JP2010100895A - Pretreatment liquid for reduction type electroless gold plating and electroless gold plating method - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method of stably performing electroless gold plating to an independent fine wiring pad part, and to provide a pretreatment liquid for reduction type electroless gold plating used therefor. <P>SOLUTION: The pretreatment liquid for reduction type electroless gold plating is obtained by blending one or more kinds of components selected from a phenyl compound, an ascorbic acid compound, a hydrazine compound and a thiourea compound into an aqueous solution comprising at least one kind of component selected from the group consisting of sulfurous acid and the salt thereof and at least one kind of component selected from the group consisting of thiosulfuric acid and the salt thereof independently or in combination. <P>COPYRIGHT: (C)2010,JPO&amp;INPIT

Description

  The present invention relates to a pretreatment liquid for reducing electroless gold plating and an electroless gold plating method.

  Many electronic parts such as printed wiring boards, semiconductor packages, ceramic electronic parts, and semiconductors are plated with gold for the purpose of improving solderability, corrosion resistance of parts, and reliability during wire bonding and flip chip bonding. Is given. Gold plating is roughly divided into electro gold plating and electroless gold plating depending on the method of construction. In recent years, due to demands for miniaturization and high performance of electronic parts, parts that need to be plated with gold have become smaller year by year and have become independent circuits. For this reason, in order to secure a limited wiring space, there is an increasing need for electroless gold plating that does not require lead wiring during gold plating.

  In general, electroless gold plating can be broadly divided into substitutional electroless gold plating (substitution gold plating) and reduction type electroless gold plating (electroless gold plating). Displacement gold plating is the difference in ionization tendency between electroless nickel plating film applied to improve corrosion resistance on copper wiring and suppressing diffusion of base copper and gold plating film and gold ions in replacement gold plating solution. Is a method of depositing gold by a substitution reaction utilizing In this displacement gold plating, gold precipitates with the dissolution of the underlying nickel, so that the portion where the nickel film can be dissolved decreases due to the growth of the gold plating film, and the precipitation reaction gradually decreases. The gold film thickness that can be deposited by displacement gold plating is about 0.05 to 0.1 μm. In solder joint applications, it is generally sufficient that the gold is as thick as a protective film, and substitution gold plating is generally used.

  However, in wire bonding bonding and flip chip bonding, the required gold film thickness is usually 0.3 to 0.7 μm because of connection reliability and bonding stability. It is necessary to perform thick gold plating by electrolytic gold plating.

  Conventional electroless gold plating contains a cyanide compound, such as an electroless gold plating solution described in JP-A-62-99477, and has a high alkaline pH range of 12 or more. The electronic parts that can be used are limited. In addition, the electroless gold plating that was originally developed and has a neutral pH and does not use a cyanide compound has a low liquid stability and cannot cope with mass production.

  Therefore, in order to realize this film thickness by substitution gold plating having high stability, substitution-type thick electroless gold plating that promotes substitution reaction like substitution gold plating solution described in JP-A-9-176864 ( Substitution-thick gold plating) and substitution-reduction-use electroless gold plating (replacement-reduction-use gold plating) in which a reducing agent that reacts with the underlying nickel is added to a substitution-type gold plating solution have been developed.

  However, since this reaction uses substitution reaction for many of them, corrosion of the underlying nickel film is locally accelerated to generate voids, peeling of wire bonding and insufficient strength, poor adhesion of flip chip bonding, Has been found to have defects that cause poor solder joints and poor connection reliability.

  On the other hand, electroless gold plating solutions that can be used in a neutral low temperature region have been improved, and many electroless gold plating solutions that have high stability and can be mass-produced have been developed and commercialized. However, there are many problems with these electroless gold platings. One of them is a phenomenon in which electroless gold plating hardly deposits on an independent fine pad.

As indicated above, many electronic components such as printed wiring boards, semiconductor packages, ceramic electronic components, and semiconductors are becoming increasingly dense and high-performance, and there is a need to apply gold plating to a small part of an independent circuit within the component. Is growing. Due to the nature of electroless gold plating, oxidation of the reducing agent occurs on the gold surface of the displacement-type gold plating film, which is a pretreatment. For this reason, as the plating area becomes smaller, the oxidizing reaction of the reducing agent is less likely to occur, and a phenomenon that the electroless gold plating does not deposit on the minute part of the independent circuit has come to be observed.
JP-A-62-99477 JP-A-9-176864

  An object of the present invention is to provide a method capable of stably performing electroless gold plating on an independent micro wiring pad portion, and a pretreatment solution for reducing electroless gold plating used therefor.

As a result of sincerity studies to achieve the above-mentioned object, the present inventor selected a phenyl compound, an ascorbic acid compound, a hydrazine compound, and a thiourea compound in an aqueous solution in which sulfite and thiosulfate were used alone or mixed. After immersing the object to be plated, which has been subjected to displacement gold plating, in the treatment liquid comprising one or more kinds of the above, by immersing directly in a reducing electroless gold plating liquid without performing a water washing step, The inventors have found that the object can be achieved and have completed the present invention.
That is, this invention is providing the invention which concerns on the following item.
(1) An aqueous solution containing at least one component selected from the group consisting of sulfurous acid and its salt and at least one component selected from the group consisting of thiosulfuric acid and its salt, alone or both, A pretreatment solution for reducing electroless gold plating, comprising one or more components selected from a compound, an ascorbic acid compound, a hydrazine compound, and a thiourea compound.
(2) The pretreatment liquid for reducing electroless gold plating according to the above (1), wherein the pH is 4 to 10.
(3) After immersing the object to be plated that has been subjected to displacement gold plating in the pretreatment liquid for reducing electroless gold plating described in (1) or (2) above, direct reduction without performing a water washing step Electroless gold plating method characterized by immersing in a type electroless gold plating solution.

  By using the pretreatment liquid for reducing electroless gold plating of the present invention, uniform electroless gold plating can be uniformly applied to isolated wire bonding pads and flip chip pads of electronic components. Therefore, by performing treatment with these treatment liquids after substitution gold plating, and performing the treatment with electroless gold plating as it is without performing a water washing step, it is possible to stably secure plating on a minute and independent pad portion, Electronic components such as package substrates and semiconductors can be further reduced in size and performance.

Hereinafter, the present invention will be described in detail.
(Pretreatment solution for reducing electroless gold plating)
The pretreatment liquid for reducing electroless gold plating of the present invention includes at least one component selected from the group consisting of sulfurous acid and its salt, and at least one component selected from the group consisting of thiosulfuric acid and its salt And one or more components (compounds) selected from a phenyl compound, an ascorbic acid compound, a hydrazine compound, and a thiourea compound.

(Sulfurous acid and its salts)
Sulphites are used to prevent oxidation reactions of reducing agents such as phenyl compounds, ascorbic acid compounds, hydrazine compounds, and thiourea compounds. Examples of sulfites that can be used include sodium sulfite, potassium sulfite, ammonium sulfite, sodium hydrogen sulfite, potassium hydrogen sulfite and the like, but are not limited to these components. The addition amount is preferably 10 to 100 g / L, but if it is less than 10 g / L, the effect of suppressing the oxidation of the added reducing agent is insufficient, the reducing agent is oxidized, and there is a risk that it cannot be used for a long time. There is sex. On the other hand, if it exceeds 100 g / L, the solubility becomes low and recrystallization may occur. Therefore, it is more preferably 20 to 60 g / L, and further preferably 30 to 50 g / L.

(Thiosulfuric acid and its salts)
Thiosulfate has the same effect as the above sulfite. Examples of the thiosulfate that can be used include sodium thiosulfate, potassium thiosulfate, and ammonium thiosulfate. However, the thiosulfate is not particularly limited to these components. The addition amount is preferably 10 to 100 g / L, but if it is less than 10 g / L, the effect of suppressing the oxidation of the added reducing agent is insufficient, and the reducing agent is oxidized, so that it cannot be used for a long time. There is sex. On the other hand, if it exceeds 100 g / L, the solubility becomes low and recrystallization may occur. Therefore, it is more preferably 20 to 60 g / L, and further preferably 30 to 50 g / L.

  In addition, when used in combination with sulfites, phenyl compounds, ascorbic acid compounds, hydrazine compounds, thiourea compounds, etc., even when the amount of sulfites and thiosulfates added is reduced due to the synergistic effect of sulfites and thiosulfates. The oxidation reaction of the reducing agent can be prevented. In addition, there is an advantage that the autooxidation reaction of the reducing agent can be prevented even when stored for a long time.

(Phenyl compounds, ascorbic acid compounds, hydrazine compounds, thiourea compounds)
These substances are generally reducing agents used in non-cyanide electroless gold plating solutions. In the electroless gold plating treatment, after the substitution gold plating, the substrate is washed with water, and further immersed in the above-described reduction type electroless gold plating treatment solution, and then enters the electroless gold plating solution as it is without performing the water washing step. For this reason, since the reducing agent is brought into the electroless gold plating solution, it is preferable to use the same components for the reducing agent used in the electroless gold plating and the reducing agent in the pretreatment solution for reducing electroless gold plating. However, it is not particularly limited to this.

  Examples of phenyl compounds that can be used include phenol, o-cresol, p-cresol, o-ethylphenol, p-ethylphenol, t-butylphenol, o-aminophenol, p-aminophenol, hydroquinone, catechol, pyrogallol, methylhydroquinone, Aniline, o-phenylenediamine, p-phenylenediamine, o-toluidine, p-toluidine, o-ethylaniline, p-ethylaniline, sodium hydroquinonesulfonate, potassium hydroquinonesulfonate, gallic acid, pyrogallol-4-carboxylic acid, Pyrogallol-4,6-dicarboxylic acid, pyrogallol monomethyl ether and the like can be used. Among these, hydroquinone, methylhydroquinone, pyrogallol, sodium hydroquinonesulfonate, potassium hydroquinonesulfonate, and the like are more preferable. However, it is not limited to the above components.

  Examples of the ascorbic acid compound that can be used include sodium ascorbate, potassium ascorbate, ammonium ascorbate, sodium isoascorbate, potassium isoascorbate, and ammonium isoascorbate.

  Further, as the hydrazine compound, hydrazine hydrate, hydrazine hydrochloride, hydrazine sulfate, hydrazine monochloride, hydrazine dichloride and the like can be used. Examples of thiourea compounds include N-methylthiourea, 1-acetylthiourea, 1,3-dimethylthiourea, and ethylenethiourea.

  Although these ascorbic acid compounds, hydrazine compounds, and thiourea compounds are listed, they are not necessarily limited to these components. These reducing agent components are preferably in the range of 0.5 to 100 g / L. If the amount of the reducing agent is less than 0.5 g / L, the surface of the displacement gold plating film cannot be sufficiently reduced. On the other hand, if the addition amount exceeds 100 g / L, there is no washing step, so that it is brought into the electroless gold plating solution, changing the reducing agent concentration and possibly reducing the solution stability. Furthermore, the range of 2-50 g / L is more preferable, and 5-20 g / L is especially preferable.

(PH)
The pH of the pretreatment liquid for reducing electroless gold plating of the present invention is preferably used in the range of 4-10. This is because, when the pH is less than 4, sodium sulfite or sodium thiosulfate, which is a stabilizer of the reducing agent component, is oxidized to change into sulfuric acid and the effect is reduced. In addition, when the pH is used above 10, it is weakly alkaline, so that it easily damages the resist of electronic parts.
In addition, there is no particular limitation when adjusting the pH, but when adjusting to acidic, adjust with a dilute solution of inorganic acids such as hydrochloric acid, sulfuric acid and nitric acid, and organic acids such as citric acid, succinic acid and malic acid. Can do. Moreover, when adjusting to alkalinity, sodium hydroxide, potassium hydroxide, ammonia solution, etc. can be used. It is preferable to dilute these solutions to some extent.

(PH buffers)
It is preferable to add a pH buffer to the pretreatment solution for reducing electroless gold plating of the present invention. The pH buffer that can be used is not particularly limited, but organic acids such as citric acid, succinic acid, malic acid and tartaric acid, water-soluble amines such as ethylenediamine, EDTA, polyaminecarboxylic acid, and ammonium chloride, phosphoric acids, Boric acids such as sodium tetraborate can also be used. The working concentration can be used in the range of 10 to 100 g / L. If it is less than 10 g / L, there is a possibility that the pH buffering action is small and the treatment liquid cannot be used stably for a long time. Moreover, when it exceeds 100 g / L, salt concentration will become high and there exists a possibility of recrystallizing in a liquid. It is preferably used at 20 to 50 g / L.

(Plating method)
In the present invention, the fine circuit of the printed wiring board, the through hole pad portion, the land and other electronic component contact portion, the wire bonding terminal of the semiconductor package, the solder ball connection portion and the terminal portion of various electronic components are to be plated. Is preferred.
In addition, the method of using the pretreatment liquid for reducing electroless gold plating of the present invention is as follows. First, the pretreatment liquid for reducing electroless gold plating described in the present invention is applied to the object to be plated on which the replacement gold plating is formed. The object to be plated is brought into contact with. Then, it is immersed in an electroless gold plating solution as it is without performing the water washing step. This is because when the water washing process is performed, the minute pad portion is reoxidized, and the electroless gold plating may not be deposited on the minute portion.

  The pretreatment liquid for reducing electroless gold plating of the present invention can be used in the range of room temperature (25 ° C.) to 90 ° C., but is more preferably used at 25 to 70 ° C. Further, when the temperature is adjusted to the operating temperature of the electroless gold plating solution, the temperature change at the time of plating is minimized, which is more preferable. Although the processing time of the pretreatment liquid for reducing electroless gold plating of the present invention is not particularly limited, it is usually 30 seconds to 10 minutes, preferably 1 to 5 minutes.

(Preparation of experimental samples)
A BGA substrate with a 5 cm × 5 cm × 1.0 mm independent copper wiring pad formed in an area array with a pad diameter of 50 μm and a pitch of 100 μm, and a comparative copper plate (2 cm × 2 cm, thickness 0.7 mm) It was used. After applying electroless nickel plating to this BGA substrate and copper plate with electroless nickel plating (medium phosphorus: 5 to 8%) generally used for processing exclusively for independent circuit boards, washing with water Further, general substitution gold plating for printed circuit boards was applied, and a substitution gold film was applied to electroless nickel by 0.05 μm. Then, after immersing in various pretreatment liquids for reduction type electroless gold plating shown in the following Table 1, it was immersed in the electroless gold plating liquid shown in the following Table 1 without performing a water washing process.

(Evaluation)
The BGA substrate and the copper plate were evaluated by visual observation with a metal microscope, and the film thickness was measured using a fluorescent X-ray film thickness meter. In addition, the 50 μm pad portion was measured at 20 locations, and the effect of the pretreatment liquid was confirmed by comparing the thinnest portion.

(Examples 1-4)
Table 1 shows Examples 1 to 4.
In Example 1, hydroquinone was used as a reducing agent as a phenyl compound.
In Example 2, sodium ascorbate was used as the reducing agent, hydrazine sulfate was used in Example 3, and thiourea was used in Example 4. The pretreatment liquid for reduction-type electroless gold plating was adjusted to 7.5 with hydrochloric acid so that the pH of the electroless gold plating would not change greatly due to the introduction of the liquid. The treatment temperature was also used at 65 ° C., which was almost the same as the electroless gold plating, so that the substrate surface temperature did not vary greatly, and the treatment time was 5 minutes.

  As shown in the evaluation results of Examples 1 to 4 in Table 1, after immersion in the pretreatment liquid for reducing electroless gold plating, the results of various electroless gold plating without performing the water washing step are for comparison. It was found that gold can be deposited with substantially the same film thickness on the copper plate treated in the same manner and the isolated pattern of the pad type 50 μm. Moreover, it was found that the storage stability (room temperature (25 ° C.) and 65 ° C. for 1 week) of the pretreatment liquid for reducing electroless gold plating was good, and the liquid was not decomposed. In addition, the stability of the electroless gold plating solution used is not impaired. Good results.

(Comparative Examples 1-4)
Table 1 shows Comparative Examples 1 to 4. In the comparative example, a pretreatment liquid for reducing electroless gold plating was prepared under the condition that sodium sulfite and sodium thiosulfate were not added as additives for stabilizing the reducing agent contained in the treatment liquid.

  In Comparative Example 1, when hydroquinone, which is a phenyl compound-based reducing agent, was dissolved, the liquid began to turn brown. This solution remained brown even when the temperature was 65 ° C., and a precipitate was formed. Moreover, although the sodium ascorbate of Example 2 was transparent at the beginning of dissolution, the pretreatment liquid changed to a deep yellow when the liquid temperature was 65 ° C. or when stored at room temperature (25 ° C.). I understood. No precipitate was generated for sodium ascorbate.

On the other hand, hydrazine sulfate of Example 3 was uniformly dissolved. Moreover, even if it preserve | saved at normal temperature (25 degreeC) and 65 degreeC, the change was not seen by the liquid.
Although the thiourea of Example 4 was initially dissolved, the liquid became cloudy as time passed. Furthermore, when it preserve | saved at normal temperature (25 degreeC) and temperature was 65 degreeC, the deposit generate | occur | produced. These chemical solutions were used for pretreatment for reduced electroless gold plating, and electroless gold plating shown in Table 1 was performed without performing a water washing step.
As a result, although the hydroquinone of Comparative Example 1, the sodium ascorbate of Comparative Example 2, the hydrazine sulfate of Comparative Example 3 and the thiourea of Comparative Example 4 were normally deposited on the copper plate, the deposition rate was 50 μm in the pad portion. Although it rose a little, compared with a normal copper plate, only about 1/4 was able to obtain a gold film thickness.
Moreover, it turned out that the hydrazine sulfate of the comparative example 3 by which neither precipitation nor turbidity generate | occur | produced in the liquid was difficult to precipitate in a micro pad part. This is presumed that, although no precipitate was produced, hydrolysis of hydrazine sulfate occurred, and the activity effect of the fine pad portion was lowered.

By using the pretreatment liquid for reducing electroless gold plating of the present invention, uniform electroless gold plating can be uniformly applied to isolated wire bonding pads and flip chip pads of electronic components.
Therefore, by performing treatment with these treatment liquids after substitution gold plating, and performing the treatment with electroless gold plating as it is without performing a water washing step, it is possible to stably secure plating on a minute and independent pad portion, Electronic components such as package substrates and semiconductors can be further reduced in size and performance.

Claims (3)

  An aqueous solution containing at least one component selected from the group consisting of sulfurous acid and its salt and at least one component selected from the group consisting of thiosulfuric acid and its salt, alone or both, in a phenyl compound, ascorbine A pretreatment solution for reducing electroless gold plating, comprising one or more components selected from an acid compound, a hydrazine compound, and a thiourea compound.   The pretreatment liquid for reducing electroless gold plating according to claim 1, wherein the pH is 4 to 10.   After the object to be plated with the displacement gold plating is immersed in the pretreatment liquid for reducing electroless gold plating according to claim 1 or 2, the reducing electroless gold plating is directly performed without performing a washing step. An electroless gold plating method characterized by immersing in a liquid.