ELECTROLESS PLATING METHOD

Information

  • Patent Application
  • 20180179633
  • Publication Number
    20180179633
  • Date Filed
    November 21, 2017
    7 years ago
  • Date Published
    June 28, 2018
    6 years ago
Abstract
A method of the present invention for performing an electroless plating on a substrate comprising the steps of: (a) putting the substrate in contact with a composition containing a compound represented by the following general formula (1):
Description
FIELD OF THE INVENTION

The present invention relates to a method of electroless metal plating on a resin substrate, particularly a printed wiring board, and more particularly relates to a method of forming a metal film having high adhesion on the surface of a resin substrate with a pretreatment solution containing a specific compound.


BACKGROUND OF THE INVENTION

Electrical connection between layers of a printed wiring board is generally performed via very small holes known as through holes. As a method of forming a conductive film on the surface of the printed wiring board and in the inner wall surface of these through holes, a method of treating with a pretreatment solution (also referred to as a conditioner) containing a cationic polymer and a surfactant, applying a catalyst containing palladium and the like, and then forming a metal film by an electroless plating method, is generally used. In order to improve the adhesion between a resin substrate and a conductive film, generally prior to conditioner treatment, a resin-swelling process using a treatment solution primarily containing solvent is performed, then a roughening process using a treatment solution primarily containing a permanganate is performed, and then a series of de-smear/roughening processes that remove the manganese by a neutralization process is performed. De-smear/roughening processes form fine unevenness on the resin surface, thereby improving adhesion between the resin substrate and the conductive film by an anchoring effect.


However, with a method that provides adhesion primarily by an anchoring effect, if the degree of roughness of the resin substrate surface is reduced, the adhesion between the substrate and the metal film will be lowered, and obtaining a plating film with high adhesion will be difficult. Accordingly, there has been a demand for a conditioner having high adhesion even on the surface of resin substrate having a low degree of roughening instead of a conventional conditioner, and an electroless plating method using this conditioner.


Japanese Laid-open Patent Publication no. 2006-77289 discloses a pretreatment solution for electroless plating containing a compound having at least two amino groups in one molecule (specifically, a vinylamine (co)polymer or an allylamine (co)polymer). Further, Japanese Laid-open Patent Publication no. 2010-106337 discloses a method of forming a metal film having high adhesion by further adding ammonium hydrogen difluoride to conditioner containing a cationic polymer and a nonionic surfactant.


SUMMARY OF THE INVENTION

Accordingly, it is an object of the present invention to provide a conditioner having adhesion higher than the conventional conditioner using a cationic polymer or the like, and an electroless plating method using the same.


The present inventors have conducted intensive studies and found that the addition of a specific nitrogen compound to the conditioner instead of cationic polymer can produce a conditioner having adhesion higher than the cationic polymer. The present invention has been accomplished based on these findings.


In other words, the present invention pertains to a method for performing electroless plating on a substrate comprising the steps of:

    • (a) putting the substrate in contact with a composition containing a compound represented by the following general formula (1):




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wherein R1 is an alkyl group having 8 to 20 carbon atoms or an aryl group having 5 to 14 carbon atoms, the alkyl group or the aryl group may be substituted with a hydroxyl group, a carboxyl group, a halogen or an alkyl group having 1 to 4 carbon atoms wherein when R1 is an aryl group, the total number of carbon atoms of the aryl group and its substituent is not less than 6, R2, R3, and R4 are each independently a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, the alkyl group of R2, R3, and R4 may be substituted by a hydroxyl group, a carboxyl group, or a halogen, wherein at least one of R2, R3, and R4 may be bonded with R1 to form a ring that may contain one or more hetero atoms and may be substituted with a hydroxyl group, a carboxyl group, a halogen or an alkyl group having 1 to 4 carbon atoms, the total number of carbon atoms of the ring and its substituent is not less than 8, X is a counter anion, and having a molecular weight not greater than 500, or a compound represented by the following general formula (2):




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wherein R5 is an alkyl group having 8 to 20 carbon atoms, the alkyl group may be substituted by a hydroxyl group, a carboxyl group, a halogen or an alkyl group having 1 to 4 carbon atoms, R6 and R7 are each independently a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, Y is a halogen, and having a molecular weight not greater than 500;

    • (b) putting the substrate in contact with a catalyst composition, and
    • (c) putting the substrate in contact with an electroless plating composition.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Example 1.



FIG. 2 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Example 2.



FIG. 3 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Example 3.



FIG. 4 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Example 4.



FIG. 5 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Example 5.



FIG. 6 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 1.



FIG. 7 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 2.



FIG. 8 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 3.



FIG. 9 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 4.



FIG. 10 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 5.



FIG. 11 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 6.



FIG. 12 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 7.



FIG. 13 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 8.



FIG. 14 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 9.



FIG. 15 is a SEM photograph (magnification: 2000 times) showing an inner wall surface of the microvia hole subjected to copper plating in Comparative Example 10.





DETAILED DESCRIPTION OF THE INVENTION

The abbreviations used throughout this specification have the following meanings unless otherwise designated.

    • g=gram; mg=milligram; ° C.=degree Centigrade; min=minute; m=meter; cm=centimeter; L=liter; mL=milliliter; and N=Newton. The range of all values includes the boundary values, and may be combined in any order. In addition, percent (%) means weight % unless otherwise stated in this specification.


In the first aspect of the method of the present invention, a composition containing a compound represented by the following general formula (1):




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and having a molecular weight not greater than 500 is used. In the general formula (1), R1 is an alkyl group having 8 to 20 carbon atoms or an aryl group having 5 to 14 carbon atoms. The alkyl group or the aryl group may be substituted by a hydroxyl group, a carboxyl group, a halogen or an alkyl group having 1 to 4 carbon atoms. If R1 is an aryl group, the total number of carbon atoms of the aryl group and its substituent is not less than 6, preferably 6 to 20. R2, R3, and R4 are each independently a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. The alkyl group may be substituted with a hydroxyl group, a carboxyl group or a halogen.


In general formula (1), at least one of R2, R3, and R4 may be bonded with Ri to form a ring that may contain one or more hetero atoms or may be substituted by a hydroxyl group, a carboxyl group, a halogen or an alkyl group having 1 to 4 carbon atoms. The total number of carbon atoms of the ring and its substituent is not less than 8, preferably 8 to 20. Those remaining of R1, R2, R3, and R4 not forming a ring are the same as defined above, and the alkyl group or the aryl group may be substituted by a hydroxyl group, a carboxyl group or a halogen.


X is a counter anion. The counter anion is not particularly limited. Examples thereof include chloride ion, bromine ion, iodide ion, fluoride ion, hydroxide ion, nitrate ion, and the like.


Specific examples of the compound represented by general formula (1) include the following compounds.




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In the second aspect of the method of the present invention, a composition containing a compound represented by the following general formula (2):




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and having a molecular weight not greater than 500 is used. In general formula (2), R5 is an alkyl group having 8 to 20 carbon atoms. The alkyl group may be substituted by a hydroxyl group, a carboxyl group, a halogen or an alkyl group having 1 to 4 carbon atoms. R6 and R7 are each independently a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. Y is a halogen.


Specific examples of the compound represented by general formula (2) include dodecylamine hydrochloride, 1-(dimethylamino) dodecane, 12-aminododecanoic acid, and the like.


The present inventor has found that the adhesion is characteristically improved by using the above compounds. Although this is not bound by theory, it is believed that compounds having only one long alkyl group and the rest having a hydrogen atom or a short alkyl group have excellent hydrophilic-lipophilic balance, are easily adsorbed on a resin substrate and at the same time, are easily bonded with the catalyst in the subsequent catalyst application step. Thus, it is possible to form a metal film with high adhesion. Further, although the commonly used cationic polymer has a high adhesion to a resin, it is believed to be easily over-adsorbed because of its large molecular weight. Thus, a relatively large amount of cationic polymer remains between the resin surface and the metal film, thereby deteriorating the adhesion.


The molecular weight of the compound, represented by general formula (1) or (2), is not greater than 500, preferably not greater than 400, more preferably not greater than 300.


The content of the compound, represented by general formula (1) or 2, in the conditioner is preferably 0.1 to 10 g/L, more preferably 1 to 8 g/L.


One of the characteristics of the conditioner used in the present invention is that the metal film having high adhesion can be formed even if it does not contain a surfactant. The conditioner containing cationic polymer usually contains a surfactant to increase penetrability of conditioner ingredients into through holes and blind vias, and to impart uniform conditioning action to glass and resin. However, depending on the use condition, the conditioner containing surfactant may produce bubbles on the liquid surface, thereby deteriorating the workability. By using the compound represented by general formula (1) or (2), the conditioner of the present invention exhibits higher adhesion than the conventional conditioner even without containing a surfactant.


The conditioner used in the present invention may contain any component other than the compound represented by general formula (1). For example, it may contain a chelating agent as an optional component. The chelating agent plays a role in extending the life of the conditioner by forming a chelate compound with the metal ion when the metal ion dissolves into the conditioner. Examples of preferred chelating agents include ethanolamine, triethanolamine, ethylenediaminetetraacetic acid (EDTA), ethylenediamine n, n 'disuccinic acid (EDDS), and iminodiacetic acid (IDA). The amount of chelating agent added is preferably 0.1 to 0.2 mol/L relative to the conditioner.


If necessary, the conditioner used in the present invention can also contain additives such as pH-adjusting agents and the like, as additional optional components. The conditioner used in the present invention preferably contains water as a solvent. Any water can be used such as deionized water, tap water, and the like. Further, a solvent such as alcohol may be mixed with water and used.


The resin substrate can be a printed wiring board, and the printed wiring board can have glass cloth/resin. The resin substrate may have small holes known as through holes or small non-through holes known as blind vias. Furthermore, with a high-density printed wiring board represented by high-performance semiconductor package boards, a functional insulative resin material board is used as the resin substrate. With the method of the present invention, plating can be uniformly deposited not only on the surface of the printed wiring board but also on the inner wall surface of holes if holes such as through holes or the like exist in the substrate.


Examples of the resin substrate include substrates made from epoxy resin, cyanate resin, bismaleimide triazine resin, polyamide, ABS, polyphenyl ether, polysulfone, fluorine resin, polycarbonate, polyacetal, polyphenylene oxide, polypropylene, and liquid crystal polymer, and the like.


Any method that brings the conditioner into contact with the resin substrate is used. For example, the treatment can be performed by immersing a substrate in the conditioner after being subjected to so-called de-smearing or roughening process if necessary, or spraying the conditioner on the substrate. At the time of immersion, the substrate may be immersed in the conditioner at a temperature of 30 to 60° C., preferably 40 to 50° C., for 1 to 10 minutes, preferably 2 to 6 minutes.


After bringing the conditioner into contact with the resin substrate, a catalyst application process is performed to bring the resin substrate into contact with the catalyst composition to adsorb the catalyst on the surface of the resin substrate. However, before bringing the resin substrate into contact with the catalyst composition, a step of immersing the resin substrate (also referred to as microetch) in an aqueous solution such as sodium persulfate, ammonium persulfate, sulfuric acid and hydrogen peroxide mixed solution and a step of washing the surface of the resin substrate with an acid such as sulfuric acid can be optionally performed. The conditioner used in the present invention can remain on the surface of the resin substrate and on the inner wall surface of the holes even after performing such steps, and a sufficient amount of catalyst can be adsorbed on the surface of the resin substrate and the inner wall surface of the holes in the subsequent catalyst application step. The microetch step can usually be performed using an aqueous solution at a temperature of 20 to 35° C. for 0.5 to 10 minutes, preferably 1 to 3 minutes, and the acid washing step can usually be performed at a temperature of 20 to 35° C., preferably 25 to 30° C., for 0.5 to 5 minutes, preferably 1 to 3 minutes.


A conventionally known catalyst composition may be used. Examples of the catalyst composition include a palladium-tin colloid solution, or a composition containing metal ions such as palladium, platinum, silver or copper, and the like. For example, CIRCUPOSIT™ ADV 8530 Catalyst and CIRCUPOSIT™ 6530 Catalyst (both manufactured by Rohm and Haas Electronic Materials Co., Ltd.) can be used. In the case of using CIRCUPOSIT™ ADV 8530 catalyst as a catalyst composition, for example, the resin substrate is immersed in the catalyst composition at a temperature of 35 to 60° C., preferably 40 to 50° C., for 1 to 10 minutes, preferably 3 to 5 minutes, and then a deduction treatment of palladium ions can be performed with CIRCUPOSIT™ 6540 reducer.


A conventionally known electroless plating composition may be used. For example, an electroless plating composition containing metals such as copper, nickel, cobalt, iron or the like or a mixture thereof can be used. Electroless copper plating is usually preferred when using a printed wiring board as the resin substrate. For example, CIRCUPOSIT™ 6550 electroless copper, CIRCUPOSIT™ ADV 8550 electroless copper, and CIRCUPOSIT™ 328 copper mix concentrate (all manufactured by Rohm and Haas Electronic Materials Co., Ltd.) can be used.


EXAMPLES

Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples.


In the following Examples and Comparative Examples, plating deposition on the inner wall surface of the through holes was evaluated by SEM observation. Adhesion strength was also evaluated according to the following procedure: The surface of the substrate subjected to the electroless plating was washed with deionized water for 3 minutes at room temperature and heated and dried (120° C., 30 minutes). Then, the surface of the material to be plated was immersed in an acid cleaner (liquid temperature of 35° C., 2 minutes) containing sulfuric acid. Thereafter, acid washing was performed, and electrolytic copper plating treatment was performed with electrolytic copper plating MICRO FILL™ EVF. The surface of the resultant plated material was washed with deionized water at room temperature for 3 minutes, and then heated and dried (180° C., 60 minutes). The resulting copper plating film had a film thickness of 20 to 25 μm, and this plating film was cut in 1-cm widths. The adhesion strength (peel strength) between the substrate resin and the plating film was measured using an INSTRON™ 5564 tester at a tensile speed of 50 mm/minute and at an angle of 90° in accordance with the JIS C5012 printed wiring board test method.


Examples 1 to 5 and Comparative Examples 1 to 10

The following resin substrates 1 to 3 were used as the resin substrate of the material to be treated.


Resin Substrates

Resin substrate 1: Ra: 100 (nm)


Resin substrate 2: Ra: 250 (nm)


Epoxy resin substrate 3: Ra: 80 (nm)


Note: Ra represents an arithmetic average roughness.


Each compound shown in Tables 1 to 3 was added to deionized water in the amounts shown in Tables 1 to 3 to prepare a conditioner. Resin substrates 1 to 3 were subjected to a de-smearing/roughening process using a permanganate salt, and then immersed in the conditioner at a temperature of 45° C. for 5 minutes. Next, soft etching was performed using sodium persulfate. After washing with acid, a catalyst imparting treatment using an alkaline palladium catalyst CIRCUPOSIT™ ADV 8530 Catalyst and a reduction treatment using a CIRCUPOSIT™ 6540 Reducer were performed. Then, electroless copper plating was performed by immersing in an electroless copper plating solution (CIRCUPOSIT™ ADV 8550 electroless copper) at a temperature of 32° C. for 20 minutes. Between each treatment, washing with deionized water was performed at room temperature for 2 minutes. The state of plating deposition in the micro via hole after electroless copper plating was observed by SEM. Next, electrolytic copper plating treatment was performed and then adhesion test was performed. The evaluation results are also shown in Tables 1 to 3.


In Examples 1 to 4, the above-mentioned compounds (3) to (6) were used, respectively, as the compounds (conditioner components) of the conditioner, and in Example 5, dodecylamine hydrochloride was used. Further, in Comparative Example 1, the test was carried out only with deionized water without adding any conditioning components. In Comparative Examples 2 to 4, glycidyltrimethylammonium chloride, 3-chloro-2-hydroxypropyl trimethylammonium chloride, and sodium dodecylbenzenesulfonate were used as conditioning components, respectively. In Comparative Examples 5 to 8, monoethanolamine, triisopropanolamine, triethanolamine, and tetramethylammonium hydroxide were used as conditioning components, respectively. In Comparative Examples 9 and 10, commercial conditioners 231 and 3328 were used, respectively, (both manufactured by Rohm and Haas Company, containing cationic polymer, chelating agent, nonionic surfactant, and water, pH: about 10 and 1).














TABLE 1





Example
1
2
3
4
5




















Compound
Compound (3)
Compound (4)
Compound (5)
Compound (6)
Dodecylamine







hydrochloride


Addition amount (g)
2.0 
2.0 
5.0 
2.0
5.0 


Copper
Good (FIG. 1)
Good (FIG. 2)
Good (FIG. 3)
Good (FIG. 4)
Good (FIG. 5)


deposition state













Peel
Resin 1
0.540
0.533
0.595

0.515


strength




(not performed)


(kN/m)
Resin 2
0.508
0.486
0.408

0.451







(not performed)



Resin 3
0.192
0.193
0.308

0.213







(not performed)












Comprehensive
Good
Good
Good
Good
Good


evaluation
(Good copper
(Good copper
(Good copper

(Good copper



deposition
deposition
deposition

deposition



with high peel
with high peel
with high peel

with high peel



strength)
strength)
strength)

strength)




















TABLE 2





Comparative Example
1
2
3
4



















Compound

Glycidyltrimethylammonium
3-chloro-2-
Sodium




chloride
hydroxypropyl
dodecylbenzenesulfonate





trimethylammonium





chloride


Addition amount (g)

5
5
18


Copper
Almost no
Almost no
Almost no
Almost no


deposition state
deposition (FIG. 6)
deposition (FIG. 7)
deposition (FIG. 8)
deposition (FIG. 9)












Peel
Resin 1
Not performed due
Not performed due
Not performed due
Not performed due


strength

to poor deposition
to poor deposition
to poor deposition
to poor deposition


(kN/m)
Resin 2
Not performed due
Not performed due
Not performed due
Not performed due




to poor deposition
to poor deposition
to poor deposition
to poor deposition



Resin 3
Not performed due
Not performed due
Not performed due
Not performed due




to poor deposition
to poor deposition
to poor deposition
to poor deposition











Comprehensive
Poor
Poor
Poor
Poor


evaluation
(Poor copper plating
(Poor copper plating
(Poor copper plating
(Poor copper plating



deposition)
deposition)
deposition)
deposition)




















TABLE 3





Comparative Example
5
6
7
8



















Compound
Monoethanola-mine
Triisopropanolamine
Triethanolamine
Tetramethylammonium






hydroxide


Addition amount (g)
20   
42
40
24


Copper
Almost no
Almost no
Almost no
Almost no


deposition state
deposition (FIG. 10)
deposition (FIG. 11)
deposition (FIG. 12)
deposition (FIG. 13)












Peel
Resin 1
0.568
Not performed due
Not performed due
Not performed due


strength


to poor deposition
to poor deposition
to poor deposition


(kN/m)
Resin 2
0.413
Not performed due
Not performed due
Not performed due





to poor deposition
to poor deposition
to poor deposition



Resin 3
0.289
Not performed due
Not performed due
Not performed due





to poor deposition
to poor deposition
to poor deposition











Comprehensive
Good peel
Poor copper plating
Poor copper plating
Poor copper plating


evaluation
strength but
deposition
deposition
deposition



poor copper



plating



deposition


















TABLE 4





Comparative Example
9
10

















Commercial
231
3328


conditioner


Copper
Good (FIG. 14)
Good (FIG. 15)


deposition state










Peel
Resin 1
0.463
0.493


strength
Resin 2
0.345
0.366


(kN/m)
Resin 3
0.176
0.125









Comprehensive
Good copper
Good copper


evaluation
deposition but low
deposition but low



adhesion strength
adhesion strength



(peel strength)
(peel strength)








Claims
  • 1. A method for performing an electroless plating on a substrate comprising the steps of: (a) putting the substrate in contact with a composition containing a compound represented by the following general formula (1):
  • 2. The method according to claim 1, wherein the content of the compound, represented by general formula (1) or (2), in the composition is from 0.1 to 10 g/L.
  • 3. The method according to claim 1, wherein the electroless plating is electroless copper plating.
  • 4. A substrate having a metal film on at least a part of its surface obtained by the method according to claim 1.
Priority Claims (1)
Number Date Country Kind
2016-250043 Dec 2016 JP national