1. Field of the Invention
Embodiments of the invention generally relate to deposition of a metal layer onto a substrate. Particularly, the invention relates to methods and systems for electrochemical deposition of a metal layer on a substrate.
2. Description of the Related Art
Submicron, multi-level metallization is one of the key technologies for very large scale integration (VLSI) and ultra large scale integration (ULSI) semiconductor devices. The multilevel interconnects that lie at the heart of this technology require the filling of contacts, vias, lines, and other features formed in high aspect ratio apertures. Reliable formation of these features is very important to the success of both VLSI and ULSI as well as to the continued effort to increase circuit density and quality on individual substrates and die.
As circuit densities increase, the widths of contacts, vias, lines and other features, as well as dielectric materials between them, may be decreased. Since the thickness of the dielectric materials remains invariable, the result is that the aspect ratios (i.e., their height divided by width) for most semiconductor features have to substantially increase. Many conventional deposition processes do not consistently fill semiconductor structures in which the aspect ratios exceed 6:1, and particularly when the aspect ratios exceed 10:1. As such, there is a great amount of ongoing effort being directed to the formation of void-free, nanometer-sized structures having aspect ratios of 6:1 or higher.
Electro-chemical deposition (ECD), such as Electro-chemical plating (ECP), originally used in other industries, has been applied in the semiconductor industry as a deposition technique for filling small features because of its ability to grow the deposited material, such as copper, on a conductive surface and fill even high aspect ratio features substantially free of voids. Typically, a metallic diffusion barrier layer is deposited over the surface of a feature, followed by the deposition of a conductive metal seed layer. Then, a conductive metal is electro-chemically plated over the conductive metal seed layer to fill the structure/feature. Finally, the surface of the feature is planarized, such as by chemical mechanical polishing (CMP), to define a conductive interconnect feature.
Copper has become the desired metal for semiconductor device fabrication, because of its lower resistivities and significantly higher electromigration resistance as compared to aluminum and good thermal conductivity. Copper electro-chemical plating systems have been developed for semiconductor fabrication of advanced interconnect structures. Typically, copper ECP uses a plating bath/electrolyte including positively charged copper ions in contact with a negatively charged substrate, as a source of electrons, to plate out the copper on the charged substrate.
All ECP electrolytes have both inorganic and organic compounds at low concentrations. Typical inorganics include copper sulfate (CuSO4), sulfuric acid (H2SO4), and trace amounts of chloride (Cl−) ions. Typical organics include accelerators, suppressors, and levelers. An accelerator is sometimes called a brightener or anti-suppressor. A suppressor may be a surfactant or wetting agent, and is sometimes called a carrier. A leveler is also called a grain refiner or an over-plate inhibitor.
Most ECP processes generally require two processes, wherein a seed layer is first formed over the surface of features on the substrate (this process may be performed in a separate system), and then the surfaces of the features are exposed to an electrolyte solution while an electrical bias is simultaneously applied between the substrate surface (serving as a cathode) and an anode positioned within the electrolyte solution.
Conventional plating practices include depositing a copper seed layer by physical vapor deposition (PVD), chemical vapor deposition (CVD), or atomic layer deposition (ALD) onto a diffusion barrier layer (e.g., tantalum or tantalum nitride). However, as the feature sizes become smaller, it becomes difficult to have adequate seed step coverage with PVD techniques, as discontinuous islands of copper agglomerates are often obtained in the feature side walls close to the feature bottom. When using a CVD or ALD deposition process in place of PVD to deposit a continuous sidewall layer throughout the depth of the high aspect ratio features, a thick copper layer is formed over the field. The thick copper layer on the field can cause the throat of the feature to close before the feature sidewalls are completely covered. When the deposition thickness on the field is reduced to prevent throat closure, ALD and CVD techniques are also prone to generate discontinuities in the seed layer. These discontinuities in the seed layer have been shown to cause plating defects in the layers plated over the seed layer. In addition, copper tends to oxidize readily in the atmosphere and copper oxide readily dissolves in the plating solution. To prevent complete dissolution of copper in the features, the copper seed layer is usually made relatively thick (as high as 800 Å), which can inhibit the plating process from filling the features. Therefore, it is desirable to have a copper plating process that allows direct electroplating of copper on suitable barrier layer(s) without a copper seed layer.
Another challenge with direct copper plating on a suitable barrier metal layer is that the resistance of the barrier metal layer is high (low resistivity) and is known to cause high edge-plating, i.e. thicker copper plating at the edge of the substrate and no copper plating in the middle of the substrate. Also, copper tends to plate on local sites of nucleation, resulting in clusters of copper nuclei, copper clusters/crystal, so deposition is not uniform on the whole surface of the substrate.
Therefore, there is a need for a copper plating process that can plate a thin copper seed layer directly on suitable barrier metals to uniformly deposit copper across the whole substrate surface and fill features before plating of a bulk copper layer.
Embodiments of the invention provide an electrochemical deposition method for plating a thin copper seed layer directly on a barrier layer and an apparatus adapted for the method.
Embodiments of the invention provide a method of plating a metal layer onto a substrate in a plating apparatus having two or more segments of an anode and an auxiliary electrode. The method includes plating a first portion of the metal layer on the surface of the substrate under a first processing condition to at least cover a large portion of the substrate, the first processing condition comprising electrically connecting a first power supply to a central segment of the anode and the substrate.
Embodiments of the invention further provide a method of plating a metal layer onto a substrate in a plating cell having a first and a second electrode. The method includes connecting a first power supply to a central segment of the first electrode and the substrate, connecting a second power supply to the second electrode and the substrate, and plating a first portion of the metal layer on the surface of the substrate at reverse polarity of the first and the second electrodes.
Embodiments of the invention may further provide a method of plating a metal layer onto a substrate in a plating cell having two or more segments of an anode and an second electrode. The method includes applying a first current pulse to the substrate to deposit a first portion of the metal layer on the surface of the substrate, the first current pulse is provided by a first power supply and a second power supply which are in electrical communication in reverse polarity with one segment of the anode and the second electrode, respectively. The method further includes applying a second current pulse to the substrate to deposit a second portion of the metal layer on the surface of the substrate, the second current pulse comprising currents provided to all segments of the anode.
Embodiments of the invention may further provide a method of plating a metal layer onto a substrate in a plating cell including plating a metal coating on the contact points of the plating cell before the substrate is placed inside the plating cell and plating a metal layer onto the surface of the substrate.
Embodiments of the invention may further provide an electrochemical plating cell configured to metallize sub 100 nanometer features on integrated circuit devices. The plating cell includes a fluid basin having an anolyte solution compartment and a catholyte solution compartment, an ionic membrane positioned between the anolyte solution compartment and the catholyte solution compartment, two or more anode segments positioned in the anolyte solution compartment, an auxiliary electrode, two or more power supplies connected to the two or more anode segments and the auxiliary electrodes, and substrate contact elements/points positioned to electrically contact and support a substrate for processing in the fluid basin.
So that the manner in which the above recited features of the present invention can be understood in detail, a more particular description of the invention, briefly summarized above, may be had by reference to embodiments, some of which are illustrated in the appended drawings. It is to be noted, however, that the appended drawings illustrate only typical embodiments of this invention and are therefore not to be considered limiting of its scope, for the invention may admit to other equally effective embodiments.
Embodiments of the invention provide a method and apparatus adapted for electrochemical deposition of a thin metal seed layer and/or a bulk metal layer on a substrate having a conductive barrier metal thereon. The metal material suitable for the bulk metal layer can be any metal materials that can be plated on a substrate surface, such as copper, nickel, etc. For example, the invention provides plating of a copper material on the surface of a barrier material or a copper seed layer during direct or indirect copper plating process to fill submicron features during semiconductor interconnect formation. In one embodiment, the invention may include at least three or more stages/steps (as will be described in detail herein) during electrochemical deposition of a conductive metal material to obtain uniform plating across the entire surface of a substrate. The three or more stages of plating can be performed in the same electrochemical deposition apparatus or in different plating tools. Particularly, the invention allows uniform plating of one or more metal layers on a substrate surface having materials with low resistivity (thus highly resistive) thereon. In addition, the invention is provided to solve high substrate surface resistance problems, to improve contact resistance and current distribution at the edges of a substrate.
The surface of the substrate can be any of the materials that can be used as a suitable seed or conductive material for plating, such as a group VIII metal or noble metal barrier layer. The substrate surface material includes, but is not limited to, copper (Cu), ruthenium (Ru), chromium (Cr), tantalum (Ta), iridium (Ir), osmium (Os), tungsten (W), palladium (Pd), platinum (Pt), and alloys thereof. For example, ruthenium (Ru) is a metal with low resistivity and can be used to coat features on a substrate as a barrier layer for direct copper plating without the need of a copper seed layer deposited by other deposition methods than plating.
In
One embodiment of the invention provides plating of a uniform copper layer on an underlying layer of a conductive material, such as a group VIII metal material, e.g., ruthenium (Ru), rhodium (Rh), palladium (Pd), osmium (Os), iridium (Ir), and platinum (Pt), among others, which are very resistive to start/nucleate plating because of their low electrical resistivity. As an example, a thin ruthenium layer of about 100 Å is about 100 times more resistant than a copper seed layer of about 1000 Å and is passive for copper to plate thereon, independent of the deposition process used to form the underlying layer.
The group VIII metal material may be used as a barrier layer or an under-layer for copper interconnect features, e.g., vias, trenches, and lines, which have aspect ratios hreater than 3:1, because most group VIII metal materials provide low electrical resistivity and high thermal stability, and are resistant to corrosion and oxidation. For example, the resistivity of ruthenium is about ˜7 μΩ-cm and its melting point is about 2300° C. In addition, the thermal and electrical conductivities of ruthenium are twice of those of tantalum (Ta), so ruthenium is a good barrier layer for copper. Ruthenium also does not form an alloy with copper at temperature below 900° C. and shows good adhesion to copper. Thus, group VIII metal or noble metal materials can also be deposited on a conventional barrier layer, such as Ta (tantalum) and/or TaN (tantalum nitride), to serve as a glue layer between the conventional barrier layer and copper. In addition, the low resistivity of ruthenium (Ru) can be an advantage when trying to fill ruthenium coated features during copper interconnect without the need for a copper PVD or CVD seed layer. Especially, ruthenium can be a good seedless diffusion barrier material between intermetal dielectrics (IMD) for a less than 45 nm copper interconnect.
Referring to
Thereafter, referring to
An electrochemical plating solution for ECP copper plating generally includes a copper source, an acid source, a chlorine ion source, and at least one plating solution additive, i.e., levelers, suppressors, accelerators, antifoaming agents, etc. For example, the plating solution may contain between about 30 and about 60 g/L of copper, between about 10 and about 50 g/L of an acid, between about 20 and about 100 ppm of chloride ions, between about 5 and about 30 ppm of an additive accelerator, between about 100 and about 1000 ppm of an additive suppressor, and between about 1 and about 6 ml/L of an additive leveler. The plating current may be in the range from about 2 mA/cm2 to about 10 mA/cm2 for filling copper into the submicron trench and/or via structures. Examples of copper plating chemistries and processes can be found in commonly assigned U.S. patent application Ser. No. 10/616,097, titled “Multiple-Step Electrodeposition Process For Direct Copper Plating On Barrier Metals”, filed on Jul. 8, 2003, and U.S. patent application No. 60/510,190, titled “Methods And Chemistry For Providing Initial Conformal Electrochemical Deposition Of Copper In Sub-Micron Features”, filed on Oct. 10, 2003. An example of an electrochemical plating (ECP) system and an exemplary plating cell are described in
Problems with group VIII barrier material, such as ruthenium (Ru), as a highly resistive thin barrier layer for copper plating is that uniform plating cannot occur on the whole surface of the substrate, especially on substrates having small features thereon. In addition, the initial overpotential to start plating must be higher than normal, for example, an additional voltage of about 30 mV or more is required for plating copper on ruthenium than on copper. In addition, there is poor contact of the substrate with substrate contact points located near the edges of the substrate resulting in hazy zone or poor plating in those locations.
Thus, one embodiment of the invention is provided to solve the problem of non-uniformity on the surface of a substrate during plating of a metal material and includes multiple stages of metal plating processes which require the use of at least two electrodes in a plating apparatus. One electrode serves as the main anode, which is aligned with the center of the substrate during plating. Another electrode is an auxiliary electrode which is located near the edge of the substrate and can serve as an additional anode or cathode during plating. The invention also contemplates the use of additional electrodes, electrode segments, or anode segments to aid in generating uniform current density during plating. Further, before plating of a thin metal seed layer on a substrate, the invention contemplates coating or pre-treating the substrate contact points/locations of a plating apparatus with a thin coating of the metal material to be plated to improve uniform metal plating on the substrate and uniform current distribution,
Next at stage 310, a thin metal layer is plated on the surface of the substrate under a first processing condition to at least cover a large portion of the substrate at stage 310. For example, a thin copper seed layer is directly plated on a substrate surface having group VIII metal or noble metal barrier materials thereon in order to generate a relative uniform and conductive surface for subsequent plating steps. The substrate surface may include a ruthenium barrier layer or a copper seed layer deposited by physical vapor deposition (PVD) technique.
The first processing condition may include a short DC current pulse provided by at least two power supplies in reverse direction. One power supply is connected to a main anode and the substrate (serving as a cathode). Another power supply is connected to one or more auxiliary electrodes and the substrate to provide a current going through the one or more auxiliary electrodes in reverse polarity to the current going through the main anode.
The main anode may be one central/inner anode segment, or several anode segments, which cover a large area of an anode assembly in a plating apparatus. In addition, the main anode may be aligned with or located near the center/middle of a substrate to be processed and the one or more auxiliary electrode may be located near the peripheral regions of the substrate such that current going through the center/middle of the substrate may be increased. The main anode connected to a first power supply is used to electrodeposit copper onto the substrate surface, preferably onto the middle of the substrate. The one or more auxiliary electrodes connected to a second power supply working in reverse direction of the first power supply is used to act as current thieves to decrease the electrodeposition near the edges of the substrate. In one embodiment, the short DC current pulse is applied under the first processing condition to increase deposition toward the center/middle region of the substrate. In another embodiment, the short DC current pulse is applied under the first processing condition to decrease deposition toward the periphery of the substrate.
Each current going through the first and the second power supplies is constant during the DC current pulse but may be different in amplitude and direction/polarity. With the use of the main anode, the one or more auxiliary electrodes, and the two or more power supplies, plating can be uniformly occurring on the whole surface of the substrate.
The short DC current density of this pulse passing through the substrate depends on the material of the barrier (or the passivity of the barrier material) used, the electrolyte used for plating, and the geometry of the electrical field near the substrate, and may be from about 40 mA/cm2 to about 50 mA/cm2, for example. Other factors which may affect the DC current density may include the diameter of the central main anode segment, conductivity of the electrolyte, etc. The short DC current density may last for a time period until a required thickness is reached. In one embodiment, a thin copper seed layer of about 30 Å to about 250 Å, such as about 50 Å to about 100 Å is formed uniformly at stage 310.
At stage 320, plating under a second processing condition is performed to at least fill gaps, features, such as the apertures 120, on the substrate surface. In one embodiment, a total thickness of the plated copper after stage 320 is more than about 50 Å, such as from about 50 Å to about 200 Å or more, or about 500 Å to about 1000 Å. The second processing condition may include a DC current pulse for plating to continue by providing one or more power supplies to one or more anodes, anode segments, or all anode segments, which are aligned to cover the surface of the substrate. The intensity for the DC current pulse under the second processing condition depends on the resitivity of the plated metal, the underlying materials on the substrate, and other plating parameter, and is not limiting. In one embodiment, the intensity for the DC current pulse under the second processing condition is less than the intensity of the DC current pulse under the first processing condition. In addition, under the second processing condition, the current intensity for the auxiliary electrode is not limiting. The auxiliary electrode may be idle, serve as an additional cathode, or serve as an additional anode. In one embodiment, current can be applied through the auxiliary electrode with less current than the current going through the substrate
At stage 330, plating is performed under a third processing condition to at least deposit a portion of a bulk metal layer on the substrate surface. In one embodiment, a total thickness of a bulk copper layer at stage 330 may be more than about 500 Å, such as from about 800 Å to about 1200 Å. The third processing condition may include plating at high throughput to continuously deposit copper to a desired total thickness. One or more power supplies are connected to the anode assembly of the plating apparatus (including one or more or all anode segments) and one or more auxiliary electrodes, and plating can be uniformly occurring on the whole surface of the substrate.
Embodiments of the invention further provide a plating apparatus adapted for electrochemical deposition of a metal layer including a thin metal seed layer and/or a bulk metal layer on a substrate. The plating apparatus or plating cell includes one or more electrodes, such as a main anode electrode/anode segment, another one or more anode electrodes, and one or more auxiliary electrodes or counter electrodes. The auxiliary electrode is positioned and configured to be electrically isolated from the anode electrodes. Exemplary plating cells may be found in commonly assigned U.S. patent application Ser. No. 10/627,336, filed Jul. 24, 2003 entitled “Electrochemical Processing Cell”, and commonly assigned U.S. patent application Ser. No. 10/880,103, filed Jun., 28, 2004 entitled “Electrochemical Plating Cell with a Counter Electrode in an Isolated Anolyte Compartment”; both are hereby incorporated by reference in their entirety.
Inside the fluid basin 408, one or more electrodes, anode assembly 422 or anode segments 422a-422c, are configured to be used as the anode for plating. Additionally one embodiment of the invention provides an auxiliary electrode assembly 424 configured to be positioned radially outward of the perimeter of the anode assembly 422 or anode segments 422a-422c. The one or more anode assembly 422, anode segments 422a-422c, and the auxiliary electrode assembly 424 may be made out of electrically conductive members. The conductive member may be manufactured from a consumable material, such as copper, or from an inconsumable material, such as platinum or another noble metal, etc.
An anolyte volume 420 generally contains an anode assembly that includes the one or more anode segments 422a-422c positioned in contact with an anolyte solution flowing therethrough. The one or more anode segments may include a main anode 422a, an anode segment 422b, and an additional anode segment 422c, etc, which will be further discussed in
The fluid basin 408 is configured to confine an inner fluid volume 410 and to receive the substrate 418 for plating in the inner fluid volume 410. Overflown plating solution from the inner fluid volume 410 is drained into the outer collection volume 412 such that the plating solution may be recirculated back to the inner fluid volume 410. Optionally, a fluid diffusion member 414 is positioned across the inner fluid volume 410 at a position below where the substrate 418 being plated is positioned and above the anode assembly 422. The fluid diffusion member 414 operates to resist fluid flow variations across the substrate 418 and in the direction between the anode assembly 422 and the substrate 418. A more thorough description of the fluid diffusion member and other plating cell components and operational characteristics may be found in commonly assigned U.S. Pat. No. 6,261,433 and commonly assigned U.S. Pat. No. 6,585,876, both of which are hereby incorporated by reference in their entireties.
Further, a membrane 416 is positioned across the fluid basin 408 and, if used, at a position below where the diffusion member 414 may be positioned and above the anode segments 422a-422c. The membrane 416 is generally an ionic membrane, and more particularly, a cationic membrane, generally configured to prevent fluid passage therethrough, while allowing ions, such as copper ions, to travel through the membrane 416 toward the substrate 418. As such, the membrane 416 generally operates to separate a catholyte volume 419 of the plating cell 400 from the anolyte volume 420 of the plating cell 400. The catholyte volume 419 is generally referred to as the fluid volume between the membrane 416 and the substrate 418, and the anolyte volume 420 is referred to as the fluid volume below the membrane 416 adjacent the anode segments 422a-422c. A more thorough description of the membrane 416 and the separation of an anolyte solution from a catholyte solution may be found in commonly assigned U.S. patent application Ser. No. 10/627,336, filed Jul. 24, 2003 entitled “Electrochemical Processing Cell”, which is hereby incorporated by reference in its entirety.
A plating solution, such as an anolyte solution, is supplied to the anolyte volume 420 by an anolyte supply conduit 431a and drained from the anolyte volume 420 by an anolyte drain conduit 431b positioned on an opposing side from the anolyte supply conduit 431a. The positioning of the anolyte supply conduit 431a and the anolyte drain conduit 431b generates directional flow of the anolyte solution across the upper surface of the anode segments 422a-422c, as described in commonly assigned U.S. patent application Ser. No. 10/268,284, filed Oct. 9, 2002 entitled “Electrochemical Processing Cell”, which is hereby incorporated by reference in its entirety.
A second anolyte supply conduit 432a is also configured to supply an anolyte solution to a volume 435 surrounding the auxiliary electrode assembly 424, while not fluidly or electrically communicating with the anolyte volume 420 contained in the volume adjacent the anode segments 422a-422c and supplied by the anolyte supply conduit 431a and the anolyte drain conduit 431b. A second anolyte drain conduit 432b is configured to drain fluid from the volume 435 near the auxiliary electrode assembly 424. The volume 435 is fluidly bound by the membrane 416 on the upper side thereof with two seals 436, such as circular o-ring-type seals, adjacent the auxiliary electrode assembly 424.
As shown in
Referring back to
A plating solution, also termed a catholyte, is supplied to the catholyte volume 419 by a fluid conduits 433a, 433b which is in fluid communication with a catholyte solution tank (not shown). The catholyte solution generally includes several constituents, including, for example, water, copper sulfate, halide ions, and one or more of a plurality of plating additives (levelers, suppressors, accelerators, etc.). The catholyte solution supplied by the fluid conduits 433a, 433b overflows the weir 409 and is collected by the collection volume 412.
Although the membrane 416 provides a fluid barrier that prevents the anolyte solution from fluidly transferring therethrough, the membrane 416 allows for ionic transfer, and more particularly, for positive ionic transfer. As such, although the anolyte cannot permeate the membrane 416, ions such as copper and hydrogen ions may transfer through the membrane 416 into vent conduit 440, which contains catholyte. Thus, the combination of the volume 435 above the auxiliary electrode assembly 424 and the catholyte in vent conduit 440 generates an electrical path for current to travel through the auxiliary electrode assembly 424.
At step 820, a first power supply is connected to a central segment of a first electrode, such as an anode positioned in a plating cell and aligned with the central region of the surface of a substrate for plating on the center/middle of the substrate. At step 830, a second power supply is connected to a second electrode positioned and aligned with the peripheral region or edges of the substrate. The second electrode can be, for example, an anode, a cathode, an auxiliary electrode, a counter electrode, etc.
At step 840, plating is performed under a first processing condition and at reverse polarity of the first and second electrodes to deposit a thin metal layer uniformly on the substrate surface. For example, one embodiment of the invention provides a plating cell 400 having a central segment, such as the anode segment 422a, which is in electrical communication with an anodic terminal of a first power supply (not shown) and the cathodic terminal of the same power supply is generally in electrical communication with the contact ring 406, which is configured to electrically contact the substrate 418, serving as the cathode. In another embodiment, the auxiliary electrode assembly 424 is in electrical communication with a cathodic terminal of a second power supply (not shown). However, although only two power supplies are discussed herein, it is understood that more than two independently controlled power supplies may be used without departing from the scope of the invention. For example, additional power supply or the same first power supply can be used to electrically connect to additional electrode segments, such as 422b and 422c, depending on the processing parameter requirements during different stages of electrochemical plating. In addition, the anode segments 422a, 422b, 422c may also be individually powered and are not limited to any particular number, i.e., there may be between 1 and about 10 or more anode segments in a plating cell. With regard to independently powering anode segments, the power density applied on the anode segment may be the same or vary, e.g., the power on the anode segment 422a may be greater than those on the anode segment 422b.
In one embodiment, the current passing through the auxiliary electrode 424 is less than the current passing through the substrate 418 and also less than the current passing through the anode assembly 422, or the anode segments 422a, 422b, or 422c. For example, the total current passing through the second power supply (PS2) is about 10% to about 60% of the total current passing through the substrate 418 (served as the cathode), as shown in
Not wishing to be bound by theory, it is thought that when the central anode segment or the main anode 422a is connected to the first power supply, during the initial plating stage of a very short time span, such as less than 4 seconds, copper deposition starts from the edges of the substrate 418 near the contact pin 403 and extend to the middle of the substrate. The distance between the growing copper front and the middle of the substrate becomes shorter and shorter and the overvoltage in the middle of the substrate increases such that nucleation becomes possible over the whole surface of the substrate. This short time span of initial nucleation generally depends not only on the characteristic or passivity of the barrier metal on the substrate but also on the average current passing through the substrate 418 and the current passing through the auxiliary electrode assembly 424. Higher current passing through the substrate 418 generally results in a larger area on the substrate where nucleation can occur.
However, the presence of a nucleation zone 910 or nucleation area on the substrate 418 is also very sensitive to the characteristic of the material already on the substrate surface. For example, Group VIII metal materials generally are very passive and require a high initial overvoltage to start nucleation for copper to plate on. Also the nucleation zone 910 on a surface of a substrate with Group VIII metal material thereon is very narrow, even at extremely high average current applied on the substrate.
The invention employs the use of an auxiliary electrode as a current thief with an optimal high reverse current passing through in order to widen the initial nucleation zone dramatically and re-distribute the current from the edges to the center/middle of the substrate. However, the current passing through the auxiliary electrode during the initial nucleation stage should be optimal and cannot otherwise make the current near the contact pins 403 become anodic, resulting in copper dissolution near substrate edges or damage of the surface of the contacts and materials on the substrate. In operation, the auxiliary electrode assembly 424 is used in combination with the anode segments 422a-422c, which may be one of the segmented anodes illustrated in
As shown in
Referring back to
At step 870, current is provided to the first electrode and plating is performed under a third processing condition to at least deposit a portion of a bulk metal layer on the substrate surface. Under the third processing condition, the central anode or, alternatively, all anode segments are in electrical communication with an anodic terminal of one or more power supplies. In addition, the current densities applied to the anode segments and the second electrode are not limiting. Alternatively, the second electrode may be idle.
It is noted that embodiments of the invention do not require the stages or steps to be performed in the order as described herein. Also, the respective parameters may be modified to perform the processes in various plating apparatus and for different substrate sizes, such as 200 mm, 300 mm substrates or square substrates, among others.
As an example,
One embodiment of the invention may include a stage 310, step 840, or any steps herein which is also a multi-staged process in order to provide better quality of the thin plated metal seed, such as a copper seed. For example, the short DC current pulse at the stage 310 may include two or more shorter steps to tune the uniformity and quality of the electroplated copper seed formed on the substrate surface.
While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof, and the scope thereof is determined by the claims that follow.
This application claims the benefit of U.S. provisional patent application Ser. No. 60/579,129, entitled “Method Of Barrier Layer Surface Treatment To Enable Direct Copper Plating”, filed on Jun. 10, 2004 and claims benefit of U.S. provisional patent application Ser. No. 60/621,215 (AMAT/9201L), filed on Oct. 21, 2004, entitled “Plating Chemistry And Method Of Single-Step Electroplating Of Copper On A Barrier Metal”. This application is a continuation-in-part of co-pending U.S. patent application Ser. No. 10/880,103 (AMAT/8556), titled “Multiple-Step Electrodeposition Process For Direct Copper Plating On Barrier Metals”, filed on Jun. 28, 2004; co-pending U.S. patent application Ser. No. 10/616,097 (AMAT/8241), titled “Multiple-Step Electrodeposition Process For Direct Copper Plating On Barrier Metals”, filed on Jul. 8, 2003; co-pending U.S. patent application Ser. No. 10/664,277 (AMAT/7735), titled “Insoluble Anode with an Auxiliary Electrode”, filed on Sep. 17, 2003; co-pending U.S. patent application Ser. No. 09/586,736 (AMAT/4256Y1), titled “Programmable Anode Apparatus and Associated Method”, filed on Jun. 5, 2000; and co-pending U.S. patent application Ser. No. 10/962,236, filed on Oct. 8, 2004, which claim benefit of U.S. provisional patent application Ser. No. 60/510,190 (AMAT/8039L), titled “Methods And Chemistry For Providing Initial Conformal Electrochemical Deposition Of Copper In Sub-Micron Features”, filed on Oct. 10, 2003. Each of the aforementioned related patent applications is herein incorporated by reference.
Number | Date | Country | |
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60579129 | Jun 2004 | US | |
60621215 | Oct 2004 | US | |
60510190 | Oct 2003 | US |
Number | Date | Country | |
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Parent | 10880103 | Jun 2004 | US |
Child | 11072473 | Mar 2005 | US |
Parent | 10616097 | Jul 2003 | US |
Child | 11072473 | Mar 2005 | US |
Parent | 10664277 | Sep 2003 | US |
Child | 11072473 | Mar 2005 | US |
Parent | 09586736 | Jun 2000 | US |
Child | 11072473 | Mar 2005 | US |
Parent | 10962236 | Oct 2004 | US |
Child | 11072473 | Mar 2005 | US |