating on Copper
CN106480437B (en) * 2015-08-31 2019-01-11 比亚迪股份有限公司 A kind of ionic palladium reducing solution, preparation method and a kind of method of Chemical Plating of Non metal Material
TWI707061B (en) * 2015-11-27 2020-10-11 德商德國艾托特克公司 Plating bath composition and method for electroless plating of palladium
JP6635304B2 (en) 2016-04-18 2020-01-22 株式会社オートネットワーク技術研究所 Relay device and in-vehicle system

Also Published As

Publication number Publication date
JP7149061B2 (en) 2022-10-06
TWI829653B (en) 2024-01-21
JP2019070172A (en) 2019-05-09
TW201925531A (en) 2019-07-01
EP3693495A4 (en) 2021-09-29
KR20200062265A (en) 2020-06-03
CN111164236A (en) 2020-05-15
WO2019069964A1 (en) 2019-04-11
US20200248312A1 (en) 2020-08-06

Similar Documents

Publication Publication Date Title
US7704307B2 (en) Electroless palladium plating liquid
US8124174B2 (en) Electroless gold plating method and electronic parts
US11946144B2 (en) Electroless palladium plating solution
KR101393477B1 (en) Electroless gold plating bath, electroless gold plating method and electronic parts
JP3892730B2 (en) Electroless gold plating solution
KR101444687B1 (en) Electroless gold plating liquid
CN106399983B (en) Cyanide-free electroless gold plating bath and electroless gold plating method
KR101393478B1 (en) Electroless gold plating bath, electroless gold plating method and electronic parts
EP3693495A1 (en) Electroless palladium plating solution, and electroless palladium plated coating
JP2007009305A (en) Electroless palladium plating liquid, and three layer-plated film terminal formed using the same
US8771409B2 (en) Electroless gold plating solution and electroless gold plating method
JP5371465B2 (en) Non-cyan electroless gold plating solution and conductor pattern plating method
JP2010196121A (en) Electroless palladium plating bath and electroless palladium plating method
TW202208683A (en) Electroless Palladium Plating Bath
JP2023527982A (en) Gold plating bath and gold plating final finish
JP2009149958A (en) Pattern plating film and method for forming pattern plating film
JP2001003179A (en) Electroless palladium-molybdenum alloy plating solution and plating method
JP2010031312A (en) Pattern plating film, and forming method thereof

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20200416

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
RIC1 Information provided on ipc code assigned before grant

Ipc: C23C 18/16 20060101ALI20210526BHEP

Ipc: C23C 18/44 20060101AFI20210526BHEP

A4 Supplementary search report drawn up and despatched

Effective date: 20210901

RIC1 Information provided on ipc code assigned before grant

Ipc: C23C 18/16 20060101ALI20210826BHEP

Ipc: C23C 18/44 20060101AFI20210826BHEP

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20230403