TECHNICAL FIELD
[0001] The present invention relates to an electroless palladium plating solution and an
electroless palladium plating film.
BACKGROUND ART
[0002] 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.
[0003] 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.
[0004] 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
SUMMARY OF THE INVENTION
PROBLEMS TO BE SOLVED BY THE INVENTION
[0006] 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.
[0007] 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
[0008] 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.
[0009] Preferable embodiment of the the present inventive electroless Pd plating solution
includes any combination of the following options (i) to (iii).
- (i) the amine borane compound is at least one selected from a group consisting of
dimethylamine borane and trimethylamine borane;
- (ii) the hydroboron compound is borohydride salt;
- (iii) the complexing agent is at least one selected from a group consisting of ammonia
and an amine compound;
[0010] 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.
[0011] The present invention includes an electronic equipment component including the electroless
Pd plating film of the present invention.
ADVANTAGEOUS EFFECTS OF INVENTION
[0012] 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
[0013] 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.
[0014] 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.
[0015] 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.
[0016] 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
[0017] 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.
[0018] 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
[0019] 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
[0020] 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
[0021] 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.
[0022] 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
[0023] 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
[0024] 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.
[0025] 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.
[0026] 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.
[0027] 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.
[0028] 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.
[0029] 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.
[0030] 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.
[0031] 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.
[0032] 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
[0033] 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.
EXAMPLES
[0035] 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.
[0036] 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
[0037] 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]
[0038] 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

[0039] 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.
[0040] 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.