This application claims priority to Taiwanese Application No. 096148408, filed Dec. 18, 2007, the disclosure of which is herein incorporated by reference.
1. Field of the Invention
This invention relates to a method of bonding a copper foil to a ceramic substrate, more particularly to a bonding method including oxidation of a copper foil to form a copper oxide layer that is subsequently bonded to a ceramic substrate through heat treatment.
2. Description of the Related Art
Direct bonding copper (DBC) or direct copper bonding (DCB) is a conventional method of bonding a copper foil to a ceramic substrate. In the conventional method, a copper foil is oxidized such that a surface of the copper foil is oxidized to a copper oxide layer. The copper foil is disposed on a surface of a ceramic substrate such that the copper oxide layer is in contact with the surface of the ceramic substrate. The copper foil and the ceramic substrate are heated together to a temperature that is lower than 1083° C. (the melting point of copper) and higher than 1063° C. (the eutectic temperature of the copper-copper oxide eutectic). Therefore, the copper foil is bonded to the surface of the ceramic substrate.
Conventionally, the surface of the copper foil is oxidized to the copper oxide layer by pre-heating the copper foil before the copper foil and the ceramic substrate are heated together. However, when the copper foil is pre-heated, two copper oxide layers are formed on two opposite surfaces of the copper foil.
Referring to
In order to avoid the aforesaid problem, the prior art suggests a method of bonding two copper foils to two surfaces of a ceramic substrate as illustrated in
Therefore, the object of the present invention is to provide a ceramic-copper foil bonding method that can eliminate the aforesaid drawbacks of the prior art and that employs wet-oxidation to oxidize a copper foil.
According to one aspect of this invention, a ceramic-copper foil bonding method comprises wet-oxidizing a first copper foil such that a first surface of the first copper foil is oxidized to a copper oxide layer, contacting the copper oxide layer with a first surface of a ceramic substrate, and bonding the copper oxide layer of the first copper foil to the first surface of the ceramic substrate by heat treatment.
According to another aspect of this invention, a ceramic-copper foil bonding method comprises: providing first and second copper foils, each of which has a first surface and a second surface opposite to the first surface; wet-oxidizing the first and second copper foils such that the first surface of each of the first and second copper foils is oxidized to a copper oxide layer and the second surface of each of the first and second copper foils is not oxidized; contacting the copper oxide layers of the first and second copper foils with opposite first and second surfaces of a ceramic substrate, respectively; and heating together the first copper foil, the second copper foil, and the ceramic substrate, thereby bonding the same together.
Other features and advantages of the present invention will become apparent in the following detailed description of the preferred embodiments of this invention, with reference to the accompanying drawings, in which:
According to the present invention, a ceramic-copper foil bonding method includes wet-oxidizing a first copper foil such that a first surface of the first copper foil is oxidized to a copper oxide layer, contacting the copper oxide layer with a first surface of a ceramic substrate, and bonding the copper oxide layer of the first copper foil to the first surface of the ceramic substrate by heat treatment.
Preferably, the ceramic-copper foil bonding method further includes providing a protective layer on a second surface of the first copper foil, which is opposite to the first surface of the first copper foil, before wet-oxidizing the first copper foil such that the second surface of the first copper foil is not oxidized during wet-oxidizing the first copper foil. The protective layer may be a tape attached to the second surface of the first copper foil. The tape may be made from a material selected from the group consisting of polyvinyl chloride, polyethylene terephthalate, and polyimide.
In an embodiment, the method further includes roughening the first copper foil before wet-oxidizing the first copper foil. Preferably, the first copper foil is roughened in a roughening solution including hydrogen peroxide, sulfuric acid, and a stabilizer. The stabilizer is one selected from the group consisting of ethylamine and acetamide. The roughening solution includes sulfuric acid in a concentration that ranges from 100 to 250 grams per liter of the roughening solution, hydrogen peroxide in a concentration that ranges from 20 to 40 grams per liter of the roughening solution, and the stabilizer in a concentration that ranges from 0.5 to 15 grams per liter of the roughening solution. The roughening solution is kept at a temperature that ranges from 25° C. to 60° C. The first copper foil is roughened in the roughening solution for 1 to 5 minutes.
The first copper foil is wet-oxidized in an oxidizing solution including an oxidizing agent selected from the group consisting of potassium persulfate, sodium phosphate, and sodium chlorite. The oxidizing solution includes the oxidizing agent in a concentration that ranges from 2 to 60 grams per liter of the oxidizing solution. In an embodiment, the oxidizing solution further includes sodium hydroxide. The oxidizing solution is kept at a temperature that ranges from 25° C. to 80° C. The first copper foil is wet-oxidized in the oxidizing solution for 10 seconds to 10 minutes.
In another embodiment, the method further includes forming an oxygen-isolation layer on a surface of the copper oxide layer of the first copper foil to prevent further oxidation before contacting the copper oxide layer with the first surface of the ceramic substrate. To this end, the copper oxide layer of the first copper foil is disposed in an anti-oxidizing solution including an antioxidant for forming the oxygen-isolation layer. The antioxidant is made from a material selected from the group consisting of benzotriazole, triazole, imidazole, and tetrazole. The anti-oxidizing solution is kept at a temperature that ranges from 25° C. to 60° C. The copper oxide layer of the first copper foil is disposed in the anti-oxidizing solution for 10 seconds to 5 minutes.
In still another embodiment, the method further includes: wet-oxidizing a second copper foil such that a first surface of the second copper foil is oxidized to a copper oxide layer, and a second surface of the second copper foil, which is opposite to the first surface of the second copper foil, is not oxidized; contacting the copper oxide layer of the second copper foil with a second surface of the ceramic substrate, which is opposite to the first surface of the ceramic substrate, before bonding the copper oxide layer of the first copper foil to the first surface of the ceramic substrate; and bonding the copper oxide layer of the second copper foil to the second surface of the ceramic substrate simultaneously with the bonding of the copper oxide layer of the first copper foil to the first surface of the ceramic substrate by heat treatment.
30 g hydrogen peroxide, 150 g sulfuric acid, and 10 g ethylamine were added to 1 L de-ionized water so as to form a roughening solution. Subsequently, the roughening solution was heated to about 50° C.
A first copper foil was cleaned. A tape was attached to one surface of the first copper foil as a protective layer, while another surface of the first copper foil was kept exposed. When the first copper foil was soaked in the roughening solution for approximately 3 minutes, the exposed surface opposite to the tape was corroded and formed into a rough layer. The chemical reaction for roughening the first copper foil is as follows:
Cu+H2O2+H2SO4→CuSO4+2H2O
The first copper foil was removed from the roughening solution and subsequently rinsed with de-ionized water.
40 g sodium chlorite and 30 g sodium hydroxide were added to 1 L de-ionized water so as to form an oxidizing solution. The oxidizing solution was heated to about 77° C. When the first copper foil was soaked in the oxidizing solution for approximately 5 minutes, the rough layer of the first copper foil was oxidized to a copper oxide layer. The chemical reaction for wet-oxidizing the first copper foil is as follows:
2Cu+NaClO2+2H2O→2Cu(OH)2+NaCl
2Cu(OH)2→2CuO+2H2O
The first copper foil having the copper oxide layer was removed from the oxidizing solution, rinsed with de-ionized water, and dried in sequence. When the first copper foil was dry, the tape was detached from the first copper foil. The first copper foil thus had one surface formed with the copper oxide layer, and another surface of the first copper foil to which the tape was attached was not oxidized during wet-oxidizing the first copper foil.
Referring to
If the bonding step is not to be conducted immediately after the wet-oxidizing step, an oxygen-isolation layer may be formed on a surface of the copper oxide layer of the first copper foil. Therefore, the copper oxide layer of the first copper foil can be isolated from oxygen by virtue of the oxygen-isolation layer so as to prevent the first copper foil from further oxidation that may result in thickening of the copper oxide layer and hence in reducing the bonding strength. To form the oxygen-isolation layer, the first copper foil having the copper oxide layer was soaked in a 10 g/L benzotriazole solution. After about 2 minutes, the first copper foil was removed from the benzotriazole solution and formed with the oxygen-isolation layer.
30 g hydrogen peroxide, 150 g sulfuric acid, and 1 g acetamide were added to 1 L de-ionized water so as to form a roughening solution. Subsequently, the roughening solution was heated to about 50° C.
A first copper foil and a second copper foil were cleaned. Each of the first and second copper foils had opposite first and second surfaces. A tape was attached to the second surface of the first copper foil as a protective layer. The first surface of the first copper foil was exposed to the roughening solution. Another tape was attached to the second surface of the second copper foil as a protective layer. The first surface of the second copper foil was exposed to the roughening solution.
The first and second copper foils were soaked in the roughening solution for approximately 5 minutes. Each of the second surfaces of the first and second copper foils was corroded so as to form a rough layer. The chemical reaction for roughening the first and second copper foils is as follows:
Cu+H2O2+H2SO4→CuSO4+2H2O
The first and second copper foils were removed from the roughening solution and subsequently rinsed with de-ionized water.
10 g potassium persulfate and 50 g sodium hydroxide were added to 1 L de-ionized water in order to form an oxidizing solution. The oxidizing solution was heated to about 60° C. The first and second copper foils were soaked in the oxidizing solution for approximately 7 minutes. Each of the rough layers of the first and second copper foils was oxidized to a copper oxide layer. The chemical reaction for wet-oxidizing the first and second copper foils is as follows:
K2S2O8+2NaOH→K2SO4+Na2SO4+H2O+[O]
Cu+2NaOH+[O]→Na2CuO2+H2O
Na2CuO2+H2O→CuO+2NaOH
The first and second copper foils were removed from the oxidizing solution, rinsed with de-ionized water, and dried in sequence. The tapes were respectively detached from the first and second copper foils when the first and second copper foils were dry. The first and second copper foils had the first surfaces thereof oxidized, and the second surfaces thereof were not oxidized.
Referring to
According to the present invention, two copper foils can be bonded to a ceramic substrate through a single heat treatment step, thereby reducing energy necessary for bonding two copper foils to a ceramic substrate compared to the conventional method. The method is simple and can be performed at a relatively low cost.
While the present invention has been described in connection with what are considered the most practical and preferred embodiments, it is understood that this invention is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretation and equivalent arrangements.
Number | Date | Country | Kind |
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096148408 | Dec 2007 | TW | national |