1. Field of the Invention
The present invention relates to a manufacturing method, and more particularly to a manufacturing method for forming circuit structure on a non-conductive carrier.
2. Description of the Related Art
Since people trends to purchase 3C products with convenience and portability, these electronic products are developed toward the tendency of small, light weight and multifunction. The circuit design and manufacturing is also developed with light weight, small size and thin thickness.
Well known manners of manufacturing circuits usually include electroplating and chemical plating. By comparing with electroplating, chemical plating is also called electroless plating or autocatalytic plating and is that metal ions within aqueous solution are chemically reduced under a controlled environment without electroplating over the substrate. The advantages of chemical plating include uniform plating, few pore rate of plating layer, and multi-element alloy. Therefore, in the electronic products requiring higher uniform degree of metal layer thickness, for example, a manner of forming circuits of circuit components, such as a cell phone and a laptop computer, usually adopts chemical plating to manufacture the circuit components.
In a process of manufacturing a moduled interconnect device, a conventional technique is to disperse a metal oxide in a non-conductive carrier and provide a base through injection molding. Subsequently, any surface of the base is irradiated by laser to form a predetermined circuit pattern. While performing laser ablation on the surface of the base, the metal oxide on the surface is simultaneously exposed and activated to release metal nuclei. In the manufacturing process, to uniformly disperse the metal oxide in the non-conductive carrier, the metal oxide with a certain ratio must be provided. However, the metal nuclei released by the metal oxide are merely provided for reduction reaction of metallization of the surface of the predetermined circuit pattern. Cost consumption caused by laser activated metal oxide may not occur, and the possibility of recycling and reutilizing it may not occur as well.
In other conventional techniques, since a portion of catalyst is exposed on the surface of a non-predetermined track, metal may also be plated over the surface of the non-predetermined track during the subsequent metallization, resulting in increasing the defective fraction.
Moreover, in U.S. Pat. No. 7,060,421, titled “method of manufacturing conductor track structure”, because applied laser power must achieve the energy as well as the metal oxide releasing the metal nuclei, the service life of the laser source is reduced. U.S. Pat. Nos. 5,945,213 and 5,076,841 may form micro-wires with three-dimensional masks on a three-dimensional curved surface, resulting in higher costs.
In view of the shortcomings of the prior art, the inventor(s) of the present invention based on years of experience in the related industry to conduct extensive researches and experiments, and finally developed a manufacturing method for forming circuit structure on a non-conductive carrier as a principle objective to achieve efficacies of simplifying a manufacturing process and reducing costs and defective fraction and to have an advantage of flexible implementation.
To achieve the foregoing objective, a manufacturing method for forming circuit structure on a non-conductive carrier is provided and comprises the following steps: providing a non-conductive carrier; dispersing a catalyst on the non-conductive carrier or in the non-conductive carrier; forming a predetermined track structure on the non-conductive carrier and exposing the catalyst on a surface of the predetermined track structure; and metalizing the predetermined track structure to form a conductive track.
A sandblasting, a laser irradiating or a chemical etching is utilized so that the predetermined track structure is formed on the non-conductive carrier to expose the catalyst on the predetermined track structure. The foregoing chemical etching does not only expose the catalyst, but also has some wetting effect to allow a face to be plated to have few hydrophilic features, thereby facilitating the proceeding of the subsequent chemical plating.
In the manufacturing method for forming circuit structure on a non-conductive carrier, a step of disposing an insulation layer on a non-conductive carrier containing the catalyst is further provided to form a composite body. Therefore, while subsequently performing the metallization, disposing the insulation layer can prevent the metal from plating on a surface of a non-predetermined track, thereby reducing the defective fraction.
The step of dispersing the catalyst over the non-conductive carrier is achieved by disposing a thin film containing the catalyst on the surface of the non-conductive carrier. The thin film can be ink, a plastic film, paint or organic polymer. Alternatively, the residual thin film can be selectively removed after forming the conductor track.
The non-conductive carrier can further include a heat conduction material, a heat column or a combination thereof to further increase the heat conduction efficiency. The heat conduction material can include a non-metal heat conduction material or a heat conduction material. The non-metal heat conduction material can be selected from a group consisting of graphite, graphene, diamond, carbon nanotube, carbon nanocapsule, nanobubble, carbon sixty, nanocone, nanohorn, carbon nanopipet, microtree, beryllium oxide, aluminum oxide, boron nitride, aluminum nitride, magnesium oxide, silicon nitride and silicon carbide. The metal heat conduction material can be selected from a group consisting of lead, aluminum, gold, copper, tungsten, magnesium, molybdenum, zinc and silver. A material of the heat column can be selected from a group consisting of lead, aluminum, gold, copper, tungsten, magnesium, molybdenum, zinc, silver, graphite, grapheme, diamond, carbon nanotube, carbon nanocapsule, nanobubble, carbon sixty, nanocone, nanohorn, carbon nanopipet, microtree, beryllium oxide, aluminum oxide, boron nitride, aluminum nitride, magnesium oxide, silicon nitride and silicon carbide.
The manufacturing method for forming circuit structure on a non-conductive carrier according to the invention has one or above two following advantages:
The foregoing and other technical characteristics of the present invention will become apparent with the detailed description of the preferred embodiments and the illustration of the related drawings.
With reference to
In the manufacturing method for forming circuit structure on non-conductive carrier of the invention, the catalyst can comprises metal elements or can be metal oxide, metal hydroxide, metal hydrate or composite metal oxide hydrate having the metal elements.
The metal elements can comprise transition metals or the mixture thereof such as titanium, antimony, silver, palladium, ferric, nickel, copper, vanadium, cobalt, zinc, platinum, iridium, osmium, rhodium, rhenium, ruthenium and tin. The metal oxide can include silver oxide or palladium oxide, etc. The metal hydroxide can include silver hydroxide, copper hydroxide, palladium hydroxide, nickel hydroxide, gold hydroxide, platinum hydroxide, indium hydroxide, rhenium hydroxide or rhodium hydroxide. The metal hydrate can include platinum oxide hydrate, silver oxide hydrate, copper oxide hydrate, palladium oxide hydrate, nickel oxide hydrate, gold oxide hydrate, indium oxide hydrate, rhenium oxide hydrate or rhodium oxide hydrate, etc. The composite metal oxide hydrate can be the following molecular formula:
M1xM2Om.n(H2O)
M1 is palladium or silver, and M2 is silicon, titanium or zirconium. When M1 is palladium, x is 1. When M1 is silver, x is 2. m and n are integers between 1 to 20. The composite metal oxide hydrate can be PdTiO3.n(H2O), Ag2TiO3.n(H2O), PdSiO3.n(H2O), PdZrO3.n(H2O) and the like.
With respect to the predetermined track structure formed on the non-conductive carrier, the forgoing carrier can be achieved by partial or overall sandblasting, laser irradiating or chemical etching to make the catalyst exposed on the predetermined track structure.
The laser manner comprises CO2 laser, Nd: YAG (neodymium-doped yttrium aluminum garnet) laser, Nd: YVO4 laser (neodymium-doped yttrium orthvanadate), EXCIMER laser or fiber laser. The wavelength range of laser is any wavelength between 248 nm and 10600 nm. The wavelength range of laser is determined according to whether the predetermined track structure is formed on the thin film or the non-conductive carrier, and the laser exposure time is regulated according to the laser intensity.
When the catalyst is directly disperse in the non-conductive carrier 21, the predetermined track structure can be directly formed on the non-conductive carrier 21 such that the catalyst 32 can be exposed on the surface of the predetermined track structure to perform metallization, thereby forming the metal layer 33 on the predetermined track structure as shown in
In another embodiment, when the catalyst is dispersed on the non-conductive carrier, the thin film containing the catalyst can be utilized, for example the palladium catalyst. In step S13, the non-conductive carrier is immersed in the electroless plating solution after being processed with laser ablation, sandblasting or chemical etching. The palladium catalyst exposed to the predetermined track structure catalyzes the metal ions within the electroless solution, and the ions are reductased and precipitated on the surface of the predetermined track structure through chemical reduction reaction to further form a metal coating layer, thereby achieving a goal of producing the structural circuit on the non-conductive carrier.
With respect to different non-conductive carriers, the laser intensity of performing laser ablation is also different, and the laser exposure time is changed in accordance with laser power. For example, while taking polymer plastic material (e.g. a thermoplastic or thermosetting plastic material) as a material of a non-conductive carrier and using laser with stronger power, laser exposure time is relatively reduced to prevent the structure of the non-conductive carrier composed of the polymer plastic material from being damaged. While performing laser ablation on the non-conductive carrier composed of the thermoplastic or thermosetting plastic material, the surface of the non-conductive carrier may be decomposed and deteriorated by being overheated. However, decomposed and deteriorated byproducts may influence the effect of the catalyst. Alternatively, the catalyst amount of the catalyst thin film on the non-conductive carrier is reduced due to over-ablation such that other metals to be plated are unable to be plated in the subsequent process or not completely plated, resulting in influencing the quality of the final products.
Therefore, when the non-conductive carrier 21 is composed of the polymer plastic material, the catalyst can also be formed on the non-conductive carrier 21 by the way of the thin film 24. In another word, the thin film 24 containing the catalyst is disposed on the non-conductive carrier 21, such that laser ablation can be performed on the thin film 24 without damaging the non-conductive carrier 21 composed of the polymer plastic material may not be damaged, as shown in
The thermoplastic material can include PE (polythene), PP (polypropylene), PS (polystyrene), PMMA (polymethyl methacrylate). PVC (polyvinylchloride), nylon, PC (polycarbonate), PU (polyurethane), PTFE (polytetrafluoroethylene), PET or PETE (polyethylene terephthalate), ABS (acrylonitrile butadiene styrene) or PC (polycarbonate)/ABS and a combination thereof. The thermosetting plastic material can be epoxy resin, phenol plastic material, aldehydes plastic material, polyimide, melamine-formaldehyde resin or a combination thereof. The non-conductive carrier can also be a liquid crystal polymer (LCP) material.
Moreover, the non-conductive carrier can be made of a ceramic material or add a glassy material in the thin film containing the catalyst on the surface of the ceramic material in order to increase the adhesive strength between the ceramic material and the catalyst after completing the sintering procedure. However, since the glassy material, which has been molten, would fill with pores on the surface of the ceramic material, laser may not easily allow the catalyst to penetrate into the non-conductive carrier made of the ceramic material. When the predetermined track structure is formed on the non-conductive carrier 21, the catalyst can be exposed on the surface of the predetermined track structure, as shown in
With reference to
Compared with the foregoing embodiment, the second embodiment of the invention has an additional insulation layer as shown in
In addition, in
With reference to
The difference between the third embodiment and the first and second embodiment is that the third embodiment utilizes the injection molding to form the composite body composed of the polymer film, the thin film containing the catalyst and the non-conductive carrier. The composite body is directly taken as a base for circuit components. In addition, the thin film can contains patterns containing the predetermined track structures. Ablation is performed according to the patterns to form the predetermined track structures on the thin film or the non-conductive carrier, and make the catalyst exposed.
In the process of forming the composite body composed of the polymer film, the thin film containing the catalyst and the non-conductive carrier by injection molding, the conductor track patterns with different structures can be produced through different injection molding molds. In addition, the disposition positions of the thin film, the polymer film and the non-conductive carrier can also have many types. For example, while performing the injection molding, the polymer film can be disposed between the non-conductive carrier and the thin film. Alternatively, the thin film can be located between the non-conductive carrier and the polymer film. Moreover, according to different kinds of the non-conductive carrier, the degree of laser ablation may also be different. Its principle is the same as that of the foregoing embodiments, and there is no need to repeat herein. What the difference is, in the embodiment, that the polymer film can be disposed between the thin film and the non-conductive carrier. Thus, the predetermined track structures can be formed on the polymer film during the ablation process.
In the foregoing embodiments, the residual thin film can be further removed. With respect to the second embodiment, after forming the conductor track, the residual thin film can be removed in order to be dissolved to extract catalyst therefrom and reuse the catalyst. Thus, raw material cost can be cut down.
With reference to
Moreover, the catalysts depicted in the second embodiment to the fourth embodiment are similar to the first embodiment, and there is no need to depict. In addition, the foregoing catalysts take the thin film as an example instead of a limitation. Alternatively, the catalysts can be directly disposed in the non-conductive carrier. The foregoing catalysts can covered over the surface of inorganic filler. After forming composite particles, the particles are mixed into the thin film to increase specific surface area thereof. Accordingly, the catalyst number that is exposed is increased after performing laser ablation. The usage quantity of the catalysts and cost can be further reduced. The inorganic filler can contain silicic acid, silicic acid derivate, carbonic acid, carbonic acid derivate, phosphoric acid, phosphoric acid derivate, active carbon, porous carbon, carbon nanotube, graphite, zeolite, clay mineral, ceramic powder, chitin or a combination.
In the foregoing embodiments, when the non-conductive carrier is composed of a material (e.g. a polymer plastic material) with low heat conductivity, the manufacturing method of the invention can further comprise disposing a heat conduction material, a heat column or a combination thereof in the non-conductive carrier to increase the heat conduction efficiency. The heat conduction material can comprise a non-metal heat conduction material or a metal heat conduction material. The non-metal heat conduction material can be selected from a group consisting of graphite, graphene, diamond, carbon nanotube, carbon nanocapsule, nanobubble, carbon sixty, nanocone, nanohorn, carbon nanopipet, microtree, beryllium oxide, aluminum oxide, boron nitride, aluminum nitride, magnesium oxide, silicon nitride and silicon carbide. The metal heat conduction material can be selected from a group consisting of lead, aluminum, gold, copper, tungsten, magnesium, molybdenum, zinc and silver. The material of the heat column can be selected from a group consisting of lead, aluminum, gold, copper, tungsten, magnesium, molybdenum, zinc, silver, graphite, grapheme, diamond, carbon nanotube, carbon nanocapsule, nanobubble, carbon sixty, nanocone, nanohorn, carbon nanopipet, microtree, beryllium oxide, aluminum oxide, boron nitride, aluminum nitride, magnesium oxide, silicon nitride and silicon carbide.
With reference to
To sum up, since an insulation film is disposed on the thin film containing the catalyst, and undesirable influence caused by the catalyst exposed on the non-predetermined track structure of the surface of the thin film can be avoid during the subsequent metallization process. In addition, the non-conductive carrier can include the heat conduction material, the heat column or the combination thereof so as to increase the heat conduction efficiency.
The invention improves over the prior art and complies with patent application requirements, and thus is duly filed for patent application. While the invention has been described by device of specific embodiments, numerous modifications and variations could be made thereto by those generally skilled in the art without departing from the scope and spirit of the invention set forth in the claims.
This application claims priority to co-pending provisional application 61/423084, filed Dec. 14, 2010, and also claims priority to co-pending provisional application 61/385,984, filed Sep. 24, 2010.
Number | Date | Country | |
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61385984 | Sep 2010 | US | |
61423084 | Dec 2010 | US |