MICRO-ETCH SOLUTION FOR PRODUCING METAL SURFACE TOPOGRAPHY

Abstract

Metal surfaces, particularly copper surfaces, which are oxidatively micro-etched to increase surface area through the use of molybdenum. The micro-etch solutions contain a proton source, e.g., a mineral acid, an oxidizer agent, e.g., hydrogen peroxide, an azole compound, and a molybdenum source.

Description

[0001] The present invention is directed to printed circuit boards, particularly multi-layer printed circuit boards. Specifically, the invention is directed to micro-etching of metal, particularly copper, printed circuitry by an oxidative process so as to improve adhesion of the metal circuitry to the dielectric layers of multi-layer circuit boards. Because the major portion of printed circuitry is copper circuitry, the invention will be discussed herein in primarily in relationship to copper printed circuitry. However, the invention is generally applicable to metal surfaces which can be oxidatively micro-etched to provide increased surface area; which correlates to increased surface roughness thus, discussions with respect to copper surfaces are to be understood to pertain to other metal surfaces which may be oxidatively micro-etched for surface area enhancement.

BACKGROUND OF THE INVENTION

[0002] Successful fabrication of multi-layer printed circuit boards requires bonding together of copper and resin layers. However, direct bonding of copper and resin layers does not provide sufficient bonding strength. Therefore, it is common to improve copper-resin bonding strength by providing surface roughness to the copper surface, whereby mechanical bonding between the copper and resin is enhanced.

[0003] One common method of providing surface roughness is by depositing on the copper surface an oxide layer, such as cuprous oxide, cupric oxide, or the like. Formation of the oxide layer, which turns the pink copper surface a black-brown color, creates minute unevenness on the copper surface which provide an interlocking effect between the copper surface and resin, thus improving bonding strength.

[0004] However, copper oxides are readily degraded and dissolved upon contact with acid. Because various acid treatments are used in later stages of fabrication of multilayer circuit boards, oxide layer deposition has been problematic at best. In particular, through-holes are drilled through multilayer circuit boards, and the through-holes plated with copper to interconnect the circuitry of the several layers. As part of the copper-plating process, the through-holes are exposed to acids, such as sulfuric acid. Acid attack on the oxide layer in the region surrounding the through-holes is commonly referred to in the industry as “pink ring”, because as acid strips the black-brown oxide layer from the surface, a ring of bare pink copper becomes evident. The problem of copper oxide vulnerability to acid has been approached in a number of patents, e.g. U.S. Pat. Nos. 4,642,161 and 4,717,439.

[0005] An alternative to building up a copper oxide coating on the copper surface is to micro-etch the copper surface to roughen the same; and it is to this method of surface roughening that the present invention is directed. Most commonly, this etching solution is an aqueous solution of a mineral acid, such as sulfuric acid, and an oxidizer agent, such as hydrogen peroxide. Such a solution is described in U.S. Pat. No. 4,751,106, the teachings of which are incorporated herein by reference. The micro-etching process roughens the copper, probably by oxidation of the metallic copper; the resulting topography on the metal surface provides better adhesion to resin. The micro-etched surface appears pink/tan to dark brown, probably the result of the topography of the surface and some residual copper oxide that is formed in the etching process. Micro-etched copper circuitry, when exposed to acid-based copper plating of through holes, is likewise subject to formation of “pink ring” through acid attack of the copper circuitry traces around the through-holes. The formation of “pink ring” is detrimental at least to appearance and is a potential indication of a failure in multi-layer printed circuit boards.

[0006] It is a primary object of the present invention to provide enhanced surface topography of micro-etched metal surfaces, particularly deeper surface etching, so as to increase bond strength between the metal surfaces and polymeric materials used in processes of producing multilayer printed circuit boards. It is further an optional object of the present invention to provide acid-resistance to micro-etched copper circuitry so as to prevent or minimize acid attack problems such as “pink ring”. In this regard, it is to be understood that there are a wide variety of possible processing steps in forming printed circuitry, and the invention, though described relative to a few common processing procedures, is generally applicable to providing increased surface topography roughness and optionally acid-resistance.

SUMMARY OF THE INVENTION

[0007] In accordance with one aspect of the invention there is provided an oxidative aqueous etching solution for micro-etching metal surfaces so as to increase the surface area of the metal surface and optionally providing acid resistance to the micro-etched metal surface. The solution contains a proton source; an oxidizer agent; an azole compound; and a source of molybdenum ions. This solution is used to micro-etch a metal, e.g., copper surface. Very substantial improvements in surface topography, i.e., differential surface etching (peak to valley height difference), is achieved through inclusion of the molybdenum ion source in conjunction with the azole compound than with a standard peroxide sulfuric acid micro-etch technology. Additionally, optional inclusion of a thiazole and/or thiocarbamide compounds provides unusually high resistance to acid attack as evidenced by significantly longer times that it takes for an HCl solution to change the color of a micro-etched board from brown to pink. This improved acid resistance translates to elimination or minimization of “pink ring” in the formation of multi-layer printed circuit boards and elimination or minimization of other acid attack related problems in printed circuit board formation.

[0008] As an alternative to providing a thiazole and/or thiaocarbamide in the micro-etch solution, the micro-etched metal surface may be post-treated with an aqueous solution of a thiazole compound, a thiocarbamide compound or a mixture thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

[0009] FIG. 1 is a 5000× photo of a copper surface micro-etched with a comparative example solution containing no molybdenum ion.

[0010] FIG. 2 is a 5000× photo of a copper surface micro-etched with a solution in accordance with the present invention containing molybdenum ion.

DETATILED DESCRIPTION OF CERTAIN PREFERRED EMBODIMENTS

[0011] As stated above, although the discussion of this invention is primarily in respect to copper and copper alloys, the invention applies to any metal surface which may be oxidatively micro-etched, including, but not limited to, copper, nickel, cadmium, zinc, iron, aluminum, and alloys thereof. For purposes of this invention, an “alloy” of a metal is a mixture of metals containing at least 50 wt % of the designated metal. Herein, when the singular is used for a component, the plural is meant in the alternative; thus molybdenum compound is intended to encompass either a single molybdenum ion or a mixture of molybdenum salts or other sources of molybdenum. Herein, the term “aqueous solution” is intended to mean a solution in which the primary solvent is water; however, the term is intended to encompass solutions containing up to about 10 wt % water-miscible co-solvents.

[0012] The micro-etching process in accordance with the present invention is to be distinguished from processes in which portions of a copper layer are etched completely through such as to form circuitry traces of a printed circuit board. In micro-etching, no portion of copper, e.g., copper circuitry traces, are etched completely away; rather, the surface is etched or oxidized only to a limited extent so as to leave intact the original pattern of the copper being etched. Typically, the surface of the copper is etched by an oxidative process only to a depth of between about 20 and about 500 micro-inches as measured from the original surface to the depths of the micro-etching. This is accomplished by limiting the extent of etching according to the parameters, e.g., concentrations, temperature, etc. of the etching solution.

[0013] Most commonly the proton source is a mineral acid, typically sulfuric acid, although other mineral acids such as nitric acid, phosphoric acid, etc. may be used as well. Also, strong organic acids, such as methanoic may be used as the proton source. Acids are typically used at between about 0.5 and about 7.5 moles per liter. Preferably, the sufficient acid is used such that the pH of the solution is about 4 or below.

[0014] Oxidizer agents include, but are not limited to peroxides, particularly hydrogen peroxide, persulfate compounds, ferric compounds, cupric compounds and nitric acid. The oxidizer agent is typically used at between about 0.2 wt % and about 5 wt % of the solution. Hydrogen peroxide, if used as the oxidizer agent is typically used at about 0.1 and about 3.5 moles per liter. The oxidizer agent in conjunction with the proton donor are the primary agents for providing the micro-etching. Depending upon the degree of micro-etching required, etching times may vary from about 0.1 to about 10.0 minutes at temperatures between about 15 and about 70° C.

[0015] Enhanced differential etching, and thereby better copper to resin adhesion is achieved by the inclusion of the azole compound at levels of between about 0.2 wt % and about 2 wt %. The preferred azole compound is benzotriazole. Suitable classes of azole compounds include triazoles (including benzotriazoles), imidazoles, and tetrazoles. Particular suitable suitable azole compounds include tolyltriazole, carbxoxytriazole, and imidazole. The preferred azole compound is benzotriazole. Additional suitable azole compounds are described, for example, in U.S. Pat. No. 3,770,530, the teachings of which are incorporated herein by reference.

[0016] The micro-etching solution includes a molybdenum source which provides molybdenum ions at a level of between about 2 and about 20,000 parts per million by weight (ppm) based on the weight of the molybdenum ion. Preferably the molybdenum ion is present at 20 to 1000 ppm, most preferably 60-200 ppm. By “molybdenum ion” is meant herein any molybdenum-containing ion soluble in the aqueous solution. Though applicants are not bound by theory, it is believed that any soluble molybdenum-containing ion in the presence of the oxidizer solution will be converted from whatever valence state it might be originally added to the solution to the +6 valence state. Preferred molybdenum sources are molybdate (MoO4−2) salts, e.g., sodium molybdate, and phosphomolybdic acid (MoO3.H3PO4). Other suitable molybdenum ion sources include, but are not limited to molybdic acid, molybdic anhydride and salts of phosphomolybdic acid. Molybdenum might be added to the solution as zero valence metal, provided the proton source and oxidizer are sufficiently strong to dissolve and ionize the metallic molybdenum.

[0017] Addition of the thiazole compound and/or thiocarbamide to the solution provides the micro-etched surface resistance to subsequent acid exposure. From the standpoint of minimizing processing steps, the thiazole and/or thiocarbamide compound is included in the micro-etching solution. If used, the total level of the thiazole compound and/or the thiocarbamide compound in the micro-etching is at least about 0.05 wt %, preferably at least about 0.3 wt %, up to saturation levels. While applicants are not bound by theory, it is believed that the thiazole and/or thiocarbamide compound bonds to the copper surface, e.g., by chelation, and thereby renders the copper (and any copper oxide) inaccessible to subsequent acid attack.

[0018] Thiocarbamide (thiourea) is the preferred thiocarbamide compound, although substituted thiocarbamide compounds, such as described in U.S. Pat. No. 4,715,894, the teachings of which are incorporated by reference, may also be utilized in accordance with the invention.

[0019] Along with thiazole, substituted thiazoles may also be used in accordance with the present invention. Suitable substituted thiazoles include, but are not limited to 2-amino thiazole and 2-mercaptobenzothiazole. Of these, 2-aminothiazole has given the best acid-resistance to date.

[0020] The aqueous solution may optionally contain between about 0.2 and about 10 wt % of a metal-chelating agent, such as ethylenediaminetetraacetate.

[0021] The aqueous solution may optionally contain a surfactant at a level of between about 0.05 and about 1.0% by weight. Suitable surfactants include, but are not limited to polyalkoxylated amnines, sulfated and sulfonated armides, sulfated and sulfonated amines, glycerides and polyalkoxylated esters, betaines, and alcohols.

[0022] The aqueous solution may optionally contain between about 0.1 and about 10 wt % of a water-miscible organic solvent.

[0023] The aqueous solution may optionally include a source of halide ion, the source of halide ion providing the halide ion at between about 2 and about 50 ppm based on the weight of the halide ion. The preferred halide ion, if used, is chloride. The halide ion source may be a salt, such as sodium chloride, an acid, such as hydrogen chloride, or any other compatible chemical which provides such halide source. Other components may also provide the halide ion. For example, ionic surfactants, may provide chlorine ions.

[0024] The aqueous solution may also contain between about 250 ppm and about 50,000 ppm of an organic polymer. Suitable organic polymers include ethylene oxide, ethylene oxide-propylene oxide copolymers, polyethylene glycols, polyproplylene oxide copolymers, polyethylene glycols, polyproplyene glycols, polyvinyl alcohols, and mixtures thereof.

[0025] The aqueous solutions in accordance with the invention contain at least 40 wt % water.

[0026] As an alternative to including the thiazole compound and/or thiocarbamide compound in the micro-etching solution, an oxidatively micro-etched surface may be post-treated with an aqueous solution of a thiazole compound and/or thiocarbamide compound. Again, the total level of the thiazole compound and/or thiazole carbamide compound is at least about 0.2 wt %, preferably at least about 1 wt %, up to saturation levels.

[0027] The micro-etch solutions of the present invention are suitable for both immersion processes in which the circuit board is immersed in the solution and the conveyorized spray systems which afford substantial processing efficiencies.

[0028] The invention will now be described in greater detail by way of specific examples.

Comparative Example 1: and Example 2 in Accordance With the Invention

[0029] Comparative Example 1 was formulated as follows:

[0030] 5% v/v sulfuric acid, 98% w/w

[0031] 3% v/v hydrogen peroxide, 50% w/w

[0032] 2.5 g/L benzotriazole

[0033] Example 2, in accordance with the invention was formulated as follows:

[0034] 5% v/v sulfuric acid, 98% w/w

[0035] 3% v/v hydrogen peroxide, 50% w/w

[0036] 5 g/L benzotriazole

[0037] 200 ppm Na2MoO4.2H2O (79 ppm Mo ion)

[0038] Copper foil samples were chemically pre-cleaned. Then the samples were micro-etched in each of the Comparative Example 1 solution and the Example 2 solution for 2 min. at ambient temperature. Photomicrographs were taken and are provided herewith as FIG. 1 (Comparative Example 1) and FIG. 2 (Example 2). As can be seen, the mico-etching of FIG. 2. is substantially deeper than that of FIG. 1.

[0039] Each of the boards of FIG. 1 and FIG. 2 were laminated to pre-preg epoxy material. The peel strength of the material laminated to the FIG. 2 micro-etched board was several times that of the peel strength of material laminated to the FIG. 1 micro-etched board.

Claims

1. An aqueous solution for increasing surface area on a metal surface, the solution comprising for the following:

a proton source;

an oxidizer agent;

a source of molybdenum ions; and

an azole compound.

2. The aqueous solution according to

claim 1 further comprising a metal-chelating agent.

3. The aqueous solution according to

claim 2 wherein said chelating agent comprises between about 0.2% and about 10.0% by weight of said aqueous solution.

4. The aqueous solution according to

claim 1 having a pH of about 4 or below.

5. The aqueous solution according to

claim 1 containing between about 0.2 to about 5.0 wt % of said oxidizer agent.

6. The aqueous solution according to

claim 1, wherein said oxidizer agent is selected from the group comprising of a peroxide compound, a persulfate compound, a ferric compound, a cupric compound, nitric acid, and mixtures thereof.

7. The aqueous solution according to

claim 1, wherein said oxidizer agent is hydrogen peroxide.

8. The aqueous solution according to

claim 1, wherein said proton source is an organic or an inorganic acid.

9. The aqueous solution according to

claim 1, wherein said proton source is selected from the group consisting of sulfuric acid, nitric acid, phosphoric acid, hydrofluoric acid, methanoic acid, phenylsulfonic acid and mixtures thereof.

10. The aqueous solution according to

claim 1 further comprising a compound selected form the group consisting of thiazole, thiocarbamide, and mixtures thereof in an amount to provide acid-resistance to the micro-etched circuitry.

11. The aqueous solution according to

claim 10, wherein said thiazole compound is selected from the group consisting of 2-aminothiazole, 2-mercaptobenothiazole and mixtures thereof.

12. The aqueous solution according to

claim 10, wherein said thiocarbamide compound is thiocarbamide (thiourea).

13. The aqueous solution according to

claim 1 wherein said thiazole compound and/or said thiocarbamide compound is present at a level of at least about 0.2 wt % of said aqueous solution up to saturation level.

14. The aqueous solution according to

claim 1 wherein said molybdenum ion source provides molybdenum ion at between about 2 and about 20,000 ppm.

15. The aqueous solution according to

claim 1 wherein said molybdenum ion source provides molybdenum ion at between about 20 and about 1000 ppm.

16. The aqueous solution according to

claim 1 wherein said molybdenum ion source provides molybdenum ion at between about 60 and about 200 ppm.

17. The aqueous solution according to

claim 1 wherein said molybdenum ion source is selected from the group consisting of molybdic acid, a salt or anhydride of molybdic acid phosphomolybdic acid and salts thereof, and mixtures thereof.

18. The aqueous solution according to

claim 1 wherein said azole compound is present in an amount of between about 0.2 and about 2.0% by weight of said aqueous solution.

19. The aqueous solution according to

claim 1 wherein said azole compound is selected from the group consisting of the classes of triazoles, tetrazoles, imidazoles, and mixtures thereof

20. the aqueous solution according to

claim 1 wherein said azole compound is benzotriazole.

21. The aqueous solution according to

claim 1 further comprising a surfactant.

22. The aqueous solution according to

claim 21, wherein said surfactant at between about 0.05 and about 1.0% by weight.

23. The aqueous solution according to

claim 1 further containing between about 0.1 and about 10 wt % of a water-miscible organic solvent.

24. The aqueous solution according to

claim 1 wherein a water soluble polymer is incorporated.

25. A composition according to

claim 24 wherein the water soluble polymer is selected form the group consisting of polymers of ethylene oxide, ethylene oxide-propylene oxide copolymers, polyethylene glycols, polyproplylene oxide copolymers, polyethylene glycols, polypropylene glycols, polyvinyl alcohols, and mixtures thereof.

26. The composition according to

claim 1 further containing between about 2 and about 50 ppm of a halogen ion.

27. The composition according to

claim 26 wherein said halogen ion is chlorine.

28. A process for creating increased surface area on a metal surface, said process comprising: Exposing the aqueous solution to a metal surface for a time sufficient to increase the surface area of said metal surface, said aqueous solution comprising:

a proton source;

an oxidizer agent;

a source of molybdenum ions; and

an azole compound.