The present invention relates generally to semiconductor fabrication and more specifically to copper interconnection fabrication.
There are currently no effect ways to recover or rework copper seed layer degraded due to exposure to air after processing in physical vapor deposition (PVD) chambers. The Q-time management of the copper seed layer deposition to the bulk copper plating over the copper seed layer impacts the production rate and product yield significantly.
U.S. Pat. No. 6,287,954 B1 to Ashley et al. describes a copper seed layer and plating process where the seed layer is converted into an intermetallic layer.
U.S. Pat. No. 6,258,710 B1 to Rathore et al. describes a method of providing sub-half-micron copper interconnections with improved electromigration and corrosion resistance.
U.S. Pat. No. 6,184,137 B1 to Ding et al. describes a structure and method for improving low temperature copper reflow in semiconductor features.
U.S. Pat. No. 6,245,676 B1 to Ueno describes a method of electroplating copper interconnects.
Accordingly, it is an object of one or more embodiments of the present invention to provide an improved method of fabricating copper interconnections by removing any copper oxide formed on the copper seed layer.
It is another object of one or more embodiments of the present invention to increase the operation window of plating and the product yield.
Other objects will appear hereinafter.
It has now been discovered that the above and other objects of the present invention may be accomplished in the following manner. Specifically, a substrate is provided and a patterned dielectric layer is formed over the substrate. The patterned dielectric layer having an opening exposing a portion of the substrate. The opening having exposed sidewalls. A copper seed layer is formed over the sidewalls of the opening. The copper seed layer is subjected to an electrochemical technique to eliminate any copper oxide formed over the copper seed layer. A bulk copper layer is electrochemically plated over the copper-oxide-free copper seed layer, filling the opening and forming the oxide-free copper interconnect.
The present invention will be more clearly understood from the following description taken in conjunction with the accompanying drawings in which like reference numerals designate similar or corresponding elements, regions and portions and in which:
Initial Structure
As shown in
Structure 10 is preferably a silicon substrate and is understood to possibly include a semiconductor wafer or substrate, active and passive devices formed within the wafer, conductive layers and dielectric layers (e.g., inter-poly oxide (IPO), intermetal dielectric (IMD), etc.) formed over the wafer surface. The term “semiconductor structure” is meant to include devices formed within a semiconductor wafer and the layers overlying the wafer.
A patterned dielectric layer 14 having opening 15 is formed over semiconductor substrate 10 and conductive structure 12 to a thickness of preferably from about 3000 to 15, 000 Å. Dielectric layer 14 is preferably comprised of a low-k dielectric material such as F-doped SiO2, a low-k CVD low-k inorganic material or a low-k organic material and is more preferably comprised of F-doped SiO2. Dielectric layer 14 exposes a portion 26 of conductive structure 12.
Opening 15 has exposed vertical and horizontal sidewalls, 19 and may include, for example, a lower via opening 22 and an M2 metal opening 24.
As shown in
A copper (Cu) seed layer 18 is then formed over barrier layer 16 to a thickness of preferably from about 20 to 90 Å and more preferably from about 50 to 70 Å. Cu seed layer 18 is preferably formed by physical vapor deposition (PVD), chemical vapor deposition (CVD) or electroless deposition and more preferably PVD.
Formation of Copper Oxide Layer 20 Over Copper Seed Layer 18
As shown in
Electrochemical Technique to Remove Copper Oxide Layer 20
As shown in
The electrochemical technique of the present invention causes the following electrochemical reduction to occur to reduce the copper oxide layer 20 to copper:
2CuO+4e−→2Cu+O2
by one of two methods: (1) a potentiostat method that uses a constant voltage of from about 0.0 to −0.3 volts (V) vs. an Ag/AgCl reference electrode; or (2) a galvanostat method that uses a constant current of from about 0.05 to 5.00 milliamps/cm2 (mA/cm2). The potentiostat method is the more preferred electrochemical technique. Precisely applying a constant voltage relative to a reference electrode can define only the electrochemical reaction of CuO reduction happens during this pretreatment process.
A CuSO4 electrolyte solution with or without additives such as an accelerator(s), a suppressor(s) and a leveler(s) is used with the electrochemical technique.
In a conventional ECP recipe, the first step is an initiation step with a current, I, if about 3.14 A (about 10 mA/cm2). However, when using the galvanostat electrochemical technique method of the present invention, for example, a lower constant current of from about 0.05 to 5.00 mA/cm2 is used first as a pre-ECP cleaning step to reduce any copper oxide 20 to copper as shown above. (Similarly, when using the potentiostat electrochemical technique method of the present invention, for example, a lower constant voltage of from about 0.0 to 0.3 V than in a conventional ECP recipe is used first as a pre-ECP cleaning step to reduce any copper oxide 20 to copper as shown above.)
Then, the normal ECP recipe is continued with a higher voltage or higher current to plate Cu from the electrolyte solution onto the surface of the wafer, i.e. the cleaned Cu seed layer 18, filling the opening 15, i.e.:
Cu2++2e−→Cu
The bulk plated copper layer may then be planarized to form a planarized copper interconnect 30 within TaN barrier layer 16/Cu seed layer 18 lined opening 15 as shown in FIG. 3.
Advantages of the Present Invention
The advantages of one or more embodiments of the present
While particular embodiments of the present invention have been illustrated and described, it is not intended to limit the invention, except as defined by the following claims.
Number | Name | Date | Kind |
---|---|---|---|
6184137 | Ding et al. | Feb 2001 | B1 |
6245676 | Ueno | Jun 2001 | B1 |
6258710 | Rathore et al. | Jul 2001 | B1 |
6287954 | Ashley et al. | Sep 2001 | B1 |
6531046 | Morrissey et al. | Mar 2003 | B2 |
20020074242 | Morrissey et al. | Jun 2002 | A1 |
20020100693 | Lu et al. | Aug 2002 | A1 |
Number | Date | Country |
---|---|---|
1005078 | May 2000 | EP |